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Kozo Tanaka

Showing results (61-70 of 71) with videos related to

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The Journal of Biological Chemistry|September 10, 2017
Dynamic feature of mitotic arrest deficient 2-like protein 2 (MAD2L2) and structural basis for its interaction with chromosome alignment-maintaining phosphoprotein (CAMP)Kodai Hara, Shota Taharazako, Masanori Ikeda, et al.
Cell Reports|October 24, 2025
BET family BRD3 initiates DSB-induced chromatin remodeling with TIP60 to promote R-loop-mediated HRJianghao Qian, Tomoko Watanabe, Reiko Watanabe, et al.
The Biochemical Journal|February 21, 2018
Phosphorylation of BACH1 switches its function from transcription factor to mitotic chromosome regulator and promotes its interaction with HMMRJie Li, Hiroki Shima, Hironari Nishizawa, et al.
Scientific Reports|December 31, 2024
CHAMP1 premature termination codon mutations found in individuals with intellectual disability cause a homologous recombination defect through haploinsufficiencyYujiro Yoshizaki, Yunosuke Ouchi, Dicky Kurniawan, et al.
Brain Communications|September 15, 2022
Deficiency of <i>CHAMP1</i>, a gene related to intellectual disability, causes impaired neuronal development and a mild behavioural phenotypeMasayoshi Nagai, Kenji Iemura, Takako Kikkawa, et al.
Biochimica Et Biophysica Acta|May 12, 2015
A novel anti-microtubule agent with carbazole and benzohydrazide structures suppresses tumor cell growth in vivoMakoto Ohira, Yuka Iwasaki, Chika Tanaka, et al.
Iscience|February 10, 2022
TORC1 inactivation promotes APC/C-dependent mitotic slippage in yeast and human cellsChihiro Yamada, Aya Morooka, Seira Miyazaki, et al.
Gastroenterology|January 16, 2017
Activation of the Hypoxia Inducible Factor 1α Subunit Pathway in Steatotic Liver Contributes to Formation of Cholesterol GallstonesYoichiro Asai, Tetsuya Yamada, Sohei Tsukita, et al.
Human Mutation|January 12, 2016
De Novo Truncating Mutations in the Kinetochore-Microtubules Attachment Gene CHAMP1 Cause Syndromic Intellectual DisabilityBertrand Isidor, Sébastien Küry, Jill A Rosenfeld, et al.
Autophagy|January 12, 2008
Guidelines for the use and interpretation of assays for monitoring autophagy in higher eukaryotesDaniel J Klionsky, Hagai Abeliovich, Patrizia Agostinis, et al.
Pageof 8

Showing results (61-70 of 71) with videos related to

Sort By:
Pageof 8
The Journal of Biological Chemistry|September 10, 2017
Dynamic feature of mitotic arrest deficient 2-like protein 2 (MAD2L2) and structural basis for its interaction with chromosome alignment-maintaining phosphoprotein (CAMP)Kodai Hara, Shota Taharazako, Masanori Ikeda, et al.
Cell Reports|October 24, 2025
BET family BRD3 initiates DSB-induced chromatin remodeling with TIP60 to promote R-loop-mediated HRJianghao Qian, Tomoko Watanabe, Reiko Watanabe, et al.
The Biochemical Journal|February 21, 2018
Phosphorylation of BACH1 switches its function from transcription factor to mitotic chromosome regulator and promotes its interaction with HMMRJie Li, Hiroki Shima, Hironari Nishizawa, et al.
Scientific Reports|December 31, 2024
CHAMP1 premature termination codon mutations found in individuals with intellectual disability cause a homologous recombination defect through haploinsufficiencyYujiro Yoshizaki, Yunosuke Ouchi, Dicky Kurniawan, et al.
Brain Communications|September 15, 2022
Deficiency of <i>CHAMP1</i>, a gene related to intellectual disability, causes impaired neuronal development and a mild behavioural phenotypeMasayoshi Nagai, Kenji Iemura, Takako Kikkawa, et al.
Biochimica Et Biophysica Acta|May 12, 2015
A novel anti-microtubule agent with carbazole and benzohydrazide structures suppresses tumor cell growth in vivoMakoto Ohira, Yuka Iwasaki, Chika Tanaka, et al.
Iscience|February 10, 2022
TORC1 inactivation promotes APC/C-dependent mitotic slippage in yeast and human cellsChihiro Yamada, Aya Morooka, Seira Miyazaki, et al.
Gastroenterology|January 16, 2017
Activation of the Hypoxia Inducible Factor 1α Subunit Pathway in Steatotic Liver Contributes to Formation of Cholesterol GallstonesYoichiro Asai, Tetsuya Yamada, Sohei Tsukita, et al.
Human Mutation|January 12, 2016
De Novo Truncating Mutations in the Kinetochore-Microtubules Attachment Gene CHAMP1 Cause Syndromic Intellectual DisabilityBertrand Isidor, Sébastien Küry, Jill A Rosenfeld, et al.
Autophagy|January 12, 2008
Guidelines for the use and interpretation of assays for monitoring autophagy in higher eukaryotesDaniel J Klionsky, Hagai Abeliovich, Patrizia Agostinis, et al.
Pageof 8