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With new method, genome editing moves toward 'prime' time

Oct. 22, 2019
By Anette Breindl
A team at the Broad Institute of Harvard and MIT has developed a genome editing method that could, in principle, correct 90% of the roughly 75,000 currently known genomic changes that are associated with genetic diseases.
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BioWorld MedTech's Cardiology Extra

Oct. 22, 2019
By Liz Hollis
Keeping you up to date on recent developments in cardiology.
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Bench Press for Oct. 21, 2019

Oct. 21, 2019
By Anette Breindl
BioWorld looks at translational medicine.
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Penn researchers develop neoantigen quality algorithm to guide immunotherapy

Oct. 21, 2019
By Stacy Lawrence
Researchers at the Abramson Cancer Center at the University of Pennsylvania have developed an algorithm to better personalize immunotherapy treatment. The algorithm works by examining neoantigen quality, not just their quantity. Neoantigens are proteins that are the result of genetic mutations in a tumor.
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BioWorld MedTech's Neurology Extra

Oct. 21, 2019
By Andrea Applegate and Anette Breindl
Keeping you up to date on recent developments in neurology.
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Penn researchers develop neoantigen quality algorithm to guide immunotherapy

Oct. 21, 2019
By Stacy Lawrence
Researchers at the Abramson Cancer Center at the University of Pennsylvania have developed an algorithm to better personalize immunotherapy treatment. The algorithm works by examining neoantigen quality, not just their quantity. Neoantigens are proteins that are the result of genetic mutations in a tumor.
Read More

BioWorld MedTech's Diagnostics Extra

Oct. 18, 2019
By Meg Bryant
Keeping you up to date on recent developments in diagnostics.
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New small-molecule inhibitors block apoptosis in mice

Oct. 16, 2019
By John Fox
Australian researchers have developed the first potent new small-molecule inhibitors capable of blocking the activation of apoptotic cell death before it causes damage to mitochondria, they reported in a study published in the Oct. 7, 2019, issue of Nature Chemical Biology.
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Australia's Orthocell ready to file interim results for Celgro

Oct. 15, 2019
By Tamra Sami
PERTH, Australia – Following stunning interim clinical results for its Celgro nerve regeneration treatment in quadriplegic patients, regenerative medicine company Orthocell Ltd. will focus all its efforts on gaining quick U.S. FDA approval based on the early results.
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Calling bias sinks CCR5 work but is 'likely unique' to variant

Oct. 15, 2019
By Nuala Moran
LONDON – A paper that raised concerns for the future health of Lulu and Nana, the world's first gene-edited babies, has been fully retracted at the request of the authors, after they failed to identify a problem in data from the U.K. Biobank on which their analysis was based. The study published in Nature Medicine in June, concluded the edits the twin girls are purported to have in their CCR5 chemokine receptor gene is associated with a 21% increase in mortality in middle and old age.
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