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Biochemical and Biophysical Research Communications|July 18, 2006
Protein expression is increased by a class III AU-rich element and tethered CUG-BP1Carine Barreau, Tanguy Watrin, H Beverley Osborne, et al.EMBO Reports|August 6, 2014
Sororin pre-mRNA splicing is required for proper sister chromatid cohesion in human cellsErwan Watrin, Maria Demidova, Tanguy Watrin, et al.The International Journal of Developmental Biology|May 5, 2009
The developing female genital tract: from genetics to epigeneticsJulie Massé, Tanguy Watrin, Audrey Laurent, et al.The International Journal of Developmental Biology|September 21, 2005
PBX1 intracellular localization is independent of MEIS1 in epithelial cells of the developing female genital tractAgnès Dintilhac, Réjane Bihan, Daniel Guerrier, et al.Gene Expression|April 2, 2013
Involvement of ITIH5, a candidate gene for congenital uterovaginal aplasia (Mayer-Rokitansky-Küster-Hauser syndrome), in female genital tract developmentKarine Morcel, Tanguy Watrin, Frédérique Jaffre, et al.Journal of Materials Science. Materials in Medicine|March 22, 2013
Spheroid model study comparing the biocompatibility of Biodentine and MTAMatthieu Pérard, Justine Le Clerc, Tanguy Watrin, et al.Traffic (Copenhagen, Denmark)|April 25, 2007
Stress-induced retrotranslocation of clusterin/ApoJ into the cytosolPhilippe Nizard, Susanne Tetley, Yves Le Dréan, et al.European Journal of Medical Genetics|November 4, 2006
Phenotypic variability of a 4q34-->qter inherited deletion: MRKH syndrome in the daughter, cardiac defect and Fallopian tube cancer in the motherClaude Bendavid, Laurent Pasquier, Tanguy Watrin, et al.Orphanet Journal of Rare Diseases|March 17, 2011
Utero-vaginal aplasia (Mayer-Rokitansky-Küster-Hauser syndrome) associated with deletions in known DiGeorge or DiGeorge-like lociKarine Morcel, Tanguy Watrin, Laurent Pasquier, et al.Pageof 1