CRISPR used to destroy the regulatory genes of HIV
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...
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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 identified a key in the road for the way the liver deals with carbohydrates, fats and protein...
Researchers have discovered that a signalling protein elevated in patients with AML plays a much wider role in the disease than previously thought...
The NIH is supporting efforts to broaden biomedical scientists’ access to cryo-electron microscopy the imaging method that is revolutionising structural biology...
Epigenomic analyses may lead to other unexpected findings and novel therapeutic drug targets for many diseases
Researchers have developed a new technique to restore retinal function in mice afflicted by a degenerative retinal disease, retinitis pigmentosa...
Researchers have carried out the largest genomic analysis of patients with SMM to explain the biology of the disease and how it unfolds through time...
Researchers create eye neuron network model to study retinal diseases, possible treatment options...
Scientists have discovered the first leukaemia protective gene that is specific to the male-only Y chromosome...
Research could help lead to the design of drugs that slow neurodegeneration...
A CAR-T-based immunotherapy successfully kills tumours and prevents metastatic growth, in final preclinical tests before human trials...
The FoxM1 gene will drive the development of new drugs to reverse a process called vascular remodelling - a key feature in pulmonary hypertension...
Scientists have identified a therapeutic RNA molecule that corrects the error in genetic processing that leads to familial dysautonomia...
Researchers have identified a protein critical for the aggressiveness of T-cell leukaemia...
Scientists have created individual cell lines in which specific blood group genes were altered to prevent the expression of blood group proteins...