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CRISPR News 🧬

@CRISPR_News

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The latest CRISPR breakthroughs @crispr-news.bsky.social

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Joined June 2015
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@CRISPR_News
CRISPR News 🧬
12 days
RT @CRISPR_News: CRISPR zeroes in on SDR42E1—a gene that supercharges vitamin D uptake and cripples colorectal cancer cells. 🔬☀️ #CRISPR #V….
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digitaljournal.com
Because gene SDR42E1 is involved in vitamin D metabolism, scientists could also target it in any of the many diseases.
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@CRISPR_News
CRISPR News 🧬
13 days
CRISPR zeroes in on SDR42E1—a gene that supercharges vitamin D uptake and cripples colorectal cancer cells. 🔬☀️ #CRISPR #VitaminD
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digitaljournal.com
Because gene SDR42E1 is involved in vitamin D metabolism, scientists could also target it in any of the many diseases.
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@CRISPR_News
CRISPR News 🧬
19 days
RT @CRISPR_News: Big news! The Chan Zuckerberg Initiative & Innovative Genomics Institute have launched the Center for Pediatric CRISPR Cur….
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chanzuckerberg.com
With the launch of the new center, we're one step closer to making personalized CRISPR cures a reality for children born with rare genetic diseases.
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@CRISPR_News
CRISPR News 🧬
22 days
Big news! The Chan Zuckerberg Initiative & Innovative Genomics Institute have launched the Center for Pediatric CRISPR Cures to develop personalized gene-editing treatments for kids with rare genetic diseases. 🌍🔬 More info:
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chanzuckerberg.com
With the launch of the new center, we're one step closer to making personalized CRISPR cures a reality for children born with rare genetic diseases.
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@CRISPR_News
CRISPR News 🧬
2 months
RT @CRISPR_News: Baby KJ, the world's first patient to receive personalized CRISPR gene editing therapy for a rare metabolic disease, is no….
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@CRISPR_News
CRISPR News 🧬
2 months
Baby KJ, the world's first patient to receive personalized CRISPR gene editing therapy for a rare metabolic disease, is now home and thriving! This groundbreaking treatment offers hope for other untreatable genetic conditions. #CRISPR #GeneEditing
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@CRISPR_News
CRISPR News 🧬
2 months
RT @CRISPR_News: Researchers at @Stanford have developed CRISPR-TO, a new tech acting like an "RNA mailman" to precisely target damaged neu….
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@CRISPR_News
CRISPR News 🧬
2 months
Researchers at @Stanford have developed CRISPR-TO, a new tech acting like an "RNA mailman" to precisely target damaged neurons. This could offer new hope for ALS & spinal injuries by promoting nerve cell repair. #CRISPR #Neuroscience
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@CRISPR_News
CRISPR News 🧬
3 months
RT @CRISPR_News: Researchers at the University of Bayreuth have used CRISPR-Cas9 to create spiders that produce red fluorescent silk. This….
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newatlas.com
For years, the CRISPR-Cas9 genome technology has been reshaping genetic engineering, a precision tool to transform everything from agriculture to medicine. With its incredible efficiency, this...
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@CRISPR_News
CRISPR News 🧬
3 months
Researchers at the University of Bayreuth have used CRISPR-Cas9 to create spiders that produce red fluorescent silk. This breakthrough could revolutionize materials science by enhancing silk's natural strength & elasticity. #Science #Biotech
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newatlas.com
For years, the CRISPR-Cas9 genome technology has been reshaping genetic engineering, a precision tool to transform everything from agriculture to medicine. With its incredible efficiency, this...
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@CRISPR_News
CRISPR News 🧬
3 months
RT @CRISPR_News: Amazing news! 🌟 Baby KJ received a custom CRISPR therapy for a life-threatening genetic disorder, developed in a record 6….
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wired.com
Scientists were able to create a bespoke treatment for KJ Muldoon’s rare genetic disorder within six months. It could be a blueprint for potentially life-saving, gene-editing Crispr therapies.
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@CRISPR_News
CRISPR News 🧬
3 months
Amazing news! 🌟 Baby KJ received a custom CRISPR therapy for a life-threatening genetic disorder, developed in a record 6 months! He's now thriving, and this breakthrough could revolutionize personalized medicine. A true game-changer! 🧬 #CRISPR .
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wired.com
Scientists were able to create a bespoke treatment for KJ Muldoon’s rare genetic disorder within six months. It could be a blueprint for potentially life-saving, gene-editing Crispr therapies.
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@CRISPR_News
CRISPR News 🧬
5 months
RT @CRISPR_News: CRISPR is revolutionizing cancer treatment! 💥 Researchers used CRISPR to eliminate 50% of head & neck tumors in mice by ta….
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insideprecisionmedicine.com
Researchers used CRISPR gene editing to target head and neck tumors, eliminating 50% of tumors in mice after three injections over 84 days.
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@CRISPR_News
CRISPR News 🧬
5 months
CRISPR is revolutionizing cancer treatment! 💥 Researchers used CRISPR to eliminate 50% of head & neck tumors in mice by targeting the SOX2 gene. Read more about this groundbreaking study: #CRISPR #CancerResearch #GeneEditing.
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insideprecisionmedicine.com
Researchers used CRISPR gene editing to target head and neck tumors, eliminating 50% of tumors in mice after three injections over 84 days.
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@CRISPR_News
CRISPR News 🧬
5 months
RT @CRISPR_News: Johns Hopkins & Cold Spring Harbor scientists use CGISPR to boost tomato & eggplant size, enhancing flavor and yields. htt….
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technologynetworks.com
Johns Hopkins and Cold Spring Harbor researchers discovered genes controlling fruit size in tomatoes and eggplants. Using CRISPR gene editing, they modified key genes to grow larger fruits.
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@CRISPR_News
CRISPR News 🧬
5 months
Johns Hopkins & Cold Spring Harbor scientists use CGISPR to boost tomato & eggplant size, enhancing flavor and yields.
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technologynetworks.com
Johns Hopkins and Cold Spring Harbor researchers discovered genes controlling fruit size in tomatoes and eggplants. Using CRISPR gene editing, they modified key genes to grow larger fruits.
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@CRISPR_News
CRISPR News 🧬
6 months
RT @CRISPR_News: Bahrain makes history as the first country outside the US to successfully treat sickle cell disease using #CRISPR-based ge….
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@CRISPR_News
CRISPR News 🧬
6 months
Bahrain makes history as the first country outside the US to successfully treat sickle cell disease using #CRISPR-based gene-editing therapy, Casgevy. @CRISPRTX
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@CRISPR_News
CRISPR News 🧬
6 months
England's NHS approves a groundbreaking gene therapy for sickle cell disease, offering new hope to thousands. Know as Exa-cel or Casgevy and developed by @CRISPRTX and @VertexPharma .#Healthcare #Innovation #SickleCellDisease #GeneTherapy 🧬.
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theguardian.com
Clinical trials find one-time gene therapy exa-cel offers ‘functional cure’ in 96.6% of patients
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@CRISPR_News
CRISPR News 🧬
6 months
RT @SickleCellUK: NEW TREATMENT APPROVED FOR SICKLE CELL! We are delighted that NICE has today approved the groundbreaking gene therapy, Ex….
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