Pages that link to "Q33821952"
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The following pages link to Atypical familial dysbetalipoproteinemia associated with apolipoprotein phenotype E3/3. (Q33821952):
Displaying 36 items.
- Familial apolipoprotein E deficiency (Q24299817) (← links)
- Apo E variants in patients with type III hyperlipoproteinemia (Q28236370) (← links)
- Genetic heterogeneity of apolipoprotein E and its influence on plasma lipid and lipoprotein levels (Q28306136) (← links)
- Sequence diversity and large-scale typing of SNPs in the human apolipoprotein E gene (Q30947195) (← links)
- Receptor-mediated mechanisms of lipoprotein remnant catabolism (Q33597635) (← links)
- Cholesteryl ester accumulation in mouse peritoneal macrophages induced by β-migrating very low density lipoproteins from patients with atypical dysbetalipoproteinemia (Q33822341) (← links)
- Type III hyperlipoproteinemic phenotype in transgenic mice expressing dysfunctional apolipoprotein E. (Q33902876) (← links)
- Variable expression of familial dysbetalipoproteinemia in apolipoprotein E*2 (Lys146-->Gln) Allele carriers (Q34185850) (← links)
- Familial dysbetalipoproteinemia associated with apolipoprotein E3-Leiden in an extended multigeneration pedigree (Q34194380) (← links)
- Molecular etiology of a dominant form of type III hyperlipoproteinemia caused by R142C substitution in apoE4 (Q34395148) (← links)
- Fat feeding in humans induces lipoproteins of density less than 1.006 that are enriched in apolipoprotein [a] and that cause lipid accumulation in macrophages (Q34522075) (← links)
- Pre-beta-very low density lipoproteins as precursors of beta-very low density lipoproteins. A model for the pathogenesis of familial dysbetalipoproteinemia (type III hyperlipoproteinemia) (Q34560246) (← links)
- Type III hyperlipoproteinemia associated with apolipoprotein E phenotype E3/3. Structure and genetics of an apolipoprotein E3 variant (Q34569772) (← links)
- High receptor binding affinity of lipoproteins in atypical dysbetalipoproteinemia (type III hyperlipoproteinemia) (Q34581286) (← links)
- A novel electrophoretic variant of human apolipoprotein E. Identification and characterization of apolipoprotein E1 (Q34607518) (← links)
- Comprehensive evaluation of the association of APOE genetic variation with plasma lipoprotein traits in U.S. whites and African blacks (Q34689708) (← links)
- Apolipoprotein E2-Christchurch (136 Arg----Ser). New variant of human apolipoprotein E in a patient with type III hyperlipoproteinemia (Q35577335) (← links)
- Dominant expression of type III hyperlipoproteinemia. Pathophysiological insights derived from the structural and kinetic characteristics of ApoE-1 (Lys146-->Glu) (Q35753304) (← links)
- NMR studies of the low-density lipoprotein receptor-binding peptide of apolipoprotein E bound to dodecylphosphocholine micelles (Q36281647) (← links)
- Exploratory data analysis of hyperlipidemia on the Macintosh: software tools for analysis of biochemical, clinical, and genetic variables in 1677 consecutive lipid clinic patients (Q36757274) (← links)
- Lipoproteins of special significance in atherosclerosis. Insights provided by studies of type III hyperlipoproteinemia (Q39498138) (← links)
- Classification of primary dyslipoproteinemias. (Q39820316) (← links)
- Apolipoprotein E: structure-function relationships (Q40737965) (← links)
- The underlying molecular mechanism of apolipoprotein E polymorphism: relationships to lipid disorders, cardiovascular disease, and Alzheimer's disease. (Q41161234) (← links)
- Apolipoprotein E polymorphism in The Netherlands and its effect on plasma lipid and apolipoprotein levels (Q41404082) (← links)
- The functional characteristics of a human apolipoprotein E variant (cysteine at residue 142) may explain its association with dominant expression of type III hyperlipoproteinemia (Q43755287) (← links)
- LDL receptor deficiency or apoE mutations prevent remnant clearance and induce hypertriglyceridemia in mice (Q43916892) (← links)
- Hypolipidemic and hyperlipidemic phenotypes in transgenic mice expressing human apolipoprotein E2. (Q45948223) (← links)
- Lipoprotein glomerulopathy associated with psoriasis vulgaris: report of 2 cases with apolipoprotein E3/3 (Q64048577) (← links)
- Apolipoprotein E-C1-C4-C2 gene cluster region and inter-individual variation in plasma lipoprotein levels: a comprehensive genetic association study in two ethnic groups (Q64121082) (← links)
- Expression of type III hyperlipoproteinemia in an adolescent patient with hypothyroidism (Q68416884) (← links)
- Pharmacological treatment of lipid disorders in diabetes mellitus (Q69126606) (← links)
- Apolipoprotein E3-Leiden. A new variant of human apolipoprotein E associated with familial type III hyperlipoproteinemia (Q69547644) (← links)
- Lipoprotein abnormalities in insulin-dependent diabetes mellitus (Q69880900) (← links)
- Familial disorders of plasma apolipoproteins (Q69951162) (← links)
- Apolipoprotein epsilon 2/3 genotype and type III hyperlipoproteinemia among Taiwanese (Q73126921) (← links)