BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

196 related articles for article (PubMed ID: 8834242)

  • 21. Novel locus for an inherited cardiomyopathy maps to chromosome 7.
    Song L; DePalma SR; Kharlap M; Zenovich AG; Cirino A; Mitchell R; McDonough B; Maron BJ; Seidman CE; Seidman JG; Ho CY
    Circulation; 2006 May; 113(18):2186-92. PubMed ID: 16651466
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Clinical and prognostic evaluation of familial hypertrophic cardiomyopathy in two South African families with different cardiac beta myosin heavy chain gene mutations.
    Posen BM; Moolman JC; Corfield VA; Brink PA
    Br Heart J; 1995 Jul; 74(1):40-6. PubMed ID: 7662452
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Mutations in cardiac myosin heavy chain genes cause familial hypertrophic cardiomyopathy.
    Seidman CE; Seidman JG
    Mol Biol Med; 1991 Apr; 8(2):159-66. PubMed ID: 1806760
    [TBL] [Abstract][Full Text] [Related]  

  • 24. The COX8 gene is not the disease gene of the CMH4 locus in familial hypertrophic cardiomyopathy.
    Bonne G; Carrier L; Schwartz K; Komajda M
    J Med Genet; 1995 Aug; 32(8):670-1. PubMed ID: 7473670
    [No Abstract]   [Full Text] [Related]  

  • 25. Hypertrophic cardiomyopathy and human leukocyte antigen linkage: differentiation of two forms of hypertrophic cardiomyopathy.
    Darsee JR; Heymsfield SB; Nutter DO
    N Engl J Med; 1979 Apr; 300(16):877-82. PubMed ID: 370596
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Molecular genetics of familial hypertrophic cardiomyopathy.
    Hengstenberg C; Schwartz K
    J Mol Cell Cardiol; 1994 Jan; 26(1):3-10. PubMed ID: 8196066
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Exclusion of genes coding for proteins of the cytoskeleton and the extracellular matrix in familial hypertrophic cardiomyopathy using a candidate gene approach.
    Dufour C; Carrier L; Hengstenberg C; Bercovici J; Dausse E; Weissenbach J; Dubourg O; Komajda M; Schwartz K; Beckmann JS
    C R Acad Sci III; 1993; 316(5):474-81. PubMed ID: 8221230
    [TBL] [Abstract][Full Text] [Related]  

  • 28. A new missense mutation, Arg719Gln, in the beta-cardiac heavy chain myosin gene of patients with familial hypertrophic cardiomyopathy.
    Consevage MW; Salada GC; Baylen BG; Ladda RL; Rogan PK
    Hum Mol Genet; 1994 Jun; 3(6):1025-6. PubMed ID: 7848441
    [No Abstract]   [Full Text] [Related]  

  • 29. Isolated familial somatotropinomas: establishment of linkage to chromosome 11q13.1-11q13.3 and evidence for a potential second locus at chromosome 2p16-12.
    Gadelha MR; Une KN; Rohde K; Vaisman M; Kineman RD; Frohman LA
    J Clin Endocrinol Metab; 2000 Feb; 85(2):707-14. PubMed ID: 10690880
    [TBL] [Abstract][Full Text] [Related]  

  • 30. [Genetic heterogeneity of hypertrophic cardiomyopathy in Japanese].
    Machida M
    Hokkaido Igaku Zasshi; 1994 Jul; 69(4):1024-34. PubMed ID: 7959583
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Apical hypertrophic cardiomyopathy of the Japanese type: occurrence with familial hypertrophic cardiomyopathy in a family.
    Ko YL; Lei MH; Chiang FT; Chen JJ; Kuan P; Lien WP
    Am Heart J; 1992 Dec; 124(6):1626-30. PubMed ID: 1462925
    [No Abstract]   [Full Text] [Related]  

  • 32. HLA linkage vs association in hypertrophic cardiomyopathy. Evidence for the absence of an association in a heterogeneous Caucasian population.
    Gardin JM; Gottdiener JS; Radvany R; Maron BJ; Lesch M
    Chest; 1982 Apr; 81(4):466-72. PubMed ID: 7200000
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Development and application of linkage analysis in genetic diagnosis of familial hypertrophic cardiomyopathy.
    Mogensen J; Andersen PS; Steffensen U; Christiansen M; Egeblad H; Gregersen N; Børglum AD
    J Med Genet; 2001 Mar; 38(3):193-8. PubMed ID: 11303515
    [No Abstract]   [Full Text] [Related]  

  • 34. Clinical and genetical heterogeneity of familial hypertrophic cardiomyopathy.
    Hengstenberg C; Carrier L; Schwartz K; Maisch B
    Herz; 1994 Apr; 19(2):84-90. PubMed ID: 8194836
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Gene mapping of familial autosomal dominant dilated cardiomyopathy to chromosome 10q21-23.
    Bowles KR; Gajarski R; Porter P; Goytia V; Bachinski L; Roberts R; Pignatelli R; Towbin JA
    J Clin Invest; 1996 Sep; 98(6):1355-60. PubMed ID: 8823300
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Variable clinical manifestation of a novel missense mutation in the alpha-tropomyosin (TPM1) gene in familial hypertrophic cardiomyopathy.
    Jongbloed RJ; Marcelis CL; Doevendans PA; Schmeitz-Mulkens JM; Van Dockum WG; Geraedts JP; Smeets HJ
    J Am Coll Cardiol; 2003 Mar; 41(6):981-6. PubMed ID: 12651045
    [TBL] [Abstract][Full Text] [Related]  

  • 37. An evaluation of ribonuclease protection assays for the detection of beta-cardiac myosin heavy chain gene mutations.
    MacRae CA; Watkins HC; Jarcho JA; Thierfelder L; McKenna WJ; Seidman JG; Seidman CE
    Circulation; 1994 Jan; 89(1):33-5. PubMed ID: 8281665
    [TBL] [Abstract][Full Text] [Related]  

  • 38. HLA gene analysis in a Japanese family with hypertrophic cardiomyopathy by restriction fragment length polymorphism.
    Kanda T; Takeuchi N; Hasegawa A; Suzuki T; Murata K
    Heart Vessels; 1992; 7(3):155-60. PubMed ID: 1354216
    [TBL] [Abstract][Full Text] [Related]  

  • 39. [Genetic linkage analysis of hypertrophic cardiomyopathy in Japanese].
    Nishi H; Kimura A
    Nihon Rinsho; 1991 Jan; 49(1):232-8. PubMed ID: 1672172
    [No Abstract]   [Full Text] [Related]  

  • 40. Refined localization of the human alpha-tropomyosin gene (TPM1) by genetic mapping.
    Mogensen J; Kruse TA; Børglum AD
    Cytogenet Cell Genet; 1999; 84(1-2):35-6. PubMed ID: 10343096
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 10.