PubMed (cited) for id: 160790

Year	Number of Results
1982	1
1988	1
1989	2
1996	1
1997	1
2001	1
2002	2
2005	1
2011	1
2024	0

1

Furthering the link between the sarcomere and primary cardiomyopathies: restrictive cardiomyopathy associated with multiple mutations in genes previously associated with hypertrophic or dilated cardiomyopathy.

Caleshu C, Sakhuja R, Nussbaum RL, Schiller NB, Ursell PC, Eng C, De Marco T, McGlothlin D, Burchard EG, Rame JE. Caleshu C, et al. Am J Med Genet A. 2011 Sep;155A(9):2229-35. doi: 10.1002/ajmg.a.34097. Epub 2011 Aug 5. Am J Med Genet A. 2011. PMID: 21823217 Free PMC article.

2

Gene mutations in apical hypertrophic cardiomyopathy.

Arad M, Penas-Lado M, Monserrat L, Maron BJ, Sherrid M, Ho CY, Barr S, Karim A, Olson TM, Kamisago M, Seidman JG, Seidman CE. Arad M, et al. Circulation. 2005 Nov 1;112(18):2805-11. doi: 10.1161/CIRCULATIONAHA.105.547448. Circulation. 2005. PMID: 16267253

3

Essential myosin light chain as a target for caspase-3 in failing myocardium.

Moretti A, Weig HJ, Ott T, Seyfarth M, Holthoff HP, Grewe D, Gillitzer A, Bott-Flügel L, Schömig A, Ungerer M, Laugwitz KL. Moretti A, et al. Proc Natl Acad Sci U S A. 2002 Sep 3;99(18):11860-5. doi: 10.1073/pnas.182373099. Epub 2002 Aug 19. Proc Natl Acad Sci U S A. 2002. PMID: 12186978 Free PMC article.

4

Myosin light chain mutation causes autosomal recessive cardiomyopathy with mid-cavitary hypertrophy and restrictive physiology.

Olson TM, Karst ML, Whitby FG, Driscoll DJ. Olson TM, et al. Circulation. 2002 May 21;105(20):2337-40. doi: 10.1161/01.cir.0000018444.47798.94. Circulation. 2002. PMID: 12021217

5

Blocking caspase-activated apoptosis improves contractility in failing myocardium.

Laugwitz KL, Moretti A, Weig HJ, Gillitzer A, Pinkernell K, Ott T, Pragst I, Städele C, Seyfarth M, Schömig A, Ungerer M. Laugwitz KL, et al. Hum Gene Ther. 2001 Nov 20;12(17):2051-63. doi: 10.1089/10430340152677403. Hum Gene Ther. 2001. PMID: 11747596

6

Substitution mutations in the myosin essential light chain lead to reduced actin-activated ATPase activity despite stoichiometric binding to the heavy chain.

Ho G, Chisholm RL. Ho G, et al. J Biol Chem. 1997 Feb 14;272(7):4522-7. doi: 10.1074/jbc.272.7.4522. J Biol Chem. 1997. PMID: 9020178 Free article.

7

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

8

Hypertrophic cardiomyopathy with ventricular septal hypertrophy localized to the apical region of the left ventricle (apical hypertrophic cardiomyopathy).

Maron BJ, Bonow RO, Seshagiri TN, Roberts WC, Epstein SE. Maron BJ, et al. Am J Cardiol. 1982 Jun;49(8):1838-48. doi: 10.1016/0002-9149(82)90200-4. Am J Cardiol. 1982. PMID: 6211078

9

Molecular cloning and complete nucleotide sequence of a human ventricular myosin light chain 1.

Hoffmann E, Shi QW, Floroff M, Mickle DA, Wu TW, Olley PM, Jackowski G. Hoffmann E, et al. Nucleic Acids Res. 1988 Mar 25;16(5):2353. doi: 10.1093/nar/16.5.2353. Nucleic Acids Res. 1988. PMID: 3357795 Free PMC article. No abstract available.

10

Human ventricular/slow twitch myosin alkali light chain gene characterization, sequence, and chromosomal location.

Fodor WL, Darras B, Seharaseyon J, Falkenthal S, Francke U, Vanin EF. Fodor WL, et al. J Biol Chem. 1989 Feb 5;264(4):2143-9. J Biol Chem. 1989. PMID: 2789520 Free article.

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