Transfection is the process of deliberately introducing nucleic acids into cells. Cell transfection is crucial in the fields of T cell and stem cell therapy. However, the existing transfection technology still faces challenges ...
Cell & Microbiology
Jun 4, 2024
0
0
Researchers have developed a novel version of a key CRISPR gene-editing protein that shows efficient editing activity and is small enough to be packaged within a non-pathogenic virus that can deliver it to target cells. Hongjian ...
Biotechnology
May 30, 2024
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213
An interdisciplinary collaboration has designed a way to "cloak" proteins so that they can be captured by lipid nanoparticles, which are akin to tiny bubbles of fat. These bubbles are small enough to sneak their hidden cargo ...
Bio & Medicine
May 28, 2024
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40
A new study has shown an advance in the treatment of antibiotic-resistant infections in animals. The research, focusing on a 5-year-old Siamese cat Squeaks with a multidrug-resistant Pseudomonas aeruginosa infection post-arthrodesis ...
Veterinary medicine
May 27, 2024
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75
A new study, titled "Cow Cuddling: Cognitive Considerations in Bovine-Assisted Therapy" published in the Human-Animal Interactions journal, reveals that cows who are cuddled as therapy animals showed a strong preference for ...
Plants & Animals
May 22, 2024
6
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Disk-related back pain may one day meet its therapeutic match: Gene therapy delivered by naturally derived nanocarriers that, a new study shows, repairs damaged disks in the spine and lowers pain symptoms in mice.
Bio & Medicine
May 16, 2024
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23
Dr. Petr Cígler and his collaborators are working on refining molecular systems for transporting ribonucleic acid (RNA) molecules into cells. The question of how to effectively deliver RNA to a designated place in the body ...
Bio & Medicine
May 15, 2024
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20
Slow electrons are used in cancer therapy as well as in microelectronics. It is very hard to observe how they behave in solids. But scientists at TU Wien have made this possible.
Condensed Matter
May 13, 2024
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6
Drug delivery researchers at Oregon State University have developed a device with the potential to improve gene therapy for patients with inherited lung diseases such as cystic fibrosis.
Bio & Medicine
May 7, 2024
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67
A collaboration has led to the identification, in a bacterium of the intestine, of new CRISPR-Cas9 molecules that could have a clinical potential to treat genetic diseases such as retinitis pigmentosa, through sub-retinal ...
Cell & Microbiology
May 7, 2024
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