نتایج جستجو برای: progeroid appearance

تعداد نتایج: 87138  

Journal: :The Journal of Clinical Endocrinology & Metabolism 2009

Journal: :Organic & biomolecular chemistry 2016
Mark C Bagley Jessica E Dwyer Mohammed Baashen Matthew C Dix Paola G S Murziani Michal J Rokicki David Kipling Terence Davis

Microwave-assisted synthesis of the pyrazolyl ketone p38 MAPK inhibitor RO3201195 in 7 steps and 15% overall yield, and the comparison of its effect upon the proliferation of Werner Syndrome cells with a library of pyrazolyl ketones, strengthens the evidence that p38 MAPK inhibition plays a critical role in modulating premature cellular senescence in this progeroid syndrome and the reversal of ...

2012
Maureen Bowles John Lally Andrew J. Fadden Stephane Mouilleron Timothy Hammonds Neil Q. McDonald

The structure-specific endonuclease activity of the human XPF-ERCC1 complex is essential for a number of DNA processing mechanisms that help to maintain genomic integrity. XPF-ERCC1 cleaves DNA structures such as stem-loops, bubbles or flaps in one strand of a duplex where there is at least one downstream single strand. Here, we define the minimal substrate requirements for cleavage of stem-loo...

2013
Lolita S. Nidadavolu Laura J. Niedernhofer Saleem A. Khan

XFE progeroid syndrome, a disease of accelerated aging caused by deficiency in the DNA repair endonuclease XPF-ERCC1, is modeled by Ercc1 knockout and hypomorphic mice. Tissues and primary cells from these mice senesce prematurely, offering a unique opportunity to identify factors that regulate senescence and aging. We compared microRNA (miRNA) expression in Ercc1-/- primary mouse embryonic fib...

Journal: :Pathobiology of Aging & Age-related Diseases 2011

Journal: :Journal of cell science 2006
Antonio E Rusiñol Michael S Sinensky

Three mammalian nuclear lamin proteins, lamin B(1), lamin B(2) and the lamin A precursor, prelamin A, undergo canonical farnesylation and processing at CAAX motifs. In the case of prelamin A, there is an additional farnesylation-dependent endoproteolysis, which is defective in two congenital diseases: Hutchinson-Gilford progeria (HGPS) and restrictive dermopathy (RD). These two diseases arise r...

نمودار تعداد نتایج جستجو در هر سال

با کلیک روی نمودار نتایج را به سال انتشار فیلتر کنید