Dan Vershkov相关文献与解析，生知库 | 链接生命科学的每一步

Comprehensive analysis of DNA replication timing across 184 cell lines suggests a role for MCM10 in replication timing regulation

对 184 个细胞系的 DNA 复制时间进行全面分析，表明 MCM10 在复制时间调控中发挥作用

Madison Caballero, Tiffany Ge, Ana Rita Rebelo, Seungmae Seo, Sean Kim, Kayla Brooks, Michael Zuccaro, Radhakrishnan Kanagaraj, Dan Vershkov, Dongsung Kim, Agata Smogorzewska, Marcus Smolka, Nissim Benvenisty, Stephen C West, Dieter Egli, Emily M Mace, Amnon Koren

细胞生物学

其它细胞

发表日期：2022

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Identifying regulators of parental imprinting by CRISPR/Cas9 screening in haploid human embryonic stem cells

利用 CRISPR/Cas9 筛选单倍体人类胚胎干细胞鉴定亲代印记的调控因子

期刊:Nature Communications

影响因子:14.7

doi:10.1038/s41467-021-26949-7

Shiran Bar，Dan Vershkov，Gal Keshet，Elyad Lezmi，Naama Meller，Atilgan Yilmaz，Ofra Yanuka，Malka Nissim-Rafinia

Delayed DNA replication in haploid human embryonic stem cells

单倍体人类胚胎干细胞的 DNA 复制延迟

期刊:Genome Research

影响因子:6.2

doi:10.1101/gr.275953.121

Matthew M Edwards, Michael V Zuccaro, Ido Sagi, Qiliang Ding, Dan Vershkov, Nissim Benvenisty, Dieter Egli, Amnon Koren

FMR1 Reactivating Treatments in Fragile X iPSC-Derived Neural Progenitors In Vitro and In Vivo

体外和体内对脆性 X iPSC 衍生神经祖细胞进行 FMR1 再激活治疗

期刊:Cell Reports

影响因子:7.5

doi:10.1016/j.celrep.2019.02.026

Dan Vershkov, Nina Fainstein, Sapir Suissa, Tamar Golan-Lev, Tamir Ben-Hur, Nissim Benvenisty

Rescue of Fragile X Syndrome Neurons by DNA Methylation Editing of the FMR1 Gene

通过 FMR1 基因的 DNA 甲基化编辑挽救脆性 X 综合征神经元

期刊:Cell

影响因子:45.5

doi:10.1016/j.cell.2018.01.012

X Shawn Liu, Hao Wu, Marine Krzisch, Xuebing Wu, John Graef, Julien Muffat, Denes Hnisz, Charles H Li, Bingbing Yuan, Chuanyun Xu, Yun Li, Dan Vershkov, Angela Cacace, Richard A Young, Rudolf Jaenisch

Culture-induced recurrent epigenetic aberrations in human pluripotent stem cells

人类多能干细胞培养诱导的复发性表观遗传畸变

期刊:PLoS Genetics

影响因子:

doi:10.1371/journal.pgen.1006979

Uri Weissbein, Omer Plotnik, Dan Vershkov, Nissim Benvenisty

Genome-wide screening for genes involved in the epigenetic basis of fragile X syndrome

全基因组筛查与脆性 X 综合征表观遗传基础相关的基因

Comprehensive analysis of DNA replication timing across 184 cell lines suggests a role for MCM10 in replication timing regulation

对 184 个细胞系的 DNA 复制时间进行全面分析，表明 MCM10 在复制时间调控中发挥作用

Identifying regulators of parental imprinting by CRISPR/Cas9 screening in haploid human embryonic stem cells

利用 CRISPR/Cas9 筛选单倍体人类胚胎干细胞鉴定亲代印记的调控因子

Delayed DNA replication in haploid human embryonic stem cells

单倍体人类胚胎干细胞的 DNA 复制延迟

FMR1 Reactivating Treatments in Fragile X iPSC-Derived Neural Progenitors In Vitro and In Vivo

体外和体内对脆性 X iPSC 衍生神经祖细胞进行 FMR1 再激活治疗

Rescue of Fragile X Syndrome Neurons by DNA Methylation Editing of the FMR1 Gene

通过 FMR1 基因的 DNA 甲基化编辑挽救脆性 X 综合征神经元

Culture-induced recurrent epigenetic aberrations in human pluripotent stem cells

人类多能干细胞培养诱导的复发性表观遗传畸变