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lamin C

an alternatively-spiced form of lamin A
Networked: 58 relevant articles (0 outcomes, 0 trials/studies)

Bio-Agent Context: Research Results

Experts

1. Fong, Loren G: 8 articles (09/2016 - 07/2005)
2. Young, Stephen G: 8 articles (09/2016 - 07/2005)
3. Yang, Shao H: 5 articles (04/2016 - 07/2005)
4. Tu, Yiping: 3 articles (09/2016 - 07/2010)
5. Bennett, C Frank: 3 articles (04/2016 - 03/2006)
6. Jung, Hea-Jin: 3 articles (04/2016 - 01/2011)
7. Vickers, Timothy A: 3 articles (04/2016 - 03/2006)
8. Aljada, Ahmad: 2 articles (11/2021 - 04/2016)
9. Garg, Abhimanyu: 2 articles (09/2017 - 05/2002)
10. Lee, John M: 2 articles (04/2016 - 08/2014)

Related Diseases

1. Progeria (Hutchinson Gilford Syndrome)
2. Laminopathies
3. Cardiomyopathies (Cardiomyopathy)
4. Lipodystrophy
10/07/2014 - "MADA with partial lipodystrophy, more marked acral, can be caused by homozygous or compound heterozygous mutation in the gene encoding lamin A and lamin C (LMNA). "
09/01/2000 - "The findings indicated that 1) a spectrum of LMNA mutations underlies FPLD; 2) aberrant lamin A, and not lamin C, is likely to underlie FPLD, as R584H occurs within LMNA sequence that is specific for lamin A; 3) the V440M mutation may not cause lipodystrophy on its own; 4) compound heterozygosity for V440M and R482Q is associated with a relatively more severe FPLD phenotype, but not with complete lipodystrophy; and 5) variation in the severity of the phenotype might be related to environmental factors."
12/01/2007 - "We have observed lower levels of lamin A isoform but normal levels of lamin C isoform in all HIV-infected patients, irrespective of the presence or absence of lipodystrophy, which reinforces the idea that an altered lamin A/C ratio could reflect a pathogenic condition. "
09/01/2017 - "While mutations in lamin A specific residues cause several diseases including lipodystrophy, progeria, muscular dystrophy, neuropathy, and cardiomyopathy, only three families with mutations in lamin C-specific residues are reported with cardiomyopathy, neuropathy, and muscular dystrophy so far. "
08/01/2014 - "Much of the work on nuclear lamins during the past 15 years has focused on mutations in LMNA (the gene for prelamin A and lamin C) that cause particular muscular dystrophy, cardiomyopathy, partial lipodystrophy, and progeroid syndromes. "
5. Neoplasms (Cancer)

Related Drugs and Biologics

1. Lamin Type A (Lamin A)
2. Proteins (Proteins, Gene)
3. Lamins
4. prelamin A
5. Lamin Type B (Lamin B)
6. Protein Isoforms (Isoforms)
7. Autoantibodies
8. Peptides (Polypeptides)
9. Antinuclear Antibodies
10. Adiponectin

Related Therapies and Procedures

1. Implantable Defibrillators (Implantable Cardioverter-Defibrillator)
2. Lasers (Laser)