ライフサイエンスコーパス: downy mildew

1 biotic stresses (watermelon mosaic virus and downy mildew).

2 ora parasitica (P.p.) races Emoy2 and Emwa1 (downy mildew).

3 een identified as a susceptibility factor to downy mildew.

4 e timing and extent of outbreaks of cucurbit downy mildew.

5 ve high levels of quantitative resistance to downy mildew.

6 esticide residues in wine grapes affected by Downy Mildew.

7 he loss of uninucleate zoospores in multiple downy mildews.

8 of the putative chromatin regulator Enhanced Downy Mildew 2 (EDM2) as a cellular antisilencing factor

9 We identified EDM2 (enhanced downy mildew 2) in a genetic screen for RPP7 suppressors

10 le, CsIVP-RNAi plants were more resistant to downy mildew and accumulated more salicylic acid (SA).

11 mMPK4-silenced plants were more resistant to downy mildew and Soybean mosaic virus compared with vect

12 ete, Peronospora parasitica (causal agent of downy mildew), and encodes an NBS-LRR type R protein wit

13 The perception of downy mildew avirulence (Arabidopsis thaliana Recognized

14 Lettuce downy mildew caused by Bremia lactucae is the most impor

15 ys broad-spectrum resistance against lettuce downy mildew caused by Bremia lactucae Regel and is cons

16 pes affected by cryptogamic diseases, namely downy mildew caused by Plasmopara viticola, and black ro

17 whose production is severely constrained by downy mildew caused by Sclerospora graminicola (Sacc.).

18 , encodes Dm3 which determines resistance to downy mildew caused by the oomycete Bremia lactucae carr

19 Grapevine downy mildew, caused by the oomycete Plasmopara viticola

20 12 activation, and reduced susceptibility to downy mildew disease (Hyaloperonospora arabidopsidis).

21 popular leafy vegetable, are susceptible to downy mildew disease caused by Bremia lactucae.

22 sity of ABA signaling affects the outcome of downy mildew disease.

23 several species of the oomycetes that cause downy mildew diseases.

24 ent biotic and abiotic stresses, among which downy mildew (DM) is a severe biotic stress that is detr

25 Cucumis sativus) is resistant to oomyceteous downy mildew (DM), bacterial angular leaf spot (ALS) and

26 Previous screens for enhanced downy mildew (edm) mutants identified the co-chaperone S

27 genes conferring resistance to the oomycete downy mildew fungus Bremia lactucae map to the major res

28 The resurgence of cucurbit downy mildew has dramatically influenced production of c

29 and RPP2B confer recognition of Arabidopsis downy mildew (Hyaloperonospora arabidopsidis [Hpa]) isol

30 that the 3221 mutant exhibited resistance to downy mildew (Hyaloperonospora arabidopsidis) and green

31 volved in R-gene-mediated resistance against downy mildew in Arabidopsis and their regulatory control

32 A recent outbreak of sorghum downy mildew in Texas has led to the discovery of both m

33 which confers resistance to Bremia lactucae (downy mildew) in 1033 accessions of Lactuca serriola (pr

34 ly divergent alleles of ATR1NdWsB from eight downy mildew isolates and demonstrate that the ATR1NdWsB

35 hum, maize, sugarcane, pearl millet and rose downy mildew isolates.

36 nome of Hyaloperonospora arabidopsidis (Hpa, downy mildew of Arabidopsis) contains at least 134 candi

37 Downy mildew of spinach is caused by the obligate oomyce

38 as well as from 5 related species that cause downy mildew on other hosts, the number of different ban

39 IP18292 in response to inoculation with the downy mildew oomycete pathogen Sclerospora graminicola.

40 ntribute to pearl millet defense against the downy mildew pathogen by activating the expression of de

41 The biotrophic downy mildew pathogen Hyaloperonospora arabidopsidis enc

42 H-induced immunity (iri) mutants against the downy mildew pathogen Hyaloperonospora arabidopsidis, yi

43 s required for successful infection with the downy mildew pathogen Hyaloperonospora arabidopsidis.

44 We study the oomycete downy mildew pathogen of Arabidopsis, Hyaloperonospora a

45 Hyaloperonospora arabidopsidis, a downy mildew pathogen of the model plant Arabidopsis, ha

46 lent/Columbia-0 (Col-0) virulent isolates of downy mildew pathogen.

47 in resolving among phylogenetically related downy mildew pathogens dramatically point out the need f

48 esponding to incursions of new or reemerging downy mildew pathogens.

49 ne confers AtSgt1b-independent resistance to downy mildew (Peronospora parasitica) isolate Hiks1.

50 targeted to Phytoene desaturase (SlPDS) and Downy mildew resistance 6 (SlDMR6) genes fused to mobile

51 mediated organ morphogenesis and SA-mediated downy mildew resistance in cucumber.

52 plicating that GB is a promising elicitor of downy mildew resistance in P. glaucum.

53 dies to assess candidate genes necessary for downy mildew resistance in spinach.

54 We also describe evidence that the downy mildew resistance loci of cultivated spinach are d

55 s (Arabidopsis thaliana) RLPs, including the downy mildew resistance protein RPP27.

56 harbor desirable alleles of genes related to downy mildew resistance, frost resistance, leaf morpholo

57 s were screened for spontaneous mutations in downy mildew resistance.

58 of several R genes that confer bacterial and downy mildew resistance.

59 cum positively correlated with the increased downy mildew resistance.

60 a resistance gene analog is associated with downy mildew resistance.

61 We also show here that DOWNY MILDEW RESISTANT6 (AtDMR6), the Arabidopsis homolo

62 rimer pairs studied in detail using DNA from downy mildews that attack maize (P. maydis & P. philippi

63 its common parasite Peronospora parasitica (downy mildew) to study the evolution of resistance speci

64 uences of three Phytophthora species and one downy mildew were identified and could serve as useful p