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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
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
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
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
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
31 ntial biomolecule that is synthesized by myo-inositol monophosphatase (IMPase) from inositol monophos
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
36 first step in inositol biosynthesis, nor the inositol monophosphatase (IMPase), which generates myo-i
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
45 oader than those of bacterial and eukaryotic inositol monophosphatases (it can also act as a fructose
48 s are pretreated with Li(+), an inhibitor of inositol monophosphatases that prevents PIP2 resynthesis
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