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Biology of the Cell|July 22, 2008
Conditional knockout of nucleolin in DT40 cells reveals the functional redundancy of its RNA-binding domainsSébastien Storck, Marc Thiry, Philippe BouvetSub-Cellular Biochemistry|May 9, 2007
Functions of the histone chaperone nucleolin in diseasesSébastien Storck, Manu Shukla, Stefan Dimitrov, et al.Current Opinion in Immunology|March 29, 2011
AID and partners: for better and (not) for worseSébastien Storck, Said Aoufouchi, Jean-Claude Weill, et al.Epigenetics & Chromatin|April 3, 2010
Histone variant macroH2A1 deletion in mice causes female-specific steatosisMathieu Boulard, Sébastien Storck, Rong Cong, et al.BMC Molecular Biology|August 19, 2007
Inactivation of nucleolin leads to nucleolar disruption, cell cycle arrest and defects in centrosome duplicationIva Ugrinova, Karine Monier, Corinne Ivaldi, et al.Nature Immunology|October 27, 2009
Multiple layers of B cell memory with different effector functionsIsmail Dogan, Barbara Bertocci, Valérie Vilmont, et al.Molecular and Cellular Biology|April 9, 2014
Somatic hypermutation at A/T-rich oligonucleotide substrates shows different strand polarities in Ung-deficient or -proficient backgroundsMarija Zivojnovic, Frédéric Delbos, Giulia Girelli Zubani, et al.Molecular and Cellular Biology|February 3, 2005
Normal immune system development in mice lacking the Deltex-1 RING finger domainSébastien Storck, Frédéric Delbos, Nicolas Stadler, et al.The Journal of Experimental Medicine|March 12, 2017
Pms2 and uracil-DNA glycosylases act jointly in the mismatch repair pathway to generate Ig gene mutations at A-T base pairsGiulia Girelli Zubani, Marija Zivojnovic, Annie De Smet, et al.DNA Repair|August 3, 2016
A single aspartate mutation in the conserved catalytic site of Rev3L generates a hypomorphic phenotype in vivo and in vitroRémi Fritzen, Frédéric Delbos, Annie De Smet, et al.Pageof 2