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Items: 1 to 20 of 385

1.
Disruption of TCF4 regulatory networks leads to abnormal cortical development and mental disabilities
Hong Li, Ying Zhu, Yury M. Morozov, Xiaoli Chen, Stephanie Cerceo Page, Matthew D. Rannals, Brady J. Maher, Pasko Rakic
Mol Psychiatry. Author manuscript; available in PMC 2024 Apr 16.
Published in final edited form as: Mol Psychiatry. 2019 Aug; 24(8): 1235–1246. Published online 2019 Jan 31. doi: 10.1038/s41380-019-0353-0
PMCID:
PMC11019556
AbstractArticlePDF–1.7M
2.
GTF2I dosage regulates neuronal differentiation and social behavior in 7q11.23 neurodevelopmental disorders
Alejandro López-Tobón, Reinald Shyti, Carlo Emanuele Villa, Cristina Cheroni, Patricio Fuentes-Bravo, Sebastiano Trattaro, Nicolò Caporale, Flavia Troglio, Erika Tenderini, Marija Mihailovich, Adrianos Skaros, William T. Gibson, Alessandro Cuomo, Tiziana Bonaldi, Ciro Mercurio, Mario Varasi, Lucy Osborne, Giuseppe Testa
Sci Adv. 2023 Dec 1; 9(48): eadh2726. Published online 2023 Nov 29. doi: 10.1126/sciadv.adh2726
PMCID:
PMC10686562
AbstractArticlePDF–2.0M
3.
Single-cell analysis reveals specific neuronal transition during mouse corticogenesis
Ziheng Zhou, Yueyang Pan, Si Zhou, Shuguang Wang, Dengwei Zhang, Ye Cao, Xiaosen Jiang, Jie Li, Linnan Zhu, Lijian Zhao, Shen Gu, Ge Lin, Zirui Dong, Hai-Xi Sun
Front Cell Dev Biol. 2023; 11: 1209320. Published online 2023 Nov 6. doi: 10.3389/fcell.2023.1209320
PMCID:
PMC10657809
AbstractArticlePDF–3.8M
4.
CUX1-related neurodevelopmental disorder: deep insights into phenotype-genotype spectrum and underlying pathology
Henry Oppermann, Elia Marcos-Grañeda, Linnea A. Weiss, Christina A. Gurnett, Anne Marie Jelsig, Susanne H. Vineke, Bertrand Isidor, Sandra Mercier, Kari Magnussen, Pia Zacher, Mona Hashim, Alistair T. Pagnamenta, Simone Race, Siddharth Srivastava, Zoë Frazier, Robert Maiwald, Matthias Pergande, Donatella Milani, Martina Rinelli, Jonathan Levy, Ilona Krey, Paolo Fontana, Fortunato Lonardo, Stephanie Riley, Jasmine Kretzer, Julia Rankin, Linda M. Reis, Elena V. Semina, Miriam S. Reuter, Stephen W. Scherer, Maria Iascone, Denisa Weis, Christina R. Fagerberg, Charlotte Brasch-Andersen, Lars Kjaersgaard Hansen, Alma Kuechler, Nathan Noble, Alice Gardham, Jessica Tenney, Geetanjali Rathore, Stefanie Beck-Woedl, Tobias B. Haack, Despoina C. Pavlidou, Isis Atallah, Julia Vodopiutz, Andreas R. Janecke, Tzung-Chien Hsieh, Hellen Lesmann, Hannah Klinkhammer, Peter M. Krawitz, Johannes R. Lemke, Rami Abou Jamra, Marta Nieto, Zeynep Tümer, Konrad Platzer
Eur J Hum Genet. 2023 Nov; 31(11): 1251–1260. Published online 2023 Aug 30. doi: 10.1038/s41431-023-01445-2
PMCID:
PMC10620399
AbstractArticlePDF–3.6M
5.
P53 independent pathogenic mechanisms contribute to BubR1 microcephaly
Noelle A. Sterling, Bethany K. Terry, Julia M. McDonnell, Seonhee Kim
Front Cell Dev Biol. 2023; 11: 1282182. Published online 2023 Oct 12. doi: 10.3389/fcell.2023.1282182
PMCID:
PMC10602889
AbstractArticlePDF–7.3M
6.
Celf4 controls mRNA translation underlying synaptic development in the prenatal mammalian neocortex
Iva Salamon, Yongkyu Park, Terezija Miškić, Janja Kopić, Paul Matteson, Nicholas F. Page, Alfonso Roque, Geoffrey W. McAuliffe, John Favate, Marta Garcia-Forn, Premal Shah, Miloš Judaš, James H. Millonig, Ivica Kostović, Silvia De Rubeis, Ronald P. Hart, Željka Krsnik, Mladen-Roko Rasin
Nat Commun. 2023; 14: 6025. Published online 2023 Sep 27. doi: 10.1038/s41467-023-41730-8
PMCID:
PMC10533865
AbstractArticlePDF–4.9M
7.
Autism-linked UBE3A gain-of-function mutation causes interneuron and behavioral phenotypes when inherited maternally or paternally in mice
Lei Xing, Jeremy M. Simon, Travis S. Ptacek, Jason J. Yi, Lipin Loo, Hanqian Mao, Justin M. Wolter, Eric S. McCoy, Smita R. Paranjape, Bonnie Taylor-Blake, Mark J. Zylka
Cell Rep. Author manuscript; available in PMC 2023 Sep 27.
Published in final edited form as: Cell Rep. 2023 Jul 25; 42(7): 112706. Published online 2023 Jun 28. doi: 10.1016/j.celrep.2023.112706
PMCID:
PMC10530456
AbstractArticlePDF–4.5M
8.
Deletion of ARGLU1 causes global defects in alternative splicing in vivo and mouse cortical malformations primarily via apoptosis
Fenyong Yao, Shisheng Huang, Jiahui Liu, Chunhua Tan, Mengqi Xu, Dengkui Wang, Maoqing Huang, Yiyao Zhu, Xingxu Huang, Shuijin He
Cell Death Dis. 2023 Aug; 14(8): 543. Published online 2023 Aug 23. doi: 10.1038/s41419-023-06071-w
PMCID:
PMC10447433
AbstractArticlePDF–9.2M
9.
An adhesion signaling axis involving Dystroglycan, β1-Integrin, and Cas adaptor proteins regulates the establishment of the cortical glial scaffold
Wenny Wong, Jason A. Estep, Alyssa M. Treptow, Niloofar Rajabli, Jennifer N. Jahncke, Teresa Ubina, Kevin M. Wright, Martin M. Riccomagno
PLoS Biol. 2023 Aug; 21(8): e3002212. Published online 2023 Aug 4. doi: 10.1371/journal.pbio.3002212
PMCID:
PMC10431685
AbstractArticlePDF–12M
10.
Notch directs telencephalic development and controls neocortical neuron fate determination by regulating microRNA levels
Jisoo S. Han, Elizabeth Fishman-Williams, Steven C. Decker, Keiko Hino, Raenier V. Reyes, Nadean L. Brown, Sergi Simó, Anna La Torre
Development. 2023 Jun 1; 150(11): dev201408. Published online 2023 Jun 5. doi: 10.1242/dev.201408
PMCID:
PMC10309580
AbstractArticle
11.
Differential Expression of the Tmem132 Family Genes in the Developing Mouse Nervous System
Yuan Wang, Graham Herzig, Cassandra Molano, Aimin Liu
Gene Expr Patterns. Author manuscript; available in PMC 2023 May 30.
Published in final edited form as: Gene Expr Patterns. 2022 Sep; 45: 119257. Published online 2022 Jun 8. doi: 10.1016/j.gep.2022.119257
PMCID:
PMC10228465
AbstractArticlePDF–2.0M
12.
Histological Analysis of a Mouse Model of the 22q11.2 Microdeletion Syndrome
Hidenori Tabata, Daisuke Mori, Tohru Matsuki, Kaichi Yoshizaki, Masato Asai, Atsuo Nakayama, Norio Ozaki, Koh-ichi Nagata
Biomolecules. 2023 May; 13(5): 763. Published online 2023 Apr 27. doi: 10.3390/biom13050763
PMCID:
PMC10216591
AbstractArticlePDF–4.2M
13.
Delayed cortical development in mice with a neural specific deletion of β1 integrin
Mamunur Rashid, Eric C. Olson
Front Neurosci. 2023; 17: 1158419. Published online 2023 May 12. doi: 10.3389/fnins.2023.1158419
PMCID:
PMC10213249
AbstractArticlePDF–4.6M
14.
RAB35 is required for murine hippocampal development and functions by regulating neuronal cell distribution
Ikuko Maejima, Taichi Hara, Satoshi Tsukamoto, Hiroyuki Koizumi, Takeshi Kawauchi, Tomoko Akuzawa, Rika Hirai, Hisae Kobayashi, Inoya Isobe, Kazuo Emoto, Hidetaka Kosako, Ken Sato
Commun Biol. 2023; 6: 440. Published online 2023 Apr 21. doi: 10.1038/s42003-023-04826-x
PMCID:
PMC10121692
AbstractArticlePDF–4.2M
15.
Epitranscriptomic regulation of cortical neurogenesis via Mettl8-dependent mitochondrial tRNA m3C modification
Feng Zhang, Kijun Yoon, Daniel Y. Zhang, Nam-Shik Kim, Guo-li Ming, Hongjun Song
Cell Stem Cell. Author manuscript; available in PMC 2024 Mar 2.
Published in final edited form as: Cell Stem Cell. 2023 Mar 2; 30(3): 300–311.e11. Published online 2023 Feb 9. doi: 10.1016/j.stem.2023.01.007
PMCID:
PMC10031801
AbstractArticlePDF–4.3M
16.
Bulk and mosaic deletions of Egfr reveal regionally defined gliogenesis in the developing mouse forebrain
Xuying Zhang, Guanxi Xiao, Caroline Johnson, Yuheng Cai, Zachary K. Horowitz, Christine Mennicke, Robert Coffey, Mansoor Haider, David Threadgill, Rebecca Eliscu, Michael C. Oldham, Alon Greenbaum, H. Troy Ghashghaei
iScience. 2023 Mar 17; 26(3): 106242. Published online 2023 Feb 20. doi: 10.1016/j.isci.2023.106242
PMCID:
PMC10006693
AbstractArticlePDF–7.6M
17.
Tip60/KAT5 Histone Acetyltransferase Is Required for Maintenance and Neurogenesis of Embryonic Neural Stem Cells
Kaoru Tominaga, Eiji Sakashita, Katsumi Kasashima, Kenji Kuroiwa, Yasumitsu Nagao, Naoki Iwamori, Hitoshi Endo
Int J Mol Sci. 2023 Feb; 24(3): 2113. Published online 2023 Jan 20. doi: 10.3390/ijms24032113
PMCID:
PMC9916716
AbstractArticlePDF–4.8M
18.
An entosis-like process induces mitotic disruption in Pals1 microcephaly pathogenesis
Noelle A. Sterling, Jun Young Park, Raehee Park, Seo-Hee Cho, Seonhee Kim
Nat Commun. 2023; 14: 82. Published online 2023 Jan 5. doi: 10.1038/s41467-022-35719-y
PMCID:
PMC9816111
AbstractArticlePDF–7.8M
19.
KIF2A deficiency causes early-onset neurodegeneration
Nuria Ruiz-Reig, Georges Chehade, Janne Hakanen, Mohamed Aittaleb, Keimpe Wierda, Joris De Wit, Laurent Nguyen, Philippe Gailly, Fadel Tissir
Proc Natl Acad Sci U S A. 2022 Nov 15; 119(46): e2209714119. Published online 2022 Nov 7. doi: 10.1073/pnas.2209714119
PMCID:
PMC9674219
AbstractArticlePDF–3.8M
20.
Conserved and Distinct Functions of the Autism-Related Chromatin Remodeler CHD8 in Embryonic and Adult Forebrain Neurogenesis
Chen Dong, Chuntao Zhao, Xiang Chen, Kalen Berry, Jiajia Wang, Feng Zhang, Yunfei Liao, Rong Han, Sean Ogurek, Lingli Xu, Li Zhang, Yifeng Lin, Wenhao Zhou, Mei Xin, Daniel A. Lim, Kenneth Campbell, Masato Nakafuku, Ronald R. Waclaw, Q. Richard Lu
J Neurosci. 2022 Nov 2; 42(44): 8373–8392. doi: 10.1523/JNEUROSCI.2400-21.2022
PMCID:
PMC9653284
AbstractArticlePDF–12M

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