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1 e, which encodes the purine recycling enzyme hypoxanthine-guanine phosphoribosyltransferase.
2 disorder caused by deficiency of the enzyme hypoxanthine-guanine phosphoribosyltransferase.
3 ntitative explanation for the specificity of hypoxanthine-guanine phosphoribosyltransferase, a key en
4 pectrum of clinical features associated with hypoxanthine-guanine phosphoribosyltransferase deficienc
5 e pathogenesis and diagnosis of all forms of hypoxanthine-guanine phosphoribosyltransferase deficienc
7 mutant fraction of 8 x 10(-3) in the nuclear hypoxanthine-guanine phosphoribosyltransferase gene, and
11 ly been shown to be good inhibitors of human hypoxanthine-guanine phosphoribosyltransferase (HGPRT) a
12 donovani salvages purines primarily through hypoxanthine-guanine phosphoribosyltransferase (HGPRT) a
13 33% amino acid identity with the L. donovani hypoxanthine-guanine phosphoribosyltransferase (HGPRT) a
15 osphate (IMP) complexes of Toxoplasma gondii hypoxanthine-guanine phosphoribosyltransferase (HGPRT) h
18 Antimutagenic activity was determined at the hypoxanthine-guanine phosphoribosyltransferase (HGPRT) l
19 Two isozymes of the purine salvage enzyme hypoxanthine-guanine phosphoribosyltransferase (HGPRT) o
22 e crystal structure of the Toxoplasma gondii hypoxanthine-guanine phosphoribosyltransferase (HGPRT)-x
23 y a deficiency of the purine salvage enzyme, hypoxanthine-guanine phosphoribosyltransferase (HGPRT).
24 thase (GMPS) or direct salvage of guanine by hypoxanthine-guanine phosphoribosyltransferase (HGPRT).
25 transferase (HGXPRT) and Schistosoma mansoni hypoxanthine-guanine phosphoribosyltransferase (HGPRT).
26 l deficiency of the purine recycling enzyme, hypoxanthine-guanine phosphoribosyltransferase (HGprt).
27 Purine nucleoside phosphorylase (PNP) and hypoxanthine-guanine phosphoribosyltransferase (HGPRTase
28 alarial enzyme are similar to those of human hypoxanthine-guanine phosphoribosyltransferase (HGPRTase
29 Hypoxanthine-guanine phosphoribosyltransferase (HGPRTase
30 Hypoxanthine-guanine phosphoribosyltransferase (HGPRTase
31 ics (MD) simulations on two enzymes: a human hypoxanthine-guanine-phosphoribosyltransferase (HGPRTase
32 city and induced mutation frequencies at the hypoxanthine guanine phosphoribosyltransferase (HPRT) lo
33 genetic disorder caused by mutations of the hypoxanthine guanine phosphoribosyltransferase (HPRT) pu
34 gene encoding the purine biosynthetic enzyme hypoxanthine-guanine phosphoribosyltransferase (HPRT) ca
35 e transcriptional promoter and exon 1 of the hypoxanthine-guanine phosphoribosyltransferase (HPRT) ge
37 junctions associated with cRSS sites at the hypoxanthine-guanine phosphoribosyltransferase (HPRT) lo
39 ype, multiple mutations were detected in the hypoxanthine-guanine phosphoribosyltransferase (HPRT) re
40 way salvages guanine through the activity of hypoxanthine-guanine phosphoribosyltransferase (HPRT) to
41 frequency of somatic mutations (Mfs) at the hypoxanthine-guanine phosphoribosyltransferase (HPRT)-re
42 d by deficiency of the purine salvage enzyme hypoxanthine-guanine phosphoribosyltransferase (HPRT).
43 catalyzed by the X chromosome-linked enzyme hypoxanthine-guanine phosphoribosyltransferase (HPRT).
44 d in human lymphoblastoid cells in the human hypoxanthine-guanine-phosphoribosyltransferase (HPRT) ge
46 lpha) and two with 17alpha or Yalpha and the hypoxanthine guanine phosphoribosyltransferase locus (HP
47 single-copy transgene (Tg; inserted into the hypoxanthine-guanine phosphoribosyltransferase locus) th
49 We have generated a cell line derived from a hypoxanthine-guanine phosphoribosyltransferase negative
50 gle Mg2+ ion and Arg(63), in contrast to the hypoxanthine-guanine phosphoribosyltransferases, which u
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