Toshiki Kurosawa

Assistant Professor

Teikyo University

Japan

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Toshiki Kurosawa is an Assistant Professor at Teikyo University in Japan. His research focuses on the mechanisms and models associated with the blood-brain barrier, particularly the transport of organic cations and the functional evaluation of endothelial cells derived from human induced pluripotent stem cells. Recent articles authored by Professor Kurosawa explore topics such as proton-coupled organic cation antiporters and the construction of advanced blood-brain barrier models.

Articles (9)

Year:

2024

Year:

2023

Year:

2022

Year:

2022

Year:

2022

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2021

Year:

2021

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2020

Year:

2020

Collaborators (6)

Tadahaya Mizuno

assistant professor

University of Tokyo

JAPAN

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Tetsuya Terasaki

JAPAN

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Takashi Nakakura

Teikyo University

JAPAN

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Yoshiyuki Kubo

Professor

Teikyo University

JAPAN

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Kei Higuchi

Assistant Professor

Tokyo University of Pharmacy and Life Sciences

JAPAN

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Yasuo Uchida

Tohoku University

JAPAN

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Toshiki Kurosawa

Research Interests

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Articles (9)

Involvement of Proton-Coupled Organic Cation Antiporter in Human Blood–Brain Barrier Transport of Mesoridazine and Metoclopramide

Development and Functional Evaluation of MDR1-Expressing Microvascular Endothelial-Like Cells Derived from Human iPS Cells as an In Vitro Blood-Brain Barrier Model

Proteomics-Based Transporter Identification by the PICK Method: Involvement of TM7SF3 and LHFPL6 in Proton-Coupled Organic Cation Antiport at the Blood–Brain Barrier

Construction and Functional Evaluation of a Three-Dimensional Blood-Brain Barrier Model Equipped With Human Induced Pluripotent Stem Cell-Derived Brain Microvascular Endothelial Cells.

Naltrexone Transport by a Proton-Coupled Organic Cation Antiporter in hCMEC/D3 Cells, an in Vitro Human Blood-Brain Barrier Model.

Fibronectin is essential for formation of fenestrae in endothelial cells of the fenestrated capillary

Transport Characteristics of 6-Mercaptopurine in Brain Microvascular Endothelial Cells Derived From Human Induced Pluripotent Stem Cells.

Functional Investigation of Solute Carrier Family 35, Member F2, in Three Cellular Models of the Primate Blood-Brain Barrier.

Structural Requirements for Uptake of Diphenhydramine Analogs into hCMEC/D3 Cells Via the Proton-Coupled Organic Cation Antiporter.

Collaborators (6)

Tadahaya Mizuno

Tetsuya Terasaki

Takashi Nakakura

Yoshiyuki Kubo

Kei Higuchi

Yasuo Uchida

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