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Featured researches published by Shinya Kubota.


FEBS Letters | 2003

Photoreceptor synaptic protein HRG4 (UNC119) interacts with ARL2 via a putative conserved domain

Akira Kobayashi; Shinya Kubota; Naoki Mori; Margaret J. McLaren; George Inana

Human retinal gene 4 (HRG4) (UNC119) is a photoreceptor synaptic protein of unknown function, shown when mutated to cause retinal degeneration in a patient and in a confirmatory transgenic model. ADP‐ribosylation factor‐like protein 2 (ARL2) was identified as an interactor of HRG4 by the yeast two‐hybrid strategy. The presence of ARL2 in the retina and co‐localization with HRG4 was confirmed by Western blot and double immunofluorescence analysis, respectively. The interaction of ARL2 with HRG4 was further confirmed by co‐immunoprecipitation and direct binding analysis. Phosphodiesterase δ (PDEδ) is an ARL2‐binding protein homologous to HRG4. Amino acid residues of PDEδ involved in binding ARL2 and forming a hydrophobic pocket were shown to be highly conserved in HRG4, suggesting similarity in binding mechanism and function.


Investigative Ophthalmology & Visual Science | 2000

HRG4 (UNC119) Mutation Found in Cone–Rod Dystrophy Causes Retinal Degeneration in a Transgenic Model

Akira Kobayashi; Tomomi Higashide; Duco I. Hamasaki; Shinya Kubota; Hitoshi Sakuma; Weijun An; Takuro Fujimaki; Margaret J. McLaren; Richard G. Weleber; George Inana


Experimental Eye Research | 2007

Targeted inactivation of synaptic HRG4 (UNC119) causes dysfunction in the distal photoreceptor and slow retinal degeneration, revealing a new function

Y. Ishiba; Tomomi Higashide; Naoki Mori; Akira Kobayashi; Shinya Kubota; Margaret J. McLaren; Hiromasa Satoh; Fulton Wong; George Inana


Investigative Ophthalmology & Visual Science | 2002

Changes in Retinal Synaptic Proteins in the Transgenic Model Expressing a Mutant HRG4 (UNC119)

Shinya Kubota; Akira Kobayashi; Naoki Mori; Tomomi Higashide; Margaret J. McLaren; George Inana


Investigative Ophthalmology & Visual Science | 2006

Truncation mutation in HRG4 (UNC119) leads to mitochondrial ANT-1-mediated photoreceptor synaptic and retinal degeneration by apoptosis

Naoki Mori; Y. Ishiba; Shinya Kubota; Akira Kobayashi; Tomomi Higashide; Margaret J. McLaren; George Inana


Investigative Ophthalmology & Visual Science | 2006

Changes in Retinal Synaptic Proteins in the Knock–Out Model of HRG4 (UNC119)

Y. Ishiba; N. Mori; Shinya Kubota; Akira Kobayashi; Tomomi Higashide; Margaret J. McLaren; George Inana


Investigative Ophthalmology & Visual Science | 2005

Mutation in HRG4 (UNC119) Leads To Mitochondrial ANT1–Mediated Apoptosis and Retinal Degeneration

Y. Ishiba; N. Mori; Shinya Kubota; Akira Kobayashi; Tomomi Higashide; Margaret J. McLaren; George Inana


Investigative Ophthalmology & Visual Science | 2004

Retinal degeneration in a knock–out model of HRG4 (UNC119)

Y. Ishiba; N. Mori; Shinya Kubota; Akira Kobayashi; Tomomi Higashide; Margaret J. McLaren; George Inana


Investigative Ophthalmology & Visual Science | 2004

Changes in BART and ANT–1 in the transgenic model expressing a mutant HRG4(UNC 119) .

Naoki Mori; Y. Ishiba; Shinya Kubota; Akira Kobayashi; Tomomi Higashide; Margaret J. McLaren; George Inana


Investigative Ophthalmology & Visual Science | 2003

Preferential Interaction of Mutant HRG4(UNC 119) With its Target Protein, ARL-2

N. Mori; Y. Ishiba; Shinya Kubota; Akira Kobayashi; Margaret J. McLaren; George Inana

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