Office of Technology Transfer and Development

I.D.

Technology

Pat. No.
(LINK TO USPTO)

ES-016

Tetracycline-Modulated Bicistronic Mammalian Expression Vector

ES-059

Plasmids DNA's for human and mouse TTP and mammalian expression vectors for same

HL-006

Use of Chimeric Murine Leukemia Virus LTRs in Expressing Retroviral Vectors

HL-016

Genetic Reassortment of Rotaviruses for Production of Vaccine and Vaccine Precursor

4,571,385

HL-062

Retroviral Vectors Containing Internal Ribosome Entry

HL-069

Adenovirus Mediated Transfer Of Genes To The Gastrointestinal Tract

HL-072

Inhibition of Cell Proliferation Using Antisense Oligonucleotides

HL-090

Improved Expression Of Human Multidrug Resistance Genes And Improved Selection

HL-116

Adenovirus Mediated Augmentation of Cell Transfection With Unmodified Plasmid Vectors

HL-121

Vector Systems For The Generation of Adeno- Associated Virus Particles

HL-122

Fusion Proteins Containing Adeno-Associated Virus Rep Proteins

HL-133

Novel Retroviral Envelope and LTR and Retroviral Vector Particles

HL-135

Gene Therapy to Promote Myocardial Blood Vessel Growth

HL-136

Adeno-Associated Virus Capable of Expressing at Least One Globin Gene and Method

HL-137

Lipid Vesicles Containing Adeno-Associated Virus Rep Protein For Transgene Integration

HL-146

Vector Particles Resistant to Inactivation by Human Serum

HL-149

Gene Therapy with Hirudin for Arterial Proliferating Disease

HL-153

Vectors Including Foreign Genes and Negative Selective Markers

HL-155

Organ Selective In Vivo Gene Transfer

HL-156

Promotion and Angiogenesis using Adenoviral-modified endothelial cells and graft

HL-161

Molecular Cloning of AAV and Use as a Transduction Vector

HL-169

High level production in vitro of human coagulation factor IX from a recombinant Adeno-associated virus.

HL-170

Genetically Engineered Endothelial Cells and uses Thereof

HL-174

"Method for Development of Localized Cell-mediated Immune Responses by Gene Transfer into Peripheral Blood Monocyte/macrophages for the Treatment of Aids and Other Infections Pathogens"

HL-176

Delivery of Therapeutic Agents by Gene Therapy

HL-187

Method for Enhancement of Cell-mediated Immune Responses by Gene Transfer into peripheral blood cells

HL-188

Molecular Cloning of AAV5 and It's use as a Transduction Vector

HL-225

In vivo transduction of ependymal cells with AAV4 vectors

HL-226

In vivo of mouse lung with AAV5 vectors

HL-230

A chimeric Lentiviral vector with enhanced gene expression.

HL-237

Vectors encoding for the interaction domains of proteins can interfere with those protein interactions

HL-240

Methods for producing recombinant AAVs in invertebrate cell lines

HL-243

Adeno-associated virus (AAV) vector encoding human coagulation factor VIII under transcription control

HL-257

Methods for producing recombinant AAVs in invertebrate cell lines

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