Results 161 to 170 of about 20,035 (219)

A polymorphic variant at the Werner helicase (WRN) gene is associated with bone density, but not spondylosis, in postmenopausal women

open access: yesA polymorphic variant at the Werner helicase (WRN) gene is associated with bone density, but not spondylosis, in postmenopausal women
Werner syndrome (WS) is a rare autosomal recessive progeroid syndrome characterized by the premature onset of multiple age-related disorders. The gene responsible for WS has been identified as WRN, a member of the RecQ family of helicase genes. Based on the fact that patients with WS exhibit osteoporosis and osteoarthritis, the present study was ...
openaire  

Werner syndrome as a model of aging:the role of wrn at telomeres and the impact of telomerase [PDF]

open access: yes, 2014
Esteve Garcia, Anna   +1 more
core  

[Case report: A case of Werner syndrome with compound heterozygous mutations of WRN gene].

open access: yesNihon Naika Gakkai zasshi. The Journal of the Japanese Society of Internal Medicine, 2011
Yoshikazu, Tamori   +8 more
openaire   +1 more source

Endothelial cell senescence shapes T cell activity in late-stage of chronic obstructive pulmonary disease. [PDF]

open access: yesCell Death Discov
Lee CM   +10 more
europepmc   +1 more source

Decreased mitochondrial NAD+ in WRN deficient cells links to dysfunctional proliferation. [PDF]

open access: yesAging (Albany NY)
Lautrup S   +18 more
europepmc   +1 more source

A case of atypical Werner syndrome without WRN gene mutations

open access: green, 2009
Ji Hoon Choi   +5 more
openalex   +1 more source

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