Zobrazeno 1 - 10
of 324
pro vyhledávání: '"P, Kwiterovich"'
Autor:
Peter O. Kwiterovich, Jr., Shirley C. Chen, Donna G. Virgil, Amy Schweitzer, Dagmar R. Arnold, Lisa E. Kratz
Publikováno v:
Journal of Lipid Research, Vol 44, Iss 6, Pp 1143-1155 (2003)
Twelve obligate heterozygotes from two kindreds were ascertained through phytosterolemic probands homozygous for molecular defects in the ATP binding cassette (ABC) half transporter, ABCG8. The response of these heterozygotes to a Step 1 diet low in
Externí odkaz:
https://doaj.org/article/baa91e6ca9f34b8b9ca19d0cb5ad3ead
Publikováno v:
Journal of Lipid Research, Vol 36, Iss 5, Pp 931-938 (1995)
Previous mutations associated with lecithin:cholesterol acyltransferase (LCAT) deficiency have been identified using genomic DNA. To facilitate mutation analysis, we used cDNA from cultured fibroblasts which were shown to express LCAT mRNA. Using rev
Externí odkaz:
https://doaj.org/article/554891dcbb424c9c84c8d941045a2863
Publikováno v:
Journal of Lipid Research, Vol 34, Iss 10, Pp 1687-1697 (1993)
Low density lipoprotein (LDL) physical-chemical characteristics were studied as nontraditional risk factors of coronary artery disease (CAD) in a well-characterized population of 98 men aged < or = 50 and 100 women aged < or = 60 who underwent electi
Externí odkaz:
https://doaj.org/article/8be61030c05b45e3b2e6e7d79c33cc07
Autor:
B. Musser, John P. Kane, K. von Bergmann, D. Lütjohann, P. Stein, Shailendra B. Patel, T. Musliner, P. Kwiterovich, G. Salen
Publikováno v:
Circulation. 109:966-971
Background— Sitosterolemia is a recessively inherited disorder that results from mutations in either ABCG5 or G8 proteins, with hyperabsorption of dietary sterols and decreased hepatic excretion of plant sterols and cholesterol. As a consequence of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1be082b8d9581b42472d4e9b00c6177b
https://doi.org/10.1161/01.cir.0000116766.31036.03
https://doi.org/10.1161/01.cir.0000116766.31036.03
Publikováno v:
Journal of Lipid Research, Vol 23, Iss 8, Pp 1236-1242 (1982)
We determined the effect of storage at -70 degrees C on the determination of plasma high density lipoprotein (HDL)-cholesterol. Plasma from 106 subjects was stored for 1, 6, and 12 months, then treated with heparin and MnCl2 to remove other lipoprote
Externí odkaz:
https://doaj.org/article/f69065c83d6c47969f79ee458d4b5d92
Publikováno v:
Journal of Lipid Research, Vol 23, Iss 4, Pp 513-522 (1982)
The content of glycosphingolipids (GSL) was studied in the urinary sediments (24-hr specimens) from seven normal subjects, a patient with Fabry's disease, and five homozygotes with familial hypercholesterolemia (FH). Normal urinary sediments containe
Externí odkaz:
https://doaj.org/article/d6ac84118a7842eb8afaafdf89ad0ccf
Publikováno v:
Journal of Lipid Research, Vol 21, Iss 5, Pp 608-616 (1980)
This study was performed to determine the effect of frozen and unfrozen storage on plasma high density lipoprotein (HDL) cholesterol analysis. HDL-cholesterol was determined, following removal of the other lipoproteins by precipitation with heparin a
Externí odkaz:
https://doaj.org/article/f72512d13f374491996204173b9b3325
Publikováno v:
Journal of Lipid Research, Vol 26, Iss 2, Pp 203-209 (1985)
We have measured plasma sterol composition in 14 subjects with sitosterolemia and xanthomatosis. In addition to elevated plasma phytosterol (campesterol 16 +/- 7 mg/dl and sitosterol 35 +/- 16 mg/dl) and normal to moderately high cholesterol levels (
Externí odkaz:
https://doaj.org/article/d72646ae98034347a6d37e99c82226e5
Publikováno v:
Journal of Lipid Research, Vol 30, Iss 3, Pp 387-394 (1989)
A pedigree consisting of 103 New Zealand White hyperlipidemic and normal rabbits was used in a genetic analysis of total cholesterol and triglyceride levels to test for Mendelian control of hyperlipidemia. The founder male of this pedigree was identi
Externí odkaz:
https://doaj.org/article/acfa467b278647c493597104148ecb2a
Publikováno v:
Journal of Lipid Research, Vol 11, Iss 4, Pp 322-330 (1970)
An analysis of the lipids in normal human liver is presented which is particularly designed to assist in the classification and study of lipid-storage diseases. Special emphasis has been given to a determination of the quantity and composition of the
Externí odkaz:
https://doaj.org/article/d1c1a66044aa4d729d31aa0ec40693db