Buendia B - Search Results

1

Muscular Dystrophy Mutations Impair the Nuclear Envelope Emerin Self-assembly Properties.

Herrada I, Samson C, Velours C, Renault L, Östlund C, Chervy P, Puchkov D, Worman HJ, Buendia B, Zinn-Justin S. Herrada I, et al. Among authors: buendia b. ACS Chem Biol. 2015 Dec 18;10(12):2733-42. doi: 10.1021/acschembio.5b00648. Epub 2015 Oct 5. ACS Chem Biol. 2015. PMID: 26415001 Free PMC article.

2

Expression of lamin A mutated in the carboxyl-terminal tail generates an aberrant nuclear phenotype similar to that observed in cells from patients with Dunnigan-type partial lipodystrophy and Emery-Dreifuss muscular dystrophy.

Favreau C, Dubosclard E, Ostlund C, Vigouroux C, Capeau J, Wehnert M, Higuet D, Worman HJ, Courvalin JC, Buendia B. Favreau C, et al. Among authors: buendia b. Exp Cell Res. 2003 Jan 1;282(1):14-23. doi: 10.1006/excr.2002.5669. Exp Cell Res. 2003. PMID: 12490190

3

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.

4

Purification and Structural Analysis of LEM-Domain Proteins.

Herrada I, Bourgeois B, Samson C, Buendia B, Worman HJ, Zinn-Justin S. Herrada I, et al. Among authors: buendia b. Methods Enzymol. 2016;569:43-61. doi: 10.1016/bs.mie.2015.07.008. Epub 2015 Aug 8. Methods Enzymol. 2016. PMID: 26778552

5

Structural analysis of the ternary complex between lamin A/C, BAF and emerin identifies an interface disrupted in autosomal recessive progeroid diseases.

Samson C, Petitalot A, Celli F, Herrada I, Ropars V, Le Du MH, Nhiri N, Jacquet E, Arteni AA, Buendia B, Zinn-Justin S. Samson C, et al. Among authors: buendia b. Nucleic Acids Res. 2018 Nov 2;46(19):10460-10473. doi: 10.1093/nar/gky736. Nucleic Acids Res. 2018. PMID: 30137533 Free PMC article.

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. 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.

7

Localization and phosphorylation of HP1 proteins during the cell cycle in mammalian cells.

Minc E, Allory Y, Worman HJ, Courvalin JC, Buendia B. Minc E, et al. Among authors: buendia b. Chromosoma. 1999 Aug;108(4):220-34. doi: 10.1007/s004120050372. Chromosoma. 1999. PMID: 10460410

8

In Situ Detection of Interactions Between Nuclear Envelope Proteins and Partners.

Barateau A, Buendia B. Barateau A, et al. Among authors: buendia b. Methods Mol Biol. 2016;1411:147-58. doi: 10.1007/978-1-4939-3530-7_9. Methods Mol Biol. 2016. PMID: 27147040

9

Expression of a mutant lamin A that causes Emery-Dreifuss muscular dystrophy inhibits in vitro differentiation of C2C12 myoblasts.

Favreau C, Higuet D, Courvalin JC, Buendia B. Favreau C, et al. Among authors: buendia b. Mol Cell Biol. 2004 Feb;24(4):1481-92. doi: 10.1128/MCB.24.4.1481-1492.2004. Mol Cell Biol. 2004. PMID: 14749366 Free PMC article.

10

A Novel Lamin A Mutant Responsible for Congenital Muscular Dystrophy Causes Distinct Abnormalities of the Cell Nucleus.

Barateau A, Vadrot N, Vicart P, Ferreiro A, Mayer M, Héron D, Vigouroux C, Buendia B. Barateau A, et al. Among authors: buendia b. PLoS One. 2017 Jan 26;12(1):e0169189. doi: 10.1371/journal.pone.0169189. eCollection 2017. PLoS One. 2017. PMID: 28125586 Free PMC article.

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