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T Oura

Showing results (51-60 of 76) with videos related to

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Human Mutation|January 1, 1992
Frequency and distribution of phenylketonuric mutations in OrientalsY Okano, Y Hase, D H Lee, et al.
Early Human Development|March 1, 1979
Seasonality of birth in sporadic cretinismK Miyai, K Ichihara, N Amino, et al.
Pediatric Research|December 1, 1984
Semiautomated enzyme immunoassay of thyrotropin as a mass screening test for neonatal hypothyroidismK Miyai, T Tsuruhara, S Kusuda, et al.
Acta Paediatrica Japonica : Overseas Edition|December 1, 1988
Neonatal hypothyroid screening using enzymeimmunoassay of thyrotropin--comparison with radioimmunoassayS Kusuda, T Tsuruhara, Y Hase, et al.
Endocrine Journal|July 8, 1999
Evaluation of highly sensitive thyrotropin assay for detecting thyroid diseases in neonatal screening: preliminary studiesK Miyai, T Miyagi, N Ashida, et al.
Oncogene|January 12, 2010
Identification of an ovarian clear cell carcinoma gene signature that reflects inherent disease biology and the carcinogenic processesK Yamaguchi, M Mandai, T Oura, et al.
Journal of Inherited Metabolic Disease|January 1, 1994
Prenatal diagnosis of 6-pyruvoyl tetrahydropterin synthase deficiency in seven subjectsH Shintaku, K J Hsiao, T T Liu, et al.
European Journal of Pediatrics|August 1, 1984
Follow-up study of a nation-wide neonatal metabolic screening program in Japan. A collaborative study group of neonatal screening for inborn errors of metabolism in JapanK Tada, H Tateda, S Arashima, et al.
Enzyme|January 1, 1987
Treatment of phenylketonuria with a formula consisting of low-phenylalanine peptide. A collaborative studyT Kitagawa, M Owada, K Aoki, et al.
American Journal of Transplantation : Official Journal of the American Society of Transplantation and the American Society of Transplant Surgeons|December 31, 2017
RNA expression profiling of nonhuman primate renal allograft rejection identifies toleranceR N Smith, M Matsunami, B A Adam, et al.
Pageof 8

Showing results (51-60 of 76) with videos related to

Sort By:
Pageof 8
Human Mutation|January 1, 1992
Frequency and distribution of phenylketonuric mutations in OrientalsY Okano, Y Hase, D H Lee, et al.
Early Human Development|March 1, 1979
Seasonality of birth in sporadic cretinismK Miyai, K Ichihara, N Amino, et al.
Pediatric Research|December 1, 1984
Semiautomated enzyme immunoassay of thyrotropin as a mass screening test for neonatal hypothyroidismK Miyai, T Tsuruhara, S Kusuda, et al.
Acta Paediatrica Japonica : Overseas Edition|December 1, 1988
Neonatal hypothyroid screening using enzymeimmunoassay of thyrotropin--comparison with radioimmunoassayS Kusuda, T Tsuruhara, Y Hase, et al.
Endocrine Journal|July 8, 1999
Evaluation of highly sensitive thyrotropin assay for detecting thyroid diseases in neonatal screening: preliminary studiesK Miyai, T Miyagi, N Ashida, et al.
Oncogene|January 12, 2010
Identification of an ovarian clear cell carcinoma gene signature that reflects inherent disease biology and the carcinogenic processesK Yamaguchi, M Mandai, T Oura, et al.
Journal of Inherited Metabolic Disease|January 1, 1994
Prenatal diagnosis of 6-pyruvoyl tetrahydropterin synthase deficiency in seven subjectsH Shintaku, K J Hsiao, T T Liu, et al.
European Journal of Pediatrics|August 1, 1984
Follow-up study of a nation-wide neonatal metabolic screening program in Japan. A collaborative study group of neonatal screening for inborn errors of metabolism in JapanK Tada, H Tateda, S Arashima, et al.
Enzyme|January 1, 1987
Treatment of phenylketonuria with a formula consisting of low-phenylalanine peptide. A collaborative studyT Kitagawa, M Owada, K Aoki, et al.
American Journal of Transplantation : Official Journal of the American Society of Transplantation and the American Society of Transplant Surgeons|December 31, 2017
RNA expression profiling of nonhuman primate renal allograft rejection identifies toleranceR N Smith, M Matsunami, B A Adam, et al.
Pageof 8