Keiko Kobayashi

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

Keiko Kobayashi, David S. Sinasac, Mikio Iijima et al. · Nature Genetics · 1999 · 409 citations

Mitochondrial Biogenesis, Mitochondrial Function, Genetic Disorder +9

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

Md. Abdul Jalil, Laila Begum, Laura Contreras et al. · Journal of Biological Chemistry · 2005 · 164 citations · Full text

Cellular Physiology, Social Sciences, Oxidative Stress +22

Developmental changes in the Ca2+-regulated mitochondrial aspartate–glutamate carrier aralar1 in brain and prominent expression in the spinal cord

Milagros Ramos, Araceli del Arco, Beatriz Pardo et al. · Developmental Brain Research · 2003 · 146 citations

Synaptic Plasticity, Developmental Biology, Molecular Neuroscience +15

Identification of two novel mutations in the SLC25A13 gene and detection of seven mutations in 102 patients with adult-onset type II citrullinemia

Tomotsugu Yasuda, Naoki Yamaguchi, Keiko Kobayashi et al. · Human Genetics · 2000 · 131 citations

Mendelian Disorder, Genetic Disorder, Genetics +8

Neonatal presentation of adult-onset type II citrullinemia

Toshihiro Ohura, Keiko Kobayashi, Yusaku Tazawa et al. · Human Genetics · 2001 · 129 citations

Neonatal Presentation, Neonatology, Paediatric Medicine +1