Zobrazeno 1 - 10 of 94 pro vyhledávání: '"B M Tracey"'
1
Subunit molecular mass assignment of 14,654 Da to the soluble beta-galactoside-binding lectin from bovine heart muscle and demonstration of intramolecular disulfide bonding associated with oxidative inactivation
Autor: R A Carruthers, B M Tracey, B N Green, W M Abbott, Alexander M. Lawson, Ten Feizi
Publikováno v: Journal of Biological Chemistry. 267:10342-10347
The soluble dimeric beta-galactoside-binding lectin (subunit molecular mass, approximately 14 kDa) of bovine heart muscle, in common with the 14-kDa lectins of several other animal species, displays carbohydrate-binding activity when it is in the red
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::541dbb3b94fc265a6a4a887737e2306c
https://doi.org/10.1016/s0021-9258(19)50024-2
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2
Enzymologic Studies on Patients with Methylmalonic Aciduria: Basis for a Clinical Trial of Deoxyadenosylcobalamin in a Hydroxocobalamin-Unresponsive Patient
Autor: J. Mistry, Ronald A. Chalmers, M D Bain, C Weaver, B. M. Tracey
Publikováno v: Pediatric Research. 30:560-563
Eleven patients with methylmalonic aciduria have been classified on the basis of detailed enzymology on cultured skin fibroblasts. Nine were classified as mutase deficiencies and were unresponsive to hydroxocobalamin in vivo or in vitro. One was clas
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f2f737a228e552ebdf7a30aad0ab286e
https://doi.org/10.1203/00006450-199112000-00014
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3
Characterization of azo coupling adducts of benzenediazonium ions with aromatic amino acids in peptides and proteins
Autor: B M, Tracey, D E, Shuker
Publikováno v: Chemical research in toxicology. 10(12)
A synthetic peptide, VLSPADKTNWGHEYRMF(cmC)QIG, was reacted with 4-chlorobenzenediazonium hexafluorophosphate as a model for reactions of aromatic diazonium ions with proteins. At a ratio of diazonium ion to peptide of 0.8:1, three products could be
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::583b165e0a75e88a7916d82a6cb94c55
https://pubmed.ncbi.nlm.nih.gov/9437529
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5
The response to l-carnitine and glycine therapy in isovaleric acidaemia
Autor: Ronald A. Chalmers, C. de Sousa, C. M. Weaver, T. E. Stacey, B. M. Tracey, D. Bradley
Publikováno v: European Journal of Pediatrics. 144:451-456
The profound metabolic disturbances which occur in isovaleric acidaemia are due to the intramitochondrial accumulation of isovaleryl coenzyme A (CoA) with a consequent reduction in the availability of free CoA. Secondary carnitine insufficiency is al
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::399d17edeba789284e7aa78b60d911ca
https://doi.org/10.1007/bf00441737
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6
Urinary C6–C12 dicarboxylic acylcarnitines in Reye's syndrome
Autor: B. M. Tracey, Ronald A. Chalmers, J. Rosankiewicz, K. N. Cheng, T.E. Stacey
Publikováno v: Clinica Chimica Acta. 175:79-87
C6-C12 dicarboxylic acylcarnitines have been identified for the first time in urine from a 2-year-old girl presenting with Reye's syndrome. The acylcarnitines were extracted by ion-exchange chromatography and analysed, both underivatised and as methy
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a555fdc9c705ca5ce61d90102801aabc
https://doi.org/10.1016/0009-8981(88)90037-x
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7
Characterization of acylcarnitines as their isobutyl ester derivatives using fast atom bombardment mass spectrometry and constant neutral loss scan
Autor: R. A. Chalmers, B. M. Tracey, K. N. Cheng, J. Rosankiewicz
Publikováno v: Biological Mass Spectrometry. 18:668-672
A simple method is described for the characterization of acylcarnitines by fast atom bombardment mass spectrometry in combination with constant neutral loss (CNL) scan. Acylcarnitines in urine are extracted using cation-exchange chromatography and de
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::69bf59873ed9cc07a112c8d099d5df8a
https://doi.org/10.1002/bms.1200180906
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8
Metabolic response to carnitine in methylmalonic aciduria. An effective strategy for elimination of propionyl groups
Autor: David S. Millington, T. E. Stacey, Charles L. Hoppel, B. M. Tracey, R A Chalmers, C R Roe
Publikováno v: Archives of Disease in Childhood. 58:916-920
Patients with methylmalonic aciduria have an excessive intramitochondrial accumulation of acylcoenzyme A compounds that may reduce the availability of free coenzyme A (CoA) for normal metabolic requirements, producing profound metabolic disturbances.
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3c44ba83aa78566d3ebbbba3a427ef40
https://doi.org/10.1136/adc.58.11.916
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9
Studies on abnormal metabolic function in Reye's syndrome
Autor: Ronald A. Chalmers, H. B. Valman, P. Purkiss, T. E. Stacey, N.R. English, A. Mehta, B. M. Tracey
Publikováno v: Journal of Inherited Metabolic Disease. 10:263-265
(1) The presence of medium chain dicarboxylic acylcarnitines and 3-hydroxydicarboxylic acids in the urine of a patient with Reye's syndrome suggests that β-oxidation of dicarboxylic acids to succinyl CoA is occurring but also being inhibited at seve
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::877035a30e2d787ef75a5c5c3ba52c4a
https://doi.org/10.1007/bf01811421
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