Influence of LDL receptor gene mutations and the R3500Q mutation of the apoB gene on lipoprotein phenotype of familial hypercholesterolemic patients from a South European population | European Journal of Human Genetics
Missense Mutation in the LDLR Gene: A Wide Spectrum in the Severity of Familial Hypercholesterolemia | IntechOpen
Spontaneous severe hypercholesterolemia and atherosclerosis lesions in rabbits with deficiency of low-density lipoprotein receptor (LDLR) on exon 7 - eBioMedicine
LDLR » COVID-19 Testing SAME DAY RESULTS
Increased LDL receptor by SREBP2 or SREBP2-induced lncRNA LDLR-AS promotes triglyceride accumulation in fish - ScienceDirect
Frontiers | Mutational Spectrum of LDLR and PCSK9 Genes Identified in Iranian Patients With Premature Coronary Artery Disease and Familial Hypercholesterolemia
Novel compound heterozygous mutations in low density lipoprotein receptor gene causes a severe phenotype in a Chinese hypercholesterolemia family
Familial hypercholesterolemia: Detect, treat, and ask about family | Cleveland Clinic Journal of Medicine
The LDL Receptor Gene Family: Neuron
Structure of LDL receptor. A) schematic representation of the human... | Download Scientific Diagram
Divergent low-density lipoprotein receptor (LDLR) linked to low VSV G-dependent viral infectivity and unique serum lipid profile in zebra finches | PNAS
Genes | Free Full-Text | The LDLR, APOB, and PCSK9 Variants of Index Patients with Familial Hypercholesterolemia in Russia
The LDLR gene. (A) The LDLR gene; exons are shown as vertical dark... | Download Scientific Diagram
Frontiers | Proteostasis Regulation in the Endoplasmic Reticulum: An Emerging Theme in the Molecular Pathology and Therapeutic Management of Familial Hypercholesterolemia
Identification of a recurrent frameshift mutation at the LDLR exon 14 (c.2027delG, p.(G676Afs*33)) causing familial hypercholesterolemia in Saudi Arab homozygous children - ScienceDirect
IJMS | Free Full-Text | Calling and Phasing of Single-Nucleotide and Structural Variants of the LDLR Gene Using Oxford Nanopore MinION
HoFH | About HoFH - Genetics and Pathogenesis
Spectrum of LDL receptor gene mutations in Denmark: implications for molecular diagnostic strategy in heterozygous familial hypercholesterolemia - ScienceDirect
Piperine Induces Hepatic Low-Density Lipoprotein Receptor Expression through Proteolytic Activation of Sterol Regulatory Element-Binding Proteins | PLOS ONE
IJMS | Free Full-Text | Validation of LDLr Activity as a Tool to Improve Genetic Diagnosis of Familial Hypercholesterolemia: A Retrospective on Functional Characterization of LDLr Variants
LDLR gene. a. Location of the LDLR gene, the short (p) arm of... | Download Scientific Diagram
Homozygous Familial Hypercholesterolemia Patients With Identical Mutations Variably Express the LDLR (Low-Density Lipoprotein Receptor) | Arteriosclerosis, Thrombosis, and Vascular Biology
LDL receptor - Wikipedia
The benign c.344G > A: p.(Arg115His) variant in the LDLR gene interpreted from a pedigree-based genetic analysis of familial hypercholesterolemia | Lipids in Health and Disease | Full Text
sgugenetics / Mechanisms of Disease: Genetic Causes
a Illustrates the five different classes for defects of LDL receptor... | Download Scientific Diagram
