Zobrazeno 1 - 10
of 17
pro vyhledávání: '"J L Adolphson"'
Publikováno v:
Journal of Lipid Research, Vol 22, Iss 8, Pp 1206-1213 (1981)
The relationship between plasma lecithin:cholesterol acyltransferase mass and enzyme activity and between mass and plasma cholesterol esterification rate was determined in 25 adult volunteers without overt disease (14 normolipidemic and 11 hyperlipid
Externí odkaz:
https://doaj.org/article/bb0326169d0b499d956515842987424c
Publikováno v:
Journal of Lipid Research, Vol 18, Iss 3, Pp 331-338 (1977)
A quantitative immunodiffusion assay demonstrated Lp(a) lipoprotein in 91% (911 of 1000) of subjects. In order to quantitate Lp(a) in all plasma, a sensitive and specific double antibody radioimmunoassay was developed. The between-assay coefficient o
Externí odkaz:
https://doaj.org/article/56431ed3aac44005a9b0bbca95420587
Publikováno v:
Journal of Lipid Research, Vol 26, Iss 8, Pp 995-1001 (1985)
Radial immunodiffusion (RID) has been used for determination of low density lipoprotein (LDL) B protein in plasma. During measurement of B protein in plasma and the d less than and d greater than 1.019 g/ml plasma fractions by RID in 1.0%, 1.5%, 2.0%
Externí odkaz:
https://doaj.org/article/49828ce50775464eb2447d1ef64ca237
Autor:
J L Adolphson, J J Albers
Publikováno v:
Journal of Lipid Research, Vol 30, Iss 4, Pp 597-606 (1989)
Normotriglyceridemic and hypertriglyceridemic samples were analyzed for apoproteins A-I and B using the Beckman Array System and the Behring Nephelometer, and the nephelometric values were compared to values obtained by highly standardized radioimmun
Externí odkaz:
https://doaj.org/article/18ed935613694ba69f16edfddcbbb8e0
Autor:
J R McNamara, H Campos, J L Adolphson, J M Ordovas, P W Wilson, J J Albers, D C Usher, E J Schaefer
Publikováno v:
Journal of Lipid Research, Vol 30, Iss 5, Pp 747-755 (1989)
Plasma was screened for the presence of lipoprotein[a] using 2-16% nondenaturing, polyacrylamide gradient gel electrophoresis. Gels were scanned with a densitometer after staining with Sudan black B. Bands that migrated above low density lipoprotein
Externí odkaz:
https://doaj.org/article/584383e6ebbb4be88b3bb54195caf97a
Autor:
J J Albers, J L Adolphson
Publikováno v:
Journal of Lipid Research, Vol 29, Iss 1, Pp 102-108 (1988)
There has recently been a proliferation of commercial kits available for apoproteins A-I and B. Since reference procedures for apoproteins have not yet been established we have elected to compare apoprotein kit methods with highly standardized apopro
Externí odkaz:
https://doaj.org/article/8cf1148f1c154a398ddbddb9e32ed665
Autor:
J R, Day, J J, Albers, C E, Lofton-Day, T L, Gilbert, A F, Ching, F J, Grant, P J, O'Hara, S M, Marcovina, J L, Adolphson
Publikováno v:
The Journal of biological chemistry. 269(12)
Phospholipid transfer protein, with an apparent molecular mass of 81 kDa, was purified from human plasma. The NH2-terminal amino acid sequence of a 51-kDa proteolytic fragment obtained from phospholipid transfer protein allowed degenerate primers to
Publikováno v:
Clinical chemistry. 36(2)
A common accuracy-based standardization program is indispensable for establishing reference intervals for the clinical use of apolipoproteins. The development and distribution of reference materials and quality-control materials that do not exhibit m
Autor:
Ernst J. Schaefer, Hannia Campos, Peter W.F. Wilson, Judith R. McNamara, Jose M. Ordovas, J. J. Albers, D. C. Usher, J. L. Adolphson
Publikováno v:
Scopus-Elsevier
Journal of Lipid Research, Vol 30, Iss 5, Pp 747-755 (1989)
Journal of Lipid Research, Vol 30, Iss 5, Pp 747-755 (1989)
Plasma was screened for the presence of lipoprotein[a] using 2-16% nondenaturing, polyacrylamide gradient gel electrophoresis. Gels were scanned with a densitometer after staining with Sudan black B. Bands that migrated above low density lipoprotein
Publikováno v:
Journal of Clinical Investigation. 67:141-148
A sensitive and precise competitive-displacement double-antibody radioimmunoassay was developed for the human plasma enzyme lecithin-cholesterol acyltransferase (LCAT; Ec 2.3 1.43). The ability of plasma from various animal species to displace labele