745 related articles for article (PubMed ID: 28669108)
1. Novel Genetic Variants in BAG3 and TNNT2 in a Swedish Family with a History of Dilated Cardiomyopathy and Sudden Cardiac Death.
Fernlund E; Österberg AW; Kuchinskaya E; Gustafsson M; Jansson K; Gunnarsson C
Pediatr Cardiol; 2017 Aug; 38(6):1262-1268. PubMed ID: 28669108
[TBL] [Abstract][Full Text] [Related]
2. Whole exome sequencing identified 1 base pair novel deletion in BCL2-associated athanogene 3 (BAG3) gene associated with severe dilated cardiomyopathy (DCM) requiring heart transplant in multiple family members.
Rafiq MA; Chaudhry A; Care M; Spears DA; Morel CF; Hamilton RM
Am J Med Genet A; 2017 Mar; 173(3):699-705. PubMed ID: 28211974
[TBL] [Abstract][Full Text] [Related]
3. Nonsense mutations in BAG3 are associated with early-onset dilated cardiomyopathy in French Canadians.
Chami N; Tadros R; Lemarbre F; Lo KS; Beaudoin M; Robb L; Labuda D; Tardif JC; Racine N; Talajic M; Lettre G
Can J Cardiol; 2014 Dec; 30(12):1655-61. PubMed ID: 25448463
[TBL] [Abstract][Full Text] [Related]
4. Dilated Cardiomyopathy Due to BLC2-Associated Athanogene 3 (BAG3) Mutations.
Domínguez F; Cuenca S; Bilińska Z; Toro R; Villard E; Barriales-Villa R; Ochoa JP; Asselbergs F; Sammani A; Franaszczyk M; Akhtar M; Coronado-Albi MJ; Rangel-Sousa D; Rodriguez-Palomares JF; Jiménez-Jáimez J; Garcia-Pinilla JM; Ripoll-Vera T; Mogollón-Jiménez MV; Fontalba-Romero A; Garcia-Medina D; Palomino-Doza J; de Gonzalo-Calvo D; Cicerchia M; Salazar-Mendiguchia J; Salas C; Pankuweit S; Hey TM; Mogensen J; Barton PJ; Charron P; Elliott P; Garcia-Pavia P;
J Am Coll Cardiol; 2018 Nov; 72(20):2471-2481. PubMed ID: 30442290
[TBL] [Abstract][Full Text] [Related]
5. Clinical and Prognostic Profiles of Cardiomyopathies Caused by Mutations in the Troponin T Gene.
Ripoll-Vera T; Gámez JM; Govea N; Gómez Y; Núñez J; Socías L; Escandell Á; Rosell J
Rev Esp Cardiol (Engl Ed); 2016 Feb; 69(2):149-58. PubMed ID: 26507537
[TBL] [Abstract][Full Text] [Related]
6. Truncating mutations on myofibrillar myopathies causing genes as prevalent molecular explanations on patients with dilated cardiomyopathy.
Janin A; N'Guyen K; Habib G; Dauphin C; Chanavat V; Bouvagnet P; Eschalier R; Streichenberger N; Chevalier P; Millat G
Clin Genet; 2017 Dec; 92(6):616-623. PubMed ID: 28436997
[TBL] [Abstract][Full Text] [Related]
7. Severe disease expression of cardiac troponin C and T mutations in patients with idiopathic dilated cardiomyopathy.
Mogensen J; Murphy RT; Shaw T; Bahl A; Redwood C; Watkins H; Burke M; Elliott PM; McKenna WJ
J Am Coll Cardiol; 2004 Nov; 44(10):2033-40. PubMed ID: 15542288
[TBL] [Abstract][Full Text] [Related]
8. Digenic inheritance of mutations in the cardiac troponin (TNNT2) and cardiac beta myosin heavy chain (MYH7) as the cause of severe dilated cardiomyopathy.
Petropoulou E; Soltani M; Firoozabadi AD; Namayandeh SM; Crockford J; Maroofian R; Jamshidi Y
Eur J Med Genet; 2017 Sep; 60(9):485-488. PubMed ID: 28642161
[TBL] [Abstract][Full Text] [Related]
9. Association of variants in MYH7, MYBPC3 and TNNT2 with sudden cardiac death-related risk factors in Brazilian patients with hypertrophic cardiomyopathy.
Mori AA; Castro LR; Bortolin RH; Bastos GM; Oliveira VF; Ferreira GM; Hirata TDC; Fajardo CM; Sampaio MF; Moreira DAR; Pachón-Mateos JC; Correia EB; Sousa AGMR; Brión M; Carracedo A; Hirata RDC; Hirata MH
Forensic Sci Int Genet; 2021 May; 52():102478. PubMed ID: 33588347
[TBL] [Abstract][Full Text] [Related]
10. The congenital disorder of glycosylation in PGM1 (PGM1-CDG) can cause severe cardiomyopathy and unexpected sudden cardiac death in childhood.
Fernlund E; Andersson O; Ellegård R; Årstrand HK; Green H; Olsson H; Gunnarsson C
Forensic Sci Int Genet; 2019 Nov; 43():102111. PubMed ID: 31563034
[TBL] [Abstract][Full Text] [Related]
11. Clinical and functional characterization of TNNT2 mutations identified in patients with dilated cardiomyopathy.
Hershberger RE; Pinto JR; Parks SB; Kushner JD; Li D; Ludwigsen S; Cowan J; Morales A; Parvatiyar MS; Potter JD
Circ Cardiovasc Genet; 2009 Aug; 2(4):306-13. PubMed ID: 20031601
[TBL] [Abstract][Full Text] [Related]
12. Reevaluating the Genetic Contribution of Monogenic Dilated Cardiomyopathy.
Mazzarotto F; Tayal U; Buchan RJ; Midwinter W; Wilk A; Whiffin N; Govind R; Mazaika E; de Marvao A; Dawes TJW; Felkin LE; Ahmad M; Theotokis PI; Edwards E; Ing AY; Thomson KL; Chan LLH; Sim D; Baksi AJ; Pantazis A; Roberts AM; Watkins H; Funke B; O'Regan DP; Olivotto I; Barton PJR; Prasad SK; Cook SA; Ware JS; Walsh R
Circulation; 2020 Feb; 141(5):387-398. PubMed ID: 31983221
[TBL] [Abstract][Full Text] [Related]
13. Dilated cardiomyopathy caused by a novel TNNT2 mutation-added value of genetic testing in the correct identification of affected subjects.
Van Acker H; De Sutter J; Vandekerckhove K; de Ravel TJ; Verhaaren H; De Backer J
Int J Cardiol; 2010 Oct; 144(2):307-9. PubMed ID: 19324435
[TBL] [Abstract][Full Text] [Related]
14. Genome-wide studies of copy number variation and exome sequencing identify rare variants in BAG3 as a cause of dilated cardiomyopathy.
Norton N; Li D; Rieder MJ; Siegfried JD; Rampersaud E; Züchner S; Mangos S; Gonzalez-Quintana J; Wang L; McGee S; Reiser J; Martin E; Nickerson DA; Hershberger RE
Am J Hum Genet; 2011 Mar; 88(3):273-82. PubMed ID: 21353195
[TBL] [Abstract][Full Text] [Related]
15. Differential expression of circulating miRNAs as a novel tool to assess BAG3-associated familial dilated cardiomyopathy.
Zaragoza C; Saura M; Hernández I; Ramirez-Carracedo R; García-García F; Zamorano JL; Mangas A; Toro R
Biosci Rep; 2019 Mar; 39(3):. PubMed ID: 30792263
[TBL] [Abstract][Full Text] [Related]
16. Poor prognosis of rare sarcomeric gene variants in patients with dilated cardiomyopathy.
Merlo M; Sinagra G; Carniel E; Slavov D; Zhu X; Barbati G; Spezzacatene A; Ramani F; Salcedo E; Di Lenarda A; Mestroni L; Taylor MR;
Clin Transl Sci; 2013 Dec; 6(6):424-8. PubMed ID: 24119082
[TBL] [Abstract][Full Text] [Related]
17. Exome Sequencing Identifies Pathogenic and Modifier Mutations in a Child With Sporadic Dilated Cardiomyopathy.
Long PA; Larsen BT; Evans JM; Olson TM
J Am Heart Assoc; 2015 Dec; 4(12):. PubMed ID: 26656454
[TBL] [Abstract][Full Text] [Related]
18. Association of Variants in BAG3 With Cardiomyopathy Outcomes in African American Individuals.
Myers VD; Gerhard GS; McNamara DM; Tomar D; Madesh M; Kaniper S; Ramsey FV; Fisher SG; Ingersoll RG; Kasch-Semenza L; Wang J; Hanley-Yanez K; Lemster B; Schwisow JA; Ambardekar AV; Degann SH; Bristow MR; Sheppard R; Alexis JD; Tilley DG; Kontos CD; McClung JM; Taylor AL; Yancy CW; Khalili K; Seidman JG; Seidman CE; McTiernan CF; Cheung JY; Feldman AM
JAMA Cardiol; 2018 Oct; 3(10):929-938. PubMed ID: 30140897
[TBL] [Abstract][Full Text] [Related]
19. Dilated cardiomyopathy-associated BAG3 mutations impair Z-disc assembly and enhance sensitivity to apoptosis in cardiomyocytes.
Arimura T; Ishikawa T; Nunoda S; Kawai S; Kimura A
Hum Mutat; 2011 Dec; 32(12):1481-91. PubMed ID: 21898660
[TBL] [Abstract][Full Text] [Related]
20. The BAG3 gene variants in Polish patients with dilated cardiomyopathy: four novel mutations and a genotype-phenotype correlation.
Franaszczyk M; Bilinska ZT; Sobieszczańska-Małek M; Michalak E; Sleszycka J; Sioma A; Małek ŁA; Kaczmarska D; Walczak E; Włodarski P; Hutnik Ł; Milanowska B; Dzielinska Z; Religa G; Grzybowski J; Zieliński T; Ploski R
J Transl Med; 2014 Jul; 12():192. PubMed ID: 25008357
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
