نتایج جستجو برای: progeroid appearance

تعداد نتایج: 87138  

Journal: :Journal of Nepal Paediatric Society 2012

2012
Fernando G. Osorio Carlos López-Otín José M. P. Freije

consequence of a stochastic process caused by the accumulative effect of damaged molecules. However, recent experimental evidences have extended this view and suggested that aging also requires active signaling programs for the maintenance of the aged state [1]. Beyond cell-autonomous alterations, age signals get systemic through changes in intercellular communication pathways [2]. The identifi...

Journal: :Trends in Glycoscience and Glycotechnology 1993

Journal: :PLoS Genetics 2006
Marieke van de Ven Jaan-Olle Andressoo Valerie B Holcomb Marieke von Lindern Willeke M. C Jong Chris I. De Zeeuw Yousin Suh Paul Hasty Jan H. J Hoeijmakers Gijsbertus T. J van der Horst James R Mitchell

How congenital defects causing genome instability can result in the pleiotropic symptoms reminiscent of aging but in a segmental and accelerated fashion remains largely unknown. Most segmental progerias are associated with accelerated fibroblast senescence, suggesting that cellular senescence is a likely contributing mechanism. Contrary to expectations, neither accelerated senescence nor acute ...

2017
Rafael R. Flores Cheryl L. Clauson Joonseok Cho Byeong‐Chel Lee Sara J. McGowan Darren J. Baker Laura J. Niedernhofer Paul D. Robbins

With aging, there is progressive loss of tissue homeostasis and functional reserve, leading to an impaired response to stress and an increased risk of morbidity and mortality. A key mediator of the cellular response to damage and stress is the transcription factor NF-κB. We demonstrated previously that NF-κB transcriptional activity is upregulated in tissues from both natural aged mice and in a...

Journal: :Indian pediatrics 2011
J P Narayan P Garg G Pareek S Narayan

Wiedemann Rautenstauch (WR) syndrome is a rare autosomal recessive neonatal progeroid syndrome with only few published case reports. We describe a neonate showing clinical features of WR syndrome with peeling of skin, and presented with weak cry and breathing difficulty since birth.

Journal: :Japanese journal of human genetics 1987

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