Exploration on Molecular Mechanism of Reversal Effect of Compound Danshen Tablets on Hepatic Fibrosis Based on Network Pharmacology by Minling Cao, Jingyue Fan, Xiaoli Yang, Meifeng Shi, Shanshan Lin, Xiaoling Chi

“…Traditional Chinese medicine systems pharmacology (TCMSP) and online Mendelian inheritance in man (OMIM) databases were searched for compound Danshen tablets’ active ingredients o and hepatic fibrosis-related genes. …”
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Research on the Protection of Battlefield Sites in the Taihang Mountain Area of Southern Hebei Province, China: A Case Study of She County by Feifei Zheng, Yuan Kuang, Yue Hu

“…This study can lay the foundation for the cultural inheritance and sustainable protection of battlefield sites in the Taihang Mountain Area of Southern Hebei Province, and provide theoretical references and practical examples for similar research.…”
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Perinatal Management for a Pregnant Woman with an MYH9 Disorder by Yuka Yamashita, Rei Matsuura, Shinji Kunishima, Yoshie Oikawa, Hirotsugu Ariizumi, Shoko Hamada, Nahoko Shirato, Ryu Matsuoka, Kohichi Ogawa, Akihiko Sekizawa

“…We provided genetic counseling, as required, which included apprising the woman of the inheritance pattern, the importance of a genetic analysis, and the potential delivery risks for the patient and her offspring. …”
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Maternal asthma imprints fetal lung ILC2s via glucocorticoid signaling leading to worsened allergic airway inflammation in murine adult offspring by Tomoaki Takao, Ako Matsui, Chie Kikutake, Keiko Kan-o, Azusa Inoue, Mikita Suyama, Isamu Okamoto, Minako Ito

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Interspecific potato hybrids as donors of durable resistance to pathogens by E. V. Rogozina, E. E. Khavkin

“…The breeding value of tuber-bearing Solanum species depends on their compatibility with the cultivated potato and the mechanism of target trait inheritance. To overcome incompatibility in crosses, breeders employ ploidy manipulation in the parental forms, bridge crosses, the mediator method and various in vitro technologies. …”
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The Relationship between Cadherin Polymorphisms and the Risk of Delayed Encephalopathy after Acute Carbon Monoxide Poisoning in the Chinese Han Population by Xuejiao Liu, Jiao Zeng, Xiaoli Zhang, Jiapeng Gu, Fan Zhang, Yongkai Han, Ping Zhang, Wenqiang Li, Renjun Gu

“…We found that rs1944294 in the N-cadherin (CDH2) gene showed significant differences in genotype frequencies between the two groups under codominant and dominant inheritance models. Similarly, rs2513796 in the cadherin-17 (CDH17) gene showed significant differences under the codominant, dominant, and overdominant genetic models. …”
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The Pathogenesis of Periodic Fever, Aphthous Stomatitis, Pharyngitis, and Cervical Adenitis Syndrome: A Review of Current Research by Barbara Kraszewska-Głomba, Agnieszka Matkowska-Kocjan, Leszek Szenborn

“…The absence of a clear monogenic trait indicates a heterogenous, polygenic, or complex inheritance of PFAPA syndrome. As two mutations with a possible functional effect on the inflammasomes (MEFV E148Q and NLRP3 Q703K) have been found in several PFAPA cohorts, the role of inflammasome-related genes in PFAPA pathogenesis cannot be excluded. …”
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Innovative Framework for Historical Architectural Recognition in China: Integrating Swin Transformer and Global Channel–Spatial Attention Mechanism by Jiade Wu, Yang Ying, Yigao Tan, Zhuliang Liu

“…The digital recognition and preservation of historical architectural heritage has become a critical challenge in cultural inheritance and sustainable urban development. While deep learning methods show promise in architectural classification, existing models often struggle to achieve ideal results due to the complexity and uniqueness of historical buildings, particularly the limited data availability in remote areas. …”
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POLYMORPHIC VARIANTS OF SUNFLOWER <i> RFL-PPR </i> GENES AS MOLECULAR GENETIC MARKERS by I. N. Anisimova, Yu. I. Karabitsina, N. V. Alpatieva, E. B. Kuznetsova, V. A. Gavrilova, E. E. Radchenko

“…However, the CAPS marker elaborated for the QHL12D20 fragment showed independent inheritance from pollen fertility restoration trait in the F2 of the hybrid VIR116xVIR740.…”
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Primary Hyperoxaluria Type 1 in 18 Children: Genotyping and Outcome by Mohamed S. Al Riyami, Badria Al Ghaithi, Nadia Al Hashmi, Naifain Al Kalbani

“…Primary hyperoxaluria belongs to a group of rare metabolic disorders with autosomal recessive inheritance. It results from genetic mutations of the AGXT gene, which is more common due to higher consanguinity rates in the developing countries. …”
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History and National Integration: A Study of Collective Memory of Tamiang Monuments in Medan 1894 by Aulia Rahman, Husaini Ibrahim, Okhaifi Prasetyo, Usman Usman, Mufti Riyani

“…Through historical methods, the study results show that the Tamiang Monument plays an essential role in the inheritance of collective memory about the conquest of Tamiang as part of the Aceh region by the Dutch colonialists. …”
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Combining Ability of Pod Yield and Related Traits of Groundnut (Arachis hypogaea L.) under Salinity Stress by Md. Abul Kalam Azad, Md. Shah-E-Alam, Md. Abdul Hamid, Mohd Y. Rafii, M. A. Malek

“…A study was performed using 6×6 F1 diallel population without reciprocals to assess the mode of inheritance of pod yield and related traits in groundnut with imposed salinity stress. …”
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An Interactive Database of Cocaine-Responsive Gene Expression by Willard M. Freeman, Kathryn E. Dougherty, Sally E. Vacca, Kent E. Vrana

“…Accompanying each gene is a description of the gene, links to the original publications, and a link to the appropriate OMIM (Online Mendelian Inheritance in Man) entry. The nature of this review allows for timely modifications and rapid inclusion of new publications, and should help researchers build second-generation hypotheses on the role of gene expression changes in the physiology and behavior of cocaine abuse. …”
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Novel Human Induced Pluripotent Stem Cell-Based Model for Retinal Pigment Epithelial Cells to Reveal Possible Disease Mechanisms for Macular Degeneration in Pseudoxanthoma Elasticu... by Taina Viheriälä, Heidi Hongisto, Lyydia Saari, Marika Oksanen, Tanja Ilmarinen, Suvi Väärämäki, Hannu Uusitalo, Pasi Nevalainen, Heli Skottman

“…Pseudoxanthoma elasticum (PXE) is a rare metabolic disease with autosomal recessive inheritance. The manifestation in PXE is represented by retinal complications, pseudoxanthomas of the skin folding areas, and arterial calcification. …”
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On the human nature (following in the steps of Belyaev) by A. L. Markel

“…In fact, we are talking about epigenetic inheritance in the evolution of culture and morality. …”
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Genetic control of traits determining phosphorus uptake by rice varieties (Oryza sativa L.) by J. K. Goncharova, E. M. Kharitonov

“…Traits determining the rate of phosphorus uptake by rice varieties and their inheritance are discussed. Polymorphism of 72 rice accessions of Russian and foreign breeding by the rate of the formation of the root system and its size at maturity is considered. …”
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Diagenesis and Fluid Flow Variability of Structural Heterogeneity Units in Tight Sandstone Carrier Beds of Dibei, Eastern Kuqa Depression by H. Shi, X. R. Luo, G. L. Lei, L. Q. Zhang, L. K. Zhang, Y. H. Lei

“…We propose that there is an inheritance relationship between the late gas and early oil migration pathways, which implies that the sweet spots develop in the reservoirs that experienced early oil emplacement.…”
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Size, spines, and primes: the drivers of collar spine numbers among echinostome trematodes by Bronwen Presswell, Priscila M. Salloum, Jerusha Bennett, Katherine E. Buschang, Robert Poulin

“…Overall, our findings indicate that the number of collar spines, a hallmark of echinostomes, is the product of conserved phylogenetic inheritance overlaid by adaptive functional adjustments. …”
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Soil and Groundwater Characteristics of a Legacy Spill Site by A Adoki

“…Families own the land and this ownership is by inheritance. In recent times, people can purchase land for use and others can also hire. …”
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Spontaneous Coronary Artery Dissection: A Rare Manifestation of Alport Syndrome by Amornpol Anuwatworn, Prince Sethi, Kelly Steffen, Orvar Jonsson, Marian Petrasko

“…Alport syndrome (AS) is a genetic disorder due to inheritance of genetic mutations which lead to production of abnormal type IV collagen. …”
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