The activity and surface presence of organic cation/carnitine transporter OCTN2 (SLC22A5) in breast cancer cells depends on AKT kinase - ScienceDirect
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
SLC22A5 - an overview | ScienceDirect Topics
![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
Genetic spectrum of pathogenic variants in the SLC22A5 gene. (A)... | Download Scientific Diagram
P 38 Mapk Inhibitor (Jena Bioscience) | Bioz | Ratings For Life-Science Research
SLC22A5 gene | Semantic Scholar
Frontiers | Biochemical, Molecular, and Clinical Characterization of Patients With Primary Carnitine Deficiency via Large-Scale Newborn Screening in Xuzhou Area
Frontiers | Newborn Screening and Genetic Analysis Identify Six Novel Genetic Variants for Primary Carnitine Deficiency in Ningbo Area, China
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
anti-SLC22A5 antibody | anti-Human SLC22A5 Antibody-NP_001295051.1
SLC22A5 Membrane Protein Introduction - Creative Biolabs
Slc22a5 ORF Vector (Mouse) (pORF) | Applied Biological Materials Inc.
SLC22A5 - Wikiwand
![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 - Wikipedia
Molecules | Free Full-Text | SLC22A5 (OCTN2) Carnitine Transporter—Indispensable for Cell Metabolism, a Jekyll and Hyde of Human Cancer
Molecular investigation in Chinese patients with primary carnitine deficiency - Zhang - 2019 - Molecular Genetics & Genomic Medicine - Wiley Online Library
Frontiers | A report of a pedigree with compound heterozygous mutations in the SLC22A5 gene
Glioma cells survival depends both on fatty acid oxidation and on functional carnitine transport by SLC22A5 - Juraszek - 2021 - Journal of Neurochemistry - Wiley Online Library
Maternal systemic primary carnitine deficiency uncovered by newborn screening: Clinical, biochemical, and molecular aspects | Genetics in Medicine
L -Carnitine and its carrier SLC22A5 mediated sensing and signaling | Download Scientific Diagram
