Origen and Plato on the Superiority and Perfection of the Soul by Zhimeng Lin

“…Origen’s theology is fundamentally rooted in the question of whether he upheld the pre-existence of the soul or focused more on the soul’s superiority over the body and its perfection. While inheriting many ideas from Plato, Origen adapted them in accordance with Christian doctrine. …”
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SOME THEORETICAL AND PRACTICAL ISSUES ON THE CONSTRUCTION AND DEVELOPMENT OF URBAN CULTURAL COMMUNITIES IN VIETNAM TODAY by Ngoc Tho Nguyen

“…It can be said that building a new urban community culture in Vietnam today requires a multidimensional approach, including two basic perspectives, a constructivist approach and a cognitive approach, to ensure the two main objectives of (1) creating a suitable and effective cultural environment for urban communities and (2) enhancing the sense of responsibility for participating in cultural creation and building an urban cultural flow that protects, inherits traditions, and fully conforms to civilized and modern standards. …”
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Thanatophoric Dysplasia: A Report of 2 Cases with Antenatal Misdiagnosis by Lamidi Audu, Amina Gambo, Tokan Silas Baduku, Bilkisu Farouk, Anisa Yahaya, Kefas Jacob

“…Thanatophoric dysplasia (TD) is a rare but uniformly lethal inherited disorder of the skeletal system resulting from defects in the fibroblast growth factor receptor-3 gene on the short arm of chromosome ##4. …”
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A Study of Social Class Conflict in Jane Austen’s Pride and Prejudice. by Atukunda, Atubangiire

“…Darcy, challenge and subvert class norms, illustrating Austen’s critique of superficial social distinctions and her advocacy for personal merit over inherited status. The study highlights how Austen uses satire and irony to address the moral limitations of the class system and to propose a more flexible social order. …”
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Targeting Herpetic Keratitis by Gene Therapy by Hossein Mostafa Elbadawy, Marine Gailledrat, Carole Desseaux, Diego Ponzin, Stefano Ferrari

“…Whereas the correction of inherited diseases was the initial goal of the field of gene therapy, here we discuss transgene expression, gene replacement, silencing, or clipping. …”
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Enhanced Inverse Model Predictive Control for EV Chargers: Solution for Rectifier-Side by Ali Sharida, Abdullah Berkay Bayindir, Sertac Bayhan, Haitham Abu-Rub

“…Inverse model predictive control (IMPC) is a control technique that was recently proposed for power electronic converters. IMPC inherits the advantages of model predictive control (MPC) in terms of ability to handle complex and nonlinear systems and achieving multiple control objectives, while adhering to various constraints. …”
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Ribosomes translocation into the spore of Bacillus subtilis is highly organised and requires peptidoglycan rearrangements by Olga Iwańska, Przemysław Latoch, Mariia Kovalenko, Małgorzata Lichocka, Joanna Hołówka, Remigiusz Serwa, Agata Grzybowska, Jolanta Zakrzewska-Czerwińska, Agata L. Starosta

“…Our results demonstrate that translation and translational machinery are temporally and spatially organised in B. subtilis during sporulation and that the forespore ‘inherits’ ribosomes from the mother cell. We propose that the movement of ribosomes in the cell may be mediated by the bacterial homologs of cytoskeletal proteins and that the cues for asymmetric division localisation may be translation-dependent. …”
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Genetics of Endometrial Cancers by Tsuyoshi Okuda, Akihiko Sekizawa, Yuditiya Purwosunu, Masaaki Nagatsuka, Miki Morioka, Masaki Hayashi, Takashi Okai

“…Lynch syndrome, which is an autosomal dominantly inherited disorder of cancer susceptibility and is characterized by a MSH2/MSH6 protein complex deficiency, is associated with the development of non-endometrioid carcinomas.…”
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Photocatalytic Oxidation of Gaseous Isopropanol Using Visible-Light Active Silver Vanadates/SBA-15 Composite by Ting-Chung Pan, Hung-Chang Chen, Guan-Ting Pan, Chao-Ming Huang

“…All the composites loaded with various amount of SVO inherit the higher adsorption capacity and larger mineralization yield than those of P-25 (commercial TiO2) and pure SVO. …”
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Interfacial coupling effects in two-dimensional ordered arrays for microwave attenuation by Yijie Liu, Jintang Zhou, Chenchen Li, Henghui Zhang, Yucheng Wang, Yi Yan, Lvtong Duan, Zhenyu Cheng, Yao Ma, Zhengjun Yao

“…The modified 2D ordered polyhedral superstructures not only inherit the atomic-level doping and well-designed shell structure, but also further amplify the loss properties to realize the multi-scale modulated MA response. …”
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FFUNet: A novel feature fusion makes strong decoder for medical image segmentation by Junsong Xie, Renju Zhu, Zezhi Wu, Jinling Ouyang

“…On the other hand, the feature gap between an encoder and decoder is also challenging for a U‐shaped network, which adopts a plain skip connection. Inherited from convolutional networks and transformers, FFUNet, a hybrid network structure with a novel module named the Feature Fusion Module (FFM) is proposed for medical image segmentation. …”
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Vitamin C-Induced Oxalate Nephropathy by Jorge Lamarche, Reji Nair, Alfredo Peguero, Craig Courville

“…Hyperoxaluria occurs as a result of inherited enzymatic deficiencies known as primary hyperoxaluria or from exogenous sources known as secondary hyperoxaluria. …”
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Neuronal Ceroid Lipofuscinosis in Border Collie Dogs in Japan: Clinical and Molecular Epidemiological Study (2000–2011) by Keijiro Mizukami, Takuji Kawamichi, Hiroshi Koie, Shinji Tamura, Satoru Matsunaga, Shigeki Imamoto, Miyoko Saito, Daisuke Hasegawa, Naoaki Matsuki, Satoshi Tamahara, Shigenobu Sato, Akira Yabuki, Hye-Sook Chang, Osamu Yamato

“…Neuronal ceroid lipofuscinosis (NCL) is an inherited, neurodegenerative lysosomal disease that causes premature death. …”
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Multifactorial Origin of Exertional Rhabdomyolysis, Recurrent Hematuria, and Episodic Pain in a Service Member with Sickle Cell Trait by Nyamkhishig Sambuughin, Mingqiang Ren, John F. Capacchione, Ognoon Mungunsukh, Kevin Chuang, Iren Horkayne-Szakaly, Francis G. O’Connor, Patricia A. Deuster

“…Individuals with Sickle Cell Trait (SCT), generally considered a benign carrier state of hemoglobin S (HbAS), are thought to be at risk for exertional rhabdomyolysis and hematuria, conditions that can also be caused by various other acquired and inherited factors. We report an SCT positive service member with an exertional rhabdomyolysis event, recurrent hematuria with transient proteinuria, and episodic burning pain in the lower extremities. …”
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The Musculoskeletal Anatomy of the Komodo Dragon’s Hindlimb (<i>Varanus komodoensis</i>, Varanidae) by Anna Tomańska, Martyna Stawinoga, Tomasz Gębarowski, Maciej Janeczek, Joanna Klećkowska-Nawrot, Karolina Goździewska-Harłajczuk, Maciej Dobrzyński

“…Additionally, these findings shed light on the evolutionary patterns inherited from the species’ ancestors, which contributed to the development of its distinctive biological adaptations.…”
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Familial Russell–Silver Syndrome like Phenotype in the PCNA Domain of the CDKN1C Gene, a Further Case by A. H. Sabir, G. Ryan, Z. Mohammed, J. Kirk, N. Kiely, M. Thyagarajan, T. Cole

“…The diagnosis was made through whole genome sequencing via the 100,000 genome project. A maternally inherited pathogenic heterozygous CDKN1C variant was found in the PCNA (proliferating cell nuclear antigen) domain. …”
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Diagnosis of Fanconi Anemia: Mutation Analysis by Multiplex Ligation-Dependent Probe Amplification and PCR-Based Sanger Sequencing by Johan J. P. Gille, Karijn Floor, Lianne Kerkhoven, Najim Ameziane, Hans Joenje, Johan P. de Winter

“…Fanconi anemia (FA) is a rare inherited disease characterized by developmental defects, short stature, bone marrow failure, and a high risk of malignancies. …”
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Wilson’s Disease: Diagnosis of Wilson’s Disease in Ethiopian Young Sisters by Nebiyu Bekele, Frew Ewnetu, Tigest Hailu, Zerubabel Tegegne, Abilo Tadesse

“…Wilson’s disease is an inherited autosomal recessive disorder of copper metabolism. …”
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Chromosome-level reference genome assembly of the gyrfalcon (Falco rusticolus) and population genomics offer insights into the falcon population in Mongolia by Farooq Omar Al-Ajli, Giulio Formenti, Olivier Fedrigo, Alan Tracey, Ying Sims, Kerstin Howe, Ikdam M. Al-Karkhi, Asmaa Ali Althani, Erich D. Jarvis, Sadequr Rahman, Qasim Ayub

“…The Altai maternally-inherited haplotypes diverged 422,000 years before present (290,000–550,000 YBP) from the ancestor of sakers and gyrfalcons, both of which, in turn, split 109,000 YBP (70,000–150,000 YBP). …”
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A Review of Complicated Cataract in Retinitis Pigmentosa: Pathogenesis and Cataract Surgery by Yingying Hong, Hongzhe Li, Yang Sun, Yinghong Ji

“…Retinitis pigmentosa (RP) is a set of inherited retinal degenerative diseases that affect photoreceptor and retinal pigment epithelial cells (RPEs), possibly associated with some ocular complications, including cataract. …”
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