Mice reconstituted with DNA polymerase beta-deficient fetal liver cells are able to mount a T cell-dependent immune response and mutate their Ig genes normally
about
Two novel human and mouse DNA polymerases of the polX familyThe role of DNA polymerase activity in human non-homologous end joiningHuman DNA polymerase theta possesses 5'-dRP lyase activity and functions in single-nucleotide base excision repair in vitroAltered nucleotide misinsertion fidelity associated with poliota-dependent replication at the end of a DNA template.poliota, a remarkably error-prone human DNA polymeraseDifferential expression of APE1 and APE2 in germinal centers promotes error-prone repair and A:T mutations during somatic hypermutationp53 Deficiency rescues neuronal apoptosis but not differentiation in DNA polymerase beta-deficient micePolymerase mu is up-regulated during the T cell-dependent immune response and its deficiency alters developmental dynamics of spleen centroblastsM17, a gene specific for germinal center (GC) B cells and a prognostic marker for GC B-cell lymphomas, is dispensable for the GC reaction in miceStructural relationship of curcumin derivatives binding to the BRCT domain of human DNA polymerase lambda.Dual functions of ASCIZ in the DNA base damage response and pulmonary organogenesisA new class of errant DNA polymerases provides candidates for somatic hypermutation.The reverse transcriptase model of somatic hypermutationTranscription, beta-like DNA polymerases and hypermutationDifferent mutation signatures in DNA polymerase eta- and MSH6-deficient mice suggest separate roles in antibody diversificationSomatic immunoglobulin hypermutation.AID and somatic hypermutation.Base excision repair in a network of defence and tolerance.DNA polymerases and somatic hypermutation of immunoglobulin genesMSH2-MSH6 stimulates DNA polymerase eta, suggesting a role for A:T mutations in antibody genes.Emerging links between hypermutation of antibody genes and DNA polymerases.AID and mismatch repair in antibody diversification.Immunoglobulin somatic hypermutation: double-strand DNA breaks, AID and error-prone DNA repair.On the molecular mechanism of somatic hypermutation of rearranged immunoglobulin genes.DNA deamination in immunity.DNA lesions and repair in immunoglobulin class switch recombination and somatic hypermutation.DNA polymerase beta is able to repair breaks in switch regions and plays an inhibitory role during immunoglobulin class switch recombination.Down-regulation of DNA polymerase beta accompanies somatic hypermutation in human BL2 cell linesThe translesion DNA polymerase zeta plays a major role in Ig and bcl-6 somatic hypermutation.Error-prone candidates vie for somatic mutationAntibody diversification caused by disrupted mismatch repair and promiscuous DNA polymerasesUbiquitylated PCNA plays a role in somatic hypermutation and class-switch recombination and is required for meiotic progression.Pol zeta ablation in B cells impairs the germinal center reaction, class switch recombination, DNA break repair, and genome stability.The roles of APE1, APE2, DNA polymerase beta and mismatch repair in creating S region DNA breaks during antibody class switchRev1 is a base excision repair enzyme with 5'-deoxyribose phosphate lyase activity.DNA polymerases β and λ do not directly affect Ig variable region somatic hypermutation although their absence reduces the frequency of mutations.Translesion DNA synthesis in the context of cancer research.Targeting Gene Function in Germinal Center B Cells: A Practical Approach.Overexpression of human DNA polymerase mu (Pol mu) in a Burkitt's lymphoma cell line affects the somatic hypermutation rate.Germinal center dysregulation by histone methyltransferase EZH2 promotes lymphomagenesis.
P2860
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P2860
Mice reconstituted with DNA polymerase beta-deficient fetal liver cells are able to mount a T cell-dependent immune response and mutate their Ig genes normally
description
2000 թուականի Փետրուարին հրատարակուած գիտական յօդուած
@hyw
2000 թվականի փետրվարին հրատարակված գիտական հոդված
@hy
article publié dans les Procee ...... f the United States of America
@fr
artículu científicu espublizáu en 2000
@ast
im Februar 2000 veröffentlichter wissenschaftlicher Artikel
@de
scientific journal article
@en
vedecký článok (publikovaný 2000/02/01)
@sk
vědecký článek publikovaný v roce 2000
@cs
wetenschappelijk artikel (gepubliceerd op 2000/02/01)
@nl
наукова стаття, опублікована в лютому 2000
@uk
name
Mice reconstituted with DNA po ...... mutate their Ig genes normally
@ast
Mice reconstituted with DNA po ...... mutate their Ig genes normally
@en
Mice reconstituted with DNA po ...... mutate their Ig genes normally
@nl
type
label
Mice reconstituted with DNA po ...... mutate their Ig genes normally
@ast
Mice reconstituted with DNA po ...... mutate their Ig genes normally
@en
Mice reconstituted with DNA po ...... mutate their Ig genes normally
@nl
prefLabel
Mice reconstituted with DNA po ...... mutate their Ig genes normally
@ast
Mice reconstituted with DNA po ...... mutate their Ig genes normally
@en
Mice reconstituted with DNA po ...... mutate their Ig genes normally
@nl
P2093
P2860
P3181
P356
P1476
Mice reconstituted with DNA po ...... mutate their Ig genes normally
@en
P2093
P2860
P304
P3181
P356
10.1073/PNAS.97.3.1166
P407
P577
2000-02-01T00:00:00Z