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Human Gene Therapy
|
July 9, 2021
Adeno-Associated Virus Vector Gene Delivery Elevates Factor I Levels and Downregulates the Complement Alternative Pathway <i>In Vivo</i>
Amina Ahmad, Mawj Mandwie, Anna K Dreismann, et al.
Circulation Research
|
May 15, 2007
Gene transfer of connexin43 mutants attenuates coupling in cardiomyocytes: novel basis for modulation of cardiac conduction by gene therapy
Eddy Kizana, Connie Y Chang, Eugenio Cingolani, et al.
Molecular Therapy. Methods & Clinical Development
|
October 27, 2021
Safety and efficacy of an engineered hepatotropic AAV gene therapy for ornithine transcarbamylase deficiency in cynomolgus monkeys
Julien Baruteau, Sharon C Cunningham, Berna Seker Yilmaz, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research
|
September 30, 2011
A murine model of neurofibromatosis type 1 tibial pseudarthrosis featuring proliferative fibrous tissue and osteoclast-like cells
Jad El-Hoss, Kate Sullivan, Tegan Cheng, et al.
Human Gene Therapy
|
March 16, 2022
Conversion of the Liver into a Biofactory for DNaseI Using Adeno-Associated Virus Vector Gene Transfer Reduces Neutrophil Extracellular Traps in a Model of Systemic Lupus Erythematosus
Amina Ahmad, Mawj Mandwie, Kim M O'Sullivan, et al.
Biorxiv : the Preprint Server for Biology
|
May 15, 2024
Structural characterization of antibody-responses from Zolgensma treatment provides the blueprint for the engineering of an AAV capsid suitable for redosing
Mario Mietzsch, Austin R Nelson, Jane Hsi, et al.
Molecular Therapy. Methods & Clinical Development
|
June 7, 2021
Single amino acid insertion allows functional transduction of murine hepatocytes with human liver tropic AAV capsids
Marti Cabanes-Creus, Renina Gale Navarro, Sophia H Y Liao, et al.
The Journal of Gene Medicine
|
March 27, 2018
Partial pancreatic transdifferentiation of primary human hepatocytes in the livers of a humanised mouse model
Binhai Ren, Que T La, Bronwyn A O'Brien, et al.
Human Gene Therapy
|
July 21, 2018
Age-Related Seroprevalence of Antibodies Against AAV-LK03 in a UK Population Cohort
Dany P Perocheau, Sharon Cunningham, Juhee Lee, et al.
Clinical and Experimental Immunology
|
March 11, 2026
A novel fusion protein reduces kidney complement in experimental C3 glomerulopathy
Talat H Malik, Karolina Kwiatkowska, Hannah J Lomax-Browne, et al.
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of 14
Search research articles
Search
Showing results (71-80 of 131) with videos related to
Sort By:
Page
of 14
Human Gene Therapy
|
July 9, 2021
Adeno-Associated Virus Vector Gene Delivery Elevates Factor I Levels and Downregulates the Complement Alternative Pathway <i>In Vivo</i>
Amina Ahmad, Mawj Mandwie, Anna K Dreismann, et al.
Circulation Research
|
May 15, 2007
Gene transfer of connexin43 mutants attenuates coupling in cardiomyocytes: novel basis for modulation of cardiac conduction by gene therapy
Eddy Kizana, Connie Y Chang, Eugenio Cingolani, et al.
Molecular Therapy. Methods & Clinical Development
|
October 27, 2021
Safety and efficacy of an engineered hepatotropic AAV gene therapy for ornithine transcarbamylase deficiency in cynomolgus monkeys
Julien Baruteau, Sharon C Cunningham, Berna Seker Yilmaz, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research
|
September 30, 2011
A murine model of neurofibromatosis type 1 tibial pseudarthrosis featuring proliferative fibrous tissue and osteoclast-like cells
Jad El-Hoss, Kate Sullivan, Tegan Cheng, et al.
Human Gene Therapy
|
March 16, 2022
Conversion of the Liver into a Biofactory for DNaseI Using Adeno-Associated Virus Vector Gene Transfer Reduces Neutrophil Extracellular Traps in a Model of Systemic Lupus Erythematosus
Amina Ahmad, Mawj Mandwie, Kim M O'Sullivan, et al.
Biorxiv : the Preprint Server for Biology
|
May 15, 2024
Structural characterization of antibody-responses from Zolgensma treatment provides the blueprint for the engineering of an AAV capsid suitable for redosing
Mario Mietzsch, Austin R Nelson, Jane Hsi, et al.
Molecular Therapy. Methods & Clinical Development
|
June 7, 2021
Single amino acid insertion allows functional transduction of murine hepatocytes with human liver tropic AAV capsids
Marti Cabanes-Creus, Renina Gale Navarro, Sophia H Y Liao, et al.
The Journal of Gene Medicine
|
March 27, 2018
Partial pancreatic transdifferentiation of primary human hepatocytes in the livers of a humanised mouse model
Binhai Ren, Que T La, Bronwyn A O'Brien, et al.
Human Gene Therapy
|
July 21, 2018
Age-Related Seroprevalence of Antibodies Against AAV-LK03 in a UK Population Cohort
Dany P Perocheau, Sharon Cunningham, Juhee Lee, et al.
Clinical and Experimental Immunology
|
March 11, 2026
A novel fusion protein reduces kidney complement in experimental C3 glomerulopathy
Talat H Malik, Karolina Kwiatkowska, Hannah J Lomax-Browne, et al.
Page
of 14