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Titlebook: Endocrine Therapy and Growth Regulation of Breast Cancer; Urs Eppenberger,Aron Goldhirsch (Vice-Primario) Conference proceedings 1989 Spri

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Representations of Internarrative Identity to a malignant phenotype. Subsequent experiments showed that this was a gene related in structure to that encoding the epidermal growth factor (EGF) receptor (Coussens et al. 1985; Yamamoto 1986). Because of its derivation from a tumour classified as a neuroblastoma, the transforming oncogene was n
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New Aspects in the Molecular Growth Regulation of Mammary Tumors,growth regulation of human breast epithelium cells. Such a transcriptional control is achieved through the interaction of transacting factors with the respective promoter elements located on the DNA. The steroid receptor proteins belong to such a family of regulatory proteins. The ability of these p
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Ribosomal Protein S6 Kinase and PKC in Human Mammary Tumor Cells, (GF-R). Such GF-Rs are likely to represent important growth-regulatory elements in the estrogen-induced autocrine or paracrine growth mechanisms of human breast cancer (Fitzpatrick et al. 1984; Macias et al. 1986; Sainsbury et al. 1985; Wyss et al. 1987; Sainsbury et al. 1987; Furlanetto and DiCarl
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Expression of the c-erbB-2 Proto-Oncogene Protein in Human Breast Cancer, to a malignant phenotype. Subsequent experiments showed that this was a gene related in structure to that encoding the epidermal growth factor (EGF) receptor (Coussens et al. 1985; Yamamoto 1986). Because of its derivation from a tumour classified as a neuroblastoma, the transforming oncogene was n
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The Transformation-Suppressive Function Is Lost in Tumorgenic Cells and Is Restored upon Transfer o1987). We have demonstrated that rat embryo fibroblasts which have often been used as recipient cells for the introduction of “dominant-acting” oncogenes are still capable of suppressing the neoplastic phenotype when fused with a H-. transformed rat cell line. The neoplastic phenotype is re-expresse
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https://doi.org/10.1057/9780230378162The establishment of numerous breast cancer cell lines in continuous culture has favored the study of the hormonal control of breast cancer proliferation in the past years.
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