525 related articles for article (PubMed ID: 19428457)
1. Telomere length in Hutchinson-Gilford progeria syndrome.
Decker ML; Chavez E; Vulto I; Lansdorp PM
Mech Ageing Dev; 2009 Jun; 130(6):377-83. PubMed ID: 19428457
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. 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]
4. A homozygous ZMPSTE24 null mutation in combination with a heterozygous mutation in the LMNA gene causes Hutchinson-Gilford progeria syndrome (HGPS): insights into the pathophysiology of HGPS.
Denecke J; Brune T; Feldhaus T; Robenek H; Kranz C; Auchus RJ; Agarwal AK; Marquardt T
Hum Mutat; 2006 Jun; 27(6):524-31. PubMed ID: 16671095
[TBL] [Abstract][Full Text] [Related]
5. Hutchinson-Gilford progeria syndrome.
Pollex RL; Hegele RA
Clin Genet; 2004 Nov; 66(5):375-81. PubMed ID: 15479179
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. Aging of Hutchinson-Gilford progeria syndrome fibroblasts is characterised by hyperproliferation and increased apoptosis.
Bridger JM; Kill IR
Exp Gerontol; 2004 May; 39(5):717-24. PubMed ID: 15130666
[TBL] [Abstract][Full Text] [Related]
8. LMNA mutations in progeroid syndromes.
Huang S; Kennedy BK; Oshima J
Novartis Found Symp; 2005; 264():197-202; discussion 202-7, 227-30. PubMed ID: 15773755
[TBL] [Abstract][Full Text] [Related]
9. The neonatal progeroid syndrome (Wiedemann-Rautenstrauch): a model for the study of human aging?
Arboleda G; Ramírez N; Arboleda H
Exp Gerontol; 2007 Oct; 42(10):939-43. PubMed ID: 17728088
[TBL] [Abstract][Full Text] [Related]
10. Targeted transgenic expression of the mutation causing Hutchinson-Gilford progeria syndrome leads to proliferative and degenerative epidermal disease.
Sagelius H; Rosengardten Y; Hanif M; Erdos MR; Rozell B; Collins FS; Eriksson M
J Cell Sci; 2008 Apr; 121(Pt 7):969-78. PubMed ID: 18334552
[TBL] [Abstract][Full Text] [Related]
11. Tethering by lamin A stabilizes and targets the ING1 tumour suppressor.
Han X; Feng X; Rattner JB; Smith H; Bose P; Suzuki K; Soliman MA; Scott MS; Burke BE; Riabowol K
Nat Cell Biol; 2008 Nov; 10(11):1333-40. PubMed ID: 18836436
[TBL] [Abstract][Full Text] [Related]
12. A progeroid syndrome in mice is caused by defects in A-type lamins.
Mounkes LC; Kozlov S; Hernandez L; Sullivan T; Stewart CL
Nature; 2003 May; 423(6937):298-301. PubMed ID: 12748643
[TBL] [Abstract][Full Text] [Related]
13. Reduced telomere length variation in healthy oldest old.
Halaschek-Wiener J; Vulto I; Fornika D; Collins J; Connors JM; Le ND; Lansdorp PM; Brooks-Wilson A
Mech Ageing Dev; 2008 Nov; 129(11):638-41. PubMed ID: 18765247
[TBL] [Abstract][Full Text] [Related]
14. Reversible phenotype in a mouse model of Hutchinson-Gilford progeria syndrome.
Sagelius H; Rosengardten Y; Schmidt E; Sonnabend C; Rozell B; Eriksson M
J Med Genet; 2008 Dec; 45(12):794-801. PubMed ID: 18708427
[TBL] [Abstract][Full Text] [Related]
15. Hutchinson-Gilford progeria syndrome through the lens of transcription.
Prokocimer M; Barkan R; Gruenbaum Y
Aging Cell; 2013 Aug; 12(4):533-43. PubMed ID: 23496208
[TBL] [Abstract][Full Text] [Related]
16. [The role of lamins and mutations of LMNA gene in physiological and premature aging].
Sliwińska MA
Postepy Biochem; 2007; 53(1):46-52. PubMed ID: 17718387
[TBL] [Abstract][Full Text] [Related]
17. The truncated prelamin A in Hutchinson-Gilford progeria syndrome alters segregation of A-type and B-type lamin homopolymers.
Delbarre E; Tramier M; Coppey-Moisan M; Gaillard C; Courvalin JC; Buendia B
Hum Mol Genet; 2006 Apr; 15(7):1113-22. PubMed ID: 16481358
[TBL] [Abstract][Full Text] [Related]
18. Molecular cytogenetic insights into the ageing syndrome Hutchinson-Gilford Progeria (HGPS).
Corso C; Parry EM; Faragher RG; Seager A; Green MH; Parry JM
Cytogenet Genome Res; 2005; 111(1):27-33. PubMed ID: 16093717
[TBL] [Abstract][Full Text] [Related]
19. A conserved splicing mechanism of the LMNA gene controls premature aging.
Lopez-Mejia IC; Vautrot V; De Toledo M; Behm-Ansmant I; Bourgeois CF; Navarro CL; Osorio FG; Freije JM; Stévenin J; De Sandre-Giovannoli A; Lopez-Otin C; Lévy N; Branlant C; Tazi J
Hum Mol Genet; 2011 Dec; 20(23):4540-55. PubMed ID: 21875900
[TBL] [Abstract][Full Text] [Related]
20. Fibroblast clones from patients with Hutchinson-Gilford progeria can senesce despite the presence of telomerase.
Wallis CV; Sheerin AN; Green MH; Jones CJ; Kipling D; Faragher RG
Exp Gerontol; 2004 Apr; 39(4):461-7. PubMed ID: 15050279
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]