Possible role of Artemis c.512C>G polymorphic variant in Omenn syndrome☆-Reference-Cited by-同舟云学术

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Possible role of Artemis c.512C>G polymorphic variant in Omenn syndrome☆

Published:2011-01-02 Issue:1 Volume:10 Page:3-4
ISSN:1568-7864
Container-title:DNA Repair
language:en
Short-container-title:DNA Repair

Author:

Mancebo Esther,Recio María José,Martínez-Busto Elena,González-Granado Luis I.,Rojo Pablo,Fernández-Díaz Eva,Ruiz-Contreras Jesús,Paz-Artal Estela,Allende Luis M.

Publisher

Elsevier BV

Subject

Cell Biology,Molecular Biology,Biochemistry

Cited by 5 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. Co-Expression Pattern of Artemis Serine 516 Phosphorylation with Indicators Involving in Differentiation, Proliferation and Apoptosis of Human Anagen Hair Follicles: An Immunofluorescence Double-Staining Study;Frontiers in Bioscience-Landmark;2023-01-16

2. Positive newborn screen: a case of a novel variant in DCLRE1C in a patient with SCID;LymphoSign Journal;2020-03-01

3. Combined Immunodeficiencies;Manual of Molecular and Clinical Laboratory Immunology;2016-01-27

4. Molecular Characteristics, Clinical and Immunologic Manifestations of 11 Children with Omenn Syndrome in East Slavs (Russia, Belarus, Ukraine);Journal of Clinical Immunology;2015-11-23

5. Omenn syndrome does not live by V(D)J recombination alone;Current Opinion in Allergy & Clinical Immunology;2011-12

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