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2. LMNA-associated cardiocutaneous progeria: an inherited autosomal dominant premature aging syndrome with late onset. Kane MS; Lindsay ME; Judge DP; Barrowman J; Ap Rhys C; Simonson L; Dietz HC; Michaelis S Am J Med Genet A; 2013 Jul; 161A(7):1599-611. PubMed ID: 23666920 [TBL] [Abstract][Full Text] [Related]
3. Hutchinson-Gilford progeria mutant lamin A primarily targets human vascular cells as detected by an anti-Lamin A G608G antibody. McClintock D; Gordon LB; Djabali K Proc Natl Acad Sci U S A; 2006 Feb; 103(7):2154-9. PubMed ID: 16461887 [TBL] [Abstract][Full Text] [Related]
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5. Towards a Drosophila model of Hutchinson-Gilford progeria syndrome. Beard GS; Bridger JM; Kill IR; Tree DR Biochem Soc Trans; 2008 Dec; 36(Pt 6):1389-92. PubMed ID: 19021561 [TBL] [Abstract][Full Text] [Related]
6. Cardiovascular pathology in Hutchinson-Gilford progeria: correlation with the vascular pathology of aging. Olive M; Harten I; Mitchell R; Beers JK; Djabali K; Cao K; Erdos MR; Blair C; Funke B; Smoot L; Gerhard-Herman M; Machan JT; Kutys R; Virmani R; Collins FS; Wight TN; Nabel EG; Gordon LB Arterioscler Thromb Vasc Biol; 2010 Nov; 30(11):2301-9. PubMed ID: 20798379 [TBL] [Abstract][Full Text] [Related]
11. Transgene silencing of the Hutchinson-Gilford progeria syndrome mutation results in a reversible bone phenotype, whereas resveratrol treatment does not show overall beneficial effects. Strandgren C; Nasser HA; McKenna T; Koskela A; Tuukkanen J; Ohlsson C; Rozell B; Eriksson M FASEB J; 2015 Aug; 29(8):3193-205. PubMed ID: 25877214 [TBL] [Abstract][Full Text] [Related]
12. Incomplete processing of mutant lamin A in Hutchinson-Gilford progeria leads to nuclear abnormalities, which are reversed by farnesyltransferase inhibition. Glynn MW; Glover TW Hum Mol Genet; 2005 Oct; 14(20):2959-69. PubMed ID: 16126733 [TBL] [Abstract][Full Text] [Related]
13. Hutchinson-Gilford progeria syndrome: clinical findings in three patients carrying the G608G mutation in LMNA and review of the literature. Mazereeuw-Hautier J; Wilson LC; Mohammed S; Smallwood D; Shackleton S; Atherton DJ; Harper JI Br J Dermatol; 2007 Jun; 156(6):1308-14. PubMed ID: 17459035 [TBL] [Abstract][Full Text] [Related]
14. Genome-scale expression profiling of Hutchinson-Gilford progeria syndrome reveals widespread transcriptional misregulation leading to mesodermal/mesenchymal defects and accelerated atherosclerosis. Csoka AB; English SB; Simkevich CP; Ginzinger DG; Butte AJ; Schatten GP; Rothman FG; Sedivy JM Aging Cell; 2004 Aug; 3(4):235-43. PubMed ID: 15268757 [TBL] [Abstract][Full Text] [Related]
15. Hutchinson-Gilford Progeria Syndrome: A premature aging disease caused by LMNA gene mutations. Gonzalo S; Kreienkamp R; Askjaer P Ageing Res Rev; 2017 Jan; 33():18-29. PubMed ID: 27374873 [TBL] [Abstract][Full Text] [Related]
16. Epigenetic involvement in Hutchinson-Gilford progeria syndrome: a mini-review. Arancio W; Pizzolanti G; Genovese SI; Pitrone M; Giordano C Gerontology; 2014; 60(3):197-203. PubMed ID: 24603298 [TBL] [Abstract][Full Text] [Related]
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19. Bilateral stenosis of carotid siphon in Hutchinson-Gilford progeria syndrome. Narazaki R; Makimura M; Sanefuji M; Fukamachi S; Akiyoshi H; So H; Yamamura K; Doisaki S; Kojima S; Ihara K; Hara T; Ohga S Brain Dev; 2013 Aug; 35(7):690-3. PubMed ID: 23141186 [TBL] [Abstract][Full Text] [Related]
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