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9561
Treatment of Severe Hypertriglyceridemia with Continuous Insulin Infusion
Published 2011-01-01“…Most patients with SH suffer primary or genetic abnormality in lipid metabolism in combination with a precipitating factor such as uncontrolled diabetes mellitus, alcoholism, and drug intake. …”
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9562
Retinoid Therapy in a Case of Harlequin Ichthyosis with a Short Literature Review
Published 2024-01-01“…Harlequin ichthyosis (HI) is a genetically inherited epidermal disorder due to the mutation of the ABCA12 gene, which is responsible for lipid transportation, and presents with large keratinised scales characterised by deep erythematous fissures, with ectropion and eclabium. …”
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9563
Le Græculus et la Chananéenne : Salammbô, le roman des traductions
Published 2012-03-01“…The other translating character in the novel, the heroine herself, practices translation like the art of seduction, until Flaubert, in a writing act that genetic analysis of the drafts can trace, casts on this novel and on its character Babel’s curse, more severe than Tanit’s. …”
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9564
Thermal Aeroelastic Tailoring for Laminated Panel with Lamination Parameters and JAYA Algorithm
Published 2022-01-01“…In the second-stage, instead of using conventional genetic algorithm, the enhanced JAYA method is extended to search the laminate configuration to target the optimal lamination parameters. …”
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9565
Array gain and phase calibration in the presence of multipath based on weighted spatial smoothing
Published 2004-01-01“…Simulation results using genetic algorithm are provided to demonstrate the effectiveness and behavior of the proposed algorithm…”
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9566
Optimal Allocation of Shared Manufacturing Resources Based on Bilevel Programming
Published 2021-01-01“…The weights of the upper indicators are determined by Analytic Hierarchy Process (AHP) and Improved Order Relation Analysis (Improved G1) combination weighting method and the bilevel programming model is solved by the Improved Fast Elitist Non-Dominated Sorting Genetic Algorithm (Improved NSGA-II). Finally, the effectiveness of the model is validated by a numerical example.…”
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9567
Klippel-Trenaunay-Weber Syndrome. Case Report and Literature Review
Published 2023-06-01“…This is a rare, infrequent disease with a not well-defined genetic inheritance pattern that requires multidisciplinary management. …”
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9568
Calcium Signaling in the Ventricular Myocardium of the Goto-Kakizaki Type 2 Diabetic Rat
Published 2018-01-01“…The GK rat is a widely used nonobese, nonhypertensive genetic model of T2DM which is characterized by insulin resistance, elevated blood glucose, alterations in blood lipid profile, and cardiac dysfunction.…”
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9569
Histological Findings of ETosis in Hermansky-Pudlak Syndrome with Pulmonary Fibrosis: A Follow-Up Case Report
Published 2025-01-01“…Hermansky-Pudlak syndrome (HPS), both alone and in conjunction with pulmonary fibrosis (HPS-PF), is a rare, genetically heterogeneous, autosomal recessive disorder that affects multiple organs, including the lungs. …”
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9570
A Brief Review on the Pathological Role of Decreased Blood Flow Affected in Retinitis Pigmentosa
Published 2018-01-01“…Retinitis pigmentosa (RP) represents a clinically and genetically heterogeneous disease characterized by progressive photoreceptor loss. …”
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9571
The three geologic regions of Puebla State, Mexico
Published 2024-12-01“…It is divided into three distinct regions: the northern region with its predominantly marine successions, where outcrops a volcano-sedimentary marine succession aged between 171.3 ± 0.5 Ma and 168.6 ± 0.4 Ma; the central region, part of the Trans-Mexican Volcanic Belt; and the southern region, mainly characterized by a multitude of continental units on crystalline basements.BULLETS:Geological regionalization, geological provinces, genetic-chronostratigraphic units, key successions tableGeological records contrast between the northern and southern regionsFirst report of Middle Jurassic marine volcano-sedimentary succession in the Sierra Madre Oriental Range…”
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9572
Cardiac achalasia: modern concepts on etiology, pathogenesis, clinical presentation and diagnostics
Published 2014-12-01“…Esophageal manometry which allows to evaluate resting pressure and relaxation phenomenon of the lower esophageal sphincter and peristaltic activity of distal part of the esophagus is the «gold standard» of diagnostics. Genetic, autoimmune and infectious theories are considered for disease etiology.Conclusion. …”
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9573
Williams-Beuren Syndrome and Congenital Lobar Emphysema: Uncommon Association with Common Pathology?
Published 2017-01-01“…A diagnosis of congenital lobar emphysema should prompt further screening for congenital heart disease and genetic deletion, and further research is needed to investigate the role of elastin gene mutation in the development of the neonatal lung.…”
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9574
Adverse Immunologically Mediated Oral Mucosal Reactions to Systemic Medication: Lichenoid Tissue Reaction/Interface Dermatitis-Stomatitis, Autoimmune Vesiculobullous Disease, and I...
Published 2018-01-01“…Drug-induced hypersensitivity immune reactions are exaggerated immunoinflammatory responses to allergenic components of the medications that occur in genetically susceptible subjects. The type of hypersensitivity immune response generated, whether antibody mediated or T cell mediated, or an immune complex reaction is determined by multiple factors, including the molecular characteristics of the allergen, the route of administration of the medication, the manner of presentation of the allergen by antigen-presenting cells to naïve T cells, the repertoire of the T cell receptors, and the cytokine profile within the microenvironment. …”
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9575
Optimization Research of the Hinge Position and Output Speed of Electromechanical Erection Device
Published 2021-08-01“…The relation between output speed and output power, the relation between output speed and output force, the relation between hinge position and output power, the relation between hinge position and output force are explored. The Genetic Algorithm is taken to optimize the output speed and the hinge position. …”
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9576
Generation of an induced pluripotent stem cell line (UCLi026-A) from a patient with ADCY5-related disease carrying the heterozygous variant c.1253G > A; (p. Arg418Gln)
Published 2025-04-01“…Adenylyl cyclase 5 (ADCY5)-related diseases are a rare group of genetic disorders that commonly present in childhood. …”
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9577
Dynamic Modeling and Parameters Optimization of Large Vibrating Screen with Full Degree of Freedom
Published 2019-01-01“…The BP neural network is used to model the relationship between beam position and maximal elastic deformation of the lateral plate. Further, the genetic algorithm is used to optimize the established neural network model, and the optimal design parameters are obtained.…”
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9578
Rolling Bearing Fault Diagnosis Based on SVM Optimized with Adaptive Quantum DE Algorithm
Published 2022-01-01“…Finally, compared with quantum genetic algorithm support vector machines (QGA-SVM) and differential evolution-support vector machines (DE-SVM), etc., the results show that the algorithm proposed in this study has a higher diagnosis accuracy and shorter running time, providing great practical engineering value in the application of rolling bearing fault diagnosis.…”
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9579
DRUG-INDUCED GINGIVAL OVERGROWTHS: AN INSIGHT INTO MOLECULAR MECHANISMS
Published 2024-06-01“…This review aims to provide an in-depth analysis of the cellular and molecular pathways implicated in DIGO, including the roles of fibroblasts, inflammatory mediators, and genetic predispositions. By elucidating the interactions between these factors, we seek to highlight potential targets for intervention. …”
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9580
Epidermolysis bullosa
Published 2024-01-01“…Epidermolysis bullosa (EB) is a hereditary multisystemic disease caused by genetic defects in the skin's structural proteins. …”
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