Á. Jáni

发表

Persistence of plasmid DNA and expression in rat brain cells in vivo

G. Acsadi, P. Felgner, J. Wolff, 1992, Experimental Neurology.

Direct gene transfer into mouse muscle in vivo.

G. Acsadi, R. Malone, P. Felgner, 1990, Science.

Gene transfer into skeletal muscles by isogenic myoblasts.

G. Acsadi, J. Huard, Á. Jáni, 1994, Human gene therapy.

Efficiency and functional consequences of adenovirus-mediated in vivo gene transfer to normal and dystrophic (mdx) mouse diaphragm.

Hanns Lochmüller, G. Acsadi, Á. Jáni, 1995, American journal of respiratory cell and molecular biology.

Increased survival and function of SOD1 mice after glial cell-derived neurotrophic factor gene therapy.

R. Lewis, G. Toth, M. Shy, 2002, Human gene therapy.

Cultured human myoblasts and myotubes show markedly different transducibility by replication-defective adenovirus recombinants.

Hanns Lochmüller, G. Acsadi, J. Huard, 1994, Gene therapy.

Direct gene transfer and expression into rat heart in vivo.

G. Acsadi, J. Wolff, S. Jiao, 1991, The New biologist.

Generation, validation, and large scale production of adenoviral recombinants with large size inserts such as a 6.3 kb human dystrophin cDNA.

Hanns Lochmüller, G. Acsadi, A. Garnier, 1997, Journal of virological methods.

Interferons impair early transgene expression by adenovirus-mediated gene transfer in muscle cells

H. Lochmüller, G. Acsadi, J. Nalbantoglu, 1998, Journal of Molecular Medicine.

A differential efficiency of adenovirus-mediated in vivo gene transfer into skeletal muscle cells of different maturity.

G. Acsadi, Á. Jáni, B. Massie, 1994, Human molecular genetics.

Overcoming Cellular Immunity to Prolong Adenoviral‐Mediated Gene Expression in Sciatic Nerve

M. Shy, J. Kamholz, G. Acsadi, 1999, Annals of the New York Academy of Sciences.

Modulation of cell-mediated immunity prolongs adenovirus-mediated transgene expression in sciatic nerve.

M. Shy, H. Jiang, J. Kamholz, 1999, Human gene therapy.

Differential short-term transduction efficiency of adult versus newborn mouse tissues by adenoviral recombinants.

Hanns Lochmüller, G. Acsadi, C. Guérin, 1995, Experimental and molecular pathology.

Human dystrophin expression in mdx mice after intramuscular injection of DNA constructs

K. Davies, F. Walsh, G. Dickson, 1991, Nature.

Emergence of Early Region 1-Containing Replication-Competent Adenovirus in Stocks of Replication-Defective Adenovirus Recombinants (ΔE1 + ΔE3) During Multiple Passages in 293 Cells

Hanns Lochmüller, G. Acsadi, J. Huard, 1994 .

Differential contribution of fimbria and fornix fibers to behavior.

G. Buzsáki, G. Acsadi, Á. Jáni, 1980, Behavioral and neural biology.

The route of administration is a major determinant of the transduction efficiency of rat tissues by adenoviral recombinants.

Hanns Lochmüller, G. Acsadi, J. Huard, 1995, Gene therapy.

Long-term persistence of plasmid DNA and foreign gene expression in mouse muscle.

G. Acsadi, J. Wolff, J. Ludtke, 1992, Human molecular genetics.

Adenovirus-mediated gene transfer into striated muscles

G. Acsadi, Á. Jáni, B. Massie, 1995, Journal of Molecular Medicine.

Charcot-Marie-Tooth disease type 1: molecular pathogenesis to gene therapy.

S. Scherer, M. Shy, J. Lilien, 2000, Brain : a journal of neurology.

Dystrophin expression in muscles of mdx mice after adenovirus-mediated in vivo gene transfer.

Hanns Lochmüller, G. Acsadi, J. Huard, 1996, Human gene therapy.

Phenotypic clustering in MPZ mutations.

Richard A Lewis, Jun Li, Michael E Shy, 2004, Brain : a journal of neurology.

Toxicity of Replication-Defective Adenoviral Recombinants in Dissociated Cultures of Nervous Tissue

Hanns Lochmüller, G. Acsadi, Á. Jáni, 1996, Experimental Neurology.

Conditions affecting direct gene transfer into rodent muscle in vivo.

G. Acsadi, J. Wolff, S. Jiao, 1991, BioTechniques.

Efficient muscle-specific transgene expression after adenovirus-mediated gene transfer in mice using a 1.35 kb muscle creatine kinase promoter/enhancer

H. Lochmüller, J. Nalbantoglu, Á. Jáni, 1997, Gene Therapy.

Myophosphorylase gene transfer in McArdle’s disease myoblasts in vitro

G. Pari, E. Shoubridge, S. Dimauro, 1999, Neurology.

Emergence of early region 1-containing replication-competent adenovirus in stocks of replication-defective adenovirus recombinants (delta E1 + delta E3) during multiple passages in 293 cells.

Hanns Lochmüller, G. Acsadi, J. Huard, 1994, Human gene therapy.