Markus Reichold
Regensburg, BY 93053, Germany
Last Updated: 09/26/2026
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Found 11 publications
CLN7/MFSD8 may be an important factor for SARS-CoV-2 cell entry.
Journal: iScience
Published: November 04, 2021
A Founder Mutation in EHD1 Presents with Tubular Proteinuria and Deafness.
Journal: Journal of the American Society of Nephrology : JASN
Published: October 06, 2021
Distinct Mitochondrial Pathologies Caused by Mutations of the Proximal Tubular Enzymes EHHADH and GATM.
Journal: Frontiers in physiology
Published: May 27, 2021
Glycine Amidinotransferase (GATM), Renal Fanconi Syndrome, and Kidney Failure.
Journal: Journal of the American Society of Nephrology : JASN
Published: November 13, 2017
Renal Fanconi Syndrome Is Caused by a Mistargeting-Based Mitochondriopathy.
Journal: Cell reports
Published: November 03, 2014
Renal Fanconi syndrome: taking a proximal look at the nephron.
Journal: Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association
Published: September 16, 2014
Mistargeting of peroxisomal EHHADH and inherited renal Fanconi's syndrome.
Journal: The New England journal of medicine
Published: January 10, 2014
Dynamics of renal electrolyte excretion in growing mice.
Journal: Nephron. Physiology
Published: September 17, 2013
TWIK1, a unique background channel with variable ion selectivity.
Journal: Proceedings of the National Academy of Sciences of the United States of America
Published: March 21, 2012
Showing 1-11 of 11
Last Updated: 09/26/2026