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6篇 您的检索式:作者名="Mafficini"
    题名 作者 年代 出处 被引量
1Targeted next‐generation sequencing of cancer genes dissects the molecular profiles of intraductal papillary neoplasms of the pancreas显示文摘Eliana Amato Marco dal Molin Andrea Mafficini Jun Yu Giuseppe Malleo Borislav Rusev Matteo Fassan Davide Antonello Yoshihiko Sadakari Paola Castelli Giuseppe Zamboni Anirban Maitra Roberto Salvia Ralph H Hruban Claudio Bassi Paola Capelli Rita T Lawlor Mi 2014J. Pathol2014,,3:2
2Elevated urinary levels of urokinase-type plasminogen activator receptor(uPAR) in pancreatic ductal adenocarcinoma identify a clinically high-risk group显示文摘Sorio C Mafficini A Furlan F 2011BMC Cancer2011,11,:1
3Both HIV- and EIAV- based lentiviral vectors mediate gene delivery to pancreatic cancer cells and human pancreatic primary patient xenografts 显示文摘Saraga G Mafficini A Ghaneh P 2007Cancer Gene Ther2007,14,9:1
4Elevated urinary levels of urokinase-type plasminogen activator receptor (uPAR) in pancreatic ductal adenocarcinoma identify a clinically high-risk group显示文摘Sorio C Mafficini A Furlan F 2011BMC Cancer2011,11,:1
5To metabolomics and beyond:a technological portfolio to investigate cancer metabolism显示文摘Tumour cells have exquisite flexibility in reprogramming their metabolism in order to support tumour initiation, progression,metastasis and resistance to therapies. These reprogrammed activities include a complete rewiring of the bioenergetic, biosyntheticand redox status to sustain the increased energetic demand of the cells. Over the last decades, the cancer metabolism field hasseen an explosion of new biochemical technologies giving more tools than ever before to navigate this complexity. Within a cell ora tissue, the metabolites constitute the direct signature of the molecular phenotype and thus their profiling has concrete clinicalapplications in oncology. Metabolomics and fluxomics, are key technological approaches that mainly revolutionized the fieldenabling researchers to have both a qualitative and mechanistic model of the biochemical activities in cancer. Furthermore, theupgrade from bulk to single-cell analysis technologies provided unprecedented opportunity to investigate cancer biology at cellularresolution allowing an in depth quantitative analysis of complex and heterogenous diseases. More recently, the advent offunctional genomic screening allowed the identification of molecular pathways, cellular processes, biomarkers and noveltherapeutic targets that in concert with other technologies allow patient stratification and identification of new treatmentregimens. This review is intended to be a guide for researchers to cancer metabolism, highlighting current and emergingtechnologies, emphasizing advantages, disadvantages and applications with the potential of leading the development ofinnovative anti-cancer therapies.Federica Danzi Raffaella Pacchiana Andrea Mafficini Maria TScupoli Aldo Scarpa Massimo Donadelli Alessandra Fiore 2023Signal Transduction and Targeted Therapy2023,8,4:1
6Elevated urinary levels of uro-kinase-type plasminogen activator receptor(u PAR)in pancreatic ductal adenocarcinoma identify a clinically highrisk group显示文摘Sorio C Mafficini A Furlan F 2011BMC Cancer2011,,11:1
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