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Hitoshi Osaka

Showing results (91-100 of 218) with videos related to

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Nucleic Acids Research|March 10, 2012
HIF2α-Sp1 interaction mediates a deacetylation-dependent FVII-gene activation under hypoxic conditions in ovarian cancer cellsShiro Koizume, Shin Ito, Etsuko Miyagi, et al.
Annals of Neurology|August 10, 2010
Disrupted SOX10 regulation of GJC2 transcription causes Pelizaeus-Merzbacher-like diseaseHitoshi Osaka, Haruka Hamanoue, Ryoko Yamamoto, et al.
Pediatric Neurology|December 22, 2023
An Open-Label Administration of Bioavailable-Form Curcumin in Patients With Pelizaeus-Merzbacher DiseaseAkiyo Yamamoto, Yuko Shimizu-Motohashi, Akihiko Ishiyama, et al.
Journal of Human Genetics|July 19, 2018
A novel SLC9A1 mutation causes cerebellar ataxiaKazuhiro Iwama, Hitoshi Osaka, Takahiro Ikeda, et al.
Human Mutation|July 29, 2010
Plectin deficiency leads to both muscular dystrophy and pyloric atresia in epidermolysis bullosa simplexKen Natsuga, Wataru Nishie, Satoru Shinkuma, et al.
No to Hattatsu = Brain and Development|September 28, 2011
[Three children with Rasmussen encephalitis showing marked improvement in daily life activity following the functional hemispherectomy]Mutsuki Shioda, Hirokazu Oguni, Yasushi Ito, et al.
Brain & Development|July 4, 2016
A female case of aromatic l-amino acid decarboxylase deficiency responsive to MAO-B inhibitionKarin Kojima, Rie Anzai, Chihiro Ohba, et al.
Brain & Development|August 29, 2020
Gallbladder cancer with ascites in a child with metachromatic leukodystrophyKiri Koshu, Takahiro Ikeda, Daisuke Tamura, et al.
Pediatric Neurology|March 18, 2014
A novel two-nucleotide deletion in the ATP7A gene associated with delayed infantile onset of Menkes diseaseTakahito Wada, Marie Reine Haddad, Ling Yi, et al.
Scientific Reports|December 3, 2024
Perampanel reduces seizure frequency in patients with developmental and epileptic encephalopathy for a long termHirokazu Yamagishi, Hitoshi Osaka, Kazuhiro Muramatsu, et al.
Pageof 22

Showing results (91-100 of 218) with videos related to

Sort By:
Pageof 22
Nucleic Acids Research|March 10, 2012
HIF2α-Sp1 interaction mediates a deacetylation-dependent FVII-gene activation under hypoxic conditions in ovarian cancer cellsShiro Koizume, Shin Ito, Etsuko Miyagi, et al.
Annals of Neurology|August 10, 2010
Disrupted SOX10 regulation of GJC2 transcription causes Pelizaeus-Merzbacher-like diseaseHitoshi Osaka, Haruka Hamanoue, Ryoko Yamamoto, et al.
Pediatric Neurology|December 22, 2023
An Open-Label Administration of Bioavailable-Form Curcumin in Patients With Pelizaeus-Merzbacher DiseaseAkiyo Yamamoto, Yuko Shimizu-Motohashi, Akihiko Ishiyama, et al.
Journal of Human Genetics|July 19, 2018
A novel SLC9A1 mutation causes cerebellar ataxiaKazuhiro Iwama, Hitoshi Osaka, Takahiro Ikeda, et al.
Human Mutation|July 29, 2010
Plectin deficiency leads to both muscular dystrophy and pyloric atresia in epidermolysis bullosa simplexKen Natsuga, Wataru Nishie, Satoru Shinkuma, et al.
No to Hattatsu = Brain and Development|September 28, 2011
[Three children with Rasmussen encephalitis showing marked improvement in daily life activity following the functional hemispherectomy]Mutsuki Shioda, Hirokazu Oguni, Yasushi Ito, et al.
Brain & Development|July 4, 2016
A female case of aromatic l-amino acid decarboxylase deficiency responsive to MAO-B inhibitionKarin Kojima, Rie Anzai, Chihiro Ohba, et al.
Brain & Development|August 29, 2020
Gallbladder cancer with ascites in a child with metachromatic leukodystrophyKiri Koshu, Takahiro Ikeda, Daisuke Tamura, et al.
Pediatric Neurology|March 18, 2014
A novel two-nucleotide deletion in the ATP7A gene associated with delayed infantile onset of Menkes diseaseTakahito Wada, Marie Reine Haddad, Ling Yi, et al.
Scientific Reports|December 3, 2024
Perampanel reduces seizure frequency in patients with developmental and epileptic encephalopathy for a long termHirokazu Yamagishi, Hitoshi Osaka, Kazuhiro Muramatsu, et al.
Pageof 22