Page last updated: 2024-08-21

pyrimidine and Abnormalities, Multiple

pyrimidine has been researched along with Abnormalities, Multiple in 2 studies

Research

Studies (2)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	0 (0.00)	18.2507
2000's	0 (0.00)	29.6817
2010's	2 (100.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Cai, C; Fan, W; Fang, Y; Hu, W; Lin, S; Meng, Y; Shu, J; Sun, B; Wang, C; Zhang, C; Zhang, X; Zhang, Y	1
Amamoto, R; Fang, J; Kang, D; Matsumoto, S; Nonaka, K; Takazaki, S; Uchiumi, T; Yagi, M; Yamaza, H	1

Other Studies

2 other study(ies) available for pyrimidine and Abnormalities, Multiple

Article	Year
Clinical and genetic analysis of 7 Chinese patients with β-ureidopropionase deficiency. Medicine, 2019, Volume: 98, Issue:1 Topics: Abnormalities, Multiple; Amidohydrolases; Aminoisobutyric Acids; Asian People; beta-Alanine; Brain Diseases; Child, Preschool; Computational Biology; Female; Genetic Testing; Humans; Infant; Infant, Newborn; Male; Metabolomics; Movement Disorders; Mutation, Missense; Purine-Pyrimidine Metabolism, Inborn Errors; Pyrimidines	2019
Dihydro-orotate dehydrogenase is physically associated with the respiratory complex and its loss leads to mitochondrial dysfunction. Bioscience reports, 2013, Feb-05, Volume: 33, Issue:2 Topics: Abnormalities, Multiple; Dihydroorotate Dehydrogenase; Electron Transport Complex II; HeLa Cells; Humans; Limb Deformities, Congenital; Mandibulofacial Dysostosis; Membrane Potential, Mitochondrial; Micrognathism; Mitochondria; Mutation; Oxidative Phosphorylation; Oxidoreductases Acting on CH-CH Group Donors; Pyrimidines; Reactive Oxygen Species; RNA, Small Interfering; Ubiquinone	2013

Article

Year

Clinical and genetic analysis of 7 Chinese patients with β-ureidopropionase deficiency.

Medicine, 2019, Volume: 98, Issue:1

Topics: Abnormalities, Multiple; Amidohydrolases; Aminoisobutyric Acids; Asian People; beta-Alanine; Brain Diseases; Child, Preschool; Computational Biology; Female; Genetic Testing; Humans; Infant; Infant, Newborn; Male; Metabolomics; Movement Disorders; Mutation, Missense; Purine-Pyrimidine Metabolism, Inborn Errors; Pyrimidines

2019

Dihydro-orotate dehydrogenase is physically associated with the respiratory complex and its loss leads to mitochondrial dysfunction.

Bioscience reports, 2013, Feb-05, Volume: 33, Issue:2

Topics: Abnormalities, Multiple; Dihydroorotate Dehydrogenase; Electron Transport Complex II; HeLa Cells; Humans; Limb Deformities, Congenital; Mandibulofacial Dysostosis; Membrane Potential, Mitochondrial; Micrognathism; Mitochondria; Mutation; Oxidative Phosphorylation; Oxidoreductases Acting on CH-CH Group Donors; Pyrimidines; Reactive Oxygen Species; RNA, Small Interfering; Ubiquinone

2013