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1  with that proposed previously for the human inositol monophosphatase.
2  beta-bulge that is conserved in related myo-inositol monophosphatases.
3 ial target of lithium action, in addition to inositol monophosphatases.
4 bundant transcript in axons was mRNA for myo-inositol monophosphatase-1 (Impa1), a key enzyme that re
5  of human inositol monophosphatase, exhibits inositol monophosphatase activity but with substrate spe
6                     The purified protein has inositol monophosphatase activity that is inhibited by t
7           In the inm1Delta:URA3 null mutant, inositol monophosphatase activity was reduced but not el
8 likely related to its known ability to block inositol monophosphatase activity.
9 ich reduces InsP3 levels by interfering with inositol monophosphatase, also failed to alter I(CRAC).
10 id sequence significantly similar to that of inositol monophosphatase, an enzyme that is not involved
11 oM and 302 microM for the wild-type, [Gln217]inositol monophosphatase and [Phe219]inositol monophosph
12 .8 mM and 29.1 mM for the wild-type, [Gln217]inositol monophosphatase and [Phe219]inositol monophosph
13  is suppressed by an inhibitor of the enzyme inositol monophosphatase and hence of the phosphatidylin
14 report that the antioxidant ebselen inhibits inositol monophosphatase and induces lithium-like effect
15 es of lithium were mediated by inhibition of inositol monophosphatase and led to free inositol deplet
16 thium also inhibits other targets, including inositol monophosphatase and structurally related phosph
17  residues are required for activation of myo-inositol monophosphatase, and enzyme activation is enhan
18                             Lithium inhibits inositol monophosphatase at therapeutically effective co
19  other Li(+)-sensitive phosphatases, such as inositol monophosphatase, but molecular modelling of I(1
20 e (ORF) YHR046c (termed INM1), which encodes inositol monophosphatase, characterized the protein Inm1
21                                              Inositol monophosphatase (EC 3.1.3.25) in hyperthermophi
22 [Gln217]inositol monophosphatase and [Phe219]inositol monophosphatase enzymes respectively.
23 [Gln217]inositol monophosphatase and [Phe219]inositol monophosphatase enzymes, respectively, each sho
24 is substantially homologous to that of human inositol monophosphatase, exhibits inositol monophosphat
25                           Candidates include inositol monophosphatases, glycogen synthase kinase-3 (G
26                                Myo-inositol (inositol) monophosphatase (IMP), an enzyme which catalyz
27 ed the expression and tissue distribution of inositol monophosphatase (IMPA1) and characterized its r
28 We previously reported that ebselen inhibits inositol monophosphatase (IMPase) and exhibits lithium-l
29 ces mTOR-independent autophagy by inhibiting inositol monophosphatase (IMPase) and reducing inositol
30                                              Inositol monophosphatase (IMPase) catalyzes the hydrolys
31 ntial biomolecule that is synthesized by myo-inositol monophosphatase (IMPase) from inositol monophos
32                        Lithium sensitive myo-inositol monophosphatase (IMPase) is a pivotal enzyme wh
33 a coli product of the suhB gene, SuhB, is an inositol monophosphatase (IMPase) that is best known as
34     During the course of our analysis of myo-inositol monophosphatase (IMPase), a key enzyme of brain
35            In this context, we examined host inositol monophosphatase (IMPase), reduced levels of whi
36 first step in inositol biosynthesis, nor the inositol monophosphatase (IMPase), which generates myo-i
37 s is that lithium acts through inhibition of inositol monophosphatase (IMPase).
38                                  Li inhibits inositol-monophosphatase (IMPase)-1.
39  previously in prokaryotes and resembles myo-inositol monophosphatases (IMPases).
40 ion of inositol metabolism, we characterized inositol monophosphatase in this yeast.
41 tial for the catalytic activity of mammalian inositol monophosphatase, increase the ellipticity in th
42  mimetic with the potential both to validate inositol monophosphatase inhibition as a treatment for b
43                                              Inositol monophosphatase is a key enzyme in the de novo
44                                              Inositol monophosphatase is a possible target but no bio
45 oader than those of bacterial and eukaryotic inositol monophosphatases (it can also act as a fructose
46 y converted to the final product, DIP, by an inositol monophosphatase-like phosphatase.
47                                              Inositol monophosphatase plays a vital role in the de no
48 s are pretreated with Li(+), an inhibitor of inositol monophosphatases that prevents PIP2 resynthesis
49 d enzymes, inositol-1-phosphate synthase and inositol monophosphatase, were identified.

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