(Q48351063)

10 February 2018

review article

1 reference

title

Renal phosphate handling and inherited disorders of phosphate reabsorption: an update (English)

1 reference

10 February 2018

2

Isabel Rubio-Aliaga

1 reference

10 February 2018

author name string

Carsten A Wagner

series ordinal

1

1 reference

10 February 2018

Nati Hernando

series ordinal

3

1 reference

10 February 2018

publication date

23 December 2017

1 reference

10 February 2018

published in

Pediatric Nephrology

1 reference

10 February 2018

https://scigraph.springernature.com/pub.10.1007/s00467-017-3873-3

exact match

0 references

cites work

Public health impact of dietary phosphorus excess on bone and cardiovascular health in the general population

1 reference

https://api.crossref.org/works/10.1007%2FS00467-017-3873-3

High dietary phosphorus intake is associated with all-cause mortality: results from NHANES III.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-017-3873-3

Vitamin D endocrine system and the intestine

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-017-3873-3

Intestinal Depletion of NaPi-IIb/Slc34a2 in Mice: Renal and Hormonal Adaptation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-017-3873-3

Regulation of intestinal phosphate transport. I. Segmental expression and adaptation to low-P(i) diet of the type IIb Na(+)-P(i) cotransporter in mouse small intestine.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-017-3873-3

Intestinal and renal adaptation to a low-Pi diet of type II NaPi cotransporters in vitamin D receptor- and 1alphaOHase-deficient mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-017-3873-3

Pulmonary alveolar microlithiasis. State-of-the-art review

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-017-3873-3

Mutations in SLC34A2 cause pulmonary alveolar microlithiasis and are possibly associated with testicular microlithiasis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-017-3873-3

Intestinal npt2b plays a major role in phosphate absorption and homeostasis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-017-3873-3

The intestinal phosphate transporter NaPi-IIb (Slc34a2) is required to protect bone during dietary phosphate restriction

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-017-3873-3

Mutations in SLC20A2 link familial idiopathic basal ganglia calcification with phosphate homeostasis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-017-3873-3

Renal control of calcium, phosphate, and magnesium homeostasis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-017-3873-3

Phosphate transporters and their function

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-017-3873-3

The SLC34 family of sodium-dependent phosphate transporters.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-017-3873-3

Functional asymmetry of phosphate transport and its regulation in opossum kidney cells: phosphate "adaptation".

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-017-3873-3

Functional asymmetry of phosphate transport and its regulation in opossum kidney cells: phosphate transport.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-017-3873-3

Structural fold and binding sites of the human Na⁺-phosphate cotransporter NaPi-II

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-017-3873-3

Phosphate transporters of the SLC20 and SLC34 families

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-017-3873-3

Genetic diseases of renal phosphate handling

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-017-3873-3

FGF23 and syndromes of abnormal renal phosphate handling

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-017-3873-3

Disorders of phosphate homeostasis and tissue mineralisation

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-017-3873-3

Heritable and acquired disorders of phosphate metabolism: Etiologies involving FGF23 and current therapeutics

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-017-3873-3

What is nephrocalcinosis?

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-017-3873-3

Idiopathic hypercalciuria and formation of calcium renal stones

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-017-3873-3

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-017-3873-3

Genetic, pathophysiological, and clinical aspects of nephrocalcinosis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-017-3873-3

Common genetic variants associate with serum phosphorus concentration

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-017-3873-3

A replication study for three nephrolithiasis loci at 5q35.3, 7p14.3 and 13q14.1 in the Japanese population

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-017-3873-3

A genome-wide association study of nephrolithiasis in the Japanese population identifies novel susceptible Loci at 5q35.3, 7p14.3, and 13q14.1

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-017-3873-3

Genetic determinants of urolithiasis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-017-3873-3

Common and rare variants associated with kidney stones and biochemical traits

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-017-3873-3

Nephrolithiasis and osteoporosis associated with hypophosphatemia caused by mutations in the type 2a sodium-phosphate cotransporter

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-017-3873-3

Exome sequencing identifies a novel homozygous mutation in the phosphate transporter SLC34A1 in hypophosphatemia and nephrocalcinosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-017-3873-3

Autosomal-Recessive Mutations in SLC34A1 Encoding Sodium-Phosphate Cotransporter 2A Cause Idiopathic Infantile Hypercalcemia

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-017-3873-3

Prevalence of Monogenic Causes in Pediatric Patients with Nephrolithiasis or Nephrocalcinosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-017-3873-3

Fourteen monogenic genes account for 15% of nephrolithiasis/nephrocalcinosis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-017-3873-3

Loss of function of NaPiIIa causes nephrocalcinosis and possibly kidney insufficiency.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-017-3873-3

A loss-of-function mutation in NaPi-IIa and renal Fanconi's syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-017-3873-3

Clinical Heterogeneity and Phenotypic Expansion of NaPi-IIa-Associated Disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-017-3873-3

Whole exome sequencing frequently detects a monogenic cause in early onset nephrolithiasis and nephrocalcinosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-017-3873-3

Sotos syndrome, infantile hypercalcemia, and nephrocalcinosis: a contiguous gene syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-017-3873-3

Biallelic mutations in CYP24A1 or SLC34A1 as a cause of infantile idiopathic hypercalcemia (IIH) with vitamin D hypersensitivity: molecular study of 11 historical IIH cases.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-017-3873-3

NPT2a gene variation in calcium nephrolithiasis with renal phosphate leak.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-017-3873-3

Functional characterization of two naturally occurring mutations in the human sodium-phosphate cotransporter type IIa.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-017-3873-3

Monitoring protein-protein interactions between the mammalian integral membrane transporters and PDZ-interacting partners using a modified split-ubiquitin membrane yeast two-hybrid system

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-017-3873-3

The functional unit of the renal type IIa Na+/Pi cotransporter is a monomer

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-017-3873-3

Calcium oxalate crystal deposition in kidneys of hypercalciuric mice with disrupted type IIa sodium-phosphate cotransporter

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-017-3873-3

Renal calcification in mice homozygous for the disrupted type IIa Na/Pi cotransporter gene Npt2.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-017-3873-3

Targeted inactivation of Npt2 in mice leads to severe renal phosphate wasting, hypercalciuria, and skeletal abnormalities

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-017-3873-3

1alpha-Hydroxylase gene ablation and Pi supplementation inhibit renal calcification in mice homozygous for the disrupted Npt2a gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-017-3873-3

Mutations in SLC34A3/NPT2c are associated with kidney stones and nephrocalcinosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-017-3873-3

Hereditary hypophosphatemic rickets with hypercalciuria is caused by mutations in the sodium-phosphate cotransporter gene SLC34A3.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-017-3873-3

SLC34A3 mutations in patients with hereditary hypophosphatemic rickets with hypercalciuria predict a key role for the sodium-phosphate cotransporter NaPi-IIc in maintaining phosphate homeostasis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-017-3873-3

A novel missense mutation in SLC34A3 that causes hereditary hypophosphatemic rickets with hypercalciuria in humans identifies threonine 137 as an important determinant of sodium-phosphate cotransport in NaPi-IIc

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-017-3873-3

A patient with hypophosphatemia, a femoral fracture, and recurrent kidney stones: report of a novel mutation in SLC34A3.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-017-3873-3

Association between compound heterozygous mutations of SLC34A3 and hypercalciuria.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-017-3873-3

Genetic and clinical peculiarities in a new family with hereditary hypophosphatemic rickets with hypercalciuria: a case report

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-017-3873-3

Processing and stability of type IIc sodium-dependent phosphate cotransporter mutations in patients with hereditary hypophosphatemic rickets with hypercalciuria

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-017-3873-3

Hereditary hypophosphatemic rickets with hypercalciuria and nephrolithiasis-identification of a novel SLC34A3/NaPi-IIc mutation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-017-3873-3

Novel SLC34A3 mutation causing hereditary hypophosphataemic rickets with hypercalciuria in a Gambian family

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-017-3873-3

Hypophosphatemic rickets with hypercalciuria due to mutation in SLC34A3/type IIc sodium-phosphate cotransporter: presentation as hypercalciuria and nephrolithiasis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-017-3873-3

Novel NaPi-IIc mutations causing HHRH and idiopathic hypercalciuria in several unrelated families: long-term follow-up in one kindred

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-017-3873-3

A compound heterozygous mutation in SLC34A3 causes hereditary hypophosphatemic rickets with hypercalciuria in a Chinese patient.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-017-3873-3

Hereditary hypophosphatemia in Norway: a retrospective population-based study of genotypes, phenotypes, and treatment complications

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-017-3873-3

Intronic deletions in the SLC34A3 gene: a cautionary tale for mutation analysis of hereditary hypophosphatemic rickets with hypercalciuria

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-017-3873-3

Type IIc sodium-dependent phosphate transporter regulates calcium metabolism

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-017-3873-3

Renal-specific and inducible depletion of NaPi-IIc/Slc34a3, the cotransporter mutated in HHRH, does not affect phosphate or calcium homeostasis in mice.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-017-3873-3

Na(+)/H(+ ) exchanger regulatory factor 2 directs parathyroid hormone 1 receptor signalling

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-017-3873-3

Defective coupling of apical PTH receptors to phospholipase C prevents internalization of the Na+-phosphate cotransporter NaPi-IIa in Nherf1-deficient mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-017-3873-3

Interaction of the type IIa Na/Pi cotransporter with PDZ proteins

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-017-3873-3

PDZ-domain interactions and apical expression of type IIa Na/P(i) cotransporters.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-017-3873-3

Role of NHERF-1 in regulation of the activity of Na-K ATPase and sodium-phosphate co-transport in epithelial cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-017-3873-3

Targeted disruption of the mouse NHERF-1 gene promotes internalization of proximal tubule sodium-phosphate cotransporter type IIa and renal phosphate wasting

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-017-3873-3

Na+/H+ exchanger-regulatory factor 1 mediates inhibition of phosphate transport by parathyroid hormone and second messengers by acting at multiple sites in opossum kidney cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-017-3873-3

The role of NHERF-1 in the regulation of renal proximal tubule sodium-hydrogen exchanger 3 and sodium-dependent phosphate cotransporter 2a.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-017-3873-3

NHERF1 mutations and responsiveness of renal parathyroid hormone

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-017-3873-3

A new human NHERF1 mutation decreases renal phosphate transporter NPT2a expression by a PTH-independent mechanism

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-017-3873-3

The Na+-Pi cotransporter PiT-2 (SLC20A2) is expressed in the apical membrane of rat renal proximal tubules and regulated by dietary Pi

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-017-3873-3

Acute parathyroid hormone differentially regulates renal brush border membrane phosphate cotransporters

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-017-3873-3

Mutations in SLC20A2 are a major cause of familial idiopathic basal ganglia calcification

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-017-3873-3

Inorganic phosphate export by the retrovirus receptor XPR1 in metazoans

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-017-3873-3

Expression of the mammalian Xenotropic Polytropic Virus Receptor 1 (XPR1) in tobacco leaves leads to phosphate export.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-017-3873-3

Control of eukaryotic phosphate homeostasis by inositol polyphosphate sensor domains

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-017-3873-3

Mutations in XPR1 cause primary familial brain calcification associated with altered phosphate export

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-017-3873-3

XPR1 mutations are a rare cause of primary familial brain calcification.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-017-3873-3

Renal Fanconi Syndrome and Hypophosphatemic Rickets in the Absence of Xenotropic and Polytropic Retroviral Receptor in the Nephron.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-017-3873-3

Fanconi-Bickel syndrome and autosomal recessive proximal tubulopathy with hypercalciuria (ARPTH) are allelic variants caused by GLUT2 mutations.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-017-3873-3

Acute metabolic acidosis in a GLUT2-deficient patient with Fanconi-Bickel syndrome: new pathophysiology insights

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-017-3873-3

Mutations in GLUT2, the gene for the liver-type glucose transporter, in patients with Fanconi-Bickel syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-017-3873-3

A common molecular basis for three inherited kidney stone diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-017-3873-3

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-017-3873-3

Multiple loci associated with indices of renal function and chronic kidney disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-017-3873-3

New loci associated with kidney function and chronic kidney disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-017-3873-3

Trans-ethnic Fine Mapping Highlights Kidney-Function Genes Linked to Salt Sensitivity

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-017-3873-3

Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-017-3873-3

Functional genomic annotation of genetic risk loci highlights inflammation and epithelial biology networks in CKD

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-017-3873-3

Relations of Serum Phosphorus and Calcium Levels to the Incidence of Cardiovascular Disease in the Community

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-017-3873-3

Absorption of Inorganic Phosphate in the Human Small Intestine

21 January 2018

1 reference

12 December 2020

Intronic deletions in the SLC34A3 gene cause hereditary hypophosphatemic rickets with hypercalciuria

1 reference

12 December 2020

Tissue-specific mRNA expression profiles of human solute carrier transporter superfamilies

1 reference

12 December 2020

NHERF1 mutations and responsiveness of renal parathyroid hormone

1 reference

12 December 2020

10.1007/S00467-017-3873-3

Identifiers

DOI

1 reference

10 February 2018

1 reference

10 February 2018