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Select item 112000121.

Menin Deficiency Induces Autism‐Like Behaviors by Regulating Foxg1 Transcription and Participates in Foxg1‐Related Encephalopathy

Kai Zhuang, Lige Leng, Xiao Su, Shuzhong Wang, Yuemin Su, Yanbing Chen, Ziqi Yuan, Liu Zi, Jieyin Li, Wenting Xie, Sihan Yan, Yujun Xia, Han Wang, Huifang Li, Zhenyi Chen, Tifei Yuan, Jie Zhang

Adv Sci (Weinh) 2024 Jun; 11(24): 2307953. Published online 2024 Apr 6. doi: 10.1002/advs.202307953

PMCID:: PMC11200012

Abstract Article PDF–5.0M

Select item 111904512.

Foxg1 bimodally tunes L1-mRNA and -DNA dynamics in the developing murine neocortex

Gabriele Liuzzi, Osvaldo Artimagnella, Simone Frisari, Antonello Mallamaci

Development. 2024 May 15; 151(10): dev202292. Published online 2024 May 23. doi: 10.1242/dev.202292

PMCID:: PMC11190451

Abstract Article

Select item 106255413.

Systemic and intrinsic functions of ATRX in glial cell fate and CNS myelination in male mice

Megan E. Rowland, Yan Jiang, Sarfraz Shafiq, Alireza Ghahramani, Miguel A. Pena-Ortiz, Vanessa Dumeaux, Nathalie G. Bérubé

Nat Commun. 2023; 14: 7090. Published online 2023 Nov 4. doi: 10.1038/s41467-023-42752-y

PMCID:: PMC10625541

Abstract Article PDF–3.8M

Select item 105454374.

DOT1L deletion impairs the development of cortical parvalbumin-expressing interneurons

Arquimedes Cheffer, Marta Garcia-Miralles, Esther Maier, Ipek Akol, Henriette Franz, Vandana Shree Vedartham Srinivasan, Tanja Vogel

Cereb Cortex. 2023 Oct 1; 33(19): 10272–10285. Published online 2023 Aug 11. doi: 10.1093/cercor/bhad281

PMCID:: PMC10545437

Abstract Article PDF–2.8M

Select item 105308925.

Conditional Deletion of Foxg1 Delayed Myelination during Early Postnatal Brain Development

Guangliang Cao, Congli Sun, Hualin Shen, Dewei Qu, Chuanlu Shen, Haiqin Lu

Int J Mol Sci. 2023 Sep; 24(18): 13921. Published online 2023 Sep 10. doi: 10.3390/ijms241813921

PMCID:: PMC10530892

Abstract Article PDF–4.2M

Select item 105220216.

Notch pathway mutants do not equivalently perturb mouse embryonic retinal development

Bernadett Bosze, Julissa Suarez-Navarro, Illiana Cajias, Joseph A. Brzezinski IV, Nadean L. Brown

PLoS Genet. 2023 Sep; 19(9): e1010928. Published online 2023 Sep 26. doi: 10.1371/journal.pgen.1010928

PMCID:: PMC10522021

Abstract Article PDF–5.9M

Select item 105064007.

Inactivation of Fgf3 and Fgf4 within the Fgf3/Fgf4/Fgf15 gene cluster reveals their redundant requirement for mouse inner ear induction and embryonic survival

Laura Zelarayan, Victor Vendrell, Elena Domínguez-Frutos, Iris López-Hernández, Kiril Schimmang-Alonso, María Teresa Alonso, Yolanda Alvarez, Hannes Maier, Matthew J. Anderson, Mark Lewandoski, Thomas Schimmang

Dev Dyn. Author manuscript; available in PMC 2023 Sep 18.

Published in final edited form as: Dev Dyn. 2022 May; 251(5): 877–884. Published online 2021 Nov 12. doi: 10.1002/dvdy.435

PMCID:: PMC10506400

Abstract Article PDF–1.3M

Select item 104859568.

Distinct requirements for Tcf3 and Tcf12 during oligodendrocyte development in the mouse telencephalon

Mary Jo Talley, Diana Nardini, Lisa A. Ehrman, Q. Richard Lu, Ronald R. Waclaw

Neural Dev. 2023; 18: 5. Published online 2023 Sep 8. doi: 10.1186/s13064-023-00173-z

PMCID:: PMC10485956

Abstract Article PDF–15M

Select item 104098009.

SNIP1 and PRC2 coordinate cell fates of neural progenitors during brain development

Yurika Matsui, Mohamed Nadhir Djekidel, Katherine Lindsay, Parimal Samir, Nina Connolly, Gang Wu, Xiaoyang Yang, Yiping Fan, Beisi Xu, Jamy C. Peng

Nat Commun. 2023; 14: 4754. Published online 2023 Aug 8. doi: 10.1038/s41467-023-40487-4

PMCID:: PMC10409800

Abstract Article PDF–5.3M

Select item 1039049210.

Three-dimensional molecular architecture of mouse organogenesis

Fangfang Qu, Wenjia Li, Jian Xu, Ruifang Zhang, Jincan Ke, Xiaodie Ren, Xiaogao Meng, Lexin Qin, Jingna Zhang, Fangru Lu, Xin Zhou, Xi Luo, Zhen Zhang, Minhan Wang, Guangming Wu, Duanqing Pei, Jiekai Chen, Guizhong Cui, Shengbao Suo, Guangdun Peng

Nat Commun. 2023; 14: 4599. Published online 2023 Jul 31. doi: 10.1038/s41467-023-40155-7

PMCID:: PMC10390492

Abstract Article PDF–13M

Select item 1033087711.

Disruption of BMP4 signaling is associated with laryngeal birth defects in a mouse model

N Bottasso-Arias, K Burra, D Sinner, T Riede

Dev Biol. Author manuscript; available in PMC 2024 Aug 1.

Published in final edited form as: Dev Biol. 2023 Aug; 500: 10–21. Published online 2023 May 23. doi: 10.1016/j.ydbio.2023.04.007

PMCID:: PMC10330877

Abstract Article PDF–2.1M

Select item 1030958012.

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

Abstract Article

Select item 1026824013.

ZBTB20 is essential for cochlear maturation and hearing in mice

Zhifang Xie, Xian-Hua Ma, Qiu-Fang Bai, Jie Tang, Jian-He Sun, Fei Jiang, Wei Guo, Chen-Ma Wang, Rui Yang, Yin-Chuan Wen, Fang-Yuan Wang, Yu-Xia Chen, Hai Zhang, David Z. He, Matthew W. Kelley, Shiming Yang, Weiping J. Zhang

Proc Natl Acad Sci U S A. 2023 Jun 13; 120(24): e2220867120. Published online 2023 Jun 6. doi: 10.1073/pnas.2220867120

PMCID:: PMC10268240

Abstract Article PDF–7.7M

Select item 1024738014.

Myelin dysfunction drives amyloid-β deposition in models of Alzheimer’s disease

Constanze Depp, Ting Sun, Andrew Octavian Sasmita, Lena Spieth, Stefan A. Berghoff, Taisiia Nazarenko, Katharina Overhoff, Agnes A. Steixner-Kumar, Swati Subramanian, Sahab Arinrad, Torben Ruhwedel, Wiebke Möbius, Sandra Göbbels, Gesine Saher, Hauke B. Werner, Alkmini Damkou, Silvia Zampar, Oliver Wirths, Maik Thalmann, Mikael Simons, Takashi Saito, Takaomi Saido, Dilja Krueger-Burg, Riki Kawaguchi, Michael Willem, Christian Haass, Daniel Geschwind, Hannelore Ehrenreich, Ruth Stassart, Klaus-Armin Nave

Nature. 2023; 618(7964): 349–357. Published online 2023 May 31. doi: 10.1038/s41586-023-06120-6

PMCID:: PMC10247380

Abstract Article PDF–19M

Select item 1018337015.

POLR1A variants underlie phenotypic heterogeneity in craniofacial, neural, and cardiac anomalies

Kelly Smallwood, Kristin E.N. Watt, Satoru Ide, Kristina Baltrunaite, Chad Brunswick, Katherine Inskeep, Corrine Capannari, Margaret P. Adam, Amber Begtrup, Debora R. Bertola, Laurie Demmer, Erin Demo, Orrin Devinsky, Emily R. Gallagher, Maria J. Guillen Sacoto, Robert Jech, Boris Keren, Jennifer Kussmann, Roger Ladda, Lisa A. Lansdon, Sebastian Lunke, Anne Mardy, Kirsty McWalters, Richard Person, Laura Raiti, Noriko Saitoh, Carol J. Saunders, Rhonda Schnur, Matej Skorvanek, Susan L. Sell, Anne Slavotinek, Bonnie R. Sullivan, Zornitza Stark, Joseph D. Symonds, Tara Wenger, Sacha Weber, Sandra Whalen, Susan M. White, Juliane Winkelmann, Michael Zech, Shimriet Zeidler, Kazuhiro Maeshima, Rolf W. Stottmann, Paul A. Trainor, K. Nicole Weaver

Am J Hum Genet. 2023 May 4; 110(5): 809–825. Published online 2023 Apr 18. doi: 10.1016/j.ajhg.2023.03.014

PMCID:: PMC10183370

Abstract Article PDF–4.3M

Select item 993437616.

Cell-autonomous requirement for ACE2 across organs in lethal mouse SARS-CoV-2 infection

Alan T. Tang, David W. Buchholz, Katherine M. Szigety, Brian Imbiakha, Siqi Gao, Maxwell Frankfurter, Min Wang, Jisheng Yang, Peter Hewins, Patricia Mericko-Ishizuka, N Adrian Leu, Stephanie Sterling, Isaac A. Monreal, Julie Sahler, Avery August, Xuming Zhu, Kellie A. Jurado, Mingang Xu, Edward E. Morrisey, Sarah E. Millar, Hector C. Aguilar, Mark L. Kahn

PLoS Biol. 2023 Feb; 21(2): e3001989. Published online 2023 Feb 6. doi: 10.1371/journal.pbio.3001989