🔬 Scientist & Co-founder of Re:Pair Genomics in Toronto. Develop gene therapy products for 8 years. Raised 20k. Bring hope and change the world🌍 Toronto, ON, CanadaJoined March 2024
🚀 Oligodendrocytes, the speed boosters of our brain! These cells create a fatty substance called myelin that provides insulation to the axons of neurons, helping them to transmit electrical signals more efficiently. Talk about a brain power-up! #PromoterDesign#RePairGenomics
🛡️ Microglia, the brain’s immune warriors! These cells are involved in the immune response in the brain, helping to clear away dead cells and other debris. They’re the guardians of our brain health! #Microglia#PromoterDesign#RePairGenomics
✨ Astrocytes: Star-shaped cells that have many functions, including providing nutrients to neurons and regulating the concentrations of ions in the area surrounding neurons. They’re the caretakers of our neurons! #PromotorDesign#Astrocytes#RePairGenomics
🌟 Did you know? Glial cells are non-neuronal cells that provide support and nutrition, maintain homeostasis, form myelin, and participate in signal transmission in the nervous system. They’re the unsung heroes of our nervous system! #PromotorDesign#RePairGenomics#Neuroscience
🧠 Diving into the world of neuroscience! Neurons, the primary functional units of the brain, are responsible for receiving sensory input from the external world, sending motor commands to our muscles, and relaying the electrical signals at every step in between. #PromotorDesign
💌 Compose with Us: Dive into the DMs, where time bends to our will. Let’s orchestrate a healthier future together, one cell at a time. 🌟🎵#RePairGenomics#HealthTech#GeneTherapy
🌟 Precision Accelerates Progress: Forget slow and steady. Our rapid promoter design pipeline churns out candidates daily. Imagine a world where gene therapy hits the right notes every time. 🎶 #GeneTherapy#RePairGenomics#PromoterDesign#CellSpecificity
🧬 Unlocking Precision: Gene therapy faces a nemesis—the off-target effect. Our tailored cell-type-specific promoters at #RePairGenomics silence rogue genes, paving the way for safer treatments. Follow us for a symphony of breakthroughs! 🚀#GeneTherapy#PrecisionMedicine
#GeneTherapy, empowered by cell type-specific promoter design, is a beacon of hope for those with #RareDiseases. Ready to explore the potential of gene therapy for your condition? Reach out to me #RePairGenomics. Let’s conquer rare diseases together! #PromoterDesign
Cell type-specific promoter design is not an option, it’s a necessity for successful gene therapy. Imagine a world where no disease is deemed incurable. That’s the world gene therapy promises. #PromoterDesign#GeneTherapy#RePairGenomics
#GeneTherapy is not just about inserting a ‘healthy’ gene. The magic lies in the design of cell type-specific promoters. A well-designed promoter ensures the gene is expressed in the right cells, just like a well-written address ensures the mail reaches the right house.
Fast forward to the present, she’s a triumphant survivor, leading a full, healthy life. From running marathons to globetrotting, she’s doing it all. Free from the disease that once overshadowed her existence, she’s a living testament to the transformative power of #GeneTherapy.
Imagine Sarah, a dynamic young woman who was once shackled by a life-threatening #RareDisease. Her life was never-ending hospital visits and treatments that barely made a difference. But then, #GeneTherapy entered the picture. A single, personalized treatment changes everything.
Without a cure, #RareDiseases like #Huntington’s threaten lives, causing physical and cognitive decline. Imagine a future where every step becomes a challenge, every thought a struggle. Enter #GeneTherapy! A revolutionary approach that uses genes to treat or prevent diseases.
🎯 Re:Pair Genomics, an award-winning innovator of promoter design, is exploring FXS specific promoters to target and treat FXS. This could lead to more effective and specific treatments. Interested in? Send DM! #RePairGenomics#FragileXSyndrome#ScienceIsCool#HopeForFXS
💉 Gene therapy shows promise for treating FXS. It works by delivering a functional FMR1 gene to cells, which can help produce the necessary protein that’s missing in FXS. This could be a game-changer! #GeneTherapy#MedicalBreakthrough#FragileXSyndrome
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44K Followers 3K Following29 February 2024 is Rare Disease Day. Raising awareness for patients, families and carers around the world that are affected by rare diseases. #RareDiseaseDay
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