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Insights into myosin regulatory and essential light chains: a focus on their roles in cardiac and skeletal muscle function, development and disease.
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Functions of myosin light chain-2 (MYL2) in cardiac muscle and disease.
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Transgenic remodeling of the regulatory myosin light chains in the mammalian heart.
Circ Res. 1997 May;80(5):655-64. doi: 10.1161/01.res.80.5.655.
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Tuning the human heart molecular motors by myosin light chains.
J Mol Med (Berl). 1999 Jul;77(7):544-55. doi: 10.1007/s001099900031.
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Myosin essential light chain in health and disease.
Am J Physiol Heart Circ Physiol. 2007 Apr;292(4):H1643-54. doi: 10.1152/ajpheart.00931.2006. Epub 2006 Dec 1.

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MYL1-Related Congenital Myopathy: Clinical, Genetic and Pathological Insights.
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Birth of protein-coding exons by ancient domestication of LINE-1 retrotransposon.
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Activation of VEGFR3 and MLC2 are Critical for GLP-2 Enhancement of Chylomicron Transport.
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In-depth characterization of S-glutathionylation in ventricular myosin light chain 1 across species by top-down proteomics.
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CircFBLN2 regulates duck myoblast proliferation and differentiation through miR-22-5p and MEF2C interaction.
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The distinctive mechanical and structural signatures of residual force enhancement in myofibers.
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Cell polarity proteins promote macropinocytosis in response to metabolic stress.
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Hyperhomocysteinemia-Induced Alterations in Protein Expression and Oxidative Stress Parameters in Rat Heart.
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Proteins with calmodulin-like domains: structures and functional roles.
Cell Mol Life Sci. 2019 Jun;76(12):2299-2328. doi: 10.1007/s00018-019-03062-z. Epub 2019 Mar 15.
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Bi-allelic mutations in MYL1 cause a severe congenital myopathy.
Hum Mol Genet. 2018 Dec 15;27(24):4263-4272. doi: 10.1093/hmg/ddy320.
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Thick Filament Protein Network, Functions, and Disease Association.
Compr Physiol. 2018 Mar 13;8(2):631-709. doi: 10.1002/cphy.c170023.
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Single cardiac ventricular myosins are autonomous motors.
Open Biol. 2018 Apr;8(4). doi: 10.1098/rsob.170240.
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Sarcomeric perturbations of myosin motors lead to dilated cardiomyopathy in genetically modified mice.
Proc Natl Acad Sci U S A. 2018 Mar 6;115(10):E2338-E2347. doi: 10.1073/pnas.1716925115. Epub 2018 Feb 20.

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