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Research

Research

BDR researchers coming from diverse research fields are working together to achieve higher goals.

Seminars & Symposia

Seminars & Symposia

BDR hosts annual symposium and regular seminars inviting international scientists in life science.

Careers & Study

Careers & Study

BDR embraces people from diverse backgrounds, and strives to create an open and supportive setting for research.

Outreach

Outreach

BDR communicates the appeal and significance of our research to society through the use of various media and activities.

News

News

From research, events, people and everything in between, find out what’s going on at RIKEN BDR.

About Us

About Us

Exploring the scientific foundations of life through interdisciplinary approaches to address society’s problems.

Principal investigator sitting in an office

Team Director
Hideyuki Okano M.D., Ph.D.

Laboratory for Brain Organoid

LocationKobe / Developmental Biology Buildings

E-mailhideyuki.okano@riken.jp

The Laboratory for Brain Organoid utilizes iPSC-derived brain organoid, assembloid, and connectoid technologies to establish human disease models that recapitulate the pathophysiology of amyotrophic lateral sclerosis (ALS), neuroimmune disorders, Alzheimer’s disease, and neurodevelopmental disorders. Using these models as a platform, we aim to elucidate disease mechanisms, advance drug discovery research, and develop novel therapeutic strategies.

Selected Publications

Okada K, Ito D, Morimoto S, et al.
Multiple lines of evidence for disruption of nuclear lamina and nucleoporins in FUS amyotrophic lateral sclerosis
Brain 147(11), 3933-3948 (2024) doi: 10.1093/brain/awae224

Morimoto S, Takahashi S, Ito D, et al.
Phase 1/2a clinical trial in ALS with ropinirole, a drug candidate identified by iPSC drug discovery
Cell Stem Cell 30(6), 766-780.e9 (2023) doi: 10.1016/j.stem.2023.04.017

Shimada H, Sato Y, Sasaki T, et al.
A next-generation iPSC-derived forebrain organoid model of tauopathy with tau fibrils by AAV-mediated gene transfer
Cell Reports Methods 2(9), 100289 (2022) doi: 10.1016/j.crmeth.2022.100289

Okano H, Morimoto S.
iPSC-based disease modeling and drug discovery in cardinal neurodegenerative disorders
Cell Stem Cell 29(2), 189-208 (2022) doi: 10.1016/j.stem.2022.01.007

Heide M, Haffner C, Murayama A, et al.
Human-specific ARHGAP11B increases size and folding of primate neocortex in the fetal marmoset
Science 369(6503), 546-550 (2020) doi: 10.1126/science.abb2401

Fujimori K, Ishikawa M, Otomo A, et al.
Modeling sporadic ALS in iPSC-derived motor neurons identifies a potential therapeutic agent
Nature Medicine 24(10), 1579-1589 (2018) doi: 10.1038/s41591-018-0140-5

Okano H, Sasaki E, Yamamori T, et al.
Brain/MINDS: A Japanese National Brain Project for Marmoset Neuroscience
Neuron 92(3), 582-590 (2016) doi: 10.1016/j.neuron.2016.10.018

Miura K, Okada Y, Aoi T, et al.
Variation in the safety of induced pluripotent stem cell lines
Nature Biotechnology 27(8), 743-745 (2009) doi: 10.1038/nbt.1554

Sasaki E, Suemizu H, Shimada A, et al.
Generation of transgenic non-human primates with germline transmission
Nature 459(7246), 523-527 (2009) doi: 10.1038/nature08090

Okada S, Nakamura M, Katoh H, et al.
Conditional ablation of Stat3 or Socs3 discloses a dual role for reactive astrocytes after spinal cord injury
Nature Medicine 12(7), 829-834 (2006) doi: 10.1038/nm1425

Members

Hideyuki Okano

Team Director

Ryo Yoshida

Technical Staff I

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