Pages that link to "Q44274905"
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The following pages link to Interaction between the LDL-receptor gene bearing a novel mutation and a variant in the apolipoprotein A-II promoter: molecular study in a 1135-member familial hypercholesterolemia kindred (Q44274905):
Displaying 19 items.
- Dissection of a QTL hotspot on mouse distal chromosome 1 that modulates neurobehavioral phenotypes and gene expression (Q33384434) (← links)
- Genomic susceptibility Loci for brain atrophy, ventricular volume, and leukoaraiosis in hypertensive sibships (Q33689539) (← links)
- APOA2, dietary fat, and body mass index: replication of a gene-diet interaction in 3 independent populations (Q33870909) (← links)
- Hypertriglyceridemia associated with amino acid variation Asn985Tyr of the RP1 gene (Q34199597) (← links)
- A promoter SNP (-1323T>C) in G-substrate gene (GSBS) correlates with hypercholesterolemia (Q34227913) (← links)
- Hypercholesterolemia associated with splice-junction variation of inter-alpha-trypsin inhibitor heavy chain 4 (ITIH4) gene (Q34281912) (← links)
- Soluble epoxide hydrolase variant (Glu287Arg) modifies plasma total cholesterol and triglyceride phenotype in familial hypercholesterolemia: intrafamilial association study in an eight-generation hyperlipidemic kindred (Q34283448) (← links)
- Heterozygous familial hypercholesterolemia: an underrecognized cause of early cardiovascular disease (Q34499298) (← links)
- Association between the APOA2 promoter polymorphism and body weight in Mediterranean and Asian populations: replication of a gene-saturated fat interaction (Q34539555) (← links)
- Studies of gene variants related to inflammation, oxidative stress, dyslipidemia, and obesity: implications for a nutrigenetic approach (Q35104849) (← links)
- Pathway-Wide Association Study Implicates Multiple Sterol Transport and Metabolism Genes in HDL Cholesterol Regulation. (Q35711232) (← links)
- A Splice Region Variant in LDLR Lowers Non-high Density Lipoprotein Cholesterol and Protects against Coronary Artery Disease (Q35761096) (← links)
- Mechanisms of disease: genetic causes of familial hypercholesterolemia (Q36767518) (← links)
- Monogenic pediatric dyslipidemias: classification, genetics and clinical spectrum (Q37006314) (← links)
- Genomic Study of Cardiovascular Continuum Comorbidity (Q40412731) (← links)
- Apolipoprotein H Variant Modifies Plasma Triglyceride Phenotype in Familial Hypercholesterolemia: A Molecular Study in an Eight-generation Hyperlipidemic Family (Q44436466) (← links)
- Functional impairment of two novel mutations detected in lipoprotein-associated phospholipase A2 (Lp-PLA2) deficiency patients (Q44899944) (← links)
- Association between the APOA2 rs3813627 Single Nucleotide Polymorphism and HDL and APOA1 Levels Through BMI (Q89975541) (← links)
- Mapping the genetic basis of diabetes mellitus in the Australian Burmese cat (Felis catus) (Q101403171) (← links)