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Biotechs Dictionary Of Toxicology
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Book Synopsis Biotech's Dictionary of Toxicology by : Dinesh Arora
Download or read book Biotech's Dictionary of Toxicology written by Dinesh Arora and published by Daya Books. This book was released on 2004 with total page 356 pages. Available in PDF, EPUB and Kindle. Book excerpt: Formally, Toxicology - Toxic + Ology - Means Science Of Poisons. But, In An Industrial Agent, Its Meaning Has Acquired Wider Connotations And Polluting Agents Like Co, Co2, Heavy Metals Which Cause Diseases Over A Long Period Rather Than Quick Death, Have Been Included As Its Subject Matter. The Ecological Concerns Of Mankind Are Reflected In It. The Biological Revolution Has Affected It Profoundly And Genetic Effects Of Various Environmental Factors Now Form A Part Of Toxicology. With No Great A Variety, It Is No Wonder That The Student Is Confused Over New And Unfamiliar Words. This Dictionary, We Hope, Will Go A Long Way Towards Solving These Problems. In Clear, Concise Manner, It Gives The Meaning Of Thousands Of Technical/Jargon Words Used In Genetics, Cytology, Pollution Study And Physiology/Medicine. It Is Hoped That Students Will Benefit Greatly From It And It Will Become A Standard Reference For Them.
Book Synopsis Dictionary of Toxicology by : Ernest Hodgson
Download or read book Dictionary of Toxicology written by Ernest Hodgson and published by Academic Press. This book was released on 2014-10-08 with total page 390 pages. Available in PDF, EPUB and Kindle. Book excerpt: Dictionary of Toxicology, Third Edition presents a compendium of definitions of all current toxicological terminology. This authoritative reference illustrates and describes words, concepts, acronyms and symbols for both the toxicological theory and applied risk assessment, as well as providing guidance on the correct selection of problematic, similar and frequently-misused terms. Written by one of the world’s foremost experts in toxicology, and with each entry peer reviewed, Dictionary of Toxicology, Third Edition is an essential reference for all scientific, medical and legal professionals who work with or encounter the toxicological effects of contaminants on biological systems. New to this edition: an update on every entry and the inclusion of all terminology and concepts relating to molecular toxicology, nanotoxicology and computational toxicology. Presents peer-reviewed definitions on the most up-to-date toxicological terms and concepts. New edition includes definitions within the fields of molecular toxicology, nanotoxicology, computational toxicology and risk assessment.
Book Synopsis Dictionary of Toxicology by : Ernest Hodgson
Download or read book Dictionary of Toxicology written by Ernest Hodgson and published by Nature Publishing Group. This book was released on 1998-01-01 with total page 504 pages. Available in PDF, EPUB and Kindle. Book excerpt: With over 4,000 insightful definitions, Dictionary of Toxicology is the only book to bring together in one place the language of toxicology. This edition contains 40% new material in areas such as molecular, environmental and regulatory toxicology. In addition, one third of the first edition entries have been revised. A new comprehensive subject area index guides users to all entries pertinent to particular topical areas. Ideal for those studying and/or working in toxicology, pharmacology, medicine, biotechnology, R&D in industry, government and science policy.
Book Synopsis Translation and Medicine by : Henry Fischbach
Download or read book Translation and Medicine written by Henry Fischbach and published by John Benjamins Publishing. This book was released on 1998-01-01 with total page 203 pages. Available in PDF, EPUB and Kindle. Book excerpt: The contributors to "Translation and Medicine" address several broad aspects of medical translation, from the cultural/historic framework of the language of medicine to pragmatic considerations of register and terminology. Their articles highlight some of the contributions translation has made to medical science and addresses some of the questions raised by those who escort the advances of medicine across language and cultural barriers and those who train the next generation of medical translators.Section 1 covers some Historical and Cultural Aspects that have characterized the language of medicine in Japan and Western Europe, with special emphasis on French and Spanish; Section 2 opens some vistas on The Medical Translator in Training with two specific university-level programs in Switzerland and in Spain, as well as an in-depth analysis of who makes the better medical translator: the medically knowledgeable linguist or the linguistically knowledgeable medical professional; and Section 3 looks at several facets of The Translator at Work, with discussions of the translator-client relationship and the art of audience-specific translating, an insider s view of the Translation Unit of the National Institutes of Health, and a detailed study of online medical terminology resources.
Book Synopsis Dictionary of Pharmaceutical Medicine by : Gerhard Nahler
Download or read book Dictionary of Pharmaceutical Medicine written by Gerhard Nahler and published by Springer Science & Business Media. This book was released on 2013-04-12 with total page 318 pages. Available in PDF, EPUB and Kindle. Book excerpt: This dictionary includes various terms typically used in pharmaceutical medicine. The 3rd edition underlines the increasing importance of this science and the changing regulatory environment, especially focusing on the research and development of new therapies as well as on conducting clinical trials, marketing authorizations for new medicinal products, and safety aspects including pharmacovigilance. The number of keywords has been considerably enlarged and is accompanied by an up to date list of the most important websites. Similar to the previous editions, this new book explains roughly 1,000 abbreviations most commonly used in pharmaceutical medicine. This volume will be a valuable tool for professionals working in the pharmaceutical industry, medical and preclinical research, regulatory affairs, marketing and marketing authorization of pharmaceuticals.
Book Synopsis Universities Press Dictionary Of Biotechnology And Genetic Engineering by : Sharon D. Cosloy
Download or read book Universities Press Dictionary Of Biotechnology And Genetic Engineering written by Sharon D. Cosloy and published by Universities Press. This book was released on 2003 with total page 244 pages. Available in PDF, EPUB and Kindle. Book excerpt: Revised And Expanded By More Than 300 New Terms, The Universities Press Dictionary Of Biotechnology And Genetic Engineering, New Edition Is An Essential Reference Tool On Modern Biotechnology And Genetic Engineering That Lucidly Articulates The Flood Of Advances And Discoveries In These Areas. In Addition To 100 Black-And-White Line Drawings, The Dictionary Includes Four Helpful Appendixes. The Universities Press Dictionary Of Biotechnology And Genetic Engineering, New Edition Will Benefit Students, Teachers, Physicians, Science And Technical Writers, Or Others Looking For A Concise Source Of Current Information On These Interdisciplinary Fields.
Book Synopsis Sarup's Dictionary of Biotechnology by : Jaishree Sharma
Download or read book Sarup's Dictionary of Biotechnology written by Jaishree Sharma and published by Sarup & Sons. This book was released on 2000 with total page 276 pages. Available in PDF, EPUB and Kindle. Book excerpt:
Book Synopsis FDA Biotechnology Inspection Guide by : United States. Food and Drug Administration
Download or read book FDA Biotechnology Inspection Guide written by United States. Food and Drug Administration and published by . This book was released on 1991 with total page 62 pages. Available in PDF, EPUB and Kindle. Book excerpt:
Download or read book Drug Information written by Bonnie Snow and published by Scarecrow Press. This book was released on 1999 with total page 772 pages. Available in PDF, EPUB and Kindle. Book excerpt: Designed for use as a self-study text, as a course text in more formal instruction programs, or as a refresher for the busy professional, the book includes valuable background data on legal and regulatory issues, as well as pharmaceutical technology.
Book Synopsis Pharmacokinetics and Pharmacodynamics of Biotech Drugs by : Bernd Meibohm
Download or read book Pharmacokinetics and Pharmacodynamics of Biotech Drugs written by Bernd Meibohm and published by John Wiley & Sons. This book was released on 2006-12-13 with total page 426 pages. Available in PDF, EPUB and Kindle. Book excerpt: This first ever coverage of the pharmacokinetic and pharmacodynamic characteristics of biopharmaceuticals meets the need for a comprehensive book in this field. It spans all topics from lead identification right up to final-stage clinical trials. Following an introduction to the role of PK and PD in the development of biotech drugs, the book goes on to cover the basics, including the pharmacokinetics of peptides, monoclonal antibodies, antisense oligonucleotides, as well as viral and non-viral gene delivery vectors. The second section discusses such challenges and opportunities as pulmonary delivery of proteins and peptides, and the delivery of oligonucleotides. The final section considers the integration of PK and PD concepts into the biotech drug development plan, taking as case studies the preclinical and clinical drug development of tasidotin, as well as the examples of cetuximab and pegfilgrastim. The result is vital reading for all pharmaceutical researchers.
Book Synopsis The Language of Biotechnology by : John M. Walker
Download or read book The Language of Biotechnology written by John M. Walker and published by . This book was released on 1988 with total page 274 pages. Available in PDF, EPUB and Kindle. Book excerpt: This dictionary attempts to define routinely used specialized language in the various areas of biotechnology, and remain suitable for use by scientists involved in unrelated disciplines. Viewing biotechnology as the practical application of biological systems to the manufacturing and service industries, and to the management of the environment, terms defined have been selected from as broad a spectrum as possible to include work accomplished by the following disciplines: (1) microbiology; (2) pharmacology; (3) biochemistry; (4) chemistry; (5) physiology; (6) chemical engineering; (7) genetic engineering; (8) enzymology; and (9) cell biology. The typical biotechnologist can utilize this dictionary to integrate specialized work with studies being carried out by collaborators in related fields, particularly with respect to differences in terminology, i.e., jargon. (JJK)
Book Synopsis Handbook on the Toxicology of Metals: Volume I: General Considerations by : Gunnar F. Nordberg
Download or read book Handbook on the Toxicology of Metals: Volume I: General Considerations written by Gunnar F. Nordberg and published by Academic Press. This book was released on 2021-11-30 with total page 798 pages. Available in PDF, EPUB and Kindle. Book excerpt: Handbook on the Toxicology of Metals, Fifth Edition, Volume I: General Considerations is the first volume of a two-volume work that gives an overview and covers topics of general importance including reviews of various health effects of trace metals. The book emphasizes toxic effects in humans, along with discussions on the toxic effects of animals and biological systems in vitro when relevant. The book has been systematically updated with the latest studies and advances in technology and contains several new chapters. As a multidisciplinary resource that integrates both human and environmental toxicology, the book is a comprehensive and valuable reference for toxicologists, physicians, pharmacologists, and environmental scientists in the fields of environmental, occupational and public health. Contains peer-reviewed chapters that deal with the effects of metallic elements and their compounds on biological systems Includes information on sources, transport and the transformation of metals in the environment Covers the ecological effects of metals to provide a basis for better understanding of the potential for adverse effects on human health Provides critical information on the properties, use, biological monitoring, dose-response relationships, diagnosis, treatment and prevention of metallic elements and compounds
Book Synopsis Rare Diseases and Orphan Products by : Institute of Medicine
Download or read book Rare Diseases and Orphan Products written by Institute of Medicine and published by National Academies Press. This book was released on 2011-04-03 with total page 442 pages. Available in PDF, EPUB and Kindle. Book excerpt: Rare diseases collectively affect millions of Americans of all ages, but developing drugs and medical devices to prevent, diagnose, and treat these conditions is challenging. The Institute of Medicine (IOM) recommends implementing an integrated national strategy to promote rare diseases research and product development.
Book Synopsis Reference Manual on Scientific Evidence by :
Download or read book Reference Manual on Scientific Evidence written by and published by . This book was released on 1994 with total page 652 pages. Available in PDF, EPUB and Kindle. Book excerpt:
Book Synopsis A Textbook of Modern Toxicology by : Ernest Hodgson
Download or read book A Textbook of Modern Toxicology written by Ernest Hodgson and published by McGraw-Hill Medical Publishing. This book was released on 1997 with total page 518 pages. Available in PDF, EPUB and Kindle. Book excerpt: This revised edition reflects changes in the core curriculum subjects covered in the basic toxicology course for graduate students. Designed as an introductory textbook, it emphasizes the fundamental basis of toxic action at the cellular and molecular levels and lays the foundation for specialized courses in toxicology. Additional topics include metabolic activation and cellular protection, clinical toxicology diagnosis and treatment, ecosystems, environmental toxicology, ecotoxicology, case histories, and future consideration for environmental and human health.
Book Synopsis Modern Methods of Clinical Investigation by : Institute of Medicine
Download or read book Modern Methods of Clinical Investigation written by Institute of Medicine and published by National Academies Press. This book was released on 1990-02-01 with total page 241 pages. Available in PDF, EPUB and Kindle. Book excerpt: The very rapid pace of advances in biomedical research promises us a wide range of new drugs, medical devices, and clinical procedures. The extent to which these discoveries will benefit the public, however, depends in large part on the methods we choose for developing and testing them. Modern Methods of Clinical Investigation focuses on strategies for clinical evaluation and their role in uncovering the actual benefits and risks of medical innovation. Essays explore differences in our current systems for evaluating drugs, medical devices, and clinical procedures; health insurance databases as a tool for assessing treatment outcomes; the role of the medical profession, the Food and Drug Administration, and industry in stimulating the use of evaluative methods; and more. This book will be of special interest to policymakers, regulators, executives in the medical industry, clinical researchers, and physicians.
Book Synopsis The Prevention and Treatment of Missing Data in Clinical Trials by : National Research Council
Download or read book The Prevention and Treatment of Missing Data in Clinical Trials written by National Research Council and published by National Academies Press. This book was released on 2010-12-21 with total page 163 pages. Available in PDF, EPUB and Kindle. Book excerpt: Randomized clinical trials are the primary tool for evaluating new medical interventions. Randomization provides for a fair comparison between treatment and control groups, balancing out, on average, distributions of known and unknown factors among the participants. Unfortunately, these studies often lack a substantial percentage of data. This missing data reduces the benefit provided by the randomization and introduces potential biases in the comparison of the treatment groups. Missing data can arise for a variety of reasons, including the inability or unwillingness of participants to meet appointments for evaluation. And in some studies, some or all of data collection ceases when participants discontinue study treatment. Existing guidelines for the design and conduct of clinical trials, and the analysis of the resulting data, provide only limited advice on how to handle missing data. Thus, approaches to the analysis of data with an appreciable amount of missing values tend to be ad hoc and variable. The Prevention and Treatment of Missing Data in Clinical Trials concludes that a more principled approach to design and analysis in the presence of missing data is both needed and possible. Such an approach needs to focus on two critical elements: (1) careful design and conduct to limit the amount and impact of missing data and (2) analysis that makes full use of information on all randomized participants and is based on careful attention to the assumptions about the nature of the missing data underlying estimates of treatment effects. In addition to the highest priority recommendations, the book offers more detailed recommendations on the conduct of clinical trials and techniques for analysis of trial data.
