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Homozygous familial hypercholesterolemia mutant with a defect in internalization of low density lipoprotein.

During studies on binding of low density lipoprotein (LDL) to fibroblasts from patients with the homozygous form of familial hypercholesterolemia (FH), a unique line was derived from subject M.N. This line could bind as much LDL as normal cells, or even more. However, like fibroblasts from other pat...

Täydet tiedot

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Bibliografiset tiedot
Päätekijät: Miyake, Y, Tajima, S, Yamamura, T, Yamamoto, A
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: 1981
Aiheet:
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC320351/
https://ncbi.nlm.nih.gov/pubmed/6272292
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