| 1 |
35058562 | Citrin mediated metabolic rewiring in response to altered basal subcellular Ca2+ homeostasis. | 2022 Jan 20 |
1 |
| 2 |
32740958 | Metabolic basis and treatment of citrin deficiency. | 2021 Jan |
1 |
| 3 |
33497735 | The mitochondrial aspartate/glutamate carrier (AGC or Aralar1) isoforms in D. melanogaster: biochemical characterization, gene structure, and evolutionary analysis. | 2021 May |
1 |
| 4 |
34228977 | Citrin deficiency: Does the reactivation of liver aralar-1 come into play and promote HCC development? | 2021 Nov |
1 |
| 5 |
31462712 | The mitochondrial carrier Citrin plays a role in regulating cellular energy during carcinogenesis. | 2020 Jan |
2 |
| 6 |
32335094 | Diabetes mellitus exacerbates citrin deficiency via glucose toxicity. | 2020 Jun |
2 |
| 7 |
32722104 | AGC2 (Citrin) Deficiency-From Recognition of the Disease till Construction of Therapeutic Procedures. | 2020 Jul 24 |
4 |
| 8 |
33176737 | Citrin deficiency mimicking mitochondrial depletion syndrome. | 2020 Nov 11 |
1 |
| 9 |
30995827 | Transcriptional Regulation Factors of the Human Mitochondrial Aspartate/Glutamate Carrier Gene, Isoform 2 (SLC25A13): USF1 as Basal Factor and FOXA2 as Activator in Liver Cells. | 2019 Apr 16 |
2 |
| 10 |
29651749 | Medium-chain triglycerides supplement therapy with a low-carbohydrate formula can supply energy and enhance ammonia detoxification in the hepatocytes of patients with adult-onset type II citrullinemia. | 2018 Sep |
2 |
| 11 |
29376577 | p.Val452Ile mutation of the SLC25A13 gene in a Turkish patient with citrin deficiency. | 2017 |
1 |
| 12 |
27132995 | AGC1/2, the mitochondrial aspartate-glutamate carriers. | 2016 Oct |
1 |
| 13 |
25533124 | Steatogenesis in adult-onset type II citrullinemia is associated with down-regulation of PPARĪ±. | 2015 Mar |
3 |
| 14 |
25947987 | Citrin deficiency: A treatable cause of acute psychosis in adults. | 2015 Mar-Apr |
1 |
| 15 |
26062589 | [Treatment and Pathomechanism of Citrin Deficiency]. | 2015 Jun |
2 |
| 16 |
24586645 | Clinical, molecular and functional investigation on an infant with neonatal intrahepatic cholestasis caused by citrin deficiency (NICCD). | 2014 |
1 |
| 17 |
25110155 | Screening for five prevalent mutations of SLC25A13 gene in Guangdong, China: a molecular epidemiologic survey of citrin deficiency. | 2014 Aug |
2 |
| 18 |
27896073 | Medium-chain triglyceride supplementation under a low-carbohydrate formula is a promising therapy for adult-onset type II citrullinemia. | 2014 |
2 |
| 19 |
24069319 | SLC25A13 gene analysis in citrin deficiency: sixteen novel mutations in East Asian patients, and the mutation distribution in a large pediatric cohort in China. | 2013 |
1 |
| 20 |
22710133 | Multiple ovarian antral follicles in a preterm infant with neonatal intrahepatic cholestasis caused by citrin deficiency: a clinical, genetic and transcriptional analysis. | 2012 Sep 1 |
2 |
| 21 |
23022256 | Molecular analysis of SLC25A13 gene in human peripheral blood lymphocytes: Marked transcript diversity, and the feasibility of cDNA cloning as a diagnostic tool for citrin deficiency. | 2012 Dec 15 |
1 |
| 22 |
23430852 | Treatment with lactose (galactose)-restricted and medium-chain triglyceride-supplemented formula for neonatal intrahepatic cholestasis caused by citrin deficiency. | 2012 |
1 |
| 23 |
26835269 | Cloning and sequence analysis of SLC25A13 transcripts in human amniocytes. | 2012 Oct |
2 |
| 24 |
21365350 | A GC/MS-based metabolomic approach for diagnosing citrin deficiency. | 2011 Jun |
2 |
| 25 |
21424115 | Genotypic and phenotypic features of citrin deficiency: five-year experience in a Chinese pediatric center. | 2011 Jul |
2 |
| 26 |
19232506 | Sustaining hypercitrullinemia, hypercholesterolemia and augmented oxidative stress in Japanese children with aspartate/glutamate carrier isoform 2-citrin-deficiency even during the silent period. | 2009 May |
2 |
| 27 |
18392553 | Identification of 13 novel mutations including a retrotransposal insertion in SLC25A13 gene and frequency of 30 mutations found in patients with citrin deficiency. | 2008 |
1 |
| 28 |
18415701 | Reduced carbohydrate intake in citrin-deficient subjects. | 2008 Jun |
1 |
| 29 |
19099775 | [Identification and diagnosis of three novel mutations in SLC25A13 gene of neonatal intrahepatic cholestasis caused by citrin deficiency]. | 2008 Jun |
2 |
| 30 |
17213189 | Ca2+ Activation kinetics of the two aspartate-glutamate mitochondrial carriers, aralar and citrin: role in the heart malate-aspartate NADH shuttle. | 2007 Mar 9 |
1 |
| 31 |
17237342 | Mitochondrial transporters as novel targets for intracellular calcium signaling. | 2007 Jan |
1 |
| 32 |
17880783 | [SLC25A13 gene mutation analysis in a pedigree of neonatal intrahepatic cholestasis caused by citrin deficiency]. | 2007 Jun |
2 |
| 33 |
18162705 | Neonatal intrahepatic cholestasis caused by citrin deficiency in Korean infants. | 2007 Dec |
1 |
| 34 |
18273444 | Downregulation of citrin, a mitochondrial AGC, is associated with apoptosis of hepatocytes. | 2007 Dec 28 |
1 |
| 35 |
16458993 | Pyruvate ameliorates the defect in ureogenesis from ammonia in citrin-deficient mice. | 2006 May |
2 |
| 36 |
16736097 | Time course of acylcarnitine elevation in neonatal intrahepatic cholestasis caused by citrin deficiency. | 2006 Aug |
1 |
| 37 |
17160946 | [Progresses and perspectives in the study on citrin deficiency]. | 2006 Dec |
2 |
| 38 |
16199199 | Metabolic derangements in deficiency of citrin, a liver-type mitochondrial aspartate-glutamate carrier. | 2005 Oct |
6 |
| 39 |
15050970 | Adult-onset type II citrullinemia and idiopathic neonatal hepatitis caused by citrin deficiency: involvement of the aspartate glutamate carrier for urea synthesis and maintenance of the urea cycle. | 2004 Apr |
2 |
| 40 |
15054102 | Identification of a novel human subfamily of mitochondrial carriers with calcium-binding domains. | 2004 Jun 4 |
1 |
| 41 |
15254020 | The calcium-binding aspartate/glutamate carriers, citrin and aralar1, are new substrates for the DDP1/TIMM8a-TIMM13 complex. | 2004 Sep 15 |
2 |
| 42 |
12111366 | Mitochondrial aspartate glutamate carrier (citrin) deficiency as the cause of adult-onset type II citrullinemia (CTLN2) and idiopathic neonatal hepatitis (NICCD). | 2002 |
3 |
| 43 |
12424587 | Neonatal intrahepatic cholestasis caused by citrin deficiency: severe hepatic dysfunction in an infant requiring liver transplantation. | 2002 Nov |
2 |
| 44 |
11566871 | Citrin and aralar1 are Ca(2+)-stimulated aspartate/glutamate transporters in mitochondria. | 2001 Sep 17 |
2 |