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Summary Expression Phenotypes Gene Literature (10) GO Terms (10) Nucleotides (98) Proteins (56) Interactants (46) Wiki
XB-GENEPAGE-958178

Papers associated with trpm6



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TRPM6 and TRPM7: Novel players in cell intercalation during vertebrate embryonic development., Runnels LW, Komiya Y., Dev Dyn. August 1, 2020; 249 (8): 912-923.        

Calcium Signaling in Vertebrate Development and Its Role in Disease., Paudel S, Sindelar R, Saha M., Int J Mol Sci. October 30, 2018; 19 (11):     

A Nonredundant Role for the TRPM6 Channel in Neural Tube Closure., Komiya Y, Bai Z, Cai N, Lou L, Al-Saadi N, Mezzacappa C, Habas R, Runnels LW., Sci Rep. November 15, 2017; 7 (1): 15623.                    

TRPM7., Fleig A, Chubanov V., Handb Exp Pharmacol. January 1, 2014; 222 521-46.

Magnesium and embryonic development., Komiya Y, Su LT, Chen HC, Habas R, Runnels LW., Magnes Res. January 1, 2014; 27 (1): 1-8.

TRPM7 is required within zebrafish sensory neurons for the activation of touch-evoked escape behaviors., Low SE, Amburgey K, Horstick E, Linsley J, Sprague SM, Cui WW, Zhou W, Hirata H, Saint-Amant L, Hume RI, Kuwada JY., J Neurosci. August 10, 2011; 31 (32): 11633-44.                  

TRPM7 regulates gastrulation during vertebrate embryogenesis., Liu W, Su LT, Khadka DK, Mezzacappa C, Komiya Y, Sato A, Habas R, Runnels LW., Dev Biol. February 15, 2011; 350 (2): 348-57.            

Hypomagnesemia with secondary hypocalcemia due to a missense mutation in the putative pore-forming region of TRPM6., Chubanov V, Schlingmann KP, Wäring J, Heinzinger J, Kaske S, Waldegger S, Mederos y Schnitzler M, Gudermann T., J Biol Chem. March 9, 2007; 282 (10): 7656-67.

Novel TRPM6 mutations in 21 families with primary hypomagnesemia and secondary hypocalcemia., Schlingmann KP, Sassen MC, Weber S, Pechmann U, Kusch K, Pelken L, Lotan D, Syrrou M, Prebble JJ, Cole DE, Metzger DL, Rahman S, Tajima T, Shu SG, Waldegger S, Seyberth HW, Konrad M., J Am Soc Nephrol. October 1, 2005; 16 (10): 3061-9.

Disruption of TRPM6/TRPM7 complex formation by a mutation in the TRPM6 gene causes hypomagnesemia with secondary hypocalcemia., Chubanov V, Waldegger S, Mederos y Schnitzler M, Vitzthum H, Sassen MC, Seyberth HW, Konrad M, Gudermann T., Proc Natl Acad Sci U S A. March 2, 2004; 101 (9): 2894-9.

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