167 related articles for article (PubMed ID: 35241752)
1. LIM domain-wide comprehensive virtual mutagenesis provides structural rationale for cardiomyopathy mutations in CSRP3.
Chauhan PK; Sowdhamini R
Sci Rep; 2022 Mar; 12(1):3562. PubMed ID: 35241752
[TBL] [Abstract][Full Text] [Related]
2. Beyond the sarcomere: CSRP3 mutations cause hypertrophic cardiomyopathy.
Geier C; Gehmlich K; Ehler E; Hassfeld S; Perrot A; Hayess K; Cardim N; Wenzel K; Erdmann B; Krackhardt F; Posch MG; Osterziel KJ; Bublak A; Nägele H; Scheffold T; Dietz R; Chien KR; Spuler S; Fürst DO; Nürnberg P; Ozcelik C
Hum Mol Genet; 2008 Sep; 17(18):2753-65. PubMed ID: 18505755
[TBL] [Abstract][Full Text] [Related]
3. Mutant Muscle LIM Protein C58G causes cardiomyopathy through protein depletion.
Ehsan M; Kelly M; Hooper C; Yavari A; Beglov J; Bellahcene M; Ghataorhe K; Poloni G; Goel A; Kyriakou T; Fleischanderl K; Ehler E; Makeyev E; Lange S; Ashrafian H; Redwood C; Davies B; Watkins H; Gehmlich K
J Mol Cell Cardiol; 2018 Aug; 121():287-296. PubMed ID: 30048712
[TBL] [Abstract][Full Text] [Related]
4. First identification of homozygous truncating CSRP3 variants in two unrelated cases with hypertrophic cardiomyopathy.
Janin A; Bessière F; Chauveau S; Chevalier P; Millat G
Gene; 2018 Nov; 676():110-116. PubMed ID: 30012424
[TBL] [Abstract][Full Text] [Related]
5. CSRP3, p.Arg122*, is responsible for hypertrophic cardiomyopathy in a Chinese family.
Huang H; Chen Y; Jin J; Du R; Tang K; Fan L; Xiang R
J Gene Med; 2022 Jan; 24(1):e3390. PubMed ID: 34558151
[TBL] [Abstract][Full Text] [Related]
6. A novel gene-trap line reveals the dynamic patterns and essential roles of cysteine and glycine-rich protein 3 in zebrafish heart development and regeneration.
Liang S; Zhou Y; Chang Y; Li J; Zhang M; Gao P; Li Q; Yu H; Kawakami K; Ma J; Zhang R
Cell Mol Life Sci; 2024 Mar; 81(1):158. PubMed ID: 38556571
[TBL] [Abstract][Full Text] [Related]
7. The p.(Cys150Tyr) variant in CSRP3 is associated with late-onset hypertrophic cardiomyopathy in heterozygous individuals.
Salazar-Mendiguchía J; Barriales-Villa R; Lopes LR; Ochoa JP; Rodríguez-Vilela A; Palomino-Doza J; Larrañaga-Moreira JM; Cicerchia M; Cárdenas-Reyes I; García-Giustiniani D; Brögger N; Fernández G; García S; Santiago L; Vélez P; Ortiz-Genga M; Elliott PM; Monserrat L
Eur J Med Genet; 2020 Dec; 63(12):104079. PubMed ID: 33035702
[TBL] [Abstract][Full Text] [Related]
8. Genotype-phenotype relationships involving hypertrophic cardiomyopathy-associated mutations in titin, muscle LIM protein, and telethonin.
Bos JM; Poley RN; Ny M; Tester DJ; Xu X; Vatta M; Towbin JA; Gersh BJ; Ommen SR; Ackerman MJ
Mol Genet Metab; 2006 May; 88(1):78-85. PubMed ID: 16352453
[TBL] [Abstract][Full Text] [Related]
9. Identification of a variant hotspot in MYBPC3 and of a novel CSRP3 autosomal recessive alteration in a cohort of Polish patients with hypertrophic cardiomyopathy.
Lipari M; Wypasek E; Karpiński M; Tomkiewicz-Pajak L; Laino L; Binni F; Giannarelli D; Rubiś P; Petkow-Dimitrow P; Undas A; Grammatico P; Bottillo I
Pol Arch Intern Med; 2020 Feb; 130(2):89-99. PubMed ID: 31919335
[TBL] [Abstract][Full Text] [Related]
10. Computational analysis of the flexibility in the disordered linker region connecting LIM domains in cysteine-glycine-rich protein.
Chauhan PK; Sowdhamini R
Front Genet; 2023; 14():1134509. PubMed ID: 37065494
[TBL] [Abstract][Full Text] [Related]
11. MLP-deficient human pluripotent stem cell derived cardiomyocytes develop hypertrophic cardiomyopathy and heart failure phenotypes due to abnormal calcium handling.
Li X; Lu WJ; Li Y; Wu F; Bai R; Ma S; Dong T; Zhang H; Lee AS; Wang Y; Lan F
Cell Death Dis; 2019 Aug; 10(8):610. PubMed ID: 31406109
[TBL] [Abstract][Full Text] [Related]
12. W4R variant in CSRP3 encoding muscle LIM protein in a patient with hypertrophic cardiomyopathy.
Newman B; Cescon D; Woo A; Rakowski H; Erikkson MJ; Sole M; Wigle ED; Siminovitch KA
Mol Genet Metab; 2005 Apr; 84(4):374-5. PubMed ID: 15781201
[No Abstract] [Full Text] [Related]
13. Zebrafish cysteine and glycine-rich protein 3 is essential for mechanical stability in skeletal muscles.
Chang Y; Geng F; Hu Y; Ding Y; Zhang R
Biochem Biophys Res Commun; 2019 Apr; 511(3):604-611. PubMed ID: 30826063
[TBL] [Abstract][Full Text] [Related]
14. Identification and in silico characterization of CSRP3 synonymous variants in dilated cardiomyopathy.
Giri P; Jain D; Kumar A; Mohapatra B
Mol Biol Rep; 2023 May; 50(5):4105-4117. PubMed ID: 36877346
[TBL] [Abstract][Full Text] [Related]
15. Mutations in the human muscle LIM protein gene in families with hypertrophic cardiomyopathy.
Geier C; Perrot A; Ozcelik C; Binner P; Counsell D; Hoffmann K; Pilz B; Martiniak Y; Gehmlich K; van der Ven PF; Fürst DO; Vornwald A; von Hodenberg E; Nürnberg P; Scheffold T; Dietz R; Osterziel KJ
Circulation; 2003 Mar; 107(10):1390-5. PubMed ID: 12642359
[TBL] [Abstract][Full Text] [Related]
16. Discriminating aspects of global metabolism of neonatal cardiomyocytes from wild type and KO-CSRP3 rats using proton magnetic resonance spectroscopy of culture media samples.
Bloise AC; Dos Santos JA; de Brito IV; Bassaneze V; Gomes LF; Alencar AM
In Vitro Cell Dev Biol Anim; 2020 Sep; 56(8):604-613. PubMed ID: 32914385
[TBL] [Abstract][Full Text] [Related]
17. Molecular cloning, characterization and tissue specificity of the expression of the ovine CSRP2 and CSRP3 genes from Small-tail Han sheep (Ovis aries).
Liu G; Zhang C; Wang G; Ji Z; Liu Z; Chao T; Zhang S; Wang J
Gene; 2016 Apr; 580(1):47-57. PubMed ID: 26779824
[TBL] [Abstract][Full Text] [Related]
18. Evidence for FHL1 as a novel disease gene for isolated hypertrophic cardiomyopathy.
Friedrich FW; Wilding BR; Reischmann S; Crocini C; Lang P; Charron P; Müller OJ; McGrath MJ; Vollert I; Hansen A; Linke WA; Hengstenberg C; Bonne G; Morner S; Wichter T; Madeira H; Arbustini E; Eschenhagen T; Mitchell CA; Isnard R; Carrier L
Hum Mol Genet; 2012 Jul; 21(14):3237-54. PubMed ID: 22523091
[TBL] [Abstract][Full Text] [Related]
19. Isolated X-linked hypertrophic cardiomyopathy caused by a novel mutation of the four-and-a-half LIM domain 1 gene.
Hartmannova H; Kubanek M; Sramko M; Piherova L; Noskova L; Hodanova K; Stranecky V; Pristoupilova A; Sovova J; Marek T; Maluskova J; Ridzon P; Kautzner J; Hulkova H; Kmoch S
Circ Cardiovasc Genet; 2013 Dec; 6(6):543-51. PubMed ID: 24114807
[TBL] [Abstract][Full Text] [Related]
20. Mutations in the muscle LIM protein and alpha-actinin-2 genes in dilated cardiomyopathy and endocardial fibroelastosis.
Mohapatra B; Jimenez S; Lin JH; Bowles KR; Coveler KJ; Marx JG; Chrisco MA; Murphy RT; Lurie PR; Schwartz RJ; Elliott PM; Vatta M; McKenna W; Towbin JA; Bowles NE
Mol Genet Metab; 2003; 80(1-2):207-15. PubMed ID: 14567970
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
