136 Article(s)Download |
PMID | Title | Pub. Year | #Total Relationships |
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 |