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Results: 1-10 |
Results: 10
CLINICAL-RESULTS FROM INTRACYTOPLASMIC SPERM INJECTION AT MONASH IVF
Authors: MCLACHLAN RI FUSCALDO G RHO H POULOS C DALRYMPLE J JACKSON P HOLDEN CA
Citation: Ri. Mclachlan et al., CLINICAL-RESULTS FROM INTRACYTOPLASMIC SPERM INJECTION AT MONASH IVF, Reproduction, fertility and development, 7(2), 1995, pp. 247-253
GR-73,632 AND [GLU(OBZL)(11)]SUBSTANCE-P ARE SELECTIVE AGONISTS FOR THE SEPTIDE-SENSITIVE TACHYKININ NK1 RECEPTOR IN THE RAT URINARY-BLADDER
Authors: MEINI S PATACCHINI R LECCI A POULOS C ROVERO P MAGGI CA
Citation: S. Meini et al., GR-73,632 AND [GLU(OBZL)(11)]SUBSTANCE-P ARE SELECTIVE AGONISTS FOR THE SEPTIDE-SENSITIVE TACHYKININ NK1 RECEPTOR IN THE RAT URINARY-BLADDER, Neuropeptides, 28(2), 1995, pp. 99-106
MICROINJECTION - CHOICE OF EMBRYO-TRANSFER TECHNIQUE
Authors: MCLACHLAN RI FUSCALDO G CALDERON I LACHAMKAPLAN O POULOS C RHO H TROUNSON A WOOD C
Citation: Ri. Mclachlan et al., MICROINJECTION - CHOICE OF EMBRYO-TRANSFER TECHNIQUE, Reproduction, fertility and development, 6(1), 1994, pp. 57-61
SYNTHESIS AND BIOLOGICAL-ACTIVITY OF LOCUST AKH-I AND ITS ANALOGS WITH MODIFICATIONS AT THE THREONINE RESIDUES
Authors: POULOS C KARAGIANNIS K LEE M GOLDSWORTHY G
Citation: C. Poulos et al., SYNTHESIS AND BIOLOGICAL-ACTIVITY OF LOCUST AKH-I AND ITS ANALOGS WITH MODIFICATIONS AT THE THREONINE RESIDUES, International journal of peptide & protein research, 44(6), 1994, pp. 589-593
ANALOGS OF THE C-TERMINAL FRAGMENTS OF NEUROKININS WITH MODIFICATIONSAT THEIR C-TERMINAL METHIONYL RESIDUE - STRUCTURE-ACTIVITY STUDIES
Authors: ANTONIOU M POULOS C
Citation: M. Antoniou et C. Poulos, ANALOGS OF THE C-TERMINAL FRAGMENTS OF NEUROKININS WITH MODIFICATIONSAT THEIR C-TERMINAL METHIONYL RESIDUE - STRUCTURE-ACTIVITY STUDIES, International journal of peptide & protein research, 43(4), 1994, pp. 344-350
SYNTHESIS OF SUBSTANCE-P C-TERMINAL HEXAPEPTIDE ANALOGS AND THEIR BIOLOGICAL-ACTIVITY - ANALOGS WITH ANTAGONISTIC ACTIVITY WITHOUT CONTAINING D-AMINO ACIDS
Authors: KARAGIANNIS K MANOLOPOULOU A POULOS C STAVROPOULOS G
Citation: K. Karagiannis et al., SYNTHESIS OF SUBSTANCE-P C-TERMINAL HEXAPEPTIDE ANALOGS AND THEIR BIOLOGICAL-ACTIVITY - ANALOGS WITH ANTAGONISTIC ACTIVITY WITHOUT CONTAINING D-AMINO ACIDS, European journal of medicinal chemistry, 29(9), 1994, pp. 667-673
SYNTHESIS AND BIOLOGICAL-ACTIVITY OF NK1 SUBSTANCE-P SELECTIVE AGONISTS BY MODIFYING THE METHIONYL RESIDUE
Authors: POULOS C ANTONIOU M PATACCHINI R MAGGI CA PEGORARO S ROVERO P
Citation: C. Poulos et al., SYNTHESIS AND BIOLOGICAL-ACTIVITY OF NK1 SUBSTANCE-P SELECTIVE AGONISTS BY MODIFYING THE METHIONYL RESIDUE, Neuropeptides, 27(1), 1994, pp. 27-29
SYNTHESIS AND BIOLOGICAL-ACTIVITY OF NK(1) TACHYKININ ANTAGONISTS NOTCONTAINING D-RESIDUES
Authors: POULOS C ANTONIOU M PATACCHINI R MAGGI CA ROVERO P
Citation: C. Poulos et al., SYNTHESIS AND BIOLOGICAL-ACTIVITY OF NK(1) TACHYKININ ANTAGONISTS NOTCONTAINING D-RESIDUES, Neuropeptides, 26(1), 1994, pp. 55-57
A CASE OF SUCCESSFUL USE OF REPRODUCTIVE TECHNOLOGY FOR A COUPLE WITHSUBFERTILITY DUE TO RETROGRADE EJACULATION, WHERE ARTIFICIAL-INSEMINATION HAD FAILED
Authors: KOVACS GT LAWRENCE M BURDEN J POULOS C
Citation: Gt. Kovacs et al., A CASE OF SUCCESSFUL USE OF REPRODUCTIVE TECHNOLOGY FOR A COUPLE WITHSUBFERTILITY DUE TO RETROGRADE EJACULATION, WHERE ARTIFICIAL-INSEMINATION HAD FAILED, Australian and New Zealand Journal of Obstetrics and Gynaecology, 34(1), 1994, pp. 116-117
SYNTHESIS OF A POTENT ANTAGONIST OF SUBSTANCE-P BY REPLACING THE CH2SCH3 AND THE ALPHA-CARBOXAMIDE GROUPS OF THE METHIONINE AT [ORN6]-SP(6-11) BY BENZYL ESTER GROUPS
Authors: KARAGIANNIS K STAVROPOULOS G POULOS C JORDAN CC HAGAN RM
Citation: K. Karagiannis et al., SYNTHESIS OF A POTENT ANTAGONIST OF SUBSTANCE-P BY REPLACING THE CH2SCH3 AND THE ALPHA-CARBOXAMIDE GROUPS OF THE METHIONINE AT [ORN6]-SP(6-11) BY BENZYL ESTER GROUPS, International journal of peptide & protein research, 42(6), 1993, pp. 565-569
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