Citations

Citation Database:
Scientific Publications with Lonza's Nucleofector™ Technology, Clonetics™ or Poietics™ Cells, Media, or Molecular Biology Products

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4493 Publications available.

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  1. Going non-viral: the Sleeping Beauty transposon system breaks on through to the clinical side.

    Authors: Hudecek M1, Izsvák Z2, Johnen S3, Renner M4, Thumann G5, Ivics Z4.

    In:  (2017) 52(4): 355(80)

    Details

  2. CRISPR-Mediated Integration of Large Gene Cassettes Using AAV Donor Vectors.

    Authors: Bak RO, Porteus MH.

    In:  (2017) 20(3): 750-756

    Details

  3. Viability of primary cultured podocytes is associated with extracellular high glucose-dependent autophagy downregulation

    Authors: Audzeyenka I, Rogacka D, Piwkowska A, Angielski S, Jankowski M.

    In:  (2017) 430(1-2): 11-19

    Details

  4. Simulation of human plasma concentration-time profiles of the partial glucokinase activator PF-04937319 and its disproportionate N-demethylated metabolite using humanized chimeric mice and semi-physiological pharmacokinetic modeling

    Authors: Kamimura H1,2, Ito S1, Chijiwa H3, Okuzono T3, Ishiguro T3, Yamamoto Y3, Nishinoaki S3, Ninomiya SI1, Mitsui M4, Kalgutkar AS5, Yamazaki H4, Suemizu H2

    In:  (2017) 47(5): 382-393

    Details

  5. Real architecture For 3D Tissue (RAFT™) culture system improves viability and maintains insulin and glucagon production of mouse pancreatic islet cells.

    Authors: Szebeni GJ, Tancos Z, Feher LZ, Alfoldi R, Kobolak J, Dinnyes A, Puskas LG

    In:  (2017) 69(2): 359-369

    Details

  6. CRISPR/Cas9-mediated PD-1 disruption enhances anti-tumor efficacy of human chimeric antigen receptor T cells.

    Authors: Rupp LJ1, Schumann K, Roybal KT, Gate RE, Ye CJ, Lim WA, Marson A.

    In:  (2017) 7 (1): 737

    Details

  7. CRISPR-Cpf1 correction of muscular dystrophy mutations in human cardiomyocytes and mice.

    Authors: Zhang Y, Long C, Li H, McAnally JR, Baskin KK1,2,3, Shelton JM4, Bassel-Duby R, Olson EN,

    In:  (2017) 12, 3(4): 1-11

    Details

  8. Targeted gene knock-in by homology-directed genome editing using Cas9 ribonucleoprotein and AAV donor delivery.

    Authors: Gaj T, Staahl BT, Rodrigues GM, Limsirichai P, Ekman FK, Doudna JA, Schaffer DV.

    In:  (2017) 45(11): 1-11

    Details

  9. A genome-wide CRISPR screen identifies a restricted set of HIV host dependency factors.

    Authors: Park RJ, Wang T, Koundakjian D, Hultquist JF, Lamothe-Molina P, Monel B, Schumann K, Yu H, Krupzcak KM, Garcia-Beltran W, Piechocka-Trocha , Krogan NJ, Marson A, Sabatini DM, Lander ES, Hacohen N, Walker BD.

    In:  (2017) 49(2): 193-203

    Details

  10. Efficient CRISPR/Cas9-assisted gene targeting enables rapid and precise genetic manipulation of mammalian neural stem cells.

    Authors: Bressan RB, Dewari PS, Kalantzaki M, Gangoso E, Matjusaitis M, Garcia-Diaz C, Blin C, Grant V, Bulstrode H, Gogolok S, Skarnes WC, Pollard SM.

    In:  (2017) 144(4): 635-648

    Details

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