Mouse growth hormone,GH ELISA KIT

1. The results indicate that increased circulating GH is associated with a reduced ovarian primordial follicle reserve and increased pFoxO3a content in oocytes. PMID: 27771355
2. These results indicate that up-regulation of GH in the lungs of DJ-1 KO mice may enhance the malignancy of B16F10 cells and nodule formation in pulmonary metastasis of melanoma. PMID: 27825319
3. Confirmation of the impairment of GH-IGF-1 release in hyperphagic MC4R KO mice suggests a role for insulin in regulating both the release of GH, but also in mediating growth during periods of physiologically suppressed GH-IGF-1 levels PMID: 27558671
4. When charged with hypoxia-ischemia, mutant brains with deleted IGF-1 receptor were broadly protected from cell damage, neuroinflammation and cerebral edema. PMID: 26762506
5. Thiol-disulfide exchange reactions in hGH and related model peptides were influenced by higher order structure, by the size of the thiol reactant and by an Arg residue adjacent to Cys in the thiol reactant. PMID: 26887678
6. Growth hormone deficient mice exhibited renal hypertrophy in tubular epithelial cells. PMID: 26997624
7. observations demonstrate that germline loss of ghrelin-O-acyltransferase alters Growth Hormone release and patterning PMID: 26442444
8. alter miR-19b concentrations in hematopoietic stem cells (HSCs) and affect HSC migration PMID: 26465715
9. Moderate elevations in circulating GH and IGF-I can directly increase basal insulin secretion without impacting beta-cell mass, independent of changes in whole body insulin sensitivity and hyperlipidemia. PMID: 25936582
10. Acylated ghrelin is not required for the surge in pituitary growth hormone observed in pregnant mice. PMID: 25645493
11. STAT5 signaling is increased in the liver in GH-transgenic mice during the growth period, with a balance between positive and negative effectors resulting in accelerated but controlled growth. PMID: 25691498
12. Our data indicate that FGF21 is important in the regulation of beta-cell proliferation and insulin synthesis, probably via modulation of GH signaling PMID: 25811804
13. Hepatic GH actions normally serve to inhibit de novo lipogenesis (DNL), where loss of this inhibitory signal may explain, in part, the inappropriate increase in hepatic DNL observed in NAFLD patients. PMID: 26015548
14. The effects of osteocalcin on testosterone and on induction of the growth hormone/insulin-like growth factor-1 axis, were investigated. PMID: 24691732
15. The development of GH excess induced liver-, kidney-, and pituitary gland-alterations in GH transgenic mice are independent of IGF1 whereas GH- stimulated body growth depends on IGF1. PMID: 25017732
16. The role of somatostatin in the expression of growth hormone in male and female mice is reported. PMID: 25551181
17. Data suggest that Gh represses H6pd (hexose-6-phosphate dehydrogenase) through locally produced Igf1 (insulin-like growth factor 1); Gh directly represses Hsd11b1 (11-beta-hydroxysteroid dehydrogenase 1) mRNA rather than acting via Igf1 receptor. PMID: 24759003
18. GH resistance dramatically exacerbates liver fibrosis in model of inflammatory cholestasis PMID: 25179284
19. These results further support a role of GH/IGF-I in regulating mammary tumorigenesis but suggest the ultimate consequences of GH/IGF-I on breast tumor development are dependent on the diet and/or metabolic status. PMID: 25085903
20. Exposure of mGH to UV light results in a wide spectrum of chemical modifications with immunogenic consequences. PMID: 24758742
21. Ghrelin is a regulator of GH pulse amplitude in growing mice. PMID: 24949662
22. robust GH-stimulated hepatic Igf1 gene transcription utilizes tissue-specific mechanisms of epigenetic regulation that are established independent of GH signaling. PMID: 24109593
23. Data (including data from knockout mice) suggest that GH/GH receptor signaling in liver plays important roles in body size and body composition throughout life; in addition, liver-derived Igf1 (somatomedin) is important for normal body growth. PMID: 24517230
24. The GH/IGF milieu does impact the growth of PTEN-deficient dysplastic prostatic cells. PMID: 23689346
25. growth hormone resistance in adipocytes reduced lipolysis and increased body fat. PMID: 23782652
26. Growth hormone seems to be necessary for the increased adipose p53 expression and for insulin resistance of obese mice. PMID: 23913444
27. In vivo knockdown of SIRT1 in the liver restored the fasting-induced decrease in serum IGF-I levels and enhanced the GH-dependent increase in IGF-I levels, indicating that SIRT1 negatively regulates GH-dependent IGF-I production in the liver. PMID: 23980167
28. the increased expression of FGF21 during chronic undernutrition inhibits GH action on chondrocytes by activating LEPROT and LEPROTL1. PMID: 23940039
29. Data from mouse strain (Y*; created by genetic recombination) suggest neural GH of hypothalamic preoptic area is involved in mechanism by which sex chromosome dosage affects appetite regulation, increase in body weight, and susceptibility to obesity. PMID: 23861378
30. The prolonged exposure to Growth hormone induces in the liver alterations in signaling pathways involved in cell growth, proliferation and survival. PMID: 23428905
31. Specific removal of GHR in adipose tissue is sufficient to increase adipose tissue and decrease circulating adipsin. PMID: 23349524
32. Microarray revealed 116 genes to be up or down regulated in the cochlea between young and old animals, the most prominent being prolactin (108.2 fold increase) and growth hormone (43.94 fold increase). PMID: 23010755
33. Increased adiposity and insulin level is associated with the suppression of pulsatile GH secretion during weight gain. PMID: 23708999
34. Data indicate a putative hypoxia response element (HRE) in the growth hormone (GH) promoter at the region -176 bp to -172 bp that contains a copy of the hypoxia-inducible factor-1 (Hif-1) binding motif (5'-ACGTG-3'). PMID: 23639351
35. Targeted deletion of growth hormone (GH) receptor in macrophage reveals novel osteopontin-mediated effects of GH on glucose homeostasis and insulin sensitivity in diet-induced obesity. PMID: 23595986
36. STAT5 proteins prevent progressive fatty liver disease and the formation of aggressive hepatocellular carcinoma in the setting of hyperactivated GH signaling. They play a key role in controlling systemic inflammation and regulating organ and body size. PMID: 22031092
37. Reciprocal relationships between GH signaling and longevity discovered in mutant mice are discussed in this review and apply also to normal mice and other mammalian species. PMID: 21852148
38. CST inhibited GH and adrenocorticotropin-hormone axes in a gender-dependent fashion. PMID: 21971153
39. Elevated endogenous GH promotes lean mass and whole-body lipid oxidation but has minimal effects on adiposity PMID: 21990313
40. GH-induced hepatic FGF21 production is mediated by FFA released from adipose tissues, and elevated FGF21 in turn acts as a negative feedback signal to terminate GH-stimulated lipolysis in adipocytes PMID: 21849508
41. Data suggest that the induction of isoforms of the GH molecule in cells of the immune system may be an important mechanism of adaptation and/or protection of lymphoid cells under conditions of oxidative stress. PMID: 21741628
42. Hepatic STAT5/GR signaling is crucial for the maintenance of systemic lipid homeostasis. PMID: 21725989
43. Data show that the pituitary gland contributes to the sexually dimorphic patterns of growth hormone secretion that play an important role in differences in growth and metabolism between the sexes. PMID: 21098290
44. sterol regulatory element-binding protein (SREBP)-1a links growth hormone action to lipid metabolism in hepatocytes PMID: 20863500
45. Nadir-to-peak distribution of plasma GH concentration in mice was similar to other mammals, and that nycthemeral and sex differences existed as well. We found handling stress to be a potent immediate downregulator of circulating GH. PMID: 21045135
46. Despite normal plasma free fatty acids and minimal obesity, absent growth hormone activation leads to steatosis because activated STAT5 prevents hepatic steatosis. PMID: 21084450
47. the actions of GH on ZEB2 and P- and E-cadherin expression play a role in the pathogenesis of microalbuminuria of DN. PMID: 20682777
48. The serum balance in liver IGF-1-deficient mice that favors GH over IGF-1 diminished the effects of ablated ovarian function on numbers of osteoclast precursors in the marrow and viability of osteocytes within the cortical matrix PMID: 19619004
49. Ghrelin O-acyltransferase (GOAT) is essential for growth hormone-mediated survival of calorie-restricted mice PMID: 20231469
50. loss of STAT5 sensitizes hepatocytes to bile acid-induced damage and apoptosis caused by disruption of GH-induced transcription of Igf-1 and down-regulation of hepatoprotective genes. PMID: 20162728

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KEGG: mmu:14599

STRING: 10090.ENSMUSP00000099360

UniGene: Mm.343934