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Kenji Amano

Showing results (1-10 of 25) with videos related to

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Advances in Experimental Medicine and Biology|March 11, 2010
Central respiratory failure in a mouse model depends on the genetic background of the hostSatoru Arata, Kenji Amano, Kazuhiro Yamakawa, et al.
Neurobiology of Disease|December 11, 2017
DYRK1A-haploinsufficiency in mice causes autistic-like features and febrile seizuresMatthieu Raveau, Atsushi Shimohata, Kenji Amano, et al.
Advances in Experimental Medicine and Biology|March 11, 2010
Loss of pre-inspiratory neuron synchroneity in mice with DSCAM deficiencyKenji Amano, Morimitsu Fujii, Satoru Arata, et al.
Elife|February 28, 2018
Alterations of in vivo CA1 network activity in Dp(16)1Yey Down syndrome model miceMatthieu Raveau, Denis Polygalov, Roman Boehringer, et al.
Cerebral Cortex (New York, N.Y. : 1991)|August 28, 2009
Enlarged brain ventricles and impaired neurogenesis in the Ts1Cje and Ts2Cje mouse models of Down syndromeKeiichi Ishihara, Kenji Amano, Eiichi Takaki, et al.
Hinyokika Kiyo. Acta Urologica Japonica|February 4, 2022
[A Case of Retroperitoneal Bronchogenic Cyst Diagnosed by Fluorescence in situ Hybridization]Kenji Amano, Hisanori Taniguchi, Junichi Ikeda, et al.
Human Molecular Genetics|January 11, 2017
Brain ventriculomegaly in Down syndrome mice is caused by Pcp4 dose-dependent cilia dysfunctionMatthieu Raveau, Takashi Nakahari, Sachie Asada, et al.
Neuroscience Letters|August 9, 2005
Transcriptional profiling of a mouse model for Lafora disease reveals dysregulation of genes involved in the expression and modification of proteinsSubramaniam Ganesh, Naomi Tsurutani, Kenji Amano, et al.
Human Molecular Genetics|May 13, 2004
Dosage-dependent over-expression of genes in the trisomic region of Ts1Cje mouse model for Down syndromeKenji Amano, Haruhiko Sago, Chiharu Uchikawa, et al.
Psychiatric Genetics|January 17, 2008
Association study between the Down syndrome cell adhesion molecule (DSCAM) gene and bipolar disorderKenji Amano, Kazuo Yamada, Yoshimi Iwayama, et al.
Pageof 3

Showing results (1-10 of 25) with videos related to

Sort By:
Pageof 3
Advances in Experimental Medicine and Biology|March 11, 2010
Central respiratory failure in a mouse model depends on the genetic background of the hostSatoru Arata, Kenji Amano, Kazuhiro Yamakawa, et al.
Neurobiology of Disease|December 11, 2017
DYRK1A-haploinsufficiency in mice causes autistic-like features and febrile seizuresMatthieu Raveau, Atsushi Shimohata, Kenji Amano, et al.
Advances in Experimental Medicine and Biology|March 11, 2010
Loss of pre-inspiratory neuron synchroneity in mice with DSCAM deficiencyKenji Amano, Morimitsu Fujii, Satoru Arata, et al.
Elife|February 28, 2018
Alterations of in vivo CA1 network activity in Dp(16)1Yey Down syndrome model miceMatthieu Raveau, Denis Polygalov, Roman Boehringer, et al.
Cerebral Cortex (New York, N.Y. : 1991)|August 28, 2009
Enlarged brain ventricles and impaired neurogenesis in the Ts1Cje and Ts2Cje mouse models of Down syndromeKeiichi Ishihara, Kenji Amano, Eiichi Takaki, et al.
Hinyokika Kiyo. Acta Urologica Japonica|February 4, 2022
[A Case of Retroperitoneal Bronchogenic Cyst Diagnosed by Fluorescence in situ Hybridization]Kenji Amano, Hisanori Taniguchi, Junichi Ikeda, et al.
Human Molecular Genetics|January 11, 2017
Brain ventriculomegaly in Down syndrome mice is caused by Pcp4 dose-dependent cilia dysfunctionMatthieu Raveau, Takashi Nakahari, Sachie Asada, et al.
Neuroscience Letters|August 9, 2005
Transcriptional profiling of a mouse model for Lafora disease reveals dysregulation of genes involved in the expression and modification of proteinsSubramaniam Ganesh, Naomi Tsurutani, Kenji Amano, et al.
Human Molecular Genetics|May 13, 2004
Dosage-dependent over-expression of genes in the trisomic region of Ts1Cje mouse model for Down syndromeKenji Amano, Haruhiko Sago, Chiharu Uchikawa, et al.
Psychiatric Genetics|January 17, 2008
Association study between the Down syndrome cell adhesion molecule (DSCAM) gene and bipolar disorderKenji Amano, Kazuo Yamada, Yoshimi Iwayama, et al.
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