Kerns JA - Search Results

1

Exclusion of melanocortin-1 receptor (mc1r) and agouti as candidates for dominant black in dogs.

Kerns JA, Olivier M, Lust G, Barsh GS. Kerns JA, et al. J Hered. 2003 Jan-Feb;94(1):75-9. J Hered. 2003. PMID: 12692166

2

Characterization of the dog Agouti gene and a nonagoutimutation in German Shepherd Dogs.

Kerns JA, Newton J, Berryere TG, Rubin EM, Cheng JF, Schmutz SM, Barsh GS. Kerns JA, et al. Mamm Genome. 2004 Oct;15(10):798-808. doi: 10.1007/s00335-004-2377-1. Mamm Genome. 2004. PMID: 15520882

3

Linkage and segregation analysis of black and brindle coat color in domestic dogs.

Kerns JA, Cargill EJ, Clark LA, Candille SI, Berryere TG, Olivier M, Lust G, Todhunter RJ, Schmutz SM, Murphy KE, Barsh GS. Kerns JA, et al. Genetics. 2007 Jul;176(3):1679-89. doi: 10.1534/genetics.107.074237. Epub 2007 May 4. Genetics. 2007. PMID: 17483404 Free PMC article.

4

A -defensin mutation causes black coat color in domestic dogs.

Candille SI, Kaelin CB, Cattanach BM, Yu B, Thompson DA, Nix MA, Kerns JA, Schmutz SM, Millhauser GL, Barsh GS. Candille SI, et al. Among authors: kerns ja. Science. 2007 Nov 30;318(5855):1418-23. doi: 10.1126/science.1147880. Epub 2007 Oct 18. Science. 2007. PMID: 17947548 Free PMC article.

5

MC1R studies in dogs with melanistic mask or brindle patterns.

Schmutz SM, Berryere TG, Ellinwood NM, Kerns JA, Barsh GS. Schmutz SM, et al. Among authors: kerns ja. J Hered. 2003 Jan-Feb;94(1):69-73. doi: 10.1093/jhered/esg014. J Hered. 2003. PMID: 12692165

6

Association of an Agouti allele with fawn or sable coat color in domestic dogs.

Berryere TG, Kerns JA, Barsh GS, Schmutz SM. Berryere TG, et al. Among authors: kerns ja. Mamm Genome. 2005 Apr;16(4):262-72. doi: 10.1007/s00335-004-2445-6. Mamm Genome. 2005. PMID: 15965787

7

Antagonism of central melanocortin receptors in vitro and in vivo by agouti-related protein.

Ollmann MM, Wilson BD, Yang YK, Kerns JA, Chen Y, Gantz I, Barsh GS. Ollmann MM, et al. Among authors: kerns ja. Science. 1997 Oct 3;278(5335):135-8. doi: 10.1126/science.278.5335.135. Science. 1997. PMID: 9311920

8

WASP gene mutations in Wiskott-Aldrich syndrome and X-linked thrombocytopenia.

Derry JM, Kerns JA, Weinberg KI, Ochs HD, Volpini V, Estivill X, Walker AP, Francke U. Derry JM, et al. Among authors: kerns ja. Hum Mol Genet. 1995 Jul;4(7):1127-35. doi: 10.1093/hmg/4.7.1127. Hum Mol Genet. 1995. PMID: 8528199

9

RBM3, a novel human gene in Xp11.23 with a putative RNA-binding domain.

Derry JM, Kerns JA, Francke U. Derry JM, et al. Among authors: kerns ja. Hum Mol Genet. 1995 Dec;4(12):2307-11. doi: 10.1093/hmg/4.12.2307. Hum Mol Genet. 1995. PMID: 8634703

10

Identification of a novel paternally expressed gene in the Prader-Willi syndrome region.

Wevrick R, Kerns JA, Francke U. Wevrick R, et al. Among authors: kerns ja. Hum Mol Genet. 1994 Oct;3(10):1877-82. doi: 10.1093/hmg/3.10.1877. Hum Mol Genet. 1994. PMID: 7849716

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

20 results

Search Page

Filters