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1 phorylase over a wide range of activities of phosphorylase a.
2 D253A:E256R) exhibited an increased K(m) for phosphorylase a.
3 e and inactive forms of human liver glycogen phosphorylase a.
4 suring Ca2+-dependent activation of glycogen phosphorylase a.
5 ion protein specifically bound either PP1 or phosphorylase a.
6 e catalytic subunit or trypsinolysis of [32P]phosphorylase a.
7 re also dephosphorylated preferentially over phosphorylase a.
8 etraacetic acid (EGTA), blocked APAP-induced phosphorylase a activation and necrotic cell death, but
9 d necrotic cell death, but failed to inhibit phosphorylase a activation by the adenosine 3',5'-cyclic
10 h vehicle infused ZDF (ZDF-V), high glycogen phosphorylase a activity was decreased and low synthase
11 vity, and relative activity against glycogen phosphorylase a and C subunit as substrates, the cellula
12 ts of phosphorylase b have been converted to phosphorylase a and examined for their efficacy as subst
15 formed complexes with phosphorylase kinase, phosphorylase a, and glycogen synthase, the primary enzy
16 struct displayed phosphatase activity toward phosphorylase a, and this activity was preferentially in
17 erature, like the phosphorylated form of GP, phosphorylase a, and unlike the dephospho-form, phosphor
18 activation of GSK-3 and dephosphorylation of phosphorylase a as alternative pathways in the stimulati
19 was timed to minimize futile cycling, since phosphorylase a became inhibited by high intracellular g
20 s increased PP1 activity against 32P-labeled phosphorylase a by decreasing the Km of PP1 for phosphor
21 or of the dephosphorylation of (32)P-labeled phosphorylase a by T. cruzi epimastigotes and metacyclic
25 with decreasing affinities to the protamine:phosphorylase a complex, free phosphorylase a, and free
29 MTAP encodes the enzyme methylthioadenosine phosphorylase, a key enzyme in the methionine salvage pa
30 lling pathway involving dephosphorylation of phosphorylase a leading to both activation and transloca
32 rotamine decreases the K(m) of PP2A1 for the phosphorylase a monomer 5-fold and increases the Vmax 17
34 f the basic polypeptide, not associated with phosphorylase a monomer, interacting with the regulatory
35 Using a negative staining approach, maltose phosphorylase, a phosphate-consuming enzyme, can also be
39 The plant VTC2 gene encodes GDP-L-galactose phosphorylase, a rate-limiting enzyme in plant vitamin C
40 lly, BMI1 coprecipitated with polynucleotide phosphorylase, a ribonuclease that is responsible for de
41 ected mutagenesis and kinetic analyses using phosphorylase a, RII peptide, Kemptide, and p-nitropheny
43 ed twofold and greater increases in glycogen phosphorylase a stimulation at 6 hours, which was revers
44 le or no contribution of the cAMP pathway to phosphorylase a stimulation during APAP-induced necrotic
46 inhibited PP1-catalyzed dephosphorylation of phosphorylase a, the GADD34-bound PP1 was an active eIF-
47 (CP-91149) that causes dephosphorylation of phosphorylase a, to determine the relative contributions
50 lytic activity toward the standard substrate phosphorylase a when this enzyme is bound to pRB contain
51 ation by phosphorylase kinase (PhK) produces phosphorylase a, which is active in the absence of AMP.
52 rotamine forms a very tight association with phosphorylase a, which is optimal at a 1:1 protamine:pho
53 of leptin were associated with inhibition of phosphorylase a, which occurred after 4 h of exposure to
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