Pathways Knowlegdes
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| Pathway | DOIs | Note |
|---|---|---|
| Purine Nucleotides De Novo Biosynthesis 2 Accession ID: PathBank:SMP0122223 |
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| Purine Metabolism Accession ID: PathBank:SMP0000050 |
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| Methionine Metabolism Accession ID: PathBank:SMP0000033 |
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| Adenosine Deaminase Deficiency Accession ID: PathBank:SMP0000144 |
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| Molybdenum Cofactor Deficiency Accession ID: PathBank:SMP0000203 |
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| Glycine N-Methyltransferase Deficiency Accession ID: PathBank:SMP0000222 |
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| Mercaptopurine Action Pathway Accession ID: PathBank:SMP0000428 |
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| Adenine Phosphoribosyltransferase Deficiency (APRT) Accession ID: PathBank:SMP0000535 |
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| Methylenetetrahydrofolate Reductase Deficiency (MTHFRD) Accession ID: PathBank:SMP0000543 |
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| Serine Metabolism Accession ID: PathBank:SMP0002323 |
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| Purine Nucleotides De Novo Biosynthesis Accession ID: PathBank:SMP0002377 |
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| Glycine Metabolism Accession ID: PathBank:SMP0002428 |
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| Folate Metabolism Accession ID: PathBank:SMP0087196 |
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| Methionine Metabolism Accession ID: PathBank:SMP0087249 |
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| Methionine Metabolism Accession ID: PathBank:SMP0063637 |
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| Folate Malabsorption, Hereditary Accession ID: PathBank:SMP0120656 |
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| Lesch-Nyhan Syndrome (LNS) Accession ID: PathBank:SMP0120728 |
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| Molybdenum Cofactor Deficiency Accession ID: PathBank:SMP0120752 |
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| Purine Nucleoside Phosphorylase Deficiency Accession ID: PathBank:SMP0120756 |
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| Xanthinuria Type I Accession ID: PathBank:SMP0120796 |
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