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MD Anderson, Artios Pharma and ShangPharma collaborate for ATR inhibitor program

MD Anderson, Artios Pharma and ShangPharma collaborate for ATR inhibitor program

CRISPR-Cas9 protein can help increase targeting accuracy in genome editing process

CRISPR-Cas9 protein can help increase targeting accuracy in genome editing process

New CRISPR-Cas9 variant has potential to increase precision during gene therapy

New CRISPR-Cas9 variant has potential to increase precision during gene therapy

Nanoparticles used to deliver CRISPR gene editing tools into the cell

Nanoparticles used to deliver CRISPR gene editing tools into the cell

Scientists use gold nanoparticles to edit genes tied to HIV, inherited blood disorders

Scientists use gold nanoparticles to edit genes tied to HIV, inherited blood disorders

Newly discovered molecules safely halt the gene editing process

Newly discovered molecules safely halt the gene editing process

New strategy for editing and repairing genetic mutation associated with microduplications

New strategy for editing and repairing genetic mutation associated with microduplications

High Throughput Nucleic Acid Purification Simplified

High Throughput Nucleic Acid Purification Simplified

Cellular protein could take on role of restriction factor for hepatitis B virus

Cellular protein could take on role of restriction factor for hepatitis B virus

IDT to demonstrate CRISPR expertise at European-focused events

IDT to demonstrate CRISPR expertise at European-focused events

Researchers deplete key protein for DNA replication using protein degradation system

Researchers deplete key protein for DNA replication using protein degradation system

Gene therapy approach could help treat mitochondrial diseases

Gene therapy approach could help treat mitochondrial diseases

Using CRISPR-Cas9 genome editing to correct mutation responsible for sickle cell disease

Using CRISPR-Cas9 genome editing to correct mutation responsible for sickle cell disease

New RNA deletion tool could help create drugs that correct genetic diseases

New RNA deletion tool could help create drugs that correct genetic diseases

LogicBio team to present data on preclinical effectiveness of GeneRide platform

LogicBio team to present data on preclinical effectiveness of GeneRide platform

Scientists uncover new answers to cell aging in children with rare, fatal disease

Scientists uncover new answers to cell aging in children with rare, fatal disease

Benson Hill Biosystems granted patent for novel genome editing system

Benson Hill Biosystems granted patent for novel genome editing system

Scientists develop ultrasound-propelled nanomotors for active delivery of Cas9-sgRNA complex

Scientists develop ultrasound-propelled nanomotors for active delivery of Cas9-sgRNA complex

Sangamo and Pfizer partner for development of new zinc finger protein gene therapy to treat ALS

Sangamo and Pfizer partner for development of new zinc finger protein gene therapy to treat ALS

Study focuses on improving pharmacokinetic properties of therapeutic aptamers

Study focuses on improving pharmacokinetic properties of therapeutic aptamers