Roe B - Search Results

1

A deletion causing spontaneous fracture identified from a candidate region of mouse Chromosome 14.

Jiao Y, Li X, Beamer WG, Yan J, Tong Y, Goldowitz D, Roe B, Gu W. Jiao Y, et al. Among authors: roe b. Mamm Genome. 2005 Jan;16(1):20-31. doi: 10.1007/s00335-004-2414-0. Mamm Genome. 2005. PMID: 15674730

2

Carbonic anhydrase-related protein VIII deficiency is associated with a distinctive lifelong gait disorder in waddles mice.

Jiao Y, Yan J, Zhao Y, Donahue LR, Beamer WG, Li X, Roe BA, Ledoux MS, Gu W. Jiao Y, et al. Genetics. 2005 Nov;171(3):1239-46. doi: 10.1534/genetics.105.044487. Epub 2005 Aug 22. Genetics. 2005. PMID: 16118194 Free PMC article.

3

Effects of carbonic anhydrase VIII deficiency on cerebellar gene expression profiles in the wdl mouse.

Yan J, Jiao Y, Jiao F, Stuart J, Donahue LR, Beamer WG, Li X, Roe BA, LeDoux MS, Gu W. Yan J, et al. Neurosci Lett. 2007 Feb 21;413(3):196-201. doi: 10.1016/j.neulet.2006.11.046. Epub 2006 Dec 15. Neurosci Lett. 2007. PMID: 17174474 Free PMC article.

4

A single nucleotide mutation in Nppc is associated with a long bone abnormality in lbab mice.

Jiao Y, Yan J, Jiao F, Yang H, Donahue LR, Li X, Roe BA, Stuart J, Gu W. Jiao Y, et al. BMC Genet. 2007 Apr 17;8:16. doi: 10.1186/1471-2156-8-16. BMC Genet. 2007. PMID: 17439653 Free PMC article.

5

A deletion mutation in Slc12a6 is associated with neuromuscular disease in gaxp mice.

Jiao Y, Jin X, Yan J, Zhang C, Jiao F, Li X, Roe BA, Mount DB, Gu W. Jiao Y, et al. Among authors: roe ba. Genomics. 2008 May;91(5):407-14. doi: 10.1016/j.ygeno.2007.12.010. Epub 2008 Mar 14. Genomics. 2008. PMID: 18343091 Free PMC article.

6

An insertion of intracisternal A-particle retrotransposon in a novel member of the phosphoglycerate mutase family in the lew allele of mutant mice.

Jiao Y, Jin X, Yan J, Jiao F, Li X, Roe BA, Jarrett HW, Gu W. Jiao Y, et al. Genes Genet Syst. 2009 Oct;84(5):327-34. doi: 10.1266/ggs.84.327. Genes Genet Syst. 2009. PMID: 20154419 Free PMC article.

7

Sequence-ready physical map of the mouse chromosome 16 region with conserved synteny to the human velocardiofacial syndrome region on 22q11.2.

Lund J, Roe B, Chen F, Budarf M, Galili N, Riblet R, Miller RD, Emanuel BS, Reeves RH. Lund J, et al. Among authors: roe b. Mamm Genome. 1999 May;10(5):438-43. doi: 10.1007/s003359901019. Mamm Genome. 1999. PMID: 10337614

8

Characterization of CDC45L: a gene in the 22q11.2 deletion region expressed during murine and human development.

Shaikh TH, Gottlieb S, Sellinger B, Chen F, Roe BA, Oakey RJ, Emanuel BS, Budarf ML. Shaikh TH, et al. Among authors: roe ba. Mamm Genome. 1999 Mar;10(3):322-6. doi: 10.1007/s003359900996. Mamm Genome. 1999. PMID: 10051334 No abstract available.

9

DQX1, an RNA-dependent ATPase homolog with a novel DEAQ box: expression pattern and genomic sequence comparison of the human and mouse genes.

Ji W, Chen F, Do T, Do A, Roe BA, Meisler MH. Ji W, et al. Among authors: roe ba. Mamm Genome. 2001 Jun;12(6):456-61. doi: 10.1007/s003350020032. Mamm Genome. 2001. PMID: 11353393 Free article.

10

Characterization of the mouse beta-prime adaptin gene; cDNA sequence, genomic structure, and chromosomal localization.

Guilbaud C, Peyrard M, Fransson I, Clifton SW, Roe BA, Carter NP, Dumanski JP. Guilbaud C, et al. Among authors: roe ba. Mamm Genome. 1997 Sep;8(9):651-6. doi: 10.1007/s003359900531. Mamm Genome. 1997. PMID: 9271666

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