■ Published papers
Original article
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1.
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Tatsuya Maegawa, Hiroyuki Akagawa, Hideaki Onda, Hidetoshi Kasuya:
Whole-exome sequencing in a Japanese multiplex family identifies new susceptibility genes for intracranial aneurysms.
PLoS ONE
17
(3)
:e0265359
, 2022.3
DOI:doi: 10.1371/journal.pone.0265359
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2.
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Hara Shoko, Mukawa Maki, Akagawa Hiroyuki, Thamamongood Thiparpa, Inaji Motoki, Tanaka Yoji, Maehara Taketoshi, Kasuya Hidetoshi, Nariai Tadashi:
Absence of the RNF213 p.R4810K variant may indicate a severe form of pediatric moyamoya disease in Japanese patients.
Journal of neurosurgery. Pediatrics
29
(1)
:48-56
, 2021.10
DOI:10.3171/2021.7.PEDS21250
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3.
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Kurokawa Yuna, Konishi Rikako, Tomioku Kanna, Tanabe Kenji, Fujita Akikazu:
The distribution of phosphatidylinositol 4,5-bisphosphate in the budding yeast plasma membrane.
Histochemistry and cell biology
156
(2)
:109-121
, 2021.8
DOI:10.1007/s00418-021-01989-8
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4.
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Kenji Tanabe:
Image-based phenotypic profiling of a chemogenomic screening library identifies novel druggable targets in the EGFR pathway.
BioRxiv
:440090
, 2021.4
DOI:https://doi.org/10.1101/2021.04.16.440090
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Case report
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1.
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Morita Shuhei, Yamaguchi Koji, Akagawa Hiroyuki, Ishikawa Tatsuya, Funatsu Takayuki, Eguchi Seiichiro, Ishikawa Tomomi, Niwa Akihiro, Nonaka Taku, Kawamata Takakazu:
Triple bypass for multisystem smooth muscle dysfunction syndrome due to Arg179His ACTA2 mutation.
Journal of stroke and cerebrovascular diseases : the official journal of National Stroke Association
31
(9)
:106402
, 2022.3
DOI:10.1016/j.jstrokecerebrovasdis.2022.106402
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2.
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Shimazaki Rui, Ikezawa Jun, Okiyama Ryoichi, Azuma Kenko, Akagawa Hiroyuki, Takahashi Kazushi:
Dystonic Tremor in Adult-onset DYT-KMT2B: A Case Report.
Internal medicine (Tokyo, Japan)
:1-5
, 2022.1
DOI:10.2169/internalmedicine.8700-21
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3.
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Yamamoto-Shimojima K†, Akagawa H, Yanagi K, Kaname T, Okamoto N, Yamamoto T*:
Deep intronic deletion in intron 3 of PLP1 associated with severe phenotype of Pelizaeus-Merzbacher disease.
Human Genome Variation
8
:14
, 2021.4
DOI:https://doi.org/10.1038/s41439-021-00144-y
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Other
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1.
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Hara Shoko, Akagawa Hiroyuki, Nariai Tadashi:
RNF213 Gene Variants in Moyamoya Disease: Questions Remain Unanswered.
World neurosurgery
162
:18-20
, 2022.3
DOI:10.1016/j.wneu.2022.03.040
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