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News
Meet the world’s first CRISPR-edited hypoallergenic hounds
1+ hour, 12+ min ago (20+ words) Using CRISPR, researchers have created a pair of hypoallergenic dogs that don’t produce the main protein that triggers dog allergies....
Red Blood Cell-Inspired Carriers Show Promise for Gene Therapy Delivery
1+ hour, 13+ min ago (724+ words) Red blood cells serve as the foundation for nanocarriers that show promise in a new study as effective and efficient vehicles for gene therapy, tumor targeting and other medical treatments. Scientists at The Ohio State University showed that the engineered…...
A novel needleless delivery of Cas9 ribonucleoprotein complex in Bemisia tabaci embryos for gene editing
2+ hour, 56+ min ago (18+ words) Springer Nature Link...
Scientists explore electromagnetic gene switch for precise, reversible control of gene expression
12+ hour, 40+ min ago (371+ words) Researchers at Dongguk University in the Republic of Korea have developed a novel electromagnetic field (EMF)-responsive gene switch that enables non-invasive, reversible and precise control of gene expression in living organisms, potentially opening new avenues for gene therapy and…...
Cracking Code Of Gene Regulation
9+ hour, 46+ min ago (394+ words) EPFL researchers help complete the largest map yet of how human cells read DNA and reveal how chemical marks can change the meaning of the genetic instructions. Every cell in the body contains essentially the same DNA; and yet, a…...
Patient-Focused Science Targets Rare Genetic Disorders
11+ hour, 7+ min ago (600+ words) Shannon Knight attributes her interest in neuroscience to an experience she had in high school. She and her sister attended a medical day for students at the nearby University of Illinois Chicago. As they were on their way out of…...
Tackling rare genetic disorders with patient-focused science
11+ hour, 10+ min ago (600+ words) Shannon Knight attributes her interest in neuroscience to an experience she had in high school. She and her sister attended a medical day for students at the nearby University of Illinois Chicago. As they were on their way out of…...
Rewriting Disease: Oligonucleotides Take Aim at the Untreatable
17+ hour, 53+ min ago (345+ words) How synthetic DNA and RNA are becoming the discovery engines behind a new generation of precision therapies By Mike May, PhD Oligonucleotides are engineered sequences of nucleic acids, typically ranging from 10 to 50 nucleotides in length. Because they can be designed…...
The Immortal Cells of Henrietta Lacks: A Story of Science, Legacy, and Ethics
17+ hour, 31+ min ago (619+ words) Henrietta Lacks In 1951, Henrietta Lacks, a 31-year old African-American woman, seeks treatment for cervical cancer at …...
Virus-like particles enable targeted gene engineering, pooled CRISPR
21+ hour, 34+ min ago (775+ words) Primary human myeloid cells are emerging as important components of next-generation immunotherapies, but they have traditionally been difficult to engineer at the scale and precision needed for modern functional genomics....