Genotype, phenotype, and outcomes of nine patients with T-B+NK+ SCID - Test2 - elhamkhani - TriplyDB

Genotype, phenotype, and outcomes of nine patients with T-B+NK+ SCID

Genotype, phenotype, and outcomes of nine patients with T-B+NK+ SCID

http://www.wikidata.org/entity/Q35387846

about

Mechanism-Based Strategies for the Management of Autoimmunity and Immune Dysregulation in Primary Immunodeficiencies Unbalanced Immune System: Immunodeficiencies and Autoimmunity Primary Immune Deficiency Treatment Consortium (PIDTC) report.

P2860

Q28066193-9EEB8187-73F8-45C7-B5D7-33FE0FE341C8 Q28075911-74270865-3C5B-4B53-8E92-8A2950C84E9F Q37649782-AAAA6411-0440-4F86-A074-5B1F539A8406

P2860

Genotype, phenotype, and outcomes of nine patients with T-B+NK+ SCID

http://www.wikidata.org/entity/Q35387846

description

2011 nî lūn-bûn

@nan

2011 թուականի Օգոստոսին հրատարակուած գիտական յօդուած

@hyw

2011 թվականի օգոստոսին հրատարակված գիտական հոդված

@hy

2011年の論文

@ja

2011年論文

@yue

2011年論文

@zh-hant

2011年論文

@zh-hk

2011年論文

@zh-mo

2011年論文

@zh-tw

2011年论文

@wuu

name

Genotype, phenotype, and outcomes of nine patients with T-B+NK+ SCID

@ast

Genotype, phenotype, and outcomes of nine patients with T-B+NK+ SCID

@en

type

label

Genotype, phenotype, and outcomes of nine patients with T-B+NK+ SCID

@ast

Genotype, phenotype, and outcomes of nine patients with T-B+NK+ SCID

@en

prefLabel

Genotype, phenotype, and outcomes of nine patients with T-B+NK+ SCID

@ast

Genotype, phenotype, and outcomes of nine patients with T-B+NK+ SCID

@en

P1433

Q35387846-03F4D1FD-CCA4-44C3-B6DE-BD83D7C82B0E

P1476

Q35387846-25C634D0-80F3-43EF-9D2F-2D3053EB798A

P2093

Q35387846-094C138E-B02C-4ECA-A771-FF862B395A6A

Q35387846-09F9145E-B29E-42CB-9143-2AC97A139247

Q35387846-21435036-921C-4C91-BB00-6DA19684CA0C

Q35387846-310CE949-3903-46B6-94A7-0E315AA30A5B

Q35387846-569907BA-9D3F-499D-91CC-9ED42AACAB1C

Q35387846-642F2167-2A96-40AA-AD0B-CBA7E7AC11BE

Q35387846-6D5A5AC4-C36D-45ED-B831-B4FD6AC9A37E

Q35387846-878ACC7F-9DEB-48B6-9376-DF596998DB27

Q35387846-924D9AF7-0AD9-4777-99C7-5CF68F6DEB4F

Q35387846-94B1D63D-CCCF-4FD5-9CC4-5D22A38CF1DE

P2860

Q35387846-0180EE1D-F247-4520-A1A9-AEB8742EB991

Q35387846-0B2DAC20-18AA-47FA-ABC2-8C34BC6F26F6

Q35387846-0F1E17B5-377E-4065-8E0D-CF23940BBFBE

Q35387846-1274EC1F-2631-4C3F-9CE8-9B0D0D34E093

Q35387846-21C8ED0A-F41E-4C30-A825-63648961C757

Q35387846-2B4519E5-37DB-4141-984D-74B97D148EB0

Q35387846-2D64F494-71F4-4509-9537-D20FA3793B6E

Q35387846-3280AD1C-62FA-4383-97C6-81FE29C00158

Q35387846-44AF379B-980E-48DC-AA46-DBF72CD4DF1D

Q35387846-4FA07804-014C-4D60-A384-CA1E8CCE0AA5

P304

Q35387846-6A41B5F3-5AB7-47B1-9378-4C6183EBA328

P31

Q35387846-26787451-C788-476D-BE57-82B81B8D72C0

P356

Q35387846-A786B2AD-EFD6-40EF-A590-69B5E7EDE131

P433

Q35387846-2F52B65B-96A1-4C47-880E-FB349FBD823A

P478

Q35387846-3ACFFDA9-8E59-4452-8398-7D3B50C6E73B

P50

Q35387846-98FBBF91-6CB9-4A03-9C38-24997112CACF

Q35387846-E24A746A-D50C-4589-AF1E-B7030B85173B

P577

Q35387846-D21D314B-4F4C-4E10-AADA-27A225EF3841

P5875

Q35387846-A9959C6B-E245-4080-940B-BA31A4B7FEE1

P698

Q35387846-C2CD5455-EB51-4129-A036-571FC5AF92CB

P932

Q35387846-20C154D3-598D-4606-9377-29D19E7C4549

P356

J.1399-3046.2011.01563.X

P1433

Pediatric Transplantation

P1476

Genotype, phenotype, and outcomes of nine patients with T-B+NK+ SCID

@en

P2093

Dale T Umetsu

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

David B Lewis

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

David R Berk

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

E Richard Stiehm

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

Elizabeth Dunn

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

Grace P Yu

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

Jennifer M Puck

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

Joseph Roberts

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

Kari C Nadeau

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

Kristina Kavanau

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

P2860

Defective IL7R expression in T(-)B(+)NK(+) severe combined immunodeficiency

Partial V(D)J recombination activity leads to Omenn syndrome

The gene for severe combined immunodeficiency disease in Athabascan-speaking Native Americans is located on chromosome 10p.

Severe combined immunodeficiency caused by deficiency in either the delta or the epsilon subunit of CD3

Primary immunodeficiency diseases: an update from the International Union of Immunological Societies Primary Immunodeficiency Diseases Classification Committee

Complete genomic organization of the human JAK3 gene and mutation analysis in severe combined immunodeficiency by single-strand conformation polymorphism

Interaction of IL-2R beta and gamma c chains with Jak1 and Jak3: implications for XSCID and XCID

Molecular defects in human severe combined immunodeficiency and approaches to immune reconstitution

Structural and functional basis for JAK3-deficient severe combined immunodeficiency

Molecular and biochemical characterization of JAK3 deficiency in a patient with severe combined immunodeficiency over 20 years after bone marrow transplantation: implications for treatment

P304

733-741

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

P31

scholarly article

P356

10.1111/J.1399-3046.2011.01563.X

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

P433

7

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

P478

15

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

P50

Geneviève de Saint Basile

Perrine Knapnougel

P577

2011-08-23T00:00:00Z

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

P5875

51612078

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

P698

21883749

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

P932

3196791

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