244 related articles for article (PubMed ID: 36293084)
1. Genotype Complements the Phenotype: Identification of the Pathogenicity of an LMNA Splice Variant by Nanopore Long-Read Sequencing in a Large DCM Family.
Sedaghat-Hamedani F; Rebs S; Kayvanpour E; Zhu C; Amr A; Müller M; Haas J; Wu J; Steinmetz LM; Ehlermann P; Streckfuss-Bömeke K; Frey N; Meder B
Int J Mol Sci; 2022 Oct; 23(20):. PubMed ID: 36293084
[TBL] [Abstract][Full Text] [Related]
2. Modeling of lamin A/C mutation premature cardiac aging using patient‐specific induced pluripotent stem cells.
Siu CW; Lee YK; Ho JC; Lai WH; Chan YC; Ng KM; Wong LY; Au KW; Lau YM; Zhang J; Lay KW; Colman A; Tse HF
Aging (Albany NY); 2012 Nov; 4(11):803-822. PubMed ID: 23362510
[TBL] [Abstract][Full Text] [Related]
3. An LMNA synonymous variant associated with severe dilated cardiomyopathy: Case report.
Gao S; Mumme-Monheit A; Chen SN; Spector EB; Slavov D; Baralle FE; Bristow MR; Mestroni L; Taylor MRG;
Am J Med Genet A; 2022 Feb; 188(2):600-605. PubMed ID: 34652067
[TBL] [Abstract][Full Text] [Related]
4. Identification of
Sedaghat-Hamedani F; Rebs S; El-Battrawy I; Chasan S; Krause T; Haas J; Zhong R; Liao Z; Xu Q; Zhou X; Akin I; Zitron E; Frey N; Streckfuss-Bömeke K; Kayvanpour E
Int J Mol Sci; 2021 Nov; 22(23):. PubMed ID: 34884792
[TBL] [Abstract][Full Text] [Related]
5.
Kato K; Ohno S; Sonoda K; Fukuyama M; Makiyama T; Ozawa T; Horie M
Circ Genom Precis Med; 2020 Oct; 13(5):435-443. PubMed ID: 32818388
[TBL] [Abstract][Full Text] [Related]
6. Genetic mutation of familial dilated cardiomyopathy based on next‑generation semiconductor sequencing.
Lin XF; Luo JW; Liu G; Zhu YB; Jin Z; Lin X
Mol Med Rep; 2018 Nov; 18(5):4271-4280. PubMed ID: 30221713
[TBL] [Abstract][Full Text] [Related]
7. Investigating
Shemer Y; Mekies LN; Ben Jehuda R; Baskin P; Shulman R; Eisen B; Regev D; Arbustini E; Gerull B; Gherghiceanu M; Gottlieb E; Arad M; Binah O
Int J Mol Sci; 2021 Jul; 22(15):. PubMed ID: 34360639
[No Abstract] [Full Text] [Related]
8. Clinical and functional characterization of a novel mutation in lamin a/c gene in a multigenerational family with arrhythmogenic cardiac laminopathy.
Forleo C; Carmosino M; Resta N; Rampazzo A; Valecce R; Sorrentino S; Iacoviello M; Pisani F; Procino G; Gerbino A; Scardapane A; Simone C; Calore M; Torretta S; Svelto M; Favale S
PLoS One; 2015; 10(4):e0121723. PubMed ID: 25837155
[TBL] [Abstract][Full Text] [Related]
9. Activation of PDGF pathway links LMNA mutation to dilated cardiomyopathy.
Lee J; Termglinchan V; Diecke S; Itzhaki I; Lam CK; Garg P; Lau E; Greenhaw M; Seeger T; Wu H; Zhang JZ; Chen X; Gil IP; Ameen M; Sallam K; Rhee JW; Churko JM; Chaudhary R; Chour T; Wang PJ; Snyder MP; Chang HY; Karakikes I; Wu JC
Nature; 2019 Aug; 572(7769):335-340. PubMed ID: 31316208
[TBL] [Abstract][Full Text] [Related]
10. Clinical trial in a dish using iPSCs shows lovastatin improves endothelial dysfunction and cellular cross-talk in LMNA cardiomyopathy.
Sayed N; Liu C; Ameen M; Himmati F; Zhang JZ; Khanamiri S; Moonen JR; Wnorowski A; Cheng L; Rhee JW; Gaddam S; Wang KC; Sallam K; Boyd JH; Woo YJ; Rabinovitch M; Wu JC
Sci Transl Med; 2020 Jul; 12(554):. PubMed ID: 32727917
[TBL] [Abstract][Full Text] [Related]
11. Multigenic Disease and Bilineal Inheritance in Dilated Cardiomyopathy Is Illustrated in Nonsegregating LMNA Pedigrees.
Cowan JR; Kinnamon DD; Morales A; Salyer L; Nickerson DA; Hershberger RE
Circ Genom Precis Med; 2018 Jul; 11(7):e002038. PubMed ID: 30012837
[TBL] [Abstract][Full Text] [Related]
12. A Novel Truncating LMNA Mutation in Patients with Cardiac Conduction Disorders and Dilated Cardiomyopathy.
Kawakami H; Ogimoto A; Tokunaga N; Nishimura K; Kawakami H; Higashi H; Iio C; Kono T; Aono J; Uetani T; Nagai T; Inoue K; Suzuki J; Ikeda S; Okura T; Ohyagi Y; Tabara Y; Higaki J
Int Heart J; 2018 May; 59(3):531-541. PubMed ID: 29628476
[TBL] [Abstract][Full Text] [Related]
13. Systematic in vivo candidate evaluation uncovers therapeutic targets for LMNA dilated cardiomyopathy and risk of Lamin A toxicity.
Tan CY; Chan PS; Tan H; Tan SW; Lee CJM; Wang JW; Ye S; Werner H; Loh YJ; Lee YL; Ackers-Johnson M; Foo RSY; Jiang J
J Transl Med; 2023 Oct; 21(1):690. PubMed ID: 37840136
[TBL] [Abstract][Full Text] [Related]
14. Severe DCM phenotype of patient harboring RBM20 mutation S635A can be modeled by patient-specific induced pluripotent stem cell-derived cardiomyocytes.
Streckfuss-Bömeke K; Tiburcy M; Fomin A; Luo X; Li W; Fischer C; Özcelik C; Perrot A; Sossalla S; Haas J; Vidal RO; Rebs S; Khadjeh S; Meder B; Bonn S; Linke WA; Zimmermann WH; Hasenfuss G; Guan K
J Mol Cell Cardiol; 2017 Dec; 113():9-21. PubMed ID: 28941705
[TBL] [Abstract][Full Text] [Related]
15. Lamin A/C mutation analysis in a cohort of 324 unrelated patients with idiopathic or familial dilated cardiomyopathy.
Parks SB; Kushner JD; Nauman D; Burgess D; Ludwigsen S; Peterson A; Li D; Jakobs P; Litt M; Porter CB; Rahko PS; Hershberger RE
Am Heart J; 2008 Jul; 156(1):161-9. PubMed ID: 18585512
[TBL] [Abstract][Full Text] [Related]
16. Exome Sequencing Identifies a Novel LMNA Splice-Site Mutation and Multigenic Heterozygosity of Potential Modifiers in a Family with Sick Sinus Syndrome, Dilated Cardiomyopathy, and Sudden Cardiac Death.
Zaragoza MV; Fung L; Jensen E; Oh F; Cung K; McCarthy LA; Tran CK; Hoang V; Hakim SA; Grosberg A
PLoS One; 2016; 11(5):e0155421. PubMed ID: 27182706
[TBL] [Abstract][Full Text] [Related]
17. Identification of mutational hot spots in LMNA encoding lamin A/C in patients with familial dilated cardiomyopathy.
Perrot A; Hussein S; Ruppert V; Schmidt HH; Wehnert MS; Duong NT; Posch MG; Panek A; Dietz R; Kindermann I; Böhm M; Michalewska-Wludarczyk A; Richter A; Maisch B; Pankuweit S; Ozcelik C
Basic Res Cardiol; 2009 Jan; 104(1):90-9. PubMed ID: 18795223
[TBL] [Abstract][Full Text] [Related]
18. The LMNA mutation p.Arg321Ter associated with dilated cardiomyopathy leads to reduced expression and a skewed ratio of lamin A and lamin C proteins.
Al-Saaidi R; Rasmussen TB; Palmfeldt J; Nissen PH; Beqqali A; Hansen J; Pinto YM; Boesen T; Mogensen J; Bross P
Exp Cell Res; 2013 Nov; 319(19):3010-9. PubMed ID: 24001739
[TBL] [Abstract][Full Text] [Related]
19. High yield of LMNA mutations in patients with dilated cardiomyopathy and/or conduction disease referred to cardiogenetics outpatient clinics.
van Tintelen JP; Hofstra RM; Katerberg H; Rossenbacker T; Wiesfeld AC; du Marchie Sarvaas GJ; Wilde AA; van Langen IM; Nannenberg EA; van der Kooi AJ; Kraak M; van Gelder IC; van Veldhuisen DJ; Vos Y; van den Berg MP;
Am Heart J; 2007 Dec; 154(6):1130-9. PubMed ID: 18035086
[TBL] [Abstract][Full Text] [Related]
20. Molecular characterization of Portuguese patients with dilated cardiomyopathy.
Sousa A; Canedo P; Azevedo O; Lopes L; Pinho T; Baixia M; Rocha-Gonçalves F; Gonçalves L; Cardoso JS; Machado JC; Martins E;
Rev Port Cardiol (Engl Ed); 2019 Feb; 38(2):129-139. PubMed ID: 30871747
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
