(Q37603366)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19780717%20AND%20SRC:MED&resulttype=core&format=json

8 February 2020

review article

1 reference

title

Hereditary tubular transport disorders: implications for renal handling of Ca2+ and Mg2+ (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19780717%20AND%20SRC:MED&resulttype=core&format=json

8 February 2020

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19780717%20AND%20SRC:MED&resulttype=core&format=json

8 February 2020

author name string

Joost G Hoenderop

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19780717%20AND%20SRC:MED&resulttype=core&format=json

8 February 2020

René J Bindels

series ordinal

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19780717%20AND%20SRC:MED&resulttype=core&format=json

8 February 2020

language of work or name

English

0 references

publication date

28 September 2009

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19780717%20AND%20SRC:MED&resulttype=core&format=json

8 February 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19780717%20AND%20SRC:MED&resulttype=core&format=json

8 February 2020

volume

118

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19780717%20AND%20SRC:MED&resulttype=core&format=json

8 February 2020

issue

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19780717%20AND%20SRC:MED&resulttype=core&format=json

8 February 2020

page(s)

1-18

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19780717%20AND%20SRC:MED&resulttype=core&format=json

Clinical review 51: Management of hypercalcemia

8 February 2020

cites work

1 reference

https://api.crossref.org/works/10.1042%2FCS20090086

Hypomagnesemia and hypermagnesemia

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FCS20090086

Calcium absorption across epithelia

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FCS20090086

Calcium transport in the rabbit superficial proximal convoluted tubule

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FCS20090086

Serum magnesium levels in the United States, 1971-1974.

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FCS20090086

Dent's disease, a renal Fanconi syndrome with nephrocalcinosis and kidney stones, is associated with a microdeletion involving DXS255 and maps to Xp11.22.

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FCS20090086

A common molecular basis for three inherited kidney stone diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FCS20090086

Chloride/proton antiporter activity of mammalian CLC proteins ClC-4 and ClC-5.

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FCS20090086

Voltage-dependent electrogenic chloride/proton exchange by endosomal CLC proteins

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FCS20090086

Intra-renal and subcellular distribution of the human chloride channel, CLC-5, reveals a pathophysiological basis for Dent's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FCS20090086

Loss of chloride channel ClC-5 impairs endocytosis by defective trafficking of megalin and cubilin in kidney proximal tubules

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FCS20090086

ClC-5 Cl- -channel disruption impairs endocytosis in a mouse model for Dent's disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FCS20090086

Mice lacking renal chloride channel, CLC-5, are a model for Dent's disease, a nephrolithiasis disorder associated with defective receptor-mediated endocytosis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FCS20090086

Mechanisms of disease: what can mouse models tell us about the molecular processes underlying Dent disease?

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FCS20090086

An endocytic pathway essential for renal uptake and activation of the steroid 25-(OH) vitamin D3

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FCS20090086

Nonsense mutations in the OCRL-1 gene in patients with the oculocerebrorenal syndrome of Lowe

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FCS20090086

Cell Lines from Kidney Proximal Tubules of a Patient with Lowe Syndrome Lack OCRL Inositol Polyphosphate 5-Phosphatase and Accumulate Phosphatidylinositol 4,5-Bisphosphate

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FCS20090086

Dent Disease with mutations in OCRL1

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FCS20090086

Magnesium transport in the cortical thick ascending limb of Henle's loop of the rabbit

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FCS20090086

Calcium transport in the thick ascending limb of Henle. Heterogeneity of function in the medullary and cortical segments

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FCS20090086

Effects of parathyroid hormone and calcitonin on Na+, Cl-, K+, Mg2+ and Ca2+ transport in cortical and medullary thick ascending limbs of mouse kidney.

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FCS20090086

The cortical thick ascending limb and early distal convoluted tubule in the urinary concentrating mechanism

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FCS20090086

Sodium chloride and water transport in the medullary thick ascending limb of Henle. Evidence for active chloride transport

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FCS20090086

Paracellin-1 and the modulation of ion selectivity of tight junctions

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FCS20090086

Hypercalcaemic and hypocalcaemic conditions due to calcium-sensing receptor mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FCS20090086

Calcium-sensing receptor: regulation of electrolyte transport in the thick ascending limb of Henle's loop.

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FCS20090086

Calcium-sensing receptor regulation of PTH-dependent calcium absorption by mouse cortical ascending limbs

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FCS20090086

Aminoglycoside antibiotics induce pH-sensitive activation of the calcium-sensing receptor

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FCS20090086

Calcium and phosphate transport in isolated segments of rabbit Henle's loop

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FCS20090086

Bartter's syndrome, hypokalaemic alkalosis with hypercalciuria, is caused by mutations in the Na-K-2Cl cotransporter NKCC2

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FCS20090086

Mechanisms of Disease: the kidney-specific chloride channels ClCKA and ClCKB, the Barttin subunit, and their clinical relevance

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FCS20090086

Mutations in the chloride channel gene, CLCNKB, cause Bartter's syndrome type III

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FCS20090086

Mutation of BSND causes Bartter syndrome with sensorineural deafness and kidney failure

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FCS20090086

Barttin is a Cl- channel beta-subunit crucial for renal Cl- reabsorption and inner ear K+ secretion

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FCS20090086

Salt wasting and deafness resulting from mutations in two chloride channels

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FCS20090086

A familial syndrome of hypocalcemia with hypercalciuria due to mutations in the calcium-sensing receptor

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FCS20090086

Autosomal dominant hypocalcaemia caused by a Ca(2+)-sensing receptor gene mutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FCS20090086

Association between activating mutations of calcium-sensing receptor and Bartter's syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FCS20090086

Mutations in the chloride channel gene, CLCNKB, leading to a mixed Bartter-Gitelman phenotype

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FCS20090086

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FCS20090086

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FCS20090086

A novel claudin 16 mutation associated with childhood hypercalciuria abolishes binding to ZO-1 and results in lysosomal mistargeting

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FCS20090086

Phosphorylation of paracellin-1 at Ser217 by protein kinase A is essential for localization in tight junctions

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FCS20090086

Salt and acid-base metabolism in claudin-16 knockdown mice: impact for the pathophysiology of FHHNC patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FCS20090086

Urinary calcium excretion in familial hypocalciuric hypercalcemia. Persistence of relative hypocalciuria after induction of hypoparathyroidism.

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FCS20090086

Extracellular calcium-sensing receptor: implications for calcium and magnesium handling in the kidney

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FCS20090086

The calcium-sensing receptor is required for normal calcium homeostasis independent of parathyroid hormone

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FCS20090086

A standard nomenclature for structures of the kidney. The Renal Commission of the International Union of Physiological Sciences (IUPS).

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FCS20090086

Molecular identification of the apical Ca2+ channel in 1, 25-dihydroxyvitamin D3-responsive epithelia

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FCS20090086

Sodium and calcium transport pathways along the mammalian distal nephron: from rabbit to human

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FCS20090086

Fluorescence isolation of mouse late distal convoluted tubules and connecting tubules: effects of vasopressin and vitamin D3 on Ca2+ signaling

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FCS20090086

Renal Ca2+ wasting, hyperabsorption, and reduced bone thickness in mice lacking TRPV5

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FCS20090086

TRPV5 gene polymorphisms in renal hypercalciuria.

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FCS20090086

Intracellular magnesium and magnesium buffering

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FCS20090086

Effect of calcium, furosemide and chlorothiazide on net volume reabsorption and basolateral membrane potential of the distal tubule

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FCS20090086

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FCS20090086

Mg2+ Homeostasis: The Mg2+nificent TRPM Chanzymes

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FCS20090086

Functional characterization of homo- and heteromeric channel kinases TRPM6 and TRPM7

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FCS20090086

Molecular determinants of Mg2+ and Ca2+ permeability and pH sensitivity in TRPM6 and TRPM7.

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FCS20090086

Hypomagnesemia with secondary hypocalcemia due to a missense mutation in the putative pore-forming region of TRPM6.

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FCS20090086

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FCS20090086

A critical role of TRPM channel-kinase for human magnesium transport

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FCS20090086

The channel kinases TRPM6 and TRPM7 are functionally nonredundant

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FCS20090086

The epithelial Mg2+ channel transient receptor potential melastatin 6 is regulated by dietary Mg2+ content and estrogens

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FCS20090086

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FCS20090086

Mutation of TRPM6 causes familial hypomagnesemia with secondary hypocalcemia

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FCS20090086

Clinical presentation and outcome in primary familial hypomagnesaemia

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FCS20090086

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FCS20090086

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FCS20090086

EGF increases TRPM6 activity and surface expression

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FCS20090086

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FCS20090086

Renal magnesium wasting in two families with autosomal dominant inheritance

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FCS20090086

The gamma subunit modulates Na(+) and K(+) affinity of the renal Na,K-ATPase

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FCS20090086

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FCS20090086

Na,K-ATPase from mice lacking the gamma subunit (FXYD2) exhibits altered Na+ affinity and decreased thermal stability

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FCS20090086

CHIF, a member of the FXYD protein family, is a regulator of Na,K-ATPase distinct from the gamma-subunit

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FCS20090086

The gamma subunit is a specific component of the Na,K-ATPase and modulates its transport function

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FCS20090086

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FCS20090086

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FCS20090086

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FCS20090086

Codependence of renal calcium and sodium transport

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FCS20090086

Thiazide-induced hypocalciuria is accompanied by a decreased expression of Ca2+ transport proteins in kidney

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FCS20090086

Altered renal distal tubule structure and renal Na(+) and Ca(2+) handling in a mouse model for Gitelman's syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FCS20090086

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FCS20090086

Thiazide treatment of rats provokes apoptosis in distal tubule cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FCS20090086

Downregulation of renal TRPM7 and increased inflammation and fibrosis in aldosterone-infused mice: effects of magnesium

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FCS20090086

Correction of hypokalemia with antialdosterone therapy in Gitelman's syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FCS20090086

Familial distal renal tubular acidosis is associated with mutations in the red cell anion exchanger (Band 3, AE1) gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FCS20090086

Mutations in the gene encoding B1 subunit of H+-ATPase cause renal tubular acidosis with sensorineural deafness

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FCS20090086

Mutations in ATP6N1B, encoding a new kidney vacuolar proton pump 116-kD subunit, cause recessive distal renal tubular acidosis with preserved hearing

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FCS20090086

Bone buffering of acid and base in humans

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FCS20090086

Acid-base status determines the renal expression of Ca2+ and Mg2+ transport proteins.

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FCS20090086

Extracellular pH dynamically controls cell surface delivery of functional TRPV5 channels

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FCS20090086

Mechanism and molecular determinant for regulation of rabbit transient receptor potential type 5 (TRPV5) channel by extracellular pH.

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FCS20090086

Micropuncture study of the effect of various diuretics on sodium reabsorption by the proximal tubules of the dog.

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FCS20090086

Acidosis increases magnesiuria in children with distal renal tubular acidosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FCS20090086

Effects of acid-base disturbances on renal handling of magnesium in the dog.

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FCS20090086

WNK1, a novel mammalian serine/threonine protein kinase lacking the catalytic lysine in subdomain II

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FCS20090086

WNK kinases, a novel protein kinase subfamily in multi-cellular organisms

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FCS20090086

Wnk1 kinase deficiency lowers blood pressure in mice: A gene-trap screen to identify potential targets for therapeutic intervention

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FCS20090086

Human hypertension caused by mutations in WNK kinases

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FCS20090086

WNK kinases regulate thiazide-sensitive Na-Cl cotransport

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FCS20090086

WNK4 regulates the balance between renal NaCl reabsorption and K+ secretion

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FCS20090086

Antagonistic regulation of ROMK by long and kidney-specific WNK1 isoforms

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FCS20090086

The thiazide-sensitive Na-Cl cotransporter is regulated by a WNK kinase signaling complex

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FCS20090086

Hypercalciuria in familial hyperkalemia and hypertension accompanies hyperkalemia and precedes hypertension: description of a large family with the Q565E WNK4 mutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FCS20090086

Tubular Mechanism for the Spontaneous Hypercalciuria in Laboratory Rat

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FCS20090086

A cluster of metabolic defects caused by mutation in a mitochondrial tRNA.

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FCS20090086

Factors governing the transepithelial potential difference across the proximal tubule of the rat kidney

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FCS20090086

21 January 2018

Identifiers

DOI

10.1042/CS20090086

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19780717%20AND%20SRC:MED&resulttype=core&format=json

8 February 2020

1 reference