Dr. Gerard C Blobe M.D.
Oncologist | Medical Oncology
Box 2631 Dumc Durham NC, 27710About
Dr. Gerard Blobe is an oncologist practicing in Durham, NC. Dr. Blobe specializes in the care and treatment of patients with cancer. As an oncologist, Dr. Blobe manages and oversees the treatment of a cancer patient after he or she has been diagnosed with the disease. Oncologists will care for their patients throughout the course of the disease. Types of oncologists include medical oncologists, surgical oncologists, radiation oncologists, gynecologic oncologists, pediatric oncologists and hematologist oncologists.
Provider Details
Expert Publications
Data provided by the National Library of Medicine- Role of transforming growth factor beta in human disease.
- Functional roles for the cytoplasmic domain of the type III transforming growth
- A novel mechanism for regulating transforming growth factor beta (TGF-beta) signaling. Functional modulation of type III TGF-beta receptor expression through interaction with the PDZ domain protein, GIPC.
- Context-specific effects of fibulin-5 (DANCE/EVEC) on cell proliferation,
- Regulation of ALK-1 signaling by the nuclear receptor LXRbeta.
- Inhibiting the TGF-beta signalling pathway as a means of cancer immunotherapy.
- Beta-arrestin 2 mediates endocytosis of type III TGF-beta receptor and down-regulation of its signaling.
- Role of transforming growth factor Beta in human cancer.
- Cell-surface co-receptors: emerging roles in signaling and human disease.
- Role of transforming growth factor-beta in hematologic malignancies.
- The type III TGF-beta receptor suppresses breast cancer progression.
- The type III transforming growth factor-beta receptor as a novel tumor suppressor gene in prostate cancer.
- Loss of betaglycan expression in ovarian cancer: role in motility and invasion.
- The interaction of endoglin with beta-arrestin2 regulates transforming growth factor-beta-mediated ERK activation and migration in endothelial cells.
- The type III TGF-beta receptor signals through both Smad3 and the p38 MAP kinase pathways to contribute to inhibition of cell proliferation.
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