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Articles published in Gene Ther

Retrieve available abstracts of 8 articles:
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Single Articles

    March 2023
  1. TOMINAGA S, Ojima T, Miyazawa M, Iwamoto H, et al
    Induced pluripotent stem cell-derived dendritic cell vaccine therapy genetically modified on the ubiquitin-proteasome system.
    Gene Ther. 2023 Mar 23. doi: 10.1038/s41434-023-00388.
    PubMed     Abstract available

    December 2022
  2. SULEMAN S, Payne A, Bowden J, Haque SA, et al
    HIV- 1 lentivirus tethering to the genome is associated with transcription factor binding sites found in genes that favour virus survival.
    Gene Ther. 2022;29:720-729.
    PubMed     Abstract available

  3. AIT BENICHOU S, Jauvin D, De Serres-Berard T, Pierre M, et al
    Antisense oligonucleotides as a potential treatment for brain deficits observed in myotonic dystrophy type 1.
    Gene Ther. 2022;29:698-709.
    PubMed     Abstract available

    October 2022
  4. COLLON K, Bell JA, Gallo MC, Chang SW, et al
    Influence of donor age and comorbidities on transduced human adipose-derived stem cell in vitro osteogenic potential.
    Gene Ther. 2022 Oct 11. pii: 10.1038/s41434-022-00367.
    PubMed     Abstract available

    July 2022
  5. SHIMADA Y, Ishii N, Higuchi T, Goto M, et al
    A novel preclinical model of mucopolysaccharidosis type II for developing human hematopoietic stem cell gene therapy.
    Gene Ther. 2022 Jul 14. pii: 10.1038/s41434-022-00357.
    PubMed     Abstract available

    February 2022
  6. LIANG G, Qin Z, Luo Y, Yin J, et al
    Exosomal microRNA-133b-3p from bone marrow mesenchymal stem cells inhibits angiogenesis and oxidative stress via FBN1 repression in diabetic retinopathy.
    Gene Ther. 2022 Feb 7. pii: 10.1038/s41434-021-00310.
    PubMed     Abstract available

    December 2021
  7. BOUGIOUKLI S, Chateau M, Morales H, Vakhshori V, et al
    Limited potential of AAV-mediated gene therapy in transducing human mesenchymal stem cells for bone repair applications.
    Gene Ther. 2021;28:729-739.
    PubMed     Abstract available

    June 2021
  8. SWEENEY CL, Pavel-Dinu M, Choi U, Brault J, et al
    Correction of X-CGD patient HSPCs by targeted CYBB cDNA insertion using CRISPR/Cas9 with 53BP1 inhibition for enhanced homology-directed repair.
    Gene Ther. 2021;28:373-390.
    PubMed     Abstract available

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