Cellular Senescence and Aging: Mechanisms, Disease Convergence, and Therapeutic Frontiers
This schematic illustrates the hierarchical and interconnected nature of the primary molecular hallmarks of aging. The progression of aging is driven by a convergence of intrinsic molecular insults. Within the nucleus, genomic instability and telomere attrition trigger persistent DDR, accompanied by extensive epigenetic alterations.
Guowei Cai +10 more
wiley +1 more source
Hutchinson Gilford Progeria Syndrome (HGPS): Potential Treatments [PDF]
The Hutchinson-Gilford Progeria syndrome is a rare genetic disease that causes an early accelerated aging in children; clinically characterized by manifestations affecting skin, musculoskeletal system and blood vessels, also other features supporting ...
Sutiono, D. R. (Dias) +1 more
core
De HGP-write aux « super-cellules » [PDF]
The HGP-write project, announced in 2016 but not really implemented yet, comes back as a project aimed at constructing an “ultra-safe” human cell line fully resistant to virus infection and with other desirable characteristics. This involves introducing 400,000 changes in the genome and raises a number of technical and financial issues, but may become ...
openaire +2 more sources
Metabolic Dysfunction‐Associated Fatty Liver Disease: From Pathogenesis to Treatment
Extracellular vesicles play a crucial role in interorgan crosstalk of adipose–liver and gut–liver axes and hold potential as therapeutic targets and drug delivery systems for metabolic dysfunction‐associated fatty liver disease (MAFLD). Abbreviations: AT: adipose tissue; EVs: extracellular vesicles; HL: healthy liver; NAFL: nonalcoholic fatty liver ...
Zhifu Cui +5 more
wiley +1 more source
Hutchinson-Gilford Progeria Syndrome: a premature aging disease caused by LMNA gene mutations
Products of the LMNA gene, primarily lamin A and C, are key components of the nuclear lamina, a proteinaceous meshwork that underlies the inner nuclear membrane and is essential for proper nuclear architecture.
S. Gonzalo, R. Kreienkamp, P. Askjaer
semanticscholar +1 more source
Targeted validation of PRPS1 shows down-regulation of transcript and protein levels in HGPS-cells and the animal model of HPGS, respectively. [PDF]
Orthogonal validation of PRPS1 modulation by targeted techniques in cell lines (A, B) and in the mouse model of HGPS (C, D). Real-Time PCR (RT-PCR) of HGPS and control cell lines (A) showing that PRPS1 transcript is down-regulated in the three HGPS cell ...
Juan Fafián-Labora (5917748) +8 more
core +1 more source
Low levels of the reverse transactivator fail to induce target transgene expression in vascular smooth muscle cells. [PDF]
Hutchinson-Gilford progeria syndrome (HGPS) is a genetic disease with multiple features that are suggestive of premature aging. Most patients with HGPS carry a mutation on one of their copies of the LMNA gene.
Nikenza Viceconte +2 more
doaj +1 more source
Hawaii Geothermal Project; HGP-A Reservoir Engineering [PDF]
Department of Energy, Contract EY-76-C-03-1093; Energy Research and Development Administration, Contract E(04-3)-1093; National Science Foundation, Grant GI 38319; State of Hawaii, Grants RCUH 5774, 5784, 5942; County of Hawaii, Grant RCUH 5773; Hawaiian Electric Company, Grants 5809, 5828.
Yuen, P. C. +4 more
openaire +2 more sources
Nucleolar expansion and elevated protein translation in premature aging
Premature aging disorders provide an opportunity to study the mechanisms that drive aging. In Hutchinson-Gilford progeria syndrome (HGPS), a mutant form of the nuclear scaffold protein lamin A distorts nuclei and sequesters nuclear proteins. We sought to
A. Buchwalter, M. Hetzer
semanticscholar +1 more source
Expression of TRP channel transcripts in IMR90-iPSC-ECs and HGPS-iPSC-ECs. [PDF]
Shown were the expressional levels of transcripts for TRPV (A), TRPC (B), TRPM (C) and TRPP (D) in IMR90-iPSC-ECs (I) and HGPS-iPSC-ECs (H).
Nelson L. Tang (515416) +8 more
core +1 more source

