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Titlebook: Basic and Clinical Applications of Flow Cytometry; Proceeding of the 24 Frederick A. Valeriote,Alexander Nakeff,Manuel Val Conference proce

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期刊全称Basic and Clinical Applications of Flow Cytometry
期刊简称Proceeding of the 24
影响因子2023Frederick A. Valeriote,Alexander Nakeff,Manuel Val
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学科分类Developments in Oncology
图书封面Titlebook: Basic and Clinical Applications of Flow Cytometry; Proceeding of the 24 Frederick A. Valeriote,Alexander Nakeff,Manuel Val Conference proce
影响因子The focus of this symposium was on the present and futurecapabilities of flow cytometry for both medical and biologicalapplications in cancer. This technology began with quite modestinstrumentation, with limited capabilities to answer biologicalquestions. Today, both the clinical workhorses and the powerfulmulti-laser, multi-detector, sorting machinery, coupled withsophisticated computers and storage devices and the increasingstorehouse of markers and dyes, are taking us to the limit and beyondin finding answers to the cause and cure of cancer. .In the past, both normal hematopoietic tissue and leukemias have beenthe tissue samples of choice in the application of flow cytometry, andsome of the most recent applications with these tissues are presentedhere. However, the book also discusses the increasingly sophisticateddisaggregation techniques which allow investigators the possibility totrain their lasers on solid tumors. Not only can we use flow cytometrywith associated fluorescent markers to understand the biology ofcancer, but also the wide array of existing and developing markersprovides us with important diagnostic tools in the detection of cancerearly in either the malignant o
Pindex Conference proceedings 1996
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Stephan Eggersglüß,Rolf Drechslerrgets (1–3). Multiple drug resistance (MDR) has been recently described as a phenomenon in which tumor cells are resistant to a variety of unrelated natural products such as alkaloids and antibiotics used as cancer chemotherapeutic agents (1,3).
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The Lithic Assemblage of Level Jram of tissue, and (4) maintain the desired phenotypes being studied. The ability to meet these goals varies with the tumor as well as with the dissociation technique. Individualization and validation of a dissociation technique, for either a fresh or fixed, paraffin-embedded tumor, is needed to meet these criteria.
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Jon Orloff,Mark Utlaut,Lynwood Swansonactical to use for routine analysis and sorting of such cell subpopulations. One simple method for processing cells at higher speeds on conventional flow cytometers has been described (9). This method triggers the data acquisition or sort signal on a rare fluorescence signal.
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Activation and Proliferation of Purified Hematopoietic Precursor Cells from Human Bone Marrow,ow such cells to display this self-renewal potential. This would in turn allow numerical expansion of stem cells . for transplantation and gene transfer experiments starting with very few (in principle a single) stem cells.
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Flow Cytometric Proliferative Fraction Analysis in Solid Tumors,and cell cycling (1). Prognosis in many clinical tumor systems is strikingly correlated to arguably pedestrian estimates of proliferation such as mitotic counts on histologic tissue sections and empirical doubling times extrapolated from serial radiographic measurements (2,3).
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