D. Valerio

发表

Isolation of cDNA clones for human adenosine deaminase.

A. van der Eb, A. de Waard, P. Meera Khan, 1983, Gene.

Gene Expression and Apoptosis Levels in Cumulus Cells of Patients with Polymorphisms of FSHR and LHB Undergoing in Vitro Fertilization Program

P. Piomboni, G. Ruvolo, D. Santi, 2017, Cellular Physiology and Biochemistry.

Optimized conditions for the production of recombinant amphotropic retroviral vector preparations

D. Valerio, L. Kaptein, A. Greijer, 1997, Gene Therapy.

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

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

IL-6 production by retrovirus packaging cells and cultured bone marrow cells.

D. Valerio, M. Einerhand, T. Bakx, 1991, Human gene therapy.

Human purine nucleoside phosphorylase and adenosine deaminase: gene transfer into cultured cells and murine hematopoietic stem cells by using recombinant amphotropic retroviruses

S. Williams, I. Verma, M. J. Johnson, 1987, Molecular and cellular biology.

Adenovirus-mediated interleukin 3 beta gene transfer by isolated limb perfusion inhibits growth of limb sarcoma in rats.

A. Eggermont, J. D. Wilt, J. D. de Wilt, 2001, Human gene therapy.

Intra-CSF administered recombinant adenovirus causes an immune response-mediated toxicity

A. Bout, C. Vecht, D. Valerio, 2000, Gene Therapy.

SA1/SA2 cohesion proteins and SIRT1-NAD+ deacetylase modulate telomere homeostasis in cumulus cells and are eligible biomarkers of ovarian aging

V. de Leo, P. Piomboni, A. Luddi, 2018, Human reproduction.

The influence of synovial fluid on adenovirus-mediated gene transfer to the synovial tissue.

F. Breedveld, P. Goossens, M. Havenga, 2001, Arthritis and rheumatism.

Cloning of human adenosine deaminase cDNA and expression in mouse cells.

S. Williams, Steven R. Williams, D. Martin, 1984, Gene.

In vitro and in vivo gene transfer to pulmonary cells mediated by cationic liposomes.

M. Zanta, E. Fortunati, M. Scarpa, 1996, Biochimica et biophysica acta.

Long-term in vivo expression of the MFG-ADA retroviral vector in rhesus monkeys transplanted with transduced bone marrow cells.

R. Mulligan, V. V. van Beusechem, I. Rivière, 1997, Human Gene Therapy.

Long-term genetic modification of rhesus monkey hematopoietic cells following transplantation of adenoassociated virus vector-transduced CD34+ cells.

D. Valerio, E. Claassen, M. Einerhand, 1998, Human gene therapy.

Regulated high-level human beta-globin gene expression in erythroid cells following recombinant adeno-associated virus-mediated gene transfer.

F. Grosveld, N. Muzyczka, S. Zolotukhin, 1995, 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.

Cloning, biological characterization and high-level expression of rat interleukin-3 using recombinant adenovirus: description of a new splicing variant.

A. Bout, D. Valerio, D. V. van Bekkum, 1998, Gene.

Distribution of recombinant adenovirus in the cerebrospinal fluid of nonhuman primates.

A. Bout, C. Vecht, D. Valerio, 1999, Human gene therapy.

Characterization of fetal haematopoietic progenitors circulating in maternal blood of seven aneuploid pregnancies

D. Valerio, F. Antonucci, V. Altieri, 1997, Prenatal diagnosis.

Retrovirus-mediated gene transfer into embryonal carcinoma and hemopoietic stem cells: expression from a hybrid long terminal repeat.

I. Verma, D. Valerio, C. Li, 1989, Gene.

Factors affecting the transduction of pluripotent hematopoietic stem cells: long-term expression of a human adenosine deaminase gene in mice.

D. Valerio, A. Kukler, M. Einerhand, 1993, Blood.

Intracerebral injection of adenovirus harboring the HSVtk gene combined with ganciclovir administration: toxicity study in nonhuman primates

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

New helper cells and matched early region 1-deleted adenovirus vectors prevent generation of replication-competent adenoviruses.

A. van der Eb, A. Bout, K. Hehir, 1998, Human gene therapy.

Factors affecting the transduction of pluripotent hematopoietic stem cells: long-term expression of a human adenosine deaminase gene in mice

D. Valerio, A. Kukler, M. Einerhand, 1993 .

Amphotropic retroviruses with a hybrid long terminal repeat as a tool for gene therapy of cystic fibrosis.

M. Wilke, B. Scholte, E. Verbeek, 1992, Biochemical and biophysical research communications.

Expression of human adenosine deaminase in mice transplanted with hemopoietic stem cells infected with amphotropic retroviruses

A. van der Eb, V. V. van Beusechem, D. Valerio, 1990, The Journal of experimental medicine.

Progress in the Development of Somatic Cell Gene Therapy for Adenosine Deaminase Deficiency

A. Eb, D. Valerio, D. Bekkum, 1990 .

Toward Gene Therapy in Hemophilia A: Introduction of Factor VIII Expression Vectors Into Somatic Cells

A. Eb, E. Briët, R. Hoeben, 1990 .

Towards Gene Therapy for Adenosine Deaminase Deficiency

I. Verma, R. Kellems, D. Valerio, 1989 .

Treatment of patients with severe combined immunodeficiency due to adenosine deaminase (ADA) deficiency by autologous transplantation of genetically modified bone marrow cells.

J. Vossen, D. Valerio, P. Hoogerbrugge, 1992, Human gene therapy.

Expression pattern of CD2 locus control region containing retroviral vectors in hemopoietic cells in vitro and in vivo

D. Valerio, L. Kaptein, V. V. Beusechem, 1998, Gene Therapy.

Gene transfer into hematopoietic stem cells: prospects for human gene therapy.

D. Valerio, M. Einerhand, 1992, Current topics in microbiology and immunology.

Somatic cell gene therapy: the model of adenosine deaminase deficiency.

V. V. van Beusechem, D. Valerio, A. Kukler, 1989, Bone marrow transplantation.

Feasibility of adenovirus-mediated nonsurgical synovectomy in collagen-induced arthritis-affected rhesus monkeys.

F. Breedveld, P. Kluin, P. Goossens, 1999, Human gene therapy.

Ganciclovir-mediated in vivo elimination of myeloid leukemic cells expressing the HSVtk gene induces HSVtk loss variants

A. Hagenbeek, R. Vogels, E. Braakman, 1999, Gene Therapy.

Simultaneous detection of NOS-3 protein expression and nitric oxide production using a flow cytometer.

P. Quax, M. Havenga, A. Bout, 2001, Analytical biochemistry.

Cell cycle state, response to hemopoietic growth factors and retroviral vector-mediated transduction of human hemopoietic stem cells.

V. V. van Beusechem, D. Valerio, S. Knaän-Shanzer, 1996, Gene therapy.

Adenosine deaminase: characterization and expression of a gene with a remarkable promoter.

A. Eb, G. Weeda, D. Valerio, 1985, The EMBO journal.

Gene transfer into hematopoietic stem cells of nonhuman primates.

V. V. van Beusechem, D. Valerio, 1996, Human gene therapy.

Propagation of Adenoviral Vectors: Use of PER. C6 Cells

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

Mosaic tetrasomy 12p: a new case

G. Delrio, D. Valerio, E. de PONTE, 1992, Prenatal diagnosis.

A new case of partial trisomy 19q (q13.2-->qter) owing to an unusual maternal translocation.

D. Valerio, M. Scalona, F. Lavorgna, 1993, Journal of medical genetics.

Retrovirus-mediated gene transfer into rhesus monkey hematopoietic stem cells: the effect of viral titers on transduction efficiency.

V. V. van Beusechem, E. Braakman, D. Valerio, 1993, Human gene therapy.

The Human Gene for Adenosine Deaminase

A. Eb, P. Khan, D. Valerio, 1985, Advances in experimental medicine and biology.

Construction and expression of an adenosine deaminase::lacZ fusion gene.

V. V. van Beusechem, D. Valerio, Q. Shen, 1991, 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.

Bone marrow transplantation and gene therapy for lysosomal storage diseases.

D. Valerio, P. Hoogerbrugge, 1998, Bone marrow transplantation.

Adenosine deaminase (ADA) deficiency in cells derived from humans with severe combined immunodeficiency is due to an aberration of the ADA protein.

A. van der Eb, P. Meera Khan, D. Valerio, 1984, Nucleic acids research.

L. Altucci, F. Cuomo, C. Dell'Aversana, 2021, Human reproduction.

Gene transfer into nonhuman primate CD34+CD11b- bone marrow progenitor cells capable of repopulating lymphoid and myeloid lineages.

V. V. van Beusechem, R. Levinsky, D. Valerio, 1994, Human gene therapy.

Detection of fetal trisomy 18 by short-term culture of maternal peripheral blood.

D. Valerio, F. Antonucci, D. Cavallo, 2000, American journal of obstetrics and gynecology.

CULTURE OF FETAL ERYTHROID PROGENITOR CELLS FROM MATERNAL BLOOD FOR NON‐INVASIVE PRENATAL GENETIC DIAGNOSIS

D. Valerio, V. Altieri, A. Fortunato, 1996 .

Biochemical and immunological status following gene therapy and PEG-ADA therapy for adenosine deaminase (ADA) deficiency.

H. Simmonds, V. V. van Beusechem, H. Gaspar, 1994, Advances in experimental medicine and biology.

One adenosine deaminase allele in a patient with severe combined immunodeficiency contains a point mutation abolishing enzyme activity.

A. Eb, D. Valerio, M. Duyvesteyn, 1986, The EMBO journal.

Bone marrow gene transfer in three patients with adenosine deaminase deficiency.

A. Fischer, R. Levinsky, V. V. van Beusechem, 1996, Gene therapy.

Isolation of fetal erythroid cells from maternal blood based on expression of erythropoietin receptors.

D. Valerio, V. Altieri, R. Aiello, 1997, Molecular human reproduction.

Percutaneous gene therapy using recombinant adenoviruses encoding human herpes simplex virus thymidine kinase, human PAI-1, and human NOS3 in balloon-injured porcine coronary arteries.

B. Iung, P. Sinnaeve, D. Collen, 2000, Human gene therapy.

Gene therapy of experimental malignant mesothelioma using adenovirus vectors encoding the HSVtk gene

A. Bout, D. Valerio, J. Noteboom, 1997, Gene Therapy.

The effect of promoter strength in adenoviral vectors in hyperplastic synovium.

F. Breedveld, P. Kluin, P. Goossens, 2000, Clinical and Experimental Rheumatology.

Preclinical testing of recombinant adenoviral herpes simplex virus-thymidine kinase gene therapy for central nervous system malignancies.

C. Avezaat, A. Bout, P. Hoogerbrugge, 1997, Neurosurgery.

Treatment of leptomeningeal metastases in a rat model using a recombinant adenovirus containing the HSV-tk gene.

C. Avezaat, A. Bout, C. Vecht, 1996, Journal of neurosurgery.

Lung gene therapy: in vivo adenovirus-mediated gene transfer to rhesus monkey airway epithelium.

M. Perricaudet, B. Scholte, A. Bout, 1994, Human gene therapy.

Aerosol-mediated delivery of recombinant adenovirus to the airways of nonhuman primates.

A. Bout, A. Pavirani, J. Imler, 1995, Human gene therapy.

In vivo adenovirus-mediated transfer of human CFTR cDNA to rhesus monkey airway epithelium: efficacy, toxicity and safety.

M. Perricaudet, A. Bout, A. Pavirani, 1994, Gene therapy.

Trans-complementation of E1-deleted adenovirus: a new vector to reduce the possibility of codissemination of wild-type and recombinant adenoviruses.

M. Mehtali, A. Bout, A. Pavirani, 1995, Human gene therapy.

Prenatal diagnosis of a partial 6q trisomy: a case report

M. Felicetti, D. Valerio, A. Borrelli, 2006, Prenatal diagnosis.

Influence of interleukin-3, interleukin-6, and stem cell factor on retroviral transduction of rhesus monkey CD34+ hematopoietic progenitor cells measured in vitro and in vivo.

V. V. van Beusechem, D. Valerio, P. Hoogerbrugge, 1995, Gene therapy.

Maternal serum screening of fetal chromosomal abnormalities by AFP, UE3, hCG and free-beta hCG. Prospective and retrospective results.

D. Valerio, V. Altieri, P. Fagnoni, 1996, Minerva ginecologica.

Intrinsic potential of phenotypically defined human hemopoietic stem cells to self-renew in short-term in vitro cultures.

V. V. van Beusechem, D. Valerio, D. V. van Bekkum, 1999, Experimental hematology.

Retrovirus vectors for gene therapy procedures

G. Kollias, F. Grosveld, D. Valerio, 1992 .

Culture of fetal erythroid progenitor cells from maternal blood for non-invasive prenatal genetic diagnosis.

D. Valerio, A. Malato, V. Altieri, 1997, Prenatal Diagnosis.

Retrovirus-mediated transfer and expression of marker genes in the BN rat acute myelocytic leukemia model for the study of minimal residual disease (MRD).

A. Hagenbeek, A. Martens, C. J. de Groot, 1993, Leukemia.

In vivo transfer and expression of the lacZ gene in the mouse lung.

B. Scholte, D. Valerio, A. Bout, 1993, Experimental lung research.

Hodgkin's disease and infectious mononucleosis.

A. Dawson, J. Green, D. Valerio, 2009, Scandinavian journal of haematology.