CYSTATHIONINURIA
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1469-1809.1959.tb01485.x/fullpdf
Reference12 articles.
1. A DISEASE, PROBABLY HEREDITARY, CHARACTERISED BY SEVERE MENTAL DEFICIENCY AND A CONSTANT GROSS ABNORMALITY OF AMINOACID METABOLISM
2. A study of the behaviour of some sixty amino-acids and other ninhydrin-reacting substances on phenol-‘collidine’ filter-paper chromatograms, with notes as to the occurrence of some of them in biological fluids
3. MICRO-ELECTROPHORESIS OF PROTEIN ON FILTER-PAPER*1
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2. Mammalian Sulfur Amino Acid Metabolism: A Nexus Between Redox Regulation, Nutrition, Epigenetics, and Detoxification;Antioxidants & Redox Signaling;2018-08
3. Role for Cystathionine γ Lyase (CSE) in an Ethanol (E)-Induced Lesion in Fetal Brain GSH Homeostasis;International Journal of Molecular Sciences;2018-05-22
4. Identification of altered brain metabolites associated with TNAP activity in a mouse model of hypophosphatasia using untargeted NMR-based metabolomics analysis;Journal of Neurochemistry;2017-03
5. Screening, morphological and molecular characterization of fungi producing cystathionine γ-lyase;Acta Biologica Hungarica;2015-03
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