(Q36081267)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15793031%20AND%20SRC:MED&resulttype=core&format=json

10 January 2020

review article

1 reference

title

Salt handling in the distal nephron: lessons learned from inherited human disorders (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15793031%20AND%20SRC:MED&resulttype=core&format=json

10 January 2020

1 reference

4

1 reference

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10 January 2020

Hannsjörg W. Seyberth

7

object named as

Hannsjörg W Seyberth

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15793031%20AND%20SRC:MED&resulttype=core&format=json

10 January 2020

author name string

Nikola Jeck

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15793031%20AND%20SRC:MED&resulttype=core&format=json

10 January 2020

Karl P Schlingmann

2

1 reference

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10 January 2020

Stephan C Reinalter

3

1 reference

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10 January 2020

Melanie Peters

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15793031%20AND%20SRC:MED&resulttype=core&format=json

10 January 2020

Siegfried Waldegger

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15793031%20AND%20SRC:MED&resulttype=core&format=json

10 January 2020

language of work or name

1 reference

1 April 2005

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15793031%20AND%20SRC:MED&resulttype=core&format=json

American Journal of Physiology - Regulatory, Integrative and Comparative Physiology

10 January 2020

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15793031%20AND%20SRC:MED&resulttype=core&format=json

10 January 2020

volume

288

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15793031%20AND%20SRC:MED&resulttype=core&format=json

10 January 2020

issue

4

1 reference

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10 January 2020

page(s)

R782-95

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15793031%20AND%20SRC:MED&resulttype=core&format=json

Pseudohypoaldosteronism in a preterm infant: Intrauterine presentation as hydramnios

10 January 2020

cites work

1 reference

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Hyperplasia of the juxtaglomerular complex with hyperaldosteronism and hypokalemic alkalosis. A new syndrome

21 January 2018

1 reference

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

21 January 2018

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Deafness and renal tubular acidosis in mice lacking the K-Cl co-transporter Kcc4.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPREGU.00600.2004

Loss of K-Cl co-transporter KCC3 causes deafness, neurodegeneration and reduced seizure threshold

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPREGU.00600.2004

Furosemide effect on isolated perfused tubules

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPREGU.00600.2004

Role of p38 in the regulation of renal cortical cyclooxygenase-2 expression by extracellular chloride

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPREGU.00600.2004

Characterization of furosemide-induced activation of the renal prostaglandin system

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPREGU.00600.2004

Evidence supporting a role for KCl cotransporter in the thick ascending limb of Henle's loop

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPREGU.00600.2004

An amino acid triplet in the NH2 terminus of rat ROMK1 determines interaction with SUR2B.

21 January 2018

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Divalent cation transport by the distal nephron: insights from Bartter's and Gitelman's syndromes

21 January 2018

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

21 January 2018

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Role of prostaglandins in the pathogenesis of Bartter's syndrome

21 January 2018

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Transient neonatal hyperkalemia in the antenatal (ROMK defective) Bartter syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPREGU.00600.2004

Immunolocalization of a microsomal prostaglandin E synthase in rabbit kidney

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPREGU.00600.2004

Primary structure and functional expression of a cDNA encoding the thiazide-sensitive, electroneutral sodium-chloride cotransporter

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPREGU.00600.2004

Hypomagnesemia and chondrocalcinosis in Gitelman syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPREGU.00600.2004

Evidence for a prostaglandin-independent defect in chloride reabsorption in the loop of henle as a proximal cause of Bartter's syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPREGU.00600.2004

Bartter's syndrome: a disorder characterized by high urinary prostaglandins and a dependence of hyperreninemia on prostaglandin synthesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPREGU.00600.2004

Ion transport mechanisms in thick ascending limb of Henle's loop of mammalian nephron

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPREGU.00600.2004

Prostaglandin E2 inhibits renal collecting duct Na+ absorption by activating the EP1 receptor

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPREGU.00600.2004

Successful management of an extreme example of neonatal hyperprostaglandin-E syndrome (Bartter???s syndrome) with the new cyclooxygenase-2 inhibitor rofecoxib

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPREGU.00600.2004

A de novo missense mutation of the beta subunit of the epithelial sodium channel causes hypertension and Liddle syndrome, identifying a proline-rich segment critical for regulation of channel activity

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPREGU.00600.2004

Hypertension caused by a truncated epithelial sodium channel gamma subunit: genetic heterogeneity of Liddle syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPREGU.00600.2004

Cyclooxygenase-2 mediates increased renal renin content induced by low-sodium diet.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPREGU.00600.2004

Cyclooxygenase-2 is associated with the macula densa of rat kidney and increases with salt restriction

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPREGU.00600.2004

Cloning and expression of an inwardly rectifying ATP-regulated potassium channel

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPREGU.00600.2004

Mutations in the gene encoding the inwardly-rectifying renal potassium channel, ROMK, cause the antenatal variant of Bartter syndrome: evidence for genetic heterogeneity. International Collaborative Study Group for Bartter-like Syndromes [published e

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPREGU.00600.2004

Functional heterogeneity of ROMK mutations linked to hyperprostaglandin E syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPREGU.00600.2004

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPREGU.00600.2004

Hypokalemic salt-losing tubulopathy with chronic renal failure and sensorineural deafness

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPREGU.00600.2004

A common sequence variation of the CLCNKB gene strongly activates ClC-Kb chloride channel activity

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPREGU.00600.2004

Activating mutation of the renal epithelial chloride channel ClC-Kb, predisposing to hypertension

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPREGU.00600.2004

Primary structure of Torpedo marmorata chloride channel isolated by expression cloning in Xenopus oocytes.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPREGU.00600.2004

Prostaglandin E2 but not I2 restores furosemide response in indomethacin-treated rats

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPREGU.00600.2004

Prenatal and postnatal management of hyperprostaglandin E syndrome after genetic diagnosis from amniocytes.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPREGU.00600.2004

Renal cyclooxygenase-2 (COX-2). Physiological, pathophysiological, and clinical implications.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPREGU.00600.2004

Clarification of the site of action of chlorothiazide in the rat nephron

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPREGU.00600.2004

Novel mutations in the thiazide-sensitive NaCl cotransporter gene in patients with Gitelman syndrome with predominant localization to the C-terminal domain

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPREGU.00600.2004

Reference intervals and developmental changes in urinary prostanoid excretion in healthy newborns, infants and children

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPREGU.00600.2004

Thiazide treatment of rats provokes apoptosis in distal tubule cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPREGU.00600.2004

Impaired renal NaCl absorption in mice lacking the ROMK potassium channel, a model for type II Bartter's syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPREGU.00600.2004

Absence of small conductance K+ channel (SK) activity in apical membranes of thick ascending limb and cortical collecting duct in ROMK (Bartter's) knockout mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPREGU.00600.2004

Molecular cloning, expression pattern, and chromosomal localization of the human Na-Cl thiazide-sensitive cotransporter (SLC12A3)

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPREGU.00600.2004

Overt nephrogenic diabetes insipidus in mice lacking the CLC-K1 chloride channel.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPREGU.00600.2004

Sensitivity of a renal K+ channel (ROMK2) to the inhibitory sulfonylurea compound glibenclamide is enhanced by coexpression with the ATP-binding cassette transporter cystic fibrosis transmembrane regulator

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPREGU.00600.2004

A single nucleotide polymorphism alters the activity of the renal Na+:Cl- cotransporter and reveals a role for transmembrane segment 4 in chloride and thiazide affinity

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPREGU.00600.2004

Upregulation of Na+ transporter abundances in response to chronic thiazide or loop diuretic treatment in rats

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPREGU.00600.2004

Pathogenetic role of cyclooxygenase-2 in hyperprostaglandin E syndrome/antenatal Bartter syndrome: therapeutic use of the cyclooxygenase-2 inhibitor nimesulide

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPREGU.00600.2004

A variant of Bartter's syndrome. Bartter's syndrome associated with hydramnios, prematurity, hypercalciuria and nephrocalcinosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPREGU.00600.2004

Clinical presentation of genetically defined patients with hypokalemic salt-losing tubulopathies.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPREGU.00600.2004

Mammalian distal tubule: physiology, pathophysiology, and molecular anatomy

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPREGU.00600.2004

Evaluation of long-term treatment with indomethacin in hereditary hypokalemic salt-losing tubulopathies

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPREGU.00600.2004

Role of cyclooxygenase-2 in hyperprostaglandin E syndrome/antenatal Bartter syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPREGU.00600.2004

Reevaluation of the criteria for the clinical diagnosis of Gitelman syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPREGU.00600.2004

Hypomagnesaemia of hereditary renal origin

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPREGU.00600.2004

Renal effects of selective cyclooxygenase-2 inhibition in normotensive salt-depleted subjects

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPREGU.00600.2004

Ion conductances of isolated cortical collecting duct cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPREGU.00600.2004

Salt wasting and deafness resulting from mutations in two chloride channels

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPREGU.00600.2004

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/10.1152%2FAJPREGU.00600.2004

Genotype/phenotype observations in African Americans with Bartter syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPREGU.00600.2004

Role of prostaglandins in hyperprostaglandin E syndrome and in selected renal tubular disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPREGU.00600.2004

Congenital hypokalemia with hypercalciuria in preterm infants: a hyperprostaglandinuric tubular syndrome different from Bartter syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPREGU.00600.2004

The neonatal variant of Bartter syndrome and deafness: preservation of renal function

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPREGU.00600.2004

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/10.1152%2FAJPREGU.00600.2004

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPREGU.00600.2004

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/10.1152%2FAJPREGU.00600.2004

Molecular basis of the long-QT syndrome associated with deafness

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPREGU.00600.2004

Regulation of renal ion transport and cell growth by sodium

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPREGU.00600.2004

Uncompensated polyuria in a mouse model of Bartter's syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPREGU.00600.2004

Rat homolog of sulfonylurea receptor 2B determines glibenclamide sensitivity of ROMK2 in Xenopus laevis oocyte

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPREGU.00600.2004

Flow-dependent activation of maxi K+ channels in apical membrane of rabbit connecting tubule

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPREGU.00600.2004

Ion and diuretic specificity of chimeric proteins between apical Na(+)-K(+)-2Cl(-) and Na(+)-Cl(-) cotransporters

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPREGU.00600.2004

Novel molecular variants of the Na-K-2Cl cotransporter gene are responsible for antenatal Bartter syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPREGU.00600.2004

Bartter's syndrome with hyperplasia of renomedullary cells: successful treatment with indomethacin

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPREGU.00600.2004

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPREGU.00600.2004

Barttin increases surface expression and changes current properties of ClC-K channels

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPREGU.00600.2004

Interference with Feedback Control of Glomerular Filtration Rate by Furosemide, Triflocin, and Cyanide

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPREGU.00600.2004

Neonatal mortality in an aquaporin-2 knock-in mouse model of recessive nephrogenic diabetes insipidus

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPREGU.00600.2004

Low chloride stimulation of prostaglandin E2 release and cyclooxygenase-2 expression in a mouse macula densa cell line

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPREGU.00600.2004

Generation and phenotype of mice harboring a nonsense mutation in the V2 vasopressin receptor gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPREGU.00600.2004

Hypokalaemic salt-losing tubulopathies: an evolving story

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPREGU.00600.2004

A novel mutation in the chloride channel gene, CLCNKB, as a cause of Gitelman and Bartter syndromes

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPREGU.00600.2004

10.1152/AJPREGU.00600.2004

21 January 2018

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15793031%20AND%20SRC:MED&resulttype=core&format=json

10 January 2020

1 reference