NGUYEN DU’S PERCEPTION ABOUT CHINA UNDER THE QING DYNASTY THROUGH BAC HANH TAP LUC by Lê Quang Trường

“…Many of his family members served in high positions in the imperial mandarin system of the Le-Trinh dynasty. Inheriting honors from his father, Nguyen Du was bestowed the titles: Hoang Tin Great Man, Guard Commandant of Origin, and Thu Nhac Count. …”
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Solving Nonnative Combinatorial Optimization Problems Using Hybrid Quantum–Classical Algorithms by Jonathan Wurtz, Stefan H. Sack, Sheng-Tao Wang

“…By designing nonnative quantum variational anosatzes that inherit some but not all problem structure, measurement outcomes from the quantum computer can act as a resource to be used by classical routines to indirectly compute optimal solutions, partially overcoming the challenges of contemporary quantum optimization approaches. …”
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Clinicoepidemiological Observational Study of Acquired Alopecias in Females Correlating with Anemia and Thyroid Function by Kirti Deo, Yugal K. Sharma, Meenakshi Wadhokar, Neha Tyagi

“…Alopecia can either be inherited or acquired; the latter, more common, can be diffuse, patterned, and focal, each having cicatricial and noncicatricial forms. …”
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Lilla’s Heritage. Cultural Sketches of the Vay Branch in Hungary by Lili Veronika Békéssy

“…There is however, little research on that topic regarding the cultural heritage Dora inherited. The lineage of this family, though only partially documented from a musicological point of view, unveils a significant impact on Dora’s abilities and sensitivities by diligently scrutinizing press and archival records from that era. …”
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Assessing Magnetic Susceptibility Profiles of Topsoils under Different Occupations by N. Bouhsane, S. Bouhlassa

“…The aims of this study were to investigate the impact of land use or human activity on χlf of soil overlying the same substrate, to discriminate allochthonous material or pollution from autochthonous or inherited ones, and to assess the origin and contribution of superparamagnetic (SP) grains to the global magnetic susceptibility χlf. …”
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Cardiac Tamponade: A Rare Manifestation of Familial Mediterranean Fever by Abdolreza Malek, Tina Zeraati, Ariane Sadr-Nabavi, Niloofar Vakili, Mohammad Reza Abbaszadegan

“…FMF is an autoinflammatory disease, usually inherited with an autosomal recessive pattern. The patients typically have biallelic mutations in the MEFV gene, located on chromosome 16. …”
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A narrative review of the literature on the pediatric orthopedic management of fibrous dysplasia by Elio Paris, Giacomo De Marco, Oscar Vazquez, Christina Steiger, Sana Boudabbous, Romain Dayer, Dimitri Ceroni

“…Fibrous dysplasia is a congenital, non-inherited, benign intramedullary bone lesion in which the normal bone marrow is replaced by abnormal fibro-osseous tissue. …”
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Clinical phenotype and trio whole exome sequencing data from a patient with glycogen storage disease IV in Indonesia(NCBI) by Ivan William Harsono, Yulia Ariani, Beben Benyamin, Fadilah Fadilah, Dwi Ari Pujianto, Cut Nurul Hafifah, Titis Prawitasari

“…GSD IV occurs once in approximately 1 in every 760,000 to 960,000 live births and is inherited in an autosomal recessive pattern. Early diagnosis of GSD IV is challenging due to non-specific symptoms, such as liver and spleen enlargement, which can overlap with other hematologic and hepatobiliary disorders. …”
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X-Linked Lymphoproliferative Syndrome and Common Variable Immunodeficiency May Not Be Differentiated by SH2D1A and XIAP/BIRC4 Genes Sequence Analysis by Nesrin Gulez, Guzide Aksu, Afig Berdeli, Neslihan Karaca, Sema Tanrıverdi, Necil Kutukculer, Elif Azarsiz

“…The X-linked lymphoproliferative syndrome (XLP) is a rare, inherited immunodeficiency characterized by recurrent episodes of hemophagocytic lymphohistiocytosis, hypogammaglobulinemia, and/or lymphomas. …”
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Dual Functions of the C5a Receptor as a Connector for the K562 Erythroblast-Like Cell-THP-1 Macrophage-Like Cell Island and as a Sensor for the Differentiation of the K562 Erythrob... by Hiroshi Nishiura, Rui Zhao, Tetsuro Yamamoto

“…In contrast to the extraribosomal functions of the RP S19, a proapoptotic signal in pro-EBs, which is caused by mutations in the RP S19 gene, is associated with the inherited erythroblastopenia, Diamond-Blackfan anaemia. …”
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Association of fatty acid desaturase 2 gene polymorphism (rs28456) with susceptibility to bipolar disorder in the Turkish population: A case-control study by Pirim Dilek, Gümüş Ceren, Boztepe Esra, Akdağ Emine Merve, Şirin Hande

“…Future studies are necessary to explore the impact of FADS2 variations on BD risk in larger study groups, considering their potential interaction with non-inherited risk factors.…”
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Preclinical use of a clinically-relevant scAAV9/SUMF1 vector for the treatment of multiple sulfatase deficiency by Maximiliano Presa, Rachel M. Bailey, Somdatta Ray, Lauren Bailey, Saurabh Tata, Tara Murphy, Pierre-Alexandre Piec, Harold Combs, Steven J. Gray, Cathleen Lutz

“…Abstract Background Multiple Sulfatase Deficiency (MSD) is a rare inherited lysosomal storage disorder characterized by loss of function mutations in the SUMF1 gene that manifests as a severe pediatric neurological disease. …”
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Approximate Solutions of Combinatorial Problems via Quantum Relaxations by Bryce Fuller, Charles Hadfield, Jennifer R. Glick, Takashi Imamichi, Toshinari Itoko, J. Richard Thompson, Yang Jiao, M. Marna Kagele, W. Blom-Schieber Adriana, Rudy Raymond, Antonio Mezzacapo

“…The proposed quantum relaxations inherit memory compression from quantum random access codes, which allowed us to test the performances of the methods presented for 3-regular random graphs and a design problem motivated by industry for sizes up to 40 nodes, on superconducting quantum processors.…”
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Unlocking the potential of sepiolite: Designing high-performance energy storage materials by Yanhuai Ding, Yizhi Jiang, Dongzhao Jin, Yunhong Jiang, Ana C.S. Alcântara

“…By utilizing sepiolite's morphological and structural characteristics, the composite materials not only inherit the form of sepiolite but also achieve a significant enhancement in electrochemical performance. …”
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A Korean Patient With Leber Congenital Amaurosis and a Homozygous RPE65 Variant Originating From a Paternal Uniparental Isodisomy by Hane Lee, Dongseok Moon, Rin Khang, Go Hun Seo, Chang Ki Yoon, Un Chul Park, Kyu Hyung Park, Eun Kyoung Lee

“…ABSTRACT Background Leber congenital amaurosis (LCA), the most severe form of inherited retinal dystrophy, is a rare, heterogeneous, genetic eye disease associated with severe congenital visual impairment. …”
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Physically engineered extracellular vesicles targeted delivering miR-21-5p to promote renoprotection after renal ischemia-reperfusion injury by Di Wu, Wenjie Ma, Liucheng Wang, Chengcheng Long, Silin Chen, Jingyu Liu, Yiguan Qian, Jun Zhao, Changcheng Zhou, Ruipeng Jia

“…In this study, we developed neutrophils (NEs) membrane-modified EVs (N-EVs) by exploiting the natural properties of NEs to target damaged endothelium. N-EVs inherited the characteristic membrane proteins of NEs along with the biological functions of EPCs-EVs. …”
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Entropy-extreme concept of data gaps filling in a small-sized collection by Viacheslav Kovtun, Krzysztof Grochla, Mohammed Al-Maitah, Saad Aldosary, Oleksii Kozachko

“…Thus, the proposed concept inherits the benefits of both parametric estimation and using a trained model of the target process and non-parametric estimation of undefined characteristics that distort data. …”
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RAISE OF HIGH FROST-RESISTANT AGROPYRON–TRITICUM HYBRIDS by E. P. Razmakhnin, T. M. Razmakhnina, V. E. Kozlov, E. I. Gordeeva, N. P. Goncharov, G. Y. Galitsyn, S. G. Veprev, V. M. Chekurov

“…When ripe, a few frost-resistant lines of winter wheat obtained displayed elevated productivity and altered morphology of ears, which had long awns, inherited in the progeny. This material is now being studied and propagated.…”
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A comparative approach of analyzing data uncertainty in parameter estimation for a Lumpy Skin Disease model by Edwiga Renald, Miracle Amadi, Heikki Haario, Joram Buza, Jean M. Tchuenche, Verdiana G. Masanja

“…Mathematical models of real-life systems inherit loss of information, and consequently, accuracy of their results is often complicated by the presence of uncertainties in data used to estimate parameter values. …”
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The mitochondrial gene order and CYTB gene evolution in insects by F. S. Sharko, A. V. Nedoluzhko, S. M. Rastorguev, S. V. Tsygankova, E. S. Boulygina, A. A. Polilov, E. B. Prokhortchouk, K. G. Skryabin

“…Mitochondrial DNA genes (mtDNA) are quite often used as markers for phylogenetic research into many organisms including arthropods, because mtDNA is multicopied, is inherited maternally, does not undergo recombination and accumulates mutations quickly enough (relative to the nuclear genome). …”
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