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Yoshio Hashizume

Showing results (151-160 of 159) with videos related to

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American Journal of Human Genetics|November 3, 2009
Spinocerebellar ataxia type 31 is associated with "inserted" penta-nucleotide repeats containing (TGGAA)nNozomu Sato, Takeshi Amino, Kazuhiro Kobayashi, et al.
Neurology International|October 25, 2024
UBL3 Interacts with PolyQ-Expanded Huntingtin Fragments and Modifies Their Intracellular SortingSoho Oyama, Hengsen Zhang, Rafia Ferdous, et al.
Brain Communications|March 1, 2021
Distinct microglial response against Alzheimer's amyloid and tau pathologies characterized by P2Y12 receptorJun Maeda, Takeharu Minamihisamatsu, Masafumi Shimojo, et al.
Metabolites|September 26, 2021
Transferrin Biosynthesized in the Brain Is a Novel Biomarker for Alzheimer's DiseaseKyoka Hoshi, Hiromi Ito, Eriko Abe, et al.
American Journal of Human Genetics|July 8, 2005
An autosomal dominant cerebellar ataxia linked to chromosome 16q22.1 is associated with a single-nucleotide substitution in the 5' untranslated region of the gene encoding a protein with spectrin repeat and Rho guanine-nucleotide exchange-factor domainsKinya Ishikawa, Shuta Toru, Taiji Tsunemi, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 6, 2014
Transcriptome analysis of distinct mouse strains reveals kinesin light chain-1 splicing as an amyloid-β accumulation modifierTakashi Morihara, Noriyuki Hayashi, Mikiko Yokokoji, et al.
Molecular and Cellular Biology|June 22, 2002
Targeted deletion of both thymidine phosphorylase and uridine phosphorylase and consequent disorders in miceMisako Haraguchi, Hiroaki Tsujimoto, Masakazu Fukushima, et al.
Brain Pathology (Zurich, Switzerland)|July 13, 2021
Multiple system atrophy variant with severe hippocampal pathologyTakashi Ando, Yuichi Riku, Akio Akagi, 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 16

Showing results (151-160 of 159) with videos related to

Sort By:
Pageof 16
You have reached the last page of results.This site can display upto 159 results.
American Journal of Human Genetics|November 3, 2009
Spinocerebellar ataxia type 31 is associated with "inserted" penta-nucleotide repeats containing (TGGAA)nNozomu Sato, Takeshi Amino, Kazuhiro Kobayashi, et al.
Neurology International|October 25, 2024
UBL3 Interacts with PolyQ-Expanded Huntingtin Fragments and Modifies Their Intracellular SortingSoho Oyama, Hengsen Zhang, Rafia Ferdous, et al.
Brain Communications|March 1, 2021
Distinct microglial response against Alzheimer's amyloid and tau pathologies characterized by P2Y12 receptorJun Maeda, Takeharu Minamihisamatsu, Masafumi Shimojo, et al.
Metabolites|September 26, 2021
Transferrin Biosynthesized in the Brain Is a Novel Biomarker for Alzheimer's DiseaseKyoka Hoshi, Hiromi Ito, Eriko Abe, et al.
American Journal of Human Genetics|July 8, 2005
An autosomal dominant cerebellar ataxia linked to chromosome 16q22.1 is associated with a single-nucleotide substitution in the 5' untranslated region of the gene encoding a protein with spectrin repeat and Rho guanine-nucleotide exchange-factor domainsKinya Ishikawa, Shuta Toru, Taiji Tsunemi, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 6, 2014
Transcriptome analysis of distinct mouse strains reveals kinesin light chain-1 splicing as an amyloid-β accumulation modifierTakashi Morihara, Noriyuki Hayashi, Mikiko Yokokoji, et al.
Molecular and Cellular Biology|June 22, 2002
Targeted deletion of both thymidine phosphorylase and uridine phosphorylase and consequent disorders in miceMisako Haraguchi, Hiroaki Tsujimoto, Masakazu Fukushima, et al.
Brain Pathology (Zurich, Switzerland)|July 13, 2021
Multiple system atrophy variant with severe hippocampal pathologyTakashi Ando, Yuichi Riku, Akio Akagi, 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 16