PubMed

Molecular ageing in progeroid syndromes: Hutchinson-Gilford progeria syndrome as a model.

Coutinho HD, Falcão-Silva VS, Gonçalves GF, da Nóbrega RB.

Immun Ageing. 2009 Apr 20;6:4.PMID: 19379495 [PubMed]Free PMC ArticleFree textRelated citations

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 [PubMed - indexed for MEDLINE]Related citations

Hutchinson-Gilford progeria syndrome.

Pollex RL, Hegele RA.

Clin Genet. 2004 Nov;66(5):375-81. Review.PMID: 15479179 [PubMed - indexed for MEDLINE]Related citations

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 [PubMed - indexed for MEDLINE]Related citations

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.PMID: 16671095 [PubMed - indexed for MEDLINE]Related citations

LMNA is mutated in Hutchinson-Gilford progeria (MIM 176670) but not in Wiedemann-Rautenstrauch progeroid syndrome (MIM 264090).

Cao H, Hegele RA.

J Hum Genet. 2003;48(5):271-4. Epub 2003 Apr 3.PMID: 12768443 [PubMed - indexed for MEDLINE]Related citations

[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 [PubMed - indexed for MEDLINE]Related citations

Prematurely aged children: molecular alterations leading to Hutchinson-Gilford progeria and Werner syndromes.

Domínguez-Gerpe L, Araújo-Vilar D.

Curr Aging Sci. 2008 Dec;1(3):202-12. Review.PMID: 20021393 [PubMed - indexed for MEDLINE]Related citations

[Hutchinson-Gilford progeria syndrome: clinical and molecular analysis in an African patient]

Mutesa L, Pierquin G, Cwiny-Ay N, Buzizi P, Bours V.

Rev Med Liege. 2007 Mar;62(3):155-8. French. PMID: 17511383 [PubMed - indexed for MEDLINE]Related citations

Dermal fibroblasts in Hutchinson-Gilford progeria syndrome with the lamin A G608G mutation have dysmorphic nuclei and are hypersensitive to heat stress.

Paradisi M, McClintock D, Boguslavsky RL, Pedicelli C, Worman HJ, Djabali K.

BMC Cell Biol. 2005 Jun 27;6:27.PMID: 15982412 [PubMed - indexed for MEDLINE]Free PMC ArticleFree textRelated citations

Evidence for the involvement of lamins in aging.

Rodríguez S, Eriksson M.

Curr Aging Sci. 2010 Jul 1;3(2):81-9.PMID: 20044904 [PubMed - in process]Related citations

Increased progerin expression associated with unusual LMNA mutations causes severe progeroid syndromes.

Moulson CL, Fong LG, Gardner JM, Farber EA, Go G, Passariello A, Grange DK, Young SG, Miner JH.

Hum Mutat. 2007 Sep;28(9):882-9.PMID: 17469202 [PubMed - indexed for MEDLINE]Related citations

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 [PubMed - indexed for MEDLINE]Related citations

An association of Hutchinson-Gilford progeria and malignancy.

Shalev SA, De Sandre-Giovannoli A, Shani AA, Levy N.

Am J Med Genet A. 2007 Aug 15;143A(16):1821-6.PMID: 17618517 [PubMed - indexed for MEDLINE]Related citations

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 [PubMed - indexed for MEDLINE]Related citations

Recurrent de novo point mutations in lamin A cause Hutchinson-Gilford progeria syndrome.

Eriksson M, Brown WT, Gordon LB, Glynn MW, Singer J, Scott L, Erdos MR, Robbins CM, Moses TY, Berglund P, Dutra A, Pak E, Durkin S, Csoka AB, Boehnke M, Glover TW, Collins FS.

Nature. 2003 May 15;423(6937):293-8. Epub 2003 Apr 25.PMID: 12714972 [PubMed - indexed for MEDLINE]Related citations

Progeroid syndrome with scleroderma-like skin changes associated with homozygous R435C LMNA mutation.

Madej-Pilarczyk A, Rosińska-Borkowska D, Rekawek J, Marchel M, Szaluś E, Jabłońska S, Hausmanowa-Petrusewicz I.

Am J Med Genet A. 2009 Nov;149A(11):2387-92.PMID: 19842191 [PubMed - indexed for MEDLINE]Related citations

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. Epub 2008 Aug 15.PMID: 18708427 [PubMed - indexed for MEDLINE]Related citations

Inhibiting farnesylation reverses the nuclear morphology defect in a HeLa cell model for Hutchinson-Gilford progeria syndrome.

Mallampalli MP, Huyer G, Bendale P, Gelb MH, Michaelis S.

Proc Natl Acad Sci U S A. 2005 Oct 4;102(40):14416-21. Epub 2005 Sep 26.PMID: 16186497 [PubMed - indexed for MEDLINE]Free PMC ArticleFree textRelated citations

Defective lamin A-Rb signaling in Hutchinson-Gilford Progeria Syndrome and reversal by farnesyltransferase inhibition.

Marji J, O'Donoghue SI, McClintock D, Satagopam VP, Schneider R, Ratner D, J Worman H, Gordon LB, Djabali K.

PLoS One. 2010 Jun 15;5(6):e11132.PMID: 20559568 [PubMed - in process]Free PMC ArticleFree textRelated citations