Results 171 to 180 of about 17,639 (297)

Ankyrin G overexpression in Hutchinson-Gilford progeria syndrome fibroblasts identified through biological filtering of expression profiles [PDF]

open access: bronze, 2006
Jian Wang   +7 more
openalex   +1 more source

Nesprin-2 giant safeguards nuclear envelope architecture in LMNA S143F progeria cells [PDF]

open access: bronze, 2007
Sebastian Kandert   +12 more
openalex   +1 more source

Progeria

open access: yesNursing & Healthcare International Journal
Progeria is a rare genetic disease with striking features that resemble accelerated aging. The inheritance pattern, paternal age effect, and lack of consanguinity argue that it is due to a sporadic dominant mutation. We have observed elevated levels of hyaluronic acid (HA) excretion in progeria patients.
openaire   +1 more source

Phenotype and Course of Hutchinson–Gilford Progeria Syndrome [PDF]

open access: bronze, 2008
Melissa A. Merideth   +24 more
openalex   +1 more source

Increasing the length of progerin's isoprenyl anchor does not worsen bone disease or survival in mice with Hutchinson-Gilford progeria syndrome [PDF]

open access: hybrid, 2008
Brandon S.J. Davies   +10 more
openalex   +1 more source

Inhibiting farnesylation of progerin prevents the characteristic nuclear blebbing of Hutchinson-Gilford progeria syndrome

open access: green, 2005
B. C. Capell   +9 more
openalex   +2 more sources

Assessing the efficacy of protein farnesyltransferase inhibitors in mouse models of progeria [PDF]

open access: hybrid, 2009
Shao H. Yang   +5 more
openalex   +1 more source

Adaptive stress response in segmental progeria resembles long-lived dwarfism and calorie restriction in mice

open access: green, 2005
Marieke van de Ven   +10 more
openalex   +1 more source

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