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glycine and Deficiency Disease, Ornithine Carbamoyltransferase

glycine has been researched along with Deficiency Disease, Ornithine Carbamoyltransferase in 11 studies

Research Excerpts

ExcerptRelevanceReference
"B6 status in a patient with OTC deficiency during the therapy with benzoate."1.27Activity of the glycine cleavage system in hyperammonemia treated with benzoate. ( Fujiwara, K; Kamoshita, S; Kodama, H; Motokawa, Y; Nose, O; Tajiri, H, 1983)

Research

Studies (11)

TimeframeStudies, this research(%)All Research%
pre-19904 (36.36)18.7374
1990's5 (45.45)18.2507
2000's1 (9.09)29.6817
2010's1 (9.09)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Auray-Blais, C1
Maranda, B1
Lavoie, P1
Marini, JC1
Erez, A1
Castillo, L1
Lee, B1
Brusilow, S1
Tinker, J1
Batshaw, ML1
Kodama, H1
Fujiwara, K1
Motokawa, Y1
Tajiri, H1
Nose, O1
Kamoshita, S1
Matsuura, T1
Hoshide, R1
Kiwaki, K1
Komaki, S1
Koike, E1
Endo, F1
Oyanagi, K1
Suzuki, Y1
Kato, I1
Ishikawa, K1
Qureshi, IA2
Leblanc, D1
Cyr, D1
Giguère, R1
Mitchell, G1
Vion-Dury, J1
Salvan, AM1
Confort-Gouny, S1
Cozzone, PJ1
Topaloglu, AK1
Sansaricq, C1
Fox, JE1
Bale, AE1
Tuchman, M1
Desnick, RJ1
Shiro, Y1
Yabuki, S1
Clermont, P1
Letarte, J2
Qureshi, I1
Rouleau, T1
Ouellet, R1

Reviews

1 review available for glycine and Deficiency Disease, Ornithine Carbamoyltransferase

ArticleYear
[A case of ornithine transcarbamylase deficiency presenting severe symptoms in adulthood].
    Rinsho shinkeigaku = Clinical neurology, 1992, Volume: 32, Issue:7

    Topics: Adult; Ammonia; Arginine; Citrulline; Consciousness Disorders; Female; Glycine; Humans; Ornithine Ca

1992

Other Studies

10 other studies available for glycine and Deficiency Disease, Ornithine Carbamoyltransferase

ArticleYear
High-throughput tandem mass spectrometry multiplex analysis for newborn urinary screening of creatine synthesis and transport disorders, Triple H syndrome and OTC deficiency.
    Clinica chimica acta; international journal of clinical chemistry, 2014, Sep-25, Volume: 436

    Topics: Biomarkers; Creatine; Creatinine; Filtration; Glycine; Humans; Hyperammonemia; Infant, Newborn; Orni

2014
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

2007
Amino acid acylation: a mechanism of nitrogen excretion in inborn errors of urea synthesis.
    Science (New York, N.Y.), 1980, Feb-08, Volume: 207, Issue:4431

    Topics: Adolescent; Amino Acid Metabolism, Inborn Errors; Amino Acids; Ammonia; Benzoates; Carbamoyl-Phospha

1980
Activity of the glycine cleavage system in hyperammonemia treated with benzoate.
    The Tohoku journal of experimental medicine, 1983, Volume: 140, Issue:3

    Topics: Ammonia; Animals; Benzoates; Benzoic Acid; Female; Folic Acid; Glycine; Humans; Liver; Male; Mice; M

1983
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 Analysi

1994
Breeding experiments to combine the X-linked sparse-fur (spf) mutation with the autosomal recessive BALB/cByJ strain: testing the biochemical phenotype of double-mutant mice as a model for ammonia: fatty acyl CoA synergism.
    Biochemical and biophysical research communications, 1993, Mar-15, Volume: 191, Issue:2

    Topics: Acyl Coenzyme A; Acyl-CoA Dehydrogenases; Ammonia; Animals; Butyryl-CoA Dehydrogenase; Crosses, Gene

1993
Atlas of brain proton magnetic resonance spectra. Part II: Inherited metabolic encephalopathies.
    Journal of neuroradiology = Journal de neuroradiologie, 1998, Volume: 25, Issue:4

    Topics: Adipates; Adult; Anatomy, Artistic; Argininosuccinic Acid; Argininosuccinic Aciduria; Brain; Brain D

1998
Prenatal molecular diagnosis of severe ornithine carbamoyltransferase deficiency due to a novel mutation, E181G.
    Journal of inherited metabolic disease, 1999, Volume: 22, Issue:1

    Topics: Female; Glutamic Acid; Glycine; Humans; Infant; Male; Ornithine Carbamoyltransferase; Ornithine Carb

1999
The importance of glyoxylate and other glycine precursors in the hepatic and renal conjugation of benzoate in normal and hyperammonemic mice.
    Canadian journal of physiology and pharmacology, 1989, Volume: 67, Issue:11

    Topics: Ammonia; Animals; Benzoates; Female; Glycine; Glyoxylates; Hippurates; In Vitro Techniques; Kidney;

1989
Significance of transported glycine in the conjugation of sodium benzoate in spf mutant mice with ornithine transcarbamylase deficiency.
    Biochemistry international, 1986, Volume: 12, Issue:6

    Topics: Animals; Benzoates; Benzoic Acid; Carbon Radioisotopes; Glycine; Kinetics; Liver; Mice; Mice, Mutant

1986