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1 ing plant infection by the pathogenic fungus Ustilago maydis.
2 t early endosome (EE) motility in the fungus Ustilago maydis.
3 chitin synthases (CHSs) in the corn pathogen Ustilago maydis.
4 nthesis from a tryptophan (Trp) precursor in Ustilago maydis.
5 resence of Brh2, the BRCA2 family protein in Ustilago maydis.
6 Rec2 is the single Rad51 paralog in Ustilago maydis.
7 al toxin secreted by the P4 killer strain of Ustilago maydis.
8 charomyces cerevisiae, Candida albicans, and Ustilago maydis.
9 A homologues have been identified to date in Ustilago maydis.
10 al toxin secreted by the P4 killer strain of Ustilago maydis.
11 ein Tsd2 is necessary for DNA replication in Ustilago maydis.
12 meiosis and gene targeting in the corn smut Ustilago maydis.
13 p, a protein required for DNA replication in Ustilago maydis.
14 combinational repair gene from the corn smut Ustilago maydis.
15 for pathogenicity of the corn smut pathogen Ustilago maydis.
16 nal regulator of siderophore biosynthesis in Ustilago maydis.
17 equired for cell proliferation in the fungus Ustilago maydis.
18 espectively, for siderophore biosynthesis in Ustilago maydis.
19 aporthe grisea and the basidiomycete fungus, Ustilago maydis.
20 double-stranded DNA gaps was investigated in Ustilago maydis.
21 matical model of early endosome transport in Ustilago maydis.
23 n/repair proteins to telomere maintenance in Ustilago maydis, a fungus that bears strong resemblance
24 r DNA repair-defective mutants in the fungus Ustilago maydis, a gene encoding a BRCA2 family member,
25 tions of ergosterol biosynthesis inhibitors, Ustilago maydis alters the ratio of linoleic to oleic ac
27 eport that an ortholog of DSS1 is present in Ustilago maydis and associates with Brh2, the BRCA2-rela
28 mology to a recombinational repair gene from Ustilago maydis and contain functional domains to hRAD51
29 iring Enzyme1 in the plant pathogenic fungus Ustilago maydis and demonstrate that the UPR is tightly
30 gens such as the phytopathogenic smut fungi, Ustilago maydis and Microbotryum violaceum, must switch
31 as teliospores of the phytopathogenic fungus Ustilago maydis and spores of the social amoeba Dictyost
32 s of the related, maize-infecting smut fungi Ustilago maydis and Sporisorium reilianum but has a larg
36 s controlling cell fate in the basidiomycete Ustilago maydis, bE5 and bE6, allows cooperative DNA bin
39 ptides from bovine protein standards, yeast, Ustilago maydis cell lysates, and Arabidopsis thaliana l
40 and basidiomycetous pathogens and mushrooms (Ustilago maydis, Coprinus cinereus, Schizophyllum commun
43 logenetically closely related plant pathogen Ustilago maydis encodes a different arsenal of extracell
48 ecific stages of this pathway in maize smut (Ustilago maydis), glucosidase I (Gls1) and glucosidase I
49 In the elongated hyphal cell of the fungus Ustilago maydis, Higuchi et al. now demonstrate that pol
57 le in the homologous recombination system of Ustilago maydis, mediating delivery of Rad51 to single-s
65 Some strains of the plant-pathogenic fungus Ustilago maydis secrete toxins (killer toxins) that are
67 oplasm of maize plants and on engineering of Ustilago maydis strains to secrete Avitagged effectors.
70 omosome ends of Saccharomyces cerevisiae and Ustilago maydis, the initial association of helicase gen
74 -arabinofuranosidases from the basidiomycete Ustilago maydis (UmAbf62A) and ascomycete Podospora anse
75 ignated SFU1 that encodes a homologue of the Ustilago maydis URBS1, a transcriptional repressor of si
76 cturally unrelated antifungal toxin KP4 from Ustilago maydis, whereas structurally similar MtDef2 and
77 he ortholog of the BRCA2 tumor suppressor in Ustilago maydis, works hand in hand with Rad51 to promot
78 ulosa is related to the model plant pathogen Ustilago maydis yet is not a phytopathogen but rather a
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