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Fuyuki Miya

Showing results (51-60 of 109) with videos related to

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Communications Biology|April 1, 2025
An organoid library of human esophageal squamous cell carcinomas (ESCCs) uncovers the chemotherapy-resistant ESCC featuresShunsaku Nakagawa, Taku Sato, Eriko Ohashi, et al.
European Journal of Human Genetics : EJHG|September 22, 2016
Novel compound heterozygous variants in PLK4 identified in a patient with autosomal recessive microcephaly and chorioretinopathyMakiko Tsutsumi, Setsuri Yokoi, Fuyuki Miya, et al.
Journal of Human Genetics|June 23, 2017
Siblings with optic neuropathy and RTN4IP1 mutationNobuhiko Okamoto, Fuyuki Miya, Yoshikazu Hatsukawa, et al.
In Vivo (Athens, Greece)|January 6, 2021
ELF3 Overexpression as Prognostic Biomarker for Recurrence of Stage II Colorectal CancerAyumi Takaoka, Toshiaki Ishikawa, Satoshi Okazaki, et al.
Human Molecular Genetics|July 21, 2022
De novo non-synonymous DPYSL2 (CRMP2) variants in two patients with intellectual disabilities and documentation of functional relevance through zebrafish rescue and cellular transfection experimentsHisato Suzuki, Simo Li, Tomoharu Tokutomi, et al.
Brain & Development|October 19, 2025
Refractory myoclonic epilepsy and progressive movement disorder arising from recurrent DHDDS variants in Japanese patients: a case seriesYu Kobayashi, Satoru Sakuma, Emiko Morimoto, et al.
European Journal of Medical Genetics|August 16, 2024
Digital clubbing without hypoxia for lysinuric protein intoleranceDaisuke Watanabe, Yuko Tsujioka, Daisuke Nakato, et al.
Iscience|February 7, 2022
Immune subtypes and neoantigen-related immune evasion in advanced colorectal cancerToshitaka Sugawara, Fuyuki Miya, Toshiaki Ishikawa, et al.
Acta Ophthalmologica|February 12, 2020
Serum anti-recoverin antibodies is found in elderly patients with retinitis pigmentosa and cancerTaimu Sato, Koji M Nishiguchi, Kosuke Fujita, et al.
American Journal of Medical Genetics. Part A|August 5, 2017
A novel genetic syndrome with STARD9 mutation and abnormal spindle morphologyNobuhiko Okamoto, Yuki Tsuchiya, Fuyuki Miya, et al.
Pageof 11

Showing results (51-60 of 109) with videos related to

Sort By:
Pageof 11
Communications Biology|April 1, 2025
An organoid library of human esophageal squamous cell carcinomas (ESCCs) uncovers the chemotherapy-resistant ESCC featuresShunsaku Nakagawa, Taku Sato, Eriko Ohashi, et al.
European Journal of Human Genetics : EJHG|September 22, 2016
Novel compound heterozygous variants in PLK4 identified in a patient with autosomal recessive microcephaly and chorioretinopathyMakiko Tsutsumi, Setsuri Yokoi, Fuyuki Miya, et al.
Journal of Human Genetics|June 23, 2017
Siblings with optic neuropathy and RTN4IP1 mutationNobuhiko Okamoto, Fuyuki Miya, Yoshikazu Hatsukawa, et al.
In Vivo (Athens, Greece)|January 6, 2021
ELF3 Overexpression as Prognostic Biomarker for Recurrence of Stage II Colorectal CancerAyumi Takaoka, Toshiaki Ishikawa, Satoshi Okazaki, et al.
Human Molecular Genetics|July 21, 2022
De novo non-synonymous DPYSL2 (CRMP2) variants in two patients with intellectual disabilities and documentation of functional relevance through zebrafish rescue and cellular transfection experimentsHisato Suzuki, Simo Li, Tomoharu Tokutomi, et al.
Brain & Development|October 19, 2025
Refractory myoclonic epilepsy and progressive movement disorder arising from recurrent DHDDS variants in Japanese patients: a case seriesYu Kobayashi, Satoru Sakuma, Emiko Morimoto, et al.
European Journal of Medical Genetics|August 16, 2024
Digital clubbing without hypoxia for lysinuric protein intoleranceDaisuke Watanabe, Yuko Tsujioka, Daisuke Nakato, et al.
Iscience|February 7, 2022
Immune subtypes and neoantigen-related immune evasion in advanced colorectal cancerToshitaka Sugawara, Fuyuki Miya, Toshiaki Ishikawa, et al.
Acta Ophthalmologica|February 12, 2020
Serum anti-recoverin antibodies is found in elderly patients with retinitis pigmentosa and cancerTaimu Sato, Koji M Nishiguchi, Kosuke Fujita, et al.
American Journal of Medical Genetics. Part A|August 5, 2017
A novel genetic syndrome with STARD9 mutation and abnormal spindle morphologyNobuhiko Okamoto, Yuki Tsuchiya, Fuyuki Miya, et al.
Pageof 11