標題: Titlebook: Cellular Heterogeneity; Methods and Protocol Natasha S. Barteneva,Ivan A. Vorobjev Book 2018 Springer Science+Business Media, LLC 2018 Live [打印本頁] 作者: 銀河 時間: 2025-3-21 19:02
書目名稱Cellular Heterogeneity影響因子(影響力)
書目名稱Cellular Heterogeneity影響因子(影響力)學科排名
書目名稱Cellular Heterogeneity網(wǎng)絡公開度
書目名稱Cellular Heterogeneity網(wǎng)絡公開度學科排名
書目名稱Cellular Heterogeneity被引頻次
書目名稱Cellular Heterogeneity被引頻次學科排名
書目名稱Cellular Heterogeneity年度引用
書目名稱Cellular Heterogeneity年度引用學科排名
書目名稱Cellular Heterogeneity讀者反饋
書目名稱Cellular Heterogeneity讀者反饋學科排名
作者: CLASH 時間: 2025-3-22 00:05 作者: 大氣層 時間: 2025-3-22 03:51
Organisation und Welterschlie?ungphages represent heterogeneous populations, which can modulate CNS environment and have different effects on neuronal regeneration. In this chapter, the main features of microglial and macrophage subsets and current methods for investigation of their heterogeneity will be discussed.作者: BILL 時間: 2025-3-22 07:27 作者: Neutral-Spine 時間: 2025-3-22 10:17
Usage of Multiparameter Flow Cytometry to Study Microglia and Macrophage Heterogeneity in the Centraphages represent heterogeneous populations, which can modulate CNS environment and have different effects on neuronal regeneration. In this chapter, the main features of microglial and macrophage subsets and current methods for investigation of their heterogeneity will be discussed.作者: LAST 時間: 2025-3-22 12:52 作者: LAST 時間: 2025-3-22 19:35 作者: Carcinogen 時間: 2025-3-22 21:23 作者: 充滿裝飾 時間: 2025-3-23 03:17
Multiparametric Analysis of Myeloid Populations by Flow Cytometryining, and analysis, which include a newly described viSNE tool to generate two-dimensional clustering within myeloid populations. We also reference the use of transgenic reporter mice on specific myeloid cells that provides enhanced specificity and profiling when defining myeloid heterogeneity.作者: 土坯 時間: 2025-3-23 06:23
Characterizing Cell Heterogeneity Using PCR Fingerprinting of Surface Multigene Families in Protozoaell populations of protozoan parasites using a combination of nested PCR amplification and capillary electrophoresis. With this workflow, in silico gels from isolated cell clones can be generated, thus providing an excellent tool for analyzing cellular heterogeneity in protozoan parasites.作者: 確保 時間: 2025-3-23 10:08
https://doi.org/10.1007/978-3-531-90872-4 control that can be used to filter out erroneous tracks and improve assessment of heterogeneity. We demonstrate possible phenotypic readouts including motility, nuclear receptor translocation, and mitosis.作者: Gobble 時間: 2025-3-23 14:23 作者: Intrepid 時間: 2025-3-23 18:01
Organisationen als Placebo-Responderg an optimized nuclear mask and similarity score parameter to correlate the location of IRF3 staining and a nuclear dye. The technique measures IRF3 activation at a single cell level and can detect small changes in the percent of activated cells providing objective quantitative data for statistical analysis.作者: Cirrhosis 時間: 2025-3-24 00:15
Image-Based Tracking of Heterogeneous Single-Cell Phenotypes control that can be used to filter out erroneous tracks and improve assessment of heterogeneity. We demonstrate possible phenotypic readouts including motility, nuclear receptor translocation, and mitosis.作者: BRIEF 時間: 2025-3-24 06:14 作者: 修改 時間: 2025-3-24 07:46 作者: 反抗者 時間: 2025-3-24 11:06 作者: blight 時間: 2025-3-24 17:35
https://doi.org/10.1007/978-3-531-90872-4re directions may include the development of nondestructive methods for dissecting molecular events in intact cells, simultaneous correlative cellular analysis of phenotypic and molecular features by hybrid technologies such as imaging flow cytometry, and further progress in supervised and non-super作者: Deceit 時間: 2025-3-24 22:37 作者: 使虛弱 時間: 2025-3-25 02:30 作者: 閑聊 時間: 2025-3-25 03:42
Strukturation und Dekonstruktion variation in MT dynamics measurement. We show that variability in MT dynamics within a cell when using repeated measurements is significantly less than between different cells in the same chamber. This approach allows better estimation of the heterogeneity of cells’ responses to different treatment作者: Keratin 時間: 2025-3-25 09:32 作者: Platelet 時間: 2025-3-25 14:46 作者: 寬宏大量 時間: 2025-3-25 17:37
Organisationen als Placebo-Respondergy of Mtb, which may contribute to the variable response of intracellular Mtb to different antimycobacterial agents. In this chapter, we describe the details of a method used in the generation of reporter strains for the measurement of the NADH/NAD. ratio in mycobacteria. Importantly, once the repor作者: 軟膏 時間: 2025-3-25 20:08
1064-3745 ods and Protocols. encourages readers to explore new ways of studying cells that will help lead to exciting new discoveries..978-1-4939-8541-8978-1-4939-7680-5Series ISSN 1064-3745 Series E-ISSN 1940-6029 作者: palpitate 時間: 2025-3-26 02:22 作者: Rebate 時間: 2025-3-26 05:51 作者: FLACK 時間: 2025-3-26 11:42 作者: IVORY 時間: 2025-3-26 13:34
Analysis of Microtubule Dynamics Heterogeneity in Cell Culture variation in MT dynamics measurement. We show that variability in MT dynamics within a cell when using repeated measurements is significantly less than between different cells in the same chamber. This approach allows better estimation of the heterogeneity of cells’ responses to different treatment作者: 制度 時間: 2025-3-26 19:03 作者: 平常 時間: 2025-3-26 21:25 作者: interrupt 時間: 2025-3-27 03:49
Quantification of the Metabolic Heterogeneity in Mycobacterial Cells Through the Measurement of the gy of Mtb, which may contribute to the variable response of intracellular Mtb to different antimycobacterial agents. In this chapter, we describe the details of a method used in the generation of reporter strains for the measurement of the NADH/NAD. ratio in mycobacteria. Importantly, once the repor作者: Obstreperous 時間: 2025-3-27 09:10 作者: 低能兒 時間: 2025-3-27 12:19 作者: 上腭 時間: 2025-3-27 15:29
Image-Based Tracking of Heterogeneous Single-Cell Phenotypess are beginning to capture the importance and interdependence of these phenomena. However, existing image analysis pipelines often fail to capture the intricate changes that occur in small subpopulations, either due to poor segmentation protocols or cell tracking errors. Here we report a pipeline de作者: Virtues 時間: 2025-3-27 20:24
Broad Immune Monitoring and Profiling of T Cell Subsets with Mass Cytometryents of protein or nucleic acid abundances by bringing together the detection capacity of atomic mass spectroscopy and the sample preparation workflow typical of regular flow cytometry. In 2014 the mass cytometer was adapted for the acquisition of samples from microscopy slides (termed imaging mass 作者: 攤位 時間: 2025-3-27 23:22 作者: 輕而薄 時間: 2025-3-28 05:02 作者: Anguish 時間: 2025-3-28 06:42
Multiparametric Analysis of Myeloid Populations by Flow Cytometryusing fluorescently conjugated antibodies for specific surface and activation markers provides a comprehensive profile of immune cells. This chapter describes the identification and characterization of myeloid populations using flow cytometric analysis in an acute model of resolving inflammation. Th作者: Medley 時間: 2025-3-28 14:20 作者: 沒血色 時間: 2025-3-28 17:46
Methods of Study of Neuron Structural Heterogeneity: Flow Cytometry vs. Laser Interferometryudying of individual neurons is the presence of long processes (axons) on differentiated adult neurons that hamper their isolation without significant damage to the cells. Therefore, the most common method to study neuronal cells is immunofluorescent microscopy of sections of the brain, which remain作者: Synovial-Fluid 時間: 2025-3-28 18:59 作者: Gum-Disease 時間: 2025-3-29 02:50 作者: 賭博 時間: 2025-3-29 05:57 作者: Relinquish 時間: 2025-3-29 09:56 作者: 四指套 時間: 2025-3-29 13:10 作者: faddish 時間: 2025-3-29 16:04
Characterizing Cell Heterogeneity Using PCR Fingerprinting of Surface Multigene Families in Protozoaes. Surface multigene protein families are defined not only by highly variable regions in length and/or sequence exposed to the outer space but also by conserved sequences codifying for the signal peptide, hydrophobic C-terminal regions necessary for GPI modifications, as well as conserved UTR regio作者: compose 時間: 2025-3-29 23:21
Natasha S. Barteneva,Ivan A. VorobjevIncludes cutting-edge techniques for the study of cellular heterogeneity.Provides step-by-step detail essential for reproducible results.Contains key implementation advice from the experts作者: 追蹤 時間: 2025-3-30 02:20
Methods in Molecular Biologyhttp://image.papertrans.cn/c/image/223030.jpg作者: TRUST 時間: 2025-3-30 05:57
Cellular Heterogeneity978-1-4939-7680-5Series ISSN 1064-3745 Series E-ISSN 1940-6029 作者: 輕率的你 時間: 2025-3-30 11:11
https://doi.org/10.1007/978-3-531-90921-9eneous cellular populations. The protocol describes a detailed step-by-step analysis of microalgae using these techniques and examples from our laboratory (. sp., ., and . sp.). Moreover, the chapter will be helpful to scientists who want to perform spectral flow cytometry and apply principal component analysis.作者: 馬籠頭 時間: 2025-3-30 15:06
https://doi.org/10.1007/978-3-531-90872-4geneity, there are four major approaches: analysis of pooled samples, single-cell analysis, high-throughput single-cell analysis, and lately integrated analysis of cellular population at a single-cell level. Recently developed high-throughput single-cell genetic analysis methods such as RNA-Seq requ作者: Compatriot 時間: 2025-3-30 18:26 作者: expdient 時間: 2025-3-30 21:39
https://doi.org/10.1007/978-3-531-90872-4s are beginning to capture the importance and interdependence of these phenomena. However, existing image analysis pipelines often fail to capture the intricate changes that occur in small subpopulations, either due to poor segmentation protocols or cell tracking errors. Here we report a pipeline de作者: 拋棄的貨物 時間: 2025-3-31 04:07
Organisation und Welterschlie?ungents of protein or nucleic acid abundances by bringing together the detection capacity of atomic mass spectroscopy and the sample preparation workflow typical of regular flow cytometry. In 2014 the mass cytometer was adapted for the acquisition of samples from microscopy slides (termed imaging mass 作者: 讓空氣進入 時間: 2025-3-31 06:40
https://doi.org/10.1007/978-3-531-90921-9eneous cellular populations. The protocol describes a detailed step-by-step analysis of microalgae using these techniques and examples from our laboratory (. sp., ., and . sp.). Moreover, the chapter will be helpful to scientists who want to perform spectral flow cytometry and apply principal compon作者: 貪婪性 時間: 2025-3-31 10:57 作者: 儲備 時間: 2025-3-31 14:14
Strukturation und Dekonstruktionusing fluorescently conjugated antibodies for specific surface and activation markers provides a comprehensive profile of immune cells. This chapter describes the identification and characterization of myeloid populations using flow cytometric analysis in an acute model of resolving inflammation. Th作者: Pelvic-Floor 時間: 2025-3-31 20:51 作者: SEEK 時間: 2025-4-1 01:30
