Join our Co-Founder and CEO, Tim Lu, today for a fireside chat at Chardan’s 8th Annual Genetic Medicines Conference as he shares company highlights. Visit the events page of our website for webcast details and archived recordings: https://lnkd.in/eC93_hEp $SNTI #celltherapy #synbio
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Pharmacogenomics expert, psychiatric pharmacist, and strategic thinker with a passion for education, developing strong relationships, and leadership.
DPYD PGx testing is an easy way to ensure you get the right dose of fluorouracil-based chemotherapy. It may not be part of clinical guidelines, but when DPYD testing has such a high level of evidence, it should be.
DPYD genetic variants could cause severe adverse effects and even death. DPYD Pharmacogenomic testing is currently in the guidelines for 5 Fluorouracil , Capecitabine and Tegafur. Ask your oncologist for genetic testing options. https://lnkd.in/grB4zFda
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DPYD genetic testing is crucial before the administration of 5-FU, capecitabine and tegafur.🙌🤞Stay on a safe side✅
DPYD genetic variants could cause severe adverse effects and even death. DPYD Pharmacogenomic testing is currently in the guidelines for 5 Fluorouracil , Capecitabine and Tegafur. Ask your oncologist for genetic testing options. https://lnkd.in/grB4zFda
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Did you miss the recent Devyser webinar with Dr. Robert Akkers highlighting the shifting distribution of hemoglobinopathy and the need for expanded thalassemia genetic testing? Now watch the on-demand webinar here: https://bit.ly/3RPitjr #thalassemia #ngs #genetictesting
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For the most part, the technology used to treat #Duchenne muscular dystrophy has been focused on exon skipping. But as is the case with many boys with the condition, my son Caffrey's mutation is not amenable to this type of treatment. That’s why we need to continue to develop additional therapeutic options for #DMD. Thank you, Rare Disease Advisor, for the opportunity to share Caffrey’s story and how his diagnosis helped me appreciate the sheer unmet medical need there is not only within the Duchenne community, but also broadly across all #rarediseases – and what we are doing at @Alltrna to accelerate #raredisease #drugdevelopment.
Alltrna’s CEO Michelle Werner discusses with Larry Luxner of Rare Disease Advisor her personal and professional mission to accelerate #raredisease #drugdevelopment and how new tRNA genetic medicines could do this: by treating many diseases at once. 🎧 Listen to the interview: https://lnkd.in/gStF48fc #tRNA #RNA #tRNAmedicines #tRNAbiology #rarediseases #StopCodonDisease #geneticmedicines #programmablemedicines
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Do you want to use ClinVar to better understand genetic testing results? Check out GenomeConnect’s recent webinar “ClinVar - How to Search and How to Track a Variant” ⬇️ https://ow.ly/2XTW50U2BmK
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Access the newest article from Pharma insights! Learn how RGD peptide-based lipids are revolutionizing mRNA delivery, offering targeted precision and enhanced efficacy in treating genetic disorders. Click here: https://ow.ly/MSIs30sCfSz #CrodaPharma #EmpoweringBiologicsDelivery #PharmaInsights
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Join our webinar at 12:00 PM on May 2nd to how Allysta Pharmaceuticals is developing a completely new treatment for Duchenne Muscular Dystrophy, a genetic disease that affects men starting in childhood. https://hubs.la/Q02tLKSK0
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Access the newest article from Pharma insights! Learn how RGD peptide-based lipids are revolutionizing mRNA delivery, offering targeted precision and enhanced efficacy in treating genetic disorders. Click here: https://ow.ly/G93Q30sCgLi #CrodaPharma #EmpoweringBiologicsDelivery #PharmaInsights
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Join our webinar at 12:00 PM on May 2nd to how Allysta Pharmaceuticals is developing a completely new treatment for Duchenne Muscular Dystrophy, a genetic disease that affects men starting in childhood. https://hubs.la/Q02tLQ270
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Join our webinar at 12:00 PM on May 2nd to how Allysta Pharmaceuticals is developing a completely new treatment for Duchenne Muscular Dystrophy, a genetic disease that affects men starting in childhood. https://hubs.la/Q02tLQjX0
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