Human FasL, evolution and plasmin cleavage
A human-specific FasL substitution creates a proteolytic vulnerability in studied solid-tumor settings.
12 projects
A human-specific FasL substitution creates a proteolytic vulnerability in studied solid-tumor settings.
A T119R sequence difference permits plasmin cleavage of macaque TIGIT in the tested systems.
Mapping a Fas/CD95 epitope clarifies antibody agonism and a CAR-T bystander response in ovarian cancer models.
A dual-specificity antibody anchors to FOLR1 and activates DR5 in preclinical ovarian cancer systems.
DR5 agonist experiments reveal a PD-L1-associated response in several studied solid-tumor settings.
A positively charged receptor patch influences the activity of tested clinical DR5 antibodies.
A published UC invention proposes dual action on DR5 apoptosis and the CD155–TIGIT axis.
A UC Davis disclosure describes a synthetic peptide designed to resist plasmin cleavage.
A UC Davis listing describes Fas epitope antibodies and bispecific formats designed for tumor selectivity.
Coauthored studies examine TRIM37-linked chemoresistance, metastasis and a population-associated variant.
A coauthored interdisciplinary study targets microRNA control of X inactivation in Rett models.
A cell-based study examines furin targeting during the viral infection cycle.
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