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Items: 1 to 20 of 69

1.

[miR-9: the sentinel of neurons in progeria].

Blondel S, Navarro C, Lévy N, Peschanski M, Nissan X.

Med Sci (Paris). 2012 Jun-Jul;28(6-7):663-6. doi: 10.1051/medsci/2012286022. Epub 2012 Jul 16. Review. French. No abstract available.

2.

Unique preservation of neural cells in Hutchinson- Gilford progeria syndrome is due to the expression of the neural-specific miR-9 microRNA.

Nissan X, Blondel S, Navarro C, Maury Y, Denis C, Girard M, Martinat C, De Sandre-Giovannoli A, Levy N, Peschanski M.

Cell Rep. 2012 Jul 26;2(1):1-9. doi: 10.1016/j.celrep.2012.05.015. Epub 2012 Jun 21.

3.

In vitro pathological modelling using patient-specific induced pluripotent stem cells: the case of progeria.

Nissan X, Blondel S, Peschanski M.

Biochem Soc Trans. 2011 Dec;39(6):1775-9. doi: 10.1042/BST20110659. Review.

PMID:
22103524
4.

The premature ageing syndromes: insights into the ageing process.

Dyer CA, Sinclair AJ.

Age Ageing. 1998 Jan;27(1):73-80. Review. No abstract available.

PMID:
9504370
5.

[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
6.

Falling apart.

Davenport RJ.

Sci Aging Knowledge Environ. 2005 Jun 29;2005(26):nf52. No abstract available.

PMID:
15994212
7.

Of hyperaging and methuselah genes.

Strauss E.

Sci Aging Knowledge Environ. 2001 Oct 3;2001(1):ns2. No abstract available.

PMID:
14602944
8.

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. Epub 2007 Jul 19. Review.

PMID:
17728088
9.

Stem cell depletion in Hutchinson-Gilford progeria syndrome.

Rosengardten Y, McKenna T, Grochová D, Eriksson M.

Aging Cell. 2011 Dec;10(6):1011-20. doi: 10.1111/j.1474-9726.2011.00743.x. Epub 2011 Oct 11.

10.
11.

Progeria: a paradigm for translational medicine.

Gordon LB, Rothman FG, López-Otín C, Misteli T.

Cell. 2014 Jan 30;156(3):400-7. doi: 10.1016/j.cell.2013.12.028.

12.

Homozygous missense mutation in the lamin A/C gene causes autosomal recessive Hutchinson-Gilford progeria syndrome.

Plasilova M, Chattopadhyay C, Pal P, Schaub NA, Buechner SA, Mueller H, Miny P, Ghosh A, Heinimann K.

J Med Genet. 2004 Aug;41(8):609-14. No abstract available.

13.

Vascular aging: insights from studies on cellular senescence, stem cell aging, and progeroid syndromes.

Minamino T, Komuro I.

Nat Clin Pract Cardiovasc Med. 2008 Oct;5(10):637-48. doi: 10.1038/ncpcardio1324. Epub 2008 Sep 2. Review.

PMID:
18762784
14.

Loose chromosomes sink cells.

Leslie M.

Sci Aging Knowledge Environ. 2005 Dec 21;2005(51):nf91. No abstract available.

PMID:
16371657
15.

[Could progeria be a model for the natural process of aging?].

Herman WA, łacka K.

Pol Merkur Lekarski. 2005 Jan;18(103):5-8. Review. Polish.

PMID:
15859537
16.

p53 and a human premature ageing disorder.

O'Neill M, Núñez F, Melton DW.

Mech Ageing Dev. 2003 May;124(5):599-603.

PMID:
12735900
17.

HGPS and related premature aging disorders: from genomic identification to the first therapeutic approaches.

Pereira S, Bourgeois P, Navarro C, Esteves-Vieira V, Cau P, De Sandre-Giovannoli A, Lévy N.

Mech Ageing Dev. 2008 Jul-Aug;129(7-8):449-59. doi: 10.1016/j.mad.2008.04.003. Epub 2008 Apr 12. Review.

PMID:
18513784
18.

Hutchinson-Gilford progeria syndrome: clinical and genetical traits.

Coutinho HD, Falcão-Silva VS, Gonçalves GF.

Panminerva Med. 2009 Jun;51(2):134-5. No abstract available.

PMID:
19776715
19.

Altered splicing in prelamin A-associated premature aging phenotypes.

De Sandre-Giovannoli A, Lévy N.

Prog Mol Subcell Biol. 2006;44:199-232. Review.

PMID:
17076270
20.

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