An inhibitory role of progerin in the gene induction network of adipocyte differentiation from iPS cells | Aging
Frontiers | Nesprins and Lamins in Health and Diseases of Cardiac and Skeletal Muscles
Mutant nuclear lamin A leads to progressive alterations of epigenetic control in premature aging | PNAS
JCI - Progerin elicits disease phenotypes of progeria in mice whether or not it is farnesylated
Mammalian SUN Protein Interaction Networks at the Inner Nuclear Membrane and Their Role in Laminopathy Disease Processes - ScienceDirect
Modulation of cytoskeleton in cardiomyopathy caused by mutations in LMNA gene | American Journal of Physiology-Cell Physiology
Permanent farnesylation of lamin A mutants linked to progeria impairs its phosphorylation at serine 22 during interphase - Figure F7 | Aging
Western blots with an antibody against lamin A/C showing that... | Download Scientific Diagram
Progerinin, an optimized progerin-lamin A binding inhibitor, ameliorates premature senescence phenotypes of Hutchinson-Gilford progeria syndrome | Communications Biology
Comparing relative stability of lamin A, progerin and lamin B1 in human... | Download Scientific Diagram
Lamin A‐mediated nuclear lamina integrity is required for proper ciliogenesis | EMBO reports
The Mutant Form of Lamin A that Causes Hutchinson-Gilford Progeria Is a Biomarker of Cellular Aging in Human Skin | PLOS ONE
Cells | Free Full-Text | Deciphering Nuclear Mechanobiology in Laminopathy
Frontiers | The Emerging Role of Lamin C as an Important LMNA Isoform in Mechanophenotype
Status of the nuclear proteins in HGPS cells. A. Representative Western... | Download Scientific Diagram
Unique Preservation of Neural Cells in Hutchinson- Gilford Progeria Syndrome Is Due to the Expression of the Neural-Specific miR-9 MicroRNA - ScienceDirect
LMNA mutation in a 45 year old Japanese subject with Hutchinson-Gilford progeria syndrome | Journal of Medical Genetics
A progeria mutation reveals functions for lamin A in nuclear assembly, architecture, and chromosome organization | PNAS
Molecular insights into the premature aging disease progeria | Histochemistry and Cell Biology
Novel LMNA mutations cause an aggressive atypical neonatal progeria without progerin accumulation | Journal of Medical Genetics
Metformin decreases progerin expression and alleviates pathological defects of Hutchinson–Gilford progeria syndrome cells | npj Aging
Hutchinson–Gilford progeria mutant lamin A primarily targets human vascular cells as detected by an anti-Lamin A G608G antibody | PNAS
Role of nuclear Lamin A/C in cardiomyocyte functions - Carmosino - 2014 - Biology of the Cell - Wiley Online Library
