List of works - Fiona E Karet

A novel missense mutation in AE1 causing autosomal dominant distal renal tubular acidosis retains normal transport function but is mistargeted in polarized epithelial cells

scientific article

An endothelin-1 mediated autocrine growth loop involved in human renal tubular regeneration

scientific article published on 01 August 1995

An extended nomenclature for mammalian V-ATPase subunit genes and splice variants

scientific article

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

scientific article

Bovril and moclobemide: a novel therapeutic strategy for central autonomic failure

scientific article published on 01 November 1994

Cellular physiology of the renal H+ATPase.

scientific article published on September 2009

Characterization of a Recurrent In-frame UMOD Indel Mutation Causing Late-onset Autosomal Dominant End-Stage Renal Failure ⬇️

scientific article published on October 27, 2011

Characterization of peptide and nonpeptide antagonists in human kidney

scientific article published on 01 January 1995

Comparative ontogeny, processing, and segmental distribution of the renal chloride channel, ClC-5

scientific article

Comparative quantification of endothelin receptor mRNA in human kidney: new tools for direct investigation of human tissue

article

Disorders of Water and Acid-Base Homeostasis ⬇️

scientific article published on November 11, 2010

Endothelin and the human kidney: a potential target for new drugs

scientific article published on 01 January 1994

Endothelin peptides and receptors in human kidney

scientific article published on 01 September 1996

Examining Patients - an introduction to clinical medicine.

scientific article published in April 1991

Genetic heterogeneity of Bartter's syndrome revealed by mutations in the K+ channel, ROMK

scientific article published on 01 October 1996

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

scientific article

Glyceraldehyde 3-phosphate dehydrogenase is required for band 3 (anion exchanger 1) membrane residency in the mammalian kidney

scientific journal article

Human H+ATPase a4 subunit mutations causing renal tubular acidosis reveal a role for interaction with phosphofructokinase-1 ⬇️

scientific article

Human kidney: endothelin isoforms detected by HPLC with radioimmunoassay and receptor subtypes detected using ligands BQ123 and BQ3020

scientific article published on 01 January 1993

Human urinary exosomes as innate immune effectors

scientific article

Hypertension

Importance of early audiologic assessment in distal renal tubular acidosis

scientific article published on 22 December 2010

Inherited distal renal tubular acidosis.

scientific article

Inherited renal acidoses.

scientific article published on June 2007

Inherited renal tubular acidosis

scientific article published on 01 January 2000

Interpretation of blood films in diagnosis of malaria.

scientific article published in September 1989

Life-threatening metabolic alkalosis in Pendred syndrome

scientific article

Lipoprotein glomerulopathy: a new role for apolipoprotein E?

scientific article published on 01 May 1997

Localization and regulation of the ATP6V0A4 (a4) vacuolar H+-ATPase subunit defective in an inherited form of distal renal tubular acidosis

scientific article

Localization of a gene for autosomal recessive distal renal tubular acidosis with normal hearing (rdRTA2) to 7q33-34

scientific article

Localization of endothelin peptides in human kidney

scientific article published on 01 February 1996

Mice deficient in H+-ATPase a4 subunit have severe hearing impairment associated with enlarged endolymphatic compartments within the inner ear.

scientific article

Molecular cloning and characterization of a novel form of the human vacuolar H+-ATPase e-subunit: an essential proton pump component

scientific article

Molecular cloning and characterization of novel tissue-specific isoforms of the human vacuolar H(+)-ATPase C, G and d subunits, and their evaluation in autosomal recessive distal renal tubular acidosis

scientific article (publication date: 4 September 2002)

Monogenic tubular salt and acid transporter disorders.

scientific article

Mutations contributing to human blood pressure variation.

scientific article

Mutations in VPS33B, encoding a regulator of SNARE-dependent membrane fusion, cause arthrogryposis-renal dysfunction-cholestasis (ARC) syndrome

scientific article

Mutations in the chloride-bicarbonate exchanger gene AE1 cause autosomal dominant but not autosomal recessive distal renal tubular acidosis

scientific article

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

scientific article

Non-polarized targeting of AE1 causes autosomal dominant distal renal tubular acidosis

scientific article

Novel ligands BQ123 and BQ3020 characterize endothelin receptor subtypes ETA and ETB in human kidney

scientific article published on 01 July 1993

PDLIM5 links kidney anion exchanger 1 (kAE1) to ILK and is required for membrane targeting of kAE1.

scientific article published on 03 January 2017

Polarisation, key to good localisation

scientific article published on 31 March 2006

Practical Guide to the Care of the Medical Patient

Regulation of the basolateral chloride/base exchangers AE1 and SLC26A7 in the kidney collecting duct in potassium depletion

scientific journal article

Revised nomenclature for mammalian vacuolar-type H+ -ATPase subunit genes

scientific article (publication date: October 2003)

RhCG is the major putative ammonia transporter expressed in the human kidney, and RhBG is not expressed at detectable levels.

scientific article published on 08 April 2009

Salt handling and hypertension.

scientific article

Targeting the renin-angiotensin system in patients with renal disease

scientific article published on 01 August 2002

Two novel missense mutations in g protein-coupled receptor 54 in a patient with hypogonadotropic hypogonadism.

scientific article published on 14 December 2004

Urinary Exosomes Contain MicroRNAs Capable of Paracrine Modulation of Tubular Transporters in Kidney

scientific article

Uromodulin exclusion list improves urinary exosomal protein identification ⬇️

scientific article published on December 1, 2011

Uromodulin mutations causing familial juvenile hyperuricaemic nephropathy lead to protein maturation defects and retention in the endoplasmic reticulum

scientific article published on 22 May 2009

Vacuolar H+-ATPase d2 subunit: molecular characterization, developmental regulation, and localization to specialized proton pumps in kidney and bone

scientific article

Vasopressin induces expression of the Cl-/HCO3- exchanger SLC26A7 in kidney medullary collecting ducts of Brattleboro rats

scientific journal article

[125I]-PD151242: a selective ligand for endothelin ETA receptors in human kidney which localizes to renal vasculature.

scientific article published on December 1994

List of works by Fiona E Karet

A novel missense mutation in AE1 causing autosomal dominant distal renal tubular acidosis retains normal transport function but is mistargeted in polarized epithelial cells

An endothelin-1 mediated autocrine growth loop involved in human renal tubular regeneration

An extended nomenclature for mammalian V-ATPase subunit genes and splice variants

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

Bovril and moclobemide: a novel therapeutic strategy for central autonomic failure

Cellular physiology of the renal H+ATPase.

Characterization of a Recurrent In-frame UMOD Indel Mutation Causing Late-onset Autosomal Dominant End-Stage Renal Failure ⬇️

Characterization of peptide and nonpeptide antagonists in human kidney

Comparative ontogeny, processing, and segmental distribution of the renal chloride channel, ClC-5

Comparative quantification of endothelin receptor mRNA in human kidney: new tools for direct investigation of human tissue

Disorders of Water and Acid-Base Homeostasis ⬇️

Endothelin and the human kidney: a potential target for new drugs

Endothelin peptides and receptors in human kidney

Examining Patients - an introduction to clinical medicine.

Genetic heterogeneity of Bartter's syndrome revealed by mutations in the K+ channel, ROMK

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

Glyceraldehyde 3-phosphate dehydrogenase is required for band 3 (anion exchanger 1) membrane residency in the mammalian kidney

Human H+ATPase a4 subunit mutations causing renal tubular acidosis reveal a role for interaction with phosphofructokinase-1 ⬇️

Human kidney: endothelin isoforms detected by HPLC with radioimmunoassay and receptor subtypes detected using ligands BQ123 and BQ3020

Human urinary exosomes as innate immune effectors

Hypertension

Importance of early audiologic assessment in distal renal tubular acidosis

Inherited distal renal tubular acidosis.

Inherited renal acidoses.

Inherited renal tubular acidosis

Interpretation of blood films in diagnosis of malaria.

Life-threatening metabolic alkalosis in Pendred syndrome

Lipoprotein glomerulopathy: a new role for apolipoprotein E?

Localization and regulation of the ATP6V0A4 (a4) vacuolar H+-ATPase subunit defective in an inherited form of distal renal tubular acidosis

Localization of a gene for autosomal recessive distal renal tubular acidosis with normal hearing (rdRTA2) to 7q33-34

Localization of endothelin peptides in human kidney

Mice deficient in H+-ATPase a4 subunit have severe hearing impairment associated with enlarged endolymphatic compartments within the inner ear.

Molecular cloning and characterization of a novel form of the human vacuolar H+-ATPase e-subunit: an essential proton pump component

Molecular cloning and characterization of novel tissue-specific isoforms of the human vacuolar H(+)-ATPase C, G and d subunits, and their evaluation in autosomal recessive distal renal tubular acidosis

Monogenic tubular salt and acid transporter disorders.

Mutations contributing to human blood pressure variation.

Mutations in VPS33B, encoding a regulator of SNARE-dependent membrane fusion, cause arthrogryposis-renal dysfunction-cholestasis (ARC) syndrome

Mutations in the chloride-bicarbonate exchanger gene AE1 cause autosomal dominant but not autosomal recessive distal renal tubular acidosis

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

Non-polarized targeting of AE1 causes autosomal dominant distal renal tubular acidosis

Novel ligands BQ123 and BQ3020 characterize endothelin receptor subtypes ETA and ETB in human kidney

PDLIM5 links kidney anion exchanger 1 (kAE1) to ILK and is required for membrane targeting of kAE1.

Polarisation, key to good localisation

Practical Guide to the Care of the Medical Patient

Regulation of the basolateral chloride/base exchangers AE1 and SLC26A7 in the kidney collecting duct in potassium depletion

Revised nomenclature for mammalian vacuolar-type H+ -ATPase subunit genes

RhCG is the major putative ammonia transporter expressed in the human kidney, and RhBG is not expressed at detectable levels.

Salt handling and hypertension.

Targeting the renin-angiotensin system in patients with renal disease

Two novel missense mutations in g protein-coupled receptor 54 in a patient with hypogonadotropic hypogonadism.

Urinary Exosomes Contain MicroRNAs Capable of Paracrine Modulation of Tubular Transporters in Kidney

Uromodulin exclusion list improves urinary exosomal protein identification ⬇️

Uromodulin mutations causing familial juvenile hyperuricaemic nephropathy lead to protein maturation defects and retention in the endoplasmic reticulum

Vacuolar H+-ATPase d2 subunit: molecular characterization, developmental regulation, and localization to specialized proton pumps in kidney and bone

Vasopressin induces expression of the Cl-/HCO3- exchanger SLC26A7 in kidney medullary collecting ducts of Brattleboro rats

[125I]-PD151242: a selective ligand for endothelin ETA receptors in human kidney which localizes to renal vasculature.