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Rachel Eiges

Showing results (21-30 of 30) with videos related to

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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.
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|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.
Stem Cell Reports|October 25, 2016
Marked Differences in C9orf72 Methylation Status and Isoform Expression between C9/ALS Human Embryonic and Induced Pluripotent Stem CellsYaara Cohen-Hadad, Gheona Altarescu, Talia Eldar-Geva, et al.
Stem Cells and Development|May 19, 2011
Female sex bias in human embryonic stem cell linesDalit Ben-Yosef, Ami Amit, Mira Malcov, et al.
Science Advances|May 29, 2024
DNMT3B splicing dysregulation mediated by SMCHD1 loss contributes to DUX4 overexpression and FSHD pathogenesisEden Engal, Aveksha Sharma, Uria Aviel, et al.
Neurobiology of Aging|July 17, 2021
A recessive S174X mutation in Optineurin causes amyotrophic lateral sclerosis through a loss of function via allele-specific nonsense-mediated decayMarc Gotkine, Martina de Majo, Chun Hao Wong, et al.
Nature Communications|June 8, 2023
Pluripotency-independent induction of human trophoblast stem cells from fibroblastsMoriyah Naama, Moran Rahamim, Valery Zayat, et al.
Nature Communications|April 16, 2024
Differentiation shifts from a reversible to an irreversible heterochromatin state at the DM1 locusTayma Handal, Sarah Juster, Manar Abu Diab, et al.
Cells|September 28, 2023
Insight and Recommendations for Fragile X-Premutation-Associated Conditions from the Fifth International Conference on <i>FMR1</i> PremutationFlora Tassone, Dragana Protic, Emily Graves Allen, et al.
Pageof 3

Showing results (21-30 of 30) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 30 results.
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.
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|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.
Stem Cell Reports|October 25, 2016
Marked Differences in C9orf72 Methylation Status and Isoform Expression between C9/ALS Human Embryonic and Induced Pluripotent Stem CellsYaara Cohen-Hadad, Gheona Altarescu, Talia Eldar-Geva, et al.
Stem Cells and Development|May 19, 2011
Female sex bias in human embryonic stem cell linesDalit Ben-Yosef, Ami Amit, Mira Malcov, et al.
Science Advances|May 29, 2024
DNMT3B splicing dysregulation mediated by SMCHD1 loss contributes to DUX4 overexpression and FSHD pathogenesisEden Engal, Aveksha Sharma, Uria Aviel, et al.
Neurobiology of Aging|July 17, 2021
A recessive S174X mutation in Optineurin causes amyotrophic lateral sclerosis through a loss of function via allele-specific nonsense-mediated decayMarc Gotkine, Martina de Majo, Chun Hao Wong, et al.
Nature Communications|June 8, 2023
Pluripotency-independent induction of human trophoblast stem cells from fibroblastsMoriyah Naama, Moran Rahamim, Valery Zayat, et al.
Nature Communications|April 16, 2024
Differentiation shifts from a reversible to an irreversible heterochromatin state at the DM1 locusTayma Handal, Sarah Juster, Manar Abu Diab, et al.
Cells|September 28, 2023
Insight and Recommendations for Fragile X-Premutation-Associated Conditions from the Fifth International Conference on <i>FMR1</i> PremutationFlora Tassone, Dragana Protic, Emily Graves Allen, et al.
Pageof 3