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Journal Abstract Search

237 related items for PubMed ID: 12642359

  • 21. Isolated X-linked hypertrophic cardiomyopathy caused by a novel mutation of the four-and-a-half LIM domain 1 gene.
    Hartmannova H, Kubanek M, Sramko M, Piherova L, Noskova L, Hodanova K, Stranecky V, Pristoupilova A, Sovova J, Marek T, Maluskova J, Ridzon P, Kautzner J, Hulkova H, Kmoch S.
    Circ Cardiovasc Genet; 2013 Dec; 6(6):543-51. PubMed ID: 24114807
    [Abstract] [Full Text] [Related]

  • 22. MLP (muscle LIM protein) as a stress sensor in the heart.
    Buyandelger B, Ng KE, Miocic S, Piotrowska I, Gunkel S, Ku CH, Knöll R.
    Pflugers Arch; 2011 Jul; 462(1):135-42. PubMed ID: 21484537
    [Abstract] [Full Text] [Related]

  • 23. Prevalence and spectrum of LRRC10 mutations associated with idiopathic dilated cardiomyopathy.
    Qu XK, Yuan F, Li RG, Xu L, Jing WF, Liu H, Xu YJ, Zhang M, Liu X, Fang WY, Yang YQ, Qiu XB.
    Mol Med Rep; 2015 Sep; 12(3):3718-3724. PubMed ID: 26017719
    [Abstract] [Full Text] [Related]

  • 24. Muscle lim protein isoform negatively regulates striated muscle actin dynamics and differentiation.
    Vafiadaki E, Arvanitis DA, Papalouka V, Terzis G, Roumeliotis TI, Spengos K, Garbis SD, Manta P, Kranias EG, Sanoudou D.
    FEBS J; 2014 Jul; 281(14):3261-79. PubMed ID: 24860983
    [Abstract] [Full Text] [Related]

  • 25. Gene mutations in apical hypertrophic cardiomyopathy.
    Arad M, Penas-Lado M, Monserrat L, Maron BJ, Sherrid M, Ho CY, Barr S, Karim A, Olson TM, Kamisago M, Seidman JG, Seidman CE.
    Circulation; 2005 Nov 01; 112(18):2805-11. PubMed ID: 16267253
    [Abstract] [Full Text] [Related]

  • 26. Structural analysis of the titin gene in hypertrophic cardiomyopathy: identification of a novel disease gene.
    Satoh M, Takahashi M, Sakamoto T, Hiroe M, Marumo F, Kimura A.
    Biochem Biophys Res Commun; 1999 Aug 27; 262(2):411-7. PubMed ID: 10462489
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  • 29. A common MLP (muscle LIM protein) variant is associated with cardiomyopathy.
    Knöll R, Kostin S, Klede S, Savvatis K, Klinge L, Stehle I, Gunkel S, Kötter S, Babicz K, Sohns M, Miocic S, Didié M, Knöll G, Zimmermann WH, Thelen P, Bickeböller H, Maier LS, Schaper W, Schaper J, Kraft T, Tschöpe C, Linke WA, Chien KR.
    Circ Res; 2010 Mar 05; 106(4):695-704. PubMed ID: 20044516
    [Abstract] [Full Text] [Related]

  • 30. Human molecular genetic and functional studies identify TRIM63, encoding Muscle RING Finger Protein 1, as a novel gene for human hypertrophic cardiomyopathy.
    Chen SN, Czernuszewicz G, Tan Y, Lombardi R, Jin J, Willerson JT, Marian AJ.
    Circ Res; 2012 Sep 14; 111(7):907-19. PubMed ID: 22821932
    [Abstract] [Full Text] [Related]

  • 31. A substitution mutation in cardiac ubiquitin ligase, FBXO32, is associated with an autosomal recessive form of dilated cardiomyopathy.
    Al-Hassnan ZN, Shinwari ZM, Wakil SM, Tulbah S, Mohammed S, Rahbeeni Z, Alghamdi M, Rababh M, Colak D, Kaya N, Al-Fayyadh M, Alburaiki J.
    BMC Med Genet; 2016 Jan 14; 17():3. PubMed ID: 26768247
    [Abstract] [Full Text] [Related]

  • 32. Structural analysis of four and half LIM protein-2 in dilated cardiomyopathy.
    Arimura T, Hayashi T, Matsumoto Y, Shibata H, Hiroi S, Nakamura T, Inagaki N, Hinohara K, Takahashi M, Manatsu SI, Sasaoka T, Izumi T, Bonne G, Schwartz K, Kimura A.
    Biochem Biophys Res Commun; 2007 May 25; 357(1):162-7. PubMed ID: 17416352
    [Abstract] [Full Text] [Related]

  • 33. 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 25; 74(1):40-6. PubMed ID: 7662452
    [Abstract] [Full Text] [Related]

  • 34. Prevalence of cardiac beta-myosin heavy chain gene mutations in patients with hypertrophic cardiomyopathy.
    Perrot A, Schmidt-Traub H, Hoffmann B, Prager M, Bit-Avragim N, Rudenko RI, Usupbaeva DA, Kabaeva Z, Imanov B, Mirrakhimov MM, Dietz R, Wycisk A, Tendera M, Gessner R, Osterziel KJ.
    J Mol Med (Berl); 2005 Jun 25; 83(6):468-77. PubMed ID: 15856146
    [Abstract] [Full Text] [Related]

  • 35. Sarcomeric protein mutations in dilated cardiomyopathy.
    Chang AN, Potter JD.
    Heart Fail Rev; 2005 Sep 25; 10(3):225-35. PubMed ID: 16416045
    [Abstract] [Full Text] [Related]

  • 36. Different expressivity of a ventricular essential myosin light chain gene Ala57Gly mutation in familial hypertrophic cardiomyopathy.
    Lee W, Hwang TH, Kimura A, Park SW, Satoh M, Nishi H, Harada H, Toyama J, Park JE.
    Am Heart J; 2001 Feb 25; 141(2):184-9. PubMed ID: 11174330
    [Abstract] [Full Text] [Related]

  • 37. Molecular genetic and functional characterization implicate muscle-restricted coiled-coil gene (MURC) as a causal gene for familial dilated cardiomyopathy.
    Rodriguez G, Ueyama T, Ogata T, Czernuszewicz G, Tan Y, Dorn GW, Bogaev R, Amano K, Oh H, Matsubara H, Willerson JT, Marian AJ.
    Circ Cardiovasc Genet; 2011 Aug 01; 4(4):349-58. PubMed ID: 21642240
    [Abstract] [Full Text] [Related]

  • 38. FHL2 expression and variants in hypertrophic cardiomyopathy.
    Friedrich FW, Reischmann S, Schwalm A, Unger A, Ramanujam D, Münch J, Müller OJ, Hengstenberg C, Galve E, Charron P, Linke WA, Engelhardt S, Patten M, Richard P, van der Velden J, Eschenhagen T, Isnard R, Carrier L.
    Basic Res Cardiol; 2014 Aug 01; 109(6):451. PubMed ID: 25358972
    [Abstract] [Full Text] [Related]

  • 39. A missense mutation in the beta myosin heavy chain gene is a predictor of premature sudden death in patients with hypertrophic cardiomyopathy.
    Marian AJ, Kelly D, Mares A, Fitzgibbons J, Caira T, Qun-Tao, Hill R, Perryman MB, Roberts R.
    J Sports Med Phys Fitness; 1994 Mar 01; 34(1):1-10. PubMed ID: 7934006
    [Abstract] [Full Text] [Related]

  • 40. Genotype phenotype correlations of cardiac beta-myosin heavy chain mutations in Indian patients with hypertrophic and dilated cardiomyopathy.
    Rai TS, Ahmad S, Bahl A, Ahuja M, Ahluwalia TS, Singh B, Talwar KK, Khullar M.
    Mol Cell Biochem; 2009 Jan 01; 321(1-2):189-96. PubMed ID: 18953637
    [Abstract] [Full Text] [Related]

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