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1دورية أكاديمية
المؤلفون: Michal Avitzour, Hagar Mor-Shaked, Shira Yanovsky-Dagan, Shira Aharoni, Gheona Altarescu, Paul Renbaum, Talia Eldar-Geva, Oshrat Schonberger, Ephrat Levy-Lahad, Silvina Epsztejn-Litman, Rachel Eiges
المصدر: Stem Cell Reports, Vol 3, Iss 5, Pp 699-706 (2014)
مصطلحات موضوعية: Medicine (General), R5-920, Biology (General), QH301-705.5
وصف الملف: electronic resource
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2دورية أكاديمية
المؤلفون: Silvina Epsztejn-Litman, Yaara Cohen-Hadad, Shira Aharoni, Gheona Altarescu, Paul Renbaum, Ephrat Levy-Lahad, Oshrat Schonberger, Talia Eldar-Geva, Sharon Zeligson, Rachel Eiges
المصدر: PLoS ONE, Vol 10, Iss 10, p e0138893 (2015)
وصف الملف: electronic resource
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3
المؤلفون: Shira Yanovsky-Dagan, Talia Eldar-Geva, Ephrat Levy-Lahad, Shira Aharoni, Rachel Eiges, Michal Avitzour, Silvina Epsztejn-Litman, Gheona Altarescu, Paul Renbaum, Hagar Mor-Shaked, Oshrat Schonberger
المصدر: Stem Cell Reports, Vol 3, Iss 5, Pp 699-706 (2014)
Stem Cell Reportsمصطلحات موضوعية: congenital, hereditary, and neonatal diseases and abnormalities, Blotting, Western, Gene Expression, Biology, Biochemistry, Methylation, X-inactivation, Cell Line, Epigenesis, Genetic, Histones, Fragile X Mental Retardation Protein, X Chromosome Inactivation, Report, Genetics, medicine, Gene silencing, Humans, Epigenetics, Gene Silencing, lcsh:QH301-705.5, Embryonic Stem Cells, lcsh:R5-920, Reverse Transcriptase Polymerase Chain Reaction, Lysine, SOXB1 Transcription Factors, Cell Biology, Sequence Analysis, DNA, DNA Methylation, medicine.disease, Embryonic stem cell, FMR1, Fragile X syndrome, lcsh:Biology (General), Fragile X Syndrome, DNA methylation, Trinucleotide repeat expansion, 5' Untranslated Regions, Trinucleotide Repeat Expansion, lcsh:Medicine (General), Octamer Transcription Factor-3, Developmental Biology
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4
المؤلفون: Shira Aharoni, Paul Renbaum, Ephrat Levy-Lahad, Silvina Epsztejn-Litman, Rachel Eiges, Yaara Cohen-Hadad, Gheona Altarescu, Sharon Zeligson, Oshrat Schonberger, Talia Eldar-Geva
المصدر: PLoS ONE
PLoS ONE, Vol 10, Iss 10, p e0138893 (2015)مصطلحات موضوعية: Mutant, Human Embryonic Stem Cells, Parthenogenesis, lcsh:Medicine, Biology, Spinal Muscular Atrophies of Childhood, Preimplantation genetic diagnosis, medicine.disease_cause, Polymorphism, Single Nucleotide, snRNP Core Proteins, 03 medical and health sciences, Genomic Imprinting, 0302 clinical medicine, medicine, Humans, lcsh:Science, 030304 developmental biology, Genetics, 0303 health sciences, Mutation, Multidisciplinary, SnRNP Core Proteins, lcsh:R, Homozygote, Proteins, Embryo, Embryonic stem cell, DNA methylation, embryonic structures, lcsh:Q, RNA, Long Noncoding, Genomic imprinting, 030217 neurology & neurosurgery, Research Article