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Autosomal dominant gain-of-function mutations in LCP1 cause syndromiceneutropenia and immunodeficiency-
IL7R depletion mitigates neuroinflammation and ischemic stroke via AKT dephosphorylation dependent LCP1 suppression in mice
IL7R depletion mitigates neuroinflammation and ischemic stroke via AKT dephosphorylation dependent LCP1 suppression in mice
To further evaluate the impact of LCP1 dysfunction on hematopoiesis, we performed single-cell RNA sequencing (scRNA-seq) for bone marrow cells from patients and two matched healthy controls. Total 39, 028 cells were included in the sequential analysis after quality control.
ORGANISM(S): Homo sapiens 
2026-03-01 | GSE252973 | GEO
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