An amplified electrochemical strategy using DNA-QDs dendrimer superstructure for the detection of thymine DNA glycosylase activity
H Liu, Y Lou, F Zhou, H Zhu, ES Abdel-Halim… - Biosensors and …, 2015 - Elsevier
A triple-signal amplification strategy was proposed for highly sensitive and selective
detection of thymine DNA glycosylase (TDG) by coupling a dendrimer-like DNA label with …
detection of thymine DNA glycosylase (TDG) by coupling a dendrimer-like DNA label with …
A sensitive, homogeneous fluorescence assay for detection of thymine DNA glycosylase activity based on exonuclease-mediated amplification
C Chen, D Zhou, H Tang, M Liang… - Chemical Communications, 2013 - pubs.rsc.org
A sensitive, homogeneous fluorescence assay for detection of thymine DNA glycosylase
activity based on exonuclease-mediated amplification - Chemical Communications (RSC …
activity based on exonuclease-mediated amplification - Chemical Communications (RSC …
Activity and crystal structure of human thymine DNA glycosylase mutant N140A with 5-carboxylcytosine DNA at low pH
H Hashimoto, X Zhang, X Cheng - DNA repair, 2013 - Elsevier
The mammalian thymine DNA glycosylase (TDG) excises 5-carboxylcytosine (5caC) when
paired with a guanine in a CpG sequence, in addition to mismatched bases. Here we …
paired with a guanine in a CpG sequence, in addition to mismatched bases. Here we …
[HTML][HTML] Inhibition of protein kinase C increases Prdm14 level to promote self-renewal of embryonic stem cells through reducing Suv39h-induced H3K9 methylation
J Ji, J Cao, P Chen, R Huang, SD Ye - Journal of Biological Chemistry, 2024 - ASBMB
Inhibition of protein kinase C (PKC) efficiently promoted the self-renewal of embryonic stem
cells (ESCs). However, information about the function of PKC inhibition remains lacking …
cells (ESCs). However, information about the function of PKC inhibition remains lacking …
[HTML][HTML] Repair and DNA Polymerase Bypass of Clickable Pyrimidine Nucleotides
AV Endutkin, AV Yudkina, TD Zharkov, AE Barmatov… - Biomolecules, 2024 - mdpi.com
Clickable nucleosides, most often 5-ethynyl-2′-deoxyuridine (EtU), are widely used in
studies of DNA replication in living cells and in DNA functionalization for bionanotechology …
studies of DNA replication in living cells and in DNA functionalization for bionanotechology …
Impact of 5-formylcytosine on the melting kinetics of DNA by 1H NMR chemical exchange
RCA Dubini, A Schön, M Müller, T Carell… - Nucleic Acids …, 2020 - academic.oup.com
Formylcytosine (5fC) is a chemically edited, naturally occurring nucleobase which appears
in the context of modified DNA strands. The understanding of the impact of 5fC on dsDNA …
in the context of modified DNA strands. The understanding of the impact of 5fC on dsDNA …
The carboxy-terminal domain of ROS1 is essential for 5-methylcytosine DNA glycosylase activity
S Hong, H Hashimoto, YW Kow, X Zhang… - Journal of molecular …, 2014 - Elsevier
Arabidopsis thaliana repressor of silencing 1 (ROS1) is a multi-domain bifunctional DNA
glycosylase/lyase, which excises 5-methylcytosine (5mC) and 5-hydroxymethylcytosine …
glycosylase/lyase, which excises 5-methylcytosine (5mC) and 5-hydroxymethylcytosine …
[HTML][HTML] UNG-1 and APN-1 are the major enzymes to efficiently repair 5-hydroxymethyluracil DNA lesions in C. elegans
A Papaluca, JR Wagner, HU Saragovi, D Ramotar - Scientific Reports, 2018 - nature.com
In Caenorhabditis elegans, two DNA glycosylases, UNG-1 and NTH-1, and two AP
endonucleases, APN-1 and EXO-3, have been characterized from the base-excision repair …
endonucleases, APN-1 and EXO-3, have been characterized from the base-excision repair …
Comparison of the absolute level of epigenetic marks 5-methylcytosine, 5-hydroxymethylcytosine, and 5-hydroxymethyluracil between human leukocytes and sperm
Methylcytosine is one of the most important epigenetic modifications and has a profound
impact on embryonic development. After gamete fusion, there is a widespread and rapid …
impact on embryonic development. After gamete fusion, there is a widespread and rapid …
[HTML][HTML] FANCD2 maintains replication fork stability during misincorporation of the DNA demethylation products 5-hydroxymethyl-2'-deoxycytidine and 5 …
MJ Peña-Gómez, P Moreno-Gordillo, M Narmontė… - Cell death & …, 2022 - nature.com
Fanconi anemia (FA) is a rare hereditary disorder caused by mutations in any one of the
FANC genes. FA cells are mainly characterized by extreme hypersensitivity to interstrand …
FANC genes. FA cells are mainly characterized by extreme hypersensitivity to interstrand …