ライフサイエンスコーパス: striata

1 s or morphological changes in their injected striata.

2 take in mGluR5 receptor-rich regions such as striata.

3 rcent decrease in D1-like binding in the two striata.

4 activity but not in PSP activity in lesioned striata.

5 t alter neuron firing in the 6-OHDA-lesioned striata.

6 nondopaminergic cells in their cortices and striata.

7 medium spiny-like neurons in 6-OHDA-lesioned striata.

8 es were detected in the quinolinate-injected striata.

9 ociated, [3H]choline-labeled, adult male rat striata.

10 ed in the lesioned and contralateral control striata.

11 n acutely dissociated neurons from adult rat striata.

12 roscopy in the ipsilateral and contralateral striata.

13 ults were used to segment the monkey and rat striata according to ACC/OFC inputs.

14 nobutyric acid-positive) isolated from mouse striata also responded to U50,488 by increasing phospho-

15 llular dopamine in both lesioned and control striata, although tissue dopamine was decreased 30-70% i

16 f an average scan, automatically locates the striata and occipital structures, locates the caudate an

17 s were positioned in both the right and left striata and perfused with artificial cerebrospinal fluid

18 s was 60% in the corpus callosum, 36% in the striata, and 18%-22% in the cortical lobes in the simula

19 blast cells were grafted in parkinsonian rat striata, and L-DOPA was systemically administered.

20 ng doublecortin-defined neuroblasts in their striata, and the new neurons expressed p27 as a marker o

21 ue dopamine was decreased 30-70% in lesioned striata, as determined subsequently by HPLC-EC.

22 -stimulated [3H]ACh release from dissociated striata, as opposed to striatal slices.

23 striatum was significantly decreased in Q140 striata, as was the abundance of VGLUT2(+) axodendritic

24 approximately half of that in contralateral striata at 3 days, and was significantly increased in IR

25 ation readily elicited DA release in control striata but not from contralateral striata when nigrostr

26 rsolateral (30-60%) and posterior (100-200%) striata, but not within the anterior ventromedial striat

27 nylacetic acid (DOPAC) were not different in striata collected from melatonin-treated versus DMSO-tre

28 eductions in TH immunoreactivity in injected striata compared with the contralateral hemisphere (inje

29 ing tumors was 1.6-fold greater than that of striata containing control tumors (p<0.05).

30 HRP enzymatic activity associated with striata containing SF/HGF-expressing tumors was 1.6-fold

31 l transitions in Bengalese finches (Lonchura striata domestica) and pre-lingual human infants.

32 tutored juvenile Bengalese finches (Lonchura striata domestica) from different genetic backgrounds wi

33 gia guttata) and Bengalese finches (Lonchura striata domestica) to detect a zebra finch or a Bengales

34 ductions in ligand binding to both D1 and D2 striata dopamine receptors in young and old rats.

35 h quantitative autoradiography in postmortem striata from 19 patients with dementia with Lewy bodies,

36 predator, the nudibranch gastropod Tritonia striata, from potential predators.

37 astructural studies of the human and Macaque striata further revealed an association of torsinA immun

38 Only denervated striata grafted with fibro-blasts possessing both TH and

39 ces were observed between medial and lateral striata in either TH+ or DA+ terminals.

40 s were differentially expressed in TgR mouse striata, including 15 known genes, 7 of which are anxiet

41 suggests that increases in dopamine (DA) in striata may participate in neurodegenerative processes d

42 iated murine neuroblastoma (NBP2) cells into striata of 6-hydroxydopamine-lesioned rats (an animal mo

43 ver, transplantation of these cells into the striata of 6-hydroxydopamine-treated rats at the neurona

44 In addition, the striata of AChE-/- mice showed dramatic reductions in le

45 PA metabolites in extracellular space in the striata of anesthetized rats was investigated using in v

46 reuptake were significantly increased in the striata of animals receiving dopamine PTEN knock-out tra

47 Receptor density (Bmax) in the striata of clinically stable spf/Y mice and +/Y litterma

48 determined for the lesioned and non-lesioned striata of each animal.

49 lished human data of increased DAT levels in striata of HAND patients and by demonstrating similar fi

50 RGS2 expression levels are reduced in the striata of LRRK2 and sporadic PD patients.

51 e receptor availability has been observed in striata of methamphetamine users as compared with contro

52 is due to intrinsic differences between the striata of mice and men.

53 th nuclear proteins from adult and embryonic striata of mice and rats.

54 anted bilaterally into the dopamine depleted striata of MitoPark mice that express a parkinsonian phe

55 cell-cycle markers typically not seen in the striata of normal mice, and these cells are preferential

56 rtalized dopamine neurons, when grafted into striata of normal rats, did not divide, did not form tum

57 ery of exogenously applied dopamine from the striata of ovariectomized female rats.

58 line receptors (nAChRs) are decreased in the striata of patients with Parkinson's disease (PD) or in

59 es, and TH expression were attenuated in the striata of pups from the dams fed with the resveratrol-s

60 The bias was increased significantly in the striata of simulated pathologic studies (P < 0.05).

61 te (NMDA) receptor-induced excitotoxicity in striata of symptomatic N171-82Q mice, a new transgenic m

62 e to the loss of medium spiny neurons in the striata of the hyperammonemic sparse fur (spf/Y) mouse,

63 d (HVA) were significantly diminished in the striata of the middle-aged and old rats as compared to l

64 howed no change in NR1, NR2A, or NR2B in the striata of the symptomatic mice, we observed a decrease

65 We followed the distribution of mHTT in the striata of transgenic R6/2-J2 HD mice as their motor fun

66 fferential changes in gene expression in the striata of wild-type and SOD-tg mice treated with neurot

67 hydroxylase-like immunohistochemistry in the striata of wild-type mice.

68 The striata on the two sides of the brain were compared over

69 The number of striata perceived as difficult to interpret decreased as

70 67% and 83% were GDNF+ in dorsal and ventral striata, respectively.

71 Biochemical fractionation of the human striata revealed a concentration of torsinA immunoreacti

72 actional [3H]ACH efflux from dissociated rat striata tested whether tonic inhibition prevents stimula

73 In rat striata, TH and AADC co-immunoprecipitate with VMAT(2),

74 geting human Htt mRNA (siRNA-Htt) into mouse striata that also received adeno-associated virus contai

75 ongbird species (Bengalese finches, Lonchura striata var. domestica) greatly reduced the magnitude of

76 tory feedback in Bengalese finches (Lonchura striata var. domestica) to create sensory errors during

77 tal extracellular [18F] radioactivity in rat striata was observed to rise and peak at 30 min post-inj

78 ased by 2.4-fold in blood-injected wild-type striata, was not altered by IRP1 knockout, but was reduc

79 Rat striata were exposed to 15 mM quinolinic acid (QUIN), or

80 The striata were isolated from the pups at postnatal days 10

81 um spiny-like neurons in the 6-OHDA-lesioned striata were significantly faster than were firing rates

82 n control striata but not from contralateral striata when nigrostriatal neurons were transduced.

83 DA release in either the control or lesioned striata when the virus was injected directly into the st

84 4%, respectively, relative to the unlesioned striata, whereas the abundance of NR2A was unchanged.

85 iculate, and, to a lesser extent, cortex and striata, which are known to contain alpha(4)beta(2) site

86 and by germline inactivation in osteopathia striata with cranial sclerosis, a bone overgrowth syndro