Axin2 coupled excessive Wnt‐glycolysis signaling mediates social defect in autism spectrum disorders
- Standort
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Deutsche Nationalbibliothek Frankfurt am Main
- Umfang
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Online-Ressource
- Sprache
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Englisch
- Erschienen in
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Axin2 coupled excessive Wnt‐glycolysis signaling mediates social defect in autism spectrum disorders ; day:20 ; month:04 ; year:2023 ; extent:20
EMBO molecular medicine / European Molecular Biology Organization ; (20.04.2023) (gesamt 20)
- Urheber
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Wang, Mengmeng
Xian, Panpan
Zheng, Weian
Li, Zhenzhen
Chen, Andi
Xiao, Haoxiang
Xu, Chao
Wang, Fei
Mao, Honghui
Meng, Han
Zhao, Youyi
Luo, Ceng
Wang, Yazhou
Wu, Shengxi
- DOI
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10.15252/emmm.202217101
- URN
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urn:nbn:de:101:1-2023042415385175252509
- Rechteinformation
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Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
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14.08.2025, 10:50 MESZ
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Beteiligte
- Wang, Mengmeng
- Xian, Panpan
- Zheng, Weian
- Li, Zhenzhen
- Chen, Andi
- Xiao, Haoxiang
- Xu, Chao
- Wang, Fei
- Mao, Honghui
- Meng, Han
- Zhao, Youyi
- Luo, Ceng
- Wang, Yazhou
- Wu, Shengxi
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