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C

C. Wright

Researcher at Newcastle University

Publications -  24
Citations -  2897

C. Wright is an academic researcher from Newcastle University. The author has contributed to research in topics: Breast cancer & Cancer. The author has an hindex of 19, co-authored 22 publications receiving 2884 citations.

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Journal Article

Expression of c-erbB-2 Oncoprotein: A Prognostic Indicator in Human Breast Cancer

TL;DR: Lymph node, epidermal growth factor receptor, and estrogen receptor status, tumor size, and histological grade also had prognostic significance but, applying multivariate analysis, only lymph node status was a more important predictor of relapse-free and overall survival than staining for the c-erbB-2 oncoprotein.
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Relationship between c-erbB-2 protein product expression and response to endocrine therapy in advanced breast cancer.

TL;DR: It is suggested that c-erbB-2 protein overexpression, a marker of poor prognosis in breast cancer, is associated with a lack of response to endocrine therapy on relapse, and particularly in combination with EGFR may be useful in directing therapeutic choices.
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c-erbB-2 protein overexpression in breast cancer is a risk factor in patients with involved and uninvolved lymph nodes

TL;DR: There was an increased risk of relapse and death associated with c-erbB-2 expression irrespective of nodal involvement and this marker thus appears to be a significant prognostic factor in the early as well as the late stages of breast cancer.
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p53 expression in human breast cancer related to survival and prognostic factors: an immunohistochemical study.

TL;DR: The data suggest p53 protein expression may be a marker of more aggressive carcinomas but that the prognostic power of expression is likely to be weak and unlikely, therefore, to be of clinical value.
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Epidermal growth factor receptors in breast cancer: association with early relapse and death, poor response to hormones and interactions with neu.

TL;DR: Epidermal growth factor receptors (EGFRs) were measured in 221 primary breast cancers by ligand binding with 125I-labelled EGF, and high-affinity sites were quantitated, and expression of neu conferred similar poor prognosis to EGFR expression in all prognostic subgroups.