Valentina Strecker

发表

Phenotypic spectrum of eleven patients and five novel MTFMT mutations identified by exome sequencing and candidate gene screening.

T. Wieland, T. Meitinger, T. Strom, 2014, Molecular genetics and metabolism.

Exome sequencing identifies ACAD9 mutations as a cause of complex I deficiency

Thomas Meitinger, Joanna Poulton, Hans-Werner Mewes, 2010, Nature Genetics.

Respiratory Chain Complexes in Dynamic Mitochondria Display a Patchy Distribution in Life Cells

Jürgen Bereiter-Hahn, Ilka Wittig, Valentina Strecker, 2010, PloS one.

Cytochrome P450 enzymes but not NADPH oxidases are the source of the NADPH‐dependent lucigenin chemiluminescence in membrane assays

R. Brandes, N. Weissmann, Nina Kurrle, 2017, Free radical biology & medicine.

Molecular diagnosis in mitochondrial complex I deficiency using exome sequencing

T. Wieland, T. Meitinger, T. Strom, 2012, Journal of Medical Genetics.

MTO1-Deficient Mouse Model Mirrors the Human Phenotype Showing Complex I Defect and Cardiomyopathy

H. Fuchs, A. Walch, M. Aichler, 2014, PloS one.

Large pore gels to separate mega protein complexes larger than 10 MDa by blue native electrophoresis: Isolation of putative respiratory strings or patches

H. Schägger, I. Wittig, Valentina Strecker, 2010, Proteomics.

Quantification of protein complexes by blue native electrophoresis.

I. Wittig, Valentina Strecker, J. Heidler, 2013, Methods in molecular biology.

Cellular responses to egg-oil (charismon©).

J. Bereiter-Hahn, A. Bernd, S. Kippenberger, 2014, Acta medica.

Clinical, biochemical and genetic spectrum of 70 patients with ACAD9 deficiency

T. Wieland, A. Munnich, H. Smeets, 2018 .

Homozygous missense mutation in BOLA3 causes multiple mitochondrial dysfunctions syndrome in two siblings

T. Meitinger, T. Strom, H. Prokisch, 2013, Journal of Inherited Metabolic Disease.

Mutant desmin substantially perturbs mitochondrial morphology, function and maintenance in skeletal muscle tissue

R. Kley, W. Kunz, I. Wittig, 2016, Acta Neuropathologica.

Supercomplex-associated Cox26 protein binds to cytochrome c oxidase.

C. Cruciat, K. Pfeiffer, R. Stuart, 2016, Biochimica et biophysica acta.

Mic13 Is Essential for Formation of Crista Junctions in Mammalian Cells

A. Reichert, I. Wittig, Ruchika Anand, 2016, PloS one.

Aging of different avian cultured cells: Lack of ROS-induced damage and quality control mechanisms

J. Bereiter-Hahn, A. Bürkle, M. Jendrach, 2010, Mechanisms of Ageing and Development.

Mutational Analysis of the QRRQ Motif in the Yeast Hig1 Type 2 Protein Rcf1 Reveals a Regulatory Role for the Cytochrome c Oxidase Complex*

R. Stuart, I. Wittig, Valentina Strecker, 2017, The Journal of Biological Chemistry.

Determination of protein mobility in mitochondrial membranes of living cells.

J. Bereiter-Hahn, I. Wittig, K. Busch, 2010, Biochimica et biophysica acta.

Biallelic Mutations in TMEM126B Cause Severe Complex I Deficiency with a Variable Clinical Phenotype

Katrien Stouffs, Melanie Bahlo, Holger Prokisch, 2016, American journal of human genetics.

Clinical, biochemical and genetic spectrum of 70 patients with ACAD9 deficiency: is riboflavin supplementation effective?

Robert W. Taylor, T. Wieland, A. Munnich, 2018, Orphanet Journal of Rare Diseases.

Coi1 is a novel assembly factor of the yeast complex III–complex IV supercomplex

I. Wittig, J. Herrmann, D. Rapaport, 2017, Molecular biology of the cell.

Large pore gels to separate mega protein complexes larger than 10 MDa by blue native electrophoresis: Isolation of putative respiratory strings or patches

H. Schägger, I. Wittig, Valentina Strecker, 2010, Proteomics.

Phenotypic spectrum of eleven patients and five novel MTFMT mutations identified by exome sequencing and candidate gene screening.

T. Wieland, T. Meitinger, T. Strom, 2014, Molecular genetics and metabolism.