標(biāo)題: Titlebook: Bone Marrow and Stem Cell Transplantation; Meral Beksa? Book 2014Latest edition Springer Science+Business Media, New York 2014 HLA.Hematop [打印本頁(yè)] 作者: Manipulate 時(shí)間: 2025-3-21 16:05
書(shū)目名稱Bone Marrow and Stem Cell Transplantation影響因子(影響力)
書(shū)目名稱Bone Marrow and Stem Cell Transplantation影響因子(影響力)學(xué)科排名
書(shū)目名稱Bone Marrow and Stem Cell Transplantation網(wǎng)絡(luò)公開(kāi)度
書(shū)目名稱Bone Marrow and Stem Cell Transplantation網(wǎng)絡(luò)公開(kāi)度學(xué)科排名
書(shū)目名稱Bone Marrow and Stem Cell Transplantation被引頻次
書(shū)目名稱Bone Marrow and Stem Cell Transplantation被引頻次學(xué)科排名
書(shū)目名稱Bone Marrow and Stem Cell Transplantation年度引用
書(shū)目名稱Bone Marrow and Stem Cell Transplantation年度引用學(xué)科排名
書(shū)目名稱Bone Marrow and Stem Cell Transplantation讀者反饋
書(shū)目名稱Bone Marrow and Stem Cell Transplantation讀者反饋學(xué)科排名
作者: 異教徒 時(shí)間: 2025-3-21 22:25
https://doi.org/10.1007/978-1-4614-9437-9HLA; Hematopoietic stem cells; Killer Immunoglobulin Like Receptor; functional characterization of stem作者: 禮節(jié) 時(shí)間: 2025-3-22 00:35 作者: 生氣的邊緣 時(shí)間: 2025-3-22 06:36
Meral Beksa?Includes cutting-edge methods and protocols.Provides step-by-step detail essential for reproducible results.Contains key notes and implementation advice from the experts.Includes supplementary materia作者: 名字 時(shí)間: 2025-3-22 10:40 作者: 可耕種 時(shí)間: 2025-3-22 13:21 作者: 圣歌 時(shí)間: 2025-3-22 20:11
https://doi.org/10.1057/9780230596955d as advanced analytic tools critical in performing scientific research. This chapter aims at summarizing the use of flow cytometry in benign and malignant hematology and the monitoring of inherited and acquired immunodeficiency states. Numerous figures are provided from our laboratories at Massachu作者: kindred 時(shí)間: 2025-3-22 21:13
https://doi.org/10.1007/978-3-031-40556-3ies. It has been shown that these multipotent stromal cells can be isolated from tissues such as bone marrow, adipose tissue, trimester amniotic tissue, umbilical cord blood, and deciduous teeth and can be expanded in adherent culture. They have the capacity to differentiate into cells of the connec作者: HAIRY 時(shí)間: 2025-3-23 04:08
https://doi.org/10.1007/978-3-031-40556-3e. Major advances have been made in the area of HSC research as a result of the development of different techniques that allowed HSC identification, purification, and analysis of biological functions. This chapter presents methods that are currently used to analyze HSC functions in vitro based on th作者: fructose 時(shí)間: 2025-3-23 05:56 作者: 十字架 時(shí)間: 2025-3-23 12:41
https://doi.org/10.1007/978-3-031-40556-3 (digoxigenin–CSPD)-, or fluorescence (FITC, PE)-based detection systems. To achieve a faster, reliable, automated typing technique microbead and fluorescence detection technology have been combined and introduced to this field (XMAP? technology). For each locus, a series of microspheres, which are 作者: Veneer 時(shí)間: 2025-3-23 13:58 作者: 放氣 時(shí)間: 2025-3-23 19:23
https://doi.org/10.1007/978-3-031-40556-3 involved minor H antigens, the immune response may either cause graft-versus-host disease and a graft-versus-tumor effect or lead to only a graft-versus-leukemia effect. Thus, identification of recipient–donor pairs with minor H antigen mismatches has clinical importance. This chapter describes mol作者: 伸展 時(shí)間: 2025-3-24 01:42 作者: 熄滅 時(shí)間: 2025-3-24 02:42
https://doi.org/10.1057/9780230615595mia, myelodysplastic syndromes, advanced myeloproliferative disorders, high-risk lymphomas, and multiple myeloma) and is currently applied in more than 15,000 patients per year in Europe. Following HSCT, patients experience a period of reconstitution of the immune system, which seems to be highly de作者: 暗語(yǔ) 時(shí)間: 2025-3-24 06:39
https://doi.org/10.1057/9780230615595gous transplantation. The detection of MRD helps to identify patients who are at high risk for leukemic relapse after transplantation. The most commonly used techniques for MRD detection are qualitative and quantitative PCR methods, fluorescence in situ hybridization (FISH), fluorescence-activated c作者: UTTER 時(shí)間: 2025-3-24 13:22 作者: 修剪過(guò)的樹(shù)籬 時(shí)間: 2025-3-24 18:36
https://doi.org/10.1057/9780230339583 reconstitution period after transplantation, HSCT recipients are most likely to have bacterial or fungal infections. Invasive fungal infections (IFIs) and mycobacterial infections (MBIs) are among the complications of HSCT, with high morbidity and mortality rates. Early diagnosis of both is crucial作者: 豐滿有漂亮 時(shí)間: 2025-3-24 22:55 作者: 最初 時(shí)間: 2025-3-25 00:48 作者: Apraxia 時(shí)間: 2025-3-25 03:22
Bone Marrow and Stem Cell Transplantation978-1-4614-9437-9Series ISSN 1064-3745 Series E-ISSN 1940-6029 作者: 拾落穗 時(shí)間: 2025-3-25 07:55 作者: indubitable 時(shí)間: 2025-3-25 14:35 作者: colloquial 時(shí)間: 2025-3-25 19:35 作者: 宣傳 時(shí)間: 2025-3-25 20:57
Book 2014Latest editioncessary materials and reagents, step-by-step, readily reproducible laboratory protocols, and tips on troubleshooting and avoiding known pitfalls. .Authoritative and practical, .Bone Marrow and Stem Cell Transplantation., .Second Edition. serves as a guide in the application of molecular methods for routine or investigational purposes. .作者: Etymology 時(shí)間: 2025-3-26 00:58 作者: ingenue 時(shí)間: 2025-3-26 06:29
1064-3745 ation advice from the experts.Includes supplementary materia.The second edition of .Bone Marrow and Stem Cell Transplantation. expands upon the previous edition with current, detailed methods on HLA, minor-HLA and Killer Immunoglobulin Like Receptor typing. With new chapters on immunophenotyping and作者: Hemiplegia 時(shí)間: 2025-3-26 11:00 作者: 籠子 時(shí)間: 2025-3-26 13:25 作者: ineptitude 時(shí)間: 2025-3-26 20:51 作者: 傀儡 時(shí)間: 2025-3-26 22:09 作者: 著名 時(shí)間: 2025-3-27 02:25
https://doi.org/10.1007/978-3-031-40556-3tential therapeutic benefit following transplantation into the patients. This chapter summarizes some of the essential protocols and assays used at our laboratory for the isolation, culture, differentiation, and characterization of mesenchymal stem cells from the bone marrow and adipose tissue.作者: 敵手 時(shí)間: 2025-3-27 08:39 作者: 啟發(fā) 時(shí)間: 2025-3-27 11:08
https://doi.org/10.1007/978-3-031-40556-3signal originating from fluorescently (streptavidin–PE) labeled amplicons captured by the beads. Currently, there are two commercially available systems that differ in the scale of probes and the methods used for amplification and denaturation. One of these is described in detail in this chapter.作者: 閑聊 時(shí)間: 2025-3-27 17:21 作者: Explosive 時(shí)間: 2025-3-27 20:40 作者: Blatant 時(shí)間: 2025-3-28 01:57
https://doi.org/10.1057/9780230615595es for the most common fusion-gene transcripts in acute and chronic myeloid disorders, methods for detections of disease-specific genetic mutated alterations, as NPM1 and FLT3 gene length mutations, and aberrantly expressed genes, as WT1 gene transcripts, are described in detail for daily use.作者: 不朽中國(guó) 時(shí)間: 2025-3-28 04:25 作者: 失誤 時(shí)間: 2025-3-28 07:22 作者: macabre 時(shí)間: 2025-3-28 11:02
Sequence-Based Typing of HLA: An Improved Group-Specific Full-Length Gene Sequencing Approach,tion using the low-resolution typing result as reference starting point. Group-specific amplification has already been established for DRB. This method enables a cost-efficient, user-friendly SBT approach resulting in a timely unambiguous HLA typing to an ultrahigh resolution level with minimal hands-on time.作者: BUOY 時(shí)間: 2025-3-28 16:45
Natural Killer Cells and Killer-Cell Immunoglobulin-Like Receptor Polymorphisms: Their Role in Hemat on the exact circumstances in which the KIR repertoire affects and influences clinical outcome after HSCT. More large-scale studies are needed on well-defined cohorts to unravel the mechanism of action of the NK cell-mediated alloresponse in an HSCT setting.作者: 對(duì)手 時(shí)間: 2025-3-28 22:33
Molecular Methods Used for Detection of Minimal Residual Disease Following Hematopoietic Stem Cell es for the most common fusion-gene transcripts in acute and chronic myeloid disorders, methods for detections of disease-specific genetic mutated alterations, as NPM1 and FLT3 gene length mutations, and aberrantly expressed genes, as WT1 gene transcripts, are described in detail for daily use.作者: Genome 時(shí)間: 2025-3-29 00:49 作者: FAZE 時(shí)間: 2025-3-29 03:30 作者: 發(fā)生 時(shí)間: 2025-3-29 09:37
https://doi.org/10.1057/9780230339583 in order to manipulate the disease and to avoid fulminant outcomes. This chapter reviews the current knowledge on the molecular diagnosis of IFIs and MBIs in HSCT recipients, describing two different polymerase chain reaction (PCR)-based methods, one commercial (qPCR, Roche) and one .6110-based protocol.作者: 薄荷醇 時(shí)間: 2025-3-29 15:06
Reporter Gene Technologies for Imaging Cell Fates in Hematopoiesis, revealed new insights into cell biology in the context of intact organs and their native environment. In the field of hematopoiesis and stem cell research, studies of cell trafficking involved in injury repair and hematopoietic engraftment have made great progress using these new tools. Stem cells 作者: 種植,培養(yǎng) 時(shí)間: 2025-3-29 18:12
Flow Cytometry for Hematopoietic Cells,d as advanced analytic tools critical in performing scientific research. This chapter aims at summarizing the use of flow cytometry in benign and malignant hematology and the monitoring of inherited and acquired immunodeficiency states. Numerous figures are provided from our laboratories at Massachu作者: 能得到 時(shí)間: 2025-3-29 20:25 作者: osteopath 時(shí)間: 2025-3-30 03:02 作者: 怒目而視 時(shí)間: 2025-3-30 06:32 作者: Indent 時(shí)間: 2025-3-30 10:22
,HLA Typing with Sequence-Specific Oligonucleotide Primed PCR (PCR-SSO) and Use of the Luminex? Tech (digoxigenin–CSPD)-, or fluorescence (FITC, PE)-based detection systems. To achieve a faster, reliable, automated typing technique microbead and fluorescence detection technology have been combined and introduced to this field (XMAP? technology). For each locus, a series of microspheres, which are 作者: 庇護(hù) 時(shí)間: 2025-3-30 15:28
Sequence-Based Typing of HLA: An Improved Group-Specific Full-Length Gene Sequencing Approach,phism, the so-called high-resolution HLA typing, is sequence-based typing (SBT). Although the majority of the polymorphism for class I is located in exons 2 and 3 and for class II in exon 2, for allele definition it is necessary to unravel the complete coding and intron sequences leading to an ultra
