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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.
The mouse mutation "thrombocytopenia and cardiomyopathy" (trac) disrupts Abcg5: a spontaneous single gene model for human hereditary phytosterolemia/sitosterolemia.
Chase TH, Lyons BL, Bronson RT, Foreman O, Donahue LR, Burzenski LM, Gott B, Lane P, Harris B, Ceglarek U, Thiery J, Wittenburg H, Thon JN, Italiano JE Jr, Johnson KR, Shultz LD. Chase TH, et al. Among authors: bronson rt. Blood. 2010 Feb 11;115(6):1267-76. doi: 10.1182/blood-2009-05-219808. Epub 2009 Oct 21. Blood. 2010. PMID: 19846887 Free PMC article.
Mutations in a P-type ATPase gene cause axonal degeneration.
Zhu X, Libby RT, de Vries WN, Smith RS, Wright DL, Bronson RT, Seburn KL, John SW. Zhu X, et al. Among authors: bronson rt. PLoS Genet. 2012;8(8):e1002853. doi: 10.1371/journal.pgen.1002853. Epub 2012 Aug 9. PLoS Genet. 2012. PMID: 22912588 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.
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.
499 results