ライフサイエンスコーパス: hut

1 ession of gdhA expression but still activate hut and ure expression normally.

2 ame, were tested for the ability to activate hut and repress gdh in vivo.

3 sed from such chimeras were able to activate hut transcription in a purified system in vitro, as were

4 5 amino acids) were functional in activating hut and repressing gdh expression in vivo.

5 An examination of dpp and hut expression in cells during exponential growth in var

6 C activates transcription of operons such as hut (histidine utilization) and ure (urea utilization),

7 ty tested: (i) it activates transcription at hut and ure; (ii) it competes with the lysine-sensitive

8 tus and gave control for 10 months in cement huts and 6 months in mud huts.

9 In cement huts application rates of 0.5 g/m(2) induced high mortal

10 required for amino acid regulation of either hut induction or the expression of proline oxidase, the

11 nalyses of bioassay studies and experimental hut trials are used to characterise how pyrethroid resis

12 pha 25 mg/m(2) in a small-scale experimental hut trial in an area of wild An. arabiensis.

13 evaluated as IRS treatments in experimental huts in an area of Benin where the mosquitoes Anopheles

14 In experimental huts the mixture of CFP 100+ Alpha 25 killed 58% of An.

15 For hut studies: low resistance, RD 0.56 (95% CI 0.43 to 0.6

16 ilar studies using the NAC-binding site from hut showed that two mutations in the promoter proximal h

17 rophobic residue activate transcription from hut and ure promoters, but fail to repress gdhA expressi

18 y generated inside the screened and grounded huts, the birds again lost their magnetic orientation ca

19 he same order as NAC(WT) (ure > gdhA > nac > hut); (v) it induces the same slight bend as dimers of N

20 28 maternity hut clusters were randomly assigned-14 to the misoprosto

21 Maternity huts that had been included in a previous study of misop

22 Maternity huts with auxiliary midwives located 3-21 km from the cl

23 ter-randomised controlled trial at maternity huts in three districts in Senegal.

24 delivered by auxiliary midwives at maternity huts.

25 1412 women delivered in the study maternity huts.

26 d by the auxiliary midwives in the maternity huts were eligible for the study.

27 prolonged activators disrupts CO(2)-mediated hut entry behaviour of Culex mosquitoes.

28 In mud huts application rates of 1 g/m(2) induced high mortalit

29 10 months in cement huts and 6 months in mud huts.

30 strate that the mfd mutation relieves CCR of hut and gnt expression at the cis-acting cre sequences l

31 An examination of hut expression in a delta codY mutant demonstrated that

32 crh mutation individually had any affect on hut CCR but that hut CCR was abolished in a ptsH1 crh do

33 obial iron regulator (rirA) has no effect on hut locus transcription.

34 rast, the ptsH1 mutation completely relieved hut CCR in cells grown in Luria-Bertani medium.

35 vergently transcribed and that the remaining hut genes are expressed as a polycistronic mRNA.

36 in electrically grounded, aluminium-screened huts, which attenuated electromagnetic noise in the freq

37 ividually had any affect on hut CCR but that hut CCR was abolished in a ptsH1 crh double mutant.

38 reverse transcriptase PCR analyses show that hut locus transcription is subject to hemin-responsive r

39 dhA; (iii) it binds to the same sites at the hut, ure, nac, and gdhA promoters as NAC(WT); (iv) the r

40 The protein Pa3175 is dislocated from the hut operon and was shown to catalyze the hydrolysis of N

41 phily (premature exit of mosquitoes from the hut), deterrence, time to 50% or 95% knock-down, and per

42 Analysis of the hut genes indicated that hutBCD, which are predicted to

43 ctions as a transcriptional repressor of the hut locus at all hemin concentrations tested.

44 es carbon catabolite repression (CCR) of the hut operon was isolated by transposon mutagenesis.

45 or, which lies immediately downstream of the hut promoter, was defective in a delta codY mutant.

46 hroid resistant An. gambiae that entered the huts.

47 ential locus dedicated to hemin utilization (hut) encoding a putative hemin receptor, HutA; a TonB-li

48 ion of the CCR of the histidine utilization (hut) enzymes in cells grown in minimal medium showed tha

49 transcription of the histidine utilization (hut) operon and to repress transcription of the glutamat

50 cid repression of the histidine utilization (hut) operon were isolated by transposon mutagenesis.

51 ocated in both of the histidine utilization (hut) operons were upregulated in both QS and flhDC mutan

52 omagnetic noise present in unscreened wooden huts at the University of Oldenburg campus, they could n