These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

210 related articles for article (PubMed ID: 32637448)

  • 1. Cerebral Organoids: A Human Model for AAV Capsid Selection and Therapeutic Transgene Efficacy in the Brain.
    Depla JA; Sogorb-Gonzalez M; Mulder LA; Heine VM; Konstantinova P; van Deventer SJ; Wolthers KC; Pajkrt D; Sridhar A; Evers MM
    Mol Ther Methods Clin Dev; 2020 Sep; 18():167-175. PubMed ID: 32637448
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Optimized Adeno-Associated Virus Vectors for Efficient Transduction of Human Retinal Organoids.
    Völkner M; Pavlou M; Büning H; Michalakis S; Karl MO
    Hum Gene Ther; 2021 Jul; 32(13-14):694-706. PubMed ID: 33752467
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Generation of Human iPSC-Derived Retinal Organoids for Assessment of AAV-Mediated Gene Delivery.
    Tso A; da Costa BL; Fehnel A; Levi SR; Jenny LA; Ragi SD; Li Y; Quinn PMJ
    Methods Mol Biol; 2023; 2560():287-302. PubMed ID: 36481905
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Assessment of AAV Vector Tropisms for Mouse and Human Pluripotent Stem Cell-Derived RPE and Photoreceptor Cells.
    Gonzalez-Cordero A; Goh D; Kruczek K; Naeem A; Fernando M; Kleine Holthaus SM; Takaaki M; Blackford SJI; Kloc M; Agundez L; Sampson RD; Borooah S; Ovando-Roche P; Mehat MS; West EL; Smith AJ; Pearson RA; Ali RR
    Hum Gene Ther; 2018 Oct; 29(10):1124-1139. PubMed ID: 29580100
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Delivering Transgenic DNA Exceeding the Carrying Capacity of AAV Vectors.
    Hirsch ML; Wolf SJ; Samulski RJ
    Methods Mol Biol; 2016; 1382():21-39. PubMed ID: 26611576
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Human
    Latour YL; Yoon R; Thomas SE; Grant C; Li C; Sena-Esteves M; Allende ML; Proia RL; Tifft CJ
    Mol Genet Metab Rep; 2019 Dec; 21():100513. PubMed ID: 31534909
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Immunoadsorption enables successful rAAV5-mediated repeated hepatic gene delivery in nonhuman primates.
    Salas D; Kwikkers KL; Zabaleta N; Bazo A; Petry H; van Deventer SJ; Aseguinolaza GG; Ferreira V
    Blood Adv; 2019 Sep; 3(17):2632-2641. PubMed ID: 31501158
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Production of iPS-Derived Human Retinal Organoids for Use in Transgene Expression Assays.
    Quinn PM; Buck TM; Ohonin C; Mikkers HMM; Wijnholds J
    Methods Mol Biol; 2018; 1715():261-273. PubMed ID: 29188520
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Modeling Herpes Simplex Virus 1 Infections in Human Central Nervous System Neuronal Cells Using Two- and Three-Dimensional Cultures Derived from Induced Pluripotent Stem Cells.
    D'Aiuto L; Bloom DC; Naciri JN; Smith A; Edwards TG; McClain L; Callio JA; Jessup M; Wood J; Chowdari K; Demers M; Abrahamson EE; Ikonomovic MD; Viggiano L; De Zio R; Watkins S; Kinchington PR; Nimgaonkar VL
    J Virol; 2019 May; 93(9):. PubMed ID: 30787148
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Direct Head-to-Head Evaluation of Recombinant Adeno-associated Viral Vectors Manufactured in Human versus Insect Cells.
    Kondratov O; Marsic D; Crosson SM; Mendez-Gomez HR; Moskalenko O; Mietzsch M; Heilbronn R; Allison JR; Green KB; Agbandje-McKenna M; Zolotukhin S
    Mol Ther; 2017 Dec; 25(12):2661-2675. PubMed ID: 28890324
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Selection of an Efficient AAV Vector for Robust CNS Transgene Expression.
    Hanlon KS; Meltzer JC; Buzhdygan T; Cheng MJ; Sena-Esteves M; Bennett RE; Sullivan TP; Razmpour R; Gong Y; Ng C; Nammour J; Maiz D; Dujardin S; Ramirez SH; Hudry E; Maguire CA
    Mol Ther Methods Clin Dev; 2019 Dec; 15():320-332. PubMed ID: 31788496
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Capsid Engineering Overcomes Barriers Toward Adeno-Associated Virus Vector-Mediated Transduction of Endothelial Cells.
    Zhang L; Rossi A; Lange L; Meumann N; Koitzsch U; Christie K; Nesbit MA; Moore CBT; Hacker UT; Morgan M; Hoffmann D; Zengel J; Carette JE; Schambach A; Salvetti A; Odenthal M; Büning H
    Hum Gene Ther; 2019 Oct; 30(10):1284-1296. PubMed ID: 31407607
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Adeno-associated virus vectors serotyped with AAV8 capsid are more efficient than AAV-1 or -2 serotypes for widespread gene delivery to the neonatal mouse brain.
    Broekman ML; Comer LA; Hyman BT; Sena-Esteves M
    Neuroscience; 2006; 138(2):501-10. PubMed ID: 16414198
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Ubiquitination of both adeno-associated virus type 2 and 5 capsid proteins affects the transduction efficiency of recombinant vectors.
    Yan Z; Zak R; Luxton GW; Ritchie TC; Bantel-Schaal U; Engelhardt JF
    J Virol; 2002 Mar; 76(5):2043-53. PubMed ID: 11836382
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Cross-packaging of a single adeno-associated virus (AAV) type 2 vector genome into multiple AAV serotypes enables transduction with broad specificity.
    Rabinowitz JE; Rolling F; Li C; Conrath H; Xiao W; Xiao X; Samulski RJ
    J Virol; 2002 Jan; 76(2):791-801. PubMed ID: 11752169
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Circulating anti-wild-type adeno-associated virus type 2 (AAV2) antibodies inhibit recombinant AAV2 (rAAV2)-mediated, but not rAAV5-mediated, gene transfer in the brain.
    Peden CS; Burger C; Muzyczka N; Mandel RJ
    J Virol; 2004 Jun; 78(12):6344-59. PubMed ID: 15163728
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Comparative AAV-eGFP Transgene Expression Using Vector Serotypes 1-9, 7m8, and 8b in Human Pluripotent Stem Cells, RPEs, and Human and Rat Cortical Neurons.
    Duong TT; Lim J; Vasireddy V; Papp T; Nguyen H; Leo L; Pan J; Zhou S; Chen HI; Bennett J; Mills JA
    Stem Cells Int; 2019; 2019():7281912. PubMed ID: 30800164
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Enhanced gene transfer efficiency in the murine striatum and an orthotopic glioblastoma tumor model, using AAV-7- and AAV-8-pseudotyped vectors.
    Harding TC; Dickinson PJ; Roberts BN; Yendluri S; Gonzalez-Edick M; Lecouteur RA; Jooss KU
    Hum Gene Ther; 2006 Aug; 17(8):807-20. PubMed ID: 16942441
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Generating CNS organoids from human induced pluripotent stem cells for modeling neurological disorders.
    Brawner AT; Xu R; Liu D; Jiang P
    Int J Physiol Pathophysiol Pharmacol; 2017; 9(3):101-111. PubMed ID: 28694921
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Expressing Transgenes That Exceed the Packaging Capacity of Adeno-Associated Virus Capsids.
    Chamberlain K; Riyad JM; Weber T
    Hum Gene Ther Methods; 2016 Feb; 27(1):1-12. PubMed ID: 26757051
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.