Exosome-based Ldlr gene therapy for familial hypercholesterolemia in a mouse model
Structure of LDL receptor. A) schematic representation of the human... | Download Scientific Diagram
Expanding the genetic spectrum for Chinese familial hypercholesterolemia population with six genetic mutations identified using a next‐generation sequencing‐based laboratory‐developed screening test - Jingxin - 2022 - Molecular Genetics & Genomic ...
Spectrum of LDL receptor gene mutations in Denmark: implications for molecular diagnostic strategy in heterozygous familial hypercholesterolemia - ScienceDirect
The LDLR gene. (A) The LDLR gene; exons are shown as vertical dark... | Download Scientific Diagram
Schematic representation of the LDLR gene and LDLR protein... | Download Scientific Diagram
Homozygous Familial Hypercholesterolemia Patients With Identical Mutations Variably Express the LDLR (Low-Density Lipoprotein Receptor) | Arteriosclerosis, Thrombosis, and Vascular Biology
Increased LDL receptor by SREBP2 or SREBP2-induced lncRNA LDLR-AS promotes triglyceride accumulation in fish - ScienceDirect
Familial Hypercholesterolemia (FH): Diagnosis, Genetics
sgugenetics / Mechanisms of Disease: Genetic Causes
The LDLR gene. Notes: exons are shown as dark bars numbered underneath.... | Download Scientific Diagram
Frontiers | Proteostasis Regulation in the Endoplasmic Reticulum: An Emerging Theme in the Molecular Pathology and Therapeutic Management of Familial Hypercholesterolemia
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
Therapeutic targets of hypercholesterolemia: HMGCR and LDLR | DMSO
Crispr Cas9 Knockout Knockin Ldl Receptor Ldlr Human Gene Knockout Kit (OriGene) | Bioz | Ratings For Life-Science Research
LDLR » Laboratory Testing and Research
Frontiers | Mutational Spectrum of LDLR and PCSK9 Genes Identified in Iranian Patients With Premature Coronary Artery Disease and Familial Hypercholesterolemia
Frontiers | The Digenic Causality in Familial Hypercholesterolemia: Revising the Genotype–Phenotype Correlations of the Disease
Missense Mutation in the LDLR Gene: A Wide Spectrum in the Severity of Familial Hypercholesterolemia | IntechOpen
The LDL Receptor Gene Family: Neuron
Genes | Free Full-Text | Identification of New Genetic Determinants in Pediatric Patients with Familial Hypercholesterolemia Using a Custom NGS Panel
Low-density lipoprotein receptor gene family - Wikipedia
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
