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Prenatal Diagnosis|June 28, 2011
Preventing mucopolysaccharidosis type II (Hunter syndrome): PGD and establishing a Hunter (46, XX) stem cell lineGheona Altarescu, Paul Renbaum, Talia Eldar-Geva, et al.Scientific Reports|October 31, 2018
Noninvasive paternal exclusion testing for cystic fibrosis in the first five to eight weeks of gestationDavid A Zeevi, Fouad Zahdeh, Yehuda Kling, et al.The Journal of Clinical Investigation|June 7, 2014
Testicular differentiation factor SF-1 is required for human spleen developmentDavid Zangen, Yotam Kaufman, Ehud Banne, et al.Stem Cell Reports|November 25, 2014
FMR1 epigenetic silencing commonly occurs in undifferentiated fragile X-affected embryonic stem cellsMichal Avitzour, Hagar Mor-Shaked, Shira Yanovsky-Dagan, et al.The Journal of Clinical Investigation|October 2, 2015
Proof-of-principle rapid noninvasive prenatal diagnosis of autosomal recessive founder mutationsDavid A Zeevi, Gheona Altarescu, Ariella Weinberg-Shukron, et al.Journal of Cell Science|November 6, 2009
p53-dependent control of transactivation of the Pen2 promoter by presenilinsJulie Dunys, Jean Sevalle, Emilie Giaime, et al.Journal of Medical Genetics|April 16, 2015
Minichromosome maintenance complex component 8 (MCM8) gene mutations result in primary gonadal failureYardena Tenenbaum-Rakover, Ariella Weinberg-Shukron, Paul Renbaum, et al.Journal of Molecular Cell Biology|January 30, 2013
Parkin differently regulates presenilin-1 and presenilin-2 functions by direct control of their promoter transcriptionEric Duplan, Jean Sevalle, Julien Viotti, et al.American Journal of Human Genetics|October 4, 2011
XX ovarian dysgenesis is caused by a PSMC3IP/HOP2 mutation that abolishes coactivation of estrogen-driven transcriptionDavid Zangen, Yotam Kaufman, Sharon Zeligson, et al.Stem Cell Reports|July 21, 2015
Uncovering the Role of Hypermethylation by CTG Expansion in Myotonic Dystrophy Type 1 Using Mutant Human Embryonic Stem CellsShira Yanovsky-Dagan, Michal Avitzour, Gheona Altarescu, et al.Pageof 8