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Hepatology (Baltimore, Md.)|May 1, 1997
Pancreatic secretory trypsin inhibitor as a diagnostic marker for adult-onset type II citrullinemiaK Kobayashi, M Horiuchi, T SahekiMolecular Genetics and Metabolism|January 4, 2001
Antagonizing effect of AP-1 on glucocorticoid induction of urea cycle enzymes: a study of hyperammonemia in carnitine-deficient, juvenile visceral steatosis miceT Saheki, M X Li, K KobayashiBiochemical Medicine and Metabolic Biology|December 1, 1987
Accumulation of large neutral amino acids in the brain of sparse-fur mice at hyperammonemic stateI Inoue, T Gushiken, K Kobayashi, et al.Journal of Inherited Metabolic Disease|October 30, 2008
Treatment of a citrin-deficient patient at the early stage of adult-onset type II citrullinaemia with arginine and sodium pyruvateK Mutoh, K Kurokawa, K Kobayashi, et al.American Journal of Human Genetics|December 1, 1994
Mutations in argininosuccinate synthetase mRNA of Japanese patients, causing classical citrullinemiaK Kobayashi, N Shaheen, H Terazono, et al.Japanese Journal of Cancer Research : Gann|August 1, 1994
Nuclear accumulation of p53 protein correlates with mutations in the p53 gene on archival paraffin-embedded tissues of human breast cancerY Umekita, K Kobayashi, T Saheki, et al.Biochimica Et Biophysica Acta|April 16, 1998
Secondary abnormality of carnitine biosynthesis results from carnitine reabsorptional system defect in juvenile visceral steatosis miceM Horiuchi, K Kobayashi, N Asaka, et al.In Vivo (Athens, Greece)|September 1, 1989
Increase of brain ammonia after microwave irradiation and its mechanismK Kobayashi, M Horiuchi, S Hagihara, et al.Biofactors (Oxford, England)|December 28, 1999
Pyruvate dehydrogenase kinase 4 mRNA is increased in the hypertrophied ventricles of carnitine-deficient juvenile visceral steatosis (JVS) miceM Horiuchi, K Kobayashi, M Masuda, et al.Human Mutation|January 1, 1997
Mutations and DNA diagnoses of classical citrullinemiaH Kakinoki, K Kobayashi, H Terazono, et al.Pageof 344