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SAMHD1, IVS14AS, G-C, -1
National Institutes of Health
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AICARDI-GOUTIERES SYNDROME 5 (disorder)
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Semantic Scholar uses AI to extract papers important to this topic.
2017
2017
A SAMHD1 mutation associated with Aicardi–Goutières syndrome uncouples the ability of SAMHD1 to restrict HIV‐1 from its ability to downmodulate type I interferon in humans
Tommy White
,
Alberto Brandariz-Nuñez
,
+5 authors
F. Diaz-Griffero
Human Mutation
2017
Corpus ID: 205923594
Mutations in the human SAMHD1 gene are known to correlate with the development of the Aicardi–Goutières syndrome (AGS), which is…
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2016
2016
Substrate Specificity of SAMHD1 Triphosphohydrolase Activity Is Controlled by Deoxyribonucleoside Triphosphates and Phosphorylation at Thr592.
Sunbok Jang
,
Xiaohong Zhou
,
Jinwoo Ahn
Biochemistry
2016
Corpus ID: 40446247
The sterile alpha motif (SAM) and histidine-aspartate (HD) domain containing protein 1 (SAMHD1) constitute a triphosphohydrolase…
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2015
2015
Vpx mediated degradation of SAMHD1 has only a very limited effect on lentiviral transduction rate in ex vivo cultured HSPCs☆
Duo Li
,
E. Schlaepfer
,
+6 authors
R. Speck
Stem Cell Research
2015
Corpus ID: 24642101
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