Hutchinson-gilford progeria is a skeletal dysplasia-Reference-Cited by-同舟云学术

Hutchinson-gilford progeria is a skeletal dysplasia

Published:2011-06-21 Issue:7 Volume:26 Page:1670-1679
ISSN:0884-0431
Container-title:Journal of Bone and Mineral Research
language:en
Short-container-title:J Bone Miner Res

Author:

Gordon Catherine M,Gordon Leslie B,Snyder Brian D,Nazarian Ara,Quinn Nicolle,Huh Susanna,Giobbie-Hurder Anita,Neuberg Donna,Cleveland Robert,Kleinman Monica,Miller David T,Kieran Mark W

Publisher

Wiley

Subject

Orthopedics and Sports Medicine,Endocrinology, Diabetes and Metabolism

Reference28 articles.

1. LMNA is mutated in Hutchinson-Gilford progeria (MIM 176670) but not in Wiedemann-Rautenstrauch progeroid syndrome (MIM 264090);Cao;J Hum Genet.,2003

2. Lamin a truncation in Hutchinson-Gilford progeria;De;Science.,2003

3. Recurrent de novo point mutations in lamin A cause Hutchinson-Gilford progeria syndrome;Eriksson;Nature.,2003

4. Accumulation of mutant lamin A causes progressive changes in nuclear architecture in Hutchinson-Gilford progeria syndrome;Goldman;Proc Natl Acad Sci. USA.,2004

5. Inhibiting farnesylation of progerin prevents the characteristic nuclear blebbing of Hutchinson-Gilford progeria syndrome;Capell;Proc Natl Acad Sci USA.,2005

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2. Skeletal phenotypes and molecular mechanisms in aging mice;Zoological Research;2024

3. Lipodystrophy as a target to delay premature aging;Trends in Endocrinology & Metabolism;2023-11

4. Intervention for Critical Aortic Stenosis in Hutchinson-Gilford Progeria Syndrome;2023-10-06

5. An infant with congenital micrognathia and upper airway obstruction was diagnosed as Hutchinson-Gilford progeria syndrome caused by a novel LMNA mutation: Case report and literature review;Heliyon;2023-10