117 related articles for article (PubMed ID: 12778156)
1. Lamin mutations come of age.
Hegele RA
Nat Med; 2003 Jun; 9(6):644-5. PubMed ID: 12778156
[No Abstract] [Full Text] [Related]
2. Nesprin-2 giant safeguards nuclear envelope architecture in LMNA S143F progeria cells.
Kandert S; Lüke Y; Kleinhenz T; Neumann S; Lu W; Jaeger VM; Munck M; Wehnert M; Müller CR; Zhou Z; Noegel AA; Dabauvalle MC; Karakesisoglou I
Hum Mol Genet; 2007 Dec; 16(23):2944-59. PubMed ID: 17881656
[TBL] [Abstract][Full Text] [Related]
3. [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]
4. 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]
5. 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]
6. Hutchinson-Gilford progeria syndrome, aging, and the nuclear lamina.
Korf B
N Engl J Med; 2008 Feb; 358(6):552-5. PubMed ID: 18256390
[No Abstract] [Full Text] [Related]
7. Lamin A-linked progerias: is farnesylation the be all and end all?
Smallwood DT; Shackleton S
Biochem Soc Trans; 2010 Feb; 38(Pt 1):281-6. PubMed ID: 20074075
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. Nuclear envelope.
Dultz E; Ellenberg J
Curr Biol; 2007 Mar; 17(5):R154-6. PubMed ID: 17339009
[No Abstract] [Full Text] [Related]
10. Accumulation of mutant lamin A causes progressive changes in nuclear architecture in Hutchinson-Gilford progeria syndrome.
Goldman RD; Shumaker DK; Erdos MR; Eriksson M; Goldman AE; Gordon LB; Gruenbaum Y; Khuon S; Mendez M; Varga R; Collins FS
Proc Natl Acad Sci U S A; 2004 Jun; 101(24):8963-8. PubMed ID: 15184648
[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. p.S143F mutation in lamin A/C: a new phenotype combining myopathy and progeria.
Kirschner J; Brune T; Wehnert M; Denecke J; Wasner C; Feuer A; Marquardt T; Ketelsen UP; Wieacker P; Bönnemann CG; Korinthenberg R
Ann Neurol; 2005 Jan; 57(1):148-51. PubMed ID: 15622532
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. 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]
15. 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]
16. Genome instability in progeria: when repair gets old.
Misteli T; Scaffidi P
Nat Med; 2005 Jul; 11(7):718-9. PubMed ID: 16015360
[No Abstract] [Full Text] [Related]
17. Mutations in the mouse Lmna gene causing progeria, muscular dystrophy and cardiomyopathy.
Kozlov S; Mounkes L; Cutler D; Sullivan T; Hernandez L; Levy N; Rottman J; Stewart CL
Novartis Found Symp; 2005; 264():246-58; discussion 258-63. PubMed ID: 15773758
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. [Progeria: fatal exchange of nucleotides].
Kaulen H
Dtsch Med Wochenschr; 2003 Jun; 128(25-26):1386. PubMed ID: 12866530
[No Abstract] [Full Text] [Related]
20. Progeria, the nucleolus and farnesyltransferase inhibitors.
Mehta IS; Bridger JM; Kill IR
Biochem Soc Trans; 2010 Feb; 38(Pt 1):287-91. PubMed ID: 20074076
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]