Works by Eiges, Rachel

Results: 15

Insight and Recommendations for Fragile X-Premutation-Associated Conditions from the Fifth International Conference on FMR1 Premutation.

Published in:

Cells (2073-4409), 2023, v. 12, n. 18, p. 2330, doi. 10.3390/cells12182330

By:

Tassone, Flora;
Protic, Dragana;
Allen, Emily Graves;
Archibald, Alison D.;
Baud, Anna;
Brown, Ted W.;
Budimirovic, Dejan B.;
Cohen, Jonathan;
Dufour, Brett;
Eiges, Rachel;
Elvassore, Nicola;
Gabis, Lidia V.;
Grudzien, Samantha J.;
Hall, Deborah A.;
Hessl, David;
Hogan, Abigail;
Hunter, Jessica Ezzell;
Jin, Peng;
Jiraanont, Poonnada;
Klusek, Jessica

Publication type:

Article

Modeling Fragile X Syndrome Using Human Pluripotent Stem Cells.

Published in:

Genes, 2016, v. 7, n. 10, p. 77, doi. 10.3390/genes7100077

By:

Mor-Shaked, Hagar;
Eiges, Rachel

Publication type:

Article

Prevention of Lysosomal Storage Diseases and Derivation of Mutant Stem Cell Lines by Preimplantation Genetic Diagnosis.

Published in:

Molecular Biology International, 2012, p. 1, doi. 10.1155/2012/797342

By:

Altarescu, Gheona;
Beeri, Rachel;
Eiges, Rachel;
Epsztejn-Litman, Silvina;
Eldar-Geva, Talia;
Elstein, Deborah;
Zimran, Ari;
Margalioth, Ehud J.;
Levy-Lahad, Ephrat;
Renbaum, Paul

Publication type:

Article

The noncoding RNA IPW regulates the imprinted DLK1-DIO3 locus in an induced pluripotent stem cell model of Prader-Willi syndrome.

Published in:

Nature Genetics, 2014, v. 46, n. 6, p. 551, doi. 10.1038/ng.2968

By:

Stelzer, Yonatan;
Sagi, Ido;
Yanuka, Ofra;
Eiges, Rachel;
Benvenisty, Nissim

Publication type:

Article

Correction of Heritable Epigenetic Defects Using Editing Tools.

Published in:

International Journal of Molecular Sciences, 2021, v. 22, n. 8, p. 3966, doi. 10.3390/ijms22083966

By:

Handal, Tayma;
Eiges, Rachel

Publication type:

Article

Pluripotency-independent induction of human trophoblast stem cells from fibroblasts.

Published in:

Nature Communications, 2023, v. 14, n. 1, p. 1, doi. 10.1038/s41467-023-39104-1

By:

Naama, Moriyah;
Rahamim, Moran;
Zayat, Valery;
Sebban, Shulamit;
Radwan, Ahmed;
Orzech, Dana;
Lasry, Rachel;
Ifrah, Annael;
Jaber, Mohammad;
Sabag, Ofra;
Yassen, Hazar;
Khatib, Areej;
Epsztejn-Litman, Silvina;
Novoselsky-Persky, Michal;
Makedonski, Kirill;
Deri, Noy;
Goldman-Wohl, Debra;
Cedar, Howard;
Yagel, Simcha;
Eiges, Rachel

Publication type:

Article

Differentiation shifts from a reversible to an irreversible heterochromatin state at the DM1 locus.

Published in:

Nature Communications, 2024, v. 15, n. 1, p. 1, doi. 10.1038/s41467-024-47217-4

By:

Handal, Tayma;
Juster, Sarah;
Diab, Manar Abu;
Yanovsky-Dagan, Shira;
Zahdeh, Fouad;
Aviel, Uria;
Sarel-Gallily, Roni;
Michael, Shir;
Bnaya, Ester;
Sebban, Shulamit;
Buganim, Yosef;
Drier, Yotam;
Mouly, Vincent;
Kubicek, Stefan;
van den Broek, Walther J. A. A.;
Wansink, Derick G.;
Epsztejn-Litman, Silvina;
Eiges, Rachel

Publication type:

Article

Reevaluation of FMR1 Hypermethylation Timing in Fragile X Syndrome.

Published in:

Frontiers in Molecular Neuroscience, 2018, p. 1, doi. 10.3389/fnmol.2018.00031

By:

Mor-Shaked, Hagar;
Eiges, Rachel

Publication type:

Article

Preventing mucopolysaccharidosis type II (Hunter syndrome): PGD and establishing a Hunter (46, XX) stem cell line.

Published in:

Prenatal Diagnosis, 2011, v. 31, n. 9, p. 853, doi. 10.1002/pd.2786

By:

Altarescu, Gheona;
Renbaum, Paul;
Eldar-Geva, Talia;
Brooks, Baruch;
Varshaver, Irit;
Avitzour, Mical;
Margalioth, Ehud J.;
Levy-Lahad, Ephrat;
Elstein, Deborah;
Epsztejn-Litman, Silvina;
Eiges, Rachel

Publication type:

Article

The Contribution of Pluripotent Stem Cell (PSC)-Based Models to the Study of Fragile X Syndrome (FXS).

Published in:

Brain Sciences (2076-3425), 2019, v. 9, n. 2, p. 42, doi. 10.3390/brainsci9020042

By:

Abu Diab, Manar;
Eiges, Rachel

Publication type:

Article

Establishment of Homozygote Mutant Human Embryonic Stem Cells by Parthenogenesis.

Published in:

PLoS ONE, 2015, v. 10, n. 10, p. 1, doi. 10.1371/journal.pone.0138893

By:

Epsztejn-Litman, Silvina;
Cohen-Hadad, Yaara;
Aharoni, Shira;
Altarescu, Gheona;
Renbaum, Paul;
Levy-Lahad, Ephrat;
Schonberger, Oshrat;
Eldar-Geva, Talia;
Zeligson, Sharon;
Eiges, Rachel

Publication type:

Article

GNE Is Involved in the Early Development of Skeletal and Cardiac Muscle.

Published in:

PLoS ONE, 2011, v. 6, n. 6, p. 1, doi. 10.1371/journal.pone.0021389

By:

Krentsis, Irit Milman;
Sela, Ilan;
Eiges, Rachel;
Blanchard, Véronique;
Berger, Markus;
Cohen, Michal Becker;
Mitrani-Rosenbaum, Stella

Publication type:

Article

The G-rich Repeats in FMR1 and C9orf72 Loci Are Hotspots for Local Unpairing of DNA.

Published in:

Genetics, 2018, v. 210, n. 4, p. 1239, doi. 10.1534/genetics.118.301672

By:

Diab, Manar Abu;
Epsztejn-Litman, Silvina;
Mor-Shaked, Hagar;
Cohen, Eliora;
Cohen-Hadad, Yaara;
Eiges, Rachel;
Ram, Oren

Publication type:

Article

A molecular view on pluripotent stem cells

Published in:

FEBS Letters, 2002, v. 529, n. 1, p. 135, doi. 10.1016/S0014-5793(02)03191-5

By:

Eiges, Rachel;
Benvenisty, Nissim

Publication type:

Article

Incomplete methylation of a germ cell tumor (Seminoma) in a Prader‐Willi male.

Published in:

Molecular Genetics & Genomic Medicine, 2018, v. 6, n. 5, p. 811, doi. 10.1002/mgg3.448

By:

Eldar‐Geva, Talia;
Gross‐Tsur, Varda;
Hirsch, Harry J.;
Altarescu, Gheona;
Segal, Reeval;
Zeligson, Sharon;
Golomb, Eliahu;
Epsztejn‐Litman, Silvina;
Eiges, Rachel

Publication type:

Article