Mukhran Khundadze
Jena, TH, Germany
Last Updated: 09/26/2026
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Found 14 publications
Metabolic acidosis causes a Fanconi-like syndrome with intracellular trafficking defects and proximal tubule dysfunction.
Journal: Science translational medicine
Published: February 11, 2026
REEP1 Accumulation Disrupts ER Integrity and Drives Spinal Motoneuron Degeneration in Distal Hereditary Motor Neuropathy.
Journal: Advanced science (Weinheim, Baden-Wurttemberg, Germany)
Published: June 23, 2025
Microglia and CD8+ T cell activation precede neuronal loss in a murine model of spastic paraplegia 15.
Journal: The Journal of experimental medicine
Published: December 21, 2023
Neuroinflammatory disease signatures in SPG11-related hereditary spastic paraplegia patients.
Journal: Acta neuropathologica
Published: October 25, 2023
RTN2 deficiency results in an autosomal recessive distal motor neuropathy with lower limb spasticity.
Journal: Brain : a journal of neurology
Published: August 30, 2023
SPG15 protein deficits are at the crossroads between lysosomal abnormalities, altered lipid metabolism and synaptic dysfunction.
Journal: Human molecular genetics
Published: January 09, 2022
Guidelines for the use and interpretation of assays for monitoring autophagy (4th edition)1.
Journal: Autophagy
Published: February 26, 2021
A mouse model for SPG48 reveals a block of autophagic flux upon disruption of adaptor protein complex five.
Journal: Neurobiology of disease
Published: January 09, 2019
The spectrum of KIAA0196 variants, and characterization of a murine knockout: implications for the mutational mechanism in hereditary spastic paraplegia type SPG8.
Journal: Orphanet journal of rare diseases
Published: July 03, 2015
Thalamic afferents influence cortical progenitors via ephrin A5-EphA4 interactions.
Journal: Development (Cambridge, England)
Published: December 07, 2014
Last Updated: 09/26/2026