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1. Interleukin‐1α promotes matrix metalloproteinase‐9 expression, cellular motility, and local invasiveness of ameloblastoma cells.

2. Interleukin‐1α promotes matrix metalloproteinase‐9 expression, cellular motility, and local invasiveness of ameloblastoma cells

6. IL-1α Promotes MMP-9 Expression, Cellular Motility and Local Invasiveness of Ameloblastoma Cells

20. Regulation of IL-6 and IL-8 production by reciprocal cell-to-cell interactions between tumor cells and stromal fibroblasts through IL-1α in ameloblastoma

22. Karyotypic analysis in the process of immortalization of human cells treated with 4-nitroquinoline 1-oxide

24. Citrin/Mitochondrial Glycerol-3-phosphate Dehydrogenase Double Knock-out Mice Recapitulate Features of Human Citrin Deficiency

27. Fasting-induced reduction in locomotor activity and reduced response of orexin neurons in carnitine-deficient mice

29. Reduced N-Acetylaspartate Levels in Mice Lacking Aralar, a Brain- and Muscle-type Mitochondrial Aspartate-glutamate Carrier

30. 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

32. Identification of 16 novel mutations in the argininosuccinate synthetase gene and genotype-phenotype correlation in 38 classical citrullinemia patients

33. Moderate citrullinaemia without hyperammonaemia in a child with mutated and deficient argininosuccinate synthetase

34. Novel mRNA molecules are induced in hypertrophied ventricles of carnitine-deficient mice and belong to a family of up-regulated gene in cells overexpressing c-erbB-2

36. Screening of SLC25A13 mutations in early and late onset patients with citrin deficiency and in the Japanese population: Identification of two novel mutations and establishment of multiple DNA diagnosis methods for nine mutations

37. Pathogenesis of adult-onset type II citrullinemia caused by deficiency of citrin, a mitochondrial solute carrier protein: tissue and subcellular localization of citrin

38. Involvement of a cis-Acting Element in the Suppression of Carbamoyl Phosphate Synthetase I Gene Expression in the Liver of Carnitine-Deficient Mice

39. The gene mutated in adult-onset type II citrullinaemia encodes a putative mitochondrial carrier protein

43. Metabolic derangements in deficiency of citrin, a liver-type mitochondrial aspartate–glutamate carrier

46. Decreased Level of Anxiety-like Behaviors and Decreased Expression of Brain Tryptophan Hydroxylase in Aralar-deficient Mice : A Preliminary Study

49. Ca2+ Activation Kinetics of the Two Aspartate-Glutamate Mitochondrial Carriers, Aralar and Citrin.

50. Living donor liver transplantation for type II citrullinemia from a heterozygous donor.

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