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Ryozo Kuwano

Showing results (81-90 of 97) with videos related to

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Acta Neuropathologica|February 9, 2010
Sporadic four-repeat tauopathy with frontotemporal lobar degeneration, Parkinsonism, and motor neuron disease: a distinct clinicopathological and biochemical disease entityYong-Juan Fu, Yasushi Nishihira, Shigetoshi Kuroda, et al.
Journal of Human Genetics|October 21, 2011
A genome-wide CNV association study on panic disorder in a Japanese populationYoshiya Kawamura, Takeshi Otowa, Asako Koike, et al.
Molecular Cytogenetics|July 3, 2015
Assessment of copy number variations in the brain genome of schizophrenia patientsMiwako Sakai, Yuichiro Watanabe, Toshiyuki Someya, et al.
BMC Medical Genomics|April 1, 2020
Sensitivity to gene dosage and gene expression affects genes with copy number variants observed among neuropsychiatric diseasesMaria Yamasaki, Takashi Makino, Seik-Soon Khor, et al.
Journal of Human Genetics|June 17, 2016
Evaluation of polygenic risks for narcolepsy and essential hypersomniaMaria Yamasaki, Taku Miyagawa, Hiromi Toyoda, et al.
Annals of Neurology|July 22, 2014
PLXNA4 is associated with Alzheimer disease and modulates tau phosphorylationGyungah Jun, Hirohide Asai, Ella Zeldich, et al.
Neurology|May 11, 2016
Distinct molecular mechanisms of HTRA1 mutants in manifesting heterozygotes with CARASILHiroaki Nozaki, Taisuke Kato, Megumi Nihonmatsu, et al.
The New England Journal of Medicine|April 24, 2009
Association of HTRA1 mutations and familial ischemic cerebral small-vessel diseaseKenju Hara, Atsushi Shiga, Toshio Fukutake, et al.
EMBO Molecular Medicine|January 6, 2010
The 28-amino acid form of an APLP1-derived Abeta-like peptide is a surrogate marker for Abeta42 production in the central nervous systemKanta Yanagida, Masayasu Okochi, Shinji Tagami, et al.
Journal of Alzheimer'S Disease : JAD|May 21, 2025
Association of rare <i>APOE</i> missense variants with Alzheimer's disease in the Japanese populationAkinori Miyashita, Ai Obinata, Norikazu Hara, et al.
Pageof 10

Showing results (81-90 of 97) with videos related to

Sort By:
Pageof 10
Acta Neuropathologica|February 9, 2010
Sporadic four-repeat tauopathy with frontotemporal lobar degeneration, Parkinsonism, and motor neuron disease: a distinct clinicopathological and biochemical disease entityYong-Juan Fu, Yasushi Nishihira, Shigetoshi Kuroda, et al.
Journal of Human Genetics|October 21, 2011
A genome-wide CNV association study on panic disorder in a Japanese populationYoshiya Kawamura, Takeshi Otowa, Asako Koike, et al.
Molecular Cytogenetics|July 3, 2015
Assessment of copy number variations in the brain genome of schizophrenia patientsMiwako Sakai, Yuichiro Watanabe, Toshiyuki Someya, et al.
BMC Medical Genomics|April 1, 2020
Sensitivity to gene dosage and gene expression affects genes with copy number variants observed among neuropsychiatric diseasesMaria Yamasaki, Takashi Makino, Seik-Soon Khor, et al.
Journal of Human Genetics|June 17, 2016
Evaluation of polygenic risks for narcolepsy and essential hypersomniaMaria Yamasaki, Taku Miyagawa, Hiromi Toyoda, et al.
Annals of Neurology|July 22, 2014
PLXNA4 is associated with Alzheimer disease and modulates tau phosphorylationGyungah Jun, Hirohide Asai, Ella Zeldich, et al.
Neurology|May 11, 2016
Distinct molecular mechanisms of HTRA1 mutants in manifesting heterozygotes with CARASILHiroaki Nozaki, Taisuke Kato, Megumi Nihonmatsu, et al.
The New England Journal of Medicine|April 24, 2009
Association of HTRA1 mutations and familial ischemic cerebral small-vessel diseaseKenju Hara, Atsushi Shiga, Toshio Fukutake, et al.
EMBO Molecular Medicine|January 6, 2010
The 28-amino acid form of an APLP1-derived Abeta-like peptide is a surrogate marker for Abeta42 production in the central nervous systemKanta Yanagida, Masayasu Okochi, Shinji Tagami, et al.
Journal of Alzheimer'S Disease : JAD|May 21, 2025
Association of rare <i>APOE</i> missense variants with Alzheimer's disease in the Japanese populationAkinori Miyashita, Ai Obinata, Norikazu Hara, et al.
Pageof 10