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Chromatin --- Chromosomes --- Nucleoproteins --- Research --- Methodology.
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Food security emerged as an issue in the first decade of the 21st Century, questioning the sustainability of the human race, which is inevitably related directly to the agricultural water management that has multifaceted dimensions and requires interdisciplinary expertise in order to be dealt with. The purpose of this book is to bring together and integrate the subject matter that deals with the equity, profitability and irrigation water pricing; modelling, monitoring and assessment techniques; sustainable irrigation development and management, and strategies for irrigation water supply and conservation in a single text. The book is divided into four sections and is intended to be a comprehensive reference for students, professionals and researchers working on various aspects of agricultural water management. The book seeks its impact from the diverse nature of content revealing situations from different continents (Australia, USA, Asia, Europe and Africa). Various case studies have been discussed in the chapters to present a general scenario of the problem, perspective and challenges of irrigation water use.
Genetics. --- Biology --- Embryology --- Mendel's law --- Adaptation (Biology) --- Breeding --- Chromosomes --- Heredity --- Mutation (Biology) --- Variation (Biology) --- Genetics (non-medical)
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refers to the way in which the environment in the wide sense participates in the regulation of gene expression. This volume is a simplified source of information for both undergraduate and working professionals interested in lifestyle medicine and life sciences in general.
Epigenetics. --- Genetics. --- Biology --- Embryology --- Mendel's law --- Adaptation (Biology) --- Breeding --- Chromosomes --- Heredity --- Mutation (Biology) --- Variation (Biology) --- Genetics
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"The sequencing of the human genome and the identification of associations between specific genetic variants and diseases have led to an explosion of genomic-based diagnostic tests. These tests have the potential to direct therapeutic interventions, predict risk or onset of disease, or detect residual disease. As research progresses and an increasing number of associations are found, further tests will be developed that can aid in providing personalized treatment options for patients. However, the adoption of genomic diagnostic tests by health care providers has been limited due to a lack of evidence regarding the clinical utility of many tests. Health funders and practitioners lack the data necessary to distinguish which tests can improve practice or the clinical settings in which tests will provide the greatest value. The Roundtable on Translating Genomic-Based Research for Health held a workshop in November 2010 to determine what evidence is needed and how it is viewed by different stakeholders in order to develop genomic diagnostic tests of clinical value. Genome-Based Diagnostics summarizes the presentations and discussions that took place throughout the workshop. Two presentations, in particular, sparked extensive discussion. One presentation proposed that all genomic diagnostic tests be reviewed and approved by the Food and Drug Administration. The other observed that venture capitalists are no longer investing substantially in the development of genomic diagnostic tests because of a lack of clarity surrounding regulatory and reimbursement pathways. Both presentations suggested the need for major changes in the systems used to develop, regulate, and reimburse genomic diagnostic tests. The report also presents the perspectives of different stakeholders in the development of genomic diagnostic tests. Each stakeholder group has a different set of needs and issues of importance, yet commonalities among them are apparent, such as the need to put patients and health outcomes at the center of discussion and action"--Publisher's description.
Congenital diseases --- Disorders, Inherited --- Genetic diseases --- Hereditary diseases --- Inherited diseases --- Human chromosome abnormalities --- Genetic disorders --- Disorders, Genetic --- Diseases --- Medical genetics --- Human chromosomes --- Chromosome abnormalities --- Diagnosis --- Abnormalities
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In 2000, with the success of the Human Genome Project, scientists declared the death of race in biology and medicine. But within five years, many of these same scientists had reversed course and embarked upon a new hunt for the biological meaning of race. Drawing on personal interviews and life stories, Race Decoded takes us into the world of elite genome scientists-including Francis Collins, director of the NIH; Craig Venter, the first person to create a synthetic genome; and Spencer Wells, National Geographic Society explorer-in-residence, among others-to show how and why they ar
Race. --- Human genome. --- Genomics --- Social justice. --- Equality --- Justice --- Genome research --- Genomes --- Molecular genetics --- Human chromosomes --- Physical anthropology --- Social aspects. --- Moral and ethical aspects. --- Research
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The deciphering of the genome and, last but not least, the development of modern sequencing methods make many people fear that their "individuality" could be lost as a result. What this means exactly, what the individual's self-image is based on and to what extent the concern is justified is examined in this volume in the interdisciplinary discourse between human genetics and law. The contributions result from an interdisciplinary workshop of the Göttingen Institute for Human Genetics in cooperation with the Center for Medical Law in January 2012. Additional contributions from both a human genetic and a legal perspective broaden the factual basis and provide a deeper insight into the current state of affairs.
Genetics --- Human genetocs --- Genomes --- Law and legislation. --- Genomics --- Haploidy --- Biology --- Embryology --- Mendel's law --- Adaptation (Biology) --- Breeding --- Chromosomes --- Heredity --- Mutation (Biology) --- Variation (Biology) --- Human Genetics --- Law --- Institute of Human Genetics --- Centre of Medical Law --- Bundesverfassungsgericht --- Desoxyribonukleinsäure --- DNA-Sequenzierung --- Grundgesetz für die Bundesrepublik Deutschland --- Human genetics
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In the fifty years since DNA was discovered, we have seen extraordinary advances. For example, genetic testing has rapidly improved the diagnosis and treatment of diseases such as Huntington's, cystic fibrosis, breast cancer, and Alzheimer's. But with this new knowledge comes difficult decisions for countless people, who wrestle with fear about whether to get tested, and if so, what to do with the results. Am I My Genes? shows how real individuals have confronted these issues in their daily lives. Robert L. Klitzman interviewed 64 people who faced Huntington's Disease, breast and ovarian cance
Human chromosome abnormalities --- Medical genetics --- Human chromosomes --- Chromosome abnormalities --- Genetic disorders --- Diagnosis --- Social aspects. --- Abnormalities --- Genetic screening --- Medical records --- Privacy, Right of --- genetische counseling --- genetische test --- #SBIB:316.334.3M13 --- #SBIB:316.334.3M51 --- Invasion of privacy --- Right of privacy --- Civil rights --- Libel and slander --- Personality (Law) --- Press law --- Computer crimes --- Confidential communications --- Data protection --- Right to be forgotten --- Secrecy --- Medical ethics --- Moral and ethical aspects --- Access control --- conseil génétique --- test génétique --- Medische sociologie: aanverwante disciplines --- Organisatie van de gezondheidszorg: modellen van therapeutisch handelen --- Law and legislation --- Physicians
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