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Year | Number of Results |
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2011 | 1 |
2014 | 2 |
2015 | 2 |
2016 | 2 |
2024 | 0 |
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Page 1
Comparing ESC and iPSC-Based Models for Human Genetic Disorders.
J Clin Med. 2014 Oct 24;3(4):1146-62. doi: 10.3390/jcm3041146.
J Clin Med. 2014.
PMID: 26237596
Free PMC article.
Review.
Molecular Characterization of Down Syndrome Embryonic Stem Cells Reveals a Role for RUNX1 in Neural Differentiation.
Halevy T, Biancotti JC, Yanuka O, Golan-Lev T, Benvenisty N.
Halevy T, et al.
Stem Cell Reports. 2016 Oct 11;7(4):777-786. doi: 10.1016/j.stemcr.2016.08.003. Epub 2016 Sep 8.
Stem Cell Reports. 2016.
PMID: 27618722
Free PMC article.
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Chromosomal Instability and Molecular Defects in Induced Pluripotent Stem Cells from Nijmegen Breakage Syndrome Patients.
Halevy T, Akov S, Bohndorf M, Mlody B, Adjaye J, Benvenisty N, Goldberg M.
Halevy T, et al.
Cell Rep. 2016 Aug 30;16(9):2499-511. doi: 10.1016/j.celrep.2016.07.071. Epub 2016 Aug 18.
Cell Rep. 2016.
PMID: 27545893
Free article.
Item in Clipboard
Molecular mechanisms regulating the defects in fragile X syndrome neurons derived from human pluripotent stem cells.
Halevy T, Czech C, Benvenisty N.
Halevy T, et al.
Stem Cell Reports. 2015 Jan 13;4(1):37-46. doi: 10.1016/j.stemcr.2014.10.015. Epub 2014 Dec 4.
Stem Cell Reports. 2015.
PMID: 25483109
Free PMC article.
Item in Clipboard
Reversion of FMR1 Methylation and Silencing by Editing the Triplet Repeats in Fragile X iPSC-Derived Neurons.
Park CY, Halevy T, Lee DR, Sung JJ, Lee JS, Yanuka O, Benvenisty N, Kim DW.
Park CY, et al. Among authors: halevy t.
Cell Rep. 2015 Oct 13;13(2):234-41. doi: 10.1016/j.celrep.2015.08.084. Epub 2015 Oct 1.
Cell Rep. 2015.
PMID: 26440889
Free article.
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MDC1 is ubiquitylated on its tandem BRCT domain and directly binds RAP80 in a UBC13-dependent manner.
Strauss C, Halevy T, Macarov M, Argaman L, Goldberg M.
Strauss C, et al. Among authors: halevy t.
DNA Repair (Amst). 2011 Aug 15;10(8):806-14. doi: 10.1016/j.dnarep.2011.04.016. Epub 2011 May 31.
DNA Repair (Amst). 2011.
PMID: 21622030
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