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S Bajusz

Showing results (71-80 of 85) with videos related to

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Life Sciences|April 1, 1977
Cross tolerance between morphine and beta-endorphin in vivoJ I Szkely, A Z Rónai, Z Dunai-Kovács, et al.
Journal of Autonomic Pharmacology|March 1, 1984
Met5-enkephalin-Arg6-Phe7 inhibition of noradrenaline and acetylcholine release from peripheral organsL G Hársing, A Z Rónai, G T Somogyi, et al.
Annals of the New York Academy of Sciences|October 28, 1977
Structure-function relationships in lipotropinsL Gráf, G Cseh, E Barát, et al.
Life Sciences|May 21, 1979
Attenuation of morphine tolerance and dependence by alpha-melanocyte stimulating hormone(alpha-MSH)J I Székely, E Miglécz, Z Dunai-Kovács, et al.
European Journal of Pharmacology|June 1, 1977
(D-met2, pro5)-enkephalinamide: a potent morphine-like analgesicJ I Székely, A Z Rónai, Z Dunai-Kovács, et al.
Seminars in Thrombosis and Hemostasis|January 1, 1996
Active site-directed thrombin inhibitors: alpha-hydroxyacyl-prolyl-arginals, new orally active stable analogues of D-Phe-Pro-Arg-HS Bajusz, E Barabas, I Fauszt, et al.
Bioorganic & Medicinal Chemistry|August 1, 1995
Active site-directed thrombin inhibitors: alpha-hydroxyacyl-prolyl-arginals. New orally active stable analogs of D-Phe-Pro-Arg-HS Bajusz, E Barabás, I Fauszt, et al.
International Journal of Peptide and Protein Research|March 1, 1992
Potent agonists of growth hormone-releasing hormone. Part IM Zarandi, P Serfozo, J Zsigo, et al.
FEBS Letters|August 11, 1980
Enkephalin analogs containing amino sulfonic acid and amino phosphonic acid residues at position 5S Bajusz, A Z Rónai, J I Székely, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 1, 1989
Highly potent analogues of luteinizing hormone-releasing hormone containing D-phenylalanine nitrogen mustard in position 6S Bajusz, T Janaky, V J Csernus, et al.
Pageof 9

Showing results (71-80 of 85) with videos related to

Sort By:
Pageof 9
Life Sciences|April 1, 1977
Cross tolerance between morphine and beta-endorphin in vivoJ I Szkely, A Z Rónai, Z Dunai-Kovács, et al.
Journal of Autonomic Pharmacology|March 1, 1984
Met5-enkephalin-Arg6-Phe7 inhibition of noradrenaline and acetylcholine release from peripheral organsL G Hársing, A Z Rónai, G T Somogyi, et al.
Annals of the New York Academy of Sciences|October 28, 1977
Structure-function relationships in lipotropinsL Gráf, G Cseh, E Barát, et al.
Life Sciences|May 21, 1979
Attenuation of morphine tolerance and dependence by alpha-melanocyte stimulating hormone(alpha-MSH)J I Székely, E Miglécz, Z Dunai-Kovács, et al.
European Journal of Pharmacology|June 1, 1977
(D-met2, pro5)-enkephalinamide: a potent morphine-like analgesicJ I Székely, A Z Rónai, Z Dunai-Kovács, et al.
Seminars in Thrombosis and Hemostasis|January 1, 1996
Active site-directed thrombin inhibitors: alpha-hydroxyacyl-prolyl-arginals, new orally active stable analogues of D-Phe-Pro-Arg-HS Bajusz, E Barabas, I Fauszt, et al.
Bioorganic & Medicinal Chemistry|August 1, 1995
Active site-directed thrombin inhibitors: alpha-hydroxyacyl-prolyl-arginals. New orally active stable analogs of D-Phe-Pro-Arg-HS Bajusz, E Barabás, I Fauszt, et al.
International Journal of Peptide and Protein Research|March 1, 1992
Potent agonists of growth hormone-releasing hormone. Part IM Zarandi, P Serfozo, J Zsigo, et al.
FEBS Letters|August 11, 1980
Enkephalin analogs containing amino sulfonic acid and amino phosphonic acid residues at position 5S Bajusz, A Z Rónai, J I Székely, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 1, 1989
Highly potent analogues of luteinizing hormone-releasing hormone containing D-phenylalanine nitrogen mustard in position 6S Bajusz, T Janaky, V J Csernus, et al.
Pageof 9