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Y Indo

Showing results (31-40 of 51) with videos related to

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Journal of Pediatric Gastroenterology and Nutrition|September 1, 1986
Conversion of thyroxine into tri-iodothyronine in zinc deficient rat liverS Fujimoto, Y Indo, A Higashi, et al.
Progress in Clinical and Biological Research|January 1, 1990
The acyl-CoA dehydrogenase family: homology and divergence of primary sequence of four acyl-CoA dehydrogenases, and consideration of their functional significanceK Tanaka, Y Matsubara, Y Indo, et al.
The Journal of Biological Chemistry|March 15, 1989
Primary structure and gene localization of human prolidaseF Endo, A Tanoue, H Nakai, et al.
Biochimica Et Biophysica Acta|February 22, 1994
Deficiency of the E1 beta subunit in the branched-chain alpha-keto acid dehydrogenase complex due to a single base substitution of the intron 5, resulting in two alternatively spliced mRNAs in a patient with maple syrup urine diseaseY Hayashida, H Mitsubuchi, Y Indo, et al.
The Journal of Clinical Investigation|May 1, 1991
Maple syrup urine disease. Complete defect of the E1 beta subunit of the branched chain alpha-ketoacid dehydrogenase complex due to a deletion of an 11-bp repeat sequence which encodes a mitochondrial targeting leader peptide in a family with the diseaseY Nobukuni, H Mitsubuchi, I Akaboshi, et al.
Human Genetics|September 12, 2000
Mutation and polymorphism analysis of the TRKA (NTRK1) gene encoding a high-affinity receptor for nerve growth factor in congenital insensitivity to pain with anhidrosis (CIPA) familiesY Miura, S Mardy, Y Awaya, et al.
Journal of Inherited Metabolic Disease|January 1, 1992
Molecular diagnosis of maple syrup urine disease: screening and identification of gene mutations in the branched-chain alpha-ketoacid dehydrogenase multienzyme complexY Nobukuni, H Mitsubuchi, K Ohta, et al.
Biochemical and Biophysical Research Communications|October 30, 1990
A T-to-A substitution in the E1 alpha subunit gene of the branched-chain alpha-ketoacid dehydrogenase complex in two cell lines derived from Menonite maple syrup urine disease patientsI Matsuda, Y Nobukuni, H Mitsubuchi, et al.
Genomics|January 15, 1996
Human ESP1/CRP2, a member of the LIM domain protein family: characterization of the cDNA and assignment of the gene locus to chromosome 14q32.3M A Karim, K Ohta, M Egashira, et al.
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.
Pageof 6

Showing results (31-40 of 51) with videos related to

Sort By:
Pageof 6
Journal of Pediatric Gastroenterology and Nutrition|September 1, 1986
Conversion of thyroxine into tri-iodothyronine in zinc deficient rat liverS Fujimoto, Y Indo, A Higashi, et al.
Progress in Clinical and Biological Research|January 1, 1990
The acyl-CoA dehydrogenase family: homology and divergence of primary sequence of four acyl-CoA dehydrogenases, and consideration of their functional significanceK Tanaka, Y Matsubara, Y Indo, et al.
The Journal of Biological Chemistry|March 15, 1989
Primary structure and gene localization of human prolidaseF Endo, A Tanoue, H Nakai, et al.
Biochimica Et Biophysica Acta|February 22, 1994
Deficiency of the E1 beta subunit in the branched-chain alpha-keto acid dehydrogenase complex due to a single base substitution of the intron 5, resulting in two alternatively spliced mRNAs in a patient with maple syrup urine diseaseY Hayashida, H Mitsubuchi, Y Indo, et al.
The Journal of Clinical Investigation|May 1, 1991
Maple syrup urine disease. Complete defect of the E1 beta subunit of the branched chain alpha-ketoacid dehydrogenase complex due to a deletion of an 11-bp repeat sequence which encodes a mitochondrial targeting leader peptide in a family with the diseaseY Nobukuni, H Mitsubuchi, I Akaboshi, et al.
Human Genetics|September 12, 2000
Mutation and polymorphism analysis of the TRKA (NTRK1) gene encoding a high-affinity receptor for nerve growth factor in congenital insensitivity to pain with anhidrosis (CIPA) familiesY Miura, S Mardy, Y Awaya, et al.
Journal of Inherited Metabolic Disease|January 1, 1992
Molecular diagnosis of maple syrup urine disease: screening and identification of gene mutations in the branched-chain alpha-ketoacid dehydrogenase multienzyme complexY Nobukuni, H Mitsubuchi, K Ohta, et al.
Biochemical and Biophysical Research Communications|October 30, 1990
A T-to-A substitution in the E1 alpha subunit gene of the branched-chain alpha-ketoacid dehydrogenase complex in two cell lines derived from Menonite maple syrup urine disease patientsI Matsuda, Y Nobukuni, H Mitsubuchi, et al.
Genomics|January 15, 1996
Human ESP1/CRP2, a member of the LIM domain protein family: characterization of the cDNA and assignment of the gene locus to chromosome 14q32.3M A Karim, K Ohta, M Egashira, et al.
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.
Pageof 6