» Articles » PMID: 15353794

What Can Progeroid Syndromes Tell Us About Human Aging?

Overview
Journal Science
Specialty Science
Date 2004 Sep 9
PMID 15353794
Citations 53
Authors
Affiliations
Soon will be listed here.
Abstract

Human genetic diseases that resemble accelerated aging provide useful models for gerontologists. They combine known single-gene mutations with deficits in selected tissues that are reminiscent of changes seen during normal aging. Here, we describe recent progress toward linking molecular and cellular changes with the phenotype seen in two of these disorders. One in particular, Werner syndrome, provides evidence to support the hypothesis that the senescence of somatic cells may be a causal agent of normal aging.

Citing Articles

Premature aging in genetic diseases: what conclusions can be drawn for physiological aging.

Milosic F, Hengstschlager M, Osmanagic-Myers S Front Aging. 2024; 4:1327833.

PMID: 38481648 PMC: 10933081. DOI: 10.3389/fragi.2023.1327833.


Seven knowledge gaps in modern biogerontology.

Rattan S Biogerontology. 2024; 25(1):1-8.

PMID: 38206540 DOI: 10.1007/s10522-023-10089-0.


Modified iPOND revealed the role of mutant p53 in promoting helicase function and telomere maintenance.

Wang Q, Hou K, Yang J, Li H, Li C, Zhang Y Aging (Albany NY). 2023; 15(19):10767-10784.

PMID: 37827695 PMC: 10599736. DOI: 10.18632/aging.205117.


Progerin, an Aberrant Spliced Form of Lamin A, Is a Potential Therapeutic Target for HGPS.

Kim B, Chung Y, Woo T, Kang S, Park S, Park B Cells. 2023; 12(18).

PMID: 37759521 PMC: 10527460. DOI: 10.3390/cells12182299.


An efficient method for cell sheet bioengineering from rBMSCs on thermo-responsive PCL-PEG-PCL copolymer.

Vaghefi Moghaddam S, Abedi F, Lotfi H, Salehi R, Barzegar A, Baghaban Eslaminejad M J Biol Eng. 2023; 17(1):27.

PMID: 37024910 PMC: 10080813. DOI: 10.1186/s13036-023-00346-8.