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Bone Coupling Factor Key To Skeletal Health
Published July 9, 2009, 3:21 pm, Science Daily
Previously, scientists had searched for but missed the biological link between bone growth and bone remodeling -- a natural give-and-take system that is crucial to skeletal health. A new study pinpoints the coupling factor as transforming growth factor beta-1, or TGF beta-1.
Bayer HealthCare Launches Hemophilia Self-Infusion Training Program
Published July 9, 2009, 1:13 pm, redOrbit
WAYNE, N.J., July 9 /PRNewswire/ -- Today, Bayer HealthCare Pharmaceuticals launched the BayCuff(TM) self-infusion training program, an educational initiative designed to make infusion of recombinant factor VIII easier for both patients with hemophilia A and for their caregivers.
157-mile bicycle ride to ‘give back’
Published July 9, 2009, 1:07 pm, Lone Tree Voice
As a former pediatric physical therapist at The Children’s Hospital, Nanci Ricks worked with many special needs children.
Discovery of key gene for bone development that when mutated lead to dwarfism
Published July 9, 2009, 12:49 pm, News-Medical-Net
Scientists have just discovered the gene behind Recessive Omodysplasia, a rare skeletal disease characterised by short-limbed dwarfism and craniofacial anomalies.
Louisiana Business: Economic Development Site, Insurance, Workforce, US Economy
Published July 9, 2009, 10:54 am, Bayou Buzz
July 8, 2009 @ 11:35
Of Yeast And Men: Unraveling The Molecular Mechanisms Of Friedreich's Ataxia
Published July 9, 2009, 10:21 am, Science Daily
Scientists have created an experimental model that produces large-scale expansion of GAA repeats during DNA replication, which is the cause of Friedreich's Ataxia. With this model, the researchers are able to analyze GAA repeat expansions and then identify cellular proteins that thwarted normal replication and promoted the elongated sequence.
Unraveling The Molecular Mechanisms Of Friedreich's Ataxia
Published July 9, 2009, 10:16 am, redOrbit
Researchers in human genetics have long known that expansions of GAA repeats – resulting in this nucleotide triplet repeating hundreds or thousands of times – cause the most common hereditary neurological disorder known as Friedreich's ataxia.
Of yeast and men: Unraveling the molecular mechanisms of Friedreich's ataxia
Published July 9, 2009, 10:05 am, PhysOrg
Researchers in human genetics have long known that expansions of GAA repeats - resulting in this nucleotide triplet repeating hundreds or thousands of times - cause the most common hereditary neurological disorder known as Friedreich's ataxia. There is no cure for this condition, which damages the nervous system and can result in heart disease.
Novel genetic finding offers new avenue for future Crohn's disease treatment
Published July 9, 2009, 9:35 am, PhysOrg
Researchers from Case Western Reserve University School of Medicine identified a novel link between ITCH, a gene known to regulate inflammation in the body and NOD2, a gene which causes the majority of genetic Crohn's Disease diagnoses. ITCH, when malfunctioning, causes widespread inflammatory diseases, including inflammatory bowel disease, gastritis, uncontrolled skin inflammation, and ...
Unraveling the Molecular Mechanisms of Friedreich's Ataxia
Published July 9, 2009, 9:24 am, Newswise
A Tufts University research team has created an experimental model that produces large-scale expansion of GAA repeats during DNA replication, which is the cause of Friedreich's Ataxia. With this model, the researchers are able to analyze GAA repeat expansions and then identify cellular proteins that thwarted normal replication and promoted the elongated sequence.
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