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Results: 1-25 | 26-29
Results: 1-25/29
COMPLEMENT DEPLETION IMPROVES NEUROLOGICAL FUNCTION IN CEREBRAL-ISCHEMIA
Authors: VASTHARE US BARONE FC SARAU HM ROSENWASSER RH DIMARTINO M YOUNG WF TUMA RF
Citation: Us. Vasthare et al., COMPLEMENT DEPLETION IMPROVES NEUROLOGICAL FUNCTION IN CEREBRAL-ISCHEMIA, Brain research bulletin, 45(4), 1998, pp. 413-419
FUNCTIONAL, EXPRESSION OF THE HUMAN C3A RECEPTOR IN HEK-293 CELLS BY COEXPRESSION WITH G-ALPHA-16
Authors: AMES RS TORNETTA MA FOLEY JJ SARAU HM GANGULY S
Citation: Rs. Ames et al., FUNCTIONAL, EXPRESSION OF THE HUMAN C3A RECEPTOR IN HEK-293 CELLS BY COEXPRESSION WITH G-ALPHA-16, Molecular immunology, 35(6-7), 1998, pp. 2-2
CHIMERIC RECEPTORS OF THE HUMAN C3A-RECEPTOR (C3AR) AND C5A-RECEPTOR (C5AR, CD88)
Authors: CRASS T AMES RS TORNETTA MA SARAU HM FOLEY JJ KOHL J KLOS A BAUTSCH W
Citation: T. Crass et al., CHIMERIC RECEPTORS OF THE HUMAN C3A-RECEPTOR (C3AR) AND C5A-RECEPTOR (C5AR, CD88), Molecular immunology, 35(6-7), 1998, pp. 143-143
HUMAN C4A ANAPHYLATOXIN ELICITS C3A-RECEPTOR MEDIATED EFFECTS IN GUINEA-PIGS BUT NOT IN MAN
Authors: LIENENKLAUS S AMES RS TORNETTA MA SARAU HM FOLEY JJ CRASS T SOHNS B RAFFETSEDER U GROVE M HOLZER A KLOS A KOHL J BAUTSCH W
Citation: S. Lienenklaus et al., HUMAN C4A ANAPHYLATOXIN ELICITS C3A-RECEPTOR MEDIATED EFFECTS IN GUINEA-PIGS BUT NOT IN MAN, Molecular immunology, 35(6-7), 1998, pp. 144-144
CUTTING EDGE - HUMAN ANAPHYLATOXIN C4A IS A POTENT AGONIST OF THE GUINEA-PIG BUT NOT THE HUMAN C3A RECEPTOR
Authors: LIENENKLAUS S AMES RS TORNETTA MA SARAU HM FOLEY JJ CRASS T SOHNS B RAFFETSEDER U GROVE M HOLZER A KLOS A KOHL J BAUTSCH W
Citation: S. Lienenklaus et al., CUTTING EDGE - HUMAN ANAPHYLATOXIN C4A IS A POTENT AGONIST OF THE GUINEA-PIG BUT NOT THE HUMAN C3A RECEPTOR, The Journal of immunology (1950), 161(5), 1998, pp. 2089-2093
IDENTIFICATION OF A POTENT, SELECTIVE NONPEPTIDE CXCR2 ANTAGONIST THAT INHIBITS INTERLEUKIN-8-INDUCED NEUTROPHIL MIGRATION
Authors: WHITE JR LEE JM YOUNG PR HERTZBERG RP JUREWICZ AJ CHAIKIN MA WIDDOWSON K FOLEY JJ MARTIN LD GRISWOLD DE SARAU HM
Citation: Jr. White et al., IDENTIFICATION OF A POTENT, SELECTIVE NONPEPTIDE CXCR2 ANTAGONIST THAT INHIBITS INTERLEUKIN-8-INDUCED NEUTROPHIL MIGRATION, The Journal of biological chemistry, 273(17), 1998, pp. 10095-10098
CLONING AND FUNCTIONAL-CHARACTERIZATION OF A NOVEL HUMAN CC-CHEMOKINETHAT BINDS TO THE CCR3 RECEPTOR AND ACTIVATES HUMAN EOSINOPHILS
Authors: WHITE JR IMBURGIA C DUL E APPELBAUM E ODONNELL K OSHANNESSY DJ BRAWNER M FORNWALD J ADAMOU J ELSHOURBAGY NA KAISER K FOLEY JJ SCHMIDT DB JOHANSON K MACPHEE C MOORES K MCNULTY D SCOTT GF SCHLEIMER RP SARAU HM
Citation: Jr. White et al., CLONING AND FUNCTIONAL-CHARACTERIZATION OF A NOVEL HUMAN CC-CHEMOKINETHAT BINDS TO THE CCR3 RECEPTOR AND ACTIVATES HUMAN EOSINOPHILS, Journal of leukocyte biology, 62(5), 1997, pp. 667-675
EVIDENCE THAT THE RECEPTOR FOR C4A IS DISTINCT FROM THE C3A RECEPTOR
Authors: AMES RS TORNETTA MA FOLEY JJ HUGLI TE SARAU HM
Citation: Rs. Ames et al., EVIDENCE THAT THE RECEPTOR FOR C4A IS DISTINCT FROM THE C3A RECEPTOR, Immunopharmacology, 38(1-2), 1997, pp. 87-92
CHARACTERIZATION OF FUNCTIONAL CHEMOKINE RECEPTORS (CCR1 AND CCR2) ONEOL-3 CELLS - A MODEL SYSTEM TO EXAMINE THE ROLE OF CHEMOKINES IN CELL-FUNCTION
Authors: SARAU HM RUSH JA FOLEY JJ BRAWNER ME SCHMIDT DB WHITE JR BARNETTE MS
Citation: Hm. Sarau et al., CHARACTERIZATION OF FUNCTIONAL CHEMOKINE RECEPTORS (CCR1 AND CCR2) ONEOL-3 CELLS - A MODEL SYSTEM TO EXAMINE THE ROLE OF CHEMOKINES IN CELL-FUNCTION, The Journal of pharmacology and experimental therapeutics, 283(1), 1997, pp. 411-418
NONPEPTIDE TACHYKININ RECEPTOR ANTAGONISTS .1. PHARMACOLOGICAL AND PHARMACOKINETIC CHARACTERIZATION OF SB-223412, A NOVEL, POTENT AND SELECTIVE NEUROKININ-3 RECEPTOR ANTAGONIST
Authors: SARAU HM GRISWOLD DE POTTS W FOLEY JJ SCHMIDT DB WEBB EF MARTIN LD BRAWNER ME ELSHOURBAGY NA MEDHURST AD GIARDINA GAM HAY DWP
Citation: Hm. Sarau et al., NONPEPTIDE TACHYKININ RECEPTOR ANTAGONISTS .1. PHARMACOLOGICAL AND PHARMACOKINETIC CHARACTERIZATION OF SB-223412, A NOVEL, POTENT AND SELECTIVE NEUROKININ-3 RECEPTOR ANTAGONIST, The Journal of pharmacology and experimental therapeutics, 281(3), 1997, pp. 1303-1311
DISCOVERY OF A NOVEL CLASS OF SELECTIVE NONPEPTIDE ANTAGONISTS FOR THE HUMAN NEUROKININ-3 RECEPTOR .1. IDENTIFICATION OF THE 4-QUINOLINECARBOXAMIDE FRAMEWORK
Authors: GIARDINA GAM SARAU HM FARINA C MEDHURST AD GRUGNI M RAVEGLIA LF SCHMIDT DB RIGOLIO R LUTTMANN M VECCHIETTI V HAY DWP
Citation: Gam. Giardina et al., DISCOVERY OF A NOVEL CLASS OF SELECTIVE NONPEPTIDE ANTAGONISTS FOR THE HUMAN NEUROKININ-3 RECEPTOR .1. IDENTIFICATION OF THE 4-QUINOLINECARBOXAMIDE FRAMEWORK, Journal of medicinal chemistry, 40(12), 1997, pp. 1794-1807
THE MOUSE ANAPHYLATOXIN C3A RECEPTOR - MOLECULAR-CLONING, GENOMIC ORGANIZATION, AND FUNCTIONAL EXPRESSION
Authors: TORNETTA MA FOLEY JJ SARAU HM AMES RS
Citation: Ma. Tornetta et al., THE MOUSE ANAPHYLATOXIN C3A RECEPTOR - MOLECULAR-CLONING, GENOMIC ORGANIZATION, AND FUNCTIONAL EXPRESSION, The Journal of immunology, 158(11), 1997, pp. 5277-5282
CLONING, IN-VITRO EXPRESSION, AND FUNCTIONAL-CHARACTERIZATION OF A NOVEL HUMAN CC CHEMOKINE OF THE MONOCYTE CHEMOTACTIC PROTEIN (MCP) FAMILY (MCP-4) THAT BINDS AND SIGNALS THROUGH THE CC CHEMOKINE RECEPTOR 2B
Authors: BERKHOUT TA SARAU HM MOORES K WHITE JR ELSHOURBAGY N APPELBAUM E REAPE TJ BRAWNER M MAKWANA J FOLEY JJ SCHMIDT DB IMBURGIA C MCNULTY D MATTHEWS J ODONNELL K OSHANNESSY D SCOTT M GROOT PHE MACPHEE C
Citation: Ta. Berkhout et al., CLONING, IN-VITRO EXPRESSION, AND FUNCTIONAL-CHARACTERIZATION OF A NOVEL HUMAN CC CHEMOKINE OF THE MONOCYTE CHEMOTACTIC PROTEIN (MCP) FAMILY (MCP-4) THAT BINDS AND SIGNALS THROUGH THE CC CHEMOKINE RECEPTOR 2B, The Journal of biological chemistry, 272(26), 1997, pp. 16404-16413
MOLECULAR CHARACTERIZATION OF A HUMAN CHEMOKINE RECEPTOR-LIKE THAT ISACTIVATED SELECTIVELY BY A UNIQUE CHEMOKINE CKB-4
Authors: EISHOURBAGY NA WHITE JR BRAWNER ME OSHANNESSY D GROOT PH RYNE P TEMPLETON L BERGSMA DJ SARAU HM
Citation: Na. Eishourbagy et al., MOLECULAR CHARACTERIZATION OF A HUMAN CHEMOKINE RECEPTOR-LIKE THAT ISACTIVATED SELECTIVELY BY A UNIQUE CHEMOKINE CKB-4, Circulation, 96(8), 1997, pp. 7-7
CHARACTERIZATION OF THE MONOCYTIC CHEMOKINE RECEPTOR HRBS11 - A POTENTIAL ROLE IN THE INFLAMMATORY RESPONSE TO VASCULAR INJURY
Authors: LOGAN TJ NUTHULAGANTI P WHITE JR OHLSTEIN EH SARAU HM DEBOUCK C BERGSMA DJ EISHOURBAGY NA
Citation: Tj. Logan et al., CHARACTERIZATION OF THE MONOCYTIC CHEMOKINE RECEPTOR HRBS11 - A POTENTIAL ROLE IN THE INFLAMMATORY RESPONSE TO VASCULAR INJURY, Circulation, 96(8), 1997, pp. 2819-2819
ETHYL]-3-(2-PHENYLETHOXY)-2-PYRIDINYL]-2-PROPENOIC ACID - A HIGH-AFFINITY LEUKOTRIENE B-4 RECEPTOR ANTAGONIST WITH ORAL ANTIINFLAMMATORY ACTIVITY
Authors: DAINES RA CHAMBERS PA FOLEY JJ GRISWOLD DE KINGSBURY WD MARTIN LD SCHMIDT DB SHAM KKC SARAU HM
Citation: Ra. Daines et al., ETHYL]-3-(2-PHENYLETHOXY)-2-PYRIDINYL]-2-PROPENOIC ACID - A HIGH-AFFINITY LEUKOTRIENE B-4 RECEPTOR ANTAGONIST WITH ORAL ANTIINFLAMMATORY ACTIVITY, Journal of medicinal chemistry, 39(19), 1996, pp. 3837-3841
MOLECULAR-CLONING AND CHARACTERIZATION OF THE HUMAN ANAPHYLATOXIN C3ARECEPTOR
Authors: AMES RS LI Y SARAU HM NUTHULAGANTI P FOLEY JJ ELLIS C ZENG ZZ SU K JUREWICZ AJ HERTZBERG RP BERGSMA DJ KUMAR C
Citation: Rs. Ames et al., MOLECULAR-CLONING AND CHARACTERIZATION OF THE HUMAN ANAPHYLATOXIN C3ARECEPTOR, The Journal of biological chemistry, 271(34), 1996, pp. 20231-20234
TIME-RELATED CHANGES IN MYELOPEROXIDASE ACTIVITY AND LEUKOTRIENE B-4 RECEPTOR-BINDING REFLECT LEUKOCYTE INFLUX IN CEREBRAL FOCAL STROKE
Authors: BARONE FC HILLEGASS LM TZIMAS MN SCHMIDT DB FOLEY JJ WHITE RF PRICE WJ FEUERSTEIN GZ CLARK RK GRISWOLD DE SARAU HM
Citation: Fc. Barone et al., TIME-RELATED CHANGES IN MYELOPEROXIDASE ACTIVITY AND LEUKOTRIENE B-4 RECEPTOR-BINDING REFLECT LEUKOCYTE INFLUX IN CEREBRAL FOCAL STROKE, Molecular and chemical neuropathology, 24(1), 1995, pp. 13-30
PHARMACOLOGICAL CHARACTERIZATION OF SB-202235, A POTENT AND SELECTIVE5-LIPOXYGENASE INHIBITOR - EFFECTS IN MODELS OF ALLERGIC-ASTHMA
Authors: CHABOTFLETCHER MC UNDERWOOD DC BRETON JJ ADAMS JL KAGEYSOBOTKA A GRISWOLD DE MARSHALL LA SARAU HM WINKLER JD HAY DWP
Citation: Mc. Chabotfletcher et al., PHARMACOLOGICAL CHARACTERIZATION OF SB-202235, A POTENT AND SELECTIVE5-LIPOXYGENASE INHIBITOR - EFFECTS IN MODELS OF ALLERGIC-ASTHMA, The Journal of pharmacology and experimental therapeutics, 273(3), 1995, pp. 1147-1155
SALBUTAMOL UP-REGULATES PDE4 ACTIVITY AND INDUCES A HETEROLOGOUS DESENSITIZATION OF U937 CELLS TO PROSTAGLANDIN E(2) - IMPLICATIONS FOR THETHERAPEUTIC USE OF BETA-ADRENOCEPTOR AGONISTS
Authors: TORPHY TJ ZHOU HL FOLEY JJ SARAU HM MANNING CD BARNETTE MS
Citation: Tj. Torphy et al., SALBUTAMOL UP-REGULATES PDE4 ACTIVITY AND INDUCES A HETEROLOGOUS DESENSITIZATION OF U937 CELLS TO PROSTAGLANDIN E(2) - IMPLICATIONS FOR THETHERAPEUTIC USE OF BETA-ADRENOCEPTOR AGONISTS, The Journal of biological chemistry, 270(40), 1995, pp. 23598-23604
EVIDENCE FOR A DISTINCT D-1-LIKE DOPAMINE-RECEPTOR THAT COUPLES TO ACTIVATION OF PHOSPHOINOSITIDE METABOLISM IN BRAIN
Authors: UNDIE AS WEINSTOCK J SARAU HM FRIEDMAN E
Citation: As. Undie et al., EVIDENCE FOR A DISTINCT D-1-LIKE DOPAMINE-RECEPTOR THAT COUPLES TO ACTIVATION OF PHOSPHOINOSITIDE METABOLISM IN BRAIN, Journal of neurochemistry, 62(5), 1994, pp. 2045-2048
)OCTYL]OXY]-2-PYRIDINYL]METHYL]THIO]METHYL]BENZOIC ACID AND RELATED-COMPOUNDS - HIGH-AFFINITY LEUKOTRIENE B-4 RECEPTOR ANTAGONISTS
Authors: DAINES RA CHAMBERS PA EGGLESTON DS FOLEY JJ GRISWOLD DE HALTIWANGER RC JAKAS DR KINGSBURY WD MARTIN LD PENDRAK I SCHMIDT DB TZIMAS MN SARAU HM
Citation: Ra. Daines et al., )OCTYL]OXY]-2-PYRIDINYL]METHYL]THIO]METHYL]BENZOIC ACID AND RELATED-COMPOUNDS - HIGH-AFFINITY LEUKOTRIENE B-4 RECEPTOR ANTAGONISTS, Journal of medicinal chemistry, 37(20), 1994, pp. 3327-3336
EFFECTS OF SCALARADIAL, A NOVEL INHIBITOR OF 14 KDA PHOSPHOLIPASE A(2), ON HUMAN NEUTROPHIL FUNCTION
Authors: BARNETTE MS RUSH J MARSHALL LA FOLEY JJ SCHMIDT DB SARAU HM
Citation: Ms. Barnette et al., EFFECTS OF SCALARADIAL, A NOVEL INHIBITOR OF 14 KDA PHOSPHOLIPASE A(2), ON HUMAN NEUTROPHIL FUNCTION, Biochemical pharmacology, 47(9), 1994, pp. 1661-1667
CARBOXYETHENYL)-5-[[8-(4-METHOXYPHENYL)OCTY-1]OXY] -2-PYRIDINYL]METHYL]THIO]METHYL]BENZOIC ACID - A NOVEL HIGH-AFFINITY LEUKOTRIENE B-4 RECEPTOR ANTAGONIST (VOL 36, PG 2703, 1 993)
Authors: DAINES RA CHAMBERS PA PENDRAK I JAKAS DR SARAU HM FOLEY JJ SCHMIDT DB GRISWOLD DE MARTIN LD TZIMAS MN KINGSBURY WD
Citation: Ra. Daines et al., CARBOXYETHENYL)-5-[[8-(4-METHOXYPHENYL)OCTY-1]OXY] -2-PYRIDINYL]METHYL]THIO]METHYL]BENZOIC ACID - A NOVEL HIGH-AFFINITY LEUKOTRIENE B-4 RECEPTOR ANTAGONIST (VOL 36, PG 2703, 1 993), Journal of medicinal chemistry, 36(25), 1993, pp. 4130-4130
SYNTHESIS OF STRUCTURAL ANALOGS OF LEUKOTRIENE-B(4) AND THEIR RECEPTOR-BINDING ACTIVITY
Authors: KINGSBURY WD PENDRAK I LEBER JD BOEHM JC MALLET B SARAU HM FOLEY JJ SCHMIDT DB DAINES RA
Citation: Wd. Kingsbury et al., SYNTHESIS OF STRUCTURAL ANALOGS OF LEUKOTRIENE-B(4) AND THEIR RECEPTOR-BINDING ACTIVITY, Journal of medicinal chemistry, 36(22), 1993, pp. 3308-3320
Risultati: 1-25 | 26-29