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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 n transcript accumulation for representative fungal genes by drug-induced elevation of cAMP levels.
13 ed significant homologies with bacterial and fungal genes encoding enzymes that metabolise acetyl gro
14 iency at the onset of saprotrophy in barley, fungal genes encoding hydrolytic enzymes and nutrient tr
15 d to investigate the origin and diversity of fungal genes encoding putative PKSs that are predicted t
17 affects C. neoformans directly, we analyzed fungal gene expression after binding of protective and n
18 matic activities of arginase and urease, and fungal gene expression in the extraradical and intraradi
20 ococcus neoformans elicit diverse effects on fungal gene expression, lipid biosynthesis, susceptibili
24 or forage grasses requires identification of fungal genes for alkaloid biosynthesis, and DNA-mediated
27 endogenous transcript levels of the targeted fungal genes indicating translocation of siRNA molecules
28 nized and natural Pgt isolates to identify a fungal gene named AvrSr35 that is required for Sr35 avir
30 nregulation of key developmentally regulated fungal genes occurs during infection, but vegetative gro
32 induced by the imposed stress on a group of fungal genes playing a key role in the water-transport p
33 N transfer from the fungus to the plant, 11 fungal genes putatively involved in the pathway were ide
34 ive in coat protein coupled with introducing fungal gene sequences simultaneously in sense and antise
35 ng dsRNA in host plants can trigger specific fungal gene silencing and confer resistance to fungal pa
36 e germline X inactivation in nematodes and a fungal gene-silencing mechanism that alters the way we v
37 noculation of BSMV RNAi constructs generated fungal gene-specific siRNA molecules in systemic leaves
39 olves both innate and adaptive immunity, but fungal genes that modulate these processes are poorly un
42 e the extent to which virus infection alters fungal gene transcript accumulation and to assess the de
43 the wild-type during early pathogenesis, 106 fungal genes were also induced in the wild-type but not
44 show that these aphid genes are derived from fungal genes, which have been integrated into the genome
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