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Robert P.C. Shiu

Researcher at Laboratory of Molecular Biology

Publications -  5
Citations -  725

Robert P.C. Shiu is an academic researcher from Laboratory of Molecular Biology. The author has contributed to research in topics: Rous sarcoma virus & Avian sarcoma virus. The author has an hindex of 5, co-authored 5 publications receiving 707 citations.

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Glucose depletion accounts for the induction of two transformation-sensitive membrane proteinsin Rous sarcoma virus-transformed chick embryo fibroblasts

TL;DR: Chick embryo fibroblasts transformed by Rous sarcoma virus have an increased content of two membrane proteins of molecular weights 78,000 and 95,000 which may have an important role in regulating the utilization of glucose in cultured cells.
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Induction of two transformation-sensitive membrane polypeptides in normal fibroblasts by a block in glycoprotein synthesis or glucose deprivation.

TL;DR: The induction of these two proteins by glucose starvation suggests that they have a role in glucose utilization, and two glucose derivatives, glucosamine and 2-deoxyglucose, are known to interfere with the glycosylation process.
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Identification of a transformation-specific protein induced by a rous sarcoma virus

TL;DR: Pulsechase experiments indicate that this 56,000 dalton molecular weight protein is extremely unstable, with a half-life of about 20 min, and does not serve as a precursor to any of the detectable virion polypeptides.
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Properties and purification of a glucose-regulated protein from chick embryo fibroblasts.

TL;DR: Immunofluorescence studies using affinity purified antibodies to GRP-78 revealed that this protein was not exposed on the cell surface but was localized in a granular vesicular network inside the cell that resembles the distribution of endoplasmic reticulum.
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Epidermal growth factor and insulin cause normal chicken heart mesenchymal cells to proliferate like their Rous sarcoma virus-infected counterparts

TL;DR: The addition of epidermal growth factor and insulin to cultures of normal chicken heart mesenchymal cells causes these cells to proliferate at a rate comparable to that of their RSV-infected counterparts.