Work part time的問題，透過圖書和論文來找解法和答案更準確安心。 我們挖掘到下列精選懶人包

Arms, Men and Society in Roman Judea

為了解決Work part time的問題，作者Stiebel, Guy D. 這樣論述：

Guy D. Stiebel provides an in-depth study of Roman weaponry as used in Judaea from the arrival of the Romans in the area in around 63 BCE until the time of the Bar Kochba Revolt (135/136 CE). The work is split into three parts. The first addresses Roman militaria and provides a study of the types of

weapon used, how they were produced, and stored, and examines the sources available for the study of weaponry in the region and period. Part two looks at how the types of weapon marked identity and at how they carried symbolic meanings which developed over time. Finally, the third part of the book

examines how the Romans dealt with the aftermath of conflict and reused and reshaped the ruins of the areas they had conquered. Guy D. Stiebel is Senior Lecturer at Tel Aviv University, Israel.

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An Integrated Approach For Uncovering Novel DNA Methylation Biomarkers For Non-small Cell Lung Carcinoma

為了解決Work part time的問題，作者VAIBHAV KUMAR SUNKARIA 這樣論述：

Introduction - Lung cancer is one of primal and ubiquitous cause of cancer related fatalities in the world. Leading cause of these fatalities is non-small cell lung cancer (NSCLC) with a proportion of 85%. The major subtypes of NSCLC are Lung Adenocarcinoma (LUAD) and Lung Small Cell Carcinoma (LUS

C). Early-stage surgical detection and removal of tumor offers a favorable prognosis and better survival rates. However, a major portion of 75% subjects have stage III/IV at the time of diagnosis and despite advanced major developments in oncology survival rates remain poor. Carcinogens produce wide

spread DNA methylation changes within cells. These changes are characterized by globally hyper or hypo methylated regions around CpG islands, many of these changes occur early in tumorigenesis and are highly prevalent across a tumor type.Structure - This research work took advantage of publicly avai

lable methylation profiling resources and relevant comorbidities for lung cancer patients extracted from meta-analysis of scientific review and journal available at PubMed and CNKI search which were combined systematically to explore effective DNA methylation markers for NSCLC. We also tried to iden

tify common CpG loci between Caucasian, Black and Asian racial groups for identifying ubiquitous candidate genes thoroughly. Statistical analysis and GO ontology were also conducted to explore associated novel biomarkers. These novel findings could facilitate design of accurate diagnostic panel for

practical clinical relevance.Methodology - DNA methylation profiles were extracted from TCGA for 418 LUAD and 370 LUSC tissue samples from patients compared with 32 and 42 non-malignant ones respectively. Standard pipeline was conducted to discover significant differentially methylated sites as prim

ary biomarkers. Secondary biomarkers were extracted by incorporating genes associated with comorbidities from meta-analysis of research articles. Concordant candidates were utilized for NSCLC relevant biomarker candidates. Gene ontology annotations were used to calculate gene-pair distance matrix fo

r all candidate biomarkers. Clustering algorithms were utilized to categorize candidate genes into different functional groups using the gene distance matrix. There were 35 CpG loci identified by comparing TCGA training cohort with GEO testing cohort from these functional groups, and 4 gene-based pa

nel was devised after finding highly discriminatory diagnostic panel through combinatorial validation of each functional cluster.Results – To evaluate the gene panel for NSCLC, the methylation levels of SCT(Secritin), FOXD3(Forkhead Box D3), TRIM58(Tripartite Motif Containing 58) and TAC1(Tachikinin

1) were tested. Individually each gene showed significant methylation difference between LUAD and LUSC training cohort. Combined 4-gene panel AUC, sensitivity/specificity were evaluated with 0.9596, 90.43%/100% in LUAD; 0.949, 86.95%/98.21% in LUSC TCGA training cohort; 0.94, 85.92%/97.37 in GEO 66

836; 0.91,89.17%/100% in GEO 83842 smokers; 0.948, 91.67%/100% in GEO83842 non-smokers independent testing cohort. Our study validates SCT, FOXD3, TRIM58 and TAC1 based gene panel has great potential in early recognition of NSCLC undetermined lung nodules. The findings can yield universally accurate

and robust markers facilitating early diagnosis and rapid severity examination.

Cationic Polymerizations Guide, Non-living Polymerization of Olefins

為了解決Work part time的問題，作者Lewis, Stewart 這樣論述：

This book is the first of a series providing a comprehensive resource on cationic polymerization. All three volumes are written in a manner that is easy to comprehend, even by undergraduate college students, and are designed to help the reader decipher an otherwise complex subject. Topics for each v

olume are presented in an order that build successively on material presented in prior books. The series is comprehensive, so even those who are well-versed in the discipline will find invaluable information in each volume. Through study of these books, the reader can become an expert in this subset

of polymer science without ever having attended courses on the subject.This first volume focuses on the most commercially-relevant technique: non-living polymerization of olefins. It provides a complete overview of methods (including those used industrially) that have been devised to effect such po

lymerizations, dating from the very inception of the technique through the present. From this, chemists can make educated choices on how to best design a polymerization system meeting their specific requirements. Mechanistic aspects of the chemistry are presented throughout the text with ample chemi

cal drawings, and this information can help the reader develop new polymerization systems. This work also emphasizes improvements (many being reported for the first time) made to the green aspects of the cationic methodology, a facet of growing importance for today's chemist. This is the only book o

n cationic polymerization that contains a section dedicated to experimental techniques. The reader can use the information contained within both to safely conduct their own bench-top to pilot plant scale experimentation.The other volumes in the 3-part set are: Vol 2: Thermodynamics/Kinetics/Spectral

Properties; Vol 3: Living Polymerizations.

關於沈浸自己，我說的其實是

為了解決Work part time的問題，作者陳冠中 這樣論述：

此書面報告書寫從個人迷戀於「音」出發，回溯「音」愛好者的身份過渡到 以「音」作為創作思考的歷程，爬梳「音」與聲音藝術間之外的研究，進而追究 「音」作為主體之下，去聲音藝術化的「音」，如何勾勒出「音」的主體性。在 此「音」主體性的建構過程，必需同時進行解構主體性化，也就是說當「音」有 了結構性的系統，「音」也就不在是「音」了。以「音」作為書寫(創作)的對 象，本身就極為弔詭，「音」是無法明確地被定義的，當本文試圖接近「音」主體 性的過程，以及「音」作為創作的思考對象，便是「音」趨向消逝死亡的時刻， 「音」始終面對自身的抵抗性，不得不提醒筆者在整個書寫過程(創作

過程)，需 要摧毀書寫結構(作品的形式內容)。以上的文字原寫於西元二零二一年三月十八日， 改寫於西元二零二一年十一月三十日，這些文字以「先將來時」的時態預言著未來， 我在西元二零二一年九月二十三日決定摧毀書寫結構的這一個動作。「只好做壞自己」，是經過疫情之後，重新梳理自我與創作的關係，原先關於「音」 的章節書寫，只保留了「噪動史」的部分放在後記裡面。書寫主軸將重新定位在新作 上面。《代號:劇場的原始積累》因疫情取消公開展演，在無法繼續往下推動進展之 下，取而代之的是，奠基在「只要不睡覺，就會有時間了」這一句話為核心發展的作 品，保留了「無線電」聲音技術作為發展，但這個作品並不是要直接以劇場的

形式去 回應有關劇場的勞動問題，《非得要錯過些什麼》透過與表演者的共創，試圖從「活」 的身體擾動展覽的界線，製造出非在場的真實。