Yearly Archives: 2015
Effects of whey protein on strength, fat free mass or lean body mass
The first case in the world of Brugada Phenocopy due to coronary anomaly
Genetically engineered mice provide a new look at sight-threatening eye disease
Are domestic pig hybrids sick more often than other wild boar?
PM2.5 pollution and respiratory diseases in Beijing
Gene sequencing as a novel tool for diagnosing Loeys-Dietz syndrome
Selectivity in acquired prosopagnosia
Repair of damaged genetic material in humans
Should we protect the brain barriers to prevent Alzheimer’s disease?
Smart legumain drugs: Blocking the right activity at the right time, at the right place
Doctors, look up! Lack of eye contact reduces trust
Importance of selenium for brain function
SOCS3 in neurons halts abnormal blood vessel formation in the eye
Methylation profile of DMPK gene in myotonic dystrophy type 1 (DM1)
Myotonic dystrophy type 1 (DM1, Steinert’s disease), is the most common muscular dystrophy in adult life, characterized by myotonia (prolonged muscle contractions), muscle weakness, cataract, cardiac disease, gastrointestinal abnormalities, and central nervous system dysfunction. The clinical spectrum
























