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Structure-Function Relationships of Apolipoprotein B-100
1993Apolipoprotein (apo) B-100 is a huge protein that has been difficult to study by traditional protein chemistry techniques. Other experimental approaches, such as investigations in cultured cells, and in human subjects with specific apoB mutations also have their limitations a novel approach using transgenic mice has yielded interesting information on ...
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Haplotype analysis of apolipoprotein B-100 in subjects with familial defective apolipoprotein B-100
2002Obiteljska pogreška u strukturi apolipoproteina B-100 je autosomno dodominantni premećaj zbog mutacije R3500Q gena za apolipoprotein B. Skupljeni su uzorci krvi 1489 ispitanika s hiperkolesterolemijom i/ili bolešću koronarnih arterija. Restrikcijskom izotipizacijom analiziran je ulomak DNA koji sadržava kodon 3500 gena za apo B.
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Atherosclerosis, 2007
The objective of this study was to examine frequency of familial defective apo-B-100 (FDB, R3500Q mutation) in probands with the phenotype of familial hypercholesterolemia (FH) and in the general population of 40-year-old subjects in Slovakia and to characterize their lipid and clinical criteria and to compare the frequency of FDB with other ...
Juraj, Gasparovic +5 more
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The objective of this study was to examine frequency of familial defective apo-B-100 (FDB, R3500Q mutation) in probands with the phenotype of familial hypercholesterolemia (FH) and in the general population of 40-year-old subjects in Slovakia and to characterize their lipid and clinical criteria and to compare the frequency of FDB with other ...
Juraj, Gasparovic +5 more
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JAMA, 1989
A 43-year-old woman with severe coronary artery disease and hyperapobetalipoproteinemia was heterozygous for an abnormal Msp I apolipoprotein B (APOB) gene fragment because of the absence of the MspI site around codon 4046 in exon 29 of the APOB gene.
J A, Ladias +7 more
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A 43-year-old woman with severe coronary artery disease and hyperapobetalipoproteinemia was heterozygous for an abnormal Msp I apolipoprotein B (APOB) gene fragment because of the absence of the MspI site around codon 4046 in exon 29 of the APOB gene.
J A, Ladias +7 more
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Familial defective apolipoprotein B-100 in Slovakia
Atherosclerosis, 2007Juraj Gašparovič +5 more
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[Apolipoprotein B-100 variants].
Ryoikibetsu shokogun shirizu, 1998A, Nohara, H, Mabuchi
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Ligand-defective Apolipoprotein B-100, Familial
2009Alexander K. C. Leung +126 more
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Familial Ligand-defective Apolipoprotein B-100
2009Robert J. Desnick +48 more
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Presence of Apolipoprotein B‐100 in Human Intestine Epithelial Cells
Annals of the New York Academy of Sciences, 1997M, Tamura +6 more
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