Skin infiltration of CD56brightCD16-natural killer cells in a case of X-SCID with Omenn syndrome-like manifestations-Reference-Cited by-同舟云学术

Skin infiltration of CD56brightCD16-natural killer cells in a case of X-SCID with Omenn syndrome-like manifestations

Published:2007-07 Issue:1 Volume:79 Page:81-85
ISSN:0902-4441
Container-title:European Journal of Haematology
language:en
Short-container-title:Eur J Haematol

Author:

Shibata Fumie,Toma Tomoko,Wada Taizo,Inoue Masayuki,Tone Yumi,Ohta Kazuhide,Kasahara Yoshihito,Sano Fumie,Kimura Mitsuaki,Ikeno Mitsuru,Koizumi Shoichi,Yachie Akihiro

Publisher

Wiley

Subject

Hematology,General Medicine

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1600-0609.2007.00874.x/fullpdf

Reference25 articles.

1. Cytokines and immunodeficiency diseases: critical roles of the gammac-dependent cytokines interleukins 2, 4, 7, 9, 15, and 21, and their signaling pathways

2. Molecular Defects in Human Severe Combined Immunodeficiency and Approaches to Immune Reconstitution

3. Transplacentally acquired maternal T lymphocytes in severe combined immunodeficiency: a study of 121 patients

4. Defective human interleukin 2 receptor gamma chain in an atypical X chromosome-linked severe combined immunodeficiency with peripheral T cells.

5. Engrafted maternal T cells in a severe combined immunodeficiency patient express T-cell receptor variable beta segments characterized by a restricted V-D-J junctional diversity

Cited by 33 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. A novel X-linked mutation in IL2RG associated with early-onset inflammatory bowel disease: a case report of twin brothers;Journal of Medical Case Reports;2023-07-18

2. Exhaustion‑like dysfunction of T and NKT cells in an X‑linked severe combined immunodeficiency patient with maternal engraftment by single‑cell analysis;International Journal of Molecular Medicine;2023-02-06

3. Inborn errors of immunity with atopic phenotypes: A practical guide for allergists;World Allergy Organization Journal;2021-02

4. Severe combined immune deficiency;Stiehm's Immune Deficiencies;2020

5. Prominent dermal Langerhans cells in an Omenn syndrome patient with a novel mutation in the IL 2 RG gene;The Journal of Dermatology;2019-11