S. Bajusz - Concepedia

Author

S. Bajusz

Also Known As

S BAJUSZ, S Bajusz, S. BAJUSZ, S. Bajusz, SANDOR BAJUSZ, Sandor BAJUSZ, Sandor Bajusz, SÁNDOR BAJUSZ, Sàndor BAJUSZ, Sàndor Bajusz

133

Publications

2.5K

Citations

H-Index

Concepts

All Affiliations

Tulane University Hungarian Academy of Sciences HUN-REN Institute of Experimental Medicine Eötvös Loránd University

About

S. Bajusz is an author at Tulane University specializing in pharmacology, medicine, and pharmacotherapy.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	24	44	2K
2	Natural Sciences	12	13	845
3	Health Sciences	10	11	569
4	Public Health	3	3	47
5	Engineering	1	1	44

S. Bajusz

Publications

2.3K

Citations

H-Index

Page 1

	Year	Citations
Highly active and selective anticoagulants: D-Phe-Pro-Arg-H, a free tripeptide aldehyde prone to spontaneous inactivation, and its stable N-methyl derivative, D-MePhe-Pro-Arg-H S. Bajusz, E. Széll, D Bagdy, Journal of Medicinal Chemistry Pharmaceutical ScienceSelective AnticoagulantsSpontaneous InactivationOrganic ChemistrySuch Inactivation	1990	170
A superactive antinociceptive pentapeptide, (D‐Met<sup>2</sup>,Pro<sup>5</sup>)‐enkephalinamide S. Bajusz, András Z. Rónai, József I. Székely, FEBS Letters Molecular PharmacologyMedicinal ChemistrySuperactive Antinociceptive PentapeptideMedicinePain Medicine	1977	156
Comparative study on analgesic effect of Met5-enkephalin and related lipotropin fragments L. Gráf, József I. Székely, András Z. Rónai, Nature Analgesic EffectAnti-inflammatoryHealth SciencesPain MedicineLipotropin Fragments	1976	147
INHIBITION OF THROMBIN AND TRYPSIN BY TRIPEPTIDE ALDEHYDES S. Bajusz, Éva Barabás, P Tolnay, International journal of peptide & protein research Bioorganic ChemistryCertain Tripeptide AldehydesAldo-keto ReductaseNatural OriginChemical Biology	1978	142
New antagonists of LHRH II. Inhibition and potentiation of LHRH by closely related analogues S. Bajusz, Valér Csernus, Tamás Janáky, International journal of peptide & protein research Pharmaceutical ScienceToxic EffectsPharmacotherapyExperimental PharmacologyPharmaceutical Chemistry	1988	137
Attenuation of morphine tolerance and dependence by α-melanocyte stimulating hormone (α-MSH) József I. Székely, Erzsèbet Miglècz, Zsuzsa Dunai-Kovàcs, Life Sciences Molecular PharmacologyMorphine ToleranceAddictionMedicinePhysiology	1979	87
Highly potent antagonists of luteinizing hormone-releasing hormone free of edematogenic effects. S. Bajusz, Magdolna Kovács, M. Gazdag, Proceedings of the National Academy of Sciences Edematogenic EffectsPharmaceutical SciencePharmacotherapyExperimental PharmacologyMolecular Pharmacology	1988	87
(D-MET2, PRO5)-enkephalinamide: a potent morphine-like analgesic József I. Székely, András Z. Rónai, Zsuzsa Dunai-Kovàcs, European Journal of Pharmacology Molecular PharmacologyHealth SciencesPain MedicineMedicineMolecular Pain	1977	84
Involvement of Brain Serotonin in the Prolactin- Releasing Effect of Opioid Peptides* Santi Spampinato, Vittorio Locatelli, Daniela Cocchi, Endocrinology Brain SerotoninSynaptic TransmissionAnesthetic MechanismPharmacotherapyExperimental Pharmacology	1979	82
Analogues of luteinizing hormone-releasing hormone containing cytotoxic groups. Tamás Janáky, Attila Juhász, S. Bajusz, Proceedings of the National Academy of Sciences Pharmaceutical SciencePharmacotherapyMolecular PharmacologyMedicinal ChemistryD Amino Acids	1992	71

Page 1