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The Nobel Prize-winning observations and discoveries of John B. Gurdon and Shinya Yamanaka have ignited an explosion of excitement around the potential use of stem cells in research and treatment of human disease.
A study reveals why people with the APOE4 gene have a higher risk of the disease...
New study uses CRISPR/Cas9 to make CD33 CAR T cells cancer-specific...
By destroying the regulatory genes of the AIDS virus HIV-1 using the genome editing system CRISPR/Cas9, researchers have succeeded in blocking the production of HIV-1 by infected cells...
Researchers have developed a new technique to restore retinal function in mice afflicted by a degenerative retinal disease, retinitis pigmentosa...
This whitepaper outlines how advances in real-time live-cell monitoring and analysis methods are addressing these changing needs.
Scientists have created individual cell lines in which specific blood group genes were altered to prevent the expression of blood group proteins...
26 April 2018 | By Charles River Laboratories
This webinar highlights cell based assays for Parkinson’s disease that include endpoints such as a-synuclein aggregation and mitophagy readouts.
Scientists have developed a breakthrough CRISPR gene-editing tool, that could allow researchers to quickly and precisely engineer multiple changes to the genetic code...
In this application note, BMG Labtech discuss how the Bioluminescence resonance energy transfer (BRET) is a versatile tool to study interactions and trafficking in proteins.
Using genetic engineering technology, a team of scientists have established an animal model of Huntington's disease...
Predictiveness is one of the key factors for success in the drug discovery workflow. Many compounds fail at late stages due to lack of predictive data or the discovery of unwanted side effects.
Study provides a roadmap for using CRISPR to investigate neurological disorders...
Genome editing could enable new strategies to prevent malaria transmission to humans...
Improvements to gene-editing techniques hold promise for inactivating the defective gene responsible for this as-yet incurable disease...
