DNA-dependent protein kinase activity is not required for immunoglobulin class switching.
about
Functional redundancy between the XLF and DNA-PKcs DNA repair factors in V(D)J recombination and nonhomologous DNA end joiningEssential role for DNA-PKcs in DNA double-strand break repair and apoptosis in ATM-deficient lymphocytesRelated Mechanisms of Antibody Somatic Hypermutation and Class Switch RecombinationDeletion of the nucleotide excision repair gene Ercc1 reduces immunoglobulin class switching and alters mutations near switch recombination junctionsMlh1 can function in antibody class switch recombination independently of Msh2Artemis-independent functions of DNA-dependent protein kinase in Ig heavy chain class switch recombination and developmentInteraction between HIV-1 Tat and DNA-PKcs modulates HIV transcription and class switch recombination.Mechanism and regulation of class switch recombinationDe novo protein synthesis is required for the activation-induced cytidine deaminase function in class-switch recombination.AID to overcome the limitations of genomic information by introducing somatic DNA alterations.Class-switch recombination: after the dawn of AID.The role of DNA breaks in genomic instability and tumorigenesis.The catalytic subunit of DNA-protein kinase (DNA-PKcs) is not required for Ig class-switch recombinationThe role of the non-homologous end-joining pathway in lymphocyte development.Hyper-immunoglobulin M syndromes caused by intrinsic B-lymphocyte defects.Role of genomic instability and p53 in AID-induced c-myc-Igh translocations.AID to overcome the limitations of genomic information.Role for DNA repair factor XRCC4 in immunoglobulin class switch recombination.H2AX is required for recombination between immunoglobulin switch regions but not for intra-switch region recombination or somatic hypermutationATM is required for efficient recombination between immunoglobulin switch regions.Mapping of a functional recombination motif that defines isotype specificity for mu-->gamma3 switch recombination implicates NF-kappaB p50 as the isotype-specific switching factorFixing DNA breaks during class switch recombination.DNA-PKcs and Artemis function in the end-joining phase of immunoglobulin heavy chain class switch recombinationV(D)J and immunoglobulin class switch recombinations: a paradigm to study the regulation of DNA end-joining.Non-homologous end joining in class switch recombination: the beginning of the endDifferent DNA End Configurations Dictate Which NHEJ Components Are Most Important for Joining Efficiency.Altered kinetics of nonhomologous end joining and class switch recombination in ligase IV-deficient B cells.NHEJ-deficient DT40 cells have increased levels of immunoglobulin gene conversion: evidence for a double strand break intermediate.Fine-structure analysis of activation-induced deaminase accessibility to class switch region R-loops.Paradigm switching in the germinal center.
P2860
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P2860
DNA-dependent protein kinase activity is not required for immunoglobulin class switching.
description
2002 nî lūn-bûn
@nan
2002年の論文
@ja
2002年学术文章
@wuu
2002年学术文章
@zh-cn
2002年学术文章
@zh-hans
2002年学术文章
@zh-my
2002年学术文章
@zh-sg
2002年學術文章
@yue
2002年學術文章
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2002年學術文章
@zh-hant
name
DNA-dependent protein kinase activity is not required for immunoglobulin class switching.
@ast
DNA-dependent protein kinase activity is not required for immunoglobulin class switching.
@en
type
label
DNA-dependent protein kinase activity is not required for immunoglobulin class switching.
@ast
DNA-dependent protein kinase activity is not required for immunoglobulin class switching.
@en
prefLabel
DNA-dependent protein kinase activity is not required for immunoglobulin class switching.
@ast
DNA-dependent protein kinase activity is not required for immunoglobulin class switching.
@en
P2093
P2860
P356
P1476
DNA-dependent protein kinase activity is not required for immunoglobulin class switching.
@en
P2093
Donna M Fath
Gayle C Bosma
Jiyoon Kim
Maria G Cotticelli
Marko Z Radic
Melvin J Bosma
Norman R Ruetsch
Teresa Urich
P2860
P304
P356
10.1084/JEM.20001871
P407
P577
2002-12-01T00:00:00Z