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

Scientific reports, 2017-01, Vol.7 (1), p.39701-39701, Article 39701

2017

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Excretory-secretory products from the brown stomach worm, Teladorsagia circumcincta, exert antimicrobial activity in in vitro growth assays

Parasites & vectors, 2022-10, Vol.15 (1), p.1-354, Article 354

2022

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HYDROchlorothiazide versus placebo to PROTECT polycystic kidney disease patients and improve their quality of life: study protocol and rationale for the HYDRO-PROTECT randomized controlled trial

Trials, 2024-02, Vol.25 (1), p.120-120, Article 120

2024

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

PloS one, 2010-03, Vol.5 (3), p.e9531

2010

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Size-Exclusion Chromatography Separation Reveals That Vesicular and Non-Vesicular Small RNA Profiles Differ in Cell Free Urine

International journal of molecular sciences, 2021-05, Vol.22 (9), p.4881

2021

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

Disease models & mechanisms, 2013-03, Vol.6 (2), p.434-442

2013

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

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

1996

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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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Cellular physiology of the renal H+ATPase

Current opinion in nephrology and hypertension, 2009-09, Vol.18 (5), p.433-438

2009

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Clinical utility of PKD2 mutation testing in a polycystic kidney disease cohort attending a specialist nephrology out-patient clinic

BMC nephrology, 2012-08, Vol.13 (1), p.79-79, Article 79

2012

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

Kidney international, 2004-01, Vol.65 (1), p.198-208

2004

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A role for VAX2 in correct retinal function revealed by a novel genomic deletion at 2p13.3 causing distal Renal Tubular Acidosis: case report

BMC medical genetics, 2015-06, Vol.16 (1), p.38-38, Article 38

2015

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Inherited disorders of the H+-ATPase

Current opinion in nephrology and hypertension, 2002-09, Vol.11 (5), p.563-568

2002

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Importance of early audiologic assessment in distal renal tubular acidosis

International medical case reports journal, 2011-01, Vol.4 (default), p.7-11

2011

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

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

Journal of cardiovascular pharmacology, 1995, Vol.26 Suppl 3, p.S268-271

1995

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Genetic heterogeneity of Barter'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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Characterization of Peptide and Nonpeptide Antagonists in Human Kidney

Journal of cardiovascular pharmacology, 1995, Vol.26 Suppl 3, p.S373-375

1995

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Localization of endothelin peptides in human kidney

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

1996

Volltextzugriff (PDF)

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

Journal of cardiovascular pharmacology, 1995, Vol.26 Suppl 3, p.S268-271

1995

Volltextzugriff (PDF)

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

Nature genetics, 1996-01, Vol.12 (1), p.24-30

1996

Volltextzugriff (PDF)

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

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

1995

Volltextzugriff (PDF)

Importance of early audiologic assessment in distal renal tubular acidosis

International medical case reports journal, 2011, Vol.4, p.7-11

2011

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

Excretory-secretory products from the brown stomach worm, Teladorsagia circumcincta, exert antimicrobial activity in in vitro growth assays

HYDROchlorothiazide versus placebo to PROTECT polycystic kidney disease patients and improve their quality of life: study protocol and rationale for the HYDRO-PROTECT randomized controlled trial

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

Size-Exclusion Chromatography Separation Reveals That Vesicular and Non-Vesicular Small RNA Profiles Differ in Cell Free Urine

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

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

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

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

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

Cellular physiology of the renal H+ATPase

Clinical utility of PKD2 mutation testing in a polycystic kidney disease cohort attending a specialist nephrology out-patient clinic

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

A role for VAX2 in correct retinal function revealed by a novel genomic deletion at 2p13.3 causing distal Renal Tubular Acidosis: case report

Inherited disorders of the H+-ATPase

Importance of early audiologic assessment in distal renal tubular acidosis

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

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

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

Characterization of Peptide and Nonpeptide Antagonists in Human Kidney

Localization of endothelin peptides in human kidney

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

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

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

Importance of early audiologic assessment in distal renal tubular acidosis

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