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 *

183 related articles for article (PubMed ID: 25125180)

  • 1. Structural implications of β-cardiac myosin heavy chain mutations in human disease.
    Colegrave M; Peckham M
    Anat Rec (Hoboken); 2014 Sep; 297(9):1670-80. PubMed ID: 25125180
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Multidimensional structure-function relationships in human β-cardiac myosin from population-scale genetic variation.
    Homburger JR; Green EM; Caleshu C; Sunitha MS; Taylor RE; Ruppel KM; Metpally RP; Colan SD; Michels M; Day SM; Olivotto I; Bustamante CD; Dewey FE; Ho CY; Spudich JA; Ashley EA
    Proc Natl Acad Sci U S A; 2016 Jun; 113(24):6701-6. PubMed ID: 27247418
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A1603P and K1617del, Mutations in β-Cardiac Myosin Heavy Chain that Cause Laing Early-Onset Distal Myopathy, Affect Secondary Structure and Filament Formation In Vitro and In Vivo.
    Parker F; Batchelor M; Wolny M; Hughes R; Knight PJ; Peckham M
    J Mol Biol; 2018 May; 430(10):1459-1478. PubMed ID: 29660325
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Dilated cardiomyopathy myosin mutants have reduced force-generating capacity.
    Ujfalusi Z; Vera CD; Mijailovich SM; Svicevic M; Yu EC; Kawana M; Ruppel KM; Spudich JA; Geeves MA; Leinwand LA
    J Biol Chem; 2018 Jun; 293(23):9017-9029. PubMed ID: 29666183
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Whole-exome sequencing identifies R1279X of MYH6 gene to be associated with congenital heart disease.
    Razmara E; Garshasbi M
    BMC Cardiovasc Disord; 2018 Jul; 18(1):137. PubMed ID: 29969989
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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. PubMed ID: 18555187
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Cardiomyopathy mutations reveal variable region of myosin converter as major element of cross-bridge compliance.
    Seebohm B; Matinmehr F; Köhler J; Francino A; Navarro-Lopéz F; Perrot A; Ozcelik C; McKenna WJ; Brenner B; Kraft T
    Biophys J; 2009 Aug; 97(3):806-24. PubMed ID: 19651039
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Novel familial dilated cardiomyopathy mutation in MYL2 affects the structure and function of myosin regulatory light chain.
    Huang W; Liang J; Yuan CC; Kazmierczak K; Zhou Z; Morales A; McBride KL; Fitzgerald-Butt SM; Hershberger RE; Szczesna-Cordary D
    FEBS J; 2015 Jun; 282(12):2379-93. PubMed ID: 25825243
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Novel mutation in the α-myosin heavy chain gene is associated with sick sinus syndrome.
    Ishikawa T; Jou CJ; Nogami A; Kowase S; Arrington CB; Barnett SM; Harrell DT; Arimura T; Tsuji Y; Kimura A; Makita N
    Circ Arrhythm Electrophysiol; 2015 Apr; 8(2):400-8. PubMed ID: 25717017
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Structural effects of the slow/b-cardiac myosin heavy chain R453C mutation in cardiac and skeletal muscle.
    Tajsharghi H; Fyhr IM
    Scand Cardiovasc J; 2008 Apr; 42(2):153-6. PubMed ID: 18365899
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Structural, functional and molecular dynamics analysis of the native and mutated actin to study its effect on congenital myopathy.
    Mohajer FS; Parvizpour S; Razmara J; Khoshkhooy Yazdi M; Shamsir MS
    J Biomol Struct Dyn; 2017 May; 35(7):1608-1614. PubMed ID: 27448459
    [No Abstract]   [Full Text] [Related]  

  • 12. Digenic mutational inheritance of the integrin alpha 7 and the myosin heavy chain 7B genes causes congenital myopathy with left ventricular non-compact cardiomyopathy.
    Esposito T; Sampaolo S; Limongelli G; Varone A; Formicola D; Diodato D; Farina O; Napolitano F; Pacileo G; Gianfrancesco F; Di Iorio G
    Orphanet J Rare Dis; 2013 Jun; 8():91. PubMed ID: 23800289
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Recessive MYH6 Mutations in Hypoplastic Left Heart With Reduced Ejection Fraction.
    Theis JL; Zimmermann MT; Evans JM; Eckloff BW; Wieben ED; Qureshi MY; O'Leary PW; Olson TM
    Circ Cardiovasc Genet; 2015 Aug; 8(4):564-71. PubMed ID: 26085007
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Surgical repair of left ventricular noncompaction in a patient with a novel mutation of the myosin heavy chain 7 gene.
    Uchiyama T; Yoshimura K; Kaneko K; Nemoto S; Ichida F; Hata Y; Nishida N
    Tohoku J Exp Med; 2012 Dec; 228(4):301-4. PubMed ID: 23117287
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Skip residues modulate the structural properties of the myosin rod and guide thick filament assembly.
    Taylor KC; Buvoli M; Korkmaz EN; Buvoli A; Zheng Y; Heinze NT; Cui Q; Leinwand LA; Rayment I
    Proc Natl Acad Sci U S A; 2015 Jul; 112(29):E3806-15. PubMed ID: 26150528
    [TBL] [Abstract][Full Text] [Related]  

  • 16. New skeletal myopathy and cardiomyopathy associated with a missense mutation in MYH7.
    Darin N; Tajsharghi H; Ostman-Smith I; Gilljam T; Oldfors A
    Neurology; 2007 Jun; 68(23):2041-2. PubMed ID: 17548557
    [No Abstract]   [Full Text] [Related]  

  • 17. The myosin mesa and the basis of hypercontractility caused by hypertrophic cardiomyopathy mutations.
    Nag S; Trivedi DV; Sarkar SS; Adhikari AS; Sunitha MS; Sutton S; Ruppel KM; Spudich JA
    Nat Struct Mol Biol; 2017 Jun; 24(6):525-533. PubMed ID: 28481356
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Genetic analysis of monoallelic double MYH7 mutations responsible for familial hypertrophic cardiomyopathy.
    Wang B; Wang J; Wang LF; Yang F; Xu L; Li WX; He Y; Zuo L; Yang QL; Shao H; Hu D; Liu LW
    Mol Med Rep; 2019 Dec; 20(6):5229-5238. PubMed ID: 31638223
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A low prevalence of MYH7/MYBPC3 mutations among familial hypertrophic cardiomyopathy patients in India.
    Bashyam MD; Purushotham G; Chaudhary AK; Rao KM; Acharya V; Mohammad TA; Nagarajaram HA; Hariram V; Narasimhan C
    Mol Cell Biochem; 2012 Jan; 360(1-2):373-82. PubMed ID: 21959974
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Novel mutations in beta-myosin heavy chain, actin and troponin-I genes associated with dilated cardiomyopathy in Indian population.
    Boda U; Vadapalli S; Calambur N; Nallari P
    J Genet; 2009 Dec; 88(3):373-7. PubMed ID: 20086309
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 10.