Up in the air的問題，透過圖書和論文來找解法和答案更準確安心。 我們找到下列懶人包和總整理

Strategic Air Command

為了解決Up in the air的問題，作者Wright, Kevin 這樣論述：

Strategic Air Command (SAC) was the pre-eminent military actor in US nuclear policy from the start to the end of the Cold War. Illustrated with over 170 photographs, this book provides an examination of SAC, covering its aircraft, operations, people and locations. It will look at the introduction

of new aircraft and early ballistic missiles with Curtis LeMay as Commander of SAC up to Cuban missile crisis. Post Cuba, the B-52 and KC-135 dominated force and second generation missiles will be covered. Then, the late 1960s/early1970s will see the pressures of the bomber force involvement in Vie

tnam, and the introduction of the FB-111A. Finally, comes the introduction of the B-1 and how, in 1980s, SAC readiness reached a peak. Interweaved through that account will be material covering new equipment, the importance of SAC strategic reconnaissance aircraft (the RB-29, RB-45, RB-50, U-2/TR-1,

SR-71, B-47 and RC-135), SAC readiness programmes (ORI), and its command and control mechanisms - especially EC-135s and E-4s and PACCS.

Up in the air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Up in the air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.

Learning to Talk: Stories

為了解決Up in the air的問題，作者Mantel, Hilary 這樣論述：

A dazzling collection of short stories from the two-time winner of the Booker Prize and #1 New York Times bestselling author of the Wolf Hall trilogy.In the wake of Hilary Mantel’s brilliant conclusion to her award-winning Wolf Hall trilogy, Learning to Talk is a collection of loosely autobiograp

hical stories that locates the transforming moments of a haunted childhood. Absorbing and evocative, these drawn-from-life stories begin in the 1950s in an insular northern village ＂scoured by bitter winds and rough gossip tongues.＂ For the young narrator, the only way to survive is to get up, get o

n, get out. In ＂King Billy Is a Gentleman,＂ the child must come to terms with the loss of a father and the puzzle of a fading Irish heritage. ＂Curved Is the Line of Beauty is a story of friendship, faith and a near-disaster in a scrap-yard. The title story sees our narrator ironing out her northern

vowels with the help of an ex-actress with one lung and a Manchester accent. In ＂Third Floor Rising, she watches, amazed, as her mother carves out a stylish new identity. With a deceptively light touch, Mantel illuminates the poignant experiences of childhood that leave each of us forever changed.

＂A book of her short stories is like a little sweet treat...Mantel’s narrators never tell everything they know, and that’s why they’re worth listening to, carefully.＂ --USA Today＂Her short stories always recognize other potential realities...Even the most straightforward of Mantel’s tales retain a f

aintly otherworldly air.＂ --The Washington Post

高功率可變出光角光子晶體面射型雷射之特性研究

為了解決Up in the air的問題，作者陳立人 這樣論述：

本論文旨在研究高功率可變出光角之光子晶體面射型雷射的設計，製作及其光電特性。光子晶體面射型雷射因具備大功率操作及發散角小等特性，近年來頗受矚目，被視為是3D感測，光達，和雷射加工等應用領域的理想光源；研究首先藉由數值模擬計算來探討磊晶結構及光子晶體結構對於雷射閾值及出光效率的影響，進而得到較佳的磊晶結構同時配合不同的光子晶體結構來進行實驗驗證，實驗與模擬的結果均顯示雷射的斜率效率隨著光子晶體結構的對稱性下降而大幅上升，實驗並針對P面向上的結構進行優化，使得光輸出功率進一步提升，同時我們也針對大功率單模操作進行探討。另一方面我們也針對改變鐳射出光角度的機制進行研究以實現光束掃描的新奇雷射結構。

先後評估了主動式的光學相位陣列，主動式光柵結構，雙調變式光子晶體結構以及超穎結構等方式，考量結構整合的便利性及發光效率等因素，我們採用雷射整合表面超穎結構的方式進行設計，超穎結構的設計使用了奈米結構陣列及反向設計兩種方式，在砷化鎵基板上實驗的結果顯示此結構可將雷射光偏轉至設計的角度並且抑制原本垂直方向上的雷射光，此超穎結構結合光子晶體面射型雷射將得到高效率且緊湊的光束偏轉雷射，進一步製作成不同出光角度的陣列並單獨控制即可實現掃描功能，預期此雷射結構在上述的應用領域有著相當大的潛力。