phenylalanine and Ornithine Carbamoyltransferase Deficiency Disease

phenylalanine has been researched along with Ornithine Carbamoyltransferase Deficiency Disease in 1 studies

Research

Studies (1)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	0 (0.00)	18.2507
2000's	1 (100.00)	29.6817
2010's	0 (0.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Castillo, L; Erez, A; Lee, B; Marini, JC	1

Other Studies

1 other study(ies) available for phenylalanine and Ornithine Carbamoyltransferase Deficiency Disease

Article	Year
Interaction between murine spf-ash mutation and genetic background yields different metabolic phenotypes. American journal of physiology. Endocrinology and metabolism, 2007, Volume: 293, Issue:6 Topics: Alanine; Ammonia; Animals; Arginine; Citrulline; Disease Models, Animal; Female; Glycine; Injections, Intravenous; Intestinal Mucosa; Liver; Male; Mice; Mice, Inbred ICR; Mice, Inbred Strains; Mice, Mutant Strains; Models, Biological; Mutation; Nitric Oxide; Ornithine; Ornithine Carbamoyltransferase; Ornithine Carbamoyltransferase Deficiency Disease; Phenotype; Phenylalanine; Urea	2007

Article

Year

Interaction between murine spf-ash mutation and genetic background yields different metabolic phenotypes.

American journal of physiology. Endocrinology and metabolism, 2007, Volume: 293, Issue:6

Topics: Alanine; Ammonia; Animals; Arginine; Citrulline; Disease Models, Animal; Female; Glycine; Injections, Intravenous; Intestinal Mucosa; Liver; Male; Mice; Mice, Inbred ICR; Mice, Inbred Strains; Mice, Mutant Strains; Models, Biological; Mutation; Nitric Oxide; Ornithine; Ornithine Carbamoyltransferase; Ornithine Carbamoyltransferase Deficiency Disease; Phenotype; Phenylalanine; Urea

2007