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Ohsawa, Ryosuke
82
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Online (82)
Mediatypes
Articles (Online) (51)
OpenAccess-fulltext (31)
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1
Optineurin deficiency impairs autophagy to cause interferon..:
Fukushi, Masaya
;
Ohsawa, Ryosuke
;
Okinaka, Yasushi
...
PLOS ONE. 18 (2023) 6 - p. e0287545 , 2023
Link:
https://doi.org/10.1371/..
?
2
Analysis of genetic risk factors in Japanese patients with ..:
Kanaya, Yuhei
;
Kume, Kodai
;
Morino, Hiroyuki
...
Journal of Human Genetics. 66 (2021) 10 - p. 957-964 , 2021
Link:
https://doi.org/10.1038/..
?
3
Optineurin defects cause TDP43-pathology with autophagic va..:
Kurashige, Takashi
;
Kuramochi, Masahito
;
Ohsawa, Ryosuke
...
Neurobiology of Disease. 148 (2021) - p. 105215 , 2021
Link:
https://doi.org/10.1016/..
?
4
Middle-age-onset cerebellar ataxia caused by a homozygous T..:
Kume, Kodai
;
Morino, Hiroyuki
;
Miyamoto, Ryosuke
...
BMC Medical Genetics. 21 (2020) 1 - p. , 2020
Link:
https://doi.org/10.1186/..
?
5
The first Japanese case of primary familial brain calcifica..:
Kume, Kodai
;
Takata, Tadayuki
;
Morino, Hiroyuki
...
Journal of Human Genetics. 65 (2020) 10 - p. 917-920 , 2020
Link:
https://doi.org/10.1038/..
?
6
Aggressive periodontitis and NOD2 variants:
Mizuno, Noriyoshi
;
Kume, Kodai
;
Nagatani, Yukiko
...
Journal of Human Genetics. 65 (2020) 10 - p. 841-846 , 2020
Link:
https://doi.org/10.1038/..
?
7
Genetic screening for potassium channel mutations in Japane..:
Tada, Yui
;
Kume, Kodai
;
Matsuda, Yukiko
...
Journal of Human Genetics. 65 (2020) 4 - p. 363-369 , 2020
Link:
https://doi.org/10.1038/..
?
8
Optineurin regulates osteoblastogenesis through STAT1:
Mizuno, Noriyoshi
;
Iwata, Tomoyuki
;
Ohsawa, Ryosuke
...
Biochemical and Biophysical Research Communications. 525 (2020) 4 - p. 889-894 , 2020
Link:
https://doi.org/10.1016/..
?
9
C-terminal mutations in SYNE1 are associated with motor neu..:
Kume, Kodai
;
Morino, Hiroyuki
;
Komure, Osamu
...
Journal of the Neurological Sciences. 402 (2019) - p. 118-120 , 2019
Link:
https://doi.org/10.1016/..
?
10
Compound heterozygote mutations in the SIGMAR1 gene in an o..:
Izumi, Yuishin
;
Morino, Hiroyuki
;
Miyamoto, Ryosuke
...
Geriatrics & Gerontology International. 18 (2018) 10 - p. 1519-1520 , 2018
Link:
https://doi.org/10.1111/..
?
11
The Commercial Antibodies Widely Used to Measure H3 K56 Ace..:
Pal, Sangita
;
Graves, Hillary
;
Ohsawa, Ryosuke
...
PLOS ONE. 11 (2016) 5 - p. e0155409 , 2016
Link:
https://doi.org/10.1371/..
?
12
A mutation in the low voltage-gated calcium channel CACNA1G..:
Morino, Hiroyuki
;
Matsuda, Yukiko
;
Muguruma, Keiko
...
Molecular Brain. 8 (2015) 1 - p. , 2015
Link:
https://doi.org/10.1186/..
?
13
Mutations in Twinkle primase-helicase cause Perrault syndro..:
Morino, Hiroyuki
;
Pierce, Sarah B.
;
Matsuda, Yukiko
...
Neurology. 83 (2014) 22 - p. 2054-2061 , 2014
Link:
https://doi.org/10.1212/..
?
14
At the intersection of non-coding transcription, DNA repair..:
Ohsawa, Ryosuke
;
Seol, Ja-Hwan
;
Tyler, Jessica K.
Frontiers in Genetics. 4 (2013) - p. , 2013
Link:
https://doi.org/10.3389/..
?
15
Epigenetic inheritance of an inducibly nucleosome-depleted ..:
Ohsawa, Ryosuke
;
Adkins, Melissa
;
Tyler, Jessica K
Epigenetics & Chromatin. 2 (2009) 1 - p. , 2009
Link:
https://doi.org/10.1186/..
1-15