AUTORADIOGRAPHIC STUDY OF BINDING AND INTERNALIZATION OF A LUTEINIZING-HORMONE-RELEASING HORMONE ANTAGONIST [D-NAL1, D-CPA2, A-D-TRP3, D-ARG6, D-ALA10]LHRH BY RAT PITUITARY GONADOTROPHS

被引：1

作者：

BADR, M ^{[1
]}

PELLETIER, G ^{[1
]}

机构：

[1] CHU LAVAL,MOLEC ENDOCRINOL GRP,MRC,QUEBEC CITY G1V 4G2,QUEBEC,CANADA

来源：

JOURNAL OF NEUROENDOCRINOLOGY | 1989年 / 1卷 / 02期

关键词：

D O I：

10.1111/j.1365-2826.1989.tb00093.x

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

引用

页码：141 / 146

页数：6

共 46 条

[21] INHIBITION BY N-METHYL-D-ASPARTIC ACID (NMDA) RECEPTOR ANTAGONIST OF LORDOSIS BEHAVIOR INDUCED BY ESTROGEN FOLLOWED BY PROGESTERONE OR LUTEINIZING-HORMONE-RELEASING HORMONE (LHRH) IN THE RAT
GARGIULO, PA
MUNOZ, V
DONOSO, AO
PHYSIOLOGY & BEHAVIOR, 1992, 52 (04) : 737 - 739
[22] REPRODUCTIVE ENDOCRINE AND ANAPHYLACTOID PROPERTIES OF AN LHRH-ANTAGONIST, ORF-18260 [AC-DNAL1(2),4FDPHE2,D-TRP3,D-ARG6]-GNRH
HAHN, DW
MCGUIRE, JL
VALE, WW
RIVIER, J
LIFE SCIENCES, 1985, 37 (06) : 505 - 514
[23] ANTIFERTILITY PROPERTIES OF A POTENT LHRH-ANTAGONIST, ORF-18260 [AC-DNAL-1(2), 4 FD PHE2,D-TRP3,D-ARG6]-GNRH
MCGUIRE, JL
VALE, WW
RIVIER, J
CONTRACEPTIVE DELIVERY SYSTEMS, 1984, 5 (03) : 37 - 37
[24] RADIOIMMUNOASSAY OF AN ANALOG OF LUTEINIZING-HORMONE-RELEASING HORMONE, [D-SER(TBU)]6DES-GLY-NH2-10 ETHYLAMIDE (BUSERELIN)
SAITO, S
SAITO, H
YAMASAKI, R
HOSOI, E
KOMATSU, M
IWAHANA, H
MAEDA, T
JOURNAL OF IMMUNOLOGICAL METHODS, 1985, 79 (02) : 173 - 183
[25] THE LUTEINIZING-HORMONE-RELEASING HORMONE (LHRH) AGONIST [D-TRP6-PRO9-NET]LHRH INCREASED RATHER THAN LOWERED LH AND ALPHA-SUBUNIT LEVELS IN A PATIENT WITH AN LH-SECRETING PITUITARY-TUMOR
ROMAN, SH
GOLDSTEIN, M
KOURIDES, IA
COMITE, F
BARDIN, CW
KRIEGER, DT
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1984, 58 (02): : 313 - 319
[26] RESULTS OF 3-TIMES-PER-WEEK LONG-TERM ADMINISTRATION OF A LUTEINIZING-HORMONE-RELEASING HORMONE (LHRH) ANALOG, D-SER-(TBU)6-LHRH-(EA)10 IN PRIMARY AMENORRHEA
BATRINOS, ML
ANAPLIOTOU, M
PANITSAFAFLIA, C
PITOULIS, S
FERTILITY AND STERILITY, 1981, 35 (05) : 515 - 520
[27] INSENSITIVITY OF BONNET MONKEYS TO (D-ALA6, DES-GLY10) LHRH ETHYLAMIDE, A POTENT NEW LUTEINIZING-HORMONE RELEASING HORMONE ANALOG IN RATS AND MICE
LEVITAN, D
BEITINS, IZ
MILTON, G
BARNES, A
MCARTHUR, JW
ENDOCRINOLOGY, 1977, 100 (04) : 918 - 922
[28] SYNTHESIS OF [1,6-CYCLO(ACETYL-1-L-GLUTAMIC ACID, 2-D-PHENYLALANINE, 3-D-TRYPTOPHAN, 6-D-LYSINE)] LUTEINIZING-HORMONE-RELEASING HORMONE ON POLY-N-ACRYLYLPYRROLIDINE RESIN
SMITH, CW
SKALA, G
WILKS, JW
INTERNATIONAL JOURNAL OF PEPTIDE AND PROTEIN RESEARCH, 1983, 21 (02): : 127 - 134
[29] MORPHOLOGICAL-STUDIES OF THE CANINE PITUITARY LUTEINIZING-HORMONE (LH) CELLS AFTER LONG-TERM TREATMENT WITH THE LH-RELEASING HORMONE (LHRH) AGONIST [D-TRP6]LHRH ETHYLAMIDE
DUBE, D
PELLETIER, G
LABRIE, F
ENDOCRINOLOGY, 1987, 120 (02) : 589 - 594
[30] THE EFFECTS OF AN LH-RH ANTAGONIST ([N-AC-D-TRP1'3,D-P-CL-PHE2,D-PHE6,D-ALA10]-LH-RH) DURING THE PREOVULATORY PERIOD OF THE RHESUS-MONKEY
BALMACEDA, JP
SCHALLY, AV
COY, D
ASCH, RH
CONTRACEPTION, 1981, 24 (03) : 275 - 281

← 1 2 3 4 5 →