Molecules | Free Full-Text | SLC22A5 (OCTN2) Carnitine Transporter—Indispensable for Cell Metabolism, a Jekyll and Hyde of Human Cancer
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
![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
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
Molecular investigation in Chinese patients with primary carnitine deficiency - Zhang - 2019 - Molecular Genetics & Genomic Medicine - Wiley Online Library
The activity and surface presence of organic cation/carnitine transporter OCTN2 (SLC22A5) in breast cancer cells depends on AKT kinase - ScienceDirect
![PDF] Identification of SLC22A5 Gene Mutation in a Family with Carnitine Uptake Defect | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/f809e8360ccae2c9351b4387e3de330e41978c2d/2-Figure1-1.png "PDF] Identification of SLC22A5 Gene Mutation in a Family with Carnitine Uptake Defect | Semantic Scholar")
PDF] Identification of SLC22A5 Gene Mutation in a Family with Carnitine Uptake Defect | Semantic Scholar
SLC22A5 - Wikiwand
Schematic representation of the molecular mechanism by which estrogen... | Download Scientific Diagram
Homepage of the SLC22A5 gene from our LOVD-China database for FAODs. | Download Scientific Diagram
L -Carnitine and its carrier SLC22A5 mediated sensing and signaling | Download Scientific Diagram
Frontiers | Newborn Screening and Genetic Analysis Identify Six Novel Genetic Variants for Primary Carnitine Deficiency in Ningbo Area, China
A novel pathogenic variant in the carnitine transporter gene, SLC22A5, in association with metabolic carnitine deficiency and cardiomyopathy features | BMC Cardiovascular Disorders | Full Text
Maternal systemic primary carnitine deficiency uncovered by newborn screening: Clinical, biochemical, and molecular aspects | Genetics in Medicine
SLC22A5 gene | Semantic Scholar
Tight junction protein ZO-1 controls organic cation/carnitine transporter OCTN2 (SLC22A5) in a protein kinase C-dependent way - ScienceDirect
SLC22A5 - Wikipedia
SLC22A5 Gene - GeneCards | S22A5 Protein | S22A5 Antibody
P 38 Mapk Inhibitor (Jena Bioscience) | Bioz | Ratings For Life-Science Research
What is SLC22A5 Gene Carnitine deficiency NGS Genetic DNA Test ?
Frontiers | Biochemical, Molecular, and Clinical Characterization of Patients With Primary Carnitine Deficiency via Large-Scale Newborn Screening in Xuzhou Area
IJMS | Free Full-Text | PGC-1α and MEF2 Regulate the Transcription of the Carnitine Transporter OCTN2 Gene in C2C12 Cells and in Mouse Skeletal Muscle
Primary carnitine deficiency in two sisters with intractable epilepsy and reversible metabolic cardiomyopathy: Two case reports
![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]")
Hong Kong Journal of Paediatrics [HK J Paediatr (New Series) 2013;18:167-173]
SLC22A5 Membrane Protein Introduction - Creative Biolabs
