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For: Tiret L, Blot S, Kessler JL, Gaillot H, Breen M, Panthier JJ. The cnm locus, a canine homologue of human autosomal forms of centronuclear myopathy, maps to chromosome 2. Hum Genet 2003;113:297-306. [PMID: 12884002 DOI: 10.1007/s00439-003-0984-7] [Cited by in Crossref: 27] [Cited by in F6Publishing: 22] [Article Influence: 1.4] [Reference Citation Analysis]
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2 Barthélémy I, Hitte C, Tiret L. The Dog Model in the Spotlight: Legacy of a Trustful Cooperation. J Neuromuscul Dis 2019;6:421-51. [PMID: 31450509 DOI: 10.3233/JND-190394] [Cited by in Crossref: 1] [Article Influence: 0.5] [Reference Citation Analysis]
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6 Pelé M, Tiret L, Kessler JL, Blot S, Panthier JJ. SINE exonic insertion in the PTPLA gene leads to multiple splicing defects and segregates with the autosomal recessive centronuclear myopathy in dogs. Hum Mol Genet 2005;14:1417-27. [PMID: 15829503 DOI: 10.1093/hmg/ddi151] [Cited by in Crossref: 103] [Cited by in F6Publishing: 90] [Article Influence: 6.1] [Reference Citation Analysis]
7 Cerda-Gonzalez S, Talarico L, Todhunter R. Noninvasive Assessment of Neuromuscular Disease in Dogs: Use of the 6-minute Walk Test to Assess Submaximal Exercise Tolerance in Dogs with Centronuclear Myopathy. J Vet Intern Med 2016;30:808-12. [PMID: 27012153 DOI: 10.1111/jvim.13939] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 0.7] [Reference Citation Analysis]
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9 Walmsley GL, Blot S, Venner K, Sewry C, Laporte J, Blondelle J, Barthélémy I, Maurer M, Blanchard-Gutton N, Pilot-Storck F, Tiret L, Piercy RJ. Progressive Structural Defects in Canine Centronuclear Myopathy Indicate a Role for HACD1 in Maintaining Skeletal Muscle Membrane Systems. Am J Pathol 2017;187:441-56. [PMID: 27939133 DOI: 10.1016/j.ajpath.2016.10.002] [Cited by in Crossref: 12] [Cited by in F6Publishing: 6] [Article Influence: 2.0] [Reference Citation Analysis]
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12 Parker HG, Shearin AL, Ostrander EA. Man's best friend becomes biology's best in show: genome analyses in the domestic dog. Annu Rev Genet 2010;44:309-36. [PMID: 21047261 DOI: 10.1146/annurev-genet-102808-115200] [Cited by in Crossref: 123] [Cited by in F6Publishing: 105] [Article Influence: 11.2] [Reference Citation Analysis]
13 García-martínez JD, Rivero MA, López-albors O, Arencibia A, Vázquez JM, Ayala I, Gil F. Late onset centronuclear myopathy with severe atrophy in an adult Labrador retriever. Journal of Applied Animal Research 2012;40:69-72. [DOI: 10.1080/09712119.2011.628237] [Reference Citation Analysis]
14 Muhammad E, Reish O, Ohno Y, Scheetz T, Deluca A, Searby C, Regev M, Benyamini L, Fellig Y, Kihara A, Sheffield VC, Parvari R. Congenital myopathy is caused by mutation of HACD1. Hum Mol Genet 2013;22:5229-36. [PMID: 23933735 DOI: 10.1093/hmg/ddt380] [Cited by in Crossref: 35] [Cited by in F6Publishing: 31] [Article Influence: 3.9] [Reference Citation Analysis]
15 Feliu-pascual AL, Shelton GD, Targett MP, Long SN, Comerford EJ, Mcmillan C, Davies D, Rusbridge C, Mellor D, Chang KC, Anderson TJ. Inherited myopathy of great Danes. J Small Animal Practice 2006;47:249-54. [DOI: 10.1111/j.1748-5827.2006.00073.x] [Cited by in Crossref: 11] [Cited by in F6Publishing: 8] [Article Influence: 0.7] [Reference Citation Analysis]
16 Maurer M, Mary J, Guillaud L, Fender M, Pelé M, Bilzer T, Olby N, Penderis J, Shelton GD, Panthier JJ, Thibaud JL, Barthélémy I, Aubin-Houzelstein G, Blot S, Hitte C, Tiret L. Centronuclear myopathy in Labrador retrievers: a recent founder mutation in the PTPLA gene has rapidly disseminated worldwide. PLoS One 2012;7:e46408. [PMID: 23071563 DOI: 10.1371/journal.pone.0046408] [Cited by in Crossref: 15] [Cited by in F6Publishing: 13] [Article Influence: 1.5] [Reference Citation Analysis]
17 Blondelle J, Ohno Y, Gache V, Guyot S, Storck S, Blanchard-Gutton N, Barthélémy I, Walmsley G, Rahier A, Gadin S, Maurer M, Guillaud L, Prola A, Ferry A, Aubin-Houzelstein G, Demarquoy J, Relaix F, Piercy RJ, Blot S, Kihara A, Tiret L, Pilot-Storck F. HACD1, a regulator of membrane composition and fluidity, promotes myoblast fusion and skeletal muscle growth. J Mol Cell Biol 2015;7:429-40. [PMID: 26160855 DOI: 10.1093/jmcb/mjv049] [Cited by in Crossref: 27] [Cited by in F6Publishing: 22] [Article Influence: 3.9] [Reference Citation Analysis]
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20 Shelton GD, Engvall E. Canine and feline models of human inherited muscle diseases. Neuromuscul Disord 2005;15:127-38. [PMID: 15694134 DOI: 10.1016/j.nmd.2004.10.019] [Cited by in Crossref: 78] [Cited by in F6Publishing: 60] [Article Influence: 4.6] [Reference Citation Analysis]
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22 Toussaint A, Cowling BS, Hnia K, Mohr M, Oldfors A, Schwab Y, Yis U, Maisonobe T, Stojkovic T, Wallgren-Pettersson C, Laugel V, Echaniz-Laguna A, Mandel JL, Nishino I, Laporte J. Defects in amphiphysin 2 (BIN1) and triads in several forms of centronuclear myopathies. Acta Neuropathol 2011;121:253-66. [PMID: 20927630 DOI: 10.1007/s00401-010-0754-2] [Cited by in Crossref: 92] [Cited by in F6Publishing: 83] [Article Influence: 7.7] [Reference Citation Analysis]
23 Gentilini F, Zambon E, Gandini G, Rosati M, Spadari A, Romagnoli N, Turba ME, Gernone F. Frequency of the allelic variant of the PTPLA gene responsible for centronuclear myopathy in Labrador Retriever dogs as assessed in Italy. J Vet Diagn Invest 2011;23:124-6. [PMID: 21217042 DOI: 10.1177/104063871102300122] [Cited by in Crossref: 6] [Cited by in F6Publishing: 4] [Article Influence: 0.5] [Reference Citation Analysis]