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For: 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]
Number Citing Articles
1 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]
2 Prola A, Blondelle J, Vandestienne A, Piquereau J, Denis RGP, Guyot S, Chauvin H, Mourier A, Maurer M, Henry C, Khadhraoui N, Gallerne C, Molinié T, Courtin G, Guillaud L, Gressette M, Solgadi A, Dumont F, Castel J, Ternacle J, Demarquoy J, Malgoyre A, Koulmann N, Derumeaux G, Giraud MF, Joubert F, Veksler V, Luquet S, Relaix F, Tiret L, Pilot-Storck F. Cardiolipin content controls mitochondrial coupling and energetic efficiency in muscle. Sci Adv 2021;7:eabd6322. [PMID: 33523852 DOI: 10.1126/sciadv.abd6322] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 4.0] [Reference Citation Analysis]
3 Kim JH, Chen EH. The fusogenic synapse at a glance. J Cell Sci 2019;132:jcs213124. [PMID: 31527149 DOI: 10.1242/jcs.213124] [Cited by in Crossref: 13] [Cited by in F6Publishing: 8] [Article Influence: 4.3] [Reference Citation Analysis]
4 Ceco E, Weinberg SE, Chandel NS, Sznajder JI. Metabolism and Skeletal Muscle Homeostasis in Lung Disease. Am J Respir Cell Mol Biol 2017;57:28-34. [PMID: 28085493 DOI: 10.1165/rcmb.2016-0355TR] [Cited by in Crossref: 11] [Cited by in F6Publishing: 9] [Article Influence: 2.2] [Reference Citation Analysis]
5 Blondelle J, Pais de Barros JP, Pilot-Storck F, Tiret L. Targeted Lipidomic Analysis of Myoblasts by GC-MS and LC-MS/MS. Methods Mol Biol 2017;1668:39-60. [PMID: 28842901 DOI: 10.1007/978-1-4939-7283-8_4] [Cited by in Crossref: 9] [Cited by in F6Publishing: 8] [Article Influence: 2.3] [Reference Citation Analysis]
6 Szcześniak KA, Ciecierska A, Ostaszewski P, Sadkowski T. Characterisation of equine satellite cell transcriptomic profile response to β-hydroxy-β-methylbutyrate (HMB). Br J Nutr 2016;116:1315-25. [PMID: 27691998 DOI: 10.1017/S000711451600324X] [Cited by in Crossref: 9] [Cited by in F6Publishing: 6] [Article Influence: 1.5] [Reference Citation Analysis]
7 Ma X, Wu J, Li Y, Liang X, Casper D, Ding W, Wang X, Shi A, Shi X, Ma L, Eer H, Lang X. Transcriptome and metabolome analyses reveal muscle changes in Tan sheep (Ovis aries) at different ages. Livestock Science 2022;255:104781. [DOI: 10.1016/j.livsci.2021.104781] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
8 Sawai M, Uchida Y, Ohno Y, Miyamoto M, Nishioka C, Itohara S, Sassa T, Kihara A. The 3-hydroxyacyl-CoA dehydratases HACD1 and HACD2 exhibit functional redundancy and are active in a wide range of fatty acid elongation pathways. J Biol Chem 2017;292:15538-51. [PMID: 28784662 DOI: 10.1074/jbc.M117.803171] [Cited by in Crossref: 12] [Cited by in F6Publishing: 5] [Article Influence: 2.4] [Reference Citation Analysis]
9 Blondelle J, Tallapaka K, Seto JT, Ghassemian M, Clark M, Laitila JM, Bournazos A, Singer JD, Lange S. Cullin-3 dependent deregulation of ACTN1 represents a new pathogenic mechanism in nemaline myopathy. JCI Insight 2019;5:125665. [PMID: 30990797 DOI: 10.1172/jci.insight.125665] [Cited by in Crossref: 8] [Cited by in F6Publishing: 8] [Article Influence: 2.7] [Reference Citation Analysis]
10 Ganassi M, Muntoni F, Zammit PS. Defining and Identifying Satellite Cell-opathies within Muscular Dystrophies and Myopathies. Exp Cell Res 2021;:112906. [PMID: 34740639 DOI: 10.1016/j.yexcr.2021.112906] [Cited by in Crossref: 6] [Cited by in F6Publishing: 4] [Article Influence: 6.0] [Reference Citation Analysis]
11 Al Amrani F, Gorodetsky C, Hazrati LN, Amburgey K, Gonorazky HD, Dowling JJ. Biallelic LINE insertion mutation in HACD1 causing congenital myopathy. Neurol Genet 2020;6:e423. [PMID: 32426512 DOI: 10.1212/NXG.0000000000000423] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
12 Papadimas GK, Xirou S, Kararizou E, Papadopoulos C. Update on Congenital Myopathies in Adulthood. Int J Mol Sci 2020;21:E3694. [PMID: 32456280 DOI: 10.3390/ijms21103694] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
13 Lee SM, Lee SH, Jung Y, Lee Y, Yoon JH, Choi JY, Hwang CY, Son YH, Park SS, Hwang GS, Lee KP, Kwon KS. FABP3-mediated membrane lipid saturation alters fluidity and induces ER stress in skeletal muscle with aging. Nat Commun 2020;11:5661. [PMID: 33168829 DOI: 10.1038/s41467-020-19501-6] [Cited by in Crossref: 6] [Cited by in F6Publishing: 6] [Article Influence: 3.0] [Reference Citation Analysis]
14 Zhang Z, Zhang L, Zhou Y, Li L, Zhao J, Qin W, Jin Z, Liu W. Increase in HDAC9 suppresses myoblast differentiation via epigenetic regulation of autophagy in hypoxia. Cell Death Dis 2019;10:552. [PMID: 31320610 DOI: 10.1038/s41419-019-1763-2] [Cited by in Crossref: 12] [Cited by in F6Publishing: 11] [Article Influence: 4.0] [Reference Citation Analysis]
15 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]
16 Raouf J, Idborg H, Englund P, Alexanderson H, Dastmalchi M, Jakobsson PJ, Lundberg IE, Korotkova M. Targeted lipidomics analysis identified altered serum lipid profiles in patients with polymyositis and dermatomyositis. Arthritis Res Ther 2018;20:83. [PMID: 29720222 DOI: 10.1186/s13075-018-1579-y] [Cited by in Crossref: 11] [Cited by in F6Publishing: 9] [Article Influence: 2.8] [Reference Citation Analysis]
17 Prokic I, Cowling BS, Kutchukian C, Kretz C, Tasfaout H, Gache V, Hergueux J, Wendling O, Ferry A, Toussaint A, Gavriilidis C, Nattarayan V, Koch C, Lainé J, Combe R, Tiret L, Jacquemond V, Pilot-Storck F, Laporte J. Differential physiological roles for BIN1 isoforms in skeletal muscle development, function and regeneration. Dis Model Mech 2020;13:dmm044354. [PMID: 32994313 DOI: 10.1242/dmm.044354] [Cited by in Crossref: 5] [Cited by in F6Publishing: 3] [Article Influence: 2.5] [Reference Citation Analysis]
18 Davignon L, Chauveau C, Julien C, Dill C, Duband-Goulet I, Cabet E, Buendia B, Lilienbaum A, Rendu J, Minot MC, Guichet A, Allamand V, Vadrot N, Fauré J, Odent S, Lazaro L, Leroy JP, Marcorelles P, Dubourg O, Ferreiro A. The transcription coactivator ASC-1 is a regulator of skeletal myogenesis, and its deficiency causes a novel form of congenital muscle disease. Hum Mol Genet 2016;25:1559-73. [PMID: 27008887 DOI: 10.1093/hmg/ddw033] [Cited by in Crossref: 16] [Cited by in F6Publishing: 14] [Article Influence: 2.7] [Reference Citation Analysis]
19 Lausser L, Siegle L, Rottbauer W, Frank D, Just S, Kestler HA. Semantic Multi-Classifier Systems Identify Predictive Processes in Heart Failure Models across Species. Biomolecules 2018;8:E158. [PMID: 30486323 DOI: 10.3390/biom8040158] [Reference Citation Analysis]
20 Butchart LC, Fox A, Shavlakadze T, Grounds MD. The long and short of non-coding RNAs during post-natal growth and differentiation of skeletal muscles: Focus on lncRNA and miRNAs. Differentiation 2016;92:237-48. [DOI: 10.1016/j.diff.2016.05.003] [Cited by in Crossref: 25] [Cited by in F6Publishing: 23] [Article Influence: 4.2] [Reference Citation Analysis]
21 Bargui R, Solgadi A, Prost B, Chester M, Ferreiro A, Piquereau J, Moulin M. Phospholipids: Identification and Implication in Muscle Pathophysiology. Int J Mol Sci 2021;22:8176. [PMID: 34360941 DOI: 10.3390/ijms22158176] [Reference Citation Analysis]
22 Kihara A. Synthesis and degradation pathways, functions, and pathology of ceramides and epidermal acylceramides. Prog Lipid Res 2016;63:50-69. [PMID: 27107674 DOI: 10.1016/j.plipres.2016.04.001] [Cited by in Crossref: 92] [Cited by in F6Publishing: 90] [Article Influence: 15.3] [Reference Citation Analysis]
23 Ravenscroft G, Davis MR, Lamont P, Forrest A, Laing NG. New era in genetics of early-onset muscle disease: Breakthroughs and challenges. Semin Cell Dev Biol 2017;64:160-70. [PMID: 27519468 DOI: 10.1016/j.semcdb.2016.08.002] [Cited by in Crossref: 13] [Cited by in F6Publishing: 11] [Article Influence: 2.2] [Reference Citation Analysis]
24 Wei L, Weng S, Lu X, Zhu S, Yang Q, Chen YQ. 3-Hydroxyacyl-CoA dehydratase 2 deficiency confers resistance to diet-induced obesity and glucose intolerance. Biochem Biophys Res Commun 2022;605:134-40. [PMID: 35325655 DOI: 10.1016/j.bbrc.2022.03.057] [Reference Citation Analysis]