624 adenovirus targeting to c erbb 2 oncoprotein by single chain antibody using recombinant adapter protein or genetic modification of viral capsid

624 Adenovirus Targeting to c erbB 2 Oncoprotein by Single Chain Antibody Using Recombinant Adapter Protein or Genetic Modification of Viral Capsid Molecular Therapy Vol 5, No 5, May 2002, Part 2 of 2[.]

Molecular Therapy Vol 5, No 5, May 2002, Part 2 of 2 Parts

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621 Highly Prostate-Specific Gene T

621 Highly Prostate-Specific Gene Transfer by a ransfer by a

Complex

Complex Adenovirus V Adenovirus V Adenovirus Vector Containing a Novel TRE- ector Containing a Novel

TRE-Probasin Control System

Jan Woraratanadharm, 1 Semyon Rubinchik, 1 Hong Yu, 1 Jian-yun

Dong 1

1 Microbiology and Immunology, Medical University of South

Carolina, Charleston, SC, United States.

622 Double Modification of Adenoviral Fiber Protein

with RGD and Polylysine Motifs

Hongju Wu, 1 Toshiro Seki, 1 Taco Uil, 1 Igor Dmitriev, 1 Elena

Kashentseva, 1 David T Curiel 1

1 Division of Human Gene Therapy, University of Alabama at

Birmingham, Birmingham, AL, United States.

623 Use of Grp78 Promoter for T

623 Use of Grp78 Promoter for Tumor Selective umor Selective Stress Inducible Regulation of V

Stress Inducible Regulation of Virus V irus V irus Vector T ector T ector Transgene ransgene Expression and Regulation

Tack-Kee L Yoon, 1 Chris Logg, 1 Toshiaki Shichinohe, 1 Chien Kuo Tai, 1 Amy S Lee, 2 Noriyuki Kasahara 1

1 Institute for Genetic Medicine, USC Keck School of Medicine, Los Angeles, CA, United States; 2 Norris Jr Comprehensive Cancer Center, USC Keck School of Medicine, Los Angeles, CA, United States.

624

624 Adenovirus T Adenovirus T Adenovirus Targeting to c-erbB-2 Oncoprotein by argeting to c-erbB-2 Oncoprotein by Single-Chain Antibody Using Recombinant Adapter Protein or Genetic Modification of Viral Capsid

Igor P Dmitriev, 1 Elena A Kashentseva, 1 David T Curiel 1,2

1 Division of Human Gene Therapy, Departments of Medicine, Pathology, and Surgery; 2 The Gene Therapy Center, University of Alabama at Birmingham, Birmingham, Alabama, United States.

Molecular Therapy Vol 5, No 5, May 2002, Part 2 of 2 Parts Copyright © The American Society of Gene Therapy

S204

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625 Design of Chemically Modified Virus for Cell

T

Targeting argeting

Hoyin S Mok, 1,2 Michael A Barry 1,2,3

1 Bioengineeering, Rice University, Houston, Texas, United States;

2 Center of Cell and Gene Therapy, Baylor College of Medicine,

Houston, Texas, United States; 3 Molecular Genetics, Baylor

College of Medicine, Houston, Texas, United States.

626 Improved

626 Improved Adenoviral V Adenoviral V Adenoviral Vectors T ectors T ectors To Enhance Gene o Enhance Gene Delivery to Human Saphenous V

Delivery to Human Saphenous Vein Grafts ein Grafts

Lorraine M Work, 1 Stuart A Nicklin, 1 Nick J R Brain, 1 Victor Krasnykh, 2 David T Curiel, 2 Paul N Reynolds, 3 Andrew H Baker 1

1 Department of Medicine & Therapeutics, University of Glasgow, Glasgow, United Kingdom; 2 Gene Therapy Center, University of Alabama at Birmingham, Birmingham, AL, United States;

3 Department of Thoracic Medicine, Royal Adelaide Hospital, Adelaide, Australia.