F. Karet

发表

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

G. Ihrke, M. Devonald, Annabel N. Smith, 2003, Nature Genetics.

Mutations in Kelch-like 3 and Cullin 3 cause hypertension and electrolyte abnormalities

Jai Radhakrishnan, Murim Choi, Robert Bjornson, 2012, Nature.

A Novel Missense Mutation in AE1 Causing Autosomal Dominant Distal Renal Tubular Acidosis Retains Normal Transport Function but Is Mistargeted in Polarized Epithelial Cells*

F. Reimann, W. Bennett, M. Devonald, 2004, Journal of Biological Chemistry.

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

F. Karet, Jamie Brown, J. Brown, 1994, The Lancet.

Cellular physiology of the renal H+ATPase

F. Karet, Katherine G. Blake-Palmer, 2009, Current opinion in nephrology and hypertension.

The d subunit plays a central role in human vacuolar H+-ATPases

R. Francis, Annabel N. Smith, F. Karet, 2008, Journal of bioenergetics and biomembranes.

Disorders of Water and Acid-Base Homeostasis

F. Karet, 2010, Nephron Physiology.

Life-threatening metabolic alkalosis in Pendred syndrome

M. Evans, F. Karet, N. Kandasamy, 2011, European journal of endocrinology.

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

Alice C. N. Brown, M. Saleem, F. Karet, 2009, American journal of physiology. Renal physiology.

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

Alice C. N. Brown, Aiwu Zhou, T. Hiemstra, 2010, American journal of physiology. Renal physiology.

Salt handling and hypertension.

F. Karet, K. O'Shaughnessy, 2006 .

Co-expression of Pendrin, Vacuolar H+-ATPase α4-Subunit and Carbonic Anhydrase II in Epithelial Cells of the Murine Endolymphatic Sac

Annabel N. Smith, F. Karet, J. Greinwald, 2004, The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society.

Targeting the Renin-Angiotensin System in Patients with Renal Disease

M. Devonald, F. Karet, 2002 .

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

J. Kere, A. Blanchard, F. Karet, 2007, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

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

P. Rorsman, C. Antignac, P. Williams, 2009, Human molecular genetics.

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

A. Davenport, F. Karet, R. Kuc, 1993, Kidney international.

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

P. Wilson, F. Jouret, O. Devuyst, 2004, Kidney international.

An Extended Nomenclature for Mammalian V-ATPase Subunit Genes and Splice Variants

K. Miranda, Dennis Brown, F. Karet, 2010, PloS one.

Distal Renal Tubular Acidosis

F. Karet, 2009 .

Inherited renal acidoses.

F. Karet, A. Fry, 2007, Physiology.

A phenocopy of CAII deficiency: a novel genetic explanation for inherited infantile osteopetrosis with distal renal tubular acidosis

W. Sly, A. Bakkaloğlu, U. Kornak, 2003, Journal of medical genetics.

The endothelin system in the kidney

F. Karet, Anthony Pdavenport, 1996 .

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

F. Karet, S. Petrovic, Xuming Sun, 2006, American journal of physiology. Renal physiology.

Molecular cloning and characterization of Atp6n1b: a novel fourth murine vacuolar H+-ATPase a-subunit gene.

R. Lifton, K. Finberg, C. Wagner, 2001, The Journal of biological chemistry.

Salt handling and hypertension.

F. Karet, K. O'Shaughnessy, K. O’Shaughnessy, 2004, The Journal of clinical investigation.

Localization of endothelin peptides in human kidney.

A. Davenport, F. Karet, 1996, Kidney international.

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

A. Davenport, F. Karet, R. Kuc, 1994, British journal of pharmacology.

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

G. Giebisch, R. Lifton, K. Finberg, 2003, Journal of the American Society of Nephrology : JASN.

Selective downregulation of ETA receptor mRNA in renal transplant recipients on cyclosporin A revealed by quantitative RT-PCR

A. Davenport, F. Karet, 1996 .

Nephroloqy Dialysis Transplantation Selective downregulation of ETA receptor mRNA in renal transplant recipients on cyclosporin A revealed by quantitative RT-PCR

A. Davenport, F. Karet, 2022 .

A serum potassium level above 10 mmol/l in a patient predisposed to hypokalemia

F. Karet, D. Phillips, Kashif Ahmad, 2006, Nature Clinical Practice Nephrology.

Characterization of Peptide and Nonpeptide Antagonists in Human Kidney

A. Davenport, F. Karet, R. Kuc, 1995, Journal of cardiovascular pharmacology.

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

A. Davenport, F. Karet, 1994, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

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

Aiwu Zhou, B. Javid, F. Karet, 2008, American journal of physiology. Renal physiology.

Inherited distal renal tubular acidosis.

F. Karet, 2002, Journal of the American Society of Nephrology : JASN.

FRONTIERS IN NEPHROLOGY Inherited Distal Renal Tubular Acidosis

F. Karet, 2002 .

Mutations contributing to human blood pressure variation.

R. Lifton, F. Karet, 1997, Recent progress in hormone research.

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

Annabel N. Smith, F. Karet, Katherine G. Blake-Palmer, 2007, Gene.

The a-Subunit of the V-type H+-ATPase Interacts with Phosphofructokinase-1 in Humans*

Aiwu Zhou, F. Karet, R. Al‐Lamki, 2003, Journal of Biological Chemistry.

Polarisation, key to good localisation.

G. Hendriks, P. Deen, M. Devonald, 2006, Biochimica et biophysica acta.

Comparative Quantification of Endothelin Receptor mRNA in Human Kidney: New Tools for Direct Investigation of Human Tissue

A. Davenport, F. Karet, 1995, Journal of cardiovascular pharmacology.

V1 and V0 Domains of the Human H+-ATPase Are Linked by an Interaction between the G and a Subunits*

Annabel N. Smith, F. Karet, R. Al‐Lamki, 2007, Journal of Biological Chemistry.

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

U. Kornak, F. Jouret, O. Devuyst, 2005, Journal of the American Society of Nephrology : JASN.

Physiological and Metabolic Implications of V-ATPase Isoforms in the Kidney

F. Karet, 2005, Journal of bioenergetics and biomembranes.

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

A. Davenport, F. Karet, F. E. Karet, 1993, Journal of cardiovascular pharmacology.

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

R. Lifton, C. Nelson-Williams, D. Ellison, 1996, Nature Genetics.

Salt handling and hypertension.

F. Karet, K. O’Shaughnessy, 2004, Annual review of nutrition.

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

J Ellery, S. O’Rahilly, I. Farooqi, 2005, The Journal of clinical endocrinology and metabolism.

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

R. Lifton, S. Sanjad, H. Trachtman, 1996, Nature Genetics.

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

R. Lifton, S. Sanjad, D. Simon, 1996, Nature genetics.

Renal epithelial traffic jams and one-way streets.

M. Devonald, F. Karet, 2004, Journal of the American Society of Nephrology : JASN.

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

Richard C Trembath, Paul Gissen, Colin A. Johnson, 2004, Nature Genetics.

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.

Annabel N. Smith, F. Karet, K. Borthwick, 2002, Gene.

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

A. di Pietro, R. Lifton, A. Nayır, 1998, Proceedings of the National Academy of Sciences of the United States of America.

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

C. Cremers, C. Morton, R. Lifton, 1999, Nature Genetics.

Novel ATP6V1B1 and ATP6V0A4 mutations in autosomal recessive distal renal tubular acidosis with new evidence for hearing loss

S. Bianca, C. Morton, V. Tasic, 2002, Journal of medical genetics.

Ubiquitous and kidney-specific subunits of vacuolar H+-ATPase are differentially expressed during nephrogenesis.

P. Courtoy, H. Debaix, F. Jouret, 2005, Journal of the American Society of Nephrology : JASN.

Mutations in ATP6N1B, encoding a new kidney vacuolar proton pump 116-kD subunit, cause recessive distal renal tubular acidosis with preserved hearing

S. Scherer, R. Lifton, A. Nayır, 2000, Nature Genetics.

Inherited disorders of the H+-ATPase

F. Karet, K. Borthwick, 2002, Current opinion in nephrology and hypertension.

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

R. Lifton, K. Finberg, A. Nayır, 1999, American journal of human genetics.

Monogenic tubular salt and acid transporter disorders.

F. Karet, 2002, Journal of nephrology.

Mechanisms in hyperkalemic renal tubular acidosis.

F. Karet, 2009, Journal of the American Society of Nephrology : JASN.

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

Ruth C Lovering, R. Lovering, Dennis Brown, 2003, Molecular cell.

Lipoprotein glomerulopathy: a new role for apolipoprotein E?

R. Lifton, F. Karet, 1997, Journal of the American Society of Nephrology : JASN.

Uromodulin exclusion list improves urinary exosomal protein identification.

K. Lilley, T. Hiemstra, F. Karet, 2011, Journal of biomolecular techniques : JBT.

Replacing the short ammonium chloride test.

F. Karet, A. Norden, A. Viljoen, 2007, Kidney international.

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

R. Lifton, S. Sanjad, A. Pietro, 1996, Nature Genetics.

Two novel missense mutations in GPR54 in a subject with hypogonadotropic hypogonadism

I. Farooqi, F. Karet, S. Aparicio, 2005 .

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

G. Giebisch, R. Lifton, K. Finberg, 2003, Journal of the American Society of Nephrology : JASN.