SAT Hosp head defends Indian-made SMA drug, rejects trial claims | Thiruvananthapuram News
Representational AI-image Thiruvananthapuram: SAT Hospital superintendent Dr R S Riyas has urged the public not to spread misinformation…
Roche cans muscle-preserving obesity drug, hands it back to Chugai
Roche has scrapped development of a muscle-building drug, ending a trial testing the experimental medicine in combination with…
Advances in chemistry and delivery are taking oligonucleotide medicines beyond rare diseases
Decades of work on RNA targeting, chemical modification, and tissue-specific delivery are reshaping what programmable genetic medicines can…
Zebrafish can play a decisive role in clinical interpretation of spinal muscular atrophy
The tiny zebrafish is helping researchers rapidly determine whether a newborn’s genetic mutation is likely to cause spinal…
A qualitative, mixed-method approach to reaching consensus on function, fatigue, and fatigability outcomes in teens and adults living with spinal muscular atrophy | Orphanet Journal of Rare Diseases
Bach JR, Baird JS, Plosky D, Navado J, Weaver B. Spinal muscular atrophy type 1: management and outcomes.…
PacBio Targets Carrier Screening, Aims to Simplify Genetic Testing
PacBio is known in the genomics space for its HiFi sequencing technology—which provides long, highly accurate reads. But…