D. Valerio

发表

Improved Adenovirus Vectors for Infection of Cardiovascular Tissues

P. Quax, M. Havenga, A. Lemckert, 2001, Journal of Virology.

Second gene expression in bicistronic constructs using short synthetic intercistrons and viral IRES sequences.

A. Hagenbeek, R. Vogels, D. Valerio, 1998, Gene.

Methotrexate selectable retroviral vectors for Gaucher disease

D. Valerio, M. Havenga, A. Werner, 1998, Gene Therapy.

Treatment of Adenosine Deaminase Deficiency

D. Valerio, P. Hoogerbrugge, J. Vossen, 1998, BioDrugs.

Human mesenchymal stem cells ectopically expressing full-length dystrophin can complement Duchenne muscular dystrophy myotubes by cell fusion.

D. Valerio, A. D. de Vries, M. Gonçalves, 2006, Human molecular genetics.

IL-1/IL-3 gene therapy of non-small cell lung cancer (NSCLC) in rats using ‘cracked’ adenoproducer cells

A. Bout, D. Valerio, J. Noteboom, 1998, Gene Therapy.

Propagation of Adenoviral Vectors: Use of PER. C6 Cells

W. W. Nichols, D. Kaslow, R. Hill, 2002 .

Highly efficient targeted transduction of undifferentiated human hematopoietic cells by adenoviral vectors displaying fiber knobs of subgroup B.

A. Lemckert, D. Valerio, A. D. de Vries, 2001, Human gene therapy.

Circumvention of chemotherapy-induced myelosuppression by transfer of themdr1 gene

D. Valerio, K. Nooter, J. Boesen, 1993, Biotherapy.

Overexpression of the MDRL gene in blast cells from patients with acute myelocytic leukemia is associated with decreased anthracycline accumulation that can be restored by cyclosporin‐A

P. Sonneveld, D. Valerio, H. Herweijer, 1990, International journal of cancer.

Full genetic rescue of adenosine deaminase-deficient mice through introduction of the human gene.

M. Hershfield, D. Valerio, A. Migchielsen, 1996, Human molecular genetics.

Retroviral transfer of the multidrug resistance‐1 gene into lineage‐committed and primitive hemopoietic cells

W. Zeller, D. Valerio, B. Löwenberg, 1995, Stem cells.

Development of safe and efficient retroviral vectors for Gaucher disease

D. Valerio, M. Havenga, H. V. Es, 1997, Gene Therapy.

Retroviral Stem Cell Gene Therapy

M. Havenga, D. Valerio, H. V. van Es, 1997, Stem cells.

Rapamycin impairs antigen uptake of human dendritic cells1

P. Allavena, L. Piemonti, D. Valerio, 2003, Transplantation.

EVIDENCE OF METABOLIC ACTIVITY OF ADULT AND FETAL RAT HEPATOCYTES TRANSPLANTED INTO SOLID SUPPORTS

P. Jansen, F. Hoek, D. Valerio, 1992, Transplantation.

Genetic correction of cultured T cells from an adenosine deaminase‐deficient patient: Characteristics of non‐transduced and transduced T cells

D. Valerio, V. V. van Beusechem, B. V. van Krimpen, 1992, European journal of immunology.

Frequency analysis of multidrug resistance-1 gene transfer into human primitive hematopoietic progenitor cells using the cobblestone area-forming cell assay and detection of vector-mediated P-glycoprotein expression by rhodamine-123.

D. Valerio, B. Löwenberg, S. Fruehauf, 1996, Human gene therapy.

Phenotypic and Functional Reversal Within the Early Human Hematopoietic Compartment

D. Valerio, A. D. de Vries, D. V. van Bekkum, 2008, Stem cells.

Transduction of myogenic cells by retargeted dual high-capacity hybrid viral vectors: robust dystrophin synthesis in duchenne muscular dystrophy muscle cells.

D. Valerio, A. D. de Vries, M. Gonçalves, 2006, Molecular therapy : the journal of the American Society of Gene Therapy.

Transfer of the Full-Length Dystrophin-Coding Sequence into Muscle Cells by a Dual High-Capacity Hybrid Viral Vector with Site-Specific Integration Ability

M. Tijssen, D. Valerio, A. D. de Vries, 2005, Journal of Virology.

The human gene for adenosine deaminase.

D. Valerio, G. Weeda, C. Breukel, 1986 .

In vivo methotrexate selection of murine hemopoietic cells transduced with a retroviral vector for Gaucher disease

D. Valerio, M. Havenga, H. V. Es, 1999, Gene Therapy.

Gene therapy for human inherited disorders: techniques and status.

A. van der Eb, D. Valerio, R. Hoeben, 1992, Critical reviews in oncology/hematology.

Toward Gene Therapy in Haemophilia A: Retrovirus-Mediated Transfer of a Factor VIII Gene into Murine Haematopoietic Progenitor Cells

A. van der Eb, D. Valerio, E. Briët, 1992, Thrombosis and Haemostasis.

A flow cytometric assay for lysosomal glucocerebrosidase.

D. Valerio, M. Havenga, H. V. van Es, 1997, Analytical biochemistry.

A flow cytometric assay enabling specific detection of the human lysosomal enzyme, beta-glucocerebrosidase.

D. Valerio, M. Havenga, H. V. van Es, 1998, Analytical biochemistry.

Isolated Limb Perfusion for Local Gene Delivery: Efficient and Targeted Adenovirus-Mediated Gene Transfer Into Soft Tissue Sarcomas

A. Eggermont, J. D. de Wilt, A. Bout, 2000, Annals of surgery.

Improved screening method for recombinant retrovirus producing clones.

D. Valerio, M. Havenga, H. V. van Es, 1996, BioTechniques.

Adenosine–deaminase–deficient mice die perinatally and exhibit liver–cell degeneration, atelectasis and small intestinal cell death

A. Berns, M. Hershfield, H. Riele, 1995, Nature Genetics.

Chapter 6 Propagation of Adenoviral Vectors Use of PER. C6 Cells

S. M. Galloway, K. Brouwer, W. W. Nichols, 2002, Adenoviral Vectors for Gene Therapy.

Mammalian Expression of Cloned cDNA Sequences Encoding Human Purine Nucleoside Phosphorylase and Adenosine Deaminase a

Steven R. Williams, A. Eb, D. Valerio, 1985, Annals of the New York Academy of Sciences.

Efficient Generation and Amplification of High-Capacity Adeno-Associated Virus/Adenovirus Hybrid Vectors

D. Opstelten, D. Valerio, A. D. de Vries, 2002, Journal of Virology.

Generation of a high-capacity hybrid vector: packaging of recombinant adenoassociated virus replicative intermediates in adenovirus capsids overcomes the limited cloning capacity of adenoassociated virus vectors.

D. Valerio, A. D. de Vries, M. Gonçalves, 2001, Virology.

Proliferative response of hepatocytes transplanted into spleen or solid support.

G. Kazemier, I. B. Borel Rinkes, D. Valerio, 1994, The Journal of surgical research.

Introduction of the Human MDR 1 Gene into Hematopoietic Stem Cells to Improve Cancer Chemotherapy

G. Hospers, D. Valerio, K. Nooter, 1995 .

Endowing Human Adenovirus Serotype 5 Vectors with Fiber Domains of Species B Greatly Enhances Gene Transfer into Human Mesenchymal Stem Cells

D. Valerio, A. D. de Vries, M. Gonçalves, 2005, Stem cells.

Stable transduction of large DNA by high-capacity adeno-associated virus/adenovirus hybrid vectors.

D. Valerio, A. D. de Vries, M. Gonçalves, 2004, Virology.

Generation of normal lymphocyte populations following transplantation of adenosine–deaminase-deficient fetal liver cells

D. Valerio, M. Hershfield, A. Migchielsen, 1997, Bone Marrow Transplantation.

Herpes simplex virus thymidine kinase gene therapy for rat malignant brain tumors.

C. Avezaat, C. Vecht, A. Bout, 1996, Human gene therapy.

Introduction of sequences encoding functional human adenosine deaminase into mouse cells using a retroviral shuttle system.

A. van der Eb, D. Valerio, D. Valerio, 1985, Gene.

Long-term expression of human adenosine deaminase in rhesus monkeys transplanted with retrovirus-infected bone-marrow cells.

D. Valerio, V. V. van Beusechem, D. Valerio, 1992, Proceedings of the National Academy of Sciences of the United States of America.