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Tucker, R P, C Hagios, R Chiquet-Ehrismann, and J Lawler. 1997. “In Situ Localization of Thrombospondin-1 and Thrombospondin-3 Transcripts in the Avian Embryo.”. Developmental Dynamics : An Official Publication of the American Association of Anatomists 208 (3): 326-37.

Adams, J C, and J Lawler. 1994. “Cell-Type Specific Adhesive Interactions of Skeletal Myoblasts With Thrombospondin-1.”. Molecular Biology of the Cell 5 (4): 423-37.

Corless, C L, A Mendoza, T Collins, and J Lawler. 1992. “Colocalization of Thrombospondin and Syndecan During Murine Development.”. Developmental Dynamics : An Official Publication of the American Association of Anatomists 193 (4): 346-58.

Lawler, J, M Duquette, and P Ferro. 1991. “Cloning and Sequencing of Chicken Thrombospondin.”. The Journal of Biological Chemistry 266 (13): 8039-43.

Lambert, S, H Yu, J T Prchal, J Lawler, P Ruff, D Speicher, M C Cheung, Y W Kan, and J Palek. 1990. “CDNA Sequence for Human Erythrocyte Ankyrin.”. Proceedings of the National Academy of Sciences of the United States of America 87 (5): 1730-4.

Cohen, A M, S C Liu, J Lawler, L Derick, and J Palek. 1988. “Identification of the Protein 4.1 Binding Site to Phosphatidylserine Vesicles.”. Biochemistry 27 (2): 614-9.

Clezardin, P, N R Hunter, J Lawler, J Dawes, and J L McGregor. 1987. “Production, Characterization, and Use of Monoclonal Antibodies Directed Against Human Blood Platelet Thrombospondin: Immunologic Comparison With Human Endothelial and Fibroblast Thrombospondins.”. Seminars in Thrombosis and Hemostasis 13 (3): 261-75.

Lawler, J, and R O Hynes. 1986. “The Structure of Human Thrombospondin, an Adhesive Glycoprotein With Multiple Calcium-Binding Sites and Homologies With Several Different Proteins.”. The Journal of Cell Biology 103 (5): 1635-48.

Lahav, J, J Lawler, and M A Gimbrone. 1984. “Thrombospondin Interactions With Fibronectin and Fibrinogen. Mutual Inhibition in Binding.”. European Journal of Biochemistry 145 (1): 151-6.

Lawler, J, S C Liu, J Palek, and J Prchal. 1984. “A Molecular Defect of Spectrin in a Subset of Patients With Hereditary Elliptocytosis. Alterations in the Alpha-Subunit Domain Involved in Spectrin Self-Association.”. The Journal of Clinical Investigation 73 (6): 1688-95.