Browse Genetics by genetic diseases

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Human Genetics: What is Genetic Imprinting?
Genetic or genomic imprinting is an important process in the mechanism of gene expression. Here genes are expressed based on the parent-of-origin. The phenomena is important for development, but it can also cause serious genetic abnormalities.

Published by Rafael B. (8,334 pts ) on Aug 17, 2009 to
Genetics Articles
How a "Silent Mutation" Can Be Harmful
Geneticists long dismissed certain mutations as "silent," believing them to have no effect. But a significant body of research has proved this assumption false: many so-called silent mutations are actually harmful mutations that are proven to cause genetic diseases in humans.

Published by Robyn Broyles (11,124 pts ) on Jun 28, 2009 to
Genetics Articles
Google Your Genome
Scientists love data. They collect it, read it, and spend hours trying to draw meaningful inferences from it. The ability of search engines such as Google to harness reams of information offers new ways of conducting research into the genetic causes of disease.

Published by Paul Arnold (15,324 pts ) on May 26, 2009 to
Genetics Articles
Introduction to Genetics: Glossary A-M
Does the field of genetics get you in a twist? Are you puzzled by some of the words, phrases, and terminology? If so, then this genetics glossary is for you. It features some of the key words used by scientists that are also found between the covers of prestigious science journals.

Published by Paul Arnold (15,324 pts ) on Apr 26, 2009 to
Genetics Articles
Genetic Disorders and Antisense Technology
Antisense technology is still in its infancy, but may prove to be one of the most important breakthroughs in the battle with genetic disorders and diseases.

Published by Jason C. Chavis (4,377 pts ) on Jan 28, 2009 to
Genetics Articles

Spina Bifida and Genetics
Spina bifida is the most common neural tube birth defect in the United States. At the present time the causes of spina bifida are unknown, though it is strongly believed that both genetics and the environment are contributing factors.

Published by Rafael B. (8,334 pts ) on Nov 18, 2008 to
Genetics Articles
Gene Discovered for Anencephaly, a Fatal Birth Defect
Anencephaly, a rare birth defect, has a genetic cause. The gene responsible for anencephaly has been discovered in mice, opening up the door to genetic testing and therapies for this genetic disorder.

Published by Rafael B. (8,334 pts ) on Oct 16, 2008 to
Genetics Articles
Kartagener’s Syndrome: A Rare Genetic Disorder
Kartagener’s syndrome is a rare genetic disorder also known as PCD. What causes it? What are the symptoms? How is PCD treated? Find out below.

Published by Rafael B. (8,334 pts ) on Oct 12, 2008 to
Genetics Articles