Novel TRPM6 mutations in 21 families with primary hypomagnesemia and secondary hypocalcemia - Wikidata - wikimedia - TriplyDB

Novel TRPM6 mutations in 21 families with primary hypomagnesemia and secondary hypocalcemia

Novel TRPM6 mutations in 21 families with primary hypomagnesemia and secondary hypocalcemia

http://www.wikidata.org/entity/Q28267778

about

Mammalian MagT1 and TUSC3 are required for cellular magnesium uptake and vertebrate embryonic development Functional characterization of homo- and heteromeric channel kinases TRPM6 and TRPM7 Proton-pump inhibitor-induced hypomagnesemia: Current research and proposed mechanisms Transient receptor potential channels as therapeutic targets Epithelial magnesium transport by TRPM6 is essential for prenatal development and adult survival Clinical review of genetic epileptic encephalopathies Common genetic variants of the ion channel transient receptor potential membrane melastatin 6 and 7 (TRPM6 and TRPM7), magnesium intake, and risk of type 2 diabetes in women.Genetic causes of hypomagnesemia, a clinical overview Differential mRNA expression and glucocorticoid-mediated regulation of TRPM6 and TRPM7 in the heart and kidney throughout murine pregnancy and development Comparative genomic analyses reveal a vast, novel network of nucleotide-centric systems in biological conflicts, immunity and signaling.Novel Alleles of gon-2, a C. elegans Ortholog of Mammalian TRPM6 and TRPM7, Obtained by Genetic Reversion Screens.Hypomagnesemia and functional hypoparathyroidism due to novel mutations in the Mg-channel TRPM6 TRPpathies.A Novel Homozygous Mutation in the Transient Receptor Potential Melastatin 6 Gene: A Case Report.Transient receptor potential melastatin 6 and 7 channels, magnesium transport, and vascular biology: implications in hypertension.Calciotropic and magnesiotropic TRP channels.Magnesium-permeable TRPM6 polymorphisms in patients with meningomyelocele.Mice defective in Trpm6 show embryonic mortality and neural tube defects New TRPM6 missense mutations linked to hypomagnesemia with secondary hypocalcemia Molecular identification of ancient and modern mammalian magnesium transporters.The role of transient receptor potential cation channels in Ca2+ signaling The transient receptor potential family of ion channels Drug-induced alterations in Mg2+ homoeostasis.TRP channels.Hypomagnesemia and proton-pump inhibitors.Inherited disorders of renal hypomagnesaemia.Addressing potential role of magnesium dyshomeostasis to improve treatment efficacy for epilepsy: A reexamination of the literature.Magnesium Deficiency and Proton-Pump Inhibitor Use: A Clinical Review.Against all odds: blended phenotypes of three single-gene defects.Changes in serum magnesium concentration after use of a proton pump inhibitor in patients undergoing percutaneous coronary intervention.Association of hypermagnesemia and blood pressure in the critically ill.Familial hypomagnesaemia with secondary hypocalcaemia.Comparing the expression patterns of placental magnesium/phosphorus-transporting channels between healthy and preeclamptic pregnancies.Behavioral disorders secondary to profound hypomagnesemia in a patient given cetuximab for metastatic colorectal cancer hypomagnesemia due to cetuximab treatment.[Electrolyte disorders as a hallmark of monogenetic diseases].Downregulation of transient receptor potential M6 channels as a cause of hypermagnesiuric hypomagnesemia in obese type 2 diabetic rats.Seizures Related to Hypomagnesemia: A Case Series and Review of the Literature.The Role of Magnesium in Neurological Disorders.Germline De Novo Mutations in ATP1A1 Cause Renal Hypomagnesemia, Refractory Seizures, and Intellectual Disability

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P2860

Novel TRPM6 mutations in 21 families with primary hypomagnesemia and secondary hypocalcemia

http://www.wikidata.org/entity/Q28267778

description

2005 nî lūn-bûn

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2005 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած

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2005 թվականի հոտեմբերին հրատարակված գիտական հոդված

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2005年の論文

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2005年論文

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2005年論文

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2005年論文

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2005年論文

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2005年論文

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2005年论文

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name

Novel TRPM6 mutations in 21 fa ...... mia and secondary hypocalcemia

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Novel TRPM6 mutations in 21 fa ...... mia and secondary hypocalcemia

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Novel TRPM6 mutations in 21 fa ...... mia and secondary hypocalcemia

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Novel TRPM6 mutations in 21 fa ...... mia and secondary hypocalcemia

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Novel TRPM6 mutations in 21 fa ...... mia and secondary hypocalcemia

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Novel TRPM6 mutations in 21 fa ...... mia and secondary hypocalcemia

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Novel TRPM6 mutations in 21 fa ...... mia and secondary hypocalcemia

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Novel TRPM6 mutations in 21 fa ...... mia and secondary hypocalcemia

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Novel TRPM6 mutations in 21 fa ...... mia and secondary hypocalcemia

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Journal of the American Society of Nephrology

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Novel TRPM6 mutations in 21 fa ...... mia and secondary hypocalcemia

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P2093

Daniel Lotan

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David E C Cole

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Hannsjoerg W Seyberth

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Jeffrey J Prebble

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Karl P Schlingmann

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Kerstin Kusch

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Lutz Pelken

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Maria Syrrou

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Martin C Sassen

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Martin Konrad

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scholarly article

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3166528

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10.1681/ASN.2004110989

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10

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16

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Daniel L Metzger

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2005-10-01T00:00:00Z

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