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» Products » KromoNews » Volume 4, Issue 19
  Published online October 12th, 2008
 

Weekly KromoNews: Volume 4, Issue 19
In this issue:
   This Week in Genetics
   Featured Genetic Test
   Upcoming Genetics Event
   Term of the Week: Histone

Editor's Note

Mobile version of Kromosoft website (incl. Pathology Central)
Did you know that the entire Kromosoft website, including the Pathology Central (which now has 570+ pathologies) is available on your BlackBerry/PDA/iPhone? When logging in, simply choose "concise" mode. It works pretty fast too.

You can contact a certified genetics counselor for free as part of your Kromosoft membership. You can submit any genetics related question. We pool the questions and get the answers back to you.
Submit a question


This Week in Genetics

New gene for male pattern baldness identified
Oct 12, 2008
Scientists have discovered an important hair-loss gene. During their study, the researchers investigated over 500,000 positions in the human genome, and found a gene variant which occurs clearly more frequently in bald men than in control persons. In 2005, the scientists had already characterized the first hair-loss gene inherited through the maternal line, which explained why hair-loss in men often reflects that of their maternal grandfathers. This newly discovered gene, on the other hand, may now account for the similarity in cranial hair growth between father and son.
[Nature Genetics]
Read Full Story

DNA strands found to have various sensitivity to ultraviolet light
Oct 10, 2008
DNA is highly resistant against alteration by ultraviolet light, but understanding the mechanism for its photostability presents some puzzling problems. A key aspect is the interaction between the four chemical bases that make up the DNA molecule. Researchers at Kiel University have succeeded in showing that DNA strands differ in their light sensitivity depending on their base sequences.
[- Other - ]
Read Full Story

Featured Genetic Test: Alpha-1 Antitrypsin Deficiency
Genetic testing for alpha-1 antitrypsin deficiency (also known as Alpha-1) tells whether a person has one of the two most common inherited changes – known as Z and S – associated with the condition.

Find more details about this test
Ask a question about this test to a certified genetics counselor

Upcoming Genetics Event

The 58th Annual Meeting of The American Society of Human Genetics (ASHG)

When:Tue Nov 11, 2008 to Sat Nov 15, 2008
Title:The 58th Annual Meeting of The American Society of Human Genetics (ASHG)
Description:The American Society of Human Genetics (ASHG) Annual Meeting is held each fall in a major U.S. or Canadian city and attracts over 5,000 attendees, plus exhibitors. ASHG members and others are selected to present their research findings at platform and poster sessions. Abstracts of work submitted for presentation at the annual meeting are published in a supplementary issue of The American Journal of Human Genetics (AJHG).

The highlights of each ASHG Annual Meeting are the scientific symposia, workshops and other sessions focusing on important research and clinical developments in human genetics that are presented by prominent professionals in the field.
Where:Philadelphia Convention Center, Philadelphia, PA, United States
Contact:Pauline Minhinnett, CMP
Email:paulinem@ashg.org
Website:http://www.ashg.org/2008meeting

Genetics Term of the Week: Histone
Histone: Histones are the chief protein components of chromatin. They are the spools around which DNA winds, and they play a role in gene regulation.
Read more



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