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Endocrinology|September 1, 1996
Inverse agonism of amino-terminally truncated parathyroid hormone (PTH) and PTH-related peptide (PTHrP) analogs revealed with constitutively active mutant PTH/PTHrP receptorsT J Gardella, M D Luck, G S Jensen, et al.
Peptides|January 1, 1994
Differences in binding affinities of human PTH(1-84) do not alter biological potency: a comparison between chemically synthesized hormone, natural and mutant formsO K Olstad, N E Morrison, R Jemtland, et al.
The Journal of Clinical Endocrinology and Metabolism|November 24, 1999
A novel immunoradiometric assay detects full-length human PTH but not amino-terminally truncated fragments: implications for PTH measurements in renal failureM R John, W G Goodman, P Gao, et al.
Kidney International|December 16, 1998
Growth of long bones in renal failure: roles of hyperparathyroidism, growth hormone and calcitriolC P Sanchez, I B Salusky, B D Kuizon, et al.
Endocrinology|April 4, 2000
Impaired growth, delayed ossification, and reduced osteoclastic activity in the growth plate of calcium-supplemented rats with renal failureC P Sanchez, B D Kuizon, P A Abdella, et al.
Endocrinology|August 1, 1996
Cell-specific signal transduction of parathyroid hormone (PTH)-related protein through stably expressed recombinant PTH/PTHrP receptors in vascular smooth muscle cellsS Maeda, S Wu, H Jüppner, et al.
Nature|April 11, 1991
A novel cyclin encoded by a bcl1-linked candidate oncogeneT Motokura, T Bloom, H G Kim, et al.
Molecular Endocrinology (Baltimore, Md.)|October 1, 1995
Homolog-scanning mutagenesis of the parathyroid hormone (PTH) receptor reveals PTH-(1-34) binding determinants in the third extracellular loopC Lee, M D Luck, H Jüppner, et al.
The Journal of Endocrinology|May 26, 2001
Extracts from tumors causing oncogenic osteomalacia inhibit phosphate uptake in opossum kidney cellsK B Jonsson, M Mannstadt, A Miyauchi, et al.
Biochemistry|July 31, 1990
Preparation and characterization of [N alpha-(4-azido-2-nitrophenyl)Ala1,Tyr36]-parathyroid hormone related peptide (1-36)amide: a high-affinity, partial agonist having high cross-linking efficiency with its receptor on ROS 17/2.8 cellsH Jüppner, A B Abou-Samra, S Uneno, et al.
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