Buendia B - Search Results

1

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. Lund E, et al. Among authors: buendia b. Genome Res. 2013 Oct;23(10):1580-9. doi: 10.1101/gr.159400.113. Epub 2013 Jul 16. Genome Res. 2013. PMID: 23861385 Free PMC article.

2

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. Håkelien AM, et al. Among authors: buendia b. Exp Cell Res. 2008 May 1;314(8):1869-80. doi: 10.1016/j.yexcr.2008.02.018. Epub 2008 Mar 7. Exp Cell Res. 2008. PMID: 18396274

3

Distinct features of lamin A-interacting chromatin domains mapped by ChIP-sequencing from sonicated or micrococcal nuclease-digested chromatin.

Lund EG, Duband-Goulet I, Oldenburg A, Buendia B, Collas P. Lund EG, et al. Among authors: buendia b. Nucleus. 2015;6(1):30-9. doi: 10.4161/19491034.2014.990855. Nucleus. 2015. PMID: 25602132 Free PMC article.

4

Chrom3D: three-dimensional genome modeling from Hi-C and nuclear lamin-genome contacts.

Paulsen J, Sekelja M, Oldenburg AR, Barateau A, Briand N, Delbarre E, Shah A, Sørensen AL, Vigouroux C, Buendia B, Collas P. Paulsen J, et al. Among authors: buendia b. Genome Biol. 2017 Jan 30;18(1):21. doi: 10.1186/s13059-016-1146-2. Genome Biol. 2017. PMID: 28137286 Free PMC article.

5

The p.R482W substitution in A-type lamins deregulates SREBP1 activity in Dunnigan-type familial partial lipodystrophy.

Vadrot N, Duband-Goulet I, Cabet E, Attanda W, Barateau A, Vicart P, Gerbal F, Briand N, Vigouroux C, Oldenburg AR, Lund EG, Collas P, Buendia B. Vadrot N, et al. Among authors: buendia b. Hum Mol Genet. 2015 Apr 1;24(7):2096-109. doi: 10.1093/hmg/ddu728. Epub 2014 Dec 18. Hum Mol Genet. 2015. PMID: 25524705

6

LBR, a chromatin and lamin binding protein from the inner nuclear membrane, is proteolyzed at late stages of apoptosis.

Duband-Goulet I, Courvalin JC, Buendia B. Duband-Goulet I, et al. Among authors: buendia b. J Cell Sci. 1998 May;111 ( Pt 10):1441-51. doi: 10.1242/jcs.111.10.1441. J Cell Sci. 1998. PMID: 9570761

7

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. Delbarre E, et al. Among authors: buendia b. Hum Mol Genet. 2006 Apr 1;15(7):1113-22. doi: 10.1093/hmg/ddl026. Epub 2006 Feb 15. Hum Mol Genet. 2006. PMID: 16481358 Free article.

8

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. Favreau C, et al. Among authors: buendia b. Exp Cell Res. 2008 Apr 1;314(6):1392-405. doi: 10.1016/j.yexcr.2008.01.018. Epub 2008 Feb 6. Exp Cell Res. 2008. PMID: 18294630

9

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. Bruston F, et al. Among authors: buendia b. FEBS Lett. 2010 Jul 16;584(14):2999-3004. doi: 10.1016/j.febslet.2010.05.032. Epub 2010 May 24. FEBS Lett. 2010. PMID: 20580717 Free PMC article.

10

Subcellular localization of SREBP1 depends on its interaction with the C-terminal region of wild-type and disease related A-type lamins.

Duband-Goulet I, Woerner S, Gasparini S, Attanda W, Kondé E, Tellier-Lebègue C, Craescu CT, Gombault A, Roussel P, Vadrot N, Vicart P, Ostlund C, Worman HJ, Zinn-Justin S, Buendia B. Duband-Goulet I, et al. Among authors: buendia b. Exp Cell Res. 2011 Dec 10;317(20):2800-13. doi: 10.1016/j.yexcr.2011.09.012. Epub 2011 Oct 4. Exp Cell Res. 2011. PMID: 21993218 Free PMC article.

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