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T Oura

Showing results (41-50 of 76) with videos related to

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Advances in Experimental Medicine and Biology|January 1, 1993
Experimental research on a new treatment for maternal phenylketonuria(PKU)T Imamura, H Shintaku, T Nakajima, et al.
American Journal of Perinatology|March 1, 1994
Fetal liver biopsy for prenatal diagnosis of carbamoyl phosphate synthetase deficiencyJ Murotsuki, S Uehara, K Okamura, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|April 1, 1994
An epidemiologic analysis of end-stage lupus nephritisK Iseki, F Miyasato, T Oura, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 18, 1997
Single amino acid residue as a functional determinant of rod and cone visual pigmentsH Imai, D Kojima, T Oura, et al.
Acta Paediatrica Japonica : Overseas Edition|August 1, 1988
Early treatment of inborn errors of biopterin metabolismY Hase, Y Okano, Y Sawada, et al.
Human Genetics|December 22, 1998
Molecular characterization of phenylketonuria in Japanese patientsY Okano, M Asada, Y Kang, et al.
Human Molecular Genetics|April 1, 1994
Molecular characterization of phenylketonuric mutations in Japanese by analysis of phenylalanine hydroxylase mRNA from lymphoblastsY Okano, Y Hase, H Shintaku, et al.
Biochemistry|February 27, 1996
Molecular properties of chimerical mutants of gecko blue and bovine rhodopsinD Kojima, T Oura, O Hisatomi, et al.
Nihon Sanka Fujinka Gakkai Zasshi|December 1, 1991
[Prenatal diagnosis of carbamyl phosphate synthetase deficiency by fetal liver biopsy]J Murotsuki, S Uehara, K Okamura, et al.
Journal of Inherited Metabolic Disease|January 1, 1994
Molecular and population genetics of phenylketonuria in Orientals: correlation between phenotype and genotypeY Okano, Y Hase, D H Lee, et al.
Pageof 8

Showing results (41-50 of 76) with videos related to

Sort By:
Pageof 8
Advances in Experimental Medicine and Biology|January 1, 1993
Experimental research on a new treatment for maternal phenylketonuria(PKU)T Imamura, H Shintaku, T Nakajima, et al.
American Journal of Perinatology|March 1, 1994
Fetal liver biopsy for prenatal diagnosis of carbamoyl phosphate synthetase deficiencyJ Murotsuki, S Uehara, K Okamura, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|April 1, 1994
An epidemiologic analysis of end-stage lupus nephritisK Iseki, F Miyasato, T Oura, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 18, 1997
Single amino acid residue as a functional determinant of rod and cone visual pigmentsH Imai, D Kojima, T Oura, et al.
Acta Paediatrica Japonica : Overseas Edition|August 1, 1988
Early treatment of inborn errors of biopterin metabolismY Hase, Y Okano, Y Sawada, et al.
Human Genetics|December 22, 1998
Molecular characterization of phenylketonuria in Japanese patientsY Okano, M Asada, Y Kang, et al.
Human Molecular Genetics|April 1, 1994
Molecular characterization of phenylketonuric mutations in Japanese by analysis of phenylalanine hydroxylase mRNA from lymphoblastsY Okano, Y Hase, H Shintaku, et al.
Biochemistry|February 27, 1996
Molecular properties of chimerical mutants of gecko blue and bovine rhodopsinD Kojima, T Oura, O Hisatomi, et al.
Nihon Sanka Fujinka Gakkai Zasshi|December 1, 1991
[Prenatal diagnosis of carbamyl phosphate synthetase deficiency by fetal liver biopsy]J Murotsuki, S Uehara, K Okamura, et al.
Journal of Inherited Metabolic Disease|January 1, 1994
Molecular and population genetics of phenylketonuria in Orientals: correlation between phenotype and genotypeY Okano, Y Hase, D H Lee, et al.
Pageof 8