Metabolomics,Unknown,Transcriptomics,Genomics,Proteomics

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SnRNA-seq of cortices from a MCT8-OATP1C1-deficient Allan-Herndon-Dudley Syndrome mouse model


ABSTRACT: Allan-Herndon-Dudley syndrome (AHDS) is a rare disorder caused by faulty thyroid hormone transport to the brain, leading to severe movement problems and intellectual disability. Our study in a murine model of the AHDS used snRNAseq to gain deep insights into individual cortical cells, aiming to unravel novel pathologies of the AHDS. Organism: Mus Musculus Tissue: cortical hemispheres and attached cerebral nuclei Groups: 3 x WT, 3x dKO (global, MCT8 & OATP1C1) Mouse Info: age at cortex extraction was 21 days, mice were on a pure C57BL/6J background. Animals were pooled from multiple litters to minimize litter effects. All mice were group-housed on a 12:12-h light-dark cycle at 23°C and fed standard chow diet ad libitum Technology: 10x Genomics

INSTRUMENT(S): Illumina NovaSeq 6000

ORGANISM(S): Mus musculus

SUBMITTER: Paul Pfluger 

PROVIDER: E-MTAB-16567 | biostudies-arrayexpress |

REPOSITORIES: biostudies-arrayexpress

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