G. Velasco

发表

Corrigendum: Mutations in CDCA7 and HELLS cause immunodeficiency–centromeric instability–facial anomalies syndrome

Yuya Ito, Jun Wang, Mikita Suyama, 2016, Nature Communications.

Overexpression of vascular endothelial growth factor 189 in breast cancer cells leads to delayed tumor uptake with dilated intratumoral vessels.

I. Bièche, M. Perrot-Applanat, S. Mourah, 2008, The American journal of pathology.

Comparative methylome analysis of ICF patients identifies heterochromatin loci that require ZBTB24, CDCA7 and HELLS for their methylated state

Laure Ferry, C. Picard, J. Deleuze, 2018, Human molecular genetics.

Three novel ZBTB24 mutations identified in Japanese and Cape Verdean type 2 ICF syndrome patients

C. Picard, M. Unoki, H. Sasaki, 2013, Journal of Human Genetics.

Regulation of telomeric function by DNA methylation differs between humans and mice.

S. Selig, L. Godley, C. Francastel, 2020, Human molecular genetics.

CDCA7 and HELLS suppress DNA:RNA hybrid-associated DNA damage at pericentromeric repeats

H. Sasaki, H. Koseki, Yuichiro Saito, 2020, Scientific Reports.

Genetic, Cellular and Clinical Features of ICF Syndrome: a French National Survey

A. Fischer, C. Picard, N. Mahlaoui, 2016, Journal of Clinical Immunology.

Germline genes hypomethylation and expression define a molecular signature in peripheral blood of ICF patients: implications for diagnosis and etiology

C. Picard, A. Mégarbané, H. Sasaki, 2014, Orphanet Journal of Rare Diseases.

New Insights into BS69 Functions*

S. Ansieau, G. Velasco, S. Grkovic, 2006, Journal of Biological Chemistry.

Loss of the Methyl-CpG-Binding Protein ZBTB4 Alters Mitotic Checkpoint, Increases Aneuploidy, and Promotes Tumorigenesis.

P. Defossez, P. Dubus, Giacomo Grillo, 2017, Cancer research.

Maintenance of DNA methylation: Dnmt3b joins the dance

C. Francastel, G. Velasco, E. Walton, 2011, Epigenetics.

Steroid receptor RNA activator protein binds to and counteracts SRA RNA-mediated activation of MyoD and muscle differentiation

Florent Hubé, Guillaume Velasco, Jérôme Rollin, 2010, Nucleic Acids Res..

Dnmt3b recruitment through E2F6 transcriptional repressor mediates germ-line gene silencing in murine somatic tissues

Damien Neuillet, E. Viégas-Péquignot, F. Hubé, 2010, Proceedings of the National Academy of Sciences.

Interplay between Histone and DNA Methylation Seen through Comparative Methylomes in Rare Mendelian Disorders

V. Cormier-Daire, C. Francastel, G. Velasco, 2021, International journal of molecular sciences.

CDCA7 and HELLS mutations undermine nonhomologous end joining in centromeric instability syndrome

H. Sasaki, C. Francastel, H. Funabiki, 2018, The Journal of clinical investigation.

Dnmt3b Prefers Germ Line Genes and Centromeric Regions: Lessons from the ICF Syndrome and Cancer and Implications for Diseases

C. Francastel, G. Velasco, E. Walton, 2014, Biology.

Genetics meets DNA methylation in rare diseases

C. Francastel, G. Velasco, Guillaume Velasco, 2019, Clinical genetics.

Subtelomeric methylation distinguishes between subtypes of Immunodeficiency, Centromeric instability and Facial anomalies syndrome

S. Selig, A. Kaindl, C. Francastel, 2018, Human molecular genetics.

Evaluation of DNA Methylation Episignatures for Diagnosis and Phenotype Correlations in 42 Mendelian Neurodevelopmental Disorders.

M. Shaw, N. de Leeuw, J. Gécz, 2020, American journal of human genetics.

MDA-MB-231 breast cancer cells overexpressing single VEGF isoforms display distinct colonisation characteristics

S. Vacher, I. Bièche, M. Pocard, 2015, British Journal of Cancer.

Genetic, Cellular and Clinical Features of ICF Syndrome: a French National Survey

A. Fischer, C. Picard, N. Mahlaoui, 2016, Journal of Clinical Immunology.

Evaluation of DNA Methylation Episignatures for Diagnosis and Phenotype Correlations in 42 Mendelian Neurodevelopmental Disorders.

M. Shaw, N. de Leeuw, J. Gécz, 2021, American journal of human genetics.

Mutations in CDCA7 and HELLS cause immunodeficiency–centromeric instability–facial anomalies syndrome

M. Suyama, C. Picard, A. Gennery, 2015, Nature Communications.

Telomeres in ICF syndrome cells are vulnerable to DNA damage due to elevated DNA:RNA hybrids

F. Chédin, S. Selig, C. Francastel, 2017, Nature Communications.

Non-coding murine centromeric transcripts associate with and potentiate Aurora B kinase

F. Hubé, C. Francastel, G. Velasco, 2009, Nucleic acids research.

Rosette Lidereau, S. Vacher, I. Bièche, 2011, PloS one.

CENP-A chromatin disassembly in stressed and senescent murine cells

Giacomo Grillo, C. Francastel, I. Ivkovic, 2017, Scientific Reports.

Xenoestrogens modulate vascular endothelial growth factor secretion in breast cancer cells through an estrogen receptor-dependent mechanism.

M. Perrot-Applanat, P. Balaguer, Patrick Balaguer, 2008, The Journal of endocrinology.