These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

214 related articles for article (PubMed ID: 33078954)

  • 1. East Asian-Specific Common Variant in
    Wu G; Liu L; Zhou Z; Liu J; Wang B; Ruan J; Yang Q; Kanchwala M; Dai P; Zhang C; Wang D; Kang L; Wang S; Hui R; Zou Y; Xing C; Song L; Wang J
    Circulation; 2020 Nov; 142(21):2086-2089. PubMed ID: 33078954
    [No Abstract]   [Full Text] [Related]  

  • 2. Genetic Studies of Hypertrophic Cardiomyopathy in Singaporeans Identify Variants in
    Pua CJ; Tham N; Chin CWL; Walsh R; Khor CC; Toepfer CN; Repetti GG; Garfinkel AC; Ewoldt JF; Cloonan P; Chen CS; Lim SQ; Cai J; Loo LY; Kong SC; Chiang CWK; Whiffin N; de Marvao A; Lio PM; Hii AA; Yang CX; Le TT; Bylstra Y; Lim WK; Teo JX; Padilha K; Silva GV; Pan B; Govind R; Buchan RJ; Barton PJR; Tan P; Foo R; Yip JWL; Wong RCC; Chan WX; Pereira AC; Tang HC; Jamuar SS; Ware JS; Seidman JG; Seidman CE; Cook SA
    Circ Genom Precis Med; 2020 Oct; 13(5):424-434. PubMed ID: 32815737
    [TBL] [Abstract][Full Text] [Related]  

  • 3. High prevalence of Arginine to Glutamine substitution at 98, 141 and 162 positions in Troponin I (TNNI3) associated with hypertrophic cardiomyopathy among Indians.
    Rani DS; Nallari P; Priyamvada S; Narasimhan C; Singh L; Thangaraj K
    BMC Med Genet; 2012 Aug; 13():69. PubMed ID: 22876777
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [A Chinese pedigree with hypertrophic cardiomyopathy caused by rare homozygous mutation of TNNI3 gene p.Arg162Gln].
    Duan LQ; Li Q; Ren Y; Xu JR; Han QH
    Zhonghua Xin Xue Guan Bing Za Zhi; 2019 Dec; 47(12):1008-1010. PubMed ID: 31877599
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Founder Mutation in N Terminus of Cardiac Troponin I Causes Malignant Hypertrophic Cardiomyopathy.
    Fahed AC; Nemer G; Bitar FF; Arnaout S; Abchee AB; Batrawi M; Khalil A; Abou Hassan OK; DePalma SR; McDonough B; Arabi MT; Ware JS; Seidman JG; Seidman CE
    Circ Genom Precis Med; 2020 Oct; 13(5):444-452. PubMed ID: 32885985
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [Cardiac troponin I gene mutation (Asp127Tyr) in a Chinese patient with hypertrophic cardiomyopathy].
    SHENG HZ; SHAN QJ; WU X; CAO KJ
    Zhonghua Xin Xue Guan Bing Za Zhi; 2008 Dec; 36(12):1063-5. PubMed ID: 19134270
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Clinical Profile and Health Disparities in a Multiethnic Cohort of Patients With Hypertrophic Cardiomyopathy.
    Butters A; Semsarian CR; Bagnall RD; Yeates L; Stafford F; Burns C; Semsarian C; Ingles J
    Circ Heart Fail; 2021 Mar; 14(3):e007537. PubMed ID: 33724884
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Frequency of cardiac troponin I mutations in families with hypertrophic cardiomyopathy in China.
    Cheng TO
    J Am Coll Cardiol; 2005 Jul; 46(1):180-1; author reply 181. PubMed ID: 15992656
    [No Abstract]   [Full Text] [Related]  

  • 9. Frequency and clinical expression of cardiac troponin I mutations in 748 consecutive families with hypertrophic cardiomyopathy.
    Mogensen J; Murphy RT; Kubo T; Bahl A; Moon JC; Klausen IC; Elliott PM; McKenna WJ
    J Am Coll Cardiol; 2004 Dec; 44(12):2315-25. PubMed ID: 15607392
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Hypertrophic Cardiomyopathy Accompanied by Spinocerebellar Atrophy With a Novel Mutation in Troponin I Gene.
    Kawai H; Morimoto S; Takakuwa Y; Ueda A; Inada K; Sarai M; Arimura T; Mutoh T; Kimura A; Ozaki Y
    Int Heart J; 2016 Jul; 57(4):507-10. PubMed ID: 27385602
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Low prevalence and variable clinical presentation of troponin I and troponin T gene mutations in hypertrophic cardiomyopathy.
    Curila K; Benesova L; Penicka M; Minarik M; Zemanek D; Veselka J; Widimsky P; Gregor P
    Genet Test Mol Biomarkers; 2009 Oct; 13(5):647-50. PubMed ID: 19645627
    [TBL] [Abstract][Full Text] [Related]  

  • 12. The cardiac troponin I gene is not associated with hypertrophic cardiomyopathy in patients from eastern Finland.
    Jääskeläinen P; Miettinen R; Silvennoinen K; Vauhkonen I; Laakso M; Kuusisto J
    J Mol Cell Cardiol; 1999 Nov; 31(11):2031-6. PubMed ID: 10591029
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [Fabry disease among hypertrophic cardiomyopathy of genetic origin].
    Bouvagnet P; Millat G; Rousson R; Gilbert G; Derumeaux G
    Rev Med Interne; 2010 Dec; 31 Suppl 2():S233-7. PubMed ID: 21211671
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Myocardial late gadolinium enhancement cardiovascular magnetic resonance in hypertrophic cardiomyopathy caused by mutations in troponin I.
    Moon JC; Mogensen J; Elliott PM; Smith GC; Elkington AG; Prasad SK; Pennell DJ; McKenna WJ
    Heart; 2005 Aug; 91(8):1036-40. PubMed ID: 16020591
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Altered regulatory properties of human cardiac troponin I mutants that cause hypertrophic cardiomyopathy.
    Elliott K; Watkins H; Redwood CS
    J Biol Chem; 2000 Jul; 275(29):22069-74. PubMed ID: 10806205
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Potential digenic inheritance of familial hypertrophic cardiomyopathy identified by whole-exome sequencing.
    Ren MB; Chai XR; Li L; Wang X; Yin C
    Mol Genet Genomic Med; 2020 Mar; 8(3):e1150. PubMed ID: 31960626
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Prevalence and spectrum of mutations in the sarcomeric troponin T and I genes in a cohort of Spanish cardiac hypertrophy patients.
    García-Castro M; Reguero JR; Morís C; Alonso-Montes C; Berrazueta JR; Sainz R; Alvarez V; Coto E
    Int J Cardiol; 2007 Sep; 121(1):115-6. PubMed ID: 17101185
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Homozygous mutation in the cardiac troponin I gene: clinical heterogeneity in hypertrophic cardiomyopathy.
    Gray B; Yeates L; Medi C; Ingles J; Semsarian C
    Int J Cardiol; 2013 Sep; 168(2):1530-1. PubMed ID: 23270746
    [No Abstract]   [Full Text] [Related]  

  • 19. Clinical outcomes associated with sarcomere mutations in hypertrophic cardiomyopathy: a meta-analysis on 7675 individuals.
    Sedaghat-Hamedani F; Kayvanpour E; Tugrul OF; Lai A; Amr A; Haas J; Proctor T; Ehlermann P; Jensen K; Katus HA; Meder B
    Clin Res Cardiol; 2018 Jan; 107(1):30-41. PubMed ID: 28840316
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Molecular epidemiology of hypertrophic cardiomyopathy.
    Morita H; DePalma SR; Arad M; McDonough B; Barr S; Duffy C; Maron BJ; Seidman CE; Seidman JG
    Cold Spring Harb Symp Quant Biol; 2002; 67():383-8. PubMed ID: 12858563
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 11.