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The Journal of Investigative Dermatology|July 2, 2016
The Exonuclease Trex2 Shapes Psoriatic PhenotypeJoan Manils, Eduard Casas, Arnau Viña-Vilaseca, et al.American Journal of Human Genetics|March 16, 2007
Heterozygous mutations in TREX1 cause familial chilblain lupus and dominant Aicardi-Goutieres syndromeGillian Rice, William G Newman, John Dean, et al.Journal of Autoimmunity|March 23, 2017
DNase-active TREX1 frame-shift mutants induce serologic autoimmunity in miceTomomi Sakai, Takuya Miyazaki, Dong-Mi Shin, et al.Oncotarget|June 20, 2015
Multifaceted role of TREX2 in the skin defense against UV-induced skin carcinogenesisJoan Manils, Diana Gómez, Mercè Salla-Martret, et al.Human Mutation|April 18, 2013
Synonymous mutations in RNASEH2A create cryptic splice sites impairing RNase H2 enzyme function in Aicardi-Goutières syndromeGillian I Rice, Martin A M Reijns, Stephanie R Coffin, et al.Nature Genetics|July 31, 2007
Mutations in the gene encoding the 3'-5' DNA exonuclease TREX1 are associated with systemic lupus erythematosusMin Ae Lee-Kirsch, Maolian Gong, Dipanjan Chowdhury, et al.Pageof 5