Discover open access scientific publications

Search, annotate, share and cite publications

Publications by Citra N.Z. Mattar

A Comparison of Intrauterine Haemopoietic Cell Transplantation and Lentiviral Gene Transfer for the Correction of Severe Β-Thalassaemia in a HbbTh3/+ Murine Model.

Experimental Hematology

English

Related publications

Haemopoietic Stem Cell Transplantation in the Treatment of Severe Autoimmune Diseases 2000

Annals of the Rheumatic Diseases

English

Comparison of Lentiviral and Sleeping Beauty Mediated Αβ T Cell Receptor Gene Transfer

PLoS ONE

Multidisciplinary

2013

English

Autologous Haemopoietic Stem Cell Transplantation in a Patient With Severe Pulmonary Hypertension Complicating Connective Tissue Disease.

Annals of the Rheumatic Diseases

English

Correction of Murine SCID-X1 by Lentiviral Gene Therapy Using a Codon-Optimized IL2RG Gene and Minimal Pretransplant Conditioning

English

Lentiviral Haemopoietic Stem/Progenitor Cell Gene Therapy for Treatment of Wiskott-Aldrich Syndrome: Interim Results of a Non-Randomised, Open-Label, Phase 1/2 Clinical Study

The Lancet Haematology

Hematology

2019

English

Outcomes of Gene Therapy for Severe Sickle Cell Disease (SCD) via Transplantation of Autologous Hematopoietic Stem Cells Transduced Ex Vivo With a Lentiviral ßAT87Q-Globin Vector

Biology of Blood and Marrow Transplantation

Transplantation

Hematology

2016

English

Virus-Specific Immunity After Gene Therapy in a Murine Model of Severe Combined Immunodeficiency

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

Multidisciplinary

1999

English

Airway Gene Transfer in a Non-Human Primate: Lentiviral Gene Expression in Marmoset Lungs

Scientific Reports

Multidisciplinary

2013

English

447. Lentiviral Gene Therapy in a Preclinical Model of Omenn Syndrome

English

Amanote Research

Discover open access scientific publications

Search, annotate, share and cite publications

Publications by Citra N.Z. Mattar

A Comparison of Intrauterine Haemopoietic Cell Transplantation and Lentiviral Gene Transfer for the Correction of Severe Β-Thalassaemia in a HbbTh3/+ Murine Model.

Related publications

Haemopoietic Stem Cell Transplantation in the Treatment of Severe Autoimmune Diseases 2000

Comparison of Lentiviral and Sleeping Beauty Mediated Αβ T Cell Receptor Gene Transfer

Autologous Haemopoietic Stem Cell Transplantation in a Patient With Severe Pulmonary Hypertension Complicating Connective Tissue Disease.

Correction of Murine SCID-X1 by Lentiviral Gene Therapy Using a Codon-Optimized IL2RG Gene and Minimal Pretransplant Conditioning

Lentiviral Haemopoietic Stem/Progenitor Cell Gene Therapy for Treatment of Wiskott-Aldrich Syndrome: Interim Results of a Non-Randomised, Open-Label, Phase 1/2 Clinical Study

Outcomes of Gene Therapy for Severe Sickle Cell Disease (SCD) via Transplantation of Autologous Hematopoietic Stem Cells Transduced Ex Vivo With a Lentiviral ßAT87Q-Globin Vector

Virus-Specific Immunity After Gene Therapy in a Murine Model of Severe Combined Immunodeficiency

Airway Gene Transfer in a Non-Human Primate: Lentiviral Gene Expression in Marmoset Lungs

447. Lentiviral Gene Therapy in a Preclinical Model of Omenn Syndrome