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Environmental News Network - UW Researchers Will Develop Gene Editing Therapy to Treat Blindness

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United statesUniversity of wisconsinWalter koroshetzNational institute of neurological disordersSomatic cell genome editing programNational institutes of healthWisconsin institute for discoveryNational institutesWisconsin instituteBest diseaseLeber congenital amaurosisNational instituteNeurological disorders

UW researchers will trial gene editing therapy to treat blindness

UW researchers will trial gene editing therapy to treat blindness
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United statesWalter koroshetzDavid gamm krishanu sahaKrishanu sahaDavid gammShaoqin sarah gongNational institutes of healthNational institute of neurological disordersSomatic cell genome editing consortiumTherapeutics incorporatedSomatic cell genome editing programWisconsin institute of discoveryMcpherson eye research instituteNational institutesWisconsin instituteBest disease

Research to develop new rare disease therapies underway at The Jackson Laboratory

Research to develop new rare disease therapies underway at The Jackson Laboratory
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United statesMark wannerCathleen lutzSteven murrayWalter koroshetzRare disease translational centerBroad instituteJackson laboratorySomatic cell genome editing programSomatic cell gene editing programUt southwestern medical centerNational institute of neurological disordersNational instituteNeurological disordersMassachusetts general hospitalBoston children

Research to develop new rare disease therapies underway at The Jackson Laboratory

/PRNewswire/ Researchers led by Cathleen Lutz, Ph.D., are using an exciting new method, preclinical genomic editing, to develop safe, effective therapies.

United statesCathleen lutzWalter koroshetzSteven murrayMark wannerSomatic cell genome editing programSomatic cell gene editing programUt southwestern medical centerNational institute of neurological disordersRare disease translational centerBroad instituteJackson laboratoryNational instituteNeurological disordersMassachusetts general hospitalBoston children

Scientists Use Lipid Nanoparticles to Precisely Target Gene Editing to Liver

Gene editing delivery method in mice suggests possible one shot treatment of high cholesterol Nanoparticles deliver gene editing package specifically.

United statesQiaobing xuCenters for diseaseBroad institute of harvardScientists at tufts universityProceedings of the national academy sciencesTuft school of engineeringSomatic cell genome editing programTufts universityBroad instituteNational academyDisease controlTuft schoolMin qiuZachary glassGene editing