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1 des the purine recycling enzyme hypoxanthine-guanine phosphoribosyltransferase.
2 sed by deficiency of the enzyme hypoxanthine-guanine phosphoribosyltransferase.
3 lanation for the specificity of hypoxanthine-guanine phosphoribosyltransferase, a key enzyme in the p
4 Mutants deficient in hypoxanthine-xanthine-guanine phosphoribosyltransferase activity were used as
5 utant parasite lacking hypoxanthine-xanthine-guanine phosphoribosyltransferase and a T. gondii cDNA l
6 ynthesis and relies primarily on adenine and guanine phosphoribosyltransferases (APRTase and GPRTase)
11 on of 8 x 10(-3) in the nuclear hypoxanthine-guanine phosphoribosyltransferase gene, and a clear and
15 adenine phosphoribosyltransferase (APRT) and guanine phosphoribosyltransferase (GPRT) that constitute
17 tains the selectable marker Escherichia coli guanine phosphoribosyltransferase (gpt) linked to a TGFb
18 Homozygous null mutants of the hypoxanthine-guanine phosphoribosyltransferase (hgprt) and adenine ph
19 to be good inhibitors of human hypoxanthine-guanine phosphoribosyltransferase (HGPRT) and Plasmodium
20 d identity with the L. donovani hypoxanthine-guanine phosphoribosyltransferase (HGPRT) and significan
21 vages purines primarily through hypoxanthine-guanine phosphoribosyltransferase (HGPRT) and xanthine p
22 We here demonstrate that human hypoxanthine guanine phosphoribosyltransferase (HGPRT) converts T-705
23 complexes of Toxoplasma gondii hypoxanthine-guanine phosphoribosyltransferase (HGPRT) have been dete
27 es of the purine salvage enzyme hypoxanthine-guanine phosphoribosyltransferase (HGPRT) of the apicomp
29 To dissect the contributions of hypoxanthine-guanine phosphoribosyltransferase (HGPRT), adenine phosp
30 ucture of the Toxoplasma gondii hypoxanthine-guanine phosphoribosyltransferase (HGPRT)-xanthosine 5'-
35 leoside phosphorylase (PNP) and hypoxanthine-guanine phosphoribosyltransferase (HGPRTase) catalyze N-
37 e are similar to those of human hypoxanthine-guanine phosphoribosyltransferase (HGPRTase) despite dis
39 lations on two enzymes: a human hypoxanthine-guanine-phosphoribosyltransferase (HGPRTase) and its ana
40 the purine biosynthetic enzyme hypoxanthine-guanine phosphoribosyltransferase (HPRT) cause the intra
42 onal promoter and exon 1 of the hypoxanthine-guanine phosphoribosyltransferase (HPRT) gene in the mou
43 ced mutation frequencies at the hypoxanthine guanine phosphoribosyltransferase (HPRT) locus in diploi
44 sociated with cRSS sites at the hypoxanthine-guanine phosphoribosyltransferase (HPRT) locus in periph
45 rder caused by mutations of the hypoxanthine guanine phosphoribosyltransferase (HPRT) purine biosynth
46 mutations were detected in the hypoxanthine-guanine phosphoribosyltransferase (HPRT) reporter gene i
48 guanine through the activity of hypoxanthine-guanine phosphoribosyltransferase (HPRT) to supply the c
49 somatic mutations (Mfs) at the hypoxanthine-guanine phosphoribosyltransferase (HPRT)-reporter gene i
52 mphoblastoid cells in the human hypoxanthine-guanine-phosphoribosyltransferase (HPRT) gene and compar
53 These genes included those for hypoxanthine-guanine phosphoribosyltransferase (hpt), adenylosuccinat
54 defined by the enzymes hypoxanthine-xanthine-guanine phosphoribosyltransferase (HXGPRT) and adenosine
55 xpression of T. gondii hypoxanthine-xanthine-guanine phosphoribosyltransferase (HXGPRT) in stable tra
58 ransgene (Tg; inserted into the hypoxanthine-guanine phosphoribosyltransferase locus) that enables in
59 One potential new target is hypoxanthine-guanine phosphoribosyltransferase (MtHGPRT), a key enzym
60 ated a cell line derived from a hypoxanthine-guanine phosphoribosyltransferase negative (HPRT-) HT108
61 and Arg(63), in contrast to the hypoxanthine-guanine phosphoribosyltransferases, which use two Mg2+ i
62 possess two purine salvage enzymes: xanthine-guanine phosphoribosyltransferase (XGPRT) and hypoxanthi
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