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Recurrent de novo point mutations in lamin A cause Hutchinson-Gilford progeria syndrome.
Eriksson M, Brown WT, Gordon LB, Glynn MW, Singer J, Scott L, Erdos MR, Robbins CM, Moses TY, Berglund P, Dutra A, Pak E, Durkin S, Csoka AB, Boehnke M, Glover TW, Collins FS. Eriksson M, et al. Among authors: gordon lb. Nature. 2003 May 15;423(6937):293-8. doi: 10.1038/nature01629. Epub 2003 Apr 25. Nature. 2003. PMID: 12714972 Free article.
Progressive vascular smooth muscle cell defects in a mouse model of Hutchinson-Gilford progeria syndrome.
Varga R, Eriksson M, Erdos MR, Olive M, Harten I, Kolodgie F, Capell BC, Cheng J, Faddah D, Perkins S, Avallone H, San H, Qu X, Ganesh S, Gordon LB, Virmani R, Wight TN, Nabel EG, Collins FS. Varga R, et al. Among authors: gordon lb. Proc Natl Acad Sci U S A. 2006 Feb 28;103(9):3250-5. doi: 10.1073/pnas.0600012103. Epub 2006 Feb 21. Proc Natl Acad Sci U S A. 2006. PMID: 16492728 Free PMC article.
New approaches to progeria.
Kieran MW, Gordon L, Kleinman M. Kieran MW, et al. Pediatrics. 2007 Oct;120(4):834-41. doi: 10.1542/peds.2007-1356. Pediatrics. 2007. PMID: 17908771 Review.
70 results