Mastrogiacomo, Frank; Université de Liège - ULiège > Département des sciences biomédicales et précliniques > Biochimie et physiologie humaine et pathologique
Koike M, Kichiko K. Structure, assembly and function of mammalian α-keto acid dehydrogenase complexes. Adv Biophys 1976;9:187-227
Yeaman SJ. The mammalian 2-oxoacid dehydrogenases: a complex family. Trends Biochem Sci 1986;11:293-296
Rice JE, Dunbar B, Lindsay JG. Sequences directing dihydrolipoamide dehydrogenase (E3) binding are located on the 2-oxoglutarate dehydrogenase (E1) component of the mammalian 2-oxoglutarate dehydrogenase multienzyme complex. EMBO J 1992;11:322-335
Gibson GE, Sheu K-FR, Blass JP, et al. Reduced activities of thiamine-dependent enzymes in the brains and peripheral tissues of patients with Alzheimer's disease. Arch Neurol 1988; 45:836-840
Butterworth RF, Besnard AM. Thiamine-dependent enzyme changes in temporal cortex of patients with Alzheimer's disease. Metab Brain Dis 1990;4:179-184
Sheu K-FR, Cooper AJL, Koike K, et al. Abnormality of the α-ketoglutarate dehydrogenase complex in fibroblasts from familial Alzheimer's disease. Ann Neurol 1994;35:312-318
Beal MF. Does impairment of energy metabolism result in excitotoxic neuronal death in neurodegenerative illnesses? Ann Neurol 1992;31:119-130
Kish SJ, Bergeron C, Rajput A, et al. Brain cytochrome oxidase in Alzheimer's disease. J Neurochem 1992;59:776-779
Mirra SS, Heyman A, McKeel D, et al. The Consortium to Establish Assessment of Alzheimer's Disease (CERAD). Part II. Standardization of the neuropathologic assessment of Alzheimer's disease. Neurology 1991;41:479-486
Kennedy AM, Newman SK, Frackowiak RSJ, et al. Chromosome 14 linked familial Alzheimer's disease. A clinicopathological study of a single pedigree. Brain 1995;118:185-205
Kish SJ, Dixon LM, Sherwin AL. Aspartic acid aminotransferase activity is increased in actively spiking compared with non-spiking human epileptic cortex. J Neurol Neurosurg Psychiatry 1988;51:552-556
Hunter A, Lindsay JG. Immunological and biosynthetic studies on the mammalian 2-oxoglutarate dehydrogenase multienzyme complex. Eur J Biochem 1986;155:103-109
Lindsay JG. Targeting of the 2-oxo acid dehydrogenase complexes to the mitochondrion. Ann NY Acad Sci 1989;573: 254-266
Fonnum F. A rapid radiochemical method for the determination of choline acetyltransferase. J Neurochem 1975;24:407-409
Sheu K-FR, Kim Y-T, Blass JP, Weksler ME. An immunochemical study of the pyruvate dehydrogenase deficit in Alzheimer's disease brain. Ann Neurol 1985;17:444-449
Calingasan NY, Baker H, Sheu K-FR, Gibson GE. Distribution of the α-ketoglutarate dehydrogenase complex in rat brain. J Comp Neurol 1994;346:461-479
Nakano K, Matuda S, Yamanaka T, et al. Purification and molecular cloning of succinyltransferase of the rat α-ketoglutarate dehydrogenase complex. J Biol Chem 1991;266:19013-19017
Perry EK, Perry RH, Tomlinson BE, et al. Coenzyme A-acetylating enzymes in Alzheimer's disease: possible cholinergic 'compartment' of pyruvate dehydrogenase. Neurosci Lett 1980; 18:105-110
Sheu K-FR, Clarke DD, Kim Y-T, et al. Studies of transketolase abnormality in Alzheimer's disease. Arch Neurol 1988; 45:841-845
Sorbi S, Bird ED, Blass JP. Decreased pyruvate dehydrogenase complex activity in Huntington and Alzheimer brain. Ann Neurol 1983;13:72-78
Yates CM, Butterworch J, Tennant MC, Gordon A. Enzyme activities in relation to pH and lactate in postmortem brain in Alzheimer-type and other dementias. J Neurochem 1990;55: 1624-1630
Mastrogiacomo F, Bettendorff L, Grisar T, Kish SJ. Brain thiamine, its phosphate esters, and its metabolizing enzymes in Alzheimer's disease. Ann Neurol 1996;39:585-591
Neagle JC, Lindsay JG. Selective proteolysis of the protein X subunit of the bovine heart pyruvate dehydrogenase complex. Biochem J 1991;278:423-427
Mizuno Y, Matuda S, Yoshino H, et al. An immunohistochemical study on α-ketoglutarate dehydrogenase complex in Parkinson's disease. Ann Neurol 1994;35:204-210
Butterworth RF, Kril JJ, Harper CG. Thiamine-dependent enzyme changes in the brains of alcoholics: relationship to the Wernicke-Korsakoff syndrome. Alcohol Clin Exp Res 1993;17: 1084-1088
Mastrogiacomo F, La Marche J, Dožić S, et al. Immunoreactive levels of α-ketoglutarate dehydrogenase subunits in Friedreich's ataxia and spinocerebellar ataxia type 1. Neurodegeneration 1996 (in press)
Al Aqeel A, Rashed M, Ozand PT, et al. A new patient with α-ketoglutaric aciduria and progressive extrapyramidal tract disease. Brain Dev 1994;16(suppl):33-37
Gabudza DH, Busciglio J, Chen LB, et al. Inhibition of energy metabolism alters the processing of amyloid precursor protein and induces a potentially amyloidogenic derivative. J Biol Chem 1994;269:13623-13628
