Familial hypercholesterolemia: Detect, treat, and ask about family | Cleveland Clinic Journal of Medicine
Translational medicine in Familial hypercholesterolaemia – the Portuguese FH Study - ICPerMed
sgugenetics / Mechanisms of Disease: Genetic Causes
Missense Mutation in the LDLR Gene: A Wide Spectrum in the Severity of Familial Hypercholesterolemia | IntechOpen
Low-density lipoprotein receptor gene family - Wikipedia
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
Pharmacogenetic aspects in familial hypercholesterolemia with the special focus on FHMarburg (FH p.W556R) | Clinical Research in Cardiology Supplements
Structure of LDL receptor. A) schematic representation of the human... | Download Scientific Diagram
Genes | Free Full-Text | Identification of New Genetic Determinants in Pediatric Patients with Familial Hypercholesterolemia Using a Custom NGS Panel
Schematic diagram of LDLR gene with all the mutations observed. Solid... | Download Scientific Diagram
The LDLR gene. (A) The LDLR gene; exons are shown as vertical dark... | Download Scientific Diagram
Dual regulation of the LDL receptor—Some clarity and new questions: Cell Metabolism
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 | Calling and Phasing of Single-Nucleotide and Structural Variants of the LDLR Gene Using Oxford Nanopore MinION
Genetic Testing for Hypercholesterolemia Improves Diagnosis - molecular-diagnostics - mobile.Labmedica.com
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
Familial Hypercholesterolemia (FH): Diagnosis, Genetics
Spontaneous severe hypercholesterolemia and atherosclerosis lesions in rabbits with deficiency of low-density lipoprotein receptor (LDLR) on exon 7 - eBioMedicine
The LDL Receptor Gene Family: Neuron
Genes | Free Full-Text | The LDLR, APOB, and PCSK9 Variants of Index Patients with Familial Hypercholesterolemia in Russia
Spectrum of LDL receptor gene mutations in Denmark: implications for molecular diagnostic strategy in heterozygous familial hypercholesterolemia - ScienceDirect
sgugenetics / Mechanisms of Disease: Genetic Causes
LDLR gene. a. Location of the LDLR gene, the short (p) arm of... | Download Scientific Diagram
Frontiers | Proteostasis Regulation in the Endoplasmic Reticulum: An Emerging Theme in the Molecular Pathology and Therapeutic Management of Familial Hypercholesterolemia
Divergent low-density lipoprotein receptor (LDLR) linked to low VSV G-dependent viral infectivity and unique serum lipid profile in zebra finches | PNAS
Frontiers | The Digenic Causality in Familial Hypercholesterolemia: Revising the Genotype–Phenotype Correlations of the Disease
LDLR » Laboratory Testing and Research
Crispr Cas9 Knockout Knockin Ldl Receptor Ldlr Human Gene Knockout Kit (OriGene) | Bioz | Ratings For Life-Science Research
