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الثقة في النظرية : نجاح لنظام التنمية (البديل) الخاص بالصين
جاء هذا الكتاب تحت عنوان «الثقة في النظرية : نجاح لنظام التنمية \"البديل\" الخاص بالصين» وهو من تأليف (مايا غيو) وترجمة عبد الرحمن النجار. يبحث الكتاب في التطور الصيني السريع خلال الستة عقود الماضية، والدور الذي لعبه الحزب الشيوعي الصيني في تحويل الصين إلى دولة اشتراكية حديثة مزدهرة وقوية وديمقراطية ومتطورة ثقافيا ويستكشف ويستكشف فيما إذا كان صعود الصين يهدد نموذج التنمية الغربي وخاصة بعد أن أضحى صعود الصين حقيقة لا جدال فيها. يعتبر هذا الكتاب من أنجح الكتب التي نشرت عن الصين اليوم. فهو يقدم حججا مقنعة حول نهوض الصين. وتستند الآراء المعبر عنها في الكتاب ليس فقط إلى 60 عاما من تاريخ جمهورية الصين الشعبية وإنجازاتها الملحوظة في العقود الثلاثة الماضية، ولكن أيضا على تاريخها الحديث منذ عام 1840، وتاريخها الذي دام 2000 عام كدولة موحدة، وحضارتها ذات ال 5000 سنة. وتعكس المقابلات التي أجرتها المؤلفة \"مايا غيو\" مراقبتها الدقيقة للصين اليوم. إذ تضمنت أشخاصا من دوائر مختلفة، تشمل مجالات خبرتهم السياسة والاقتصاد والمجتمع والوضع الوطني وتاريخ دبلوماسية الحزب الشيوعي الصيني والاستراتيجية العسكرية وإدارة ممتلكات الدولة والرعاية الصحية والأعمال التجارية الخاصة. وتختلف موضوعات المقابلات على نطاق واسع؛ فمن النظم والنظرية والتطوير والإصلاح، إلى نوعية الحياة والاستراتيجية والدبلوماسية وجميع من كان فيها يؤيدون التعلم من الحضارات الإنسانية، ولكنهم يصرون في الوقت نفسه على ضرورة اتخاذ مسار يناسب الصين بدلا من استنساخ النموذج الغربي. يأتي هذا الكتاب من ضمن سلسلة تتألف من ثلاثة كتب وهي : الثقة في المسار : نموذج جديد لقوة صاعدة، الثقة في النظرية : فلسفة الصين لنظام دولي جديد، والثقة في النظام : نجاح نظام التنمية \"البديل\" في الصين. بما يوفر للقارئ مقاربة نظرية وواقعية لمسار الصين ونظريتها ونظامها، ويشرح أسباب ثقة الدولة الصينية في خياراتها.
Book
Regulating the T7 RNA polymerase expression in E. coli BL21 (DE3) to provide more host options for recombinant protein production
Escherichia coli
is the most widely used bacterium in prokaryotic expression system for the production of recombinant proteins. In BL21 (DE3), the gene encoding the T7 RNA polymerase (T7 RNAP) is under control of the strong lacUV5 promoter (P
lacUV5
), which is leakier and more active than wild-type lac promoter (P
lacWT
) under certain growth conditions. These characteristics are not advantageous for the production of those recombinant proteins with toxic or growth-burdened. On the one hand, leakage expression of T7 RNAP leads to rapid production of target proteins under non-inducing period, which sucks resources away from cellular growth. Moreover, in non-inducing or inducing period, high expression of T7 RNAP production leads to the high-production of hard-to-express proteins, which may all lead to loss of the expression plasmid or the occurrence of mutations in the expressed gene. Therefore, more BL21 (DE3)-derived variant strains with rigorous expression and different expression level of T7 RNAP should be developed. Hence, we replaced P
lacUV5
with other inducible promoters respectively, including arabinose promoter (P
araBAD
), rhamnose promoter (P
rhaBAD
), tetracycline promoter (P
tet
), in order to optimize the production of recombinant protein by regulating the transcription level and the leakage level of T7 RNAP. Compared with BL21 (DE3), the constructed engineered strains had higher sensitivity to inducers, among which rhamnose and tetracycline promoters had the lowest leakage ability. In the production of glucose dehydrogenase (GDH), a protein that causes host autolysis, the engineered strain BL21 (DE3::ara) exhibited higher biomass, cell survival rate and foreign protein expression level than that of BL21 (DE3). In addition, these engineered strains had been successfully applied to improve the production of membrane proteins, including
E. coli
cytosine transporter protein (CodB), the
E. coli
membrane protein insertase/foldase (YidC), and the
E. coli
F-ATPase subunit b (Ecb). The engineered strains constructed in this paper provided more host choices for the production of recombinant proteins.
Journal Article
Comparative analysis of cell lineage differentiation during hepatogenesis in humans and mice at the single-cell transcriptome level
During embryogenesis, the liver is the site of hepatogenesis and hematopoiesis and contains many cell lineages derived from the endoderm and mesoderm. However, the characteristics and developmental programs of many of these cell lineages remain unclear, especially in humans. Here, we performed single-cell RNA sequencing of whole human and mouse fetal livers throughout development. We identified four cell lineage families of endoderm-derived, erythroid, non-erythroid hematopoietic, and mesoderm-derived non-hematopoietic cells, and defined the developmental pathways of the major cell lineage families. In both humans and mice, we identified novel markers of hepatic lineages and an ID3
+
subpopulation of hepatoblasts as well as verified that hepatoblast differentiation follows the “default-directed” model. Additionally, we found that human but not mouse fetal hepatocytes display heterogeneity associated with expression of metabolism-related genes. We described the developmental process of erythroid progenitor cells during human and mouse hematopoiesis. Moreover, despite the general conservation of cell differentiation programs between species, we observed different cell lineage compositions during hematopoiesis in the human and mouse fetal livers. Taken together, these results reveal the dynamic cell landscape of fetal liver development and illustrate the similarities and differences in liver development between species, providing an extensive resource for inducing various liver cell lineages in vitro.
Journal Article
TranSIC-Net: An End-to-End Transformer Network for OFDM Symbol Demodulation with Validation on DroneID Signals
Demodulating Orthogonal Frequency Division Multiplexing (OFDM) signals in complex wireless environments remains a fundamental challenge, especially when traditional receiver designs rely on explicit channel estimation under adverse conditions such as low signal-to-noise ratio (SNR) or carrier frequency offset (CFO). Motivated by practical challenges in decoding DroneID—a proprietary OFDM-like signaling format used by DJI drones with a nonstandard frame structure—we present TranSIC-Net, a Transformer-based end-to-end neural network that unifies channel estimation and symbol detection within a single architecture. Unlike conventional methods that treat these steps separately, TranSIC-Net implicitly learns channel dynamics from pilot patterns and exploits the attention mechanism to capture inter-subcarrier correlations. While initially developed to tackle the unique structure of DroneID, the model demonstrates strong generalizability: with minimal adaptation, it can be applied to a wide range of OFDM systems. Extensive evaluations on both synthetic OFDM waveforms and real-world unmanned aerial vehicle (UAV) signals show that TranSIC-Net consistently outperforms least-squares plus zero-forcing (LS+ZF) and leading deep learning baselines such as ProEsNet in terms of bit error rate (BER), estimation accuracy, and robustness—highlighting its effectiveness and flexibility in practical wireless communication scenarios.
Journal Article
Strategies for efficient production of recombinant proteins in Escherichia coli: alleviating the host burden and enhancing protein activity
Escherichia coli
, one of the most efficient expression hosts for recombinant proteins (RPs), is widely used in chemical, medical, food and other industries. However, conventional expression strains are unable to effectively express proteins with complex structures or toxicity. The key to solving this problem is to alleviate the host burden associated with protein overproduction and to enhance the ability to accurately fold and modify RPs at high expression levels. Here, we summarize the recently developed optimization strategies for the high-level production of RPs from the two aspects of host burden and protein activity. The aim is to maximize the ability of researchers to quickly select an appropriate optimization strategy for improving the production of RPs.
Journal Article
Motion-unrestricted dynamic electrocardiogram system utilizing imperceptible electronics
Electrocardiogram (ECG) plays a vital role in the prevention, diagnosis, and prognosis of cardiovascular diseases (CVDs). However, the lack of a user-friendly and accurate long-term dynamic electrocardiogram (DCG) device in motion has made it challenging to perform many daily cardiovascular risk screenings and assessments, such as sudden cardiac arrest, resulting in additional economic burdens on society. Here, we present a motion-unrestricted dynamic electrocardiogram (MU-DCG) system, which employs skin-conformal, imperceptible electronics for long-term, comfortable, and accurate 12-lead DCG monitoring. To facilitate assembly for use on the skin, the MU-DCG system features a pressure-activated flexible skin socket for stably soft-connecting the on-skin soft module and the off-skin stiff module during dynamic movements. Crucially, blinded cardiologist evaluations confirm minimal motion artifacts in MU-DCG-acquired ECG signals. Our results demonstrate that the MU-DCG system, with large-area, ultra-thin on-skin electrodes/leads, and an off-skin module, accomplishes anti-motion interference acquisition and in-situ analysis while retaining wearing imperceptibility.
Electrocardiogram is crucial for cardiovascular disease prevention, diagnosis, and prognosis. Here, the authors present a motion-unrestricted dynamic electrocardiogram system utilizing skin-conformal, imperceptible electronics for long-term, comfortable, and accurate 12-lead monitoring.
Journal Article
The Litsea genome and the evolution of the laurel family
The laurel family within the Magnoliids has attracted attentions owing to its scents, variable inflorescences, and controversial phylogenetic position. Here, we present a chromosomelevel assembly of the Litsea cubeba genome, together with low-coverage genomic and transcriptomic data for many other Lauraceae. Phylogenomic analyses show phylogenetic discordance at the position of Magnoliids, suggesting incomplete lineage sorting during the divergence of monocots, eudicots, and Magnoliids. An ancient whole-genome duplication (WGD) event occurred just before the divergence of Laurales and Magnoliales; subsequently, independent WGDs occurred almost simultaneously in the three Lauralean lineages. The phylogenetic relationships within Lauraceae correspond to the divergence of inflorescences, as evidenced by the phylogeny of FUWA, a conserved gene involved in determining panicle architecture in Lauraceae. Monoterpene synthases responsible for production of specific volatile compounds in Lauraceae are functionally verified. Our work sheds light on the evolution of the Lauraceae, the genetic basis for floral evolution and specific scents.
Journal Article
Stresses as First-Line Tools for Enhancing Lipid and Carotenoid Production in Microalgae
Microalgae can produce high-value-added products such as lipids and carotenoids using light or sugars, and their biosynthesis mechanism can be triggered by various stress conditions. Under nutrient deprivation or environmental stresses, microalgal cells accumulate lipids as an energy-rich carbon storage battery and generate additional amounts of carotenoids to alleviate the oxidative damage induced by stress conditions. Though stressful conditions are unfavorable for biomass accumulation and can induce oxidative damage, stress-based strategies are widely used in this field due to their effectiveness and economy. For the overproduction of different target products, it is required and meaningful to deeply understand the effects and mechanisms of various stress conditions so as to provide guidance on choosing the appropriate stress conditions. Moreover, the underlying molecular mechanisms under stress conditions can be clarified by omics technologies, which exhibit enormous potential in guiding rational genetic engineering for improving lipid and carotenoid biosynthesis.
Journal Article
Supramolecular metal-organic frameworks that display high homogeneous and heterogeneous photocatalytic activity for H2 production
Self-assembly has a unique presence when it comes to creating complicated, ordered supramolecular architectures from simple components under mild conditions. Here, we describe a self-assembly strategy for the generation of the first homogeneous supramolecular metal-organic framework (SMOF-1) in water at room temperature from a hexaarmed [Ru(bpy)
3
]
2+
-based precursor and cucurbit[8]uril (CB[8]). The solution-phase periodicity of this cubic transition metal-cored supramolecular organic framework (MSOF) is confirmed by small-angle X-ray scattering and diffraction experiments, which, as supported by TEM imaging, is commensurate with the periodicity in the solid state. We further demonstrate that SMOF-1 adsorbs anionic Wells−Dawson-type polyoxometalates (WD-POMs) in a one-cage-one-guest manner to give WD-POM@SMOF-1 hybrid assemblies. Upon visible-light (500 nm) irradiation, such hybrids enable fast multi-electron injection from photosensitive [Ru(bpy)
3
]
2+
units to redox-active WD-POM units, leading to efficient hydrogen production in aqueous media and in organic media. The demonstrated strategy opens the door for the development of new classes of liquid-phase and solid-phase ordered porous materials.
Self-assembly is robust in creating advanced, homogeneous architectures under mild conditions. Here, the authors describe the generation of the first 3D metal-cored supramolecular organic framework using this strategy and illustrate its capacity in catalysing visible light-induced H
2
production.
Journal Article
Emerging Role and Mechanism of the FTO Gene in Cardiovascular Diseases
The fat mass and obesity-associated (FTO) gene was the first obesity-susceptibility gene identified through a genome-wide association study (GWAS). A growing number of studies have suggested that genetic variants of FTO are strongly associated with the risk of cardiovascular diseases, including hypertension and acute coronary syndrome. In addition, FTO was also the first N6-methyladenosine (m6A) demethylase, suggesting the reversible nature of m6A modification. m6A is dynamically deposited, removed, and recognized by m6A methylases, demethylases, and m6A binding proteins, respectively. By catalyzing m6A demethylation on mRNA, FTO may participate in various biological processes by modulating RNA function. Recent studies demonstrated that FTO plays a pivotal role in the initiation and progression of cardiovascular diseases such as myocardial fibrosis, heart failure, and atherosclerosis and may hold promise as a potential therapeutic target for treating or preventing a variety of cardiovascular diseases. Here, we review the association between FTO genetic variants and cardiovascular disease risk, summarize the role of FTO as an m6A demethylase in cardiovascular disorders, and discuss future research directions and possible clinical implications.
Journal Article