Single nucleotide polymorphisms in DNA glycosylases: From function to disease-Reference-Cited by-同舟云学术

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Single nucleotide polymorphisms in DNA glycosylases: From function to disease

Published:2017-06 Issue: Volume:107 Page:278-291
ISSN:0891-5849
Container-title:Free Radical Biology and Medicine
language:en
Short-container-title:Free Radical Biology and Medicine

Author:

D’Errico Mariarosaria,Parlanti Eleonora,Pascucci Barbara,Fortini Paola,Baccarini Sara,Simonelli Valeria,Dogliotti Eugenia

Funder

AIRC, Italy

European Union's Seventh Programme for Research, Technological Development and Demonstration

Publisher

Elsevier BV

Subject

Physiology (medical),Biochemistry

Reference221 articles.

1. Early steps in the DNA base excision/single-strand interruption repair pathway in mammalian cells;Hegde;Cell Res.,2008

2. Base excision repair;Krokan;Cold Spring Harb. Perspect. Biol.,2013

3. The alpha/beta fold uracil DNA glycosylases: a common origin with diverse fates;Aravind;Genome Biol.,2000

4. MBD4 and TDG: multifaceted DNA glycosylases with ever expanding biological roles;Sjolund;Mutat. Res.,2013

5. Nuclear and mitochondrial uracil-DNA glycosylases are generated by alternative splicing and transcription from different positions in the UNG gene;Nilsen;Nucleic Acids Res.,1997

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4. Activatable Self-Dissociation of Watson–Crick Structures with Fluorescent Nucleotides for Sensing Multiple Human Glycosylases at Single-Cell Level;Analytical Chemistry;2022-12-08

5. Activatable Self-Dissociation of Watson-Crick Structures with Fluorescent Nucleotides for Sensing Multiple Human Glycosylases at Single-Cell Level;ANAL CHEM;2022

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