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Chikashi Obuse

Showing results (81-90 of 93) with videos related to

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Science Translational Medicine|July 18, 2014
An annexin A1-FPR1 interaction contributes to necroptosis of keratinocytes in severe cutaneous adverse drug reactionsNao Saito, Hongjiang Qiao, Teruki Yanagi, et al.
The EMBO Journal|July 26, 2012
Histone chaperone activity of Fanconi anemia proteins, FANCD2 and FANCI, is required for DNA crosslink repairKoichi Sato, Masamichi Ishiai, Kazue Toda, et al.
Scientific Reports|July 5, 2020
Rare variant of the epigenetic regulator SMCHD1 in a patient with pituitary hormone deficiencyKenichi Kinjo, Keisuke Nagasaki, Koji Muroya, et al.
Developmental Cell|January 12, 2010
The E3 ligase TTC3 facilitates ubiquitination and degradation of phosphorylated AktFutoshi Suizu, Yosuke Hiramuki, Fumihiko Okumura, et al.
Nature Communications|December 15, 2025
scRepli-RamDA-seq: a multi-omics technology enabling the analysis of gene expression dynamics during S-phaseRawin Poonperm, Taiki Yoneda, Taito Imada, et al.
Cell Reports|January 12, 2017
BRCA1 Directs the Repair Pathway to Homologous Recombination by Promoting 53BP1 DephosphorylationMayu Isono, Atsuko Niimi, Takahiro Oike, et al.
Molecular Cell|July 6, 2011
SHP2 tyrosine phosphatase converts parafibromin/Cdc73 from a tumor suppressor to an oncogenic driverAtsushi Takahashi, Ryouhei Tsutsumi, Ippei Kikuchi, et al.
Scientific Reports|August 15, 2013
Genetically encoded system to track histone modification in vivoYuko Sato, Masanori Mukai, Jun Ueda, et al.
Scientific Reports|April 12, 2016
Histone H4 lysine 20 acetylation is associated with gene repression in human cellsJun-Ya Kaimori, Kazumitsu Maehara, Yoko Hayashi-Takanaka, et al.
Neurology|May 30, 2020
Homozygous nonsense variant in <i>LRIF1</i> associated with facioscapulohumeral muscular dystrophyKohei Hamanaka, Darina Šikrová, Satomi Mitsuhashi, et al.
Pageof 10

Showing results (81-90 of 93) with videos related to

Sort By:
Pageof 10
Science Translational Medicine|July 18, 2014
An annexin A1-FPR1 interaction contributes to necroptosis of keratinocytes in severe cutaneous adverse drug reactionsNao Saito, Hongjiang Qiao, Teruki Yanagi, et al.
The EMBO Journal|July 26, 2012
Histone chaperone activity of Fanconi anemia proteins, FANCD2 and FANCI, is required for DNA crosslink repairKoichi Sato, Masamichi Ishiai, Kazue Toda, et al.
Scientific Reports|July 5, 2020
Rare variant of the epigenetic regulator SMCHD1 in a patient with pituitary hormone deficiencyKenichi Kinjo, Keisuke Nagasaki, Koji Muroya, et al.
Developmental Cell|January 12, 2010
The E3 ligase TTC3 facilitates ubiquitination and degradation of phosphorylated AktFutoshi Suizu, Yosuke Hiramuki, Fumihiko Okumura, et al.
Nature Communications|December 15, 2025
scRepli-RamDA-seq: a multi-omics technology enabling the analysis of gene expression dynamics during S-phaseRawin Poonperm, Taiki Yoneda, Taito Imada, et al.
Cell Reports|January 12, 2017
BRCA1 Directs the Repair Pathway to Homologous Recombination by Promoting 53BP1 DephosphorylationMayu Isono, Atsuko Niimi, Takahiro Oike, et al.
Molecular Cell|July 6, 2011
SHP2 tyrosine phosphatase converts parafibromin/Cdc73 from a tumor suppressor to an oncogenic driverAtsushi Takahashi, Ryouhei Tsutsumi, Ippei Kikuchi, et al.
Scientific Reports|August 15, 2013
Genetically encoded system to track histone modification in vivoYuko Sato, Masanori Mukai, Jun Ueda, et al.
Scientific Reports|April 12, 2016
Histone H4 lysine 20 acetylation is associated with gene repression in human cellsJun-Ya Kaimori, Kazumitsu Maehara, Yoko Hayashi-Takanaka, et al.
Neurology|May 30, 2020
Homozygous nonsense variant in <i>LRIF1</i> associated with facioscapulohumeral muscular dystrophyKohei Hamanaka, Darina Šikrová, Satomi Mitsuhashi, et al.
Pageof 10