Page last updated: 2024-08-17

nad and Argininosuccinate Synthase Deficiency Disease

nad has been researched along with Argininosuccinate Synthase Deficiency Disease in 4 studies

Research

Studies (4)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's3 (75.00)29.6817
2010's0 (0.00)24.3611
2020's1 (25.00)2.80

Authors

AuthorsStudies
Chen, GB; Francisco, JC; Li, S; Singh, BK; Thimmukonda, NK; Yau, WW; Yen, PM; Zhou, J1
Begum, L; Horiuchi, M; Iijima, M; Jalil, MA; Kobayashi, K; Li, MX; Moriyama, M; Robinson, BH; Saheki, T; Sinasac, DS; Tsui, LC1
Kobayashi, K; Saheki, T1
Fujimoto, H; Hattori, T; Inui, A; Kizaki, Z; Kobayashi, K; Mutoh, K; Ohura, T; Okano, Y; Saheki, T; Terashi, M; Yanagawa, Y1

Reviews

1 review(s) available for nad and Argininosuccinate Synthase Deficiency Disease

ArticleYear
[Molecular basis of citrin deficiency].
    Seikagaku. The Journal of Japanese Biochemical Society, 2004, Volume: 76, Issue:12

    Topics: Aspartic Acid; Calcium; Calcium-Binding Proteins; Cholestasis, Intrahepatic; Chromosome Mapping; Citrullinemia; Gene Frequency; Homozygote; Humans; Infant, Newborn; Maleates; Membrane Transport Proteins; Mitochondria; Mitochondrial Membrane Transport Proteins; Mitochondrial Proteins; Mutation; NAD; Organic Anion Transporters

2004

Other Studies

3 other study(ies) available for nad and Argininosuccinate Synthase Deficiency Disease

ArticleYear
Nicotinamide riboside rescues dysregulated glycolysis and fatty acid β-oxidation in a human hepatic cell model of citrin deficiency.
    Human molecular genetics, 2023, 05-18, Volume: 32, Issue:11

    Topics: Aspartic Acid; Citrullinemia; Fatty Acids; Glycolysis; Hepatocytes; Humans; Hyperammonemia; Malates; Mitochondrial Membrane Transport Proteins; NAD; Urea

2023
Slc25a13-knockout mice harbor metabolic deficits but fail to display hallmarks of adult-onset type II citrullinemia.
    Molecular and cellular biology, 2004, Volume: 24, Issue:2

    Topics: Amino Acids; Ammonia; Animals; Argininosuccinate Synthase; Aspartic Acid; Base Sequence; Citrullinemia; Disease Models, Animal; DNA; Female; Gluconeogenesis; Humans; Liver; Male; Membrane Transport Proteins; Mice; Mice, Knockout; Mitochondrial Membrane Transport Proteins; Mitochondrial Proteins; Mutation; NAD; Phenotype; RNA, Messenger; Urea

2004
Reduced carbohydrate intake in citrin-deficient subjects.
    Journal of inherited metabolic disease, 2008, Volume: 31, Issue:3

    Topics: Adolescent; Adult; Calcium-Binding Proteins; Child; Child, Preschool; Cholestasis, Intrahepatic; Citrullinemia; Dietary Carbohydrates; Dietary Fats; Energy Intake; Female; Food Preferences; Glucose; Humans; Infant; Male; Middle Aged; NAD; Organic Anion Transporters

2008