Results were compared to biopsy specimens without myopathic changes (n=9) and hereditary muscular dystrophy (n=9). Results: The mRNA expression of BAFF, APRIL, and CXCL-13 was significantly higher in ...

Imaging Fibrous Structure Abnormalities of the White of the Eye in Myopathic Patients May 16, 2024 — Abnormalities in the shape of the sclera, the white of the eye, can cause various ...

Vatche and Tamar Manoukian Division of Digestive Diseases, G. Oppenheimer Center for Neurobiology of Stress and Resilience, ...

Elamipretide is also under evaluation for primary mitochondrial myopathy, a rare skeletal myopathic disease, with pivotal ...

We are also evaluating a topical ophthalmic formulation of our second-generation clinical-stage candidate, bevemipretide (SBT ...

and have a deep pipeline of novel compounds under evaluation for rare neurological and myopathic diseases.

Overall, an understanding of all of the genes involved in the dystrophic phenotype should lead to insights on correction of the myopathic condition, the major goal of the laboratory.

JAMA Ophthalmology (formerly Archives of Ophthalmology) is a monthly professional medical journal published by the American Medical Association. Archives of Ophthalmology publishes peer-reviewed ...

Researchers at the Center for Genomic Regulation in Barcelona and the University of Cologne in Germany have developed a new experimental strategy to tackle scarring and fibrosis. Experiments with ...

1 Department of Rheumatology, Ren Ji Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China 2 Department of Rheumatology, Zhongshan Hospital Fudan University, Shanghai, China ...