Published in Gene Therapy Weekly, September 23rd, 2004
According to a study from Germany, "in mammalian cells, factor VIII (FVIII) secretion depends upon its interaction with chaperones of the endoplasmic reticulum (ER) and requires a unique ATP-dependent step to dissociate aggregates formed within the ER. To further elucidate mechanisms which might account for the inefficient secretion of recombinant FVIII (rFVIII), we have analyzed the pathways of recombinant full length (rFVIII-FL) and B-domain deleted (rFVIIIDeltaB) FVIII and compared these to the secretion route of native FVIII in primary hepatocytes."
"Using confocal laser scanning...
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Source: Gene Therapy Weekly (2004-09-23)
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