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Kate Dishart

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Angelika B Kritz; Campbell G Nicol; Kate L Dishart; Ruth Nelson; Susan Holbeck; Dan J Von Seggern; Lorraine M Work; John H McVey; Stuart A Nicklin; Andrew H Baker
Adenovirus 5 fibers mutated at the putative HSPG-binding site show restricted retargeting with targeting peptides in the HI loop.
Lorraine M Work; Stuart A Nicklin; Nick J R Brain; Kate L Dishart; Dan J Von Seggern; Michael Hallek; Hildegard Büning; Andrew H Baker
Development of efficient viral vectors selective for vascular smooth muscle cells.
Stuart A Nicklin; Kate L Dishart; Hildegard Buening; Paul N Reynolds; Michael Hallek; Glen R Nemerow; Dan J Von Seggern; Andrew H Baker
Transductional and transcriptional targeting of cancer cells using genetically engineered viral vectors.

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All Publications

2007: Angelika B Kritz; Campbell G Nicol; Kate L Dishart; Ruth Nelson; Susan Holbeck; Dan J Von Seggern; Lorraine M Work; John H McVey; Stuart A Nicklin; Andrew H Baker
Adenovirus 5 fibers mutated at the putative HSPG-binding site show restricted retargeting with targeting peptides in the HI loop.
Molecular therapy : the journal of the American Society of Gene Therapy 2007;15(4):741-9.
2004: Lorraine M Work; Stuart A Nicklin; Nick J R Brain; Kate L Dishart; Dan J Von Seggern; Michael Hallek; Hildegard Büning; Andrew H Baker
Development of efficient viral vectors selective for vascular smooth muscle cells.
Molecular therapy : the journal of the American Society of Gene Therapy 2004;9(2):198-208.
2003: Stuart A Nicklin; Kate L Dishart; Hildegard Buening; Paul N Reynolds; Michael Hallek; Glen R Nemerow; Dan J Von Seggern; Andrew H Baker
Transductional and transcriptional targeting of cancer cells using genetically engineered viral vectors.
Cancer letters 2003;201(2):165-73.
2003: Kate L Dishart; Laura Denby; Sarah George; Stuart A Nicklin; Satya Yendluri; Melanie J Tuerk; Michael P Kelley; Brian A Donahue; Andrew C Newby; Thomas C Harding; Andrew H Baker
Third-generation lentivirus vectors efficiently transduce and phenotypically modify vascular cells: implications for gene therapy.
Journal of molecular and cellular cardiology 2003;35(7):739-48.
2001: Stuart A Nicklin; Hildegard Buening; Kate L Dishart; Mahesh De Alwis; A Girod; Ulrich T Hacker; Adrian J Thrasher; Robin R Ali; Michael Hallek; Andrew H Baker
Efficient and selective AAV2-mediated gene transfer directed to human vascular endothelial cells.
Molecular therapy : the journal of the American Society of Gene Therapy 2001;4(3):174-81.