Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Ester Bnaya"'
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:
Ester Bnaya, Shay Shilo, Tzah Feldman, Tal Bacharach, Yoni Moskovitz, Aditee Kadam, Paz Yedidim, Hadas Azogy, Nathali Kaushansky, Noa Chapal-Ilani, Liran I. Shlush
DNA double strand breaks (DSBs) are a major source of mutations. Both non-homologous-end-joining (NHEJ) and microhomology-mediated-end-joining (MMEJ) DSB repair pathways are error prone and produce deletions, which can lead to cancer. DSBs also lead
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3ed620f641d75a1d6821a060f9dd8db6
https://doi.org/10.1101/2022.07.21.500965
https://doi.org/10.1101/2022.07.21.500965
