Found: 13
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Regulation of growth-hormone-receptor gene expression by growth hormone and pegvisomant in human mesangial cells.
- Published in:
- 2003
- By:
- Publication type:
- journal article
Allelic variations in the human growth hormone-1 gene promoter of growth hormone-deficient patients and normal controls.
- Published in:
- European Journal of Endocrinology, 1997, v. 137, n. 5, p. 474, doi. 10.1530/eje.0.1370474
- By:
- Publication type:
- Article
IGHD II: A Novel GH-1 Gene Mutation (GH-L76P) Severely Affects GH Folding, Stability, and Secretion.
- Published in:
- 2015
- By:
- Publication type:
- journal article
Butyrate Increases Intracellular Calcium Levels and Enhances Growth Hormone Release from Rat Anterior Pituitary Cells via the G-Protein-Coupled Receptors GPR41 and 43.
- Published in:
- PLoS ONE, 2014, v. 9, n. 10, p. 1, doi. 10.1371/journal.pone.0107388
- By:
- Publication type:
- Article
Influence of Growth Hormone (GH) Receptor Deletion of Exon 3 and Full-Length Isoforms on GH Response and Final Height in Patients with Severe GH Deficiency.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2008, v. 93, n. 3, p. 974, doi. 10.1210/jc.2007-1382
- By:
- Publication type:
- Article
Exon splice enhancer mutation (GH-E32A) causes autosomal dominant growth hormone deficiency.
- Published in:
- 2007
- By:
- Publication type:
- journal article
Evaluation of the Biological Activity of a Growth Hormone (GH) Mutant (R77C) and Its Impact on GH Responsiveness and Stature.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2007, v. 92, n. 8, p. 2893, doi. 10.1210/jc.2006-2238
- By:
- Publication type:
- Article
Short Stature Caused by a Biologically Inactive Mutant Growth Hormone (GH-C53S).
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2005, v. 90, n. 5, p. 2493, doi. 10.1210/jc.2004-1838
- By:
- Publication type:
- Article
Phenotypic Variability in Familial Combined Pituitary Hormone Deficiency Caused by a PROP1 Gene Mutation Resulting in the Substitution of Arg3Cys at Codon 120 (R120C)
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 1998, v. 83, n. 10, p. 3727, doi. 10.1210/jcem.83.10.5172
- By:
- Publication type:
- Article
Short stature in two siblings heterozygous for a novel bioinactive GH mutant (GH-P59S) suggesting that the mutant also affects secretion of the wild-type GH.
- Published in:
- European Journal of Endocrinology, 2013, v. 168, n. 3, p. K35, doi. 10.1530/EJE-12-0847
- By:
- Publication type:
- Article
GH mutant (R77C) in a pedigree presenting with the delay of growth and pubertal development: structural analysis of the mutant and evaluation of the biological activity.
- Published in:
- European Journal of Endocrinology, 2007, v. 157, p. S67, doi. 10.1530/EJE-07-0339
- By:
- Publication type:
- Article
Alteration of ZnT5-Mediated Zinc Import into the Early Secretory Pathway Affects the Secretion of Growth Hormone from Rat Pituitary Cells.
- Published in:
- Hormone Research in Paediatrics, 2014, v. 82, n. 4, p. 245, doi. 10.1159/000365924
- By:
- Publication type:
- Article
Transient Neonatal Zinc Deficiency Caused by a Heterozygous G87R Mutation in the Zinc Transporter ZnT-2 (SLC30A2) Gene in the Mother Highlighting the Importance of Zn<sup>2+</sup> for Normal Growth and Development.
- Published in:
- International Journal of Endocrinology, 2013, p. 1, doi. 10.1155/2013/259189
- By:
- Publication type:
- Article