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Items: 10


The E22K mutation of myosin RLC that causes familial hypertrophic cardiomyopathy increases calcium sensitivity of force and ATPase in transgenic mice.

Szczesna-Cordary D, Guzman G, Zhao J, Hernandez O, Wei J, Diaz-Perez Z.

J Cell Sci. 2005 Aug 15;118(Pt 16):3675-83. Epub 2005 Aug 2.


Systematic analysis of the regulatory and essential myosin light chain genes: genetic variants and mutations in hypertrophic cardiomyopathy.

Kabaeva ZT, Perrot A, Wolter B, Dietz R, Cardim N, Correia JM, Schulte HD, Aldashev AA, Mirrakhimov MM, Osterziel KJ.

Eur J Hum Genet. 2002 Nov;10(11):741-8.


The overall pattern of cardiac contraction depends on a spatial gradient of myosin regulatory light chain phosphorylation.

Davis JS, Hassanzadeh S, Winitsky S, Lin H, Satorius C, Vemuri R, Aletras AH, Wen H, Epstein ND.

Cell. 2001 Nov 30;107(5):631-41.


Familial hypertrophic cardiomyopathy mutations in the regulatory light chains of myosin affect their structure, Ca2+ binding, and phosphorylation.

Szczesna D, Ghosh D, Li Q, Gomes AV, Guzman G, Arana C, Zhi G, Stull JT, Potter JD.

J Biol Chem. 2001 Mar 9;276(10):7086-92. Epub 2000 Dec 1.


Identification of two novel mutations in the ventricular regulatory myosin light chain gene (MYL2) associated with familial and classical forms of hypertrophic cardiomyopathy.

Flavigny J, Richard P, Isnard R, Carrier L, Charron P, Bonne G, Forissier JF, Desnos M, Dubourg O, Komajda M, Schwartz K, Hainque B.

J Mol Med (Berl). 1998 Mar;76(3-4):208-14.


Mutations in either the essential or regulatory light chains of myosin are associated with a rare myopathy in human heart and skeletal muscle.

Poetter K, Jiang H, Hassanzadeh S, Master SR, Chang A, Dalakas MC, Rayment I, Sellers JR, Fananapazir L, Epstein ND.

Nat Genet. 1996 May;13(1):63-9.


Interaction of a conserved peptide domain in recombinant human ventricular myosin light chain-2 with myosin heavy chain.

Wadgaonkar R, Shafiq S, Rajmanickam C, Siddiqui MA.

Cell Mol Biol Res. 1993;39(1):13-26.


Isolation and nucleotide sequence of the cDNA encoding human ventricular myosin light chain 2.

Dalla Libera L, Hoffmann E, Floroff M, Jackowski G.

Nucleic Acids Res. 1989 Mar 25;17(6):2360. No abstract available.


Localization of the gene coding for ventricular myosin regulatory light chain (MYL2) to human chromosome 12q23-q24.3.

Macera MJ, Szabo P, Wadgaonkar R, Siddiqui MA, Verma RS.

Genomics. 1992 Jul;13(3):829-31.


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