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Kidney International|April 1, 1994
Reduced hepatic growth hormone (GH) receptor gene expression and increased plasma GH binding protein in experimental uremiaB Tönshoff, S Edén, E Weiser, et al.
European Journal of Endocrinology|November 22, 1997
Serum leptin in short children born small for gestational age: relationship with the growth response to growth hormone treatment. The Swedish Study Group for Growth Hormone TreatmentM Boguszewski, J Dahlgren, R Bjarnason, et al.
Scandinavian Journal of Immunology|January 1, 1976
Suppressor cell activity in a male infant with T-and B-lymphocyte dysfunction treated with thymosinL A Hanson, L Lindholm, B Carlsson, et al.
Diabetes Research and Clinical Practice|April 13, 2010
Differences in associations between HSD11B1 gene expression and metabolic parameters in subjects with and without impaired glucose homeostasisC Karlsson, M Jernås, B Olsson, et al.
Endocrinology|May 1, 1996
Differential long-term effects of insulin-like growth factor-I (IGF-I) growth hormone (GH), and IGF-I plus GH on body growth and IGF binding proteins in hypophysectomized ratsP J Fielder, D L Mortensen, P Mallet, et al.
Growth Hormone & IGF Research : Official Journal of the Growth Hormone Research Society and the International IGF Research Society|January 29, 2003
The effect of treatment with the oral growth hormone (GH) secretagogue MK-677 on GH isoformsJ Svensson, C L Boguszewski, F Shibata, et al.
Endocrinology|March 1, 1997
Comparison of the ligand binding specificity and transcript tissue distribution of estrogen receptors alpha and betaG G Kuiper, B Carlsson, K Grandien, et al.
Pediatric Research|August 1, 1993
The effect of caloric supplementation on selected milk protective factors in undernourished Guatemalan mothersM V Herías, J R Cruz, T González-Cossío, et al.
CPT: Pharmacometrics & Systems Pharmacology|May 31, 2017
Translational Modeling to Guide Study Design and Dose Choice in Obesity Exemplified by AZD1979, a Melanin-concentrating Hormone Receptor 1 AntagonistP Gennemark, M Trägårdh, D Lindén, et al.
Human Molecular Genetics|July 1, 1997
Missense mutations in the human glutathione synthetase gene result in severe metabolic acidosis, 5-oxoprolinuria, hemolytic anemia and neurological dysfunctionN Dahl, M Pigg, E Ristoff, et al.
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