Compounds > ornithine

ornithine and Citrullinemia

ornithine has been researched along with Citrullinemia in 5 studies

Research

Studies (5)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's1 (20.00)18.2507
2000's3 (60.00)29.6817
2010's1 (20.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Eto, K; Funahashi, A; Furuie, S; Furukawa, T; Gao, Q; Horiuchi, M; Kadowaki, T; Kuroda, E; Moriyama, M; Nakamura, Y; Saheki, T; Setogawa, Y; Sinasac, DS; Tai, YH; Takano, K; Ushikai, M; Yamamura, KI; Yasuda, I1
Camacho, JA; Rioseco-Camacho, N1
Aupetit, J; Bardet, J; Blanc, A; Chabli, A; Chadefaux-Vekemans, B; Kamoun, P; Rabier, D1
Andrade, D; Camacho, JA; Cederbaum, SD; Derbeneva, O; Mardach, R; Qu, Y; Rioseco-Camacho, N; Ruiz-Pesini, E; Zaldivar, F1
Sass, JO; Skladal, D1

Other Studies

5 other study(ies) available for ornithine and Citrullinemia

ArticleYear
Pivotal role of inter-organ aspartate metabolism for treatment of mitochondrial aspartate-glutamate carrier 2 (citrin) deficiency, based on the mouse model.
    Scientific reports, 2019, 03-12, Volume: 9, Issue:1

    Topics: Amino Acids; Ammonia; Ammonium Chloride; Animals; Aspartic Acid; Citrulline; Citrullinemia; Disease Models, Animal; Glycerolphosphate Dehydrogenase; Hyperammonemia; Intestine, Small; Lactates; Liver; Mice, Inbred C57BL; Mice, Knockout; Mitochondrial Membrane Transport Proteins; Organ Specificity; Ornithine; Perfusion; Portal Vein; Pyruvic Acid; Urea

2019
The human and mouse SLC25A29 mitochondrial transporters rescue the deficient ornithine metabolism in fibroblasts of patients with the hyperornithinemia-hyperammonemia-homocitrullinuria (HHH) syndrome.
    Pediatric research, 2009, Volume: 66, Issue:1

    Topics: Amino Acid Transport Systems, Basic; Animals; Astrocytes; Carnitine Acyltransferases; Central Nervous System; Citrullinemia; DNA Primers; Fibroblasts; Fluorescent Antibody Technique, Indirect; Humans; Hyperammonemia; Mice; Mitochondrial Proteins; Ornithine; Reverse Transcriptase Polymerase Chain Reaction; Syndrome

2009
Improving the prenatal diagnosis of citrullinemia using citrulline/ornithine+arginine ratio in amniotic fluid.
    Prenatal diagnosis, 2002, Volume: 22, Issue:6

    Topics: Amniocentesis; Amniotic Fluid; Arginine; Argininosuccinate Synthase; Chorionic Villi Sampling; Citrulline; Citrullinemia; Female; Humans; Ornithine; Pregnancy; Sensitivity and Specificity

2002
Clinical and functional characterization of a human ORNT1 mutation (T32R) in the hyperornithinemia-hyperammonemia-homocitrullinuria (HHH) syndrome.
    Pediatric research, 2006, Volume: 60, Issue:4

    Topics: Adolescent; Adult; Amino Acid Transport Systems, Basic; Child; Citrullinemia; DNA, Mitochondrial; Female; Haplotypes; Humans; Hyperammonemia; Male; Metabolic Diseases; Mitochondrial Membrane Transport Proteins; Mutation; Ornithine; Pedigree; Phenotype; Polymorphism, Genetic; Proteins; RNA, Messenger; Syndrome

2006
Plasma concentrations and renal clearance of orotic acid in argininosuccinic acid synthetase deficiency.
    Pediatric nephrology (Berlin, Germany), 1999, Volume: 13, Issue:9

    Topics: Amino Acids; Arginine; Child; Chromatography, Gas; Citrulline; Citrullinemia; Creatinine; Glutamine; Humans; Male; Ornithine; Orotic Acid; Quaternary Ammonium Compounds; Time Factors

1999