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Publications by G Denning

Generation of an Optimized Lentiviral Vector Encoding a High-Expression Factor VIII Transgene for Gene Therapy of Hemophilia A

Gene Therapy

English

A Simple Trypsin Resistance Assay for Muscle and Other Cell Fusion.

Journal of Histochemistry and Cytochemistry

Anatomy

Histology

1986

English

Related publications

Expression of Human Coagulation Factor VIII in Adipocytes Transduced With the Simian Immunodeficiency Virus agmTYO1-based Vector for Hemophilia a Gene Therapy

English

244. Factor VIII Immunogenicity Is a Barrier to AAV Gene Therapy for Hemophilia A

English

Liver-Directed Lentiviral Gene Therapy in a Dog Model of Hemophilia B

Science Translational Medicine

Medicine

2015

English

Lentivirus-Mediated Platelet Gene Therapy of Murine Hemophilia a With Pre-Existing Anti-Factor VIII Immunity

Journal of Thrombosis and Haemostasis

Medicine

Hematology

2012

English

Creating a DDAVP Releasable Pool of Factor VIII: Its Impact on the Gene Therapy of Hemophilia a † 786

English

Long-Term Expression of Human Coagulation Factor VIII and Correction of Hemophilia a After in Vivo Retroviral Gene Transfer in Factor VIII-deficient Mice

Proceedings of the National Academy of Sciences of the United States of America

Multidisciplinary

1999

English

Optimized Lentiviral Vectors for HIV Gene Therapy: Multiplexed Expression of Small RNAs and Inclusion of MGMTP140K Drug Resistance Gene

English

Generation of a High Titre Retroviral Vector for Endothelial Cell-Specific Gene Expression in Vivo

English

Postpartum Acquired Hemophilia Factor VIII �nhibitors and Response to Therapy

Turkish Journal of Haematology

Hematology

2012

English

Amanote Research

Discover open access scientific publications

Search, annotate, share and cite publications

Publications by G Denning

Generation of an Optimized Lentiviral Vector Encoding a High-Expression Factor VIII Transgene for Gene Therapy of Hemophilia A

A Simple Trypsin Resistance Assay for Muscle and Other Cell Fusion.

Related publications

Expression of Human Coagulation Factor VIII in Adipocytes Transduced With the Simian Immunodeficiency Virus agmTYO1-based Vector for Hemophilia a Gene Therapy

244. Factor VIII Immunogenicity Is a Barrier to AAV Gene Therapy for Hemophilia A

Liver-Directed Lentiviral Gene Therapy in a Dog Model of Hemophilia B

Lentivirus-Mediated Platelet Gene Therapy of Murine Hemophilia a With Pre-Existing Anti-Factor VIII Immunity

Creating a DDAVP Releasable Pool of Factor VIII: Its Impact on the Gene Therapy of Hemophilia a † 786

Long-Term Expression of Human Coagulation Factor VIII and Correction of Hemophilia a After in Vivo Retroviral Gene Transfer in Factor VIII-deficient Mice

Optimized Lentiviral Vectors for HIV Gene Therapy: Multiplexed Expression of Small RNAs and Inclusion of MGMTP140K Drug Resistance Gene

Generation of a High Titre Retroviral Vector for Endothelial Cell-Specific Gene Expression in Vivo

Postpartum Acquired Hemophilia Factor VIII �nhibitors and Response to Therapy