Download e-book for iPad: Hutchinson-Gilford Progeria Syndrome - A Bibliography and by Philip M. Parker

By Philip M. Parker

ISBN-10: 0497112361

ISBN-13: 9780497112363

ISBN-10: 1429497068

ISBN-13: 9781429497060

In March 2001, the nationwide Institutes of health and wellbeing issued the next caution: ''The variety of sites providing health-related assets grows each day. Many websites offer worthwhile details, whereas others can have details that's unreliable or misleading.'' in addition, as a result of the fast raise in Internet-based details, many hours will be wasted looking, making a choice on, and printing. considering the fact that in simple terms the smallest fraction of data facing Hutchinson-Gilford progeria syndrome is listed in se's, reminiscent of www.google.com or others, a non-systematic method of web learn should be not just time eating, but in addition incomplete. This e-book was once created for doctors, scholars, and individuals of most of the people who are looking to behavior scientific examine utilizing the main complicated instruments to be had and spending the smallest amount of time doing so.

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Extra info for Hutchinson-Gilford Progeria Syndrome - A Bibliography and Dictionary for Physicians, Patients, and Genome Researchers

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The journey from gene to protein is complex and tightly controlled within each cell. It consists of two major steps: transcription and translation. Together, transcription and translation are known as gene expression. During the process of transcription, the information stored in a gene’s DNA is transferred to a similar molecule called RNA (ribonucleic acid) in the cell nucleus. Both RNA and DNA are made up of a chain of nucleotide bases, but they have slightly different chemical properties. The type of RNA that contains the information for making a protein is called messenger RNA (mRNA) because it carries the information, or message, from the DNA out of the nucleus into the cytoplasm.

When a mutation alters a protein that plays a critical role in the body, it can disrupt normal development or cause a medical condition. A condition caused by mutations in one or more genes is called a genetic disorder. In some cases, gene mutations are so severe that they prevent an embryo from surviving until birth. These changes occur in genes that are essential for development, and often disrupt the development of an embryo in its earliest stages. Because these mutations have very serious effects, they are incompatible with life.

The following multimedia has been indexed on Hutchinson-Gilford progeria syndrome: • Demystifying medicine, progeria, cardiovascular disease, and aging [electronic resource] Source: Francis S. Collins, Elizabeth G. : Films for the Humanities & Sciences, c1998 31 APPENDICES 32 APPENDIX A. 6 The Basics: Genes and How They Work This section gives you information on the basics of cells, DNA, genes, chromosomes, and proteins. What Is a Cell? Cells are the basic building blocks of all living things. The human body is composed of trillions of cells.

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Hutchinson-Gilford Progeria Syndrome - A Bibliography and Dictionary for Physicians, Patients, and Genome Researchers by Philip M. Parker


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