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Arginine 206 of the C5a receptor is critical for ligand recognition and receptor activation by C-terminal hexapeptide analogs
Arginine 206 of the C5a receptor is critical for ligand recognition and receptor activation by C-terminal hexapeptide analogs
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Arginine 206 of the C5a receptor is critical for ligand recognition and receptor activation by C-terminal hexapeptide analogs

Demartino, J A ; Konteatis, Z D ; Siciliano, S J ; Van Riper, G ; Underwood, D J ; Fischer, P A ; Springer, M S

The Journal of biological chemistry, 07 July 1995, Vol.270(27), pp.15966-9 [Peer Reviewed Journal]

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Two-site binding of C5a by its receptor: an alternative binding paradigm for G protein-coupled receptors
Two-site binding of C5a by its receptor: an alternative binding paradigm for G protein-coupled receptors
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Two-site binding of C5a by its receptor: an alternative binding paradigm for G protein-coupled receptors

Siciliano, S J ; Rollins, T E ; Demartino, J ; Konteatis, Z ; Malkowitz, L ; Van Riper, G ; Bondy, S ; Rosen, H ; Springer, M S

Proceedings of the National Academy of Sciences of the United States of America, 15 February 1994, Vol.91(4), pp.1214-8 [Peer Reviewed Journal]

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3
The amino terminus of the human C5a receptor is required for high affinity C5a binding and for receptor activation by C5a but not C5a analogs
The amino terminus of the human C5a receptor is required for high affinity C5a binding and for receptor activation by C5a but not C5a analogs
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The amino terminus of the human C5a receptor is required for high affinity C5a binding and for receptor activation by C5a but not C5a analogs

Demartino, J A ; Van Riper, G ; Siciliano, S J ; Molineaux, C J ; Konteatis, Z D ; Rosen, H ; Springer, M S

The Journal of biological chemistry, 20 May 1994, Vol.269(20), pp.14446-50 [Peer Reviewed Journal]

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4
Construction and phosphorylation of a fusion protein Hu-IFN-alpha A/gamma
Construction and phosphorylation of a fusion protein Hu-IFN-alpha A/gamma
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Construction and phosphorylation of a fusion protein Hu-IFN-alpha A/gamma

Zhao, X X ; Li, B L ; Langer, J A ; Van Riper, G ; Pestka, S

Analytical biochemistry, 01 May 1989, Vol.178(2), pp.342-7 [Peer Reviewed Journal]

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A modified risk assessment to establish molybdenum standards for land application of biosolids
A modified risk assessment to establish molybdenum standards for land application of biosolids
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A modified risk assessment to establish molybdenum standards for land application of biosolids

O'Connor, G A ; Brobst, R B ; Chaney, R L ; Kincaid, R L ; Mcdowell, L R ; Pierzynski, G M ; Rubin, A ; Van Riper, G G

Journal of environmental quality, 2001, Vol.30(5), pp.1490-507 [Peer Reviewed Journal]

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Characterization and species distribution of high affinity GTP-coupled receptors for human rantes and monocyte chemoattractant protein 1
Characterization and species distribution of high affinity GTP-coupled receptors for human rantes and monocyte chemoattractant protein 1
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Characterization and species distribution of high affinity GTP-coupled receptors for human rantes and monocyte chemoattractant protein 1

Van Riper, G ; Siciliano, S ; Fischer, P A ; Meurer, R ; Springer, M S ; Rosen, H

The Journal of experimental medicine, 01 March 1993, Vol.177(3), pp.851-6 [Peer Reviewed Journal]

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7
Formation of eosinophilic and monocytic intradermal inflammatory sites in the dog by injection of human RANTES but not human monocyte chemoattractant protein 1, human macrophage inflammatory protein 1 alpha, or human interleukin 8
Formation of eosinophilic and monocytic intradermal inflammatory sites in the dog by injection of human RANTES but not human monocyte chemoattractant protein 1, human macrophage inflammatory protein 1 alpha, or human interleukin 8
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Formation of eosinophilic and monocytic intradermal inflammatory sites in the dog by injection of human RANTES but not human monocyte chemoattractant protein 1, human macrophage inflammatory protein 1 alpha, or human interleukin 8

Meurer, R ; Van Riper, G ; Feeney, W ; Cunningham, P ; Hora, D ; Springer, M S ; Macintyre, D E ; Rosen, H

The Journal of experimental medicine, 01 December 1993, Vol.178(6), pp.1913-21 [Peer Reviewed Journal]

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8
The discovery of sulfonylated dipeptides as potent VLA-4 antagonists
The discovery of sulfonylated dipeptides as potent VLA-4 antagonists
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The discovery of sulfonylated dipeptides as potent VLA-4 antagonists

Hagmann, W K ; Durette, P L ; Lanza, T ; Kevin, N J ; De Laszlo, S E ; Kopka, I E ; Young, D ; Magriotis, P A ; Li, B ; Lin, L S ; Yang, G ; Kamenecka, T ; Chang, L L ; Wilson, J ; Maccoss, M ; Mills, S G ; Van Riper, G ; Mccauley, E ; Egger, L A ; Kidambi, U ; Lyons, K ; Vincent, S ; Stearns, R ; Colletti, A ; Teffera, J ; Tong, S ; Fenyk-Melody, J ; Owens, K ; Levorse, D ; Kim, P ; Schmidt, J A ; Mumford, R A

Bioorganic & medicinal chemistry letters, 22 October 2001, Vol.11(20), pp.2709-13 [Peer Reviewed Journal]

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