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1 anism for catalysis in one of these enzymes, adenine phosphoribosyltransferase.
2 nes for primosomal replication protein N and adenine phosphoribosyltransferase.
3 opurine as a fluorescent substrate for yeast adenine phosphoribosyltransferase.
4 ream of a gene (apt) that apparently encodes adenine phosphoribosyltransferase and is transcribed fro
5 ic activities, Km values, and Vmax values of adenine phosphoribosyltransferase and of hypoxanthine ph
6 recycling MTA from the polyamine pathway via adenine phosphoribosyltransferase and recycling MTR to m
7                                    Using the adenine phosphoribosyltransferase (APRT(+)) --> APRT(-)
8 rts to the contrary, we found no evidence of adenine phosphoribosyltransferase (APRT) activity when p
9 ated two major parallel pathways mediated by adenine phosphoribosyltransferase (APRT) and guanine pho
10                                              Adenine phosphoribosyltransferase (APRT) and hypoxanthin
11                                              Adenine phosphoribosyltransferase (APRT) deficiency in h
12                                              Adenine phosphoribosyltransferase (APRT) deficiency is a
13                                              Adenine phosphoribosyltransferase (APRT) deficiency is a
14                                   The enzyme adenine phosphoribosyltransferase (APRT) functions to sa
15  chromosomal copies of the 3' portion of the adenine phosphoribosyltransferase (APRT) gene (targets)
16 ense codons in four of the five exons of the adenine phosphoribosyltransferase (aprt) gene and have f
17             The promoter region of the mouse adenine phosphoribosyltransferase (aprt) gene contains o
18 ranscribed and nontranscribed strands of the adenine phosphoribosyltransferase (APRT) gene in Chinese
19 us in situ hybridization with a Z-4-specific adenine phosphoribosyltransferase (APRT) gene revealed t
20           Partial tandem duplications of the adenine phosphoribosyltransferase (APRT) gene then were
21 finity to a specific site within the hamster adenine phosphoribosyltransferase (APRT) gene was modifi
22 o contain a tandem duplication of the native adenine phosphoribosyltransferase (APRT) gene with an I-
23 rked amplification and overexpression of the adenine phosphoribosyltransferase (APRT) gene.
24 tion of the CpG island upstream of the mouse adenine phosphoribosyltransferase (Aprt) gene.
25         Administration of drugs that inhibit adenine phosphoribosyltransferase (APRT) in HPRT-deficie
26 uanine phosphoribosyltransferase (hgprt) and adenine phosphoribosyltransferase (aprt) loci were creat
27  recombination between direct repeats at the adenine phosphoribosyltransferase (APRT) locus in ERCC1-
28 lation-associated silencing of the autosomal adenine phosphoribosyltransferase (Aprt) locus occurs in
29  are efficiently repaired in both strands of adenine phosphoribosyltransferase (APRT) locus, in eithe
30                                Knockdown for adenine phosphoribosyltransferase (APRT) or nicotinamide
31 nRNP A1 was demonstrated with mutant hamster adenine phosphoribosyltransferase (aprt) transcripts tha
32 e-guanine phosphoribosyltransferase (HGPRT), adenine phosphoribosyltransferase (APRT), and adenosine
33 at encode two potentially different forms of adenine phosphoribosyltransferase (APRT).
34                                              Adenine phosphoribosyltransferase (APRT, EC 2.4.2.7) cat
35                                          The adenine phosphoribosyltransferase (APRTase) from Giardia
36                                              Adenine phosphoribosyltransferase (APRTase) is a widely
37                        Here, we developed an adenine phosphoribosyltransferase (APT)-based RNAi techn
38 om the altered expression of a gene encoding adenine phosphoribosyltransferase (APT1), an enzyme that
39                     Hereditary deficiency of adenine phosphoribosyltransferase causes 2,8-dihydroxyad
40  allograft loss in patients with undiagnosed adenine phosphoribosyltransferase deficiency and the nee
41 f ES cells led to accumulation of cells with adenine phosphoribosyltransferase deficiency and UPD.
42                                              Adenine phosphoribosyltransferase deficiency is a rare a
43                                Patients with adenine phosphoribosyltransferase deficiency showed simi
44                   We describe a patient with adenine phosphoribosyltransferase deficiency who was dia
45                               The reversible adenine phosphoribosyltransferase enzyme (APRT) is essen
46                             We have used the adenine phosphoribosyltransferase gene (APRT; 16q24) to
47 erozygous deficiency for the autosomal Aprt (adenine phosphoribosyltransferase) gene was tested for i
48                In this paper we show how the adenine phosphoribosyltransferase locus in CHO cells can
49                     On the chromosome at the adenine phosphoribosyltransferase locus, however, this s
50  knockout mutations for the selectable Aprt (adenine phosphoribosyltransferase) locus and the Atm loc
51                          The catalysis of an adenine phosphoribosyltransferase reaction by this mutan
52                   Mice heterozygous at Aprt (adenine phosphoribosyltransferase) were used as a model