#crispr

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Daily briefing: How synthetic 'mirror life' bacteria could infect the world

Elon Musk's influence on US science could lead to budget cuts that may hinder innovation.
New CRISPR treatment shows long-term potential but raises accessibility concerns.
The creation of synthetic organisms with reversed handedness poses ecological risks.
#gene-editing

CRISPR genome-editing grows up: advanced therapies head for the clinic

Gene-editing therapies like Casgevy show long-lasting benefits for blood disorders but face challenges in accessibility due to complexity and cost.

No CRISPR: oddball 'jumping gene' enzyme edits genomes without breaking DNA

A molecular oddity in bacteria could lead to precise genome redesign through jumping genes, surpassing CRISPR limitations.

Jennifer Doudna on the Brave New World Being Ushered In by Gene Editing

CRISPR technology offers transformative potential for medicine and agriculture but raises significant ethical and societal concerns.

Why Jennifer Doudna is one of Fast Company's 10 most innovative people of the last 10 years

CRISPR technology has revolutionized gene editing in medicine, impacting various diseases and treatment methodologies.

New technique opens the door to large-scale DNA editing to cure diseases

Gene editing corrects diseases like sickle cell anemia by replacing a defective gene with a working one using CRISPR technology.
New genetic editing mechanism uses jumping genes to introduce long DNA sequences with potential for higher precision in editing and genome alteration.

From cloning to CRISPR: The center that created Dolly designs epidemic-resistant animals

Roslin Institute has shifted focus from cloning to CRISPR gene editing to enhance animal disease resistance and improve livestock health.

CRISPR genome-editing grows up: advanced therapies head for the clinic

Gene-editing therapies like Casgevy show long-lasting benefits for blood disorders but face challenges in accessibility due to complexity and cost.

No CRISPR: oddball 'jumping gene' enzyme edits genomes without breaking DNA

A molecular oddity in bacteria could lead to precise genome redesign through jumping genes, surpassing CRISPR limitations.

Jennifer Doudna on the Brave New World Being Ushered In by Gene Editing

CRISPR technology offers transformative potential for medicine and agriculture but raises significant ethical and societal concerns.

Why Jennifer Doudna is one of Fast Company's 10 most innovative people of the last 10 years

CRISPR technology has revolutionized gene editing in medicine, impacting various diseases and treatment methodologies.

New technique opens the door to large-scale DNA editing to cure diseases

Gene editing corrects diseases like sickle cell anemia by replacing a defective gene with a working one using CRISPR technology.
New genetic editing mechanism uses jumping genes to introduce long DNA sequences with potential for higher precision in editing and genome alteration.

From cloning to CRISPR: The center that created Dolly designs epidemic-resistant animals

Roslin Institute has shifted focus from cloning to CRISPR gene editing to enhance animal disease resistance and improve livestock health.
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Combining AI and Crispr Will Be Transformational

AI and machine learning are set to enhance Crispr genome editing's impact across multiple fields by 2025.

Daily briefing: Big tomatoes get sweeter thanks to CRISPR editing

Genetic modifications can significantly enhance the sweetness of tomatoes without altering their size.
Mobile phone data can improve the mapping and understanding of the ionosphere and navigation systems.

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.

Other Barks & Bites for Friday, September 27: FTC Appeals Ruling on Noncompete Ban; the TTAB Cancels Four DC and Marvel SUPER HERO Trademarks; OpenAI Agrees to Share Training Data with Authors Suing for Copyright Infringement

The TTAB has canceled superhero trademarks from Marvel and DC after legal challenges, impacting their intellectual property ownership.
Nobel winners seek to preemptively cancel their CRISPR patent to avoid its invalidation.

A Rose Without Thorns? How Gene Editing Is Giving Plants A Glow-Up

The discovery of a gene controlling prickliness can lead to the development of smooth, prickle-free plants without compromising fruit and flower quality.

Crispr-Enhanced Viruses Are Being Deployed Against UTIs

Locus's phage therapy effectively targets and degrades E. coli bacteria, showing promising results in treating urinary tract infections (UTIs).

Leadership essentials: "Inspire, motivate, and cultivate"

Scribe Therapeutics, led by CEO Benjamin Oakes, aims to revolutionize genetic medicine through innovative genome editing technology.

CRISPR therapy restores some vision to people with blindness

CRISPR-based gene therapy improved vision in individuals with inherited blindness.

Rat Neurons Repair Mouse Brains That Lack a Sense of Smell

Chimeras in the form of mice with rat neurons exhibit brain adaptability for potential disease study and tissue transplantation.

Generative A.I. Arrives in the Gene Editing World of CRISPR

Generative A.I. technology can create blueprints for microscopic biological mechanisms to edit DNA for battling illnesses with precision and speed.

Here Are the New Drugs and Treatments We Could See in 2024

2023 was a strong year for innovative new drugs, but 2024 is also shaping up to be a milestone year for some exciting therapies.
Eli Lilly could debut a new treatment for Alzheimer's disease that targets amyloid, the protein that builds up in the brains of patients.

Revolutionary gene therapy may offer new life for patients battling chronic sickle cell disease

Gene therapy using CRISPR/Cas9 has been approved by federal regulators as a potential treatment for sickle cell disease.
The University of Chicago Medicine and the University of Illinois at Chicago are among the first medical centers to offer this groundbreaking therapy.

People with Sickle Cell Deserve More Respect from Health Care Providers

The recent approval of gene-editing treatments for sickle cell disease provides hope for relief from pain and reduced lifespan.
Access to these high-tech treatments remains uncertain and marginalized communities must continue to be supported in their healthcare.

'It's Transformed My Life': FDA Approves First Gene-Editing Treatment for Illness | KQED

The CRISPR treatment for sickle cell disease involves editing a gene with CRISPR and infusing the modified cells back into patients.
The therapy, Casgevy, is designed to be a one-time treatment that alleviates symptoms for a lifetime.

FDA Approves First CRISPR Treatment in U.S.

The U.S. FDA has approved the first gene therapy treatment based on CRISPR technology.
The treatment, called exa-cel, is approved for sickle cell disease and may also be approved for beta thalassemia.

FDA approves first CRISPR gene editing treatment that may cure sickle cell disease

Regulators have approved two new gene therapies for sickle cell disease that could potentially cure the inherited blood disorder.
The treatments are the first to be approved based on CRISPR, the gene editing tool that won its inventors the Nobel Prize in 2020.

Breakthrough Gene Treatments For Sickle Cell Disease Approved

Regulators have approved two new gene therapies for sickle cell disease, offering hope for a cure for the painful blood disorder
The treatments are designed for patients 12 and older with severe forms of the disease, and one of them is the first therapy based on CRISPR gene editing

The CRISPR Era Is Here

Gene-editing technology CRISPR has successfully treated a patient with sickle-cell disease, providing hope for future treatments.
The treatment resulted in the patient living virtually symptom-free, with 29 out of 30 eligible patients experiencing zero pain crises after treatment.
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