Heather Holl, Ph.D.

 

 

Publications:

 

Evidence for a retroviral insertion in TRPM1 as the cause of congenital stationary night blindness and leopard complex spotting in the horse.

Bellone RR, Holl H, Setaluri V, Devi S, Maddodi N, Archer S, Sandmeyer L, Ludwig A, Foerster D, Pruvost M, Reissmann M, Bortfeldt R, Adelson DL, Lim SL, Nelson J, Haase B, Engensteiner M, Leeb T, Forsyth G, Mienaltowski MJ, Mahadevan P, Hofreiter M, Paijmans JL, Gonzalez-Fortes G, Grahn B, Brooks SA.

PLoS One. 2013 Oct 22;8(10):e78280. doi: 10.1371/journal.pone.0078280. eCollection 2013.

 

Novel variants in the KIT and PAX3 genes in horses with white-spotted coat colour phenotypes.

Hauswirth R, Jude R, Haase B, Bellone RR, Archer S, Holl H, Brooks SA, Tozaki T, Penedo MC, Rieder S, Leeb T.

Anim Genet. 2013 Dec;44(6):763-5. doi: 10.1111/age.12057. Epub 2013 May 9.

 

Detection of two equine trisomies using SNP-CGH.

Holl HM, Lear TL, Nolen-Walston RD, Slack J, Brooks SA.

Mamm Genome. 2013 Jun;24(5-6):252-6. doi: 10.1007/s00335-013-9450-6. Epub 2013 Mar 21.

 

Related Media and Articles of Interest:

Write up about an interesting genetic mutation causing lack of pigmentation in a Thoroughbred

http://www.thehorse.com/articles/26587/genetic-mutation-caused-nonhereditary-white-coat-color-pattern

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