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Fiona Karet

Research Profile

Disorders

Anatomy

Kidneys

Chemicals & Drugs

Concepts & Ideas

Genes & Molecular Sequences

Physiology

Mutation

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Publications

TOP 3
Thomas F Hiemstra; Fiona E Karet; Philip D Charles; Svenja S Hester; Kathryn S Lilley
Uromodulin exclusion list improves urinary exosomal protein identification.
Narayanan Kandasamy; Krishna Chatterjee; Mark Evans; Laura Fugazzola; Fiona E Karet
Life-threatening metabolic alkalosis in Pendred syndrome.
Fiona E Karet
Disorders of water and acid-base homeostasis.

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All Publications

2011: Thomas F Hiemstra; Fiona E Karet; Philip D Charles; Svenja S Hester; Kathryn S Lilley
Uromodulin exclusion list improves urinary exosomal protein identification.
Journal of biomolecular techniques : JBT 2011;22(4):136-45.
2011: Narayanan Kandasamy; Krishna Chatterjee; Mark Evans; Laura Fugazzola; Fiona E Karet
Life-threatening metabolic alkalosis in Pendred syndrome.
European journal of endocrinology / European Federation of Endocrine Societies 2011;165(1):167-70.
2011: Fiona E Karet
Disorders of water and acid-base homeostasis.
Nephron. Physiology 2011;118(1):p28-34.
2011: Ya Su; Katherine G Blake-Palmer; Andrew C Fry; Alison Best; Alice C N Brown; Thomas F Hiemstra; Shoko Horita; Aiwu Zhou; Ashley M Toye; Fiona E Karet
Glyceraldehyde 3-phosphate dehydrogenase is required for band 3 (anion exchanger 1) membrane residency in the mammalian kidney.
American journal of physiology. Renal physiology 2011;300(1):F157-66.
2010: Kevin C Miranda; Fiona E Karet; Dennis Brown
An extended nomenclature for mammalian V-ATPase subunit genes and splice variants.
PloS one 2010;5(3):e9531.
2009: Katherine G Blake-Palmer; Fiona E Karet
Cellular physiology of the renal H+ATPase.
Current opinion in nephrology and hypertension 2009;18(5):433-8.
2009: Siân E Williams; Anita A C Reed; Juris Galvanovskis; Corinne Antignac; Tim Goodship; Fiona E Karet; Peter Kotanko; Karl Lhotta; Vincent Morinière; Paul Williams; William Wong; Patrik Rorsman; Rajesh V Thakker
Uromodulin mutations causing familial juvenile hyperuricaemic nephropathy lead to protein maturation defects and retention in the endoplasmic reticulum.
Human molecular genetics 2009;18(16):2963-74.
2009: Alice C N Brown; Dalila Hallouane; William J Mawby; Fiona E Karet; Moin A Saleem; Alexander J Howie; Ashley M Toye
RhCG is the major putative ammonia transporter expressed in the human kidney, and RhBG is not expressed at detectable levels.
American journal of physiology. Renal physiology 2009;296(6):F1279-90.
2009: Fiona E Karet
Mechanisms in hyperkalemic renal tubular acidosis.
Journal of the American Society of Nephrology : JASN 2009;20(2):251-4.
2008: Ya Su; Katherine G Blake-Palmer; Sara Sorrell; Babak Javid; Katherine Bowers; Aiwu Zhou; Simon H Chang; Seema Qamar; Fiona E Karet
Human H+ATPase a4 subunit mutations causing renal tubular acidosis reveal a role for interaction with phosphofructokinase-1.
American journal of physiology. Renal physiology 2008;295(4):F950-8.
2008: Annabel N Smith; Richard W Francis; Sara L Sorrell; Fiona E Karet
The d subunit plays a central role in human vacuolar H(+)-ATPases.
Journal of bioenergetics and biomembranes 2008;40(4):371-80.
2007: Sharon Barone; Hassane Amlal; Minna Kujala; Jie Xu; Fiona E Karet; Ann Blanchard; Juha Kere; Manoocher Soleimani
Regulation of the basolateral chloride/base exchangers AE1 and SLC26A7 in the kidney collecting duct in potassium depletion.
Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association 2007;22(12):3462-70.
2007: Andrew C Fry; Fiona E Karet
Inherited renal acidoses.
Physiology (Bethesda, Md.) 2007;22():202-11.
2007: Katherine G Blake-Palmer; Ya Su; Annabel N Smith; Fiona E Karet
Molecular cloning and characterization of a novel form of the human vacuolar H+-ATPase e-subunit: an essential proton pump component.
Gene 2007;393(1-2):94-100.
2007: Elizabeth E Norgett; Katherine Borthwick; Rafia S Al-Lamki; Ya Su; Annabel N Smith; Fiona E Karet
V1 and V0 domains of the human H+-ATPase are linked by an interaction between the G and a subunits.
The Journal of biological chemistry 2007;282(19):14421-7.
2006: Moniek van Beest; Joris H Robben; Paul J M Savelkoul; Giel Hendriks; Mark A J Devonald; Irene B M Konings; Anne K Lagendijk; Fiona E Karet; Peter M T Deen
Polarisation, key to good localisation.
Biochimica et biophysica acta 2006;1758(8):1126-33.
2006: David R Phillips; Kashif I Ahmad; Sarah J Waller; Peter Meisner; Fiona E Karet
A serum potassium level above 10 mmol/l in a patient predisposed to hypokalemia.
Nature clinical practice. Nephrology 2006;2(6):340-6; quiz 347.
2006: Snezana Petrovic; Hassane Amlal; Xuming Sun; Fiona E Karet; Sharon Barone; Manoocher Soleimani
Vasopressin induces expression of the Cl-/HCO3- exchanger SLC26A7 in kidney medullary collecting ducts of Brattleboro rats.
American journal of physiology. Renal physiology 2006;290(5):F1194-201.
2006: Kevin M O'Shaughnessy; Fiona E Karet
Salt handling and hypertension.
Annual review of nutrition 2006;26():343-65.
2005: Fiona E Karet
Physiological and metabolic implications of V-ATPase isoforms in the kidney.
Journal of bioenergetics and biomembranes 2005;37(6):425-9.
2005: François Jouret; Céline Auzanneau; Huguette Debaix; Ge-Hong Sun Wada; Chrystel Pretto; Etienne Marbaix; Fiona E Karet; Pierre J Courtoy; Olivier Devuyst
Ubiquitous and kidney-specific subunits of vacuolar H+-ATPase are differentially expressed during nephrogenesis.
Journal of the American Society of Nephrology : JASN 2005;16(11):3235-46.
2005: Annabel N Smith; François Jouret; Sharyn Bord; Katherine Borthwick; Rafia S Al-Lamki; Carsten A Wagner; Deborah C Ireland; Valérie Cormier-Daire; Annalisa Frattini; Anna Villa; Uwe Kornak; Olivier Devuyst; Fiona E Karet
Vacuolar H+-ATPase d2 subunit: molecular characterization, developmental regulation, and localization to specialized proton pumps in kidney and bone.
Journal of the American Society of Nephrology : JASN 2005;16(5):1245-56.
2005: Robert K Semple; J C Achermann; J Ellery; I Sadaf Farooqi; Fiona E Karet; Richard Stanhope; Stephen O'Rahilly; Samuel A J R Aparicio
Two novel missense mutations in g protein-coupled receptor 54 in a patient with hypogonadotropic hypogonadism.
The Journal of clinical endocrinology and metabolism 2005;90(3):1849-55.
2004: Hongwei Dou; Jie Xu; Zhaohui Wang; Annabel N Smith; Manoocher Soleimani; Fiona E Karet; John H Greinwald; Daniel I Choo
Co-expression of pendrin, vacuolar H+-ATPase alpha4-subunit and carbonic anhydrase II in epithelial cells of the murine endolymphatic sac.
The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society 2004;52(10):1377-84.
2004: Mark A J Devonald; Fiona E Karet
Renal epithelial traffic jams and one-way streets.
Journal of the American Society of Nephrology : JASN 2004;15(6):1370-81.
2004: Nanyawan Rungroj; Mark A J Devonald; Alan W Cuthbert; Frank Reimann; Varaporn Akkarapatumwong; Pa-thai Yenchitsomanus; William M Bennett; 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.
The Journal of biological chemistry 2004;279(14):13833-8.
2004: Kevin M O'Shaughnessy; Fiona E Karet
Salt handling and hypertension.
The Journal of clinical investigation 2004;113(8):1075-81.
2004: Paul Gissen; Colin A Johnson; Neil V Morgan; Janneke M Stapelbroek; Tim Forshew; Wendy N Cooper; Patrick J McKiernan; Leo W J Klomp; Andrew A M Morris; James Wraith; Patricia McClean; Sally A Lynch; Richard John Thompson; Bryan Lo; Oliver W Quarrell; Maja Di Rocco; Richard C Trembath; Hanna Mandel; S Wali; Fiona E Karet; Alex S Knisely; Roderick H J Houwen; Deirdre A Kelly; Eamonn R Maher
Mutations in VPS33B, encoding a regulator of SNARE-dependent membrane fusion, cause arthrogryposis-renal dysfunction-cholestasis (ARC) syndrome.
Nature genetics 2004;36(4):400-4.
2004: François Jouret; Takashi Igarashi; Francoise Gofflot; Patricia D Wilson; Fiona E Karet; Rajesh V Thakker; Olivier Devuyst
Comparative ontogeny, processing, and segmental distribution of the renal chloride channel, ClC-5.
Kidney international 2004;65(1):198-208.
2003: Paul A Stehberger; Nicole Schulz; Karin E Finberg; Fiona E Karet; Gerhard Giebisch; Richard P Lifton; John Peter Geibel; Carsten A Wagner
Localization and regulation of the ATP6V0A4 (a4) vacuolar H+-ATPase subunit defective in an inherited form of distal renal tubular acidosis.
Journal of the American Society of Nephrology : JASN 2003;14(12):3027-38.
2003: Annabel N Smith; Ruth C Lovering; Masamitsu Futai; Jun Takeda; Dennis Brown; Fiona E Karet
Revised nomenclature for mammalian vacuolar-type H+ -ATPase subunit genes.
Molecular cell 2003;12(4):801-3.
2003: Ya Su; Aiwu Zhou; Rafia S Al-Lamki; Fiona E Karet
The a-subunit of the V-type H+-ATPase interacts with phosphofructokinase-1 in humans.
The Journal of biological chemistry 2003;278(22):20013-8.
2003: Katherine Borthwick; Nurgun Kandemir; R Topaloglu; Uwe Kornak; A Bakkaloglu; Nursen Yordam; S Ozen; H Mocan; G N Shah; W S Sly; Fiona E Karet
A phenocopy of CAII deficiency: a novel genetic explanation for inherited infantile osteopetrosis with distal renal tubular acidosis.
Journal of medical genetics 2003;40(2):115-21.
2003: Mark A J Devonald; Annabel N Smith; Jenny P Poon; Gudrun Ihrke; Fiona E Karet
Non-polarized targeting of AE1 causes autosomal dominant distal renal tubular acidosis.
Nature genetics 2003;33(2):125-7.
2002: Fiona E Karet
Monogenic tubular salt and acid transporter disorders.
Journal of nephrology 2002;15 Suppl 6():S57-68.
2002: Annabel N Smith; Katherine Borthwick; Fiona E Karet
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.
Gene 2002;297(1-2):169-77.
2002: Katherine Borthwick; Fiona E Karet
Inherited disorders of the H+-ATPase.
Current opinion in nephrology and hypertension 2002;11(5):563-8.
2002: Mark A J Devonald; Fiona E Karet
Targeting the renin-angiotensin system in patients with renal disease.
Journal of the Royal Society of Medicine 2002;95(8):391-7.
2002: Fiona E Karet
Inherited distal renal tubular acidosis.
Journal of the American Society of Nephrology : JASN 2002;13(8):2178-84.
2001: Annabel N Smith; Karin E Finberg; Carsten A Wagner; Richard P Lifton; Mark A J Devonald; Ya Su; Fiona E Karet
Molecular cloning and characterization of Atp6n1b: a novel fourth murine vacuolar H+-ATPase a-subunit gene.
The Journal of biological chemistry 2001;276(45):42382-8.
2000: Annabel N Smith; J Skaug; Keith Choate; AHMET NAYIR; A Bakkaloglu; S Ozen; SA Hulton; Sami A Sanjad; EA al-Sabban; Richard P Lifton; S W Scherer; Fiona E Karet
Mutations in ATP6N1B, encoding a new kidney vacuolar proton pump 116-kD subunit, cause recessive distal renal tubular acidosis with preserved hearing.
Nature genetics 2000;26(1):71-5.
2000: Fiona E Karet
Inherited renal tubular acidosis.
Advances in nephrology from the Necker Hospital 2000;30():147-62.
1999: Fiona E Karet; Karin E Finberg; AHMET NAYIR; A Bakkaloglu; S Ozen; SA Hulton; Sami A Sanjad; EA al-Sabban; J F Medina; Richard P Lifton
Localization of a gene for autosomal recessive distal renal tubular acidosis with normal hearing (rdRTA2) to 7q33-34.
American journal of human genetics 1999;65(6):1656-65.
1999: Fiona E Karet; Karin E Finberg; R D Nelson; AHMET NAYIR; H Mocan; Sami A Sanjad; Juan Rodriguez Soriano; F Santos; C W Cremers; A Di Pietro; B I Hoffbrand; J Winiarski; A Bakkaloglu; S Ozen; R Dusunsel; P Goodyer; SA Hulton; D K Wu; A B Skvorak; C C Morton; M J Cunningham; V Jha; Richard P Lifton
Mutations in the gene encoding B1 subunit of H+-ATPase cause renal tubular acidosis with sensorineural deafness.
Nature genetics 1999;21(1):84-90.
1998: Fiona E Karet; F J Gainza; A Z Györy; Robert J Unwin; Oliver Wrong; Michael Tanner; AHMET NAYIR; H Alpay; F Santos; SA Hulton; A Bakkaloglu; S Ozen; M J Cunningham; A di Pietro; W G Walker; Richard P Lifton
Mutations in the chloride-bicarbonate exchanger gene AE1 cause autosomal dominant but not autosomal recessive distal renal tubular acidosis.
Proceedings of the National Academy of Sciences of the United States of America 1998;95(11):6337-42.
1997: Fiona E Karet; R P Lifton
Lipoprotein glomerulopathy: a new role for apolipoprotein E?
Journal of the American Society of Nephrology : JASN 1997;8(5):840-2.
1997: Fiona E Karet; Richard P Lifton
Mutations contributing to human blood pressure variation.
Recent progress in hormone research 1997;52():263-76; discussion 276-7.
1996: Fiona E Karet; Anthony P Davenport
Selective downregulation of ETA receptor mRNA in renal transplant recipients on cyclosporin A revealed by quantitative RT-PCR.
Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association 1996;11(10):1976-82.
1996: DB Simon; Fiona E Karet; Juan Rodriguez Soriano; J H Hamdan; A DiPietro; Howard Trachtman; Sami A Sanjad; R P Lifton
Genetic heterogeneity of Bartter's syndrome revealed by mutations in the K+ channel, ROMK.
Nature genetics 1996;14(2):152-6.
1996: Fiona E Karet
Endothelin peptides and receptors in human kidney.
Clinical science (London, England : 1979) 1996;91(3):267-73.
1996: DB Simon; Fiona E Karet; J M Hamdan; A DiPietro; Sami A Sanjad; R P Lifton
Bartter's syndrome, hypokalaemic alkalosis with hypercalciuria, is caused by mutations in the Na-K-2Cl cotransporter NKCC2.
Nature genetics 1996;13(2):183-8.
1996: Fiona E Karet; Anthony P Davenport
Localization of endothelin peptides in human kidney.
Kidney international 1996;49(2):382-7.
1996: DB Simon; C Nelson-Williams; M J Bia; David H Ellison; Fiona E Karet; A M Molina; I Vaara; F Iwata; H M Cushner; M Koolen; F J Gainza; H J Gitleman; R P Lifton
Gitelman's variant of Bartter's syndrome, inherited hypokalaemic alkalosis, is caused by mutations in the thiazide-sensitive Na-Cl cotransporter.
Nature genetics 1996;12(1):24-30.
1995: Rhoda E Kuc; Fiona E Karet; Anthony P Davenport
Characterization of peptide and nonpeptide antagonists in human kidney.
Journal of cardiovascular pharmacology 1995;26 Suppl 3():S373-5.
1995: Fiona E Karet; Anthony P Davenport
Comparative quantification of endothelin receptor mRNA in human kidney: new tools for direct investigation of human tissue.
Journal of cardiovascular pharmacology 1995;26 Suppl 3():S268-71.
1994: Anthony P Davenport; Rhoda E Kuc; S L Hoskins; Fiona E Karet; F Fitzgerald
[125I]-PD151242: a selective ligand for endothelin ETA receptors in human kidney which localizes to renal vasculature.
British journal of pharmacology 1994;113(4):1303-10.
1994: Fiona E Karet; J E Dickerson; J Brown; Morris J Brown
Bovril and moclobemide: a novel therapeutic strategy for central autonomic failure.
Lancet 1994;344(8932):1263-5.
1994: Fiona E Karet; D Stephen Charnock-Jones; M L Harrison-Woolrych; G O'Reilly; Anthony P Davenport; Stephen K Smith
Quantification of mRNA in human tissue using fluorescent nested reverse-transcriptase polymerase chain reaction.
Analytical biochemistry 1994;220(2):384-90.
1994: Fiona E Karet; Morris J Brown
Phaeochromocytoma: diagnosis and management.
Postgraduate medical journal 1994;70(823):326-8.
1993: Fiona E Karet; Rhoda E Kuc; Anthony P Davenport
Novel ligands BQ123 and BQ3020 characterize endothelin receptor subtypes ETA and ETB in human kidney.
Kidney international 1993;44(1):36-42.
1993: Fiona E Karet; Anthony P Davenport
Human kidney: endothelin isoforms detected by HPLC with radioimmunoassay and receptor subtypes detected using ligands BQ123 and BQ3020.
Journal of cardiovascular pharmacology 1993;22 Suppl 8():S29-33.