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Query author contributions in Reactome

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Details on Person Hollis, Thomas

Class:IdPerson:3244615
_displayNameHollis, Thomas
_timestamp2013-03-28 05:14:38
created[InstanceEdit:3244632] Shamovsky, V, 2013-03-28
firstnameThomas
initialT
surnameHollis
(author)[LiteratureReference:3244662] The TREX1 exonuclease R114H mutation in Aicardi-Goutières syndrome and lupus reveals dimeric structure requirements for DNA degradation activity
[LiteratureReference:3247886] The crystal structure of TREX1 explains the 3' nucleotide specificity and reveals a polyproline II helix for protein partnering
[LiteratureReference:3247919] Dominant mutation of the TREX1 exonuclease gene in lupus and Aicardi-Goutieres syndrome
[LiteratureReference:3247939] Mutations in the gene encoding the 3'-5' DNA exonuclease TREX1 are associated with systemic lupus erythematosus
[LiteratureReference:3247960] Defects in DNA degradation revealed in crystal structures of TREX1 exonuclease mutations linked to autoimmune disease
[LiteratureReference:3247963] The human TREX2 3' -> 5'-exonuclease structure suggests a mechanism for efficient nonprocessive DNA catalysis
[LiteratureReference:3247970] The TREX1 double-stranded DNA degradation activity is defective in dominant mutations associated with autoimmune disease
[LiteratureReference:3247972] DNA binding induces active site conformational change in the human TREX2 3'-exonuclease
[LiteratureReference:3248000] Heterozygous mutations in TREX1 cause familial chilblain lupus and dominant Aicardi-Goutieres syndrome
[LiteratureReference:8866603] Aicardi-Goutieres syndrome gene and HIV-1 restriction factor SAMHD1 is a dGTP-regulated deoxynucleotide triphosphohydrolase
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No pathways have been reviewed or authored by Hollis, Thomas (3244615)