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S-Allyl-L-Cysteine Affects Cell Proliferation and Expression of H2S-Synthetizing Enzymes in MCF-7 and MDA-MB-231 Adenocarcinoma Cell Lines. [PDF]
BiomoleculesBentke-Imiolek A +4 more
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Why Symptoms Linger in Quiescent Crohn's Disease: Investigating the Impact of Sulfidogenic Microbes and Sulfur Metabolic Pathways. [PDF]
Inflamm Bowel DisGolob J +10 more
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The therapeutic potential of hydrogen sulfide and its donors, a new discovery in vascular diseases. [PDF]
J Cardiovasc PharmacolPu Y, Lin W, Ren S, Gao Y, Wang G.
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Molecular Mechanisms and Novel Therapeutics Targeting Ferroptosis in Gastric Cancer: A Literature Review. [PDF]
J CancerHsieh HL +4 more
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Human Genetics, 2003
Hereditary cystathioninuria (MIM 219500) is presumed to be caused by deficiency of the activity of cystathionine gamma-lyase (cystathionase; CTH EC 4.4.1.1), which is normally required for the conversion of methionine into cysteine. To date, no mutations have been described among patients with cystathioninuria.
Jian, Wang, Robert A, Hegele
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Hereditary cystathioninuria (MIM 219500) is presumed to be caused by deficiency of the activity of cystathionine gamma-lyase (cystathionase; CTH EC 4.4.1.1), which is normally required for the conversion of methionine into cysteine. To date, no mutations have been described among patients with cystathioninuria.
Jian, Wang, Robert A, Hegele
openaire +2 more sources