Understanding of pathogenesis of autism and development of its therapeutic way based on epigenomic information
Understanding of pathogenesis of autism and development of its therapeutic way based on epigenomic information
批准号:
20390295
负责人:
KUBOTA Takeo
金额:
$11.32万
依托单位:
依托单位国家:
日本
项目类别:
Grant-in-Aid for Scientific Research (B)
财政年份:
2008
资助国家:
日本
项目状态:
已结题
起止时间:
2008 至 2010
中文摘要
表观遗传异常以及基因突变现在被认为是遗传病的原因。其中之一是一种自闭症,雷特综合征,由MECP2基因突变引起。在本研究中,我们发现了与神经细胞黏附相关的新的MECP2靶基因。此外,我们还了解了利用营养因子和基因靶向表观基因组试剂治疗表观基因组病的方法学。
英文摘要
Epigenetic abnormalities, as well as genetic mutations, are now considered to be causes of genetic diseases. One of those is an autistic disorder, Rett syndrome, which is caused byMECP2 gene mutations. In this study, we found new MECP2 target genes, which is involved in neuronal cell adhesion. Furthermore, we obtained some knowledge of the therapeutic methodology for epigenomic diseases with nutritional factors and gene-targeting epigenomic reagents.
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Idenfiticaiton of MeCP2-target synaptic molecules associated with pathogenesis of Rett syndrome
与 Rett 综合征发病机制相关的 MeCP2 靶标突触分子的鉴定
DOI:
--
发表时间:
2011
期刊:
影响因子:
--
作者:
[Miyake K, Hirasawa T, Kubota T]
通讯作者:
Kubota T
総説「エピジェネティクス臨床検査の展望」
回顾“表观遗传学临床测试的前景”
DOI:
--
发表时间:
2011
期刊:
臨床化学 40
影响因子:
--
作者:
[Mitsuya H, Maeda K, Das D, Ghosh AK., 久保田健夫]
通讯作者:
久保田健夫
小児神経学(有馬正高・加我牧子・稲垣真澄編)(遺伝子診断入門)
小儿神经病学(有马正孝、加贺真希子、稻垣真澄主编)(基因诊断导论)
DOI:
--
发表时间:
2008
期刊:
影响因子:
--
作者:
[三宅邦夫, 久保田健夫, 久保田健夫, 久保田健夫]
通讯作者:
久保田健夫
Rett症候群の責任蛋白質MeCP2の標的遺伝子探索-自閉症マーカー遺伝子の同定に向けて-
寻找与 Rett 综合征有关的蛋白质 MeCP2 的目标基因 - 致力于识别自闭症标记基因 -
DOI:
--
发表时间:
2008
期刊:
影响因子:
--
作者:
[久保田健夫, 伊藤雅之, 後藤雄一, 稲澤譲治]
通讯作者:
稲澤譲治
ICF, an immunodeficiency syndrome: DNA methyltransferase 3B involvement, chromosome anomalies, and gene dysregulation.
ICF,一种免疫缺陷综合征:DNA甲基转移酶3B受累,染色体异常和基因失调。
DOI:
10.1080/08916930802024202
发表时间:
2008-05
期刊:
AUTOIMMUNITY
影响因子:
3.5
作者:
[Ehrlich, Melanie, Sanchez, Cecilia, Shao, Chunbo, Nishiyama, Rie, Kehrl, John, Kuick, Rork, Kubota, Takeo, Hanash, Samir M.]
通讯作者:
Hanash, Samir M.
共 41 条
Identification of genomic changes and their therapeutic effects in neuronally-differentiated induced pluripotent stem cells of autistic patients
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批准号:25670473
-
项目类别:Grant-in-Aid for Challenging Exploratory Research
-
资助金额:$2.33万
-
财政年份:2013
-
负责人:KUBOTA Takeo
-
依托单位:
Development epigenomic restoration therapy for autistic disorders
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批准号:23390272
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项目类别:Grant-in-Aid for Scientific Research (B)
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资助金额:$11.73万
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财政年份:2011
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负责人:KUBOTA Takeo
-
依托单位:
Comparison of genomic and epigenomicexpression in monozygotic twins using next-generation sequencing.
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批准号:23659519
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项目类别:Grant-in-Aid for Challenging Exploratory Research
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资助金额:$2.5万
-
财政年份:2011
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负责人:KUBOTA Takeo
-
依托单位:
Investigation of A Child Disease with Epigenetic Disorder -Rett Syndrome-
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批准号:15390330
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项目类别:Grant-in-Aid for Scientific Research (B)
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资助金额:$9.41万
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财政年份:2003
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负责人:KUBOTA Takeo
-
依托单位:
Investigation of the imprinted domain located at the chromosomal deletion associated with Prader-Willi syndrome
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批准号:13670858
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项目类别:Grant-in-Aid for Scientific Research (C)
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资助金额:$2.43万
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财政年份:2001
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负责人:KUBOTA Takeo
-
依托单位:
Establishment of carrier detection method of X-linked diseases by methylation-specific PCR
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批准号:11670752
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项目类别:Grant-in-Aid for Scientific Research (C)
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资助金额:$1.86万
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财政年份:1999
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负责人:KUBOTA Takeo
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依托单位:
海外基金