A Spectrum of Mutations in SH2D1A That Causes X-linked Lymphoproliferative Disease and Other Epstein-Barr Virus-associated Illnesses-Reference-Cited by-同舟云学术

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A Spectrum of Mutations in SH2D1A That Causes X-linked Lymphoproliferative Disease and Other Epstein-Barr Virus-associated Illnesses

Published:2002-01 Issue:6 Volume:43 Page:1189-1201
ISSN:1042-8194
Container-title:Leukemia & Lymphoma
language:en
Short-container-title:Leukemia & Lymphoma

Author:

Sumegi Janos,Seemayer Thomas A.,Huang Dali,Davis Jack R.,Morra Massimo,Gross Thomas G.,Yin Luo,Romco Giovanni,Klein Eva,Terhorst Cox,Lanyi Arpad

Publisher

Informa UK Limited

Subject

Cancer Research,Oncology,Hematology

Link

http://www.tandfonline.com/doi/pdf/10.1080/10428190290026240

Reference78 articles.

1. X-LINKED RECESSIVE PROGRESSIVE COMBINED VARIABLE IMMUNODEFICIENCY (DUNCAN'S DISEASE)

2. Helper T cell differentiation: a role for SAP?

3. X-Linked Lymphoproliferative Disease: Twenty-Five Years after the Discovery

4. Epstein--Barr Virus-Negative Boys With Non-Hodgkin Lymphoma Are Mutated in the Sh2D1A Gene, as Are Patients With X-Linked Lymphoproliferative Disease (XLP)

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1. Genetics of Primary Hemophagocytic Lymphohistiocytosis;Advances in Experimental Medicine and Biology;2024

2. Potential pathogenic mechanism of type 1 X-linked lymphoproliferative syndrome caused by a mutation of SH2D1A gene in an infant: A case report;Medicine;2022-10-14

3. Exon skipping caused by a complex structural variation in SH2D1A resulted in X‐linked lymphoproliferative syndrome type 1;Molecular Genetics & Genomic Medicine;2022-01-29

4. Chromosome X-wide Analysis of Positive Selection in Human Populations: Common and Private Signals of Selection and its Impact on Inactivated Genes and Enhancers;Frontiers in Genetics;2021-09-27

5. Chromosome X-wide analysis of positive selection in human populations: from common and private signals to selection impact on inactivated genes and enhancers-like signatures;2021-05-28

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