Shen C, Cui W, Xiong W, Mei L
J Comp Neurol. 2025; 533(3):e70030.
PMID: 40034091
PMC: 11877257.
DOI: 10.1002/cne.70030.
Micoli E, Ferrero Restelli F, Barbiera G, Moors R, Nouboers E, Du J
bioRxiv. 2025; .
PMID: 40027755
PMC: 11870569.
DOI: 10.1101/2025.02.19.636192.
Wang C, Liu J, Su L, Wang X, Bian Y, Wang Z
Adv Sci (Weinh). 2025; 12(10):e2411972.
PMID: 39823534
PMC: 11904963.
DOI: 10.1002/advs.202411972.
Feng X, Gao Y, Chu F, Shan Y, Liu M, Wang Y
Nat Commun. 2025; 16(1):672.
PMID: 39809789
PMC: 11733295.
DOI: 10.1038/s41467-025-56058-8.
Yin L, Xu X, Conacher B, Lin Y, Carrillo G, Cun Y
bioRxiv. 2024; .
PMID: 39605670
PMC: 11601525.
DOI: 10.1101/2024.11.21.624733.
Brain state and cortical layer-specific mechanisms underlying perception at threshold.
Morton M, Denagamage S, Blume I, Reynolds J, Jadi M, Nandy A
Elife. 2024; 12.
PMID: 39556415
PMC: 11573349.
DOI: 10.7554/eLife.91722.
FOXR2 Targets LHX6+/DLX+ Neural Lineages to Drive Central Nervous System Neuroblastoma.
Jessa S, De Cola A, Chandarana B, McNicholas M, Hebert S, Ptack A
Cancer Res. 2024; 85(2):231-250.
PMID: 39495206
PMC: 11733536.
DOI: 10.1158/0008-5472.CAN-24-2248.
Pathogenesis of Germinal Matrix Hemorrhage: Insights from Single-Cell Transcriptomics.
Chen J, Choi J, Lin P, Huang E
Annu Rev Pathol. 2024; 20(1):221-243.
PMID: 39401848
PMC: 11759652.
DOI: 10.1146/annurev-pathmechdis-111523-023446.
Inhibitory Systems in Brain Evolution: Pathways of Vulnerability in Neurodevelopmental Disorders.
Hanson K, Greiner D, Schumann C, Semendeferi K
Brain Behav Evol. 2024; 100(1):29-48.
PMID: 39137740
PMC: 11822052.
DOI: 10.1159/000540865.
Developmental dynamics of the prefrontal cortical SST and PV interneuron networks: Insights from the monkey highlight human-specific features.
Fin N, Yip A, Teo L, Homman-Ludiye J, Bourne J
bioRxiv. 2024; .
PMID: 39026896
PMC: 11257587.
DOI: 10.1101/2024.07.10.602904.
The Principle of Cortical Development and Evolution.
Yang Z
Neurosci Bull. 2024; 41(3):461-485.
PMID: 39023844
PMC: 11876516.
DOI: 10.1007/s12264-024-01259-2.
Rapid rebalancing of co-tuned ensemble activity in the auditory cortex.
Kang H, Babola T, Kanold P
bioRxiv. 2024; .
PMID: 38948779
PMC: 11212947.
DOI: 10.1101/2024.06.17.599418.
Human Brain In Vitro Model for Pathogen Infection-Related Neurodegeneration Study.
Yan Y, Cho A
Int J Mol Sci. 2024; 25(12).
PMID: 38928228
PMC: 11204318.
DOI: 10.3390/ijms25126522.
Defining cis-regulatory elements and transcription factors that control human cortical interneuron development.
Chapman G, Determan J, Jetter H, Kaushik K, Prakasam R, Kroll K
iScience. 2024; 27(6):109967.
PMID: 38827400
PMC: 11140214.
DOI: 10.1016/j.isci.2024.109967.
Complimentary vertebrate models exhibit phenotypes relevant to DeSanto-Shinawi Syndrome.
Lee K, Stafford A, Pacheco-Vergara M, Cichewicz K, Canales C, Seban N
bioRxiv. 2024; .
PMID: 38826421
PMC: 11142245.
DOI: 10.1101/2024.05.26.595966.
SIMS: A deep-learning label transfer tool for single-cell RNA sequencing analysis.
Gonzalez-Ferrer J, Lehrer J, OFarrell A, Paten B, Teodorescu M, Haussler D
Cell Genom. 2024; 4(6):100581.
PMID: 38823397
PMC: 11228957.
DOI: 10.1016/j.xgen.2024.100581.
Parietal-Frontal Pathway Controls Relapse of Fear Memory in a Novel Context.
Joo B, Xu S, Park H, Kim K, Rah J, Koo J
Biol Psychiatry Glob Open Sci. 2024; 4(4):100315.
PMID: 38726036
PMC: 11078648.
DOI: 10.1016/j.bpsgos.2024.100315.
Interaction between Oligodendrocytes and Interneurons in Brain Development and Related Neuropsychiatric Disorders.
Liu Y, Yuan J, Dong Y, Jiang S, Zhang M, Zhao X
Int J Mol Sci. 2024; 25(7).
PMID: 38612430
PMC: 11011273.
DOI: 10.3390/ijms25073620.
Cell-type-resolved mosaicism reveals clonal dynamics of the human forebrain.
Chung C, Yang X, Hevner R, Kennedy K, Vong K, Liu Y
Nature. 2024; 629(8011):384-392.
PMID: 38600385
PMC: 11194162.
DOI: 10.1038/s41586-024-07292-5.
Multiple parallel cell lineages in the developing mammalian cerebral cortex.
Del-Valle-Anton L, Amin S, Cimino D, Neuhaus F, Dvoretskova E, Fernandez V
Sci Adv. 2024; 10(13):eadn9998.
PMID: 38536915
PMC: 10971412.
DOI: 10.1126/sciadv.adn9998.