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Archivum Immunologiae Et Therapiae Experimentalis|July 27, 2000

A burgeoning family of biological mediators: chemokines and chemokine receptorsY Le, W Gong, W Shen, et al.

Forum (Genoa, Italy)|December 28, 1999

A new insight into the role of "old" chemotactic peptide receptors FPR and FPRL1: down-regulation of chemokine receptors CCR5 and CXCR4Y Le, W Shen, B Li, et al.

The Journal of General Virology|October 1, 1982

Persistence of one species of oncovirus in mixed infection after antiserum treatment or transspecies rescueP J Fischinger, W G Robey, D G Blair, et al.

Journal of Immunology (Baltimore, Md. : 1950)|June 15, 1990

Epitopes recognized by the neutralizing antibodies of an HIV-1-infected individualA T Profy, P A Salinas, L I Eckler, et al.

Journal of Leukocyte Biology|July 4, 2001

Synthetic peptide MMK-1 is a highly specific chemotactic agonist for leukocyte FPRL1J Y Hu, Y Le, W Gong, et al.

Immunological Reviews|January 4, 2001

Novel pathophysiological role of classical chemotactic peptide receptors and their communications with chemokine receptorsY Le, B Li, W Gong, et al.

Science (New York, N.Y.)|August 5, 1988

Synthetic CD4 peptide derivatives that inhibit HIV infection and cytopathicityJ D Lifson, K M Hwang, P L Nara, et al.

Journal of Immunology (Baltimore, Md. : 1950)|December 10, 1999

Utilization of two seven-transmembrane, G protein-coupled receptors, formyl peptide receptor-like 1 and formyl peptide receptor, by the synthetic hexapeptide WKYMVm for human phagocyte activationY Le, W Gong, B Li, et al.

Clinical Immunology (Orlando, Fla.)|August 31, 2000

N36, a synthetic N-terminal heptad repeat domain of the HIV-1 envelope protein gp41, is an activator of human phagocytesY Le, S Jiang, J Hu, et al.

Journal of Immunology (Baltimore, Md. : 1950)|May 7, 1999

T21/DP107, A synthetic leucine zipper-like domain of the HIV-1 envelope gp41, attracts and activates human phagocytes by using G-protein-coupled formyl peptide receptorsS B Su, J l Gao, W h Gong, et al.

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Showing results (11-20 of 26) with videos related to

Sort By:

Pageof 3

Archivum Immunologiae Et Therapiae Experimentalis|July 27, 2000

A burgeoning family of biological mediators: chemokines and chemokine receptorsY Le, W Gong, W Shen, et al.

Forum (Genoa, Italy)|December 28, 1999

A new insight into the role of "old" chemotactic peptide receptors FPR and FPRL1: down-regulation of chemokine receptors CCR5 and CXCR4Y Le, W Shen, B Li, et al.

The Journal of General Virology|October 1, 1982

Persistence of one species of oncovirus in mixed infection after antiserum treatment or transspecies rescueP J Fischinger, W G Robey, D G Blair, et al.

Journal of Immunology (Baltimore, Md. : 1950)|June 15, 1990

Epitopes recognized by the neutralizing antibodies of an HIV-1-infected individualA T Profy, P A Salinas, L I Eckler, et al.

Journal of Leukocyte Biology|July 4, 2001

Synthetic peptide MMK-1 is a highly specific chemotactic agonist for leukocyte FPRL1J Y Hu, Y Le, W Gong, et al.

Immunological Reviews|January 4, 2001

Novel pathophysiological role of classical chemotactic peptide receptors and their communications with chemokine receptorsY Le, B Li, W Gong, et al.

Science (New York, N.Y.)|August 5, 1988

Synthetic CD4 peptide derivatives that inhibit HIV infection and cytopathicityJ D Lifson, K M Hwang, P L Nara, et al.

Journal of Immunology (Baltimore, Md. : 1950)|December 10, 1999

Utilization of two seven-transmembrane, G protein-coupled receptors, formyl peptide receptor-like 1 and formyl peptide receptor, by the synthetic hexapeptide WKYMVm for human phagocyte activationY Le, W Gong, B Li, et al.

Clinical Immunology (Orlando, Fla.)|August 31, 2000

N36, a synthetic N-terminal heptad repeat domain of the HIV-1 envelope protein gp41, is an activator of human phagocytesY Le, S Jiang, J Hu, et al.

Journal of Immunology (Baltimore, Md. : 1950)|May 7, 1999

T21/DP107, A synthetic leucine zipper-like domain of the HIV-1 envelope gp41, attracts and activates human phagocytes by using G-protein-coupled formyl peptide receptorsS B Su, J l Gao, W h Gong, et al.

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