J. Marshall-Neff

A Genetically Modified Adenoviral Vector Exhibits Enhanced Gene Transfer of Human Smooth Muscle Cells

E. Su, M. Rollence, S. Stevenson, 2001, Journal of Vascular Research.

Overexpression of Soluble Fas Attenuates Transplant Arteriosclerosis in Rat Aortic Allografts

R. Michler, E. Herderick, P. Goldschmidt-Clermont, 2002, Circulation.

vessel wall and reduces the severity of transplant arteriosclerosis . Methods Construction of Adenoviral Vectors

R. Michler, E. Herderick, P. Goldschmidt-Clermont, 2002 .

Phenotypic correction of hypercholesterolemia in apoE-deficient mice by adenovirus-mediated in vivo gene transfer.

A. Mcclelland, S. Stevenson, B. Teng, 1995, Arteriosclerosis, thrombosis, and vascular biology.

Selective targeting of human cells by a chimeric adenovirus vector containing a modified fiber protein

M. Rollence, A. Mcclelland, S. Stevenson, 1997, Journal of virology.

Adenovirus serotype 5 fiber shaft influences in vivo gene transfer in mice.

G. Nemerow, M. Rollence, M. Kaleko, 2003, Human Gene Therapy.

Receptor interactions involved in adenoviral-mediated gene delivery after systemic administration in non-human primates.

J. Markovits, M. Rollence, M. Kaleko, 2003, Human gene therapy.

Inhibition of Accelerated Graft Arteriosclerosis by Gene Transfer of Soluble Fibroblast Growth Factor Receptor-1 in Rat Aortic Transplants

R. Hruban, J. Black, B. Ballermann, 2004, Arteriosclerosis, thrombosis, and vascular biology.