טוען...
A Glycine N-methyltransferase knockout mouse model for humans with deficiency of this enzyme
Three human cases having mutations in the glycine N-methyltransferase (GNMT) gene have been reported. This enzyme transfers a methyl group from S-adenosylmethionine (SAM) to glycine to form S-adenosylhomocysteine (SAH) and N-methylglycine (sarcosine) and is believed to be involved in the regulation...
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| Main Authors: | , , , |
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| פורמט: | Artigo |
| שפה: | Inglês |
| יצא לאור: |
2006
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| נושאים: | |
| גישה מקוונת: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2792375/ https://ncbi.nlm.nih.gov/pubmed/16779654 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s11248-006-0008-1 |
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