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Gene Information

Gene symbol: NAMPT

Gene name: nicotinamide phosphoribosyltransferase

HGNC ID: 30092

Synonyms: PBEF

Related Genes

# Gene Symbol Number of hits
1 ADIPOQ 1 hits
2 AGT 1 hits
3 AKT1 1 hits
4 CCL2 1 hits
5 COL1A1 1 hits
6 INS 1 hits
7 INSR 1 hits
8 LEP 1 hits
9 MAPK1 1 hits
10 MAPK3 1 hits
11 RETN 1 hits
12 SERPINE1 1 hits
13 SIRT1 1 hits
14 SIRT3 1 hits
15 SLC2A1 1 hits

Related Sentences

# PMID Sentence
1 20375985 Visfatin (also known as pre-B cell colony-enhancing factor) is a newly discovered adipocytokine that is preferentially produced by visceral fat and regulated by cytokines promoting insulin resistance.
2 20375985 Further, in both renal cells, visfatin synthesis was significantly increased by high glucose in the media but not by angiotensin II.
3 20375985 Additionally, visfatin treatment induced rapid uptake of glucose and was associated with increased translocation of GLUT-1 to the cellular membrane of both renal cell types.
4 20375985 Furthermore, visfatin induced tyrosine phosphorylation of the insulin receptor, activated downstream insulin signaling pathways such as Erk-1, Akt, and p38 MAPK, and markedly increased the levels of TGFbeta1, PAI-1, type I collagen, and MCP-1 in both renal cells.
5 20375985 Visfatin (also known as pre-B cell colony-enhancing factor) is a newly discovered adipocytokine that is preferentially produced by visceral fat and regulated by cytokines promoting insulin resistance.
6 20375985 Further, in both renal cells, visfatin synthesis was significantly increased by high glucose in the media but not by angiotensin II.
7 20375985 Additionally, visfatin treatment induced rapid uptake of glucose and was associated with increased translocation of GLUT-1 to the cellular membrane of both renal cell types.
8 20375985 Furthermore, visfatin induced tyrosine phosphorylation of the insulin receptor, activated downstream insulin signaling pathways such as Erk-1, Akt, and p38 MAPK, and markedly increased the levels of TGFbeta1, PAI-1, type I collagen, and MCP-1 in both renal cells.
9 20375985 Visfatin (also known as pre-B cell colony-enhancing factor) is a newly discovered adipocytokine that is preferentially produced by visceral fat and regulated by cytokines promoting insulin resistance.
10 20375985 Further, in both renal cells, visfatin synthesis was significantly increased by high glucose in the media but not by angiotensin II.
11 20375985 Additionally, visfatin treatment induced rapid uptake of glucose and was associated with increased translocation of GLUT-1 to the cellular membrane of both renal cell types.
12 20375985 Furthermore, visfatin induced tyrosine phosphorylation of the insulin receptor, activated downstream insulin signaling pathways such as Erk-1, Akt, and p38 MAPK, and markedly increased the levels of TGFbeta1, PAI-1, type I collagen, and MCP-1 in both renal cells.
13 20375985 Visfatin (also known as pre-B cell colony-enhancing factor) is a newly discovered adipocytokine that is preferentially produced by visceral fat and regulated by cytokines promoting insulin resistance.
14 20375985 Further, in both renal cells, visfatin synthesis was significantly increased by high glucose in the media but not by angiotensin II.
15 20375985 Additionally, visfatin treatment induced rapid uptake of glucose and was associated with increased translocation of GLUT-1 to the cellular membrane of both renal cell types.
16 20375985 Furthermore, visfatin induced tyrosine phosphorylation of the insulin receptor, activated downstream insulin signaling pathways such as Erk-1, Akt, and p38 MAPK, and markedly increased the levels of TGFbeta1, PAI-1, type I collagen, and MCP-1 in both renal cells.
17 24107418 Altered levels of the adipokines leptin, adiponectin, resistin, and visfatin can decrease the glomerular filtration rate and increase albuminuria, which are pathophysiological changes typical of CKD.
18 24107418 In addition, the adipokines leptin and adiponectin can act on tubular networks.
19 29608912 In addition, histological, western blot and PCR analysis of the Tg26 mice kidneys showed a downregulation of NAMPT, SIRT1, and SIRT3 expressions levels.