Results 221 to 230 of about 4,239 (280)

Epilepsy‐associated SCN2A‐L1342P mutation drives network hyperexcitability and widespread transcriptomic changes in human cortical organoids

open access: yesEpilepsia, Volume 67, Issue 10, Page 5514-5530, October 2026.
Abstract Objective SCN2A pathogenic mutations, such as the recurrent heterozygous Nav1.2‐L1342P, are monogenic causes of epilepsy. In this human‐induced pluripotent stem cell–derived model system, we aim to investigate the molecular and cellular mechanisms underlying SCN2A‐L1342P‐associated pathology. Methods Using a human male induced pluripotent stem
Maria I. Olivero‐Acosta   +26 more
wiley   +1 more source

Mapping of uterine-related neurons in central nervous system of mice by <i>trans</i>-synaptic tracing with pseudorabies virus. [PDF]

open access: yesBiochem Biophys Rep
Wang H   +10 more
europepmc   +1 more source

Visualizing α‐synuclein pathology in live brain: A new platform for Parkinson's disease research

open access: yes
Clinical and Translational Medicine, Volume 16, Issue 10, October 2026.
Minhui Yu, Peng Cao
wiley   +1 more source

A cortical pathway to sleep: Role of long‐range inhibition

open access: yes
Clinical and Translational Medicine, Volume 16, Issue 10, October 2026.
Geoffrey Terral, Renata Batista‐Brito
wiley   +1 more source

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