<HashMap><database>GEO</database><file_versions><headers><Content-Type>application/xml</Content-Type></headers><body><files><Other>ftp://ftp.ncbi.nlm.nih.gov/geo/series/GSE307nnn/GSE307945/</Other></files><type>primary</type></body><statusCode>OK</statusCode><statusCodeValue>200</statusCodeValue></file_versions><scores/><additional><omics_type>Transcriptomics</omics_type><species>Mus musculus</species><gds_type>Expression profiling by high throughput sequencing</gds_type><full_dataset_link>https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE307945</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>Caspase-4 transgenic mice exhibit cytoplasmic TDP-43 accumulation and age-dependent neuropathology</name><description>TAR DNA-binding protein (TDP-43) is a multifunctional protein that binds DNA and RNA within the nucleus. However, in human brains affected by Amyotrophic Lateral Sclerosis (ALS) or other pathological conditions, TDP-43 is often mislocalized in the cytoplasm, forming cytoplasmic inclusions. Existing TDP-43 transgenic mouse models have generally failed to exhibit significant cytoplasmic accumulation and loss of nuclear TDP-43, limiting the study of cytoplasmic TDP-43 pathology. In the current study, we developed a transgenic mouse model that expresses the human CASP4 and replicates the cytoplasmic mislocalization of endogenous TDP-43 and motor dysfunction in an age-dependent manner.</description><dates><publication>2026/05/08</publication></dates><accession>GSE307945</accession><cross_references><GSM>GSM9234451</GSM><GSM>GSM9234450</GSM><GSM>GSM9234453</GSM><GSM>GSM9234452</GSM><GSM>GSM9234448</GSM><GSM>GSM9234447</GSM><GSM>GSM9234449</GSM><GSM>GSM9234455</GSM><GSM>GSM9234444</GSM><GSM>GSM9234454</GSM><GSM>GSM9234446</GSM><GSM>GSM9234445</GSM><GPL>28330</GPL><GSE>307945</GSE><taxon>Mus musculus</taxon></cross_references></HashMap>