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A spontaneous mutation in contactin 1 in the mouse.
Davisson MT, Bronson RT, Tadenev AL, Motley WW, Krishnaswamy A, Seburn KL, Burgess RW. Davisson MT, et al. Among authors: bronson rt. PLoS One. 2011;6(12):e29538. doi: 10.1371/journal.pone.0029538. Epub 2011 Dec 29. PLoS One. 2011. PMID: 22242131 Free PMC article.
A mouse model for Meckel syndrome type 3.
Cook SA, Collin GB, Bronson RT, Naggert JK, Liu DP, Akeson EC, Davisson MT. Cook SA, et al. Among authors: bronson rt. J Am Soc Nephrol. 2009 Apr;20(4):753-64. doi: 10.1681/ASN.2008040412. Epub 2009 Feb 11. J Am Soc Nephrol. 2009. PMID: 19211713 Free PMC article.
Fine Mapping of a Deafness Mutation hml on Mouse Chromosome 10.
Zheng QY, Harris BS, Ward-Bailey PF, Yu H, Bronson RT, Davisson MT, Johnson KR. Zheng QY, et al. Among authors: bronson rt. Acad J Xian Jiaotong Univ. 2004 Jun;25(3):209-212. Acad J Xian Jiaotong Univ. 2004. PMID: 21179397 Free PMC article.
Trak1 mutation disrupts GABA(A) receptor homeostasis in hypertonic mice.
Gilbert SL, Zhang L, Forster ML, Anderson JR, Iwase T, Soliven B, Donahue LR, Sweet HO, Bronson RT, Davisson MT, Wollmann RL, Lahn BT. Gilbert SL, et al. Among authors: bronson rt. Nat Genet. 2006 Feb;38(2):245-50. doi: 10.1038/ng1715. Epub 2005 Dec 25. Nat Genet. 2006. PMID: 16380713
ZFP191 is required by oligodendrocytes for CNS myelination.
Howng SY, Avila RL, Emery B, Traka M, Lin W, Watkins T, Cook S, Bronson R, Davisson M, Barres BA, Popko B. Howng SY, et al. Genes Dev. 2010 Feb 1;24(3):301-11. doi: 10.1101/gad.1864510. Epub 2010 Jan 15. Genes Dev. 2010. PMID: 20080941 Free PMC article.
Discovery and characterization of spontaneous mouse models of craniofacial dysmorphology.
Palmer K, Fairfield H, Borgeia S, Curtain M, Hassan MG, Dionne L, Yong Karst S, Coombs H, Bronson RT, Reinholdt LG, Bergstrom DE, Donahue LR, Cox TC, Murray SA. Palmer K, et al. Among authors: bronson rt. Dev Biol. 2016 Jul 15;415(2):216-227. doi: 10.1016/j.ydbio.2015.07.023. Epub 2015 Jul 31. Dev Biol. 2016. PMID: 26234751 Free PMC article.
548 results