186 related articles for article (PubMed ID: 37492967)
21. FLNC pathogenic variants in patients with cardiomyopathies: Prevalence and genotype-phenotype correlations.
Ader F; De Groote P; Réant P; Rooryck-Thambo C; Dupin-Deguine D; Rambaud C; Khraiche D; Perret C; Pruny JF; Mathieu-Dramard M; Gérard M; Troadec Y; Gouya L; Jeunemaitre X; Van Maldergem L; Hagège A; Villard E; Charron P; Richard P
Clin Genet; 2019 Oct; 96(4):317-329. PubMed ID: 31245841
[TBL] [Abstract][Full Text] [Related]
22. Novel Mutation in
Tucker NR; McLellan MA; Hu D; Ye J; Parsons VA; Mills RW; Clauss S; Dolmatova E; Shea MA; Milan DJ; Scott NS; Lindsay M; Lubitz SA; Domian IJ; Stone JR; Lin H; Ellinor PT
Circ Cardiovasc Genet; 2017 Dec; 10(6):. PubMed ID: 29212899
[TBL] [Abstract][Full Text] [Related]
23. Filamin actin-binding and titin-binding fulfill distinct functions in Z-disc cohesion.
González-Morales N; Holenka TK; Schöck F
PLoS Genet; 2017 Jul; 13(7):e1006880. PubMed ID: 28732005
[TBL] [Abstract][Full Text] [Related]
24. Overexpression of filamin c in chronic intermittent hypoxia-induced cardiomyocyte apoptosis is a potential cardioprotective target for obstructive sleep apnea.
Yang X; Shi Y; Zhang L; Liu H; Shao Y; Zhang S
Sleep Breath; 2019 Jun; 23(2):493-502. PubMed ID: 30194514
[TBL] [Abstract][Full Text] [Related]
25. Filamin C variants are associated with a distinctive clinical and immunohistochemical arrhythmogenic cardiomyopathy phenotype.
Hall CL; Akhtar MM; Sabater-Molina M; Futema M; Asimaki A; Protonotarios A; Dalageorgou C; Pittman AM; Suarez MP; Aguilera B; Molina P; Zorio E; Hernández JP; Pastor F; Gimeno JR; Syrris P; McKenna WJ
Int J Cardiol; 2020 May; 307():101-108. PubMed ID: 31627847
[TBL] [Abstract][Full Text] [Related]
26. Cardiomyopathy, Proximal Myopathy, Camptocormia, and Novel Filamin C (FLNC) Variant: A Case Report.
Hooshmand SJ; Govindarajan R; Bostick BP
Am J Case Rep; 2021 Sep; 22():e932648. PubMed ID: 34526477
[TBL] [Abstract][Full Text] [Related]
27. A CRISPR/Cas9 strategy for the generation of a FLNC knockout hESC line (WAe009-A-70) to model dilated cardiomyopathy and arrhythmogenic right ventricular cardiomyopathy.
Qin Z; Sun L; Sun X; Su H; Gao X
Stem Cell Res; 2021 Oct; 56():102562. PubMed ID: 34634758
[TBL] [Abstract][Full Text] [Related]
28. Reduction in Filamin C transcript is associated with arrhythmogenic cardiomyopathy in Ashkenazi Jews.
Oz S; Yonath H; Visochyk L; Ofek E; Landa N; Reznik-Wolf H; Ortiz-Genga M; Monserrat L; Ben-Gal T; Goitein O; Beinart R; Glikson M; Freimark D; Pras E; Arad M; Nof E
Int J Cardiol; 2020 Oct; 317():133-138. PubMed ID: 32532510
[TBL] [Abstract][Full Text] [Related]
29. Homozygous expression of the myofibrillar myopathy-associated p.W2710X filamin C variant reveals major pathomechanisms of sarcomeric lesion formation.
Schuld J; Orfanos Z; Chevessier F; Eggers B; Heil L; Uszkoreit J; Unger A; Kirfel G; van der Ven PFM; Marcus K; Linke WA; Clemen CS; Schröder R; Fürst DO
Acta Neuropathol Commun; 2020 Sep; 8(1):154. PubMed ID: 32887649
[TBL] [Abstract][Full Text] [Related]
30. Generation of a pluripotent stem cell line (UMGi270-A) and a corresponding CRISPR/Cas9 modified isogenic control (UMGi270-A-1) from a patient with sudden onset dilated cardiomyopathy harboring a FLNC p.R2187P mutation.
Maurer W; Rebs S; Köhne S; Eberl H; Wollnik B; Zibat A; Streckfuss-Bömeke K
Stem Cell Res; 2024 Jun; 77():103409. PubMed ID: 38583294
[TBL] [Abstract][Full Text] [Related]
31. Novel pathogenic variants in filamin C identified in pediatric restrictive cardiomyopathy.
Schubert J; Tariq M; Geddes G; Kindel S; Miller EM; Ware SM
Hum Mutat; 2018 Dec; 39(12):2083-2096. PubMed ID: 30260051
[TBL] [Abstract][Full Text] [Related]
32. F-actin clustering and cell dysmotility induced by the pathological W148R missense mutation of filamin B at the actin-binding domain.
Zhao Y; Shapiro SS; Eto M
Am J Physiol Cell Physiol; 2016 Jan; 310(1):C89-98. PubMed ID: 26491051
[TBL] [Abstract][Full Text] [Related]
33. Identification of CAP as a costameric protein that interacts with filamin C.
Zhang M; Liu J; Cheng A; Deyoung SM; Saltiel AR
Mol Biol Cell; 2007 Dec; 18(12):4731-40. PubMed ID: 17898075
[TBL] [Abstract][Full Text] [Related]
34. Mutations in FLNC are Associated with Familial Restrictive Cardiomyopathy.
Brodehl A; Ferrier RA; Hamilton SJ; Greenway SC; Brundler MA; Yu W; Gibson WT; McKinnon ML; McGillivray B; Alvarez N; Giuffre M; Schwartzentruber J; ; Gerull B
Hum Mutat; 2016 Mar; 37(3):269-79. PubMed ID: 26666891
[TBL] [Abstract][Full Text] [Related]
35. Rare clinical phenotype of filaminopathy presenting as restrictive cardiomyopathy and myopathy in childhood.
Muravyev A; Vershinina T; Tesner P; Sjoberg G; Fomicheva Y; Čajbiková NN; Kozyreva A; Zhuk S; Mamaeva E; Tarnovskaya S; Jornholt J; Sokolnikova P; Pervunina T; Vasichkina E; Sejersen T; Kostareva A
Orphanet J Rare Dis; 2022 Sep; 17(1):358. PubMed ID: 36104822
[TBL] [Abstract][Full Text] [Related]
36. Filamin C plays an essential role in the maintenance of the structural integrity of cardiac and skeletal muscles, revealed by the medaka mutant zacro.
Fujita M; Mitsuhashi H; Isogai S; Nakata T; Kawakami A; Nonaka I; Noguchi S; Hayashi YK; Nishino I; Kudo A
Dev Biol; 2012 Jan; 361(1):79-89. PubMed ID: 22020047
[TBL] [Abstract][Full Text] [Related]
37. Congenital dilated cardiomyopathy caused by biallelic mutations in Filamin C.
Reinstein E; Gutierrez-Fernandez A; Tzur S; Bormans C; Marcu S; Tayeb-Fligelman E; Vinkler C; Raas-Rothschild A; Irge D; Landau M; Shohat M; Puente XS; Behar DM; Lopez-Otın C
Eur J Hum Genet; 2016 Dec; 24(12):1792-1796. PubMed ID: 27601210
[TBL] [Abstract][Full Text] [Related]
38. Loss of FilaminC (FLNc) results in severe defects in myogenesis and myotube structure.
Dalkilic I; Schienda J; Thompson TG; Kunkel LM
Mol Cell Biol; 2006 Sep; 26(17):6522-34. PubMed ID: 16914736
[TBL] [Abstract][Full Text] [Related]
39. FLNC Expression Level Influences the Activity of TEAD-YAP/TAZ Signaling.
Knyazeva A; Khudiakov A; Vaz R; Muravyev A; Sukhareva K; Sejersen T; Kostareva A
Genes (Basel); 2020 Nov; 11(11):. PubMed ID: 33202721
[TBL] [Abstract][Full Text] [Related]
40. A novel familial truncating mutation in the filamin C gene associated with cardiac arrhythmias.
Mangum KD; Ferns SJ
Eur J Med Genet; 2019 Apr; 62(4):282-285. PubMed ID: 30118858
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
