Fragile X-like behaviors and abnormal cortical dendritic spines in cytoplasmic FMR1-interacting protein 2-mutant mice |
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A gene network regulating lysosomal biogenesis and function |
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Human-specific regulation of MeCP2 levels in fetal brains by microRNA miR-483-5p |
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Loss of Ataxin-1 Potentiates Alzheimer's Pathogenesis by Elevating Cerebral BACE1 Transcription |
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MicroRNA target prediction by expression analysis of host genes |
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microRNAs and genetic diseases |
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A Mild PUM1 Mutation Is Associated with Adult-Onset Ataxia, whereas Haploinsufficiency Causes Developmental Delay and Seizures. |
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miRNeye: a microRNA expression atlas of the mouse eye. |
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NUDT21-spanning CNVs lead to neuropsychiatric disease and altered MeCP2 abundance via alternative polyadenylation |
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Promiscuity of enhancer, coding and non-coding transcription functions in ultraconserved elements |
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Protocol for recording epileptiform discharges of EEG and behavioral seizures in freely moving mice |
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Protocol to assess the effect of disease-driving variants on mouse brain morphology and primary hippocampal neurons |
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Pumilio proteins utilize distinct regulatory mechanisms to achieve complementary functions required for pluripotency and embryogenesis |
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Pumilio1 haploinsufficiency leads to SCA1-like neurodegeneration by increasing wild-type Ataxin1 levels |
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RBM17 Interacts with U2SURP and CHERP to Regulate Expression and Splicing of RNA-Processing Proteins |
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UTRdb and UTRsite (RELEASE 2010): a collection of sequences and regulatory motifs of the untranslated regions of eukaryotic mRNAs |
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