Development and evolution of thalamocortical connectivity

Z Molnár, KY Kwan - Cold Spring Harbor Perspectives in …, 2024 - cshperspectives.cshlp.org
Conscious perception in mammals depends on precise circuit connectivity between cerebral
cortex and thalamus; the evolution and development of these structures are closely linked …

Human cerebral organoids—a new tool for clinical neurology research

OL Eichmüller, JA Knoblich - Nature Reviews Neurology, 2022 - nature.com
The current understanding of neurological diseases is derived mostly from direct analysis of
patients and from animal models of disease. However, most patient studies do not capture …

SWI/SNF complex connects signaling and epigenetic state in cells of nervous system

VK Chmykhalo, RV Deev, AT Tokarev… - Molecular …, 2025 - Springer
SWI/SNF protein complexes are evolutionarily conserved epigenetic regulators described in
all eukaryotes. In metameric animals, the complexes are involved in all processes occurring …

Tissue-and cell-type-specific molecular and functional signatures of 16p11. 2 reciprocal genomic disorder across mouse brain and human neuronal models

DJC Tai, P Razaz, S Erdin, D Gao, J Wang… - The American Journal of …, 2022 - cell.com
Summary Chromosome 16p11. 2 reciprocal genomic disorder, resulting from recurrent copy-
number variants (CNVs), involves intellectual disability, autism spectrum disorder (ASD) …

Postmitotic accumulation of histone variant H3. 3 in new cortical neurons establishes neuronal chromatin, transcriptome, and identity

OH Funk, Y Qalieh, DZ Doyle… - Proceedings of the …, 2022 - National Acad Sciences
Histone variants, which can be expressed outside of S-phase and deposited DNA synthesis-
independently, provide long-term histone replacement in postmitotic cells, including …

Congenital hydrocephalus: new Mendelian mutations and evidence for oligogenic inheritance

V Jacquemin, N Versbraegen, S Duerinckx, A Massart… - Human genomics, 2023 - Springer
Background Congenital hydrocephalus is characterized by ventriculomegaly, defined as a
dilatation of cerebral ventricles, and thought to be due to impaired cerebrospinal fluid (CSF) …

The chromatin remodeler ADNP regulates neurodevelopmental disorder risk genes and neocortical neurogenesis

S Clémot-Dupont, JA Lourenço Fernandes… - Proceedings of the …, 2025 - pnas.org
Although chromatin remodelers are among the most important risk genes associated with
neurodevelopmental disorders (NDDs), the roles of these complexes during brain …

PfARID Regulates P. falciparum Malaria Parasite Male Gametogenesis and Female Fertility and Is Critical for Parasite Transmission to the Mosquito Vector

S Kumar, VK Baranwal, MT Haile, KMZ Oualim… - Mbio, 2022 - Am Soc Microbiol
Sexual reproduction of Plasmodium falciparum parasites is critical to the spread of malaria
in the human population. The factors that regulate gene expression underlying formation of …

ARID1B controls transcriptional programs of axon projection in an organoid model of the human corpus callosum

C Martins-Costa, A Wiegers, VA Pham, J Sidhaye… - Cell Stem Cell, 2024 - cell.com
Mutations in ARID1B, a member of the mSWI/SNF complex, cause severe
neurodevelopmental phenotypes with elusive mechanisms in humans. The most common …

[HTML][HTML] A facile method to generate cerebral organoids from human pluripotent stem cells

S Simorgh, SA Mousavi, V Pasque, K Wierda… - EXCLI …, 2023 - ncbi.nlm.nih.gov
Human cerebral organoids (COs) are self-organizing three-dimensional (3D) neural
structures that provide a human-specific platform to study the cellular and molecular …