The team found that a slight change in the expression phase of a gene called orthodenticle (otd) can cause a significant difference in the size of the ommatidia, individual hexagonal-shaped units that...
Read moreEl Hospital público Universitario 12 de Octubre de la Comunidad de Madrid lidera un ensayo clínico en adolescentes con cáncer para estudiar los resultados de una intervención basada en ejercicio f...
Read moreLos resultados del estudio muestran una aparente tendencia decreciente en las concentraciones de PCBs en cetáceos a lo largo de los años, pero aún así, el 51.28% de los individuos analizados prese...
Read moreIt contains twelve pollutants, the impacts of which have been identified as having the possibility for widespread concern for the environment and human health.
Read moreThermo Fisher Scientific Inc, today announced the launch of the CorEvitas Systemic Lupus Erythematosus (SLE) Registry. The multi-center, prospective registry leverages the CorEvitas rheumatology physi...
Read moreThis Dot-Blot protocol wants to be an easy and basic guide for researchers to help them through the process. It contains a list of materials, the steps to follow and even a list of common problems and...
Read moreLeading US psychiatric experts join Oryzon’s Clinical Advisory Board (CAB) to advance Phase III development of vafidemstat in Borderline Personality Disorder (BPD)
Read moreAgarose Bead Technologies (ABT) is a leading European manufacturer of agarose resins supporting the biopharmaceutical industry. Agarose resins are manufactured under a rigorous Quality Management Syst...
Read moreOryzon Genomics, S.A, a clinical-stage biopharmaceutical company leveraging epigenetics to develop therapies in diseases with strong unmet medical need, today reported financial results for the fou...
Read moreThe researchers demonstrate that TANGO2 directly binds to a key fat molecule called acyl-CoA, transporting them like a shuttle inside cells. The authors of the study made the findings by tagging TANGO...
Read moreMyhre syndrome is a rare genetic disorder marked by a range of clinical features that affect both physical development and organ function. It is primarily caused by five specific SMAD variants, which ...
Read moreOn Rare Disease Day, the Sant Pau Research Institute (IR Sant Pau) reaffirms the significance of scientific and clinical advancements in improving the diagnosis and treatment of these little-known con...
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