نتایج جستجو برای: progeroid appearance

تعداد نتایج: 87138  

Journal: :Genes & development 2015
Andres J Lopez-Contreras Julia Specks Jacqueline H Barlow Chiara Ambrogio Claus Desler Svante Vikingsson Sara Rodrigo-Perez Henrik Green Lene Juel Rasmussen Matilde Murga André Nussenzweig Oscar Fernandez-Capetillo

In Saccharomyces cerevisiae, absence of the checkpoint kinase Mec1 (ATR) is viable upon mutations that increase the activity of the ribonucleotide reductase (RNR) complex. Whether this pathway is conserved in mammals remains unknown. Here we show that cells from mice carrying extra alleles of the RNR regulatory subunit RRM2 (Rrm2(TG)) present supraphysiological RNR activity and reduced chromoso...

2009
Baomin Li Sonali Jog Jose Candelario Sita Reddy Lucio Comai

Syndromes of accelerated aging could provide an entry point for identifying and dissecting the cellular pathways that are involved in the development of age-related pathologies in the general population. However, their usefulness for aging research has been controversial, as it has been argued that these diseases do not faithfully reflect the process of natural aging. Here we review recent find...

2011
Eriko Koshimizu Shintaro Imamura Jie Qi Jamal Toure Delgado M. Valdez Christopher E. Carr Jun-ichi Hanai Shuji Kishi

BACKGROUND Mutations that disrupt the conversion of prelamin A to mature lamin A cause the rare genetic disorder Hutchinson-Gilford progeria syndrome and a group of laminopathies. Our understanding of how A-type lamins function in vivo during early vertebrate development through aging remains limited, and would benefit from a suitable experimental model. The zebrafish has proven to be a tractab...

2008
Lynne S. Cox

The premature ageing Werner syndrome (WS) is characterized by the early onset of many age related phenotypes, including graying of hair, cataracts, atherosclerosis, cancer and type 2 diabetes. Type 2 diabetes (DM2) is the loss of blood glucose homeostastis, due to insulin resistance and a failure of acute glucose-stimulated insulin secretion (GSIS) by pancreatic cells. Early compensation for in...

Journal: :Cancer research 2002
Junko Oshima Shurong Huang Chong Pae Judith Campisi Robert H Schiestl

Loss of WRN causes the genomic instability progeroid syndrome, Werner syndrome. WRN encodes a multifunctional nuclear protein with 3'-->5' exonuclease and 3'-->5' helicase activities. Linear plasmids with noncompatible ends introduced to Werner syndrome cells underwent extensive deletions at nonhomologous joining ends, particularly at the 3' protruding single-stranded end. This extensive deleti...

Journal: :Hormones 2008
George A Garinis

The physicochemical constitution of DNA cannot warrant lifelong stability. Yet, unlike all other macromolecules, nuclear DNA must last the lifetime of a cell ensuring that its vital genetic information is preserved and faithfully transmitted to progeny. An increasing body of evidence suggests that progressive genome instability likely contributes to aging and shortens lifespan. In support, defe...

Journal: :The Journals of Gerontology Series A: Biological Sciences and Medical Sciences 2005

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