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The Journal of Biological Chemistry
|
March 15, 1989
Primary structure and gene localization of human prolidase
F 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 girl
S 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 disease
Y 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 disease
Y 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 F
F 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) families
Y 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 scintigraphy
T 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 complex
Y 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 patients
I Matsuda, Y Nobukuni, H Mitsubuchi, et al.
Page
of 20
Search research articles
Search
Showing results (121-130 of 197) with videos related to
Sort By:
Page
of 20
The Journal of Biological Chemistry
|
March 15, 1989
Primary structure and gene localization of human prolidase
F 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 girl
S 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 disease
Y 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 disease
Y 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 F
F 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) families
Y 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 scintigraphy
T 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 complex
Y 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 patients
I Matsuda, Y Nobukuni, H Mitsubuchi, et al.
Page
of 20