March的問題，透過圖書和論文來找解法和答案更準確安心。 我們找到下列各種有用的問答集和懶人包

Dowding & Churchill: The Dark Side of the Battle of Britain

為了解決March的問題，作者Dixon, Jack 這樣論述：

Air Chief Marshal Sir Hugh - later Lord - Dowding was one of the greatest Englishmen of the 20th century. He created Fighter Command with its unique early warning system (radar) from nothing in 1936 to the efficient defensive force it became in 1940. In consequence Fighter Command was the only ar

m that was properly prepared for battle when war was declared against Germany. Hugh Dowding led Fighter Command in the Battle of Britain, and was victorious. The campaign, although a series of defensive engagements, was one of the decisive battles of Western Civilization. The strategic importance of

the Battle of Britain was recognized at the time, yet, the moment it was won Dowding was summarily relieved of his command and shuffled into retirement without recognition, reward or promotion. This book reveals that this was the result of a shabby conspiracy by fellow officers. The Air Ministry pu

blished a brief account of the Battle in March 1941 and in it there was no mention of Dowding. Churchill was furiously indignant. But in November 1940 he had acquiesced in Dowding's removal. Why? And what are the factors that led to Dowding's dismissal in the first place? In this thought-provoking a

nd authoritative book Jack Dixon answers these questions and explains Dowding's true greatness

March進入發燒排行的影片

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

為了解決March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.

Beyond Love and Light: A Reimagining of Solidarity and Self

為了解決March的問題，作者Cargle, Rachel Elizabeth 這樣論述：

A deeply personal and illuminating approach to antiracism and allyship, revealing the power of imagination and action to dismantle oppressive systems and build liberating ones, from a highly lauded lecturer, public academic, writer, and activist.In A Renaissance of Our Own, Rachel Cargle details

the seminal event that put her on the map--her viral 2017 Women’s March appearance that thrust her into the national conversation on feminism and allyship--and how she soon woke up to the fallacies of a movement she had believed in. Discovering and unpacking the white-washed lies she’d been fed abou

t intersectional ＂solidarity,＂ Cargle’s awakening, although painful and seismic, gifted her the opportunity to see the world through a new lens. Now, Cargle shares her journey, depicting a framework for allyship, and beyond, that she developed along the way. In creating KEA (Knowledge, Empathy, Acti

on), or as she calls them ＂from the head to the heart to the feet,＂ Cargle learned to craft a world independent of oppressive constructs that allowed her to critically examine her surroundings. Alongside KEA, she established a set of intentional values based on an individual sense of purpose, known

as higher values, and through the combination of these tools, reimagined her approach to the personal, societal, and structural components of life that are often stifled. She provides the same tools and prompts that she used to unearth and align her own values so anyone can wield them, and ultimatel

y, identify the structures and mindsets that hold them back and learn to move forward. A Renaissance of Our Own serves as a reminder of the power of reimagining as an engine for critical learning, radical empathizing, and intentional action.

關於沈浸自己，我說的其實是

為了解決March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。