High-level serum B-cell activating factor and promoter polymorphisms in patients with idiopathic thrombocytopenic purpura.
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Advances in Diagnosis and Treatments for Immune ThrombocytopeniaContemporary management of primary immune thrombocytopenia in adultsPiecing together the humoral and cellular mechanisms of immune thrombocytopeniaElevated pretransplantation soluble BAFF is associated with an increased risk of acute antibody-mediated rejectionCD16 and CD32 Gene Polymorphisms May Contribute to Risk of Idiopathic Thrombocytopenic Purpura.Gene expression and pathway analysis of immune thrombocytopenic purpura.BAFF and BAFF-R of peripheral blood and spleen mononuclear cells in idiopathic thrombocytopenic purpura.The ITP syndrome: pathogenic and clinical diversity.Raised expression of APRIL in Chinese patients with immune thrombocytopenia and its clinical implications.Genetic studies in pediatric ITP: outlook, feasibility, and requirements.Direct B-cell stimulation by peripheral blood monocyte-derived dendritic cells in idiopathic thrombocytopenic purpura patients.ITP: a historical perspective.Investigation of TNF-alpha, TGF-beta 1, IL-10, IL-6, IFN-gamma, MBL, GPIA, and IL1A gene polymorphisms in patients with idiopathic thrombocytopenic purpura.Reduced expression of transforming growth factor-β1 and correlated elevation of interleukin-17 and interferon-γ in pediatric patients with chronic primary immune thrombocytopenia (ITP).Defective regulatory B-cell compartment in patients with immune thrombocytopeniaImmune thrombocytopenic purpura: historical perspective, current status, recent advances and future directions.Cellular immune dysfunction in immune thrombocytopenia (ITP).Oxidative stress is predominant in female but not in male patients with autoimmune thrombocytopenia.Immune thrombocytopaenic purpura: an autoimmune cross-link between infections and vaccines.Reduced tumour necrosis factor receptor superfamily 13C inversely correlated with tumour necrosis factor superfamily 13B in patients with immune thrombocytopenia.CD86 +1057G/A polymorphism and risk of chronic immune thrombocytopenia.Immune thrombocytopenic purpura (ITP) associated with vaccinations: a review of reported cases.B-cell hyperfunction in children with immune thrombocytopenic purpura persists after splenectomy.Identification of novel biomarkers in chronic immune thrombocytopenia (ITP) by microarray-based serum protein profiling.Spectrum of clinical and genetic features of patients with inherited platelet disorder with suspected predisposition to hematological malignancies: a nationwide survey in Japan.A distinct plasmablast and naïve B-cell phenotype in primary immune thrombocytopenia.Pathogenesis and Therapeutic Mechanisms in Immune Thrombocytopenia (ITP)Emerging drugs for immune thrombocytopenia (ITP).Serum levels of beta2-microglobulin and free light chains of immunoglobulins are associated with systemic disease activity in primary Sjögren's syndrome. Data at enrollment in the prospective ASSESS cohort.Analysis of Associations of Human BAFF Gene Polymorphisms with Autoimmune Thyroid Diseases.High serum levels of BAFF, APRIL, and TACI in common variable immunodeficiency.BAFF is increased in renal transplant patients following treatment with alemtuzumabManipulating B cell homeostasis: a key component in the advancement of targeted strategiesGenetic variation in B-cell-activating factor is associated with an increased risk of developing B-cell non-Hodgkin lymphoma.Markers of B-lymphocyte activation are elevated in patients with early rheumatoid arthritis and correlated with disease activity in the ESPOIR cohort.Association of variants in BAFF (rs9514828 and rs1041569) and BAFF-R (rs61756766) genes with the risk of chronic lymphocytic leukemia.Biomarkers as tools for improved diagnostic and therapeutic monitoring in systemic lupus erythematosisEffect of FCGR polymorphism on the occurrence of late-onset neutropenia and flare-free survival in rheumatic patients treated with rituximab.B-cell biomarkers in transplantation--from genes to therapy.A gain-of-function mutation in TNFRSF13B is a candidate for predisposition to familial or sporadic immune thrombocytopenia.
P2860
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P2860
High-level serum B-cell activating factor and promoter polymorphisms in patients with idiopathic thrombocytopenic purpura.
description
2006 nî lūn-bûn
@nan
2006 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած
@hyw
2006 թվականի նոյեմբերին հրատարակված գիտական հոդված
@hy
2006年の論文
@ja
2006年論文
@yue
2006年論文
@zh-hant
2006年論文
@zh-hk
2006年論文
@zh-mo
2006年論文
@zh-tw
2006年论文
@wuu
name
High-level serum B-cell activa ...... thic thrombocytopenic purpura.
@ast
High-level serum B-cell activa ...... thic thrombocytopenic purpura.
@en
type
label
High-level serum B-cell activa ...... thic thrombocytopenic purpura.
@ast
High-level serum B-cell activa ...... thic thrombocytopenic purpura.
@en
prefLabel
High-level serum B-cell activa ...... thic thrombocytopenic purpura.
@ast
High-level serum B-cell activa ...... thic thrombocytopenic purpura.
@en
P2093
P2860
P1476
High-level serum B-cell activa ...... thic thrombocytopenic purpura.
@en
P2093
Abdulgabar Salama
Alaa Barakat
Caroline Mühle
Florian Emmerich
Julian Milz
Lorena Martinez-Gamboa
Thomas Dörner
P2860
P304
P356
10.1111/J.1365-2141.2006.06431.X
P407
P50
P577
2006-11-30T00:00:00Z