Ontology highlight
ABSTRACT:
INSTRUMENT(S):
ORGANISM(S): Mus Musculus (mouse)
TISSUE(S): Brain
SUBMITTER: Shuzhong Wang
LAB HEAD: Jie Zhang
PROVIDER: PXD042795 | Pride | 2024-07-03
REPOSITORIES: Pride
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ZK-1_Slot2-11_1_3103.d.rar | Other | |||
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ZK-3_Slot2-13_1_3107.d.rar | Other | |||
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ZK-5_Slot2-15_1_3111.d.rar | Other |
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Advanced science (Weinheim, Baden-Wurttemberg, Germany) 20240406 24
FOXG1 syndrome is a developmental encephalopathy caused by FOXG1 (Forkhead box G1) mutations, resulting in high phenotypic variability. However, the upstream transcriptional regulation of Foxg1 expression remains unclear. This report demonstrates that both deficiency and overexpression of Men1 (protein: menin, a pathogenic gene of MEN1 syndrome known as multiple endocrine neoplasia type 1) lead to autism-like behaviors, such as social defects, increased repetitive behaviors, and cognitive impair ...[more]