| Year |
Citation |
Score |
| 2020 |
Hall EG, Wenger LW, Wilson NR, Undurty-Akella SS, Standley J, Augustine-Akpan EA, Kousa YA, Acevedo DS, Goering JP, Pitstick L, Natsume N, Paroya SM, Busch TD, Ito M, Mori A, ... ... Schutte BC, et al. SPECC1L regulates palate development downstream of IRF6. Human Molecular Genetics. PMID 31943082 DOI: 10.1093/Hmg/Ddaa002 |
0.741 |
|
| 2019 |
Bonner J, Fisher R, Wilch E, Schutte D, Schutte B. Mitochondrial Haplogroups and Lifespan in a Population Isolate. Mitochondrion. PMID 31887371 DOI: 10.1016/J.Mito.2019.12.004 |
0.669 |
|
| 2019 |
Kousa YA, Zhu H, Fakhouri WD, Lei Y, Kinoshita A, Roushangar RR, Patel NK, Agopian AJ, Yang W, Leslie EJ, Busch TD, Mansour TA, Li X, Smith AL, Li EB, ... ... Schutte BC, et al. The TFAP2A-IRF6-GRHL3 genetic pathway is conserved in neurulation. Human Molecular Genetics. PMID 30689861 DOI: 10.1093/Hmg/Ddz010 |
0.763 |
|
| 2018 |
Kousa YA, Fuller E, Schutte BC. IRF6 and AP2A Interaction Regulates Epidermal Development. The Journal of Investigative Dermatology. PMID 29913133 DOI: 10.1016/J.Jid.2018.05.030 |
0.72 |
|
| 2017 |
Li EB, Truong D, Hallett SA, Mukherjee K, Schutte BC, Liao EC. Rapid functional analysis of computationally complex rare human IRF6 gene variants using a novel zebrafish model. Plos Genetics. 13: e1007009. PMID 28945736 DOI: 10.1371/Journal.Pgen.1007009 |
0.393 |
|
| 2017 |
Fakhouri WD, Metwalli K, Naji A, Bakhiet S, Quispe-Salcedo A, Nitschke L, Kousa YA, Schutte BC. Intercellular Genetic Interaction Between Irf6 and Twist1 during Craniofacial Development. Scientific Reports. 7: 7129. PMID 28769044 DOI: 10.1038/S41598-017-06310-Z |
0.754 |
|
| 2017 |
Kousa YA, Roushangar R, Patel N, Walter A, Marangoni P, Krumlauf R, Klein OD, Schutte BC. IRF6 and SPRY4 Signaling Interact in Periderm Development. Journal of Dental Research. 22034517719870. PMID 28732181 DOI: 10.1177/0022034517719870 |
0.733 |
|
| 2017 |
Kousa YA, Moussa D, Schutte BC. IRF6 expression in basal epithelium partially rescues Irf6 knockout mice. Developmental Dynamics : An Official Publication of the American Association of Anatomists. PMID 28643456 DOI: 10.1002/Dvdy.24537 |
0.726 |
|
| 2017 |
Smith AL, Kousa YA, Kinoshita A, Fodor K, Yang B, Schutte BC. Generation and Characterization of a Conditional Allele of Interferon regulatory factor 6. Genesis (New York, N.Y. : 2000). PMID 28481036 DOI: 10.1002/Dvg.23038 |
0.775 |
|
| 2016 |
Kousa YA, Mansour TA, Seada H, Matoo S, Schutte BC. Shared molecular networks in orofacial and neural tube development. Birth Defects Research. Part a, Clinical and Molecular Teratology. PMID 27933721 DOI: 10.1002/Bdra.23598 |
0.698 |
|
| 2016 |
Chu EY, Tamasas B, Fong H, Foster BL, LaCourse MR, Tran AB, Martin JF, Schutte BC, Somerman MJ, Cox TC. Full Spectrum of Postnatal Tooth Phenotypes in a Novel Irf6 Cleft Lip Model. Journal of Dental Research. PMID 27369589 DOI: 10.1177/0022034516656787 |
0.398 |
|
| 2016 |
Kousa YA, Schutte BC. Toward an orofacial gene regulatory network. Developmental Dynamics : An Official Publication of the American Association of Anatomists. 245: 220-32. PMID 26332872 DOI: 10.1002/Dvdy.24341 |
0.724 |
|
| 2015 |
Leslie EJ, Koboldt DC, Kang CJ, Ma L, Hecht JT, Wehby GL, Christensen K, Czeizel AE, Deleyiannis FW, Fulton RS, Wilson RK, Beaty TH, Schutte BC, Murray JC, Marazita ML. IRF6 mutation screening in nonsyndromic orofacial clefting: analysis of 1521 families. Clinical Genetics. PMID 26346622 DOI: 10.1111/Cge.12675 |
0.372 |
|
| 2015 |
Leslie EJ, Taub MA, Liu H, Steinberg KM, Koboldt DC, Zhang Q, Carlson JC, Hetmanski JB, Wang H, Larson DE, Fulton RS, Kousa YA, Fakhouri WD, Naji A, Ruczinski I, ... ... Schutte BC, et al. Identification of functional variants for cleft lip with or without cleft palate in or near PAX7, FGFR2, and NOG by targeted sequencing of GWAS loci. American Journal of Human Genetics. 96: 397-411. PMID 25704602 DOI: 10.1016/J.Ajhg.2015.01.004 |
0.719 |
|
| 2014 |
Bonner JD, Fisher R, Klein J, Lu Q, Wilch E, Friderici KH, Elfenbein JL, Schutte DL, Schutte BC. Pedigree structure and kinship measurements of a mid-Michigan community: a new North American population isolate identified. Human Biology. 86: 59-68. PMID 25401987 DOI: 10.3378/027.086.0103 |
0.682 |
|
| 2014 |
Biggs LC, Naridze RL, DeMali KA, Lusche DF, Kuhl S, Soll DR, Schutte BC, Dunnwald M. Interferon regulatory factor 6 regulates keratinocyte migration. Journal of Cell Science. 127: 2840-8. PMID 24777480 DOI: 10.1242/Jcs.139246 |
0.355 |
|
| 2014 |
Fakhouri WD, Rahimov F, Attanasio C, Kouwenhoven EN, Ferreira De Lima RL, Felix TM, Nitschke L, Huver D, Barrons J, Kousa YA, Leslie E, Pennacchio LA, Van Bokhoven H, Visel A, Zhou H, ... ... Schutte BC, et al. An etiologic regulatory mutation in IRF6 with loss- and gain-of-function effects. Human Molecular Genetics. 23: 2711-20. PMID 24442519 DOI: 10.1093/Hmg/Ddt664 |
0.731 |
|
| 2014 |
Peyrard-Janvid M, Leslie EJ, Kousa YA, Smith TL, Dunnwald M, Magnusson M, Lentz BA, Unneberg P, Fransson I, Koillinen HK, Rautio J, Pegelow M, Karsten A, Basel-Vanagaite L, Gordon W, ... ... Schutte BC, et al. Dominant mutations in GRHL3 cause Van der Woude Syndrome and disrupt oral periderm development. American Journal of Human Genetics. 94: 23-32. PMID 24360809 DOI: 10.1016/J.Ajhg.2013.11.009 |
0.733 |
|
| 2014 |
Aerts A, DeVolder I, Weinberg SM, Thedens D, Dunnwald M, Schutte BC, Nopoulos P. Haploinsufficiency of interferon regulatory factor 6 alters brain morphology in the mouse. American Journal of Medical Genetics. Part A. 164: 655-60. PMID 24357509 DOI: 10.1002/Ajmg.A.36333 |
0.346 |
|
| 2013 |
Leslie EJ, Mancuso JL, Schutte BC, Cooper ME, Durda KM, L'heureux J, Zucchero TM, Marazita ML, Murray JC. Search for genetic modifiers of IRF6 and genotype-phenotype correlations in Van der Woude and popliteal pterygium syndromes. American Journal of Medical Genetics. Part A. 161: 2535-44. PMID 23949966 DOI: 10.1002/Ajmg.A.36133 |
0.458 |
|
| 2013 |
Aldhamen YA, Seregin SS, Kousa YA, Rastall DP, Appledorn DM, Godbehere S, Schutte BC, Amalfitano A. Improved cytotoxic T-lymphocyte immune responses to a tumor antigen by vaccines co-expressing the SLAM-associated adaptor EAT-2. Cancer Gene Therapy. 20: 564-75. PMID 23949283 DOI: 10.1038/Cgt.2013.53 |
0.666 |
|
| 2013 |
Boell L, Pallares LF, Brodski C, Chen Y, Christian JL, Kousa YA, Kuss P, Nelsen S, Novikov O, Schutte BC, Wang Y, Tautz D. Exploring the effects of gene dosage on mandible shape in mice as a model for studying the genetic basis of natural variation. Development Genes and Evolution. 223: 279-87. PMID 23563729 DOI: 10.1007/S00427-013-0443-Y |
0.709 |
|
| 2013 |
Goudy S, Angel P, Jacobs B, Hill C, Mainini V, Smith AL, Kousa YA, Caprioli R, Prince LS, Baldwin S, Schutte BC. Cell-autonomous and non-cell-autonomous roles for IRF6 during development of the tongue. Plos One. 8: e56270. PMID 23451037 DOI: 10.1371/Journal.Pone.0056270 |
0.76 |
|
| 2013 |
Leslie EJ, Standley J, Compton J, Bale S, Schutte BC, Murray JC. Comparative analysis of IRF6 variants in families with Van der Woude syndrome and popliteal pterygium syndrome using public whole-exome databases Genetics in Medicine. 15: 338-344. PMID 23154523 DOI: 10.1038/Gim.2012.141 |
0.372 |
|
| 2013 |
de la Garza G, Schleiffarth JR, Dunnwald M, Mankad A, Weirather JL, Bonde G, Butcher S, Mansour TA, Kousa YA, Fukazawa CF, Houston DW, Manak JR, Schutte BC, Wagner DS, Cornell RA. Interferon regulatory factor 6 promotes differentiation of the periderm by activating expression of Grainyhead-like 3. The Journal of Investigative Dermatology. 133: 68-77. PMID 22931925 DOI: 10.1038/Jid.2012.269 |
0.721 |
|
| 2013 |
Garza GDL, Schleiffarth JR, Dunnwald M, Mankad A, Weirather JL, Bonde G, Butcher S, Mansour TA, Kousa YA, Fukazawa CF, Houston DW, Manak JR, Schutte BC, Wagner DS, Cornell RA. Erratum: Interferon regulatory factor 6 promotes differentiation of the periderm by activating expression of grainyhead-like 3 (Journal of Investigative Dermatology (2013) 133 (68-77) DOI: 10.1038/jid.2012.269) Journal of Investigative Dermatology. 133. DOI: 10.1038/Jid.2012.380 |
0.694 |
|
| 2012 |
Letra A, Fakhouri W, Fonseca RF, Menezes R, Kempa I, Prasad JL, McHenry TG, Lidral AC, Moreno L, Murray JC, Daack-Hirsch S, Marazita ML, Castilla EE, Lace B, Orioli IM, ... ... Schutte BC, et al. Interaction between IRF6 and TGFA genes contribute to the risk of nonsyndromic cleft lip/palate. Plos One. 7: e45441. PMID 23029012 DOI: 10.1371/Journal.Pone.0045441 |
0.332 |
|
| 2012 |
Blackburn J, Ohazama A, Kawasaki K, Otsuka-Tanaka Y, Liu B, Honda K, Rountree RB, Hu Y, Kawasaki M, Birchmeier W, Schmidt-Ullrich R, Kinoshita A, Schutte BC, Hammond NL, Dixon MJ, et al. The role of Irf6 in tooth epithelial invagination. Developmental Biology. 365: 61-70. PMID 22366192 DOI: 10.1016/J.Ydbio.2012.02.009 |
0.355 |
|
| 2012 |
Mitchell K, O'Sullivan J, Missero C, Blair E, Richardson R, Anderson B, Antonini D, Murray JC, Shanske AL, Schutte BC, Romano RA, Sinha S, Bhaskar SS, Black GC, Dixon J, et al. Exome sequence identifies RIPK4 as the Bartsocas-Papas syndrome locus. American Journal of Human Genetics. 90: 69-75. PMID 22197488 DOI: 10.1016/J.Ajhg.2011.11.013 |
0.408 |
|
| 2012 |
Fakhouri WD, Rhea L, Du T, Sweezer E, Morrison H, Fitzpatrick D, Yang B, Dunnwald M, Schutte BC. MCS9.7 enhancer activity is highly, but not completely, associated with expression of Irf6 and p63. Developmental Dynamics : An Official Publication of the American Association of Anatomists. 241: 340-9. PMID 22113860 DOI: 10.1002/Dvdy.22786 |
0.398 |
|
| 2012 |
Biggs LC, Rhea L, Schutte BC, Dunnwald M. Interferon regulatory factor 6 is necessary, but not sufficient, for keratinocyte differentiation. The Journal of Investigative Dermatology. 132: 50-8. PMID 21918538 DOI: 10.1038/Jid.2011.272 |
0.382 |
|
| 2012 |
Schutte BC, Fakhouri WD, Zemke D. Regulatory mutations leading to cleft lip and palate Gene Regulatory Sequences and Human Disease. 2147483647: 95-122. DOI: 10.1007/978-1-4614-1683-8_6 |
0.338 |
|
| 2011 |
Kahr WH, Hinckley J, Li L, Schwertz H, Christensen H, Rowley JW, Pluthero FG, Urban D, Fabbro S, Nixon B, Gadzinski R, Storck M, Wang K, Ryu GY, Jobe SM, ... Schutte BC, et al. Mutations in NBEAL2, encoding a BEACH protein, cause gray platelet syndrome. Nature Genetics. 43: 738-40. PMID 21765413 DOI: 10.1038/Ng.884 |
0.359 |
|
| 2011 |
Rorick NK, Kinoshita A, Weirather JL, Peyrard-Janvid M, de Lima RL, Dunnwald M, Shanske AL, Moretti-Ferreira D, Koillinen H, Kere J, Mansilla MA, Murray JC, Goudy SL, Schutte BC. Genomic strategy identifies a missense mutation in WD-repeat domain 65 (WDR65) in an individual with Van der Woude syndrome. American Journal of Medical Genetics. Part A. 155: 1314-21. PMID 21574244 DOI: 10.1002/Ajmg.A.33980 |
0.477 |
|
| 2011 |
Fabbro S, Kahr WH, Hinckley J, Wang K, Moseley J, Ryu GY, Nixon B, White JG, Bair T, Schutte B, Di Paola J. Homozygosity mapping with SNP arrays confirms 3p21 as a recessive locus for gray platelet syndrome and narrows the interval significantly. Blood. 117: 3430-4. PMID 21263149 DOI: 10.1182/Blood-2010-12-322990 |
0.308 |
|
| 2009 |
Bailey CM, Margaryan NV, Abbott DE, Schutte BC, Yang B, Khalkhali-Ellis Z, Hendrix MJ. Temporal and spatial expression patterns for the tumor suppressor Maspin and its binding partner interferon regulatory factor 6 during breast development. Development, Growth & Differentiation. 51: 473-81. PMID 19527266 DOI: 10.1111/J.1440-169X.2009.01110.X |
0.358 |
|
| 2009 |
de Lima RL, Hoper SA, Ghassibe M, Cooper ME, Rorick NK, Kondo S, Katz L, Marazita ML, Compton J, Bale S, Hehr U, Dixon MJ, Daack-Hirsch S, Boute O, Bayet B, ... ... Schutte BC, et al. Prevalence and nonrandom distribution of exonic mutations in interferon regulatory factor 6 in 307 families with Van der Woude syndrome and 37 families with popliteal pterygium syndrome. Genetics in Medicine : Official Journal of the American College of Medical Genetics. 11: 241-7. PMID 19282774 DOI: 10.1097/Gim.0B013E318197A49A |
0.365 |
|
| 2009 |
Little HJ, Rorick NK, Su LI, Baldock C, Malhotra S, Jowitt T, Gakhar L, Subramanian R, Schutte BC, Dixon MJ, Shore P. Missense mutations that cause Van der Woude syndrome and popliteal pterygium syndrome affect the DNA-binding and transcriptional activation functions of IRF6. Human Molecular Genetics. 18: 535-45. PMID 19036739 DOI: 10.1093/Hmg/Ddn381 |
0.411 |
|
| 2009 |
Sabel JL, d'Alençon C, O'Brien EK, Van Otterloo E, Lutz K, Cuykendall TN, Schutte BC, Houston DW, Cornell RA. Maternal Interferon Regulatory Factor 6 is required for the differentiation of primary superficial epithelia in Danio and Xenopus embryos. Developmental Biology. 325: 249-62. PMID 19013452 DOI: 10.1016/J.Ydbio.2008.10.031 |
0.422 |
|
| 2009 |
Little HJ, Rorick NK, Su LI, Baldock C, Malhotra S, Jowitt T, Gakhar L, Subramanian R, Schutte BC, Dixon MJ, Shore P. Erratum: Missense mutations that cause Van der Woude syndrome and popliteal pterygium syndrome affect the DNA-binding and transcriptional activation functions of IRF6 (Human Molecular Genetics (2009) vol. 18(3) (535-545) 10.1093/hmg/ddn381) Human Molecular Genetics. 18. DOI: 10.1093/Hmg/Ddp056 |
0.413 |
|
| 2008 |
Rahimov F, Marazita ML, Visel A, Cooper ME, Hitchler MJ, Rubini M, Domann FE, Govil M, Christensen K, Bille C, Melbye M, Jugessur A, Lie RT, Wilcox AJ, Fitzpatrick DR, ... ... Schutte BC, et al. Disruption of an AP-2alpha binding site in an IRF6 enhancer is associated with cleft lip. Nature Genetics. 40: 1341-7. PMID 18836445 DOI: 10.1038/Ng.242 |
0.36 |
|
| 2008 |
Del Frari B, Amort M, Janecke AR, Schutte BC, Piza-Katzer H. Van-der-Woude Syndrome Klinische Padiatrie. 220: 26-28. PMID 18095255 DOI: 10.1055/S-2007-971049 |
0.392 |
|
| 2008 |
Osoegawa K, Vessere GM, Utami KH, Mansilla MA, Johnson MK, Riley BM, L'Heureux J, Pfundt R, Staaf J, van der Vliet WA, Lidral AC, Schoenmakers EF, Borg A, Schutte BC, Lammer EJ, et al. Identification of novel candidate genes associated with cleft lip and palate using array comparative genomic hybridisation. Journal of Medical Genetics. 45: 81-6. PMID 17873121 DOI: 10.1136/Jmg.2007.052191 |
0.32 |
|
| 2006 |
Ingraham CR, Kinoshita A, Kondo S, Yang B, Sajan S, Trout KJ, Malik MI, Dunnwald M, Goudy SL, Lovett M, Murray JC, Schutte BC. Abnormal skin, limb and craniofacial morphogenesis in mice deficient for interferon regulatory factor 6 (Irf6). Nature Genetics. 38: 1335-40. PMID 17041601 DOI: 10.1038/Ng1903 |
0.418 |
|
| 2006 |
Knight AS, Schutte BC, Jiang R, Dixon MJ. Developmental expression analysis of the mouse and chick orthologues of IRF6: the gene mutated in Van der Woude syndrome. Developmental Dynamics : An Official Publication of the American Association of Anatomists. 235: 1441-7. PMID 16245336 DOI: 10.1002/Dvdy.20598 |
0.459 |
|
| 2006 |
Sabel J, d'Alencon C, Rorick N, Hemerson P, Schutte B, Cornell R. Inhibition of oral–facial clefting gene Interferon Regulatory Factor 6 disrupts gastrulation, pectoral fin formation, and somite boundary formation in zebrafish Developmental Biology. 295: 394. DOI: 10.1016/J.Ydbio.2006.04.208 |
0.32 |
|
| 2005 |
Bailey CM, Khalkhali-Ellis Z, Kondo S, Margaryan NV, Seftor RE, Wheaton WW, Amir S, Pins MR, Schutte BC, Hendrix MJ. Mammary serine protease inhibitor (Maspin) binds directly to interferon regulatory factor 6: identification of a novel serpin partnership. The Journal of Biological Chemistry. 280: 34210-7. PMID 16049006 DOI: 10.1074/Jbc.M503523200 |
0.376 |
|
| 2004 |
Zucchero TM, Cooper ME, Maher BS, Daack-Hirsch S, Nepomuceno B, Ribeiro L, Caprau D, Christensen K, Suzuki Y, Machida J, Natsume N, Yoshiura K, Vieira AR, Orioli IM, Castilla EE, ... ... Schutte BC, et al. Interferon regulatory factor 6 (IRF6) gene variants and the risk of isolated cleft lip or palate. The New England Journal of Medicine. 351: 769-80. PMID 15317890 DOI: 10.1056/Nejmoa032909 |
0.418 |
|
| 2004 |
Shanske AL, Hoper SA, Krahn K, Schutte BC. Mutations in IRF6 do not cause Bartsocas-Papas syndrome in a family with two affected sibs [1] American Journal of Medical Genetics. 128: 431-433. PMID 15264293 DOI: 10.1002/Ajmg.A.30096 |
0.349 |
|
| 2004 |
Murray JC, Schutte BC. Cleft palate: players, pathways, and pursuits. The Journal of Clinical Investigation. 113: 1676-8. PMID 15199400 DOI: 10.1172/Jci22154 |
0.345 |
|
| 2003 |
Kayano S, Kure S, Suzuki Y, Kanno K, Aoki Y, Kondo S, Schutte BC, Murray JC, Yamada A, Matsubara Y. Novel IRF6 mutations in Japanese patients with Van der Woude syndrome: two missense mutations (R45Q and P396S) and a 17-kb deletion. Journal of Human Genetics. 48: 622-8. PMID 14618417 DOI: 10.1007/S10038-003-0089-0 |
0.396 |
|
| 2002 |
Scheetz T, Bartlett JA, Walters JD, Schutte BC, Casavant TL, McCray PB. Genomics-based approaches to gene discovery in innate immunity. Immunological Reviews. 190: 137-45. PMID 12493011 DOI: 10.1034/J.1600-065X.2002.19010.X |
0.317 |
|
| 2002 |
Arreola J, Begenisich T, Nehrke K, Nguyen HV, Park K, Richardson L, Yang B, Schutte BC, Lamb FS, Melvin JE. Secretion and cell volume regulation by salivary acinar cells from mice lacking expression of the Clcn3 Cl- channel gene. The Journal of Physiology. 545: 207-16. PMID 12433961 DOI: 10.1113/Jphysiol.2002.021980 |
0.301 |
|
| 2002 |
Kondo S, Schutte BC, Richardson RJ, Bjork BC, Knight AS, Watanabe Y, Howard E, de Lima RL, Daack-Hirsch S, Sander A, McDonald-McGinn DM, Zackai EH, Lammer EJ, Aylsworth AS, Ardinger HH, et al. Mutations in IRF6 cause Van der Woude and popliteal pterygium syndromes. Nature Genetics. 32: 285-9. PMID 12219090 DOI: 10.1038/Ng985 |
0.445 |
|
| 2002 |
Kantaputra PN, Sumitsawan Y, Schutte BC, Tochareontanaphol C. Van der Woude syndrome with sensorineural hearing loss, large craniofacial sinuses, dental pulp stones, and minor limb anomalies: report of a four-generation Thai family. American Journal of Medical Genetics. 108: 275-80. PMID 11920830 DOI: 10.1002/Ajmg.10276 |
0.32 |
|
| 2002 |
Schutte BC, Mitros JP, Bartlett JA, Walters JD, Jia HP, Welsh MJ, Casavant TL, McCray PB. Discovery of five conserved beta -defensin gene clusters using a computational search strategy. Proceedings of the National Academy of Sciences of the United States of America. 99: 2129-33. PMID 11854508 DOI: 10.1073/Pnas.042692699 |
0.303 |
|
| 2001 |
Watanabe Y, Murray JC, Bjork BC, Bird CP, Chiang PW, Gregory SG, Kurnit DM, Schutte BC. Matroshka and ectopic polymorphisms: Two new classes of DNA sequence variation identified at the van der woude syndrome locus on 1q32-q41 Human Mutation. 18: 422-434. PMID 11668635 DOI: 10.1002/Humu.1213 |
0.33 |
|
| 2001 |
Peng Jia H, Schutte BC, Schudy A, Linzmeier R, Guthmiller JM, Johnson GK, Tack BF, Mitros JP, Rosenthal A, Ganz T, McCray PB. Discovery of new human β-defensins using a genomics-based approach Gene. 263: 211-218. PMID 11223260 DOI: 10.1016/S0378-1119(00)00569-2 |
0.342 |
|
| 2000 |
Arbour NC, Lorenz E, Schutte BC, Zabner J, Kline JN, Jones M, Frees K, Watt JL, Schwartz DA. TLR4 mutations are associated with endotoxin hyporesponsiveness in humans Nature Genetics. 25: 187-191. PMID 10835634 DOI: 10.1038/76048 |
0.332 |
|
| 2000 |
Lamb FS, Barna TJ, Goud C, Marenholz I, Mischke D, Schutte BC. Complex RNA processing of TDRKH, a novel gene encoding the putative RNA-binding Tudor and KH domains Gene. 246: 209-218. PMID 10767542 DOI: 10.1016/S0378-1119(00)00087-1 |
0.342 |
|
| 2000 |
Schutte BC, Bjork BC, Coppage KB, Malik MI, Gregory SG, Scott DJ, Brentzell LM, Watanabe Y, Dixon MJ, Murray JC. A preliminary gene map for the Van der Woude syndrome critical region derived from 900 kb of genomic sequence at 1q32-q41 Genome Research. 10: 81-94. PMID 10645953 DOI: 10.1101/Gr.10.1.81 |
0.35 |
|
| 1999 |
Raymond MH, Schutte BC, Torner JC, Burns TL, Willing MC. Osteocalcin: Genetic and physical mapping of the human gene BGLAP and its potential role in postmenopausal osteoporosis Genomics. 60: 210-217. PMID 10486212 DOI: 10.1006/Geno.1999.5893 |
0.307 |
|
| 1999 |
Schutte BC, Murray JC. The many faces and factors of orofacial clefts Human Molecular Genetics. 8: 1853-1859. PMID 10469837 DOI: 10.1093/Hmg/8.10.1853 |
0.413 |
|
| 1999 |
L'Ecuyer TJ, Schutte BC, Mendel KA, Morris E, Fulton AB. Muscle-specific transcription factors in fibroblasts expressing the α- striated tropomyosin 3' untranslated region Molecular Genetics and Metabolism. 67: 213-226. PMID 10381329 DOI: 10.1006/Mgme.1999.2858 |
0.341 |
|
| 1999 |
Schutte BC, Basart AM, Watanabe Y, Laffin JJS, Coppage K, Bjork BC, Daack-Hirsch S, Patil S, Dixon MJ, Murray JC. Microdeletions at chromosome bands 1q32-q41 as a cause of Van der Woude syndrome American Journal of Medical Genetics. 84: 145-150. PMID 10323740 DOI: 10.1002/(Sici)1096-8628(19990521)84:2<145::Aid-Ajmg11>3.0.Co;2-L |
0.394 |
|
| 1999 |
Lamb FS, Clayton GH, Liu BX, Smith RL, Barna TJ, Schutte BC. Expression of CLCN voltage-gated chloride channel genes in human blood vessels Journal of Molecular and Cellular Cardiology. 31: 657-666. PMID 10198195 DOI: 10.1006/Jmcc.1998.0901 |
0.311 |
|
| 1999 |
Widness JA, Lambert DJ, Schmidt RL, Schutte BC. Erythropoietin Receptor Gene Expression in Humans Is Greater in the Fetus Compared to the Adult Pediatric Research. 45: 265A-265A. DOI: 10.1203/00006450-199904020-01579 |
0.301 |
|
| 1998 |
Liu L, Wang L, Jia HP, Zhao C, Heng HHQ, Schutte BC, McCray PB, Ganz T. Structure and mapping of the human β-defensin HBD-2 gene and its expression at sites of inflammation Gene. 222: 237-244. PMID 9831658 DOI: 10.1016/S0378-1119(98)00480-6 |
0.323 |
|
| 1998 |
Brennan TM, Landau D, Shalev H, Lamb F, Schutte BC, Walder RY, Mark AL, Carmi R, Sheffield VC. Linkage of infantile Bartter syndrome with sensorineural deafness to chromosome 1p. American Journal of Human Genetics. 62: 355-61. PMID 9463315 DOI: 10.1086/301708 |
0.409 |
|
| 1997 |
Tymms MJ, Ng AY, Thomas RS, Schutte BC, Zhou J, Eyre HJ, Sutherland GR, Seth A, Rosenberg M, Papas T, Debouck C, Kola I. A novel epithelial-expressed ETS gene, ELF3: human and murine cDNA sequences, murine genomic organization, human mapping to 1q32.2 and expression in tissues and cancer. Oncogene. 15: 2449-62. PMID 9395241 DOI: 10.1038/Sj.Onc.1201427 |
0.36 |
|
| 1997 |
Schutte BC, Coppage KB, Bjork B, Malik M, Sander A, Murray JC. Physical mapping and candidate gene analysis of the Van der Woude locus on Ch1q32. † 624 Pediatric Research. 41: 106-106. DOI: 10.1203/00006450-199704001-00644 |
0.349 |
|
| 1997 |
Klein JM, McCarthy TA, Keese ME, Schutte BC. THE EFFECTS OF SEX HORMONES ON HUMAN PULMONARY EGF RECEPTOR PROMOTER ACTIVITY. † 271 Pediatric Research. 41: 48-48. DOI: 10.1203/00006450-199704001-00291 |
0.315 |
|
| 1996 |
Schutte BC, Sander A, Malik M, Murray JC. Refinement of the Van der Woude gene location and construction of a 3.5- Mb YAC contig and STS map spanning the critical region in 1q32-q41 Genomics. 36: 507-514. PMID 8884274 DOI: 10.1006/Geno.1996.0496 |
0.31 |
|
| 1995 |
Robillard JE, Page WV, Mathews MS, Schutte BC, Nuyt AM, Segar JL. Differential gene expression and regulation of renal angiotensin ii receptor subtypes (AT<inf>1</inf> and AT<inf>2</inf>) during fetal life in sheep Pediatric Research. 38: 896-904. PMID 8618791 DOI: 10.1203/00006450-199512000-00012 |
0.315 |
|
| 1994 |
Weiffenbach B, Dubois J, Manning S, Ma NS, Schutte BC, Winokur ST, Altherr MR, Jacobsen SJ, Stanton VP, Yokoyama K, Moir D. YAC Contigs for 4q35 in the Region of the Facioscapulohumeral Muscular Dystrophy (FSHD) Gene Genomics. 19: 532-541. PMID 8188296 DOI: 10.1006/Geno.1994.1103 |
0.31 |
|
| 1994 |
Robillard JE, Schutte BC, Page WV, Fedderson JA, Porter CC, Segar JL. Ontogenic changes and regulation of renal angiotensin ii type 1 receptor gene expression during fetal and newborn life Pediatric Research. 36: 755-762. PMID 7898984 DOI: 10.1203/00006450-199412000-00013 |
0.301 |
|
| 1989 |
Pugh BF, Schutte BC, Cox MM. Extent of duplex DNA underwinding induced by RecA protein binding in the presence of ATP. Journal of Molecular Biology. 205: 487-92. PMID 2538631 DOI: 10.1016/0022-2836(89)90219-2 |
0.447 |
|
| 1988 |
Schutte BC, Cox MM. Homology-dependent underwinding of duplex DNA in recA protein generated paranemic complexes Biochemistry. 27: 7886-7894. PMID 3061463 DOI: 10.1021/Bi00420A046 |
0.443 |
|
| 1987 |
Schutte BC, Cox MM. Homology-dependent changes in adenosine 5′-triphosphate hydrolysis during recA protein promoted DNA strand exchange: Evidence for long paranemic complexes Biochemistry. 26: 5616-5625. PMID 3314992 DOI: 10.1021/Bi00392A006 |
0.434 |
|
| 1987 |
Brenner SL, Mitchell RS, Morrical SW, Neuendorf SK, Schutte BC, Cox MM. recA protein-promoted ATP hydrolysis occurs throughout recA nucleoprotein filaments Journal of Biological Chemistry. 262: 4011-4016. PMID 2951381 |
0.606 |
|
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