| 1 |
35622436 | Acylcarnitines and Genetic Variation in Fat Oxidation Genes in HIV-infected, Antiretroviral-treated Children With and Without Myopathy. | 2022 May 25 |
2 |
| 2 |
32654140 | Glioma cells survival depends both on fatty acid oxidation and on functional carnitine transport by SLC22A5. | 2021 Mar |
6 |
| 3 |
33181153 | Newborn screening for primary carnitine deficiency in Quanzhou, China. | 2021 Jan |
2 |
| 4 |
33334877 | Cholesterol stimulates the cellular uptake of L-carnitine by the carnitine/organic cation transporter novel 2 (OCTN2). | 2021 Jan-Jun |
10 |
| 5 |
34249102 | Newborn Screening and Genetic Analysis Identify Six Novel Genetic Variants for Primary Carnitine Deficiency in Ningbo Area, China. | 2021 |
2 |
| 6 |
34478916 | Organic cation transporters (OCTs/OCTNs) in human primary alveolar epithelial cells. | 2021 Oct 22 |
1 |
| 7 |
34603016 | The Role of the Carnitine/Organic Cation Transporter Novel 2 in the Clinical Outcome of Patients With Locally Advanced Esophageal Carcinoma Treated With Oxaliplatin. | 2021 |
1 |
| 8 |
34824054 | Urinary metabotype of severe asthma evidences decreased carnitine metabolism independent of oral corticosteroid treatment in the U-BIOPRED study. | 2021 Nov 25 |
2 |
| 9 |
31864849 | Carnitine uptake defect due to a 5'UTR mutation in a pedigree with false positives and false negatives on Newborn screening. | 2020 Mar |
1 |
| 10 |
31913724 | OCTN2-targeted nanoparticles for oral delivery of paclitaxel: differential impact of the polyethylene glycol linker size on drug delivery in vitro, in situ, and in vivo. | 2020 Dec |
2 |
| 11 |
32027707 | Functional analysis of OCTN2 and ATB0,+ in normal human airway epithelial cells. | 2020 |
6 |
| 12 |
32256846 | Intestinal OCTN2- and MCT1-targeted drug delivery to improve oral bioavailability. | 2020 Mar |
1 |
| 13 |
32306775 | l-Carnitine conjugated chitosan-stearic acid polymeric micelles for improving the oral bioavailability of paclitaxel. | 2020 Dec |
4 |
| 14 |
32620667 | Sorafenib Might Induce Sarcopenia in Patients With Hepatocellular Carcinoma by Inhibiting Carnitine Absorption. | 2020 Jul |
1 |
| 15 |
33268576 | Biochemical and genetic characteristics of 40 neonates with carnitine deficiency. | 2020 Oct 28 |
2 |
| 16 |
30523710 | OCTN: A Small Transporter Subfamily with Great Relevance to Human Pathophysiology, Drug Discovery, and Diagnostics. | 2019 Feb |
2 |
| 17 |
30670496 | L-Carnitine-Mediated Tumor Cell Protection and Poor Patient Survival Associated with OCTN2 Overexpression in Glioblastoma Multiforme. | 2019 May 1 |
4 |
| 18 |
30735677 | The inhibitory effect of antiretroviral drugs on the L-carnitine uptake in human placenta. | 2019 Apr 1 |
6 |
| 19 |
30858625 | SLC22A5 polymorphism associated with risk of extra-articular manifestations in rheumatoid arthritis patients. | 2019 |
2 |
| 20 |
30863740 | Biochemical, Molecular, and Clinical Characterization of Patients With Primary Carnitine Deficiency via Large-Scale Newborn Screening in Xuzhou Area. | 2019 |
3 |
| 21 |
31187905 | A mutation creating an upstream translation initiation codon in SLC22A5 5'UTR is a frequent cause of primary carnitine deficiency. | 2019 Oct |
1 |
| 22 |
31200524 | First Case Report of Primary Carnitine Deficiency Manifested as Intellectual Disability and Autism Spectrum Disorder. | 2019 Jun 13 |
2 |
| 23 |
31364285 | Molecular investigation in Chinese patients with primary carnitine deficiency. | 2019 Sep |
3 |
| 24 |
31394757 | OCTN2-Mediated Acetyl-l-Carnitine Transport in Human Pulmonary Epithelial Cells In Vitro. | 2019 Aug 7 |
1 |
| 25 |
31500110 | Carnitine Inborn Errors of Metabolism. | 2019 Sep 6 |
1 |
| 26 |
31861504 | SLC22A5 (OCTN2) Carnitine Transporter-Indispensable for Cell Metabolism, a Jekyll and Hyde of Human Cancer. | 2019 Dec 19 |
7 |
| 27 |
28974108 | L-Carnitine-conjugated nanoparticles to promote permeation across blood-brain barrier and to target glioma cells for drug delivery via the novel organic cation/carnitine transporter OCTN2. | 2018 Dec |
4 |
| 28 |
29614331 | Carnitine levels and mutations in the SLC22A5 gene in Faroes patients with Parkinson's disease. | 2018 May 14 |
1 |
| 29 |
30016594 | Recent advances in drug delivery via the organic cation/carnitine transporter 2 (OCTN2/SLC22A5). | 2018 Aug |
3 |
| 30 |
27581592 | Primary Carnitine Deficiency - A Rare Treatable Cause of Cardiomyopathy and Massive Hepatomegaly. | 2017 Jan |
2 |
| 31 |
27733576 | Human macrophage differentiation induces OCTN2-mediated L-carnitine transport through stimulation of mTOR-STAT3 axis. | 2017 Mar |
2 |
| 32 |
28234466 | Combination of l-Carnitine with Lipophilic Linkage-Donating Gemcitabine Derivatives as Intestinal Novel Organic Cation Transporter 2-Targeting Oral Prodrugs. | 2017 Mar 23 |
1 |
| 33 |
28295041 | Exome sequencing identifies primary carnitine deficiency in a family with cardiomyopathy and sudden death. | 2017 Jun |
1 |
| 34 |
28365301 | Species specificity profiling of rat and human organic cation/carnitine transporter Slc22a5/SLC22A5 (Octn2/OCTN2). | 2017 Jun |
3 |
| 35 |
28711408 | Biochemical characteristics of newborns with carnitine transporter defect identified by newborn screening in California. | 2017 Nov |
1 |
| 36 |
28911246 | Dual targeting of l-carnitine-conjugated nanoparticles to OCTN2 and ATB0,+ to deliver chemotherapeutic agents for colon cancer therapy. | 2017 Nov |
3 |
| 37 |
29132460 | [Genetic diagnosis of 10 neonates with primary carnitine deficiency]. | 2017 Nov |
1 |
| 38 |
26607009 | Functional activity of L-carnitine transporters in human airway epithelial cells. | 2016 Feb |
6 |
| 39 |
26828774 | Carnitine transport and fatty acid oxidation. | 2016 Oct |
5 |
| 40 |
26850121 | Pharmacological effects of meldonium: Biochemical mechanisms and biomarkers of cardiometabolic activity. | 2016 Nov |
2 |
| 41 |
26994919 | Wide tolerance to amino acids substitutions in the OCTN1 ergothioneine transporter. | 2016 Jun |
4 |
| 42 |
27931018 | Primary Carnitine Deficiency and Newborn Screening for Disorders of the Carnitine Cycle. | 2016 |
2 |
| 43 |
25269560 | Strategies for skeletal muscle targeting in drug discovery. | 2015 |
1 |
| 44 |
25827849 | Multiple acyl-CoA dehydrogenation deficiency as decreased acyl-carnitine profile in serum. | 2015 Jun |
1 |
| 45 |
25857234 | Memantine transport by a proton-coupled organic cation antiporter in hCMEC/D3 cells, an in vitro human blood-brain barrier model. | 2015 Apr |
1 |
| 46 |
26043725 | Acetylcarnitine potentiates the anticarcinogenic effects of butyrate on SW480 colon cancer cells. | 2015 Aug |
1 |
| 47 |
26075114 | Identification of SLC22A5 Gene Mutation in a Family with Carnitine Uptake Defect. | 2015 |
1 |
| 48 |
23379544 | Primary carnitine deficiency: novel mutations and insights into the cardiac phenotype. | 2014 Feb |
2 |
| 49 |
23877104 | Functional expression of organic cation/carnitine transporter 2 (OCTN2/SLC22A5) in human brain capillary endothelial cell line hCMEC/D3, a human blood-brain barrier model. | 2014 |
3 |
| 50 |
25132046 | Analysis of genetic mutations in Chinese patients with systemic primary carnitine deficiency. | 2014 Oct |
1 |