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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

115 related items for PubMed ID: 21118319

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  • 25. Mutation in cyclophilin B that causes hyperelastosis cutis in American Quarter Horse does not affect peptidylprolyl cis-trans isomerase activity but shows altered cyclophilin B-protein interactions and affects collagen folding.
    Ishikawa Y, Vranka JA, Boudko SP, Pokidysheva E, Mizuno K, Zientek K, Keene DR, Rashmir-Raven AM, Nagata K, Winand NJ, Bächinger HP.
    J Biol Chem; 2012 Jun 22; 287(26):22253-65. PubMed ID: 22556420
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  • 27. An inherited connective tissue disease in the horse.
    Hardy MH, Fisher KR, Vrablic OE, Yager JA, Nimmo-Wilkie JS, Parker W, Keeley FW.
    Lab Invest; 1988 Aug 22; 59(2):253-62. PubMed ID: 3404977
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  • 29. A 2-Year-Old Filly With Hereditary Equine Regional Dermal Asthenia: The First Case Report From China.
    Li 李靖 J, Liu B, Yu F, Liu T, Peng Y, Fu Y.
    J Equine Vet Sci; 2018 May 22; 64():1-4. PubMed ID: 30973143
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  • 30. Connective Tissue Disorders in Domestic Animals.
    Roberts JH, Halper J.
    Adv Exp Med Biol; 2021 May 22; 1348():325-335. PubMed ID: 34807427
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  • 31. Evaluation of FOXC2 as a candidate gene for chronic progressive lymphedema in draft horses.
    Young AE, Bower LP, Affolter VK, De Cock HE, Ferraro GL, Bannasch DL.
    Vet J; 2007 Sep 22; 174(2):397-9. PubMed ID: 16884936
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  • 32. Evaluation of the Filum Terminale in Hereditary Equine Regional Dermal Asthenia.
    McElroy A, Klinge PM, Sledge D, Donahue JE, Glabman RA, Rashmir A.
    Vet Pathol; 2021 Nov 22; 58(6):1100-1106. PubMed ID: 34056982
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  • 33. Polysaccharide storage myopathy phenotype in quarter horse-related breeds is modified by the presence of an RYR1 mutation.
    McCue ME, Valberg SJ, Jackson M, Borgia L, Lucio M, Mickelson JR.
    Neuromuscul Disord; 2009 Jan 22; 19(1):37-43. PubMed ID: 19056269
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  • 35. Hereditary equine regional dermal asthenia in a quarter horse bred in the United Kingdom.
    Rendle DI, Durhma AE, Smith KC.
    Vet Rec; 2008 Jan 05; 162(1):20-2. PubMed ID: 18178934
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  • 36. Population screening of endangered horse breeds for the foal immunodeficiency syndrome mutation.
    Fox-Clipsham LY, Brown EE, Carter SD, Swinburne JE.
    Vet Rec; 2011 Dec 17; 169(25):655. PubMed ID: 22016514
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  • 37. The epitheliogenesis imperfecta locus maps to equine chromosome 8 in American Saddlebred horses.
    Lieto LD, Cothran EG.
    Cytogenet Genome Res; 2003 Dec 17; 102(1-4):207-10. PubMed ID: 14970704
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  • 38. A GYS1 gene mutation is highly associated with polysaccharide storage myopathy in Cob Normand draught horses.
    Herszberg B, McCue ME, Larcher T, Mata X, Vaiman A, Chaffaux S, Chérel Y, Valberg SJ, Mickelson JR, Guérin G.
    Anim Genet; 2009 Feb 17; 40(1):94-6. PubMed ID: 18822097
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  • 39. Familial basis of exertional rhabdomyolysis in quarter horse-related breeds.
    Valberg SJ, Geyer C, Sorum SA, Cardinet GH.
    Am J Vet Res; 1996 Mar 17; 57(3):286-90. PubMed ID: 8669756
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  • 40. Periodic paralysis in quarter horses: a sodium channel mutation disseminated by selective breeding.
    Rudolph JA, Spier SJ, Byrns G, Rojas CV, Bernoco D, Hoffman EP.
    Nat Genet; 1992 Oct 17; 2(2):144-7. PubMed ID: 1338908
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