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Journal Abstract Search

83 related items for PubMed ID: 21070280

  • 1. A genome-wide scan for tying-up syndrome in Japanese Thoroughbreds.
    Tozaki T, Hirota K, Sugita S, Ishida N, Miyake T, Oki H, Hasegawa T.
    Anim Genet; 2010 Dec; 41 Suppl 2():80-6. PubMed ID: 21070280
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  • 2. Heritability of recurrent exertional rhabdomyolysis in Thoroughbred racehorses.
    MacLeay JM, Valberg SJ, Sorum SA, Sorum MD, Kassube T, Santschi EM, Mickelson JR, Geyer CJ.
    Am J Vet Res; 1999 Feb; 60(2):250-6. PubMed ID: 10048561
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  • 3. Exclusion of linkage of the RYR1, CACNA1S, and ATP2A1 genes to recurrent exertional rhabdomyolysis in Thoroughbreds.
    Dranchak PK, Valberg SJ, Onan GW, Gallant EM, Binns MM, Swinburne JE, Mickelson JR.
    Am J Vet Res; 2006 Aug; 67(8):1395-400. PubMed ID: 16881852
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  • 6. Heritability of Recurrent Exertional Rhabdomyolysis in Standardbred and Thoroughbred Racehorses Derived From SNP Genotyping Data.
    Norton EM, Mickelson JR, Binns MM, Blott SC, Caputo P, Isgren CM, McCoy AM, Moore A, Piercy RJ, Swinburne JE, Vaudin M, McCue ME.
    J Hered; 2016 Nov; 107(6):537-43. PubMed ID: 27489252
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  • 10. Epidemiologic analysis of factors influencing exertional rhabdomyolysis in Thoroughbreds.
    MacLeay JM, Sorum SA, Valberg SJ, Marsh WE, Sorum MD.
    Am J Vet Res; 1999 Dec; 60(12):1562-6. PubMed ID: 10622169
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  • 11. Transcriptome analysis of muscle in horses suffering from recurrent exertional rhabdomyolysis revealed energetic pathway alterations and disruption in the cytosolic calcium regulation.
    Barrey E, Jayr L, Mucher E, Gospodnetic S, Joly F, Benech P, Alibert O, Gidrol X, Mata X, Vaiman A, Guérin G.
    Anim Genet; 2012 Jun; 43(3):271-81. PubMed ID: 22486498
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  • 12. Refinement of a quantitative trait locus on equine chromosome 5 responsible for fetlock osteochondrosis in Hanoverian warmblood horses.
    Lampe V, Dierks C, Distl O.
    Anim Genet; 2009 Aug; 40(4):553-5. PubMed ID: 19392821
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  • 13. Calcium sensitivity of force production and myofibrillar ATPase activity in muscles from Thoroughbreds with recurrent exertional rhabdomyolysis.
    Mlekoday JA, Mickelson JR, Valberg SJ, Horton JH, Gallant EM, Thompson LV.
    Am J Vet Res; 2001 Oct; 62(10):1647-52. PubMed ID: 11592334
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  • 14. Fine mapping of a quantitative trait locus for osteochondrosis on horse chromosome 2.
    Dierks C, Komm K, Lampe V, Distl O.
    Anim Genet; 2010 Dec; 41 Suppl 2():87-90. PubMed ID: 21070281
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  • 16. Whole-genome scan identifies quantitative trait loci for chronic pastern dermatitis in German draft horses.
    Mittmann EH, Mömke S, Distl O.
    Mamm Genome; 2010 Feb; 21(1-2):95-103. PubMed ID: 20039044
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  • 17. Exertional rhabdomyolysis in quarter horses and thoroughbreds: one syndrome, multiple aetiologies.
    Valberg SJ, Mickelson JR, Gallant EM, MacLeay JM, Lentz L, de la Corte F.
    Equine Vet J Suppl; 1999 Jul; (30):533-8. PubMed ID: 10659313
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  • 18. Identification of a new quantitative trait locus on equine chromosome 18 responsible for osteochondrosis in Hanoverian warmblood horses.
    Lampe V, Dierks C, Komm K, Distl O.
    J Anim Sci; 2009 Nov; 87(11):3477-81. PubMed ID: 19684265
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  • 20. A genome-wide association study for racing performances in Thoroughbreds clarifies a candidate region near the MSTN gene.
    Tozaki T, Miyake T, Kakoi H, Gawahara H, Sugita S, Hasegawa T, Ishida N, Hirota K, Nakano Y.
    Anim Genet; 2010 Dec; 41 Suppl 2():28-35. PubMed ID: 21070273
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