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Cytogenetic and genome research2006; 114(1); 93A; doi: 10.1159/000091935

Comparative mapping of oculocutaneous albinism type II (OCA2), transient receptor potential cation channel, subfamily M member 1 (TRPM1) and two equine microsatellites, ASB08 and 1CA43, among four equid species by fluorescence in situ hybridization.

Abstract: No abstract available
Publication Date: 2006-05-24 PubMed ID: 16717457DOI: 10.1159/000091935Google Scholar: Lookup
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  • Journal Article

Cite This Article

APA
Bellone R, Lear T, Adelson DL, Bailey E. (2006). Comparative mapping of oculocutaneous albinism type II (OCA2), transient receptor potential cation channel, subfamily M member 1 (TRPM1) and two equine microsatellites, ASB08 and 1CA43, among four equid species by fluorescence in situ hybridization. Cytogenet Genome Res, 114(1), 93A. https://doi.org/10.1159/000091935

Publication

ISSN: 1424-859X
NlmUniqueID: 101142708
Country: Switzerland
Language: English
Volume: 114
Issue: 1
Pages: 93A

Researcher Affiliations

Bellone, R
  • Department of Biology, University of Tampa, Tampa, FL, USA.
Lear, T
    Adelson, D L
      Bailey, E

        MeSH Terms

        • Albinism, Oculocutaneous / genetics
        • Albinism, Oculocutaneous / veterinary
        • Amino Acid Transport Systems, Neutral / genetics
        • Animals
        • Chromosome Mapping
        • Horse Diseases / genetics
        • Horses / genetics
        • In Situ Hybridization, Fluorescence
        • TRPM Cation Channels / genetics

        Citations

        This article has been cited 3 times.
        1. Grilz-Seger G, Neuditschko M, Ricard A, Velie B, Lindgren G, Mesarič M, Cotman M, Horna M, Dobretsberger M, Brem G, Druml T. Genome-Wide Homozygosity Patterns and Evidence for Selection in a Set of European and Near Eastern Horse Breeds.. Genes (Basel) 2019 Jun 28;10(7).
          doi: 10.3390/genes10070491pubmed: 31261764google scholar: lookup
        2. Haase B, Signer-Hasler H, Binns MM, Obexer-Ruff G, Hauswirth R, Bellone RR, Burger D, Rieder S, Wade CM, Leeb T. Accumulating mutations in series of haplotypes at the KIT and MITF loci are major determinants of white markings in Franches-Montagnes horses.. PLoS One 2013;8(9):e75071.
          doi: 10.1371/journal.pone.0075071pubmed: 24098679google scholar: lookup
        3. Bellone RR, Brooks SA, Sandmeyer L, Murphy BA, Forsyth G, Archer S, Bailey E, Grahn B. Differential gene expression of TRPM1, the potential cause of congenital stationary night blindness and coat spotting patterns (LP) in the Appaloosa horse (Equus caballus).. Genetics 2008 Aug;179(4):1861-70.
          doi: 10.1534/genetics.108.088807pubmed: 18660533google scholar: lookup