Title | Total cells | ||
1 | A spatially resolved atlas of the human lung characterizes a gland-associated immune niche Dataset 1: All cells and nuclei cell type: NK_CD56bright expressed genes: SMG6 | ||
2 | Blood and immune development in human fetal bone marrow and Down syndrome Dataset 1: Fetal Bone Marrow (10x) cell type: CD56 bright NK expressed genes: SMG6 Dataset 3: Fetal Bone Marrow (10x) - Down Syndrome cell type: CD56 bright NK expressed genes: SMG6 Dataset 4: Human Fetal Bone Marrow (CITE-seq) cell type: CD56 bright NK expressed genes: SMG6 | ||
3 | Local and systemic responses to SARS-CoV-2 infection in children and adults Dataset 2: Airway cell type: NK cd56hi expressed genes: SMG6 | ||
4 | Pathogenic variants damage cell composition and single cell transcription in cardiomyopathies Dataset 6: DCM/ACM heart cell atlas: Lymphoids cell type: NK_CD56hi expressed genes: SMG6 | ||
5 | 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: NK_56hi expressed genes: SMG6 | ||
6 | 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: CD56_NK expressed genes: SMG6 | ||
7 | Spatially resolved multiomics of human cardiac niches Dataset 1: Combined single cell and single nuclei RNA-Seq data - Heart Global cell type: NK_CD56hi expressed genes: SMG6 | ||
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: NK_CD56++ expressed genes: SMG6 |