Hebbel, Robert P.

Heme triggers TLR4 signaling leading to endothelial cell activation and vaso-occlusion in murine sickle cell disease

Belcher, J. D., Chen, C., Nguyen, J., Milbauer, L., Abdulla, F., Alayash, A. I., Smith, A., Nath, K. A., Hebbel, R. P., & Vercellotti, G. M. (2014) · Blood

Hemoglobinopathies and Related DisordersHemoglobin structure and function

Cited by 695

Vasculopathy in sickle cell disease: Biology, pathophysiology, genetics, translational medicine, and new research directions

Kato, G. J., Hebbel, R. P., Steinberg, M. H., & Gladwin, M. T. (2009) · American Journal of Hematology

Hemoglobinopathies and Related DisordersBlood properties and coagulation

Cited by 349

Accelerated autoxidation and heme loss due to instability of sickle hemoglobin.

Hebbel, R. P., Morgan, W. T., Eaton, J. W., & Hedlund, B. E. (1988) · Proceedings of the National Academy of Sciences

Hemoglobinopathies and Related DisordersHemoglobin structure and function

Cited by 306

Human llamas: adaptation to altitude in subjects with high hemoglobin oxygen affinity.

Hebbel, R. P., Eaton, J. W., Kronenberg, R. S., Zanjani, E. D., Moore, L. G., & Berger, E. M. (1978) · Journal of Clinical Investigation

High Altitude and HypoxiaHemoglobin structure and function

Cited by 135

Differential Expression of E‐ and P‐Selectin in the Microvasculature of Sickle Cell Transgenic Mice

Wood, K., Russell, J., Hebbel, R. P., & Granger, D. N. (2004) · Microcirculation

Hemoglobinopathies and Related DisordersBlood properties and coagulation

Cited by 42