by admin | Jul 28, 2023 | Bernie Siegel’s WORLD STEM CELL SUMMIT BLOG, News and Opinions
by LAURA UNGAR and FREIDA FRISARO – MedicalXpress Dr. Alfonso Sabater pulled up two photos of Antonio Vento Carvajal’s eyes. One showed cloudy scars covering both eyeballs. The other, taken after months of gene therapy given through eyedrops, revealed no...
by admin | Jul 27, 2023 | Bernie Siegel’s WORLD STEM CELL SUMMIT BLOG, News and Opinions
By Saikiran Chandha – Live Science In the future, research labs will embrace the transformative potential of artificial intelligence to tackle wicked problems and speed up scientific discovery. Scientific laboratories of the future probably won’t have...
by admin | Jul 26, 2023 | Bernie Siegel’s WORLD STEM CELL SUMMIT BLOG, News and Opinions
by David McManus – Disability Support Guide A new breakthrough in Parkinson’s disease research has moved scientists one step closer to a significant treatment. Researchers were able to yield significant results through transplanting the skin cells of two people...
by admin | Jul 25, 2023 | Bernie Siegel’s WORLD STEM CELL SUMMIT BLOG, News and Opinions
By Center for Breakthrough Medicine – BIOPHARMADIVE The enormous impact the pandemic had on the biopharma industry is unmistakable, as evidenced by the unprecedented investments that took place in the cell and gene therapy (CGT) space. In January 2022, the...
by admin | Jul 24, 2023 | Bernie Siegel’s WORLD STEM CELL SUMMIT BLOG, News and Opinions
By Bronwyn Thompson – New Atlas A new stem cell therapy for Parkinson’s disease is one step closer to human trials after scientists were able to successfully rebuild neural damage in an animal model. Researchers from Scripps Research and Cardiff University used...
by admin | Jul 21, 2023 | Bernie Siegel’s WORLD STEM CELL SUMMIT BLOG, News and Opinions
By Andrew Joseph – Stat News When the genome-editing tool CRISPR is thought of as a potential medicine, the targets that first come to mind are diseases like sickle cell or other conditions caused by particular mutations. Use CRISPR to fix that mutation, the...