Activating the synthesis of progerin, the mutant prelamin A in Hutchinson–Gilford progeria syndrome, with antisense oligonucleotides-Reference-Cited by-同舟云学术

Activating the synthesis of progerin, the mutant prelamin A in Hutchinson–Gilford progeria syndrome, with antisense oligonucleotides

Published:2009-04-17 Issue:13 Volume:18 Page:2462-2471
ISSN:1460-2083
Container-title:Human Molecular Genetics
language:en
Short-container-title:

Author:

Fong Loren G.,Vickers Timothy A.,Farber Emily A.,Choi Christine,Yun Ui Jeong,Hu Yan,Yang Shao H.,Coffinier Catherine,Lee Roger,Yin Liya,Davies Brandon S.J.,Andres Douglas A.,Spielmann H. Peter,Bennett C. Frank,Young Stephen G.

Publisher

Oxford University Press (OUP)

Subject

Genetics (clinical),Genetics,Molecular Biology,General Medicine

Link

http://academic.oup.com/hmg/article-pdf/18/13/2462/17247078/ddp184.pdf

Reference36 articles.

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2. Lamin A truncation in Hutchinson–Gilford progeria;de Sandre-Giovannoli;Science,2003

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

4. Reversal of the cellular phenotype in the premature aging disease Hutchinson–Gilford progeria syndrome;Scaffidi;Nat. Med.,2005

5. Correction of cellular phenotypes of Hutchinson–Gilford Progeria cells by RNA interference;Huang;Hum. Genet.,2005

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