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F Endo

Showing results (121-130 of 197) with videos related to

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The Journal of Biological Chemistry|March 15, 1989
Primary structure and gene localization of human prolidaseF Endo, A Tanoue, H Nakai, et al.
Nihon Hinyokika Gakkai Zasshi. the Japanese Journal of Urology|March 11, 1998
[Inflammatory pseudotumor of the ureter: a case report]F Endo, S Matsumoto, A Naka, et al.
Pediatric Radiology|June 17, 1999
Reversibility of hyperintense globus pallidus on T 1-weighted MRI follow- ing surgery for a portosystemic shunt in an 8-year-old girlS Ikeda, Y Sera, M Yoshida, 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.
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.
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.
Annals of Nuclear Medicine|August 2, 2000
Evaluation of persistence of ductus venosus with tc-99m DTPA galactosyl human serum albumin liver scintigraphy and I-123 iodoamphetamine per-rectal portal scintigraphyT Kira, S Ikeda, Y Sera, 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.
Pageof 20

Showing results (121-130 of 197) with videos related to

Sort By:
Pageof 20
The Journal of Biological Chemistry|March 15, 1989
Primary structure and gene localization of human prolidaseF Endo, A Tanoue, H Nakai, et al.
Nihon Hinyokika Gakkai Zasshi. the Japanese Journal of Urology|March 11, 1998
[Inflammatory pseudotumor of the ureter: a case report]F Endo, S Matsumoto, A Naka, et al.
Pediatric Radiology|June 17, 1999
Reversibility of hyperintense globus pallidus on T 1-weighted MRI follow- ing surgery for a portosystemic shunt in an 8-year-old girlS Ikeda, Y Sera, M Yoshida, 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.
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.
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.
Annals of Nuclear Medicine|August 2, 2000
Evaluation of persistence of ductus venosus with tc-99m DTPA galactosyl human serum albumin liver scintigraphy and I-123 iodoamphetamine per-rectal portal scintigraphyT Kira, S Ikeda, Y Sera, 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.
Pageof 20