protoporphyrinogen has been researched along with Porphyria, Variegate in 1 studies
*Porphyria, Variegate: An autosomal dominant porphyria that is due to a deficiency of protoporphyrinogen oxidase (EC 1.3.3.4) in the LIVER, the seventh enzyme in the 8-enzyme biosynthetic pathway of HEME. Clinical features include both neurological symptoms and cutaneous lesions. Patients excrete increased levels of porphyrin precursors, COPROPORPHYRINS and protoporphyrinogen. [MeSH]
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 1 (100.00) | 2.80 |
| Authors | Studies |
|---|---|
| Barinka, C; Havlinova, B; Kasparek, P; Korandova, Z; Kutil, Z; Milosevic, M; Novakova, Z; Ondrakova, M; Rohlena, J; Sandoval-Acuña, C; Truksa, J; Vrbacky, M | 1 |
1 other study(ies) available for protoporphyrinogen and Porphyria, Variegate
| Article | Year |
|---|---|
Generation and characterization of human U-2 OS cell lines with the CRISPR/Cas9-edited protoporphyrinogen oxidase IX gene.
Topics: Aminolevulinic Acid; Cell Line; CRISPR-Cas Systems; Heme; Humans; Oxidoreductases; Porphyria, Variegate; Protoporphyrinogen Oxidase; Protoporphyrins | 2022 |