Pages that link to "Q34576724"
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The following pages link to Genetic analysis of a kindred with familial hypobetalipoproteinemia. Evidence for two separate gene defects: one associated with an abnormal apolipoprotein B species, apolipoprotein B-37; and a second associated with low plasma concentrations of apo (Q34576724):
Displaying 22 items.
- A gene-targeted mouse model for familial hypobetalipoproteinemia. Low levels of apolipoprotein B mRNA in association with a nonsense mutation in exon 26 of the apolipoprotein B gene (Q28512923) (← links)
- Whole-exome sequencing identifies rare and low-frequency coding variants associated with LDL cholesterol (Q30411390) (← links)
- Genetic basis of lipoprotein disorders (Q33847743) (← links)
- A truncated species of apolipoprotein B (B67) in a kindred with familial hypobetalipoproteinemia (Q34189158) (← links)
- Phenotypes of apolipoprotein B and apolipoprotein E after liver transplantation (Q34225777) (← links)
- Familial hypobetalipoproteinemia caused by a mutation in the apolipoprotein B gene that results in a truncated species of apolipoprotein B (B-31). A unique mutation that helps to define the portion of the apolipoprotein B molecule required for the f (Q34246106) (← links)
- Familial defective apolipoprotein B-100: low density lipoproteins with abnormal receptor binding (Q34350695) (← links)
- Inference of a molecular defect of apolipoprotein B in hypobetalipoproteinemia by linkage analysis in a large kindred (Q34561886) (← links)
- Characterization of an abnormal species of apolipoprotein B, apolipoprotein B-37, associated with familial hypobetalipoproteinemia (Q34576682) (← links)
- Genetic evidence from two families that the apolipoprotein B gene is not involved in abetalipoproteinemia (Q35593754) (← links)
- Pathway-Wide Association Study Implicates Multiple Sterol Transport and Metabolism Genes in HDL Cholesterol Regulation. (Q35711232) (← links)
- Truncated variants of apolipoprotein B cause hypobetalipoproteinaemia (Q36065192) (← links)
- Familial hypobetalipoproteinemia-induced nonalcoholic steatohepatitis (Q36098448) (← links)
- Mutations and Variants of Apolipoprotein B that Affect Plasma Cholesterol Levels (Q37201866) (← links)
- Reading-frame restoration with an apolipoprotein B gene frameshift mutation. (Q37324226) (← links)
- Insights from human congenital disorders of intestinal lipid metabolism (Q38267212) (← links)
- Transcriptional regulation of the apolipoprotein B100 gene: purification and characterization of trans-acting factor BRF-2 (Q38327727) (← links)
- A single in vitro point mutation in the first non-translated exon silences transcription of the human apolipoprotein B gene in HepG2 cells (Q40973516) (← links)
- Identification and characterization of truncated forms of apolipoprotein B in hypobetalipoproteinemia (Q41250782) (← links)
- Receptor-dependent and -independent catabolism of low-density lipoprotein in a kindred with familial hypobetalipoproteinemia (Q44386028) (← links)
- Complex genetic architecture in severe hypobetalipoproteinemia. (Q52355653) (← links)
- Reading-frame restoration by transcriptional slippage at long stretches of adenine residues in mammalian cells. (Q53969208) (← links)