Galina V Mikheeva

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An Adenovirus Vector with Genetically Modified Fibers Demonstrates Expanded Tropism via Utilization of a Coxsackievirus and Adenovirus Receptor-Independent Cell Entry Mechanism

C. Miller, D. Curiel, Minghui Wang, 1998, Journal of Virology.

Genetic modification of liver grafts with an adenoviral vector encoding the Bcl-2 gene improves organ preservation.

J. Contreras, D. Curiel, J. Thomas, 1999, Transplantation.

Treatment of ovarian cancer with a tropism modified oncolytic adenovirus.

D. Nettelbeck, R. Alemany, D. Curiel, 2002, Cancer research.

Characterization of an Adenovirus Vector Containing a Heterologous Peptide Epitope in the HI Loop of the Fiber Knob

C. Miller, D. Curiel, I. Dmitriev, 1998, Journal of Virology.

A system for the propagation of adenoviral vectors with genetically modified receptor specificities

C. Miller, D. Curiel, I. Dmitriev, 1999, Nature Biotechnology.

Adenovirus-Mediated Gene Expression In Vivo Is Enhanced by the Antiapoptotic Bcl-2 Gene

J. Contreras, D. Curiel, G. Bilbao, 1999, Journal of Virology.

Targeting ofAdenovirus via Genetic Modification of the Viral Capsid Combined with aProteinBridge

D. Curiel, V. Krasnykh, G. Mikheeva, 2003, Journal of Virology.

Genetic Targeting of an Adenovirus Vector via Replacement of the Fiber Protein with the Phage T4 Fibritin

D. Curiel, V. Krasnykh, G. Mikheeva, 2001, Journal of Virology.

Development of a generic adenovirus delivery system based on structure-guided design of bispecific trimeric DARPin adapters

A. Plückthun, A. Honegger, M. Grütter, 2013, Proceedings of the National Academy of Sciences.

Generation of recombinant adenovirus vectors with modified fibers for altering viral tropism

D. Curiel, V. Krasnykh, J. Douglas, 1996, Journal of virology.

Native and engineered tropism of vectors derived from a rare species D adenovirus serotype 43

C. Xiong, Chun Xing Li, P. Fox, 2016, Oncotarget.

Approaches to Utilize Mesenchymal Progenitor Cells as Cellular Vehicles

D. Curiel, V. Krasnykh, L. Pereboeva, 2003, Stem cells.

Targeting adenovirus to the serotype 3 receptor increases gene transfer efficiency to ovarian cancer cells.

D. Curiel, A. Hemminki, A. Kanerva, 2002, Clinical cancer research : an official journal of the American Association for Cancer Research.

Adenoviral-mediated delivery of herpes simplex virus thymidine kinase results in tumor reduction and prolonged survival in a SCID mouse model of human ovarian carcinoma

D. Curiel, M. Wang, G. Siegal, 1996, Journal of Molecular Medicine.

A Strategy for Adenovirus Vector Targeting with a Secreted Single Chain Antibody

D. Curiel, V. Krasnykh, G. Mikheeva, 2009, PloS one.

Advances in Brief Treatment of Ovarian Cancer with a Tropism Modified Oncolytic Adenovirus 1

D. Nettelbeck, R. Alemany, D. Curiel, 2002 .

Her2-specific multivalent adapters confer designed tropism to adenovirus for gene targeting.

A. Plückthun, P. Forrer, I. Jelesarov, 2011, Journal of molecular biology.

Development of a Targeted Gene Vector Platform Based on Simian Adenovirus Serotype 24

L. Bidaut, C. Xiong, Chun Xing Li, 2010, Journal of Virology.

Reduction of ischemia-reperfusion injury of the liver by in vivo adenovirus-mediated gene transfer of the antiapoptotic Bcl-2 gene.

J. Contreras, D. Curiel, J. Thomas, 1999, Annals of surgery.

Development of a generic adenovirus delivery system based on structure-guided design of bispecific trimeric DARPin adapters

A. Plückthun, A. Honegger, M. Grütter, 2013, Proceedings of the National Academy of Sciences.

Genetically Targeted Adenovirus Vector Directed to CD40-Expressing Cells

D. Curiel, V. Krasnykh, G. Mikheeva, 2003, Journal of Virology.

Modification of Adenovirus Capsid with a Designed Protein Ligand Yields a Gene Vector Targeted to a Major Molecular Marker of Cancer

V. Krasnykh, G. Mikheeva, J. Gelovani, 2007, Journal of Virology.