897 related articles for article (PubMed ID: 17718387)
1. [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]
2. Hutchinson-Gilford progeria syndrome.
Pollex RL; Hegele RA
Clin Genet; 2004 Nov; 66(5):375-81. PubMed ID: 15479179
[TBL] [Abstract][Full Text] [Related]
3. A-type nuclear lamins, progerias and other degenerative disorders.
Smith ED; Kudlow BA; Frock RL; Kennedy BK
Mech Ageing Dev; 2005 Apr; 126(4):447-60. PubMed ID: 15722103
[TBL] [Abstract][Full Text] [Related]
4. Aging and nuclear organization: lamins and progeria.
Mounkes LC; Stewart CL
Curr Opin Cell Biol; 2004 Jun; 16(3):322-7. PubMed ID: 15145358
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. 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]
7. 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]
8. 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]
9. Molecular insights into the premature aging disease progeria.
Vidak S; Foisner R
Histochem Cell Biol; 2016 Apr; 145(4):401-17. PubMed ID: 26847180
[TBL] [Abstract][Full Text] [Related]
10. Laminopathies and atherosclerosis.
Al-Shali KZ; Hegele RA
Arterioscler Thromb Vasc Biol; 2004 Sep; 24(9):1591-5. PubMed ID: 15205220
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. 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]
13. 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]
14. 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]
15. Nuclear matrix, nuclear envelope and premature aging syndromes in a translational research perspective.
Cau P; Navarro C; Harhouri K; Roll P; Sigaudy S; Kaspi E; Perrin S; De Sandre-Giovannoli A; Lévy N
Semin Cell Dev Biol; 2014 May; 29():125-47. PubMed ID: 24662892
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. Nuclear lamins, diseases and aging.
Mattout A; Dechat T; Adam SA; Goldman RD; Gruenbaum Y
Curr Opin Cell Biol; 2006 Jun; 18(3):335-41. PubMed ID: 16632339
[TBL] [Abstract][Full Text] [Related]
18. Nuclear lamins: laminopathies and their role in premature ageing.
Broers JL; Ramaekers FC; Bonne G; Yaou RB; Hutchison CJ
Physiol Rev; 2006 Jul; 86(3):967-1008. PubMed ID: 16816143
[TBL] [Abstract][Full Text] [Related]
19. [Laminopathies: one gene, several diseases].
Bertrand AT; Chikhaoui K; Ben Yaou R; Bonne G
Biol Aujourdhui; 2011; 205(3):147-62. PubMed ID: 21982404
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]
