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1 te the conversion of l-serine to d-serine by serine racemase.
2 porin 4, actin, and glutamine synthetase and serine racemase.
3 nd is created by conversion from L-serine by serine racemase.
4 zation of L- to D-serine by a membrane-bound serine racemase.
6 lacking the predicted transmembrane domain, serine racemase activity was detected in the cytoplasm.
7 n was overexpressed in Escherichia coli, and serine racemase activity was detected in the membrane bu
9 the astrocytic d-serine-synthesizing enzyme serine racemase after CCI injury improved synaptic plast
10 reversibly converting l-serine to d-serine, serine racemase also deaminates serine via beta-eliminat
12 -8)), whereas a variant in SRR (that encodes serine racemase and is associated with schizophrenia) co
13 d-serine is synthesized from its l-isomer by serine racemase and is metabolized by the D-amino acid o
14 oxyaspartate follow this trend, with both WT serine racemase and the S84N mutant being competitively
16 urial components of rat spinal nerve contain serine racemase, and western blot analysis detected the
17 tions of D-serine and it biosynthetic enzyme serine racemase approximate the distribution of NMDA rec
19 and fibroblasts, and both cell types showed serine racemase expression by immunofluorescence and Wes
20 d modulate neuronal activity in the CNS, but serine racemase expression in the PNS has not been repor
23 two genetically modified mouse strains: the serine racemase homozygous knockout (SR-/-) and glycine
27 tected d-serine and its synthesizing enzyme, serine racemase, in the retinas of several vertebrate sp
28 ded periods, the broad expression pattern of serine racemase indicates it to be a host enzyme whose a
30 enzymatically depleting D-serine or by using serine racemase knock-out (SR-KO) mice, confirming its s
31 increase the NMDAR potentials in slices from serine racemase knock-out mice, which are devoid of D-se
32 We utilized two genetic mouse models, the serine racemase knockout (SR-/-) and the glycine transpo
34 blished model of chronic NMDAR hypofunction, serine racemase knockout (SRKO) mice, and their wild-typ
36 O-Lys(114) hydrogen-bonding network in human serine racemase lowers the pKa of the Ser(84)re-face bas
38 olymerase chain reaction, further confirming serine racemase mRNA in Schwann cells and fibroblasts.
39 ptor (NMDAR) hypofunction, and thus used the serine racemase-null mutant mouse (SR(-/-)), which has l
40 e enzyme responsible for D-serine synthesis (serine racemase) or blocking NMDA receptor glycine coago
46 ow that the biosynthetic enzyme of d-serine, serine racemase (SR), is expressed almost entirely by ne
49 ale genome-wide association study identified serine racemase (SR), the enzyme that produces the NMDAR
56 ession quantitative trait locus of the human serine racemase (SRR) gene, was associated with fear-rel
59 There is currently great interest in human serine racemase, the enzyme responsible for producing th
61 pe mice as well mice deficient in microglial serine racemase (TMEM119creErt2:SRRfl/fl) or neuronal Gl