Philip M. Parker's Nonsyndromic Deafness - A Bibliography and Dictionary for PDF

By Philip M. Parker

ISBN-10: 0497113813

ISBN-13: 9780497113810

ISBN-10: 1429495553

ISBN-13: 9781429495554

In March 2001, the nationwide Institutes of healthiness issued the subsequent caution: "The variety of sites providing health-related assets grows each day. Many websites supply invaluable details, whereas others could have details that's unreliable or misleading." in addition, end result of the speedy elevate in Internet-based info, many hours may be wasted looking, settling on, and printing. on account that in simple terms the smallest fraction of data facing Nonsyndromic deafness is listed in se's, similar to or others, a non-systematic method of net learn will be not just time eating, but in addition incomplete. This publication was once created for doctors, scholars, and individuals of most people who are looking to behavior scientific learn utilizing the main complicated instruments to be had and spending the smallest amount of time doing so.

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Additional resources for Nonsyndromic Deafness - A Bibliography and Dictionary for Physicians, Patients, and Genome Researchers

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The MT-TS1 gene provides instructions for a specific form of transfer RNA that is designated as tRNASer(UCN). This molecule attaches to a particular amino acid, serine (Ser), and inserts it into the appropriate locations in many different proteins. The tRNASer(UCN) molecule is present only in cellular structures called mitochondria. These structures convert energy from food into a form that cells can use. Through a process called oxidative phosphorylation, mitochondria use oxygen and simple sugars to create adenosine triphosphate (ATP), the cell's main energy source.

The size of the gap junction and the types of particles that move through it are determined by the particular connexin proteins that make up the channel. Gap junctions made with connexin 30 transport potassium ions and certain small molecules. Connexin 30 is found in several different tissues throughout the body, including the brain, skin, and inner ear. Because of its presence in the inner ear, researchers are interested in this protein's role in hearing. Hearing requires the conversion of sound waves to electrical nerve impulses.

Ear Hear. 2003 Aug;24(4):303-13. Review. PubMed citation • Gene Review: Nonsyndromic Hearing Loss and Deafness, Mitochondrial • Grafakou O, Hol FA, Otfried Schwab K, Siers MH, ter Laak H, Trijbels F, Ensenauer R, Boelen C, Smeitink J. Exercise intolerance, muscle pain and lactic acidaemia associated with a 7497G>A mutation in the tRNASer(UCN) gene. J Inherit Metab Dis. 2003;26(6):593-600. PubMed citation 46 Nonsyndromic Deafness • Guan MX. Molecular pathogenetic mechanism of maternally inherited deafness.

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Nonsyndromic Deafness - A Bibliography and Dictionary for Physicians, Patients, and Genome Researchers by Philip M. Parker

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