What are genes? | Animation | Minute to Understanding | The Jackson Laboratory
1:56
YouTubeThe Jackson Laboratory
What are genes? | Animation | Minute to Understanding | The Jackson Laboratory
Learn what genes are and how they shape each and every one of us. 🏆 Viddy Awards 2022 Gold Winner: https://enter.viddyawards.com/entry/what-are-genes-2/
143.1K viewsAug 26, 2020
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DNA, genes and genomes
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Garvan Institute of Medical
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Genome editing Gene Therapy
We’ve mapped the genome. Now we’re rewriting it. The fusion of gene editing, tissue engineering, and cell therapy is creating a post-genomics era where we can program biology to heal, regenerate, and reverse aging. PMID: 40763736 PMID: 39905264 #GeneEditing #CellTherapy #TissueEngineering #PostGenomics #RegenerativeMedicine #LongevityScience #ReverseAging #FutureOfMedicine #BiotechInnovation #Healthspan #PersonalizedMedicine #Genomics #MedicalBreakthroughs #EternaHealth #reels | Adeel Khan, MD
We’ve mapped the genome. Now we’re rewriting it. The fusion of gene editing, tissue engineering, and cell therapy is creating a post-genomics era where we can program biology to heal, regenerate, and reverse aging. PMID: 40763736 PMID: 39905264 #GeneEditing #CellTherapy #TissueEngineering #PostGenomics #RegenerativeMedicine #LongevityScience #ReverseAging #FutureOfMedicine #BiotechInnovation #Healthspan #PersonalizedMedicine #Genomics #MedicalBreakthroughs #EternaHealth #reels | Adeel Khan, MD
FacebookAdeel Khan, MD
376 views1 week ago
Gene Editing Mechanism of CRISPR-Cas9
2:09
Gene Editing Mechanism of CRISPR-Cas9
harvard.edu
Nov 24, 2014
Scientists have achieved a monumental milestone in medicine: using CRISPR gene-editing technology to remove HIV DNA from infected human cells permanently. Unlike traditional treatments that suppress the virus, this therapy targets and excises the viral genome, preventing HIV from returning. The breakthrough, demonstrated in laboratory settings, could revolutionize the fight against AIDS, potentially providing a functional cure. CRISPR’s precision allows it to selectively remove harmful sequences
Scientists have achieved a monumental milestone in medicine: using CRISPR gene-editing technology to remove HIV DNA from infected human cells permanently. Unlike traditional treatments that suppress the virus, this therapy targets and excises the viral genome, preventing HIV from returning. The breakthrough, demonstrated in laboratory settings, could revolutionize the fight against AIDS, potentially providing a functional cure. CRISPR’s precision allows it to selectively remove harmful sequences
FacebookFloyd Buñag
93 views1 week ago
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