1 ed within plant roots upon infection by both
root-knot and cyst nematodes.
2 nomically important plant parasites, such as
root-knot,
cyst, and lesion nematodes.
3 etween KRP6 overexpression cell cultures and
root-knot morphology point toward the involvement of KRP
4 rial associate of nematodes, possibly as the
root knot nematode evolved to be a highly specialized pa
5 indicate that R. reniformis has replaced the
root-knot nematode (Meloidogyne incognita) as the major
6 In addition, SILIP is compatible with
root-knot nematode (Meloidogyne spp.) development, and t
7 um is effective and widely used for limiting
root-knot nematode (Meloidogyne spp.) yield loss in toma
8 e to diverse stresses such as water deficit,
root-knot nematode (RKN) infection, and UV exposure, wit
9 e organic compounds used by the subterranean
root-knot nematode (RKN) Meloidogyne incognita for host
10 t quantitative trait loci (QTL) for southern
root-knot nematode (RKN) resistance into individual gene
11 Root penetration and migration of
root-knot nematode (RKN) second-stage larvae (L2) did no
12 ematode (BCN), Heterodera schachtii, and the
root-knot nematode (RKN), Meloidogyne incognita.
13 Root-knot nematode (RKN; Meloidogyne spp.) is a major cr
14 Aphid and
root-knot nematode assays of Sgt1-2-silenced plants indi
15 Both
root-knot nematode genomes have compacted gene families
16 The recent completion of two
root-knot nematode genomes opens the way for a comparati
17 r genotypes using root tissue harvested from
root-knot nematode infected plants at 0, 3, 7 days after
18 yst nematode Heterodera schachtii and by the
root-knot nematode Meloidogyne incognita.
19 sceptibility to H. schachtii, but not to the
root-knot nematode Meloidogyne incognita.
20 T5 function increases resistance against the
root-knot nematode Meloidogyne javanica and suggests a p
21 The
root-knot nematode resistance gene Mi from tomato encode
22 rovide a resource for broadening the base of
root-knot nematode resistance in tomato and other crops.
23 TRV-Mi construct, Mi-9-mediated heat-stable
root-knot nematode resistance was compromised at 32 degr
24 timulated efforts to identify new sources of
root-knot nematode resistance.
25 ions were generated and screened for altered
root-knot nematode resistance.
26 Resistance to
root-knot nematode was introgressed into cultivated pean
27 et-cyst nematode) and Meloidogyne incognita (
root-knot nematode).
28 ich confers resistance to several species of
root-knot nematode, is present in many modern tomato cul
29 infestation of roots by the plant-parasitic
root-knot nematode, Meloidogyne incognita.
30 es have revealed the cellular changes inside
root-knot nematode-induced feeding sites, both in the co
31 It is an obligate parasite of
root knot nematodes (Meloidogyne spp.) and preferentiall
32 Root knot nematodes (RKNs) penetrate into the root vascu
33 Root knot nematodes are devastating root pests of econom
34 cognized as a potential biocontrol agent for
root knot nematodes, but the fastidious life cycle and t
35 The Mi locus of tomato confers resistance to
root knot nematodes.
36 tomato (Lycopersicon esculentum Mill.) with
root-knot nematodes (Meloidogyne javanica) encodes a pro
37 tomato Mi-1 gene confers resistance against
root-knot nematodes (Meloidogyne spp.) and a biotype of
38 Mi-1 confers resistance to
root-knot nematodes (Meloidogyne spp.), potato aphids (M
39 two additional phloem-feeding insects and to
root-knot nematodes (Meloidogyne spp.).
40 resistance as well as basal defense against
root-knot nematodes (RKN) and potato aphids.
41 Remarkably, plant-parasitic
root-knot nematodes (RKN) invoke a cytoskeletal response
42 ediate infection and parasitism of plants by
root-knot nematodes (RKN).
43 Most apomictic
root-knot nematodes (RKN; Meloidogyne spp.) have host ra
44 Root-knot nematodes (RKNs) (Meloidogyne spp.) are obliga
45 Root-knot nematodes (RKNs; Meloidogyne spp.) are plant p
46 he tomato Mi gene confers resistance against
root-knot nematodes and potato aphids.
47 The giant cells of
root-knot nematodes are formed by repeated karyokinesis
48 Cyst and
root-knot nematodes are obligate parasites of economic i
49 Cyst nematodes and
root-knot nematodes elaborately transform cells within t
50 d and important group of plant pathogens-the
root-knot nematodes Meloidogyne species-which attack mos
51 e expression analysis provides evidence that
root-knot nematodes modulate biological pathways involve
52 Plant-parasitic cyst and
root-knot nematodes synthesize and secrete a suite of ef
53 to SCN in a way similar to that reported for
root-knot nematodes, but opposite to that suggested for
54 Mi-1 confers resistance to Meloidogyne spp. (
root-knot nematodes, RKNs) and three phloem-feeding inse
55 ression in roots infected by plant-parasitic
root-knot nematodes.
56 this field, with a focus on the best-studied
root-knot nematodes.
57 parasitism and plant nurse cells in cyst and
root-knot nematodes.
58 nts were not significantly more resistant to
root-knot nematodes.