Translational data from adeno-associated virus-mediated gene therapy of hemophilia B in dogs - Wikidata - wikimedia - TriplyDB

Translational data from adeno-associated virus-mediated gene therapy of hemophilia B in dogs

Translational data from adeno-associated virus-mediated gene therapy of hemophilia B in dogs

http://www.wikidata.org/entity/Q30891500

about

Gene therapy in an era of emerging treatment options for hemophilia B Evaluation of engineered AAV capsids for hepatic factor IX gene transfer in murine and canine models Successful Phenotype Improvement following Gene Therapy for Severe Hemophilia A in Privately Owned Dogs.Sustained correction of FVII deficiency in dogs using AAV-mediated expression of zymogen FVII Preparation for a first-in-man lentivirus trial in patients with cystic fibrosis.Canine models of inherited bleeding disorders in the development of coagulation assays, novel protein replacement and gene therapies.Complexity of immune responses to AAV transgene products - Example of factor IX.Adeno-Associated Virus Type 2 and Hepatocellular Carcinoma?Systemic AAV Gene Therapy Close to Clinical Trials for Several Neuromuscular Diseases.Hemophilia B Gene Therapy with a High-Specific-Activity Factor IX Variant.Gene Therapy for Hemophilia.

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Translational data from adeno-associated virus-mediated gene therapy of hemophilia B in dogs

http://www.wikidata.org/entity/Q30891500

description

2015 nî lūn-bûn

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2015 թուականի Փետրուարին հրատարակուած գիտական յօդուած

@hyw

2015 թվականի փետրվարին հրատարակված գիտական հոդված

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2015年の論文

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2015年論文

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2015年論文

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2015年論文

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2015年論文

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2015年論文

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2015年论文

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name

Translational data from adeno- ...... herapy of hemophilia B in dogs

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Translational data from adeno- ...... herapy of hemophilia B in dogs

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Translational data from adeno- ...... herapy of hemophilia B in dogs

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Human gene therapy. Clinical development

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Translational data from adeno- ...... herapy of hemophilia B in dogs

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Hansell H Stedman

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Margaret H Whitford

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Mark A Kay

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Timothy C Nichols

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Valder R Arruda

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P2860

Successful transduction of liver in hemophilia by AAV-Factor IX and limitations imposed by the host immune response

Ledipasvir and sofosbuvir for untreated HCV genotype 1 infection

The Chapel Hill hemophilia A dog colony exhibits a factor VIII gene inversion.

Aberrant splicing and premature termination of transcription of the FVIII gene as a cause of severe canine hemophilia A: similarities with the intron 22 inversion mutation in human hemophilia.

Isolated limb infusion with cytotoxic agents: a simple alternative to isolated limb perfusion.

Current uses of isolated limb perfusion in the clinic and a model system for new strategies.

Expression of human alpha1-antitrypsin in mice and dogs following AAV6 vector-mediated gene transfer to the lungs.

Peripheral transvenular delivery of adeno-associated viral vectors to skeletal muscle as a novel therapy for hemophilia B.

Safety of AAV factor IX peripheral transvenular gene delivery to muscle in hemophilia B dogs.

AAV-mediated factor IX gene transfer to skeletal muscle in patients with severe hemophilia B.

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5-14

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scholarly article

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10.1089/HUMC.2014.153

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1

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26

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Katherine A High

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25675273

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