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《肿瘤与内分泌》.2005年.第2期
 * Development of strategies for the use of anti-growth factor treatments
 * Inhibitors of growth factor signalling
 * Intrinsic and acquired resistance to EGFR inhibitors in human cancer therapy
 * Clinical trials of intracellular signal transductions inhibitors for breast cancer — a strategy to overcome endocrine resistance
 * Overview of tyrosine kinase inhibitors in clinical breast cancer
 * Growth factor signalling in clinical breast cancer and its impact on response to conventional therapies: a review of chemotherapy
 * Growth factor signalling in clinical breast cancer and its impact on response to conventional therapies: the Edinburgh experience
 * Growth factor signalling and response to endocrine therapy: the Royal Marsden Experience
 * Epidermal growth factor receptor/HER2/insulin-like growth factor receptor signalling and oestrogen receptor activity in clinical breast canc
 * Acquired resistance to oestrogen deprivation: role for growth factor signalling kinases/oestrogen receptor cross-talk revealed in new MCF-7X
 * Downstream targets of growth factor and oestrogen signalling and endocrine resistance: the potential roles of c-Myc, cyclin D1 and cyclin E
 * Elevated ERK1/ERK2/estrogen receptor cross-talk enhances estrogen-mediated signaling during long-term estrogen deprivation
 * Long-term estradiol deprivation in breast cancer cells up-regulates growth factor signaling and enhances estrogen sensitivity
 * The NFB pathway and endocrine-resistant breast cancer
 * Growth factor signalling and resistance to selective oestrogen receptor modulators and pure anti-oestrogens: the use of anti-growth factor t
 * The epidermal growth factor receptor family
 * Overview of the impact of conventional systemic therapies on breast cancer
 * Polymer–drug conjugates: towards a novel approach for the treatment of endrocine-related cancer
 * ER is a potent inhibitor of cell proliferation in the HCT8 human colon cancer cell line through regulation of cell cycle components
 * Malign cystic glucagonoma presented with diabetic ketoacidosis: case report with an update
 * Chromosomal instability predicts metastatic disease in patients with insulinomas
 * Enhanced protein kinase B/Akt signalling in pituitary tumours
 * Gonadotropins upregulate the epidermal growth factor receptor through activation of mitogen-activated protein kinases and phosphatidyl-inosi
 * The 67 kDa laminin receptor increases tumor aggressiveness by remodeling laminin-1
 * Cytotoxic and antiproliferative activity of the single agent epirubicin versus epirubicin plus tamoxifen as primary chemotherapy in human br
 * Evidence for specific TRPM8 expression in human prostate secretory epithelial cells: functional androgen receptor requirement
 * Alterations in the regulatory volume decrease (RVD) and swelling-activated Cl–current associated with neuroendocrine differentiation of pros
 * Identification of growth factor independent-1 (GFI1) as a repressor of 25-hydroxyvitamin D 1-alpha hydroxylase (CYP27B1) gene expression in
 * BRAF mutation in thyroid cancer
 * Mechanisms of endocrine therapy-responsive and -unresponsive prostate tumours
 * Characterization of thyroid ‘follicular neoplasms’ in fine-needle aspiration cytological specimens using a panel of immunohistochemical mark
 * Action of thiazolidinediones on differentiation, proliferation and apoptosis of normal and transformed thyrocytes in culture
 * Medullary and papillary carcinoma of the thyroid gland occurring as a collision tumour: report of three cases with molecular analysis and re
 * Life expectancy in differentiated thyroid cancer: a novel approach to survival analysis
 * Low molecular weight proteomic information distinguishes metastatic from benign pheochromocytoma
 * Tissue inhibitor of metalloproteinases-1 in breast cancer
 * Breast-tissue sampling for risk assessment and prevention
 * Gefitinib inhibits the ability of human bone marrow stromal cells to induce osteoclast differentiation: implications for the pathogenesis an