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Methods in Molecular Biology (Clifton, N.J.)|November 13, 2009
Genetic manipulation of human embryonic stem cellsSilvina Epsztejn-Litman, Rachel Eiges
Methods in Molecular Biology (Clifton, N.J.)|March 23, 2019
Monitoring for Epigenetic Modifications at the FMR1 LocusSilvina Epsztejn-Litman, Rachel Eiges
Genetics|November 7, 2018
The G-rich Repeats in FMR1 and C9orf72 Loci Are Hotspots for Local Unpairing of DNAManar Abu Diab, Hagar Mor-Shaked, Eliora Cohen, et al.
European Journal of Human Genetics : EJHG|November 15, 2021
DMPK hypermethylation in sperm cells of myotonic dystrophy type 1 patientsShira Yanovsky-Dagan, Eliora Cohen, Pauline Megalli, et al.
Molecular Genetics & Genomic Medicine|July 14, 2018
Incomplete methylation of a germ cell tumor (Seminoma) in a Prader-Willi maleTalia Eldar-Geva, Varda Gross-Tsur, Harry J Hirsch, et al.
Nature Structural & Molecular Biology|October 28, 2008
De novo DNA methylation promoted by G9a prevents reprogramming of embryonically silenced genesSilvina Epsztejn-Litman, Nirit Feldman, Monther Abu-Remaileh, et al.
Plos One|October 17, 2015
Establishment of Homozygote Mutant Human Embryonic Stem Cells by ParthenogenesisSilvina Epsztejn-Litman, Yaara Cohen-Hadad, Shira Aharoni, et al.
Molecular Biology International|January 16, 2013
Prevention of lysosomal storage diseases and derivation of mutant stem cell lines by preimplantation genetic diagnosisGheona Altarescu, Rachel Beeri, Rachel Eiges, et al.
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.
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.
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