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Molecular biology of cancer

https://bccalibrary.andornot.com/en/permalink/catalog18469
Hoboken, NJ: John Wiley & Sons, Inc. , 2009.
Audience
Professional
Introduction by Stella Pelengaris and Mike Khan; The Burden of cancer by William Steward and Anne Thomas; Nature and nurture in oncogenesis by Stella Pelengaris and Mike Khan; DNA replication and the cell cycle by Stella Pelengaris and Mike Khan; Regulation of growth : growth factors, receptors, an…
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Editor
Pelengaris, Stella.
Khan, Michael
Place of Publication
Hoboken, NJ
Publisher
John Wiley & Sons, Inc.
Publication Date
2009
Series
Proquest Ebook Central
Subjects
Neoplasms - genetics
Molecular Biology
Abstract
Introduction by Stella Pelengaris and Mike Khan
The Burden of cancer by William Steward and Anne Thomas
Nature and nurture in oncogenesis by Stella Pelengaris and Mike Khan
DNA replication and the cell cycle by Stella Pelengaris and Mike Khan
Regulation of growth : growth factors, receptors, and signaling pathways by Stella Pelengaris and Mike Khan
Oncogenes by Stella Pelengaris and Mike Khan
Tumor suppressor genes by Martine Roussel
Apoptosis by Stella Pelengaris and Mike Khan
Telomeres and senescence by Maria Blasco and Mike Khan
Genetic instability, chromosomes, and repair by Stella Pelengaris and Mike Khan
Cancer is more than a genetic condition by Stella Pelengaris and Mike Khan
Cell?matrix adhesion, cell?cell interactions, and malignancy by Charles Streuli
Tumor immunity and immunotherapy by Cassian Yee
Angiogenesis by David T. Shima and Christiana Ruhrberg
Diagnosis of cancer by Anne Thomas and William Steward
Treatment of cancer : chemotherapy and radiotherapy by A.L. Thomas, R.A. Sharma, and W.P. Steward
Caring for the cancer patient by Nicky Rudd and Esther Waterhouse
Genomics and proteomics in cancer research and diagnosis by Norbert C.J. de Wit.
ISBN
9781444309089 (e-ISBN)
Language
English
Material Type
Ebook
Audience
Professional
Location
Internet
Website Notes
This Proquest title is licensed for ONE BC Cancer staff user at a time. If you are denied access while on a network computer, please try again later.
Authentication via HealthBC sign in required. Use your BC Cancer staff username and ID when prompted.
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https://login.bccancer.idm.oclc.org/login?url=https://ebookcentral.proquest.com/lib/bccancer-ebooks/detail.action?docID=428083
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Quick guide to good clinical practice : how to meet international quality standard in clinical research

https://bccalibrary.andornot.com/en/permalink/catalog120841
Cingi, Cemal, Muluk, Nuray Bayar. Cham, Switzerland: Springer , 2016.
Audience
Professional
Table of Contents:; Chapter 1: Clinical Trials: Historical Aspects and Importance and New Drug Developments -- Chapter 2: The Definition of GCP -- Chapter 3: The Principles of GCP -- Chapter 4: The Drug Development Process and Evolution of Regulations -- Chapter 5: Planning Clinical Research -- Cha…
More Information
  1 read online  
Alternate Title
How to meet international quality standard in clinical research
Author
Cingi, Cemal
Muluk, Nuray Bayar
Place of Publication
Cham, Switzerland
Publisher
Springer
Publication Date
2016
Series
EBSCOhost eBook
Subjects
Clinical Trials as Topic
Biomedical Research
Ethics, Research
Data Accuracy
Total Quality Management - standards
Internationality
Practice Guideline
Abstract
Table of Contents:
Chapter 1: Clinical Trials: Historical Aspects and Importance and New Drug Developments -- Chapter 2: The Definition of GCP -- Chapter 3: The Principles of GCP -- Chapter 4: The Drug Development Process and Evolution of Regulations -- Chapter 5: Planning Clinical Research -- Chapter 6: Preparation of Ethics Committee (IRB) Proposal -- Chapter 7: Preparation of Informed Consent -- Chapter 8: Preparation of Findings Tables -- Chapter 9: Setting the Ideal Statistical Methods -- Chapter 10: The Duties of a Clinical Research Coordinator
-- Chapter 11: The Duties of Clinical Researchers -- Chapter 12: The Phases of Clinical Studies -- Chapter 13: Safety in Clinical Trials -- Chapter 14: Setting the Size -- Chapter 15: Setting the Ideal Method -- Chapter 16: Ethics of Clinical Research -- Chapter 17: Recruitment and Enrolment -- Chapter 18: Why We Need Clinical Consent and Other Documentation -- Chapter 19: Monitoring the Trial -- Chapter 20: Inspection -- Chapter 21: Ethics: Institutional Review Board/Independent Ethics Committee (IRB/IEC) -- Chapter 22: Responsibilities of the Investigator -- Chapter 23: Responsibilities of the Sponsor -- Chapter 24: Clinical Trial Protocols
ISBN
9783319443430
9783319443447
Language
English
Material Type
Ebook
Audience
Professional
Location
Internet
Website Notes
This EBSCO title is licensed for one BC Cancer staff user at a time only. Authentication via HealthBC sign in required. Use your BC Cancer staff username and ID when prompted.
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https://login.bccancer.idm.oclc.org/login?url=http://search.ebscohost.com/login.aspx?direct=true&scope=site&db=nlebk&db=nlabk&AN=1288302
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