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Showing results (101-110 of 197) with videos related to
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The Journal of Pediatrics
|
April 1, 1989
Late neonatal vitamin K deficiency associated with subclinical liver dysfunction in human milk-fed infants
I Matsuda, S Nishiyama, K Motohara, et al.
Gastroenterology
|
June 1, 1996
Three brothers with progressive hepatic dysfunction and severe hepatic steatosis due to a patent ductus venosus
T Uchino, F Endo, S Ikeda, et al.
Biochimica Et Biophysica Acta
|
July 31, 1996
Cloning of mouse prolidase cDNA: predominant expression of prolidase mRNA in kidney
T Ishii, S Tsujino, S Matsunobu, et al.
The Journal of Clinical Investigation
|
April 1, 1991
Maple syrup urine disease caused by a partial deletion in the inner E2 core domain of the branched chain alpha-keto acid dehydrogenase complex due to aberrant splicing. A single base deletion at a 5'-splice donor site of an intron of the E2 gene disrupts the consensus sequence in this region
H Mitsubuchi, Y Nobukuni, I Akaboshi, et al.
American Journal of Human Genetics
|
September 1, 1987
Structural analysis of normal and mutant insulin receptors in fibroblasts cultured from families with leprechaunism
F Endo, N Nagata, J H Priest, et al.
The Journal of Clinical Investigation
|
July 1, 1990
Maple syrup urine disease. Complete primary structure of the E1 beta subunit of human branched chain alpha-ketoacid dehydrogenase complex deduced from the nucleotide sequence and a gene analysis of patients with this disease
Y Nobukuni, H Mitsubuchi, F Endo, et al.
American Journal of Human Genetics
|
January 1, 1985
Leprechaunism: an inherited defect in a high-affinity insulin receptor
L J Elsas, F Endo, E Strumlauf, et al.
Gene
|
November 15, 1991
Cloning and sequence of a cDNA encoding human carbamyl phosphate synthetase I: molecular analysis of hyperammonemia
Y Haraguchi, T Uchino, M Takiguchi, et al.
Biochimica Et Biophysica Acta
|
May 25, 1994
Structural organization and analysis of the human fumarylacetoacetate hydrolase gene in tyrosinemia type I
H Awata, F Endo, A Tanoue, et al.
The Journal of Biological Chemistry
|
March 31, 1995
Excess copper and ceruloplasmin biosynthesis in long-term cultured hepatocytes from Long-Evans Cinnamon (LEC) rats, a model of Wilson disease
K Nakamura, F Endo, T Ueno, et al.
Page
of 20
Search research articles
Search
Showing results (101-110 of 197) with videos related to
Sort By:
Page
of 20
The Journal of Pediatrics
|
April 1, 1989
Late neonatal vitamin K deficiency associated with subclinical liver dysfunction in human milk-fed infants
I Matsuda, S Nishiyama, K Motohara, et al.
Gastroenterology
|
June 1, 1996
Three brothers with progressive hepatic dysfunction and severe hepatic steatosis due to a patent ductus venosus
T Uchino, F Endo, S Ikeda, et al.
Biochimica Et Biophysica Acta
|
July 31, 1996
Cloning of mouse prolidase cDNA: predominant expression of prolidase mRNA in kidney
T Ishii, S Tsujino, S Matsunobu, et al.
The Journal of Clinical Investigation
|
April 1, 1991
Maple syrup urine disease caused by a partial deletion in the inner E2 core domain of the branched chain alpha-keto acid dehydrogenase complex due to aberrant splicing. A single base deletion at a 5'-splice donor site of an intron of the E2 gene disrupts the consensus sequence in this region
H Mitsubuchi, Y Nobukuni, I Akaboshi, et al.
American Journal of Human Genetics
|
September 1, 1987
Structural analysis of normal and mutant insulin receptors in fibroblasts cultured from families with leprechaunism
F Endo, N Nagata, J H Priest, et al.
The Journal of Clinical Investigation
|
July 1, 1990
Maple syrup urine disease. Complete primary structure of the E1 beta subunit of human branched chain alpha-ketoacid dehydrogenase complex deduced from the nucleotide sequence and a gene analysis of patients with this disease
Y Nobukuni, H Mitsubuchi, F Endo, et al.
American Journal of Human Genetics
|
January 1, 1985
Leprechaunism: an inherited defect in a high-affinity insulin receptor
L J Elsas, F Endo, E Strumlauf, et al.
Gene
|
November 15, 1991
Cloning and sequence of a cDNA encoding human carbamyl phosphate synthetase I: molecular analysis of hyperammonemia
Y Haraguchi, T Uchino, M Takiguchi, et al.
Biochimica Et Biophysica Acta
|
May 25, 1994
Structural organization and analysis of the human fumarylacetoacetate hydrolase gene in tyrosinemia type I
H Awata, F Endo, A Tanoue, et al.
The Journal of Biological Chemistry
|
March 31, 1995
Excess copper and ceruloplasmin biosynthesis in long-term cultured hepatocytes from Long-Evans Cinnamon (LEC) rats, a model of Wilson disease
K Nakamura, F Endo, T Ueno, et al.
Page
of 20