Increased formation of methylglyoxal and protein glycation, oxidation and nitrosation in triosephosphate isomerase deficiency

scientific article published in October 2003

Increased formation of methylglyoxal and protein glycation, oxidation and nitrosation in triosephosphate isomerase deficiency is …
instance of (P31):
scholarly articleQ13442814

External links are
P356DOI10.1016/J.BBADIS.2003.08.002
P698PubMed publication ID14559119
P5875ResearchGate publication ID9051172

P50authorPaul J ThornalleyQ56810389
P2093author name stringSinan Battah
Naila Ahmed
Margit Horányi
Roya Babaei-Jadidi
Klára Baróti
Nikolaos Karachalias
Susan Hollan
P2860cites workCharacterization of glycated hemoglobin in diabetic patients: usefulness of electrospray mass spectrometry in monitoring the extent and distribution of glycation.Q43703551
P433issue2
P304page(s)121-132
P577publication date2003-10-01
P1433published inBiochimica et Biophysica ActaQ864239
P1476titleIncreased formation of methylglyoxal and protein glycation, oxidation and nitrosation in triosephosphate isomerase deficiency
P478volume1639

Reverse relations

cites work (P2860)
Q389466443-Bromopyruvate induces rapid human prostate cancer cell death by affecting cell energy metabolism, GSH pool and the glyoxalase system.
Q83749501A simple and robust LC-MS/MS method for quantification of free 3-nitrotyrosine in human plasma from patients receiving on-pump CABG surgery
Q35767234A53T-alpha-synuclein-overexpression in the mouse nigrostriatal pathway leads to early increase of 14-3-3 epsilon and late increase of GFAP
Q37800424Advanced glycation endproducts and their pathogenic roles in neurological disorders
Q37760069Analytical methods for 3-nitrotyrosine quantification in biological samples: the unique role of tandem mass spectrometry
Q37142377Assay of 3-nitrotyrosine in tissues and body fluids by liquid chromatography with tandem mass spectrometric detection
Q55420913Bone marrow transplantation corrects haemolytic anaemia in a novel ENU mutagenesis mouse model of TPI deficiency.
Q26766024Carbonyl Stress in Bacteria: Causes and Consequences
Q41335123Characterization of stress and methylglyoxal inducible triose phosphate isomerase (OscTPI) from rice
Q47813249Comparative Examination of Temporal Glyoxalase 1 Variations Following Perforant Pathway Transection, Excitotoxicity, and Controlled Cortical Impact Injury.
Q92553107Crystal structures of Triosephosphate Isomerases from Taenia solium and Schistosoma mansoni provide insights for vaccine rationale and drug design against helminth parasites
Q36724350Degradation of functional triose phosphate isomerase protein underlies sugarkill pathology
Q21146753Dynamic rerouting of the carbohydrate flux is key to counteracting oxidative stress
Q36773904Early mitochondrial dysfunction leads to altered redox chemistry underlying pathogenesis of TPI deficiency
Q41964977Energy metabolism, altered proteins, sirtuins and ageing: converging mechanisms?
Q89976584Excess Copper-Induced Alterations of Protein Profiles and Related Physiological Parameters in Citrus Leaves
Q92451047Glycation of macrophages induces expression of pro-inflammatory cytokines and reduces phagocytic efficiency
Q37421997Glycation potentiates neurodegeneration in models of Huntington's disease.
Q38631878Glycation, Oxidation and Glycoxidation of IgG: A Biophysical, Biochemical, Immunological and Hematological study.
Q35112759Glyoxalase I polymorphism rs2736654 causing the Ala111Glu substitution modulates enzyme activity--implications for autism
Q31049371Glyoxalase II of African trypanosomes is trypanothione-dependent
Q38019452Good mass spectrometry and its place in good science
Q28539333Hydrogen sulfide releasing aspirin, ACS14, attenuates high glucose-induced increased methylglyoxal and oxidative stress in cultured vascular smooth muscle cells
Q43138020Immunological detection of fructose-derived advanced glycation end-products
Q46367798In vitro nonenzymatic glycation of guanosine 5'-triphosphate by dihydroxyacetone phosphate
Q37277390Inhibition of Non-flux-Controlling Enzymes Deters Cancer Glycolysis by Accumulation of Regulatory Metabolites of Controlling Steps
Q36396524Inhibition of enzyme activity of Rhipicephalus (Boophilus) microplus triosephosphate isomerase and BME26 cell growth by monoclonal antibodies
Q38156144Mass spectrometry and 3-nitrotyrosine: strategies, controversies, and our current perspective
Q39313466Methylglyoxal alters glucose metabolism and increases AGEs content in C6 glioma cells
Q36653426Methylglyoxal in food and living organisms.
Q42811134Methylglyoxal induces oxidative stress and mitochondrial dysfunction in osteoblastic MC3T3-E1 cells
Q35063131Methylglyoxal, the dark side of glycolysis
Q48178370Methylglyoxal-induced cytotoxicity in neonatal rat brain: a role for oxidative stress and MAP kinases
Q37530715NAD+ availability and proteotoxicity
Q58710364Novel and Selective Triosephosphate Isomerase Inhibitors with Acaricidal Activity
Q64880222On the molecular and cellular effects of omeprazole to further support its effectiveness as an antigiardial drug.
Q36072507Pathological significance of mitochondrial glycation
Q39441306Phenotyping of tianma-stimulated differentiated rat neuronal b104 cells by quantitative proteomics
Q33615740Plasma amino acids and metabolic profiling of dairy cows in response to a bolus duodenal infusion of leucine
Q40973301Protein modification by dicarbonyl molecular species in neurodegenerative diseases
Q28578850Proteomic analysis of rat retina in a steroid-induced ocular hypertension model: potential vulnerability to oxidative stress
Q34215123Pyruvate kinase triggers a metabolic feedback loop that controls redox metabolism in respiring cells
Q38205957Rare hereditary red blood cell enzymopathies associated with hemolytic anemia - pathophysiology, clinical aspects, and laboratory diagnosis.
Q28588521Role of the glyoxalase system in astrocyte-mediated neuroprotection
Q27309025Structural and Genetic Studies Demonstrate Neurologic Dysfunction in Triosephosphate Isomerase Deficiency Is Associated with Impaired Synaptic Vesicle Dynamics
Q27650882Structural basis of human triosephosphate isomerase deficiency: mutation E104D is related to alterations of a conserved water network at the dimer interface
Q59336853Superhydrophobic lab-on-chip measures secretome protonation state and provides a personalized risk assessment of sporadic tumour
Q30317530Temporal dynamics of glyoxalase 1 in secondary neuronal injury
Q46927087The structural modification of DNA nucleosides by nonenzymatic glycation: an in vitro study based on the reactions of glyoxal and methylglyoxal with 2'-deoxyguanosine
Q40679294Triosephosphate isomerase deficiency: consequences of an inherited mutation at mRNA, protein and metabolic levels
Q35056697wasted away, a Drosophila mutation in triosephosphate isomerase, causes paralysis, neurodegeneration, and early death

Search more.