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Impedance-based sensor for potassium ions

Analytica chimica acta, 2018-11, Vol.1034, p.39-45

2018

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Two Novel Missense Mutations in G Protein-Coupled Receptor 54 in a Patient with Hypogonadotropic Hypogonadism

The journal of clinical endocrinology and metabolism, 2005-03, Vol.90 (3), p.1849-1855

2005

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High water vs. ad libitum water intake for autosomal dominant polycystic kidney disease: a randomized controlled feasibility trial

QJM : An International Journal of Medicine, 2020-04, Vol.113 (4), p.258-265

2020

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Urinary extracellular vesicles as a source of protein‐based biomarkers in feline chronic kidney disease and hypertension

Journal of small animal practice, 2023-01, Vol.64 (1), p.3-11

2023

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

Journal of medical genetics, 2002-11, Vol.39 (11), p.796-803

2002

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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 - PNAS, 1998-05, Vol.95 (11), p.6337-6342

1998

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

Nature genetics, 1999-01, Vol.21 (1), p.84-90

1999

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

Journal of medical genetics, 2003-02, Vol.40 (2), p.115-121

2003

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

Nature genetics, 1996-10, Vol.14 (2), p.152-156

1996

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

Nature genetics, 1996, Vol.12 (1), p.24-30

1996

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Unexpected clinical sequelae of Gitelman syndrome: hypertension in adulthood is common and females have higher potassium requirements

Nephrology, dialysis, transplantation, 2013-06, Vol.28 (6), p.1533-1542

2013

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

Nature genetics, 2004-04, Vol.36 (4), p.400-404

2004

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High water vs. ad libitum water intake for autosomal dominant polycystic kidney disease: a randomized controlled feasibility trial

QJM : An International Journal of Medicine, 2020-04, Vol.113 (4), p.306-306

2020

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Localization of a Gene for Autosomal Recessive Distal Renal Tubular Acidosis with Normal Hearing ( rdRTA2 ) to 7q33-34

American journal of human genetics, 1999-12, Vol.65 (6), p.1656-1665

1999

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

Nature genetics, 2000-09, Vol.26 (1), p.71-75

2000

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

Nature genetics, 2003-02, Vol.33 (2), p.125-127

2003

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Localization of endothelin peptides in human kidney

Kidney international, 1996-02, Vol.49 (2), p.382-387

1996

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

Nature genetics, 1996-06, Vol.13 (2), p.183-188

1996

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

Kidney international, 1995-08, Vol.48 (2), p.390-401

1995

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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, 2004-04, Vol.279 (14), p.13833-13838

2004

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Replacing the short ammonium chloride test

Kidney international, 2007-11, Vol.72 (9), p.1163-1163

2007

Volltextzugriff (PDF)

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

The Journal of biological chemistry, 2001-11, Vol.276 (45), p.42382-42388

2001

Volltextzugriff (PDF)

Endothelin peptides and receptors in human kidney

Clinical science (1979), 1996-09, Vol.91 (3), p.267-273

Karet, F E

1996

Volltextzugriff (PDF)

Lipoprotein glomerulopathy: a new role for apolipoprotein E?

Journal of the American Society of Nephrology, 1997-05, Vol.8 (5), p.840-842

1997

Volltextzugriff (PDF)

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

Nephrology, dialysis, transplantation, 1994, Vol.9 (5), p.465-468

1994

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Impedance-based sensor for potassium ions

Two Novel Missense Mutations in G Protein-Coupled Receptor 54 in a Patient with Hypogonadotropic Hypogonadism

High water vs. ad libitum water intake for autosomal dominant polycystic kidney disease: a randomized controlled feasibility trial

Urinary extracellular vesicles as a source of protein‐based biomarkers in feline chronic kidney disease and hypertension

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

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

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

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

Unexpected clinical sequelae of Gitelman syndrome: hypertension in adulthood is common and females have higher potassium requirements

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

High water vs. ad libitum water intake for autosomal dominant polycystic kidney disease: a randomized controlled feasibility trial

Localization of a Gene for Autosomal Recessive Distal Renal Tubular Acidosis with Normal Hearing ( rdRTA2 ) to 7q33-34

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

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

Localization of endothelin peptides in human kidney

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

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

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

Replacing the short ammonium chloride test

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

Endothelin peptides and receptors in human kidney

Lipoprotein glomerulopathy: a new role for apolipoprotein E?

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

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