Development of induced pluripotent stem cells from a patient with hypertrophic cardiomyopathy who carries the pathogenic myosin heavy chain 7 mutation p.Arg403Gln

Những quyển sách tương tự

• Cell-Intrinsic Functional Effects of the α-Cardiac Myosin Arg-403-Gln Mutation in Familial Hypertrophic Cardiomyopathy
  Bằng: Chuan, Peiying, et al.
  Được phát hành: (2012)
• The L‐type Ca(2+) channel facilitates abnormal metabolic activity in the cTnI‐G203S mouse model of hypertrophic cardiomyopathy
  Bằng: Viola, Helena, et al.
  Được phát hành: (2016)
• Neonatal cardiomyopathy in mice homozygous for the Arg403Gln mutation in the α cardiac myosin heavy chain gene
  Bằng: Fatkin, Diane, et al.
  Được phát hành: (1999)
• Meningeal siderosis in a patient carrying the p.Arg92Gln variant TNFRSF1A gene
  Bằng: F.J. Nicolás-Sánchez, et al.
  Được phát hành: (2022-04-01)
• The cardiac myosin heavy chain Arg-403-->Gln mutation that causes hypertrophic cardiomyopathy does not affect the actin- or ATP-binding capacities of two size-limited recombinant myosin heavy chain fragments.
  Bằng: Eldin, P, et al.
  Được phát hành: (1995)