B-cell deficiency and severe autoimmunity caused by deficiency of protein kinase C δ.
about
Discovery of single-gene inborn errors of immunity by next generation sequencingProtein Kinase C δ: a Gatekeeper of Immune HomeostasisUnbalanced Immune System: Immunodeficiencies and AutoimmunityProtein kinase C in the immune system: from signalling to chromatin regulationGermline mutations in NFKB2 implicate the noncanonical NF-κB pathway in the pathogenesis of common variable immunodeficiencyAutoimmunity in primary T-cell immunodeficiencies.Trichuris suis induces human non-classical patrolling monocytes via the mannose receptor and PKC: implications for multiple sclerosis.Autoimmune and other cytopenias in primary immunodeficiencies: pathomechanisms, novel differential diagnoses, and treatmentProtein kinase C δ deficiency enhances megakaryopoiesis and recovery from thrombocytopenia.Guidelines for genetic studies in single patients: lessons from primary immunodeficiencies.Severe Early-Onset Combined Immunodeficiency due to Heterozygous Gain-of-Function Mutations in STAT1Biallelic loss-of-function mutation in NIK causes a primary immunodeficiency with multifaceted aberrant lymphoid immunity.Cancer-associated protein kinase C mutations reveal kinase's role as tumor suppressorThe expanding spectrum of the autoimmune lymphoproliferative syndromesUtility of next generation sequencing in clinical primary immunodeficiencies.Protein kinase Cδ promotes transitional B cell-negative selection and limits proximal B cell receptor signaling to enforce toleranceProtein kinase C inhibitors for immune disorders.Genetics of common variable immunodeficiency: role of transmembrane activator and calcium modulator and cyclophilin ligand interactor.Genes associated with common variable immunodeficiency: one diagnosis to rule them all?Autoimmunity in Primary Antibody Deficiencies.Reversing the Paradigm: Protein Kinase C as a Tumor Suppressor.Protein kinase C as a tumor suppressor.Potentially Beneficial Effect of Hydroxychloroquine in a Patient with a Novel Mutation in Protein Kinase Cδ Deficiency.Association of CLEC16A with human common variable immunodeficiency disorder and role in murine B cells.Monozygotic twins discordant for common variable immunodeficiency reveal impaired DNA demethylation during naïve-to-memory B-cell transition.[Common variable immunodeficiency: a clinical challenge].Editorial: entering the age of whole-exome sequencing in rheumatic diseases: novel insights into disease pathogenicity.Value of allohaemagglutinins in the diagnosis of a polysaccharide antibody deficiency.Regulation of FcRγ function by site-specific serine phosphorylation.Protein kinase C: perfectly balanced.Rare autoimmune disorders with Mendelian inheritance.Successful use of ofatumumab in two cases of early-onset juvenile SLE with thrombocytopenia caused by a mutation in protein kinase C δ
P2860
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P2860
B-cell deficiency and severe autoimmunity caused by deficiency of protein kinase C δ.
description
2013 nî lūn-bûn
@nan
2013年の論文
@ja
2013年論文
@yue
2013年論文
@zh-hant
2013年論文
@zh-hk
2013年論文
@zh-mo
2013年論文
@zh-tw
2013年论文
@wuu
2013年论文
@zh
2013年论文
@zh-cn
name
B-cell deficiency and severe autoimmunity caused by deficiency of protein kinase C δ.
@ast
B-cell deficiency and severe autoimmunity caused by deficiency of protein kinase C δ.
@en
type
label
B-cell deficiency and severe autoimmunity caused by deficiency of protein kinase C δ.
@ast
B-cell deficiency and severe autoimmunity caused by deficiency of protein kinase C δ.
@en
prefLabel
B-cell deficiency and severe autoimmunity caused by deficiency of protein kinase C δ.
@ast
B-cell deficiency and severe autoimmunity caused by deficiency of protein kinase C δ.
@en
P2093
P2860
P50
P1433
P1476
B-cell deficiency and severe autoimmunity caused by deficiency of protein kinase C δ
@en
P2093
Andreas Heitger
Arnold Pollak
Elisangela Santos-Valente
Franz Eitelberger
Heidrun Boztug
Kaan Boztug
Klaus Arbeiter
Leonhard Müllauer
Nina Kathrin Prengemann
Renate Kain
P2860
P304
P356
10.1182/BLOOD-2012-10-460741
P407
P577
2013-01-14T00:00:00Z