TRPM6 Antibody

1. Results identified high expression of TRPM6 to be indicative of a prolonged overall survival in colorectal patients. Computational analysis suggest that TRPM6 may be targeted by hsalet7g and hsalet7f1. PMID:30272358
2. Spectrometric analysis identified phosphorylation sites in TRPM6 protein. PMID:28220887
3. Knockout of TRPM6 or inactivation of its kinase results in global changes in histone S/T phosphorylation and changes the transcription of hundreds of genes. PMID:28784805
4. Results found that the haplotype containing two common TRPM6 SNPs (rs3750425 and rs2274924) increases the risk for proton pump inhibitor-induced hypomagnesemia. PMID:27926584
5. TNF-alpha rescues the EGFR tyrosine kinase inhibitor-induced decrease in TRPM6 expression and Mg2+ influx mediated via the activation of an NF-kappaB signaling pathway. PMID:27925186
6. A homozygous frame-shift mutation in the TRPM6 gene is associated with Hereditary hypomagnesemia with secondary hypocalcemia. PMID:26759217
7. we showed that two serum magnesium associated loci, MUC1 and TRPM6, had significant effect modification with progestin use and insulin levels, respectively, in European Americans. PMID:26058915
8. TRPM6 mRNA and protein levels in atrial fibrillation group were elevated markedly in comparison with sinus rhythm group. PMID:25796343
9. Knowledge of TRPM6 functioning is of vital importance to decipher its role in Mg handling and will, in particular, provide a molecular basis for achieving a better understanding of Mg mal(re)absorption and hence systemic Mg balance. PMID:24906182
10. We conclude that the new TRPM6 missense mutations lead to dysregulated intestinal/renal Mg(2+) (re)absorption as a consequence of loss of TRPM6 channel function. PMID:23942199
11. TRPM6 kinase activity is linked to channel activity through a kinase-independent mechanism involving the dimerization motif binding to a pocket within the kinase domain. PMID:24650431
12. Two novel mutations in Chinese sisters with familial hypomagnesemia with secondary hypocalcemia were found: one frameshift mutation (c.1196delC) and one non-sense mutation (c.4577G>A). Both patients were compound heterozygotes for these mutations. PMID:23689795
13. PIP2 is required for TRPM6 channel function; hydrolysis of PIP2 by PLC-coupled hormones/agonists may constitute an important pathway for TRPM6 gating, and perhaps Mg2+ homeostasis. PMID:22180838
14. Case Report: Resolving basal ganglia calcification in hereditary hypomagnesemia with secondary hypocalcemia due to a novel TRPM6 gene mutation. PMID:22982920
15. Loss of insulin-induced activation of TRPM6 magnesium channels results in impaired glucose tolerance during pregnancy PMID:22733750
16. A novel mutation of TRPM6 gene is responsible for the development of familial hypommagnesaemia in Turkish children. PMID:21669885
17. Results suggest that TRPM6 expression is up-regulated by a PI3K/Akt/mTOR pathway . PMID:21073857
18. Loss-of-function mutations cause hypomagnesemia with secondary hypocalcemia. PMID:20395377
19. Up-regulation of TRPM6 transcriptional activity by AP-1 in renal epithelial cells. PMID:19937979
20. Deficiency /mutations of TRPM6 causes hypomagnesemia with secondary hypocalcemia PMID:12032568
21. Individuals with TRPM6 mutations have abnormal renal magnesium excretion. Deficiency causes hypomagnesemia with secondary hypocalcemia. PMID:12032570
22. TRPM6 is specifically localized along the apical membrane of the renal distal convoluted tubule and the brush-border membrane of the small intestine and is specific for Mg2+ absoprtion. PMID:14576148
23. TRPM6 specifically interacted with its closest homolog, the Mg(2+)-permeable cation channel TRPM7, resulting in the assembly of functional TRPM6/TRPM7 complexes at the cell surface. PMID:14976260
24. In patients with primary hypomagnesaemia and secondary hypocalcaemia (HSH), a combined defect of intestinal magnesium absorption and renal magnesium conservation TRPM6 is the first component involved directly in epithelial magnesium reabsorption[review] PMID:16075242
25. data demonstrate that amino acid residues E1024, I1030 and D1031 are important for channel function and that subtle amino acid variation in the pore region accounts for TRPM6 permeation properties PMID:17098283
26. TRPM6 mutants are found in patients with a rare but severe hereditary disease called hypomagnesaemia with secondary hypocalcaemia --{REVIEW} PMID:17217065
27. This review discusses the importance of magnesium in vascular biology and implications in hypertension and highlights the transport systems, particularly TRPM6--REVIEW PMID:18192217
28. intracellular ATP regulates TRPM6 channel activity via its alpha-kinase domain independently of alpha-kinase activity PMID:18490453
29. diverse molecular regulation of TRPM6 by magnesiotropic hormones, intracellular factors and its fused alpha-kinase domain disclosed novel regulatory mechanisms of active magnesium reabsorption--REVIEW PMID:18660673
30. These findings clearly outline the activation of TRPM6 by EGF, a process fundamental to Mg2+ homeostasis. PMID:19073827
31. Our results provide suggestive evidence that two common non-synonymous TRPM6 coding region variants, Ile1393Val and Lys1584Glu polymorphisms, might confer susceptibility to type 2 diabetes in women with low magnesium intake PMID:19149903
32. REA operates as a negative feedback modulator of TRPM6 in the regulation of active Mg(2+) (re)absorption and provides new insight into the molecular mechanism of renal transepithelial Mg(2+) transport. PMID:19329436

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HGNC: 17995

UNIGENE: Hs.272225

KEGG: hsa:140803

STRING: 9606.ENSP00000354006

OMIM: 602014