Researchers have achieved the first demonstration in mice of using gene therapy to reverse hallmark symptoms of SYNGAP1-related disorder, a devastating condition affecting an estimated 1 million ...
In May, a historic moment in science and medicine was captured in a single photo that circulated across news outlets ...
At the Cell and Gene Meeting on the Mesa, a panel discussion was held on advanced therapy production and how it demands ...
News-Medical.Net on MSN
Errors in EPG5 gene implicated in rare infant condition and adult neurodegenerative diseases
Errors in a gene known to cause a serious neurodevelopmental condition in infants are also linked to the development of Parkinson's disease in adolescence and adulthood, according to new research.
Scientists have discovered that mutations in the EPG5 gene—known for causing the rare childhood disorder Vici syndrome—also increase the risk of Parkinson’s disease and dementia later in life.
2don MSN
Study reveals genetic link between childhood brain disorder and Parkinson's disease in adults
Errors in a gene known to cause a serious neurodevelopmental condition in infants are also linked to the development of ...
BDX teams with Opentrons to automate single-cell sequencing, advancing its multiomics and biosciences strategy.
Each year I like to write a post about the Nobel Prize in Physiology or Medicine. While advocating for higher standards of science in medicine we tend to spend much of our time criticizing pseudoscie ...
American researchers have successfully generated early-stage human embryos using adult skin cells, a major reproductive science breakthrough. This innovative technique, which bypasses traditional egg ...
Phase 2 Trial in Multiple Myeloma Nears Key ReadoutPreparing for Expansion into Sickle Cell Disease and Acute Myeloid ...
Researchers at Spain’s CNIO have mapped 20,000 distinct DNA repair “scars,” building the first human REPAIRome. This atlas ...
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