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The human TREX2 3' -> 5'-exonuclease structure suggests a mechanism for efficient nonprocessive DNA catalysis.
Functional consequences of the RNase H2A subunit mutations that cause Aicardi-Goutieres syndrome.
Lesion bypass of N2-ethylguanine by human DNA polymerase iota.
RNaseH2 mutants that cause Aicardi-Goutieres syndrome are active nucleases.
DNA binding induces active site conformational change in the human TREX2 3'-exonuclease.
The structure of the mammalian RNase H2 complex provides insight into RNA.NA hybrid processing to prevent immune dysfunction.
Defects in DNA degradation revealed in crystal structures of TREX1 exonuclease mutations linked to autoimmune disease.
The SAMHD1 dNTP Triphosphohydrolase Is Controlled by a Redox Switch.