V. Pichard

发表

Demonstration of direct lineage between hepatocytes and hepatocellular carcinoma in diethylnitrosamine‐treated rats

N. Ferry, M. Bralet, V. Pichard, 2002, Hepatology.

Effect of retinol dehydrogenase gene transfer in a novel rat model of Stargardt disease

C. Audrain, M. Croyal, V. Pichard, 2021, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.

Critical assessment of lifelong phenotype correction in hyperbilirubinemic Gunn rats after retroviral mediated gene transfer

D. Aubert, T. Nguyen, N. Ferry, 2007, Gene Therapy.

Therapeutic lentivirus-mediated neonatal in vivo gene therapy in hyperbilirubinemic Gunn rats.

D. Trono, D. Aubert, N. Ferry, 2005, Molecular therapy : the journal of the American Society of Gene Therapy.

Factors influencing immune response after in vivo retrovirus‐mediated gene transfer to the liver

D. Aubert, N. Ferry, V. Pichard, 2004, The journal of gene medicine.

Priming of Hepatocytes EnhancesIn VivoLiver Transduction with Lentiviral Vectors in Adult Mice

N. Ferry, V. Pichard, T. Nguyen, 2011 .

Transient increase in intrahepatic pressure mediates successful treatment of the Gunn rat with reduced doses of lentiviral vector.

N. Ferry, V. Pichard, T. Nguyen, 2010, Human gene therapy.

Lentiviral vectors that express UGT1A1 in liver and contain miR-142 target sequences normalize hyperbilirubinemia in Gunn rats.

S. Remy, C. Usal, I. Anegon, 2010, Gastroenterology.

Successful gene therapy of the Gunn rat by in vivo neonatal hepatic gene transfer using murine oncoretroviral vectors

D. Aubert, N. Ferry, F. Trivin, 2005, Hepatology.

AAV-mediated Gene Therapy Halts Retinal Degeneration in PDE6β-deficient Dogs.

F. Rolling, V. Pichard, G. Le Meur, 2016, Molecular therapy : the journal of the American Society of Gene Therapy.

Mature hepatocytes are the source of small hepatocyte-like progenitor cells in the retrorsine model of liver injury.

N. Ferry, M. Bralet, V. Pichard, 2004, Journal of hepatology.

AAV8 locoregional delivery induces long-term expression of an immunogenic transgene in macaques despite persisting local inflammation

V. Pichard, O. Adjali, Adrien Léger, 2021, Molecular therapy. Methods & clinical development.

Detection, Isolation, and Characterization of α-fetoprotein-specific T Cell Populations and Clones Using MHC Class I Multimer Magnetic Sorting

A. Gaignerie, N. Ferry, M. Grégoire, 2008, Journal of immunotherapy.

Direct In Vivo Cell Lineage Analysis in the Retrorsine and 2AAF Models of Liver Injury after Genetic Labeling in Adult and Newborn Rats

D. Aubert, N. Ferry, V. Pichard, 2009, PloS one.

in vivo Cell Lineage Analysis During Chemical Hepatocarcinogenesis in Rats Using Retroviral-Mediated Gene Transfer: Evidence for Dedifferentiation of Mature Hepatocytes

N. Ferry, M. Bralet, V. Pichard, 2002, Laboratory Investigation.

Efficient retroviral gene transfer to the liver in vivo using nonpolypeptidic mitogens.

D. Aubert, N. Ferry, V. Pichard, 2001, Biochemical and biophysical research communications.

A new surgical approach to improve gene transfer in liver using lentiviral vectors.

D. Aubert, N. Ferry, V. Pichard, 2009, Journal of pediatric surgery.

In-vivo retroviral gene transfer to the liver is cancelled by an immune response against the corrected cells. Can it be avoided?

D. Aubert, N. Ferry, V. Pichard, 2002, Pediatric Surgery International.

Long term transgene expression by hepatocytes transduced with retroviral vectors requires induction of immune tolerance to the transgene.

I. Anegon, N. Ferry, M. Cuturi, 2004, Journal of hepatology.

No tumour-initiating risk associated with scAAV transduction in newborn rat liver

D. Aubert, N. Ferry, S. Conchon, 2013, Gene Therapy.

Priming of hepatocytes enhances in vivo liver transduction with lentiviral vectors in adult mice.

N. Ferry, V. Pichard, T. Nguyen, 2012, Human gene therapy methods.

In vivo cell lineage analysis in cyproterone acetate–treated rat liver using genetic labeling of hepatocytes

D. Aubert, N. Ferry, N. Robillard, 2002, Hepatology.

AAV gene transfer to the retina does not protect retrovirally transduced hepatocytes from the immune response

D. Aubert, N. Ferry, F. Rolling, 2004, Journal of Molecular Medicine.

Polyploidization without mitosis improves in vivo liver transduction with lentiviral vectors.

N. Ferry, C. Desdouets, V. Pichard, 2013, Human gene therapy.

A transgenic mouse with beta-Galactosidase as a fetal liver self-antigen for immunotherapy studies.

D. Aubert, J. Cany, N. Ferry, 2007, Journal of hepatology.

Vitrectomy Before Intravitreal Injection of AAV2/2 Vector Promotes Efficient Transduction of Retinal Ganglion Cells in Dogs and Nonhuman Primates.

S. Nedellec, F. Rolling, V. Pichard, 2016, Human gene therapy methods.

Specific Micro RNA-Regulated TetR-KRAB Transcriptional Control of Transgene Expression in Viral Vector-Transduced Cells

D. Aubert, P. Arbuthnot, N. Ferry, 2012, PloS one.

Transient expression of genes delivered to newborn rat liver using recombinant adeno‐associated virus 2/8 vectors

D. Aubert, N. Ferry, Manfred Schmidt, 2009, The journal of gene medicine.

Cells of origin of small hepatocyte-like progenitor cells in the retrorsine model of rat liver injury and regeneration

N. Ferry, V. Pichard, 2008 .

Cytotoxic immune response blunts long-term transgene expression after efficient retroviral-mediated hepatic gene transfer in rat.

D. Aubert, L. Tesson, S. Ménoret, 2002, Molecular therapy : the journal of the American Society of Gene Therapy.

Mixed hematopoietic molecular chimerism results in permanent transgene expression from retrovirally transduced hepatocytes in mice

N. Ferry, V. Pichard, M. Bellodi-Privato, 2006, The journal of gene medicine.

In the rat liver, Adenoviral gene transfer efficiency is comparable to AAV

P. Bosma, D. Aubert, N. Ferry, 2013, Gene Therapy.

Long term phenobarbital administration does not promote the multiplication of hepatocytes replicating after single cyproterone acetate administration.

N. Ferry, V. Pichard, 2005, Life sciences.

Cytotoxic immune response after retroviral-mediated hepatic gene transfer in rat does not preclude expression from adeno-associated virus 1 transduced muscles.

D. Aubert, N. Ferry, V. Pichard, 2003, Human gene therapy.

Identification of Tribbles-1 as a Novel Binding Partner of Foxp3 in Regulatory T Cells*

E. Kiss-Toth, S. Conchon, S. Brouard, 2013, The Journal of Biological Chemistry.

Mannose-coupled AAV2: a second generation AAV vector for increased retinal gene therapy efficiency

E. Ayuso, A. Galy, M. Mével, 2022, bioRxiv.

Intravitreal air tamponade after AAV2 subretinal injection modifies retinal EGFP distribution

A. Galy, M. Mével, V. Pichard, 2023, Molecular therapy. Methods & clinical development.

Long-term expression of melanopsin and channelrhodopsin causes no gross alterations in the dystrophic dog retina

C. Guihal, S. Picaud, V. Pichard, 2017, Gene Therapy.

lacZ transgenic rats tolerant for beta-galactosidase: recipients for gene transfer studies using lacZ as a reporter gene.

D. Aubert, L. Tesson, S. Ménoret, 2002, Human gene therapy.

Brief Report lacZ Transgenic Rats Tolerant for b-Galactosidase: Recipients for Gene Transfer Studies Using lacZ as a Reporter Gene

D. Aubert, L. Tesson, I. Anegon, 2002 .