An exploration of causative genes of focal cortical dysplasia with intractable epilepsy, using advanced technologies
Project/Area Number |
22659197
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Research Category |
Grant-in-Aid for Challenging Exploratory Research
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Allocation Type | Single-year Grants |
Research Field |
Pediatrics
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Research Institution | National Center of Neurology and Psychiatry |
Principal Investigator |
ITO Masayuki 独立行政法人国立精神・神経医療研究センター, 神経研究所疾病研究第二部, 室長 (50243407)
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Project Period (FY) |
2010 – 2012
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Project Status |
Completed (Fiscal Year 2012)
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Budget Amount *help |
¥3,280,000 (Direct Cost: ¥2,800,000、Indirect Cost: ¥480,000)
Fiscal Year 2012: ¥1,040,000 (Direct Cost: ¥800,000、Indirect Cost: ¥240,000)
Fiscal Year 2011: ¥1,040,000 (Direct Cost: ¥800,000、Indirect Cost: ¥240,000)
Fiscal Year 2010: ¥1,200,000 (Direct Cost: ¥1,200,000)
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Keywords | 難治性てんかん / 大脳皮質異形成 / 遺伝子 |
Research Abstract |
Intractable epilepsy in childhood has other problems and leads to be difficult to spend daily ability. The major cause of the epilepsy is focal cortical dysplasia (FCD), which shows characteristic dysplasia in a part of cerebral cortex. In the present study, we explore causative genes of FCD formation, using cell sorting technique and CGH (Comparative genomic hybridization)array analysis. We used DNA samples of 4 FCD patients, whose parents agreed with the research usage under an informed consent. As a result, we obtained no 4-patient common abnormal gene, two 3-patient common abnormal genes and thirteen 2-patient common abnormal genes. Among them, we could pick up six genes for the candidates. We advance further analyses for the goal.
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Report
(4 results)
Research Products
(23 results)
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[Journal Article] A case of severe progressive early-onset epileptic encephalopathy: unique GABAergic interneuron distribution and imagings2013
Author(s)
Inoue T, Kawawakia H, Kuki I, Nabatame S, Tomonoh Y, Sukigara S, Horino A, Nukui M, Okazaki S, Tomiwa K, Kimura-Ohba S, Inoue T, Hirose S, Shiomi M, Itoh M.
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Journal Title
J Neurol Sci
Volume: 327
Issue: 1-2
Pages: 65-72
DOI
Related Report
Peer Reviewed
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[Journal Article] Hypoalbuminemia in early-onset dentatorubralpallidoluysian atrophy due to leakage of albumin in multiple organs2013
Author(s)
Nagai S, Saito Y, Endo Y, Saito T, Kenji Sugai K, Ishiyama A, Komaki H, Nakagawa E, Sasaki M, Ito K, Saito Y, Sukigara S, Ito M, Goto Y, Ito S, Matsuoka K
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Journal Title
J Neurol
Volume: 260
Issue: 5
Pages: 1263-1271
DOI
Related Report
Peer Reviewed
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[Journal Article] Abnormal maturation and differentiation of neocortical neurons in epileptogenic cortical malformation: unique distribution of layer-specific marker cells of focal cortical dysplasia and hemimegalencephaly2012
Author(s)
Arai A, Saito T, Hanai S, Otsuki T, Nakagawa E, Takahashi A, Kaneko Y, Kaido T, Saito Y, Sugai K, Sasaki M, Goto Y, Itoh M
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Journal Title
Brain Res
Volume: 1470
Pages: 89-97
DOI
Related Report
Peer Reviewed
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[Journal Article] Imbalance of interneuron distribution between neocortex and basal ganglia: Consideration of epileptogenesis of focal cortical dysplasia2012
Author(s)
Sakakibara T, Sukigara S, Otsuki T, Takahashi A, Kaneko Y, Kaido T, Saito Y, Sato N, Nakagawa E, Sugai K, Sasaki M, Goto Y, Itoh M
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Journal Title
J Neurol Sci
Volume: 323
Issue: 1-2
Pages: 128-133
DOI
Related Report
Peer Reviewed
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[Journal Article] Delayed maturation of neurons of focal cortical dysplasia IIA and IIB: consideration from specific neocortical-layer marker expression2012
Author(s)
Sakakibara T, Saito T, Otsuk T, Takahashi A, Kaneko Y, Kaido T, Saito Y, Sato N, Nakagawa E, Sugai K, Sasaki M, Goto Y, Itoh M
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Journal Title
J Neuropathol Exp Neurol 2012
Volume: 71(8)
Issue: 8
Pages: 741-749
DOI
Related Report
Peer Reviewed
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[Journal Article] Methyl CpG-binding protein isoform MeCP2_e2 is dispensable for Rett syndrome phenotypes but essential for embryo viability and placenta development2012
Author(s)
Itoh, M., Tahimic, C.G.T., Ide,S., Otsuki, A., Sasaoka, T., Noguchi, S., Oshimura, M., Goto, Y., and Kurimasa, A
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Journal Title
Journal of Biological Chemistry
Volume: 287(17)
Issue: 17
Pages: 13859-13867
DOI
Related Report
Peer Reviewed
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[Journal Article] Neocortical layer-formation of the human developing brains and lissencephalies : consideration of layer-specific markers expression.2011
Author(s)
Saito T, Hanai S, Takashima S, Nakagawa E, Okazaki S, Inoue T, Miyata R, Hoshino K, Akashi T, Sasaki M, Goto Y, Hayashi M, Itoh M.
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Journal Title
Cereb Cortex
Volume: 21
Pages: 588-596
Related Report
Peer Reviewed
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[Journal Article] Neocortical layer-formation of the human developing brains and lissencephalies: consideration of layer-specific markers expression2010
Author(s)
Saito T, Hanai S, Takashima S, Nakagawa E, Okazaki S, Inoue T, Miyata R, Hoshino K, Akashi T, Sasaki M, Goto Y, Hayashi M, Itoh M
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Journal Title
Cereb Cortex 2011
Volume: 21
Issue: 3
Pages: 588-596
DOI
Related Report
Peer Reviewed
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[Presentation] Defferent pathophysiology of focal cortical dysplasia IIA and IIB: specific neocortical-layer marker expression2011
Author(s)
Sakakibara T, Saito T, Otsuki T, Takahashi A, Kaneko Y, Kaido T, Saito Y, Nakagawa E, Sugai K, Sasaki K, Goto Y, Itoh M
Organizer
The 29th International Epilepsy Congress
Place of Presentation
Rome, Italy
Related Report
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