ライフサイエンスコーパス: brain neuron

1 an RGS protein at the level of an individual brain neuron.

2 2-AG accumulation in primary cultures of rat brain neurons.

3 extent of axonal regeneration of descending brain neurons.

4 a prenylated SNARE selectively expressed in brain neurons.

5 volved in survival and maintenance of mature brain neurons.

6 ther it also modulates Ca(2+) homeostasis in brain neurons.

7 ting the Kv1.2 localization observed in many brain neurons.

8 overed no coexpression of FRU(M) and 5-HT in brain neurons.

9 in the somatodendritic membrane of mammalian brain neurons.

10 ied on the basis of their rapid induction in brain neurons.

11 cesses, as well as during normal function of brain neurons.

12 in the spontaneously hypertensive rat (SHR) brain neurons.

13 ansduction pathway in Wistar Kyoto (WKY) rat brain neurons.

14 essed by using double labeling of descending brain neurons.

15 functional GLT-1 protein can be expressed in brain neurons.

16 and probably the developmental maturation of brain neurons.

17 tization of the mu-opioid receptor (MOPr) in brain neurons.

18 reatment with lithium and VPA in primary rat brain neurons.

19 surements from a small population of central brain neurons.

20 the soma and proximal dendrites of mammalian brain neurons.

21 gene LanCL1 that is prominently enriched in brain neurons.

22 eractions supply selenium for maintenance of brain neurons.

23 e to hyperexcitability and hypersynchrony of brain neurons.

24 ts of hyperphosphorylated tau protein within brain neurons.

25 e, consistent with its expression in central brain neurons.

26 as TH1-AC1) and four newly identified local brain neurons.

27 odulation of ethanol inhibition of NMDARs in brain neurons.

28 ptors for estrogen in hypothalamic and other brain neurons.

29 ated receptor tyrosine kinase B signaling in brain neurons.

30 aling and Trk-mediated survival signaling in brain neurons.

31 ain and retina, as well as isolated cultured brain neurons.

32 thylation between retinal photoreceptors and brain neurons.

33 es, where Na(V)1.2 channels are expressed in brain neurons.

34 unit expressed in many but not all mammalian brain neurons.

35 re we show that Kv2.1 clusters on the AIS of brain neurons across diverse mammalian species including

36 on of newly freed time and a large number of brain neurons affordable on a cooked diet may thus have

37 on, mu-opioid receptors were examined in rat brain neurons after treatment of animals with opioid dru

38 IP10 mRNAs were found to be expressed in rat brain neurons also expressing PAM proteins.

39 oth genes are coexpressed in most if not all brain neurons, although their patterns of expression var

40 arinic acetylcholine receptor subtype in the brain (neurons and glial cells; Br-M3-KO mice) showed a

41 xic foci in the lung (endothelial cells) and brain (neurons and neuropil).

42 different subtypes of Gi are involved in the brain neurones and in the endocrine cells: Gi2 in locus

43 receptors (mGluRs) are densely expressed in brain neurons and are actively involved in various cellu

44 (Nav) channels initiate action potentials in brain neurons and are primary therapeutic targets for an

45 hemoglobin chains are expressed in mammalian brain neurons and are regulated by a mitochondrial toxin

46 ATF5 is not detectably expressed by mature brain neurons and astrocytes, but is expressed by reacti

47 kinase is associated with sodium channels in brain neurons and can modulate Na(V)1.2 channels by tyro

48 ructural integrity of dendritic terminals in brain neurons and delay locomotor dysfunction.

49 PEI mediates transgene expression in brain neurons and glia.

50 creased aneuploidy and apoptosis in the same brain neurons and glia.

51 trated the replication of a group 1 virus in brain neurons and glial cells and in cardiac myofibers.

52 glutamate-induced excitotoxicity in cultured brain neurons and in an animal model of cerebral ischemi

53 (PKA) decreases peak Na+ current in cultured brain neurons and in mammalian cells and Xenopus oocytes

54 agocytic lineage, pancreatic beta cells, and brain neurons and is activated under oxidative stress.

55 ith the inner side of the plasma membrane in brain neurons and rat PC12 cells in vitro; they are pres

56 Here we describe four descending brain neurons and two with the soma in the subesophageal

57 d spatial manner with expression in specific brain neurons and visceral cell types.

58 ated PI3-kinase activity in both WKY and SHR brain neurons and was accompanied by its translocation f

59 d be due to axonal elongation by preexisting brain neurons and/or descending projections from new neu

60 dies of genomic DNA from the human and mouse brain, neurons and from mouse embryonic stem cells found

61 issues or cells in these body parts, such as brain, neurons and muscles, which have been identified a

62 and myoglobin, is expressed predominantly in brain neurons, and appears to modulate hypoxic-ischemic

63 odium channels initiate action potentials in brain neurons, and sodium channel blockers are used in t

64 ythmic expression of clock genes in specific brain neurons appears to control behavioral rhythms in a

65 Finally, we show that brain neurons are necessary and sufficient for sensing a

66 In the adult mammalian brain, neurons are continuously generated in two structu

67 In the developing brain, neurons are produced from neural stem cells terme

68 hich initiate action potentials in mammalian brain neurons, are modulated functionally by cAMP-depend

69 neration for the total numbers of descending brain neurons as well as neurons in certain brain cell g

70 lly administered prolactin rapidly activates brain neurons, as evidenced by prolactin-induced phospho

71 ctive downregulation of L-VSCC expression in brain neurons at the same, lower concentrations.

72 One local brain neuron, B-LI4, received inhibitory as well as exci

73 or role in basal neurotransmitter release in brain neurons but contribute significantly after inducti

74 d a role as homophilic adhesion molecules in brain neurons, but the in vivo functions remain unknown.

75 Chronic stimulation of brain neurons by angiotensin II (Ang II) results in a in

76 ydroxylase and norepinephrine transporter in brain neurons by angiotensin II (Ang II).

77 Selective overexpression of Nrf2 in brain neurons by lentiviral gene transfer was sufficient

78 channel could regulate synaptic efficacy in brain neurons by modulating Ca2+ levels in response to c

79 boration of dendrites among major classes of brain neurons by PKC-dependent mechanisms.

80 hat the control of excitatory and inhibitory brain neurons by type-1 cannabinoid (CB(1)) receptors is

81 We found that nuclear extracts from adult brain neurons can correct G.T and G.U mismatches, restor

82 neurons (forming the vast majority of adult brain neurons) can be assigned to genetically and develo

83 diction results from adaptations in specific brain neurons caused by repeated exposure to a drug of a

84 Four collybistin isoforms are expressed in brain neurons; CB2 and CB3 differ in the C terminus and

85 ions in many locations, including subsets of brain neurons (clock neurons) within the central nervous

86 lar granule cells, which outnumber all other brain neurons combined.

87 Deletion of SOCS3 from brain neurons delays the onset of diet-induced infertili

88 intracellular [Ca(2+)](i) is altered in aged brain neurons during synaptically activated neuronal act

89 hered 51 human and mouse DNA methylomes from brain neurons, embryonic stem cells and induced pluripot

90 Subsets of brain neurons expressing the clock genes period (per) an

91 In several areas of the macaque brain, neurons fire during delayed-response tasks at a r

92 The neurites of all brain neurons formed a ring-like branching pattern in th

93 play an important role in the protection of brain neurons from ischemic and hypoxic injuries.

94 Then brain neurons from mice homozygous or heterozygous for t

95 r studies indicate that the Gr43a-expressing brain neurons function as a nutrient sensor for hemolymp

96 In the vertebrate brain, neurons grouped in parallel laminae receive disti

97 ve all in crustaceans, continuous genesis of brain neurons has also been shown, namely for soma clust

98 lase and norepinephrine transporter genes in brain neurons; however, the signal-transduction mechanis

99 we show that Drosophila ring neurons-central brain neurons implicated in navigation-display visual st

100 c treatment with VDH was reported to protect brain neurons in both aging and animal models of stroke.

101 serotonergic phenotypic traits in developing brain neurons in culture.

102 Excessive inhibition of brain neurons in primary or slice cultures can induce ho

103 t unique sequences in PRO1- and PRO2-labeled brain neurons in situ, indicative of bicistronic gene ex

104 rizing the effects of stimulating individual brain neurons in the isolated nervous system of the leec

105 ide, similar to what is believed to occur in brain neurons, in the initial phases of AD.

106 of 49% and 68%, respectively, of descending brain neurons, including many unidentified RS neurons, w

107 demonstrate that the majority of descending brain neurons, including small, unidentified RS neurons,

108 Select brain neurons increase their firing rate when ambient gl

109 ight facilitates MIP secretion from specific brain neurons innervating pdf neurons.

110 Accumulation of beta-amyloid (Abeta) inside brain neurons is an early and crucial event in Alzheimer

111 that CB1 receptor signaling in many specific brain neurons is dispensable for the acute hypophagic ef

112 Light-responsive neural activity in central brain neurons is generally conveyed through opsin-based

113 ate that anandamide internalization in mouse brain neurons is independent of FAAH activity.

114 In brain neurons, it was found that active long intersperse

115 er, although DPP10 is also expressed in some brain neurons lacking Kv4 (such as parvalbumin- and soma

116 r, knockdown of XRCC1 in primary human fetal brain neurons leads to enhanced sensitivity to menadione

117 CB(1) receptor deletion from GABAergic brain neurons led to the opposite phenotype, characteriz

118 neuronal tissues, including a set of lateral brain neurons (LNs) that mediate rhythms in locomotor ac

119 and parrots have much higher proportions of brain neurons located in the pallial telencephalon compa

120 ila has defined two populations of circadian brain neurons, morning cells (M-cells) and evening cells

121 ceptor (RyR) Ca2+ -release channels in mouse brain neurons, most prominently in medium spiny neurons

122 al lamprey, the large, identified descending brain neurons (Muller and Mauthner cells) are capable of

123 re caused by a heterogeneous degeneration of brain neurons not only in substantia nigra pars compacta

124 duct of the Drosophila period (per) gene, in brain neurons of the adult fly are strongly involved in

125 In brain neurons, P- and Q-type Ca(2+) channels both appear

126 ginning at 16 days post coitum in developing brain neurons, primitive inner ear cells, and seminifero

127 d lamprey, axonal regeneration of descending brain neurons probably contributes significantly to the

128 arval lamprey, significantly more descending brain neurons projected to specific rostral levels of th

129 suppress eye toxicity, reduce cell death in brain neurons, protect the structural integrity of dendr

130 Moreover, genetic control over gut-to-brain neurons provides a molecular framework for underst

131 cent stain that labels injured, degenerating brain neurons, quantifies the extent of hippocampal inju

132 l lamprey, axonal regeneration by descending brain neurons, rather than the relatively slow addition

133 covery of locomotor behavior, and descending brain neurons regenerate their axons for progressively g

134 cent work has identified sensory and central brain neurons required for larval visual behaviors, incl

135 All brain neurons responded phasically to the sound pulses o

136 Starting from 5 months, brain neurons showed enlarged, structurally abnormal mit

137 sic action, we generated a mutant mouse with brain neuron-specific reductions in P450 activity; these

138 To delineate insulin actions in the brain, neuron-specific insulin receptor knockout (NIRKO)

139 The distribution of these PRV-labeled brain neurons strongly resembled that obtained after the

140 of postnatal cell death in several different brain neuron subtypes.

141 However, smaller, unidentified descending brain neurons, such as many of the reticulospinal (RS) n

142 elin and LGI1 co-localize in a subset of rat brain neurons, supporting an involvement of both protein

143 ic opiate use produces persistent changes in brain neurons that are expressed as adverse effects, inc

144 rectly communicates metabolic information to brain neurons that control reproduction, using GABAergic

145 isease, and are among the few populations of brain neurons that express p75NTR throughout life.

146 trigeminal sensory fibers made synapses with brain neurons that have direct or indirect inputs to ret

147 ring the development of a lineage of central brain neurons that innervate the optic lobes and are req

148 leuc and lkr genes identify small groups of brain neurons that regulate this behavior.

149 Our results demonstrate in adult mouse brain neurons that the mPTP functions to enhance ROS pro

150 l of the two kidneys is provided by the same brain neurons, the central circuitry involved in the inn

151 o acid catabolism and ammoniagenesis; and in brain neurons, the maintenance of glutamate neurotransmi

152 expression was observed in 3-4 pairs of the brain neurons: the anterior dorso-lateral interneurons,

153 These brain neurons therefore contain an identified deep brain

154 pacity of nuclear extracts from adult rodent brain neurons to carry out DNA mismatch repair.

155 asing hormone (GnRH)-mediated signaling from brain neurons to pituitary gonadotropes.

156 ated axons can electrically couple groups of brain neurons to synchronise fi ring and contribute to r

157 ly sends new cells to different areas of the brain: neurons to the olfactory bulbs and glial cells to

158 stitute a dominant Ca(2+) entry pathway into brain neurons, triggering downstream Ca(2+) -dependent p

159 ional tissue-specific expression of ttll1 in brain neurons, ttll4 in muscle, and ttll7 in otic placod

160 ses serotonin-immunoreactivity in identified brain neurons under limiting food conditions thereby lea

161 esent necrosis, but it now appears that many brain neurons undergo apoptosis after either global or f

162 In the rodent brain, neurons vary significantly in katanin levels, dep

163 that conditioning lesions "prime" descending brain neurons via cell body responses and enhance subseq

164 dish peroxidase (HRP) labeling of descending brain neurons was performed in "young" and "old" larval

165 n polymerization in Alzheimer's disease (AD) brain neurons, we examined protein and gene expression f

166 nd artificial activation of Gr43a-expressing brain neurons, we show that Gr43a is both necessary and

167 d at 20% BL, an average of 98% of descending brain neurons were double labeled.

168 Voltage-gated sodium channels in brain neurons were found to associate with receptor prot

169 evious reports of PTHrP expression in normal brain, neurons were the primary site of immunoreactive P

170 etermine the neurochemical identities of rat brain neurons which are activated by a low dose (0.175 m

171 e a tradeoff between body size and number of brain neurons, which explains the small brain size of gr

172 Most recent projects focus on only brain neurons, with the exception of an early effort to

173 does not have a relatively larger number of brain neurons yet is remarkable in its cognitive abiliti