A novel lymphoproliferative/autoimmune syndrome resembling murine lpr/gld disease. - Wikidata - awgldk - TriplyDB

A novel lymphoproliferative/autoimmune syndrome resembling murine lpr/gld disease.

A novel lymphoproliferative/autoimmune syndrome resembling murine lpr/gld disease.

http://www.wikidata.org/entity/Q35604700

about

Regulation of Fas (CD95)-induced apoptosis by nuclear factor-KB and tumor necrosis factor- alpha in macrophages Using biomarkers to predict the presence of FAS mutations in patients with features of the autoimmune lymphoproliferative syndrome Advances in the management and understanding of autoimmune lymphoproliferative syndrome (ALPS)Revised diagnostic criteria and classification for the autoimmune lymphoproliferative syndrome (ALPS): report from the 2009 NIH International Workshop How I treat autoimmune lymphoproliferative syndrome Use of rituximab for refractory cytopenias associated with autoimmune lymphoproliferative syndrome (ALPS)Primary immunodeficiencies associated with eosinophilia Approaches to Managing Autoimmune Cytopenias in Novel Immunological Disorders with Genetic Underpinnings Like Autoimmune Lymphoproliferative Syndrome Reversion of autoimmune lymphoproliferative syndrome with an antimalarial drug: preliminary results of a clinical cohort study and molecular observations FAS haploinsufficiency is a common disease mechanism in the human autoimmune lymphoproliferative syndrome Autoimmune lymphoproliferative syndrome misdiagnosed as hemophagocytic lymphohistiocytosis Causes and consequences of the autoimmune lymphoproliferative syndrome RBC autoantibodies in autoimmune lymphoproliferative syndrome.Autoimmune lymphoproliferative syndrome (ALPS): a case with congenital onset.Updated Understanding of Autoimmune Lymphoproliferative Syndrome (ALPS).The spectrum of Evans' syndrome.Constitutive expression of murine c-FLIPR causes autoimmunity in aged mice Development of disseminated histiocytic sarcoma in a patient with autoimmune lymphoproliferative syndrome and associated Rosai-Dorfman disease.The molecular basis for apoptotic defects in patients with CD95 (Fas/Apo-1) mutations Human TCR-alpha beta+ CD4- CD8- T cells can derive from CD8+ T cells and display an inflammatory effector phenotype Elevated interleukin-10: a new cause of dyslipidemia leading to severe HDL deficiency Somatic FAS mutations are common in patients with genetically undefined autoimmune lymphoproliferative syndrome.The power and the promise of restimulation-induced cell death in human immune diseases.Genetic basis of the complex pathological manifestations of collagen disease: lessons from MRL/lpr and related mouse models.The apoptosis-1/Fas protein in human systemic lupus erythematosus.Somatic KRAS mutations associated with a human nonmalignant syndrome of autoimmunity and abnormal leukocyte homeostasis New advances in the diagnosis and treatment of autoimmune lymphoproliferative syndrome Autoimmune lymphoproliferative syndrome type III: an indefinite disorder.Autoimmune lymphoproliferative syndrome type III, an indefinite disorder.Autoimmune lymphoproliferative syndrome with defective Fas: genotype influences penetrance Clues to immune tolerance: the monogenic autoimmune syndromes IL-10/Janus kinase/signal transducer and activator of transcription 3 signaling dysregulates Bim expression in autoimmune lymphoproliferative syndrome Defective CD95/APO-1/Fas signal complex formation in the human autoimmune lymphoproliferative syndrome, type Ia.Double negative (DN) αβ T cells: misperception and overdue recognition FAS mRNA editing in Human Systemic Lupus Erythematosus.Pathological findings in human autoimmune lymphoproliferative syndrome New take on comparative immunology: relevance to immunotherapy.Expansion of cytokine-producing CD4-CD8- T cells associated with abnormal Fas expression and hypereosinophilia.Fas and the art of lymphocyte maintenance.Spontaneous development of plasmacytoid tumors in mice with defective Fas-Fas ligand interactions.

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P2860

A novel lymphoproliferative/autoimmune syndrome resembling murine lpr/gld disease.

http://www.wikidata.org/entity/Q35604700

description

1992 nî lūn-bûn

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1992年の論文

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1992年論文

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1992年論文

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1992年論文

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1992年論文

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1992年論文

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1992年论文

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1992年论文

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1992年论文

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name

A novel lymphoproliferative/autoimmune syndrome resembling murine lpr/gld disease.

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A novel lymphoproliferative/autoimmune syndrome resembling murine lpr/gld disease.

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type

label

A novel lymphoproliferative/autoimmune syndrome resembling murine lpr/gld disease.

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A novel lymphoproliferative/autoimmune syndrome resembling murine lpr/gld disease.

@en

prefLabel

A novel lymphoproliferative/autoimmune syndrome resembling murine lpr/gld disease.

@ast

A novel lymphoproliferative/autoimmune syndrome resembling murine lpr/gld disease.

@en

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Journal of Clinical Investigation

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A novel lymphoproliferative/autoimmune syndrome resembling murine lpr/gld disease.

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Fleisher TA

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Jaffe ES

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Jaffe JS

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Sneller MC

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Stetler-Stevenson M

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Straus SE

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Strober W

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P2860

Structure of the human immunoglobulin mu locus: characterization of embryonic and rearranged J and D genes

Double-negative (CD4-CD8-) lymphocytes bearing T-cell receptor alpha and beta chains in normal human skin.

Recognition of cluster of differentiation 1 antigens by human CD4-CD8-cytolytic T lymphocytes.

Lpr and gld: single gene models of systemic autoimmunity and lymphoproliferative disease.

Identification of a 145,000 Mr membrane protein as the C3d receptor (CR2) of human B lymphocytes.

Configuration and expression of the T cell receptor beta chain gene in human T-lymphotrophic virus I-infected cells.

Transgenic rearranged T cell receptor gene inhibits lymphadenopathy and accumulation of CD4-CD8-B220+ T cells in lpr/lpr mice

Deletion of autospecific T cells in T cell receptor (TCR) transgenic mice spares cells with normal TCR levels and low levels of CD8 molecules.

Interleukin 2 promotes growth and cytolytic activity in human T3+4-8- thymocytes.

Role of the CD28 receptor in T-cell activation.

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443107

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