about
The Bloom's syndrome helicase (BLM) interacts physically and functionally with p12, the smallest subunit of human DNA polymerase deltaAlkyladenine DNA glycosylase (AAG) localizes to mitochondria and interacts with mitochondrial single-stranded binding protein (mtSSB)Ribonucleotide incorporation by human DNA polymerase η impacts translesion synthesis and RNase H2 activity.Effect of 8-oxoguanine and abasic site DNA lesions on in vitro elongation by human DNA polymerase in the presence of replication protein A and proliferating-cell nuclear antigen.Pharmacological Inhibition of poly(ADP-ribose) polymerases improves fitness and mitochondrial function in skeletal muscle.Involvement of Werner syndrome protein in MUTYH-mediated repair of oxidative DNA damage.Agnoprotein of polyomavirus BK interacts with proliferating cell nuclear antigen and inhibits DNA replication.DNA damage response and DNA repair - dog as a model?Regulation of oxidative DNA damage repair by DNA polymerase λ and MutYH by cross-talk of phosphorylation and ubiquitination.Base excision repair in physiology and pathology of the central nervous systemSilencing of human DNA polymerase λ causes replication stress and is synthetically lethal with an impaired S phase checkpoint.The human Tim-Tipin complex interacts directly with DNA polymerase epsilon and stimulates its synthetic activity.HUWE1 mutations in Juberg-Marsidi and Brooks syndromes: the results of an X-chromosome exome sequencing study.Replication protein A and proliferating cell nuclear antigen coordinate DNA polymerase selection in 8-oxo-guanine repair.The block of DNA polymerase delta strand displacement activity by an abasic site can be rescued by the concerted action of DNA polymerase beta and Flap endonuclease 1.DNA polymerase δ-interacting protein 2 is a processivity factor for DNA polymerase λ during 8-oxo-7,8-dihydroguanine bypassAn 8-oxo-guanine repair pathway coordinated by MUTYH glycosylase and DNA polymerase lambda.The interaction between ALKBH2 DNA repair enzyme and PCNA is direct, mediated by the hydrophobic pocket of PCNA and perturbed in naturally-occurring ALKBH2 variants.Oxygen as a friend and enemy: How to combat the mutational potential of 8-oxo-guanine.Ubiquitylation of DNA polymerase λ.Genomic and functional integrity of the hematopoietic system requires tolerance of oxidative DNA lesions.Impact of ribonucleotide incorporation by DNA polymerases β and λ on oxidative base excision repair.Nucleotides with altered hydrogen bonding capacities impede human DNA polymerase η by reducing synthesis in the presence of the major cisplatin DNA adduct.Handling the 3-methylcytosine lesion by six human DNA polymerases members of the B-, X- and Y-families.Living on the Edge: DNA Polymerase Lambda between Genome Stability and Mutagenesis.HUWE1 variants cause dominant X-linked intellectual disability: a clinical study of 21 patients.Genotype-phenotype analysis of S326C OGG1 polymorphism: a risk factor for oxidative pathologies.Bypass of Mutagenic O(6)-Carboxymethylguanine DNA Adducts by Human Y- and B-Family Polymerases.Negative effects of oxidative stress in bovine spermatozoa on in vitro development and DNA integrity of embryos.DNA polymerases: Biology, diseases and biomedical applications.Regulation of oxidative DNA damage repair: The adenine:8-oxo-guanine problemCharacterization of FGD5 Expression in Primary Breast Cancers and Lymph Node MetastasesAlkyladenine DNA glycosylase associates with transcription elongation to coordinate DNA repair with gene expression
P50
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P50
description
hulumtuese
@sq
onderzoeker
@nl
researcher
@en
հետազոտող
@hy
name
Barbara van Loon
@ast
Barbara van Loon
@en
Barbara van Loon
@es
Barbara van Loon
@nl
type
label
Barbara van Loon
@ast
Barbara van Loon
@en
Barbara van Loon
@es
Barbara van Loon
@nl
prefLabel
Barbara van Loon
@ast
Barbara van Loon
@en
Barbara van Loon
@es
Barbara van Loon
@nl
P106
P21
P31
P496
0000-0002-7597-207X