Zobrazeno 1 - 10
of 109
pro vyhledávání: '"Herbert J. Kayden"'
Publikováno v:
Journal of Lipid Research, Vol 47, Iss 6, Pp 1261-1273 (2006)
In hepatocytes, vitamin E is secreted via the efflux pathway and is believed to associate with apolipoprotein B (apoB)-lipoproteins extracellularly. The molecular mechanisms involved in the uptake, intracellular trafficking, and secretion of dietary
Externí odkaz:
https://doaj.org/article/0ccb30c5db3f4f72b2cf250afd822400
Publikováno v:
Journal of Lipid Research, Vol 14, Iss 5, Pp 533-540 (1973)
A relatively rapid procedure is described for the spectrophotometric determination of total tocopherol in red blood cells (RBC) based on a modification of the original Emmerie-Engel reaction. The critical feature in this method is the presence of a l
Externí odkaz:
https://doaj.org/article/6aa7a7b8e2fb4db2a712e0dbbf218f41
Publikováno v:
Journal of Lipid Research, Vol 47, Iss 6, Pp 1261-1273 (2006)
In hepatocytes, vitamin E is secreted via the efflux pathway and is believed to associate with apolipoprotein B (apoB)-lipoproteins extracellularly. The molecular mechanisms involved in the uptake, intracellular trafficking, and secretion of dietary
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::69d4c001865f9b497242ee0fb6dc87f2
https://doi.org/10.1194/jlr.m500523-jlr200
https://doi.org/10.1194/jlr.m500523-jlr200
Autor:
J. L. Mandel, Herbert J. Kayden, Laurence Reutenauer, Stephano Di Donato, L. Cavalier, Karim Ouahchi, Michel Koenig
Publikováno v:
The American Journal of Human Genetics. 62:301-310
Ataxia with vitamin E deficiency (AVED), or familial isolated vitamin E deficiency, is a rare autosomal recessive neurodegenerative disease characterized clinically by symptoms with often striking resemblance to those of Friedreich ataxia. We recentl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bed26aaf512e5fc64e2c18d3a5c1968c
https://doi.org/10.1086/301699
https://doi.org/10.1086/301699
Autor:
Herbert J. Kayden, Joseph E. Zerwekh, Erik G. Lund, Joachim Herz, Ingemar Björkhem, David W. Russell, Kenneth D.R. Setchell, Margrit Schwarz
Publikováno v:
Journal of Biological Chemistry. 271:18024-18031
Past experiments and current paradigms of cholesterol homeostasis suggest that cholesterol 7alpha-hydroxylase plays a crucial role in sterol metabolism by controlling the conversion of cholesterol into bile acids. Consistent with this conclusion, we
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d2de4b0a9d43c788db378b93fa66bf80
https://doi.org/10.1074/jbc.271.30.18024
https://doi.org/10.1074/jbc.271.30.18024
Autor:
Gustave A. Aguie, Daniel J. Rader, Véronique Clavey, Maret G. Traber, Graciela Castro, H. Bryan Brewer, Herbert J. Kayden, Jean Charles Fruchart, Gérard Torpier
Publikováno v:
Atherosclerosis. 118:183-191
Abetalipoproteinemia (ABL) and homozygous hypobetalipoproteinemia (HBL) are inherited disorders which are classically characterized by progressive retinal and spinocerebellar disease, fat-soluble vitamin deficiency, and absence of apolipoprotein (apo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a6d2accc4e69060d25725fe22a59b2d1
https://doi.org/10.1016/0021-9150(95)05605-x
https://doi.org/10.1016/0021-9150(95)05605-x
Autor:
Herbert J. Kayden, Maret G. Traber, Kathleen K. Sulik, Deborah B. Dehart, Gregg E. Homanics, Nobuyo Maeda
Publikováno v:
Teratology. 51:1-10
Apolipoprotein B (apoB) is a key structural component of several lipoproteins. These lipoproteins transport cholesterol, lipids, and vitamin E in the circulation. Humans that produce truncated forms of apoB have low plasma concentrations of apoB, bet
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3083b4621780d19682d6ae3215a3b3f0
https://doi.org/10.1002/tera.1420510102
https://doi.org/10.1002/tera.1420510102