BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

544 related articles for article (PubMed ID: 36899921)

  • 1. Various AAV Serotypes and Their Applications in Gene Therapy: An Overview.
    Issa SS; Shaimardanova AA; Solovyeva VV; Rizvanov AA
    Cells; 2023 Mar; 12(5):. PubMed ID: 36899921
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Infectivity of adeno-associated virus serotypes in mouse testis.
    Rajasekaran S; Thatte J; Periasamy J; Javali A; Jayaram M; Sen D; Krishnagopal A; Jayandharan GR; Sambasivan R
    BMC Biotechnol; 2018 Nov; 18(1):70. PubMed ID: 30384832
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Heparan Sulfate Binding Promotes Accumulation of Intravitreally Delivered Adeno-associated Viral Vectors at the Retina for Enhanced Transduction but Weakly Influences Tropism.
    Woodard KT; Liang KJ; Bennett WC; Samulski RJ
    J Virol; 2016 Nov; 90(21):9878-9888. PubMed ID: 27558418
    [TBL] [Abstract][Full Text] [Related]  

  • 4. New recombinant serotypes of AAV vectors.
    Gao G; Vandenberghe LH; Wilson JM
    Curr Gene Ther; 2005 Jun; 5(3):285-97. PubMed ID: 15975006
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Adeno-associated virus serotypes for gene therapeutics.
    Lisowski L; Tay SS; Alexander IE
    Curr Opin Pharmacol; 2015 Oct; 24():59-67. PubMed ID: 26291407
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [Adeno-associated viral vectors: methods for production and purification for gene therapy applications].
    Mena-Enriquez M; Flores-Contreras L; Armendáriz-Borunda J
    Rev Invest Clin; 2012; 64(5):487-94. PubMed ID: 23544311
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Cellular selectivity of AAV serotypes for gene delivery in neurons and astrocytes by neonatal intracerebroventricular injection.
    Hammond SL; Leek AN; Richman EH; Tjalkens RB
    PLoS One; 2017; 12(12):e0188830. PubMed ID: 29244806
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Comparative analysis of adeno-associated virus serotypes for gene transfer in organotypic heart slices.
    Liu Z; Klose K; Neuber S; Jiang M; Gossen M; Stamm C
    J Transl Med; 2020 Nov; 18(1):437. PubMed ID: 33208161
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Adeno-Associated Virus (AAV) Vectors in the CNS.
    McCown TJ
    Curr Gene Ther; 2011 Jun; 11(3):181-8. PubMed ID: 21453285
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Next Generation of Adeno-Associated Virus Vectors for Gene Therapy for Human Liver Diseases.
    Berns KI; Srivastava A
    Gastroenterol Clin North Am; 2019 Jun; 48(2):319-330. PubMed ID: 31046978
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Systemic gene transfer to skeletal muscle using reengineered AAV vectors.
    Phillips JL; Hegge J; Wolff JA; Samulski RJ; Asokan A
    Methods Mol Biol; 2011; 709():141-51. PubMed ID: 21194026
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Transduction Efficiency of Adeno-Associated Virus Serotypes After Local Injection in Mouse and Human Skeletal Muscle.
    Muraine L; Bensalah M; Dhiab J; Cordova G; Arandel L; Marhic A; Chapart M; Vasseur S; Benkhelifa-Ziyyat S; Bigot A; Butler-Browne G; Mouly V; Negroni E; Trollet C
    Hum Gene Ther; 2020 Feb; 31(3-4):233-240. PubMed ID: 31880951
    [TBL] [Abstract][Full Text] [Related]  

  • 13. AAV Serotypes and Their Suitability for Retinal Gene Therapy.
    Ebner LJA; Grimm C
    Adv Exp Med Biol; 2023; 1415():131-134. PubMed ID: 37440025
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Transduction of rat and human adipose-tissue derived mesenchymal stromal cells by adeno-associated viral vector serotype DJ.
    Zubkova ES; Beloglazova IB; Ratner EI; Dyikanov DT; Dergilev KV; Menshikov MY; Parfyonova YV
    Biol Open; 2021 Sep; 10(9):. PubMed ID: 34494647
    [TBL] [Abstract][Full Text] [Related]  

  • 15. The state of the art of adeno-associated virus-based vectors in gene therapy.
    Coura Rdos S; Nardi NB
    Virol J; 2007 Oct; 4():99. PubMed ID: 17939872
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Generation of Targeted Adeno-Associated Virus (AAV) Vectors for Human Gene Therapy.
    Liu Y; Siriwon N; Rohrs JA; Wang P
    Curr Pharm Des; 2015; 21(22):3248-56. PubMed ID: 26027561
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Gene therapy for the CNS using AAVs: The impact of systemic delivery by AAV9.
    Saraiva J; Nobre RJ; Pereira de Almeida L
    J Control Release; 2016 Nov; 241():94-109. PubMed ID: 27637390
    [TBL] [Abstract][Full Text] [Related]  

  • 18. The Influence of Murine Genetic Background in Adeno-Associated Virus Transduction of the Mouse Brain.
    He T; Itano MS; Earley LF; Hall NE; Riddick N; Samulski RJ; Li C
    Hum Gene Ther Clin Dev; 2019 Dec; 30(4):169-181. PubMed ID: 31749390
    [TBL] [Abstract][Full Text] [Related]  

  • 19. AAV vectors for hemophilia B gene therapy.
    Chao H; Walsh CE
    Mt Sinai J Med; 2004 Oct; 71(5):305-13. PubMed ID: 15543431
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Recombinant vectors based on porcine adeno-associated viral serotypes transduce the murine and pig retina.
    Puppo A; Bello A; Manfredi A; Cesi G; Marrocco E; Della Corte M; Rossi S; Giunti M; Bacci ML; Simonelli F; Surace EM; Kobinger GP; Auricchio A
    PLoS One; 2013; 8(3):e59025. PubMed ID: 23520549
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 28.