Richard C. Mulligan

Generation and characterization of urokinase receptor-deficient mice.

P. Carmeliet, R. Mulligan, L. Moons, 1996, The Journal of clinical investigation.

Ovulation efficiency is reduced in mice that lack plasminogen activator gene function: functional redundancy among physiological plasminogen activators.

P. Carmeliet, R. Mulligan, D. Collen, 1995, Proceedings of the National Academy of Sciences of the United States of America.

Biological Effects of Disruption of the Tissue‐Type Plasminogen Activator, Urokinase‐Type Plasminogen Activator, and Plasminogen Activator Inhibitor‐1 Genes in Mice a

P. Carmeliet, C. Clercq, R. Mulligan, 1994, Annals of the New York Academy of Sciences.

Effects of retroviral vector design on expression of human adenosine deaminase in murine bone marrow transplant recipients engrafted with genetically modified cells.

R. Mulligan, I. Rivière, K. Brose, 1995, Proceedings of the National Academy of Sciences of the United States of America.

Plasminogen activator inhibitor-1 gene-deficient mice. I. Generation by homologous recombination and characterization.

P. Carmeliet, M. Cole, G. Prendergast, 1993, The Journal of clinical investigation.

Dispensable sequence motifs in the RAG-1 and RAG-2 genes for plasmid V(D)J recombination.

D. Baltimore, R. Mulligan, D. Silver, 1993, Proceedings of the National Academy of Sciences of the United States of America.

High-efficiency gene transfer into mammalian cells: generation of helper-free recombinant retrovirus with broad mammalian host range.

R. Mulligan, R. Cone, Richard C. Mulligan, 1984, Proceedings of the National Academy of Sciences of the United States of America.

Retroviral-mediated transfer and expression of human beta-globin genes in cultured murine and human erythroid cells.

I. London, R. Mulligan, R. Cone, 1988, The Journal of biological chemistry.

Retroviral transfer of a murine cDNA for multidrug resistance confers pleiotropic drug resistance to cells without prior drug selection.

D. Housman, R. Mulligan, P. Gros, 1988, Proceedings of the National Academy of Sciences of the United States of America.

Genetically modified keratinocytes transplanted to wounds reconstitute the epidermis.

P. Vogt, R. Mulligan, E. Eriksson, 1994, Proceedings of the National Academy of Sciences of the United States of America.

Two dominant-acting selectable markers for gene transfer studies in mammalian cells.

R. Mulligan, S. Hartman, Richard C. Mulligan, 1988, Proceedings of the National Academy of Sciences of the United States of America.