T-cell receptor repertoire of mice with organ-specific autoimmunity resulting from a partial defect in T cell negative selection and dendritic cell enhancement. Read more about T-cell receptor repertoire of mice with organ-specific autoimmunity resulting from a partial defect in T cell negative selection and dendritic cell enhancement.
Correlation of autoantigen-specific Treg frequency with development of spontaneous organ-specific autoimmunity in a mouse model of uveitis. Read more about Correlation of autoantigen-specific Treg frequency with development of spontaneous organ-specific autoimmunity in a mouse model of uveitis.
Ikaros regulates gene expression programs required for proper BCR-activation in mature B cells. Read more about Ikaros regulates gene expression programs required for proper BCR-activation in mature B cells.
The phosphatidinositol-transfer protein Nir3 is a modulator of T cell development. Read more about The phosphatidinositol-transfer protein Nir3 is a modulator of T cell development.
CD4+ T cells are more sensitive to inhibition of TCR signaling under Th17 polarizing conditions. Read more about CD4+ T cells are more sensitive to inhibition of TCR signaling under Th17 polarizing conditions.
Basal TCR signaling drives the functional heterogeneity of naïve CD4+ T cells. Read more about Basal TCR signaling drives the functional heterogeneity of naïve CD4+ T cells.
Development of allergic airway immunity depends on MARCH1-mediated ubiquitination of MHCII and CD86 in dendritic cells. Read more about Development of allergic airway immunity depends on MARCH1-mediated ubiquitination of MHCII and CD86 in dendritic cells.
DNA-scaffolded biomaterials enable modular and tunable presentation of proteins to control immune cell therapies. Read more about DNA-scaffolded biomaterials enable modular and tunable presentation of proteins to control immune cell therapies.
Ikaros mutations can bypass the requirement for second co-stimulatory signal and lead to break of B-cell tolerance. Read more about Ikaros mutations can bypass the requirement for second co-stimulatory signal and lead to break of B-cell tolerance.
Adventitial stromal cells define group 2 innate lymphoid cell tissue niches. Read more about Adventitial stromal cells define group 2 innate lymphoid cell tissue niches.
