☰

Laura L. Baxter - Publications

Affiliations: 
1995-2000 Physiology Johns Hopkins University School of Medicine, Baltimore, MD, United States 
Tree Info Similar researchers PubMed Report error

37 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
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  0.48
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  0.522
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  0.541
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  0.564
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  0.502
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  0.559
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  0.544
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  0.655
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  0.674
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  0.64
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  0.662
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, 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  0.661
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  0.645
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  0.66
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  0.657
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, 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  0.683
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  0.476
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  0.578
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  0.662
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  0.64
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  0.56
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  0.683
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, 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  0.535
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  0.693
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  0.653
2006 Roper RJ, Baxter LL, Saran NG, Klinedinst DK, Beachy PA, Reeves RH. Defective cerebellar response to mitogenic Hedgehog signaling in Down [corrected] syndrome mice. Proceedings of the National Academy of Sciences of the United States of America. 103: 1452-6. PMID 16432181 DOI: 10.1073/Pnas.0510750103  0.743
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  0.597
2006 Roper RJ, Baxter LL, Saran NG, Klinedinst DK, Beachy PA, Reeves RH. Erratum: Defective cerebellar response to mitogenic Hedgehog signaling in Down's syndrome mice (Proceedings of the National Academy of Sciences of the United States of America (January 31, 2006) 103, 5 (1452-1456) 10.1073/pnas.0510750103)) Proceedings of the National Academy of Sciences of the United States of America. 103. DOI: 10.1073/Pnas.0601630103  0.708
2004 Olson LE, Roper RJ, Baxter LL, Carlson EJ, Epstein CJ, Reeves RH. Down syndrome mouse models Ts65Dn, Ts1Cje, and Ms1Cje/Ts65Dn exhibit variable severity of cerebellar phenotypes. Developmental Dynamics : An Official Publication of the American Association of Anatomists. 230: 581-9. PMID 15188443 DOI: 10.1002/Dvdy.20079  0.743
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  0.6
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  0.544
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  0.598
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  0.595
2001 Reeves RH, Baxter LL, Richtsmeier JT. Too much of a good thing: Mechanisms of gene action in Down syndrome Trends in Genetics. 17: 83-88. PMID 11173117 DOI: 10.1016/S0168-9525(00)02172-7  0.539
2000 Richtsmeier JT, Baxter LL, Reeves RH. Parallels of craniofacial maldevelopment in Down syndrome and Ts65Dn mice Developmental Dynamics. 217: 137-145. PMID 10706138 DOI: 10.1002/(Sici)1097-0177(200002)217:2<137::Aid-Dvdy1>3.0.Co;2-N  0.61
2000 Baxter LL, Moran TH, Richtsmeier JT, Troncoso J, Reeves RH. Discovery and genetic localization of Down syndrome cerebellar phenotypes using the Ts65Dn mouse. Human Molecular Genetics. 9: 195-202. PMID 10607830 DOI: 10.1093/Hmg/9.2.195  0.585
1999 Moore CS, Lee JS, Birren B, Stetten G, Baxter LL, Reeves RH. Integration of cytogenetic with recombinational and physical maps of mouse chromosome 16 Genomics. 59: 1-5. PMID 10395793 DOI: 10.1006/geno.1999.5812  0.456
Show low-probability matches.