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Ling Fu

Researcher at Genentech

Publications -  30
Citations -  4933

Ling Fu is an academic researcher from Genentech. The author has contributed to research in topics: Cancer & Ovarian cancer. The author has an hindex of 20, co-authored 28 publications receiving 4608 citations.

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Treatment of Medulloblastoma with Hedgehog Pathway Inhibitor GDC-0449

TL;DR: A 26-year-old man with metastatic medulloblastoma that was refractory to multiple therapies was treated with a novel hedgehog pathway inhibitor, GDC-0449; treatment resulted in rapid (although transient) regression of the tumor and reduction of symptoms.
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A paracrine requirement for hedgehog signalling in cancer

TL;DR: This article showed that although ligand-dependent activation of the hedgehog signalling pathway has been associated with tumorigenesis in a number of human tissues, Hh ligands failed to activate signalling in tumour epithelial cells.
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Transgenic mice expressing human fibroblast growth factor-19 display increased metabolic rate and decreased adiposity.

TL;DR: It is reported that FGF19 transgenic mice had a significant and specific reduction in fat mass that resulted from an increase in energy expenditure and did not become obese or diabetic on a high fat diet.
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Epithelial versus mesenchymal phenotype determines in vitro sensitivity and predicts clinical activity of erlotinib in lung cancer patients.

TL;DR: Examination of expression of the epithelial marker E-cadherin by immunohistochemistry on primary tumor samples from subjects enrolled in a randomized NSCLC clinical trial in which erlotinib in combination with chemotherapy previously failed to show clinical activity supports a potential role for EMT as a determinant of EGFR activity in NSCLCs tumor cells.
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Fibroblast growth factor 19 increases metabolic rate and reverses dietary and leptin-deficient diabetes.

TL;DR: Treatment with FGF19 prevented or reversed the diabetes that develops in mice made obese by genetic ablation of brown adipose tissue or genetic absence of leptin, and profiled the F GF19-induced gene expression changes in the liver and brown fat.