Results 111 to 120 of about 13,916 (214)
Validation of modulated proteins due to progerin over-expression in Progeria Syndrome (HGPS) cell lines [PDF]
El síndrome de la progeria de Hutchinson-Gilford (HGPS), una enfermedad de envejecimiento prematuro, se caracteriza por la sobreexpresión de una isoforma mutada de la lamina A, la progerina o lamina AΔ50.
Palla Pérez, Sandra
core +1 more source
Characterization of the craniofacial abnormalities of the homozygous G608G progeria mouse model
IntroductionHutchinson-Gilford Progeria Syndrome (HGPS) is a rare genetic condition characterized by premature aging, impacting multiple organ systems, including cardiovascular, musculoskeletal, and integumentary.
Indeevar Beeram +13 more
doaj +1 more source
Charles F. Harris, Robert Hutohison
openaire +1 more source
Potential Role of p53 in Huchinson-Gilford Progeria Syndrome [PDF]
Undergraduate ...
Eschedor, Danielle +2 more
core
Hutchinson-Gilford syndrome (progeria)
Progeria is a rare, autosomal dominant, progeroid disorder. In the world literature less than 100 cases have been reported to date. We present this case because of its rarity.
Surjushe Amar +3 more
doaj
LAV-BPIFB4 reverses progeria-associated cardiac aging by restoring diastolic function and reducing senescence. [PDF]
Chae U +4 more
europepmc +1 more source
Transcriptional profiling of Hutchinson-Gilford progeria patients identifies primary target pathways of progerin. [PDF]
Vidak S, Kim S, Misteli T.
europepmc +1 more source
Author Correction: p300 nucleocytoplasmic shuttling underlies mTORC1 hyperactivation in Hutchinson-Gilford progeria syndrome. [PDF]
Son SM +4 more
europepmc +1 more source

