Search the collection

49 results for Kawakami,+Hideshi

Sort by:

Sort by

Limit results to:

20 per page

49 results for Kawakami,+Hideshi

Export to excel

Export record to excel

File type to download

Beta version

Export this record
Export to excel
Print
Export record to excel
File type to download
Beta version
Select record 1
ArticlesPeer ReviewedFull Text
Optineurin deficiency impairs autophagy to cause interferon beta overproduction and increased survival of mice following viral infection
Author / Creator:Fukushi, Masaya ; Ohsawa, Ryosuke ; Okinaka, Yasushi ; Oikawa, Daisuke ; Kiyono, Tohru ; Moriwaki, Masaya ; Irie, Takashi ; Oda, Kosuke ; Kamei, Yasuhiro ; Tokunaga, Fuminori ; Sotomaru, Yusuke ; Maruyama, Hirofumi ; Kawakami, Hideshi ; Sakaguchi, Takemasa
Publisher:United States: Public Library of Science
Journal title:PloS one, 2023-06, Vol.18 (6), p.e0287545-e0287545
View online as a Library member
Access ebook if you are in the Library. Registered NSW residents may log in from home.
Export this record
Export to excel
Print
Export record to excel
File type to download
Beta version
Select record 2
ArticlesPeer ReviewedFull Text
Linear ubiquitination is involved in the pathogenesis of optineurin-associated amyotrophic lateral sclerosis
Author / Creator:Nakazawa, Seshiru ; Oikawa, Daisuke ; Ishii, Ryohei ; Ayaki, Takashi ; Takahashi, Hirotaka ; Takeda, Hiroyuki ; Ishitani, Ryuichiro ; Kamei, Kiyoko ; Takeyoshi, Izumi ; Kawakami, Hideshi ; Iwai, Kazuhiro ; Hatada, Izuho ; Sawasaki, Tatsuya ; Ito, Hidefumi ; Nureki, Osamu ; Tokunaga, Fuminori
Publisher:London: Nature Publishing Group UK
Journal title:Nature communications, 2016-08, Vol.7 (1), p.12547-12547, Article 12547
View online as a Library member
Access ebook if you are in the Library. Registered NSW residents may log in from home.
Export this record
Export to excel
Print
Export record to excel
File type to download
Beta version
Select record 3
ArticlesPeer ReviewedFull Text
The first Japanese case of primary familial brain calcification caused by an MYORG variant
Author / Creator:Kume, Kodai ; Takata, Tadayuki ; Morino, Hiroyuki ; Matsuda, Yukiko ; Ohsawa, Ryosuke ; Tada, Yui ; Kurashige, Takashi ; Kawakami, Hideshi
Publisher:England: Nature Publishing Group
Journal title:Journal of human genetics, 2020-10, Vol.65 (10), p.917-920
View online as a Library member
Access ebook if you are in the Library. Registered NSW residents may log in from home.
Export this record
Export to excel
Print
Export record to excel
File type to download
Beta version
Select record 4
ArticlesPeer ReviewedFull Text
Mutations of optineurin in amyotrophic lateral sclerosis
Author / Creator:Maruyama, Hirofumi ; Morino, Hiroyuki ; Ito, Hidefumi ; Izumi, Yuishin ; Kato, Hidemasa ; Watanabe, Yasuhito ; Kinoshita, Yoshimi ; Kamada, Masaki ; Nodera, Hiroyuki ; Suzuki, Hidenori ; Komure, Osamu ; Matsuura, Shinya ; Kobatake, Keitaro ; Morimoto, Nobutoshi ; Abe, Koji ; Suzuki, Naoki ; Aoki, Masashi ; Kawata, Akihiro ; Hirai, Takeshi ; Kato, Takeo ; Ogasawara, Kazumasa ; Hirano, Asao ; Takumi, Toru ; Kusaka, Hirofumi ; Hagiwara, Koichi ; Kaji, Ryuji ; Kawakami, Hideshi
Publisher:London: Nature Publishing Group UK
Journal title:Nature (London), 2010-05, Vol.465 (7295), p.223-226
View online as a Library member
Access ebook if you are in the Library. Registered NSW residents may log in from home.
Export this record
Export to excel
Print
Export record to excel
File type to download
Beta version
Select record 5
ArticlesPeer ReviewedFull Text
Genome-wide association study identifies common variants at four loci as genetic risk factors for Parkinson's disease
Author / Creator:Satake, Wataru ; Nakabayashi, Yuko ; Mizuta, Ikuko ; Hirota, Yushi ; Ito, Chiyomi ; Kubo, Michiaki ; Kawaguchi, Takahisa ; Tsunoda, Tatsuhiko ; Watanabe, Masahiko ; Takeda, Atsushi ; Tomiyama, Hiroyuki ; Nakashima, Kenji ; Hasegawa, Kazuko ; Obata, Fumiya ; Yoshikawa, Takeo ; Kawakami, Hideshi ; Sakoda, Saburo ; Yamamoto, Mitsutoshi ; Hattori, Nobutaka ; Murata, Miho ; Nakamura, Yusuke ; Toda, Tatsushi
Publisher:New York: Nature Publishing Group US
Journal title:Nature genetics, 2009-12, Vol.41 (12), p.1303-1307
View online as a Library member
Access ebook if you are in the Library. Registered NSW residents may log in from home.
Export this record
Export to excel
Print
Export record to excel
File type to download
Beta version
Select record 6
ArticlesPeer ReviewedFull Text
Second derivative of the finger photoplethysmogram and cardiovascular mortality in middle-aged and elderly Japanese women
Author / Creator:Inoue, Noriko ; Kawakami, Hideshi ; Yamamoto, Hideya ; Ito, Chikako ; Fujiwara, Saeko ; Sasaki, Hideo ; Kihara, Yasuki
Publisher:England: Nature Publishing Group
Journal title:Hypertension research, 2017-02, Vol.40 (2), p.207-211
View online as a Library member
Access ebook if you are in the Library. Registered NSW residents may log in from home.
Export this record
Export to excel
Print
Export record to excel
File type to download
Beta version
Select record 7
ArticlesPeer ReviewedFull Text
Genetic screening for potassium channel mutations in Japanese autosomal dominant spinocerebellar ataxia
Author / Creator:Tada, Yui ; Kume, Kodai ; Matsuda, Yukiko ; Kurashige, Takashi ; Kanaya, Yuhei ; Ohsawa, Ryosuke ; Morino, Hiroyuki ; Tabu, Hayato ; Kaneko, Satoshi ; Suenaga, Toshihiko ; Kakizuka, Akira ; Kawakami, Hideshi
Publisher:England: Nature Publishing Group
Journal title:Journal of human genetics, 2020-04, Vol.65 (4), p.363-369
View online as a Library member
Access ebook if you are in the Library. Registered NSW residents may log in from home.
Export this record
Export to excel
Print
Export record to excel
File type to download
Beta version
Select record 8
ArticlesPeer ReviewedFull Text
Prospects and status of the dosimetry system for atomic bomb survivor cohort study conducted at Research Institute for Radiation Biology and Medicine of Hiroshima University
Author / Creator:Hirota, Seiko ; Yasuda, Hiroshi ; Kawakami, Hideshi ; Yoshinaga, Shinji
Publisher:England: Oxford University Press
Journal title:Journal of radiation research, 2021-05, Vol.62 (Supplement_1), p.i107-i113
View online as a Library member
Access ebook if you are in the Library. Registered NSW residents may log in from home.
Export this record
Export to excel
Print
Export record to excel
File type to download
Beta version
Select record 9
ArticlesPeer ReviewedFull Text
Analysis of genetic risk factors in Japanese patients with Parkinson’s disease
Author / Creator:Kanaya, Yuhei ; Kume, Kodai ; Morino, Hiroyuki ; Ohsawa, Ryosuke ; Kurashige, Takashi ; Kamada, Masaki ; Torii, Tsuyoshi ; Izumi, Yuishin ; Maruyama, Hirofumi ; Kawakami, Hideshi
Publisher:England: Nature Publishing Group
Journal title:Journal of human genetics, 2021-10, Vol.66 (10), p.957-964
View online as a Library member
Access ebook if you are in the Library. Registered NSW residents may log in from home.
Export this record
Export to excel
Print
Export record to excel
File type to download
Beta version
Select record 10
ArticlesPeer ReviewedFull Text
Aggressive periodontitis and NOD2 variants
Author / Creator:Mizuno, Noriyoshi ; Kume, Kodai ; Nagatani, Yukiko ; Matsuda, Shinji ; Iwata, Tomoyuki ; Ouhara, Kazuhisa ; Kajiya, Mikihito ; Takeda, Katsuhiro ; Matsuda, Yukiko ; Tada, Yui ; Ohsawa, Ryosuke ; Morino, Hiroyuki ; Mihara, Keichiro ; Fujita, Tsuyoshi ; Kawaguchi, Hiroyuki ; Shiba, Hideki ; Kawakami, Hideshi ; Kurihara, Hidemi
Publisher:England: Nature Publishing Group
Journal title:Journal of human genetics, 2020-10, Vol.65 (10), p.841-846
View online as a Library member
Access ebook if you are in the Library. Registered NSW residents may log in from home.
Export this record
Export to excel
Print
Export record to excel
File type to download
Beta version
Select record 11
ArticlesPeer ReviewedFull Text
FXTAS is difficult to differentiate from neuronal intranuclear inclusion disease through skin biopsy: a case report
Author / Creator:Toko, Megumi ; Ohshita, Tomohiko ; Kurashige, Takashi ; Morino, Hiroyuki ; Kume, Kodai ; Yamashita, Hiroshi ; Sobue, Gen ; Iwasaki, Yasushi ; Sone, Jun ; Kawakami, Hideshi ; Maruyama, Hirofumi
Publisher:London: BioMed Central Ltd
Journal title:BMC neurology, 2021-10, Vol.21 (1), p.1-396, Article 396
View online as a Library member
Access ebook if you are in the Library. Registered NSW residents may log in from home.
Export this record
Export to excel
Print
Export record to excel
File type to download
Beta version
Select record 12
ArticlesPeer ReviewedFull Text
First report of a Japanese family with spinocerebellar ataxia type 10: The second report from Asia after a report from China
Author / Creator:Naito, Hiroyuki ; Takahashi, Tetsuya ; Kamada, Masaki ; Morino, Hiroyuki ; Yoshino, Hiroyo ; Hattori, Nobutaka ; Maruyama, Hirofumi ; Kawakami, Hideshi ; Matsumoto, Masayasu
Publisher:United States: Public Library of Science
Journal title:PloS one, 2017-05, Vol.12 (5), p.e0177955-e0177955
View online as a Library member
Access ebook if you are in the Library. Registered NSW residents may log in from home.
Export this record
Export to excel
Print
Export record to excel
File type to download
Beta version
Select record 13
ArticlesPeer ReviewedFull Text
A mutation in the low voltage-gated calcium channel CACNA1G alters the physiological properties of the channel, causing spinocerebellar ataxia
Author / Creator:Morino, Hiroyuki ; Matsuda, Yukiko ; Muguruma, Keiko ; Miyamoto, Ryosuke ; Ohsawa, Ryosuke ; Ohtake, Toshiyuki ; Otobe, Reiko ; Watanabe, Masahiko ; Maruyama, Hirofumi ; Hashimoto, Kouichi ; Kawakami, Hideshi
Publisher:England: BioMed Central Ltd
Journal title:Molecular brain, 2015-12, Vol.8 (1), p.89-89, Article 89
View online as a Library member
Access ebook if you are in the Library. Registered NSW residents may log in from home.
Export this record
Export to excel
Print
Export record to excel
File type to download
Beta version
Select record 14
ArticlesPeer ReviewedFull Text
Retinitis pigmentosa prior to familial ALS caused by a homozygous cilia and flagella-associated protein 410 mutation
Author / Creator:Kurashige, Takashi ; Morino, Hiroyuki ; Matsuda, Yukiko ; Mukai, Tomoya ; Murao, Tomomi ; Toko, Megumi ; Kume, Kodai ; Ohsawa, Ryosuke ; Torii, Tsuyoshi ; Tokinobu, Hiroshi ; Maruyama, Hirofumi ; Kawakami, Hideshi
Publisher:England: BMJ Publishing Group Ltd
Journal title:Journal of neurology, neurosurgery and psychiatry, 2020-02, Vol.91 (2), p.220-222
View online as a Library member
Access ebook if you are in the Library. Registered NSW residents may log in from home.
Export this record
Export to excel
Print
Export record to excel
File type to download
Beta version
Select record 15
ArticlesPeer ReviewedFull Text
Long-term MRI findings of adult-onset neuronal intranuclear inclusion disease
Author / Creator:Tachi, Kisaki ; Takata, Tadayuki ; Kume, Kodai ; Sone, Jun ; Kobara, Hideki ; Deguchi, Kazushi ; Kawakami, Hideshi ; Masaki, Tsutomu
Publisher:Netherlands: Elsevier B.V
Journal title:Clinical neurology and neurosurgery, 2021-02, Vol.201, p.106456-106456, Article 106456
View online as a Library member
Access ebook if you are in the Library. Registered NSW residents may log in from home.
Export this record
Export to excel
Print
Export record to excel
File type to download
Beta version
Select record 16
ArticlesPeer ReviewedFull Text
Comparison of two families with and without ataxia harboring novel variants in PRKCG
Author / Creator:Tada, Yui ; Kume, Kodai ; Noguchi, Soma ; Sekiya, Tomoko ; Nishinaka, Kazuto ; Ishiguchi, Hiroshi ; Koh, Jinsoo ; Emori, Seiji ; Nakayama, Yoshiaki ; Kurashige, Takashi ; Izumi, Yuishin ; Ito, Hidefumi ; Sakai, Norio ; Kawakami, Hideshi
Publisher:London: Nature Publishing Group
Journal title:Journal of human genetics, 2022-10, Vol.67 (10), p.595-599
View online as a Library member
Access ebook if you are in the Library. Registered NSW residents may log in from home.
Export this record
Export to excel
Print
Export record to excel
File type to download
Beta version
Select record 17
ArticlesPeer ReviewedFull Text
Middle-age-onset cerebellar ataxia caused by a homozygous TWNK variant: a case report
Author / Creator:Kume, Kodai ; Morino, Hiroyuki ; Miyamoto, Ryosuke ; Matsuda, Yukiko ; Ohsawa, Ryosuke ; Kanaya, Yuhei ; Tada, Yui ; Kurashige, Takashi ; Kawakami, Hideshi
Publisher:England: BioMed Central Ltd
Journal title:BMC medical genetics, 2020-03, Vol.21 (1), p.68-4, Article 68
View online as a Library member
Access ebook if you are in the Library. Registered NSW residents may log in from home.
Export this record
Export to excel
Print
Export record to excel
File type to download
Beta version
Select record 18
ArticlesPeer ReviewedFull Text
Zonisamide can ameliorate the voltage-dependence alteration of the T-type calcium channel CaV3.1 caused by a mutation responsible for spinocerebellar ataxia
Author / Creator:Hara, Naoyuki ; Morino, Hiroyuki ; Matsuda, Yukiko ; Satoh, Kenichi ; Hashimoto, Kouichi ; Maruyama, Hirofumi ; Kawakami, Hideshi
Publisher:London: BioMed Central Ltd
Journal title:Molecular brain, 2020-11, Vol.13 (1), p.1-163, Article 163
View online as a Library member
Access ebook if you are in the Library. Registered NSW residents may log in from home.
Export this record
Export to excel
Print
Export record to excel
File type to download
Beta version
Select record 19
ArticlesPeer ReviewedFull Text
Spinocerebellar ataxia type 17-digenic TBP/STUB1 disease: neuropathologic features of an autopsied patient
Author / Creator:Saito, Rie ; Tada, Yui ; Oikawa, Daisuke ; Sato, Yusuke ; Seto, Makiko ; Satoh, Akira ; Kume, Kodai ; Ueki, Nozomi ; Nakashima, Masahiro ; Hayashi, Shintaro ; Toyoshima, Yasuko ; Tokunaga, Fuminori ; Kawakami, Hideshi ; Kakita, Akiyoshi
Publisher:England: BioMed Central Ltd
Journal title:Acta neuropathologica communications, 2022-12, Vol.10 (1), p.177-177, Article 177
View online as a Library member
Access ebook if you are in the Library. Registered NSW residents may log in from home.
Export this record
Export to excel
Print
Export record to excel
File type to download
Beta version
Select record 20
ArticlesPeer ReviewedFull Text
Exome sequencing reveals a novel TTC19 mutation in an autosomal recessive spinocerebellar ataxia patient
Author / Creator:Morino, Hiroyuki ; Miyamoto, Ryosuke ; Ohnishi, Shizuo ; Maruyama, Hirofumi ; Kawakami, Hideshi
Publisher:England: BioMed Central Ltd
Journal title:BMC neurology, 2014-01, Vol.14 (1), p.5-5, Article 5
View online as a Library member
Access ebook if you are in the Library. Registered NSW residents may log in from home.

Showing 1 to 20 of 49 results

Export record to excel

Export this record

Export record to excel

Optineurin deficiency impairs autophagy to cause interferon beta overproduction and increased survival of mice following viral infection

Export this record

Export record to excel

Linear ubiquitination is involved in the pathogenesis of optineurin-associated amyotrophic lateral sclerosis

Export this record

Export record to excel

The first Japanese case of primary familial brain calcification caused by an MYORG variant

Export this record

Export record to excel

Mutations of optineurin in amyotrophic lateral sclerosis

Export this record

Export record to excel

Genome-wide association study identifies common variants at four loci as genetic risk factors for Parkinson's disease

Export this record

Export record to excel

Second derivative of the finger photoplethysmogram and cardiovascular mortality in middle-aged and elderly Japanese women

Export this record

Export record to excel

Genetic screening for potassium channel mutations in Japanese autosomal dominant spinocerebellar ataxia

Export this record

Export record to excel

Prospects and status of the dosimetry system for atomic bomb survivor cohort study conducted at Research Institute for Radiation Biology and Medicine of Hiroshima University

Export this record

Export record to excel

Analysis of genetic risk factors in Japanese patients with Parkinson’s disease

Export this record

Export record to excel

Aggressive periodontitis and NOD2 variants

Export this record

Export record to excel

FXTAS is difficult to differentiate from neuronal intranuclear inclusion disease through skin biopsy: a case report

Export this record

Export record to excel

First report of a Japanese family with spinocerebellar ataxia type 10: The second report from Asia after a report from China

Export this record

Export record to excel

A mutation in the low voltage-gated calcium channel CACNA1G alters the physiological properties of the channel, causing spinocerebellar ataxia

Export this record

Export record to excel

Retinitis pigmentosa prior to familial ALS caused by a homozygous cilia and flagella-associated protein 410 mutation

Export this record

Export record to excel

Long-term MRI findings of adult-onset neuronal intranuclear inclusion disease

Export this record

Export record to excel

Comparison of two families with and without ataxia harboring novel variants in PRKCG

Export this record

Export record to excel

Middle-age-onset cerebellar ataxia caused by a homozygous TWNK variant: a case report

Export this record

Export record to excel

Zonisamide can ameliorate the voltage-dependence alteration of the T-type calcium channel CaV3.1 caused by a mutation responsible for spinocerebellar ataxia

Export this record

Export record to excel

Spinocerebellar ataxia type 17-digenic TBP/STUB1 disease: neuropathologic features of an autopsied patient

Export this record

Export record to excel

Exome sequencing reveals a novel TTC19 mutation in an autosomal recessive spinocerebellar ataxia patient

Refine your search