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يتناول كتاب (المتاحف الصينية) والذي قام بتأليفه (لي شيا نياو، لوه تشهون) في حوالي (195) صفحة من القطع المتوسط موضوع (المتاحف) مستعرضا المحتويات التالية : قراءة حضارة الأمة الصينية من المتاحف-الكنوز في الوطن-المساهمات من الأقليات القومية في الصين-البحث عن أصل التاريخ-كنوز الكهوف الحجرية الصينية-القصورتحت الأرض-الحضارة الصينية-البلوارت الإنسانية-أم الحدائق-موطن الأسلاف-السماء السوداء والأرض الصفراء.‪‪‪‪‪‪‪‪‪‪‪

Since early December 2019, the 2019 novel coronavirus disease (COVID-19) has caused pneumonia epidemic in Wuhan, Hubei province of China. This study aimed to investigate the factors affecting the progression of pneumonia in COVID-19 patients. Associated results will be used to evaluate the prognosis and to find the optimal treatment regimens for COVID-19 pneumonia. Patients tested positive for the COVID-19 based on nucleic acid detection were included in this study. Patients were admitted to 3 tertiary hospitals in Wuhan between December 30, 2019, and January 15, 2020. Individual data, laboratory indices, imaging characteristics, and clinical data were collected, and statistical analysis was performed. Based on clinical typing results, the patients were divided into a progression group or an improvement/stabilization group. Continuous variables were analyzed using independent samples t-test or Mann-Whitney U test. Categorical variables were analyzed using Chi-squared test or Fisher's exact test. Logistic regression analysis was performed to explore the risk factors for disease progression. Seventy-eight patients with COVID-19-induced pneumonia met the inclusion criteria and were included in this study. Efficacy evaluation at 2 weeks after hospitalization indicated that 11 patients (14.1%) had deteriorated, and 67 patients (85.9%) had improved/stabilized. The patients in the progression group were significantly older than those in the disease improvement/stabilization group (66 [51, 70] vs. 37 [32, 41] years, U = 4.932, P = 0.001). The progression group had a significantly higher proportion of patients with a history of smoking than the improvement/stabilization group (27.3% vs. 3.0%, χ = 9.291, P = 0.018). For all the 78 patients, fever was the most common initial symptom, and the maximum body temperature at admission was significantly higher in the progression group than in the improvement/stabilization group (38.2 [37.8, 38.6] vs. 37.5 [37.0, 38.4]°C, U = 2.057, P = 0.027). Moreover, the proportion of patients with respiratory failure (54.5% vs. 20.9%, χ = 5.611, P = 0.028) and respiratory rate (34 [18, 48] vs. 24 [16, 60] breaths/min, U = 4.030, P = 0.004) were significantly higher in the progression group than in the improvement/stabilization group. C-reactive protein was significantly elevated in the progression group compared to the improvement/stabilization group (38.9 [14.3, 64.8] vs. 10.6 [1.9, 33.1] mg/L, U = 1.315, P = 0.024). Albumin was significantly lower in the progression group than in the improvement/stabilization group (36.62 ± 6.60 vs. 41.27 ± 4.55 g/L, U = 2.843, P = 0.006). Patients in the progression group were more likely to receive high-level respiratory support than in the improvement/stabilization group (χ = 16.01, P = 0.001). Multivariate logistic analysis indicated that age (odds ratio [OR], 8.546; 95% confidence interval [CI]: 1.628-44.864; P = 0.011), history of smoking (OR, 14.285; 95% CI: 1.577-25.000; P = 0.018), maximum body temperature at admission (OR, 8.999; 95% CI: 1.036-78.147, P = 0.046), respiratory failure (OR, 8.772, 95% CI: 1.942-40.000; P = 0.016), albumin (OR, 7.353, 95% CI: 1.098-50.000; P = 0.003), and C-reactive protein (OR, 10.530; 95% CI: 1.224-34.701, P = 0.028) were risk factors for disease progression. Several factors that led to the progression of COVID-19 pneumonia were identified, including age, history of smoking, maximum body temperature at admission, respiratory failure, albumin, and C-reactive protein. These results can be used to further enhance the ability of management of COVID-19 pneumonia.

هذا العمل الجماعي المشترك، كما يشير عنوانه : (التاريخ المديني الحضري للصين) هو كتاب حضاري بامتياز. كتاب ‏يستعرض جوانب أساسية من حضارة الشعب الصيني القديمة-المتجددة الراسخة، الضاربة جذورها عميقا في تربة التاريخ ‏البشري الشامل.‏‎ يعد الكتاب سفر حضاري قيم وبحث متصل رصين حول التطور التاريخي العمراني في المدن الصينية وهو إذ ‏يتناول بشكل أساسي، فن العمارة والبناء والتصميم وتخطيط المدن والشوارع والأحياء والأسواق والمقار الحكومية ‏والحدائق والمعابد والساحات ومسالك الملاحة النهرية والري، فإنه لا يغفل في الوقت نفسه عن ما يتصل به هذا ‏الموضوع، من عشرات المواضيع الحضارية والثقافية والمعيشية الأخرى، مثل : العبادات والاعتقادات والتقاليد ‏والعادات والآداب والطقوس والحرف والفنون والنظم الاجتماعية والصراع السياسي والغزو الخارجي والتنظيم ‏الحكومي والقبلي والاجتماعي والطبقي والعسكري والإداري والإنمائي والعمراني والإسكاني والتعليمي والتجاري ‏والأدبي والفني والموسيقي والفولكلوري. إنه كتاب جميل يقدم العديد من اللوحات الرشيقة الرحبة المتقابلة المتلاحقة ‏المتكاملة التي ترحل بنا بين القصور والأنهار والأسوار والأحياء والمعاهد والمعابد وهياكل عبادة الأجداد ومواقع ‏التنقيب والساحات والحدائق والميادين ودواوين الشعر وسجلات التاريخ ولا يخلو كل ذلك من جولات من البحث ‏المقارن في غير أمر من هذه الأمور ولن نطيل عليكم في الإضاءة على مواضيع هذا الكتاب لأكثر من ذلك، آملين ‏لكم سلاسة القراءة ومتعة الاكتشاف.

Emerging infectious diseases, such as severe acute respiratory syndrome (SARS) and Zika virus disease, present a major threat to public health 1 – 3 . Despite intense research efforts, how, when and where new diseases appear are still a source of considerable uncertainty. A severe respiratory disease was recently reported in Wuhan, Hubei province, China. As of 25 January 2020, at least 1,975 cases had been reported since the first patient was hospitalized on 12 December 2019. Epidemiological investigations have suggested that the outbreak was associated with a seafood market in Wuhan. Here we study a single patient who was a worker at the market and who was admitted to the Central Hospital of Wuhan on 26 December 2019 while experiencing a severe respiratory syndrome that included fever, dizziness and a cough. Metagenomic RNA sequencing 4 of a sample of bronchoalveolar lavage fluid from the patient identified a new RNA virus strain from the family Coronaviridae , which is designated here ‘WH-Human 1’ coronavirus (and has also been referred to as ‘2019-nCoV’). Phylogenetic analysis of the complete viral genome (29,903 nucleotides) revealed that the virus was most closely related (89.1% nucleotide similarity) to a group of SARS-like coronaviruses (genus Betacoronavirus, subgenus Sarbecovirus) that had previously been found in bats in China 5 . This outbreak highlights the ongoing ability of viral spill-over from animals to cause severe disease in humans. Phylogenetic and metagenomic analyses of the complete viral genome of a new coronavirus from the family Coronaviridae reveal that the virus is closely related to a group of SARS-like coronaviruses found in bats in China.

Background The majority of breast cancer patients die of metastasis rather than primary tumors, whereas the molecular mechanisms orchestrating cancer metastasis remains poorly understood. Long noncoding RNAs (lncRNA) have been shown to regulate cancer occurrence and progression. However, the lncRNAs that drive metastasis in cancer patients and their underlying mechanisms are still largely unknown. Methods lncRNAs highly expressed in metastatic lymph nodes were identified by microarray. Survival analysis were made by Kaplan-Meier method. Cell proliferation, migration, and invasion assay was performed to confirm the phenotype of LINC02273. Tail vein model and mammary fat pad model were used for in vivo study. RNA pull-down and RIP assay were used to confirm the interaction of hnRNPL and LINC02273. Chromatin isolation by RNA purification followed by sequencing (ChIRP-seq), RNA-seq, ChIP-seq, and luciferase reporter assay reveal hnRNPL-LINC02273 regulates AGR2. Antisense oligonucleotides were used for in vivo treatment. Results We identified a novel long noncoding RNA LINC02273, whose expression was significantly elevated in metastatic lesions compared to the primary tumors, by genetic screen of matched tumor samples. Increased LINC02273 promoted breast cancer metastasis in vitro and in vivo. We further showed that LINC02273 was stabilized by hnRNPL, a protein increased in metastatic lesions, in breast cancer cells. Mechanistically, hnRNPL-LINC02273 formed a complex which activated AGR2 transcription and promoted cancer metastasis. The recruitment of hnRNPL-LINC02273 complex to AGR2 promoter region epigenetically upregulated AGR2 by augmenting local H3K4me3 and H3K27ac levels. Combination of AGR2 and LINC02273 was an independent prognostic factor for predicting breast cancer patient survival. Moreover, our data revealed that LINC02273-targeting antisense oligonucleotides (ASO) substantially inhibited breast cancer metastasis in vivo. Conclusions Our findings uncover a key role of LINC02273-hnRNPL-AGR2 axis in breast cancer metastasis and provide potential novel therapeutic targets for metastatic breast cancer intervention.

Chirality, an intrinsic degree of freedom, has been barely exploited as the information carriers in data transmission, processing, computing, etc. Recently the magnons in antiferromagnets were proposed to carry both right-handed and left-handed chiralities, shedding a light on chirality-based spintronics in which chirality-based computing architectures and chiral magnonic devices may become feasible. However, the practical platform for chirality-based spintronics remains absent yet. Here we report an artificial ferrimagnetic Py/Gd/Py/Gd/Py/Pt multilayer by which the switching, reading, and modulation of magnon chirality are demonstrated. In particular, the coexisting resonance modes of ferromagnetic and antiferromagnetic characteristics permit the high adjustability and easy control of magnon chirality. As a main result, we unambiguously demonstrated that Py precessions with opposite chiralities pump spin currents of opposite spin polarizations into the Pt layer. Our result manifests the chirality as an independent degree of freedom and illustrates a practical magnonic platform for exploiting chirality, paving the way for chirality-based spintronics. Magnons in antiferromagnets hold potential for chirality-based spintronics, but a practical platform remains absent. Here, the authors demonstrate possible magnon chirality switching, reading and modulation in an artificial ferrimagnet Py/Gd/Py/Gd/Py/Pt multilayer, manifesting the chirality as an independent degree of freedom.

The rapid application of digital technology in rural areas has been carried out worldwide, but academic research on the theme of digital villages is still in its infancy. The academia is still unclear about the construction content, theoretical framework and realization path of the digital village construction. Against this background, this paper studies how villages can transform into digital villages and achieve a sustainable development. Firstly, this paper builds a digital village technology architecture system from four levels: infrastructure system, village brain, application support system and application service system. The system points out the specific construction content from the technical point of view, and provides scientific guidance for construction activities. Secondly, with the help of digital empowerment theory, the theoretical framework of the digital village construction to promote a sustainable rural development, is constructed from five fields: industry, ecology, culture, service and governance. Finally, the theoretical framework is verified through five Chinese cases, and two characteristics of a digital village construction are summarized to provide reference and guidance for digital village practice activities. The digital village construction should use data, digital technology and digital platform as the base, attract multiple subjects to participate and form symbiotic relationships, and achieve a rural sustainable development.

Chiral aldehyde catalysis is a burgeoning strategy for the catalytic asymmetric α-functionalization of aminomethyl compounds. However, the reaction types are limited and to date include no examples of stereodivergent catalysis. In this work, we disclose two chiral aldehyde-catalysed diastereodivergent reactions: a 1,6-conjugate addition of amino acids to para -quinone methides and a bio-inspired Mannich reaction of pyridinylmethanamines and imines. Both the syn - and anti -products of these two reactions can be obtained in moderate to high yields, diastereo- and enantioselectivities. Four potential reaction models produced by DFT calculations are proposed to explain the observed stereoselective control. Our work shows that chiral aldehyde catalysis based on a reversible imine formation principle is applicable for the α-functionalization of both amino acids and aryl methylamines, and holds potential to promote a range of asymmetric transformations diastereoselectively. Chiral aldehyde catalysis is a useful strategy in the catalytic asymmetric α-functionalization of amino methyl compounds but these reaction types are limited. Here, the authors report two chiral aldehyde-catalysed diastereodivergent reactions, namely, a 1,6-conjugate addition and a bio-inspired Mannich reaction.

Autism spectrum disorder (ASD) is a common neurodevelopmental disorder. The mechanisms underlying ASD are unclear. Astrocyte alterations are noted in ASD patients and animal models. However, whether astrocyte dysfunction is causal or consequential to ASD-like phenotypes in mice is unresolved. Type 2 inositol 1,4,5-trisphosphate 6 receptors (IP3R2)-mediated Ca 2+ release from intracellular Ca 2+ stores results in the activation of astrocytes. Mutations of the IP3R2 gene are associated with ASD. Here, we show that both IP3R2-null mutant mice and astrocyte-specific IP3R2 conditional knockout mice display ASD-like behaviors, such as atypical social interaction and repetitive behavior. Furthermore, we show that astrocyte-derived ATP modulates ASD-like behavior through the P2X2 receptors in the prefrontal cortex and possibly through GABAergic synaptic transmission. These findings identify astrocyte-derived ATP as a potential molecular player in the pathophysiology of ASD. Astrocytes contribute to autism spectrum disorder (ASD) pathophysiology. Here, the authors show that IP3R2 conditional KO mice show ASD-like behaviours and identify astrocyte-derived ATP as a modulator of these behaviours in mice.