A Tanoue|F Endo|I Matsuda - JoVE Visualize

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Rinsho Byori. the Japanese Journal of Clinical Pathology|May 1, 1993

[Gene analysis of maple syrup urine disease (MSUD)]H Mitsubuchi, Y Nobukuni, Y Hayashida, et al.

Biochemical and Biophysical Research Communications|December 15, 1992

Mutations in the Pit-1 gene in children with combined pituitary hormone deficiencyK Ohta, Y Nobukuni, H Mitsubuchi, et al.

Journal of Inherited Metabolic Disease|January 1, 1992

Gene analysis of Mennonite maple syrup urine disease kindred using primer-specified restriction map modificationH Mitsubuchi, I Matsuda, Y Nobukuni, et al.

Biochimica Et Biophysica Acta|November 25, 1993

Heterogeneity of mutations in maple syrup urine disease (MSUD): screening and identification of affected E1 alpha and E1 beta subunits of the branched-chain alpha-keto-acid dehydrogenase multienzyme complexY Nobukuni, H Mitsubuchi, Y Hayashida, et al.

Pediatrics|March 1, 1988

Vitamin K effect in low birth weight infantsT Ogata, K Motohara, F Endo, et al.

Journal of Inherited Metabolic Disease|January 1, 1995

Identification of two new aberrant splicings in the ornithine carbamoyltransferase (OCT) gene in two patients with early and late onset OCT deficiencyT Matsuura, R Hoshide, S Komaki, et al.

Pediatric Research|February 1, 1983

Four-hydroxyphenylpyruvic acid oxidase deficiency with normal fumarylacetoacetase: a new variant form of hereditary hypertyrosinemiaF Endo, A Kitano, I Uehara, et al.

Gene|December 15, 1992

Characterization of the gene encoding human pituitary-specific transcription factor, Pit-1K Ohta, Y Nobukuni, H Mitsubuchi, et al.

Human Genetics|February 1, 1994

Expression of four mutant human ornithine transcarbamylase genes in cultured Cos 1 cells relates to clinical phenotypesT Matsuura, R Hoshide, C Setoyama, et al.

American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|November 1, 1995

Splicing mutations in the COL4A5 gene in Alport's syndrome: different mRNA expression between leukocytes and fibroblastsH Nakazato, S Hattori, T Ushijima, et al.

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Showing results (61-70 of 494) with videos related to

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Pageof 50

Rinsho Byori. the Japanese Journal of Clinical Pathology|May 1, 1993

[Gene analysis of maple syrup urine disease (MSUD)]H Mitsubuchi, Y Nobukuni, Y Hayashida, et al.

Biochemical and Biophysical Research Communications|December 15, 1992

Mutations in the Pit-1 gene in children with combined pituitary hormone deficiencyK Ohta, Y Nobukuni, H Mitsubuchi, et al.

Journal of Inherited Metabolic Disease|January 1, 1992

Gene analysis of Mennonite maple syrup urine disease kindred using primer-specified restriction map modificationH Mitsubuchi, I Matsuda, Y Nobukuni, et al.

Biochimica Et Biophysica Acta|November 25, 1993

Heterogeneity of mutations in maple syrup urine disease (MSUD): screening and identification of affected E1 alpha and E1 beta subunits of the branched-chain alpha-keto-acid dehydrogenase multienzyme complexY Nobukuni, H Mitsubuchi, Y Hayashida, et al.

Pediatrics|March 1, 1988

Vitamin K effect in low birth weight infantsT Ogata, K Motohara, F Endo, et al.

Journal of Inherited Metabolic Disease|January 1, 1995

Identification of two new aberrant splicings in the ornithine carbamoyltransferase (OCT) gene in two patients with early and late onset OCT deficiencyT Matsuura, R Hoshide, S Komaki, et al.

Pediatric Research|February 1, 1983

Four-hydroxyphenylpyruvic acid oxidase deficiency with normal fumarylacetoacetase: a new variant form of hereditary hypertyrosinemiaF Endo, A Kitano, I Uehara, et al.

Gene|December 15, 1992

Characterization of the gene encoding human pituitary-specific transcription factor, Pit-1K Ohta, Y Nobukuni, H Mitsubuchi, et al.

Human Genetics|February 1, 1994

Expression of four mutant human ornithine transcarbamylase genes in cultured Cos 1 cells relates to clinical phenotypesT Matsuura, R Hoshide, C Setoyama, et al.

American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|November 1, 1995

Splicing mutations in the COL4A5 gene in Alport's syndrome: different mRNA expression between leukocytes and fibroblastsH Nakazato, S Hattori, T Ushijima, et al.

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