#crispr

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fromwww.nature.com
1 week ago

Rescuing dendritic cell interstitial motility sustains antitumour immunity

The study shows that conventional dendritic cells (DCs) are critical for T cell responses against tumors, underscoring the need for effective DC migration to lymph nodes.
Miscellaneous
fromSilicon Canals
2 weeks ago

Wageningen-based Scope Biosciences lands fresh capital to advance CRISPR-based molecular diagnostics platform - Silicon Canals

Scope Biosciences has secured €6 million to advance its CRISPR-based diagnostics platform, aiming for more effective detection technology for agriculture and healthcare.
European startups
#patent-law
fromPatently-O
3 weeks ago
Intellectual property law

Federal Circuit Clarifies Enablement Standards: Amgen Doesn't Apply to Anticipatory Prior Art

fromPatently-O
3 weeks ago
Intellectual property law

Federal Circuit Clarifies Enablement Standards: Amgen Doesn't Apply to Anticipatory Prior Art

more#patent-law
#genetic-disorders
OMG science
fromHarvard Gazette
1 month ago

Science that gives humans more say over their destinies - Harvard Gazette

David Liu's gene-editing technologies demonstrate significant potential, notably in treating a severe genetic condition using CRISPR for the first time.
Parenting
fromTODAY.com
1 month ago

EXCLUSIVE: Baby KJ, Saved by New Gene Editing Therapy, Goes Home After 300 Days in Hospital

KJ Muldoon is the first patient treated with customized CRISPR gene therapy, successfully overcoming a rare genetic disorder.
OMG science
fromHarvard Gazette
1 month ago

Science that gives humans more say over their destinies - Harvard Gazette

David Liu's gene-editing technologies demonstrate significant potential, notably in treating a severe genetic condition using CRISPR for the first time.
Parenting
fromTODAY.com
1 month ago

EXCLUSIVE: Baby KJ, Saved by New Gene Editing Therapy, Goes Home After 300 Days in Hospital

KJ Muldoon is the first patient treated with customized CRISPR gene therapy, successfully overcoming a rare genetic disorder.
more#genetic-disorders
#genetic-engineering
NYC startup
fromWIRED
4 months ago

Your Next Pet Could Be a Glowing Rabbit

The Los Angeles Project seeks to genetically engineer pets like glow-in-the-dark rabbits and hypoallergenic dogs, guided by biohacker Josie Zayner.
OMG science
fromenglish.elpais.com
2 months ago

The company that created woolly mice announces the de-extinction' of the dire wolf

Colossal Biosciences has reportedly de-extincted the dire wolf using genetic engineering techniques.
OMG science
fromFuturism
1 month ago

Scientists Gene-Hack Spider to Produce Bright-Red Silk

CRISPR-Cas9 can successfully modify spider silk, leading to new potential applications in materials science.
NYC startup
fromWIRED
4 months ago

Your Next Pet Could Be a Glowing Rabbit

The Los Angeles Project seeks to genetically engineer pets like glow-in-the-dark rabbits and hypoallergenic dogs, guided by biohacker Josie Zayner.
OMG science
fromenglish.elpais.com
2 months ago

The company that created woolly mice announces the de-extinction' of the dire wolf

Colossal Biosciences has reportedly de-extincted the dire wolf using genetic engineering techniques.
OMG science
fromFuturism
1 month ago

Scientists Gene-Hack Spider to Produce Bright-Red Silk

CRISPR-Cas9 can successfully modify spider silk, leading to new potential applications in materials science.
more#genetic-engineering
Alternative medicine
fromNatural Health News
1 month ago

Mutant Rice and Lab Rats: Bill Gates Sparks Outrage After Referring to India as 'Testing Ground' for Experiments

Bill Gates' comments on India prompted outrage, with many viewing the country as exploited for Western experimentation.
#medical-breakthrough
OMG science
fromNature
1 month ago

Daily briefing: The world's first human bladder transplant

A 41-year-old man received the first bladder transplant during an eight-hour surgery, marking a significant medical achievement.
fromNature
1 month ago
OMG science

Daily briefing: Meet the baby who received the world's first personalized CRISPR therapy

OMG science
fromNature
1 month ago

Daily briefing: The world's first human bladder transplant

A 41-year-old man received the first bladder transplant during an eight-hour surgery, marking a significant medical achievement.
OMG science
fromNature
1 month ago

Daily briefing: Meet the baby who received the world's first personalized CRISPR therapy

A baby boy is thriving after receiving a personalized CRISPR gene-editing therapy for a severe genetic disease.
more#medical-breakthrough
#gene-editing
OMG science
fromFuturism
3 months ago

Scientist Who Gene-Hacked Human Babies Says Ethics Are "Holding Back" Scientific Progress

He Jiankui argues that ethics restrains scientific innovation, claiming that his controversial actions in gene editing should not dissuade progress.
Venture
fromSFGATE
4 months ago

Bay Area biotech company that raised $66 million shuts down

Spotlight Therapeutics has closed down due to inadequate research outcomes and ongoing financial challenges.
OMG science
fromHarvard Gazette
2 months ago

Weighing cure for sick kids against troubling ethical questions - Harvard Gazette

CRISPR technology offers potential to cure diseases like sickle cell anemia but raises critical ethical questions about altering human genetics.
OMG science
fromThe Washington Post
1 month ago

How the race to invent a drug for one sick baby made medical history

KJ Muldoon was diagnosed with a severe genetic disorder, CPS 1 deficiency, leading to groundbreaking gene-editing treatment efforts.
OMG science
fromWIRED
6 months ago

The World's First Crispr Drug Gets a Slow Start

Casgevy is the first approved CRISPR gene-editing treatment available, but complexities hinder widespread patient access.
OMG science
fromFuturism
3 months ago

Scientist Who Gene-Hacked Human Babies Says Ethics Are "Holding Back" Scientific Progress

He Jiankui argues that ethics restrains scientific innovation, claiming that his controversial actions in gene editing should not dissuade progress.
Venture
fromSFGATE
4 months ago

Bay Area biotech company that raised $66 million shuts down

Spotlight Therapeutics has closed down due to inadequate research outcomes and ongoing financial challenges.
OMG science
fromHarvard Gazette
2 months ago

Weighing cure for sick kids against troubling ethical questions - Harvard Gazette

CRISPR technology offers potential to cure diseases like sickle cell anemia but raises critical ethical questions about altering human genetics.
OMG science
fromThe Washington Post
1 month ago

How the race to invent a drug for one sick baby made medical history

KJ Muldoon was diagnosed with a severe genetic disorder, CPS 1 deficiency, leading to groundbreaking gene-editing treatment efforts.
OMG science
fromWIRED
6 months ago

The World's First Crispr Drug Gets a Slow Start

Casgevy is the first approved CRISPR gene-editing treatment available, but complexities hinder widespread patient access.
more#gene-editing
#gene-therapy
Growth hacking
fromFuturism
1 month ago

In a World First, CRISPR Drug Tailored for One Baby Shows Life-Saving Promise

CRISPR technology successfully healed a newborn with a rare genetic disorder, indicating a breakthrough in personalized gene therapy for genetic diseases.
NYC parents
fromWIRED
1 month ago

A Baby Received a Custom Crispr Treatment in Record Time

CRISPR technology provides a personalized treatment option for patients with life-threatening genetic disorders.
Alternative medicine
fromtime.com
1 month ago

A Baby Receives the First Customized CRISPR Treatment

CRISPR technology shows potential in customized gene therapy for rare diseases, specifically in treating a patient with liver mutations.
OMG science
fromWIRED
5 months ago

Correcting Genetic Spelling Errors With Next-Generation Crispr

Sam Berns' life epitomizes the urgent need for advancements in genetic treatments, particularly for disorders like progeria that code for rapid aging.
Parenting
fromNature
1 month ago

World's first personalized CRISPR therapy given to baby with genetic disease

CRISPR therapy shows promise for treating ultra-rare genetic diseases, demonstrated by KJ Muldoon, the first recipient of tailored gene-editing treatment.
Growth hacking
fromFuturism
1 month ago

In a World First, CRISPR Drug Tailored for One Baby Shows Life-Saving Promise

CRISPR technology successfully healed a newborn with a rare genetic disorder, indicating a breakthrough in personalized gene therapy for genetic diseases.
NYC parents
fromWIRED
1 month ago

A Baby Received a Custom Crispr Treatment in Record Time

CRISPR technology provides a personalized treatment option for patients with life-threatening genetic disorders.
Alternative medicine
fromtime.com
1 month ago

A Baby Receives the First Customized CRISPR Treatment

CRISPR technology shows potential in customized gene therapy for rare diseases, specifically in treating a patient with liver mutations.
OMG science
fromWIRED
5 months ago

Correcting Genetic Spelling Errors With Next-Generation Crispr

Sam Berns' life epitomizes the urgent need for advancements in genetic treatments, particularly for disorders like progeria that code for rapid aging.
Parenting
fromNature
1 month ago

World's first personalized CRISPR therapy given to baby with genetic disease

CRISPR therapy shows promise for treating ultra-rare genetic diseases, demonstrated by KJ Muldoon, the first recipient of tailored gene-editing treatment.
more#gene-therapy
OMG science
fromNature
2 months ago

Powerful protein editors offer new ways of probing living cells

A novel protein editing technique using inteins enhances the study of protein function and localization in living cells.
OMG science
fromTechCrunch
4 months ago

On a quest to revive the woolly mammoth, Colossal Biosciences has created a woolly mouse | TechCrunch

Colossal Biosciences is progressing in its effort to resurrect the woolly mammoth by creating genetically engineered mice with mammoth-like fur.
OMG science
fromNews Center
4 months ago

Reprogramming Compromised Immune Cells to Fight Cancer - News Center

Researchers have found a way to reprogram immune cells to combat tumors by targeting specific signaling proteins.
Inhibiting proteins AhR and IRAK1 can help convert pro-tumor macrophages back into anti-tumor cells.
OMG science
fromInsideHook
9 months ago

Scientists Made a CRISPR Breakthrough for Autoimmune Diseases

Promising CRISPR treatments using donor cells may revolutionize the management of autoimmune conditions for millions of Americans.
fromBig Think
9 months ago

Leadership essentials: "Inspire, motivate, and cultivate"

The concept that the near future could look very different - and the far future could be near unimaginable - has always fascinated and challenged me to consistently seek out new ways I could imagine the universe unfolding.
UX design
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