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8. Hypomagnesemia with secondary hypocalcemia is caused by mutations in TRPM6, a new member of the TRPM gene family. Schlingmann KP; Weber S; Peters M; Niemann Nejsum L; Vitzthum H; Klingel K; Kratz M; Haddad E; Ristoff E; Dinour D; Syrrou M; Nielsen S; Sassen M; Waldegger S; Seyberth HW; Konrad M Nat Genet; 2002 Jun; 31(2):166-70. PubMed ID: 12032568 [TBL] [Abstract][Full Text] [Related]
9. TRPM6: A Janus-like protein. Bödding M Handb Exp Pharmacol; 2007; (179):299-311. PubMed ID: 17217065 [TBL] [Abstract][Full Text] [Related]
10. TRPM3. Oberwinkler J; Philipp SE Handb Exp Pharmacol; 2014; 222():427-59. PubMed ID: 24756716 [TBL] [Abstract][Full Text] [Related]
11. Kinase and channel activity of TRPM6 are co-ordinated by a dimerization motif and pocket interaction. van der Wijst J; Blanchard MG; Woodroof HI; Macartney TJ; Gourlay R; Hoenderop JG; Bindels RJ; Alessi DR Biochem J; 2014 Jun; 460(2):165-75. PubMed ID: 24650431 [TBL] [Abstract][Full Text] [Related]
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13. The epithelial Mg2+ channel transient receptor potential melastatin 6 is regulated by dietary Mg2+ content and estrogens. Groenestege WM; Hoenderop JG; van den Heuvel L; Knoers N; Bindels RJ J Am Soc Nephrol; 2006 Apr; 17(4):1035-43. PubMed ID: 16524949 [TBL] [Abstract][Full Text] [Related]
14. TRPM6 kinase activity regulates TRPM7 trafficking and inhibits cellular growth under hypomagnesic conditions. Brandao K; Deason-Towne F; Zhao X; Perraud AL; Schmitz C Cell Mol Life Sci; 2014 Dec; 71(24):4853-67. PubMed ID: 24858416 [TBL] [Abstract][Full Text] [Related]
15. Functional characterization of homo- and heteromeric channel kinases TRPM6 and TRPM7. Li M; Jiang J; Yue L J Gen Physiol; 2006 May; 127(5):525-37. PubMed ID: 16636202 [TBL] [Abstract][Full Text] [Related]
16. The TRPM6 kinase domain determines the Mg·ATP sensitivity of TRPM7/M6 heteromeric ion channels. Zhang Z; Yu H; Huang J; Faouzi M; Schmitz C; Penner R; Fleig A J Biol Chem; 2014 Feb; 289(8):5217-27. PubMed ID: 24385424 [TBL] [Abstract][Full Text] [Related]
17. New TRPM6 missense mutations linked to hypomagnesemia with secondary hypocalcemia. Lainez S; Schlingmann KP; van der Wijst J; Dworniczak B; van Zeeland F; Konrad M; Bindels RJ; Hoenderop JG Eur J Hum Genet; 2014 Apr; 22(4):497-504. PubMed ID: 23942199 [TBL] [Abstract][Full Text] [Related]
18. Mice defective in Trpm6 show embryonic mortality and neural tube defects. Walder RY; Yang B; Stokes JB; Kirby PA; Cao X; Shi P; Searby CC; Husted RF; Sheffield VC Hum Mol Genet; 2009 Nov; 18(22):4367-75. PubMed ID: 19692351 [TBL] [Abstract][Full Text] [Related]
19. 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; 2005 Oct; 16(10):3061-9. PubMed ID: 16107578 [TBL] [Abstract][Full Text] [Related]