Related references
Note: Only part of the references are listed.A Mitochondrial Polymorphism Alters Immune Cell Metabolism and Protects Mice from Skin Inflammation
Paul Schilf et al.
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES (2021)
Galectin-7 downregulation in lesional keratinocytes contributes to enhanced IL-17A signaling and skin pathology in psoriasis
Hung-Lin Chen et al.
JOURNAL OF CLINICAL INVESTIGATION (2021)
ETF dehydrogenase advances in molecular genetics and impact on treatment
Sara Missaglia et al.
CRITICAL REVIEWS IN BIOCHEMISTRY AND MOLECULAR BIOLOGY (2021)
Emerging views of mitophagy in immunity and autoimmune diseases
Ye Xu et al.
AUTOPHAGY (2020)
Bi-allelic Variants in TKFC Encoding Triokinase/FMN Cyclase Are Associated with Cataracts and Multisystem Disease
Saskia B. Wortmann et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2020)
A Variant of SLC1A5 Is a Mitochondrial Glutamine Transporter for Metabolic Reprogramming in Cancer Cells
Hee Chan Yoo et al.
CELL METABOLISM (2020)
Skin damage in a patient with lipid storage myopathy with a novel ETFDH mutation responsive to riboflavin
Hongliang Xu et al.
INTERNATIONAL JOURNAL OF NEUROSCIENCE (2020)
A pneumonia outbreak associated with a new coronavirus of probable bat origin
Peng Zhou et al.
NATURE (2020)
Spondyloepimetaphyseal dysplasia with elevated plasma lysosomal enzymes caused by homozygous variant in MBTPS1
Daniel R. Carvalho et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART A (2020)
Cytosolic Events in the Biogenesis of Mitochondrial Proteins
Yury S. Bykov et al.
TRENDS IN BIOCHEMICAL SCIENCES (2020)
Angiotensin-converting enzyme 2 (ACE2),SARS-CoV-2 and the pathophysiology of coronavirus disease 2019 (COVID-19)
Arno R. Bourgonje et al.
JOURNAL OF PATHOLOGY (2020)
Mutations in SREBF1, Encoding Sterol Regulatory Element Binding Transcription Factor 1, Cause Autosomal-Dominant IFAP Syndrome
Huijun Wang et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2020)
Calcinosis Biomarkers in Adult and Juvenile Dermatomyositis
Melody P. Chung et al.
AUTOIMMUNITY REVIEWS (2020)
Mitochondrial electron transport chain: Oxidative phosphorylation, oxidant production, and methods of measurement
Deirdre Nolfi-Donegan et al.
REDOX BIOLOGY (2020)
Patient with an autosomal-recessiveMBTPS1-linked phenotype and clinical features ofSilver-Russellsyndrome
Robert Meyer et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART A (2020)
Disorders of riboflavin metabolism
Shanti Balasubramaniam et al.
JOURNAL OF INHERITED METABOLIC DISEASE (2019)
Loss of MPC1 reprograms retinal metabolism to impair visual function
Allison Grenell et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2019)
A mutation in Site-1 Protease is associated with a complex phenotype that includes episodic hyperCKemia and focal myoedema
George G. Schweitzer et al.
MOLECULAR GENETICS & GENOMIC MEDICINE (2019)
A novel CHCHD10 mutation implicates a Mia40-dependent mitochondrial import deficit in ALS
Carina Lehmer et al.
EMBO MOLECULAR MEDICINE (2018)
OXA1L mutations cause mitochondrial encephalopathy and a combined oxidative phosphorylation defect
Kyle Thompson et al.
EMBO MOLECULAR MEDICINE (2018)
Site-1 protease deficiency causes human skeletal dysplasia due to defective inter-organelle protein trafficking
Yuji Kondo et al.
JCI INSIGHT (2018)
Clinical, pathological and functional characterization of riboflavin-responsive neuropathy
Andreea Manole et al.
BRAIN (2017)
Deletion of Mbtps1 (Pcsk8, S1p, Ski-1) Gene in Osteocytes Stimulates Soleus Muscle Regeneration and Increased Size and Contractile Force with Age
Jeff P. Gorski et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2016)
A novel index of protein-protein interface propensity improves interface residue recognition
Wentao Dai et al.
BMC SYSTEMS BIOLOGY (2016)
Disease-Causing SDHAF1 Mutations Impair Transfer of Fe-S Clusters to SDHB
Nunziata Maio et al.
CELL METABOLISM (2016)
New protein-protein interactions of mitochondrial connexin 43 in mouse heart
Amanda Denuc et al.
JOURNAL OF CELLULAR AND MOLECULAR MEDICINE (2016)
Mitochondrial Protein Interaction Mapping Identifies Regulators of Respiratory Chain Function
Brendan J. Floyd et al.
MOLECULAR CELL (2016)
Molecular architecture of the active mitochondrial protein gate
Takuya Shiota et al.
SCIENCE (2015)
Quantitative Interaction Proteomics of Neurodegenerative Disease Proteins
Fabian Hosp et al.
CELL REPORTS (2015)
Human METTL20 Is a Mitochondrial Lysine Methyltransferase That Targets the β Subunit of Electron Transfer Flavoprotein (ETFβ) and Modulates Its Activity
Jedrzej Malecki et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2015)
A Protease-Independent Function for SPPL3 in NFAT Activation
Stefanie L. Makowski et al.
MOLECULAR AND CELLULAR BIOLOGY (2015)
ZDOCK server: interactive docking prediction of protein-protein complexes and symmetric multimers
Brian G. Pierce et al.
BIOINFORMATICS (2014)
The Disulfide Relay of the Intermembrane Space Oxidizes the Ribosomal Subunit Mrp10 on Its Transit into the Mitochondrial Matrix
Sebastian Longen et al.
DEVELOPMENTAL CELL (2014)
Improvement in Low-Homology Template-Based Modeling by Employing a Model Evaluation Method with Focus on Topology
Wentao Dai et al.
PLOS ONE (2014)
Mitochondrial Encephalomyopathy Due to a Novel Mutation in ACAD9
Caterina Garone et al.
JAMA NEUROLOGY (2013)
Mechanism of superoxide and hydrogen peroxide generation by human electron-transfer flavoprotein and pathological variants
Joao V. Rodrigues et al.
FREE RADICAL BIOLOGY AND MEDICINE (2012)
Molecular mechanisms of riboflavin responsiveness in patients with ETF-QO variations and multiple acyl-CoA dehydrogenation deficiency
Nanna Cornelius et al.
HUMAN MOLECULAR GENETICS (2012)
HIPPIE: Integrating Protein Interaction Networks with Experiment Based Quality Scores
Martin H. Schaefer et al.
PLOS ONE (2012)
Ichthyosis follicularis, alopecia, and photophobia (IFAP) syndrome
Hala Megarbane et al.
ORPHANET JOURNAL OF RARE DISEASES (2011)
Protease Sets Site-1 on Lysosomes
Jin Ye
SCIENCE (2011)
A Key Enzyme in the Biogenesis of Lysosomes Is a Protease That Regulates Cholesterol Metabolism
Katrin Marschner et al.
SCIENCE (2011)
Riboflavin-responsive lipid-storage myopathy caused by ETFDH gene mutations
Bing Wen et al.
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY (2010)
Role of Flavinylation in a Mild Variant of Multiple Acyl-CoA Dehydrogenation Deficiency A MOLECULAR RATIONALE FOR THE EFFECTS OF RIBOFLAVIN SUPPLEMENTATION
Barbara J. Henriques et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2009)
SDH5, a Gene Required for Flavination of Succinate Dehydrogenase, Is Mutated in Paraganglioma
Huai-Xiang Hao et al.
SCIENCE (2009)
Clinical and molecular investigations of Japanese cases of glutaric acidemia type 2
Yuka Yotsumoto et al.
MOLECULAR GENETICS AND METABOLISM (2008)
ETFDH mutations as a major cause of riboflavin-responsive multiple acyl-CoA dehydrogenation deficiency
Rikke K. J. Olsen et al.
BRAIN (2007)
The myopathic form of coenzyme Q10 deficiency is caused by mutations in the electron-transferring-flavoprotein dehydrogenase (ETFDH) gene
Klaus Gempel et al.
BRAIN (2007)
Structure of electron transfer flavoprotein-ubiquinone oxidoreductase and electron transfer to the mitochondrial ubiquinone pool
Jian Zhang et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2006)
Tissue-type plasminogen activator rescues neurones from serum deprivation-induced apoptosis through a mechanism independent of its proteolytic activity
Geraldine Liot et al.
JOURNAL OF NEUROCHEMISTRY (2006)
Improved prediction of critical residues for protein function based on network and phylogenetic analyses
B Thibert et al.
BMC BIOINFORMATICS (2005)
Acyl-CoA dehydrogenases and acyl-CoA oxidases - Structural basis for mechanistic similarities and differences
JJP Kim et al.
EUROPEAN JOURNAL OF BIOCHEMISTRY (2004)
Identification of SLC39A4, a gene involved in acrodermatitis enteropathica
S Küry et al.
NATURE GENETICS (2002)
Ichthyosis follicularis with atrichia and photophobia (IFAP) syndrome in two unrelated female patients
S Cambiaghi et al.
JOURNAL OF THE AMERICAN ACADEMY OF DERMATOLOGY (2002)
Decreased lipid synthesis in livers of mice with disrupted Site-1 protease gene
J Yang et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2001)
Ichthyosis follicularis with alopecia and photophobia in a mother and daughter
KC Sato-Matsumura et al.
BRITISH JOURNAL OF DERMATOLOGY (2000)