Matches in Nanopublications for { ?s ?p "[By enzymatically characterizing Aicardi-Goutières syndrome (AGS)-associated SAMHD1 mutations and mutations in the allosteric dGTP-binding site of SAMHD1 for defects in RNase or dNTPase activity, we identify SAMHD1 point mutants that cause loss of one or both functions.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP1202879.RAAsEO-FGqJ6JGBJp0nvEUJIcjiyUE50J9YScTToUUa1U130_assertion description "[By enzymatically characterizing Aicardi-Goutières syndrome (AGS)-associated SAMHD1 mutations and mutations in the allosteric dGTP-binding site of SAMHD1 for defects in RNase or dNTPase activity, we identify SAMHD1 point mutants that cause loss of one or both functions.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1202879.RAAsEO-FGqJ6JGBJp0nvEUJIcjiyUE50J9YScTToUUa1U130_provenance.
- NP880399.RAeZwu0Ske161R24ETjpYXW7vJqJRyrPPRC_GoMe141jc130_assertion description "[By enzymatically characterizing Aicardi-Goutières syndrome (AGS)-associated SAMHD1 mutations and mutations in the allosteric dGTP-binding site of SAMHD1 for defects in RNase or dNTPase activity, we identify SAMHD1 point mutants that cause loss of one or both functions.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP880399.RAeZwu0Ske161R24ETjpYXW7vJqJRyrPPRC_GoMe141jc130_provenance.
- NP1202878.RA8vOTx0by8z_DGLzTaTfMYPuPXnXjs97I1ET8OMZU5To130_assertion description "[By enzymatically characterizing Aicardi-Goutières syndrome (AGS)-associated SAMHD1 mutations and mutations in the allosteric dGTP-binding site of SAMHD1 for defects in RNase or dNTPase activity, we identify SAMHD1 point mutants that cause loss of one or both functions.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1202878.RA8vOTx0by8z_DGLzTaTfMYPuPXnXjs97I1ET8OMZU5To130_provenance.
- NP880389.RAr8kWfjvjV6qmeWEOgAxB4kLwdMtEebVbvPGjONE1eBc130_assertion description "[By enzymatically characterizing Aicardi-Goutières syndrome (AGS)-associated SAMHD1 mutations and mutations in the allosteric dGTP-binding site of SAMHD1 for defects in RNase or dNTPase activity, we identify SAMHD1 point mutants that cause loss of one or both functions.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP880389.RAr8kWfjvjV6qmeWEOgAxB4kLwdMtEebVbvPGjONE1eBc130_provenance.