Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Manar Abu Diab"'
Autor:
Tayma Handal, Sarah Juster, Manar Abu Diab, Shira Yanovsky-Dagan, Fouad Zahdeh, Uria Aviel, Roni Sarel-Gallily, Shir Michael, Ester Bnaya, Shulamit Sebban, Yosef Buganim, Yotam Drier, Vincent Mouly, Stefan Kubicek, Walther J. A. A. van den Broek, Derick G. Wansink, Silvina Epsztejn-Litman, Rachel Eiges
Publikováno v:
Nature Communications, Vol 15, Iss 1, Pp 1-13 (2024)
Abstract Epigenetic defects caused by hereditary or de novo mutations are implicated in various human diseases. It remains uncertain whether correcting the underlying mutation can reverse these defects in patient cells. Here we show by the analysis o
Externí odkaz:
https://doaj.org/article/f2f26f7be8be43019350e3bc09541979
Autor:
Manar Abu Diab, Rachel Eiges
Publikováno v:
Brain Sciences, Vol 9, Iss 2, p 42 (2019)
Fragile X syndrome (FXS) is the most common heritable form of cognitive impairment. It results from a deficiency in the fragile X mental retardation protein (FMRP) due to a CGG repeat expansion in the 5′-UTR of the X-linked FMR1 gene. When CGGs exp
Externí odkaz:
https://doaj.org/article/8e9055735e9c4680911f08d59de6bc6c
Autor:
Hagar Mor-Shaked, Manar Abu Diab, Yaara Cohen-Hadad, Eliora Cohen, Silvina Epsztejn-Litman, Rachel Eiges, Oren Ram
Publikováno v:
Genetics. 210:1239-1252
Pathological mutations involving noncoding microsatellite repeats are typically located near promoters in CpG islands and are coupled with extensive repeat instability when sufficiently long. What causes these regions to be prone to repeat instabilit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::561de9111881ce9311e51679df6e38be
https://doi.org/10.1534/genetics.118.301672
https://doi.org/10.1534/genetics.118.301672
Autor:
Rachel Eiges, Manar Abu Diab
Publikováno v:
Brain Sciences, Vol 9, Iss 2, p 42 (2019)
Brain Sciences
Brain Sciences
Fragile X syndrome (FXS) is the most common heritable form of cognitive impairment. It results from a deficiency in the fragile X mental retardation protein (FMRP) due to a CGG repeat expansion in the 5′-UTR of the X-linked FMR1 gene. When CGGs exp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::000f27439fdfb586443e43fbf8eda0e7
https://www.mdpi.com/2076-3425/9/2/42
https://www.mdpi.com/2076-3425/9/2/42
Autor:
Manar, Abu Diab, Hagar, Mor-Shaked, Eliora, Cohen, Yaara, Cohen-Hadad, Oren, Ram, Silvina, Epsztejn-Litman, Rachel, Eiges
Publikováno v:
Genetics. 210(4)
Pathological mutations involving noncoding microsatellite repeats are typically located near promoters in CpG islands and are coupled with extensive repeat instability when sufficiently long. What causes these regions to be prone to repeat instabilit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::26aeba6dd0ea7bdfb2ab92fa2eb26c88
https://pubmed.ncbi.nlm.nih.gov/30396881
https://pubmed.ncbi.nlm.nih.gov/30396881