Advanced Brain Science Project
高级脑科学项目
基本信息
- 批准号:12209001
- 负责人:
- 金额:$ 997.25万
- 依托单位:
- 依托单位国家:日本
- 项目类别:Grant-in-Aid for Scientific Research on Priority Areas
- 财政年份:2000
- 资助国家:日本
- 起止时间:2000 至 2005
- 项目状态:已结题
- 来源:
- 关键词:
项目摘要
By this project, many papers with the highest impact have been published, which have clearly shown that the level of neuroscience in Japan is very high. When the project was initiated in 2000, goals were set for each field, and I believe all of us have reached them. Among the excellent publications, the following ones are exceptional: "Brain repair" by Dr. M. Nakafuku; identification of guidance molecules by Dr. K. Kaibuchi, discovery of neprilysin as a AB-degrading protease by Dr. T. Saido, and clinical trial of a new drug for X-linked spinal and bulbar muscular atrophy by Dr. G. Sobue. In addition, steady progress in the research of higher cortical function using monkey by Dr. J. Tanji should be mentioned here. Finally, identification of one susceptibility gene for Alzheimer's disease is a milestone in this kind of research in Japan.It is often claimed that interdisciplinary interaction is required to significantly advance science, and indeed this project provided such opportunity. This can partly explain why A01 investigators have obtained the most striking data: excellent investigators majoring development in general, neurobiology and stem cells have got together under the flag of neurogenesis, and heavily interacted with each another.
通过该项目,发表了许多具有最高影响力的论文,这些论文清楚地表明日本的神经科学水平非常高。当这个项目在2000年启动时,为每个领域设定了目标,我相信我们所有人都达到了目标。在优秀的出版物中,以下是例外:M.导向分子的鉴定。Kaibuchi博士发现脑啡肽酶是一种AB降解蛋白酶。Saido博士和G.索布江此外,在此应提及J.Tanji博士使用猴子进行的高级皮质功能研究的稳步进展。最后,阿尔茨海默病易感基因的确定是日本这类研究的里程碑。人们常说,要想使科学取得重大进展,就需要跨学科的相互作用,而这一项目确实提供了这样的机会。这可以部分解释为什么A01研究人员获得了最惊人的数据:一般发育、神经生物学和干细胞专业的优秀研究人员在神经发生的旗帜下聚集在一起,并相互作用。
项目成果
期刊论文数量(98)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
Brain-derived neurotrophic factor increases inhibitory synapses, revealed in solitary neurons cultured from rat visual cortex
- DOI:10.1016/j.neuroscience.2004.03.053
- 发表时间:2004-12
- 期刊:
- 影响因子:3.3
- 作者:M. Palizvan;K. Sohya;K. Kohara;A. Maruyama;H. Yasuda;F. Kimura;T. Tsumoto
- 通讯作者:M. Palizvan;K. Sohya;K. Kohara;A. Maruyama;H. Yasuda;F. Kimura;T. Tsumoto
Interference of CREB-dependent transcriptional activation by expanded polyglutamine stretches - Augmentation of transcriptional activation as a potential therapeutic strategy for polyglutamine diseases
扩展多聚谷氨酰胺延伸段干扰 CREB 依赖性转录激活 - 增强转录激活作为多聚谷氨酰胺疾病的潜在治疗策略
- DOI:
- 发表时间:2005
- 期刊:
- 影响因子:0
- 作者:Shimohata;M;Shimohata T;Igarashi;S;Naruse;S;Tsujil;S
- 通讯作者:S
Itami C., Kimura F., Kohno T., Matsuoka M., Ichikawa M., Tsumoto T., Nakamura S.: "Brain-derived neurotrophic factor-dependent unmasking of "silent" synapses in the developing mouse barrel cortex"Proc Natl Acad Sci USA. 100. 13069-13074 (2003)
Itami C.、Kimura F.、Kohno T.、Matsuoka M.、Ichikawa M.、Tsumoto T.、Nakamura S.:“脑源性神经营养因子依赖性揭示发育中的小鼠桶状皮质中的“沉默”突触”Proc
- DOI:
- 发表时间:
- 期刊:
- 影响因子:0
- 作者:
- 通讯作者:
Gu Y, Misoinou H, Sato T, Dohmae N, Takio K, Ihara Y: "Distinct intramembrane cleavage of the beta-amyloid precursor protein family resembling gamma-secretase-like cleavage of Notch"Journal of Biological Chemistry. 276. 35235-35238 (2001)
Gu Y、Misoinou H、Sato T、Dohmae N、Takio K、Ihara Y:“β-淀粉样前体蛋白家族的独特膜内裂解类似于 Notch 的γ-分泌酶样裂解”生物化学杂志。
- DOI:
- 发表时间:
- 期刊:
- 影响因子:0
- 作者:
- 通讯作者:
Matsuda H, et al.: "Chaotic stimulus dependent long-term potentiation in the hippocampal CA1 area."Biosystems. 58. 273-279 (2000)
Matsuda H 等人:“海马 CA1 区域的混沌刺激依赖性长期增强。”Biosystems。
- DOI:
- 发表时间:
- 期刊:
- 影响因子:0
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IHARA Yasuo其他文献
IHARA Yasuo的其他文献
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{{ truncateString('IHARA Yasuo', 18)}}的其他基金
A theoretical study on cultural evolution of human maladaptive behaviors
人类适应不良行为的文化演化理论研究
- 批准号:
18770217 - 财政年份:2006
- 资助金额:
$ 997.25万 - 项目类别:
Grant-in-Aid for Young Scientists (B)
Characterization of the enzymatic properties of γ-secretase
γ-分泌酶酶学特性的表征
- 批准号:
17025008 - 财政年份:2005
- 资助金额:
$ 997.25万 - 项目类别:
Grant-in-Aid for Scientific Research on Priority Areas
Hyperphosphorylation and aggregation of tau protein, and neuronal death
tau 蛋白的过度磷酸化和聚集以及神经元死亡
- 批准号:
12210005 - 财政年份:2000
- 资助金额:
$ 997.25万 - 项目类别:
Grant-in-Aid for Scientific Research on Priority Areas
Studies on beta-amyloidogenesis-isolation of membrane-bound Abeta
β-淀粉样蛋白生成的研究-膜结合 Abeta 的分离
- 批准号:
07408025 - 财政年份:1995
- 资助金额:
$ 997.25万 - 项目类别:
Grant-in-Aid for Scientific Research (A)
Identification of posttranslational modification of the tau in paired helical filaments
成对螺旋丝中 tau 蛋白翻译后修饰的鉴定
- 批准号:
03102008 - 财政年份:1991
- 资助金额:
$ 997.25万 - 项目类别:
Grant-in-Aid for Specially Promoted Research
Identification of the components of paired helical filaments
成对螺旋丝成分的鉴定
- 批准号:
62480210 - 财政年份:1987
- 资助金额:
$ 997.25万 - 项目类别:
Grant-in-Aid for General Scientific Research (B)
Identification of proteolytic fragments derived from Alzheimer's paired helical filaments with proteases
用蛋白酶鉴定源自阿尔茨海默病配对螺旋丝的蛋白水解片段
- 批准号:
60480224 - 财政年份:1985
- 资助金额:
$ 997.25万 - 项目类别:
Grant-in-Aid for General Scientific Research (B)
相似海外基金
Pathological roles of immune guidance molecules that induce granulocytic cell death
诱导粒细胞死亡的免疫引导分子的病理作用
- 批准号:
22K16361 - 财政年份:2022
- 资助金额:
$ 997.25万 - 项目类别:
Grant-in-Aid for Early-Career Scientists
Guidance molecules interact to orchestrate dopamine plasticity in adulthood
引导分子相互作用以协调成年期的多巴胺可塑性
- 批准号:
RGPIN-2015-04819 - 财政年份:2019
- 资助金额:
$ 997.25万 - 项目类别:
Discovery Grants Program - Individual
Guidance molecules interact to orchestrate dopamine plasticity in adulthood
引导分子相互作用以协调成年期的多巴胺可塑性
- 批准号:
RGPIN-2015-04819 - 财政年份:2018
- 资助金额:
$ 997.25万 - 项目类别:
Discovery Grants Program - Individual
Investigation on pathological implications of guidance molecules in neuro-immune-metabolism.
神经免疫代谢中引导分子的病理学意义的研究。
- 批准号:
18H05282 - 财政年份:2018
- 资助金额:
$ 997.25万 - 项目类别:
Grant-in-Aid for Scientific Research (S)
The relationship between the guidance molecules Draxin-Neogenin pathway and tumorigenicity of the small cell lung cancer
引导分子Draxin-Neogenin通路与小细胞肺癌致瘤性的关系
- 批准号:
19K21287 - 财政年份:2018
- 资助金额:
$ 997.25万 - 项目类别:
Grant-in-Aid for Research Activity Start-up
Guidance molecules interact to orchestrate dopamine plasticity in adulthood
引导分子相互作用以协调成年期的多巴胺可塑性
- 批准号:
RGPIN-2015-04819 - 财政年份:2017
- 资助金额:
$ 997.25万 - 项目类别:
Discovery Grants Program - Individual
The role of long-term memory formation in axon guidance molecules
长期记忆形成在轴突引导分子中的作用
- 批准号:
17K14964 - 财政年份:2017
- 资助金额:
$ 997.25万 - 项目类别:
Grant-in-Aid for Young Scientists (B)
Guidance molecules interact to orchestrate dopamine plasticity in adulthood
引导分子相互作用以协调成年期的多巴胺可塑性
- 批准号:
RGPIN-2015-04819 - 财政年份:2016
- 资助金额:
$ 997.25万 - 项目类别:
Discovery Grants Program - Individual
Regulation of small cell lung carcinoma cells by interference between axon guidance molecules and their receptors
轴突引导分子与其受体之间的干扰对小细胞肺癌细胞的调节
- 批准号:
16K15459 - 财政年份:2016
- 资助金额:
$ 997.25万 - 项目类别:
Grant-in-Aid for Challenging Exploratory Research
Guidance molecules interact to orchestrate dopamine plasticity in adulthood
引导分子相互作用以协调成年期的多巴胺可塑性
- 批准号:
RGPIN-2015-04819 - 财政年份:2015
- 资助金额:
$ 997.25万 - 项目类别:
Discovery Grants Program - Individual