ライフサイエンスコーパス: behavioral analyses

1 e ventral tegmental area and psychotomimetic behavioral analyses.

2 ctical and theoretical limitations of common behavioral analyses.

3 A total of 21 participants were included in behavioral analyses; 17 purchased cannabis and were thus

4 Using a combination of behavioral analyses and single-cell Ca(2+) imaging in wi

5 proaches, building from molecular targets to behavioral analyses and vice versa, respectively.

6 Neuronal time-lapse imaging, behavioral analyses, and electrophysiological recordings

7 Histological, electrophysiological, and behavioral analyses demonstrate that MEF2C-directed neur

8 Behavioral analyses demonstrated higher basal locomotor

9 Behavioral analyses demonstrated that pan-neural loss of

10 Behavioral analyses have long indicated that additional,

11 her, our cellular, electrophysiological, and behavioral analyses highlight the importance of axonal t

12 histochemistry, in vivo Ca(2+) imaging, and behavioral analyses in a mouse model of AD, we demonstra

13 It also reveals the importance of behavioral analyses in studies aimed at understanding th

14 r, histological, and biochemical methods and behavioral analyses in vivo we demonstrate, to our knowl

15 In this study, both recordings in vitro and behavioral analyses in vivo were used to examine cellula

16 Through a battery of behavioral analyses, including primate-unique eye-tracki

17 ls overall, but computational model fits and behavioral analyses indicate that these deficits could b

18 -imaging, hormone-measurement, and cognitive-behavioral analyses indicate the importance of mentaliza

19 Our behavioral analyses indicated that DJ-1 deficiency led t

20 This approach combined with molecular and behavioral analyses, led us to recognize, in hippocampus

21 when combined with electrophysiological and behavioral analyses, make this an attractive model syste

22 Electrophysiological, imaging, and behavioral analyses of Caenorhabditis elegans mutants la

23 Behavioral analyses of optomotor head-turning reflex, vi

24 , electrophysiological, and vision-dependent behavioral analyses of the mouse model revealed a unique

25 ly amenable to molecular, physiological, and behavioral analyses of the neural features responsible f

26 Behavioral analyses of the ontogeny of memory have shown

27 Behavioral analyses of the R6/2 mouse reveal age-related

28 hat can now be used to correlate with future behavioral analyses of these compounds and may provide i

29 Comprehensive behavioral analyses of transgenic and knockout mice have

30 High-throughput behavioral analyses of trpa1a and trpa1b mutant larvae i

31 We used a combination of molecular and behavioral analyses, pharmacology, and in vivo amperomet

32 ed a combination of slice electrophysiology, behavioral analyses, pharmacology, in vivo microdialysis

33 Microarray, imaging, and behavioral analyses reveal that tomatidine maintains mit

34 endrite patterning in the cerebellar cortex, behavioral analyses reveal that TRPC5 knockout mice have

35 Behavioral analyses revealed no differences from wild ty

36 Our behavioral analyses revealed that formoterol, a long-act

37 Behavioral analyses revealed that humans executed a hier

38 Behavioral analyses revealed that mice lacking CRFR1 dis

39 Behavioral analyses revealed that poker players were fas

40 Behavioral analyses revealed that suppression of GAD1 in

41 Genetic and behavioral analyses revealed that tank acts in the adult

42 Consistent with these observations, behavioral analyses show that bitter-compound-mediated i

43 Furthermore, behavioral analyses show that PRMT8 conditional knock-ou

44 Similarly, behavioral analyses showed impaired auditory and context

45 Motor behavioral analyses showed no changes in reach rate acro

46 Human genetic and mouse behavioral analyses suggest that ENGRAILED-2 (EN2) contr

47 Our genetic, pharmacological, and behavioral analyses suggest that in sir-2.1(0) and older

48 Behavioral analyses suggest that serotonin facilitates l

49 Genetic and behavioral analyses suggest that the NCA channels enable

50 ophysiological recordings were combined with behavioral analyses to assess whether removal of AKAP150

51 Based on this finding, we performed behavioral analyses to determine whether a gain-of-funct

52 graphical, morphological, physiological, and behavioral analyses to determine whether key functional

53 mouse genetics, single-cell dye tracing, and behavioral analyses to determine whether Tbr2 regulates

54 Such information may be correlated with pain behavioral analyses to help shed light on the complex mo

55 approach using high-throughput, quantitative behavioral analyses to identify the neural substrates of

56 ng brain imaging with social, cognitive, and behavioral analyses to understand how parental brain cir

57 Behavioral analyses using video microscopy revealed that

58 With combined brain-imaging and cognitive-behavioral analyses, we are in the early phases of under

59 ular, biochemical, electrophysiological, and behavioral analyses, we demonstrate that NRG1-IV/NSE-tTA

60 Using newly developed quantitative behavioral analyses, we demonstrate that the T(S) repres

61 Using genetic and behavioral analyses, we show that apt mediates sensitivi

62 genetics, cell-specific ablation- and mutant behavioral analyses, we show that the male makes this sh

63 analysis, calcium imaging, optogenetics and behavioral analyses, we uncovered a circuit specific for

64 Behavioral analyses were conducted using a newly-develop

65 ohistochemical, biochemical, functional, and behavioral analyses were performed in nerves harvested f

66 In the present work we combined behavioral analyses with calcium imaging of odor induced

67 Combining behavioral analyses with in vivo synaptic imaging, we sh