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Results: 1-25 |
Results: 25
PALLIATIVE CARE EDUCATION FOR COMMUNITY-BASED FAMILY PHYSICIANS - THEDEVELOPMENT OF A PROGRAM, THE EVALUATION, AND ITS CONSEQUENCES
Authors: HALL P HUPE D SCOTT J
Citation: P. Hall et al., PALLIATIVE CARE EDUCATION FOR COMMUNITY-BASED FAMILY PHYSICIANS - THEDEVELOPMENT OF A PROGRAM, THE EVALUATION, AND ITS CONSEQUENCES, Journal of palliative care, 14(3), 1998, pp. 69-74
INTERDISCIPLINARY TEAMWORK IN PALLIATIVE CARE - SIMPLE IN CONCEPT BUTDIFFICULT IN PRACTICE
Authors: ELLIOTTMILLER P HUPE D SEELY JF
Citation: P. Elliottmiller et al., INTERDISCIPLINARY TEAMWORK IN PALLIATIVE CARE - SIMPLE IN CONCEPT BUTDIFFICULT IN PRACTICE, Journal of palliative care, 14(3), 1998, pp. 109-110
COMPLEMENTARY THERAPIES - A FRAMEWORK FOR THEIR INTEGRATION WITHIN INTERDISCIPLINARY PRACTICE
Authors: HUPE D LAVOIE M
Citation: D. Hupe et M. Lavoie, COMPLEMENTARY THERAPIES - A FRAMEWORK FOR THEIR INTEGRATION WITHIN INTERDISCIPLINARY PRACTICE, Journal of palliative care, 14(3), 1998, pp. 111-111
ACTINOMYCIN-D INHIBITION OF DNA STRAND TRANSFER-REACTIONS CATALYZED BY HIV-1 REVERSE-TRANSCRIPTASE AND NUCLEOCAPSID PROTEIN
Authors: DAVIS WR GABBARA S HUPE D PELISKA JA
Citation: Wr. Davis et al., ACTINOMYCIN-D INHIBITION OF DNA STRAND TRANSFER-REACTIONS CATALYZED BY HIV-1 REVERSE-TRANSCRIPTASE AND NUCLEOCAPSID PROTEIN, Biochemistry (Easton), 37(40), 1998, pp. 14213-14221
NOVEL SELECTIVE QUINAZOLINE INHIBITORS OF ENDOTHELIN-CONVERTING ENZYME-1
Authors: AHN K SISNEROS AM HERMAN SB PAN SM HUPE D LEE C NIKAM S CHENG XM DOHERTY AM SCHROEDER RL HALEEN SJ KAW S EMOTO N YANAGISAWA M
Citation: K. Ahn et al., NOVEL SELECTIVE QUINAZOLINE INHIBITORS OF ENDOTHELIN-CONVERTING ENZYME-1, Biochemical and biophysical research communications, 243(1), 1998, pp. 184-190
A NEW CLASS OF ANTI-HIV-1 AGENTS TARGETED TOWARD THE NUCLEOCAPSID PROTEIN NCP7 - THE 2,2'-DITHIOBISBENZAMIDES
Authors: DOMAGALA JM BADER JP GOGLIOTTI RD SANCHEZ JP STIER MA SONG YT PRASAD JVNV TUMMINO PJ SCHOLTEN J HARVEY P HOLLER T GRACHECK S HUPE D RICE WG SCHULTZ R
Citation: Jm. Domagala et al., A NEW CLASS OF ANTI-HIV-1 AGENTS TARGETED TOWARD THE NUCLEOCAPSID PROTEIN NCP7 - THE 2,2'-DITHIOBISBENZAMIDES, Bioorganic & medicinal chemistry, 5(3), 1997, pp. 569-579
DISCOVERING NONPEPTIDIC INHIBITORS FOR MATRIX METALLOPROTEINASES WITHTHEIR RECOMBINANT CATALYTIC DOMAINS
Authors: YE QZ JOHNSON L HUPE D
Citation: Qz. Ye et al., DISCOVERING NONPEPTIDIC INHIBITORS FOR MATRIX METALLOPROTEINASES WITHTHEIR RECOMBINANT CATALYTIC DOMAINS, The FASEB journal, 11(9), 1997, pp. 3171-3171
THE HUMAN-IMMUNODEFICIENCY-VIRUS TYPE-1 (HIV-1) NUCLEOCAPSID PROTEIN ZINC EJECTION ACTIVITY OF DISULFIDE BENZAMIDES AND BENZISOTHIAZOLONES - CORRELATION WITH ANTI-HIV AND VIRUCIDAL ACTIVITIES
Authors: TUMMINO PJ HARVEY PJ MCQUADE T DOMAGALA J GOGLIOTTI R SANCHEZ J SONG YT HUPE D
Citation: Pj. Tummino et al., THE HUMAN-IMMUNODEFICIENCY-VIRUS TYPE-1 (HIV-1) NUCLEOCAPSID PROTEIN ZINC EJECTION ACTIVITY OF DISULFIDE BENZAMIDES AND BENZISOTHIAZOLONES - CORRELATION WITH ANTI-HIV AND VIRUCIDAL ACTIVITIES, Antimicrobial agents and chemotherapy, 41(2), 1997, pp. 394-400
SYNTHESIS OF 5,6-DIHYDRO-4-HYDROXY-2-PYRONES AS HIV-1 PROTEASE INHIBITORS - THE PROFOUND EFFECT OF POLARITY ON ANTIVIRAL ACTIVITY
Authors: HAGEN SE PRASAD JVNV BOYER FE DOMAGALA JM ELLSWORTH EL GAJDA C HAMILTON HW MARKOSKI LJ STEINBAUGH BA TAIT BD LUNNEY EA TUMMINO PJ FERGUSON D HUPE D NOUHAN C GRACHECK SJ SAUNDERS JM VANDERROEST S
Citation: Se. Hagen et al., SYNTHESIS OF 5,6-DIHYDRO-4-HYDROXY-2-PYRONES AS HIV-1 PROTEASE INHIBITORS - THE PROFOUND EFFECT OF POLARITY ON ANTIVIRAL ACTIVITY, Journal of medicinal chemistry, 40(23), 1997, pp. 3707-3711
4-HYDROXY-5,6-DIHYDROPYRONES .2. POTENT NONPEPTIDE INHIBITORS OF HIV PROTEASE
Authors: TAIT BD HAGEN S DOMAGALA J ELLSWORTH EL GAJDA C HAMILTON HW PRASAD JVNV FERGUSON D GRAHAM N HUPE D NOUHAN C TUMMINO PJ HUMBLET C LUNNEY EA PAVLOVSKY A RUBIN J GRACHECK SJ BALDWIN ET BHAT TN ERICKSON JW GULNIK SV LIU BS
Citation: Bd. Tait et al., 4-HYDROXY-5,6-DIHYDROPYRONES .2. POTENT NONPEPTIDE INHIBITORS OF HIV PROTEASE, Journal of medicinal chemistry, 40(23), 1997, pp. 3781-3792
NOVEL QUINAZOLINE ENDOTHELIN-CONVERTING ENZYME-INHIBITORS
Authors: AHN KG SISNEROS AM PAN S HUPE D NIKAM S LEE C DOHERTY A KAW S EMOTO N YANAGISAWA M
Citation: Kg. Ahn et al., NOVEL QUINAZOLINE ENDOTHELIN-CONVERTING ENZYME-INHIBITORS, The FASEB journal, 10(6), 1996, pp. 2331-2331
THE CONTRIBUTION OF ANIONS TO SYNERGY OF INHIBITION AGAINST FARNESYL-PROTEIN TRANSFERASE
Authors: ZIMMERMAN K SCHOLTEN J OXENDER M LEONARD D GOWEN R SEBOLTLEOPOLD J HUPE D
Citation: K. Zimmerman et al., THE CONTRIBUTION OF ANIONS TO SYNERGY OF INHIBITION AGAINST FARNESYL-PROTEIN TRANSFERASE, The FASEB journal, 10(6), 1996, pp. 2885-2885
THE IN-VITRO EJECTION OF ZINC FROM HUMAN-IMMUNODEFICIENCY-VIRUS (HIV)TYPE-1 NUCLEOCAPSID PROTEIN BY DISULFIDE BENZAMIDES WITH CELLULAR ANTI-HIV ACTIVITY
Authors: TUMMINO PJ SCHOLTEN JD HARVEY PJ HOLLER TP MALONEY L GOGLIOTTI R DOMAGALA J HUPE D
Citation: Pj. Tummino et al., THE IN-VITRO EJECTION OF ZINC FROM HUMAN-IMMUNODEFICIENCY-VIRUS (HIV)TYPE-1 NUCLEOCAPSID PROTEIN BY DISULFIDE BENZAMIDES WITH CELLULAR ANTI-HIV ACTIVITY, Proceedings of the National Academy of Sciences of the United Statesof America, 93(3), 1996, pp. 969-973
A PERMANENT HUMAN CELL-LINE (EA.HY926) PRESERVES THE CHARACTERISTICS OF ENDOTHELIN-CONVERTING ENZYME FROM PRIMARY HUMAN UMBILICAL VEIN ENDOTHELIAL-CELLS
Authors: AHN K PAN S BENINGO K HUPE D
Citation: K. Ahn et al., A PERMANENT HUMAN CELL-LINE (EA.HY926) PRESERVES THE CHARACTERISTICS OF ENDOTHELIN-CONVERTING ENZYME FROM PRIMARY HUMAN UMBILICAL VEIN ENDOTHELIAL-CELLS, Life sciences, 56(26), 1995, pp. 2331-2341
RECONSTRUCTED 19-KDA CATALYTIC DOMAIN OF GELATINASE-A IS AN ACTIVE PROTEINASE
Authors: YE QZ JOHNSON LL YU AE HUPE D
Citation: Qz. Ye et al., RECONSTRUCTED 19-KDA CATALYTIC DOMAIN OF GELATINASE-A IS AN ACTIVE PROTEINASE, Biochemistry, 34(14), 1995, pp. 4702-4708
COMPETITIVE-INHIBITION OF HIV-1 PROTEASE BY BIPHENYL CARBOXYLIC-ACIDS
Authors: TUMMINO PJ FERGUSON D JACOBS CM TAIT B HUPE L LUNNEY E HUPE D
Citation: Pj. Tummino et al., COMPETITIVE-INHIBITION OF HIV-1 PROTEASE BY BIPHENYL CARBOXYLIC-ACIDS, Archives of biochemistry and biophysics, 316(1), 1995, pp. 523-528
NONPEPTIDE COMPETITIVE INHIBITORS OF HIV-1 PROTEASE
Authors: TUMMINO PJ FERGUSON D HUPE L TAIT B HUPE D
Citation: Pj. Tummino et al., NONPEPTIDE COMPETITIVE INHIBITORS OF HIV-1 PROTEASE, The FASEB journal, 8(7), 1994, pp. 10001373-10001373
A RECOMBINANT HUMAN STROMELYSIN CATALYTIC DOMAIN IDENTIFIES TRYPTOPHAN DERIVATIVES AS HUMAN STROMELYSIN INHIBITORS
Authors: YE QZ JOHNSON LL NORDAN I HUPE D HUPE L
Citation: Qz. Ye et al., A RECOMBINANT HUMAN STROMELYSIN CATALYTIC DOMAIN IDENTIFIES TRYPTOPHAN DERIVATIVES AS HUMAN STROMELYSIN INHIBITORS, Journal of cellular biochemistry, 1994, pp. 149-149
A NOVEL NONPEPTIDE HIV-1 PROTEASE INHIBITOR - ELUCIDATION OF THE BINDING MODE AND ITS APPLICATION IN THE DESIGN OF RELATED ANALOGS
Authors: LUNNEY EA HAGEN SE DOMAGALA JM HUMBLET C KOSINSKI J TAIT BD WARMUS JS WILSON M FERGUSON D HUPE D TUMMINO PJ BALDWIN ET BHAT TN LIU BS ERICKSON JW
Citation: Ea. Lunney et al., A NOVEL NONPEPTIDE HIV-1 PROTEASE INHIBITOR - ELUCIDATION OF THE BINDING MODE AND ITS APPLICATION IN THE DESIGN OF RELATED ANALOGS, Journal of medicinal chemistry, 37(17), 1994, pp. 2664-2677
A RECOMBINANT HUMAN STROMELYSIN CATALYTIC DOMAIN IDENTIFYING TRYPTOPHAN DERIVATIVES AS HUMAN STROMELYSIN INHIBITORS
Authors: YE QZ JOHNSON LL NORDAN I HUPE D HUPE L
Citation: Qz. Ye et al., A RECOMBINANT HUMAN STROMELYSIN CATALYTIC DOMAIN IDENTIFYING TRYPTOPHAN DERIVATIVES AS HUMAN STROMELYSIN INHIBITORS, Journal of medicinal chemistry, 37(1), 1994, pp. 206-209
COMPETITIVE-INHIBITION OF HIV-1 PROTEASE BY WARFARIN DERIVATIVES
Authors: TUMMINO PJ FERGUSON D HUPE D
Citation: Pj. Tummino et al., COMPETITIVE-INHIBITION OF HIV-1 PROTEASE BY WARFARIN DERIVATIVES, Biochemical and biophysical research communications, 201(1), 1994, pp. 290-294
COMPETITIVE-INHIBITION OF HIV-1 PROTEASE BY 4-HYDROXY-BENZOPYRAN-2-ONES AND BY 4-HYDROXY-6-PHENYLPYRAN-2-ONES
Authors: TUMMINO PJ FERGUSON D HUPE L HUPE D
Citation: Pj. Tummino et al., COMPETITIVE-INHIBITION OF HIV-1 PROTEASE BY 4-HYDROXY-BENZOPYRAN-2-ONES AND BY 4-HYDROXY-6-PHENYLPYRAN-2-ONES, Biochemical and biophysical research communications, 200(3), 1994, pp. 1658-1664
NOVEL SERIES OF ACHIRAL, LOW-MOLECULAR-WEIGHT, AND POTENT HIV-1 PROTEASE INHIBITORS
Authors: PRASAD JVNV PARA KS LUNNEY EA ORTWINE DF DUNBAR JB FERGUSON D TUMMINO PJ HUPE D TAIT BD DOMAGALA JM HUMBLET C BHAT TN LIU BS GUERIN DMA BALDWIN ET ERICKSON JW SAWYER TK
Citation: Jvnv. Prasad et al., NOVEL SERIES OF ACHIRAL, LOW-MOLECULAR-WEIGHT, AND POTENT HIV-1 PROTEASE INHIBITORS, Journal of the American Chemical Society, 116(15), 1994, pp. 6989-6990
COMPETITIVE-INHIBITION OF HIV-1-PROTEASE BY BIPHENYL CARBOXYLIC-ACIDS
Authors: TUMMINO PJ STROUP D HUPE D
Citation: Pj. Tummino et al., COMPETITIVE-INHIBITION OF HIV-1-PROTEASE BY BIPHENYL CARBOXYLIC-ACIDS, The FASEB journal, 7(7), 1993, pp. 1183-1183
ENDOTHELIN CONVERTING ENZYME FROM TRANSFORMED HUMAN UMBILICAL VEIN ENDOTHELIAL-CELLS (EA-HY-926)
Authors: AHN K BENINGO K PAN S HUPE D
Citation: K. Ahn et al., ENDOTHELIN CONVERTING ENZYME FROM TRANSFORMED HUMAN UMBILICAL VEIN ENDOTHELIAL-CELLS (EA-HY-926), The FASEB journal, 7(7), 1993, pp. 1209-1209
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