A Stable Mixed Chimera After SCT with RIC in an Infant with IκBα Hypermorphic Mutation.

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Human IκBα Gain of Function: a Severe and Syndromic Immunodeficiency.

P2860

Q39361295-1A821015-90F3-47E6-9A16-BFE1B2A3284D

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A Stable Mixed Chimera After SCT with RIC in an Infant with IκBα Hypermorphic Mutation.

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http://www.wikidata.org/entity/Q50215511

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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

@yue

2017年學術文章

@zh-hant

name

A Stable Mixed Chimera After SCT with RIC in an Infant with IκBα Hypermorphic Mutation.

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A Stable Mixed Chimera After SCT with RIC in an Infant with IκBα Hypermorphic Mutation.

@nl

type

Item

label

A Stable Mixed Chimera After SCT with RIC in an Infant with IκBα Hypermorphic Mutation.

@en

A Stable Mixed Chimera After SCT with RIC in an Infant with IκBα Hypermorphic Mutation.

@nl

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A Stable Mixed Chimera After SCT with RIC in an Infant with IκBα Hypermorphic Mutation.

@en

A Stable Mixed Chimera After SCT with RIC in an Infant with IκBα Hypermorphic Mutation.

@nl

P1476

A Stable Mixed Chimera After SCT with RIC in an Infant with IκBα Hypermorphic Mutation.

@en

P2093

Kohsuke Imai

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

Masatoshi Takagi

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

Teppei Ohkawa

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

P2860

Defective lymphoid organogenesis underlies the immune deficiency caused by a heterozygous S32I mutation in IκBα.

A hypermorphic IkappaBalpha mutation is associated with autosomal dominant anhidrotic ectodermal dysplasia and T cell immunodeficiency.

Reduced-intensity conditioning for allogeneic stem cell transplant in primary immune deficiencies.

Reduced-intensity conditioning hematopoietic SCT for pediatric patients with LAD-1: clinical efficacy and importance of chimerism.

Hematopoietic stem cell transplantation for 30 patients with primary immunodeficiency diseases: 20 years experience of a single team.

A rapid screening method to detect autosomal-dominant ectodermal dysplasia with immune deficiency syndrome.

Long-term outcome following hematopoietic stem-cell transplantation in Wiskott-Aldrich syndrome: collaborative study of the European Society for Immunodeficiencies and European Group for Blood and Marrow Transplantation

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s10875-017-0375-9

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413-414

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scholarly article

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10.1007/S10875-017-0375-9

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

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

P478

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

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Tomohiro Morio

M Nagasawa

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2017-02-21T00:00:00Z

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

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28224354

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

A Stable Mixed Chimera After SCT with RIC in an Infant with IκBα Hypermorphic Mutation.

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P2860

P2860

A Stable Mixed Chimera After SCT with RIC in an Infant with IκBα Hypermorphic Mutation.

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P2888

P304

P31

P356

P433

P478

P50

P577

P698

P356

P1433

P1476

P2093

P2860

P2888

P304

P31

P356

P433

P478

P50

P577

P698