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B cells secreting antibodies that target virus particles.
Stem Cell Editing Repairs Severe Immunodeficiency
Scientists hoping to treat immunodeficiencies using gene therapy have found a way to edit stem cells in mice without disrupting gene regulation.
Stem Cell Editing Repairs Severe Immunodeficiency
Stem Cell Editing Repairs Severe Immunodeficiency

Scientists hoping to treat immunodeficiencies using gene therapy have found a way to edit stem cells in mice without disrupting gene regulation.

Scientists hoping to treat immunodeficiencies using gene therapy have found a way to edit stem cells in mice without disrupting gene regulation.

homology directed repair

Base Editing Now Able to Convert Adenine-Thymine to Guanine-Cytosine
Catherine Offord | Oct 25, 2017 | 8 min read
With the arrival of a new class of single-nucleotide editors, researchers can target the most common type of pathogenic SNP in humans.
Nonviral CRISPR Delivery a Success
Abby Olena, PhD | Oct 2, 2017 | 3 min read
Researchers use gold nanoparticles to deliver CRISPR-Cas9 and correct a point mutation in a mouse model of Duchenne muscular dystrophy. 
Scientists Doubt Results of CRISPR’d Embryos
Aggie Mika | Aug 31, 2017 | 2 min read
Six scientists question the authors’ conclusions about the DNA repair process that led to the human embryos’ correction of a defective gene.
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