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    Results: 1 to 20 of 112

    1.

    Expression patterns of cardiac myofilament proteins: genomic and protein analysis of surgical myectomy tissue from patients with obstructive hypertrophic cardiomyopathy.

    Theis JL, Bos JM, Theis JD, Miller DV, Dearani JA, Schaff HV, Gersh BJ, Ommen SR, Moss RL, Ackerman MJ.

    Circ Heart Fail. 2009 Jul;2(4):325-33. Epub 2009 May 13.PMID: 19808356 [PubMed - indexed for MEDLINE]Related articles

    2.

    Sarcomere mutations in cardiogenesis and ventricular noncompaction.

    McNally E, Dellefave L.

    Trends Cardiovasc Med. 2009 Jan;19(1):17-21. Review.PMID: 19467449 [PubMed - indexed for MEDLINE]Related articles

    3.

    Thick filament diseases.

    Oldfors A, Lamont PJ.

    Adv Exp Med Biol. 2008;642:78-91. Review.PMID: 19181095 [PubMed - indexed for MEDLINE]Related articles

    4.

    Striking phenotypic variability in two familial cases of myosin storage myopathy with a MYH7 Leu1793pro mutation.

    Uro-Coste E, Arné-Bes MC, Pellissier JF, Richard P, Levade T, Heitz F, Figarella-Branger D, Delisle MB.

    Neuromuscul Disord. 2009 Feb;19(2):163-6. Epub 2009 Jan 12.PMID: 19138847 [PubMed - indexed for MEDLINE]Related articles

    5.

    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.PMID: 19035361 [PubMed - indexed for MEDLINE]Related articles

    6.

    Adverse events in families with hypertrophic or dilated cardiomyopathy and mutations in the MYBPC3 gene.

    Ehlermann P, Weichenhan D, Zehelein J, Steen H, Pribe R, Zeller R, Lehrke S, Zugck C, Ivandic BT, Katus HA.

    BMC Med Genet. 2008 Oct 28;9:95.PMID: 18957093 [PubMed - indexed for MEDLINE]Related articlesFree article

    7.

    Impact of multiple gene mutations in determining the severity of cardiomyopathy and heart failure.

    Tsoutsman T, Bagnall RD, Semsarian C.

    Clin Exp Pharmacol Physiol. 2008 Nov;35(11):1349-57. Epub 2008 Aug 29. Review.PMID: 18761664 [PubMed - indexed for MEDLINE]Related articles

    8.

    Bioinformatics assessment of beta-myosin mutations reveals myosin's high sensitivity to mutations.

    Buvoli M, Hamady M, Leinwand LA, Knight R.

    Trends Cardiovasc Med. 2008 May;18(4):141-9. Review.PMID: 18555187 [PubMed - indexed for MEDLINE]Related articlesFree article

    9.

    Evaluation of the flanking nucleotide sequences of sarcomeric hypertrophic cardiomyopathy substitution mutations.

    Meurs KM, Mealey KL.

    Mutat Res. 2008 Jul 3;642(1-2):86-9. Epub 2008 Apr 24.PMID: 18539302 [PubMed - indexed for MEDLINE]Related articles

    10.

    Mutations in sarcomere protein genes in left ventricular noncompaction.

    Klaassen S, Probst S, Oechslin E, Gerull B, Krings G, Schuler P, Greutmann M, Hürlimann D, Yegitbasi M, Pons L, Gramlich M, Drenckhahn JD, Heuser A, Berger F, Jenni R, Thierfelder L.

    Circulation. 2008 Jun 3;117(22):2893-901. Epub 2008 May 27.PMID: 18506004 [PubMed - indexed for MEDLINE]Related articlesFree article

    11.

    A PCR-based integrated protocol for the structural analysis of the 13th exon of the human beta-myosin heavy chain gene (MYH7): development of a diagnostic tool for HCM disease.

    Stravopodis DJ, Zapheiropoulos AZ, Voutsinas G, Margaritis LH, Papassideri IS.

    Exp Mol Pathol. 2008 Jun;84(3):245-50. Epub 2008 Apr 16.PMID: 18499102 [PubMed - indexed for MEDLINE]Related articles

    12.

    Familial and sporadic hypertrophic myopathy: differences and similarities in a genotyped population. A long follow-up study.

    Brito D, Richard P, Komajda M, Madeira H.

    Rev Port Cardiol. 2008 Feb;27(2):147-73. English, Portuguese. PMID: 18488914 [PubMed - indexed for MEDLINE]Related articles

    13.

    A DNA resequencing array for pathogenic mutation detection in hypertrophic cardiomyopathy.

    Fokstuen S, Lyle R, Munoz A, Gehrig C, Lerch R, Perrot A, Osterziel KJ, Geier C, Beghetti M, Mach F, Sztajzel J, Sigwart U, Antonarakis SE, Blouin JL.

    Hum Mutat. 2008 Jun;29(6):879-85.PMID: 18409188 [PubMed - indexed for MEDLINE]Related articles

    14.

    Shared genetic causes of cardiac hypertrophy in children and adults.

    Morita H, Rehm HL, Menesses A, McDonough B, Roberts AE, Kucherlapati R, Towbin JA, Seidman JG, Seidman CE.

    N Engl J Med. 2008 May 1;358(18):1899-908. Epub 2008 Apr 9.PMID: 18403758 [PubMed - indexed for MEDLINE]Related articlesFree article

    15.

    Worse prognosis with gene mutations of beta-myosin heavy chain than myosin-binding protein C in Chinese patients with hypertrophic cardiomyopathy.

    Wang S, Zou Y, Fu C, Xu X, Wang J, Song L, Wang H, Chen J, Wang J, Huan T, Hui R.

    Clin Cardiol. 2008 Mar;31(3):114-8.PMID: 18383048 [PubMed - indexed for MEDLINE]Related articles

    16.

    A de novo mutation of the beta cardiac myosin heavy chain gene in an infantile restrictive cardiomyopathy.

    Karam S, Raboisson MJ, Ducreux C, Chalabreysse L, Millat G, Bozio A, Bouvagnet P.

    Congenit Heart Dis. 2008 Mar;3(2):138-43.PMID: 18380764 [PubMed - indexed for MEDLINE]Related articles

    17.

    Array-based resequencing assay for mutations causing hypertrophic cardiomyopathy.

    Waldmüller S, Müller M, Rackebrandt K, Binner P, Poths S, Bonin M, Scheffold T.

    Clin Chem. 2008 Apr;54(4):682-7. Epub 2008 Feb 7.PMID: 18258667 [PubMed - indexed for MEDLINE]Related articlesFree article

    18.

    Familial hypertrophic cardiomyopathy associated with cardiac beta-myosin heavy chain and troponin I mutations.

    Frazier A, Judge DP, Schulman SP, Johnson N, Holmes KW, Murphy AM.

    Pediatr Cardiol. 2008 Jul;29(4):846-50. Epub 2008 Jan 4.PMID: 18175163 [PubMed - indexed for MEDLINE]Related articles

    19.

    Noncompaction of the ventricular myocardium is associated with a de novo mutation in the beta-myosin heavy chain gene.

    Budde BS, Binner P, Waldmüller S, Höhne W, Blankenfeldt W, Hassfeld S, Brömsen J, Dermintzoglou A, Wieczorek M, May E, Kirst E, Selignow C, Rackebrandt K, Müller M, Goody RS, Vosberg HP, Nürnberg P, Scheffold T.

    PLoS One. 2007 Dec 26;2(12):e1362.PMID: 18159245 [PubMed - indexed for MEDLINE]Related articlesFree article

    20.

    Troponin T and beta-myosin mutations have distinct cardiac functional effects in hypertrophic cardiomyopathy patients without hypertrophy.

    Revera M, van der Merwe L, Heradien M, Goosen A, Corfield VA, Brink PA, Moolman-Smook JC.

    Cardiovasc Res. 2008 Mar 1;77(4):687-94. Epub 2007 Nov 20.PMID: 18029407 [PubMed - indexed for MEDLINE]Related articlesFree article

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