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ABOUT JoVE

Overview Leadership Blog JoVE Help Center

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Publishing Process Editorial Board Scope & Policies Peer Review FAQ Submit

LIBRARIANS

Testimonials Subscriptions Access Resources Library Advisory Board FAQ

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JoVE Journal Methods Collections JoVE Encyclopedia of Experiments Archive

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Ryuta Fujioka

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The Plant Cell|April 17, 2012

An inducible RNA interference system in Physcomitrella patens reveals a dominant role of augmin in phragmoplast microtubule generationYuki Nakaoka, Tomohiro Miki, Ryuta Fujioka, et al.

European Journal of Medical Genetics|December 4, 2018

TDRKH is a candidate gene for an autosomal dominant distal hereditary motor neuropathyShiroh Miura, Kengo Kosaka, Takuo Nomura, et al.

Molecular Brain|April 25, 2014

Comprehensive behavioral study of mGluR3 knockout mice: implication in schizophrenia related endophenotypesRyuta Fujioka, Takenobu Nii, Akiko Iwaki, et al.

Journal of Human Genetics|April 29, 2020

Intronic variant in IQGAP3 associated with hereditary neuropathy with proximal lower dominancy, urinary disturbance, and paroxysmal dry coughShiroh Miura, Kengo Kosaka, Tomofumi Shimojo, et al.

Journal of the Neurological Sciences|June 30, 2015

A novel missense mutation of RYR1 in familial idiopathic hyper CK-emiaKen Sano, Shiroh Miura, Toshiya Fujiwara, et al.

Bioscience Reports|February 18, 2021

Ddhd1 knockout mouse as a model of locomotive and physiological abnormality in familial spastic paraplegiaTakuya Morikawa, Hiroaki Ohishi, Kengo Kosaka, et al.

Pageof 2

Search research articles

Showing results (11-20 of 16) with videos related to

Sort By:

Pageof 2

You have reached the last page of results.This site can display upto 16 results.

The Plant Cell|April 17, 2012

An inducible RNA interference system in Physcomitrella patens reveals a dominant role of augmin in phragmoplast microtubule generationYuki Nakaoka, Tomohiro Miki, Ryuta Fujioka, et al.

European Journal of Medical Genetics|December 4, 2018

TDRKH is a candidate gene for an autosomal dominant distal hereditary motor neuropathyShiroh Miura, Kengo Kosaka, Takuo Nomura, et al.

Molecular Brain|April 25, 2014

Comprehensive behavioral study of mGluR3 knockout mice: implication in schizophrenia related endophenotypesRyuta Fujioka, Takenobu Nii, Akiko Iwaki, et al.

Journal of Human Genetics|April 29, 2020

Intronic variant in IQGAP3 associated with hereditary neuropathy with proximal lower dominancy, urinary disturbance, and paroxysmal dry coughShiroh Miura, Kengo Kosaka, Tomofumi Shimojo, et al.

Journal of the Neurological Sciences|June 30, 2015

A novel missense mutation of RYR1 in familial idiopathic hyper CK-emiaKen Sano, Shiroh Miura, Toshiya Fujiwara, et al.

Bioscience Reports|February 18, 2021

Ddhd1 knockout mouse as a model of locomotive and physiological abnormality in familial spastic paraplegiaTakuya Morikawa, Hiroaki Ohishi, Kengo Kosaka, et al.

Pageof 2