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The International Journal of Biochemistry & Cell Biology|September 13, 2008
Lessons from two human chromatin diseases, ICF syndrome and Rett syndromeM R Matarazzo, M L De Bonis, M Vacca, et al.Human Molecular Genetics|February 28, 2006
Maintenance of X- and Y-inactivation of the pseudoautosomal (PAR2) gene SPRY3 is independent from DNA methylation and associated to multiple layers of epigenetic modificationsM L De Bonis, A Cerase, M R Matarazzo, et al.Journal of Cellular Physiology|November 30, 2006
Multiple binding of methyl-CpG and polycomb proteins in long-term gene silencing eventsM R Matarazzo, M L De Bonis, M Strazzullo, et al.Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|October 19, 2010
BDNF Val66Met polymorphism and brain volumes in multiple sclerosisD Dinacci, A Tessitore, A Russo, et al.Brain & Development|December 12, 2001
MECP2 gene mutation analysis in the British and Italian Rett Syndrome patients: hot spot map of the most recurrent mutations and bioinformatic analysis of a new MECP2 conserved regionM Vacca, F Filippini, A Budillon, et al.Pageof 1