| scholarly article | Q13442814 |
| P8978 | DBLP publication ID | journals/bmcsb/SmithR11 |
| P6179 | Dimensions Publication ID | 1042195708 |
| P356 | DOI | 10.1186/1752-0509-5-102 |
| P953 | full work available at URL | https://bmcsystbiol.biomedcentral.com/counter/pdf/10.1186/1752-0509-5-102 |
| https://europepmc.org/articles/PMC3152903 | ||
| https://europepmc.org/articles/PMC3152903?pdf=render | ||
| P932 | PMC publication ID | 3152903 |
| P698 | PubMed publication ID | 21714867 |
| P5875 | ResearchGate publication ID | 51453458 |
| P2093 | author name string | Anthony C. Smith | |
| Alan J. Robinson | |||
| P2860 | cites work | Computational prediction of human metabolic pathways from the complete human genome | Q21092879 |
| An expanded genome-scale model of Escherichia coli K-12 (iJR904 GSM/GPR) | Q21194867 | ||
| Mutation of a nuclear succinate dehydrogenase gene results in mitochondrial respiratory chain deficiency | Q24308632 | ||
| Mutation of the fumarase gene in two siblings with progressive encephalopathy and fumarase deficiency | Q24316130 | ||
| Cytoscape: a software environment for integrated models of biomolecular interaction networks | Q24515682 | ||
| How mitochondria produce reactive oxygen species | Q24643882 | ||
| KEGG for representation and analysis of molecular networks involving diseases and drugs | Q24644514 | ||
| BRENDA, AMENDA and FRENDA the enzyme information system: new content and tools in 2009 | Q24655817 | ||
| Deficient fumarase activity in an infant with fumaricacidemia and its distribution between the different forms of the enzyme seen on isoelectric focusing | Q24676169 | ||
| Bioenergetic cost of making an adenosine triphosphate molecule in animal mitochondria | Q27664534 | ||
| Fumaric aciduria: clinical and imaging features | Q28144047 | ||
| The mitochondrial transporter family (SLC25): physiological and pathological implications | Q28181828 | ||
| The systems biology markup language (SBML): a medium for representation and exchange of biochemical network models | Q28212902 | ||
| A novel mutation in the dihydrolipoamide dehydrogenase E3 subunit gene (DLD) resulting in an atypical form of alpha-ketoglutarate dehydrogenase deficiency | Q28235105 | ||
| Succinate dehydrogenase deficiency in human | Q28270821 | ||
| What is flux balance analysis? | Q28275348 | ||
| Fumarase deficiency is an autosomal recessive encephalopathy affecting both the mitochondrial and the cytosolic enzymes | Q28279115 | ||
| Minimum information requested in the annotation of biochemical models (MIRIAM) | Q28285448 | ||
| The Universal Protein Resource (UniProt) in 2010 | Q28749229 | ||
| Quantitative prediction of cellular metabolism with constraint-based models: the COBRA Toolbox | Q29615372 | ||
| Reconstruction of metabolic networks from genome data and analysis of their global structure for various organisms | Q30763008 | ||
| Reconstruction and functional characterization of the human mitochondrial metabolic network based on proteomic and biochemical data | Q30939059 | ||
| Flux-balance analysis of mitochondrial energy metabolism: consequences of systemic stoichiometric constraints | Q31920157 | ||
| MitoMiner, an integrated database for the storage and analysis of mitochondrial proteomics data | Q33408082 | ||
| The molecular basis of dominance. | Q34283978 | ||
| Mitochondrial disease | Q34543745 | ||
| Alpha-ketoglutarate dehydrogenase deficiency presenting as congenital lactic acidosis | Q34564054 | ||
| 2-Ketoglutarate dehydrogenase deficiency, a rare cause of primary hyperlactataemia: report of a new case | Q34729219 | ||
| Inborn errors of the Krebs cycle: a group of unusual mitochondrial diseases in human | Q34742947 | ||
| The role and structure of mitochondrial carriers | Q35757351 | ||
| Alterations of myocardial amino acid metabolism in chronic ischemic heart disease | Q35905152 | ||
| Fumarase deficiency: two siblings with enlarged cerebral ventricles and polyhydramnios in utero. | Q35968221 | ||
| Myocardial substrate metabolism in the normal and failing heart | Q36179008 | ||
| Group contribution method for thermodynamic analysis of complex metabolic networks | Q36783787 | ||
| Role of cardiolipin peroxidation and Ca2+ in mitochondrial dysfunction and disease | Q37445214 | ||
| The Gene Ontology Annotation (GOA) Database--an integrated resource of GO annotations to the UniProt Knowledgebase | Q38522030 | ||
| Glucose-free fatty acid cycle operates in human heart and skeletal muscle in vivo | Q40343651 | ||
| Gamma-aminobutyric acid (GABA) metabolism in mammalian neural and nonneural tissues | Q40429762 | ||
| Glutamine metabolism and transport in skeletal muscle and heart and their clinical relevance | Q40994124 | ||
| A familial progressive neurodegenerative disease with 2-oxoglutaric aciduria | Q42468171 | ||
| Extreme pathways and Kirchhoff's second law. | Q43122158 | ||
| Non-invasive measurements of myocardial carbon metabolism using in vivo 13C NMR spectroscopy | Q43968220 | ||
| Succinate in dystrophic white matter: a proton magnetic resonance spectroscopy finding characteristic for complex II deficiency | Q44060064 | ||
| Profiling substrate fluxes in the isolated working mouse heart using 13C-labeled substrates: focusing on the origin and fate of pyruvate and citrate carbons | Q44689992 | ||
| Mitochondrial pH monitored by a new engineered green fluorescent protein mutant. | Q44710648 | ||
| Candidate metabolic network states in human mitochondria. Impact of diabetes, ischemia, and diet. | Q45168694 | ||
| The effect of hyperpolarized tracer concentration on myocardial uptake and metabolism | Q46103916 | ||
| Complex I is the major site of mitochondrial superoxide production by paraquat | Q46881393 | ||
| A general computational model of mitochondrial metabolism in a whole organelle scale | Q47205738 | ||
| Fumarate hydratase deficiency in monozygotic twins | Q48459949 | ||
| Effects of riboflavin in children with complex II deficiency | Q48515664 | ||
| Fumaric aciduria: a new organic aciduria, associated with mental retardation and speech impairment | Q52094819 | ||
| Single muscle fibre analyses in 2 brothers with succinate dehydrogenase deficiency. | Q54432742 | ||
| Fumaric aciduria: Clinical and imaging features | Q56018001 | ||
| Kearns-Sayre syndrome and complex II deficiency | Q69591998 | ||
| Biochemical investigations and immunoblot analyses of two unrelated patients with an isolated deficiency in complex II of the mitochondrial respiratory chain | Q71004601 | ||
| Myocardial Exchanges of Glutamate, Alanine and Citrate in Controls and Patients with Coronary Artery Disease | Q72543442 | ||
| Glucose and fatty acid metabolism in the isolated working mouse heart | Q73071219 | ||
| Altered metabolism causes cardiac dysfunction in perfused hearts from diabetic (db/db) mice | Q73127304 | ||
| Effects of aminooxyacetate on glutamate compartmentation and TCA cycle kinetics in rat hearts | Q74255333 | ||
| Import of lipids into mitochondria | Q74640249 | ||
| P4510 | describes a project that uses | Cytoscape | Q3699942 |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | tricarboxylic acid cycle | Q133895 |
| mitochondrion | Q39572 | ||
| modelling biological systems | Q4299308 | ||
| P304 | page(s) | 102 | |
| P577 | publication date | 2011-06-29 | |
| P1433 | published in | BMC Systems Biology | Q4835949 |
| P1476 | title | A metabolic model of the mitochondrion and its use in modelling diseases of the tricarboxylic acid cycle | |
| P478 | volume | 5 |
| Q51175854 | A design automation framework for computational bioenergetics in biological networks. |
| Q34906417 | A panoramic overview of mitochondria and mitochondrial redox biology |
| Q28384122 | Bioanalysis of Eukaryotic Organelles |
| Q36228895 | Cancer cell growth and survival as a system-level property sustained by enhanced glycolysis and mitochondrial metabolic remodeling |
| Q34396816 | CardioNet: a human metabolic network suited for the study of cardiomyocyte metabolism |
| Q39428664 | Deficits in the mitochondrial enzyme α-ketoglutarate dehydrogenase lead to Alzheimer's disease-like calcium dysregulation |
| Q39316985 | Effect of essential fatty acids on glucose-induced cytotoxicity to retinal vascular endothelial cells |
| Q47603942 | Fumarase Deficiency: A Safe and Potentially Disease Modifying Effect of High Fat/Low Carbohydrate Diet |
| Q35859412 | Fumarate is cardioprotective via activation of the Nrf2 antioxidant pathway. |
| Q38711911 | Genome-scale metabolic models applied to human health and disease |
| Q34447034 | Ischaemic accumulation of succinate controls reperfusion injury through mitochondrial ROS. |
| Q47954316 | Isolation of Functional Mitochondria from Cultured Cells and Mouse Tissues |
| Q38056722 | Mechanistic modeling of aberrant energy metabolism in human disease |
| Q41840468 | Metabolic flexibility of mitochondrial respiratory chain disorders predicted by computer modelling |
| Q34781444 | Metabolomic profiling analysis reveals chamber-dependent metabolite patterns in the mouse heart |
| Q47151205 | MitoCore: a curated constraint-based model for simulating human central metabolism |
| Q34084587 | MitoMiner: a data warehouse for mitochondrial proteomics data |
| Q36877638 | Mitochondrial Reactive Oxygen Species Mediate Cardiac Structural, Functional, and Mitochondrial Consequences of Diet-Induced Metabolic Heart Disease |
| Q46368801 | Modeling oxygen requirements in ischemic cardiomyocytes. |
| Q44501708 | Modelling pyruvate dehydrogenase under hypoxia and its role in cancer metabolism. |
| Q35777348 | Multi-Target Analysis and Design of Mitochondrial Metabolism. |
| Q44448314 | On the role of the mitochondrial 2-oxoglutarate dehydrogenase complex in amino acid metabolism |
| Q50783539 | Pedagogical view of model metabolic cycles |
| Q91815266 | Rescue of TCA Cycle Dysfunction for Cancer Therapy |
| Q57462280 | Screening of candidate substrates and coupling ions of transporters by thermostability shift assays |
| Q46637268 | Succinate: A Promising Therapeutic Target for Reperfusion Injury |
| Q61803767 | Systems Biology Approaches Toward Understanding Primary Mitochondrial Diseases |
| Q39076595 | Traditional and novel tools to probe the mitochondrial metabolism in health and disease |
| Q34032854 | Up-regulation of 2-oxoglutarate dehydrogenase as a stress response |
| Q37412089 | l-Citrulline Protects from Kidney Damage in Type 1 Diabetic Mice |
Search more.