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1 nfirm function of the protein encoded by the fungal gene.
2 large number of introns for, we believe, any fungal gene.
3 cilitated identification of highly expressed fungal genes.
4 n predicted from homologies to bacterial and fungal genes.
5 evidence for RNA-directed DNA methylation of fungal genes.
6 n to affect the transcription of a number of fungal genes.
7 to be closely related to any other animal or fungal genes, and instead are closely related to pks gen
8 ons match plant positions) when aligned with fungal genes are also highly enriched for triple matches
9 ilability structures the distribution of ECM fungal genes associated with SOM decay and, specifically
10 n transcript accumulation for representative fungal genes by drug-induced elevation of cAMP levels.
11 med phcA, that has homology to a filamentous fungal gene called het-c.
12 lassezia spp. accounting for the majority of fungal gene copies.
13                                          The fungal gene encoding 6-methylsalicylic acid synthase fro
14 ed significant homologies with bacterial and fungal genes encoding enzymes that metabolise acetyl gro
15 iency at the onset of saprotrophy in barley, fungal genes encoding hydrolytic enzymes and nutrient tr
16 d to investigate the origin and diversity of fungal genes encoding putative PKSs that are predicted t
17                                              Fungal genes encoding putative secondary metabolite clus
18  affects C. neoformans directly, we analyzed fungal gene expression after binding of protective and n
19 base for mycologists to conveniently explore fungal gene expression and alternative splicing.
20  analysis revealed major temporal changes in fungal gene expression during plant infection.
21 matic activities of arginase and urease, and fungal gene expression in the extraradical and intraradi
22          Determination and interpretation of fungal gene expression profiles based on digital reconst
23 ococcus neoformans elicit diverse effects on fungal gene expression, lipid biosynthesis, susceptibili
24 in N transport is orchestrated by changes in fungal gene expression.
25 mulation in hypovirus-mediated alteration of fungal gene expression.
26 s a significant and persistent alteration of fungal gene expression/transcript accumulation.
27 or forage grasses requires identification of fungal genes for alkaloid biosynthesis, and DNA-mediated
28                                         Some fungal genes for trichothecene biosynthesis (Tri genes)
29 on indicated the likely involvement of these fungal genes in pathogenicity.
30 duce double-stranded RNAs (dsRNAs) targeting fungal genes in the foliar and postharvest pathogen Botr
31 ntify the presence of histoplasmosis causing fungal genes, in whole blood or bronchoalveolar lavage (
32 endogenous transcript levels of the targeted fungal genes indicating translocation of siRNA molecules
33 luminescence pathway that combines plant and fungal genes is more compact, not dependent on availabil
34 nized and natural Pgt isolates to identify a fungal gene named AvrSr35 that is required for Sr35 avir
35                    In this study, four rumen fungal genes (nf2152, nf2215, nf2523, and pr2455) were i
36 nregulation of key developmentally regulated fungal genes occurs during infection, but vegetative gro
37                To better reflect features of fungal gene organization, we enhanced the intron submode
38  induced by the imposed stress on a group of fungal genes playing a key role in the water-transport p
39  N transfer from the fungus to the plant, 11 fungal genes putatively involved in the pathway were ide
40 riation in the data (70-79%), with plant and fungal gene regions providing the clearest distinction b
41                       We have identified the fungal genes related to sexual reproduction in desert tr
42 ive in coat protein coupled with introducing fungal gene sequences simultaneously in sense and antise
43 ng dsRNA in host plants can trigger specific fungal gene silencing and confer resistance to fungal pa
44 e germline X inactivation in nematodes and a fungal gene-silencing mechanism that alters the way we v
45 noculation of BSMV RNAi constructs generated fungal gene-specific siRNA molecules in systemic leaves
46                                  Many of the fungal genes that have been the focus of this co-evoluti
47 olves both innate and adaptive immunity, but fungal genes that modulate these processes are poorly un
48     In view of its homology to these related fungal genes, the pH-dependent expression of P. carinii
49 e used homology to characterize bacterial or fungal genes to predict the genes involved in the beta-k
50                                          The fungal gene ToxA encodes a 17.2-kD pre-pro-protein that
51 e the extent to which virus infection alters fungal gene transcript accumulation and to assess the de
52 the wild-type during early pathogenesis, 106 fungal genes were also induced in the wild-type but not
53 show that these aphid genes are derived from fungal genes, which have been integrated into the genome