Narrow your search

Library

FARO (3)

KU Leuven (3)

LUCA School of Arts (3)

Odisee (3)

Thomas More Kempen (3)

Thomas More Mechelen (3)

UCLL (3)

ULiège (3)

VIVES (3)

Vlaams Parlement (3)

More...

Resource type

book (4)


Language

English (4)


Year
From To Submit

2020 (2)

2019 (2)

Listing 1 - 4 of 4
Sort by

Book
Plant Organelle DNA Maintenance
Authors: ---
Year: 2020 Publisher: Basel, Switzerland MDPI - Multidisciplinary Digital Publishing Institute

Loading...
Export citation

Choose an application

Bookmark

Abstract

This book provides reviews and primary research articles that discuss the replication, repair, maintenance, and structures of plant organelle genomes. Rearrangements of these genomes are common and provide a way to distinguish closely related plant species. Some articles in the book discuss recent advances in identifying specific proteins and potential mechanisms involved in DNA replication, recombination, and repair in plant mitochondria and chloroplasts.


Book
Plant Organelle DNA Maintenance
Authors: ---
Year: 2020 Publisher: Basel, Switzerland MDPI - Multidisciplinary Digital Publishing Institute

Loading...
Export citation

Choose an application

Bookmark

Abstract

This book provides reviews and primary research articles that discuss the replication, repair, maintenance, and structures of plant organelle genomes. Rearrangements of these genomes are common and provide a way to distinguish closely related plant species. Some articles in the book discuss recent advances in identifying specific proteins and potential mechanisms involved in DNA replication, recombination, and repair in plant mitochondria and chloroplasts.

Keywords

Research & information: general --- Biology, life sciences --- DNA replication --- recombination-dependent replication (RDR) --- plant mitochondrial DNA --- chloroplast DNA --- DNA repair --- divergent inverted repeats --- short-globose cacti --- novel gene rearrangements --- pseudogenization --- sunflower --- cytoplasmic male sterility (CMS) --- mitochondrial genome --- reorganizations --- next generation sequencing (NGS) --- evolution --- replisome --- recombination-dependent replication --- Lilium --- phylogenomics --- plastome --- molecular markers --- gene tree --- species tree --- chloroplast --- mitochondrion --- genome stability --- homologous recombination repair --- repeated sequence --- Physcomitrella patens --- mitochondria --- double-strand break repair --- uracil-N-glycosylase --- Piperales --- Hydnoraceae --- Hydnora --- Prosopanche --- parasitic plants --- holoparasite --- plastid genome --- organelles --- plastid phylogenetics --- DNA recombination --- plant organelle genome structure --- DNA replication --- recombination-dependent replication (RDR) --- plant mitochondrial DNA --- chloroplast DNA --- DNA repair --- divergent inverted repeats --- short-globose cacti --- novel gene rearrangements --- pseudogenization --- sunflower --- cytoplasmic male sterility (CMS) --- mitochondrial genome --- reorganizations --- next generation sequencing (NGS) --- evolution --- replisome --- recombination-dependent replication --- Lilium --- phylogenomics --- plastome --- molecular markers --- gene tree --- species tree --- chloroplast --- mitochondrion --- genome stability --- homologous recombination repair --- repeated sequence --- Physcomitrella patens --- mitochondria --- double-strand break repair --- uracil-N-glycosylase --- Piperales --- Hydnoraceae --- Hydnora --- Prosopanche --- parasitic plants --- holoparasite --- plastid genome --- organelles --- plastid phylogenetics --- DNA recombination --- plant organelle genome structure


Book
Towards Mechanism-based Treatments for Fragile X Syndrome
Authors: ---
ISBN: 303921506X 3039215051 Year: 2019 Publisher: MDPI - Multidisciplinary Digital Publishing Institute

Loading...
Export citation

Choose an application

Bookmark

Abstract

It has been more than 25 years since the identification of the FMR1 gene and the demonstration of the causative role of CGG-repeat expansion in the disease pathology of fragile X syndrome (FXS), but the underlying mechanisms involved in the expansion mutation and the resulting gene silencing still remain elusive. Our understanding of the pathways impacted by the loss of FMRP function has grown tremendously, and has opened new avenues for targeted treatments for FXS. However, the failure of recent clinical trials that were based on successful preclinical studies using the Fmr1 knockout mouse model has forced the scientific community to revisit clinical trial design and identify objective outcome measures. There has also been a renewed interest in restoring FMR1 gene expression as a possible treatment approach for FXS. This special issue of Brain Sciences highlights the progress that has been made towards understanding the disease mechanisms and how this has informed the development of treatment strategies that are being explored for FXS.

Keywords

n/a --- lymphoblast --- pluripotent stem cells --- FMR1 --- Gene editing --- X chromosome --- Fmr1 --- epigenetic gene silencing --- FMR1 gene --- Fragile X syndrome 1 --- repeat instability --- characteristics that have the greatest impact --- DNA instability --- working memory --- language development --- mosaicism --- CRISPR 3 --- clinical trials --- autism spectrum disorders --- Fmr1 KO mouse --- automated vocal analysis --- base excision repair (BER) --- inhibitory control --- cerebral spinal fluid --- iPSC --- drug development --- targeted treatments --- molecular biomarkers --- viral vector --- avoidance --- biomarker --- set-shifting --- early identification --- expansion --- anxiety --- planning --- voice of the person --- mismatch repair (MMR) --- gene reactivation --- double-strand break repair (DSBR) --- newborn screening --- intellectual disability --- processing speed --- voice of the patient --- fragile X syndrome --- adeno-associated virus --- neurodevelopmental disorders --- histone methylation --- Non-homologous end-joining (NHEJ) --- ASD --- Fxr2 --- Fragile X-associated Tremor/Ataxia Syndrome 2 --- Trinucleotide Repeat 4 --- CGG Repeat Expansion Disease --- DNA methylation --- contraction --- fragile X mental retardation protein --- RNA:DNA hybrid --- behavior --- developmental disorders --- cognition --- females --- FMRP --- Fragile X Syndrome --- unstable repeat diseases --- protein synthesis --- brain --- cognitive flexibility --- treatment development --- fibroblast --- PRC2 --- transcription coupled repair (TCR) --- best practices --- attention --- Fragile X --- executive function


Book
DNA Replication Stress
Author:
ISBN: 3039213903 303921389X Year: 2019 Publisher: MDPI - Multidisciplinary Digital Publishing Institute

Loading...
Export citation

Choose an application

Bookmark

Abstract

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.

Keywords

Werner Syndrome --- n/a --- A549 cells --- epigenetic --- neurodegeneration --- Genome integrity --- adaptation --- cellular senescence --- genome instability --- Werner Syndrome Protein --- lipofuscin --- cell cycle checkpoints --- exonuclease 1 --- template-switching --- energy metabolism --- mutation frequency --- DNA replication --- fork regression --- motor neuron disease --- Microsatellites --- Alzheimer’s disease --- chromatin remodeler --- repair of DNA damage --- AP site analogue --- mutagens --- replication timing --- Thermococcus eurythermalis --- nucleolar stress --- gene expression --- mutations spectra --- origin firing --- Fanconi Anemia --- superfamily 2 ATPase --- DNA translocation --- DNA repair --- SSB signaling --- homologous recombination --- common fragile sites --- 8-chloro-adenosine --- replication --- genome stability --- mutagenicity --- fork reversal --- multiple sclerosis --- non-B DNA --- protein stability --- heterogeneity --- ubiquitin --- SenTraGorTM (GL13) --- replication restart --- EdU --- ?-arrestin --- NER --- aging --- SSB end resection --- oxidative stress --- ATR --- dormant origins --- R loops --- DNA damage response --- Difficult-to-Replicate Sequences --- DNA double-strand repair --- endonuclease IV --- ALS --- double strand break repair --- premature aging --- replication stress --- EXO1 --- POL? --- translesion synthesis --- strand displacements --- G2-arrest --- DNA replication pattern --- SSB repair --- genome integrity --- G protein-coupled receptor kinase interacting protein 2 (GIT2) --- MMR --- replicative stress --- senolytics --- spacer --- interactome --- ATR-Chk1 DDR pathway --- C9orf72 --- replication fork restart --- translesion DNA synthesis --- DNA damage --- mismatch repair --- DNA replication stress --- DNA helicase --- Polymerase kappa --- DNA fiber assay --- H1299 cells --- TLS --- APE2 --- ageing --- cell death --- chromosome --- TopBP1 --- barley --- clock proteins --- post-translational modification --- 8-oxoG --- S phase --- ataxia telangiectasia mutated (ATM) --- G protein-coupled receptor (GPCR) --- Polymerase eta --- cancer --- G protein-coupled receptor kinase (GRK) --- helicase --- genomic instability --- Parkinson’s disease --- nucleotide excision repair --- SupF --- Alzheimer's disease --- Parkinson's disease

Listing 1 - 4 of 4
Sort by