Frontiers | Biochemical, Molecular, and Clinical Characterization of Patients With Primary Carnitine Deficiency via Large-Scale Newborn Screening in Xuzhou Area
Molecules | Free Full-Text | SLC22A5 (OCTN2) Carnitine Transporter—Indispensable for Cell Metabolism, a Jekyll and Hyde of Human Cancer
![PDF] 20 Years After Discovery of the Causative Gene of Primary Carnitine Deficiency, How Much More Have We Known About the Disease? | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/651ba513a258b0a57dc15c728599dfc387fb11ea/3-Figure1-1.png "PDF] 20 Years After Discovery of the Causative Gene of Primary Carnitine Deficiency, How Much More Have We Known About the Disease? | Semantic Scholar")
PDF] 20 Years After Discovery of the Causative Gene of Primary Carnitine Deficiency, How Much More Have We Known About the Disease? | Semantic Scholar
SLC22A5 Membrane Protein Introduction - Creative Biolabs
A mutation creating an upstream translation initiation codon in SLC22A5 5′UTR is a frequent cause of primary carnitine deficiency - Ferdinandusse - 2019 - Human Mutation - Wiley Online Library
Functional Genetic Diversity in the High-Affinity Carnitine Transporter OCTN2 (SLC22A5) | Molecular Pharmacology
Molecules | Free Full-Text | SLC22A5 (OCTN2) Carnitine Transporter—Indispensable for Cell Metabolism, a Jekyll and Hyde of Human Cancer
Phenotype and genotype variation in primary carnitine deficiency - ScienceDirect
Phenotype and genotype variation in primary carnitine deficiency | Genetics in Medicine
SLC22A5 - Wikiwand
Tight junction protein ZO-1 controls organic cation/carnitine transporter OCTN2 (SLC22A5) in a protein kinase C-dependent way - ScienceDirect
anti-SLC22A5 antibody | anti-Human SLC22A5 Antibody-NP_001295051.1
Glioma cells survival depends both on fatty acid oxidation and on functional carnitine transport by SLC22A5 - Juraszek - 2021 - Journal of Neurochemistry - Wiley Online Library
SLC22A5 - an overview | ScienceDirect Topics
Genetic spectrum of pathogenic variants in the SLC22A5 gene. (A)... | Download Scientific Diagram
Molecular investigation in Chinese patients with primary carnitine deficiency - Zhang - 2019 - Molecular Genetics & Genomic Medicine - Wiley Online Library
L -Carnitine and its carrier SLC22A5 mediated sensing and signaling | Download Scientific Diagram
Frontiers | A report of a pedigree with compound heterozygous mutations in the SLC22A5 gene
Schematic representation of the molecular mechanism by which estrogen... | Download Scientific Diagram
proteins - How can carnitine enter the mitochondrial matrix without OCTN2? - Biology Stack Exchange
SLC22A5 gene | Semantic Scholar
P 38 Mapk Inhibitor (Jena Bioscience) | Bioz | Ratings For Life-Science Research
![Hong Kong Journal of Paediatrics [HK J Paediatr (New Series) 2013;18:167-173]](https://www.hkjpaed.org/figure/2013;18;167-173-fig1.jpg "Hong Kong Journal of Paediatrics [HK J Paediatr (New Series) 2013;18:167-173]")