Results 141 to 150 of about 21,295 (232)

Model of human aging: Recent findings on Werner’s and Hutchinson-Gilford progeria syndromes

Clinical Interventions in Aging, 2008
Shian-ling Ding1, Chen-Yang Shen2,3,41Department of Nursing, Kang-Ning Junior College of Medical Care and Management, Taipei, Taiwan; 2Institute of Biomedical Sciences, and 3Life Science Library, Academia Sinica, Taipei, Taiwan; 4Graduate Institute of ...
Shian-ling Ding, Chen-Yang Shen
doaj  

Roles of Werner syndrome protein in protection of genome integrity

, 2010
Werner syndrome protein (WRN) is one of a family of five human RecQ helicases implicated in the maintenance of genome stability. The conserved RecQ family also includes RecQ1, Bloom syndrome protein (BLM), RecQ4, and RecQ5 in humans, as well as Sgs1 in ...
Avik K. Ghosh, Marie L. Rossi, Vilhelm A. Bohr, Ghosh, Avik K, Rossi, Marie L, Bohr, Vilhelm A   +5 more
core   +1 more source

Flame-like Calcifications in Werner Syndrome. [PDF]

JCEM Case Rep, 2023
Tsujimoto Y, Bando H.
europepmc   +1 more source

Chondrosarcoma of the mandibular condyle in a patient with Werner syndrome: A case report

, 2013
Werner syndrome, also called progeria of the adult and pangeria is a rare autosomal recessive disorder that affects connective tissue throughout the body. It is associated with premature ageing and an increased risk of cancer and other diseases. The mean
Goutzanis, Labros, Papadogeorgakis, Nick, Petsinis, Vassilis, Kalfarentzos, Evagelos F.   +3 more
core  

A Case of Werner's Syndrome [PDF]

Postgraduate Medical Journal, 1962
openaire   +2 more sources

Senescence-associated inflammation and inhibition of adipogenesis in subcutaneous fat in Werner syndrome. [PDF]

Aging (Albany NY), 2023
Sawada D, Kato H, Kaneko H, Kinoshita D, Funayama S, Minamizuka T, Takasaki A, Igarashi K, Koshizaka M, Takada-Watanabe A, Nakamura R, Aono K, Yamaguchi A, Teramoto N, Maeda Y, Ohno T, Hayashi A, Ide K, Ide S, Shoji M, Kitamoto T, Endo Y, Ogata H, Kubota Y, Mitsukawa N, Iwama A, Ouchi Y, Takayama N, Eto K, Fujii K, Takatani T, Shiohama T, Hamada H, Maezawa Y, Yokote K.   +34 more
europepmc   +1 more source

The gene responsible for Werner syndrome may be a cell division "counting" gene

, 1993
Werner syndrome is a rare, autosomal, recessive condition that is frequently studied as a model of some aspects of human aging, although the behavioral changes that are usually associated with old age are only seen very infrequently.
Shall, S, Tannock, C, Faragher, RG, Kill, IR, Pope, FM, Hunter, JA   +5 more
core  

? Werner's Syndrome ? Acrogeria [PDF]

Proceedings of the Royal Society of Medicine, 1972
openaire   +2 more sources

Werner syndrome in a Lebanese family. [PDF]

Am J Med Genet A, 2022
Jaafar B, Nasrallah M, Sievers B, Oshima J, Lessel D.   +4 more
europepmc   +1 more source

Werner syndrome protein works as a dimer for unwinding and replication fork regression. [PDF]

Nucleic Acids Res, 2023
Shin S, Hyun K, Lee J, Joo D, Kulikowicz T, Bohr VA, Kim J, Hohng S.   +7 more
europepmc   +1 more source