O. ter Brake

发表

Towards a durable RNAi gene therapy for HIV-AIDS.

B. Berkhout, O. ter Brake, 2009, Expert opinion on biological therapy.

Optimization of shRNA inhibitors by variation of the terminal loop sequence.

B. Berkhout, Y. Liu, P. Konstantinova, 2010, Antiviral research.

Purification of recombinant adeno-associated virus by iodixanol gradient ultracentrifugation allows rapid and reproducible preparation of vector stocks for gene transfer in the nervous system.

P. Dijkhuizen, D. Grimm, J. Kleinschmidt, 1999, Human gene therapy.

Histatin 5-Derived Peptide with Improved Fungicidal Properties Enhances Human Immunodeficiency Virus Type 1 Replication by Promoting Viral Entry

B. Berkhout, R. Sanders, E. Veerman, 2006, Journal of Virology.

Inhibition of HIV-1 by multiple siRNAs expressed from a single microRNA polycistron

B. Berkhout, J. Haasnoot, Y. Liu, 2008, Nucleic acids research.

RNAi-inducing lentiviral vectors for anti-HIV-1 gene therapy.

B. Berkhout, Y. Liu, O. ter Brake, 2011, Methods in molecular biology.

Inhibition of human immunodeficiency virus type 1 by RNA interference using long-hairpin RNA

B. Berkhout, J. Haasnoot, P. D. Haan, 2006, Gene Therapy.

ESF-EMBO Symposium: Antiviral Applications of RNA Interference

B. Berkhout, J. Haasnoot, J. Kurreck, 2008, Retrovirology.

Silencing of HIV-1 with RNA interference: a multiple shRNA approach.

Ben Berkhout, Pavlina Konstantinova, Mustafa Ceylan, 2006, Molecular therapy : the journal of the American Society of Gene Therapy.

The virion-associated incoming HIV-1 RNA genome is not targeted by RNA interference

B. Berkhout, O. ter Brake, E. M. Westerhout, 2006, Retrovirology.

Titers of lentiviral vectors encoding shRNAs and miRNAs are reduced by different mechanisms that require distinct repair strategies.

B. Berkhout, Y. Liu, P. Konstantinova, 2010, RNA.

Anticipating and blocking HIV-1 escape by second generation antiviral shRNAs

B. Berkhout, N. Schopman, O. ter Brake, 2010, Retrovirology.

A novel approach for inhibition of HIV-1 by RNA interference: counteracting viral escape with a second generation of siRNAs

B. Berkhout, O. ter Brake, 2005, Journal of RNAi and gene silencing : an international journal of RNA and gene targeting research.

Lentiviral vector engineering for anti-HIV RNAi gene therapy.

B. Berkhout, O. ter Brake, Jan-Tinus Westerink, 2010, Methods in molecular biology.

Lentiviral vectors that carry anti‐HIV shRNAs: problems and solutions

B. Berkhout, O. ter Brake, 2007, The journal of gene medicine.

Towards a durable RNAi gene therapy for HIV-AIDS

B. Berkhout, O. ter Brake, 2009, Expert opinion on biological therapy.

SHAPE-directed discovery of potent shRNA inhibitors of HIV-1.

K. Weeks, B. Berkhout, Joseph M. Watts, 2012, Molecular therapy : the journal of the American Society of Gene Therapy.

Stringent testing identifies highly potent and escape‐proof anti‐HIV short hairpin RNAs

B. Berkhout, O. ter Brake, K. V. von Eije, 2009, The journal of gene medicine.

Probing the sequence space available for HIV-1 evolution

B. Berkhout, O. ter Brake, K. V. von Eije, 2008, AIDS.

Trans-inhibition of HIV-1 by a long hairpin RNA expressed within the viral genome

B. Berkhout, J. Haasnoot, P. Konstantinova, 2006, Retrovirology.

Optimization of shRNA inhibitors by variation of the terminal loop sequence.

B. Berkhout, P. Konstantinova, N. Schopman, 2010, Antiviral research.

Titers of lentiviral vectors encoding shRNAs and miRNAs are reduced by different mechanisms that require distinct repair strategies.

B. Berkhout, P. Konstantinova, O. ter Brake, 2010, RNA.

RNAi-inducing lentiviral vectors for anti-HIV-1 gene therapy.

B. Berkhout, O. ter Brake, Jan-Tinus Westerink, 2011, Methods in molecular biology.

Probing the sequence space available for HIV-1 evolution

B. Berkhout, O. ter Brake, K. V. von Eije, 2008, AIDS (London).

Life after death?

R. Verwer, J. Verhaagen, W. Hermens, 2002, Neurology.