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Title | Total cells | ||
1 | A cell atlas of human thymic development defines T cell repertoire formation Dataset 1: Figure 1 - A cell atlas of human thymic development defines T cell repertoire formation cell type: memory B cell expressed genes: SEMA4B | ||
2 | A spatially resolved atlas of the human lung characterizes a gland-associated immune niche Dataset 1: All cells and nuclei cell type: B_memory expressed genes: SEMA4B | ||
3 | Local and systemic responses to SARS-CoV-2 infection in children and adults Dataset 2: Airway cell type: B mem B mem activated B mem exhausted expressed genes: SEMA4B | ||
4 | Mapping single-cell transcriptomes in the intra-tumoral and associated territories of kidney cancer Dataset 1: Single-cell transcriptomic datasets of Renal cell carcinoma patients cell type: class switched memory B cell unswitched memory B cell expressed genes: SEMA4B | ||
5 | Single-Cell Sequencing of Developing Human Gut Reveals Transcriptional Links to Childhood Crohn’s Disease Dataset 2: Paediatric Human Gut (4-14y) cell type: Memory B cell expressed genes: SEMA4B | ||
6 | Single-cell multi-omics analysis of the immune response in COVID-19 Dataset 1: Single-cell multi-omics analysis of the immune response in COVID-19 cell type: B_non-switched_memory B_switched_memory expressed genes: SEMA4B | ||
7 | Single-cell proteo-genomic reference maps of the hematopoietic system enable the purification and massive profiling of precisely defined cell states Dataset 4: healthy young bone marrow donor cell type: Class switched memory B cells Nonswitched memory B cells expressed genes: SEMA4B | ||
8 | Type I interferon autoantibodies are associated with systemic immune alterations in patients with COVID-19 Dataset 1: Type I interferon autoantibodies are associated with systemic immune alterations in patients with COVID-19 cell type: B_Mem B_Mem_Prolif_Early B_Mem_Prolif_Late expressed genes: SEMA4B |