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Items: 1 to 20 of 95

1.

Human longevity and common variations in the LMNA gene: a meta-analysis.

Conneely KN, Capell BC, Erdos MR, Sebastiani P, Solovieff N, Swift AJ, Baldwin CT, Budagov T, Barzilai N, Atzmon G, Puca AA, Perls TT, Geesaman BJ, Boehnke M, Collins FS.

Aging Cell. 2012 Jun;11(3):475-81. doi: 10.1111/j.1474-9726.2012.00808.x. Epub 2012 Mar 27.

2.

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
3.
4.

Increased expression of the Hutchinson-Gilford progeria syndrome truncated lamin A transcript during cell aging.

Rodriguez S, Coppedè F, Sagelius H, Eriksson M.

Eur J Hum Genet. 2009 Jul;17(7):928-37. doi: 10.1038/ejhg.2008.270. Epub 2009 Jan 28.

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.

Epigenetic involvement in Hutchinson-Gilford progeria syndrome: a mini-review.

Arancio W, Pizzolanti G, Genovese SI, Pitrone M, Giordano C.

Gerontology. 2014;60(3):197-203. doi: 10.1159/000357206. Epub 2014 Feb 28. Review.

7.

p.Pro4Arg mutation in LMNA gene: a new atypical progeria phenotype without metabolism abnormalities.

Guo H, Luo N, Hao F, Bai Y.

Gene. 2014 Aug 1;546(1):35-9. doi: 10.1016/j.gene.2014.05.042. Epub 2014 May 23.

PMID:
24861648
8.

Hutchinson-Gilford progeria syndrome.

Pollex RL, Hegele RA.

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

PMID:
15479179
9.
10.

Polymorphisms in the superoxidase dismutase genes reveal no association with human longevity in Germans: a case-control association study.

Gentschew L, Flachsbart F, Kleindorp R, Badarinarayan N, Schreiber S, Nebel A.

Biogerontology. 2013 Dec;14(6):719-27. doi: 10.1007/s10522-013-9470-3. Epub 2013 Oct 22.

PMID:
24146173
11.

Eliminating the synthesis of mature lamin A reduces disease phenotypes in mice carrying a Hutchinson-Gilford progeria syndrome allele.

Yang SH, Qiao X, Farber E, Chang SY, Fong LG, Young SG.

J Biol Chem. 2008 Mar 14;283(11):7094-9. doi: 10.1074/jbc.M708138200. Epub 2008 Jan 4.

12.

Hutchinson-Gilford progeria syndrome through the lens of transcription.

Prokocimer M, Barkan R, Gruenbaum Y.

Aging Cell. 2013 Aug;12(4):533-43. doi: 10.1111/acel.12070. Epub 2013 Apr 19. Review.

13.

Hutchinson-Gilford progeria mutant lamin A primarily targets human vascular cells as detected by an anti-Lamin A G608G antibody.

McClintock D, Gordon LB, Djabali K.

Proc Natl Acad Sci U S A. 2006 Feb 14;103(7):2154-9. Epub 2006 Feb 6.

14.

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
15.

C1824T mutation in the LMNA gene has no association with senile cataract.

Sadikov T, Simon AJ, Avraham-Lubin BC, Dratviman-Storobinsky O, Cohen Y, Goldenberg-Cohen N.

Neurobiol Aging. 2012 Jul;33(7):1487.e15-9. doi: 10.1016/j.neurobiolaging.2011.09.034. Epub 2011 Nov 10.

PMID:
22079058
16.

Embryonic senescence and laminopathies in a progeroid zebrafish model.

Koshimizu E, Imamura S, Qi J, Toure J, Valdez DM Jr, Carr CE, Hanai J, Kishi S.

PLoS One. 2011 Mar 30;6(3):e17688. doi: 10.1371/journal.pone.0017688.

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.

An inherited LMNA gene mutation in atypical Progeria syndrome.

Doubaj Y, De Sandre-Giovannoli A, Vera EV, Navarro CL, Elalaoui SC, Tajir M, Lévy N, Sefiani A.

Am J Med Genet A. 2012 Nov;158A(11):2881-7. doi: 10.1002/ajmg.a.35557. Epub 2012 Sep 18.

PMID:
22991222
19.

Genetic Association Analysis of Common Variants in FOXO3 Related to Longevity in a Chinese Population.

Lin R, Zhang Y, Yan D, Liao X, Wang X, Fu Y, Cai W.

PLoS One. 2016 Dec 9;11(12):e0167918. doi: 10.1371/journal.pone.0167918. eCollection 2016.

20.

Association of the FOXO3A locus with extreme longevity in a southern Italian centenarian study.

Anselmi CV, Malovini A, Roncarati R, Novelli V, Villa F, Condorelli G, Bellazzi R, Puca AA.

Rejuvenation Res. 2009 Apr;12(2):95-104. doi: 10.1089/rej.2008.0827.

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