Davisson MT - Search Results

1

Forebrain overgrowth (fog): a new mutation in the mouse affecting neural tube development.

Harris BS, Franz T, Ullrich S, Cook S, Bronson RT, Davisson MT. Harris BS, et al. Among authors: davisson mt. Teratology. 1997 Apr;55(4):231-40. doi: 10.1002/(SICI)1096-9926(199704)55:4<231::AID-TERA3>3.0.CO;2-3. Teratology. 1997. PMID: 9216040

2

Mesenchymal dysplasia: a recessive mutation on chromosome 13 of the mouse.

Sweet HO, Bronson RT, Donahue LR, Davisson MT. Sweet HO, et al. Among authors: davisson mt. J Hered. 1996 Mar-Apr;87(2):87-95. doi: 10.1093/oxfordjournals.jhered.a022981. J Hered. 1996. PMID: 8830098

3

Scrambler, a new neurological mutation of the mouse with abnormalities of neuronal migration.

Sweet HO, Bronson RT, Johnson KR, Cook SA, Davisson MT. Sweet HO, et al. Among authors: davisson mt. Mamm Genome. 1996 Nov;7(11):798-802. doi: 10.1007/s003359900240. Mamm Genome. 1996. PMID: 8875886

4

Megencephaly: a new mouse mutation on chromosome 6 that causes hypertrophy of the brain.

Donahue LR, Cook SA, Johnson KR, Bronson RT, Davisson MT. Donahue LR, et al. Among authors: davisson mt. Mamm Genome. 1996 Dec;7(12):871-6. doi: 10.1007/s003359900259. Mamm Genome. 1996. PMID: 8995755

5

Cerebellar deficient folia (cdf): a new mutation on mouse chromosome 6.

Cook SA, Bronson RT, Donahue LR, Ben-Arie N, Davisson MT. Cook SA, et al. Among authors: davisson mt. Mamm Genome. 1997 Feb;8(2):108-12. doi: 10.1007/s003359900368. Mamm Genome. 1997. PMID: 9060409

6

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: davisson mt. 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.

7

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: davisson mt. Acad J Xian Jiaotong Univ. 2004 Jun;25(3):209-212. Acad J Xian Jiaotong Univ. 2004. PMID: 21179397 Free PMC article.

8

Curly bare (cub), a new mouse mutation on chromosome 11 causing skin and hair abnormalities, and a modifier gene (mcub) on chromosome 5.

Johnson KR, Lane PW, Cook SA, Harris BS, Ward-Bailey PF, Bronson RT, Lyons BL, Shultz LD, Davisson MT. Johnson KR, et al. Among authors: davisson mt. Genomics. 2003 Jan;81(1):6-14. doi: 10.1016/s0888-7543(02)00013-7. Genomics. 2003. PMID: 12573256

9

Neuromuscular degeneration (nmd): a mutation on mouse chromosome 19 that causes motor neuron degeneration.

Cook SA, Johnson KR, Bronson RT, Davisson MT. Cook SA, et al. Among authors: davisson mt. Mamm Genome. 1995 Mar;6(3):187-91. doi: 10.1007/BF00293010. Mamm Genome. 1995. PMID: 7749225

10

Identification and genetic mapping of 151 dispersed members of 16 ribosomal protein multigene families in the mouse.

Johnson KR, Cook SA, Davisson MT. Johnson KR, et al. Among authors: davisson mt. Mamm Genome. 1994 Nov;5(11):670-87. doi: 10.1007/BF00426073. Mamm Genome. 1994. PMID: 7873877

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