Title | Total cells | ||
1 | A blood atlas of COVID-19 defines hallmarks of disease severity and specificity Dataset 1: COMBAT project: single cell gene expression data from COVID-19, sepsis and flu patient PBMCs cell type: NK.CD16hi NK.CD16int expressed genes: BTN3A3 | ||
2 | Local and systemic responses to SARS-CoV-2 infection in children and adults Dataset 2: Airway cell type: NK cd56lo expressed genes: BTN3A3 | ||
3 | Prolonged cytopenia following CD19 CAR T cell therapy is linked with bone marrow infiltration of clonally expanded IFNγ-expressing CD8 T cells Dataset 1: Single cell RNA sequencing of bone marrow mononuclear cells from healthy donors and B-cell lymphoma patients following CD19 CAR T-cell therapy cell type: C09:CD16 NK expressed genes: BTN3A3 | ||
4 | Single-cell Atlas of common variable immunodeficiency shows germinal center-associated epigenetic dysregulation in B-cell responses Dataset 2: Activated PBMCs - Twins scRNA-seq cell type: NK_CD16_bright NK_CD16_bright_activated expressed genes: BTN3A3 | ||
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_16hi expressed genes: BTN3A3 | ||
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: CD16_NK expressed genes: BTN3A3 | ||
7 | 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_CD16+ expressed genes: BTN3A3 |