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I Matsuda

Showing results (281-290 of 433) with videos related to

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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.
Acta Paediatrica Japonica : Overseas Edition|February 1, 1993
Irradiated fetal thymus transplantation in a patient with combined immunodeficiency with predominant T cell defectS Higuchi, Y Yanabe, H Tsuchiya, et al.
Atherosclerosis|February 1, 1996
The heparin-bound fraction of human lipoprotein-deficient serum inhibits endocytic uptake of oxidized low density lipoprotein by macrophagesY Suginohara, A Miyazaki, H Hakamata, 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.
The Journal of Biological Chemistry|December 5, 1992
Primary structure deduced from complementary DNA sequence and expression in cultured cells of mammalian 4-hydroxyphenylpyruvic acid dioxygenase. Evidence that the enzyme is a homodimer of identical subunits homologous to rat liver-specific alloantigen FF Endo, H Awata, A Tanoue, et al.
Brain & Development|January 1, 1986
Unusual case of diffuse connective tissue disease with nodule formations in muscle, lung, kidney and brainY Nobukuni, T Miike, Y Ohtani, 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.
Biochemical and Biophysical Research Communications|May 15, 1992
Leukocyte adhesion deficiency: identification of novel mutations in two Japanese patients with a severe formS Matsuura, F Kishi, M Tsukahara, et al.
Pediatric Pharmacology (New York, N.Y.)|January 1, 1980
Serum vitamin E concentration in patients with severe multiple handicaps treated with anticonvulsantsA Higashi, H Tamari, T Ikeda, et al.
Nihon Jinzo Gakkai Shi|July 1, 1992
[Clinicopathological survey of persistent hypocomplementemic glomerulonephritis in children; correlation of DPGN and MPGN type I]S Hattori, M Hiramatsu, T Ushijima, et al.
Pageof 44

Showing results (281-290 of 433) with videos related to

Sort By:
Pageof 44
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.
Acta Paediatrica Japonica : Overseas Edition|February 1, 1993
Irradiated fetal thymus transplantation in a patient with combined immunodeficiency with predominant T cell defectS Higuchi, Y Yanabe, H Tsuchiya, et al.
Atherosclerosis|February 1, 1996
The heparin-bound fraction of human lipoprotein-deficient serum inhibits endocytic uptake of oxidized low density lipoprotein by macrophagesY Suginohara, A Miyazaki, H Hakamata, 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.
The Journal of Biological Chemistry|December 5, 1992
Primary structure deduced from complementary DNA sequence and expression in cultured cells of mammalian 4-hydroxyphenylpyruvic acid dioxygenase. Evidence that the enzyme is a homodimer of identical subunits homologous to rat liver-specific alloantigen FF Endo, H Awata, A Tanoue, et al.
Brain & Development|January 1, 1986
Unusual case of diffuse connective tissue disease with nodule formations in muscle, lung, kidney and brainY Nobukuni, T Miike, Y Ohtani, 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.
Biochemical and Biophysical Research Communications|May 15, 1992
Leukocyte adhesion deficiency: identification of novel mutations in two Japanese patients with a severe formS Matsuura, F Kishi, M Tsukahara, et al.
Pediatric Pharmacology (New York, N.Y.)|January 1, 1980
Serum vitamin E concentration in patients with severe multiple handicaps treated with anticonvulsantsA Higashi, H Tamari, T Ikeda, et al.
Nihon Jinzo Gakkai Shi|July 1, 1992
[Clinicopathological survey of persistent hypocomplementemic glomerulonephritis in children; correlation of DPGN and MPGN type I]S Hattori, M Hiramatsu, T Ushijima, et al.
Pageof 44