Mitochondria and Diabetes: Genetic, Biochemical, and Clinical Implications of the Cellular Energy Circuit

No abstract is available for this paper.

• Publication year

  1996

• Venue

  Diabetes

• Publication date

  1996-02-01

• Fields of study

  Biology, Medicine

• Identifiers
  DOI 10.2337/diab.45.2.113
• External record

  Open on Semantic Scholar

• Source metadata

  Semantic Scholar

• No claims are published for this paper.

• No concepts are published for this paper.

• Decreased muscle glucose transport/phosphorylation is an early defect in the pathogenesis of non-insulin-dependent diabetes mellitus.

  1995cited by this paper
• Abnormal calcium homeostasis and mitochondrial polarization in a human encephalomyopathy.

  1995cited by this paper
• A subtype of diabetes mellitus associated with a mutation in the mitochondrial gene

  1995cited by this paper
• Mitochondrial diabetes mellitus—glucose‐induced signaling defects and β‐cell loss

  1995cited by this paper
• Mitochondrial diabetes mellitus: a review.

  1995influential reference
• Segregation patterns of a novel mutation in the mitochondrial tRNA glutamic acid gene associated with myopathy and diabetes mellitus.

  1995cited by this paper
• Identification of Four Amino Acid Substitutions in Hexokinase II and Studies of Relationships to NIDDM, Glucose Effectiveness, and Insulin Sensitivity

  1995cited by this paper
• Co‐localization of L‐type Ca2+ channels and insulin‐containing secretory granules and its significance for the initiation of exocytosis in mouse pancreatic B‐cells.

  1995cited by this paper
• An autosomal locus predisposing to deletions of mitochondrial DNA

  1995cited by this paper
• Amino Acid Substitutions in Hexokinase II Among Patients With NIDDM

  1995cited by this paper
• Analysis of the Hexokinase II Gene in Subjects With Insulin Resistance and NIDDM and Detection of a Gln142→His Substitution

  1995cited by this paper
• Clinical features of melas and mitochondrial DNA mutations

  1995cited by this paper
• DIDMOAD or Wolfram Syndrome: A mitochondrial-mediated disorder?

  1995cited by this paper
• Reduced Expression of Hexokinase II in Insulin-Resistant Diabetes

  1995cited by this paper
• Non‐insulin‐dependent Diabetes Mellitus and Islet B‐cell Mitochondrial Glycerophosphate Dehydrogenase Deficiency

  1995cited by this paper
• Reactive oxygen species and the regulation of cell death by the Bcl-2 gene family.

  1995cited by this paper
• Congenital encephalomyopathy and adult-onset myopathy and diabetes mellitus: different phenotypic associations of a new heteroplasmic mtDNA tRNA glutamic acid mutation.

  1995cited by this paper
• Maternally inherited diabetes and deafness (MIDD): A distinct subtype of diabetes associated with a mitochondrial tRNALeu(UUR) gene point mutation

  1995cited by this paper
• Increased expression of mitochondrial-encoded genes in skeletal muscle of humans with diabetes mellitus.

  1995cited by this paper
• Mitochondrial creatine kinase: a major constituent of pathological inclusions seen in mitochondrial myopathies.

  1994cited by this paper
• Creatine treatment in MELAS.

  1994cited by this paper
• Mitochondrial DNA sequence variation in human evolution and disease.

  1994cited by this paper
• The role of Ca2+ in the release of pancreatic islet hormones.

  1994cited by this paper
• Microcompartmentation of energy metabolism at the outer mitochondrial membrane: Role in diabetes mellitus and other diseases

  1994cited by this paper
• Maternally inherited diabetes and deafness is a distinct subtype of diabetes and associates with a single point mutation in the mitochondrial tRNA Leu(UUR) gene

  1994cited by this paper
• Function of the outer mitochondrial compartment in regulation of energy metabolism.

  1994cited by this paper
• mtDNA and the origin of Caucasians: identification of ancient Caucasian-specific haplogroups, one of which is prone to a recurrent somatic duplication in the D-loop region.

  1994cited by this paper
• Local ATP regeneration is important for sarcoplasmic reticulum Ca2+ pump function.

  1994cited by this paper
• Porin proteins in mitochondria from rat pancreatic islet cells and white adipocytes: identification and regulation of hexokinase binding by the sulfonylurea glimepiride.

  1994cited by this paper
• More Direct Evidence for a Malonyl-CoA–Carnitine Palmitoyltransferase I Interaction as a Key Event in Pancreatic β-Cell Signaling

  1994cited by this paper
• Lack of voltage-dependent anion channel in human mitochondrial myopathies.

  1994cited by this paper
• The high prevalence of the diabetic patients with a mutation in the mitochondrial gene in Japan.

  1994cited by this paper
• Are duplications of mitochondrial DNA characteristic of Kearns-Sayre syndrome?

  1994cited by this paper
• Mitochondrial DNA: does more lead to less?

  1994cited by this paper
• Diabetes With Mitochondrial Gene tRNALYS Mutation

  1994cited by this paper
• Multisite control of insulin release by glucose.

  1994cited by this paper
• Effect of macromolecules on the regulation of the mitochondrial outer membrane pore and the activity of adenylate kinase in the inter-membrane space.

  1993cited by this paper
• Prevalence of mitochondrial gene mutations in families with diabetes mellitus.

  1993cited by this paper
• Maternally transmitted partial direct tandem duplication of mitochondrial DNA associated with diabetes mellitus.

  1993cited by this paper
• Two novel pathogenic mitochondrial DNA mutations affecting organelle number and protein synthesis. Is the tRNA(Leu(UUR)) gene an etiologic hot spot?

  1993cited by this paper
• Hexokinase II mRNA and gene structure, regulation by insulin, and evolution.

  1993cited by this paper
• Glucokinase as pancreatic beta cell glucose sensor and diabetes gene.

  1993cited by this paper
• Substrate-dependent changes in mitochondrial function, intracellular free calcium concentration and membrane channels in pancreatic beta-cells.

  1993cited by this paper
• Japanese case of diabetes mellitus and deafness with mutation in mitochondrial tRNA(Leu(UUR)) gene.

  1993cited by this paper
• Families of mtDNA re-arrangements can be detected in patients with mtDNA deletions: duplications may be a transient intermediate form.

  1993cited by this paper
• Effect of macromolecules on the structure of the mitochondrial inter-membrane space and the regulation of hexokinase.

  1993cited by this paper
• Wolfram syndrome: a mitochondrial-mediated disorder?

  1993cited by this paper
• A tandem duplication in the D–loop of human mitochondrial DNA is associated with deletions in mitochondrial myopathies

  1993cited by this paper
• A new point mutation associated with mitochondrial encephalomyopathy.

  1993cited by this paper
• Human Islet Glucokinase Gene: Isolation and Sequence Analysis of Full-Length cDNA

  1992cited by this paper
• Endocrine dysfunction in Kearns‐Sayre syndrome

  1992cited by this paper
• Mutation in mitochondrial tRNALeu(UUR) gene in a large pedigree with maternally transmitted type II diabetes mellitus and deafness

  1992cited by this paper
• Intracellular compartmentation, structure and function of creatine kinase isoenzymes in tissues with high and fluctuating energy demands: the 'phosphocreatine circuit' for cellular energy homeostasis.

  1992cited by this paper
• In situ hybridization of mitochondrial DNA in the heart of a patient with Kearns-Sayre syndrome and dilatative cardiomyopathy.

  1992cited by this paper
• Expression of yeast hexokinase in pancreatic beta cells of transgenic mice reduces blood glucose, enhances insulin secretion, and decreases diabetes.

  1992cited by this paper
• Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke‐like episodes (MELAS)

  1992cited by this paper
• A new mtDNA mutation in the tRNA(Lys) gene associated with myoclonic epilepsy and ragged-red fibers (MERRF).

  1992cited by this paper
• The cation-selective substate of the mitochondrial outer membrane pore: Single-channel conductance and influence on intermembrane and peripheral kinases

  1992cited by this paper
• Nonsense mutation in the glucokinase gene causes early-onset non-insulin-dependent diabetes mellitus

  1992cited by this paper
• Compartmentation of hexokinase in rat heart. A critical factor for tracer kinetic analysis of myocardial glucose metabolism.

  1992cited by this paper
• The principal islet of the coho salmon (Oncorhyncus kisutch) contains the BB isoenzyme of creatine kinase

  1992cited by this paper
• Diabetes mellitus associated with a pathogenic point mutation in mitochondrial DNA.

  1992cited by this paper
• Localization of the ATP/ADP translocator in the inner membrane and regulation of contact sites between mitochondrial envelope membranes by ADP. A study on freeze-fractured isolated liver mitochondria.

  1991cited by this paper
• The role of ATP and free ADP in metabolic coupling during fuel-stimulated insulin release from islet beta-cells in the isolated perfused rat pancreas.

  1991cited by this paper
• Inhibition of electrical activity in mouse pancreatic β‐cells by the ATP/ADP translocase inhibitor, bongkrekic acid

  1991cited by this paper
• Congenital Hypoplastic Anemia, Diabetes, and Severe Renal Tubular Dysfunction Associated with a Mitochondrial DNA Deletion

  1991cited by this paper
• Maternally inherited myopathy and cardiomyopathy: association with mutation in mitochondrial DNA tRNA(Leu)(UUR).

  1991cited by this paper
• Adult rat cardiomyocytes cultured in creatine-deficient medium display large mitochondria with paracrystalline inclusions, enriched for creatine kinase

  1991cited by this paper
• Hexokinase bound to rat brain mitochondria uses externally added ATP more efficiently than internally generated ATP.

  1991cited by this paper
• Introduction of disease-related mitochondrial DNA deletions into HeLa cells lacking mitochondrial DNA results in mitochondrial dysfunction.

  1991cited by this paper
• Myoclonic epilepsy and ragged-red fiber disease (MERRF) is associated with a mitochondrial DNA tRNA(Lys) mutation.

  1990cited by this paper
• Tetrameric structure of mitochondrially bound rat brain hexokinase: a crosslinking study.

  1990cited by this paper
• Different copy numbers of apparently identically deleted mitochondrial DNA in tissues from a patient with Kearns-Sayre syndrome detected by PCR.

  1990cited by this paper
• Further characterization of mitochondrial contact sites: effect of short-chain alcohols on membrane fluidity and activity.

  1990cited by this paper
• Mutations of the Mitochondrial DNA: The Contribution of DNA Techniques to the Diagnosis of Mitochondrial Encephalomyopathies

  1990cited by this paper
• Muscle-type MM creatine kinase is specifically bound to sarcoplasmic reticulum and can support Ca2+ uptake and regulate local ATP/ADP ratios.

  1990cited by this paper
• The high Km glucose transporter of islets of Langerhans is functionally similar to the low affinity transporter of liver and has an identical primary sequence.

  1990cited by this paper
• The theory of diazymes and functional coupling of pyruvate kinase and creatine kinase.

  1990cited by this paper
• Human cells lacking mtDNA: repopulation with exogenous mitochondria by complementation.

  1989cited by this paper
• Molecular aspects of the adenine nucleotide carrier from mitochondria.

  1989cited by this paper
• Genetically Programmed Selective Islet β-Cell Loss in Diabetic Subjects With Wolfram's Syndrome

  1989cited by this paper
• Mitochondrial DNA deletions in progressive external ophthalmoplegia and Kearns-Sayre syndrome.

  1989cited by this paper
• Localization of the pancreatic beta cell glucose transporter to specific plasma membrane domains.

  1989cited by this paper
• Mitochondrial boundary membrane contact sites in brain: points of hexokinase and creatine kinase location, and control of Ca2+ transport.

  1988cited by this paper
• Normal oxidative damage to mitochondrial and nuclear DNA is extensive.

  1988cited by this paper
• Adenosine 5'-triphosphate-sensitive potassium channels.

  1988cited by this paper
• Activation of low Km hexokinases in purified hepatocytes by binding to mitochondria.

  1988cited by this paper
• Only one of the two interconvertible forms of mitochondrial creatine kinase binds to heart mitoplasts.

  1987cited by this paper
• Microcompartmentation at the mitochondrial surface: its function in metabolic regulation.

  1986cited by this paper
• Enrichment and biochemical characterization of boundary membrane contact sites from rat-liver mitochondria.

  1986cited by this paper
• An intact hydrophobic N-terminal sequence is critical for binding of rat brain hexokinase to mitochondria.

  1985cited by this paper
• The regulation of mitochondrial-bound hexokinases in the liver.

  1985cited by this paper
• Function of M-line-bound creatine kinase as intramyofibrillar ATP regenerator at the receiving end of the phosphorylcreatine shuttle in muscle.

  1984cited by this paper
• New perspectives on pancreatic islet glucokinase.

  1984cited by this paper
• Evidence for identity between the hexokinase-binding protein and the mitochondrial porin in the outer membrane of rat liver mitochondria.

  1982cited by this paper
• The comparative isozymology of vertebrate hexokinases.

  1982cited by this paper
• Determinants of the selective toxicity of alloxan to the pancreatic B cell.

  1982cited by this paper
• Pore protein and the hexokinase‐binding protein from the outer membrane of rat liver mitochondria are identical

  1982cited by this paper
• Sequence and organization of the human mitochondrial genome

  1981cited by this paper
• Mapping of metabolites in whole animals by 31P NMR using surface coils

  1980cited by this paper

• Mondo family proteins in diabetes

  2026cites this paper
• Estrogen promotes fetal skeletal muscle mitochondrial distribution and ATP synthase activity important for insulin sensitivity in offspring

  2024cites this paper
• Exploring the Pathophysiology of ATP-Dependent Potassium Channels in Insulin Resistance

  2024cites this paper
• Immunometabolism in Endocrine Disorders Leads to a High Frequency of Diabetes Mellitus Caused by Heteroplasmic mtDNA Mutations

  2024cites this paper
• Mapping the mitochondrial landscape in T2DM: key findings from 2003-2023

  2024cites this paper
• Mitochondrial Diabetes Mellitus With Mitochondrial DNA 3316G>A Mutation: A Unique Autopsy Case Presenting With Sepsis-Associated Cholestasis

  2024cites this paper
• Redox imbalance and metabolic defects in the context of Alzheimer disease

  2024cites this paper
• Toward Ameliorating Insulin Resistance: Targeting a Novel PAK1 Signaling Pathway Required for Skeletal Muscle Mitochondrial Function

  2023cites this paper
• ProSE-Pero: Peroxisomal Protein Localization Identification Model Based on Self-Supervised Multi-Task Language Pre-Training Model.

  2023cites this paper
• Variants in the Control Region of Mitochondrial Genome Associated with type 2 Diabetes in a Cohort of Mexican Mestizos.

  2023cites this paper
• Prediction of submitochondrial proteins localization based on Gene Ontology

  2023cites this paper
• The Role of Lactate Exercise Test and Fasting Plasma C-Peptide Levels in the Diagnosis of Mitochondrial Diabetes: Analysis of Clinical Characteristics of 12 Patients With Mitochondrial Diabetes in a Single Center With Long-Term Follow-Up

  2022cites this paper
• Kearns–Sayre Syndrome Minus: Two Cases of Identical Large-Scale Mitochondrial DNA Deletions with Presentations outside the Classical Triad

  2022cites this paper
• Mitochondrial ATP6 and ND3 genes are associated with type 2 diabetic peripheral neuropathy.

  2022cites this paper
• MicroRNA-21 promotes pancreatic β cell function through modulating glucose uptake

  2022cites this paper
• 5-aminolevulinic acid and sodium ferrous citrate decreased cell viability of gastric cancer cells by enhanced ROS generation through improving COX activity.

  2022cites this paper
• The insulin receptor family in the heart: new light on old insights

  2022cites this paper
• Uncoupling protein 2 and aldolase B impact insulin release by modulating mitochondrial function and Ca2+ release from the ER

  2022cites this paper
• Alterations of Mitochondrial Network by Cigarette Smoking and E-Cigarette Vaping

  2022cites this paper
• The Mitochondrial Pyruvate Carrier at the Crossroads of Intermediary Metabolism.

  2022cites this paper
• The interplay among oxidative stress, brain insulin resistance and AMPK dysfunction contribute to neurodegeneration in type 2 diabetes and Alzheimer disease.

  2021cites this paper
• Clinical and molecular features of two diabetes families carrying mitochondrial ND1 T3394C mutation

  2021cites this paper
• Genomic Analysis Reveals Human-Mediated Introgression From European Commercial Pigs to Henan Indigenous Pigs

  2021cites this paper
• Mutational Analysis of Mitochondrial tRNA Genes in 200 Patients with Type 2 Diabetes Mellitus

  2021cites this paper
• Evaluation of hyperglycemia

  2021cites this paper
• Role of ketone bodies in diabetes-induced dementia: sirtuins, insulin resistance, synaptic plasticity, mitochondrial dysfunction, and neurotransmitter

  2021cites this paper
• Nucleus-mitochondria positive feedback loop formed by ERK5 S496 phosphorylation-mediated poly (ADP-ribose) polymerase activation provokes persistent pro-inflammatory senescent phenotype and accelerates coronary atherosclerosis after chemo-radiation

  2021cites this paper
• Fructose tolerance test in obese people with and without type 2 diabetes

  2020cites this paper
• Clinical phenotype of mitochondrial diabetes due to rare mitochondrial DNA mutations.

  2020cites this paper
• Lactate activation of α-cell KATP channels inhibits glucagon secretion by hyperpolarizing the membrane potential and reducing Ca2+ entry

  2020cites this paper
• Cytotoxicity of metformin against HT29 colon cancer cells contributes to mitochondrial Sirt3 upregulation

  2020cites this paper
• High rate of hypertension in patients with m.3243A>G MELAS mutations and POLG variants.

  2020cites this paper
• Molecular genetic analysis of leucine tRNA in relevance to type 2 diabetes mellitus

  2020cites this paper
• AMPD1 C34T Polymorphism (rs17602729) Is Not Associated with Post-Exercise Changes of Body Weight, Body Composition, and Biochemical Parameters in Caucasian Females

  2020cites this paper
• The Invisible Rainbow: A History of Electricity and Life

  2020cites this paper
• Mitochondrial DNA copy number and diabetes: the Atherosclerosis Risk in Communities (ARIC) study

  2020cites this paper
• Interaction of ApoMyoglobin with Heme-hIAPP complex.

  2020cites this paper
• A Systematic Review of Childhood Diabetes Research in the Middle East Region

  2019cites this paper
• Analyzing Mitochondrial Dysfunction, Oxidative Stress, and Apoptosis: Potential Role of L-carnitine.

  2019cites this paper
• Tortuous Paths of Insulin Signaling and Mitochondria in Alzheimer's Disease.

  2019cites this paper
• SubMito-XGBoost: predicting protein submitochondrial localization by fusing multiple feature information and eXtreme gradient boosting

  2019cites this paper
• Energy systems: a new look at aerobic metabolism in stressful exercise

  2018cites this paper
• Cellular pathways affected by carbon nanopowder-benzo(α)pyrene complex in human skin fibroblasts identified by proteomics.

  2018cites this paper
• Antidiabetic and Antioxidant Effects of Apple Cider Vinegar on Normal and Streptozotocin-Induced Diabetic Rats.

  2018cites this paper
• The Triangle of Death in Alzheimer's Disease Brain: The Aberrant Cross-Talk Among Energy Metabolism, Mammalian Target of Rapamycin Signaling, and Protein Homeostasis Revealed by Redox Proteomics

  2017cites this paper
• Étude phénotypique des mutations rares responsables de diabète mitochondrial

  2017cites this paper
• Targeting NAD+ in Metabolic Disease: New Insights Into an Old Molecule

  2017cites this paper
• The clinical characteristics of patients with mitochondrial tRNA Leu(UUR)m.3243A > G mutation: Compared with type 1 diabetes and early onset type 2 diabetes.

  2017cites this paper
• Familial longevity study reveals a significant association of mitochondrial DNA copy number between centenarians and their offspring.

  2016cites this paper
• Mitochondrial complex I and V gene polymorphisms in type II diabetes mellitus among high risk Mizo-Mongoloid population, Northeast India

  2016cites this paper
• Mitochondrial Ultrastructure and Glucose Signaling Pathways Attributed to the Kv1.3 Ion Channel

  2016cites this paper
• Developmental Programming and Life Course Regulation of Skeletal Muscle Inflammation and Oxidative Function

  2016cites this paper
• From the Cover: Thirdhand Cigarette Smoke Causes Stress-Induced Mitochondrial Hyperfusion and Alters the Transcriptional Profile of Stem Cells.

  2016cites this paper
• heartof the roles of hexokinase I and II in the

  2016cites this paper
• Association between the C34T polymorphism of the AMPD1 gene and essential hypertension in Malaysian patients.

  2016cites this paper
• Insulin signalling in Alzheimer′s disease and diabetes: from epidemiology to molecular links

  2016cites this paper
• Mitochondrial DNA variant at HVI region as a candidate of genetic markers of type 2 diabetes

  2016cites this paper
• Mitochondrial ND1 gene mutation analysis in type II diabetes of Karaikudi population

  2015cites this paper
• Plasma Lactate Levels Increase during Hyperinsulinemic Euglycemic Clamp and Oral Glucose Tolerance Test

  2015cites this paper
• Tau Hyperphosphorylation and Oxidative Stress, a Critical Vicious Circle in Neurodegenerative Tauopathies?

  2015cites this paper
• Neurobiology of Disease

  2015cites this paper
• Molecular and biochemical trajectories from diabetes to Alzheimer's disease: A critical appraisal.

  2015cites this paper
• Why is Qi-Invigorating Therapy in Chinese Medicine Suitable for Mitochondrial Diseases? A Bioenergetic Perspective

  2015cites this paper
• Insulin resistance in Alzheimer disease: Is heme oxygenase-1 an Achille's heel?

  2015cites this paper
• The role of type 2 diabetes in neurodegeneration.

  2015cites this paper
• muscle contribute to insulin resistance in NIDDM Altered glycolytic and oxidative capacities of skeletal

  2015cites this paper
• Elevated risk of type 2 diabetes for development of Alzheimer disease: a key role for oxidative stress in brain.

  2014cites this paper
• ESTUDIOS ESTRUCTURALES DE ENZIMAS INVOLUCRADAS EN EL METABOLISMO DE NUCLEÓTIDOS DE CAMARÓN BLANCO Litopenaeus vannamei

  2014cites this paper
• Diabetes in pediatric patients with Kearns-Sayre syndrome: clinical presentation of 2 cases and a review of pathophysiology.

  2014cites this paper
• Free fatty acids and skeletal muscle insulin resistance.

  2014cites this paper
• Extrahepatic targets and cellular reactivity of drug metabolites.

  2014cites this paper
• A Preliminary Fastview of Mitochondrial Protein Profile from Healthy and Type 2 Diabetic Subjects

  2014cites this paper
• Mitochondrial DNA mutations in diabetes mellitus patients in Chinese Han population.

  2013cites this paper
• Next-Generation Sequencing of Human Mitochondrial Reference Genomes Uncovers High Heteroplasmy Frequency

  2012cites this paper
• Protection from palmitate-induced mitochondrial DNA damage prevents from mitochondrial oxidative stress, mitochondrial dysfunction, apoptosis, and impaired insulin signaling in rat L6 skeletal muscle cells.

  2012cites this paper
• Glucose sensing by ChREBP/MondoA-Mlx transcription factors.

  2012cites this paper
• Chapter 3 - Pathogenesis of Type 2 Diabetes—A Comprehensive Analysis

  2012cites this paper
• Infantile Progressive Hepatoencephalomyopathy with Combined OXPHOS Deficiency due to Mutations in the Mitochondrial Translation Elongation Factor Gene GFM1.

  2012cites this paper
• Standardized mitochondrial analysis gives new insights into mitochondrial dynamics and OPA1 function.

  2012cites this paper
• Mito-GSAAC: mitochondria prediction using genetic ensemble classifier and split amino acid composition

  2012cites this paper
• Enhanced brain performance in mice following postnatal stress.

  2012cites this paper
• Chitooligosaccharide Induces Mitochondrial Biogenesis and Increases Exercise Endurance through the Activation of Sirt1 and AMPK in Rats

  2012cites this paper
• Pathobiochemical Changes in Diabetic Skeletal Muscle as Revealed by Mass-Spectrometry-Based Proteomics

  2012cites this paper
• Métabolisme énergétique cardiaque fœtal dans un modèle de restriction de croissance intra-utérine chez le rat

  2011cites this paper
• Orchestrated downregulation of genes involved in oxidative metabolic pathways in obese vs. lean high-fat young male consumers

  2011cites this paper
• Physical activity in the management of type 2 diabetes mellitus

  2011cites this paper
• The Starving Cell: Metabolic Syndrome as an Adaptive Process

  2011cites this paper
• Diabetes mellitus: Metabolic effects and oxidative stress

  2011cites this paper
• Pathogenesis of type 2 diabetes

  2011cites this paper
• Oxidative Stress and Hypoxia in the Pathogenesis of Diabetic Nephropathy

  2011cites this paper
• Lost in translation: genetic defects underlying combined OXPHOS complex I, III and IV deficiencies

  2011cites this paper
• Aspects cliniques et diagnostiques du diabète de l'enfant

  2011cites this paper
• in late

  2011cites this paper
• Protective effects of Annona muricata Linn. (Annonaceae) leaf aqueous extract on serum lipid profiles and oxidative stress in hepatocytes of streptozotocin-treated diabetic rats.

  2010cites this paper
• Oxidative stress and beta-cell dysfunction

  2010cites this paper
• Glycolytic network restructuring integral to the energetics of embryonic stem cell cardiac differentiation.

  2010cites this paper
• AMPD1 gene mutations are associated with obesity and diabetes in Polish patients with cardiovascular diseases

  2010cites this paper
• Electrophysiology of islet cells.

  2010cites this paper
• Effects of selection for low residual feed intake and feed restriction on gene expression profiles and thyroid axis in pigs

  2010cites this paper
• Mitochondrial Translation and Beyond: Processes Implicated in Combined Oxidative Phosphorylation Deficiencies

  2010cites this paper