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Results: 1-8 |
Results: 8
Design, synthesis, and evaluation of a long-acting, potent analogue of gonadotropin-releasing hormone
Authors: Rahimipour, S Ben-Aroya, N Fridkin, M Koch, Y
Citation: S. Rahimipour et al., Design, synthesis, and evaluation of a long-acting, potent analogue of gonadotropin-releasing hormone, J MED CHEM, 44(22), 2001, pp. 3645-3652
Transcriptional regulation of the human GnRH II gene is mediated by a putative cAMP response element
Authors: Chen, A Laskar-Levy, O Ben-Aroya, N Koch, Y
Citation: A. Chen et al., Transcriptional regulation of the human GnRH II gene is mediated by a putative cAMP response element, ENDOCRINOL, 142(8), 2001, pp. 3483-3492
Two isoforms of gonadotropin-releasing hormone are coexpressed in neuronalcell lines
Authors: Chen, AL Yahalom, D Laskar-Levy, O Rahimipour, S Ben-Aroya, N Koch, Y
Citation: Al. Chen et al., Two isoforms of gonadotropin-releasing hormone are coexpressed in neuronalcell lines, ENDOCRINOL, 142(2), 2001, pp. 830-837
Hexapeptide and cyclic pentapeptide endothelin antagonists directly activate pituitary gonadotropin-releasing hormone receptors
Authors: Yahalom, D Koch, Y Ben-Aroya, N Fridkin, M
Citation: D. Yahalom et al., Hexapeptide and cyclic pentapeptide endothelin antagonists directly activate pituitary gonadotropin-releasing hormone receptors, MOLEC PHARM, 57(4), 2000, pp. 718-724
Structure-activity studies of reduced-size gonadotropin-releasing hormone agonists derived from the sequence of an endothelin antagonist
Authors: Yahalom, D Rahimipour, S Koch, Y Ben-Aroya, N Fridkin, M
Citation: D. Yahalom et al., Structure-activity studies of reduced-size gonadotropin-releasing hormone agonists derived from the sequence of an endothelin antagonist, J MED CHEM, 43(15), 2000, pp. 2824-2830
Design and synthesis of potent hexapeptide and heptapeptide gonadotropin-releasing hormone antagonists by truncation of a decapeptide analogue sequence
Authors: Yahalom, D Rahimipour, S Koch, Y Ben-Aroya, N Fridkin, M
Citation: D. Yahalom et al., Design and synthesis of potent hexapeptide and heptapeptide gonadotropin-releasing hormone antagonists by truncation of a decapeptide analogue sequence, J MED CHEM, 43(15), 2000, pp. 2831-2836
Synthesis and bioactivity of fatty acid-conjugated GnRH derivatives
Authors: Yahalom, D Koch, Y Ben-Aroya, N Fridkin, M
Citation: D. Yahalom et al., Synthesis and bioactivity of fatty acid-conjugated GnRH derivatives, LIFE SCI, 64(17), 1999, pp. 1543-1552
The gonadotropin-releasing hormone family of neuropeptides in the brain ofhuman, bovine and rat: identification of a third isoform
Authors: Yahalom, D Chen, A Ben-Aroya, N Rahimipour, S Kaganovsky, E Okon, E Fridkin, M Koch, Y
Citation: D. Yahalom et al., The gonadotropin-releasing hormone family of neuropeptides in the brain ofhuman, bovine and rat: identification of a third isoform, FEBS LETTER, 463(3), 1999, pp. 289-294
Risultati: 1-8 |