Dr. L.G.J. Nijtmans

Update Persondata

• activity
• cell
• cells
• complexes
• disease
• gene
• genes
• membrane
• mutations
• protein
• transcription

Publications

(the most recent at the top)

Solute diffusion is hindered in the mitochondrial matrix

NDUFA10 mutations cause complex I deficiency in a patient with Leigh disease

Respiratory chain complex I deficiency due to NDUFA12 mutations as a new cause of Leigh syndrome

A mutation in C2orf64 causes impaired cytochrome c oxidase assembly and mitochondrial cardiomyopathy

Defective mitochondrial translation differently affects the live cell dynamics of complex I subunits

All publications..

Enhanced publications

(the most recent at the top)

Doctoral Thesis: The assembly of mitochondrial Complex I : A product of nuclear-mitochondrial synergy

Completed research projects

(the most recent research is at the top)
Researcher	Identification and characterization of novel proteins involved in the coupling of mitochondrial translation to the macromolecular assembly of human mitochondrial complex I
Co-supervisor	The assembly of Mitochondrial Complex I: A product of nuclear-mitochondrial synergy