S. Fuess

发表

Unrestricted Hepatocyte Transduction with Adeno-Associated Virus Serotype 8 Vectors in Mice

Theresa A. Storm, M. Kay, H. Nakai, 2005, Journal of Virology.

Extrachromosomal Recombinant Adeno-Associated Virus Vector Genomes Are Primarily Responsible for Stable Liver Transduction In Vivo

Theresa A. Storm, M. Kay, H. Nakai, 2001, Journal of Virology.

AAV serotype 2 vectors preferentially integrate into active genes in mice

Theresa A. Storm, Eugenio Montini, M. Kay, 2003, Nature Genetics.

13. Hot Spots for rAAV2 Vector Integration in Mice

M. Kay, S. Burgess, M. Grompe, 2004 .

Helper-independent and AAV-ITR-independent chromosomal integration of double-stranded linear DNA vectors in mice.

Theresa A. Storm, M. Kay, M. Grompe, 2003, Molecular therapy : the journal of the American Society of Gene Therapy.

Preclinical in vivo evaluation of pseudotyped adeno-associated virus vectors for liver gene therapy.

Theresa A. Storm, M. Kay, D. Grimm, 2003, Blood.

BAR: An apoptosis regulator at the intersection of caspases and Bcl-2 family proteins.

A. Godzik, John Calvin Reed, S. Krajewski, 2000, Proceedings of the National Academy of Sciences of the United States of America.

Robust systemic transduction with AAV9 vectors in mice: efficient global cardiac gene transfer superior to that of AAV8.

Theresa A. Storm, M. Kay, H. Nakai, 2006, Molecular therapy : the journal of the American Society of Gene Therapy.

A Limited Number of Transducible Hepatocytes Restricts a Wide-Range Linear Vector Dose Response in Recombinant Adeno-Associated Virus-Mediated Liver Transduction

Theresa A. Storm, M. Kay, J. F. Wright, 2002, Journal of Virology.

DNA Palindromes with a Modest Arm Length of (cid:1) 20 Base Pairs Are a Signiﬁcant Target for Recombinant Adeno-Associated Virus Vector Integration in the Liver, Muscles, and Heart in Mice (cid:1)

M. Kay, S. Lewis, H. Nakai, 2007 .

Pathways of removal of free DNA vector ends in normal and DNA-PKcs-deficient SCID mouse hepatocytes transduced with rAAV vectors.

Theresa A. Storm, M. Kay, H. Nakai, 2003, Human gene therapy.

Large-Scale Molecular Characterization of Adeno-Associated Virus Vector Integration in Mouse Liver

Theresa A. Storm, Shawn M. Burgess, Eugenio Montini, 2005, Journal of Virology.

DNA Palindromes with a Modest Arm Length of ≳20 Base Pairs Are a Significant Target for Recombinant Adeno-Associated Virus Vector Integration in the Liver, Muscles, and Heart in Mice

Theresa A. Storm, M. Kay, S. Lewis, 2007, Journal of Virology.

Hepatic parenchymal replacement in mice by transplanted allogeneic hepatocytes is facilitated by bone marrow transplantation and mediated by CD4 cells

C. Trautwein, H. Blau, M. Kay, 2008, Hepatology.

Free DNA ends are essential for concatemerization of synthetic double-stranded adeno-associated virus vector genomes transfected into mouse hepatocytes in vivo.

M. Kay, H. Nakai, S. Fuess, 2003, Molecular therapy : the journal of the American Society of Gene Therapy.

A Two-hybrid Screen Identifies Cathepsins B and L as Uncoating Factors for Adeno-associated Virus 2 and 8

Dariya S. Glazer, M. Kay, D. Grimm, 2007, Molecular Therapy.

DNA palindromes with a modest arm length of greater, similar 20 base pairs are a significant target for recombinant adeno-associated virus vector integration in the liver, muscles, and heart in mice.

Theresa A. Storm, M. Kay, S. Lewis, 2007, Journal of virology.