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Mashup Score: 122Experimental gene therapy restores some vision in patients with inherited blindness | CNN - 11 day(s) ago
For her entire life, college student Olivia Cook had only a small degree of central vision. It was as if she was watching the world through a straw hole, and in dimly lit places, she could not make out peopleβs faces, only their silhouettes.
Source: edition.cnn.comCategories: General Medicine News, Future of MedicineTweet
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Mashup Score: 763
Doctors say the patient, a 62-year-old-man is recovering well from the surgery. It is seen as a milestone and a potential solution to the worldwide shortage of human organs for patients who need transplants.
Source: www.wbur.orgCategories: General Medicine News, Future of MedicineTweet
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Mashup Score: 450Eliminating the HIV virus from infected cells with CRISPR-Cas - 2 month(s) ago
The proof-of-concept study could lead to a cure for HIV that inactivates diverse β¦
Source: www.drugtargetreview.comCategories: General Medicine News, Future of MedicineTweet
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Mashup Score: 258CRISPR gene therapy seems to cure dangerous inflammatory condition - 3 month(s) ago
Nine out of ten people in a trial of a CRISPR treatment for potentially life-threatening inflammatory reactions seem to have been cured
Source: www.newscientist.comCategories: General Medicine News, Future of MedicineTweet
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Mashup Score: 171CRISPR engineered viruses could render other viruses harmless - 3 month(s) ago
A virus engineered using CRISPR technology spread its DNA to other viruses in mice, which could be used to make viral pathogens harmless
Source: www.newscientist.comCategories: General Medicine News, Future of MedicineTweet
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Mashup Score: 50A new RNA editing tool could enhance cancer treatment - 3 month(s) ago
Cell therapies for cancer can be potentially enhanced using a CRISPR RNA-editing platform, according to a new study published Feb. 21 in Cell.
Source: phys.orgCategories: General Medicine News, Future of MedicineTweet
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Mashup Score: 43Junk DNA in birds may hold key to safe, efficient gene therapy - 3 month(s) ago
For many genetic diseases, disabling or editing a gene using CRISPR is insufficient to overcome the effects of the underlying genetic mutation. A corrective gene needs to be added to the genome to fix the problem. Researchers have discovered a way to use a bird retrotransposon — a type of junk DNA — to insert whole transgenes into the human genome in a targeted way that does not risk damaging other genes.
Source: www.sciencedaily.comCategories: General Medicine News, Future of MedicineTweet
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Mashup Score: 319New toolbox allows engineering of genomes without CRISPR - 3 month(s) ago
Belgian researchers from VIB-KULeuven Center for Microbiology and VIB-UGent Center for Plant Systems Biology have developed a new toolbox of 16 different short DNA sequences that allow triggering controlled …
Source: phys.orgCategories: General Medicine News, Future of MedicineTweet
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Mashup Score: 114New CRISPR tool accelerates and optimizes genome editing - 3 month(s) ago
CRISPR/Cas systems have undergone tremendous advancement in the past decade. These precise genome editing tools have applications ranging from transgenic crop development to gene therapy and beyond. And …
Source: phys.orgCategories: General Medicine News, Future of MedicineTweet
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Mashup Score: 286CRISPR gene therapy seems to cure dangerous inflammatory condition - 4 month(s) ago
Nine out of ten people in a trial of a CRISPR treatment for potentially life-threatening inflammatory reactions seem to have been cured
Source: www.newscientist.comCategories: General Medicine News, Future of MedicineTweet
π College student Olivia Cook, born with an inherited retinal disorder, gained new vision after experimental CRISPR treatment. Using CRISPR, her left eye now sees in dimmer lighting. A groundbreaking proof of concept! ποΈβπ¨οΈ #Science #CRISPR https://t.co/H0rnw04QjD