B. Buendia

发表

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

Jonas Paulsen, M. Sekelja, A. Oldenburg, 2017, Genome Biology.

The core of the mammalian centriole contains γ-tubulin

R. Wepf, B. Gowen, B. Buendia, 1995, Current Biology.

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

Alice Barateau, C. Vigouroux, B. Buendia, 2017, PloS one.

Domain-specific disassembly and reassembly of nuclear membranes during mitosis.

B. Buendia, J. Courvalin, 1997, Experimental cell research.

Cytoskeletal control of centrioles movement during the establishment of polarity in Madin-Darby canine kidney cells

B. Buendia, E. Karsenti, G. Griffiths, 1990, The Journal of cell biology.

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

E. Delbarre, B. Buendia, H. Worman, 2010, FEBS letters.

Clinical significance of autoantibodies to the pericentromeric heterochromatin protein 1a protein.

B. Buendia, K. Lassoued, P. Coppo, 2013, European journal of internal medicine.

The core of the mammalian centriole contains gamma-tubulin.

R. Wepf, B. Gowen, B. Buendia, 1995, Current biology : CB.

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

B. Buendia, J. Courvalin, I. Duband-Goulet, 1998, Journal of cell science.

Dynamics of the nuclear envelope at mitosis and during apoptosis

B. Buendia, P. Collas, J. Courvalin, 2001, Cellular and Molecular Life Sciences CMLS.

Postembedding α-tubulin immunolabelling of isolated centrosomes

B. Gowen, B. Buendia, S. Fuller, 1995, The Histochemical Journal.

Tobacco BY-2 cell-free extracts induce the recovery of microtubule nucleating activity of inactivated mammalian centrosomes.

B. Buendia, E. Karsenti, A. Lambert, 1999, Biochimica et biophysica acta.

Reconstruction of the centrosome cycle from cryoelectron micrographs.

B. Buendia, S. Fuller, E. Karsenti, 1997, Journal of structural biology.

The transcription coactivator ASC-1 is a regulator of skeletal myogenesis, and its deficiency causes a novel form of congenital muscle disease.

B. Buendia, J. Rendu, O. Dubourg, 2016, Human molecular genetics.

Retinoic acid induction of nuclear envelope-limited chromatin sheets in HL-60.

D. E. Olins, P. Lichter, B. Buendia, 1998, Experimental cell research.

Regulation of the microtubule nucleating activity of centrosomes in Xenopus egg extracts: role of cyclin A-associated protein kinase

B. Buendia, E. Karsenti, G. Draetta, 1992, The Journal of cell biology.

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.

C. Vigouroux, B. Buendia, J. Capeau, 2003, Experimental cell research.

Regulation of protein kinases associated with cyclin A and cyclin B and their effect on microtubule dynamics and nucleation in Xenopus egg extracts.

M. Félix, B. Buendia, E. Karsenti, 1991, Cold Spring Harbor symposia on quantitative biology.

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

E. Delbarre, B. Buendia, P. Collas, 2013, Genome Research.

HP1γ associates with euchromatin and heterochromatin in mammalian nuclei and chromosomes

B. Buendia, J. Courvalin, E. Minc, 2000, Cytogenetic and Genome Research.

Immunolocalization of HP1 proteins in metaphasic mammalian chromosomes.

Y. Allory, B. Buendia, J. Courvalin, 2001, Methods in cell science : an official journal of the Society for In Vitro Biology.

Abnormal Cellular Phenotypes Induced by Three TMPO/LAP2 Variants Identified in Men with Cardiomyopathies

F. Chapon, B. Buendia, C. Rooryck, 2023, Cells.

Ribosomal protein phosphorylation in vivo and in vitro by vaccinia virus.

B. Buendia, J. Madjar, G. Beaud, 1987, European journal of biochemistry.

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

Y. Allory, B. Buendia, H. Worman, 1999, Chromosoma.

Caspase-dependent proteolysis of integral and peripheral proteins of nuclear membranes and nuclear pore complex proteins during apoptosis.

B. Buendia, J. Courvalin, A. Santa-Maria, 1999, Journal of cell science.

Regulation of Centrosome Function During Mitosis

B. Buendia, E. Karsenti, 1995 .

C. López-Otín, B. Buendia, J. Ávila, 1994, Journal of cell science.

Enzymatic cycling assay for D-carnitine determination.

M. Cánovas, B. Buendia, J. M. Obón, 1999, Analytical biochemistry.

A new clinical condition linked to a novel mutation in lamins A and C with generalized lipoatrophy, insulin-resistant diabetes, disseminated leukomelanodermic papules, liver steatosis, and cardiomyopathy.

A. Cohen, C. Vigouroux, B. Buendia, 2003, The Journal of clinical endocrinology and metabolism.

Impaired nuclear functions lead to increased senescence and inefficient differentiation in human myoblasts with a dominant p.R545C mutation in the LMNA gene.

M. Dabauvalle, B. Buendia, M. Wehnert, 2009, European journal of cell biology.

Nuclear envelope disorganization in fibroblasts from lipodystrophic patients with heterozygous R482Q/W mutations in the lamin A/C gene.

C. Vigouroux, B. Buendia, J. Capeau, 2001, Journal of cell science.

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

Alice Barateau, N. Briand, C. Vigouroux, 2015, Human molecular genetics.

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

B. Buendia, P. Collas, Eivind G. Lund, 2015, Nucleus.

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

B. Buendia, S. Zinn-Justin, E. Jacquet, 2018, Nucleic acids research.

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

Jonas Paulsen, M. Sekelja, Alice Barateau, 2017, Genome Biology.

Purification and Structural Analysis of LEM-Domain Proteins.

B. Buendia, S. Zinn-Justin, H. Worman, 2016, Methods in enzymology.

The truncated prelamin A in Hutchinson-Gilford progeria syndrome alters segregation of A-type and B-type lamin homopolymers.

E. Delbarre, B. Buendia, C. Gaillard, 2006, Human molecular genetics.

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

E. Delbarre, B. Buendia, P. Collas, 2008, Experimental cell research.

Distinct Fiber Type Signature in Mouse Muscles Expressing a Mutant Lamin A Responsible for Congenital Muscular Dystrophy in a Patient

Alice Barateau, B. Buendia, S. Batonnet-Pichon, 2017, Cells.

Expression of a Mutant Lamin A That Causes Emery-Dreifuss Muscular Dystrophy Inhibits In Vitro Differentiation of C2C12 Myoblasts

B. Buendia, J. Courvalin, C. Favreau, 2004, Molecular and Cellular Biology.

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

B. Buendia, P. Roussel, S. Zinn-Justin, 2011, Experimental cell research.

Postembedding α-tubulin immunolabelling of isolated centrosomes

B. Gowen, B. Buendia, S. Fuller, 2004, The Histochemical Journal.

A centrosomal antigen localized on intermediate filaments and mitotic spindle poles.

M. Bornens, B. Buendia, E. Karsenti, 1990, Journal of cell science.

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.

E. Delbarre, B. Buendia, J. Courvalin, 2008, Experimental cell research.

Membrane cell retention systems for continuous production of l-carnitine using Proteus sp.

M. Cánovas, B. Buendia, J. Iborra, 2003 .

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

Alice Barateau, B. Buendia, 2016, Methods in molecular biology.

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

B. Buendia, S. Zinn-Justin, H. Worman, 2015, ACS chemical biology.

E. Delbarre, B. Buendia, J. Courvalin, 2008, Experimental cell research.

The transcription coactivator ASC-1 is a regulator of skeletal myogenesis, and its deficiency causes a novel form of congenital muscle disease.

B. Buendia, J. Rendu, O. Dubourg, 2016, Human molecular genetics.