Up, Down, and All Around: Diagnosis and Treatment of Novel STAT3 Variant. - Wikidata - awgldk - TriplyDB

Up, Down, and All Around: Diagnosis and Treatment of Novel STAT3 Variant.

Up, Down, and All Around: Diagnosis and Treatment of Novel STAT3 Variant.

http://www.wikidata.org/entity/Q37695336

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Autoimmune lymphoproliferative syndrome: more than a FAScinating disease.Bacille Calmette–Guerin Complications in Newly Described Primary Immunodeficiency Diseases: 2010–2017.

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Up, Down, and All Around: Diagnosis and Treatment of Novel STAT3 Variant.

http://www.wikidata.org/entity/Q37695336

description

article científic

@ca

article scientifique

@fr

articolo scientifico

@it

artigo científico

@pt

bilimsel makale

@tr

scientific article published on 13 March 2017

@en

vedecký článok

@sk

vetenskaplig artikel

@sv

videnskabelig artikel

@da

vědecký článek

@cs

name

Up, Down, and All Around: Diagnosis and Treatment of Novel STAT3 Variant.

@en

Up, Down, and All Around: Diagnosis and Treatment of Novel STAT3 Variant.

@nl

type

label

Up, Down, and All Around: Diagnosis and Treatment of Novel STAT3 Variant.

@en

Up, Down, and All Around: Diagnosis and Treatment of Novel STAT3 Variant.

@nl

prefLabel

Up, Down, and All Around: Diagnosis and Treatment of Novel STAT3 Variant.

@en

Up, Down, and All Around: Diagnosis and Treatment of Novel STAT3 Variant.

@nl

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FPED.2017.00049

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Frontiers in pediatrics

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Up, Down, and All Around: Diagnosis and Treatment of Novel STAT3 Variant.

@en

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Joshua D Milner

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Michael Alexander Weinreich

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Tiphanie P Vogel

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V Koneti Rao

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P2860

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

Phosphoinositide 3-kinase δ gene mutation predisposes to respiratory infection and airway damage

Approaches to Managing Autoimmune Cytopenias in Novel Immunological Disorders with Genetic Underpinnings Like Autoimmune Lymphoproliferative Syndrome

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

Immune dysregulation in human subjects with heterozygous germline mutations in CTLA4

Early-onset lymphoproliferation and autoimmunity caused by germline STAT3 gain-of-function mutations

A general framework for estimating the relative pathogenicity of human genetic variants

Rituximab salvage therapy in adults with immune thrombocytopenia: retrospective study on efficacy and safety profiles.

A human immunodeficiency caused by mutations in the PIK3R1 gene.

Dominant-activating germline mutations in the gene encoding the PI(3)K catalytic subunit p110δ result in T cell senescence and human immunodeficiency

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49

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scholarly article

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10.3389/FPED.2017.00049

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5

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2017-03-13T00:00:00Z

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