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Fermenting Made Simple

為了解決Mould的問題，作者 這樣論述：

Shortlisted for the Gourmand World Cookbook AwardsLooking to improve your gut health in a fun and flavourful way? This collection of 80+ recipes is a friendly, no-fuss primer on the joys of fermented foods.In this down-to-earth, no-fuss primer on fermented foods, Emillie Parrish introduces home c

ooks to deliciously easy DIY cultured foods and the principles of probiotics for health and well-being.Organized into chapters on fermented vegetables; nuts, seeds, and beans; grains; dairy; sourdough; and beverages (plus ideas for adding your ferments to snacks and meals) the book’s 80+ recipes emp

hasize simplicity over specialized ingredients or equipment. The book is entirely vegetarian and includes a number of recipes specifically for gluten-free or vegan diets. From kimchi, pickles, and salsa to ginger bug, yogurt, and spreads, you’ll soon have a kitchen full of tasty fermented foods.With

beautiful photography, thorough guidelines on sanitizing, advice on mould (it’s not all bad!), and best practices for storing your ferments for the short- and long-term, Fermenting Made Simple will teach you how to make affordable, no-cook and zero-waste pickles, condiments, snacks, and treats. All

of your meals will burst with flavour!

Mould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Mould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.

Lessons in Chemistry: THE Debut of 2022

為了解決Mould的問題，作者Bonnie Garmus 這樣論述：

　　'Elizabeth Zott is an iconic heroine - a feminist who refuses to be quashed, a mother who believes that her child is a person to behold, rather than to mould, and who will leave you, and the lens through which you see the world, quite changed' PANDORA SYKES 　　'A book that sparks joy with every pa

ge' ELIZABETH DAY 　　____________ 　　'Your ability to change everything - including yourself - starts here' ELIZABETH ZOTT 　　Chemist Elizabeth Zott is not your average woman. In fact, Elizabeth Zott would be the first to point out that there is no such thing. 　　But it's the early 1960s and her all-m

ale team at Hastings Research Institute take a very unscientific view of equality. Except for one: Calvin Evans; the lonely, brilliant, Nobel-prize nominated grudge-holder who falls in love with - of all things - her mind. True chemistry results.

基於曲電與介電效應之三穩態切換負型膽固醇液晶元件的光電響應

為了解決Mould的問題，作者陳冠然 這樣論述：

本研究於負型液晶DV10001中添加右旋手性分子R5011形成負型膽固醇液晶，接著經由摻雜不同配比濃度之彎曲型液晶分子CB7CB使配製完成之液晶材料具有不同程度的曲電特性，筆者藉此探討負型膽固醇液晶在摻雜彎曲型液晶分子後於不同電場條件下的紋理形成種類以及其光電響應。實驗結果分析中，對於形成紋理之介電頻譜進行首要之探討，透過均勻橫向螺紋態（ULH）紋理於介電實部之曲電鬆弛訊號判斷此材料之曲電特性，接著將其鬆弛強度90%與10%所對應於介電頻譜上之頻率點進行紋理切換頻率區間的劃分，並作為此研究之三穩態紋理切換中操作頻率區間的依據。當操作頻率f < fL，液晶分子因強烈的電流體效應及曲電強度而得以

形成ULH態；在頻率fL < f < fH區間中，曲電特性隨著頻率的增加逐漸變小，漸漸的由介電效應主導，此時液晶分子於電場驅動下形成焦錐態（FC）；當頻率f > fH，此時曲電效應幾乎完全消失，液晶分子受介電效應主導而形成平面態（P）。筆者藉由本研究提供了讀者一套於負型膽固醇液晶達成三穩態紋理切換的分析方法，並透過介電頻譜與光電特性量測詳細地說明其紋理背後的形成機制與應用。