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Nicolas Ferry

Researcher at French Institute of Health and Medical Research

Publications -  75
Citations -  2244

Nicolas Ferry is an academic researcher from French Institute of Health and Medical Research. The author has contributed to research in topics: Transgene & Genetic enhancement. The author has an hindex of 26, co-authored 75 publications receiving 2176 citations. Previous affiliations of Nicolas Ferry include École Normale Supérieure & Pasteur Institute.

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Efficient Transfer of Regulated Genes in Adipocytes and Hepatoma Cells by the Combination of Liposomes and Replication‐Deficient Adenovirus

TL;DR: The association of liposomes and adenovirus is an efficient method for transient or stable transfer of regulated genes in adipocytes and hepatoma cells.
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Different gamma-glutamyl transpeptidase mRNAs are expressed in human liver and kidney.

TL;DR: The sequencing of a human genomic clone reveals that this type II GGT mRNA is encoded by a different gene than the type I GGT RNA, which is expressed in human liver, while almost exclusively type Two GGTRNA is detected in human kidney.
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Transient expression of genes delivered to newborn rat liver using recombinant adeno-associated virus 2/8 vectors.

TL;DR: Transgene expression after AAV8 delivery of a therapeutic or a marker gene to newborn rat liver is analysed and it is suggested that AAV delivery to the newborn liver may result in transient expression.
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Critical assessment of lifelong phenotype correction in hyperbilirubinemic Gunn rats after retroviral mediated gene transfer

TL;DR: The present results document the lifelong safety of gene therapy for CN-1 with retroviral vectors and offer a better delineation of liver gene correction level required to achieve complete correction of bilirubinemia and pave the way for future clinical application of gene Therapy for inherited liver disorders.
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Alloantigen gene transfer to hepatocytes promotes tolerance to pancreatic islet graft by inducing CD8+ regulatory T cells.

TL;DR: It is demonstrated for the first time that the in vivo gene transfer of an allogeneic antigen with an adeno-associated viral vector to mouse hepatocytes induces the expansion of a population of CD8+ regulatory T lymphocytes.