Christina W. Sterner

Regensburg, BY, Germany

Last Updated: 09/26/2026

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Found 13 publications

A missense mutation in Ehd1 associated with defective spermatogenesis and male infertility.

A missense mutation in Ehd1 associated with defective spermatogenesis and male infertility.

Journal: Frontiers in cell and developmental biology

Published: June 16, 2023

A Founder Mutation in EHD1 Presents with Tubular Proteinuria and Deafness.

A Founder Mutation in EHD1 Presents with Tubular Proteinuria and Deafness.

Journal: Journal of the American Society of Nephrology : JASN

Published: October 06, 2021

Validation of the Rainbow Model of Integrated Care Measurement Tools (RMIC-MTs) in renal care for patient and care providers.

Validation of the Rainbow Model of Integrated Care Measurement Tools (RMIC-MTs) in renal care for patient and care providers.

Journal: PloS one

Published: January 11, 2019

Glycine Amidinotransferase (GATM), Renal Fanconi Syndrome, and Kidney Failure.

Glycine Amidinotransferase (GATM), Renal Fanconi Syndrome, and Kidney Failure.

Journal: Journal of the American Society of Nephrology : JASN

Published: November 13, 2017

Person-Centered Integrated Care for Chronic Kidney Disease: A Systematic Review and Meta-Analysis of Randomized Controlled Trials.

Person-Centered Integrated Care for Chronic Kidney Disease: A Systematic Review and Meta-Analysis of Randomized Controlled Trials.

Journal: Clinical journal of the American Society of Nephrology : CJASN

Published: September 13, 2017

Sex-dependent differences in the in vivo respiratory phenotype of the TASK-1 potassium channel knockout mouse.

Sex-dependent differences in the in vivo respiratory phenotype of the TASK-1 potassium channel knockout mouse.

Journal: Respiratory physiology & neurobiology

Published: May 28, 2016

Pathogenesis of Adrenal Aldosterone-Producing Adenomas Carrying Mutations of the Na(+)/K(+)-ATPase.

Pathogenesis of Adrenal Aldosterone-Producing Adenomas Carrying Mutations of the Na(+)/K(+)-ATPase.

Journal: Endocrinology

Published: September 30, 2015

Diastrophic dysplasia sulfate transporter (SLC26A2) is expressed in the adrenal cortex and regulates aldosterone secretion.

Diastrophic dysplasia sulfate transporter (SLC26A2) is expressed in the adrenal cortex and regulates aldosterone secretion.

Journal: Hypertension (Dallas, Tex. : 1979)

Published: March 05, 2014

Pharmacology and pathophysiology of mutated KCNJ5 found in adrenal aldosterone-producing adenomas.

Pharmacology and pathophysiology of mutated KCNJ5 found in adrenal aldosterone-producing adenomas.

Journal: Endocrinology

Published: February 11, 2014

Mistargeting of peroxisomal EHHADH and inherited renal Fanconi's syndrome.

Mistargeting of peroxisomal EHHADH and inherited renal Fanconi's syndrome.

Journal: The New England journal of medicine

Published: January 10, 2014

a Novel Y152C KCNJ5 mutation responsible for familial hyperaldosteronism type III.

a Novel Y152C KCNJ5 mutation responsible for familial hyperaldosteronism type III.

Journal: The Journal of clinical endocrinology and metabolism

Published: September 17, 2013

Dynamics of renal electrolyte excretion in growing mice.

Dynamics of renal electrolyte excretion in growing mice.

Journal: Nephron. Physiology

Published: September 17, 2013

Showing 1-12 of 13

Last Updated: 09/26/2026