The Molecular Mechanism for the Genetic Disorder Familial Defective Apolipoprotein B100
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Molecular Biology,Biochemistry
Reference38 articles.
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2. The Metabolic and Molecular Bases of Inherited Disease;Havel,1995
3. Identification of the low density lipoprotein receptor-binding site in apolipoprotein B100 and the modulation of its binding activity by the carboxyl terminus in familial defective apo-B100.
4. Familial defective apolipoprotein B-100: low density lipoproteins with abnormal receptor binding.
5. Familial defective apolipoprotein B-100: detection in the United Kingdom and Scandinavia, and clinical characteristics of ten cases
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1. Unveiling Familial Hypercholesterolemia—Review, Cardiovascular Complications, Lipid-Lowering Treatment and Its Efficacy;International Journal of Molecular Sciences;2024-01-29
2. Predictive Modeling and Structure Analysis of Genetic Variants in Familial Hypercholesterolemia: Implications for Diagnosis and Protein Interaction Studies;Current Atherosclerosis Reports;2023-10-17
3. Identification and Functional Analysis of APOB Variants in a Cohort of Hypercholesterolemic Patients;International Journal of Molecular Sciences;2023-04-21
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5. A Low-Frequency APOB p.(Pro955Ser) Variant Contributes to the Severity of/Variability in Familial Hypercholesterolemia;The Journal of Clinical Endocrinology & Metabolism;2022-10-03
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