Gene therapy helps dogs with muscle dystrophyThe HinduDuchenne muscular dystrophy is caused by genetic mutations that interfere with production of dystrophin, a protein needed for healthy muscles. The international team developed a new type of gene tra… Continue reading
KUOW News and InformationUsing CRISPR, scientists edit genome of viable human embryosThe Boston GlobeThe first experiment using CRISPR to alter the DNA of human embryos, in 2015, used embryos obtained from fertility clinics that had such serious geneti… Continue reading
Study: Immune-cell numbers predict response to combination immunotherapy in melanomaXinhuaSAN FRANCISCO, June 26 (Xinhua) — A nestudy indicates w that whether a melanoma patient will better respond to a single immunotherapy drug or two in combination … Continue reading
Next Big FutureGene therapy cures Duchenne muscular dystrophy in dogsNext Big FutureDuchenne muscular dystrophy (DMD) is an incurable X-linked muscle-wasting disease caused by mutations in the dystrophin gene. Gene therapy using highly functional micro… Continue reading
MIT Technology ReviewFirst Human Embryos Edited in USMIT Technology ReviewThe effort, led by Shoukhrat Mitalipov of Oregon Health and Science University, involved changing the DNA of a large number of one-cell embryos with the gene-editing technique … Continue reading
Safeguarding GenesHarvard Medical School (registration)Such chemicals could propel the development of therapeutic applications of genome editors by limiting off-target effects, or they could protect against future biological threats. The team will also… Continue reading
Yahoo News |
Gene therapy helps dogs with muscular dystrophy, humans next?
Yahoo News Paris (AFP) – Researchers have used gene editing to reverse symptoms in dogs of Duchenne muscular dystrophy (DMD) — a muscle-wasting and life-shortening disease that affects one in 5,000 baby boys. The dogs’ symptoms remained in check two years … Gene therapy cures Duchenne muscular dystrophy in dogs …Next Big Future Gene transfer corrects severe muscle defects in mice with Duchenne muscular dystrophyMedical Xpress A Gene Fix for a Mouse Model of Duchenne?Genetic Engineering & Biotechnology News (blog) |
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A step forward for gene editing: CRISPR-Cas9 and HD
HDBuzz CRISPR-Cas9 is an experimental gene editing technique used to make precise changes in DNA. For the first time, scientists have used this approach to attack the Huntington’s Disease mutation in the brain cells of a mouse. Other researchers are refining … GE Healthcare offers a virtual workshop for precise HDR-mediated genome engineeringDOTmed.com |