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Team led by A*Star scientist finds cause of rare disorder - Straits Times

This is the first time a mutation in the IRX family of genes has been found in humans. The team's work could help scientists understand how the body develops, and point the way to treatments for osteoporosis, heart disease and anaemia.
15 May 2012, 12:12 am
Key Found to Rare Genetic Disease Hamamy Syndrome - LiveScience.com

IRX genes have been repeatedly co-opted during evolution, and small variation in their activity could underlie fine alterations in the way we look, or perhaps even drastic ones such as the traits seen in an elephant, whale, turtle or frog body pattern ...
14 May 2012, 4:26 pm
Groundbreaking Discovery On Mutation-Causing Genetic Disorder in Humans - Science Daily

This is the first time that a mutation in IRX5 (and the family of IRX genes) has ever been discovered in man. IRX5 is part of a family of transcription factors that is highly conserved in all animals, meaning that this gene is present not only in humans ...
14 May 2012, 3:44 pm
Former USF engineering dean Mike Kovac dies at 70 - St. Petersburg Times

The companies included AT&T, the Harris Corp., Draper Laboratories, IRX Therapeutics and dozens of others. The idea was that the companies would work with university students and researchers, and in the process spur economic development.
11 May 2012, 12:52 am