Across the continuing state.

Across the continuing state, with a giant inflatable Rx bottle as a backdrop, AARP people are sending a ‘message in a bottle’ to Illinois members of Congress, delivering a large number of prescription bottles filled with constituents’ health care stories along with a strong message: HEALTHCARE Reform Today! Related StoriesInnovative single-use torque instruments utilize hard polycarbonate from BayerNHS ‘hourglass’ structure holds back development of support workforcePreventing falls in care homes: an interview with Professor Pip LoganHolding ‘Rx for healthcare reform’ press conferences through the entire state, hosting community occasions and forums targeted at debunking the health care reform myths and assisting the public to obtain the facts on the problem, AARP associates are urging Congress to tackle the presssing issue when they return to Washington later on this month.

Interestingly, the ERK2 gene can be central to a well-known pathway already associated with a different specific band of cardiac and craniofacial syndromes that include Noonan, Costello, Cardiofaciocutaneous syndrome, and LEOPARD syndrome. Landreth enlisted the help of Michiko Watanabe, Ph.D., professor of Pediatrics at Case Western Reserve University School of Medicine to check out the mouse hearts. She and her team discovered that they had characteristic heart defects resembling those observed in the individuals with ERK2 deletions. Sulagna Saitta, a human geneticist at Children’s Medical center of Philadelphia had identified children who had comparable center defects along with subtle facial variations.Interestingly, the ERK2 gene can be central to a well-known pathway already associated with a different specific band of cardiac and craniofacial syndromes that include Noonan, Costello, Cardiofaciocutaneous syndrome, and LEOPARD syndrome. Landreth enlisted the help of Michiko Watanabe, Ph.D., professor of Pediatrics at Case Western Reserve University School of Medicine to check out the mouse hearts. She and her team discovered that they had characteristic heart defects resembling those observed in the individuals with ERK2 deletions. Sulagna Saitta, a human geneticist at Children’s Medical center of Philadelphia had identified children who had comparable center defects along with subtle facial variations.