Crispr
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India's BioE3 Policy Is Advancing GeneEditing And Cell Therapy: Minister
The first-in-human Phase-I clinical trial for gene therapy of Hemophilia A has shown clinically significant outcomes.
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Top Scientific Discoveries Of 2025: A Year of Quantum Leaps And Cosmic Revelations
Here's a look at scientific discoveries and breakthroughs that made headlines in 2025, spanning space, biology, ecology, and fundamental physics.
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Indian Scientists Create Protein That Lights Up During Gene Editing, May Aid Cancer Treatment
Scientists from Kolkata-based Bose Institute have created GlowCas9--a CRISPR protein that lights up while performing gene editing -- to help boost treatment of genetic diseases and cancer, said the Ministry of Science and T
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CRISPR Explained: How Gene Editing Is Reshaping Medicine
CRISPR is revolutionizing medicine by enabling precise DNA edits, treating genetic diseases like sickle cell anemia and beta-thalassemia, and pioneering in vivo editing and personalized therapies.
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Scientists Revive Dire Wolves Using Ancient DNA and Modern Gene Editing
In a landmark scientific achievement, three dire wolf pups have been born using reconstructed DNA from fossils, marking the species’ return after being extinct for over 12,000 years. Dallas-based Colossal Biosciences led the project, using gene editing to implant dire wolf traits into grey wolf embryos, which were then carried by domestic dog sur...
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AI-Powered Evo-2 Model Generates DNA, Advances Genome Research
Evo-2, an AI model developed by the Arc Institute, Stanford University, and NVIDIA, has been trained on 128,000 genomes, enabling it to generate DNA sequences and predict mutations. It analyses both coding and non-coding DNA, helping researchers understand gene functions and diseases. The model has already demonstrated capabilities in designing CRI...
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How To Reproduce With Two Fathers - And No Biological Mother
At the International Summit on Human Genome Editing, held in March 2023 at the Francis Crick Institute in London, Japanese researcher Katsuhiko Hayashi stunned attendees when he explained how he had successfully reproduced mice from two male parents.
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Profluent Announces AI Gene Editor Generator OpenCRISPR to Enable Creating Bespoke Cures for Diseases
Profluent, a California-based artificial intelligence (AI)-first protein design company, announced its AI model that can generate CRISPR-like proteins that do not occur in nature on Tuesday. CRISPR or Clustered Regularly Interspaced Short Palindromic Repeats is a complex containing important proteins that scientists can use for precise gene editing...
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Scientists Edit HIV Out Of Cells, Paving The Way For A Potential Cure
The University of Amsterdam presents early HIV research at a medical conference, emphasising it's a "proof of concept," not a cure.
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New Study Might Lead to New Therapeutic Approach for Treating Alzheimer’s Disease
Researchers have used a new CRISPR technology that enables them to control these microglia cells. This, according to the team, can lead to a new approach to the treatment of Alzheimer's disease. The team geared up to detect the genes that were responsible for specific states of the microglial activity. With this, they could switch the genes on and ...
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India's BioE3 Policy Is Advancing GeneEditing And Cell Therapy: Minister
The first-in-human Phase-I clinical trial for gene therapy of Hemophilia A has shown clinically significant outcomes.
-
Top Scientific Discoveries Of 2025: A Year of Quantum Leaps And Cosmic Revelations
Here's a look at scientific discoveries and breakthroughs that made headlines in 2025, spanning space, biology, ecology, and fundamental physics.
-
Indian Scientists Create Protein That Lights Up During Gene Editing, May Aid Cancer Treatment
Scientists from Kolkata-based Bose Institute have created GlowCas9--a CRISPR protein that lights up while performing gene editing -- to help boost treatment of genetic diseases and cancer, said the Ministry of Science and T
-
CRISPR Explained: How Gene Editing Is Reshaping Medicine
CRISPR is revolutionizing medicine by enabling precise DNA edits, treating genetic diseases like sickle cell anemia and beta-thalassemia, and pioneering in vivo editing and personalized therapies.
-
Scientists Revive Dire Wolves Using Ancient DNA and Modern Gene Editing
In a landmark scientific achievement, three dire wolf pups have been born using reconstructed DNA from fossils, marking the species’ return after being extinct for over 12,000 years. Dallas-based Colossal Biosciences led the project, using gene editing to implant dire wolf traits into grey wolf embryos, which were then carried by domestic dog sur...
-
AI-Powered Evo-2 Model Generates DNA, Advances Genome Research
Evo-2, an AI model developed by the Arc Institute, Stanford University, and NVIDIA, has been trained on 128,000 genomes, enabling it to generate DNA sequences and predict mutations. It analyses both coding and non-coding DNA, helping researchers understand gene functions and diseases. The model has already demonstrated capabilities in designing CRI...
-
How To Reproduce With Two Fathers - And No Biological Mother
At the International Summit on Human Genome Editing, held in March 2023 at the Francis Crick Institute in London, Japanese researcher Katsuhiko Hayashi stunned attendees when he explained how he had successfully reproduced mice from two male parents.
-
Profluent Announces AI Gene Editor Generator OpenCRISPR to Enable Creating Bespoke Cures for Diseases
Profluent, a California-based artificial intelligence (AI)-first protein design company, announced its AI model that can generate CRISPR-like proteins that do not occur in nature on Tuesday. CRISPR or Clustered Regularly Interspaced Short Palindromic Repeats is a complex containing important proteins that scientists can use for precise gene editing...
-
Scientists Edit HIV Out Of Cells, Paving The Way For A Potential Cure
The University of Amsterdam presents early HIV research at a medical conference, emphasising it's a "proof of concept," not a cure.
-
New Study Might Lead to New Therapeutic Approach for Treating Alzheimer’s Disease
Researchers have used a new CRISPR technology that enables them to control these microglia cells. This, according to the team, can lead to a new approach to the treatment of Alzheimer's disease. The team geared up to detect the genes that were responsible for specific states of the microglial activity. With this, they could switch the genes on and ...
