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Stem Cell Research

Free Subscription Articles published in Gene Ther Retrieve available abstracts of 8 articles: HTML format

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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