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Items: 13

1.

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.

2.

Induced pluripotent stem cells reveal functional differences between drugs currently investigated in patients with hutchinson-gilford progeria syndrome.

Blondel S, Jaskowiak AL, Egesipe AL, Le Corf A, Navarro C, Cordette V, Martinat C, Laabi Y, Djabali K, de Sandre-Giovannoli A, Levy N, Peschanski M, Nissan X.

Stem Cells Transl Med. 2014 Apr;3(4):510-9. doi: 10.5966/sctm.2013-0168. Epub 2014 Mar 5.

3.

Naïve adult stem cells isolation from primary human fibroblast cultures.

Wenzel V, Roedl D, Ring J, Djabali K.

J Vis Exp. 2013 May 3;(75):e50185. doi: 10.3791/50185.

4.

Naïve adult stem cells from patients with Hutchinson-Gilford progeria syndrome express low levels of progerin in vivo.

Wenzel V, Roedl D, Gabriel D, Gordon LB, Herlyn M, Schneider R, Ring J, Djabali K.

Biol Open. 2012 Jun 15;1(6):516-26. doi: 10.1242/bio.20121149. Epub 2012 Apr 16.

5.

Cardiovascular pathology in Hutchinson-Gilford progeria: correlation with the vascular pathology of aging.

Olive M, Harten I, Mitchell R, Beers JK, Djabali K, Cao K, Erdos MR, Blair C, Funke B, Smoot L, Gerhard-Herman M, Machan JT, Kutys R, Virmani R, Collins FS, Wight TN, Nabel EG, Gordon LB.

Arterioscler Thromb Vasc Biol. 2010 Nov;30(11):2301-9. doi: 10.1161/ATVBAHA.110.209460. Epub 2010 Aug 26.

6.

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, Worman HJ, Gordon LB, Djabali K.

PLoS One. 2010 Jun 15;5(6):e11132. doi: 10.1371/journal.pone.0011132.

7.

Epidermal expression of the truncated prelamin A causing Hutchinson-Gilford progeria syndrome: effects on keratinocytes, hair and skin.

Wang Y, Panteleyev AA, Owens DM, Djabali K, Stewart CL, Worman HJ.

Hum Mol Genet. 2008 Aug 1;17(15):2357-69. doi: 10.1093/hmg/ddn136. Epub 2008 Apr 28.

8.

Ligand-independent regulation of the hairless promoter by vitamin D receptor.

Engelhard A, Bauer RC, Casta A, Djabali K, Christiano AM.

Photochem Photobiol. 2008 Mar-Apr;84(2):515-21. doi: 10.1111/j.1751-1097.2008.00301.x. Epub 2008 Feb 7.

9.

The mutant form of lamin A that causes Hutchinson-Gilford progeria is a biomarker of cellular aging in human skin.

McClintock D, Ratner D, Lokuge M, Owens DM, Gordon LB, Collins FS, Djabali K.

PLoS One. 2007 Dec 5;2(12):e1269.

10.

A lamin A protein isoform overexpressed in Hutchinson-Gilford progeria syndrome interferes with mitosis in progeria and normal cells.

Cao K, Capell BC, Erdos MR, Djabali K, Collins FS.

Proc Natl Acad Sci U S A. 2007 Mar 20;104(12):4949-54. Epub 2007 Mar 14.

11.

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.

12.

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.

13.

Peripherin expression in hippocampal neurons induced by muscle soluble factor(s).

Djabali K, Zissopoulou A, de Hoop MJ, Georgatos SD, Dotti CG.

J Cell Biol. 1993 Dec;123(5):1197-206.

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