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1 r neurons (GRNs) confers responsiveness to L-canavanine.
2 at GR8a contributes to the specificity for L-canavanine.
3 suming plant-derived insecticides, such as L-canavanine.
4 been reported to be required for detecting L-canavanine.
5 r Gr66a resulted in an inability to detect L-canavanine.
6 ress and limited growth in the presence of l-canavanine.
7 ced sensitivity to the toxic arginine analog canavanine.
8 a, can1-100 cells to grow in the presence of canavanine.
9 of upf1Delta, can1-100 cells is inhibited by canavanine.
10 H(2)O(2), ethanol, and the amino acid analog canavanine.
11 es and sensitivity to the arginine analogue, canavanine.
12 type of cpp1(-) mutants, hypersensitivity to canavanine.
13 lps confer resistance to the arginine analog canavanine.
14 salt- or sweet-sensing GRNs to respond to L-canavanine.
15 plied to the separation of L-arginine from L-canavanine (a close analogue of arginine where the termi
16 Delta significantly increased sensitivity to canavanine, a phenotype associated with an rpn10Delta si
18 he resistance phenotype of an ypq2 mutant to canavanine, a toxic analog of arginine efficiently trans
19 al coaggregation by the arginine homologue l-canavanine, abrogated the increased S. cristatus adhesio
20 nd GR98b in Drosophila S2 cells induces an L-canavanine-activated nonselective cation conductance.
24 d that GRs are essential for responding to L-canavanine and that flies missing DmXR displayed normal
25 ssion of these mutants confers resistance to canavanine and thialysine, phenotypes which are similar
26 persensitive to growth inhibitory effects of canavanine and thialysine, which are analogues of argini
27 d that flies missing DmXR displayed normal L-canavanine avoidance and L-canavanine-evoked action pote
29 own to protect cells against the toxicity of canavanine (Can), a nonproteinogenic amino acid synthesi
31 onal DnaJ, whereas Lon-dependent turnover of canavanine-containing proteins was slower in dnaJ mutant
32 ependent degradation was affected; abnormal, canavanine-containing proteins were similarly affected.
34 eCO(2) reduced the antinutritional factor l-canavanine content in Ismailia 1 cultivar and improved t
35 , targeted gene knockouts and treatment with canavanine demonstrated a catalytic linkage between casp
37 f these Grs in sweet-sensing GRNs switches L-canavanine from an aversive to an attractive compound.
40 ain of ScRheb are incapable of complementing canavanine hypersensitivity of scrheb disruptant cells.
41 reduced the ability of ScRheb to complement canavanine hypersensitivity of ScRheb-deficient yeast.
42 8a was narrowly required for responding to L-canavanine, in contrast to Gr66a, which was broadly requ
46 ion of the isosteric, titratable Arg analog, canavanine, into a neurotransmitter receptor in a living
47 ed bitter-sensitive cells failed to detect L-canavanine mixed with sucrose in three different feeding
48 py expression of POL30 (PCNA) suppresses the canavanine mutation rate of all the rad27 alleles, inclu
49 some ((DeltaUbL)rad23) does not suppress the canavanine or cold-sensitive defects of rad23Delta rpn10
50 est that GR8a and GR66a are subunits of an L-canavanine receptor and that GR8a contributes to the spe
53 type and a high rate of forward mutations to canavanine resistance that result primarily from duplica
55 20-fold increase in frequency of mutation to canavanine-resistance, which was further elevated in a u
56 pear to be due to a bias caused by selecting canavanine resistant isolates in the different HTA1-HTB1
57 process can be detected by the production of canavanine-resistant (can1) mutants among the TRP1 recom
59 UPR-inducing compounds tunicamycin, DTT, and canavanine results in a Hac1-dependent increase in GPC1
60 isiae in the presence of the arginine analog canavanine results in increased SUMOylation and Slx5-Slx
62 nalysis of P. aeruginosa ADI inhibition by L-canavanine showed that two competing pathways are follow
63 order to demonstrate the generality of the L-canavanine slow substrate inhibition and to distinguish
66 emental arginine and the arginine antagonist canavanine, we show that arginine availability is a dete
67 ells and inhibits sugar detection) or with L-canavanine (which only activates bitter-sensitive cells)
68 ion intermediate formed in the reaction of L-canavanine with Bacillus cereus ADI partitions between t
69 , a mutant resistant to the toxic effects of canavanine, with low levels of transport activities and