Genetic defects of apoptosis and primary immunodeficiency. - Wikidata - awgldk - TriplyDB

Genetic defects of apoptosis and primary immunodeficiency.

Genetic defects of apoptosis and primary immunodeficiency.

http://www.wikidata.org/entity/Q37142878

about

Whole-exome-sequencing-based discovery of human FADD deficiency Fueling the flames: Mammalian programmed necrosis in inflammatory diseases Activity of Uncleaved Caspase-8 Controls Anti-bacterial Immune Defense and TLR-Induced Cytokine Production Independent of Cell Death Caspase-8: not so silently deadly.Staying alive: cell death in antiviral immunity.30 Years of NF-κB: A Blossoming of Relevance to Human Pathobiology.Metabolic reprogramming and apoptosis sensitivity: defining the contours of a T cell response.Glucocorticoid-induced activation of caspase-8 protects the glucocorticoid-induced protein Gilz from proteasomal degradation and induces its binding to SUMO-1 in murine thymocytes A missense mutation in the extracellular domain of Fas: the most common change in Argentinean patients with autoimmune lymphoproliferative syndrome represents a founder effect.Autoimmune lymphoproliferative syndrome: more than a FAScinating disease.

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Genetic defects of apoptosis and primary immunodeficiency.

http://www.wikidata.org/entity/Q37142878

description

article científic

@ca

article scientifique

@fr

articolo scientifico

@it

artigo científico

@pt

bilimsel makale

@tr

scientific article published on May 2008

@en

vedecký článok

@sk

vetenskaplig artikel

@sv

videnskabelig artikel

@da

vědecký článek

@cs

name

Genetic defects of apoptosis and primary immunodeficiency.

@en

Genetic defects of apoptosis and primary immunodeficiency.

@nl

type

label

Genetic defects of apoptosis and primary immunodeficiency.

@en

Genetic defects of apoptosis and primary immunodeficiency.

@nl

prefLabel

Genetic defects of apoptosis and primary immunodeficiency.

@en

Genetic defects of apoptosis and primary immunodeficiency.

@nl

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J.IAC.2008.01.002

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Immunology and Allergy Clinics of North America

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Genetic defects of apoptosis and primary immunodeficiency.

@en

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Helen C Su

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Michael J Lenardo

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P2860

Inherited human Caspase 10 mutations underlie defective lymphocyte and dendritic cell apoptosis in autoimmune lymphoproliferative syndrome type II

Fas preassociation required for apoptosis signaling and dominant inhibition by pathogenic mutations

Rapamycin improves lymphoproliferative disease in murine autoimmune lymphoproliferative syndrome (ALPS)

Fas ligand mutation in a patient with systemic lupus erythematosus and lymphoproliferative disease

Autoimmune lymphoproliferative syndrome

Pleiotropic defects in lymphocyte activation caused by caspase-8 mutations lead to human immunodeficiency

A composite picture of TcR alpha/beta(+) CD4(-)CD8(-) T Cells (alpha/beta-DNTCs) in humans with autoimmune lymphoproliferative syndrome

Pyrimethamine treatment does not ameliorate lymphoproliferation or autoimmune disease in MRL/lpr-/- mice or in patients with autoimmune lymphoproliferative syndrome

Use of mycophenolate mofetil for chronic, refractory immune cytopenias in children with autoimmune lymphoproliferative syndrome

Classification of cell death: recommendations of the Nomenclature Committee on Cell Death

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329-51, ix

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scholarly article

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10.1016/J.IAC.2008.01.002

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2

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28

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2008-05-01T00:00:00Z

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5429013

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18424336

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apoptotic process

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2671802

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