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Journal Abstract Search


100 related items for PubMed ID: 27210062

  • 1. Structural study of skeletal muscle fibres in healthy and pseudomyotonia affected cattle.
    Mascarello F, Sacchetto R.
    Ann Anat; 2016 Sep; 207():21-6. PubMed ID: 27210062
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  • 2. Inhibition of ubiquitin proteasome system rescues the defective sarco(endo)plasmic reticulum Ca2+-ATPase (SERCA1) protein causing Chianina cattle pseudomyotonia.
    Bianchini E, Testoni S, Gentile A, Calì T, Ottolini D, Villa A, Brini M, Betto R, Mascarello F, Nissen P, Sandonà D, Sacchetto R.
    J Biol Chem; 2014 Nov 28; 289(48):33073-82. PubMed ID: 25288803
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  • 3. Fast-twitch skeletal muscle fiber adaptation to SERCA1 deficiency in a Dutch Improved Red and White calf pseudomyotonia case.
    Dorotea T, Grünberg W, Murgiano L, Plattet P, Drögemüller C, Mascarello F, Sacchetto R.
    Neuromuscul Disord; 2015 Nov 28; 25(11):888-97. PubMed ID: 26482047
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  • 4. Differential Analysis of Gly211Val and Gly286Val Mutations Affecting Sarco(endo)plasmic Reticulum Ca2+-ATPase (SERCA1) in Congenital Pseudomyotonia Romagnola Cattle.
    Akyürek EE, Busato F, Murgiano L, Bianchini E, Carotti M, Sandonà D, Drögemüller C, Gentile A, Sacchetto R.
    Int J Mol Sci; 2022 Oct 15; 23(20):. PubMed ID: 36293223
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  • 6. Pseudomyotonia in Romagnola cattle caused by novel ATP2A1 mutations.
    Murgiano L, Sacchetto R, Testoni S, Dorotea T, Mascarello F, Liguori R, Gentile A, Drögemüller C.
    BMC Vet Res; 2012 Oct 09; 8():186. PubMed ID: 23046865
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  • 7. A defective SERCA1 protein is responsible for congenital pseudomyotonia in Chianina cattle.
    Sacchetto R, Testoni S, Gentile A, Damiani E, Rossi M, Liguori R, Drögemüller C, Mascarello F.
    Am J Pathol; 2009 Feb 09; 174(2):565-73. PubMed ID: 19116366
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  • 8. Identification of a missense mutation in the bovine ATP2A1 gene in congenital pseudomyotonia of Chianina cattle: an animal model of human Brody disease.
    Drögemüller C, Drögemüller M, Leeb T, Mascarello F, Testoni S, Rossi M, Gentile A, Damiani E, Sacchetto R.
    Genomics; 2008 Dec 09; 92(6):474-7. PubMed ID: 18786632
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  • 9. Brody disease: insights into biochemical features of SERCA1 and identification of a novel mutation.
    Vattemi G, Gualandi F, Oosterhof A, Marini M, Tonin P, Rimessi P, Neri M, Guglielmi V, Russignan A, Poli C, van Kuppevelt TH, Ferlini A, Tomelleri G.
    J Neuropathol Exp Neurol; 2010 Mar 09; 69(3):246-52. PubMed ID: 20142766
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  • 11. Targeted disruption of the ATP2A1 gene encoding the sarco(endo)plasmic reticulum Ca2+ ATPase isoform 1 (SERCA1) impairs diaphragm function and is lethal in neonatal mice.
    Pan Y, Zvaritch E, Tupling AR, Rice WJ, de Leon S, Rudnicki M, McKerlie C, Banwell BL, MacLennan DH.
    J Biol Chem; 2003 Apr 11; 278(15):13367-75. PubMed ID: 12556521
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  • 13. Identification of Small Ankyrin 1 as a Novel Sarco(endo)plasmic Reticulum Ca2+-ATPase 1 (SERCA1) Regulatory Protein in Skeletal Muscle.
    Desmond PF, Muriel J, Markwardt ML, Rizzo MA, Bloch RJ.
    J Biol Chem; 2015 Nov 13; 290(46):27854-67. PubMed ID: 26405035
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  • 14. The Accordion Zebrafish tq206 Mutant in the Assessment of a Novel Pharmaceutical Approach to Brody Myopathy.
    Akyürek EE, Greco F, Tesoriero C, Dalla Barba F, Carotti M, Gorni G, Sandonà D, Vettori A, Sacchetto R.
    Int J Mol Sci; 2024 Aug 25; 25(17):. PubMed ID: 39273176
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  • 15. Mutations in the gene-encoding SERCA1, the fast-twitch skeletal muscle sarcoplasmic reticulum Ca2+ ATPase, are associated with Brody disease.
    Odermatt A, Taschner PE, Khanna VK, Busch HF, Karpati G, Jablecki CK, Breuning MH, MacLennan DH.
    Nat Genet; 1996 Oct 25; 14(2):191-4. PubMed ID: 8841193
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  • 16. Interactions between small ankyrin 1 and sarcolipin coordinately regulate activity of the sarco(endo)plasmic reticulum Ca2+-ATPase (SERCA1).
    Desmond PF, Labuza A, Muriel J, Markwardt ML, Mancini AE, Rizzo MA, Bloch RJ.
    J Biol Chem; 2017 Jun 30; 292(26):10961-10972. PubMed ID: 28487373
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  • 19. Characterization of cDNA and genomic DNA encoding SERCA1, the Ca(2+)-ATPase of human fast-twitch skeletal muscle sarcoplasmic reticulum, and its elimination as a candidate gene for Brody disease.
    Zhang Y, Fujii J, Phillips MS, Chen HS, Karpati G, Yee WC, Schrank B, Cornblath DR, Boylan KB, MacLennan DH.
    Genomics; 1995 Dec 10; 30(3):415-24. PubMed ID: 8825625
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  • 20. accordion, a zebrafish behavioral mutant, has a muscle relaxation defect due to a mutation in the ATPase Ca2+ pump SERCA1.
    Hirata H, Saint-Amant L, Waterbury J, Cui W, Zhou W, Li Q, Goldman D, Granato M, Kuwada JY.
    Development; 2004 Nov 10; 131(21):5457-68. PubMed ID: 15469975
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