BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

261 related articles for article (PubMed ID: 36749382)

  • 1. Transcriptome studies of inherited dilated cardiomyopathies.
    Koslow M; Mondaca-Ruff D; Xu X
    Mamm Genome; 2023 Jun; 34(2):312-322. PubMed ID: 36749382
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. Genetic compensation prevents myopathy and heart failure in an in vivo model of Bag3 deficiency.
    Diofano F; Weinmann K; Schneider I; Thiessen KD; Rottbauer W; Just S
    PLoS Genet; 2020 Nov; 16(11):e1009088. PubMed ID: 33137814
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. 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]  

  • 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. Transcriptome analysis of human heart failure reveals dysregulated cell adhesion in dilated cardiomyopathy and activated immune pathways in ischemic heart failure.
    Sweet ME; Cocciolo A; Slavov D; Jones KL; Sweet JR; Graw SL; Reece TB; Ambardekar AV; Bristow MR; Mestroni L; Taylor MRG
    BMC Genomics; 2018 Nov; 19(1):812. PubMed ID: 30419824
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. Application of an F0-based genetic assay in adult zebrafish to identify modifier genes of an inherited cardiomyopathy.
    Ding Y; Wang M; Bu H; Li J; Lin X; Xu X
    Dis Model Mech; 2023 May; 16(5):. PubMed ID: 35481478
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. 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]  

  • 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. 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]  

  • 14. 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]  

  • 15. 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]  

  • 16. Genetic evaluation of dilated cardiomyopathy.
    Morales A; Hershberger RE
    Curr Cardiol Rep; 2013 Jul; 15(7):375. PubMed ID: 23686784
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Meta-Analysis of Dilated Cardiomyopathy Using Cardiac RNA-Seq Transcriptomic Datasets.
    Alimadadi A; Munroe PB; Joe B; Cheng X
    Genes (Basel); 2020 Jan; 11(1):. PubMed ID: 31948008
    [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-linked heat shock protein family D member 1 mutations cause up-regulation of reactive oxygen species and autophagy through mitochondrial dysfunction.
    Enomoto H; Mittal N; Inomata T; Arimura T; Izumi T; Kimura A; Fukuda K; Makino S
    Cardiovasc Res; 2021 Mar; 117(4):1118-1131. PubMed ID: 32520982
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Cardiac transcriptome and dilated cardiomyopathy genes in zebrafish.
    Shih YH; Zhang Y; Ding Y; Ross CA; Li H; Olson TM; Xu X
    Circ Cardiovasc Genet; 2015 Apr; 8(2):261-9. PubMed ID: 25583992
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 14.