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Asako Otomo

Showing results (1-10 of 40) with videos related to

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Neurology Research International|August 2, 2012
Dysregulation of the autophagy-endolysosomal system in amyotrophic lateral sclerosis and related motor neuron diseasesAsako Otomo, Lei Pan, Shinji Hadano
Genomics|November 1, 2002
Identification and characterization of novel members of the CREG family, putative secreted glycoproteins expressed specifically in brainRyota Kunita, Asako Otomo, Joh-E Ikeda
FEBS Open Bio|May 31, 2016
Sexually dimorphic expression of Dmrt1 and γH2AX in germ stem cells during gonadal development in Xenopus laevisKazuko Fujitani, Asako Otomo, Mikako Wada, et al.
Neuroscience Research|April 2, 2011
Loss of glial fibrillary acidic protein marginally accelerates disease progression in a SOD1(H46R) transgenic mouse model of ALSYasuhiro Yoshii, Asako Otomo, Lei Pan, et al.
Genes to Cells : Devoted to Molecular & Cellular Mechanisms|July 1, 2026
The SQSTM1 L341V Variant Associated With Sporadic ALS Promotes the Accumulation of Enlarged Ubiquitin-Positive SQSTM1 BodiesKento Shimakura, Akira Oka, Haruka Yudahira, et al.
Biochemical and Biophysical Research Communications|July 9, 2021
The N-terminal intrinsically disordered region mediates intracellular localization and self-oligomerization of ALS2Kento Shimakura, Kai Sato, Shun Mitsui, et al.
Neurochemistry International|June 15, 2007
Molecular and cellular function of ALS2/alsin: implication of membrane dynamics in neuronal development and degenerationShinji Hadano, Ryota Kunita, Asako Otomo, et al.
FEBS Letters|February 9, 2011
Defective relocalization of ALS2/alsin missense mutants to Rac1-induced macropinosomes accounts for loss of their cellular function and leads to disturbed amphisome formationAsako Otomo, Ryota Kunita, Kyoko Suzuki-Utsunomiya, et al.
Molecules (Basel, Switzerland)|October 27, 2022
Personalized Treatment for Infantile Ascending Hereditary Spastic Paralysis Based on In Silico StrategiesMatteo Rossi Sebastiano, Giuseppe Ermondi, Kai Sato, et al.
Biochemical and Biophysical Research Communications|January 22, 2020
ALS2, the small GTPase Rab17-interacting protein, regulates maturation and sorting of Rab17-associated endosomesSuzuka Ono, Asako Otomo, Shuji Murakoshi, et al.
Pageof 4

Showing results (1-10 of 40) with videos related to

Sort By:
Pageof 4
Neurology Research International|August 2, 2012
Dysregulation of the autophagy-endolysosomal system in amyotrophic lateral sclerosis and related motor neuron diseasesAsako Otomo, Lei Pan, Shinji Hadano
Genomics|November 1, 2002
Identification and characterization of novel members of the CREG family, putative secreted glycoproteins expressed specifically in brainRyota Kunita, Asako Otomo, Joh-E Ikeda
FEBS Open Bio|May 31, 2016
Sexually dimorphic expression of Dmrt1 and γH2AX in germ stem cells during gonadal development in Xenopus laevisKazuko Fujitani, Asako Otomo, Mikako Wada, et al.
Neuroscience Research|April 2, 2011
Loss of glial fibrillary acidic protein marginally accelerates disease progression in a SOD1(H46R) transgenic mouse model of ALSYasuhiro Yoshii, Asako Otomo, Lei Pan, et al.
Genes to Cells : Devoted to Molecular & Cellular Mechanisms|July 1, 2026
The SQSTM1 L341V Variant Associated With Sporadic ALS Promotes the Accumulation of Enlarged Ubiquitin-Positive SQSTM1 BodiesKento Shimakura, Akira Oka, Haruka Yudahira, et al.
Biochemical and Biophysical Research Communications|July 9, 2021
The N-terminal intrinsically disordered region mediates intracellular localization and self-oligomerization of ALS2Kento Shimakura, Kai Sato, Shun Mitsui, et al.
Neurochemistry International|June 15, 2007
Molecular and cellular function of ALS2/alsin: implication of membrane dynamics in neuronal development and degenerationShinji Hadano, Ryota Kunita, Asako Otomo, et al.
FEBS Letters|February 9, 2011
Defective relocalization of ALS2/alsin missense mutants to Rac1-induced macropinosomes accounts for loss of their cellular function and leads to disturbed amphisome formationAsako Otomo, Ryota Kunita, Kyoko Suzuki-Utsunomiya, et al.
Molecules (Basel, Switzerland)|October 27, 2022
Personalized Treatment for Infantile Ascending Hereditary Spastic Paralysis Based on In Silico StrategiesMatteo Rossi Sebastiano, Giuseppe Ermondi, Kai Sato, et al.
Biochemical and Biophysical Research Communications|January 22, 2020
ALS2, the small GTPase Rab17-interacting protein, regulates maturation and sorting of Rab17-associated endosomesSuzuka Ono, Asako Otomo, Shuji Murakoshi, et al.
Pageof 4