Brian C. Schutte - Publications

Affiliations: 
Biochemistry and Molecular Biology - Doctor of Philosophy Michigan State University, East Lansing, MI 
Area:
Human Development, Medicine and Surgery, Biochemistry

97 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any innacuracies, 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
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  0.6
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  0.6
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  0.6
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  0.6
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  0.6
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  0.6
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  0.92
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  0.92
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  0.92
2015 Goris ED, Schutte DL, Rivard JL, Schutte BC. Community leader perceptions of the health needs of older adults. Western Journal of Nursing Research. 37: 599-618. PMID 24757048 DOI: 10.1177/0193945914530046  0.92
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: 10.1353/hub.2014.0002  0.92
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  0.92
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  0.92
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  0.92
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  0.92
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  0.92
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  0.92
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  0.92
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  0.92
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  0.92
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  0.92
2012 Le M, Naridze R, Morrison J, Biggs LC, Rhea L, Schutte BC, Kaartinen V, Dunnwald M. Transforming growth factor Beta 3 is required for excisional wound repair in vivo. Plos One. 7: e48040. PMID 23110169 DOI: 10.1371/journal.pone.0048040  0.92
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  0.92
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  0.92
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  0.92
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  0.92
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  0.92
2012 Ragina NP, Schlosser K, Knott JG, Senagore PK, Swiatek PJ, Chang EA, Fakhouri WD, Schutte BC, Kiupel M, Cibelli JB. Downregulation of H19 improves the differentiation potential of mouse parthenogenetic embryonic stem cells. Stem Cells and Development. 21: 1134-44. PMID 21793658 DOI: 10.1089/scd.2011.0152  0.92
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  0.92
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  0.92
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  0.92
2010 Jones JL, Canady JW, Brookes JT, Wehby GL, L'Heureux J, Schutte BC, Murray JC, Dunnwald M. Wound complications after cleft repair in children with Van der Woude syndrome. The Journal of Craniofacial Surgery. 21: 1350-3. PMID 20856020 DOI: 10.1097/SCS.0b013e3181ec6aad  0.92
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  0.92
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  0.92
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  0.92
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  0.92
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  0.92
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  0.92
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  0.92
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  0.92
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  0.92
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  0.92
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  0.92
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  0.92
2004 Ralphe JC, Segar JL, Schutte BC, Scholz TD. Localization and function of the brain excitatory amino acid transporter type 1 in cardiac mitochondria. Journal of Molecular and Cellular Cardiology. 37: 33-41. PMID 15242733 DOI: 10.1016/j.yjmcc.2004.04.008  0.92
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  0.92
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  0.92
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  0.92
2002 Dickerson LW, Bonthius DJ, Schutte BC, Yang B, Barna TJ, Bailey MC, Nehrke K, Williamson RA, Lamb FS. Altered GABAergic function accompanies hippocampal degeneration in mice lacking ClC-3 voltage-gated chloride channels. Brain Research. 958: 227-50. PMID 12470859 DOI: 10.1016/S0006-8993(02)03519-9  0.92
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  0.92
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  0.92
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  0.92
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  0.92
2002 Schutte BC, McCray PB. [beta]-defensins in lung host defense. Annual Review of Physiology. 64: 709-48. PMID 11826286 DOI: 10.1146/annurev.physiol.64.081501.134340  0.92
2001 Naimeh LG, Schutte BC, Hamilton WS, Tsalikian E. Ontogeny of the H19 gene in sheep and effect of maternal fasting on its expression in the fetus Endocrine Research. 27: 417-431. PMID 11794466 DOI: 10.1081/ERC-100107866  0.92
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  0.92
2001 Schutte BC, Carpten JD, Forus A, Gregory SG, Horii A, White PS. Report and abstracts of the sixth international workshop on human chromosome 1 mapping 2000. Iowa City, Iowa, USA. 30 September-3 October 2000 Cytogenetics and Cell Genetics. 92: 23-41. PMID 11306795  0.92
2001 Lamb FS, Graeff RW, Clayton GH, Smith RL, Schutte BC, McCray PB. Ontogeny of CLCN3 chloride channel gene expression in human pulmonary epithelium. American Journal of Respiratory Cell and Molecular Biology. 24: 376-81. PMID 11306429 DOI: 10.1165/ajrcmb.24.4.4114  0.92
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  0.92
2001 Schutte BC, Carpten JD, Forus A, Gregory SG, Horii A, White PS. Report of the sixth international workshop on human chromosome 1 mapping 2000 Cytogenetics and Cell Genetics. 92: 23-48.  0.92
2000 Rupert BE, Segar JL, Schutte BC, Scholz TD. Metabolic adaptation of the hypertrophied heart: Role of the malate/aspartate and α-glycerophosphate shuttles Journal of Molecular and Cellular Cardiology. 32: 2287-2297. PMID 11113004 DOI: 10.1006/jmcc.2000.1257  0.92
2000 Jia HP, Wowk SA, Schutte BC, Lee SK, Vivado A, Tack BF, Bevins CL, McCray PB. A novel murine β-defensin expressed in tongue, esophagus, and trachea* Journal of Biological Chemistry. 275: 33314-33320. PMID 10922379 DOI: 10.1074/jbc.M006603200  0.92
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  0.92
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  0.92
2000 Scholz TD, Teneyck CJ, Schutte BC. Thyroid hormone regulation of the NADH shuttles in liver and cardiac mitochondria Journal of Molecular and Cellular Cardiology. 32: 1-10. PMID 10652185 DOI: 10.1006/jmcc.1999.1047  0.92
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  0.92
1999 White PS, Forus A, Matise TC, Schutte BC, Spieker N, Stanier P, Vance JM, Gregory SG. Report of the fifth international workshop on human chromosome 1 mapping 1999 Cytogenetics and Cell Genetics. 87: 143-171. PMID 10702659  0.92
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  0.92
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  0.92
1999 Kline JN, Cowden JD, Hunninghake GW, Schutte BC, Watt JL, Wohlford-Lenane CL, Powers LS, Jones MP, Schwartz DA. Variable airway responsiveness to inhaled lipopolysaccharide American Journal of Respiratory and Critical Care Medicine. 160: 297-303. PMID 10390415  0.92
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  0.92
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  0.92
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  0.92
1999 White PS, Forus A, Matise TC, Schutte BC, Spieker N, Stanier P, Vance JM, Gregory SG. Fifth International Workshop on Human Chromosome 1 Mapping 1999, the Sanger Centre, Cambridge, UK, August 5-7 1999: Report Cytogenetics and Cell Genetics. 87: 143-163.  0.92
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  0.92
1998 Goldman FD, Ballas ZK, Schutte BC, Kemp J, Hollenback C, Noraz N, Taylor N. Defective expression of p561ck in an infant with severe combined immunodeficiency Journal of Clinical Investigation. 102: 421-429. PMID 9664084  0.92
1998 Scholz TD, Koppenhafer SL, TenEyck CJ, Schutte BC. Ontogeny of malate-aspartate shuttle capacity and gene expression in cardiac mitochondria American Journal of Physiology - Cell Physiology. 274. PMID 9530110  0.92
1998 Schutte DL, Williams J, Schutte BC, Maas M. Alzheimer's disease genetics. Practice and education implications for special care unit nurses Journal of Gerontological Nursing. 24. PMID 9510720  0.92
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  0.92
1998 Gregory SG, Vaudin M, Wooster R, Coleman M, Mischke D, Porter C, Schutte BC, White P, Vance JM. Fourth International Workshop on Human Chromosome 1 Mapping 1998, Sanger Centre, Cambridge, United Kingdom, June 25-27 1998: Report Cytogenetics and Cell Genetics. 83: 147-167.  0.92
1997 Vance JM, Matise TC, Wooster R, Schutte BC, Bruns GA, van Roy N, Brodeur GM, Tao YX, Gregory S, Weith A, Vaudin M, White P. Report and abstracts of the third international workshop on human chromosome 1 mapping 1997 Cytogenetics and Cell Genetics. 78: 154-182. PMID 9465885  0.92
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  0.92
1997 Peiffer-Schneider S, Schutte BC, Murray JC, Frees KL, Williamson K, Leysens NJ, Schwartz DA. Exclusion of Ifa and Ifb as the Lps gene and mapping of three markers near the Lps locus Mammalian Genome. 8: 785-786. PMID 9321479 DOI: 10.1007/s003359900569  0.92
1997 Scholz TD, Koppenhafer SL, TenEyck CJ, Schutte BC. Developmental regulation of the α-glycerophosphate shuttle in porcine myocardium Journal of Molecular and Cellular Cardiology. 29: 1605-1613. PMID 9220346 DOI: 10.1006/jmcc.1997.0394  0.92
1997 Atkins DL, Krumm PA, Schutte BC, Harrison JD, Green SH. Regulation of rat cardiac myocyte growth by a neuronal factor secreted by PC12 cells. Pediatric Research. 41: 832-41. PMID 9167196 DOI: 10.1203/00006450-199706000-00007  0.92
1997 Schutte BC, Ranade K, Pruessner J, Dracopoli N. Optimized conditions for cloning PCR products into an XcmI T-vector. Biotechniques. 22: 40-2, 44. PMID 8994642  0.92
1997 Vance JM, Matise TC, Wooster R, Schutte BC, Bruns GAP, Van Roy N, Brodeur GM, Tao YX, Gregory S, Weith A, Vaudin M, White P. Third International Chromosome 1 Maping Workshop, Duke University, Durham, NC, USA, 25-27 April 1997: Report of the third international workshop on human chromosome 1 mapping 1997 Cytogenetics and Cell Genetics. 78: 154-179.  0.92
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  0.92
1996 Lamb FS, Mathews K, Mills K, Barna T, Preussner J, Schutte BC. COlocalization of icln and clcn3 to human 4q32, and to mouse 8 in the candidate region for tottering (tg) Faseb Journal. 10.  0.92
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  0.92
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  0.92
1994 Winokur ST, Bengtsson U, Feddersen J, Mathews KD, Weiffenbach B, Bailey H, Markovich RP, Murray JC, Wasmuth JJ, Altherr MR. The DNA rearrangement associated with facioscapulohumeral muscular dystrophy involves a heterochromatin-associated repetitive element: implications for a role of chromatin structure in the pathogenesis of the disease. Chromosome Research : An International Journal On the Molecular, Supramolecular and Evolutionary Aspects of Chromosome Biology. 2: 225-34. PMID 8069466 DOI: 10.1007/BF01553323  0.92
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  0.92
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  0.92
1988 Schutte BC, Cox MM. Homology-dependent underwinding of duplex DNA in recA protein generated paranemic complexes Biochemistry. 27: 7886-7894. PMID 3061463  0.92
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  0.92
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  0.92
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