Brown SD - Search Results

1

A STS content physical and transcription map across the ky, kyphoscoliosis, nonrecombinant region.

Blanco G, Nikitopoulou A, Kraus M, Mason RM, Coulton GR, Brown SD. Blanco G, et al. Among authors: brown sd. Genomics. 1998 Dec 15;54(3):415-23. doi: 10.1006/geno.1998.5614. Genomics. 1998. PMID: 9878244

2

Genetic mapping of the mouse neuromuscular mutation kyphoscoliosis.

Skynner MJ, Gangadharan U, Coulton GR, Mason RM, Nikitopoulou A, Brown SD, Blanco G. Skynner MJ, et al. Among authors: brown sd. Genomics. 1995 Jan 1;25(1):207-13. doi: 10.1016/0888-7543(95)80127-8. Genomics. 1995. PMID: 7774920

3

The kyphoscoliosis (ky) mouse is deficient in hypertrophic responses and is caused by a mutation in a novel muscle-specific protein.

Blanco G, Coulton GR, Biggin A, Grainge C, Moss J, Barrett M, Berquin A, Maréchal G, Skynner M, van Mier P, Nikitopoulou A, Kraus M, Ponting CP, Mason RM, Brown SD. Blanco G, et al. Among authors: brown sd. Hum Mol Genet. 2001 Jan 1;10(1):9-16. doi: 10.1093/hmg/10.1.9. Hum Mol Genet. 2001. PMID: 11136708

4

Molecular and genetic mapping of the mouse mdx locus.

Cavanna JS, Coulton G, Morgan JE, Brockdorff N, Forrest SM, Davies KE, Brown SD. Cavanna JS, et al. Among authors: brown sd. Genomics. 1988 Nov;3(4):337-41. doi: 10.1016/0888-7543(88)90124-3. Genomics. 1988. PMID: 3243547

5

Genetic mapping of protein kinase C theta (Pkcq) to mouse chromosome 2.

Blanco G, Brown SD. Blanco G, et al. Among authors: brown sd. Mamm Genome. 1997 Jan;8(1):70-1. doi: 10.1007/s003359900355. Mamm Genome. 1997. PMID: 9021158 No abstract available.

6

Molecular phenotyping of the mouse ky mutant reveals UCP1 upregulation at the neuromuscular junctions of dystrophic soleus muscle.

Blanco G, Pritchard C, Underhill P, Breeds S, Townsend KM, Greenfield A, Brown SD. Blanco G, et al. Among authors: brown sd. Neuromuscul Disord. 2004 Mar;14(3):217-28. doi: 10.1016/j.nmd.2003.09.008. Neuromuscul Disord. 2004. PMID: 15036332

7

Mapping of the human and murine X11-like genes (APBA2 and apba2), the murine Fe65 gene (Apbb1), and the human Fe65-like gene (APBB2): genes encoding phosphotyrosine-binding domain proteins that interact with the Alzheimer's disease amyloid precursor protein.

Blanco G, Irving NG, Brown SD, Miller CC, McLoughlin DM. Blanco G, et al. Among authors: brown sd. Mamm Genome. 1998 Jun;9(6):473-5. doi: 10.1007/s003359900800. Mamm Genome. 1998. PMID: 9585438 No abstract available.

8

A high-resolution genetic, physical, and comparative gene map of the doublefoot (Dbf) region of mouse chromosome 1 and the region of conserved synteny on human chromosome 2q35.

Hayes C, Rump A, Cadman MR, Harrison M, Evans EP, Lyon MF, Morriss-Kay GM, Rosenthal A, Brown SD. Hayes C, et al. Among authors: brown sd. Genomics. 2001 Dec;78(3):197-205. doi: 10.1006/geno.2001.6657. Genomics. 2001. PMID: 11735226

9

Genetic and physical mapping of a gene encoding a methyl CpG binding protein, Mecp2, to the mouse X chromosome.

Quaderi NA, Meehan RR, Tate PH, Cross SH, Bird AP, Chatterjee A, Herman GE, Brown SD. Quaderi NA, et al. Among authors: brown sd. Genomics. 1994 Aug;22(3):648-51. doi: 10.1006/geno.1994.1442. Genomics. 1994. PMID: 8001979

10

Defects in whirlin, a PDZ domain molecule involved in stereocilia elongation, cause deafness in the whirler mouse and families with DFNB31.

Mburu P, Mustapha M, Varela A, Weil D, El-Amraoui A, Holme RH, Rump A, Hardisty RE, Blanchard S, Coimbra RS, Perfettini I, Parkinson N, Mallon AM, Glenister P, Rogers MJ, Paige AJ, Moir L, Clay J, Rosenthal A, Liu XZ, Blanco G, Steel KP, Petit C, Brown SD. Mburu P, et al. Among authors: brown sd. Nat Genet. 2003 Aug;34(4):421-8. doi: 10.1038/ng1208. Nat Genet. 2003. PMID: 12833159

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