Genetics and disease. [Translated from the Danish by Elisabeth Aagesen] by Tage Kemp

Cover of: Genetics and disease. | Tage Kemp

Published by Munskgaard in Copenhagen .

Written in English

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  • Heredity,
  • Heredity of disease,
  • Human genetics

Book details

LC ClassificationsQH431 K4513
The Physical Object
Number of Pages330
ID Numbers
Open LibraryOL18629499M

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The Epigenetics Revolution and millions of other books are available for instant access. view Kindle eBook | view Audible audiobook. The Epigenetics Revolution: How Modern Biology Is Rewriting Our Understanding of Genetics, Disease, and Inheritance 1st Edition by /5().

Genetics and Genomics of Eye Disease: Advancing to Precision Medicine thoroughly examines the latest genomics methods for studying eye disease, including complex eye disorders associated with multiple genes.

GWAS, WES, WGS, RNA-sequencing, and transcriptome analysis as employed in ocular genomics are discussed in-depth, as are genomics findings. A genetic disease is any disease caused by an abnormality in the genetic makeup of an individual.

The genetic abnormality can range from minuscule to major -- from a discrete mutation in a single base in the DNA of a single gene to a gross chromosomal abnormality involving the addition or subtraction of an entire chromosome or set of chromosomes.

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Genetics of Bone Biology and Skeletal Disease, Second Edition, is aimed at students of bone biology and genetics and includes general introductory chapters on bone biology and genetics. More specific disease orientated chapters comprehensively summarize the clinical, genetic, molecular, animal model, molecular pathology, diagnostic, counseling, and treatment aspects of each disorder.

Genes and Disease is a collection of articles that discuss genes and the diseases that they cause. These genetic disorders are organized by the parts of the body that they affect. As some diseases affect various body systems, they appear in more than one chapter. With each genetic disorder, the. Best disease, Genetics and disease.

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The New Genetics is a science education booklet that explains the role of genes in health and disease, the basics of DNA and its molecular cousin RNA, and new directions in genetic research.

Please note the publication date of this resource. There may be more recent developments that are not captured here.

We are working to update our science education content and encourage you to check. Genes & Diseases is an international journal for molecular and translational medicine. The journal primarily focuses on publishing investigations on the molecular bases and experimental therapeutics of human diseases.

Publication formats include full length research article, review article, short communication, correspondence, perspectives. This book is the proceedings of the Falk Symposium No on ‘Genetics in Liver Disease’, part of the XIII International Liver Week held in Freiburg, Germany, 7 October The first section covers the basic aspects of genetic diagnosis, pharmacogenetics, micro-arrays and their relevance for.

Parkinson's disease (PD) is a chronic progressive neurodegenerative movement disorder characterized by a profound and selective loss of nigrostriatal dopaminergic neurons. Clinical manifestations of this complex disease include motor impairments involving resting tremor, bradykinesia, postural instability, gait difficulty and rigidity.

Up to date and extensively revised to reflect recent advances in the genetics of common diseases, as well as current progress in gene therapy, Medical Genetics, 6th Edition, delivers easy-to-read, highly visual coverage of this rapidly changing accessible, practical text integrates key concepts with clinical practice, highlighted by numerous illustrations, tables, concept summaries Pages: Additional Physical Format: Online version: Kemp, Tage, Genetics and disease.

Copenhagen: Ejnar Munksgaard, (OCoLC) Document Type. Written by more than 60 international experts in the field, Muscle Disease embodies the explosion of new concepts and information on the pathology and genetics of muscle disease that has occurred in recent years.

In order to accommodate the new complex principles involved, the book is organized around the motor unit and the inherited disorders, in particular, are centered on the. Genetics is the study of genes and tries to explain what they are and how they work. Genes are how living organisms inherit features or traits from their ancestors; for example, children usually look like their parents because they have inherited their parents' genes.

Genetics tries to identify which traits are inherited, and explain how these traits are passed from generation to generation. Biochemical Genetics and Newborn Screening Follow-up. Shodair’s Biochemical Genetics Program in collaboration with Children’s Hospital Colorado cares for children and adults with inborn errors of metabolism or mitochondrial disease.

Metabolic disorders are rare and often diagnosed through newborn screening such as the “heel prick test.”. Understanding the connection between Parkinson's and genetics can help us understand how the disease develops and ultimately how it can be treated or cured. This is why studies like the Parkinson's Foundation PD GENEration study that is linking genetics to Parkinson's are essential.

An introduction to fundamental topics related to human genetics, including illustrations and basic explanations of genetics concepts. Printable PDF (7MB) Open All Close All. What is a cell. What is a gene. What is a chromosome. How many chromosomes do people have.

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Genetics is a branch of biology concerned with the study of genes, genetic variation, and heredity in organisms. Though heredity had been observed for millennia, Gregor Mendel, a scientist and Augustinian friar working in the 19th century, was the first to study genetics scientifically.

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While genetics is one of the risk factors is, that alone is usually not enough to cause coronary heart disease. If someone has a family history of coronary disease, heart attacks, strokes and elevated cholesterol levels, we know this can increase that person’s risk of coronary heart disease.

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Genetic epidemiology is a relatively new discipline that seeks to elucidate the role of genetic factors and their interaction with environmental factors in the occurrence of disease in populations (Khoury et al., ). The term genetic epidemiology appeared in the literature only recently (Figure).

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Encyclopedia of Human Genetics and Disease features nearly entries, including well-known genetic diseases, rare and lesser-known genetic diseases, and the genetic factors that may contribute to common diseases and health conditions, such as breast cancer and obesity.

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Diagnostic Techniques in Genetics offers an important overview of how DNA or RNA technology may be applied to a large set of genetic diagnoses. The first part of the book focuses on DNA/RNA applications and includes many of the latest developments in the field combined with routine procedures of genetic diagnoses, for example cloning and.

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Can knowing about genetics help treat disease. Every year, more than two million Americans have serious side effects from prescription medicines and as many as one hundred thousand die.

A "one-size-fits-all" approach to medicine might lead to some of. The Genetics Society of America (GSA), founded inis the professional membership organization for scientific researchers and educators in the field of genetics.

Our members work to advance knowledge in the basic mechanisms of inheritance, from the molecular. Other diseases caused by changes to your genes -- the doctor will call the changes "mutations" -- include cystic fibrosis, sickle cell disease, and Huntington’s : Hope Cristol.

The Epigenetics Revolution. How Modern Biology Is Rewriting Our Understanding of Genetics, Disease, and Inheritance. Nessa Carey. Columbia University Press. Biography. Muntaser Ibrahim is a Professor at the Department of Molecular Biology, Institute of Endemic Diseases at the University of Khartoum, Sudan.

He established the Unit of Diseases and Diversity at the University in He is a founding member of the African Society of Human Genetics and, inwon the CNR Rao Prize for Scientific Research. Book Description.

Genetics of Complex Disease examines how the identification of genetic variations that increase or reduce the risk of common, genetically complex, diseases can be used to improve our understanding of the pathology of many common diseases; enable better patient management and care; and help with differential diagnosis.

It starts with the questions of "what", "why" and "how. Autosomal Dominant (AD) When a disease is caused by a dominant allele of a gene, every person with that allele will show symptoms of the disease (assuming complete penetrance), and only one disease allele needs to be inherited for an individual to be affected.

Genetics of Complex Disease examines how the identification of genetic variations that increase or reduce the risk of common, genetically complex, diseases can be used to improve our understanding of the pathology of many common diseases; enable better patient management and care; and help with differential : Peter Donaldson, Ann Daly, Luca Ermini, Debra Bevitt.

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