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2 ted into aspartate (a nucleotide precursor), uridine monophosphate (a precursor of pyrimidine nucleos
3 l formyltransferase domain in a complex with uridine monophosphate and N-5-formyltetrahydrofolate.
4 ructures of DT in complex with adenyly(3'-5')uridine monophosphate (ApUp) and DT in complex with nico
5 tidine monophosphate (cCMP) and 3',5'-cyclic uridine monophosphate (cUMP) have been reported in multi
6 e), fluoride, or a nucleoside monophosphate (uridine monophosphate, deoxyadenosine monophosphate, and
8 iarrhea virus (PEDV) and identified cytidine/uridine monophosphate kinase 2 (CMPK2) as a potential ho
9 orotate phosphoribosyltransferase, 2.3-fold; uridine monophosphate kinase, 3.2-fold; pyrimidine nucle
10 ng allosteric and substrate binding sites of uridine monophosphate kinase, and suggested that in solu
13 the genome, we determined that the conserved uridine monophosphate phosphoribosyltransferase (UMPS),
14 We find that uric acid directly inhibits uridine monophosphate synthase (UMPS) and consequently r
15 TP1), isocitrate dehydrogenase 1 (IDH1), and uridine monophosphate synthase (UMPS) using CRISPR inter
16 and selected against, such as deficiency of uridine monophosphate synthase, complex vertebral malfor
17 Using genome editing methods, we disrupt uridine monophosphate synthetase (UMPS) in the pyrimidin
18 oorotate dehydrogenase (quinone) (DHODH) and uridine monophosphate synthetase (UMPS), as well as lact
21 AICAr increases orotate levels and decreases uridine monophosphate (UMP) levels, consistent with inhi
22 ated 5'-adenosine monophosphate (AMP) and 5'-uridine monophosphate (UMP) molecules confined in multi-
23 T3Gal-II also catalyzed the conversion of 5'-uridine monophosphate (UMP) to UMP-NeuAc, which was foun
24 ntrations of inosine monophosphate (IMP) and uridine monophosphate (UMP) were only 30% of those found
25 unds 5'-adenosine monophosphate (AMP) and 5'-uridine monophosphate (UMP) were subsequently identified
26 showcase our workflow by annotating N-methyl-uridine monophosphate (UMP), lysomonogalactosyl-monopalm
30 eads to build-up of the pathway intermediate uridine monophosphate, which is in turn degraded by a co