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For: Biel A, Castanza AS, Rutherford R, Fair SR, Chifamba L, Wester JC, Hester ME, Hevner RF. AUTS2 Syndrome: Molecular Mechanisms and Model Systems. Front Mol Neurosci 2022;15:858582. [DOI: 10.3389/fnmol.2022.858582] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
Number Citing Articles
1 Lepagnol-bestel A, Duchon A, Viard J, Kvajo M, Daudin R, Khelfaoui M, Haziza S, Loe-mie Y, Aime M, Suizu F, Birling M, Bensaid M, Jacquot S, Koebel P, Reverdy C, Rain J, Noguchi M, Marquez X, Triller A, Humeau Y, Hérault Y, Karayiorgou M, Gogos JA, Simonneau M. AUTS2 gene dosage affects synaptic AMPA receptors via a local dendritic spine AUTS2-TTC3-AKT-mTORC1 signaling dysfunction.. [DOI: 10.1101/2022.12.01.518705] [Reference Citation Analysis]
2 Duński E, Pękowska A. Keeping the balance: Trade-offs between human brain evolution, autism, and schizophrenia. Front Genet 2022;13. [DOI: 10.3389/fgene.2022.1009390] [Reference Citation Analysis]
3 Merdrignac C, Clément AE, Montfort J, Murat F, Bobe J. auts2 Features and Expression Are Highly Conserved during Evolution Despite Different Evolutionary Fates Following Whole Genome Duplication. Cells 2022;11:2694. [DOI: 10.3390/cells11172694] [Reference Citation Analysis]
4 Anikiej-Wiczenbach P, Mański A, Milska-Musa K, Limanówka M, Wierzba J, Jamsheer A, Cyske Z, Gaffke L, Pierzynowska K, Węgrzyn G. Highly diverse phenotypes of mucopolysaccharidosis type IIIB sibling patients: effects of an additional mutation in the AUTS2 gene. J Appl Genet 2022. [PMID: 35525889 DOI: 10.1007/s13353-022-00702-2] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]