Zobrazeno 1 - 10
of 130
pro vyhledávání: '"Wenyi Feng"'
Autor:
Sravan Kodali, Silvia Meyer-Nava, Stephen Landry, Arijita Chakraborty, Juan Carlos Rivera-Mulia, Wenyi Feng
Publikováno v:
Frontiers in Genetics, Vol 13 (2022)
Common fragile sites (CFSs) are specific regions of all individuals’ genome that are predisposed to DNA double strand breaks (DSBs) and undergo subsequent rearrangements. CFS formation can be induced in vitro by mild level of DNA replication stress
Externí odkaz:
https://doaj.org/article/27dd44996eaf4511b53034ed211719df
Publikováno v:
Frontiers in Molecular Biosciences, Vol 9 (2022)
Externí odkaz:
https://doaj.org/article/eea90fd461b44bf181fcd97213309c11
Publikováno v:
PLoS ONE, Vol 17, Iss 2 (2022)
We performed a comparative analysis of replication origin activation by genome-wide single-stranded DNA mapping in two yeast strains challenged by hydroxyurea, an inhibitor of the ribonucleotide reductase. We gained understanding of the impact on ori
Externí odkaz:
https://doaj.org/article/5437efdc41d74f3ebbd7698a525ce61a
Autor:
Leonardo G. Dettori, Diego Torrejon, Arijita Chakraborty, Arijit Dutta, Mohamed Mohamed, Csaba Papp, Vladimir A. Kuznetsov, Patrick Sung, Wenyi Feng, Alaji Bah
Publikováno v:
Frontiers in Molecular Biosciences, Vol 8 (2021)
R-loops are non-canonical, three-stranded nucleic acid structures composed of a DNA:RNA hybrid, a displaced single-stranded (ss)DNA, and a trailing ssRNA overhang. R-loops perform critical biological functions under both normal and disease conditions
Externí odkaz:
https://doaj.org/article/3bb66076549b4dee8876f201be381aaa
Publikováno v:
STAR Protocols, Vol 2, Iss 2, Pp 100554- (2021)
Summary: We describe a genome-wide DNA double-strand break (DSB) mapping technique, Break-seq. In this protocol, we provide step-by-step instructions for cell embedment in agarose, in-gel DSB labeling and subsequent capture, followed by standard Illu
Externí odkaz:
https://doaj.org/article/12d0c7d64e33488eb0851ac7e4883c1e
Autor:
Arijita Chakraborty, Piroon Jenjaroenpun, Jing Li, Sami El Hilali, Andrew McCulley, Brian Haarer, Elizabeth A. Hoffman, Aimee Belak, Audrey Thorland, Heidi Hehnly, Carl L. Schildkraut, Chun-long Chen, Vladimir A. Kuznetsov, Wenyi Feng
Publikováno v:
Cell Reports, Vol 34, Iss 12, Pp 108838- (2021)
Externí odkaz:
https://doaj.org/article/705565a0d22c47bc86d0c4bb31d7898a
Autor:
Arijita Chakraborty, Piroon Jenjaroenpun, Jing Li, Sami El Hilali, Andrew McCulley, Brian Haarer, Elizabeth A. Hoffman, Aimee Belak, Audrey Thorland, Heidi Hehnly, Carl Schildkraut, Chun-long Chen, Vladimir A. Kuznetsov, Wenyi Feng
Publikováno v:
Cell Reports, Vol 32, Iss 12, Pp 108179- (2020)
Summary: Fragile X syndrome (FXS) is a neurodevelopmental disorder caused by mutations in the FMR1 gene and deficiency of a functional FMRP protein. FMRP is known as a translation repressor whose nuclear function is not understood. We investigated th
Externí odkaz:
https://doaj.org/article/17e03ba499cf463582b53bebc5c45501
Autor:
Wenyi Feng, Zhe Wang
Publikováno v:
Applied Intelligence. 53:12908-12924
Publikováno v:
IEEE Transactions on Transportation Electrification. 8:3960-3976
Publikováno v:
Current Genetics. 68:253-265
Dbf4 is the cyclin-like subunit for the Dbf4-dependent protein kinase (DDK), required for activating the replicative helicase at DNA replication origin that fire during S phase. Dbf4 also functions as an adaptor, targeting the DDK to different groups