| 1 | MYL2
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| Mybl2 expression is under genetic control and contributes to determine a hepatocellular carcinoma susceptible phenotype.
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| Frau M, Ladu S, Calvisi DF, Simile MM, Bonelli P, Daino L, Tomasi ML, Seddaiu MA, Feo F, Pascale RM.
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| J Hepatol 55(1):111-9. Epub 2010 Dec 7.
2011
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| 2 | MYL2
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| Slow cardiac myosin regulatory light chain 2 (MYL2) was down-expressed in chronic heart failure patients.
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| Li Y, Wu G, Tang Q, Huang C, Jiang H, Shi L, Tu X, Huang J, Zhu X, Wang H.
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| Clin Cardiol 34(1):30-4. doi: 10.1002/clc.20832. Epub 2010 Dec 10.
2011
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| 3 | CMH10, MYL2
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| Cardiomyopathy-linked myosin regulatory light chain mutations disrupt myosin strain-dependent biochemistry.
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| Greenberg MJ, Kazmierczak K, Szczesna-Cordary D, Moore JR.
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| Proc Natl Acad Sci U S A 107(40):17403-8. Epub 2010 Sep 20.
2010
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| 4 | MYL2
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| Malignant familial hypertrophic cardiomyopathy D166V mutation in the ventricular myosin regulatory light chain causes profound effects in skinned and intact papillary muscle fibers from transgenic mice.
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| Kerrick WG, Kazmierczak K, Xu Y, Wang Y, Szczesna-Cordary D.
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| FASEB J 23(3):855-65. Epub 2008 Nov 5.
2009
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| 5 | ACTC1, CFMH4, CMH1, CMH11, MYBPC3, MYH7, MYL2, MYL3, PRKAG2, TNNI3, TNNT2, TPM1
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| Shared genetic causes of cardiac hypertrophy in children and adults.
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| Morita H, Rehm HL, Menesses A, McDonough B, Roberts AE, Kucherlapati R, Towbin JA, Seidman JG, Seidman CE.
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| N Engl J Med 358(18):1899-908. Epub 2008 Apr 9. 2008
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| 6 | MYL2
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| Cardiac myosin light chain-2: a novel essential component of thick-myofilament assembly and contractility of the heart.
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| Rottbauer W, Wessels G, Dahme T, Just S, Trano N, Hassel D, Burns CG, Katus HA, Fishman MC.
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| Circ Res 99(3):323-31. Epub 2006 Jun 29. 2006
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| 7 | CMH10, MYL2
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| Familial hypertrophic cardiomyopathy-linked alterations in Ca2+ binding of human cardiac myosin regulatory light chain affect cardiac muscle contraction.
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| Szczesna-Cordary D, Guzman G, Ng SS, Zhao J.
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| J Biol Chem 279(5):3535-42. Epub 2003 Nov 1. 2004
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| 8 | MYL1, MYL2, MYL3, PITX2
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| Multiple transcriptional domains, with distinct left and right components, in the atrial chambers of the developing heart.
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| Franco D, Campione M, Kelly R, Zammit PS, Buckingham M, Lamers WH, Moorman AF.
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| Circ Res 87(11):984-91. 2000
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| 9 | CMH8, CMH10, MYL2, MYL3
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| Mutations in either the essential or regulatory light chains of myosin are associated with a rare myopathy in human heart and skeletal muscle.
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| Poetter K, et al.
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| Nat Genet 13 : 63-68. 1996
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| 10 | MYL2
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| Localization of the gene coding for ventricular myosin regulatory light chain (MYL2) to human chromosome 12q23-q24.3.
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| Macera MJ, et al.
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| Genomics 13 : 829-831. 1992
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