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Items: 1 to 20 of 363

1.
2.

Progeria of stem cells: stem cell exhaustion in Hutchinson-Gilford progeria syndrome.

Halaschek-Wiener J, Brooks-Wilson A.

J Gerontol A Biol Sci Med Sci. 2007 Jan;62(1):3-8. Review.

PMID:
17301031
3.
4.
5.

Telomere length in Hutchinson-Gilford progeria syndrome.

Decker ML, Chavez E, Vulto I, Lansdorp PM.

Mech Ageing Dev. 2009 Jun;130(6):377-83. doi: 10.1016/j.mad.2009.03.001. Epub 2009 Mar 20.

PMID:
19428457
6.

Aggrecan expression is substantially and abnormally upregulated in Hutchinson-Gilford Progeria Syndrome dermal fibroblasts.

Lemire JM, Patis C, Gordon LB, Sandy JD, Toole BP, Weiss AS.

Mech Ageing Dev. 2006 Aug;127(8):660-9. Epub 2006 May 2.

PMID:
16650460
7.
8.

Identification of mitochondrial dysfunction in Hutchinson-Gilford progeria syndrome through use of stable isotope labeling with amino acids in cell culture.

Rivera-Torres J, Acín-Perez R, Cabezas-Sánchez P, Osorio FG, Gonzalez-Gómez C, Megias D, Cámara C, López-Otín C, Enríquez JA, Luque-García JL, Andrés V.

J Proteomics. 2013 Oct 8;91:466-77. doi: 10.1016/j.jprot.2013.08.008. Epub 2013 Aug 20.

PMID:
23969228
9.

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 15;423(6937):298-301.

PMID:
12748643
11.

Hutchinson-Gilford progeria syndrome.

Pollex RL, Hegele RA.

Clin Genet. 2004 Nov;66(5):375-81. Review.

PMID:
15479179
12.

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 1;121(Pt 7):969-78. doi: 10.1242/jcs.022913. Epub 2008 Mar 11.

13.

Ankyrin G overexpression in Hutchinson-Gilford progeria syndrome fibroblasts identified through biological filtering of expression profiles.

Wang J, Robinson JF, O'Neil CH, Edwards JY, Williams CM, Huff MW, Pickering JG, Hegele RA.

J Hum Genet. 2006;51(11):934-42. Epub 2006 Oct 11.

PMID:
17033732
14.

[The role of lamins and mutations of LMNA gene in physiological and premature aging].

Sliwińska MA.

Postepy Biochem. 2007;53(1):46-52. Review. Polish.

PMID:
17718387
15.

Laminopathies and atherosclerosis.

Al-Shali KZ, Hegele RA.

Arterioscler Thromb Vasc Biol. 2004 Sep;24(9):1591-5. Epub 2004 Jun 17. Review.

16.

Hutchinson-Gilford progeria syndrome: review of the phenotype.

Hennekam RC.

Am J Med Genet A. 2006 Dec 1;140(23):2603-24. Review.

PMID:
16838330
17.

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. Epub 2007 Apr 25. Review.

PMID:
17459035
18.

Progeria: a new kind of Laminopathy-- report of the First European Symposium on Progeria and creation of EURO-Progeria, a European Consortium on Progeria and related disorders.

Brune T, Bonne G, Denecke J, Elcioglu N, Hennekam RC, Marquardt T, Ozgen H, Stamsnijder M, Steichen E, Steinmann B, Wehnert M, Levy N.

Pediatr Endocrinol Rev. 2004 Sep;2(1):39-45.

PMID:
16429102
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 1;20(23):4540-55. doi: 10.1093/hmg/ddr385. Epub 2011 Aug 29.

PMID:
21875900
20.

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