Fei-Ming Li

Genetic correction of p67phox deficient chronic granulomatous disease using peripheral blood progenitor cells as a target for retrovirus mediated gene transfer.

H. Malech, N. Whiting-Theobald, G. Linton, 1997, Blood.

CD34+ peripheral blood progenitors as a target for genetic correction of the two flavocytochrome b558 defective forms of chronic granulomatous disease

H. Malech, N. Whiting-Theobald, G. Linton, 1994 .

Genetic Correction of p 67 phox Deficient Chronic Granulomatous Disease Using Peripheral Blood Progenitor Cells as a Target for Retrovirus Mediated Gene Transfer

H. Malech, N. Whiting-Theobald, G. Linton, 1997 .

Altered MARCH1 ubiquination-regulated dendritic cell immune functions during the early stage of zymosan-induced multiple organ dysfunction syndrome (MODS) in mice.

Hong-wei Wang, Qian Liu, Fei-Ming Li, 2013, Immunology letters.

CD 34 + Peripheral Blood Progenitors as a Target for Genetic Correction of the Two Flavocytochrome bSs 8 Defective Forms of Chronic Granulomatous Disease

Harry, John, Julie, 2000 .

The granulocyte macrophage-colony stimulating factor surface modified MB49 bladder cancer stem cells vaccine against metastatic bladder cancer.

Cheng-yong Lei, Yong-tong Zhu, Wan-long Tan, 2014, Stem cell research.

Prolonged production of NADPH oxidase-corrected granulocytes after gene therapy of chronic granulomatous disease.

S. Holland, T. Fleisher, C. Maack, 1997, Proceedings of the National Academy of Sciences of the United States of America.

A bicistronic retrovirus vector containing a picornavirus internal ribosome entry site allows for correction of X-linked CGD by selection for MDR1 expression.

M. Gottesman, Y. Sugimoto, H. Malech, 1996, Blood.