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Aberrant base excision repair pathway of oxidatively damaged DNA: Implications for degenerative diseases.

artículo científico publicado en 2016

Aberrant repair initiated by mismatch-specific thymine-DNA glycosylases provides a mechanism for the mutational bias observed in CpG islands.

artículo científico publicado en 2014

Aberrant repair initiated by the adenine-DNA glycosylase does not play a role in UV-induced mutagenesis in

artículo científico publicado en 2018

Apoptotic and genotoxic effects of low-intensity ultrasound on healthy and leukemic human peripheral mononuclear blood cells.

artículo científico publicado en 2017

Biological effects of non-ionizing electromagnetic fields: Two sides of a coin

scientific article published on 17 July 2018

CTHRC1: A New Candidate Biomarker for Improved Rheumatoid Arthritis Diagnosis.

artículo científico publicado en 2019

Characterization of DNA ADP-ribosyltransferase activities of PARP2 and PARP3: new insights into DNA ADP-ribosylation.

artículo científico publicado en 2018

Ile351, Leu355 and Ile461 residues are essential for catalytic activity of bovine cytochrome P450scc (CYP11A1)

scientific article published on 11 January 2019

Oxidatively Generated Guanine(C8)-Thymine(N3) Intrastrand Cross-links in Double-stranded DNA Are Repaired by Base Excision Repair Pathways

artículo científico publicado en 2015

Poly(ADP-ribose) polymerases covalently modify strand break termini in DNA fragments in vitro.

scientific article published on 28 July 2016

Structural comparison of AP endonucleases from the exonuclease III family reveals new amino acid residues in human AP endonuclease 1 that are involved in incision of damaged DNA

artículo científico publicado en 2016

The Human DNA glycosylases NEIL1 and NEIL3 Excise Psoralen-Induced DNA-DNA Cross-Links in a Four-Stranded DNA Structure.

artículo científico publicado en 2017

The role of the N-terminal domain of human apurinic/apyrimidinic endonuclease 1, APE1, in DNA glycosylase stimulation

artículo científico publicado en 2018

XPC deficiency increases risk of hematologic malignancies through mutator phenotype and characteristic mutational signature

artículo científico publicado en 2020

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