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1 lindemuthianum, causal agent of common bean anthracnose.
2 nd quantitative trait loci for resistance to anthracnose, a damaging fungal pathogen of yam, and seve
3 nt, seed alkaloid content, and resistance to anthracnose and Phomopsis stem blight; and, (iii) define
5 eir antifungal activity against post-harvest anthracnose and their effects on the storage behaviour (
7 bacterial angular leaf spot (ALS) and fungal anthracnose (AR) pathogens, but the underlying molecular
12 ategy to elucidate metabolome changes in the anthracnose-causing hemibiotrophic sorghum pathogen, Col
13 duced weight loss, oxidative stress, and the anthracnose (Colletotrichum gloeosporioides) incidence,
15 cnose resistance locus identified in another anthracnose-differential line, SC414-12E, indicating thi
16 nt inbred lines (RILs) derived from crossing anthracnose-differentials QL3 (96 RILs) and IS18760 (127
19 crop globally; its production is hampered by anthracnose disease caused by the fungal pathogen Collet
21 hemi-biotrophic fungal pathogen that causes anthracnose disease in Medicago and other closely relate
22 sion dataset of pepper fruits in response to anthracnose disease in order to contribute for future pe
23 provided a total systemic protection against anthracnose disease in strawberry, accompanied by the ex
26 fumigation had positive effects on enhancing anthracnose disease resistance during storage and also g
29 that the transgenic lines were resistant to anthracnose disease-causing C. gloeosporioides in compar
32 h RIL populations were highly susceptible to anthracnose in Florida and Georgia, while in Puerto Rico
34 Hass and Ryan avocados significantly reduced anthracnose incidence compared to prochloraz and the unt
35 Although TO fumigation significantly reduced anthracnose incidence in both naturally infected cultiva
36 cantly up- and down-regulated in response to anthracnose infection, whereas polyploid duplicates are
38 Colletotrichum destructivum, showed necrotic anthracnose lesions in non-transformed control leaves, w
39 wing drosophila, Drosophila suzukii, and the anthracnose pathogen Colletotrichum fioriniae are an imp
40 imately, the ability of the maize (Zea mays) anthracnose pathogen Colletotrichum graminicola to infec
41 a pachyrhizi and Puccinia emaculata, and one anthracnose pathogen, Colletotrichum trifolii, on the ab
42 sis, known to be elicited by Colletotrichum (anthracnose) pathogen infection in avocado, is one enric
43 recombination events were evaluated against anthracnose pathotypes from Arkansas (2), Puerto Rico (2
44 eport identification and characterization of ANTHRACNOSE RESISTANCE GENE 2 (ARG2) encoding a nucleoti
45 de-binding leucine-rich repeat receptor gene ANTHRACNOSE RESISTANCE GENE1 (ARG1) that is completely n
48 omic region on chromosome 4 overlaps with an anthracnose resistance locus identified in another anthr
52 of plant R genes and confers broad-spectrum anthracnose resistance when transferred into susceptible
53 control of vernalization responsiveness and anthracnose resistance, as well as a single locus regula
54 loci conferring vernalization independence, anthracnose resistance, low alkaloids and Phomopsis stem
55 s, RCT1 provides a novel resource to develop anthracnose-resistant alfalfa cultivars and contributes
57 n choice tests, blueberry fruit treated with anthracnose solutions containing spores from either fiel
58 resistance to both southern leaf blight and anthracnose stalk rot caused by Cochliobolis heterostrop