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A progeria mutation reveals functions for lamin A in nuclear assembly, architecture, and chromosome organization.
Taimen P, Pfleghaar K, Shimi T, Möller D, Ben-Harush K, Erdos MR, Adam SA, Herrmann H, Medalia O, Collins FS, Goldman AE, Goldman RD. Taimen P, et al. Among authors: erdos mr. Proc Natl Acad Sci U S A. 2009 Dec 8;106(49):20788-93. doi: 10.1073/pnas.0911895106. Epub 2009 Nov 19. Proc Natl Acad Sci U S A. 2009. PMID: 19926845 Free PMC article.
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: erdos mr. Nature. 2003 May 15;423(6937):293-8. doi: 10.1038/nature01629. Epub 2003 Apr 25. Nature. 2003. PMID: 12714972 Free PMC 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: erdos mr. 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.
A farnesyltransferase inhibitor prevents both the onset and late progression of cardiovascular disease in a progeria mouse model.
Capell BC, Olive M, Erdos MR, Cao K, Faddah DA, Tavarez UL, Conneely KN, Qu X, San H, Ganesh SK, Chen X, Avallone H, Kolodgie FD, Virmani R, Nabel EG, Collins FS. Capell BC, et al. Among authors: erdos mr. Proc Natl Acad Sci U S A. 2008 Oct 14;105(41):15902-7. doi: 10.1073/pnas.0807840105. Epub 2008 Oct 6. Proc Natl Acad Sci U S A. 2008. PMID: 18838683 Free PMC article.
141 results