標(biāo)題: Titlebook: Cancer Cytogenetics; Methods and Protocol Thomas S.K. Wan Book 2017 Springer Science+Business Media, LLC, part of Springer Nature 2017 Arra [打印本頁(yè)] 作者: panache 時(shí)間: 2025-3-21 18:46
書(shū)目名稱Cancer Cytogenetics影響因子(影響力)
作者: 有其法作用 時(shí)間: 2025-3-21 20:33
Chromosome Preparation for Myeloid Malignancies,, and disclose subsequent clonal evolution. Three different cell culture methods: direct harvest, nonsynchronized culture, and synchronized culture are usually prepared if the nucleated cell counts in marrow blood are sufficient. Synchronized culture is the first choice of method in myeloid malignan作者: GEON 時(shí)間: 2025-3-22 03:33 作者: 染色體 時(shí)間: 2025-3-22 06:20
Cytogenetic Harvesting of Cancer Cells and Cell Lines,ize the utility of both cell culture—to maximize the yields of the dividing cells needed to harvest mitotic metaphase chromosome preparations and how an empirical evaluation of hypotonic treatments enables optimal conditions to be efficiently determined.作者: 禁止 時(shí)間: 2025-3-22 10:34
Chromosome Bandings,oses. Giemsa (G)-, reverse (R)-, and centromere (C)-banding are the most commonly dye-based chromosome-banding techniques. G-banding involves the staining of trypsin-treated chromosomes and R-banding involves denaturing in hot acidic saline followed by Giemsa staining. C-banding is specifically used作者: Foreshadow 時(shí)間: 2025-3-22 16:07
Chromosome Recognition,cisely by recognition of its morphological characteristics and staining patterns according to specific landmarks, regions, and bands as described in the ideogram. Since the quality of metaphases obtained from malignant cells is generally poor for karyotyping, a practical and accurate chromosome reco作者: Foreshadow 時(shí)間: 2025-3-22 19:23
Applications of Fluorescence In Situ Hybridization Technology in Malignancies,and lymphoid malignancies. Cytogenetic analysis has become essential for disease diagnosis, classification, prognostic stratification, and treatment guidance. Fluorescence in situ hybridization (FISH) has greatly enhanced the field and enabled a more precise determination of the presence and frequen作者: 慢跑鞋 時(shí)間: 2025-3-22 21:29
Fluorescence In Situ Hybridization Probe Preparation, kb to 300 kb, were identified and finely mapped with respect to the Sequence Tagged Site (STS) physical map and with respect to each other. A “golden path” of BACs, covering the entire human genome, was then selected and each clone was fully sequenced. The large number of remaining BACs was not ful作者: employor 時(shí)間: 2025-3-23 02:41 作者: 男生戴手銬 時(shí)間: 2025-3-23 06:10 作者: –吃 時(shí)間: 2025-3-23 12:33
Cytoplasmic Immunoglobulin Light Chain Revelation and Interphase Fluorescence In Situ Hybridizationc options can be discussed. Owing to the patchy nature of the disease in the bone marrow (BM), the low proliferative activity of plasma cells and the cryptic nature of some PCM-associated cytogenetic changes, karyotypic analysis in this disease should be augmented with targeted interphase fluorescen作者: 陶器 時(shí)間: 2025-3-23 15:40 作者: 極微小 時(shí)間: 2025-3-23 21:33
High Resolution Fiber-Fluorescence In Situ Hybridization,probe hybridizing on DNA molecules and chromosomal regions. Since various types of DNA and chromatin fibers can be generated reflecting different degrees of DNA/chromatin packaging status, fiber-FISH technology has been successfully used in diverse molecular cytogenetic/cytogenomic studies. Followin作者: white-matter 時(shí)間: 2025-3-24 01:24 作者: Keratectomy 時(shí)間: 2025-3-24 06:16
Multicolor Karyotyping and Fluorescence In Situ Hybridization-Banding (MCB/mBAND),t approach when thinking about mFISH is multicolor karyotyping using human whole chromosome paints as probes; this can be achieved by narrow-band filter-based multiplex-FISH (M-FISH) or interferometer/spectroscopy-based spectral karyotyping (SKY). Besides, various FISH-based banding approaches were 作者: 流出 時(shí)間: 2025-3-24 07:07
Cytogenetics for Biological Dosimetry,erged, but none are as specific as cytogenetic approaches, particularly the dicentric assay. Here, we will focus on the principal cytogenetic techniques used for biological dosimetry: the dicentric assay in metaphase cells, the micronuclei assay in binucleated cells, and the premature condensed chro作者: 方便 時(shí)間: 2025-3-24 12:10 作者: reserve 時(shí)間: 2025-3-24 17:07
Recurrent Cytogenetic Abnormalities in Acute Myeloid Leukemia,onic myeloid leukemia and other myeloid neoplasms. Recurrent chromosomal translocations such as t(8;21), t(15;17), and inv(16) are frequently detected, but hundreds of other uncommon chromosomal aberrations from AML also exist. This chapter discusses 22 chromosomal abnormalities that are common stru作者: Antecedent 時(shí)間: 2025-3-24 19:24 作者: Immunoglobulin 時(shí)間: 2025-3-25 01:44 作者: antenna 時(shí)間: 2025-3-25 07:04
https://doi.org/10.1007/978-3-319-04981-6able bands for each chromosome are described in detail in this chapter with an aim to facilitate quick and accurate karyotyping in cancers. This is an indispensable chromosome recognition guide used in a cancer cytogenetics laboratory.作者: airborne 時(shí)間: 2025-3-25 07:37
MR Imaging of Vascular Malformationsds, measuring relative DNA content at chromosomal loci and identifying parental origin of homologous chromosomes. Here, a QFISH protocol suitable for the majority of DNA probes using the popular US National Institute of Health developed ImageJ software is described.作者: 不遵守 時(shí)間: 2025-3-25 15:15
Jie Sun,Niranjan Balu,Chun Yuanlitated the analysis of the dicentric assay and have permitted to assess the dose a long time after irradiation by translocation analysis (such as by Tri-color FISH or Multiplex-FISH). Telomere centromere staining of PCCs will make it possible to perform dose assessment within 24 h of exposure in the near future.作者: TRACE 時(shí)間: 2025-3-25 17:10 作者: braggadocio 時(shí)間: 2025-3-25 20:37 作者: 使苦惱 時(shí)間: 2025-3-26 03:23
Chromosome Recognition,able bands for each chromosome are described in detail in this chapter with an aim to facilitate quick and accurate karyotyping in cancers. This is an indispensable chromosome recognition guide used in a cancer cytogenetics laboratory.作者: Synapse 時(shí)間: 2025-3-26 05:26 作者: 蝕刻術(shù) 時(shí)間: 2025-3-26 08:45 作者: 虛假 時(shí)間: 2025-3-26 15:07 作者: exhibit 時(shí)間: 2025-3-26 18:07 作者: choleretic 時(shí)間: 2025-3-26 22:31 作者: Obvious 時(shí)間: 2025-3-27 02:18
Book 2017rposes. The chapters in this book cover topics such as chromosome preparation for myeloid malignancies; chromosome bandings; fluorescence in situ hybridization probe preparation; array-based comparative genomic hybridization; and cytogenetic nomenclature and reporting. The updated reviews on chromos作者: macrophage 時(shí)間: 2025-3-27 07:14 作者: 易受騙 時(shí)間: 2025-3-27 10:47 作者: 去才蔑視 時(shí)間: 2025-3-27 15:41 作者: defenses 時(shí)間: 2025-3-27 18:38 作者: BURSA 時(shí)間: 2025-3-27 23:14
Chromosome Bandings, for identifying heterochromatin by denaturing chromosomes in a saturated alkaline solution followed by Giemsa staining. Different banding techniques may be selected for the identification of chromosomes.作者: 該得 時(shí)間: 2025-3-28 05:15
High Resolution Fiber-Fluorescence In Situ Hybridization,g a brief review of this technology, including its major development and increasing applications, typical protocols to generate DNA/chromatin fiber will be described, coupled with rationales, as well as technical tips. These released DNA/chromatin fibers are suitable for an array of cytogenetic/cytogenomic analyses.作者: trigger 時(shí)間: 2025-3-28 08:01 作者: Matrimony 時(shí)間: 2025-3-28 12:45
1064-3745 ation advice from the experts.Includes supplementary materia.This volume provides readers with detailed protocols covering the main cancer cytogenetics techniques needed for clinical utilization and research purposes. The chapters in this book cover topics such as chromosome preparation for myeloid 作者: Resistance 時(shí)間: 2025-3-28 16:47
Jie Sun,Niranjan Balu,Chun Yuannomic hybridization (aCGH), PCR-based assays, and next-generation sequencing (NGS). In this chapter, we describe a microarray method that has been used for the detection of genome-wide CNVs, loss of heterozygosity (LOH), and uniparental disomy (UPD) associated with constitutional and neoplastic disorders.作者: 鋼盔 時(shí)間: 2025-3-28 19:05
Array-Based Comparative Genomic Hybridization (aCGH),nomic hybridization (aCGH), PCR-based assays, and next-generation sequencing (NGS). In this chapter, we describe a microarray method that has been used for the detection of genome-wide CNVs, loss of heterozygosity (LOH), and uniparental disomy (UPD) associated with constitutional and neoplastic disorders.作者: LURE 時(shí)間: 2025-3-29 00:13
Mingrui Zhao,Hongtao Ma,Theodore H. Schwartzassociated with chronic myeloid leukemia. Over the past five decades, innovative technical advances in the field of cancer cytogenetics have greatly enhanced the detection ability of chromosomal alterations, and have facilitated the research and diagnostic potential of chromosomal studies in neoplas作者: Lumbar-Stenosis 時(shí)間: 2025-3-29 06:53 作者: SAGE 時(shí)間: 2025-3-29 10:07
Mingrui Zhao,Hongtao Ma,Theodore H. Schwartzence in situ hybridization (FISH) and molecular analysis. Presence of particular chromosomal alterations in chronic lymphocytic leukemia enables patients’ stratification into appropriate cytogenetic risk groups and influences treatment decisions. In other non-Hodgkin lymphomas cytogenetic analyses a作者: 新星 時(shí)間: 2025-3-29 14:55
Acta Neurochirurgica Supplementize the utility of both cell culture—to maximize the yields of the dividing cells needed to harvest mitotic metaphase chromosome preparations and how an empirical evaluation of hypotonic treatments enables optimal conditions to be efficiently determined.作者: 窒息 時(shí)間: 2025-3-29 17:49
Acta Neurochirurgica Supplementoses. Giemsa (G)-, reverse (R)-, and centromere (C)-banding are the most commonly dye-based chromosome-banding techniques. G-banding involves the staining of trypsin-treated chromosomes and R-banding involves denaturing in hot acidic saline followed by Giemsa staining. C-banding is specifically used作者: 防銹 時(shí)間: 2025-3-29 23:12
https://doi.org/10.1007/978-3-319-04981-6cisely by recognition of its morphological characteristics and staining patterns according to specific landmarks, regions, and bands as described in the ideogram. Since the quality of metaphases obtained from malignant cells is generally poor for karyotyping, a practical and accurate chromosome reco作者: 低位的人或事 時(shí)間: 2025-3-30 02:41 作者: uveitis 時(shí)間: 2025-3-30 07:50
Sarah Milla,Jennifer Vaughn,Nilesh K. Desai kb to 300 kb, were identified and finely mapped with respect to the Sequence Tagged Site (STS) physical map and with respect to each other. A “golden path” of BACs, covering the entire human genome, was then selected and each clone was fully sequenced. The large number of remaining BACs was not ful作者: 微不足道 時(shí)間: 2025-3-30 10:17 作者: Macronutrients 時(shí)間: 2025-3-30 12:49 作者: 古老 時(shí)間: 2025-3-30 20:13
Shoki Takahashi,Shunji Mugikurac options can be discussed. Owing to the patchy nature of the disease in the bone marrow (BM), the low proliferative activity of plasma cells and the cryptic nature of some PCM-associated cytogenetic changes, karyotypic analysis in this disease should be augmented with targeted interphase fluorescen作者: Ischemia 時(shí)間: 2025-3-31 00:43
MR Imaging of Vascular Malformationsechnique that can be used for chromosomal DNA analysis in all cell types, at all stages of the cell cycle, and at molecular resolution. Recent developments in microscopy and imaging systems have allowed quantification of digital FISH images (quantitative FISH or QFISH) and have provided a new way fo作者: 前奏曲 時(shí)間: 2025-3-31 03:42
Cerebrovascular Development and Evolutionprobe hybridizing on DNA molecules and chromosomal regions. Since various types of DNA and chromatin fibers can be generated reflecting different degrees of DNA/chromatin packaging status, fiber-FISH technology has been successfully used in diverse molecular cytogenetic/cytogenomic studies. Followin作者: expeditious 時(shí)間: 2025-3-31 05:48 作者: 團(tuán)結(jié) 時(shí)間: 2025-3-31 12:57 作者: 分解 時(shí)間: 2025-3-31 15:50
Jie Sun,Niranjan Balu,Chun Yuanerged, but none are as specific as cytogenetic approaches, particularly the dicentric assay. Here, we will focus on the principal cytogenetic techniques used for biological dosimetry: the dicentric assay in metaphase cells, the micronuclei assay in binucleated cells, and the premature condensed chro作者: 約會(huì) 時(shí)間: 2025-3-31 18:45
DSA Imaging Protocol and Techniqueies are sufficiently characteristic of MDS to be considered MDS defining in the appropriate clinical context. MDS with isolated del(5q) is the only molecularly defined MDS subtype. The genes responsible for many aspects of 5q- syndrome, the distinct clinical phenotype associated with this condition,作者: THE 時(shí)間: 2025-3-31 21:45
DSA Imaging Protocol and Techniqueonic myeloid leukemia and other myeloid neoplasms. Recurrent chromosomal translocations such as t(8;21), t(15;17), and inv(16) are frequently detected, but hundreds of other uncommon chromosomal aberrations from AML also exist. This chapter discusses 22 chromosomal abnormalities that are common stru作者: Verify 時(shí)間: 2025-4-1 03:47
Cancer Cytogenetics978-1-4939-6703-2Series ISSN 1064-3745 Series E-ISSN 1940-6029 作者: MORPH 時(shí)間: 2025-4-1 08:57 作者: 雕鏤 時(shí)間: 2025-4-1 13:24
Cytogenetic Harvesting of Cancer Cells and Cell Lines,ize the utility of both cell culture—to maximize the yields of the dividing cells needed to harvest mitotic metaphase chromosome preparations and how an empirical evaluation of hypotonic treatments enables optimal conditions to be efficiently determined.作者: milligram 時(shí)間: 2025-4-1 17:45
https://doi.org/10.1007/978-1-4939-6703-2Array Comparative Genomic Hybridization (aCGH); FISH; lymphoid; myelodysplastic syndromes; myeloid leuke作者: defibrillator 時(shí)間: 2025-4-1 22:26
978-1-4939-8278-3Springer Science+Business Media, LLC, part of Springer Nature 2017作者: AWRY 時(shí)間: 2025-4-1 23:32 作者: 詞匯 時(shí)間: 2025-4-2 04:26
