ライフサイエンスコーパス: synergist

1 rload from surgical ablation of a functional synergist.

2 the independently expressed HDt is a potent synergist.

3 yrifos and parathion and was not affected by synergists.

4 dual responses to the presence of non-lethal synergists.

5 edict the joint effect of mixtures including synergists.

6 These chemicals are called synergists.

7 %), 1 insect repellent (3%), and 1 pesticide synergist (3%).

8 ough chronic overload of skeletal muscle via synergist ablation (SA) strongly induces hypertrophy and

9 In response to muscle overload after synergist ablation in mice, we show that myomaker, a mus

10 Synergist ablation surgery, where removal of synergist m

11 We then show that SUnSET can detect the same synergist ablation-induced increase in PS when used in v

12 a [(3)H]phenylalanine method when detecting synergist ablation-induced increases in skeletal muscle

13 uced in mouse plantaris muscle by unilateral synergist ablation.

14 hal pathogen and the ability to tolerate the synergist affect the likelihood of coexistence and the e

15 y lead to altered activation of the agonist, synergist and antagonist muscles.

16 Piperonyl butoxide (PBO) synergist and biochemical assays further support a role

17 the antagonist triceps brachii and to other synergist and non-synergist muscles of the upper limb oc

18 used, with Ia excitation restricted to close synergists and Ia reciprocal inhibition only shared betw

19 e of the azole fungicide, propiconazole (the synergist), and the insecticide, alpha-cypermethrin, on

20 o the genera Fusobacterium, Cardiobacterium, Synergistes, and Selenomonas, as well as respiratory pat

21 ngth during stance of walking when intact SO synergists are actively contracting.

22 imultaneously in neurons that are functional synergists but alternate with bursts in their antagonist

23 n how investing in tolerance to a non-lethal synergist can lead to a broad range of different populat

24 Synergists can counteract metabolic insecticide resistan

25 her supported by the genetic interaction and synergist cyst formation in the zebrafish pronephros mod

26 pathogen speed of kill and the presence of a synergist favour parasites that have faster speeds of ki

27 ly active when the same muscle was used as a synergist, fixator, or antagonist.

28 Here, we use a surprising pair of synergists in humans, the flexor hallucis longus (FHL, a

29 diac transplantation model demonstrated that synergist interactions of PDGF-AB plus VEGF plus Ang-2 (

30 . halys aggregation pheromone, and pheromone synergist, methyl (2E, 4E, 6Z)-decatrienoate when compar

31 inkages between denervated SO and its active synergists might affect its fascicle length changes.

32 The model predicts that synergist motor neurons are electrically coupled, wherea

33 Most (87%) pairs of synergist motor neurons tested made weak, noninverting c

34 Overloading the rat plantaris muscle by synergist muscle ablation, which promotes hypertrophy of

35 chanical overload by surgical removal of the synergist muscle.

36 tent of shared versus independent control of synergist muscles at the motor neuron level.

37 e nervous system coordinates the activity of synergist muscles is not well understood.

38 Neural control of synergist muscles is not well understood.

39 iceps brachii and to other synergist and non-synergist muscles of the upper limb occur in the newborn

40 Synergist ablation surgery, where removal of synergist muscles places functional overload on the plan

41 standing of how neural drive is delivered to synergist muscles.

42 tion, the remarkably potent OP neonicotinoid synergist, O-propyl O-(2-propynyl) phenylphosphonate, in

43 Inhibition of cathepsin F, the functional synergist of cathepsin S, was not observed.

44 expressed in Escherichia coli functions as a synergist of Cry1A toxicity against lepidopteran larvae.

45 The effects of the synergist on pathogen fitness are explored through a ser

46 However, the effect of synergists on genome-wide transcription in arthropods is

47 kdr mutations suggests that addition of the synergist PBO to pyrethroids could improve the efficacy

48 f standard bednets, and those containing the synergist piperonyl butoxide (PBO), and assess its impac

49 %), active ingredients (pyrethrins, 43%) and synergists (piperonyl butoxide, 42%).

50 Evolutionary analysis of tolerance of the synergist (strength of synergy) and lethal pathogen yiel

51 er mite Tetranychus urticae upon exposure to synergists such as S,S,S-tributyl phosphorotrithioate (D

52 are explored in the presence of a non-lethal synergist that hosts must tolerate.

53 ection by a lethal pathogen and a non-lethal synergist (that only acts to enhance the infectivity of

54 DL) was overloaded by (a) extirpation of the synergist tibialis anterior (TA), (b) sectioning the dis

55 on of IFN-gamma and TNF-alpha results in the synergist uniform polarization of MSCs toward a primaril