ライフサイエンスコーパス: guanosine 5'-monophosphate

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1 e or guanylate, inosine 5'-monophosphate and guanosine-5'-monophosphate).

2 is independent of global elevation of cyclic guanosine 5'-monophosphate.

3 Evidence is presented for complexation of guanosine 5'-monophosphate 2-methylimidazolide (2-MeImpG

4 dazolide derivatives of nucleotides, such as guanosine 5'-monophosphate 2-methylimidazolide (2-MeImpG

5 olycytidylic acid-directed polymerization of guanosine 5'-monophosphate 2-methylimidazolide (2-MeImpG

6 the concentration of the activated monomer, guanosine 5'-monophosphate 2-methylimidazolide, 2-MeImpG

7 These derivatives are guanosine 5'-monophosphate (5'GMP), guanosine 5'-monopho

8 s potentiation by 5'-ribonucleotides such as guanosine-5'-monophosphate and inosine 5'-monophosphate,

9 where TMA is [(CH(3))(4)N](+) and 5'-GMP is guanosine 5'-monophosphate, and K(2)(5'-GMP), containing

10 '-monophosphate, thymidine-5'-monophosphate, guanosine-5'-monophosphate, and cytidine-5'-monophosphat

11 ells to H(2)S increases intracellular cyclic guanosine 5'-monophosphate (cGMP) in a NO-dependent mann

12 Cyclic guanosine 5'-monophosphate (cGMP) phosphodiesterase (PDE

13 to synthesize a N-acetyl-(2-aminofluorenyl)-guanosine 5'-monophosphate (dGpAAF) adduct, which was su

14 nd is responsible for the phosphorylation of guanosine 5'-monophosphate (GMP) and dGMP to guanosine 5

15 The crystal structures of the guanosine 5'-monophosphate (GMP) and inosine 5'-monophos

16 arkbound in a fashion similar to that of the guanosine 5'-monophosphate (GMP) and inosine 5'-monophos

17 osphate (ADP) and guanosine conformations of guanosine 5'-monophosphate (GMP) bound to wild type and

18 the hypothesis that nitric oxide (NO) cyclic guanosine 5'-monophosphate (GMP) signaling is deficient

19 Specifically, a known competitive inhibitor, guanosine 5'-monophosphate (GMP), and a synthetic, trans

20 hway is redundant and contains two routes to guanosine-5'-monophosphate (GMP) formation: conversion f

21 inone (H2Q), N-acetyl-tyrosine (N-Ac-Tyr) or guanosine-5'-monophosphate (GMP) was investigated at var

22 del for SurE bound to a potential substrate, guanosine-5'-monophosphate (GMP).

23 onophosphate 2-methylimidazolide (2-MeImpG), guanosine 5'-monophosphate imidazolide (ImpG), and adeno

24 ives are guanosine 5'-monophosphate (5'GMP), guanosine 5'-monophosphate imidazolide (ImpG), and guano

25 In mice, exposure to CS reduced sGC, cyclic guanosine 5'-monophosphate levels, and protein kinase G

26 ine 5'-monophosphate imidazolide (ImpG), and guanosine 5'-monophosphate morpholidate (morpG).

27 ility of G-quartet stacks formed by disodium guanosine 5'-monophosphate (Na25'-GMP).

28 The free energy of binding guanosine 5'-monophosphate (pG) at 30 degrees C is simil

29 lla pneumoniae BlrP1, a light-activated c-di-guanosine 5'-monophosphate phosphodiesterase which consi

30 The Leishmania guanosine 5'-monophosphate reductase (GMPR) and inosine

31 Guanosine-5'-monophosphate reductase (GMPR) catalyzes th

32 f either MLL exon 7 or exon 8 with the GMPS (GUANOSINE 5'-MONOPHOSPHATE SYNTHETASE) gene from chromos

33 its platelet activation by generating cyclic guanosine 5'-monophosphate, which is metabolized by phos

34 itro in reactions supplemented with biotinyl-guanosine 5'-monophosphate, which led to the specific ad

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