|1.||Kobayashi, Keiko: 10 articles (01/2012 - 01/2002)|
|2.||Saheki, Takeyori: 8 articles (05/2009 - 01/2002)|
|3.||Iijima, Mikio: 7 articles (01/2008 - 01/2004)|
|4.||Ushikai, Miharu: 4 articles (01/2008 - 04/2004)|
|5.||Li, Meng Xian: 4 articles (05/2006 - 01/2004)|
|6.||Moriyama, Mitsuaki: 4 articles (05/2006 - 01/2004)|
|7.||Buxbaum, Joseph D: 3 articles (05/2010 - 04/2004)|
|8.||Ramoz, Nicolas: 3 articles (05/2010 - 04/2004)|
|9.||Tabata, Ayako: 3 articles (01/2008 - 04/2004)|
|10.||Horiuchi, Masahisa: 3 articles (05/2006 - 01/2004)|
|1.||Pervasive Child Development Disorders
05/01/2010 - "SLC25A12, a susceptibility gene for autism spectrum disorders that is mutated in a neurodevelopmental syndrome, encodes a mitochondrial aspartate-glutamate carrier (aspartate-glutamate carrier isoform 1 [AGC1]). "
04/05/2008 - "Evidence for a genetic association between autism and two single nucleotide polymorphisms (SNPs), rs2056202 and rs2292813, in the mitochondrial aspartate/glutamate carrier (SLC25A12) gene led us to ask whether any of the four previously identified familial traits in autism spectrum disorders (ASD) varied by these SNPs. "
01/01/2010 - "Altered calcium homeostasis in autism-spectrum disorders: evidence from biochemical and genetic studies of the mitochondrial aspartate/glutamate carrier AGC1."
06/01/2015 - "The solute carrier family 25 (aspartate/glutamate carrier), member 12 gene (SLC25A12) has been strongly posed as a candidate gene for autism spectrum disorder (ASD) given its important role in mitochondrial function and adenosine triphosphate (ATP) synthesis. "
|2.||Schizophrenia (Dementia Praecox)
03/01/2015 - "SLC25A13 (citrin or aspartate-glutamate carrier 2) is located in the mitochondrial membrane in the liver and its genetic deficiency causes adult-onset type II citrullinemia (CTLN2). "
01/01/2012 - "Mutation(s) of human SLC25A13 gene encoding a mitochondrial aspartate/glutamate carrier isoform 2 (AGC2), can lead to AGC2 deficiency, resulting in NICCD and an adult-onset fatal disease namely citrullinemia type II (CTLN2). "
05/01/2006 - "Mutations in SLC25A13, encoding the mitochondrial aspartate-glutamate carrier citrin, cause adult-onset type II citrullinemia (CTLN2) in humans. "
01/01/2004 - "Adult-onset type II citrullinemia (CTLN2) is an autosomal recessive disease caused by mutations in SLC25A13, the gene encoding the mitochondrial aspartate/glutamate carrier citrin. "
12/01/2007 - "Citrin is a liver-type mitochondrial aspartate-glutamate carrier encoded by the SLC25A13 gene, and its deficiency causes adult-onset type II citrullinemia and neonatal intrahepatic cholestasis caused by citrin deficiency (NICCD). "
|4.||Autistic Disorder (Autism)
06/01/2008 - "Two single nucleotide polymorphisms (SNP) within Mitochondrial Aspartate/Glutamate Carrier SLC25A12 gene have recently shown to be strongly associated with autism. "
06/01/2008 - "Mitochondrial aspartate/glutamate carrier SLC25A12 gene is associated with autism."
04/05/2008 - "Autism-related routines and rituals associated with a mitochondrial aspartate/glutamate carrier SLC25A12 polymorphism."
11/01/2006 - "We further examine the involvement of the mitochondrial aspartate/glutamate carrier gene (SLC25A12) in mitochondrial dysfunction associated with autism. "
11/01/2005 - "Confirmation of association between autism and the mitochondrial aspartate/glutamate carrier SLC25A12 gene on chromosome 2q31."
01/01/2008 - "Deficiency of citrin, liver-type mitochondrial aspartate-glutamate carrier, is an autosomal recessive disorder caused by mutations of the SLC25A13 gene on chromosome 7q21.3 and has two phenotypes: neonatal intrahepatic cholestatic hepatitis (NICCD) and adult-onset type II citrullinemia (CTLN2). "
04/01/2004 - "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."
01/01/2002 - "Mitochondrial aspartate glutamate carrier (citrin) deficiency as the cause of adult-onset type II citrullinemia (CTLN2) and idiopathic neonatal hepatitis (NICCD)."
01/01/2005 - "Deficiency of citrin, a liver-type mitochondrial aspartate-glutamate carrier (AGC), encoded by the SLC25A13 gene on chromosome 7q21.3, causes autosomal recessive disorders: adult-onset type II citrullinemia (CTLN2) and neonatal hepatitis associated with intrahepatic cholestasis (NICCD). "
|3.||Neonatal-onset citrullinemia type 2
|4.||Protein Isoforms (Isoforms)
|6.||Biological Markers (Surrogate Marker)
|8.||Messenger RNA (mRNA)
|9.||Malate Dehydrogenase (Dehydrogenase, Malate)
|10.||Adenosine Triphosphate (ATP)