Title | Total cells | ||
1 | A human fetal lung cell atlas uncovers proximal-distal gradients of differentiation and key regulators of epithelial fates Dataset 1: All cells cell type: non-classical monocyte expressed genes: SPOPL | ||
2 | A spatially resolved atlas of the human lung characterizes a gland-associated immune niche Dataset 1: All cells and nuclei cell type: Monocyte_CD16 expressed genes: SPOPL | ||
3 | Immunophenotyping of COVID-19 and influenza highlights the role of type I interferons in development of severe COVID-19 Dataset 1: Immunophenotyping of COVID-19 and influenza highlights the role of type I interferons in development of severe COVID-19 cell type: nonclassical Monocyte expressed genes: SPOPL | ||
4 | Multiomic Profiling of Human Clonal Hematopoiesis Reveals Genotype and Cell-Specific Inflammatory Pathway Activation Dataset 1: Single Cell Sequencing of Human PBMCs in Clonal Hematopoeisis of Indeterminant Potential cell type: Non-classical monocytes expressed genes: SPOPL | ||
5 | Single-cell multiomics reveals increased plasticity, resistant populations, and stem-cell–like blasts in KMT2A-rearranged leukemia Dataset 1: Global dataset of infant KMT2Ar B-ALL cell type: CD16_Monocyte expressed genes: SPOPL | ||
6 | 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: Non-classical monocytes expressed genes: SPOPL | ||
7 | Spatially resolved multiomics of human cardiac niches Dataset 1: Combined single cell and single nuclei RNA-Seq data - Heart Global cell type: CD16+Mo expressed genes: SPOPL | ||
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: ncM ncM_1006 expressed genes: SPOPL |