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Attila Nagy

Research Profile

Chemicals & Drugs

Living Beings

Anatomy

Tumor Cells, Cultured

Procedures

Physiology

Cell Divisions

Disorders

Prostatic Neoplasms

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Publications

TOP 3
Gunhild Keller; Andrew V Schally; Attila Nagy; Ben Baker; Gabor Halmos; Jörg Engel
Effective therapy of experimental human malignant melanomas with a targeted cytotoxic somatostatin analogue without induction of multi-drug resistance proteins.
Anton Stangelberger; Andrew V Schally; Attila Nagy; Karoly Szepeshazi; Celia A Kanashiro; Gabor Halmos
Inhibition of human experimental prostate cancers by a targeted cytotoxic luteinizing hormone-releasing hormone analog AN-207.
Anton Stangelberger; Andrew V Schally; Markus Letsch; Karoly Szepeshazi; Attila Nagy; Gabor Halmos; Celia A Kanashiro; Eva Corey; Robert L Vessella
Targeted chemotherapy with cytotoxic bombesin analogue AN-215 inhibits growth of experimental human prostate cancers.

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All Publications

2006: Gunhild Keller; Andrew V Schally; Attila Nagy; Ben Baker; Gabor Halmos; Jörg Engel
Effective therapy of experimental human malignant melanomas with a targeted cytotoxic somatostatin analogue without induction of multi-drug resistance proteins.
International journal of oncology 2006;28(6):1507-13.
2006: Anton Stangelberger; Andrew V Schally; Attila Nagy; Karoly Szepeshazi; Celia A Kanashiro; Gabor Halmos
Inhibition of human experimental prostate cancers by a targeted cytotoxic luteinizing hormone-releasing hormone analog AN-207.
The Prostate 2006;66(2):200-10.
2006: Anton Stangelberger; Andrew V Schally; Markus Letsch; Karoly Szepeshazi; Attila Nagy; Gabor Halmos; Celia A Kanashiro; Eva Corey; Robert L Vessella
Targeted chemotherapy with cytotoxic bombesin analogue AN-215 inhibits growth of experimental human prostate cancers.
International journal of cancer. Journal international du cancer 2006;118(1):222-9.
2005: Jörg Engel; Andrew V Schally; Gabor Halmos; Ben Baker; Attila Nagy; Gunhild Keller
Targeted cytotoxic bombesin analog AN-215 effectively inhibits experimental human breast cancers with a low induction of multi-drug resistance proteins.
Endocrine-related cancer 2005;12(4):999-1009.
2005: Gunhild Keller; Andrew V Schally; Attila Nagy; Gabor Halmos; Ben Baker; Jörg Engel
Targeted chemotherapy with cytotoxic bombesin analogue AN-215 can overcome chemoresistance in experimental renal cell carcinomas.
Cancer 2005;104(10):2266-74.
2005: Attila Nagy; Andrew V Schally
Targeting of cytotoxic luteinizing hormone-releasing hormone analogs to breast, ovarian, endometrial, and prostate cancers.
Biology of reproduction 2005;73(5):851-9.
2005: Karoly Szepeshazi; Andrew V Schally; Attila Nagy; Gabor Halmos
Inhibition of growth of experimental human and hamster pancreatic cancers in vivo by a targeted cytotoxic bombesin analog.
Pancreas 2005;31(3):275-82.
2005: Jörg Engel; Andrew V Schally; Gabor Halmos; Ben Baker; Attila Nagy; Gunhild Keller
Targeted therapy with a cytotoxic somatostatin analog, AN-238, inhibits growth of human experimental endometrial carcinomas expressing multidrug resistance protein MDR-1.
Cancer 2005;104(6):1312-21.
2005: Gunhild Keller; Andrew V Schally; Timo Gaiser; Attila Nagy; Ben Baker; Gabor Halmos; Jörg Engel
Receptors for luteinizing hormone releasing hormone (LHRH) expressed in human non-Hodgkin's lymphomas can be targeted for therapy with the cytotoxic LHRH analogue AN-207.
European journal of cancer (Oxford, England : 1990) 2005;41(14):2196-202.
2005: Gunhild Keller; Andrew V Schally; Timo Gaiser; Attila Nagy; Ben Baker; Gabor Halmos; Jörg Engel
Receptors for luteinizing hormone releasing hormone expressed on human renal cell carcinomas can be used for targeted chemotherapy with cytotoxic luteinizing hormone releasing hormone analogues.
Clinical cancer research : an official journal of the American Association for Cancer Research 2005;11(15):5549-57.
2005: Jörg Engel; Andrew V Schally; Gabor Halmos; Ben Baker; Attila Nagy; Gunhild Keller
Experimental therapy of human endometrial cancers with a targeted cytotoxic bombesin analog AN-215: low induction of multidrug resistance proteins.
European journal of cancer (Oxford, England : 1990) 2005;41(12):1824-30.
2005: Gunhild Keller; Andrew V Schally; Timo Gaiser; Attila Nagy; Ben Baker; Gabriela Westphal; Gabor Halmos; Jörg Engel
Human malignant melanomas express receptors for luteinizing hormone releasing hormone allowing targeted therapy with cytotoxic luteinizing hormone releasing hormone analogue.
Cancer research 2005;65(13):5857-63.
2005: Celia A Kanashiro; Andrew V Schally; Attila Nagy; Gabor Halmos
Inhibition of experimental U-118MG glioblastoma by targeted cytotoxic analogs of bombesin and somatostatin is associated with a suppression of angiogenic and antiapoptotic mechanisms.
International journal of oncology 2005;27(1):169-74.
2005: Gunhild Keller; Jörg Engel; Andrew V Schally; Attila Nagy; Brian D Hammann; Gabor Halmos
Growth inhibition of experimental non-Hodgkin's lymphomas with the targeted cytotoxic somatostatin analogue AN-238.
International journal of cancer. Journal international du cancer 2005;114(5):831-5.
2005: Jörg Engel; Gunhild Keller; Andrew V Schally; Attila Nagy; David D Chism; Gabor Halmos
Effective treatment of experimental human endometrial cancers with targeted cytotoxic luteinizing hormone-releasing hormone analogues AN-152 and AN-207.
Fertility and sterility 2005;83 Suppl 1():1125-33.
2005: Jörg Engel; Gunhild Keller; Andrew V Schally; Gabor Halmos; Brian D Hammann; Attila Nagy
Effective inhibition of experimental human ovarian cancers with a targeted cytotoxic bombesin analogue AN-215.
Clinical cancer research : an official journal of the American Association for Cancer Research 2005;11(6):2408-15.
2005: Attila Nagy; Andrew V Schally
Targeting cytotoxic conjugates of somatostatin, luteinizing hormone-releasing hormone and bombesin to cancers expressing their receptors: a "smarter" chemotherapy.
Current pharmaceutical design 2005;11(9):1167-80.
2004: Andrew V Schally; Attila Nagy
Chemotherapy targeted to cancers through tumoral hormone receptors.
Trends in endocrinology and metabolism: TEM 2004;15(7):300-10.
2004: Andrew V Schally; Karoly Szepeshazi; Attila Nagy; Ana Maria Comaru-Schally; Gabor Halmos
New approaches to therapy of cancers of the stomach, colon and pancreas based on peptide analogs.
Cellular and molecular life sciences : CMLS 2004;61(9):1042-68.
2003: Markus Letsch; Andrew V Schally; Karoly Szepeshazi; Gabor Halmos; Attila Nagy
Preclinical evaluation of targeted cytotoxic luteinizing hormone-releasing hormone analogue AN-152 in androgen-sensitive and insensitive prostate cancers.
Clinical cancer research : an official journal of the American Association for Cancer Research 2003;9(12):4505-13.
2003: Karoly Szepeshazi; Andrew V Schally; Attila Nagy; Brady W Wagner; Ana M Bajo; Gabor Halmos
Preclinical evaluation of therapeutic effects of targeted cytotoxic analogs of somatostatin and bombesin on human gastric carcinomas.
Cancer 2003;98(7):1401-10.
2003: Ana M Bajo; Andrew V Schally; Gabor Halmos; Attila Nagy
Targeted doxorubicin-containing luteinizing hormone-releasing hormone analogue AN-152 inhibits the growth of doxorubicin-resistant MX-1 human breast cancers.
Clinical cancer research : an official journal of the American Association for Cancer Research 2003;9(10 Pt 1):3742-8.
2003: Zoltan Szereday; Andrew V Schally; Karoly Szepeshazi; Ana M Bajo; Francine Hebert; Gabor Halmos; Attila Nagy
Effective treatment of H838 human non-small cell lung carcinoma with a targeted cytotoxic somatostatin analog, AN-238.
International journal of oncology 2003;22(5):1141-6.
2003: Gabor Halmos; Andrew V Schally; Ana Maria Comaru-Schally; Attila Nagy; Anand Irimpen
Absence of binding of targeted analogs of somatostatin carrying cytotoxic radicals or radionuclides to growth hormone secretagogue receptors on human myocardium.
Life sciences 2003;72(23):2669-74.
2003: Andrew V Schally; Attila Nagy
New approaches to treatment of various cancers based on cytotoxic analogs of LHRH, somatostatin and bombesin.
Life sciences 2003;72(21):2305-20.
2002: Jose M Arencibia; Ana M Bajo; Andrew V Schally; Magdalena Krupa; Ioulia Chatzistamou; Attila Nagy
Effective treatment of experimental ES-2 human ovarian cancers with a cytotoxic analog of luteinizing hormone-releasing hormone AN-207.
Anti-cancer drugs 2002;13(9):949-56.
2002: Zoltan Szereday; Andrew V Schally; Attila Nagy; Artur Plonowski; Ana M Bajo; Gabor Halmos; Karoly Szepeshazi; Kate Groot
Effective treatment of experimental U-87MG human glioblastoma in nude mice with a targeted cytotoxic bombesin analogue, AN-215.
British journal of cancer 2002;86(8):1322-7.
2002: Artur Plonowski; Andrew V Schally; Attila Nagy; Kate Groot; Magdalena Krupa; Nora M Navone; Christopher Logothetis
Inhibition of in vivo proliferation of MDA-PCa-2b human prostate cancer by a targeted cytotoxic analog of luteinizing hormone-releasing hormone AN-207.
Cancer letters 2002;176(1):57-63.
2002: Karoly Szepeshazi; Andrew V Schally; Gabor Halmos; Patricia Armatis; Francine Hebert; Baodong Sun; Anita Feil; Hippokratis Kiaris; Attila Nagy
Targeted cytotoxic somatostatin analogue AN-238 inhibits somatostatin receptor-positive experimental colon cancers independently of their p53 status.
Cancer research 2002;62(3):781-8.
2002: Artur Plonowski; Andrew V Schally; Attila Nagy; Baodong Sun; Gabor Halmos
Effective treatment of experimental DU-145 prostate cancers with targeted cytotoxic somatostatin analog AN-238.
International journal of oncology 2002;20(2):397-402.
2002: Magdolna Kovacs; Andrew V Schally; Balazs Csernus; Rebeca Busto; Zoltan Rekasi; Attila Nagy
Targeted cytotoxic analogue of luteinizing hormone-releasing hormone (LH-RH) only transiently decreases the gene expression of pituitary receptors for LH-RH.
Journal of neuroendocrinology 2002;14(1):5-13.
2001: Andrew V Schally; Ana Maria Comaru-Schally; Attila Nagy; Magdolna Kovacs; Karoly Szepeshazi; Artur Plonowski; Jozsef Varga; Gabor Halmos
Hypothalamic hormones and cancer.
Frontiers in neuroendocrinology 2001;22(4):248-91.
2001: Artur Plonowski; Andrew V Schally; Miklos Koppan; Attila Nagy; Jose M Arencibia; Balazs Csernus; Gabor Halmos
Inhibition of the UCI-107 human ovarian carcinoma cell line by a targeted cytotoxic analog of somatostatin, AN-238.
Cancer 2001;92(5):1168-76.
2001: Karoly Szepeshazi; Andrew V Schally; Gabor Halmos; Baodong Sun; Francine Hebert; Balazs Csernus; Attila Nagy
Targeting of cytotoxic somatostatin analog AN-238 to somatostatin receptor subtypes 5 and/or 3 in experimental pancreatic cancers.
Clinical cancer research : an official journal of the American Association for Cancer Research 2001;7(9):2854-61.
2001: Jose M Arencibia; Andrew V Schally; Magdalena Krupa; Ana M Bajo; Attila Nagy; Karoly Szepeshazi; Artur Plonowski
Targeting of doxorubicin to ES-2 human ovarian cancers in nude mice by linking to an analog of luteinizing hormone-releasing hormone improves its effectiveness.
International journal of oncology 2001;19(3):571-7.
2001: Hippokratis Kiaris; Andrew V Schally; Attila Nagy; Karoly Szepeshazi; Francine Hebert; Gabor Halmos
A targeted cytotoxic somatostatin (SST) analogue, AN-238, inhibits the growth of H-69 small-cell lung carcinoma (SCLC) and H-157 non-SCLC in nude mice.
European journal of cancer (Oxford, England : 1990) 2001;37(5):620-8.
2001: Jose M Arencibia; Andrew V Schally; Gabor Halmos; Attila Nagy; Hippokratis Kiaris
In vitro targeting of a cytotoxic analog of luteinizing hormone-releasing hormone AN-207 to ES-2 human ovarian cancer cells as demonstrated by microsatellite analyses.
Anti-cancer drugs 2001;12(1):71-8.
2000: Artur Plonowski; Attila Nagy; Andrew V Schally; Baodong Sun; Kate Groot; Gabor Halmos
In vivo inhibition of PC-3 human androgen-independent prostate cancer by a targeted cytotoxic bombesin analogue, AN-215.
International journal of cancer. Journal international du cancer 2000;88(4):652-7.
2000: Gabor Halmos; Baodong Sun; Andrew V Schally; Francine Hebert; Attila Nagy
Human ovarian cancers express somatostatin receptors.
The Journal of clinical endocrinology and metabolism 2000;85(10):3509-12.
2000: L Chatzistamou; Andrew V Schally; Attila Nagy; Patricia Armatis; Karoly Szepeshazi; Gabor Halmos
Effective treatment of metastatic MDA-MB-435 human estrogen-independent breast carcinomas with a targeted cytotoxic analogue of luteinizing hormone-releasing hormone AN-207.
Clinical cancer research : an official journal of the American Association for Cancer Research 2000;6(10):4158-65.
2000: Andrew V Schally; Ana Maria Comaru-Schally; Artur Plonowski; Attila Nagy; Gabor Halmos; Zoltan Rekasi
Peptide analogs in the therapy of prostate cancer.
The Prostate 2000;45(2):158-66.
2000: Artur Plonowski; Andrew V Schally; Attila Nagy; Hippokratis Kiaris; Francine Hebert; Gabor Halmos
Inhibition of metastatic renal cell carcinomas expressing somatostatin receptors by a targeted cytotoxic analogue of somatostatin AN-238.
Cancer research 2000;60(11):2996-3001.
2000: Z Kahán; Attila Nagy; Andrew V Schally; Gabor Halmos; Jose M Arencibia; Kate Groot
Administration of a targeted cytotoxic analog of luteinizing hormone-releasing hormone inhibits growth of estrogen-independent MDA-MB-231 human breast cancers in nude mice.
Breast cancer research and treatment 2000;59(3):255-62.
2000: Hippokratis Kiaris; Andrew V Schally; Attila Nagy; Baodong Sun; Karoly Szepeshazi; Gabor Halmos
Regression of U-87 MG human glioblastomas in nude mice after treatment with a cytotoxic somatostatin analog AN-238.
Clinical cancer research : an official journal of the American Association for Cancer Research 2000;6(2):709-17.
2000: Attila Nagy; Artur Plonowski; Andrew V Schally
Stability of cytotoxic luteinizing hormone-releasing hormone conjugate (AN-152) containing doxorubicin 14-O-hemiglutarate in mouse and human serum in vitro: implications for the design of preclinical studies.
Proceedings of the National Academy of Sciences of the United States of America 2000;97(2):829-34.
1999: Hippokratis Kiaris; Andrew V Schally; Attila Nagy; Baodong Sun; Patricia Armatis; Karoly Szepeshazi
Targeted cytotoxic analogue of bombesin/gastrin-releasing peptide inhibits the growth of H-69 human small-cell lung carcinoma in nude mice.
British journal of cancer 1999;81(6):966-71.
1999: Z Kahán; Attila Nagy; Andrew V Schally; Francine Hebert; Baodong Sun; Kate Groot; Gabor Halmos
Inhibition of growth of MX-1, MCF-7-MIII and MDA-MB-231 human breast cancer xenografts after administration of a targeted cytotoxic analog of somatostatin, AN-238.
International journal of cancer. Journal international du cancer 1999;82(4):592-8.
1999: Karoly Szepeshazi; Andrew V Schally; Attila Nagy
Effective treatment of advanced estrogen-independent MXT mouse mammary cancers with targeted cytotoxic LH-RH analogs.
Breast cancer research and treatment 1999;56(3):267-76.
1999: Andrew V Schally; Attila Nagy
Cancer chemotherapy based on targeting of cytotoxic peptide conjugates to their receptors on tumors.
European journal of endocrinology / European Federation of Endocrine Societies 1999;141(1):1-14.
1999: Z Kahán; Attila Nagy; Andrew V Schally; Gabor Halmos; Jose M Arencibia; Kate Groot
Complete regression of MX-1 human breast carcinoma xenografts after targeted chemotherapy with a cytotoxic analog of luteinizing hormone-releasing hormone, AN-207.
Cancer 1999;85(12):2608-15.
1999: M Miyazaki; Andrew V Schally; Attila Nagy; N Lamharzi; Gabor Halmos; Karoly Szepeshazi; Patricia Armatis
Targeted cytotoxic analog of luteinizing hormone-releasing hormone AN-207 inhibits growth of OV-1063 human epithelial ovarian cancers in nude mice.
American journal of obstetrics and gynecology 1999;180(5):1095-103.
1999: Artur Plonowski; Andrew V Schally; Attila Nagy; Baodong Sun; Karoly Szepeshazi
Inhibition of PC-3 human androgen-independent prostate cancer and its metastases by cytotoxic somatostatin analogue AN-238.
Cancer research 1999;59(8):1947-53.
1999: Gabor Halmos; Attila Nagy; N Lamharzi; Andrew V Schally
Cytotoxic analogs of luteinizing hormone-releasing hormone bind with high affinity to human breast cancers.
Cancer letters 1999;136(2):129-36.
1999: M Koppán; Attila Nagy; Andrew V Schally; Artur Plonowski; Gabor Halmos; Jose M Arencibia; Kate Groot
Targeted cytotoxic analog of luteinizing hormone-releasing hormone AN-207 inhibits the growth of PC-82 human prostate cancer in nude mice.
The Prostate 1999;38(2):151-8.
1998: Miklos Koppan; Attila Nagy; Andrew V Schally; Jose M Arencibia; Artur Plonowski; Gabor Halmos
Targeted cytotoxic analogue of somatostatin AN-238 inhibits growth of androgen-independent Dunning R-3327-AT-1 prostate cancer in rats at nontoxic doses.
Cancer research 1998;58(18):4132-7.
1998: Attila Nagy; Andrew V Schally; Gabor Halmos; Patricia Armatis; Renzhi Cai; VJ Csernus; M Kovács; M Koppán; K Szepesházi; Z Kahán
Synthesis and biological evaluation of cytotoxic analogs of somatostatin containing doxorubicin or its intensely potent derivative, 2-pyrrolinodoxorubicin.
Proceedings of the National Academy of Sciences of the United States of America 1998;95(4):1794-9.
1998: K Toth; Magdolna Kovacs; Marta Zarandi; Gabor Halmos; Kate Groot; Attila Nagy; Z Kele; Andrew V Schally
New analogs of human growth hormone-releasing hormone (1-29) with high and prolonged antagonistic activity.
The journal of peptide research : official journal of the American Peptide Society 1998;51(2):134-41.
1997: M Miyazaki; Attila Nagy; Andrew V Schally; N Lamharzi; Gabor Halmos; Karoly Szepeshazi; Kate Groot; Patricia Armatis
Growth inhibition of human ovarian cancers by cytotoxic analogues of luteinizing hormone-releasing hormone.
Journal of the National Cancer Institute 1997;89(23):1803-9.
1997: Karoly Szepeshazi; Andrew V Schally; Attila Nagy; Gabor Halmos; Kate Groot
Targeted cytotoxic luteinizing hormone releasing hormone (LH-RH) anlalogs inhibit growth of estrogen independent MXT mouse mammary cancers in vivo by decreasing cell proliferation and inducing apoptosis.
Anti-cancer drugs 1997;8(10):974-87.
1997: Magdolna Kovacs; Andrew V Schally; Attila Nagy; Miklos Koppan; Kate Groot
Recovery of pituitary function after treatment with a targeted cytotoxic analog of luteinizing hormone-releasing hormone.
Proceedings of the National Academy of Sciences of the United States of America 1997;94(4):1420-5.
1997: Attila Nagy; Patricia Armatis; Renzhi Cai; Karoly Szepeshazi; Gabor Halmos; Andrew V Schally
Design, synthesis, and in vitro evaluation of cytotoxic analogs of bombesin-like peptides containing doxorubicin or its intensely potent derivative, 2-pyrrolinodoxorubicin.
Proceedings of the National Academy of Sciences of the United States of America 1997;94(2):652-6.
1997: Marta Zarandi; Magdolna Kovacs; Judit E Horvath; K Toth; Gabor Halmos; Kate Groot; Attila Nagy; Z Kele; Andrew V Schally
Synthesis and in vitro evaluation of new potent antagonists of growth hormone-releasing hormone (GH-RH).
Peptides 1997;18(3):423-30.
1996: Attila Nagy; Andrew V Schally; Patricia Armatis; Karoly Szepeshazi; Gabor Halmos; Magdolna Kovacs; Marta Zarandi; Kate Groot; M Miyazaki; Andreas Jungwirth; J Horvath
Cytotoxic analogs of luteinizing hormone-releasing hormone containing doxorubicin or 2-pyrrolinodoxorubicin, a derivative 500-1000 times more potent.
Proceedings of the National Academy of Sciences of the United States of America 1996;93(14):7269-73.
1996: Attila Nagy; Patricia Armatis; Andrew V Schally
High yield conversion of doxorubicin to 2-pyrrolinodoxorubicin, an analog 500-1000 times more potent: structure-activity relationship of daunosamine-modified derivatives of doxorubicin.
Proceedings of the National Academy of Sciences of the United States of America 1996;93(6):2464-9.
1996: Karoly Szepeshazi; Andrew V Schally; Gabor Halmos; B Szoke; Kate Groot; Attila Nagy
Effect of a cytotoxic analog of LH-RH (T-98) on the growth of estrogen-dependent MXT mouse mammary cancers: correlations between growth characteristics and EGF receptor content of tumors.
Breast cancer research and treatment 1996;40(2):129-39.
1994: Marta Zarandi; Judit E Horvath; Gabor Halmos; Jacek Pinski; Attila Nagy; Kate Groot; Z Rekasi; Andrew V Schally
Synthesis and biological activities of highly potent antagonists of growth hormone-releasing hormone.
Proceedings of the National Academy of Sciences of the United States of America 1994;91(25):12298-302.
1994: B Szöke; J Horváth; Gabor Halmos; Z Rékási; Kate Groot; Attila Nagy; Andrew V Schally
LH-RH analogue carrying a cytotoxic radical is internalized by rat pituitary cells in vitro.
Peptides 1994;15(2):359-66.
1993: Attila Nagy; B Szoke; Andrew V Schally
Selective coupling of methotrexate to peptide hormone carriers through a gamma-carboxamide linkage of its glutamic acid moiety: benzotriazol-1-yloxytris(dimethylamino)phosphonium hexafluorophosphate activation in salt coupling.
Proceedings of the National Academy of Sciences of the United States of America 1993;90(13):6373-6.
1993: Z Rékási; B Szöke; Attila Nagy; Kate Groot; E S Rékási; Andrew V Schally
Effect of luteinizing hormone-releasing hormone analogs containing cytotoxic radicals on the function of rat pituitary cells: tests in a long term superfusion system.
Endocrinology 1993;132(5):1991-2000.
1993: Jacek Pinski; T Yano; T Janaky; Attila Nagy; A Juhasz; L Bokser; Kate Groot; Andrew V Schally
Evaluation of biological activities of new LH-RH antagonists (T-series) in male and female rats.
International journal of peptide and protein research 1993;41(1):66-73.
1993: Jacek Pinski; Andrew V Schally; T Yano; Karoly Szepeshazi; Gabor Halmos; Kate Groot; A M Comaru-Schally; Sinisa Radulovic; Attila Nagy
Inhibition of growth of experimental prostate cancer in rats by LH-RH analogs linked to cytotoxic radicals.
The Prostate 1993;23(2):165-78.
1992: Karoly Szepeshazi; Andrew V Schally; A Juhasz; Attila Nagy; T Janaky
Effect of luteinizing hormone-releasing hormone analogs containing cytotoxic radicals on growth of estrogen-independent MXT mouse mammary carcinoma in vivo.
Anti-cancer drugs 1992;3(2):109-16.
1992: Sinisa Radulovic; Attila Nagy; B Szoke; Andrew V Schally
Cytotoxic analog of somatostatin containing methotrexate inhibits growth of MIA PaCa-2 human pancreatic cancer xenografts in nude mice.
Cancer letters 1992;62(3):263-71.
1992: Renzhi Cai; Sinisa Radulovic; Jacek Pinski; Attila Nagy; T W Redding; D B Olsen; Andrew V Schally
Pseudononapeptide bombesin antagonists containing C-terminal Trp or Tpi.
Peptides 1992;13(2):267-71.
1992: Tamás Janáky; A Juhász; S Bajusz; V Csernus; G Srkalovic; L Bokser; S Milovanovic; T W Redding; Z Rékási; Attila Nagy
Analogues of luteinizing hormone-releasing hormone containing cytotoxic groups.
Proceedings of the National Academy of Sciences of the United States of America 1992;89(3):972-6.

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