| P50 | author | Johannes Graumann | Q55278397 |
| | Ulrike Topf | Q55743543 |
| | Carsten T Kuenne | Q56383974 |
| | Anna Magdalena Sokol | Q58094882 |
| | Barbara Uszczyńska-Ratajczak | Q58205446 |
| | Pia Lundegaard | Q58423862 |
| | Sreedevi Sugunan | Q59576269 |
| | Michal Bazała | Q90238532 |
| | Agnieszka Chacińska | Q21252754 |
| | Didier Stainier | Q36832398 |
| P2093 | author name string | Michelle M Collins | |
| | Stefan Guenther | |
| | Sherine S L Chan | |
| P2860 | cites work | MIA40 is an oxidoreductase that catalyzes oxidative protein folding in mitochondria | Q24324109 |
| | A novel mitochondrial matrix serine/threonine protein phosphatase regulates the mitochondria permeability transition pore and is essential for cellular survival and development | Q24674156 |
| | Control of muscle fibre-type diversity during embryonic development: the zebrafish paradigm | Q26823743 |
| | Remodeling of Mitochondrial Flashes in Muscular Development and Dystrophy in Zebrafish | Q27302888 |
| | Opa1 is required for proper mitochondrial metabolism in early development | Q27334237 |
| | Structural basis of yeast Tim40/Mia40 as an oxidative translocator in the mitochondrial intermembrane space | Q27656955 |
| | Molecular recognition and substrate mimicry drive the electron-transfer process between MIA40 and ALR | Q27667208 |
| | Mia40 is a trans-site receptor that drives protein import into the mitochondrial intermembrane space by hydrophobic substrate binding | Q27934445 |
| | Essential role of Mia40 in import and assembly of mitochondrial intermembrane space proteins | Q27936684 |
| | Oxidative folding in the mitochondrial intermembrane space: A regulated process important for cell physiology and disease | Q28076268 |
| | The Ca(2+)-Dependent Release of the Mia40-Induced MICU1-MICU2 Dimer from MCU Regulates Mitochondrial Ca(2+) Uptake | Q28118964 |
| | Analyzing real-time PCR data by the comparative C(T) method | Q28131831 |
| | A new syndrome of refractory sideroblastic anemia with vacuolization of marrow precursors and exocrine pancreatic dysfunction | Q28249352 |
| | Perinuclear, perigranular and sub-plasmalemmal mitochondria have distinct functions in the regulation of cellular calcium transport. | Q28362214 |
| | Bioenergetic profiling of zebrafish embryonic development | Q28477289 |
| | Autophagy induction is a Tor- and Tp53-independent cell survival response in a zebrafish model of disrupted ribosome biogenesis | Q28486076 |
| | Mitochondrial DNA polymerase gamma is essential for mammalian embryogenesis | Q28511104 |
| | Multi-organ abnormalities and mTORC1 activation in zebrafish model of multiple acyl-CoA dehydrogenase deficiency | Q28533885 |
| | The ProteomeXchange consortium in 2017: supporting the cultural change in proteomics public data deposition | Q28584437 |
| | 2016 update of the PRIDE database and its related tools | Q28603110 |
| | Augmenter of liver regeneration (alr) promotes liver outgrowth during zebrafish hepatogenesis | Q28732410 |
| | MaxQuant enables high peptide identification rates, individualized p.p.b.-range mass accuracies and proteome-wide protein quantification | Q29547200 |
| | Trimmomatic: a flexible trimmer for Illumina sequence data | Q29547278 |
| | Moderated estimation of fold change and dispersion for RNA-seq data with DESeq2 | Q29547403 |
| | Mitochondria: in sickness and in health | Q29614825 |
| | STAR: ultrafast universal RNA-seq aligner | Q29615052 |
| | Efficient design and assembly of custom TALEN and other TAL effector-based constructs for DNA targeting | Q29616145 |
| | Importing mitochondrial proteins: machineries and mechanisms | Q29616477 |
| | Translocation of proteins into mitochondria | Q29616478 |
| | High-resolution in situ hybridization to whole-mount zebrafish embryos | Q29617529 |
| | limma powers differential expression analyses for RNA-sequencing and microarray studies | Q29617988 |
| | The zebrafish embryo as a dynamic model of anoxia tolerance | Q30499819 |
| | Making sense of anti-sense data | Q30884297 |
| | Method for isolation of PCR-ready genomic DNA from zebrafish tissues. | Q50654450 |
| | Multiplex peptide stable isotope dimethyl labeling for quantitative proteomics. | Q51758332 |
| | Mitochondrial DNA metabolism in early development of zebrafish (Danio rerio). | Q51797736 |
| | Developmental analysis of ceruloplasmin gene and liver formation in zebrafish. | Q52135848 |
| | The disulfide relay of the intermembrane space oxidizes the ribosomal subunit mrp10 on its transit into the mitochondrial matrix. | Q53077102 |
| | Mistargeted mitochondrial proteins activate a proteostatic response in the cytosol. | Q53394237 |
| | Biochemical abnormalities in Pearson syndrome. | Q53612700 |
| | Pancreatic exocrine dysfunction associated with mitochondrial tRNA(Leu)(UUR) mutation | Q33680431 |
| | Gene and genome duplications in vertebrates: the one-to-four (-to-eight in fish) rule and the evolution of novel gene functions | Q33796382 |
| | Mitochondrial fusion is required for mtDNA stability in skeletal muscle and tolerance of mtDNA mutations | Q33877979 |
| | The mitochondrial import gene tomm22 is specifically required for hepatocyte survival and provides a liver regeneration model | Q33967786 |
| | A small molecule inhibitor of redox-regulated protein translocation into mitochondria | Q34036402 |
| | featureCounts: an efficient general purpose program for assigning sequence reads to genomic features | Q34384848 |
| | Simple methods for generating and detecting locus-specific mutations induced with TALENs in the zebrafish genome | Q34390580 |
| | Dynamic glucoregulation and mammalian-like responses to metabolic and developmental disruption in zebrafish | Q34459211 |
| | Reverse genetic screening reveals poor correlation between morpholino-induced and mutant phenotypes in zebrafish. | Q35806361 |
| | TAL Effector-Nucleotide Targeter (TALE-NT) 2.0: tools for TAL effector design and target prediction | Q36088336 |
| | Mitochondria: the next (neurode)generation | Q36124905 |
| | Oxygen deprivation causes suspended animation in the zebrafish embryo | Q36304805 |
| | In vivo evidence for cooperation of Mia40 and Erv1 in the oxidation of mitochondrial proteins. | Q36312207 |
| | Transcriptome analysis of pancreatic cells across distant species highlights novel important regulator genes | Q36317537 |
| | Zebrafish lacking functional DNA polymerase gamma survive to juvenile stage, despite rapid and sustained mitochondrial DNA depletion, altered energetics and growth | Q36337679 |
| | MitoCarta2.0: an updated inventory of mammalian mitochondrial proteins | Q36434534 |
| | Whole-organism screening for gluconeogenesis identifies activators of fasting metabolism. | Q36553321 |
| | Polarized calcium signaling in exocrine gland cells | Q36938402 |
| | The mitochondrial citrate transporter, CIC, is essential for mitochondrial homeostasis | Q37031290 |
| | Mitochondrial biogenesis, switching the sorting pathway of the intermembrane space receptor Mia40. | Q37142533 |
| | Mechanisms underlying metabolic and neural defects in zebrafish and human multiple acyl-CoA dehydrogenase deficiency (MADD). | Q37468328 |
| | UniProt: the universal protein knowledgebase | Q37556842 |
| | The clinical maze of mitochondrial neurology | Q37648911 |
| | Inhibition of the mitochondrial calcium uniporter rescues dopaminergic neurons in pink1-/- zebrafish | Q37664178 |
| | Mitochondrial diseases: a cross-talk between mitochondrial and nuclear genomes | Q37708099 |
| | Somatic mitochondrial DNA mutations in mammalian aging | Q37720726 |
| | Mitochondrial disulfide relay: redox-regulated protein import into the intermembrane space | Q37966824 |
| | Mitochondrial protein translocases for survival and wellbeing | Q38215345 |
| | Unlocking the presequence import pathway | Q38301169 |
| | Mitochondrial Proteins Containing Coiled-Coil-Helix-Coiled-Coil-Helix (CHCH) Domains in Health and Disease | Q38702029 |
| | Multi-omics analysis identifies ATF4 as a key regulator of the mitochondrial stress response in mammals | Q38752693 |
| | Mammalian Mitochondria and Aging: An Update | Q38769687 |
| | Interaction between AIF and CHCHD4 Regulates Respiratory Chain Biogenesis | Q38871524 |
| | Mitochondrial disulfide relay and its substrates: mechanisms in health and disease. | Q38932389 |
| | Mitochondrial Machineries for Protein Import and Assembly | Q39182116 |
| | Complex I deficiency and dopaminergic neuronal cell loss in parkin-deficient zebrafish (Danio rerio). | Q39979942 |
| | Active mitochondria surrounding the pancreatic acinar granule region prevent spreading of inositol trisphosphate-evoked local cytosolic Ca(2+) signals. | Q42477596 |
| | Mitochondrial protein import: Mia40 facilitates Tim22 translocation into the inner membrane of mitochondria | Q42730868 |
| | TigarB causes mitochondrial dysfunction and neuronal loss in PINK1 deficiency | Q42860533 |
| | Abnormal nuclear pore formation triggers apoptosis in the intestinal epithelium of elys-deficient zebrafish | Q42939187 |
| | Real-time imaging of mitochondria in transgenic zebrafish expressing mitochondrially targeted GFP. | Q46381659 |
| | Stable isotope labeling by amino acids in cell culture (SILAC) and proteome quantitation of mouse embryonic stem cells to a depth of 5,111 proteins | Q46876645 |
| | Processing tissue and cells for transmission electron microscopy in diagnostic pathology and research | Q46941953 |
| | Exocrine pancreas development in zebrafish | Q47073643 |
| | A zebrafish model of human Barth syndrome reveals the essential role of tafazzin in cardiac development and function | Q47073745 |
| | Developmental defects and neuromuscular alterations due to mitofusin 2 gene (MFN2) silencing in zebrafish: a new model for Charcot-Marie-Tooth type 2A neuropathy | Q47073965 |
| | Early developmental pathology due to cytochrome c oxidase deficiency is revealed by a new zebrafish model | Q47074213 |
| | Pancreas development in zebrafish: early dispersed appearance of endocrine hormone expressing cells and their convergence to form the definitive islet | Q47074218 |
| | Proteinopathies and OXPHOS dysfunction in neurodegenerative diseases | Q47372795 |
| | Transcriptomic and proteomic landscape of mitochondrial dysfunction reveals secondary coenzyme Q deficiency in mammals | Q47408311 |
| | Mitochondrial diseases: the contribution of organelle stress responses to pathology | Q47974129 |
| | The cellular retinol-binding protein genes are duplicated and differentially transcribed in the developing and adult zebrafish (Danio rerio). | Q48808962 |
| | Quantitative proteomics identifies redox switches for global translation modulation by mitochondrially produced reactive oxygen species | Q49178955 |
| P275 | copyright license | Creative Commons Attribution 4.0 International | Q20007257 |
| P6216 | copyright status | copyrighted | Q50423863 |
| P4510 | describes a project that uses | ImageJ | Q1659584 |
| | limma | Q112236343 |
| | DESeq2 | Q113018293 |
| | edgeR | Q113334690 |
| P433 | issue | 11 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | molecular biology | Q7202 |
| P304 | page(s) | e1007743 | |
| P577 | publication date | 2018-11-20 | |
| P1433 | published in | PLOS Genetics | Q1893441 |
| P1476 | title | Loss of the Mia40a oxidoreductase leads to hepato-pancreatic insufficiency in zebrafish | |
| P478 | volume | 14 | |