Increased LDL receptor by SREBP2 or SREBP2-induced lncRNA LDLR-AS promotes triglyceride accumulation in fish - ScienceDirect
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
LDLR Gene - GeneCards | LDLR Protein | LDLR Antibody
Divergent low-density lipoprotein receptor (LDLR) linked to low VSV G-dependent viral infectivity and unique serum lipid profile in zebra finches | PNAS
HoFH | About HoFH - Genetics and Pathogenesis
Frontiers | The Digenic Causality in Familial Hypercholesterolemia: Revising the Genotype–Phenotype Correlations of the Disease
Mutation type classification and pathogenicity assignment of sixteen missense variants located in the EGF-precursor homology domain of the LDLR | Scientific Reports
sgugenetics / Mechanisms of Disease: Genetic Causes
LDLR » COVID-19 Testing SAME DAY RESULTS
sgugenetics / Mechanisms of Disease: Genetic Causes
Structure of LDL receptor. A) schematic representation of the human... | Download Scientific Diagram
Schematic representation of the LDLR gene and LDLR protein... | Download Scientific Diagram
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
Analysis of mutations causing familial hypercholesterolaemia in black South African patients of different ancestry
LDLR/LDL Receptor Gene Sequence, Family, Fuction and Expression Information | Sino Biological
Frontiers | Proteostasis Regulation in the Endoplasmic Reticulum: An Emerging Theme in the Molecular Pathology and Therapeutic Management of Familial Hypercholesterolemia
LDLR gene. a. Location of the LDLR gene, the short (p) arm of... | Download Scientific Diagram
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 | Mutational Spectrum of LDLR and PCSK9 Genes Identified in Iranian Patients With Premature Coronary Artery Disease and Familial Hypercholesterolemia
Missense Mutation in the LDLR Gene: A Wide Spectrum in the Severity of Familial Hypercholesterolemia | IntechOpen
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
Functional Analysis of LDLR (Low-Density Lipoprotein Receptor) Variants in Patient Lymphocytes to Assess the Effect of Evinacumab in Homozygous Familial Hypercholesterolemia Patients With a Spectrum of LDLR Activity | Arteriosclerosis, Thrombosis, and
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
IJMS | Free Full-Text | Calling and Phasing of Single-Nucleotide and Structural Variants of the LDLR Gene Using Oxford Nanopore MinION
Diagram of LDLR gene showing the mutations identified in this study.... | Download Scientific Diagram