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Items: 1 to 20 of 154

1.

Correlated alterations in genome organization, histone methylation, and DNA-lamin A/C interactions in Hutchinson-Gilford progeria syndrome.

McCord RP, Nazario-Toole A, Zhang H, Chines PS, Zhan Y, Erdos MR, Collins FS, Dekker J, Cao K.

Genome Res. 2013 Feb;23(2):260-9. doi: 10.1101/gr.138032.112. Epub 2012 Nov 14.

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.

Loss of a DNA binding site within the tail of prelamin A contributes to altered heterochromatin anchorage by progerin.

Bruston F, Delbarre E, Ostlund C, Worman HJ, Buendia B, Duband-Goulet I.

FEBS Lett. 2010 Jul 16;584(14):2999-3004. doi: 10.1016/j.febslet.2010.05.032. Epub 2010 May 24.

4.

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.

5.

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.

6.

Rescue of heterochromatin organization in Hutchinson-Gilford progeria by drug treatment.

Columbaro M, Capanni C, Mattioli E, Novelli G, Parnaik VK, Squarzoni S, Maraldi NM, Lattanzi G.

Cell Mol Life Sci. 2005 Nov;62(22):2669-78.

7.

All-trans retinoic acid and rapamycin normalize Hutchinson Gilford progeria fibroblast phenotype.

Pellegrini C, Columbaro M, Capanni C, D'Apice MR, Cavallo C, Murdocca M, Lattanzi G, Squarzoni S.

Oncotarget. 2015 Oct 6;6(30):29914-28. doi: 10.18632/oncotarget.4939.

8.

Activating the synthesis of progerin, the mutant prelamin A in Hutchinson-Gilford progeria syndrome, with antisense oligonucleotides.

Fong LG, Vickers TA, Farber EA, Choi C, Yun UJ, Hu Y, Yang SH, Coffinier C, Lee R, Yin L, Davies BS, Andres DA, Spielmann HP, Bennett CF, Young SG.

Hum Mol Genet. 2009 Jul 1;18(13):2462-71. doi: 10.1093/hmg/ddp184. Epub 2009 Apr 17.

9.
10.

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.

11.

Mutant nuclear lamin A leads to progressive alterations of epigenetic control in premature aging.

Shumaker DK, Dechat T, Kohlmaier A, Adam SA, Bozovsky MR, Erdos MR, Eriksson M, Goldman AE, Khuon S, Collins FS, Jenuwein T, Goldman RD.

Proc Natl Acad Sci U S A. 2006 Jun 6;103(23):8703-8. Epub 2006 May 31.

12.

Inhibiting farnesylation of progerin prevents the characteristic nuclear blebbing of Hutchinson-Gilford progeria syndrome.

Capell BC, Erdos MR, Madigan JP, Fiordalisi JJ, Varga R, Conneely KN, Gordon LB, Der CJ, Cox AD, Collins FS.

Proc Natl Acad Sci U S A. 2005 Sep 6;102(36):12879-84. Epub 2005 Aug 29.

13.

Mapping of lamin A- and progerin-interacting genome regions.

Kubben N, Adriaens M, Meuleman W, Voncken JW, van Steensel B, Misteli T.

Chromosoma. 2012 Oct;121(5):447-64. doi: 10.1007/s00412-012-0376-7. Epub 2012 May 19.

14.

Hutchinson-Gilford progeria syndrome.

Pollex RL, Hegele RA.

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

PMID:
15479179
15.

Sulforaphane enhances progerin clearance in Hutchinson-Gilford progeria fibroblasts.

Gabriel D, Roedl D, Gordon LB, Djabali K.

Aging Cell. 2015 Feb;14(1):78-91. doi: 10.1111/acel.12300. Epub 2014 Dec 16.

16.

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.

17.
18.

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 1;15(7):1113-22. Epub 2006 Feb 15.

PMID:
16481358
19.

Molecular insights into the premature aging disease progeria.

Vidak S, Foisner R.

Histochem Cell Biol. 2016 Apr;145(4):401-17. doi: 10.1007/s00418-016-1411-1. Epub 2016 Feb 4. Review.

20.

Truncated prelamin A expression in HGPS-like patients: a transcriptional study.

Barthélémy F, Navarro C, Fayek R, Da Silva N, Roll P, Sigaudy S, Oshima J, Bonne G, Papadopoulou-Legbelou K, Evangeliou AE, Spilioti M, Lemerrer M, Wevers RA, Morava E, Robaglia-Schlupp A, Lévy N, Bartoli M, De Sandre-Giovannoli A.

Eur J Hum Genet. 2015 Aug;23(8):1051-61. doi: 10.1038/ejhg.2014.239. Epub 2015 Feb 4.

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