Rare autoimmune disorders with Mendelian inheritance.

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Susceptibility to chronic inflammation: an update.Clinical manifestations of Behçet's disease depending on sex and age: results from Japanese nationwide registration.SAMHD1: Recurring roles in cell cycle, viral restriction, cancer, and innate immunity.

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Rare autoimmune disorders with Mendelian inheritance.

Item

http://www.wikidata.org/entity/Q53086157

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2016 nî lūn-bûn

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2016年の論文

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2016年学术文章

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2016年学术文章

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2016年学术文章

@zh-cn

2016年学术文章

@zh-hans

2016年学术文章

@zh-my

2016年学术文章

@zh-sg

2016年學術文章

@yue

2016年學術文章

@zh-hant

name

Rare autoimmune disorders with Mendelian inheritance.

@en

Rare autoimmune disorders with Mendelian inheritance.

@nl

type

Item

label

Rare autoimmune disorders with Mendelian inheritance.

@en

Rare autoimmune disorders with Mendelian inheritance.

@nl

prefLabel

Rare autoimmune disorders with Mendelian inheritance.

@en

Rare autoimmune disorders with Mendelian inheritance.

@nl

P1476

Rare autoimmune disorders with Mendelian inheritance.

@en

P2093

Bernadette Kalman

http://www.w3.org/2001/XMLSchema#string

Mark Plander

http://www.w3.org/2001/XMLSchema#string

P2860

Activation-induced cytidine deaminase (AID) deficiency causes the autosomal recessive form of the Hyper-IgM syndrome (HIGM2)

Genome-wide association scan in women with systemic lupus erythematosus identifies susceptibility variants in ITGAM, PXK, KIAA1542 and other loci

Whole-exome-sequencing-based discovery of human FADD deficiency

Human immune disorder arising from mutation of the alpha chain of the interleukin-2 receptor

Complementation cloning of an MHC class II transactivator mutated in hereditary MHC class II deficiency (or bare lymphocyte syndrome)

Mutations involved in Aicardi-Goutières syndrome implicate SAMHD1 as regulator of the innate immune response

Selective regulatory function of Socs3 in the formation of IL-17-secreting T cells

Combined immunodeficiency associated with DOCK8 mutations

Revised diagnostic criteria and classification for the autoimmune lymphoproliferative syndrome (ALPS): report from the 2009 NIH International Workshop

Monoclonal antibody therapies for the treatment of relapsing-remitting multiple sclerosis: differentiating mechanisms and clinical outcomes

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285-297

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P31

scholarly article

review article

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10.1080/08916934.2016.1183658

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P433

http://www.w3.org/2001/XMLSchema#string

P478

http://www.w3.org/2001/XMLSchema#string

P577

2016-05-20T00:00:00Z

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P698

27207228

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Rare autoimmune disorders with Mendelian inheritance.

about

P2860

P2860

Rare autoimmune disorders with Mendelian inheritance.

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P577

P698

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P577

P698