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Endocytic depletion of L-MAG from CNS myelin in quaking mice

Quaking is an autosomal recessive hypo/dysmyelinating mutant mouse which has a 1-Mbp deletion on chromosome 17. The mutation exhibits pleiotrophy and does not include genes encoding characterized myelin proteins. The levels of the 67-kD isoform of the myelin-associated glycoprotein (S-MAG) relative...

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Gorde:
Xehetasun bibliografikoak
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: The Rockefeller University Press 1995
Gaiak:
Sarrera elektronikoa:https://ncbi.nlm.nih.gov/pmc/articles/PMC2120655/
https://ncbi.nlm.nih.gov/pubmed/8557747
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