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Mari Yoshida

Showing results (301-310 of 376) with videos related to

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Plos One|February 2, 2013
Early detection of abnormal prion protein in genetic human prion diseases now possible using real-time QUIC assayKazunori Sano, Katsuya Satoh, Ryuichiro Atarashi, et al.
Rinsho Shinkeigaku = Clinical Neurology|February 10, 2009
[Frontotemporal dementia (FTD) and genetic mutations including progranulin gene]Tetsuaki Arai, Masato Hasegawa, Masugi Nishihara, et al.
Frontiers in Neuroscience|November 30, 2020
Comparison of Common and Disease-Specific Post-translational Modifications of Pathological Tau Associated With a Wide Range of TauopathiesFuyuki Kametani, Mari Yoshida, Tomoyasu Matsubara, et al.
Acta Neuropathologica Communications|August 23, 2024
Genetic and pathophysiological insights from autopsied patient with primary familial brain calcification: novel MYORG variants and astrocytic implicationsTakahiro Hobara, Yujiro Higuchi, Mari Yoshida, et al.
Experimental Cell Research|August 10, 2018
Hippo, Drosophila MST, is a novel modifier of motor neuron degeneration induced by knockdown of Caz, Drosophila FUSYumiko Azuma, Takahiko Tokuda, Yukie Kushimura, et al.
Brain Communications|September 21, 2020
Two distinct prions in fatal familial insomnia and its sporadic formAtsuko Takeuchi, Shirou Mohri, Hideaki Kai, et al.
Journal of Nuclear Medicine : Official Publication, Society of Nuclear Medicine|January 8, 2026
Serotonin Transporter Distribution in the Brainstem of Multiple-System Atrophy-Parkinsonian Type: Insights from Pathology and <sup>123</sup>I-FP-CIT SPECT FindingsCong Shang, Ryunosuke Nagao, Yuichi Riku, et al.
Neuropathology : Official Journal of the Japanese Society of Neuropathology|January 28, 2010
Phosphorylated and cleaved TDP-43 in ALS, FTLD and other neurodegenerative disorders and in cellular models of TDP-43 proteinopathyTetsuaki Arai, Masato Hasegawa, Takashi Nonoka, et al.
Clinical Neurology and Neurosurgery|March 11, 2020
Steroid-responsive recurrent tumefactive demyelination with multiple petechial hemorrhages along non-displaced medullary veinsTakashi Tsuboi, Yumiko Harada, Masashi Suzuki, et al.
Internal Medicine (Tokyo, Japan)|July 17, 2024
Histopathological Investigation of Progressive Encephalomyelitis with Rigidity and Myoclonus: An Autopsy Case Characterized by Oculomotor Dysfunction and Autonomic FailureHiroyuki Yabata, Ryutaro Nakamura, Seiji Sugiyama, et al.
Pageof 38

Showing results (301-310 of 376) with videos related to

Sort By:
Pageof 38
Plos One|February 2, 2013
Early detection of abnormal prion protein in genetic human prion diseases now possible using real-time QUIC assayKazunori Sano, Katsuya Satoh, Ryuichiro Atarashi, et al.
Rinsho Shinkeigaku = Clinical Neurology|February 10, 2009
[Frontotemporal dementia (FTD) and genetic mutations including progranulin gene]Tetsuaki Arai, Masato Hasegawa, Masugi Nishihara, et al.
Frontiers in Neuroscience|November 30, 2020
Comparison of Common and Disease-Specific Post-translational Modifications of Pathological Tau Associated With a Wide Range of TauopathiesFuyuki Kametani, Mari Yoshida, Tomoyasu Matsubara, et al.
Acta Neuropathologica Communications|August 23, 2024
Genetic and pathophysiological insights from autopsied patient with primary familial brain calcification: novel MYORG variants and astrocytic implicationsTakahiro Hobara, Yujiro Higuchi, Mari Yoshida, et al.
Experimental Cell Research|August 10, 2018
Hippo, Drosophila MST, is a novel modifier of motor neuron degeneration induced by knockdown of Caz, Drosophila FUSYumiko Azuma, Takahiko Tokuda, Yukie Kushimura, et al.
Brain Communications|September 21, 2020
Two distinct prions in fatal familial insomnia and its sporadic formAtsuko Takeuchi, Shirou Mohri, Hideaki Kai, et al.
Journal of Nuclear Medicine : Official Publication, Society of Nuclear Medicine|January 8, 2026
Serotonin Transporter Distribution in the Brainstem of Multiple-System Atrophy-Parkinsonian Type: Insights from Pathology and <sup>123</sup>I-FP-CIT SPECT FindingsCong Shang, Ryunosuke Nagao, Yuichi Riku, et al.
Neuropathology : Official Journal of the Japanese Society of Neuropathology|January 28, 2010
Phosphorylated and cleaved TDP-43 in ALS, FTLD and other neurodegenerative disorders and in cellular models of TDP-43 proteinopathyTetsuaki Arai, Masato Hasegawa, Takashi Nonoka, et al.
Clinical Neurology and Neurosurgery|March 11, 2020
Steroid-responsive recurrent tumefactive demyelination with multiple petechial hemorrhages along non-displaced medullary veinsTakashi Tsuboi, Yumiko Harada, Masashi Suzuki, et al.
Internal Medicine (Tokyo, Japan)|July 17, 2024
Histopathological Investigation of Progressive Encephalomyelitis with Rigidity and Myoclonus: An Autopsy Case Characterized by Oculomotor Dysfunction and Autonomic FailureHiroyuki Yabata, Ryutaro Nakamura, Seiji Sugiyama, et al.
Pageof 38