Titlebook: Chemosensitivity; Volume II: In Vivo M Rosalyn D. Blumenthal Book 2005 Humana Press 2005 DNA.apoptosis.cell.cell death.chemoresistance.geno

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書目名稱Chemosensitivity影響因子(影響力)




書目名稱Chemosensitivity影響因子(影響力)學(xué)科排名




書目名稱Chemosensitivity網(wǎng)絡(luò)公開度




書目名稱Chemosensitivity網(wǎng)絡(luò)公開度學(xué)科排名




書目名稱Chemosensitivity被引頻次




書目名稱Chemosensitivity被引頻次學(xué)科排名




書目名稱Chemosensitivity年度引用




書目名稱Chemosensitivity年度引用學(xué)科排名




書目名稱Chemosensitivity讀者反饋




書目名稱Chemosensitivity讀者反饋學(xué)科排名

導(dǎo)師

Immunodetecting Members of the Bcl-2 Family of Proteinsacellular levels of multiple members of the Bcl-2 protein family can be analyzed simultaneously by immunoblotting and how protein-protein interactions can be studied using immunoprecipitation techniques. In addition, the methodology describes how conformational changes can be observed by immunofluor

instructive

Correlation of Telomerase Activity and Telomere Length to Chemosensitivityerapeutic intervention. Although a telomerase-specific inhibitor has not been found yet, the possible effect of anticancer agents on telomerase inhibition or the alteration of telomere length has been proposed. Recent development of TRAP assay not only increased the sensitivity but also allowed fast

Dendritic-Cells

CRACK

Overview of Tumor Cell Chemoresistance Mechanismsression. The relevant mechanisms that can contribute to cellular resistance include: increased expression of defense factors involved in reducing intracellular drug concentration; alterations in drug-target interaction; and changes in cellular response, in particular increased cell ability to repair

debunk

Flow Cytometric Monitoring of Fluorescent Drug Retention and Effluxnce in the presence or absence of an efflux blocker such as verapamil. The present chapter discusses some of the flow cytometric methods used for the study of cellular drug retention and the artifacts that may arise in such analysis.

debunk

Limit Cycles and Structural Stability,tic damage, screening of chemicals for genotoxic potential, and for specific purposes such as prediction of the radiosensitivity of tumors and interindividual variation in radiosensi tivity. In its current basic form the CBMN assay can provide, using simple morphological crite ria, the following mea

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https://doi.org/10.1007/978-3-540-33308-1acellular levels of multiple members of the Bcl-2 protein family can be analyzed simultaneously by immunoblotting and how protein-protein interactions can be studied using immunoprecipitation techniques. In addition, the methodology describes how conformational changes can be observed by immunofluor

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Bj?rn Rasch,Wilhelm Hofmann,Ewald Naumannerapeutic intervention. Although a telomerase-specific inhibitor has not been found yet, the possible effect of anticancer agents on telomerase inhibition or the alteration of telomere length has been proposed. Recent development of TRAP assay not only increased the sensitivity but also allowed fast

climax

Varianzanalyse mit Messwiederholung,tion. Basically, three procedures are described: (1) tissue dissociation and further cultivation on the sensor chip or on Transwell inserts; (2) preparation of tissue slices (300 μm thick) and attachment to the sensor chip or to inserts, and (3) cultivation of cells in dialysis tubes, a procedure ne