545 related articles for article (PubMed ID: 28211974)
1. 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]
2. 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]
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. 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]
5. 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]
6. Decreased levels of BAG3 in a family with a rare variant and in idiopathic dilated cardiomyopathy.
Feldman AM; Begay RL; Knezevic T; Myers VD; Slavov DB; Zhu W; Gowan K; Graw SL; Jones KL; Tilley DG; Coleman RC; Walinsky P; Cheung JY; Mestroni L; Khalili K; Taylor MR
J Cell Physiol; 2014 Nov; 229(11):1697-702. PubMed ID: 24623017
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. 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]
9. 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]
10. 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]
11. 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]
12. Generation of two human iPSC lines with Exon 3 mutations in BCL2-Associated Athanogene 3 (BAG3) from dilated cardiomyopathy patients.
Zushin PH; Zhou Y; Li A; Ashley EA; Wheeler MT; Wu JC
Stem Cell Res; 2023 Mar; 67():103019. PubMed ID: 36642055
[TBL] [Abstract][Full Text] [Related]
13. Whole exome sequencing in a large pedigree with DCM identifies a novel mutation in
Robyns T; Willems R; Van Cleemput J; Jhangiani S; Muzny D; Gibbs R; Lupski JR; Breckpot J; Devriendt K; Corveleyn A
Acta Cardiol; 2020 Dec; 75(8):748-753. PubMed ID: 31583969
[No Abstract] [Full Text] [Related]
14. A genome-wide association study identifies two loci associated with heart failure due to dilated cardiomyopathy.
Villard E; Perret C; Gary F; Proust C; Dilanian G; Hengstenberg C; Ruppert V; Arbustini E; Wichter T; Germain M; Dubourg O; Tavazzi L; Aumont MC; DeGroote P; Fauchier L; Trochu JN; Gibelin P; Aupetit JF; Stark K; Erdmann J; Hetzer R; Roberts AM; Barton PJ; Regitz-Zagrosek V; ; Aslam U; Duboscq-Bidot L; Meyborg M; Maisch B; Madeira H; Waldenström A; Galve E; Cleland JG; Dorent R; Roizes G; Zeller T; Blankenberg S; Goodall AH; Cook S; Tregouet DA; Tiret L; Isnard R; Komajda M; Charron P; Cambien F
Eur Heart J; 2011 May; 32(9):1065-76. PubMed ID: 21459883
[TBL] [Abstract][Full Text] [Related]
15. A substitution mutation in cardiac ubiquitin ligase, FBXO32, is associated with an autosomal recessive form of dilated cardiomyopathy.
Al-Hassnan ZN; Shinwari ZM; Wakil SM; Tulbah S; Mohammed S; Rahbeeni Z; Alghamdi M; Rababh M; Colak D; Kaya N; Al-Fayyadh M; Alburaiki J
BMC Med Genet; 2016 Jan; 17():3. PubMed ID: 26768247
[TBL] [Abstract][Full Text] [Related]
16. Familial Dilated Cardiomyopathy Caused by a Novel Frameshift in the BAG3 Gene.
Toro R; Pérez-Serra A; Campuzano O; Moncayo-Arlandi J; Allegue C; Iglesias A; Mangas A; Brugada R
PLoS One; 2016; 11(7):e0158730. PubMed ID: 27391596
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. Whole exome sequencing identifies a KCNJ12 mutation as a cause of familial dilated cardiomyopathy.
Yuan HX; Yan K; Hou DY; Zhang ZY; Wang H; Wang X; Zhang J; Xu XR; Liang YH; Zhao WS; Xu L; Zhang L
Medicine (Baltimore); 2017 Aug; 96(33):e7727. PubMed ID: 28816949
[TBL] [Abstract][Full Text] [Related]
19. Haploinsufficiency of mechanistic target of rapamycin ameliorates
Ding Y; Dvornikov AV; Ma X; Zhang H; Wang Y; Lowerison M; Packard RR; Wang L; Chen J; Zhang Y; Hsiai T; Lin X; Xu X
Dis Model Mech; 2019 Oct; 12(10):. PubMed ID: 31492659
[TBL] [Abstract][Full Text] [Related]
20. Exome Sequencing Identifies a Novel DES Mutation (R227C) in a Chinese Dilated Cardiomyopathy Family.
Yu R; Liu L; Chen C; Shen JM
Cardiology; 2017; 137(2):78-82. PubMed ID: 28171858
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
