OBESE
发表于 2025-3-21 19:53:03
书目名称Cancer Cytogenetics and Cytogenomics影响因子(影响力)<br> http://impactfactor.cn/if/?ISSN=BK0242017<br><br> <br><br>书目名称Cancer Cytogenetics and Cytogenomics影响因子(影响力)学科排名<br> http://impactfactor.cn/ifr/?ISSN=BK0242017<br><br> <br><br>书目名称Cancer Cytogenetics and Cytogenomics网络公开度<br> http://impactfactor.cn/at/?ISSN=BK0242017<br><br> <br><br>书目名称Cancer Cytogenetics and Cytogenomics网络公开度学科排名<br> http://impactfactor.cn/atr/?ISSN=BK0242017<br><br> <br><br>书目名称Cancer Cytogenetics and Cytogenomics被引频次<br> http://impactfactor.cn/tc/?ISSN=BK0242017<br><br> <br><br>书目名称Cancer Cytogenetics and Cytogenomics被引频次学科排名<br> http://impactfactor.cn/tcr/?ISSN=BK0242017<br><br> <br><br>书目名称Cancer Cytogenetics and Cytogenomics年度引用<br> http://impactfactor.cn/ii/?ISSN=BK0242017<br><br> <br><br>书目名称Cancer Cytogenetics and Cytogenomics年度引用学科排名<br> http://impactfactor.cn/iir/?ISSN=BK0242017<br><br> <br><br>书目名称Cancer Cytogenetics and Cytogenomics读者反馈<br> http://impactfactor.cn/5y/?ISSN=BK0242017<br><br> <br><br>书目名称Cancer Cytogenetics and Cytogenomics读者反馈学科排名<br> http://impactfactor.cn/5yr/?ISSN=BK0242017<br><br> <br><br>
bacteria
发表于 2025-3-22 00:07:58
Methods of Detection and Mechanisms of Origin of Complex Structural Genome Variationsor “complex” (with more than two breakpoints). Studying the breakpoints of SVs at nucleotide resolution revealed additional, subtle structural variations, such that even “simple” SVs turned out to be “complex.” Genome-wide sequencing methods, such as fosmid and paired-end mapping, short-read and lon
铁砧
发表于 2025-3-22 03:39:02
A Paradoxical Role for Somatic Chromosomal Mosaicism and Chromosome Instability in Cancer: Theoreticcompassing chromosomal mosaicism and instability) in cancer yields paradoxical results. Firstly, somatic mosaicism for specific chromosomal rearrangement causes cancer per se. Secondly, chromosomal mosaicism and instability are associated with a variety of diseases (chromosomal disorders demonstrati
Misnomer
发表于 2025-3-22 05:40:21
The Importance of Monitoring Non-clonal Chromosome Aberrations (NCCAs) in Cancer Researchromosome aberrations, or NCCAs, as insignificant noise. Our decade-long karyotype evolutionary studies have unexpectedly demonstrated otherwise. Not only the baseline of NCCAs is associated with fuzzy inheritance, but the frequencies of NCCAs can also be used to reliably measure genome or chromosome
Foregery
发表于 2025-3-22 08:46:30
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ostrish
发表于 2025-3-22 16:24:05
Cell Culture and Slide Preparation for Cytogenetic Studies of Hematological Neoplasmse essential steps to enrich and collect sufficient neoplastic cells for cytogenetic studies of the neoplasms. This chapter describes methods that are commonly used for culturing hematological neoplastic cells and preparing cytogenetic slides for clinical diagnosis and research of the neoplasms.
ostrish
发表于 2025-3-22 20:01:24
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独行者
发表于 2025-3-22 23:43:24
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或者发神韵
发表于 2025-3-23 04:20:24
Multitarget Fluorescence In Situ Hybridization Diagnostic Applications in Tumorsspectrally distinct fluorophore labels. The mFISH approach is currently a useful assay in the oncologic field for the detection of predictive, prognostic, and diagnostic biomarkers. In this chapter, we summarize the application of mFISH in the identification of target genetic aberrations in formalin
stroke
发表于 2025-3-23 08:38:58
High-Resolution FISH Analysis Using DNA Fibers Generated by Molecular Combingsepairs per micrometer. The combination of this approach with fluorescent in situ hybridization (FISH) has enabled the direct visualization of DNA structure and variations at an unprecedent high resolution. This technique has been successfully used in various studies such as the identification of co