(Q44664165)

5 December 2017

title

Induction of microsomal prostaglandin E2 synthase in the macula densa in children with hypokalemic salt-losing tubulopathies (English)

1 reference

5 December 2017

1 reference

Hannsjörg W. Seyberth

series ordinal

4

object named as

Hannsjörg W Seyberth

1 reference

5 December 2017

Martin Kömhoff

1

1 reference

5 December 2017

Stephan C Reinalter

series ordinal

2

1 reference

5 December 2017

Hermann J Gröne

series ordinal

3

1 reference

5 December 2017

language of work or name

English

0 references

publication date

19 November 2003

1 reference

5 December 2017

1 reference

5 December 2017

volume

55

1 reference

5 December 2017

issue

2

1 reference

5 December 2017

page(s)

261-266

1 reference

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

5 December 2017

cites work

1 reference

https://api.crossref.org/works/10.1203%2F01.PDR.0000101747.09626.6B

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/10.1203%2F01.PDR.0000101747.09626.6B

Characterization of furosemide-induced activation of the renal prostaglandin system

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F01.PDR.0000101747.09626.6B

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/10.1203%2F01.PDR.0000101747.09626.6B

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/10.1203%2F01.PDR.0000101747.09626.6B

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F01.PDR.0000101747.09626.6B

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F01.PDR.0000101747.09626.6B

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F01.PDR.0000101747.09626.6B

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/10.1203%2F01.PDR.0000101747.09626.6B

Prostaglandin synthase 2.

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F01.PDR.0000101747.09626.6B

Cyclooxygenase 2 and the kidney

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F01.PDR.0000101747.09626.6B

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F01.PDR.0000101747.09626.6B

Molecular identification of cytosolic prostaglandin E2 synthase that is functionally coupled with cyclooxygenase-1 in immediate prostaglandin E2 biosynthesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F01.PDR.0000101747.09626.6B

Identification of human prostaglandin E synthase: a microsomal, glutathione-dependent, inducible enzyme, constituting a potential novel drug target

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F01.PDR.0000101747.09626.6B

Coupling between cyclooxygenase, terminal prostanoid synthase, and phospholipase A2.

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F01.PDR.0000101747.09626.6B

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F01.PDR.0000101747.09626.6B

Functional heterogeneity of ROMK mutations linked to hyperprostaglandin E syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F01.PDR.0000101747.09626.6B

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/10.1203%2F01.PDR.0000101747.09626.6B

Microsomal prostaglandin E synthase is regulated by proinflammatory cytokines and glucocorticoids in primary rheumatoid synovial cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F01.PDR.0000101747.09626.6B

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/10.1203%2F01.PDR.0000101747.09626.6B

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/10.1203%2F01.PDR.0000101747.09626.6B

Gene expression of prostanoid forming enzymes along the rat nephron

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F01.PDR.0000101747.09626.6B

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/10.1203%2F01.PDR.0000101747.09626.6B

A new chapter in cardiac PKC signaling studies: searching for isoform-specific molecular targets. Focus on: “Isoenzyme-selective regulation of SERCA2 gene expression by protein kinase C in neonatal rat ventricular myocytes”

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F01.PDR.0000101747.09626.6B

10.1203/01.PDR.0000101747.09626.6B

21 January 2018

Identifiers

DOI

1 reference

Dimensions Publication ID

5 December 2017

1045649401

0 references

1 reference