Zobrazeno 1 - 10
of 18
pro vyhledávání: '"Lætitia Gressin"'
Autor:
Lise M. Hardy, Yosra Bouyacoub, Antoine Daunay, Mourad Sahbatou, Laura G. Baudrin, Laetitia Gressin, Mathilde Touvier, Hélène Blanché, Jean-François Deleuze, Alexandre How-Kit
Publikováno v:
Scientific Reports, Vol 12, Iss 1, Pp 1-12 (2022)
Abstract Lymphoblastoid cell lines (LCLs) derive from blood infected in vitro by Epstein–Barr virus and were used in several genetic, transcriptomic and epigenomic studies. Although few changes were shown between LCL and blood genotypes (SNPs) vali
Externí odkaz:
https://doaj.org/article/e6cec636107e4e92b9fda246c4445060
Autor:
Lise M. Hardy, Yosra Bouyacoub, Antoine Daunay, Mourad Sahbatou, Laura G. Baudrin, Laetitia Gressin, Mathilde Touvier, Hélène Blanché, Jean-François Deleuze, Alexandre How-Kit
Publikováno v:
Scientific reports. 12(1)
Lymphoblastoid cell lines (LCLs) derive from blood infected in vitro by Epstein–Barr virus and were used in several genetic, transcriptomic and epigenomic studies. Although few changes were shown between LCL and blood genotypes (SNPs) validating th
Autor:
Isabelle Devaux, Gilles Hetet, Laetitia Gressin, Etienne Vilmer, Nathalie Couque, Laurence Cattolico, Simone Duprat, Hélène Cavé, Valérie Bardet, Bernard Grandchamp
Publikováno v:
Genes, Chromosomes and Cancer. 33:178-187
Acute lymphoblastic leukemia is the most common malignancy in childhood. High-resolution allelotyping performed in our laboratory showed new chromosomal sites of nonrandom deletions. We have focused our work on 8q12 deletions, which we have found in
Autor:
Maryvonne Busson-Le Coniat, Thomas Mercher, Florence Nguyen Khac, Nicole Dastugue, Roland Berger, Lætitia Gressin, Olivier Bernard, Thierry Leblanc, M. Mauchauffe, Richard Monni, Francine Mugneret
Publikováno v:
Proceedings of the National Academy of Sciences. 98:5776-5779
The recurrent t(1;22)(p13;q13) translocation is exclusively associated with infant acute megakaryoblastic leukemia. We have identified the two genes involved in this translocation. Both genes possess related sequences in the Drosophila genome. The ch
Autor:
Alain Kitzis, Jean-Claude Chomel, Isabelle Callebaut, Francis Karst, Thierry Bergès, Vincent Thoreau, Zuzana Guillier-Gencik, Laetitia Gressin, Alain Bernheim, Jean-Paul Mornon
Publikováno v:
Biochemical and Biophysical Research Communications. 257:577-583
We report the cloning of a cDNA encoding human syntaxin 8 (STX8), using the regulator (R) domain of the cystic fibrosis transmembrane conductance regulator (CFTR) as a bait to screen a human fetal lung cDNA library by the yeast two-hybrid system. Thi
Autor:
Sylviane Olschwang, Guy Zeitoun, Emmanuel Tiret, Emmanuel Tubacher, Laetitia Gressin, Gilles Thomas, Jean-François Fléjou, Guillaume Portier, Hélène Blanché, Najat Mourra
Publikováno v:
Diagnostic molecular pathology : the American journal of surgical pathology, part B. 17(2)
The prognosis of patients with colorectal cancer is largely determined by the tumor stage. In this respect, colorectal cancer with lymph node metastases has the worst prognosis. Accordingly, there is considerable clinical interest in understanding th
Autor:
Valérie, Bardet, Nathalie, Couque, Laurence, Cattolico, Gilles, Hetet, Isabelle, Devaux, Simone, Duprat, Laetitia, Gressin, Etienne, Vilmer, Hélène, Cavé, Bernard, Grandchamp
Publikováno v:
Genes, chromosomescancer. 33(2)
Acute lymphoblastic leukemia is the most common malignancy in childhood. High-resolution allelotyping performed in our laboratory showed new chromosomal sites of nonrandom deletions. We have focused our work on 8q12 deletions, which we have found in
Autor:
Laetitia Gressin, Patricia Legoix, M Cengiz Yakicier, Frédérique Capron, Emmanuel Tubacher, Claude Degott, Charles Balabaud, Christelle Vaury, Jessica Zucman-Rossi, Jan Bayer
Publikováno v:
Oncogene. 20(37)
Loss of heterozygosity (LOH) represents the most frequent genetic alteration observed in hepatocellular carcinoma (HCC). Chromosome 16q is of particular interest as it exhibits LOH in 29% of HCC tumors and is frequently lost in breast, prostate, ovar
Publikováno v:
Virology. 279(2)
The HERV-H family is one of the largest human endogenous retrovirus families, with approximately 1000 elements. Using a direct coupled in vitro transcription/translation approach (PTT for protein truncation test) and an extended series of primers on
Autor:
Laetitia Gressin, Marie-Josèphe Pébusque, Valérie Soenen-Cornu, Max Chaffanet, Claude Preudhomme, Daniel Birnbaum
Publikováno v:
Genes, Chromosomes & Cancer
Genes, Chromosomes & Cancer, 2000, 28 (2), pp.138-144. ⟨10.1002/(SICI)1098-2264(200006)28:23.0.CO;2-2⟩
Genes, Chromosomes & Cancer, 2000, 28 (2), pp.138-144. ⟨10.1002/(SICI)1098-2264(200006)28:23.0.CO;2-2⟩
We report on the fusion of the monocytic leukemia zinc finger protein (MOZ) gene to the adenoviral E1A-associated protein p300 (p300) gene in acute monocytic leukemia M5 associated with a t(8;22)(p11;q13) translocation. We studied two patients with d