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Vanessa Chisholm

Researcher at Genentech

Publications -  10
Citations -  3172

Vanessa Chisholm is an academic researcher from Genentech. The author has contributed to research in topics: Chinese hamster ovary cell & Vascular endothelial growth factor A. The author has an hindex of 8, co-authored 10 publications receiving 3124 citations.

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Journal Article

Humanization of an Anti-Vascular Endothelial Growth Factor Monoclonal Antibody for the Therapy of Solid Tumors and Other Disorders

TL;DR: Rec recombinant humanized MAb V EGF is suitable to test the hypothesis that inhibition of VEGF-induced angiogenesis is a valid strategy for the treatment of solid tumors and other disorders in humans.
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Vascular endothelial growth factor is essential for corpus luteum angiogenesis

TL;DR: The unexpected finding that treatment with truncated soluble Flt-1 receptors, which inhibit vascular endothelial growth factor (VEGF) bioac-tivity, resulted in virtually complete suppression of CL angiogenesis in a rat model of hormonally induced ovulation is reported.
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Engineering Chinese hamster ovary cells to maximize sialic acid content of recombinant glycoproteins.

TL;DR: The experiments demonstrate the feasibility of genetically engineering cell lines to produce therapeutics with desired glycosylation patterns and resulted in reduction of oligosaccharides terminating with GlcNAc, whereas overexpression of ST resulted in sialylation of ≥90% of available branches.
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High-level production of recombinant proteins in CHO cells using a dicistronic DHFR intron expression vector.

TL;DR: These vectors produce stable CHO cell clones that, when pooled, produce abundant amounts of secreted recombinant proteins compared with the amounts produced by conventional expression approaches that have selectable marker and the cDNA of interest under control of separate transcription units.
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Green fluorescent protein as a second selectable marker for selection of high producing clones from transfected CHO cells.

TL;DR: This work evaluated using green fluorescent protein (GFP) for selection of high producing clones by fluorescence-activated cell sorter (FACS) to reduce screening effort in Chinese hamster ovary cells and found that productivity correlated very well with RNA of the desired protein.