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3,013 Possible Causes for cysteine

  • Skin Infection

    Cysteine protease (Exotoxin B) Pyoderma strains of S. pyogenes can colonize or survive on normal skin surfaces for extended periods.[]

  • Streptococcal Infection

    Cysteine protease (Exotoxin B) Pyoderma strains of S. pyogenes can colonize or survive on normal skin surfaces for extended periods.[] SPE B is a precursor of a cysteine protease, another determinant of virulence. [12] Group A streptococcal isolates associated with streptococcal TSS encode certain SPEs (ie[]

  • Idiopathic Pulmonary Fibrosis

    NAC (N-acetyl cysteine)—Mucomyst A recent study showed that this medication is not helpful.[]

  • Aging

    […] ligase catalytic subunit, glutamate-cysteine ligase modifier subunit, and NAD(P)H quinone oxidoreductase 1 in the liver of an aging mice.[] […] nuclear factor erythroid-2-related factor 2 and upregulated the expressions of several antioxidant genes such as glutathione reductase, glutathione S-transferase, glutamate-cysteine[]

  • Pulmonary Tuberculosis

    Single nucleotide polymorphism of glutamate-cysteine ligase subunit catalytic (GCLC) gene namely -129C/T GCLC has been reported to have an association with a risk factor of[]

  • Nasal Polyp

    The effect of hypoxia on the expressions of angiogenesis factors as cysteine-rich 61 (Cyr61) and vascular endothelial growth factor (VEGF) and neutrophil chemoattractant as[]

  • Vinyl Ether

    In rats in vivo, FDVE undergoes glutathione conjugation and metabolism to cysteine conjugates, whose bioactivation by renal cysteine conjugate beta-lyase has been implicated[] Cytosolic cysteine S-conjugates metabolism by renal beta-lyase predominated over N-acetylation (ratio of activities was 0.2-6 and 3-146 for the alkane and alkene cysteine[] The FDVE-cysteine conjugates S-(1,1-difluoro-2-fluoromethoxy-2-(trifluoromethyl) ethyl)-L-cysteine (DFEC) and (Z)-S-(1-fluoro-2-fluoromethoxy-2-(trifluoromethyl) vinyl)-L-cysteine[]

  • Calcium Gluconate

    The purpose of this study was to do compatibility testing for solutions containing calcium chloride and calcium gluconate without cysteine.[] Solutions of TrophAmine and Premasol (2.5% amino acids), containing calcium chloride or calcium gluconate were compounded without cysteine.[] This study presents data in order to evaluate options for adding calcium and phosphate to neonatal parenteral nutrition solutions during shortages of calcium and cysteine.[]

  • Li-Fraumeni Syndrome

    Genetic analysis showed a germline TP53 mutation in codon 220 exon 6, which changed TAT -- TGT and resulted in a tyrosine-to-cysteine amino acid substitution (Tyr220Cys).[]

  • Piebaldism

    The first mutation, found in two apparently unrelated probands with mild piebaldism and English ancestry, substitutes an arginine for a highly conserved cysteine at codon[] The apparent clustering of these uncommon mutations at or near the conserved cysteines for the D2 Ig-like loop further suggests a critical role for this region in Kit receptor[] , detected in a piebald kindred characterized by unusually limited depigmentation, substitutes a threonine for an alanine at codon 178, a site just proximal to conserved cysteines[]

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