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EMBO Molecular Medicine, ISSN 1757-4676, 09/2017, Volume 9, Issue 9, pp. 1294 - 1313
Hutchinson–Gilford progeria syndrome (HGPS) is a lethal premature and accelerated aging disease caused by a de novo point mutation in LMNA encoding A‐type... 
Promyeloid leukemia | Splicing | Transcription | Progeria | Point mutation | Cell lines | Children | Lamins | Nuclei | Autophagy | Phagocytosis | Skeletal muscle
Journal Article
Seminars in Cell and Developmental Biology, ISSN 1084-9521, 2014
Lamin A-related progeroid syndromes are genetically determined, extremely rare and severe. In the past 10 years, our knowledge and perspectives for these... 
Progeria | Aging | Aging diseases | Lamins | Nuclear matrix
Journal Article
Orphanet Journal of Rare Diseases, ISSN 1750-1172, 2015, Volume 10, Issue Suppl 2, p. I1
Journal Article
Pediatric Dermatology, ISSN 0736-8046, 07/2011, Volume 28, Issue 4, pp. 408 - 411
Journal Article
Journal Article
Nucleus, ISSN 1949-1034, 12/2018, Volume 9, Issue 1, pp. 265 - 276
Hutchinson-Gilford progeria syndrome (HGPS) is a sporadic, autosomal dominant disorder characterized by premature and accelerated aging symptoms leading to... 
AON | HGPS | ZOPRA | Progerin | MG132 | FTI | Rapamycin | Metformin | FARNESYLTRANSFERASE INHIBITOR | DISEASE PHENOTYPES | NUCLEAR LAMINA | CELL BIOLOGY | TRUNCATED PRELAMIN | MOUSE MODEL | FARNESYLATION INHIBITORS | CELLULAR PHENOTYPES | MUTANT LAMIN-A | PROTEASOME INHIBITOR | NF-KAPPA-B
Journal Article
Journal Article
The American Journal of Human Genetics, ISSN 0002-9297, 2002, Volume 70, Issue 3, pp. 726 - 736
Journal Article
Journal Article