Donahue LR - Search Results

1

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: donahue lr. 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.

2

Congenital hypothyroidism, dwarfism, and hearing impairment caused by a missense mutation in the mouse dual oxidase 2 gene, Duox2.

Johnson KR, Marden CC, Ward-Bailey P, Gagnon LH, Bronson RT, Donahue LR. Johnson KR, et al. Among authors: donahue lr. Mol Endocrinol. 2007 Jul;21(7):1593-602. doi: 10.1210/me.2007-0085. Epub 2007 Apr 17. Mol Endocrinol. 2007. PMID: 17440044

3

Grey intense: a new mouse mutation affecting pigmentation.

Davisson MT, Johnson KR, Bronson RT, Ward-Bailey PF, Cook SA, Harris BS, Donahue LR. Davisson MT, et al. Among authors: donahue lr. Mamm Genome. 2000 Dec;11(12):1139-41. doi: 10.1007/s003350010165. Mamm Genome. 2000. PMID: 11130986 No abstract available.

4

A missense mutation in the mouse Col2a1 gene causes spondyloepiphyseal dysplasia congenita, hearing loss, and retinoschisis.

Donahue LR, Chang B, Mohan S, Miyakoshi N, Wergedal JE, Baylink DJ, Hawes NL, Rosen CJ, Ward-Bailey P, Zheng QY, Bronson RT, Johnson KR, Davisson MT. Donahue LR, et al. J Bone Miner Res. 2003 Sep;18(9):1612-21. doi: 10.1359/jbmr.2003.18.9.1612. J Bone Miner Res. 2003. PMID: 12968670 Free PMC article.

5

Neuromuscular ataxia: a new spontaneous mutation in the mouse.

Ward-Bailey PF, Wood B, Johnson KR, Bronson RT, Donahue LR, Davisson MT. Ward-Bailey PF, et al. Among authors: donahue lr. Mamm Genome. 2000 Oct;11(10):820-3. doi: 10.1007/s003350010167. Mamm Genome. 2000. PMID: 11003693

6

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: donahue lr. J Hered. 1996 Mar-Apr;87(2):87-95. doi: 10.1093/oxfordjournals.jhered.a022981. J Hered. 1996. PMID: 8830098

7

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. Mamm Genome. 1996 Dec;7(12):871-6. doi: 10.1007/s003359900259. Mamm Genome. 1996. PMID: 8995755

8

A new spontaneous mouse mutation of Hoxd13 with a polyalanine expansion and phenotype similar to human synpolydactyly.

Johnson KR, Sweet HO, Donahue LR, Ward-Bailey P, Bronson RT, Davisson MT. Johnson KR, et al. Among authors: donahue lr. Hum Mol Genet. 1998 Jun;7(6):1033-8. doi: 10.1093/hmg/7.6.1033. Hum Mol Genet. 1998. PMID: 9580668

9

Neuronal ceroid lipofuscinosis (nclf), a new disorder of the mouse linked to chromosome 9.

Bronson RT, Donahue LR, Johnson KR, Tanner A, Lane PW, Faust JR. Bronson RT, et al. Among authors: donahue lr. Am J Med Genet. 1998 May 26;77(4):289-97. doi: 10.1002/(sici)1096-8628(19980526)77:4<289::aid-ajmg8>3.0.co;2-i. Am J Med Genet. 1998. PMID: 9600738

10

Juvenile bare: a new hair loss mutation on chromosome 7 of the mouse.

Lane PW, Bronson RT, Cook SA, Ward-Bailey P, Donahue LR, Davisson MT. Lane PW, et al. Among authors: donahue lr. J Hered. 1998 May-Jun;89(3):254-7. doi: 10.1093/jhered/89.3.254. J Hered. 1998. PMID: 9656467

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