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Rachel M. Patterson

Researcher at National Institutes of Health

Publications -  28
Citations -  1001

Rachel M. Patterson is an academic researcher from National Institutes of Health. The author has contributed to research in topics: Carcinogenesis & Estrogen. The author has an hindex of 14, co-authored 28 publications receiving 968 citations.

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Differential Effects of Trivalent and Pentavalent Arsenicals on Cell Proliferation and Cytokine Secretion in Normal Human Epidermal Keratinocytes

TL;DR: The data suggest that methylated arsenicals, products of the metabolic conversion of inorganic arsenic, can significantly affect viability and proliferation of human keratinocytes and modify their secretion of inflammatory and growth-promoting cytokines.
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Activated Oncogenes in B6C3F1 Mouse Liver Tumors: Implications for Risk Assessment

TL;DR: The B6C3F1 mouse liver may provide a sensitive assay system to detect various classes of proto-oncogenes that are susceptible to activation by carcinogenic insult and will provide information at a molecular level to aid in the use of rodent carcinogenesis data for risk assessment.
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Arsenic-induced alterations in the contact hypersensitivity response in Balb/c mice.

TL;DR: It is demonstrated that repeated, prolonged exposure to nontoxic concentrations of sodium arsenite alters immune cell populations and results in functional changes in immune responses, specifically attenuation of contact hypersensitivity.
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Baculovirus and insect cell gene expression: review of baculovirus biotechnology.

TL;DR: The BEVS continues to evolve as a powerful, flexible tool for molecular biology, protein function, and biomedical research, and the prospect of new biopharmaceuticals, in particular human therapeutics and vaccines, to improve human health and increase the quality of life for millions of people.
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HSP binding and mitochondrial localization of p53 protein in human HT1080 and mouse C3H10T1/2 cell lines

TL;DR: P53:HSP complexes represent components of a chaperone program which affects the subcellular distribution of p53 protein in these transformed lines, and suggest that p53 might be found in these cytoplasmic organelles.