Taru Hilander
Helsinki, 00014, Finland
Last Updated: 09/26/2026
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Found 11 publications
GTPBP8 is required for mitoribosomal biogenesis and mitochondrial translation.
Journal: Cellular and molecular life sciences : CMLS
Published: July 05, 2023
The roles of assembly factors in mammalian mitoribosome biogenesis.
Journal: Mitochondrion
Published: May 13, 2021
A patient with pontocerebellar hypoplasia type 6: Novel RARS2 mutations, comparison to previously published patients and clinical distinction from PEHO syndrome.
Journal: European journal of medical genetics
Published: December 21, 2018
Analysis of Mitochondrial Protein Synthesis: De Novo Translation, Steady-State Levels, and Assembled OXPHOS Complexes.
Journal: Current protocols in toxicology
Published: August 01, 2018
Redox regulation of GRPEL2 nucleotide exchange factor for mitochondrial HSP70 chaperone.
Journal: Redox biology
Published: June 20, 2018
Instability of the mitochondrial alanyl-tRNA synthetase underlies fatal infantile-onset cardiomyopathy.
Journal: Human molecular genetics
Published: June 12, 2018
Editing activity for eliminating mischarged tRNAs is essential in mammalian mitochondria.
Journal: Nucleic acids research
Published: October 17, 2017
Exposure to arginine analog canavanine induces aberrant mitochondrial translation products, mitoribosome stalling, and instability of the mitochondrial proteome.
Journal: The international journal of biochemistry & cell biology
Published: March 16, 2015
Truncated HSPB1 causes axonal neuropathy and impairs tolerance to unfolded protein stress.
Journal: BBA clinical
Published: January 13, 2015
Selenoprotein biosynthesis defect causes progressive encephalopathy with elevated lactate.
Journal: Neurology
Published: November 17, 2014
Deficiency of the E3 ubiquitin ligase TRIM2 in early-onset axonal neuropathy.
Journal: Human molecular genetics
Published: April 09, 2013
Showing 1-11 of 11
Last Updated: 09/26/2026