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For: Vasli N, Harris E, Karamchandani J, Bareke E, Majewski J, Romero NB, Stojkovic T, Barresi R, Tasfaout H, Charlton R, Malfatti E, Bohm J, Marini-Bettolo C, Choquet K, Dicaire MJ, Shao YH, Topf A, O'Ferrall E, Eymard B, Straub V, Blanco G, Lochmüller H, Brais B, Laporte J, Tétreault M. Recessive mutations in the kinase ZAK cause a congenital myopathy with fibre type disproportion. Brain 2017;140:37-48. [PMID: 27816943 DOI: 10.1093/brain/aww257] [Cited by in Crossref: 9] [Cited by in F6Publishing: 11] [Article Influence: 1.5] [Reference Citation Analysis]
Number Citing Articles
1 Rossi D, Catallo MR, Pierantozzi E, Sorrentino V. Mutations in proteins involved in E-C coupling and SOCE and congenital myopathies. J Gen Physiol 2022;154:e202213115. [PMID: 35980353 DOI: 10.1085/jgp.202213115] [Reference Citation Analysis]
2 Nordgaard C, Vind AC, Stonadge A, Kjøbsted R, Snieckute G, Antas P, Blasius M, Reinert MS, Del Val AM, Bekker-Jensen DB, Haahr P, Miroshnikova YA, Mazouzi A, Falk S, Perrier-Groult E, Tiedje C, Li X, Jakobsen JR, Jørgensen NO, Wojtaszewski JF, Mallein-Gerin F, Andersen JL, Pennisi CP, Clemmensen C, Kassem M, Jafari A, Brummelkamp T, Li VS, Wickström SA, Olsen JV, Blanco G, Bekker-Jensen S. ZAKβ is activated by cellular compression and mediates contraction-induced MAP kinase signaling in skeletal muscle. EMBO J 2022;:e111650. [PMID: 35899396 DOI: 10.15252/embj.2022111650] [Reference Citation Analysis]
3 Kreienkamp HJ, Wagner M, Weigand H, McConkie-Rossell A, McDonald M, Keren B, Mignot C, Gauthier J, Soucy JF, Michaud JL, Dumas M, Smith R, Löbel U, Hempel M, Kubisch C, Denecke J, Campeau PM, Bain JM, Lessel D. Variant-specific effects define the phenotypic spectrum of HNRNPH2-associated neurodevelopmental disorders in males. Hum Genet 2021. [PMID: 34907471 DOI: 10.1007/s00439-021-02412-x] [Reference Citation Analysis]
4 Labrecque M, Touma L, Bhérer C, Duquette A, Tétreault M. Estimated prevalence of Niemann-Pick type C disease in Quebec. Sci Rep 2021;11:22621. [PMID: 34799641 DOI: 10.1038/s41598-021-01966-0] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
5 Gómez-Oca R, Cowling BS, Laporte J. Common Pathogenic Mechanisms in Centronuclear and Myotubular Myopathies and Latest Treatment Advances. Int J Mol Sci 2021;22:11377. [PMID: 34768808 DOI: 10.3390/ijms222111377] [Cited by in F6Publishing: 4] [Reference Citation Analysis]
6 He J, Xue Y, Wang Q, Zhou X, Liu L, Zhang T, Shang C, Ma J, Ma T. Long non-coding RNA MIAT regulates blood tumor barrier permeability by functioning as a competing endogenous RNA. Cell Death Dis 2020;11:936. [PMID: 33127881 DOI: 10.1038/s41419-020-03134-0] [Cited by in Crossref: 4] [Cited by in F6Publishing: 7] [Article Influence: 2.0] [Reference Citation Analysis]
7 Radke J, Stenzel W, Goebel HH. Corrigendum to "Recently Identified Congenital Myopathies" [Semin Pediatr Neurol 29 (2019) 83-90]. Semin Pediatr Neurol 2019;32:100775. [PMID: 31813515 DOI: 10.1016/j.spen.2019.100775] [Reference Citation Analysis]
8 Moreno CAM, Estephan EP, Fappi A, Monges S, Lubieniecki F, Lopes Abath Neto O, Reed UC, Donkervoort S, Harms MB, Bonnemann C, Zanoteli E. Congenital fiber type disproportion caused by TPM3 mutation: A report of two atypical cases. Neuromuscul Disord 2020;30:54-8. [PMID: 31866162 DOI: 10.1016/j.nmd.2019.11.001] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
9 Tasfaout H, Cowling BS, Laporte J. Centronuclear myopathies under attack: A plethora of therapeutic targets. J Neuromuscul Dis 2018;5:387-406. [PMID: 30103348 DOI: 10.3233/JND-180309] [Cited by in Crossref: 19] [Cited by in F6Publishing: 22] [Article Influence: 6.3] [Reference Citation Analysis]
10 Pelin K, Wallgren-Pettersson C. Update on the Genetics of Congenital Myopathies. Semin Pediatr Neurol 2019;29:12-22. [PMID: 31060721 DOI: 10.1016/j.spen.2019.01.005] [Cited by in Crossref: 10] [Cited by in F6Publishing: 9] [Article Influence: 3.3] [Reference Citation Analysis]
11 Harris E, Topf A, Barresi R, Hudson J, Powell H, Tellez J, Hicks D, Porter A, Bertoli M, Evangelista T, Marini-Betollo C, Magnússon Ó, Lek M, MacArthur D, Bushby K, Lochmüller H, Straub V. Exome sequences versus sequential gene testing in the UK highly specialised Service for Limb Girdle Muscular Dystrophy. Orphanet J Rare Dis 2017;12:151. [PMID: 28877744 DOI: 10.1186/s13023-017-0699-9] [Cited by in Crossref: 23] [Cited by in F6Publishing: 28] [Article Influence: 4.6] [Reference Citation Analysis]