Editing TRPM6

''currently, see'' [[http://mg.moremed.org/w/index.php?title=Magnesium_intestinal_(TRPM7)]]

{{tp|p=29912157|t=2018. TRPM6 is Essential for Magnesium Uptake and Epithelial Cell Function in the Colon.|pdf=|usr=}}{{29912157}}
{{tp|p=28784805|t=2017. Histone phosphorylation by TRPM6's cleaved kinase attenuates adjacent arginine methylation to regulate gene expression.|pdf=|usr=}}{{28784805}}
{{tp|p=26705539|t=2015. Mesendogen, a novel inhibitor of TRPM6, promotes mesoderm and definitive endoderm differentiation of human embryonic stem cells through alteration of magnesium homeostasis.|pdf=|usr=}}{{26705539}}
{{tp|p=24519337|t=2014. Expression of transcripts related to intestinal ion and nutrient absorption in pregnant and lactating rats as determined by custom-designed cDNA microarray.|pdf=|usr=}}{{24519337}}
{{tp|p=24413910|t=2014. P2X4 receptor regulation of transient receptor potential melastatin type 6 (TRPM6) Mg2+ channels.|pdf=|usr=}}{{24413910}}
{{tp|p=19890837|t=2010. Modulation of TRPM6 and Na(+)/Mg(2+) exchange in mammary epithelial cells in response to variations of magnesium availability.|pdf=|usr=}}{{19890837}}
{{tp|p=18301276|t=2008. Recent developments in intestinal magnesium absorption.|pdf=|usr=}}{{18301276}}
{{tp|p=36329098|t=2022. Butyrate reduces cellular magnesium absorption independently of metabolic regulation in Caco-2 human colon cells.|pdf=|usr=}}{{36329098}}
{{tp|p=21951649|t=2011. Dietary Mg2+ regulates the epithelial Mg2+ channel TRPM6 in rat mammary tissue.|pdf=|usr=}}{{21951649}}
{{tp|p=19329436|t=2009. Regulation of the epithelial Mg2+ channel TRPM6 by estrogen and the associated repressor protein of estrogen receptor activity (REA).|pdf=|usr=}}{{19329436}}
{{tp|p=19073827|t=2009. EGF increases TRPM6 activity and surface expression.|pdf=|usr=}}{{19073827}}
{{tp|p=18490453|t=2008. Role of the alpha-kinase domain in transient receptor potential melastatin 6 channel and regulation by intracellular ATP.|pdf=|usr=}}{{18490453}}
{{tp|p=17197439|t=2007. Hypomagnesemia with secondary hypocalcemia due to a missense mutation in the putative pore-forming region of TRPM6.|pdf=|usr=}}{{17197439}}
{{tp|p=14976260|t=2004. Disruption of TRPM6/TRPM7 complex formation by a mutation in the TRPM6 gene causes hypomagnesemia with secondary hypocalcemia.|pdf=|usr=}}{{14976260}}
{{tp|p=12032568|t=2002. Hypomagnesemia with secondary hypocalcemia is caused by mutations in TRPM6, a new member of the TRPM gene family.|pdf=|usr=}}{{12032568}}
{{tp|p=30810438|t=2019. Overexpression of microRNA-202-3p protects against myocardial ischemia-reperfusion injury through activation of TGF-beta1/Smads signaling pathway by targeting TRPM6.|pdf=|usr=}}{{30810438}}