Valentina Strecker
Frankfurt Am Main, HE, Germany
Last Updated: 09/26/2026
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Found 14 publications
Clinical, biochemical and genetic spectrum of 70 patients with ACAD9 deficiency: is riboflavin supplementation effective?
Journal: Orphanet journal of rare diseases
Published: November 05, 2017
Coi1 is a novel assembly factor of the yeast complex III-complex IV supercomplex.
Journal: Molecular biology of the cell
Published: February 06, 2017
Mutational Analysis of the QRRQ Motif in the Yeast Hig1 Type 2 Protein Rcf1 Reveals a Regulatory Role for the Cytochrome c Oxidase Complex.
Journal: The Journal of biological chemistry
Published: September 09, 2016
Cytochrome P450 enzymes but not NADPH oxidases are the source of the NADPH-dependent lucigenin chemiluminescence in membrane assays.
Journal: Free radical biology & medicine
Published: July 14, 2016
Mic13 Is Essential for Formation of Crista Junctions in Mammalian Cells.
Journal: PloS one
Published: April 25, 2016
Biallelic Mutations in TMEM126B Cause Severe Complex I Deficiency with a Variable Clinical Phenotype.
Journal: American journal of human genetics
Published: March 04, 2016
Supercomplex-associated Cox26 protein binds to cytochrome c oxidase.
Journal: Biochimica et biophysica acta
Published: January 19, 2016
Cellular responses to egg-oil (charismon©).
Journal: Acta medica (Hradec Kralove)
Published: September 27, 2014
MTO1-deficient mouse model mirrors the human phenotype showing complex I defect and cardiomyopathy.
Journal: PloS one
Published: January 08, 2014
Phenotypic spectrum of eleven patients and five novel MTFMT mutations identified by exome sequencing and candidate gene screening.
Journal: Molecular genetics and metabolism
Published: December 18, 2013
Quantification of protein complexes by blue native electrophoresis.
Journal: Methods in molecular biology (Clifton, N.J.)
Published: September 03, 2013
Last Updated: 09/26/2026