Zobrazeno 1 - 10
of 25
pro vyhledávání: '"Madison B Adolph"'
Autor:
Gabriel J. Starrett, Elizabeth M. Luengas, Jennifer L. McCann, Diako Ebrahimi, Nuri A. Temiz, Robin P. Love, Yuqing Feng, Madison B. Adolph, Linda Chelico, Emily K. Law, Michael A. Carpenter, Reuben S Harris
Publikováno v:
Nature Communications, Vol 7, Iss 1, Pp 1-13 (2016)
The APOBEC family of enzymes are cytidine deaminases with APOBEC3A and APOBEC3B thought to contribute to DNA damage signatures detected in cancer genomes. Here, the authors demonstrate an unappreciated role for APOBEC3H haplotype I in the generation
Externí odkaz:
https://doaj.org/article/341af74da85247c89f420036391ce4bf
Publikováno v:
PLoS Pathogens, Vol 12, Iss 10, p e1005865 (2016)
Humans express seven human APOBEC3 proteins, which can inhibit viruses and endogenous retroelements through cytidine deaminase activity. The seven paralogs differ in the potency of their antiviral effects, as well as in their antiviral targets. One A
Externí odkaz:
https://doaj.org/article/8c1ebe9e16a6497285fc401a3c48e6d0
Autor:
Madison B. Adolph, Robin P. Love, Nazanin Mohammadzadeh, Linda Chelico, Louis M. Mansky, Yumeng Z McDaniel, Dake Wang
Publikováno v:
Nucleic Acids Research
The human apolipoprotein B mRNA editing enzyme, catalytic polypeptide-like 3 (APOBEC3, A3) family member proteins can deaminate cytosines in single-strand (ss) DNA, which restricts human immunodeficiency virus type 1 (HIV-1), retrotransposons, and ot
Autor:
Florian Morati, Madison B. Adolph, Chaoyou Xue, Eric C. Greene, Swati Balakrishnan, Walter J. Chazin, Taha M. Mohamed, David Cortez, Mauro Modesti
Publikováno v:
Molecular Cell
Molecular Cell, Elsevier, 2021, 81 (5), pp.1074-1083.e5. ⟨10.1016/j.molcel.2020.12.036⟩
Mol Cell
Molecular Cell, 2021, 81 (5), pp.1074-1083.e5. ⟨10.1016/j.molcel.2020.12.036⟩
Molecular Cell, Elsevier, 2021, 81 (5), pp.1074-1083.e5. ⟨10.1016/j.molcel.2020.12.036⟩
Mol Cell
Molecular Cell, 2021, 81 (5), pp.1074-1083.e5. ⟨10.1016/j.molcel.2020.12.036⟩
The RAD51 recombinase forms nucleoprotein filaments to promote double-strand break repair, replication fork reversal, and fork stabilization. The stability of these filaments is highly regulated since both too little and too much RAD51 activity can c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a5c5b95b3ec381eed0bcd2c15d461636
https://hal-amu.archives-ouvertes.fr/hal-03438611
https://hal-amu.archives-ouvertes.fr/hal-03438611
Publikováno v:
PLoS ONE, Vol 8, Iss 5, p e64196 (2013)
It is well established that the cytosine deaminase APOBEC3G can restrict HIV-1 virions in the absence of the virion infectivity factor (Vif) by inducing genome mutagenesis through deamination of cytosine to uracil in single-stranded HIV-1 (-)DNA. How
Externí odkaz:
https://doaj.org/article/de0677f8b0f3425085cb01f5f2feef30
Autor:
Linda Chelico, Seongho Kim, Kayla L. Conner, Ashley M. Floyd, Michele L. Cote, Wen Lei, Jacob Lindquist, Steve M. Patrick, Akshada Sawant, Ashok S. Bhagwat, Asra N. Shaik, Madison B. Adolph, Sachini U. Siriwardena, Katie A Marshall, Elmira Ekinci
Publikováno v:
Nar Cancer
Identifying the mechanisms mediating cisplatin response is essential for improving patient response. Previous research has identified base excision repair (BER) and mismatch repair (MMR) activity in sensitizing cells to cisplatin. Cisplatin forms DNA
Publikováno v:
Journal of Biological Chemistry. 298:101672
Genome integrity requires complete and accurate DNA replication once per cell division cycle. Replication stress poses obstacles to this process that must be overcome to prevent replication fork collapse. An important regulator of replication fork st
Autor:
Madison B. Adolph, David Cortez, Alessandro Vindigni, Jessica Jackson, Taha M. Mohamed, Archana Krishnamoorthy
Publikováno v:
Mol Cell
RAD51 facilitates replication fork reversal and protects reversed forks from nuclease degradation. Although potentially a useful replication stress response mechanism, unregulated fork reversal can cause genome instability. Here we show that RADX, a
Publikováno v:
Journal of molecular biology. 431(7)
The APOBEC3 family of deoxycytidine deaminases has the ability to restrict HIV-1 through deamination-dependent and deamination-independent mechanisms. Although the generation of mutations through deamination of cytosine to uracil in single-stranded H
Publikováno v:
ACS infectious diseases. 4(3)
The Apolipoprotein B mRNA editing complex (APOBEC) family of enzymes contains single-stranded polynucleotide cytidine deaminases. These enzymes catalyze the deamination of cytidine in RNA or single-stranded DNA, which forms uracil. From this 11 membe