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Jun Mitsui

Showing results (81-90 of 183) with videos related to

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Frontiers in Neurology|September 5, 2022
Multi-type <i>RFC1</i> repeat expansions as the most common cause of hereditary sensory and autonomic neuropathyJun-Hui Yuan, Yujiro Higuchi, Masahiro Ando, et al.
Cerebellum (London, England)|September 13, 2022
Clinical and Genetic Features of Multiplex Families with Multiple System Atrophy and Parkinson's DiseaseTakashi Matsukawa, Kristine Joyce L Porto, Jun Mitsui, et al.
Digestive Diseases (Basel, Switzerland)|July 4, 2018
Host MICA Polymorphism as a Potential Predictive Marker in Response to Chemotherapy for Colorectal Liver MetastasesYujiro Nishioka, Junichi Shindoh, Yoshinori Inagaki, et al.
Annals of Clinical and Translational Neurology|November 14, 2025
Dorsolateral Cervical Cord T2 Hyperintensity in KIF1C-Related Disease (Spastic Paraplegia 58): Two Long-Duration CasesAkihiko Mitsutake, Masao Osaki, Takashi Matsukawa, et al.
BMC Neurology|November 4, 2022
Valosin-containing protein Asp395Gly mutation in a patient with frontotemporal dementia: a case reportRyota Kobayashi, Hiroya Naruse, Shinobu Kawakatsu, et al.
Annals of Clinical and Translational Neurology|June 8, 2017
Partial duplication of <i>DHH</i> causes minifascicular neuropathy: A novel mutation detection of <i>DHH</i>Naoko Saito Sato, Risa Maekawa, Hiroyuki Ishiura, et al.
Neuropathology : Official Journal of the Japanese Society of Neuropathology|March 29, 2020
An autopsy case of G<sub>M1</sub> gangliosidosis type II in a patient who survived a long duration with artificial respiratory supportAkiko Uchino, Makiko Nagai, Naomi Kanazawa, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|September 3, 2013
A recurrent de novo FAM111A mutation causes Kenny-Caffey syndrome type 2Tsuyoshi Isojima, Koichiro Doi, Jun Mitsui, et al.
Human Genome Variation|February 28, 2025
In-frame deletion variant of ABCD1 in a sporadic case of adrenoleukodystrophyTakashi Matsukawa, Atsushi Sudo, Toshiyuki Kakumoto, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|May 13, 2010
Two distinct mechanisms of augmented antitumor activity by modulation of immunostimulatory/inhibitory signalsJun Mitsui, Hiroyoshi Nishikawa, Daisuke Muraoka, et al.
Pageof 19

Showing results (81-90 of 183) with videos related to

Sort By:
Pageof 19
Frontiers in Neurology|September 5, 2022
Multi-type <i>RFC1</i> repeat expansions as the most common cause of hereditary sensory and autonomic neuropathyJun-Hui Yuan, Yujiro Higuchi, Masahiro Ando, et al.
Cerebellum (London, England)|September 13, 2022
Clinical and Genetic Features of Multiplex Families with Multiple System Atrophy and Parkinson's DiseaseTakashi Matsukawa, Kristine Joyce L Porto, Jun Mitsui, et al.
Digestive Diseases (Basel, Switzerland)|July 4, 2018
Host MICA Polymorphism as a Potential Predictive Marker in Response to Chemotherapy for Colorectal Liver MetastasesYujiro Nishioka, Junichi Shindoh, Yoshinori Inagaki, et al.
Annals of Clinical and Translational Neurology|November 14, 2025
Dorsolateral Cervical Cord T2 Hyperintensity in KIF1C-Related Disease (Spastic Paraplegia 58): Two Long-Duration CasesAkihiko Mitsutake, Masao Osaki, Takashi Matsukawa, et al.
BMC Neurology|November 4, 2022
Valosin-containing protein Asp395Gly mutation in a patient with frontotemporal dementia: a case reportRyota Kobayashi, Hiroya Naruse, Shinobu Kawakatsu, et al.
Annals of Clinical and Translational Neurology|June 8, 2017
Partial duplication of <i>DHH</i> causes minifascicular neuropathy: A novel mutation detection of <i>DHH</i>Naoko Saito Sato, Risa Maekawa, Hiroyuki Ishiura, et al.
Neuropathology : Official Journal of the Japanese Society of Neuropathology|March 29, 2020
An autopsy case of G<sub>M1</sub> gangliosidosis type II in a patient who survived a long duration with artificial respiratory supportAkiko Uchino, Makiko Nagai, Naomi Kanazawa, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|September 3, 2013
A recurrent de novo FAM111A mutation causes Kenny-Caffey syndrome type 2Tsuyoshi Isojima, Koichiro Doi, Jun Mitsui, et al.
Human Genome Variation|February 28, 2025
In-frame deletion variant of ABCD1 in a sporadic case of adrenoleukodystrophyTakashi Matsukawa, Atsushi Sudo, Toshiyuki Kakumoto, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|May 13, 2010
Two distinct mechanisms of augmented antitumor activity by modulation of immunostimulatory/inhibitory signalsJun Mitsui, Hiroyoshi Nishikawa, Daisuke Muraoka, et al.
Pageof 19