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Aminolevulinic acid dehydratase (porphobilinogen synthase, or ALA dehydratase, or aminolevulinate dehydratase) is an enzyme (EC 4.2.1.24) that in humans is encoded by the …

2022年6月1日 · Learn about ALAD Porphyria, including symptoms, causes, and treatments. If you or a loved one is affected by this condition, visit NORD to find resources and Patients & …

ALAD Porphyria (ADP) is a very rare genetic metabolic disease characterized by almost complete deficiency of the enzyme delta-aminolevulinic acid (ALA) dehydratase. In ADP, the gene …

2024年12月24日 · ALAD (Aminolevulinate Dehydratase) is a Protein Coding gene. Diseases associated with ALAD include Porphyria, Acute Hepatic and Porphyria Due To Ala …

The ALAD gene provides instructions for making an enzyme known as delta-aminolevulinate dehydratase. Learn about this gene and related health conditions.

ALAD Function and Purpose δ-aminolevulinic acid dehydrogenase (ALAD) (also called Porphobilinogen Synthase (PBGS)) is an enzyme considered to be one of lead’s main targets. …

2025年1月4日 · The ALAD enzyme is composed of 8 identical subunits and catalyzes the condensation of 2 molecules of delta-aminolevulinate to form porphobilinogen (a precursor of …

2025年2月8日 · The ALAD enzyme is composed of 8 identical subunits and catalyzes the condensation of 2 molecules of delta-aminolevulinate to form porphobilinogen (a precursor of …

Aminolevulinic acid dehydratase (ALAD) activity can be inhibited in situations including hereditary tyrosinemia type 1, lead intoxication, and exposure to styrene, trichloroethylene, or …