(Q37610746)

21 August 2017

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title

New molecular players facilitating Mg(2+) reabsorption in the distal convoluted tubule (English)

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21 August 2017

2

Nine V A M Knoers

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21 August 2017

Bob Glaudemans

1

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21 August 2017

Joost G J Hoenderop

series ordinal

3

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21 August 2017

René J M Bindels

series ordinal

4

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21 August 2017

language of work or name

English

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publication date

1 January 2010

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21 August 2017

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21 August 2017

77

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21 August 2017

17-22

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21 August 2017

1

1 reference

https://scigraph.springernature.com/pub.10.1038/ki.2009.358

21 August 2017

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cites work

Hypomagnesemia in acute and chronic care patient populations

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7 January 2021

Association between cyclosporin neurotoxicity and hypomagnesaemia

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7 January 2021

Severe hypomagnesaemia in long-term users of proton-pump inhibitors

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7 January 2021

Proton-pump inhibitors and hypomagnesemic hypoparathyroidism

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7 January 2021

Cetuximab therapy and symptomatic hypomagnesemia

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7 January 2021

Magnesium wasting associated with epidermal-growth-factor receptor-targeting antibodies in colorectal cancer: a prospective study

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https://api.crossref.org/works/10.1038%2FKI.2009.358

7 January 2021

Hypomagnesemia and Renal Magnesium Wasting in Patients Receiving Cisplatin

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https://api.crossref.org/works/10.1038%2FKI.2009.358

7 January 2021

IV magnesium sulfate in the treatment of acute severe asthma: a multicenter randomized controlled trial

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7 January 2021

A preliminary report on the intravenous use of magnesium sulphate in puerperal eclampsia. 1925.

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https://api.crossref.org/works/10.1038%2FKI.2009.358

7 January 2021

Magnesium absorption in human subjects from leafy vegetables, intrinsically labeled with stable 26Mg.

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7 January 2021

Intestinal absorption of magnesium from food and supplements

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https://api.crossref.org/works/10.1038%2FKI.2009.358

7 January 2021

Magnesium deficiency: a cause of heterogeneous disease in humans

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https://api.crossref.org/works/10.1038%2FKI.2009.358

7 January 2021

Magnesium deficiency and osteoporosis: animal and human observations

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https://api.crossref.org/works/10.1038%2FKI.2009.358

7 January 2021

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

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https://api.crossref.org/works/10.1038%2FKI.2009.358

7 January 2021

Mutations in the tight-junction gene claudin 19 (CLDN19) are associated with renal magnesium wasting, renal failure, and severe ocular involvement

1 reference

https://api.crossref.org/works/10.1038%2FKI.2009.358

7 January 2021

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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https://api.crossref.org/works/10.1038%2FKI.2009.358

7 January 2021

Evidence for parathyroid failure in magnesium deficiency

1 reference

https://api.crossref.org/works/10.1038%2FKI.2009.358

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FKI.2009.358

7 January 2021

Mutation of TRPM6 causes familial hypomagnesemia with secondary hypocalcemia

1 reference

https://api.crossref.org/works/10.1038%2FKI.2009.358

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FKI.2009.358

7 January 2021

Insight into the molecular regulation of the epithelial magnesium channel TRPM6.

1 reference

https://api.crossref.org/works/10.1038%2FKI.2009.358

7 January 2021

Impaired basolateral sorting of pro-EGF causes isolated recessive renal hypomagnesemia

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https://api.crossref.org/works/10.1038%2FKI.2009.358

7 January 2021

Immunohistochemical localization of epidermal growth factor in rat and man

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https://api.crossref.org/works/10.1038%2FKI.2009.358

7 January 2021

Apical enrichment of human EGF precursor in Madin-Darby canine kidney cells involves preferential basolateral ectodomain cleavage sensitive to a metalloprotease inhibitor

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https://api.crossref.org/works/10.1038%2FKI.2009.358

7 January 2021

EGF increases TRPM6 activity and surface expression

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https://api.crossref.org/works/10.1038%2FKI.2009.358

7 January 2021

A missense mutation in the Kv1.1 voltage-gated potassium channel-encoding gene KCNA1 is linked to human autosomal dominant hypomagnesemia

1 reference

https://api.crossref.org/works/10.1038%2FKI.2009.358

7 January 2021

Intracellular magnesium and magnesium buffering

1 reference

https://api.crossref.org/works/10.1038%2FKI.2009.358

7 January 2021

Electrophysiological characterization of rabbit distal convoluted tubule cell.

1 reference

https://api.crossref.org/works/10.1038%2FKI.2009.358

7 January 2021

Dominant isolated renal magnesium loss is caused by misrouting of the Na(+),K(+)-ATPase gamma-subunit

1 reference

https://api.crossref.org/works/10.1038%2FKI.2009.358

7 January 2021

Distribution and oligomeric association of splice forms of Na(+)-K(+)-ATPase regulatory gamma-subunit in rat kidney

1 reference

https://api.crossref.org/works/10.1038%2FKI.2009.358

7 January 2021

Dominant isolated renal magnesium loss is caused by misrouting of the Na+,K+-ATPase gamma-subunit

1 reference

https://api.crossref.org/works/10.1038%2FKI.2009.358

7 January 2021

Human FXYD2 G41R mutation responsible for renal hypomagnesemia behaves as an inward-rectifying cation channel

1 reference

https://api.crossref.org/works/10.1038%2FKI.2009.358

7 January 2021

HNF1B mutations associate with hypomagnesemia and renal magnesium wasting

1 reference

https://api.crossref.org/works/10.1038%2FKI.2009.358

7 January 2021

Gitelman's variant of Bartter's syndrome, inherited hypokalaemic alkalosis, is caused by mutations in the thiazide-sensitive Na-Cl cotransporter

1 reference

https://api.crossref.org/works/10.1038%2FKI.2009.358

7 January 2021

Enhanced passive Ca2+ reabsorption and reduced Mg2+ channel abundance explains thiazide-induced hypocalciuria and hypomagnesemia

1 reference

https://api.crossref.org/works/10.1038%2FKI.2009.358

7 January 2021

https://api.crossref.org/works/10.1038%2FKI.2009.358

1 reference

7 January 2021

Salt handling in the distal nephron: lessons learned from inherited human disorders.

1 reference

https://api.crossref.org/works/10.1038%2FKI.2009.358

7 January 2021

Epilepsy, ataxia, sensorineural deafness, tubulopathy, and KCNJ10 mutations

1 reference

https://api.crossref.org/works/10.1038%2FKI.2009.358

7 January 2021

Seizures, sensorineural deafness, ataxia, mental retardation, and electrolyte imbalance (SeSAME syndrome) caused by mutations in KCNJ10.

1 reference

https://api.crossref.org/works/10.1038%2FKI.2009.358

7 January 2021

Fine mapping of a seizure susceptibility locus on mouse Chromosome 1: nomination of Kcnj10 as a causative gene.

1 reference

https://api.crossref.org/works/10.1038%2FKI.2009.358

7 January 2021

Kir4.1 potassium channel subunit is crucial for oligodendrocyte development and in vivo myelination.

1 reference

https://api.crossref.org/works/10.1038%2FKI.2009.358

7 January 2021

KCNJ10 (Kir4.1) potassium channel knockout abolishes endocochlear potential

1 reference

https://api.crossref.org/works/10.1038%2FKI.2009.358

7 January 2021

Immunolocalization of an inwardly rectifying K+ channel, K(AB)-2 (Kir4.1), in the basolateral membrane of renal distal tubular epithelia

1 reference

https://api.crossref.org/works/10.1038%2FKI.2009.358

7 January 2021

Identifiers

DOI

10.1038/KI.2009.358

1 reference

21 August 2017

1 reference