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1 us' phytoplasma, rust fungi, Ustilago smuts, root knot and cyst nematodes, and gall midges.
2                                         Both root-knot and cyst nematodes are endoparasites that have
3           Sedentary endoparasitic nematodes, root-knot and cyst nematodes in particular, as well as g
4 ed within plant roots upon infection by both root-knot and cyst nematodes.
5 nomically important plant parasites, such as root-knot, cyst, and lesion nematodes.
6                   Chlamydosporia in managing root knot disease in eggplant.
7 etween KRP6 overexpression cell cultures and root-knot morphology point toward the involvement of KRP
8  rice agroecosystems of Southeast Asia, rice root knot nematode (Meloidogyne graminicola) significant
9 ntally friendly alternatives for controlling root knot nematode and have the potential to reduce reli
10 rial associate of nematodes, possibly as the root knot nematode evolved to be a highly specialized pa
11 PCR) assay to detect Meloidogyne javanica, a root knot nematode specifically infectious to eggplant.
12 indicate that R. reniformis has replaced the root-knot nematode (Meloidogyne incognita) as the major
13        In addition, SILIP is compatible with root-knot nematode (Meloidogyne spp.) development, and t
14 um is effective and widely used for limiting root-knot nematode (Meloidogyne spp.) yield loss in toma
15                         Here, we report that root-knot nematode (RKN) attack induced a phyB-dependent
16 e to diverse stresses such as water deficit, root-knot nematode (RKN) infection, and UV exposure, wit
17 e organic compounds used by the subterranean root-knot nematode (RKN) Meloidogyne incognita for host
18                     Here, we report that the root-knot nematode (RKN) Meloidogyne incognita induces t
19 mechanisms of Pc for chitosan resistance and root-knot nematode (RKN) parasitism, using transcriptomi
20 t quantitative trait loci (QTL) for southern root-knot nematode (RKN) resistance into individual gene
21            Root penetration and migration of root-knot nematode (RKN) second-stage larvae (L2) did no
22 ematode (BCN), Heterodera schachtii, and the root-knot nematode (RKN), Meloidogyne incognita.
23                           Here, we show that root-knot nematode (RKN; Meloidogyne incognita) infectio
24                                              Root-knot nematode (RKN; Meloidogyne spp.) is a major cr
25                                    Aphid and root-knot nematode assays of Sgt1-2-silenced plants indi
26 ntially secreted proteins may have a role as root-knot nematode effectors that are induced by plant l
27                                         Both root-knot nematode genomes have compacted gene families
28                 The recent completion of two root-knot nematode genomes opens the way for a comparati
29 r genotypes using root tissue harvested from root-knot nematode infected plants at 0, 3, 7 days after
30  early responses of many oxylipins following root-knot nematode infection.
31                                              Root-knot nematode is a very destructive pathogen, to wh
32 ts to analyse the effect of infection by the root-knot nematode Meloidogyne graminicola or treatment
33 e against foliar microbial pathogens and the root-knot nematode Meloidogyne graminicola.
34 ed callose deposition in potato roots during root-knot nematode Meloidogyne hapla infection was inves
35 e cyst nematode Heterodera schachtii and the root-knot nematode Meloidogyne incognita.
36 sceptibility to H. schachtii, but not to the root-knot nematode Meloidogyne incognita.
37 yst nematode Heterodera schachtii and by the root-knot nematode Meloidogyne incognita.
38 T5 function increases resistance against the root-knot nematode Meloidogyne javanica and suggests a p
39              At the same time, the sedentary root-knot nematode Meloidogyne spp. secretes numerous ef
40                In this study, a total of 244 root-knot nematode populations from various hosts from 3
41                                          The root-knot nematode resistance gene Mi from tomato encode
42 rovide a resource for broadening the base of root-knot nematode resistance in tomato and other crops.
43  TRV-Mi construct, Mi-9-mediated heat-stable root-knot nematode resistance was compromised at 32 degr
44 timulated efforts to identify new sources of root-knot nematode resistance.
45 ions were generated and screened for altered root-knot nematode resistance.
46                 A corresponding peptide from root-knot nematode trehalase enabled the identification
47                                Resistance to root-knot nematode was introgressed into cultivated pean
48 et-cyst nematode) and Meloidogyne incognita (root-knot nematode).
49 ich confers resistance to several species of root-knot nematode, is present in many modern tomato cul
50  infestation of roots by the plant-parasitic root-knot nematode, Meloidogyne incognita.
51 es have revealed the cellular changes inside root-knot nematode-induced feeding sites, both in the co
52                It is an obligate parasite of root knot nematodes (Meloidogyne spp.) and preferentiall
53                                              Root knot nematodes (RKNs) penetrate into the root vascu
54 or its morphological similarities with other root knot nematodes (RKNs).
55                                              Root knot nematodes are devastating root pests of econom
56                                          The root knot nematodes Meloidogyne incognita are the most s
57 cognized as a potential biocontrol agent for root knot nematodes, but the fastidious life cycle and t
58 The Mi locus of tomato confers resistance to root knot nematodes.
59  tomato (Lycopersicon esculentum Mill.) with root-knot nematodes (Meloidogyne javanica) encodes a pro
60  tomato Mi-1 gene confers resistance against root-knot nematodes (Meloidogyne spp.) and a biotype of
61                                              Root-knot nematodes (Meloidogyne spp.) are highly evolve
62                                              Root-knot nematodes (Meloidogyne spp.) are the most comm
63                   Mi-1 confers resistance to root-knot nematodes (Meloidogyne spp.), potato aphids (M
64 two additional phloem-feeding insects and to root-knot nematodes (Meloidogyne spp.).
65  resistance as well as basal defense against root-knot nematodes (RKN) and potato aphids.
66                  Remarkably, plant-parasitic root-knot nematodes (RKN) invoke a cytoskeletal response
67                                              Root-knot nematodes (RKN) such as Meloidogyne spp. are a
68 ediate infection and parasitism of plants by root-knot nematodes (RKN).
69                                              Root-knot nematodes (RKN; Meloidogyne species) are plant
70                               Most apomictic root-knot nematodes (RKN; Meloidogyne spp.) have host ra
71                                              Root-knot nematodes (RKNs) (Meloidogyne spp.) are obliga
72                                              Root-knot nematodes (RKNs) induce giant cells (GCs) with
73 chanism by which plants defend against plant root-knot nematodes (RKNs) is largely unknown.
74                                              Root-knot nematodes (RKNs; Meloidogyne spp.) are plant p
75 he tomato Mi gene confers resistance against root-knot nematodes and potato aphids.
76                                              Root-knot nematodes are a major global agricultural pest
77  provided and evolutionary trends within the root-knot nematodes are discussed.
78                           The giant cells of root-knot nematodes are formed by repeated karyokinesis
79                                     Cyst and root-knot nematodes are obligate parasites of economic i
80 hough feeding sites induced by both cyst and root-knot nematodes are surrounded by endodermis during
81                           Cyst nematodes and root-knot nematodes elaborately transform cells within t
82 nd sustainable management strategies against root-knot nematodes in Arkansas.
83                                Both cyst and root-knot nematodes induce specialized long-term feeding
84 d and important group of plant pathogens-the root-knot nematodes Meloidogyne species-which attack mos
85 e expression analysis provides evidence that root-knot nematodes modulate biological pathways involve
86                                          The root-knot nematodes of the genus Meloidogyne are highly
87 , we report the identification of genes from root-knot nematodes predicted to encode PSY-like peptide
88 eviously reported related cyst nematodes and root-knot nematodes revealed a subset of esophageal glan
89                     Plant-parasitic cyst and root-knot nematodes synthesize and secrete a suite of ef
90 to SCN in a way similar to that reported for root-knot nematodes, but opposite to that suggested for
91 Mi-1 confers resistance to Meloidogyne spp. (root-knot nematodes, RKNs) and three phloem-feeding inse
92 ing plant responses to infection by cyst and root-knot nematodes, with a focus on the functions of mi
93 dentary endoparasites that includes cyst and root-knot nematodes.
94 ression in roots infected by plant-parasitic root-knot nematodes.
95 this field, with a focus on the best-studied root-knot nematodes.
96 parasitism and plant nurse cells in cyst and root-knot nematodes.
97 nts were not significantly more resistant to root-knot nematodes.
98 s potential for enhancing crop resistance to root-knot nematodes.
99 ate pathways mediates plant immunity against root-knot nematodes.