Výsledky vyhledávání - "M E Balestra"

Akademický článek

Isolation of allele-specific, receptor-binding-defective low density lipoproteins from familial defective apolipoprotein B-100 subjects.

Autor: K S Arnold, M E Balestra, R M Krauss, L K Curtiss, S G Young, T L Innerarity

Publikováno v: Journal of Lipid Research, Vol 35, Iss 8, Pp 1469-1476 (1994)

Familial defective apolipoprotein B-100 (FDB) is a genetic disorder apparently caused by a single amino acid substitution (Arg3500–>Gln) that disrupts the binding of low density lipoproteins (LDL) to the LDL receptor. The plasma of FDB heterozygote

Externí odkaz: https://doaj.org/article/b80692fa64d2496c8a5b1a82a01aefe9

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DGAT1 promoter polymorphism associated with alterations in body mass index, high density lipoprotein levels and blood pressure in Turkish women

Autor: Erwin H, Ludwig, R W, Mahley, E, Palaoglu, S, Ozbayrakçi, M E, Balestra, I B, Borecki, T L, Innerarity, R V, Farese

Publikováno v: Clinical genetics. 62(1)

Triglyceride synthesis is catalyzed by acyl CoA:diacylglycerol acyltransferases (DGAT), microsomal enzymes that use diacylglycerol and fatty acyl CoAs as substrates. Because DGAT1 expression is up-regulated during adipocyte differentiation and DGAT1

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::9ca4e332c5a3ea83c3449b55fe955907
https://pubmed.ncbi.nlm.nih.gov/12123490

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Human apolipoprotein E7:lysine mutations in the carboxy-terminal domain are directly responsible for preferential binding to very low density lipoproteins

Autor: J, Dong, M E, Balestra, Y M, Newhouse, K H, Weisgraber

Publikováno v: Journal of lipid research. 41(11)

Apolipoprotein E7 (apoE7) (apoE3 E244K/E245K) is a naturally occurring mutant in humans that is associated with increased plasma lipid levels and accelerated atherosclerosis. It is reported to display defective binding to low density lipoprotein (LDL

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::ff110e803eec1e722179a0febbf2b204
https://pubmed.ncbi.nlm.nih.gov/11060347

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Cloning and mutagenesis of the rabbit ApoB mRNA editing protein. A zinc motif is essential for catalytic activity, and noncatalytic auxiliary factor(s) of the editing complex are widely distributed

Autor: S, Yamanaka, K S, Poksay, M E, Balestra, G Q, Zeng, T L, Innerarity

Publikováno v: The Journal of biological chemistry. 269(34)

Apolipoprotein (apo) B mRNA editing is the specific deamination of cytidine (nucleotide 6666) to uridine in apoB mRNA. We isolated a full-length cDNA clone encoding the rabbit apoB mRNA editing protein (REPR), a subunit of the editing complex. Rabbit

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::f970637526bd1710f632a21536f12bdd
https://pubmed.ncbi.nlm.nih.gov/8063816

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