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Results: 12

1.

Transcription outcome of promoters enriched in histone variant H3.3 defined by positioning of H3.3 and local chromatin marks.

Lund EG, Collas P, Delbarre E.

Biochem Biophys Res Commun. 2015 Mar 14. pii: S0006-291X(15)00472-6. doi: 10.1016/j.bbrc.2015.03.037. [Epub ahead of print]

PMID:
25783056
2.

The PML-associated protein DEK regulates the balance of H3.3 loading on chromatin and is important for telomere integrity.

Ivanauskiene K, Delbarre E, McGhie JD, Küntziger T, Wong LH, Collas P.

Genome Res. 2014 Oct;24(10):1584-94. doi: 10.1101/gr.173831.114. Epub 2014 Jul 21.

PMID:
25049225
3.

Deregulation of Fragile X-related protein 1 by the lipodystrophic lamin A p.R482W mutation elicits a myogenic gene expression program in preadipocytes.

Oldenburg AR, Delbarre E, Thiede B, Vigouroux C, Collas P.

Hum Mol Genet. 2014 Mar 1;23(5):1151-62. doi: 10.1093/hmg/ddt509. Epub 2013 Oct 9.

4.

Lamin A/C-promoter interactions specify chromatin state-dependent transcription outcomes.

Lund E, Oldenburg AR, Delbarre E, Freberg CT, Duband-Goulet I, Eskeland R, Buendia B, Collas P.

Genome Res. 2013 Oct;23(10):1580-9. doi: 10.1101/gr.159400.113. Epub 2013 Jul 16.

5.

DAXX-dependent supply of soluble (H3.3-H4) dimers to PML bodies pending deposition into chromatin.

Delbarre E, Ivanauskiene K, Küntziger T, Collas P.

Genome Res. 2013 Mar;23(3):440-51. doi: 10.1101/gr.142703.112. Epub 2012 Dec 5.

6.

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.

7.

Chromatin environment of histone variant H3.3 revealed by quantitative imaging and genome-scale chromatin and DNA immunoprecipitation.

Delbarre E, Jacobsen BM, Reiner AH, Sørensen AL, Küntziger T, Collas P.

Mol Biol Cell. 2010 Jun 1;21(11):1872-84. doi: 10.1091/mbc.E09-09-0839. Epub 2010 Apr 7. Erratum in: Mol Biol Cell. 2010 Nov;21(21):3759.

8.

Expression of the myodystrophic R453W mutation of lamin A in C2C12 myoblasts causes promoter-specific and global epigenetic defects.

Håkelien AM, Delbarre E, Gaustad KG, Buendia B, Collas P.

Exp Cell Res. 2008 May 1;314(8):1869-80. doi: 10.1016/j.yexcr.2008.02.018. Epub 2008 Mar 7.

PMID:
18396274
9.

Differentiation of C2C12 myoblasts expressing lamin A mutated at a site responsible for Emery-Dreifuss muscular dystrophy is improved by inhibition of the MEK-ERK pathway and stimulation of the PI3-kinase pathway.

Favreau C, Delbarre E, Courvalin JC, Buendia B.

Exp Cell Res. 2008 Apr 1;314(6):1392-405. doi: 10.1016/j.yexcr.2008.01.018. Epub 2008 Feb 6.

PMID:
18294630
10.

Actin polymerisation at the cytoplasmic face of eukaryotic nuclei.

Münter S, Enninga J, Vazquez-Martinez R, Delbarre E, David-Watine B, Nehrbass U, Shorte SL.

BMC Cell Biol. 2006 May 23;7:23.

11.

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.

12.

[Antihyaluronidasic action of aurintricarboxylic acid].

COSTE F, DELBARRE E.

C R Seances Soc Biol Fil. 1956 Sep 26;150(5):876-9. French. No abstract available.

PMID:
13374968
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