Lataa...
In vivo metabolism of proapolipoprotein A-I in Tangier disease.
Tangier disease is a rare familial disorder characterized by extremely low levels of apolipoprotein A-I (apoA-I) and high density lipoproteins (HDL). In normal subjects, proapoA-I is secreted into plasma and converted to mature apoA-I by the cleavage of the amino-terminal six amino acids with the ma...
Tallennettuna:
| Päätekijät: | , , , , , , |
|---|---|
| Aineistotyyppi: | Artikkeli |
| Kieli: | en |
| Julkaistu: |
1987
|
| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC442448/ https://ncbi.nlm.nih.gov/pubmed/3119665 |
| Tagit: |
Lisää tagi
Ei tageja, Lisää ensimmäinen tagi!
|