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1. BIOLOGIE
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1.1 BIOLOGIE - GÉNOME
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1.4 BIOLOGIE - TECHNOS, MODÈLES
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The newest gene editor radically improves on CRISPR [MIT Technology Review]
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The new technology, which delivers a wider menu of edits with more finesse, is already worth untold sums of money. Even before the paper was published, a syndicate of venture capitalists, including Newpath, Google’s venture arm, and F-Prime, had formed a company, Prime Medicine, and bought rights to it from the Broad Institute, where Liu has a lab.
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Scientists Create New, More Powerful Technique To Edit Genes [NPR]
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One advantage of the new editing technique is that, unlike CRISPR, prime editing doesn't rely on the ability of a cell to divide to help make the desired changes in DNA. That means it could be used to correct genetic mutations in cells that often don't divide, such as cells in the nervous system.
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New gene editing technology – Expert Reaction [Science Media Centre]
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They tested their technique over 175 times in cells, and were able to correct the primary genetic causes of sickle cell disease and Tay Sachs disease, and they say they could use it to correct around 89 per cent of genetic diseases. The SMC gathered expert comment on the report.
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2. ETIOLOGIE
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2.6 ETIOLOGIE - ENVIRONNEMENT
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3.1.1 PRÉVENTION - TABAC - E-CIGS
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4. DÉPISTAGE, DIAGNOSTIC ET PRONOSTIC
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5.10 TRAITEMENTS - ESSAIS
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5.12.5 IMMUNOTHÉRAPIES - PHARMA
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5.12.7 IMMUNOTHÉRAPIES - VACCINS
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5.16 TRAITEMENTS - CHIRURGIE
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5.2 PHARMA
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5.3 TRAITEMENTS - FDA, EMA, NICE...
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6.1 OBSERVATION
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6.12 ETHIQUE
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The Ethical Conundrums of Ultra-personalized Drugs [Bill of Health]
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The problem for the researcher has traditionally been phrased as whether it is ethical to subordinate the good of the individual to benefit the common good. By contrast, the problem of custom drugs is whether to subordinate the common good for the interests of the individual by dedicating scarce medical resources to research that stands to benefit only one person.
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