TRPM6

currently, see [[1]]

29912157 PDF 2018. TRPM6 is Essential for Magnesium Uptake and Epithelial Cell Function in the Colon.Template:29912157
28784805 PDF 2017. Histone phosphorylation by TRPM6's cleaved kinase attenuates adjacent arginine methylation to regulate gene expression.Template:28784805
26705539 PDF 2015. Mesendogen, a novel inhibitor of TRPM6, promotes mesoderm and definitive endoderm differentiation of human embryonic stem cells through alteration of magnesium homeostasis.Template:26705539
24519337 PDF 2014. Expression of transcripts related to intestinal ion and nutrient absorption in pregnant and lactating rats as determined by custom-designed cDNA microarray.Template:24519337
24413910 PDF 2014. P2X4 receptor regulation of transient receptor potential melastatin type 6 (TRPM6) Mg2+ channels.Template:24413910
19890837 PDF 2010. Modulation of TRPM6 and Na(+)/Mg(2+) exchange in mammary epithelial cells in response to variations of magnesium availability.Template:19890837
18301276 PDF 2008. Recent developments in intestinal magnesium absorption.Template:18301276
36329098 PDF 2022. Butyrate reduces cellular magnesium absorption independently of metabolic regulation in Caco-2 human colon cells.Template:36329098
21951649 PDF 2011. Dietary Mg2+ regulates the epithelial Mg2+ channel TRPM6 in rat mammary tissue.Template:21951649
19329436 PDF 2009. Regulation of the epithelial Mg2+ channel TRPM6 by estrogen and the associated repressor protein of estrogen receptor activity (REA).Template:19329436
19073827 PDF 2009. EGF increases TRPM6 activity and surface expression.Template:19073827
18490453 PDF 2008. Role of the alpha-kinase domain in transient receptor potential melastatin 6 channel and regulation by intracellular ATP.Template:18490453
17197439 PDF 2007. Hypomagnesemia with secondary hypocalcemia due to a missense mutation in the putative pore-forming region of TRPM6.Template:17197439
14976260 PDF 2004. Disruption of TRPM6/TRPM7 complex formation by a mutation in the TRPM6 gene causes hypomagnesemia with secondary hypocalcemia.Template:14976260
12032568 PDF 2002. Hypomagnesemia with secondary hypocalcemia is caused by mutations in TRPM6, a new member of the TRPM gene family.Template:12032568
30810438 PDF 2019. Overexpression of microRNA-202-3p protects against myocardial ischemia-reperfusion injury through activation of TGF-beta1/Smads signaling pathway by targeting TRPM6.Template:30810438