Results 131 to 140 of about 5,892 (251)

Hutchinson–Gilford progeria syndrome: unraveling the genetic basis, symptoms, and advancements in therapeutic approaches

open access: yesTherapeutic Advances in Rare Disease
Hutchinson–Gilford Progeria syndrome (HGPS) serves as a prominent model for Progeroid syndromes, a group of rare genetic disorders characterized by accelerated aging.
Akhil Arun   +3 more
doaj   +1 more source

Endothelial YAP/TAZ activation promotes atherosclerosis in a mouse model of Hutchinson-Gilford progeria syndrome

open access: yesThe Journal of Clinical Investigation
Hutchinson-Gilford progeria syndrome (HGPS) is an extremely rare disease caused by the expression of progerin, an aberrant protein produced by a point mutation in the LMNA gene.
Ana Barettino   +16 more
doaj   +1 more source

Human immunodeficiency virus contains an epitope immunoreactive with thymosin alpha 1 and the 30-amino acid synthetic p17 group-specific antigen peptide HGP-30.

open access: green, 1987
Paul H. Naylor   +8 more
openalex   +2 more sources

Discordant Gene Expression Signatures and Related Phenotypic Differences in Lamin A- and A/C-Related Hutchinson-Gilford Progeria Syndrome (HGPS)

open access: gold, 2011
Martina Plášilová   +9 more
openalex   +2 more sources

HGP-30, a synthetic analogue of human immunodeficiency virus (HIV) p17, is a target for cytotoxic lymphocytes in HIV-infected individuals.

open access: green, 1990
Adnane Achour   +6 more
openalex   +1 more source

Complicações cardiovasculares e os impactos na qualidade de vida dos pacientes portadores da síndrome de Hutchinson-Gilford (HGPS)

open access: diamond, 2020
Pedro Antonio Rodrigues Dias   +9 more
openalex   +2 more sources

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