Nikol Voutsina
Exeter, ENG EX25DW, United Kingdom
Last Updated: 09/26/2026
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Found 10 publications
Membrane curvature elastic stress triggers recruitment of PML-II onto the inner nuclear membrane.
Journal: Molecular biology of the cell
Published: December 10, 2025
Challenges in Genomic Variant Interpretation Within Pakistani Populations due to Genomic Healthcare Inequalities.
Journal: American journal of medical genetics. Part A
Published: January 30, 2025
Expanding the genetic spectrum of hereditary motor sensory neuropathies in Pakistan.
Journal: BMC neurology
Published: December 13, 2023
TECPR2-related hereditary sensory and autonomic neuropathy in two siblings from Palestine.
Journal: American journal of medical genetics. Part A
Published: October 11, 2023
TMEM63C mutations cause mitochondrial morphology defects and underlie hereditary spastic paraplegia.
TMEM63C mutations cause mitochondrial morphology defects and underlie hereditary spastic paraplegia.
Journal: Brain : a journal of neurology
Published: July 07, 2021
Datasets of whole cell and mitochondrial oxysterols derived from THP-1, SH-SY5Y and human peripheral blood mononuclear cells using targeted metabolomics.
Journal: Data in brief
Published: June 04, 2020
Dominant mitochondrial membrane protein-associated neurodegeneration (MPAN) variants cluster within a specific C19orf12 isoform.
Journal: Parkinsonism & related disorders
Published: May 26, 2020
A quantitative LC-MS/MS method for analysis of mitochondrial -specific oxysterol metabolism.
Journal: Redox biology
Published: April 11, 2020
Showing 1-10 of 10
Last Updated: 09/26/2026