Deficiency of base excision repair enzyme NEIL3 drives increased predisposition to autoimmunity-Reference-Cited by-同舟云学术

Deficiency of base excision repair enzyme NEIL3 drives increased predisposition to autoimmunity

Published:2016-10-17 Issue:11 Volume:126 Page:4219-4236
ISSN:0021-9738
Container-title:Journal of Clinical Investigation
language:en
Short-container-title:

Author:

Massaad Michel J.,Zhou Jia,Tsuchimoto Daisuke,Chou Janet,Jabara Haifa,Janssen Erin,Glauzy Salomé,Olson Brennan G.,Morbach Henner,Ohsumi Toshiro K.,Schmitz Klaus,Kyriacos Markianos,Kane Jennifer,Torisu Kumiko,Nakabeppu Yusaku,Notarangelo Luigi D.,Chouery Eliane,Megarbane Andre,Kang Peter B.,Al-Idrissi Eman,Aldhekri Hasan,Meffre Eric,Mizui Masayuki,Tsokos George C.,Manis John P.,Al-Herz Waleed,Wallace Susan S.,Geha Raif S.

Publisher

American Society for Clinical Investigation

Subject

General Medicine

Reference82 articles.

1. Clearing the Dead: Apoptotic Cell Sensing, Recognition, Engulfment, and Digestion

2. Apoptosis and autoimmunity

3. Loss-of-function variant in DNASE1L3 causes a familial form of systemic lupus erythematosus

4. GENETIC DISORDERS OF PROGRAMMED CELL DEATH IN THE IMMUNE SYSTEM

5. Accelerated in vitro apoptosis of lymphocytes from patients with systemic lupus erythematosus;Emlen;J Immunol,1994

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