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Maintenance of neurotransmitter identity by Hox proteins through a homeostatic mechanism

Weidong Feng, Honorine Destain, Jayson J Smith, et al.

Selected by Chee Kiang Ewe

Defensive and offensive behaviors in social interaction settings in a Kleefstra syndrome mouse model

Alejandra Alonso, Anumita Samanta, Jacqueline van der Meij, et al.

Selected by Nándor Lipták

A cell fate decision map reveals abundant direct neurogenesis in the human developing neocortex

Laure Coquand, Anne-Sophie Macé, Sarah Farcy, et al.

Selected by Juan Moriano

Microglia integration into human midbrain organoids leads to increased neuronal maturation and functionality

Sonia Sabate-Soler, Sarah Louise Nickels, Cláudia Saraiva, et al.

Selected by Emma Wilson

Isolation disrupts social interactions and destabilizes brain development in bumblebees

Z Yan Wang, Grace C. McKenzie-Smith, Weijie Liu, et al.

Selected by Niveda Udaykumar

Young transposable elements rewired gene regulatory networks in human and chimpanzee hippocampal intermediate progenitors

Sruti Patoori, Samantha Barnada, Marco Trizzino

Selected by Julia Grzymkowski

TEMPO: A system to sequentially label and genetically manipulate vertebrate cell lineages

Isabel Espinosa-Medina, Daniel Feliciano, Carla Belmonte-Mateos, et al.

Selected by Julia Grzymkowski

Real-time visualization of mRNA synthesis during memory formation in live animals

Byung Hun Lee, Jae Youn Shim, Hyungseok C. Moon, et al.

Selected by Kristina Kuhbandner et al.

Self-organized morphogenesis of a human neural tube in vitro by geometric constraints

Eyal Karzbrun, Aimal H. Khankhel, Heitor C. Megale, et al.

Selected by Srivatsava Viswanadha

Ageing-associated myelin dysfunction drives amyloid deposition in mouse models of Alzheimer’s disease

Constanze Depp, Ting Sun, Andrew Octavian Sasmita, et al.

Selected by Kristina Kuhbandner

After traumatic brain injury oligodendrocytes regain a plastic phenotype and can become astrocytes

Xianshu Bai, Na Zhao, Wenhui Huang, et al.

Selected by Ranabir Chakraborty

Functional characterization of RELN missense mutations involved in recessive and dominant forms of Neuronal Migration Disorders

Martina Riva, Sofia Ferreira, Vera P. Medvedeva, et al.

Selected by Ana Uzquiano