Prospects for modulating the CD40/CD40L pathway in the therapy of the hyper-IgM syndrome.

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Prospects for modulating the CD40/CD40L pathway in the therapy of the hyper-IgM syndrome.

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2017 nî lūn-bûn

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2017年の論文

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年學術文章

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2017年學術文章

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Prospects for modulating the CD40/CD40L pathway in the therapy of the hyper-IgM syndrome.

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Prospects for modulating the CD40/CD40L pathway in the therapy of the hyper-IgM syndrome.

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Item

label

Prospects for modulating the CD40/CD40L pathway in the therapy of the hyper-IgM syndrome.

@en

Prospects for modulating the CD40/CD40L pathway in the therapy of the hyper-IgM syndrome.

@nl

prefLabel

Prospects for modulating the CD40/CD40L pathway in the therapy of the hyper-IgM syndrome.

@en

Prospects for modulating the CD40/CD40L pathway in the therapy of the hyper-IgM syndrome.

@nl

P1476

Prospects for modulating the CD40/CD40L pathway in the therapy of the hyper-IgM syndrome

@en

P2093

Bin Yang

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Wen-Chen Suen

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Xiangxue Meng

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P2860

CD40 AND CD154 IN CELL-MEDIATED IMMUNITY

A novel X-linked disorder of immune deficiency and hypohidrotic ectodermal dysplasia is allelic to incontinentia pigmenti and due to mutations in IKK-gamma (NEMO)

Mutations in activation-induced cytidine deaminase in patients with hyper IgM syndrome

X-linked anhidrotic ectodermal dysplasia with immunodeficiency is caused by impaired NF-kappaB signaling

The role of activation-induced cytidine deaminase in antibody diversification, immunodeficiency, and B-cell malignancies

Repeated gene transfer of naked prostacyclin synthase plasmid into skeletal muscles attenuates monocrotaline-induced pulmonary hypertension and prolongs survival in rats

Update on the hyper immunoglobulin M syndromes

The two NF-kappaB activation pathways and their role in innate and adaptive immunity

Clinical, immunologic and genetic analysis of 29 patients with autosomal recessive hyper-IgM syndrome due to Activation-Induced Cytidine Deaminase deficiency.

Mutations of CD40 gene cause an autosomal recessive form of immunodeficiency with hyper IgM.

P304

4-10

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P31

scholarly article

P356

10.1177/1753425917739681

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P433

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

P478

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

P577

2017-11-13T00:00:00Z

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P698

29132233

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P932

6830763

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