Convenient solid-phase synthesis of diethylenetriaminepenta-acetic acid (DTPA)- conjugated cyclic RGD peptide analogues.

MLA

Wang, Wei, et al. “Convenient Solid-Phase Synthesis of Diethylenetriaminepenta-Acetic Acid (DTPA)- Conjugated Cyclic RGD Peptide Analogues.” Cancer Biotherapy & Radiopharmaceuticals, vol. 20, no. 5, Oct. 2005, pp. 547–56. EBSCOhost, https://doi.org/10.1089/cbr.2005.20.547.

APA

Wang, W., McMurray, J. S., Wu, Q., Campbell, M. L., & Li, C. (2005). Convenient solid-phase synthesis of diethylenetriaminepenta-acetic acid (DTPA)- conjugated cyclic RGD peptide analogues. Cancer Biotherapy & Radiopharmaceuticals, 20(5), 547–556. https://doi.org/10.1089/cbr.2005.20.547

Chicago

Wang, Wei, John S McMurray, Qingping Wu, Martin L Campbell, and Chun Li. 2005. “Convenient Solid-Phase Synthesis of Diethylenetriaminepenta-Acetic Acid (DTPA)- Conjugated Cyclic RGD Peptide Analogues.” Cancer Biotherapy & Radiopharmaceuticals 20 (5): 547–56. doi:10.1089/cbr.2005.20.547.