標(biāo)題: Titlebook: In Vitro Differentiation of T-Cells; Methods and Protocol Shin Kaneko Book 2019 Springer Science+Business Media, LLC, part of Springer Natu [打印本頁] 作者: 灰塵 時(shí)間: 2025-3-21 19:16
書目名稱In Vitro Differentiation of T-Cells影響因子(影響力)
書目名稱In Vitro Differentiation of T-Cells影響因子(影響力)學(xué)科排名
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書目名稱In Vitro Differentiation of T-Cells網(wǎng)絡(luò)公開度學(xué)科排名
書目名稱In Vitro Differentiation of T-Cells被引頻次
書目名稱In Vitro Differentiation of T-Cells被引頻次學(xué)科排名
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書目名稱In Vitro Differentiation of T-Cells年度引用學(xué)科排名
書目名稱In Vitro Differentiation of T-Cells讀者反饋
書目名稱In Vitro Differentiation of T-Cells讀者反饋學(xué)科排名
作者: 前奏曲 時(shí)間: 2025-3-21 20:16
978-1-4939-9730-5Springer Science+Business Media, LLC, part of Springer Nature 2019作者: 不可救藥 時(shí)間: 2025-3-22 04:03
In Vitro Differentiation of T-Cells978-1-4939-9728-2Series ISSN 1064-3745 Series E-ISSN 1940-6029 作者: Metamorphosis 時(shí)間: 2025-3-22 06:09 作者: 1FAWN 時(shí)間: 2025-3-22 09:51
Methods in Molecular Biologyhttp://image.papertrans.cn/i/image/463012.jpg作者: 土產(chǎn) 時(shí)間: 2025-3-22 13:18 作者: Mirage 時(shí)間: 2025-3-22 21:06 作者: Popcorn 時(shí)間: 2025-3-22 22:47 作者: CLAIM 時(shí)間: 2025-3-23 02:44 作者: 新手 時(shí)間: 2025-3-23 08:31 作者: Irremediable 時(shí)間: 2025-3-23 12:07 作者: 小歌劇 時(shí)間: 2025-3-23 14:36 作者: Accessible 時(shí)間: 2025-3-23 18:20 作者: CORD 時(shí)間: 2025-3-23 23:35
Generation of Hematopoietic Stem and Progenitor Cells from Human Pluripotent Stem Cells,stained self-renewal and multilineage differentiation capacities upon transplantation. In this review, recent promising advances in the efforts to generate HSCs and hematopoietic progenitors from human PSCs in vitro and in vivo or from somatic cells are discussed.作者: 吸氣 時(shí)間: 2025-3-24 02:45
In Vitro Differentiation of T Cells: From Human Embryonic Stem Cells and Induced Pluripotent Stem Com PSCs involves three steps: induction of PSCs to hematopoietic progenitor cells (HPCs), differentiation of HPCs into progenitor T cells, and maturation of progenitor T cells into mature T cells (CD8 single-positive (SP) or CD4 SP).作者: PANEL 時(shí)間: 2025-3-24 08:35 作者: BARGE 時(shí)間: 2025-3-24 13:04
,Differentiating CD8αβ T Cells from TCR-Transduced iPSCs for Cancer Immunotherapy,ed iPSCs (TCR-iPSCs). These T cells express monoclonal expression of the transduced TCR. Generating CD8αβ CTLs from TCR-iPSC could contribute to safe and effective allogeneic regenerative T cell immunotherapies.作者: jealousy 時(shí)間: 2025-3-24 17:16
In Vitro Differentiation of T Cell: From CAR-Modified T-iPSC, this approach. CAR-engineered iPSCs are demonstrated to give rise to CAR-engineered T cell and exert their effector function. In this section, we describe the method to generate CAR-engineered iPSCs and differentiate them into T cells.作者: 吊胃口 時(shí)間: 2025-3-24 21:01 作者: 吹牛大王 時(shí)間: 2025-3-25 03:06
1064-3745 expertsThis book explores the vital importance of T-cell differentiation in areas as wide-ranging as pathological analysis, drug development, and cell therapy of human T-cells. Focusing on human embryonic stem cells and human induced pluripotent stem cells, the chapters explore a variety of .in vit作者: fixed-joint 時(shí)間: 2025-3-25 06:54 作者: 思考而得 時(shí)間: 2025-3-25 09:05 作者: 裝入膠囊 時(shí)間: 2025-3-25 13:59 作者: PURG 時(shí)間: 2025-3-25 18:55
,Redifferentiation of Adaptive Na?ve-Like CTL from T-Cell-Derived iPSC, capacity while retaining equivalent effector function compared to parental T-cell clones. Here, we demonstrate the methodology to produce na?ve-like T-iPSC-Ts, which could be potent cell source for adoptive immunotherapy.作者: Morose 時(shí)間: 2025-3-25 20:25 作者: lymphoma 時(shí)間: 2025-3-26 02:02
Flow Cytometry Analysis to Identify Human CD8+ T Cells,ity, cell components (DNA, mRNA), surface receptors, intracellular proteins, and signaling events. The flow cytometer operates via three main systems: the fluidics, optics, and electronics, which work together to analyze the physical and chemical properties of your sample. The first system, the flui作者: 你不公正 時(shí)間: 2025-3-26 08:13
Flow Cytometry Analysis to Identify Human CD4+ T Cell Subsets,he expression of cell surface markers and intracellular molecules to define cells into different populations using cell size, granularity, and fluorescently labeled antibodies. Thus, flow cytometry enables simultaneous and mutliparameter analysis of single cells..During the staining procedure, a sin作者: START 時(shí)間: 2025-3-26 11:19
Gene Modification and Immunological Analyses for the Development of Immunotherapy Utilizing T Cells antigen-specific antitumor receptors, such as T-cell receptor (TCR) and chimeric antigen receptor (CAR), has demonstrated clinical benefits even in patients with refractory malignancies. To advance this treatment modality, both generation of gene-modified T cells and evaluation of their reactivity 作者: Generalize 時(shí)間: 2025-3-26 14:10
In Vitro Conversion of Activated T Cells into Stem Cell Memory-Like T Cells,cells from patients may effectively destroy the original tumor cells. One of the limitations is a rapid acquisition of tolerant (anergy, deletion, dysfunctional, and/or exhausted) phenotypes. We and others found that stem cell memory T (T.) cells are strongly resistant to tolerance, showing strong e作者: Celiac-Plexus 時(shí)間: 2025-3-26 18:47 作者: notification 時(shí)間: 2025-3-27 00:51
In Vitro Differentiation of T Cells: From Human Embryonic Stem Cells and Induced Pluripotent Stem C) and induced pluripotent stem cells (iPSCs) derived from non-T cells, followed by the differentiation of the T-cell lineage. Derivation of T cells from PSCs involves three steps: induction of PSCs to hematopoietic progenitor cells (HPCs), differentiation of HPCs into progenitor T cells, and maturat作者: 補(bǔ)角 時(shí)間: 2025-3-27 04:13
,Redifferentiation of Adaptive Na?ve-Like CTL from T-Cell-Derived iPSC,re is derived from T-cell clone (T-iPSC), which has lost na?ve phenotype and acquired exhaustion/senescence phenotype during cloning process?(.). On the other hand, redifferentiated T cells (T-iPSC-Ts) reacquire na?ve phenotype (CD45RA.CD45RO.CCR7.CD62L.), which are reportedly critical for in vivo p作者: 一條卷發(fā) 時(shí)間: 2025-3-27 09:01
In Vitro Differentiation of T Cell: From Human iPS Cells in Feeder-Free Condition,cribe a feeder-free culture condition for differentiating T cells from hematopoietic cells that are cultured on Fc-DLL4-coated plate with T-lineage cytokines. This condition is capable of efficiently differentiating hematopoietic progenitor cells (HPCs) to immature T cells expressing both CD4 and CD作者: LITHE 時(shí)間: 2025-3-27 10:49 作者: 最小 時(shí)間: 2025-3-27 16:37
In Vitro Differentiation of T Cell: From CAR-Modified T-iPSC,al malignancies. Allogeneic transplantation approach is promising for broaden application of CART therapy. iPSCs are one of the ideal cell sources for this approach. CAR-engineered iPSCs are demonstrated to give rise to CAR-engineered T cell and exert their effector function. In this section, we des作者: 明智的人 時(shí)間: 2025-3-27 20:28 作者: 音樂會(huì) 時(shí)間: 2025-3-28 01:18 作者: aggravate 時(shí)間: 2025-3-28 04:12
In Vitro Detection of Cellular Adjuvant Properties of Human Invariant Natural Killer T Cells, by their specific ligand α-galactosylceramide (α-GalCer) induces the activation of dendritic cells (DCs) via reciprocal interaction, which results in the generation of cellular immunity against cancer. Here we describe a method to detect DC-mediated cellular adjuvant properties of human iNKT cells 作者: 減少 時(shí)間: 2025-3-28 09:18 作者: 導(dǎo)師 時(shí)間: 2025-3-28 10:42 作者: 慷慨不好 時(shí)間: 2025-3-28 16:41 作者: nutrients 時(shí)間: 2025-3-28 19:46
Structural Modeling of Lymphocyte Receptors and Their Antigens,question is: which antigens and epitopes are targeted? With emerging B cell receptor (BCR) and T cell receptor (TCR) sequencing methods improving in both breadth and depth, there is a growing need for methods that can help answer this question. Since lymphocyte-antigen recognition depends on complem作者: Iniquitous 時(shí)間: 2025-3-28 23:30 作者: Budget 時(shí)間: 2025-3-29 04:31
Generation of Hematopoietic Stem and Progenitor Cells from Human Pluripotent Stem Cells,h recent advances in genome editing technologies, human PSCs could offer various approaches that enable gene therapy, drug discovery, disease modeling, and in vitro modeling of human development. De novo generation of hematopoietic stem cells (HSCs) from human PSCs is an important focus in the field作者: 兇殘 時(shí)間: 2025-3-29 09:08
production, distribution and commercialisation. It has been edited by Professors Miguel Tú?ez-López (Universidade de Santiago de Compostela, Spain), Valentín-Alejandro Martínez-Fernández (Universidade da Coru?a, Spain), Xosé López-García (Universidade de Santiago de Compostela, Spain), Xosé Rúas-Ara作者: nullify 時(shí)間: 2025-3-29 13:06 作者: Pillory 時(shí)間: 2025-3-29 16:32 作者: GLUE 時(shí)間: 2025-3-29 20:52
Willem Van Der Byl,Simone Rizzetto,Jerome Samir,Curtis Cai,Auda A. Eltahla,Fabio Lucianientury. The two previous meetings have been concerned with housing and waste treat- ment. The subject of the third meeting, communications, is no less critical to life, but it offers particular problems and uncertainties, especially in the forecasting of future trends. Indeed, some have doubted if t作者: 華而不實(shí) 時(shí)間: 2025-3-30 01:38 作者: Graves’-disease 時(shí)間: 2025-3-30 04:03
Tinhinane Fali,Camille K’Ros,Victor Appay,Delphine Saucee Internet and the digitalrevolution, that much more needs to be done, and that new approaches,both at the Federal Communications Commission and in Congress, will berequired to complete the task. In this volume, the Progress andFreedom Foundation presents nine papers by communications policyexperts 作者: ACTIN 時(shí)間: 2025-3-30 12:07 作者: crumble 時(shí)間: 2025-3-30 13:36 作者: GUILE 時(shí)間: 2025-3-30 20:17 作者: 惡臭 時(shí)間: 2025-3-30 23:05
Miho Sekai,Jianwei Wang,Yoko Hamazakiasp. We had also not assessed the thirst of the popUlation for more and better ways of talking and writing to each other. It was the combination of market need and technical capability that created the com- munications revolution.978-1-4613-6338-5978-1-4615-3066-4作者: 休閑 時(shí)間: 2025-3-31 03:54 作者: 貨物 時(shí)間: 2025-3-31 08:48
Songling Li,Jan Wilamowski,Shunsuke Teraguchi,Floris J. van Eerden,John Rozewicki,Ana Davila,Zichangkmakes possible the best recommendations about the exact nature ofthose necessary changes. In this volume, the most difficult andpolitically-charged hot-button issues involving local and longdistance competition, universal service, spectrum allocation, programcontent regulation, and the public inter作者: NICE 時(shí)間: 2025-3-31 09:15
Tinhinane Fali,Camille K’Ros,Victor Appay,Delphine Saucekmakes possible the best recommendations about the exact nature ofthose necessary changes. In this volume, the most difficult andpolitically-charged hot-button issues involving local and longdistance competition, universal service, spectrum allocation, programcontent regulation, and the public inter作者: Fissure 時(shí)間: 2025-3-31 15:51
Hideyuki Ogurof communication in a sensor network. Also, by varying range of transmission radii and observing its impact on SNR we demonstrate that SNR-values, SNR-variance and pre-defined network threshold of SNR-variance, together can be useful in security assessment of WSN.作者: caldron 時(shí)間: 2025-3-31 18:42 作者: 可耕種 時(shí)間: 2025-4-1 00:33 作者: Acetabulum 時(shí)間: 2025-4-1 05:06
Rong Zhang,Shuichi Kitayama,Tianyi Liu,Norihiro Ueda,Yumi Tokumitsu,Hiroaki Mashima,Hideki Ohdan,Shi作者: 乳白光 時(shí)間: 2025-4-1 08:28 作者: lanugo 時(shí)間: 2025-4-1 10:17
Flow Cytometry Analysis to Identify Human CD8+ T Cells,the photocurrent from the detector system to be changed into electronic pulses to be processed by a computer and analyzed by flow cytometry software. Flow cytometry is thus a powerful technique, which is commonly used to determine the expression of cell surface markers and intracellular molecules to作者: motor-unit 時(shí)間: 2025-4-1 14:56 作者: 可能性 時(shí)間: 2025-4-1 19:51
1064-3745 ntiation of T-Cells: Methods and Protocols. serves as an ideal guide for researchers seeking to differentiate T-cells from pluripotent stem cells in order to achieve any number of significant goals..978-1-4939-9730-5978-1-4939-9728-2Series ISSN 1064-3745 Series E-ISSN 1940-6029
