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Items: 1 to 20 of 104

1.

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 15;18(22):4367-75. doi: 10.1093/hmg/ddp392. Epub 2009 Aug 18.

2.

TRPM6.

Chubanov V, Gudermann T.

Handb Exp Pharmacol. 2014;222:503-20. doi: 10.1007/978-3-642-54215-2_20. Review.

PMID:
24756719
3.

Transient receptor potential melastatin 6 knockout mice are lethal whereas heterozygous deletion results in mild hypomagnesemia.

Woudenberg-Vrenken TE, Sukinta A, van der Kemp AW, Bindels RJ, Hoenderop JG.

Nephron Physiol. 2011;117(2):p11-9. doi: 10.1159/000320580. Epub 2010 Sep 1.

PMID:
20814221
4.

Magnesium and embryonic development.

Komiya Y, Su LT, Chen HC, Habas R, Runnels LW.

Magnes Res. 2014 Jan-Mar;27(1):1-8. doi: 10.1684/mrh.2014.0356. Review.

5.

Mini-review: toward understanding mechanisms of genetic neural tube defects in mice.

Harris MJ, Juriloff DM.

Teratology. 1999 Nov;60(5):292-305. Review.

PMID:
10525207
7.

Relationship between low magnesium status and TRPM6 expression in the kidney and large intestine.

Rondón LJ, Groenestege WM, Rayssiguier Y, Mazur A.

Am J Physiol Regul Integr Comp Physiol. 2008 Jun;294(6):R2001-7. doi: 10.1152/ajpregu.00153.2007. Epub 2008 Apr 2.

8.

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. Epub 2006 Mar 8.

9.

Analysis of the embryonic phenotype of Bent tail, a mouse model for X-linked neural tube defects.

Franke B, Klootwijk R, Hekking JW, de Boer RT, ten Donkelaar HJ, Mariman EC, van Straaten HW.

Anat Embryol (Berl). 2003 Oct;207(3):255-62. Epub 2003 Oct 2.

PMID:
14523648
10.

TRPM6 and TRPM7: A Mul-TRP-PLIK-cation of channel functions.

Runnels LW.

Curr Pharm Biotechnol. 2011 Jan 1;12(1):42-53. Review.

11.

Decreased renal mRNA expression of TRPM6 is associated with hypomagnesemia in C57BL/6 asthmatic mice.

Jiang SP, Wu YM, Guo SE, Lv ZQ.

Eur Rev Med Pharmacol Sci. 2010 Nov;14(11):935-40.

PMID:
21284342
12.

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. Epub 2005 Aug 17.

13.

Neural tube defects and abnormal brain development in F52-deficient mice.

Wu M, Chen DF, Sasaoka T, Tonegawa S.

Proc Natl Acad Sci U S A. 1996 Mar 5;93(5):2110-5.

14.

Untargeted metabolite profiling of murine embryos to reveal metabolic perturbations associated with neural tube closure defects.

Hansler A, Chen Q, Gray JD, Ross ME, Finnell RH, Gross SS.

Birth Defects Res A Clin Mol Teratol. 2014 Aug;100(8):623-32. doi: 10.1002/bdra.23272. Epub 2014 Aug 13.

15.

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. 2007 Mar 9;282(10):7656-67. Epub 2006 Dec 29.

16.

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 1;460(2):165-75. doi: 10.1042/BJ20131639.

17.

Folic acid supplementation can adversely affect murine neural tube closure and embryonic survival.

Marean A, Graf A, Zhang Y, Niswander L.

Hum Mol Genet. 2011 Sep 15;20(18):3678-83. doi: 10.1093/hmg/ddr289. Epub 2011 Jun 21.

18.

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. doi: 10.1038/ejhg.2013.178. Epub 2013 Aug 14.

19.

A case of hypomagnesemia with secondary hypocalcemia caused by Trpm6 gene mutation.

Apa H, Kayserili E, Agin H, Hizarcioglu M, Gulez P, Berdeli A.

Indian J Pediatr. 2008 Jun;75(6):632-4. doi: 10.1007/s12098-008-0121-7. Epub 2008 Aug 31.

PMID:
18759094
20.

A genetic risk factor for mouse neural tube defects: defining the embryonic basis.

Fleming A, Copp AJ.

Hum Mol Genet. 2000 Mar 1;9(4):575-81.

PMID:
10699180

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