Essential role for TRPM6 in epithelial magnesium transport and body magnesium homeostasis (Q34439658)

2 August 2017

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title

Essential role for TRPM6 in epithelial magnesium transport and body magnesium homeostasis (English)

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2 August 2017

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Vladimir Chubanov

1

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2 August 2017

Thomas Gudermann

series ordinal

2

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2 August 2017

Karl P Schlingmann

series ordinal

3

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2 August 2017

17 June 2005

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2 August 2017

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2 August 2017

451

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2 August 2017

1

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2 August 2017

228-234

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https://scigraph.springernature.com/pub.10.1007/s00424-005-1470-y

2 August 2017

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cites work

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12 December 2020

Hormonal regulation of Mg2+ transport and homeostasis in eukaryotic cells

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12 December 2020

Disruption of TRPM6/TRPM7 complex formation by a mutation in the TRPM6 gene causes hypomagnesemia with secondary hypocalcemia

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Cell physiology of magnesium

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Primary infantile hypomagnesaemia: outcome after 21 years and treatment with continuous nocturnal nasogastric magnesium infusion

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Current understanding of mammalian TRP homologues

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Intracellular magnesium and magnesium buffering

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12 December 2020

Hypomagnesemia with secondary hypocalcemia is caused by mutations in TRPM6, a new member of the TRPM gene family

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12 December 2020

Familial Hypomagnesemia—A Follow-Up Examination of Three Patients After 9 to 12 Years of Treatment

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12 December 2020

Identification and characterization of a novel mammalian Mg2+ transporter with channel-like properties

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12 December 2020

Mg2+ Homeostasis: The Mg2+nificent TRPM Chanzymes

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12 December 2020

Evidence for parathyroid failure in magnesium deficiency

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12 December 2020

LTRPC7 is a Mg.ATP-regulated divalent cation channel required for cell viability

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12 December 2020

Phosphorylation of annexin I by TRPM7 channel-kinase

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12 December 2020

Novel type of signaling molecules: protein kinases covalently linked to ion channels

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12 December 2020

Subunit composition of mammalian transient receptor potential channels in living cells

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12 December 2020

Regulation of vertebrate cellular Mg2+ homeostasis by TRPM7.

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12 December 2020

Familial hypomagnesemia maps to chromosome 9q, not to the X chromosome: genetic linkage mapping and analysis of a balanced translocation breakpoint

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Recent advances in molecular genetics of hereditary magnesium-losing disorders

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Renal magnesium handling: new insights in understanding old problems

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12 December 2020

Functional characterization of human SLC41A1, a Mg2+ transporter with similarity to prokaryotic MgtE Mg2+ transporters

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12 December 2020

Dual-function ion channel/protein kinases: novel components of vertebrate magnesium regulatory mechanisms.

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Intestinal absorption of magnesium from food and supplements

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Mutation of TRPM6 causes familial hypomagnesemia with secondary hypocalcemia

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12 December 2020

The human solute carrier SLC41A1 belongs to a novel eukaryotic subfamily with homology to prokaryotic MgtE Mg2+ transporters

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12 December 2020

TRP-PLIK, a bifunctional protein with kinase and ion channel activities

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Hypomagnesaemia of hereditary renal origin

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Insights into the molecular nature of magnesium homeostasis

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Genetics of hereditary disorders of magnesium homeostasis

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Novel paracellin-1 mutations in 25 families with familial hypomagnesemia with hypercalciuria and nephrocalcinosis

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Channel function is dissociated from the intrinsic kinase activity and autophosphorylation of TRPM7/ChaK1.

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12 December 2020

Studies in primary hypomagnesaemia: evidence for defective carrier-mediated small intestinal transport of magnesium

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Defective skeletogenesis with kidney stone formation in dwarf zebrafish mutant for trpm7.

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12 December 2020

Primary hypomagnesemia with secondary hypocalcemia in an infant

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12 December 2020

Inherited disorders of renal magnesium handling

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12 December 2020

TRPM6 forms the Mg2+ influx channel involved in intestinal and renal Mg2+ absorption

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12 December 2020

Annexins--unique membrane binding proteins with diverse functions

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12 December 2020

Primary hypomagnesemia with a probable double magnesium transport defect

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12 December 2020

Involvement of TRPM7 in cell growth as a spontaneously activated Ca2+ entry pathway in human retinoblastoma cells.

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12 December 2020

Primary hypomagnesemia. I. Absorption Studies

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12 December 2020

Paracellin-1, a renal tight junction protein required for paracellular Mg2+ resorption

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12 December 2020

A key role for TRPM7 channels in anoxic neuronal death

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12 December 2020

Annexin 1 and neutrophil apoptosis

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12 December 2020

TRPM7 provides an ion channel mechanism for cellular entry of trace metal ions

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12 December 2020

10.1007/S00424-005-1470-Y

Identifiers

DOI

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Dimensions Publication ID

2 August 2017

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