Zobrazeno 1 - 10
of 144
pro vyhledávání: '"C.J. Danpure"'
Publikováno v:
Nephron. 55:336-337
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::10539f4edbacad93648ab7dff5f288ab
https://doi.org/10.1159/000185987
https://doi.org/10.1159/000185987
Publikováno v:
Pediatric Neurology. 11:144
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a5d9b26174e0baa3c728dff3cf5c6b65
https://doi.org/10.1016/0887-8994(94)90375-1
https://doi.org/10.1016/0887-8994(94)90375-1
Publikováno v:
Clinical Science. 70:417-425
1. The subcellular distribution of 2-oxoglutarate:glyoxylate carboligase was investigated in a normal human liver, a liver from a patient with pyridoxine-resistant primary hyperoxaluria type I and rat livers subjected to various degrees and types of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e734a1c96e1ee175231398a226c694a4
https://doi.org/10.1042/cs0700417
https://doi.org/10.1042/cs0700417
Publikováno v:
FEBS Letters. 222:17-20
Immunoblotting of human liver sonicates, after SDS-polyacrylamide gel electrophoresis, demonstrated the presence of a 40 kDa protein, corresponding to the subunit of alanine:glyoxylate aminotransferase, in six controls and three patients with primary
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7499c28adc208825a5ebaa2cbe2bc524
https://doi.org/10.1016/0014-5793(87)80183-7
https://doi.org/10.1016/0014-5793(87)80183-7
Publikováno v:
Clinica Chimica Acta. 81:87-97
Three techniques of gold analysis, flame and electrothermal atomic absorption spectrometry and neutron activation analysis, have been compared, using plasma and plasma fractions (derived by gel chromatography) from rheumatoid patients receiving aurot
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bb849877f65a61e36ee8e8b4c873fd53
https://doi.org/10.1016/0009-8981(77)90416-8
https://doi.org/10.1016/0009-8981(77)90416-8
Publikováno v:
Journal of Inherited Metabolic Disease. 12:286-288
Primary hyperoxaluria type 1 (PH1; McKusick 25990) is an autosomal recessive inborn error of glyoxylate metabolism which leads to excessive synthesis of oxalate and glycolate. The low solubility of calcium oxalate causes all the pathological manifest
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ede04c1ca832f1d7a00708413a5b7a9f
https://doi.org/10.1007/bf03335400
https://doi.org/10.1007/bf03335400
Autor:
M.A. Mansell, C.J. Danpure, Keith Rolles, Richard W. E. Watts, Roger Williams, R. Y. Calne, P. Purkiss, S.H. Morgan
Publikováno v:
Lancet (London, England). 2(8557)
A patient with primary hyperoxaluria type 1 (hepatic peroxisomal alanine:glyoxylate aminotransferase [EC 2.6.1.44] deficiency) was successfully treated by combined hepatic and renal transplantation. The metabolic lesion was corrected by replacement o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ba8c4374d01149f5a3d64c3fadfddb16
https://pubmed.ncbi.nlm.nih.gov/2887776
https://pubmed.ncbi.nlm.nih.gov/2887776
Autor:
C.J. Danpure, P.R Jennings
Publikováno v:
FEBS letters. 201(1)
Activities of alanine:glyoxylate aminotransferase in the livers of two patients with primary hyperoxaluria type I were substantially lower than those found in five control human livers. Detailed subcellular fractionation of one of the hyperoxaluric l
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4888fedc28382bcb0d1320e7ef01de83
https://pubmed.ncbi.nlm.nih.gov/3709805
https://pubmed.ncbi.nlm.nih.gov/3709805
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