Defect in IgV gene somatic hypermutation in common variable immuno-deficiency syndrome
about
Selective IgA deficiency (SIgAD) and common variable immunodeficiency (CVID)Altered dendritic cell distribution in patients with common variable immunodeficiency.Immunoglobulin class switch recombination: will genetics provide new clues to mechanism?Transcription, beta-like DNA polymerases and hypermutationMutations of CD40 gene cause an autosomal recessive form of immunodeficiency with hyper IgM.Role of B cells in common variable immune deficiency.Exhaustion of bacteria-specific CD4 T cells and microbial translocation in common variable immunodeficiency disorders.Hyper-IgM syndrome type 4 with a B lymphocyte-intrinsic selective deficiency in Ig class-switch recombination.Clinical and laboratory aspects of common variable immunodeficiency.IgH sequences in common variable immune deficiency reveal altered B cell development and selection.TLR-mediated B cell defects and IFN-α in common variable immunodeficiencyDNA polymerase eta is involved in hypermutation occurring during immunoglobulin class switch recombination.Somatic diversification in the absence of antigen-driven responses is the hallmark of the IgM+ IgD+ CD27+ B cell repertoire in infantsHigh serum levels of BAFF, APRIL, and TACI in common variable immunodeficiency.B-cell activating factor receptor deficiency is associated with an adult-onset antibody deficiency syndrome in humans.Pathogenesis and treatment of gastrointestinal disease in antibody deficiency syndromes.Specific NEMO mutations impair CD40-mediated c-Rel activation and B cell terminal differentiation.Highly frequent frameshift DNA synthesis by human DNA polymerase muAID-dependent somatic hypermutation occurs as a DNA single-strand event in the BL2 cell line.Human blood IgM "memory" B cells are circulating splenic marginal zone B cells harboring a prediversified immunoglobulin repertoire.Expression of activation-induced cytidine deaminase gene in B lymphocytes of patients with common variable immunodeficiency.Somatic Hypermutation Defects in Common Variable Immune Deficiency.Gene Conversion-Like Events in the Diversification of Human Rearranged IGHV3-23*01 Gene Sequences.Long-term follow-up on affinity maturation and memory B-cell generation in patients with common variable immunodeficiency.Non-functional immunoglobulin G transcripts in a case of hyper-immunoglobulin M syndrome similar to type 4.B-cell receptor repertoire sequencing in patients with primary immunodeficiency: a review.Levels of somatic hypermutations in B cell receptors increase during childhood.Impaired up-regulation of CD70 and CD86 in naive (CD27-) B cells from patients with common variable immunodeficiency (CVID).Measurement of peripheral B cell subpopulations in common variable immunodeficiency (CVID) using a whole blood method.Selection and Neutral Mutations Drive Pervasive Mutability Losses in Long-Lived Anti-HIV B-Cell Lineages.
P2860
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P2860
Defect in IgV gene somatic hypermutation in common variable immuno-deficiency syndrome
description
1998 nî lūn-bûn
@nan
1998年の論文
@ja
1998年論文
@yue
1998年論文
@zh-hant
1998年論文
@zh-hk
1998年論文
@zh-mo
1998年論文
@zh-tw
1998年论文
@wuu
1998年论文
@zh
1998年论文
@zh-cn
name
Defect in IgV gene somatic hypermutation in common variable immuno-deficiency syndrome
@ast
Defect in IgV gene somatic hypermutation in common variable immuno-deficiency syndrome
@en
type
label
Defect in IgV gene somatic hypermutation in common variable immuno-deficiency syndrome
@ast
Defect in IgV gene somatic hypermutation in common variable immuno-deficiency syndrome
@en
prefLabel
Defect in IgV gene somatic hypermutation in common variable immuno-deficiency syndrome
@ast
Defect in IgV gene somatic hypermutation in common variable immuno-deficiency syndrome
@en
P2093
P2860
P356
P1476
Defect in IgV gene somatic hypermutation in common variable immuno-deficiency syndrome
@en
P2093
Le Deist F
Reynaud CA
P2860
P304
13135-13140
P356
10.1073/PNAS.95.22.13135
P407
P577
1998-10-01T00:00:00Z