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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
1989 | 1 |
1992 | 1 |
1996 | 1 |
2000 | 1 |
2001 | 1 |
2002 | 1 |
2005 | 1 |
2024 | 0 |
PubMed (OMIM) for id: 1794147
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The E22K mutation of myosin RLC that causes familial hypertrophic cardiomyopathy increases calcium sensitivity of force and ATPase in transgenic mice.
J Cell Sci. 2005 Aug 15;118(Pt 16):3675-83. doi: 10.1242/jcs.02492. Epub 2005 Aug 2.
J Cell Sci. 2005.
PMID: 16076902
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.
Kabaeva ZT, et al.
Eur J Hum Genet. 2002 Nov;10(11):741-8. doi: 10.1038/sj.ejhg.5200872.
Eur J Hum Genet. 2002.
PMID: 12404107
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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.
Szczesna D, et al.
J Biol Chem. 2001 Mar 9;276(10):7086-92. doi: 10.1074/jbc.M009823200. Epub 2000 Dec 1.
J Biol Chem. 2001.
PMID: 11102452
Free article.
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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.
Poetter K, Jiang H, Hassanzadeh S, Master SR, Chang A, Dalakas MC, Rayment I, Sellers JR, Fananapazir L, Epstein ND.
Poetter K, et al.
Nat Genet. 1996 May;13(1):63-9. doi: 10.1038/ng0596-63.
Nat Genet. 1996.
PMID: 8673105
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Isolation and nucleotide sequence of the cDNA encoding human ventricular myosin light chain 2.
Dalla Libera L, Hoffmann E, Floroff M, Jackowski G.
Dalla Libera L, et al.
Nucleic Acids Res. 1989 Mar 25;17(6):2360. doi: 10.1093/nar/17.6.2360.
Nucleic Acids Res. 1989.
PMID: 2704627
Free PMC article.
No abstract available.
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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.
Macera MJ, et al.
Genomics. 1992 Jul;13(3):829-31. doi: 10.1016/0888-7543(92)90161-k.
Genomics. 1992.
PMID: 1386340
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