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EGF receptor family : targets for cancer therapeutics / Tony Burgess.
- Format:
- Video
- Author/Creator:
- Burgess, Antony, 1946- speaker, author.
- Series:
- Henry Stewart talks. Biomedical & life sciences collection. Signal transduction via protein tyrosine kinase receptors : structures, function, regulation, mechanisms and role in disease.
- Signal transduction via protein tyrosine kinase receptors : structures, function, regulation, mechanisms and role in disease, 2056-452X
- Language:
- English
- Subjects (All):
- Cells.
- Receptor Protein-Tyrosine Kinases.
- ErbB Receptors.
- Signal Transduction.
- Tumor Cells, Cultured.
- Medical Subjects:
- Cells.
- Receptor Protein-Tyrosine Kinases.
- ErbB Receptors.
- Signal Transduction.
- Tumor Cells, Cultured.
- Genre:
- Video recordings.
- Physical Description:
- 1 online resource (1 streaming video file (45 min.)) : color, sound.
- polychrome
- Other Title:
- Title on publisher web site: Signaling from the EGF receptor family in normal and cancer cells
- Place of Publication:
- London : Henry Stewart Talks, 2007.
- System Details:
- Mode of access: World Wide Web.
- video file
- Contents:
- Contents: The association of the Epidermal Growth Factor Receptor (EGFR) with the tumorigenic state
- The four related members of the EGFR family (EGFR, erbB2, erbB3 and erbB4)
- Signaling of the activated receptors as either homo- or heteromeric oligomers
- Activation of the EGFR by excess ligand stimulation, receptor over-expression and/or mutation in many carcinomas
- Utility of antibodies and receptor kinase inhibitors which interfere with signaling from the EGFR family as agents in cancer therapy
- The three-dimensional structures for the extracellular domains of EGFR, erbB2, erbB3 and erbB4 and the discovery that EGFR, erbB3 and erbB4 undergo major conformational transitions when interacting with their ligands
- Development of antibodies (mab806) which reduce tumor formation from cells expressing either truncated D2-7 EGFR or over-expressed EGFR by binding to the receptor in a region normally masked by the dimerization of the EGFR extracellular domain
- Use of EGFR antagonists or inhibitors to increase tumor killing by cytotoxic anti-cancer drugs and/or radiation
- Improvement of tumor killing by combining EGFR antagonists and EGFR kinase inhibitors.
- Notes:
- Animated audio-visual presentation with synchronized narration.
- Title from title frames.
- Publisher Number:
- 1074 Henry Stewart Talks
- Access Restriction:
- Restricted for use by site license.
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