Global ETD Search
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Showing 1 to 2 of 2 for “"CDKL5 deficiency disorder"”.
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Ampa Receptor Dysregulation And Therapeutic Interventions In A Mouse Model Of Cdkl5 Deficiency Disorder
CDKL5 Deficiency Disorder (CDD) is a rare disease that presents as a set of neurological deficits including early-life epilepsy, intellectual disability, and autistic-like behaviors. It results from pathogenic mutations in the gene for cyclin-dependent kinase-like 5 (CDKL5), a protein that is …
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Quantitative spatial transcriptomics of the developing brain
… transcriptomic developmental biology of Cdkl5: I further developed LaST into QST for cell type-specific quantifications of a single subject gene and analysed the expression of Cyclin-dependent kinase-like 5 (Cdkl5) during forebrain development. CDKL5 mutations cause a severe human …