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S Bajusz

Showing results (41-50 of 85) with videos related to

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FEBS Letters|March 1, 1977
Differential behaviour of LPH-(61-91)-peptide in different model systems: comparison of the opioid activities of LPH-(61-91)-peptide and its fragmentsA Rónai, L Gráf, I Székely, et al.
Experientia|December 15, 1978
Prolactin and growth hormone releasing activity of [D-Met2, Pro5]-enkephalinamide in the rat after systemic administrationV Locatelli, D Cocchi, S Bajusz, et al.
European Journal of Biochemistry|April 1, 1981
Study of the specificity of thrombin with tripeptidyl-p-nitroanilide substratesM Pozsgay, G Szabó, S Bajusz, et al.
Neuroscience|November 4, 2008
Binding studies of novel, non-mammalian enkephalins, structures predicted from frog and lungfish brain cDNA sequencesE Bojnik, A Magyar, G Tóth, et al.
FEBS Letters|January 28, 1980
Further enhancment of analgesic activity: enkephalin analogs with terminal guanidino groupS Bajusz, A Z Rónai, J I Székely, et al.
European Journal of Biochemistry|April 1, 1981
Investigation of the substrate-binding site of trypsin by the aid of tripeptidyl-p-nitroanilide substratesM Pozsgay, G Szabó, S Bajusz, et al.
Endocrinology|February 1, 1989
Comparison of different agonists and antagonists of luteinizing hormone-releasing hormone for receptor-binding ability to rat pituitary and human breast cancer membranesM Fekete, S Bajusz, K Groot, et al.
Pharmacology|January 1, 1979
Kinetic studies in isolated organs: tools to design analgesic peptides and to analyze their receptor effectsA Z Rónai, I Berzétei, J I Székely, et al.
Biochemical and Biophysical Research Communications|December 28, 1979
Tetrapeptide-amide analogues of enkephalin: the role of C-terminus in determining the character of opioid activityA Z Rónai, J I Székely, I Berzétei, et al.
Bioorganic & Medicinal Chemistry Letters|January 5, 1999
Peptidyl beta-homo-aspartals: specific inhibitors of interleukin-1 beta converting enzyme and its homologues (caspases)S Bajusz, I Fauszt, K Németh, et al.
Pageof 9

Showing results (41-50 of 85) with videos related to

Sort By:
Pageof 9
FEBS Letters|March 1, 1977
Differential behaviour of LPH-(61-91)-peptide in different model systems: comparison of the opioid activities of LPH-(61-91)-peptide and its fragmentsA Rónai, L Gráf, I Székely, et al.
Experientia|December 15, 1978
Prolactin and growth hormone releasing activity of [D-Met2, Pro5]-enkephalinamide in the rat after systemic administrationV Locatelli, D Cocchi, S Bajusz, et al.
European Journal of Biochemistry|April 1, 1981
Study of the specificity of thrombin with tripeptidyl-p-nitroanilide substratesM Pozsgay, G Szabó, S Bajusz, et al.
Neuroscience|November 4, 2008
Binding studies of novel, non-mammalian enkephalins, structures predicted from frog and lungfish brain cDNA sequencesE Bojnik, A Magyar, G Tóth, et al.
FEBS Letters|January 28, 1980
Further enhancment of analgesic activity: enkephalin analogs with terminal guanidino groupS Bajusz, A Z Rónai, J I Székely, et al.
European Journal of Biochemistry|April 1, 1981
Investigation of the substrate-binding site of trypsin by the aid of tripeptidyl-p-nitroanilide substratesM Pozsgay, G Szabó, S Bajusz, et al.
Endocrinology|February 1, 1989
Comparison of different agonists and antagonists of luteinizing hormone-releasing hormone for receptor-binding ability to rat pituitary and human breast cancer membranesM Fekete, S Bajusz, K Groot, et al.
Pharmacology|January 1, 1979
Kinetic studies in isolated organs: tools to design analgesic peptides and to analyze their receptor effectsA Z Rónai, I Berzétei, J I Székely, et al.
Biochemical and Biophysical Research Communications|December 28, 1979
Tetrapeptide-amide analogues of enkephalin: the role of C-terminus in determining the character of opioid activityA Z Rónai, J I Székely, I Berzétei, et al.
Bioorganic & Medicinal Chemistry Letters|January 5, 1999
Peptidyl beta-homo-aspartals: specific inhibitors of interleukin-1 beta converting enzyme and its homologues (caspases)S Bajusz, I Fauszt, K Németh, et al.
Pageof 9