Endothelial cell-specific progerin expression does not cause cardiovascular alterations and premature death. [PDF]
AbstractHutchinson‐Gilford progeria syndrome (HGPS) is a rare genetic disorder caused by a mutation in the LMNA gene that provokes the synthesis of progerin, a mutant version of the nuclear protein lamin A that accelerates aging and precipitates death.
Benedicto I +11 more
europepmc +6 more sources
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
A combination of both proteomic and genetic approach to indentify de-regulated pathway in progeria, an accelerated aging disorder [PDF]
Comunicaciones a ...
Arufe, M.C. +8 more
core
Induced pluripotent stem cell models of frontotemporal dementia [PDF]
The increasing prevalence of dementia in the ageing population combined with the lack of treatments and the burden on national healthcare systems globally, make dementia a public health priority.
Hardy, J, Preza, E, Warner, T, Wray, S
core
Vascular cells derived from Hutchinson-Gilford progeria syndrome (HGPS) inducible pluripotent stem cells [PDF]
To study the vulnerability of smooth muscle cells (SMCs) in Hutchinson-Gilford Progeria Syndrome (HGPS)
Ferreira, Lino +4 more
core
Senescent endothelial cells promote pathogenic neutrophil trafficking in inflamed tissues
Cellular senescence is a hallmark of advanced age and a major instigator of numerous inflammatory pathologies. While endothelial cell (EC) senescence is aligned with defective vascular functionality, its impact on fundamental inflammatory responses in ...
Loïc Rolas +21 more
doaj +1 more source
LAV-BPIFB4 reverses progeria-associated cardiac aging by restoring diastolic function and reducing senescence. [PDF]
Chae U +4 more
europepmc +1 more source
Why and How Are Infants with Hutchinson-Gilford Progeria Syndrome Born Without Severe Manifestations? [PDF]
Erokhina MA +3 more
europepmc +1 more source
Potential therapeutic approaches for modulating expression and accumulation of defective lamin A in laminopathies and age-related diseases [PDF]
core +1 more source
Hutchinson-Gilford progeria syndrome alters the endothelial genetic response to laminar shear stress. [PDF]
Kennedy CC, Carter JL, Truskey GA.
europepmc +1 more source

