<HashMap><database>GEO</database><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=GSE326887</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>An Isoform-resolved Single-cell Atlas of the Murine Placenta: Gestational Dynamics During Syngeneic and Semi-allogeneic Pregnancy</name><description>The maternal-fetal interface requires precise immune tolerance followed by coordinated inflammation at term. While single-cell studies defined placental cellular diversity, alternative splicing's contribution to immune regulation remains poorly understood. Here, we present an isoform-resolved single-cell transcriptomic resource of the murine placenta across mid- and late gestation in syngeneic and semi-allogeneic pregnancies. We identify global suppression of cytokine networks during mid-gestation semi-allogeneic pregnancies, accompanied by erythroid populations co-expressing immune programs. Isoform-level analysis reveals the coordinated generation of alternatively spliced cytokine receptor variants, including soluble decoys and intracellular traps, lacking necessary signaling domains. These variants co-express with canonical receptors, decoupling ligand binding from downstream signal transduction to fine-tune immune responses. At term, this landscape shifts to coordinated pro-inflammatory signaling. This interactive dataset provides a systems-level framework for understanding how post-transcriptional mechanisms shape immune adaptation during murine pregnancy.</description><dates><publication>2026/04/15</publication></dates><accession>GSE326887</accession><cross_references><GSM>GSM9642100</GSM><GSM>GSM9642099</GSM><GSM>GSM9642096</GSM><GSM>GSM9642098</GSM><GSM>GSM9642097</GSM><GPL>34328</GPL><GSE>326887</GSE><taxon>Mus musculus</taxon></cross_references></HashMap>