Year |
Citation |
Score |
2023 |
Berns HM, Watkins-Chow DE, Lu S, Louphrasitthiphol P, Zhang T, Brown KM, Moura-Alves P, Goding CR, Pavan WJ. Single-cell profiling of MC1R-inhibited melanocytes. Pigment Cell & Melanoma Research. PMID 37972124 DOI: 10.1111/pcmr.13141 |
0.369 |
|
2023 |
Loftus SK, Gillis MF, Lundh L, Baxter LL, Wedel JC, Watkins-Chow DE, Donovan FX, Sergeev YV, Oetting WS, Pavan WJ, Adams DR. Haplotype-based analysis resolves missing heritability in oculocutaneous albinism type 1B. American Journal of Human Genetics. PMID 37327787 DOI: 10.1016/j.ajhg.2023.05.012 |
0.628 |
|
2023 |
Berns HM, Watkins-Chow DE, Lu S, Louphrasitthiphol P, Zhang T, Brown KM, Moura-Alves P, Goding CR, Pavan WJ. Loss of MC1R signaling implicates TBX3 in pheomelanogenesis and melanoma predisposition. Biorxiv : the Preprint Server For Biology. PMID 37090624 DOI: 10.1101/2023.03.10.532018 |
0.342 |
|
2022 |
Baxter LL, Watkins-Chow DE, Johnson NL, Farhat NY, Platt FM, Dale RK, Porter FD, Pavan WJ, Rodriguez-Gil JL. Correlation of age of onset and clinical severity in Niemann-Pick disease type C1 with lysosomal abnormalities and gene expression. Scientific Reports. 12: 2162. PMID 35140266 DOI: 10.1038/s41598-022-06112-y |
0.662 |
|
2021 |
Davidson CD, Gibson AL, Gu T, Baxter LL, Deverman BE, Beadle K, Incao AA, Rodriguez-Gil JL, Fujiwara H, Jiang X, Chandler RJ, Ory DS, Gradinaru V, Venditti CP, Pavan WJ. Improved systemic AAV gene therapy with a neurotrophic capsid in Niemann-Pick disease type C1 mice. Life Science Alliance. 4. PMID 34407999 DOI: 10.26508/lsa.202101040 |
0.66 |
|
2021 |
Rodriguez-Gil JL, Baxter LL, Watkins-Chow DE, Johnson NL, Davidson CD, Carlson SR, Incao AA, Wallom KL, Farhat NY, Platt FM, Dale RK, Porter FD, Pavan WJ. Transcriptome of HPβCD-treated Niemann-pick disease type C1 cells highlights GPNMB as a biomarker for therapeutics. Human Molecular Genetics. PMID 34296265 DOI: 10.1093/hmg/ddab194 |
0.681 |
|
2021 |
Loftus SK, Lundh L, Watkins-Chow DE, Baxter LL, Pairo-Castineira E, Program NCS, Jackson IJ, Oetting WS, Pavan WJ, Adams DR. A custom capture sequence approach for oculocutaneous albinism identifies structural variant alleles at the OCA2 locus. Human Mutation. PMID 34246199 DOI: 10.1002/humu.24257 |
0.645 |
|
2020 |
Rodriguez-Gil JL, Watkins-Chow DE, Baxter LL, Elliot G, Harper UL, Wincovitch SM, Wedel JC, Incao AA, Huebecker M, Boehm FJ, Garver WS, Porter FD, Broman KW, Platt FM, Pavan WJ. Genetic background modifies phenotypic severity and longevity in a mouse model of Niemann-Pick disease type C1. Disease Models & Mechanisms. PMID 31996359 DOI: 10.1242/Dmm.042614 |
0.671 |
|
2019 |
Rodriguez-Gil JL, Watkins-Chow DE, Baxter LL, Yokoyama T, Zerfas PM, Starost MF, Gahl WA, Malicdan MCV, Porter FD, Platt FM, Pavan WJ. NPC1 Deficiency in Mice is Associated with Fetal Growth Restriction, Neonatal Lethality and Abnormal Lung Pathology. Journal of Clinical Medicine. 9. PMID 31861571 DOI: 10.3390/jcm9010012 |
0.645 |
|
2019 |
Fufa TD, Baxter LL, Wedel JC, Gildea DE, Loftus SK, Pavan WJ. MEK inhibition remodels the active chromatin landscape and induces SOX10 genomic recruitment in BRAF(V600E) mutant melanoma cells. Epigenetics & Chromatin. 12: 50. PMID 31399133 DOI: 10.1186/s13072-019-0297-2 |
0.661 |
|
2019 |
Fufa TD, Baxter LL, Wedel JC, Gildea DE, Loftus SK, Pavan WJ. MEK inhibition remodels the active chromatin landscape and induces SOX10 genomic recruitment in BRAF(V600E) mutant melanoma cells. Epigenetics & Chromatin. 12: 50. PMID 31399133 DOI: 10.1186/s13072-019-0297-2 |
0.661 |
|
2018 |
Baxter LL, Watkins-Chow DE, Pavan WJ, Loftus SK. A curated gene list for expanding the horizons of pigmentation biology. Pigment Cell & Melanoma Research. PMID 30339321 DOI: 10.1111/pcmr.12743 |
0.698 |
|
2018 |
Baxter LL, Watkins-Chow DE, Pavan WJ, Loftus SK. A curated gene list for expanding the horizons of pigmentation biology. Pigment Cell & Melanoma Research. PMID 30339321 DOI: 10.1111/pcmr.12743 |
0.698 |
|
2018 |
Zhang T, Choi J, Kovacs MA, Shi J, Xu M, Goldstein AM, Trower AJ, Bishop DT, Iles MM, Duffy DL, MacGregor S, Amundadottir LT, Law MH, ... ... Pavan WJ, et al. Cell-type-specific eQTL of primary melanocytes facilitates identification of melanoma susceptibility genes. Genome Research. PMID 30333196 DOI: 10.1101/Gr.233304.117 |
0.33 |
|
2018 |
Zhang T, Choi J, Kovacs MA, Shi J, Xu M, Goldstein AM, Trower AJ, Bishop DT, Iles MM, Duffy DL, MacGregor S, Amundadottir LT, Law MH, ... ... Pavan WJ, et al. Cell-type-specific eQTL of primary melanocytes facilitates identification of melanoma susceptibility genes. Genome Research. PMID 30333196 DOI: 10.1101/Gr.233304.117 |
0.33 |
|
2018 |
Cronin JC, Loftus SK, Baxter LL, Swatkoski S, Gucek M, Pavan WJ. Identification and functional analysis of SOX10 phosphorylation sites in melanoma. Plos One. 13: e0190834. PMID 29315345 DOI: 10.1371/journal.pone.0190834 |
0.666 |
|
2018 |
Cronin JC, Loftus SK, Baxter LL, Swatkoski S, Gucek M, Pavan WJ. Identification and functional analysis of SOX10 phosphorylation sites in melanoma. Plos One. 13: e0190834. PMID 29315345 DOI: 10.1371/journal.pone.0190834 |
0.666 |
|
2017 |
Marshall CA, Watkins-Chow DE, Palladino G, Deutsch G, Chandran K, Pavan WJ, Erickson RP. In Niemann-Pick C1 mouse models, glial-only expression of the normal gene extends survival much further than do changes in genetic background or treatment with hydroxypropyl-beta-cyclodextrin. Gene. PMID 29223359 DOI: 10.1016/j.gene.2017.12.006 |
0.314 |
|
2017 |
Marshall CA, Watkins-Chow DE, Palladino G, Deutsch G, Chandran K, Pavan WJ, Erickson RP. In Niemann-Pick C1 mouse models, glial-only expression of the normal gene extends survival much further than do changes in genetic background or treatment with hydroxypropyl-beta-cyclodextrin. Gene. PMID 29223359 DOI: 10.1016/j.gene.2017.12.006 |
0.314 |
|
2017 |
Ruiz R, Jahid S, Harris M, Marzese DM, Espitia F, Vasudeva P, Chen CF, de Feraudy S, Wu J, Gillen DL, Krasieva TB, Tromberg BJ, Pavan WJ, Hoon DS, Ganesan AK. The RhoJ-BAD signaling network: An Achilles' heel for BRAF mutant melanomas. Plos Genetics. 13: e1006913. PMID 28753606 DOI: 10.1371/Journal.Pgen.1006913 |
0.302 |
|
2017 |
Ruiz R, Jahid S, Harris M, Marzese DM, Espitia F, Vasudeva P, Chen CF, de Feraudy S, Wu J, Gillen DL, Krasieva TB, Tromberg BJ, Pavan WJ, Hoon DS, Ganesan AK. The RhoJ-BAD signaling network: An Achilles' heel for BRAF mutant melanomas. Plos Genetics. 13: e1006913. PMID 28753606 DOI: 10.1371/Journal.Pgen.1006913 |
0.302 |
|
2017 |
Marathe HG, Watkins-Chow DE, Weider M, Hoffmann A, Mehta G, Trivedi A, Aras S, Basuroy T, Mehrotra A, Bennett DC, Wegner M, Pavan WJ, de la Serna IL. BRG1 interacts with SOX10 to establish the melanocyte lineage and to promote differentiation. Nucleic Acids Research. PMID 28431046 DOI: 10.1093/nar/gkx259 |
0.392 |
|
2017 |
Marathe HG, Watkins-Chow DE, Weider M, Hoffmann A, Mehta G, Trivedi A, Aras S, Basuroy T, Mehrotra A, Bennett DC, Wegner M, Pavan WJ, de la Serna IL. BRG1 interacts with SOX10 to establish the melanocyte lineage and to promote differentiation. Nucleic Acids Research. PMID 28431046 DOI: 10.1093/nar/gkx259 |
0.392 |
|
2017 |
Seberg HE, Van Otterloo E, Loftus SK, Liu H, Bonde G, Sompallae R, Gildea DE, Santana JF, Manak JR, Pavan WJ, Williams T, Cornell RA. TFAP2 paralogs regulate melanocyte differentiation in parallel with MITF. Plos Genetics. 13: e1006636. PMID 28249010 DOI: 10.1371/Journal.Pgen.1006636 |
0.419 |
|
2017 |
Seberg HE, Van Otterloo E, Loftus SK, Liu H, Bonde G, Sompallae R, Gildea DE, Santana JF, Manak JR, Pavan WJ, Williams T, Cornell RA. TFAP2 paralogs regulate melanocyte differentiation in parallel with MITF. Plos Genetics. 13: e1006636. PMID 28249010 DOI: 10.1371/Journal.Pgen.1006636 |
0.419 |
|
2017 |
Loftus SK, Baxter LL, Cronin JC, Fufa TD, Pavan WJ. Hypoxia-induced HIF1α targets in melanocytes reveal a molecular profile associated with poor melanoma prognosis. Pigment Cell & Melanoma Research. PMID 28168807 DOI: 10.1111/pcmr.12579 |
0.69 |
|
2017 |
Loftus SK, Baxter LL, Cronin JC, Fufa TD, Pavan WJ. Hypoxia-induced HIF1α targets in melanocytes reveal a molecular profile associated with poor melanoma prognosis. Pigment Cell & Melanoma Research. PMID 28168807 DOI: 10.1111/pcmr.12579 |
0.69 |
|
2015 |
Watkins-Chow DE, Cooke J, Pidsley R, Edwards A, Slotkin R, Leeds KE, Mullen R, Baxter LL, Campbell TG, Salzer MC, Biondini L, Gibney G, Tuy FP, Chelly J, Morris HD, ... ... Pavan WJ, et al. Correction: Mutation of the Diamond-Blackfan Anemia Gene Rps7 in Mouse Results in Morphological and Neuroanatomical Phenotypes. Plos Genetics. 11: e1005682. PMID 26584186 DOI: 10.1371/journal.pgen.1005682 |
0.68 |
|
2015 |
Watkins-Chow DE, Cooke J, Pidsley R, Edwards A, Slotkin R, Leeds KE, Mullen R, Baxter LL, Campbell TG, Salzer MC, Biondini L, Gibney G, Tuy FP, Chelly J, Morris HD, ... ... Pavan WJ, et al. Correction: Mutation of the Diamond-Blackfan Anemia Gene Rps7 in Mouse Results in Morphological and Neuroanatomical Phenotypes. Plos Genetics. 11: e1005682. PMID 26584186 DOI: 10.1371/journal.pgen.1005682 |
0.68 |
|
2015 |
Fufa TD, Harris ML, Watkins-Chow DE, Levy D, Gorkin DU, Gildea DE, Song L, Safi A, Crawford GE, Sviderskaya EV, Bennett DC, Mccallion AS, Loftus SK, Pavan WJ. Genomic analysis reveals distinct mechanisms and functional classes of SOX10-regulated genes in melanocytes. Human Molecular Genetics. 24: 5433-50. PMID 26206884 DOI: 10.1093/Hmg/Ddv267 |
0.352 |
|
2015 |
Fufa TD, Harris ML, Watkins-Chow DE, Levy D, Gorkin DU, Gildea DE, Song L, Safi A, Crawford GE, Sviderskaya EV, Bennett DC, Mccallion AS, Loftus SK, Pavan WJ. Genomic analysis reveals distinct mechanisms and functional classes of SOX10-regulated genes in melanocytes. Human Molecular Genetics. 24: 5433-50. PMID 26206884 DOI: 10.1093/Hmg/Ddv267 |
0.352 |
|
2015 |
Saldana-Caboverde A, Perera EM, Watkins-Chow DE, Hansen NF, Vemulapalli M, Mullikin JC, Pavan WJ, Kos L. The transcription factors Ets1 and Sox10 interact during murine melanocyte development. Developmental Biology. 407: 300-12. PMID 25912689 DOI: 10.1016/J.Ydbio.2015.04.012 |
0.396 |
|
2015 |
Saldana-Caboverde A, Perera EM, Watkins-Chow DE, Hansen NF, Vemulapalli M, Mullikin JC, Pavan WJ, Kos L. The transcription factors Ets1 and Sox10 interact during murine melanocyte development. Developmental Biology. 407: 300-12. PMID 25912689 DOI: 10.1016/J.Ydbio.2015.04.012 |
0.396 |
|
2015 |
Loftus S, Cronin J, Fufa T, McCallion A, Crawford G, Pavan W. Abstract A23: Epigenetic Cis-regulatory interactions in HIF1a-activated melanocytes Cancer Research. 75. DOI: 10.1158/1538-7445.Mel2014-A23 |
0.318 |
|
2014 |
Hwang HW, Baxter LL, Loftus SK, Cronin JC, Trivedi NS, Borate B, Pavan WJ. Distinct microRNA expression signatures are associated with melanoma subtypes and are regulated by HIF1A. Pigment Cell & Melanoma Research. 27: 777-87. PMID 24767210 DOI: 10.1111/Pcmr.12255 |
0.671 |
|
2014 |
Hwang HW, Baxter LL, Loftus SK, Cronin JC, Trivedi NS, Borate B, Pavan WJ. Distinct microRNA expression signatures are associated with melanoma subtypes and are regulated by HIF1A. Pigment Cell & Melanoma Research. 27: 777-87. PMID 24767210 DOI: 10.1111/Pcmr.12255 |
0.671 |
|
2013 |
Praetorius C, Grill C, Stacey SN, Metcalf AM, Gorkin DU, Robinson KC, Van Otterloo E, Kim RS, Bergsteinsdottir K, Ogmundsdottir MH, Magnusdottir E, Mishra PJ, Davis SR, Guo T, Zaidi MR, ... ... Pavan WJ, et al. A polymorphism in IRF4 affects human pigmentation through a tyrosinase-dependent MITF/TFAP2A pathway. Cell. 155: 1022-33. PMID 24267888 DOI: 10.1016/J.Cell.2013.10.022 |
0.317 |
|
2013 |
Praetorius C, Grill C, Stacey SN, Metcalf AM, Gorkin DU, Robinson KC, Van Otterloo E, Kim RS, Bergsteinsdottir K, Ogmundsdottir MH, Magnusdottir E, Mishra PJ, Davis SR, Guo T, Zaidi MR, ... ... Pavan WJ, et al. A polymorphism in IRF4 affects human pigmentation through a tyrosinase-dependent MITF/TFAP2A pathway. Cell. 155: 1022-33. PMID 24267888 DOI: 10.1016/J.Cell.2013.10.022 |
0.317 |
|
2013 |
Baxter LL, Pavan WJ. The etiology and molecular genetics of human pigmentation disorders. Wiley Interdisciplinary Reviews. Developmental Biology. 2: 379-92. PMID 23799582 DOI: 10.1002/wdev.72 |
0.674 |
|
2013 |
Baxter LL, Pavan WJ. The etiology and molecular genetics of human pigmentation disorders. Wiley Interdisciplinary Reviews. Developmental Biology. 2: 379-92. PMID 23799582 DOI: 10.1002/wdev.72 |
0.674 |
|
2013 |
Fu R, Wassif CA, Yanjanin NM, Watkins-Chow DE, Baxter LL, Incao A, Liscum L, Sidhu R, Firnkes S, Graham M, Ory DS, Porter FD, Pavan WJ. Efficacy of N-acetylcysteine in phenotypic suppression of mouse models of Niemann-Pick disease, type C1. Human Molecular Genetics. 22: 3508-23. PMID 23666527 DOI: 10.1093/Hmg/Ddt206 |
0.675 |
|
2013 |
Fu R, Wassif CA, Yanjanin NM, Watkins-Chow DE, Baxter LL, Incao A, Liscum L, Sidhu R, Firnkes S, Graham M, Ory DS, Porter FD, Pavan WJ. Efficacy of N-acetylcysteine in phenotypic suppression of mouse models of Niemann-Pick disease, type C1. Human Molecular Genetics. 22: 3508-23. PMID 23666527 DOI: 10.1093/Hmg/Ddt206 |
0.675 |
|
2013 |
Watkins-Chow DE, Cooke J, Pidsley R, Edwards A, Slotkin R, Leeds KE, Mullen R, Baxter LL, Campbell TG, Salzer MC, Biondini L, Gibney G, Phan Dinh Tuy F, Chelly J, Morris HD, ... ... Pavan WJ, et al. Mutation of the diamond-blackfan anemia gene Rps7 in mouse results in morphological and neuroanatomical phenotypes. Plos Genetics. 9: e1003094. PMID 23382688 DOI: 10.1371/Journal.Pgen.1003094 |
0.704 |
|
2013 |
Watkins-Chow DE, Cooke J, Pidsley R, Edwards A, Slotkin R, Leeds KE, Mullen R, Baxter LL, Campbell TG, Salzer MC, Biondini L, Gibney G, Phan Dinh Tuy F, Chelly J, Morris HD, ... ... Pavan WJ, et al. Mutation of the diamond-blackfan anemia gene Rps7 in mouse results in morphological and neuroanatomical phenotypes. Plos Genetics. 9: e1003094. PMID 23382688 DOI: 10.1371/Journal.Pgen.1003094 |
0.704 |
|
2013 |
Silver DL, Leeds KE, Hwang HW, Miller EE, Pavan WJ. The EJC component Magoh regulates proliferation and expansion of neural crest-derived melanocytes. Developmental Biology. 375: 172-81. PMID 23333945 DOI: 10.1016/J.Ydbio.2013.01.004 |
0.313 |
|
2013 |
Silver DL, Leeds KE, Hwang HW, Miller EE, Pavan WJ. The EJC component Magoh regulates proliferation and expansion of neural crest-derived melanocytes. Developmental Biology. 375: 172-81. PMID 23333945 DOI: 10.1016/J.Ydbio.2013.01.004 |
0.313 |
|
2013 |
Harris ML, Pavan WJ. Postnatal lineage mapping of follicular melanocytes with the Tyr:: CreERT2 transgene Pigment Cell and Melanoma Research. 26: 269-274. PMID 23176440 DOI: 10.1111/pcmr.12048 |
0.339 |
|
2013 |
Harris ML, Pavan WJ. Postnatal lineage mapping of follicular melanocytes with the Tyr:: CreERT2 transgene Pigment Cell and Melanoma Research. 26: 269-274. PMID 23176440 DOI: 10.1111/pcmr.12048 |
0.339 |
|
2013 |
Fu R, Wassif CA, Yanjanin NM, Watkins-Chow DE, Baxter LL, Incao A, Liscum L, Sidhu R, Firnkes S, Graham M, Ory DS, Porter FD, Pavan WJ. Efficacy of N-acetylcysteine in phenotypic suppression of mouse models of niemann-pick disease, type C1 Human Molecular Genetics. 22: 3508-3523. DOI: 10.1093/hmg/ddt206 |
0.614 |
|
2012 |
Baxter LL, Marugan JJ, Xiao J, Incao A, McKew JC, Zheng W, Pavan WJ. Plasma and tissue concentrations of α-tocopherol and δ-tocopherol following high dose dietary supplementation in mice. Nutrients. 4: 467-90. PMID 22822447 DOI: 10.3390/nu4060467 |
0.584 |
|
2012 |
Baxter LL, Marugan JJ, Xiao J, Incao A, McKew JC, Zheng W, Pavan WJ. Plasma and tissue concentrations of α-tocopherol and δ-tocopherol following high dose dietary supplementation in mice. Nutrients. 4: 467-90. PMID 22822447 DOI: 10.3390/nu4060467 |
0.584 |
|
2012 |
Cluzeau CV, Watkins-Chow DE, Fu R, Borate B, Yanjanin N, Dail MK, Davidson CD, Walkley SU, Ory DS, Wassif CA, Pavan WJ, Porter FD. Microarray expression analysis and identification of serum biomarkers for Niemann-Pick disease, type C1. Human Molecular Genetics. 21: 3632-46. PMID 22619379 DOI: 10.1093/Hmg/Dds193 |
0.329 |
|
2012 |
Cluzeau CV, Watkins-Chow DE, Fu R, Borate B, Yanjanin N, Dail MK, Davidson CD, Walkley SU, Ory DS, Wassif CA, Pavan WJ, Porter FD. Microarray expression analysis and identification of serum biomarkers for Niemann-Pick disease, type C1. Human Molecular Genetics. 21: 3632-46. PMID 22619379 DOI: 10.1093/Hmg/Dds193 |
0.329 |
|
2010 |
Antonellis A, Dennis MY, Burzynski G, Huynh J, Maduro V, Hodonsky CJ, Khajavi M, Szigeti K, Mukkamala S, Bessling SL, Pavan WJ, McCallion AS, Lupski JR, Green ED. A rare myelin protein zero (MPZ) variant alters enhancer activity in vitro and in vivo. Plos One. 5: e14346. PMID 21179557 DOI: 10.1371/Journal.Pone.0014346 |
0.325 |
|
2010 |
Antonellis A, Dennis MY, Burzynski G, Huynh J, Maduro V, Hodonsky CJ, Khajavi M, Szigeti K, Mukkamala S, Bessling SL, Pavan WJ, McCallion AS, Lupski JR, Green ED. A rare myelin protein zero (MPZ) variant alters enhancer activity in vitro and in vivo. Plos One. 5: e14346. PMID 21179557 DOI: 10.1371/Journal.Pone.0014346 |
0.325 |
|
2010 |
Baxter LL, Moreland RT, Nguyen AD, Wolfsberg TG, Pavan WJ. A curated online resource for SOX10 and pigment cell molecular genetic pathways. Database : the Journal of Biological Databases and Curation. 2010: baq025. PMID 20974870 DOI: 10.1093/database/baq025 |
0.682 |
|
2010 |
Baxter LL, Moreland RT, Nguyen AD, Wolfsberg TG, Pavan WJ. A curated online resource for SOX10 and pigment cell molecular genetic pathways. Database : the Journal of Biological Databases and Curation. 2010: baq025. PMID 20974870 DOI: 10.1093/database/baq025 |
0.682 |
|
2010 |
Harris ML, Baxter LL, Loftus SK, Pavan WJ. Sox proteins in melanocyte development and melanoma. Pigment Cell & Melanoma Research. 23: 496-513. PMID 20444197 DOI: 10.1111/j.1755-148X.2010.00711.x |
0.667 |
|
2010 |
Harris ML, Baxter LL, Loftus SK, Pavan WJ. Sox proteins in melanocyte development and melanoma. Pigment Cell & Melanoma Research. 23: 496-513. PMID 20444197 DOI: 10.1111/j.1755-148X.2010.00711.x |
0.667 |
|
2009 |
Baxter LL, Loftus SK, Pavan WJ. Networks and pathways in pigmentation, health, and disease. Wiley Interdisciplinary Reviews. Systems Biology and Medicine. 1: 359-71. PMID 20161540 DOI: 10.1002/wsbm.20 |
0.678 |
|
2009 |
Loftus SK, Baxter LL, Buac K, Watkins-Chow DE, Larson DM, Pavan WJ. Comparison of melanoblast expression patterns identifies distinct classes of genes. Pigment Cell & Melanoma Research. 22: 611-22. PMID 19493314 DOI: 10.1111/j.1755-148X.2009.00584.x |
0.714 |
|
2009 |
Loftus SK, Baxter LL, Buac K, Watkins-Chow DE, Larson DM, Pavan WJ. Comparison of melanoblast expression patterns identifies distinct classes of genes. Pigment Cell & Melanoma Research. 22: 611-22. PMID 19493314 DOI: 10.1111/j.1755-148X.2009.00584.x |
0.714 |
|
2009 |
Loftus SK, Antonellis A, Matera I, Renaud G, Baxter LL, Reid D, Wolfsberg TG, Chen Y, Wang C, Prasad MK, Bessling SL, McCallion AS, Green ED, Bennett DC, ... Pavan WJ, et al. Gpnmb is a melanoblast-expressed, MITF-dependent gene. Pigment Cell & Melanoma Research. 22: 99-110. PMID 18983539 DOI: 10.1111/J.1755-148X.2008.00518.X |
0.682 |
|
2008 |
Dutton JR, Antonellis A, Carney TJ, Rodrigues FS, Pavan WJ, Ward A, Kelsh RN. An evolutionarily conserved intronic region controls the spatiotemporal expression of the transcription factor Sox10. Bmc Developmental Biology. 8: 105. PMID 18950534 DOI: 10.1186/1471-213X-8-105 |
0.333 |
|
2008 |
Dutton JR, Antonellis A, Carney TJ, Rodrigues FS, Pavan WJ, Ward A, Kelsh RN. An evolutionarily conserved intronic region controls the spatiotemporal expression of the transcription factor Sox10. Bmc Developmental Biology. 8: 105. PMID 18950534 DOI: 10.1186/1471-213X-8-105 |
0.333 |
|
2008 |
Buac K, Watkins-Chow DE, Loftus SK, Larson DM, Incao A, Gibney G, Pavan WJ. A Sox10 expression screen identifies an amino acid essential for Erbb3 function Plos Genetics. 4. PMID 18773073 DOI: 10.1371/journal.pgen.1000177 |
0.387 |
|
2008 |
Buac K, Watkins-Chow DE, Loftus SK, Larson DM, Incao A, Gibney G, Pavan WJ. A Sox10 expression screen identifies an amino acid essential for Erbb3 function Plos Genetics. 4. PMID 18773073 DOI: 10.1371/journal.pgen.1000177 |
0.387 |
|
2008 |
Antonellis A, Huynh JL, Lee-Lin SQ, Vinton RM, Renaud G, Loftus SK, Elliot G, Wolfsberg TG, Green ED, McCallion AS, Pavan WJ. Identification of neural crest and glial enhancers at the mouse Sox10 locus through transgenesis in zebrafish Plos Genetics. 4. PMID 18773071 DOI: 10.1371/Journal.Pgen.1000174 |
0.358 |
|
2008 |
Antonellis A, Huynh JL, Lee-Lin SQ, Vinton RM, Renaud G, Loftus SK, Elliot G, Wolfsberg TG, Green ED, McCallion AS, Pavan WJ. Identification of neural crest and glial enhancers at the mouse Sox10 locus through transgenesis in zebrafish Plos Genetics. 4. PMID 18773071 DOI: 10.1371/Journal.Pgen.1000174 |
0.358 |
|
2008 |
Matera I, Watkins-Chow DE, Loftus SK, Hou L, Incao A, Silver DL, Rivas C, Elliott EC, Baxter LL, Pavan WJ. A sensitized mutagenesis screen identifies Gli3 as a modifier of Sox10 neurocristopathy. Human Molecular Genetics. 17: 2118-31. PMID 18397875 DOI: 10.1093/Hmg/Ddn110 |
0.683 |
|
2008 |
Matera I, Watkins-Chow DE, Loftus SK, Hou L, Incao A, Silver DL, Rivas C, Elliott EC, Baxter LL, Pavan WJ. A sensitized mutagenesis screen identifies Gli3 as a modifier of Sox10 neurocristopathy. Human Molecular Genetics. 17: 2118-31. PMID 18397875 DOI: 10.1093/Hmg/Ddn110 |
0.683 |
|
2007 |
Baxter LL, Hsu BJ, Umayam L, Wolfsberg TG, Larson DM, Frith MC, Kawai J, Hayashizaki Y, Carninci P, Pavan WJ. Informatic and genomic analysis of melanocyte cDNA libraries as a resource for the study of melanocyte development and function. Pigment Cell Research / Sponsored by the European Society For Pigment Cell Research and the International Pigment Cell Society. 20: 201-9. PMID 17516927 DOI: 10.1111/J.1600-0749.2007.00372.X |
0.688 |
|
2007 |
Baxter LL, Hsu BJ, Umayam L, Wolfsberg TG, Larson DM, Frith MC, Kawai J, Hayashizaki Y, Carninci P, Pavan WJ. Informatic and genomic analysis of melanocyte cDNA libraries as a resource for the study of melanocyte development and function. Pigment Cell Research / Sponsored by the European Society For Pigment Cell Research and the International Pigment Cell Society. 20: 201-9. PMID 17516927 DOI: 10.1111/J.1600-0749.2007.00372.X |
0.688 |
|
2006 |
Hou L, Arnheiter H, Pavan WJ. Interspecies difference in the regulation of melanocyte development by SOX10 and MITF. Proceedings of the National Academy of Sciences of the United States of America. 103: 9081-5. PMID 16757562 DOI: 10.1073/pnas.0603114103 |
0.423 |
|
2006 |
Hou L, Arnheiter H, Pavan WJ. Interspecies difference in the regulation of melanocyte development by SOX10 and MITF. Proceedings of the National Academy of Sciences of the United States of America. 103: 9081-5. PMID 16757562 DOI: 10.1073/pnas.0603114103 |
0.423 |
|
2006 |
Hakami RM, Hou L, Baxter LL, Loftus SK, Southard-Smith EM, Incao A, Cheng J, Pavan WJ. Genetic evidence does not support direct regulation of EDNRB by SOX10 in migratory neural crest and the melanocyte lineage. Mechanisms of Development. 123: 124-34. PMID 16412618 DOI: 10.1016/J.Mod.2005.11.004 |
0.707 |
|
2006 |
Antonellis A, Bennett WR, Menheniott TR, Prasad AB, Lee-Lin SQ, Green ED, Paisley D, Kelsh RN, Pavan WJ, Ward A. Deletion of long-range sequences at Sox10 compromises developmental expression in a mouse model of Waardenburg-Shah (WS4) syndrome. Human Molecular Genetics. 15: 259-71. PMID 16330480 DOI: 10.1093/Hmg/Ddi442 |
0.339 |
|
2005 |
Loftus SK, Cannons JL, Incao A, Pak E, Chen A, Zerfas PM, Bryant MA, Biesecker LG, Schwartzberg PL, Pavan WJ. Acinar cell apoptosis in Serpini2-deficient mice models pancreatic insufficiency. Plos Genetics. 1: e38. PMID 16184191 DOI: 10.1371/journal.pgen.0010038 |
0.308 |
|
2004 |
Jiao Z, Mollaaghababa R, Pavan WJ, Antonellis A, Green ED, Hornyak TJ. Direct interaction of Sox10 with the promoter of murine Dopachrome Tautomerase (Dct) and synergistic activation of Dct expression with Mitf. Pigment Cell Research / Sponsored by the European Society For Pigment Cell Research and the International Pigment Cell Society. 17: 352-62. PMID 15250937 DOI: 10.1111/J.1600-0749.2004.00154.X |
0.339 |
|
2004 |
Hou L, Pavan WJ, Shin MK, Arnheiter H. Cell-autonomous and cell non-autonomous signaling through endothelin receptor B during melanocyte development. Development (Cambridge, England). 131: 3239-47. PMID 15201217 DOI: 10.1242/dev.01193 |
0.306 |
|
2004 |
Hou L, Pavan WJ, Shin MK, Arnheiter H. Cell-autonomous and cell non-autonomous signaling through endothelin receptor B during melanocyte development. Development (Cambridge, England). 131: 3239-47. PMID 15201217 DOI: 10.1242/dev.01193 |
0.306 |
|
2004 |
Baxter LL, Hou L, Loftus SK, Pavan WJ. Spotlight on spotted mice: a review of white spotting mouse mutants and associated human pigmentation disorders. Pigment Cell Research / Sponsored by the European Society For Pigment Cell Research and the International Pigment Cell Society. 17: 215-24. PMID 15140066 DOI: 10.1111/j.1600-0749.2004.00147.x |
0.706 |
|
2004 |
Hou L, Loftus SK, Incao A, Chen A, Pavan WJ. Complementation of melanocyte development in SOX10 mutant neural crest using lineage-directed gene transfer. Developmental Dynamics : An Official Publication of the American Association of Anatomists. 229: 54-62. PMID 14699577 DOI: 10.1002/dvdy.10468 |
0.384 |
|
2004 |
Hou L, Loftus SK, Incao A, Chen A, Pavan WJ. Complementation of melanocyte development in SOX10 mutant neural crest using lineage-directed gene transfer. Developmental Dynamics : An Official Publication of the American Association of Anatomists. 229: 54-62. PMID 14699577 DOI: 10.1002/dvdy.10468 |
0.384 |
|
2003 |
Baxter LL, Pavan WJ. Pmel17 expression is Mitf-dependent and reveals cranial melanoblast migration during murine development. Gene Expression Patterns : Gep. 3: 703-7. PMID 14643677 |
0.684 |
|
2003 |
Schriml LM, Hill DP, Blake JA, Bono H, Wynshaw-Boris A, Pavan WJ, Ring BZ, Beisel K, Setou M, Okazaki Y. Human disease genes and their cloned mouse orthologs: exploration of the FANTOM2 cDNA sequence data set. Genome Research. 13: 1496-500. PMID 12819148 DOI: 10.1101/Gr.979503 |
0.306 |
|
2003 |
Schriml LM, Hill DP, Blake JA, Bono H, Wynshaw-Boris A, Pavan WJ, Ring BZ, Beisel K, Setou M, Okazaki Y. Human disease genes and their cloned mouse orthologs: exploration of the FANTOM2 cDNA sequence data set. Genome Research. 13: 1496-500. PMID 12819148 DOI: 10.1101/Gr.979503 |
0.306 |
|
2003 |
Mollaaghababa R, Pavan WJ. The importance of having your SOX on: role of SOX10 in the development of neural crest-derived melanocytes and glia. Oncogene. 22: 3024-34. PMID 12789277 DOI: 10.1038/sj.onc.1206442 |
0.344 |
|
2003 |
Mollaaghababa R, Pavan WJ. The importance of having your SOX on: role of SOX10 in the development of neural crest-derived melanocytes and glia. Oncogene. 22: 3024-34. PMID 12789277 DOI: 10.1038/sj.onc.1206442 |
0.344 |
|
2003 |
Pollock PM, Cohen-Solal K, Sood R, Namkoong J, Martino JJ, Koganti A, Zhu H, Robbins C, Makalowska I, Shin SS, Marin Y, Roberts KG, Yudt LM, Chen A, Cheng J, ... ... Pavan WJ, et al. Melanoma mouse model implicates metabotropic glutamate signaling in melanocytic neoplasia. Nature Genetics. 34: 108-12. PMID 12704387 DOI: 10.1038/Ng1148 |
0.322 |
|
2002 |
Baxter LL, Pavan WJ. The oculocutaneous albinism type IV gene Matp is a new marker of pigment cell precursors during mouse embryonic development. Mechanisms of Development. 116: 209-12. PMID 12128226 DOI: 10.1016/S0925-4773(02)00130-2 |
0.714 |
|
2002 |
Loftus SK, Larson DM, Baxter LL, Antonellis A, Chen Y, Wu X, Jiang Y, Bittner M, Hammer JA, Pavan WJ. Mutation of melanosome protein RAB38 in chocolate mice. Proceedings of the National Academy of Sciences of the United States of America. 99: 4471-6. PMID 11917121 DOI: 10.1073/Pnas.072087599 |
0.7 |
|
2000 |
Dunn KJ, Williams BO, Li Y, Pavan WJ. Neural crest-Directed gene transfer demonstrates Wnt1 role in melanocyte expansion and differentiation during mouse development Proceedings of the National Academy of Sciences of the United States of America. 97: 10050-10055. PMID 10963668 DOI: 10.1073/Pnas.97.18.10050 |
0.305 |
|
2000 |
Loftus SK, Pavan WJ. The use of expression profiling to study pigment cell biology and dysfunction. Pigment Cell Research. 13: 141-6. PMID 10885671 DOI: 10.1034/J.1600-0749.2000.130304.X |
0.37 |
|
1999 |
Khan J, Bittner ML, Saal LH, Teichmann U, Azorsa DO, Gooden GC, Pavan WJ, Trent JM, Meltzer PS. cDNA microarrays detect activation of a myogenic transcription program by the PAX3-FKHR fusion oncogene Proceedings of the National Academy of Sciences of the United States of America. 96: 13264-13269. PMID 10557309 DOI: 10.1073/Pnas.96.23.13264 |
0.302 |
|
1999 |
Loftus SK, Chen Y, Gooden G, Ryan JF, Birznieks G, Hilliard M, Baxevanis AD, Bittner M, Meltzer P, Trent J, Pavan W. Informatic selection of a neural crest-melanocyte cDNA set for microarray analysis. Proceedings of the National Academy of Sciences of the United States of America. 96: 9277-80. PMID 10430933 DOI: 10.1038/14355 |
0.306 |
|
1999 |
Guru SC, Crabtree JS, Brown KD, Dunn KJ, Manickam P, Prasad NB, Wangsa D, Burns AL, Spiegel AM, Marx SJ, Pavan WJ, Collins FS, Chandrasekharappa SC. Isolation, genomic organization, and expression analysis of Men1, the murine homolog of the MEN1 gene. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 10: 592-6. PMID 10341092 DOI: 10.1007/S003359901051 |
0.304 |
|
1999 |
Southard-Smith EM, Angrist M, Ellison JS, Agarwala R, Baxevanis AD, Chakravarti A, Pavan WJ. The Sox10Dom Mouse: Modeling the Genetic Variation of Waardenburg-Shah (WS4) Syndrome Genome Research. 9: 215-225. DOI: 10.1101/Gr.9.3.215 |
0.383 |
|
1999 |
Teichmann U, Schuler G, Moore T, Otsuka T, Merlino G, Khan J, Chen Y, Bittner M, Meltzer P, Trent J, Pavan W. Development of a mouse-specific cDNA set for microarray gene expression analysis: differential gene expression in melanocyte lineage samples of the neural crest Nature Genetics. 23: 78-78. DOI: 10.1038/14414 |
0.317 |
|
1998 |
Southard-Smith EM, Kos L, Pavan WJ. Sox10 mutation disrupts neural crest development in Dom Hirschsprung mouse model. Nature Genetics. 18: 60-4. PMID 9425902 DOI: 10.1038/ng0198-60 |
0.336 |
|
1995 |
Pavan WJ, Liddell RA, Wright A, Thibaudeau G, Matteson PG, McHugh KM, Siracusa LD. A high-resolution linkage map of the lethal spotting locus: a mouse model for Hirschsprung disease. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 6: 1-7. PMID 7719019 DOI: 10.1007/BF00350885 |
0.352 |
|
1992 |
Reeves RH, Pavan WJ, Hieter P. [49] Yeast artificial chromosome modification and manipulation Methods in Enzymology. 216: 584-603. PMID 1336105 DOI: 10.1016/0076-6879(92)16051-K |
0.498 |
|
1991 |
Pavan WJ, Hieter P, Sears D, Burkhoff A, Reeves RH. High-efficiency yeast artificial chromosome fragmentation vectors Gene. 106: 125-127. PMID 1937033 DOI: 10.1016/0378-1119(91)90576-W |
0.466 |
|
1991 |
Pavan WJ, Reeves RH. Integrative selection of human chromosome-specific yeast artificial chromosomes Proceedings of the National Academy of Sciences of the United States of America. 88: 7788-7791. PMID 1881915 DOI: 10.1073/PNAS.88.17.7788 |
0.472 |
|
1990 |
Pavan WJ, Hieter P, Reeves RH. Generation of deletion derivatives by targeted transformation of human-derived yeast artificial chromosomes Proceedings of the National Academy of Sciences of the United States of America. 87: 1300-1304. PMID 2406718 DOI: 10.1073/Pnas.87.4.1300 |
0.487 |
|
1990 |
Pavan WJ, Hieter P, Reeves RH. Modification and transfer into an embryonal carcinoma cell line of a 360-kilobase human-derived yeast artificial chromosome Molecular and Cellular Biology. 10: 4163-4169. PMID 2196449 DOI: 10.1128/mcb.10.8.4163-4169.1990 |
0.506 |
|
1990 |
Reeves RH, Pavan WJ, Hieter P. Modification and manipulation of mammalian DNA cloned as YACs Gene Analysis Techniques. 7: 107-113. PMID 2091692 DOI: 10.1016/0735-0651(90)90015-8 |
0.412 |
|
1989 |
Reeves RH, Crowley MR, Lorenzon N, Pavan WJ, Smeyne RJ, Goldowitz D. The mouse neurological mutant weaver maps within the region of chromosome 16 that is homologous to human chromosome 21. Genomics. 5: 522-6. PMID 2575584 DOI: 10.1016/0888-7543(89)90018-9 |
0.49 |
|
1988 |
Reeves RH, O'Hara BF, Pavan WJ, Gearhart JD, Haller O. Genetic mapping of the Mx influenza virus resistance gene within the region of mouse chromosome 16 that is homologous to human chromosome 21. Journal of Virology. 62: 4372-5. PMID 2902234 DOI: 10.1128/Jvi.62.11.4372-4375.1988 |
0.491 |
|
Low-probability matches (unlikely to be authored by this person) |
2007 |
Brooks BP, Larson DM, Chan CC, Kjellstrom S, Smith RS, Crawford MA, Lamoreux L, Huizing M, Hess R, Jiao X, Hejtmancik JF, Maminishkis A, John SW, Bush R, Pavan WJ. Analysis of ocular hypopigmentation in Rab38cht/cht mice. Investigative Ophthalmology & Visual Science. 48: 3905-13. PMID 17724166 DOI: 10.1167/Iovs.06-1464 |
0.299 |
|
2007 |
Matera I, Cockroft JL, Moran JL, Beier DR, Goldowitz D, Pavan WJ. A mouse model of Waardenburg syndrome type IV resulting from an ENU-induced mutation in endothelin 3. Pigment Cell Research / Sponsored by the European Society For Pigment Cell Research and the International Pigment Cell Society. 20: 210-5. PMID 17516928 DOI: 10.1111/J.1600-0749.2007.00371.X |
0.299 |
|
2017 |
Crawford NG, Kelly DE, Hansen MEB, Beltrame MH, Fan S, Bowman SL, Jewett E, Ranciaro A, Thompson S, Lo Y, Pfeifer SP, Jensen JD, Campbell MC, Beggs W, Hormozdiari F, ... ... Pavan WJ, et al. Loci associated with skin pigmentation identified in African populations. Science (New York, N.Y.). PMID 29025994 DOI: 10.1126/Science.Aan8433 |
0.298 |
|
2017 |
Crawford NG, Kelly DE, Hansen MEB, Beltrame MH, Fan S, Bowman SL, Jewett E, Ranciaro A, Thompson S, Lo Y, Pfeifer SP, Jensen JD, Campbell MC, Beggs W, Hormozdiari F, ... ... Pavan WJ, et al. Loci associated with skin pigmentation identified in African populations. Science (New York, N.Y.). PMID 29025994 DOI: 10.1126/Science.Aan8433 |
0.298 |
|
1998 |
Teichmann U, Ray ME, Ellison J, Graham C, Wistow G, Meltzer PS, Trent JM, Pavan WJ. Cloning and tissue expression of the mouse ortholog of AIM1, a βγ-crystallin superfamily member Mammalian Genome. 9: 715-720. PMID 9716656 DOI: 10.1007/S003359900852 |
0.295 |
|
1997 |
Hirotsune S, Pack SD, Chong SS, Robbins CM, Pavan WJ, Ledbetter DH, Wynshaw-Boris A. Genomic organization of the murine Miller-Dieker/lissencephaly region: conservation of linkage with the human region. Genome Research. 7: 625-34. PMID 9199935 DOI: 10.1101/Gr.7.6.625 |
0.294 |
|
2015 |
Chandler RJ, Williams IM, Incao AA, Porter FD, Pavan WJ, Venditti CP. 198. Adeno-Associated Viral Gene Therapy To Treat Niemann-Pick Disease, Type C1 Molecular Therapy. 23: S79. DOI: 10.1016/S1525-0016(16)33803-5 |
0.29 |
|
2016 |
Gibson AL, Chandler RJ, Williams IM, Incao AA, Porter FD, Pavan WJ, Venditti CP. 613. A Comparison of CNS Transduction After Systemic versus Cranial Delivery of an AAV2/9 CamKII Promoter-eGFP Vector in Mice Molecular Therapy. 24: S243. DOI: 10.1016/S1525-0016(16)33421-9 |
0.289 |
|
2006 |
Silver DL, Hou L, Pavan WJ. The genetic regulation of pigment cell development. Advances in Experimental Medicine and Biology. 589: 155-69. PMID 17076280 DOI: 10.1007/978-0-387-46954-6_9 |
0.289 |
|
2006 |
Silver DL, Hou L, Pavan WJ. The genetic regulation of pigment cell development. Advances in Experimental Medicine and Biology. 589: 155-69. PMID 17076280 DOI: 10.1007/978-0-387-46954-6_9 |
0.289 |
|
2001 |
Potterf SB, Mollaaghababa R, Hou L, Southard-Smith EM, Hornyak TJ, Arnheiter H, Pavan WJ. Analysis of SOX10 function in neural crest-derived melanocyte development: SOX10-dependent transcriptional control of dopachrome tautomerase. Developmental Biology. 237: 245-57. PMID 11543611 DOI: 10.1006/Dbio.2001.0372 |
0.288 |
|
2019 |
Fialkowski AC, Levy DJ, Watkins-Chow DE, Palmer JW, Darji R, Tiwari HK, Pavan WJ, Harris ML. Identification of Gene Variants Associated with Melanocyte Stem Cell Differentiation in Mice Predisposed for Hair Graying. G3 (Bethesda, Md.). PMID 30651286 DOI: 10.1534/g3.118.200965 |
0.286 |
|
2019 |
Fialkowski AC, Levy DJ, Watkins-Chow DE, Palmer JW, Darji R, Tiwari HK, Pavan WJ, Harris ML. Identification of Gene Variants Associated with Melanocyte Stem Cell Differentiation in Mice Predisposed for Hair Graying. G3 (Bethesda, Md.). PMID 30651286 DOI: 10.1534/g3.118.200965 |
0.286 |
|
2013 |
Cronin JC, Watkins-Chow DE, Incao A, Hasskamp JH, Schönewolf N, Aoude LG, Hayward NK, Bastian BC, Dummer R, Loftus SK, Pavan WJ. SOX10 ablation arrests cell cycle, induces senescence, and suppresses melanomagenesis. Cancer Research. 73: 5709-18. PMID 23913827 DOI: 10.1158/0008-5472.CAN-12-4620 |
0.284 |
|
2013 |
Cronin JC, Watkins-Chow DE, Incao A, Hasskamp JH, Schönewolf N, Aoude LG, Hayward NK, Bastian BC, Dummer R, Loftus SK, Pavan WJ. SOX10 ablation arrests cell cycle, induces senescence, and suppresses melanomagenesis. Cancer Research. 73: 5709-18. PMID 23913827 DOI: 10.1158/0008-5472.CAN-12-4620 |
0.284 |
|
1997 |
Loftus SK, Morris JA, Carstea ED, Gu JZ, Cummings C, Brown A, Ellison J, Ohno K, Rosenfeld MA, Tagle DA, Pentchev PG, Pavan WJ. Murine model of Niemann-Pick C disease: mutation in a cholesterol homeostasis gene. Science (New York, N.Y.). 277: 232-5. PMID 9211850 DOI: 10.1126/SCIENCE.277.5323.232 |
0.284 |
|
2000 |
Potterf SB, Furumura M, Dunn KJ, Arnheiter H, Pavan WJ. Transcription factor hierarchy in Waardenburg syndrome: regulation of MITF expression by SOX10 and PAX3. Human Genetics. 107: 1-6. PMID 10982026 DOI: 10.1007/s004390000328 |
0.283 |
|
2001 |
Dunn KJ, Incao A, Watkins-Chow D, Li Y, Pavan WJ. In utero complementation of a neural crest-derived melanocyte defect using cell directed gene transfer Genesis. 30: 70-76. PMID 11416866 DOI: 10.1002/Gene.1035 |
0.283 |
|
2009 |
Cronin JC, Wunderlich J, Loftus SK, Prickett TD, Wei X, Ridd K, Vemula S, Burrell AS, Agrawal NS, Lin JC, Banister CE, Buckhaults P, Rosenberg SA, Bastian BC, Pavan WJ, et al. Frequent mutations in the MITF pathway in melanoma. Pigment Cell & Melanoma Research. 22: 435-44. PMID 19422606 DOI: 10.1111/J.1755-148X.2009.00578.X |
0.281 |
|
2009 |
Cronin JC, Wunderlich J, Loftus SK, Prickett TD, Wei X, Ridd K, Vemula S, Burrell AS, Agrawal NS, Lin JC, Banister CE, Buckhaults P, Rosenberg SA, Bastian BC, Pavan WJ, et al. Frequent mutations in the MITF pathway in melanoma. Pigment Cell & Melanoma Research. 22: 435-44. PMID 19422606 DOI: 10.1111/J.1755-148X.2009.00578.X |
0.281 |
|
2011 |
Gildea DE, Luetkemeier ES, Bao X, Loftus SK, Mackem S, Yang Y, Pavan WJ, Biesecker LG. The pleiotropic mouse phenotype extra-toes spotting is caused by translation initiation factor Eif3c mutations and is associated with disrupted sonic hedgehog signaling. Faseb Journal : Official Publication of the Federation of American Societies For Experimental Biology. 25: 1596-605. PMID 21292980 DOI: 10.1096/Fj.10-169771 |
0.28 |
|
2011 |
Gildea DE, Luetkemeier ES, Bao X, Loftus SK, Mackem S, Yang Y, Pavan WJ, Biesecker LG. The pleiotropic mouse phenotype extra-toes spotting is caused by translation initiation factor Eif3c mutations and is associated with disrupted sonic hedgehog signaling. Faseb Journal : Official Publication of the Federation of American Societies For Experimental Biology. 25: 1596-605. PMID 21292980 DOI: 10.1096/Fj.10-169771 |
0.28 |
|
1997 |
Mishra L, Tully RE, Monga SP, Yu P, Cai T, Makalowski W, Mezey E, Pavan WJ, Mishra B. Praja1, a novel gene encoding a RING-H2 motif in mouse development. Oncogene. 15: 2361-8. PMID 9393880 DOI: 10.1038/sj.onc.1201405 |
0.279 |
|
2003 |
Rao C, Foernzler D, Loftus SK, Liu S, McPherson JD, Jungers KA, Apte SS, Pavan WJ, Beier DR. A defect in a novel ADAMTS family member is the cause of the belted white-spotting mutation. Development (Cambridge, England). 130: 4665-72. PMID 12925592 DOI: 10.1242/Dev.00668 |
0.277 |
|
2008 |
Hou L, Pavan WJ. Transcriptional and signaling regulation in neural crest stem cell-derived melanocyte development: do all roads lead to Mitf? Cell Research. 18: 1163-76. PMID 19002157 DOI: 10.1038/cr.2008.303 |
0.276 |
|
2008 |
Hou L, Pavan WJ. Transcriptional and signaling regulation in neural crest stem cell-derived melanocyte development: do all roads lead to Mitf? Cell Research. 18: 1163-76. PMID 19002157 DOI: 10.1038/cr.2008.303 |
0.276 |
|
2014 |
Harmacek L, Watkins-Chow DE, Chen J, Jones KL, Pavan WJ, Salbaum JM, Niswander L. A unique missense allele of BAF155, a core BAF chromatin remodeling complex protein, causes neural tube closure defects in mice. Developmental Neurobiology. 74: 483-97. PMID 24170322 DOI: 10.1002/Dneu.22142 |
0.276 |
|
2014 |
Harmacek L, Watkins-Chow DE, Chen J, Jones KL, Pavan WJ, Salbaum JM, Niswander L. A unique missense allele of BAF155, a core BAF chromatin remodeling complex protein, causes neural tube closure defects in mice. Developmental Neurobiology. 74: 483-97. PMID 24170322 DOI: 10.1002/Dneu.22142 |
0.276 |
|
2001 |
Loftus SK, Larson DM, Watkins-Chow D, Church DM, Pavan WJ. Generation of RCAS vectors useful for functional genomic analyses. Dna Research : An International Journal For Rapid Publication of Reports On Genes and Genomes. 8: 221-6. PMID 11759842 DOI: 10.1093/DNARES/8.5.221 |
0.275 |
|
2016 |
Chandler RJ, Williams IM, Gibson AL, Davidson CD, Incao AA, Hubbard BT, Porter FD, Pavan WJ, Venditti CP. Systemic AAV9 gene therapy improves the lifespan of mice with Niemann-Pick disease, type C1. Human Molecular Genetics. PMID 27798114 DOI: 10.1093/Hmg/Ddw367 |
0.269 |
|
2016 |
Chandler RJ, Williams IM, Gibson AL, Davidson CD, Incao AA, Hubbard BT, Porter FD, Pavan WJ, Venditti CP. Systemic AAV9 gene therapy improves the lifespan of mice with Niemann-Pick disease, type C1. Human Molecular Genetics. PMID 27798114 DOI: 10.1093/Hmg/Ddw367 |
0.269 |
|
2009 |
Buac K, Xu M, Cronin J, Weeraratna AT, Hewitt SM, Pavan WJ. NRG1 / ERBB3 signaling in melanocyte development and melanoma: inhibition of differentiation and promotion of proliferation. Pigment Cell & Melanoma Research. 22: 773-84. PMID 19659570 DOI: 10.1111/j.1755-148X.2009.00616.x |
0.268 |
|
2009 |
Buac K, Xu M, Cronin J, Weeraratna AT, Hewitt SM, Pavan WJ. NRG1 / ERBB3 signaling in melanocyte development and melanoma: inhibition of differentiation and promotion of proliferation. Pigment Cell & Melanoma Research. 22: 773-84. PMID 19659570 DOI: 10.1111/j.1755-148X.2009.00616.x |
0.268 |
|
2008 |
Silver DL, Hou L, Somerville R, Young ME, Apte SS, Pavan WJ. The secreted metalloprotease ADAMTS20 is required for melanoblast survival. Plos Genetics. 4: e1000003. PMID 18454205 DOI: 10.1371/Journal.Pgen.1000003 |
0.267 |
|
2008 |
Silver DL, Hou L, Somerville R, Young ME, Apte SS, Pavan WJ. The secreted metalloprotease ADAMTS20 is required for melanoblast survival. Plos Genetics. 4: e1000003. PMID 18454205 DOI: 10.1371/Journal.Pgen.1000003 |
0.267 |
|
2015 |
Efthymiou AG, Steiner J, Pavan WJ, Wincovitch S, Larson DM, Porter FD, Rao MS, Malik N. Rescue of an in vitro neuron phenotype identified in Niemann-Pick disease, type C1 induced pluripotent stem cell-derived neurons by modulating the WNT pathway and calcium signaling. Stem Cells Translational Medicine. 4: 230-8. PMID 25637190 DOI: 10.5966/sctm.2014-0127 |
0.267 |
|
2015 |
Efthymiou AG, Steiner J, Pavan WJ, Wincovitch S, Larson DM, Porter FD, Rao MS, Malik N. Rescue of an in vitro neuron phenotype identified in Niemann-Pick disease, type C1 induced pluripotent stem cell-derived neurons by modulating the WNT pathway and calcium signaling. Stem Cells Translational Medicine. 4: 230-8. PMID 25637190 DOI: 10.5966/sctm.2014-0127 |
0.267 |
|
2012 |
Gorkin DU, Lee D, Reed X, Fletez-Brant C, Bessling SL, Loftus SK, Beer MA, Pavan WJ, McCallion AS. Integration of ChIP-seq and machine learning reveals enhancers and a predictive regulatory sequence vocabulary in melanocytes. Genome Research. 22: 2290-301. PMID 23019145 DOI: 10.1101/Gr.139360.112 |
0.265 |
|
2012 |
Gorkin DU, Lee D, Reed X, Fletez-Brant C, Bessling SL, Loftus SK, Beer MA, Pavan WJ, McCallion AS. Integration of ChIP-seq and machine learning reveals enhancers and a predictive regulatory sequence vocabulary in melanocytes. Genome Research. 22: 2290-301. PMID 23019145 DOI: 10.1101/Gr.139360.112 |
0.265 |
|
2002 |
Loftus SK, Erickson RP, Walkley SU, Bryant MA, Incao A, Heidenreich RA, Pavan WJ. Rescue of neurodegeneration in Niemann-Pick C mice by a prion-promoter-driven Npc1 cDNA transgene. Human Molecular Genetics. 11: 3107-14. PMID 12417532 DOI: 10.1093/Hmg/11.24.3107 |
0.264 |
|
2011 |
Prasad MK, Reed X, Gorkin DU, Cronin JC, McAdow AR, Chain K, Hodonsky CJ, Jones EA, Svaren J, Antonellis A, Johnson SL, Loftus SK, Pavan WJ, McCallion AS. SOX10 directly modulates ERBB3 transcription via an intronic neural crest enhancer. Bmc Developmental Biology. 11: 40. PMID 21672228 DOI: 10.1186/1471-213X-11-40 |
0.259 |
|
2011 |
Prasad MK, Reed X, Gorkin DU, Cronin JC, McAdow AR, Chain K, Hodonsky CJ, Jones EA, Svaren J, Antonellis A, Johnson SL, Loftus SK, Pavan WJ, McCallion AS. SOX10 directly modulates ERBB3 transcription via an intronic neural crest enhancer. Bmc Developmental Biology. 11: 40. PMID 21672228 DOI: 10.1186/1471-213X-11-40 |
0.259 |
|
1994 |
Pavan WJ, Tilghman SM. Piebald lethal (sl) acts early to disrupt the development of neural crest-derived melanocytes Proceedings of the National Academy of Sciences of the United States of America. 91: 7159-7163. PMID 8041763 |
0.256 |
|
2018 |
Harris ML, Fufa TD, Palmer JW, Joshi SS, Larson DM, Incao A, Gildea DE, Trivedi NS, Lee AN, Day CP, Michael HT, Hornyak TJ, Merlino G, Pavan WJ. A direct link between MITF, innate immunity, and hair graying. Plos Biology. 16: e2003648. PMID 29723194 DOI: 10.1371/journal.pbio.2003648 |
0.25 |
|
2018 |
Harris ML, Fufa TD, Palmer JW, Joshi SS, Larson DM, Incao A, Gildea DE, Trivedi NS, Lee AN, Day CP, Michael HT, Hornyak TJ, Merlino G, Pavan WJ. A direct link between MITF, innate immunity, and hair graying. Plos Biology. 16: e2003648. PMID 29723194 DOI: 10.1371/journal.pbio.2003648 |
0.25 |
|
2006 |
Riazuddin S, Khan SN, Ahmed ZM, Ghosh M, Caution K, Nazli S, Kabra M, Zafar AU, Chen K, Naz S, Antonellis A, Pavan WJ, Green ED, Wilcox ER, Friedman PL, et al. Mutations in TRIOBP, which encodes a putative cytoskeletal-organizing protein, are associated with nonsyndromic recessive deafness. American Journal of Human Genetics. 78: 137-43. PMID 16385457 DOI: 10.1086/499164 |
0.247 |
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2012 |
Xu M, Liu K, Swaroop M, Porter FD, Sidhu R, Firnkes S, Finkes S, Ory DS, Marugan JJ, Xiao J, Southall N, Pavan WJ, Davidson C, Walkley SU, Remaley AT, et al. δ-Tocopherol reduces lipid accumulation in Niemann-Pick type C1 and Wolman cholesterol storage disorders. The Journal of Biological Chemistry. 287: 39349-60. PMID 23035117 DOI: 10.1074/Jbc.M112.357707 |
0.246 |
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2012 |
Xu M, Liu K, Swaroop M, Porter FD, Sidhu R, Firnkes S, Finkes S, Ory DS, Marugan JJ, Xiao J, Southall N, Pavan WJ, Davidson C, Walkley SU, Remaley AT, et al. δ-Tocopherol reduces lipid accumulation in Niemann-Pick type C1 and Wolman cholesterol storage disorders. The Journal of Biological Chemistry. 287: 39349-60. PMID 23035117 DOI: 10.1074/Jbc.M112.357707 |
0.246 |
|
2013 |
Harris ML, Buac K, Shakhova O, Hakami RM, Wegner M, Sommer L, Pavan WJ. A dual role for SOX10 in the maintenance of the postnatal melanocyte lineage and the differentiation of melanocyte stem cell progenitors. Plos Genetics. 9: e1003644. PMID 23935512 DOI: 10.1371/journal.pgen.1003644 |
0.243 |
|
2013 |
Harris ML, Buac K, Shakhova O, Hakami RM, Wegner M, Sommer L, Pavan WJ. A dual role for SOX10 in the maintenance of the postnatal melanocyte lineage and the differentiation of melanocyte stem cell progenitors. Plos Genetics. 9: e1003644. PMID 23935512 DOI: 10.1371/journal.pgen.1003644 |
0.243 |
|
2009 |
Stine ZE, Huynh JL, Loftus SK, Gorkin DU, Salmasi AH, Novak T, Purves T, Miller RA, Antonellis A, Gearhart JP, Pavan WJ, McCallion AS. Oligodendroglial and pan-neural crest expression of Cre recombinase directed by Sox10 enhancer. Genesis (New York, N.Y. : 2000). 47: 765-70. PMID 19830815 DOI: 10.1002/Dvg.20559 |
0.241 |
|
2009 |
Stine ZE, Huynh JL, Loftus SK, Gorkin DU, Salmasi AH, Novak T, Purves T, Miller RA, Antonellis A, Gearhart JP, Pavan WJ, McCallion AS. Oligodendroglial and pan-neural crest expression of Cre recombinase directed by Sox10 enhancer. Genesis (New York, N.Y. : 2000). 47: 765-70. PMID 19830815 DOI: 10.1002/Dvg.20559 |
0.241 |
|
2011 |
Whiteman DC, Pavan WJ, Bastian BC. The melanomas: a synthesis of epidemiological, clinical, histopathological, genetic, and biological aspects, supporting distinct subtypes, causal pathways, and cells of origin. Pigment Cell & Melanoma Research. 24: 879-97. PMID 21707960 DOI: 10.1111/j.1755-148X.2011.00880.x |
0.241 |
|
2011 |
Whiteman DC, Pavan WJ, Bastian BC. The melanomas: a synthesis of epidemiological, clinical, histopathological, genetic, and biological aspects, supporting distinct subtypes, causal pathways, and cells of origin. Pigment Cell & Melanoma Research. 24: 879-97. PMID 21707960 DOI: 10.1111/j.1755-148X.2011.00880.x |
0.241 |
|
1995 |
Pavan WJ, Mac S, Cheng M, Tilghman SM. Quantitative trait loci that modify the severity of spotting in piebald mice Genome Research. 5: 29-41. PMID 8717053 DOI: 10.1101/gr.5.1.29 |
0.239 |
|
2019 |
Pavan WJ, Sturm RA. The Genetics of Human Skin and Hair Pigmentation. Annual Review of Genomics and Human Genetics. PMID 31100995 DOI: 10.1146/annurev-genom-083118-015230 |
0.239 |
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2019 |
Pavan WJ, Sturm RA. The Genetics of Human Skin and Hair Pigmentation. Annual Review of Genomics and Human Genetics. PMID 31100995 DOI: 10.1146/annurev-genom-083118-015230 |
0.239 |
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2005 |
Carninci P, Kasukawa T, Katayama S, Gough J, Frith MC, Maeda N, Oyama R, Ravasi T, Lenhard B, Wells C, Kodzius R, Shimokawa K, Bajic VB, Brenner SE, Batalov S, ... ... Pavan WJ, et al. The transcriptional landscape of the mammalian genome. Science (New York, N.Y.). 309: 1559-63. PMID 16141072 DOI: 10.1126/Science.1112014 |
0.234 |
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1998 |
Opdecamp K, Kos L, Arnheiter H, Pavan WJ. Endothelin signalling in the development of neural crest-derived melanocytes Biochemistry and Cell Biology. 76: 1093-1099. DOI: 10.1139/O99-006 |
0.232 |
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2012 |
Pavan WJ, Raible DW. Specification of neural crest into sensory neuron and melanocyte lineages. Developmental Biology. 366: 55-63. PMID 22465373 DOI: 10.1016/J.Ydbio.2012.02.038 |
0.231 |
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2012 |
Pavan WJ, Raible DW. Specification of neural crest into sensory neuron and melanocyte lineages. Developmental Biology. 366: 55-63. PMID 22465373 DOI: 10.1016/J.Ydbio.2012.02.038 |
0.231 |
|
2018 |
Tseng WC, Loeb HE, Pei W, Tsai-Morris CH, Xu L, Cluzeau CV, Wassif CA, Feldman B, Burgess SM, Pavan WJ, Porter FD. Modeling Niemann-Pick disease type C1 in zebrafish: a robust platform for screening of candidate therapeutic compounds. Disease Models & Mechanisms. 11. PMID 30135069 DOI: 10.1242/dmm.034165 |
0.23 |
|
2018 |
Tseng WC, Loeb HE, Pei W, Tsai-Morris CH, Xu L, Cluzeau CV, Wassif CA, Feldman B, Burgess SM, Pavan WJ, Porter FD. Modeling Niemann-Pick disease type C1 in zebrafish: a robust platform for screening of candidate therapeutic compounds. Disease Models & Mechanisms. 11. PMID 30135069 DOI: 10.1242/dmm.034165 |
0.23 |
|
2023 |
Aman AJ, Saunders LM, Carr AA, Srivatasan S, Eberhard C, Carrington B, Watkins-Chow D, Pavan WJ, Trapnell C, Parichy DM. Transcriptomic profiling of tissue environments critical for post-embryonic patterning and morphogenesis of zebrafish skin. Elife. 12. PMID 37695017 DOI: 10.7554/eLife.86670 |
0.229 |
|
2008 |
Watkins-Chow DE, Pavan WJ. Genomic copy number and expression variation within the C57BL/6J inbred mouse strain. Genome Research. 18: 60-6. PMID 18032724 DOI: 10.1101/gr.6927808 |
0.228 |
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2008 |
Watkins-Chow DE, Pavan WJ. Genomic copy number and expression variation within the C57BL/6J inbred mouse strain. Genome Research. 18: 60-6. PMID 18032724 DOI: 10.1101/gr.6927808 |
0.228 |
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2016 |
Westbroek W, Nguyen M, Siebert M, Lindstrom T, Burnett RA, Aflaki E, Jung O, Tamargo R, Rodriguez-Gil JL, Acosta W, Hendrix A, Behre B, Tayebi N, Fujiwara H, Sidhu R, ... ... Pavan WJ, et al. A new glucocerebrosidase-deficient neuronal cell model provides a tool to probe pathophysiology and therapeutics for Gaucher disease. Disease Models & Mechanisms. 9: 769-778. PMID 27482815 DOI: 10.1242/Dmm.024588 |
0.227 |
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2016 |
Westbroek W, Nguyen M, Siebert M, Lindstrom T, Burnett RA, Aflaki E, Jung O, Tamargo R, Rodriguez-Gil JL, Acosta W, Hendrix A, Behre B, Tayebi N, Fujiwara H, Sidhu R, ... ... Pavan WJ, et al. A new glucocerebrosidase-deficient neuronal cell model provides a tool to probe pathophysiology and therapeutics for Gaucher disease. Disease Models & Mechanisms. 9: 769-778. PMID 27482815 DOI: 10.1242/Dmm.024588 |
0.227 |
|
2023 |
Watkins-Chow DE, Incao AA, Rivas C, Elliott G, Garrett LJ, Pavan WJ. The MFSD12 p.Tyr182His common variant is sufficient to alter mouse agouti coat color. Pigment Cell & Melanoma Research. PMID 37874775 DOI: 10.1111/pcmr.13144 |
0.226 |
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2016 |
Francis KR, Ton AN, Xin Y, O'Halloran PE, Wassif CA, Malik N, Williams IM, Cluzeau CV, Trivedi NS, Pavan WJ, Cho W, Westphal H, Porter FD. Modeling Smith-Lemli-Opitz syndrome with induced pluripotent stem cells reveals a causal role for Wnt/β-catenin defects in neuronal cholesterol synthesis phenotypes. Nature Medicine. PMID 26998835 DOI: 10.1038/Nm.4067 |
0.223 |
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2016 |
Francis KR, Ton AN, Xin Y, O'Halloran PE, Wassif CA, Malik N, Williams IM, Cluzeau CV, Trivedi NS, Pavan WJ, Cho W, Westphal H, Porter FD. Modeling Smith-Lemli-Opitz syndrome with induced pluripotent stem cells reveals a causal role for Wnt/β-catenin defects in neuronal cholesterol synthesis phenotypes. Nature Medicine. PMID 26998835 DOI: 10.1038/Nm.4067 |
0.223 |
|
1990 |
Pavan WJ, Hieter P, Reeves RH. Modification and transfer into an embryonal carcinoma cell line of a 360-kilobase human-derived yeast artificial chromosome. Molecular and Cellular Biology. 10: 4163-4169. DOI: 10.1128/MCB.10.8.4163 |
0.219 |
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2015 |
Harris ML, Levy DJ, Watkins-Chow DE, Pavan WJ. Ectopic differentiation of melanocyte stem cells is influenced by genetic background. Pigment Cell & Melanoma Research. 28: 223-8. PMID 25495036 DOI: 10.1111/pcmr.12344 |
0.219 |
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2015 |
Harris ML, Levy DJ, Watkins-Chow DE, Pavan WJ. Ectopic differentiation of melanocyte stem cells is influenced by genetic background. Pigment Cell & Melanoma Research. 28: 223-8. PMID 25495036 DOI: 10.1111/pcmr.12344 |
0.219 |
|
2002 |
Okazaki Y, Furuno M, Kasukawa T, Adachi J, Bono H, Kondo S, Nikaido I, Osato N, Saito R, Suzuki H, Yamanaka I, Kiyosawa H, Yagi K, Tomaru Y, Hasegawa Y, ... ... Pavan WJ, et al. Analysis of the mouse transcriptome based on functional annotation of 60,770 full-length cDNAs. Nature. 420: 563-73. PMID 12466851 DOI: 10.1038/Nature01266 |
0.212 |
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2016 |
Nicoli ER, Al Eisa N, Cluzeau CV, Wassif CA, Gray J, Burkert KR, Smith DA, Morris L, Cologna SM, Peer CJ, Sissung TM, Uscatu CD, Figg WD, Pavan WJ, Vite CH, et al. Defective Cytochrome P450-Catalysed Drug Metabolism in Niemann-Pick Type C Disease. Plos One. 11: e0152007. PMID 27019000 DOI: 10.1371/Journal.Pone.0152007 |
0.209 |
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2016 |
Nicoli ER, Al Eisa N, Cluzeau CV, Wassif CA, Gray J, Burkert KR, Smith DA, Morris L, Cologna SM, Peer CJ, Sissung TM, Uscatu CD, Figg WD, Pavan WJ, Vite CH, et al. Defective Cytochrome P450-Catalysed Drug Metabolism in Niemann-Pick Type C Disease. Plos One. 11: e0152007. PMID 27019000 DOI: 10.1371/Journal.Pone.0152007 |
0.209 |
|
1999 |
Kos L, Aronzon A, Takayama H, Maina F, Ponzetto C, Merlino G, Pavan W. Hepatocyte growth factor/scatter factor-MET signaling in neural crest-derived melanocyte development. Pigment Cell Research / Sponsored by the European Society For Pigment Cell Research and the International Pigment Cell Society. 12: 13-21. PMID 10193678 DOI: 10.1111/j.1600-0749.1999.tb00503.x |
0.209 |
|
1997 |
Carstea ED, Morris JA, Coleman KG, Loftus SK, Zhang D, Cummings C, Gu J, Rosenfeld MA, Pavan WJ, Krizman DB, Nagle J, Polymeropoulos MH, Sturley SL, Ioannou YA, Higgins ME, et al. Niemann-Pick C1 disease gene: homology to mediators of cholesterol homeostasis. Science (New York, N.Y.). 277: 228-31. PMID 9211849 DOI: 10.1126/Science.277.5323.228 |
0.204 |
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2013 |
Rusmini M, Griseri P, Lantieri F, Matera I, Hudspeth KL, Roberto A, Mikulak J, Avanzini S, Rossi V, Mattioli G, Jasonni V, Ravazzolo R, Pavan WJ, Pini-Prato A, Ceccherini I, et al. Induction of RET dependent and independent pro-inflammatory programs in human peripheral blood mononuclear cells from Hirschsprung patients. Plos One. 8: e59066. PMID 23527089 DOI: 10.1371/journal.pone.0059066 |
0.203 |
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2013 |
Rusmini M, Griseri P, Lantieri F, Matera I, Hudspeth KL, Roberto A, Mikulak J, Avanzini S, Rossi V, Mattioli G, Jasonni V, Ravazzolo R, Pavan WJ, Pini-Prato A, Ceccherini I, et al. Induction of RET dependent and independent pro-inflammatory programs in human peripheral blood mononuclear cells from Hirschsprung patients. Plos One. 8: e59066. PMID 23527089 DOI: 10.1371/journal.pone.0059066 |
0.203 |
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2019 |
Cougnoux A, Fellmeth M, Gu T, Davidson CD, Gibson AL, Pavan WJ, Porter FD. Maternal immune activation modifies the course of Niemann-pick disease, type C1 in a gender specific manner. Molecular Genetics and Metabolism. PMID 31668555 DOI: 10.1016/j.ymgme.2019.10.004 |
0.197 |
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2000 |
Pavan WJ. “Neural crest mutants: Microarrays, gut manifestations-a moving story’ Gastroenterology. 118: A1072. DOI: 10.1016/S0016-5085(00)80084-0 |
0.195 |
|
2000 |
Rhim H, Dunn KJ, Aronzon A, Susanna M, Cheng M, Lamoreux ML, Tilghman SM, Pavan WJ. Spatially restricted hypopigmentation associated with an Ednrb(s)-modifying locus on mouse chromosome 10 Genome Research. 10: 17-29. PMID 10645946 |
0.195 |
|
2005 |
Dunn KJ, Brady M, Ochsenbauer-Jambor C, Snyder S, Incao A, Pavan WJ. WNT1 and WNT3a promote expansion of melanocytes through distinct modes of action. Pigment Cell Research. 18: 167-80. PMID 15892713 DOI: 10.1111/j.1600-0749.2005.00226.x |
0.194 |
|
2013 |
Rodriguez-Gil JL, Larson DM, Wassif CA, Yanjanin NM, Anderson SM, Kirby MR, Trivedi NS, Porter FD, Pavan WJ. A somatic cell defect is associated with the onset of neurological symptoms in a lysosomal storage disease. Molecular Genetics and Metabolism. 110: 188-90. PMID 23850077 DOI: 10.1016/j.ymgme.2013.06.010 |
0.194 |
|
2013 |
Rodriguez-Gil JL, Larson DM, Wassif CA, Yanjanin NM, Anderson SM, Kirby MR, Trivedi NS, Porter FD, Pavan WJ. A somatic cell defect is associated with the onset of neurological symptoms in a lysosomal storage disease. Molecular Genetics and Metabolism. 110: 188-90. PMID 23850077 DOI: 10.1016/j.ymgme.2013.06.010 |
0.194 |
|
2018 |
Davidson C, Gibson A, Gu T, Chandler R, Deverman B, Gradinaru V, Venditti C, Pavan W. Gene therapy for the treatment of Niemann-Pick disease type C1: Comparison of AAV9 to a novel serotype, AAV-PHP.B Molecular Genetics and Metabolism. 123: S36-S37. DOI: 10.1016/J.Ymgme.2017.12.075 |
0.192 |
|
1997 |
Gu JZ, Carstea ED, Cummings C, Morris JA, Loftus SK, Zhang D, Coleman KG, Cooney AM, Comly ME, Fandino L, Roff C, Tagle DA, Pavan WJ, Pentchev PG, Rosenfeld MA. Substantial narrowing of the Niemann-Pick C candidate interval by yeast artificial chromosome complementation. Proceedings of the National Academy of Sciences of the United States of America. 94: 7378-83. PMID 9207099 DOI: 10.1073/PNAS.94.14.7378 |
0.189 |
|
2016 |
Watkins-Chow DE, Varshney GK, Garrett LJ, Chen Z, Jimenez EA, Rivas C, Bishop KS, Sood R, Harper UL, Pavan WJ, Burgess SM. Highly-Efficient Cpf1-Mediated Gene Targeting in Mice Following High Concentration Pronuclear Injection. G3 (Bethesda, Md.). PMID 28040780 DOI: 10.1534/g3.116.038091 |
0.188 |
|
2016 |
Watkins-Chow DE, Varshney GK, Garrett LJ, Chen Z, Jimenez EA, Rivas C, Bishop KS, Sood R, Harper UL, Pavan WJ, Burgess SM. Highly-Efficient Cpf1-Mediated Gene Targeting in Mice Following High Concentration Pronuclear Injection. G3 (Bethesda, Md.). PMID 28040780 DOI: 10.1534/g3.116.038091 |
0.188 |
|
2014 |
Ottinger EA, Kao ML, Carrillo-Carrasco N, Yanjanin N, Shankar RK, Janssen M, Brewster M, Scott I, Xu X, Cradock J, Terse P, Dehdashti SJ, Marugan J, Zheng W, Portilla L, ... ... Pavan WJ, et al. Collaborative development of 2-hydroxypropyl-β-cyclodextrin for the treatment of Niemann-Pick type C1 disease. Current Topics in Medicinal Chemistry. 14: 330-9. PMID 24283970 DOI: 10.2174/1568026613666131127160118 |
0.185 |
|
2014 |
Ottinger EA, Kao ML, Carrillo-Carrasco N, Yanjanin N, Shankar RK, Janssen M, Brewster M, Scott I, Xu X, Cradock J, Terse P, Dehdashti SJ, Marugan J, Zheng W, Portilla L, ... ... Pavan WJ, et al. Collaborative development of 2-hydroxypropyl-β-cyclodextrin for the treatment of Niemann-Pick type C1 disease. Current Topics in Medicinal Chemistry. 14: 330-9. PMID 24283970 DOI: 10.2174/1568026613666131127160118 |
0.185 |
|
2003 |
Carninci P, Waki K, Shiraki T, Konno H, Shibata K, Itoh M, Aizawa K, Arakawa T, Ishii Y, Sasaki D, Bono H, Kondo S, Sugahara Y, Saito R, Osato N, ... ... Pavan W, et al. Targeting a complex transcriptome: the construction of the mouse full-length cDNA encyclopedia. Genome Research. 13: 1273-89. PMID 12819125 DOI: 10.1101/Gr.1119703 |
0.185 |
|
2003 |
Carninci P, Waki K, Shiraki T, Konno H, Shibata K, Itoh M, Aizawa K, Arakawa T, Ishii Y, Sasaki D, Bono H, Kondo S, Sugahara Y, Saito R, Osato N, ... ... Pavan W, et al. Targeting a complex transcriptome: the construction of the mouse full-length cDNA encyclopedia. Genome Research. 13: 1273-89. PMID 12819125 DOI: 10.1101/Gr.1119703 |
0.185 |
|
2007 |
Buac K, Pavan WJ. Stem cells of the melanocyte lineage. Cancer Biomarkers : Section a of Disease Markers. 3: 203-9. PMID 17917150 DOI: 10.3233/cbm-2007-34-505 |
0.182 |
|
2007 |
Buac K, Pavan WJ. Stem cells of the melanocyte lineage. Cancer Biomarkers : Section a of Disease Markers. 3: 203-9. PMID 17917150 DOI: 10.3233/cbm-2007-34-505 |
0.182 |
|
2010 |
Silver DL, Watkins-Chow DE, Schreck KC, Pierfelice TJ, Larson DM, Burnetti AJ, Liaw HJ, Myung K, Walsh CA, Gaiano N, Pavan WJ. The exon junction complex component Magoh controls brain size by regulating neural stem cell division. Nature Neuroscience. 13: 551-8. PMID 20364144 DOI: 10.1038/Nn.2527 |
0.176 |
|
2010 |
Silver DL, Watkins-Chow DE, Schreck KC, Pierfelice TJ, Larson DM, Burnetti AJ, Liaw HJ, Myung K, Walsh CA, Gaiano N, Pavan WJ. The exon junction complex component Magoh controls brain size by regulating neural stem cell division. Nature Neuroscience. 13: 551-8. PMID 20364144 DOI: 10.1038/Nn.2527 |
0.176 |
|
1999 |
Southard-Smith EM, Collins JE, Ellison JS, Smith KJ, Baxevanis AD, Touchman JW, Green ED, Dunham I, Pavan WJ. Comparative analyses of the Dominant megacolon-SOX10 genomic interval in mouse and human. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 10: 744-9. PMID 10384052 DOI: 10.1007/S003359901083 |
0.172 |
|
2019 |
Lona-Durazo F, Hernandez-Pacheco N, Fan S, Zhang T, Choi J, Kovacs MA, Loftus SK, Le P, Edwards M, Fortes-Lima CA, Eng C, Huntsman S, Hu D, Gómez-Cabezas EJ, Marín-Padrón LC, ... ... Pavan WJ, et al. Meta-analysis of GWA studies provides new insights on the genetic architecture of skin pigmentation in recently admixed populations. Bmc Genetics. 20: 59. PMID 31315583 DOI: 10.1186/S12863-019-0765-5 |
0.171 |
|
2019 |
Lona-Durazo F, Hernandez-Pacheco N, Fan S, Zhang T, Choi J, Kovacs MA, Loftus SK, Le P, Edwards M, Fortes-Lima CA, Eng C, Huntsman S, Hu D, Gómez-Cabezas EJ, Marín-Padrón LC, ... ... Pavan WJ, et al. Meta-analysis of GWA studies provides new insights on the genetic architecture of skin pigmentation in recently admixed populations. Bmc Genetics. 20: 59. PMID 31315583 DOI: 10.1186/S12863-019-0765-5 |
0.171 |
|
1999 |
Khan J, Bittner ML, Chen Y, Faller AJ, Saal LH, Azorsa DA, Teichman U, Pavan W, Trent JM, Meltzer PS. Elucidation of the Downstream Targets of the PAX3-FKHR Fusion Oncogene Found in Aveolar Rhabdomyosarcoma Using cDNA Microarrays Pediatric Research. 45: 148A-148A. DOI: 10.1203/00006450-199904020-00880 |
0.162 |
|
2016 |
Ibiza S, García-Cassani B, Ribeiro H, Carvalho T, Almeida L, Marques R, Misic AM, Bartow-McKenney C, Larson DM, Pavan WJ, Eberl G, Grice EA, Veiga-Fernandes H. Glial-cell-derived neuroregulators control type 3 innate lymphoid cells and gut defence. Nature. PMID 27409807 DOI: 10.1038/Nature18644 |
0.155 |
|
2016 |
Ibiza S, García-Cassani B, Ribeiro H, Carvalho T, Almeida L, Marques R, Misic AM, Bartow-McKenney C, Larson DM, Pavan WJ, Eberl G, Grice EA, Veiga-Fernandes H. Glial-cell-derived neuroregulators control type 3 innate lymphoid cells and gut defence. Nature. PMID 27409807 DOI: 10.1038/Nature18644 |
0.155 |
|
2017 |
Ory DS, Ottinger EA, Farhat NY, King KA, Jiang X, Weissfeld L, Berry-Kravis E, Davidson CD, Bianconi S, Keener LA, Rao R, Soldatos A, Sidhu R, Walters KA, Xu X, ... ... Pavan WJ, et al. Intrathecal 2-hydroxypropyl-β-cyclodextrin decreases neurological disease progression in Niemann-Pick disease, type C1: a non-randomised, open-label, phase 1-2 trial. Lancet (London, England). PMID 28803710 DOI: 10.1016/S0140-6736(17)31465-4 |
0.149 |
|
2017 |
Ory DS, Ottinger EA, Farhat NY, King KA, Jiang X, Weissfeld L, Berry-Kravis E, Davidson CD, Bianconi S, Keener LA, Rao R, Soldatos A, Sidhu R, Walters KA, Xu X, ... ... Pavan WJ, et al. Intrathecal 2-hydroxypropyl-β-cyclodextrin decreases neurological disease progression in Niemann-Pick disease, type C1: a non-randomised, open-label, phase 1-2 trial. Lancet (London, England). PMID 28803710 DOI: 10.1016/S0140-6736(17)31465-4 |
0.149 |
|
2008 |
Gemmill RM, Bolin R, Strauss WM, Pavan W. Purification and characterization of YACs containing large inserts. Current Protocols in Human Genetics. Unit 5.7. PMID 18428294 DOI: 10.1002/0471142905.hg0507s00 |
0.141 |
|
1998 |
Rhim H, Savagner P, Thibaudeau G, Thiery JP, Pavan WJ. Localization of a neural crest transcription factor, Slug, to mouse chromosome 16 and human chromosome 8. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 8: 872-3. PMID 9337409 DOI: 10.1007/S003359900601 |
0.141 |
|
2010 |
Hwang HW, Pavan WJ. Melanocytes don't always take the high road. Pigment Cell & Melanoma Research. 23: 11-3. PMID 20025712 DOI: 10.1111/J.1755-148X.2009.00665.X |
0.139 |
|
2010 |
Hwang HW, Pavan WJ. Melanocytes don't always take the high road. Pigment Cell & Melanoma Research. 23: 11-3. PMID 20025712 DOI: 10.1111/J.1755-148X.2009.00665.X |
0.139 |
|
1996 |
Pavan WJ. Genetic Mapping in the Mouse Current Protocols in Human Genetics. 9. DOI: 10.1002/0471142905.hg0101s09 |
0.131 |
|
1999 |
Khan J, Bittner ML, Saal LH, Faller AJ, Teichmann U, Azorsa DO, Gooden GC, Pavan WJ, Trent JM, Meltzer PS. cDNA microarrays detect activation of a myogenic transcription program by the PAX3-FKHR fusion oncogene Nature Genetics. 23: 55-55. DOI: 10.1038/14339 |
0.125 |
|
2020 |
Green ED, Gunter C, Biesecker LG, Di Francesco V, Easter CL, Feingold EA, Felsenfeld AL, Kaufman DJ, Ostrander EA, Pavan WJ, Phillippy AM, Wise AL, Dayal JG, Kish BJ, Mandich A, et al. Strategic vision for improving human health at The Forefront of Genomics. Nature. 586: 683-692. PMID 33116284 DOI: 10.1038/s41586-020-2817-4 |
0.124 |
|
2010 |
Yanjanin NM, Vélez JI, Gropman A, King K, Bianconi SE, Conley SK, Brewer CC, Solomon B, Pavan WJ, Arcos-Burgos M, Patterson MC, Porter FD. Linear clinical progression, independent of age of onset, in Niemann-Pick disease, type C. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 153: 132-40. PMID 19415691 DOI: 10.1002/ajmg.b.30969 |
0.122 |
|
2010 |
Yanjanin NM, Vélez JI, Gropman A, King K, Bianconi SE, Conley SK, Brewer CC, Solomon B, Pavan WJ, Arcos-Burgos M, Patterson MC, Porter FD. Linear clinical progression, independent of age of onset, in Niemann-Pick disease, type C. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 153: 132-40. PMID 19415691 DOI: 10.1002/ajmg.b.30969 |
0.122 |
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2008 |
Yanjanin N, Brewer C, King K, Pavan W, Gropman A, Patterson M, Porter F. 115. Disease progression in Niemann-Pick disease, type C: Longitudinal Molecular Genetics and Metabolism. 93: 44. DOI: 10.1016/J.YMGME.2007.10.127 |
0.117 |
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2019 |
Leachman SA, Hornyak TJ, Barsh G, Bastian BC, Brash DE, Cleaver JE, Cooper CD, D'Orazio JA, Fujita M, Holmen SL, Indra AK, Kramer KH, Le Poole IC, Lo RS, Lund AW, ... ... Pavan WJ, et al. Melanoma to Vitiligo: The Melanocyte in Biology & Medicine-Joint Montagna Symposium on the Biology of Skin/PanAmerican Society for Pigment Cell Research Annual Meeting. The Journal of Investigative Dermatology. PMID 31348921 DOI: 10.1016/J.Jid.2019.03.1164 |
0.116 |
|
2019 |
Leachman SA, Hornyak TJ, Barsh G, Bastian BC, Brash DE, Cleaver JE, Cooper CD, D'Orazio JA, Fujita M, Holmen SL, Indra AK, Kramer KH, Le Poole IC, Lo RS, Lund AW, ... ... Pavan WJ, et al. Melanoma to Vitiligo: The Melanocyte in Biology & Medicine-Joint Montagna Symposium on the Biology of Skin/PanAmerican Society for Pigment Cell Research Annual Meeting. The Journal of Investigative Dermatology. PMID 31348921 DOI: 10.1016/J.Jid.2019.03.1164 |
0.116 |
|
2010 |
Fu R, Yanjanin NM, Bianconi S, Pavan WJ, Porter FD. Oxidative stress in Niemann-Pick disease, type C. Molecular Genetics and Metabolism. 101: 214-8. PMID 20667755 DOI: 10.1016/j.ymgme.2010.06.018 |
0.113 |
|
2010 |
Fu R, Yanjanin NM, Bianconi S, Pavan WJ, Porter FD. Oxidative stress in Niemann-Pick disease, type C. Molecular Genetics and Metabolism. 101: 214-8. PMID 20667755 DOI: 10.1016/j.ymgme.2010.06.018 |
0.113 |
|
1999 |
Loftus S, Chen Y, Gooden G, Ryan J, Birznieks G, Hilliard M, Baxevanis A, Bittner M, Meltzer P, Trent J, Pavan W. Informatic selection of a neural crest-melanocyte cDNA set for microarray analysis Nature Genetics. 23: 59-59. DOI: 10.1038/14355 |
0.107 |
|
2019 |
Davidson C, Gibson A, Gu T, Ali N, Chandler R, Venditti C, Walkley SU, Pavan W. Improved disease amelioration with combination therapy for Niemann-Pick disease type C1 Molecular Genetics and Metabolism. 126: S46. DOI: 10.1016/J.Ymgme.2018.12.100 |
0.104 |
|
1997 |
Wright A, Kawakami Y, Pavan W. Mart1 is located on mouse Chromosome 19 and is excluded as a candidate for ep and ru Mammalian Genome. 8: 377-378. PMID 9107690 DOI: 10.1007/S003359900446 |
0.104 |
|
2006 |
Silver DL, Pavan WJ. The origin and development of neural crest-derived melanocytes From Melanocytes to Melanoma: the Progression to Malignancy. 3-26. DOI: 10.1007/978-1-59259-994-3_1 |
0.096 |
|
2015 |
Chen X, Bi Y, Wang T, Li P, Yan X, Hou S, Bammert CE, Ju J, Gibson KM, Pavan WJ, Bi L. Lysosomal targeting with stable and sensitive fluorescent probes (Superior LysoProbes): applications for lysosome labeling and tracking during apoptosis. Scientific Reports. 5: 9004. PMID 25758662 DOI: 10.1038/Srep09004 |
0.095 |
|
2015 |
Chen X, Bi Y, Wang T, Li P, Yan X, Hou S, Bammert CE, Ju J, Gibson KM, Pavan WJ, Bi L. Lysosomal targeting with stable and sensitive fluorescent probes (Superior LysoProbes): applications for lysosome labeling and tracking during apoptosis. Scientific Reports. 5: 9004. PMID 25758662 DOI: 10.1038/Srep09004 |
0.095 |
|
2015 |
Yapici NB, Bi Y, Li P, Chen X, Yan X, Mandalapu SR, Faucett M, Jockusch S, Ju J, Gibson KM, Pavan WJ, Bi L. Highly stable and sensitive fluorescent probes (LysoProbes) for lysosomal labeling and tracking. Scientific Reports. 5: 8576. PMID 25715948 DOI: 10.1038/Srep08576 |
0.094 |
|
2015 |
Yapici NB, Bi Y, Li P, Chen X, Yan X, Mandalapu SR, Faucett M, Jockusch S, Ju J, Gibson KM, Pavan WJ, Bi L. Highly stable and sensitive fluorescent probes (LysoProbes) for lysosomal labeling and tracking. Scientific Reports. 5: 8576. PMID 25715948 DOI: 10.1038/Srep08576 |
0.094 |
|
1998 |
Lenz O, Teichmann U, Langers A, Striker LJ, Striker GE, Pavan WJ. Linkage disequilibrium mapping reveals suppressed recombination at the Os locus Mammalian Genome. 9: 681-682. PMID 9680395 DOI: 10.1007/s003359900847 |
0.094 |
|
2013 |
Rusmini M, Griseri P, Lantieri F, Matera I, Hudspeth KL, Roberto A, Mikulak J, Avanzini S, Rossi V, Mattioli G, Jasonni V, Ravazzolo R, Pavan WJ, Pini-Prato A, Ceccherini I, et al. Correction: Induction of RET dependent and independent pro-inflammatory programs in human peripheral blood mononuclear cells from hirschsprung patients (PLoS ONE) Plos One. 8. DOI: 10.1371/annotation/d3a96ff5-2a66-4454-8d8d-932ad4cfe906 |
0.093 |
|
2019 |
Pini Prato A, Bartow-McKenney C, Hudspeth K, Mosconi M, Rossi V, Avanzini S, Faticato MG, Ceccherini I, Lantieri F, Mattioli G, Larson D, Pavan W, De Filippo C, Di Paola M, Mavilio D, et al. A Metagenomics Study on Hirschsprung's Disease Associated Enterocolitis: Biodiversity and Gut Microbial Homeostasis Depend on Resection Length and Patient's Clinical History. Frontiers in Pediatrics. 7: 326. PMID 31448249 DOI: 10.3389/fped.2019.00326 |
0.091 |
|
2019 |
Pini Prato A, Bartow-McKenney C, Hudspeth K, Mosconi M, Rossi V, Avanzini S, Faticato MG, Ceccherini I, Lantieri F, Mattioli G, Larson D, Pavan W, De Filippo C, Di Paola M, Mavilio D, et al. A Metagenomics Study on Hirschsprung's Disease Associated Enterocolitis: Biodiversity and Gut Microbial Homeostasis Depend on Resection Length and Patient's Clinical History. Frontiers in Pediatrics. 7: 326. PMID 31448249 DOI: 10.3389/fped.2019.00326 |
0.091 |
|
2013 |
Xu M, Liu K, Swaroop M, Porter FD, Sidhu R, Firnkes S, Ory DS, Marugan JJ, Xiao J, Southall N, Pavan WJ, Davidson C, Walkley SU, Remaley AT, Baxa U, et al. δ-Tocopherol reduces lipid accumulation in Niemann-Pick type C1 and Wolman cholesterol storage disorders (Journal of Biological Chemistry (2012) 287, (39349-39360)) Journal of Biological Chemistry. 288: 296. DOI: 10.1074/Jbc.A112.357707 |
0.086 |
|
2021 |
Marks MS, Pavan WJ. How a membrane transporter keeps melanocytes in the red. Pigment Cell & Melanoma Research. 34: 666-669. PMID 33750024 DOI: 10.1111/pcmr.12973 |
0.035 |
|
2021 |
Marks MS, Pavan WJ. How a membrane transporter keeps melanocytes in the red. Pigment Cell & Melanoma Research. 34: 666-669. PMID 33750024 DOI: 10.1111/pcmr.12973 |
0.035 |
|
2014 |
Fufa TD, Pavan WJ. Axing the cancer loop. Pigment Cell & Melanoma Research. 27: 691-3. PMID 24953508 DOI: 10.1111/pcmr.12286 |
0.021 |
|
2014 |
Fufa TD, Pavan WJ. Axing the cancer loop. Pigment Cell & Melanoma Research. 27: 691-3. PMID 24953508 DOI: 10.1111/pcmr.12286 |
0.021 |
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