| 1 |
35360862 | Newborn Screening for Mitochondrial Carnitine-Acylcarnitine Cycle Disorders in Zhejiang Province, China. | 2022 |
1 |
| 2 |
35563000 | NMR Characterization of Long-Chain Fatty Acylcarnitine Binding to the Mitochondrial Carnitine/Acylcarnitine Carrier. | 2022 Apr 21 |
2 |
| 3 |
33807231 | The Mitochondrial Carnitine Acyl-carnitine Carrier (SLC25A20): Molecular Mechanisms of Transport, Role in Redox Sensing and Interaction with Drugs. | 2021 Mar 31 |
1 |
| 4 |
32337051 | A novel homozygous missense SLC25A20 mutation in three CACT-deficient patients: clinical and autopsy data. | 2020 |
1 |
| 5 |
33194920 | Late-Onset Carnitine-Acylcarnitine Translocase Deficiency With SLC25A20 c.199-10T>G Variation: Case Report and Pathologic Analysis of Liver Biopsy. | 2020 |
3 |
| 6 |
30401918 | Management and diagnosis of mitochondrial fatty acid oxidation disorders: focus on very-long-chain acyl-CoA dehydrogenase deficiency. | 2019 Feb |
1 |
| 7 |
31108048 | Clinical and molecular characteristics of carnitine-acylcarnitine translocase deficiency: Experience with six patients in Guangdong China. | 2019 Aug |
1 |
| 8 |
28132459 | [Carnitine - mitochondria and beyond]. | 2016 |
3 |
| 9 |
23948593 | Glutathione controls the redox state of the mitochondrial carnitine/acylcarnitine carrier Cys residues by glutathionylation. | 2013 Nov |
1 |
| 10 |
21130740 | Role of FOXA and Sp1 in mitochondrial acylcarnitine carrier gene expression in different cell lines. | 2011 Jan 7 |
1 |
| 11 |
22020112 | The mitochondrial carnitine/acylcarnitine carrier: function, structure and physiopathology. | 2011 Aug |
4 |
| 12 |
19748481 | Regulation of the human SLC25A20 expression by peroxisome proliferator-activated receptor alpha in human hepatoblastoma cells. | 2009 Nov 20 |
2 |
| 13 |
18307102 | Functional characterization of residues within the carnitine/acylcarnitine translocase RX2PANAAXF distinct motif. | 2008 Feb |
1 |
| 14 |
16602102 | Disorders of carnitine transport and the carnitine cycle. | 2006 May 15 |
3 |
| 15 |
15057979 | Response to therapy in carnitine/acylcarnitine translocase (CACT) deficiency due to a novel missense mutation. | 2004 Apr 15 |
1 |
| 16 |
15363639 | Carnitine-acylcarnitine translocase deficiency, clinical, biochemical and genetic aspects. | 2004 Oct-Dec |
2 |
| 17 |
12882971 | A novel mitochondrial carnitine-acylcarnitine translocase induced by partial hepatectomy and fasting. | 2003 Oct 3 |
2 |
| 18 |
11257506 | Molecular enzymology of carnitine transfer and transport. | 2001 Mar 9 |
1 |
| 19 |
11826365 | Lethal cardiac tachyarrhythmia in a patient with neonatal carnitine-acylcarnitine translocase deficiency. | 2001 Nov-Dec |
1 |
| 20 |
10697964 | Identification of two novel mutations of the carnitine/acylcarnitine translocase (CACT) gene in a patient with CACT deficiency. | 2000 |
1 |
| 21 |
9837782 | The structure and organization of the human carnitine/acylcarnitine translocase (CACT1) gene2. | 1998 Nov 27 |
1 |