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histidine and Deficiency Disease, Ornithine Carbamoyltransferase

histidine has been researched along with Deficiency Disease, Ornithine Carbamoyltransferase in 3 studies

Research

Studies (3)

Timeframe	Studies, this research(%)	All Research%
pre-1990	1 (33.33)	18.7374
1990's	2 (66.67)	18.2507
2000's	0 (0.00)	29.6817
2010's	0 (0.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Scriver, CR	1
Endo, F; Hoshide, R; Ishikawa, K; Kato, I; Kiwaki, K; Koike, E; Komaki, S; Matsuura, T; Oyanagi, K; Suzuki, Y	1
Freisinger, P; Hässler, A; Pontz, BF; Staudt, M; Wermuth, B	1

Reviews

1 review(s) available for histidine and Deficiency Disease, Ornithine Carbamoyltransferase

Article	Year
Garrod's legacy to the nations of mice and men. Progress in clinical and biological research, 1981, Volume: 45 Topics: Amino Acid Metabolism, Inborn Errors; Animals; Biological Transport; Cell Membrane; Disease Models, Animal; Histidine; Humans; Hypophosphatemia, Familial; Metabolism, Inborn Errors; Mice; Mice, Mutant Strains; Ornithine Carbamoyltransferase Deficiency Disease; Phosphates; Proline Oxidase	1981

Article

Year

Garrod's legacy to the nations of mice and men.

Progress in clinical and biological research, 1981, Volume: 45

Topics: Amino Acid Metabolism, Inborn Errors; Animals; Biological Transport; Cell Membrane; Disease Models, Animal; Histidine; Humans; Hypophosphatemia, Familial; Metabolism, Inborn Errors; Mice; Mice, Mutant Strains; Ornithine Carbamoyltransferase Deficiency Disease; Phosphates; Proline Oxidase

1981

Other Studies

2 other study(ies) available for histidine and Deficiency Disease, Ornithine Carbamoyltransferase

Article	Year
Four newly identified ornithine transcarbamylase (OTC) mutations (D126G, R129H, I172M and W332X) in Japanese male patients with early-onset OTC deficiency. Human mutation, 1994, Volume: 3, Issue:4 Topics: Amino Acid Metabolism, Inborn Errors; Arginine; Aspartic Acid; Base Sequence; DNA Mutational Analysis; DNA Primers; DNA, Single-Stranded; Glycine; Histidine; Humans; Infant; Infant, Newborn; Isoleucine; Male; Methionine; Molecular Epidemiology; Molecular Sequence Data; Nucleic Acid Conformation; Ornithine Carbamoyltransferase; Ornithine Carbamoyltransferase Deficiency Disease; Pedigree; Point Mutation; Polymerase Chain Reaction; Polymorphism, Genetic; Tryptophan; X Chromosome	1994
Symptomatic ornithine carbamoyltransferase deficiency (point mutation H202P) with normal in vitro activity. Journal of inherited metabolic disease, 1998, Volume: 21, Issue:1 Topics: Child, Preschool; Female; Histidine; Humans; Liver; Metabolism, Inborn Errors; Ornithine Carbamoyltransferase; Ornithine Carbamoyltransferase Deficiency Disease; Point Mutation; Proline	1998

Article

Year

Four newly identified ornithine transcarbamylase (OTC) mutations (D126G, R129H, I172M and W332X) in Japanese male patients with early-onset OTC deficiency.

Human mutation, 1994, Volume: 3, Issue:4

Topics: Amino Acid Metabolism, Inborn Errors; Arginine; Aspartic Acid; Base Sequence; DNA Mutational Analysis; DNA Primers; DNA, Single-Stranded; Glycine; Histidine; Humans; Infant; Infant, Newborn; Isoleucine; Male; Methionine; Molecular Epidemiology; Molecular Sequence Data; Nucleic Acid Conformation; Ornithine Carbamoyltransferase; Ornithine Carbamoyltransferase Deficiency Disease; Pedigree; Point Mutation; Polymerase Chain Reaction; Polymorphism, Genetic; Tryptophan; X Chromosome

1994

Symptomatic ornithine carbamoyltransferase deficiency (point mutation H202P) with normal in vitro activity.

Journal of inherited metabolic disease, 1998, Volume: 21, Issue:1

Topics: Child, Preschool; Female; Histidine; Humans; Liver; Metabolism, Inborn Errors; Ornithine Carbamoyltransferase; Ornithine Carbamoyltransferase Deficiency Disease; Point Mutation; Proline

1998