PERSONALIZED (AKA PRECISION) THERAPY-A SYSTEMS ANALYSIS OF CAPTURED MOLECULAR DATA

There are eight hallmark biological capabilities necessary for cancer development and persistence: (1) sustained proliferation, (2) evasion of growth suppressors, (3) death resistance …

LIVING WITH CANCER, WEIGHING THE PRICE: DALLAS-AREA PATIENTS DISCUSS HARD CHOICES

Mike Hernandez did well for himself and his family. He retired to his home in Coppell at 47 after a career with Lucent Technologies. Five years later, though, doctors found cancer in his throat.

MARY CROWLEY QUARTERLY: VOLUME 5 ISSUE 2

TARGETING CANCER

The personalization of oncology treatments demands the alignment of patients’ molecular cancer growth mechanisms with the drugs which have been designed to target the cancer specific molecular signals.

MARY CROWLEY QUARTERLY: VOLUME 5 ISSUE 1

MARY CROWLEY QUARTERLY: VOLUME 4 ISSUE 2

VERTICALLY INTEGRATED TRANSLATIONAL STUDIES OF PDX1 AS A THERAPEUTIC TARGET FOR PANCREATIC CANCER VIA A NOVEL BIFUNCTIONAL RNAI PLATFORM

Vertically Integrated Translational Studies of PDX1 as a Therapeutic Target for Pancreatic Cancer via a Novel Bifunctional RNAi Platform.

PHASE I STUDY OF INTRAVENOUSLY ADMINISTERED ATI-1123, A LIPOSOMAL DOCETAXEL FORMULATION IN PATIENTS WITH ADVANCED SOLID TUMORS

Phase I study of intravenously administered ATI-1123, a liposomal docetaxel formulation in patients with advanced solid tumors.

PHASE I STUDY OF INTRAVENOUSLY ADMINISTERED ATI-1123, A LIPOSOMAL DOCETAXEL FORMULATION IN PATIENTS WITH ADVANCED SOLID TUMORS

Phase I study of intravenously administered ATI-1123, a liposomal docetaxel formulation in patients with advanced solid tumors.

SUMMARY OF BI-SHRNA FURIN/GM-CSF AUGMENTED AUTOLOGOUS TUMOR CELL IMMUNOTHERAPY (FANG™) IN ADVANCED CANCER OF THE LIVER

Summary of bi-shRNAfurin/GM-CSF Augmented Autologous Tumor Cell Immunotherapy (FANG™) in Advanced Cancer of the Liver.