Julia C. Hennings

Jena, TH 07747, Germany

Last Updated: 09/26/2026

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Found 21 publications

Metabolic acidosis causes a Fanconi-like syndrome with intracellular trafficking defects and proximal tubule dysfunction.

Metabolic acidosis causes a Fanconi-like syndrome with intracellular trafficking defects and proximal tubule dysfunction.

Journal: Science translational medicine
Published: February 11, 2026

Reduced Expression of Magnesium Transport Proteins in the Distal Convoluted Tubule of Clcnkb-Deficient Mice May Explain Urinary Magnesium Wasting in Classical Bartter Syndrome.

Reduced Expression of Magnesium Transport Proteins in the Distal Convoluted Tubule of Clcnkb-Deficient Mice May Explain Urinary Magnesium Wasting in Classical Bartter Syndrome.

Journal: Acta physiologica (Oxford, England)
Published: December 02, 2025

Urinary sodium wasting and disrupted collecting duct function in mice with distal renal tubular acidosis mutations.

Urinary sodium wasting and disrupted collecting duct function in mice with distal renal tubular acidosis mutations.

Journal: Disease models & mechanisms
Published: October 04, 2024

Biallelic NUDT2 variants defective in mRNA decapping cause a neurodevelopmental disease.

Biallelic NUDT2 variants defective in mRNA decapping cause a neurodevelopmental disease.

Journal: Brain : a journal of neurology
Published: July 12, 2023

Bi-allelic HPDL Variants Cause a Neurodegenerative Disease Ranging from Neonatal Encephalopathy to Adolescent-Onset Spastic Paraplegia.

Bi-allelic HPDL Variants Cause a Neurodegenerative Disease Ranging from Neonatal Encephalopathy to Adolescent-Onset Spastic Paraplegia.

Journal: American journal of human genetics
Published: May 18, 2020

Pharmacological Inhibition of Cyclin-Dependent Kinases Triggers Anti-Fibrotic Effects in Hepatic Stellate Cells In Vitro.

Pharmacological Inhibition of Cyclin-Dependent Kinases Triggers Anti-Fibrotic Effects in Hepatic Stellate Cells In Vitro.

Journal: International journal of molecular sciences
Published: April 24, 2020

GMPPA defects cause a neuromuscular disorder with α-dystroglycan hyperglycosylation.

GMPPA defects cause a neuromuscular disorder with α-dystroglycan hyperglycosylation.

Journal: The Journal of clinical investigation
Published: April 17, 2020

Intestinal dysbiosis augments liver disease progression via NLRP3 in a murine model of primary sclerosing cholangitis.

Intestinal dysbiosis augments liver disease progression via NLRP3 in a murine model of primary sclerosing cholangitis.

Journal: Gut
Published: April 23, 2018

The Na+/H+ Exchanger Nhe1 Modulates Network Excitability via GABA Release.

The Na+/H+ Exchanger Nhe1 Modulates Network Excitability via GABA Release.

Journal: Cerebral cortex (New York, N.Y. : 1991)
Published: December 22, 2017

Notch inhibition counteracts Paneth cell death in absence of caspase-8.

Notch inhibition counteracts Paneth cell death in absence of caspase-8.

Journal: Virchows Archiv : an international journal of pathology
Published: June 30, 2017

Salivary MMP-9 in the detection of oral squamous cell carcinoma.

Salivary MMP-9 in the detection of oral squamous cell carcinoma.

Journal: Medicina oral, patologia oral y cirugia bucal
Published: September 06, 2016

Intercalated Cell Depletion and Vacuolar H+-ATPase Mistargeting in an Ae1 R607H Knockin Model.

Intercalated Cell Depletion and Vacuolar H+-ATPase Mistargeting in an Ae1 R607H Knockin Model.

Journal: Journal of the American Society of Nephrology : JASN
Published: February 02, 2016
Showing 1-12 of 21

Last Updated: 09/26/2026