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 *

209 related articles for article (PubMed ID: 8358441)

  • 1. Mapping of a novel gene for familial hypertrophic cardiomyopathy to chromosome 11.
    Carrier L; Hengstenberg C; Beckmann JS; Guicheney P; Dufour C; Bercovici J; Dausse E; Berebbi-Bertrand I; Wisnewsky C; Pulvenis D
    Nat Genet; 1993 Jul; 4(3):311-3. PubMed ID: 8358441
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Familial hypertrophic cardiomyopathy. Microsatellite haplotyping and identification of a hot spot for mutations in the beta-myosin heavy chain gene.
    Dausse E; Komajda M; Fetler L; Dubourg O; Dufour C; Carrier L; Wisnewsky C; Bercovici J; Hengstenberg C; al-Mahdawi S
    J Clin Invest; 1993 Dec; 92(6):2807-13. PubMed ID: 8254035
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. [Hypertrophic cardiomyopathy: practical application of genetic research].
    Guicheney P; Schwartz K; Komajda M
    Arch Mal Coeur Vaiss; 1995 Apr; 88(4 Suppl):569-71. PubMed ID: 7487301
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. Genetic heterogeneity of familial hypertrophic cardiomyopathy.
    Dausse E; Schwartz K
    Neuromuscul Disord; 1993; 3(5-6):483-6. PubMed ID: 8186698
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Genetic linkage analysis of familial amyotrophic lateral sclerosis using human chromosome 21 microsatellite DNA markers.
    Rosen DR; Sapp P; O'Regan J; McKenna-Yasek D; Schlumpf KS; Haines JL; Gusella JF; Horvitz HR; Brown RH
    Am J Med Genet; 1994 May; 51(1):61-9. PubMed ID: 7913294
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [An analysis of the linkage of hypertrophic cardiomyopathy and the delta locus of the T-cell receptor (TCRD) chain in the family of P].
    Miakotkin VA; Finogenova SA; Krylov MIu; Moshnina MA; Korovina EP; Moiseev VS
    Ter Arkh; 1999; 71(5):67-70. PubMed ID: 10399236
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. 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]  

  • 11. Identification of a mutation near a functional site of the beta cardiac myosin heavy chain gene in a family with hypertrophic cardiomyopathy.
    Dufour C; Dausse E; Fetler L; Dubourg O; Bouhour JB; Vosberg HP; Guicheney P; Komajda M; Schwartz K
    J Mol Cell Cardiol; 1994 Sep; 26(9):1241-7. PubMed ID: 7815466
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Missense mutation of the beta-cardiac myosin heavy-chain gene in hypertrophic cardiomyopathy.
    Arai S; Matsuoka R; Hirayama K; Sakurai H; Tamura M; Ozawa T; Kimura M; Imamura S; Furutani Y; Joh-o K
    Am J Med Genet; 1995 Sep; 58(3):267-76. PubMed ID: 8533830
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Mapping a gene for familial hypertrophic cardiomyopathy to chromosome 14q1.
    Jarcho JA; McKenna W; Pare JA; Solomon SD; Holcombe RF; Dickie S; Levi T; Donis-Keller H; Seidman JG; Seidman CE
    N Engl J Med; 1989 Nov; 321(20):1372-8. PubMed ID: 2811944
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Mapping of a gene predisposing to early-onset Alzheimer's disease to chromosome 14q24.3.
    Van Broeckhoven C; Backhovens H; Cruts M; De Winter G; Bruyland M; Cras P; Martin JJ
    Nat Genet; 1992 Dec; 2(4):335-9. PubMed ID: 1303290
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Double heterozygosity for mutations in the beta-myosin heavy chain and in the cardiac myosin binding protein C genes in a family with hypertrophic cardiomyopathy.
    Richard P; Isnard R; Carrier L; Dubourg O; Donatien Y; Mathieu B; Bonne G; Gary F; Charron P; Hagege M; Komajda M; Schwartz K; Hainque B
    J Med Genet; 1999 Jul; 36(7):542-5. PubMed ID: 10424815
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A rapid protocol for cardiac troponin T gene mutation detection in familial hypertrophic cardiomyopathy.
    Gerull B; Osterziel KJ; Witt C; Dietz R; Thierfelder L
    Hum Mutat; 1998; 11(2):179-82. PubMed ID: 9482583
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A complex bilateral polysyndactyly disease locus maps to chromosome 7q36.
    Tsukurov O; Boehmer A; Flynn J; Nicolai JP; Hamel BC; Traill S; Zaleske D; Mankin HJ; Yeon H; Ho C
    Nat Genet; 1994 Mar; 6(3):282-6. PubMed ID: 8012391
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. A missense mutation of cardiac beta-myosin heavy chain gene linked to familial hypertrophic cardiomyopathy in affected Japanese families.
    Harada H; Kimura A; Nishi H; Sasazuki T; Toshima H
    Biochem Biophys Res Commun; 1993 Jul; 194(2):791-8. PubMed ID: 8343162
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Familial hypertrophic cardiomyopathy is a genetically heterogeneous disease.
    Solomon SD; Jarcho JA; McKenna W; Geisterfer-Lowrance A; Germain R; Salerni R; Seidman JG; Seidman CE
    J Clin Invest; 1990 Sep; 86(3):993-9. PubMed ID: 1975599
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.