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glycerol and Porphyria Cutanea Tarda

glycerol has been researched along with Porphyria Cutanea Tarda in 1 studies

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Porphyria Cutanea Tarda: An autosomal dominant or acquired porphyria due to a deficiency of UROPORPHYRINOGEN DECARBOXYLASE in the LIVER. It is characterized by photosensitivity and cutaneous lesions with little or no neurologic symptoms. Type I is the acquired form and is strongly associated with liver diseases and hepatic toxicities caused by alcohol or estrogenic steroids. Type II is the familial form.

Research Excerpts

ExcerptRelevanceReference
"Heme biosynthesis pathway is conserved in yeast and humans and hem12 yeast mutants mimic porphyria cutanea tarda (PCT), a hereditary human disease caused by mutations in the UROD gene."3.81Hem12, an enzyme of heme biosynthesis pathway, is monoubiquitinated by Rsp5 ubiquitin ligase in yeast cells. ( Chelstowska, A; Jastrzebska, Z; Kaminska, J; Plochocka, D; Rytka, J; Sadurska, A; Zoladek, T, 2015)

Research

Studies (1)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's1 (100.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Chelstowska, A1
Jastrzebska, Z1
Kaminska, J1
Sadurska, A1
Plochocka, D1
Rytka, J1
Zoladek, T1

Other Studies

1 other study available for glycerol and Porphyria Cutanea Tarda

ArticleYear
Hem12, an enzyme of heme biosynthesis pathway, is monoubiquitinated by Rsp5 ubiquitin ligase in yeast cells.
    Acta biochimica Polonica, 2015, Volume: 62, Issue:3

    Topics: Amino Acid Motifs; Amino Acid Sequence; Down-Regulation; Endosomal Sorting Complexes Required for Tr

2015