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I Matsuda

Showing results (291-300 of 433) with videos related to

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Journal of Oral Rehabilitation|January 30, 2013
Determinants of change in oral health-related quality of life over 7 years among older JapaneseK Enoki, K Ikebe, K-I Matsuda, et al.
Biochimica Et Biophysica Acta|January 2, 1995
Structural organization of the gene for CD40 ligand: molecular analysis for diagnosis of X-linked hyper-IgM syndromeM Shimadzu, H Nunoi, H Terasaki, et al.
The Journal of Pediatrics|April 1, 1976
Leukocyte glutathione peroxidase deficiency in a male patient with chronic granulomatous diseaseI Matsuda, Y Oka, N Taniguchi, et al.
American Journal of Human Genetics|July 1, 1989
Ornithine transcarbamylase deficiency resulting from a C-to-T substitution in exon 5 of the ornithine transcarbamylase geneA Hata, C Setoyama, K Shimada, et al.
Blood|July 1, 1995
AG dinucleotide insertion in a patient with chronic granulomatous disease lacking cytosolic 67-kD proteinH Nunoi, M Iwata, S Tatsuzawa, et al.
Humangenetik|October 20, 1975
Prenatal diagnosis of I-cell diseaseI Matsuda, S Arashima, T Mitsuyama, et al.
Human Genetics|May 1, 1991
A novel missense mutation in exon 8 of the ornithine transcarbamylase gene in two unrelated male patients with mild ornithine transcarbamylase deficiencyA Hata, T Matsuura, C Setoyama, et al.
Pediatric Research|October 1, 1979
Lysine intolerance in a variant form of citrullinemiaI Matsuda, S Arashima, Y Imanishi, et al.
Human Genetics|August 14, 1998
Prenatal diagnosis of ornithine transcarbamylase deficiency by using a single nucleated erythrocyte from maternal bloodA Watanabe, A Sekizawa, A Taguchi, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 21, 1999
A heterozygous mutation of beta-actin associated with neutrophil dysfunction and recurrent infectionH Nunoi, T Yamazaki, H Tsuchiya, et al.
Pageof 44

Showing results (291-300 of 433) with videos related to

Sort By:
Pageof 44
Journal of Oral Rehabilitation|January 30, 2013
Determinants of change in oral health-related quality of life over 7 years among older JapaneseK Enoki, K Ikebe, K-I Matsuda, et al.
Biochimica Et Biophysica Acta|January 2, 1995
Structural organization of the gene for CD40 ligand: molecular analysis for diagnosis of X-linked hyper-IgM syndromeM Shimadzu, H Nunoi, H Terasaki, et al.
The Journal of Pediatrics|April 1, 1976
Leukocyte glutathione peroxidase deficiency in a male patient with chronic granulomatous diseaseI Matsuda, Y Oka, N Taniguchi, et al.
American Journal of Human Genetics|July 1, 1989
Ornithine transcarbamylase deficiency resulting from a C-to-T substitution in exon 5 of the ornithine transcarbamylase geneA Hata, C Setoyama, K Shimada, et al.
Blood|July 1, 1995
AG dinucleotide insertion in a patient with chronic granulomatous disease lacking cytosolic 67-kD proteinH Nunoi, M Iwata, S Tatsuzawa, et al.
Humangenetik|October 20, 1975
Prenatal diagnosis of I-cell diseaseI Matsuda, S Arashima, T Mitsuyama, et al.
Human Genetics|May 1, 1991
A novel missense mutation in exon 8 of the ornithine transcarbamylase gene in two unrelated male patients with mild ornithine transcarbamylase deficiencyA Hata, T Matsuura, C Setoyama, et al.
Pediatric Research|October 1, 1979
Lysine intolerance in a variant form of citrullinemiaI Matsuda, S Arashima, Y Imanishi, et al.
Human Genetics|August 14, 1998
Prenatal diagnosis of ornithine transcarbamylase deficiency by using a single nucleated erythrocyte from maternal bloodA Watanabe, A Sekizawa, A Taguchi, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 21, 1999
A heterozygous mutation of beta-actin associated with neutrophil dysfunction and recurrent infectionH Nunoi, T Yamazaki, H Tsuchiya, et al.
Pageof 44