Publications by authors named "Takuya Morikawa"

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Hexanucleotide repeat expansion in SCA36 reduces the expression of genes involved in ribosome biosynthesis and protein translation.
Takuya Morikawa, Shiroh Miura, Yusuke Uchiyama, Shigeyoshi Hiruki, Yinrui Sun

J Hum Genet· September 2024

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Episodic ataxia type 2 with a novel missense variant (Leu602Arg) in CACNA1A.
Shiroh Miura, Emina Watanabe, Kensuke Senzaki, Shigeyoshi Hiruki, Sayaka Matsumoto, Takuya Morikawa

Hum Genome Var· January 2024

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Evolutionary activation of acidic chitinase in herbivores through the H128R mutation in ruminant livestock.
Eri Tabata, Ikuto Kobayashi, Takuya Morikawa, Akinori Kashimura, Peter O Bauer

iScience· August 2023

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Oleic Acid-Containing Phosphatidylinositol Is a Blood Biomarker Candidate for SPG28.
Takuya Morikawa, Masatomo Takahashi, Yoshihiro Izumi, Takeshi Bamba, Kosei Moriyama

Biomedicines· April 2023

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Hereditary Congenital Methemoglobinemia Diagnosed at the Age of 79 Years: A Case Report.
Marohito Nakata, Naoko Yokota, Kazuhiko Tabata, Takuya Morikawa, Hiroki Shibata

Medicina (Kaunas)· March 2023

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A Japanese family with dystonia due to a pathogenic variant in SGCE.
Takuya Morikawa, Shiroh Miura, Luoming Fan, Emina Watanabe, Ryuta Fujioka

Hum Genome Var· August 2022

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Familial paroxysmal kinesigenic dyskinesia with a novel missense variant (Arg2866Trp) in NBEA.
Shiroh Miura, Tomofumi Shimojo, Takuya Morikawa, Takashi Kamada, Yusuke Uchiyama

J Hum Genet· August 2021

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A Japanese hereditary spastic paraplegia family with a rare nonsynonymous variant in the SPAST gene.
Takuya Morikawa, Shiroh Miura, Takahisa Tateishi, Kazuhito Noda, Hiroki Shibata

Hum Genome Var· May 2021

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Ddhd1 knockout mouse as a model of locomotive and physiological abnormality in familial spastic paraplegia.
Takuya Morikawa, Hiroaki Ohishi, Kengo Kosaka, Tomofumi Shimojo, Akihiro Nagano

Biosci Rep· February 2021

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TDRKH is a candidate gene for an autosomal dominant distal hereditary motor neuropathy.
Shiroh Miura, Kengo Kosaka, Takuo Nomura, Shuji Nagata, Tomofumi Shimojo, Takuya Morikawa

Eur J Med Genet· December 2019

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Spinocerebellar ataxia 27 with a novel nonsense variant (Lys177X) in FGF14.
Shiroh Miura, Kengo Kosaka, Ryuta Fujioka, Yusuke Uchiyama, Tomofumi Shimojo, Takuya Morikawa

Eur J Med Genet· March 2019

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A new mutation of congenital methemoglobinemia exacerbated after methylene blue treatment.
Fuminori Yamaji, Akio Soeda, Hiroki Shibata, Takuya Morikawa, Kodai Suzuki

Acute Med Surg· April 2018

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A novel missense variant (Gln220Arg) of GNB4 encoding guanine nucleotide-binding protein, subunit beta-4 in a Japanese family with autosomal dominant motor and sensory neuropathy.
Shiroh Miura, Takuya Morikawa, Ryuta Fujioka, Kazuhito Noda, Kengo Kosaka

Eur J Med Genet· September 2017

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Effect of decompression drying treatment on physical properties of solid foods.
Takuya Morikawa, Norihisa Takada, Makoto Miura

Biosci Biotechnol Biochem· April 2017

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Performance evaluation of the compounding robot, APOTECAchemo, for injectable anticancer drugs in a Japanese hospital.
Takuya Iwamoto, Takuya Morikawa, Miki Hioki, Hirofumi Sudo, Demis Paolucci

J Pharm Health Care Sci· April 2017

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A novel frameshift mutation of DDHD1 in a Japanese patient with autosomal recessive spastic paraplegia.
Shiroh Miura, Takuya Morikawa, Ryuta Fujioka, Kengo Kosaka, Kohei Yamada

Eur J Med Genet· August 2016

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Olopatadine, a non-sedating H1 antihistamine, decreases the nocturnal scratching without affecting sleep quality in atopic dermatitis.
Keiichi Yamanaka, Eishi Motomura, Yuichi Noro, Koji Umeda, Takuya Morikawa

Exp Dermatol· March 2015

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Effects of the NMDA receptor antagonists on deltamethrin-induced striatal dopamine release in conscious unrestrained rats.
Takuya Morikawa, Kazuhisa Furuhama

J Vet Med Sci· August 2009

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Chronobiological disturbances with hyperthermia and hypercortisolism induced by chronic mild stress in rats.
Kentarou Ushijima, Takuya Morikawa, Hideto To, Shun Higuchi, Shigehiro Ohdo

Behav Brain Res· October 2006

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