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TMTC4 is a hair-cell-specific human deafness gene.
Human hepatic organoids for the analysis of human genetic diseases.
Homeostatic cytokines reciprocally modulate the emergence of prenatal effector PLZF+CD4+ T cells in humans.
Structural and functional analyses of a germline KRAS T50I mutation provide insights into Raf activation.
Lymphatic disorders caused by mosaic, activating KRAS variants respond to MEK inhibition.
GATOR2-dependent mTORC1 activity is a therapeutic vulnerability in FOXO1 fusion-positive rhabdomyosarcoma.
αVβ8 integrin targeting to prevent posterior capsular opacification (PCO).
The effects of low-dose IL-2 on Treg adoptive cell therapy in patients with Type 1 diabetes.
SLC26A6-selective inhibitor identified in a small-molecule screen blocks fluid absorption in small intestine.
MYH9 facilitates autoregulation of adipose tissue depot development.