BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

93 related articles for article (PubMed ID: 32602800)

  • 1. Evolutionary dissection of mtDNA hg H: a susceptibility factor for hypertrophic cardiomyopathy.
    Hagen CM; Elson JL; Hedley PL; Aidt FH; Havndrup O; Jensen MK; Kanters JK; Atherton JJ; McGaughran J; Bundgaard H; Christiansen M
    Mitochondrial DNA A DNA Mapp Seq Anal; 2020 Aug; 31(6):238-244. PubMed ID: 32602800
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Mitochondrial haplogroups modify the risk of developing hypertrophic cardiomyopathy in a Danish population.
    Hagen CM; Aidt FH; Hedley PL; Jensen MK; Havndrup O; Kanters JK; Moolman-Smook JC; Larsen SO; Bundgaard H; Christiansen M
    PLoS One; 2013; 8(8):e71904. PubMed ID: 23940792
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Private mitochondrial DNA variants in danish patients with hypertrophic cardiomyopathy.
    Hagen CM; Aidt FH; Havndrup O; Hedley PL; Jensen MK; Kanters JK; Pham TT; Bundgaard H; Christiansen M
    PLoS One; 2015; 10(4):e0124540. PubMed ID: 25923817
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Mitochondrial DNA variations associated with hypertrophic cardiomyopathy.
    Govindaraj P; Khan NA; Rani B; Rani DS; Selvaraj P; Jyothi V; Bahl A; Narasimhan C; Rakshak D; Premkumar K; Khullar M; Thangaraj K
    Mitochondrion; 2014 May; 16():65-72. PubMed ID: 24215792
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Mitochondrial DNA haplogroups in Spanish patients with hypertrophic cardiomyopathy.
    Castro MG; Huerta C; Reguero JR; Soto MI; Doménech E; Alvarez V; Gómez-Zaera M; Nunes V; González P; Corao A; Coto E
    Int J Cardiol; 2006 Sep; 112(2):202-6. PubMed ID: 16313983
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Coexistence of mitochondrial DNA and beta myosin heavy chain mutations in hypertrophic cardiomyopathy with late congestive heart failure.
    Arbustini E; Fasani R; Morbini P; Diegoli M; Grasso M; Dal Bello B; Marangoni E; Banfi P; Banchieri N; Bellini O; Comi G; Narula J; Campana C; Gavazzi A; Danesino C; Viganò M
    Heart; 1998 Dec; 80(6):548-58. PubMed ID: 10065021
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Novel mitochondrial DNA mutations associated with Chinese familial hypertrophic cardiomyopathy.
    Wei YL; Yu CA; Yang P; Li AL; Wen JY; Zhao SM; Liu HX; Ke YN; Campbell W; Zhang YG; Li XH; Liao WQ
    Clin Exp Pharmacol Physiol; 2009 Sep; 36(9):933-9. PubMed ID: 19473338
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Mitochondrial dysfunction caused by m.2336T>C mutation with hypertrophic cardiomyopathy in cybrid cell lines.
    Li D; Sun Y; Zhuang Q; Song Y; Wu B; Jia Z; Pan H; Zhou H; Hu S; Zhang B; Qiu Y; Dai Y; Chen S; Xu X; Zhu X; Lin A; Huang W; Liu Z; Yan Q
    Mitochondrion; 2019 May; 46():313-320. PubMed ID: 30196098
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Prognostic predictive value of TLR4 polymorphisms in Han Chinese population with hypertrophic cardiomyopathy.
    Han K; Li YP
    Kaohsiung J Med Sci; 2018 Oct; 34(10):569-575. PubMed ID: 30309485
    [TBL] [Abstract][Full Text] [Related]  

  • 10. A homoplasmic mitochondrial transfer ribonucleic acid mutation as a cause of maternally inherited hypertrophic cardiomyopathy.
    Taylor RW; Giordano C; Davidson MM; d'Amati G; Bain H; Hayes CM; Leonard H; Barron MJ; Casali C; Santorelli FM; Hirano M; Lightowlers RN; DiMauro S; Turnbull DM
    J Am Coll Cardiol; 2003 May; 41(10):1786-96. PubMed ID: 12767666
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Diagnostic yield, interpretation, and clinical utility of mutation screening of sarcomere encoding genes in Danish hypertrophic cardiomyopathy patients and relatives.
    Andersen PS; Havndrup O; Hougs L; Sørensen KM; Jensen M; Larsen LA; Hedley P; Thomsen AR; Moolman-Smook J; Christiansen M; Bundgaard H
    Hum Mutat; 2009 Mar; 30(3):363-70. PubMed ID: 19035361
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Nationwide study on hypertrophic cardiomyopathy in Iceland: evidence of a MYBPC3 founder mutation.
    Adalsteinsdottir B; Teekakirikul P; Maron BJ; Burke MA; Gudbjartsson DF; Holm H; Stefansson K; DePalma SR; Mazaika E; McDonough B; Danielsen R; Seidman JG; Seidman CE; Gunnarsson GT
    Circulation; 2014 Sep; 130(14):1158-67. PubMed ID: 25078086
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Cardiac mitochondrial dysfunction and DNA depletion in children with hypertrophic cardiomyopathy.
    Marin-Garcia J; Ananthakrishnan R; Goldenthal MJ; Filiano JJ; Perez-Atayde A
    J Inherit Metab Dis; 1997 Sep; 20(5):674-80. PubMed ID: 9323562
    [TBL] [Abstract][Full Text] [Related]  

  • 14. The haplotype block, NFKBIL1-ATP6V1G2-BAT1-MICB-MICA, within the class III-class I boundary region of the human major histocompatibility complex may control susceptibility to hepatitis C virus-associated dilated cardiomyopathy.
    Shichi D; Kikkawa EF; Ota M; Katsuyama Y; Kimura A; Matsumori A; Kulski JK; Naruse TK; Inoko H
    Tissue Antigens; 2005 Sep; 66(3):200-8. PubMed ID: 16101831
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Structural and biochemical evidence of mitochondrial depletion in pigs with hypertrophic cardiomyopathy.
    Lin CS; Sun YL; Liu CY
    Res Vet Sci; 2003 Jun; 74(3):219-26. PubMed ID: 12726740
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Genetic Dissection of Hypertrophic Cardiomyopathy with Myocardial RNA-Seq.
    Gao J; Collyer J; Wang M; Sun F; Xu F
    Int J Mol Sci; 2020 Apr; 21(9):. PubMed ID: 32344918
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Dissection of mitochondrial superhaplogroup H using coding region SNPs.
    Brandstätter A; Salas A; Niederstätter H; Gassner C; Carracedo A; Parson W
    Electrophoresis; 2006 Jul; 27(13):2541-50. PubMed ID: 16721903
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Myocardial fibrosis in patients with symptomatic obstructive hypertrophic cardiomyopathy: correlation with echocardiographic measurements, sarcomeric genotypes, and pro-left ventricular hypertrophy polymorphisms involving the renin-angiotensin-aldosterone system.
    Blauwet LA; Ackerman MJ; Edwards WD; Riehle DL; Ommen SR
    Cardiovasc Pathol; 2009; 18(5):262-8. PubMed ID: 18835191
    [TBL] [Abstract][Full Text] [Related]  

  • 19. mtDNA Haplogroup N9a Increases the Risk of Type 2 Diabetes by Altering Mitochondrial Function and Intracellular Mitochondrial Signals.
    Fang H; Hu N; Zhao Q; Wang B; Zhou H; Fu Q; Shen L; Chen X; Shen F; Lyu J
    Diabetes; 2018 Jul; 67(7):1441-1453. PubMed ID: 29735607
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Association of mitochondrial haplogroups H and R with keratoconus in Saudi Arabian patients.
    Abu-Amero KK; Azad TA; Sultan T; Kalantan H; Kondkar AA; Al-Muammar AM
    Invest Ophthalmol Vis Sci; 2014 May; 55(5):2827-31. PubMed ID: 24722698
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 5.