about
The human REV1 gene codes for a DNA template-dependent dCMP transferaseThe human RAD18 gene product interacts with HHR6A and HHR6BFanconi anemia complementation group A (FANCA) protein has intrinsic affinity for nucleic acids with preference for single-stranded formsSpecificity of DNA lesion bypass by the yeast DNA polymerase eta.FANCI protein binds to DNA and interacts with FANCD2 to recognize branched structuresCrystal structure of a Fanconi anemia-associated nuclease homolog bound to 5' flap DNA: basis of interstrand cross-link repair by FAN1.Error-free and error-prone lesion bypass by human DNA polymerase kappa in vitro.Response of human REV1 to different DNA damage: preferential dCMP insertion opposite the lesion.Histone deacetylase 10 regulates DNA mismatch repair and may involve the deacetylation of MutS homolog 2.Reconstitution of 5'-directed human mismatch repair in a purified system.Regulation of replication protein A functions in DNA mismatch repair by phosphorylation.Human DNA polymerase kappa synthesizes DNA with extraordinarily low fidelity.ATR-ATRIP kinase complex triggers activation of the Fanconi anemia DNA repair pathway.Mouse DNA polymerase kappa has a functional role in the repair of DNA strand breaksDamage-dependent regulation of MUS81-EME1 by Fanconi anemia complementation group A protein.Human Fanconi anemia complementation group a protein stimulates the 5' flap endonuclease activity of FEN1.Identification and characterization of OGG1 mutations in patients with Alzheimer's disease.SLX4 contributes to telomere preservation and regulated processing of telomeric joint molecule intermediatesHuman DNA Exonuclease TREX1 Is Also an Exoribonuclease That Acts on Single-stranded RNA.Identification of regulatory factor X as a novel mismatch repair stimulatory factorCoordinated processing of 3' slipped (CAG)n/(CTG)n hairpins by DNA polymerases β and δ preferentially induces repeat expansions.Maintenance of genome stability by Fanconi anemia proteins.Base excision repair of oxidative DNA damage coupled with removal of a CAG repeat hairpin attenuates trinucleotide repeat expansion.Assembling an orchestra: Fanconi anemia pathway of DNA repair.Does a helicase activity help mismatch repair in eukaryotes?8-(Hydroxymethyl)-3,N(4)-etheno-C, a potential carcinogenic glycidaldehyde product, miscodes in vitro using mammalian DNA polymerases.Effects of base sequence context on translesion synthesis past a bulky (+)-trans-anti-B[a]P-N2-dG lesion catalyzed by the Y-family polymerase pol kappa.Response of human DNA polymerase iota to DNA lesions.Highly frequent frameshift DNA synthesis by human DNA polymerase muError-prone lesion bypass by human DNA polymerase eta.Roles of Rad23 protein in yeast nucleotide excision repair.The catalytic function of the Rev1 dCMP transferase is required in a lesion-specific manner for translesion synthesis and base damage-induced mutagenesis.In vitro FANCD2 monoubiquitination by HHR6 and hRad18.trans-Lesion synthesis past bulky benzo[a]pyrene diol epoxide N2-dG and N6-dA lesions catalyzed by DNA bypass polymerases.Lesion bypass activities of human DNA polymerase mu.Two-step error-prone bypass of the (+)- and (-)-trans-anti-BPDE-N2-dG adducts by human DNA polymerases eta and kappa.Activities of human DNA polymerase kappa in response to the major benzo[a]pyrene DNA adduct: error-free lesion bypass and extension synthesis from opposite the lesion.Differential requirement for proliferating cell nuclear antigen in 5' and 3' nick-directed excision in human mismatch repair.The p-benzoquinone DNA adducts derived from benzene are highly mutagenic.Measuring strand discontinuity-directed mismatch repair in yeast Saccharomyces cerevisiae by cell-free nuclear extracts.
P50
Q22010721-28D3B915-B268-4AB3-8B0A-923D4DD24C87Q22254654-C890D717-1C44-47D2-ACF8-70939D3FB12BQ24631719-1BDEB3B9-65B5-4724-9FC9-F6B0D8DE27D8Q27933149-E466FAF4-4C0A-475A-A979-1888467F61E1Q28250124-B253F095-4315-4583-A70F-4887CA6E95B7Q28492645-FCD6C1D5-7B02-4F65-8CAF-CDEC582D0D93Q28646677-F12A8F33-C486-4E52-B9ED-CD7E68DBACBCQ28646698-9C4C5401-F83E-4B0F-85C9-A88466A52AA1Q30356611-D2223D21-0DE5-4C0F-B086-E80C9876EA72Q33222844-77C4FF89-E4DD-4146-9CAC-A243A60956DCQ33244982-5FDBFCFA-2ECC-47FD-AA2D-FF52A5B4E423Q33826153-23E3FC80-ED08-4379-A106-572DFE6EA2FEQ34132768-B0B8AF14-DE79-4F1D-9966-597AFD2A57C5Q34633078-2A42885F-F4F5-4A9B-B120-394D42BF21BCQ35028557-A5267B53-574F-4122-99F2-063CD67E9863Q35070427-43C8539D-1835-4AE4-A75C-8900251067BBQ35829350-F896214E-1FE7-4899-B73D-0A55644C6160Q35842523-428BD8A0-8898-4110-8D24-925BD870F261Q35860984-4A3F933E-C92D-4726-961D-65FE09F47A81Q36741556-6E8334F9-8DF8-4CFC-86AC-A62C3D82B07EQ36873632-CFAC3010-0060-4D13-918A-621B68B343A9Q37658498-23959CA4-3CBB-48D4-AE71-BDCA825AC3A4Q37680431-D6372FF7-5357-4B4C-9CE3-FE4619E1F45DQ37761980-A18D265D-035C-48D7-93F3-BF7C26E6810EQ37765533-0CE7815B-834D-4546-A407-8A97AE5516EBQ38292359-CE5068F7-5133-4095-8448-7DAD14FF1A23Q38357392-0027AE9F-F5DF-414F-9025-8B02AD1A5496Q38658428-5F71B8F5-59B8-470A-A37E-8B774BF5207AQ39529040-2668BEA1-A7C9-471F-8D5B-0E13B6A51209Q39607351-05840F45-3AAE-4C53-90E4-CFBF768FF8A7Q40605830-C1DB3374-967C-4CDE-9A2F-FFE9CF0F5502Q41761731-92A6FD85-6F96-45DB-B3DE-60DBD10283E6Q42739182-86796C0E-B27A-4252-96F2-BB6B59B0334AQ44026918-1879181F-F62B-4227-B074-694938CB2744Q44135115-8E761304-B7C0-42DF-BAA0-C6095C070F2FQ44234552-C4FB3287-21BF-4B09-A899-3175248DDFFAQ44267593-43821A93-8636-462C-89C8-77204F7E66EDQ44761854-91A56E61-C152-483D-A738-3DD5A14B9310Q46718719-7152653B-7E64-4A6E-AE1C-8B0F4F4B3DF8Q51793302-D1ED92B2-516F-4BB2-B611-A84A6CC258ED
P50
description
onderzoeker
@nl
researcher
@en
հետազոտող
@hy
name
Yanbin Zhang
@ast
Yanbin Zhang
@en
Yanbin Zhang
@es
Yanbin Zhang
@nl
Yanbin Zhang
@sl
type
label
Yanbin Zhang
@ast
Yanbin Zhang
@en
Yanbin Zhang
@es
Yanbin Zhang
@nl
Yanbin Zhang
@sl
prefLabel
Yanbin Zhang
@ast
Yanbin Zhang
@en
Yanbin Zhang
@es
Yanbin Zhang
@nl
Yanbin Zhang
@sl
P1053
F-2998-2011
P106
P31
P3829
P496
0000-0002-7263-5510