Zobrazeno 1 - 10
of 62
pro vyhledávání: '"June K Lloyd"'
Publikováno v:
Acta Medica Scandinavica. 224:135-139
The lecithin: cholesterol acyltransferase (LCAT) activity of lipoprotein-depleted plasma from a patient with abetalipoproteinemia has been assayed in a modified Glomset-Wright incubation system with three different normal lipoprotein substrates consi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c08858887bb30a316a275271ff1977ca
https://doi.org/10.1111/j.0954-6820.1988.tb16751.x
https://doi.org/10.1111/j.0954-6820.1988.tb16751.x
Publikováno v:
Journal of Lipid Research, Vol 9, Iss 5, Pp 661-666 (1968)
Analysis of serum free fatty acids by gas-liquid chromatography showed high proportions (27-57%) of octanoic acid for up to 4 hr after the ingestion of a single oral load of medium-chain triglyceride (approximately 1 g/kg body weight) in four volunte
Externí odkaz:
https://doaj.org/article/dbd72923f5f54e45bcc3edcb5ce52341
Autor:
F. Mailly, Paul N. Durrington, Francesco Angelico, P.J. Talmud, John Betteridge, Jutta Palmen, John D. Brunzell, Gerald F. Watts, T Gibbs, Hans Lithell, DP Muller, S. E. Humphries, K.A. Mitropoulos, June K. Lloyd
Publikováno v:
Human Mutation. 10:465-473
The aim of this study was to identify mutations in the lipoprotein lipase (LPL) gene in 20 unrelated patients with familial lipoprotein deficiency (FLLD) and to investigate the genotype/phenotype relationship. The previously reported G188E mutation (
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1272ba52a943d658dce080b3935e0988
https://doi.org/10.1002/(sici)1098-1004(1997)10:6<465::aid-humu8>3.0.co
https://doi.org/10.1002/(sici)1098-1004(1997)10:6<465::aid-humu8>3.0.co
Autor:
June K. Lloyd
Publikováno v:
Acta Paediatrica. 79:6-11
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9ec38de7857d949057e26aeb1681909e
https://doi.org/10.1111/j.1651-2227.1990.tb11322.x
https://doi.org/10.1111/j.1651-2227.1990.tb11322.x
Publikováno v:
ResearcherID
A boy with a total plasma cholesterol concentration of 20.9 mmol/l which fell significantly with a low fat diet, cholestyramine and simvastatin, was shown to have two different mutations in the low density lipoprotein receptor gene, demonstrating tha
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::61635c8c2c946ff5985d1ecad3e4ca59
https://doi.org/10.1136/adc.73.6.538
https://doi.org/10.1136/adc.73.6.538
Autor:
June K. Lloyd
Publikováno v:
Acta paediatrica Scandinavica. Supplement. 373
Hypercholesterolemia is a major risk factor for coronary heart disease and may present during childhood. Dietary measures can reduce plasma cholesterol and may thus delay or prevent the development of the atherosclerotic process. Although plasma chol
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cc3073bf5b478c6136e11fe93047e3ef
https://pubmed.ncbi.nlm.nih.gov/1927531
https://pubmed.ncbi.nlm.nih.gov/1927531
Autor:
June K. Lloyd
Publikováno v:
European Journal of Vascular Surgery. 4:435-436
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::85792f68ac6e806c91277cbe6b6bf6eb
https://doi.org/10.1016/s0950-821x(05)80883-7
https://doi.org/10.1016/s0950-821x(05)80883-7
Autor:
June K. Lloyd, Hans Lithell, M.I. Mackness, P.J. Talmud, P.A. Durrington, S. Mc Carthy, S.E. Humiphries, John Betteridge, F. Mailly, DP Muller
Publikováno v:
Atherosclerosis. 98:118-118
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8c2c8790de12334df4fae82f8d8cf6de
https://doi.org/10.1016/0021-9150(93)90240-u
https://doi.org/10.1016/0021-9150(93)90240-u
Autor:
Ross W. Milne, Sally Robertson, James F. Scott, Clive R. Pullinger, Timothy J. Knott, L. M. Powell, D. P. R. Muller, Norman E. Miller, Philippa J. Talmud, Steve E. Humphries, Yves L. Marcel, S. Wallis, David R. Collins, Richard J. Pease, June K. Lloyd
Publikováno v:
Nucleic Acids Research. 16:8361-8375
Familial hypobetalipoproteinaemia is a rare autosomal dominant disorder in which levels of apo-B-containing plasma lipoproteins are approximately half-normal in heterozygotes and virtually absent in homozygotes. Here we describe mutations of the apo-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a7a1132225689b3dd60818b749a9e39d
https://doi.org/10.1093/nar/16.17.8361
https://doi.org/10.1093/nar/16.17.8361