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Genome-wide erasure of DNA methylation in mouse primordial germ cells is affected by AID deficiency
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Reprogramming towards pluripotency requires AID-dependent DNA demethylation
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Activation-Induced Cytidine Deaminase Expression and Activity in the Absence of Germinal Centers: Insights into Hyper-IgM Syndrome
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Activation-Induced Cytidine Deaminase Deficiency Causes Organ-Specific Autoimmune Disease
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Therapeutic B cell depletion impairs adaptive and autoreactive CD4+ T cell activation in mice
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CD40 ligand and MHC class II expression are essential for human peripheral B cell tolerance
Maxime Herve et al.
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T-independent activation-induced cytidine deaminase expression, class-switch recombination, and antibody production by immature/transitional 1 B cells
Yoshihiro Ueda et al.
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CD127 expression inversely correlates with FoxP3 and suppressive function of human CD4+ T reg cells
Weihong Liu et al.
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Expression of interleukin (IL)-2 and IL-7 receptors discriminates between human regulatory and activated T cells
Nabila Seddiki et al.
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A checkpoint for autoreactivity in human IgM+ memory B cell development
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TACI-BLyS signaling via B-cell-dendritic cell cooperation is required for naive CD8+ T-cell priming in vivo
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Hassall's corpuscles instruct dendritic cells to induce CD4+CD25+ regulatory T cells in human thymus
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Molecular analysis of a large cohort of patients with the hyper immunoglobulin M (IgM) syndrome
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Surrogate light chain expressing human peripheral B cells produce self-reactive antibodies
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Bruton's tyrosine kinase is essential for human B cell tolerance
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Clinical, immunologic and genetic analysis of 29 patients with autosomal recessive hyper-IgM syndrome due to Activation-Induced Cytidine Deaminase deficiency
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Human uracil-DNA glycosylase deficiency associated with profoundly impaired immunoglobulin class-switch recombination
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Predominant autoantibody production by early human B cell precursors
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AID mutant analyses indicate requirement for class-switch-specific cofactors
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Critical roles of activation-induced cytidine deaminase in the homeostasis of gut flora
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An essential role for BAFF in the normal development of B cells through a BCMA-independent pathway
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X-linked neonatal diabetes mellitus, enteropathy and endocrinopathy syndrome is the human equivalent of mouse scurfy
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Disruption of a new forkhead/winged-helix protein, scurfin, results in the fatal lymphoproliferative disorder of the scurfy mouse
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The immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome (IPEX) is caused by mutations of FOXP3
CL Bennett et al.
NATURE GENETICS (2001)
Activation-induced cytidine deaminase (AID) deficiency causes the autosomal recessive form of the hyper-IgM syndrome (HIGM2)
P Revy et al.
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Class switch recombination and hypermutation require activation-induced cytidine deaminase (AID), a potential RNA editing enzyme
M Muramatsu et al.
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