AUTS2 Controls Neuronal Lineage Choice Through a Novel PRC1-Independent Complex and BMP Inhibition-Reference-Cited by-同舟云学术

AUTS2 Controls Neuronal Lineage Choice Through a Novel PRC1-Independent Complex and BMP Inhibition

Published:2022-10-18 Issue:2 Volume:19 Page:531-549
ISSN:2629-3269
Container-title:Stem Cell Reviews and Reports
language:en
Short-container-title:Stem Cell Rev and Rep

Author:

Geng Zhuangzhuang,Wang Qiang,Miao Weili,Wolf Trevor,Chavez Jessenia,Giddings Emily,Hobbs Ryan,DeGraff David J.,Wang Yinsheng,Stafford James,Gao Zhonghua^ORCID

Funder

NIH

Publisher

Springer Science and Business Media LLC

Subject

General Medicine

Link

https://link.springer.com/content/pdf/10.1007/s12015-022-10459-0.pdf

Reference37 articles.

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4. Beunders, G., Voorhoeve, E., Golzio, C., Pardo, L. M., Rosenfeld, J. A., Talkowski, M. E., Simonic, I., Lionel, A. C., Vergult, S., Pyatt, R. E., et al. (2013). Exonic deletions in AUTS2 cause a syndromic form of intellectual disability and suggest a critical role for the C terminus. American Journal of Human Genetics, 92, 210–220.

5. Beunders, G., van de Kamp, J., Vasudevan, P., Morton, J., Smets, K., Kleefstra, T., de Munnik, S. A., Schuurs-Hoeijmakers, J., Ceulemans, B., Zollino, M., et al. (2016). A detailed clinical analysis of 13 patients with AUTS2 syndrome further delineates the phenotypic spectrum and underscores the behavioural phenotype. Journal of Medical Genetics, 53, 523–532.

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1. AUTS2 disruption causes neuronal differentiation defects in human cerebral organoids through hyperactivation of the WNT/β-catenin pathway;Scientific Reports;2024-08-22

2. Silencing of the PHLDA1 leads to global proteome changes and differentiation pathways of human neuroblastoma cells;Frontiers in Pharmacology;2024-03-01

3. A foundational atlas of autism protein interactions reveals molecular convergence;2023-12-03

4. A homozygous variant in INTS11 links mitosis and neurogenesis defects to a severe neurodevelopmental disorder;Cell Reports;2023-12

5. Isolated loss of the AUTS2 long isoform, brain-wide or targeted to Calbindin-lineage cells, generates a specific suite of brain, behavioral, and molecular pathologies;GENETICS;2023-10-10