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  2. CRISPR gene editing - Wikipedia

    en.wikipedia.org/wiki/CRISPR_gene_editing

    CRISPR gene editing (CRISPR, pronounced / ˈ k r ɪ s p ə r / (crisper), refers to a clustered regularly interspaced short palindromic repeats") is a genetic engineering technique in molecular biology by which the genomes of living organisms may be modified.

  3. CRISPR - Wikipedia

    en.wikipedia.org/wiki/CRISPR

    CRISPR gene editing is a revolutionary technology that allows for precise, targeted modifications to the DNA of living organisms. Developed from a natural defense mechanism found in bacteria, CRISPR-Cas9 is the most commonly used system, that allows "cutting" of DNA at specific locations and either delete, modify, or insert genetic material.

  4. Human germline engineering - Wikipedia

    en.wikipedia.org/wiki/Human_germline_engineering

    The impact of human gene editing on resistance to HIV infection and other body functions in experimental infants remains controversial. The World Health Organization has issued three reports on the guidelines of human genome editing since 2019, [41] and the Chinese government has prepared regulations since May 2019. [42]

  5. FDA moves closer to sickle cell cure that uses gene editing - AOL

    www.aol.com/news/fda-moves-closer-sickle-cell...

    The gene-editing drug, from Vertex along with CRISPR Therapeutics, would eliminate the need for a donor. Instead, it works by changing the DNA in the patient’s blood cells.

  6. Gene therapy - Wikipedia

    en.wikipedia.org/wiki/Gene_therapy

    This is one of the first studies of a CRISPR-based in vivo human gene editing therapy, where the editing takes place inside the human body. [266] The first injection of the CRISPR-Cas System was confirmed in March 2020. [267] Exagamglogene autotemcel, a CRISPR-based human gene editing therapy, was used for sickle cell and thalassemia in ...

  7. CRISPR Gene Editing Is Being Tested in Human Patients, and ...

    www.aol.com/news/crispr-gene-editing-being...

    Editing genes in patients could lead to cures for a number of devastating genetic diseases, including vision disorders and sickle cell anemia

  8. Victoria Gray - Wikipedia

    en.wikipedia.org/wiki/Victoria_Gray

    Victoria Gray was the first patient ever to be treated with the gene-editing tool CRISPR for sickle-cell disease. [1]This marked the initial indication that a cure is attainable for individuals born with sickle-cell disease and another severe blood disorder, beta-thalassemia.

  9. FDA considers first CRISPR gene editing treatment that may ...

    www.aol.com/fda-considers-first-crispr-gene...

    CRISPR, or clustered regularly interspaced short palindromic repeats, is a technology researchers use to selectively modify DNA, the carrier of genetic information that the body uses to function ...