DNA Replication Stress

This Special Issue of International Journal of Molecular Sciences (IJMS) is dedicated to the mechanisms mediated at the molecular and cellular levels in response to adverse genomic perturbations and DNA replication stress. The relevant proteins and processes play paramount roles in nucleic acid tran...

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Bibliographic Details
Main Author: Brosh Jr, Robert M. (auth)
Format: Book Chapter
Published: MDPI - Multidisciplinary Digital Publishing Institute 2019
Subjects:
n/a
EdU
NER
ATR
ALS
MMR
TLS
Online Access:Get Fullteks
DOAB: description of the publication
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020 |a books978-3-03921-390-0 
020 |a 9783039213900 
020 |a 9783039213894 
024 7 |a 10.3390/books978-3-03921-390-0  |c doi 
041 0 |a English 
042 |a dc 
100 1 |a Brosh Jr, Robert M.  |4 auth 
245 1 0 |a DNA Replication Stress 
260 |b MDPI - Multidisciplinary Digital Publishing Institute  |c 2019 
300 |a 1 electronic resource (368 p.) 
506 0 |a Open Access  |2 star  |f Unrestricted online access 
520 |a This Special Issue of International Journal of Molecular Sciences (IJMS) is dedicated to the mechanisms mediated at the molecular and cellular levels in response to adverse genomic perturbations and DNA replication stress. The relevant proteins and processes play paramount roles in nucleic acid transactions to maintain genomic stability and cellular homeostasis. A total of 18 articles are presented which encompass a broad range of highly relevant topics in genome biology. These include replication fork dynamics, DNA repair processes, DNA damage signaling and cell cycle control, cancer biology, epigenetics, cellular senescence, neurodegeneration, and aging. As Guest Editor for this IJMS Special Issue, I am very pleased to offer this collection of riveting articles centered on the theme of DNA replication stress. The blend of articles builds upon a theme that DNA damage has profound consequences for genomic stability and cellular homeostasis that affect tissue function, disease, cancer, and aging at multiple levels and through unique mechanisms. I thank the authors for their excellent contributions, which provide new insight into this fascinating and highly relevant area of genome biology. 
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546 |a English 
653 |a Werner Syndrome 
653 |a n/a 
653 |a A549 cells 
653 |a epigenetic 
653 |a neurodegeneration 
653 |a Genome integrity 
653 |a adaptation 
653 |a cellular senescence 
653 |a genome instability 
653 |a Werner Syndrome Protein 
653 |a lipofuscin 
653 |a cell cycle checkpoints 
653 |a exonuclease 1 
653 |a template-switching 
653 |a energy metabolism 
653 |a mutation frequency 
653 |a DNA replication 
653 |a fork regression 
653 |a motor neuron disease 
653 |a Microsatellites 
653 |a Alzheimer's disease 
653 |a chromatin remodeler 
653 |a repair of DNA damage 
653 |a AP site analogue 
653 |a mutagens 
653 |a replication timing 
653 |a Thermococcus eurythermalis 
653 |a nucleolar stress 
653 |a gene expression 
653 |a mutations spectra 
653 |a origin firing 
653 |a Fanconi Anemia 
653 |a superfamily 2 ATPase 
653 |a DNA translocation 
653 |a DNA repair 
653 |a SSB signaling 
653 |a homologous recombination 
653 |a common fragile sites 
653 |a 8-chloro-adenosine 
653 |a replication 
653 |a genome stability 
653 |a mutagenicity 
653 |a fork reversal 
653 |a multiple sclerosis 
653 |a non-B DNA 
653 |a protein stability 
653 |a heterogeneity 
653 |a ubiquitin 
653 |a SenTraGorTM (GL13) 
653 |a replication restart 
653 |a EdU 
653 |a ?-arrestin 
653 |a NER 
653 |a aging 
653 |a SSB end resection 
653 |a oxidative stress 
653 |a ATR 
653 |a dormant origins 
653 |a R loops 
653 |a DNA damage response 
653 |a Difficult-to-Replicate Sequences 
653 |a DNA double-strand repair 
653 |a endonuclease IV 
653 |a ALS 
653 |a double strand break repair 
653 |a premature aging 
653 |a replication stress 
653 |a EXO1 
653 |a POL? 
653 |a translesion synthesis 
653 |a strand displacements 
653 |a G2-arrest 
653 |a DNA replication pattern 
653 |a SSB repair 
653 |a genome integrity 
653 |a G protein-coupled receptor kinase interacting protein 2 (GIT2) 
653 |a MMR 
653 |a replicative stress 
653 |a senolytics 
653 |a spacer 
653 |a interactome 
653 |a ATR-Chk1 DDR pathway 
653 |a C9orf72 
653 |a replication fork restart 
653 |a translesion DNA synthesis 
653 |a DNA damage 
653 |a mismatch repair 
653 |a DNA replication stress 
653 |a DNA helicase 
653 |a Polymerase kappa 
653 |a DNA fiber assay 
653 |a H1299 cells 
653 |a TLS 
653 |a APE2 
653 |a ageing 
653 |a cell death 
653 |a chromosome 
653 |a TopBP1 
653 |a barley 
653 |a clock proteins 
653 |a post-translational modification 
653 |a 8-oxoG 
653 |a S phase 
653 |a ataxia telangiectasia mutated (ATM) 
653 |a G protein-coupled receptor (GPCR) 
653 |a Polymerase eta 
653 |a cancer 
653 |a G protein-coupled receptor kinase (GRK) 
653 |a helicase 
653 |a genomic instability 
653 |a Parkinson's disease 
653 |a nucleotide excision repair 
653 |a SupF 
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856 4 0 |a www.oapen.org  |u https://directory.doabooks.org/handle/20.500.12854/45331  |7 0  |z DOAB: description of the publication