Zobrazeno 1 - 10
of 78
pro vyhledávání: '"L, Bokser"'
Autor:
Oscar Levalle, L. Fiszlejder, Chervin Ab, Abraham Guitelman, L. Bokser, N.A Pacenza, G. Aszenmil
Publikováno v:
Andrologia. 16:303-309
Summary: Both gonadotropins are necessary to induce spermatogenesis in man and to recover hypophysectomized males. The patients who suffer from tumoral or traumatic hypothalamo-hypophyseal lesion use to have low endogenous gonadotropins (opposite to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0d52ac67e70ad89f29170dc474e89370
https://doi.org/10.1111/j.1439-0272.1984.tb00288.x
https://doi.org/10.1111/j.1439-0272.1984.tb00288.x
Autor:
Marta Zarandi, Jozsef Zsigo, Tamás Janáky, Donald B. Olsen, Sandor Bajusz, Andrew V. Schally, L Bokser, P. Serfozo
Publikováno v:
Europe PubMed Central
Scopus-Elsevier
Scopus-Elsevier
Analogs of the 29 amino acid sequence of growth hormone-releasing hormone (GH-RH) with agmatine (Agm) in position 29 have been synthesized by the solid phase method, purified, and tested in vitro and in vivo. The majority of the analogs contained des
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::370384bc4c487db0c9ae0fa494962eb7
https://doi.org/10.1111/j.1399-3011.1992.tb00791.x
https://doi.org/10.1111/j.1399-3011.1992.tb00791.x
Autor:
Kate Groot, Attila Juhasz, Tetsu Yano, Tamás Janáky, Attila Nagy, Jacek Pinski, Andrew V. Schally, L Bokser
Publikováno v:
Europe PubMed Central
Scopus-Elsevier
Scopus-Elsevier
A series of new highly potent LH-RH antagonists (T-series) has been synthesized in our laboratory. Among these analogs, antagonists [Ac-D-Nal(2), D-Phe(4Cl)2, D-Pal(3)3, D-Lys(A2pr(Car)2)6, D-Ala10]LH-RH (T-140); [Ac-D-Nal(2)1, D-Phe(4Cl)2, D-Pal(3)3
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9686b85d6932b4d023c4a09d8346fc72
https://doi.org/10.1111/j.1399-3011.1993.tb00116.x
https://doi.org/10.1111/j.1399-3011.1993.tb00116.x
Publikováno v:
Biochemical and Biophysical Research Communications. 207:105-110
EGFR-T17 cells were pretreated with oleic acid and 5-10 minutes later stimulated with EGF, to study if early ionic signals are instrumental in inducing metabolic cellular response. Oleic acid blocks EGF-induced [Ca2+]i rise and Ca2+ influx without al
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5008e110f1464eeb69d6dae44865f230
https://doi.org/10.1006/bbrc.1995.1159
https://doi.org/10.1006/bbrc.1995.1159
Publikováno v:
SEMERGEN - Medicina de Familia. 27:40-42
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c0637b7b79e86a7ffeed1a5bed6d44fc
https://doi.org/10.1016/s1138-3593(01)73672-6
https://doi.org/10.1016/s1138-3593(01)73672-6
Autor:
Valér J. Csernus, L. Bokser, Tamás Janáky, S. Milovanovic, G. Srkalovic, Zoltan Rekasi, A. Juhász, S. Bajusz, Attila Nagy, T. W. Redding
Publikováno v:
Proceedings of the National Academy of Sciences. 89:972-976
In an attempt to produce better cytotoxic analogues, chemotherapeutic antineoplastic radicals including an alkylating nitrogen mustard derivative of D-phenylalanine (D-melphalan), reactive cyclopropane, anthraquinone derivatives [2-(hydroxymethyl)ant
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9c94418271f13cce16647309ce400e76
https://doi.org/10.1073/pnas.89.3.972
https://doi.org/10.1073/pnas.89.3.972
Publikováno v:
Endocrinology. 127:3052-3060
Membrane receptors for LHRH were evaluated in Dunning R3327 prostate cancers and rat anterior pituitaries. The receptors were characterized both in untreated animals and after in vivo treatment with microcapsules of the agonist D-Trp6-LHRH and a sust
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a95fbb2c6c325a5a5302cfd8ba8808d2
https://doi.org/10.1210/endo-127-6-3052
https://doi.org/10.1210/endo-127-6-3052
Autor:
Attila Juhasz, Ana Maria Comaru-Schally, Kate Groot, Gordan Srkalovic, E. Korkut, Siniša Radulović, Karoly Szepeshazi, Renzhi Cai, L Bokser, Tamás Janáky, Andrew V. Schally, Szende Bela, P. Serfozo, Tommie W. Redding
Publikováno v:
The Journal of Steroid Biochemistry and Molecular Biology. 37:1061-1067
Many clinical approaches for the treatment of hormone-sensitive tumors are being developed based on analogs of LH-RH and somatostatin. Inhibition of the pituitary-gonadal axis forms the basis for oncological applications of LH-RH agonists like [ d -T
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a48a8855b4b0c7d924dfe45b0c9f3492
https://doi.org/10.1016/0960-0760(90)90466-x
https://doi.org/10.1016/0960-0760(90)90466-x
Publikováno v:
Scopus-Elsevier
Inhibitory effects of the potent antagonist of luteinizing hormone-releasing hormone N-Ac-[3-(2-naphthyl)-D-alanine1,4-chloro-D-phenylalanine2,3- (3-pyridyl)-D- alanine3,D-citrulline6,D-alanine10]luteinizing hormone-releasing hormone (SB-75) free of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9a085e4b4c4ddc594bdc8903739e1106
https://doi.org/10.1073/pnas.87.18.7100
https://doi.org/10.1073/pnas.87.18.7100
Publikováno v:
Scopus-Elsevier
British Journal of Cancer
British Journal of Cancer
The possible protective effect of an agonist of luteinising hormone-releasing hormone (LH-RH) against the ovarian damage caused by cyclophosphamide was investigated in rats. D-Trp6-LH-RH microcapsules were injected once a month for 3 months, in a dos
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a1bccae82d5279a6ad156b482ac57a72
https://doi.org/10.1038/bjc.1990.192
https://doi.org/10.1038/bjc.1990.192