UCSF Macromolecular Structure Group

Abstract 1896: Patient-derived HER3 mutations transform ER+ and HER2+ breast cancer cells via MAPK pathway activation.

Rosalin Mishra,Samar Alanazi,Long Yuan,Thomas Solomon,Tarjani M. Thaker,Natalia Jura,Joan T. Garrett

Mobile-CRISPRi: Enabling Genetic Analysis of Diverse Bacteria.

A genetically encoded biosensor reveals location bias of opioid drug action.

Platform for rapid nanobody discovery in vitro.

The design principles of biochemical timers: circuits that discriminate between transient and sustained stimulation.

Abstract B101: Engineered PD-1 variants as immunotherapies for cancer.

Sydney R. Gordon,Roy Maute,Aaron Mayer,Melissa McCracken,Arutselvan Natarajan,Nan Guo,Richard Kimura,Jonathan M. Tsai,Aashish Manglik,Andrew Kruse,Sanjiv Gambhir,Irving L. Weissman,Aaron M. Ring

Structural Insights into the Dynamic Process of ß2-Adrenergic Receptor Signaling.

Structural Features of the Kinase Domain.

UCSF Macromolecular Structure Group

Abstract 1896: Patient-derived HER3 mutations transform ER+ and HER2+ breast cancer cells via MAPK pathway activation.

Abstract 1896: Patient-derived HER3 mutations transform ER+ and HER2+ breast cancer cells via MAPK pathway activation.

Mobile-CRISPRi: Enabling Genetic Analysis of Diverse Bacteria.

A genetically encoded biosensor reveals location bias of opioid drug action.

Platform for rapid nanobody discovery in vitro.

The design principles of biochemical timers: circuits that discriminate between transient and sustained stimulation.

Abstract B101: Engineered PD-1 variants as immunotherapies for cancer.

Abstract B101: Engineered PD-1 variants as immunotherapies for cancer.

Structural Insights into the Dynamic Process of ß2-Adrenergic Receptor Signaling.

Structural Features of the Kinase Domain.

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