17 results on '"Pajukanta P"'
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2. Plasma acylation stimulating protein and C3 in FCHL families
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3. Fine mapping of the human familial combined hyperlipidemia locus on chromosome 1q21-q23 using conserved synteny to the mouse locus on chromosome 3
4. Small low density lipoprotein particles in familial combined hyperlipidemia
5. A Genome-wide scan for low HDL-Cholesterol in genetically isolated finnish families with premature coronary heart disease
6. Isolated low HDL-cholesterol syndrome in finnish families with premature CAD
7. 1.P.131 The occurrence of small dense low density lipoprotein particles in familial combined hyperlipidemia
8. 1.P.260 Candidate gene analysis in familial combined hyperlipidemia
9. Reduced hormone-sensitive lipase activity is not a major metabolic defect in Finnish FCHL families
10. Phenotype expression in familial combined hyperlipidemia
11. Serum complement and familial combined hyperlipidemia
12. Association between the apolipoprotein B signal peptide insertion/deletion and Xbal polymorphisms and plasma lipid response to diet intervention
13. XbaI polymorphism of apolipoprotein B and factor VII coagulant activity: a dietary intervention study
14. Family-specific aggregation of lipid GWAS variants confers the susceptibility to familial hypercholesterolemia in a large Austrian family.
15. A novel nonsense apolipoprotein A-I mutation (apoA-I(E136X)) causes low HDL cholesterol in French Canadians.
16. A candidate gene study in low HDL-cholesterol families provides evidence for the involvement of the APOA2 gene and the APOA1C3A4 gene cluster.
17. The effects of the apolipoprotein B signal peptide (ins/del) and XbaI polymorphisms on plasma lipid responses to dietary change.
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