Harvard Medicine home webweekly
May 2, 2008

In Print

Morten Sommer and Gautam Dantas
Graham Ramsay

Human Gene Tied to Rare Iron-deficiency Disorder
Researchers have identified the genetic defect that causes a rare iron-deficiency disorder called iron-refractory iron deficiency anemia (IRIDA). The team, including co–senior author Mark Fleming, has not yet found a molecular mechanism by which the implicated gene acts. Yet they did determine that mutations in the gene cause inappropriately high levels of hepcidin, effectively turning off the body’s ability to absorb and recycle iron. The researchers hypothesize that these mutations may be involved in less severe forms of iron deficiency. And the discovery may open up new approaches for treating iron deficiency.

Upcoming

Polycystic Kidney Disease Symposium 2008

Friday, May 9
8 a.m.–5 p.m.

Speakers:
•Jing Zhou
•Ted Steinman
•Jagesh Shah
•Stephen Doxsey
•Iain Drummond
•David Beier
•Jordan Kreidberg
•Bradley Denker
•Peter Vassilev
•Herbert T. Cohen
•Andy McMahon

Lab Works

A multimedia site featuring Harvard Medical research.

Science Progress

How discovery happens.


 

 

 

 

 




 

 

 

 

Spotlight

Gary Ruvkun
Suzanne Camarata

Armenise Foundation Funds Chairs in Neurology and Basic Research
The Giovanni Armenise–Harvard Foundation, established by Count Giovanni Auletta Armenise, has endowed two new professorships at HMS and Massachusetts General Hospital.

Student Scene

Jason Sanders
Graham Ramsay

Is Pharm-free the Right Move?

Jason Sanders traces the line between what’s best for the patient and what’s best for the pharmaceutical industry.

 


Jeff Thiebauth

Reflection in Action Steps Up on Stage
The Young Fly Steppers, from the Jackson/Mann School in Allston, perform their winning dance routine at HMS as part of Reflection in Action. The program blends health issues with the arts and attracts participants from schools across Boston and Cambridge.

StudenTalk

Personal takes on issues inside and outside the classroom.

 

 


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