D. Curiel

发表

A cyclooxygenase-2 promoter-based conditionally replicating adenovirus with enhanced infectivity for treatment of ovarian adenocarcinoma

D. Curiel, A. Hemminki, A. Kanerva, 2004, Gene Therapy.

Fractionated radiation therapy in combination with adenoviral delivery of the cytosine deaminase gene and 5-fluorocytosine enhances cytotoxic and antitumor effects in human colorectal and cholangiocarcinoma models

M. Mayo, J. Gebert, D. Curiel, 2000, Gene Therapy.

A tropism-modified adenoviral vector increased the effectiveness of gene therapy for arthritis

D. Curiel, L. Joosten, I. Dmitriev, 2001, Gene Therapy.

Imaging and tissue biodistribution of 99mTc-labeled adenovirus knob (serotype 5)

K. Zinn, D. Curiel, J. Douglas, 1998, Gene Therapy.

Blood clearance rates of adenovirus type 5 in mice.

R. Alemany, D. Curiel, K. Suzuki, 2000, The Journal of general virology.

Selective elimination (purging) of contaminating malignant cells from hematopoietic stem cell autografts using recombinant adenovirus.

T. Meeker, P. Seth, D. Curiel, 1996, Cancer gene therapy.

Gene therapy strategies for asthma

J. Bousquet, P. Demoly, D. Curiel, 1997, Gene Therapy.

A novel system for mitigation of ectopic transgene expression induced by adenoviral vectors

D. Curiel, L. Kaliberova, Y. Adachi, 2001, Gene Therapy.

CAR-binding ablation does not change biodistribution and toxicity of adenoviral vectors

R. Alemany, D. Curiel, 2001, Gene Therapy.

Fiber shaft extension in combination with HI loop ligands augments infectivity for CAR-negative tumor targets but does not enhance hepatotropism in vivo

M. Rots, M. Wang, K. Takayama, 2002, Gene Therapy.

Incorporation of β-globin untranslated regions into a Sindbis virus vector for augmentation of heterologous mRNA expression

G. Bilbao, D. Curiel, I. Louro, 1997, Gene Therapy.

An intracellular anti-erbB-2 single-chain antibody is specifically cytotoxic to human breast carcinoma cells overexpressing erbB-2

M. Kim, J. Grim, G. Siegal, 1997, Gene Therapy.

Improved gene transfer efficiency to primary and established human pancreatic carcinoma target cells via epidermal growth factor receptor and integrin-targeted adenoviral vectors

P. Bosma, D. Curiel, P. Reynolds, 2001, Gene Therapy.

A three-dimensional assay for measurement of viral-induced oncolysis

R. Desmond, A. Hemminki, A. Kanerva, 2007, Cancer Gene Therapy.

Pulmonary prostacyclin synthase overexpression by adenovirus transfection and in transgenic mice.

N. Voelkel, B. Gao, D. Curiel, 1998, Chest.

Phenotypic knock-out of the latent membrane protein 1 of Epstein–Barr virus by an intracellular single-chain antibody

T. Curiel, K. Kasono, D. Curiel, 1998, Gene Therapy.

Humoral and cellular immune responses of dogs immunized with a nucleic acid vaccine encoding human carcinoembryonic antigen

D. Curiel, R. Conry, W. Jiang, 1998, Gene Therapy.

Transductional and transcriptional targeting of adenovirus for clinical applications.

A. Hemminki, G. Bauerschmitz, D. Curiel, 2004, Current gene therapy.

Gene therapy for gliomas: molecular targets, adenoviral vectors, and oncolytic adenoviruses.

C. Balagué, R. Alemany, D. Curiel, 1999, Experimental cell research.

Efficient gene delivery into epstein-barr virus (EBV)-transformed human B cells mediated by replication-defective herpes simplex virus-1 (HSV-1): A gene therapy model for EBV-related B cell malignancy.

T. Curiel, K. Kasono, J. Xiang, 1998, Biochemical and biophysical research communications.

Combining high selectivity of replication with fiber chimerism for effective adenoviral oncolysis of CAR-negative melanoma cells

D. Nettelbeck, A. Rivera, D. Curiel, 2004, Gene Therapy.

Use of a novel cross-linking method to modify adenovirus tropism

D. Curiel, J. Douglas, C. Ahlem, 1997, Gene Therapy.

Effective single chain antibody (scFv) concentrations in vivo via adenoviral vector mediated expression of secretory scFv

D. Nettelbeck, J. Xiang, A. Hemminki, 2002, Gene Therapy.

Functional knock-out of c-myb by an intracellular anti-c-Myb single-chain antibody.

K. Kasono, K. Moelling, G. Bilbao, 1998, Biochemical and biophysical research communications.

Immunization with a plasmid expressing pneumococcal surface protein A (PspA) can elicit protection against fatal infection with Streptococcus pneumoniae

F. Loechel, D. Curiel, C. Benedict, 1997, Gene Therapy.

Transcriptional targeting of adenoviral vector through the CXCR4 tumor-specific promoter

D. Nettelbeck, M. Wang, R. Alvarez, 2004, Gene Therapy.

Gene therapy strategies for AIDS-related malignancies

K. Kasono, D. Curiel, A. Piché, 1997, Gene Therapy.

An ex vivo human model system to evaluate specificity of replicating and non‐replicating gene therapy agents

M. Rots, P. Olinga, G. Groothuis, 2006, The journal of gene medicine.