Defects in hair cells disrupt the development of auditory peripheral circuitry

Bottom, R.T., Coin, Y., Siebald, C. et al. Defects in hair cells disrupt the development of auditory peripheral circuitry. Nat Commun 15, 10899 (2024). https://doi.org/10.1038/s41467-024-55275-x

Role of TMEM100 in mechanically insensitive nociceptor un-silencing.

Nees, T.A., Wang, N., Adamek, P. et al. Nat Commun 14, 1899 (2023). https://doi.org/10.1038/s41467-023-37602-w

Embryonically active piriform cortex neurons promote intracortical recurrent connectivity during development.

DC money, Santos-Valencia F, Song JH, Franks KM, Luo L.

Neuron.. 2024 June 27:S0896-6273(24)00414-8. doi: 10.1016/j.neuron.2024.06.007. Epub ahead of print. PMID: 38964330.

The developmental timing of spinal touch processing alterations predicts behavioral changes in genetic mouse models of autism spectrum disorders.

Tasnim, A., Cheers, I., Hakim, R. et al.

Nat Neurosci 27, 484–496 (2024). https://doi.org/10.1038/s41593-023-01552-9

Lateral olivocochlear neurons modulate cochlear responses to noise exposure

Austin A. Sitko1 *, Michelle M. Frank1 *, Gabriel E. Romero1 *, Lisa V. Goodrich1

1 Department of Neurobiology, Harvard Medical School, Boston, MA 02115, USA

https://doi.org/10.1101/2024.03.04.583418

γ-Protocadherins control synapse formation and peripheral branching of touch sensory neurons

Shan Meltzer, Katelyn C. Boulanger, you M. Cyrillic, Emmanuella Osei-Asante, Michelle DeLisle, Qiyu Zhang, Brian T. Kalish, Anika Tasnim, Erica L. Huey, Leah C. Fuller, Erin K. Flaherty, Tom Maniatis, Andrew M. Garrett, Joshua A. Weiner, David D.. Ginty.

ASH1L haploinsufficiency results in autistic-like phenotypes in mice and links Eph receptor gene to autism spectrum disorder

ASH1L haploinsufficiency results in autistic-like phenotypes in mice and links Eph receptor gene to autism spectrum disorder, ASH1L haploinsufficiency results in autistic-like phenotypes in mice and links Eph receptor gene to autism spectrum disorder, ASH1L haploinsufficiency results in autistic-like phenotypes in mice and links Eph receptor gene to autism spectrum disorder,1 ASH1L haploinsufficiency results in autistic-like phenotypes in mice and links Eph receptor gene to autism spectrum disorder, ASH1L haploinsufficiency results in autistic-like phenotypes in mice and links Eph receptor gene to autism spectrum disorder, ASH1L haploinsufficiency results in autistic-like phenotypes in mice and links Eph receptor gene to autism spectrum disorder, ASH1L haploinsufficiency results in autistic-like phenotypes in mice and links Eph receptor gene to autism spectrum disorder, ASH1L haploinsufficiency results in autistic-like phenotypes in mice and links Eph receptor gene to autism spectrum disorder, ASH1L haploinsufficiency results in autistic-like phenotypes in mice and links Eph receptor gene to autism spectrum disorder, ASH1L haploinsufficiency results in autistic-like phenotypes in mice and links Eph receptor gene to autism spectrum disorder, ASH1L haploinsufficiency results in autistic-like phenotypes in mice and links Eph receptor gene to autism spectrum disorder, ASH1L haploinsufficiency results in autistic-like phenotypes in mice and links Eph receptor gene to autism spectrum disorder, ASH1L haploinsufficiency results in autistic-like phenotypes in mice and links Eph receptor gene to autism spectrum disorder, ASH1L haploinsufficiency results in autistic-like phenotypes in mice and links Eph receptor gene to autism spectrum disorder, ASH1L haploinsufficiency results in autistic-like phenotypes in mice and links Eph receptor gene to autism spectrum disorder

ASH1L haploinsufficiency results in autistic-like phenotypes in mice and links Eph receptor gene to autism spectrum disorder2022 Jan 20;S0896-6273(21)01090-4. doi: 10.1016/ASH1L haploinsufficiency results in autistic-like phenotypes in mice and links Eph receptor gene to autism spectrum disorderASH1L haploinsufficiency results in autistic-like phenotypes in mice and links Eph receptor gene to autism spectrum disorder.

Female-specific synaptic dysfunction and cognitive impairment in a mouse model of PCDH19 disorder

Naosuke Hoshina, Erin M. Johnson-Venkatesh, Miyuki Hoshina, Hisashi Umemori

DOI: 10.1126/science.aaz3893

Nature Neuroscience, July 13, 2020

The endogenous neuronal complement inhibitor SRPX2 protects against complement-mediated synapse elimination during development

Qifei Cong, Breeanne M. Soteros, Mackenna Wollet, Jun Hee Kim, Crazy Ming Sia

https://doi.org/10.1038/s41593-020-0672-0

DOI：10.1038/s41593-020-0672-0

We start reading "Principles of neurobiology 2nd edition"。

Dr. Liqun Luo, a leading figure in the field of neuroscience、wrote this book based on her 20-year's of teaching neurobiology class at Stanford University.。2020The second edition was published in September as a revised edition for the first time in five years.。If you are interested in neurobiology、or English、join our reading circle。

Please e-mail us to attend。10First meeting wil be held at 18:00 on Thursday, 15th of March、.。

※ For further information、please contact Mari*.。

[Place] Held online

[Target] Anyone who wants to learn neurophysiology、or English、and who is interested in reading circle。Individuals of any backgrounds and ages are welcome。

Department of Neurophysiology, Keio University School of Medicine (Yuzaki Lab)  .

*Mari Shiozaki：mari.z6@keio.jp