Altered brain microRNA biogenesis contributes to phenotypic deficits in a 22q11-deletion mouse model
By K. Stark, Bin Xu, A. Bagchi, W. Lai, Hui Liu, Ruby Hsu, Xiang Wan, Paul Pavlidis, A. Mills, M. Karayiorgou and 1 more. Nature Genetics, 2008
609 citations recorded by the source corpus.
Subfields: Cancer Research, Genetics, Molecular Biology
View Paper: https://www.semanticscholar.org/paper/55e89b5753e4fb6e53c7b9b796bccfe0ec1d2480
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Citations in the corpus
- Dendritic spine pathology in neuropsychiatric disorders (2011, background): “2 microdeletion syndrome is the most common CNV associated with schizophrenia, accounting for 1–2% of case”
- MicroRNAs in development and disease. (2011, background): “(579) generated a mouse model with an equivalent deletion that spans a 1.”
- Strong association of de novo copy number mutations with sporadic schizophrenia (2008, background): “2 microdeletion removes one copy of another key gene in this pathway, DGCR8 /( PASHA ), and the resulting abnormality in miRNA biogenesis contributes to the behavioral and neuronal deficits associated with this CN mutation in a mouse mode”