| scholarly article | Q13442814 |
| P50 | author | Marni Falk | Q57158385 |
| P2093 | author name string | Z Zhang | |
| I Nissim | |||
| M Yudkoff | |||
| M M Sedensky | |||
| P G Morgan | |||
| E Daikhin | |||
| J R Rosenjack | |||
| P2860 | cites work | o-Phthaldialdehyde precolumn derivatization and reversed-phase high-performance liquid chromatography of polypeptide hydrolysates and physiological fluids | Q71071219 |
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| Mitochondrial complex I function modulates volatile anesthetic sensitivity in C. elegans. | Q36811391 | ||
| Systems analysis of energy metabolism elucidates the affected respiratory chain complex in Leigh's syndrome | Q40163676 | ||
| Mitochondrial expression and function of GAS-1 in Caenorhabditis elegans | Q43559952 | ||
| Mitochondrial electron transport is a key determinant of life span in Caenorhabditis elegans | Q43799857 | ||
| Mitochondrial disorders: a proposal for consensus diagnostic criteria in infants and children | Q44213543 | ||
| Mitochondrial complex I mutations in Caenorhabditis elegans produce cytochrome c oxidase deficiency, oxidative stress and vitamin-responsive lactic acidosis | Q44684852 | ||
| A mutation in succinate dehydrogenase cytochrome b causes oxidative stress and ageing in nematodes | Q47068796 | ||
| GAS-1: a mitochondrial protein controls sensitivity to volatile anesthetics in the nematode Caenorhabditis elegans | Q47069075 | ||
| The nutritive function of glia is regulated by signals released by neurons | Q48627683 | ||
| Diagnostic accuracy of blood lactate-to-pyruvate molar ratio in the differential diagnosis of congenital lactic acidosis. | Q54221299 | ||
| P433 | issue | 4 | |
| P921 | main subject | metabolic pathway | Q68685 |
| Caenorhabditis elegans | Q91703 | ||
| P304 | page(s) | 388-397 | |
| P577 | publication date | 2008-02-21 | |
| P1433 | published in | Molecular Genetics and Metabolism | Q6895949 |
| P1476 | title | Metabolic pathway profiling of mitochondrial respiratory chain mutants in C. elegans | |
| P478 | volume | 93 |
| Q33653914 | A Select Subset of Electron Transport Chain Genes Associated with Optic Atrophy Link Mitochondria to Axon Regeneration in Caenorhabditis elegans |
| Q43145237 | A dual role of the Wnt signaling pathway during aging in Caenorhabditis elegans |
| Q33667520 | A plasma signature of human mitochondrial disease revealed through metabolic profiling of spent media from cultured muscle cells |
| Q27312436 | A regulated response to impaired respiration slows behavioral rates and increases lifespan in Caenorhabditis elegans |
| Q33545200 | A universal nonmonotonic relationship between gene compactness and expression levels in multicellular eukaryotes |
| Q46274966 | Adaptive Evolution under Extreme Genetic Drift in Oxidatively Stressed Caenorhabditis elegans |
| Q33888328 | Applications of mass spectrometry to metabolomics and metabonomics: detection of biomarkers of aging and of age-related diseases |
| Q28708978 | Bacteria, yeast, worms, and flies: exploiting simple model organisms to investigate human mitochondrial diseases |
| Q46142843 | Cell Biology of the Mitochondrion |
| Q34364415 | Characterization of taurine as anti-obesity agent in C. elegans |
| Q34791301 | Collaboration between mitochondria and the nucleus is key to long life in Caenorhabditis elegans |
| Q41987031 | Comparative transcriptomic analysis of Bombyx mori fat body tissue following dietary restriction |
| Q41661219 | Comparison of proteomic and metabolomic profiles of mutants of the mitochondrial respiratory chain in Caenorhabditis elegans |
| Q39747691 | From the Cover: Arsenite Uncouples Mitochondrial Respiration and Induces a Warburg-like Effect in Caenorhabditis elegans |
| Q41578025 | Genome-wide RNAi Screen for Fat Regulatory Genes in C. elegans Identifies a Proteostasis-AMPK Axis Critical for Starvation Survival |
| Q34743627 | Genome-wide analysis of primary CD4+ and CD8+ T cell transcriptomes shows evidence for a network of enriched pathways associated with HIV disease |
| Q37526768 | Glutathione S-transferase mediates an ageing response to mitochondrial dysfunction |
| Q37626877 | In vivo metabolic flux profiling with stable isotopes discriminates sites and quantifies effects of mitochondrial dysfunction in C. elegans. |
| Q34405677 | In vivo quantification reveals extensive natural variation in mitochondrial form and function in Caenorhabditis briggsae |
| Q35924054 | Inhibiting cytosolic translation and autophagy improves health in mitochondrial disease. |
| Q33617779 | Integrated transcriptome analysis across mitochondrial disease etiologies and tissues improves understanding of common cellular adaptations to respiratory chain dysfunction |
| Q30834218 | Integrative analysis of independent transcriptome data for rare diseases |
| Q34352864 | Long-lived mitochondrial (Mit) mutants of Caenorhabditis elegans utilize a novel metabolism |
| Q41840468 | Metabolic flexibility of mitochondrial respiratory chain disorders predicted by computer modelling |
| Q33796289 | Mitochondrial DNA variant in COX1 subunit significantly alters energy metabolism of geographically divergent wild isolates in Caenorhabditis elegans |
| Q35672641 | Mitochondrial Morphology and Fundamental Parameters of the Mitochondrial Respiratory Chain Are Altered in Caenorhabditis elegans Strains Deficient in Mitochondrial Dynamics and Homeostasis Processes |
| Q33721238 | Mitochondrial dysfunction confers resistance to multiple drugs in Caenorhabditis elegans |
| Q28830026 | Mitochondrial dysfunction remodels one-carbon metabolism in human cells |
| Q89106395 | Mitochondrial medicine in the omics era |
| Q37266318 | Mitochondrial respiratory chain disease discrimination by retrospective cohort analysis of blood metabolites |
| Q30539297 | Mitochondrial respiratory chain dysfunction variably increases oxidant stress in Caenorhabditis elegans. |
| Q36763341 | Molecular profiling of mitochondrial dysfunction in Caenorhabditis elegans |
| Q52360003 | N-acetylcysteine and vitamin E rescue animal longevity and cellular oxidative stress in pre-clinical models of mitochondrial complex I disease. |
| Q33791348 | Natural variation in life history and aging phenotypes is associated with mitochondrial DNA deletion frequency in Caenorhabditis briggsae |
| Q37784963 | Neurodevelopmental manifestations of mitochondrial disease. |
| Q34037654 | Novel interactions between mitochondrial superoxide dismutases and the electron transport chain |
| Q47988632 | Nutritional Interventions for Mitochondrial OXPHOS Deficiencies: Mechanisms and Model Systems. |
| Q38963725 | Nutritional interventions in primary mitochondrial disorders: Developing an evidence base. |
| Q39987996 | Optical reversal of halothane-induced immobility in C. elegans |
| Q39032373 | Pharmacologic targeting of sirtuin and PPAR signaling improves longevity and mitochondrial physiology in respiratory chain complex I mutant Caenorhabditis elegans. |
| Q33330854 | Primary coenzyme Q deficiency in Pdss2 mutant mice causes isolated renal disease |
| Q28534824 | Primary respiratory chain disease causes tissue-specific dysregulation of the global transcriptome and nutrient-sensing signaling network |
| Q36088905 | Probucol ameliorates renal and metabolic sequelae of primary CoQ deficiency in Pdss2 mutant mice |
| Q93185763 | Profiling of remote skeletal muscle gene changes resulting from stimulation of atopic dermatitis disease in NC/Nga mouse model |
| Q34430855 | Profiling the anaerobic response of C. elegans using GC-MS |
| Q46257387 | Propionyl-CoA carboxylase pcca-1 and pccb-1 gene deletions in Caenorhabditis elegans globally impair mitochondrial energy metabolism |
| Q27333486 | Protective coupling of mitochondrial function and protein synthesis via the eIF2α kinase GCN-2 |
| Q42603351 | Quality improvement of mitochondrial respiratory chain complex enzyme assays using Caenorhabditis elegans |
| Q34986923 | RNAi screens to identify components of gene networks that modulate aging in Caenorhabditis elegans |
| Q34966704 | Regulation of life span by mitochondrial respiration: the HIF-1 and ROS connection |
| Q33531334 | Regulation of metabolism in Caenorhabditis elegans longevity |
| Q38018051 | Research on plants for the understanding of diseases of nuclear and mitochondrial origin |
| Q33690581 | SLR-2 and JMJC-1 regulate an evolutionarily conserved stress-response network |
| Q35396081 | Stable isotopic profiling of intermediary metabolic flux in developing and adult stage Caenorhabditis elegans |
| Q30872225 | Subcomplex Ilambda specifically controls integrated mitochondrial functions in Caenorhabditis elegans. |
| Q27333680 | Succinate dehydrogenase upregulation destabilize complex I and limits the lifespan of gas-1 mutant |
| Q55080516 | The UBR-1 ubiquitin ligase regulates glutamate metabolism to generate coordinated motor pattern in Caenorhabditis elegans. |
| Q47415130 | The high-production volume fungicide pyraclostrobin induces triglyceride accumulation associated with mitochondrial dysfunction, and promotes adipocyte differentiation independent of PPARγ activation, in 3T3-L1 cells. |
| Q33945482 | The homeobox protein CEH-23 mediates prolonged longevity in response to impaired mitochondrial electron transport chain in C. elegans |
| Q34413560 | The paradox of mitochondrial dysfunction and extended longevity |
| Q40988793 | Transcription factors CEP-1/p53 and CEH-23 collaborate with AAK-2/AMPK to modulate longevity in Caenorhabditis elegans |
| Q46387198 | Uncoupling of oxidative stress resistance and lifespan in long-lived isp-1 mitochondrial mutants in Caenorhabditis elegans |
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