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8701
Vera Petrovna Tsarenko (1940–2022): (in memory of the scientist)
Published 2022-06-01Get full text
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8702
Assessment of grain starch content and responses to CMS-S and CMS-C in high-starch maize hybrids
Published 2024-10-01Get full text
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8703
Association of Differing Qatari Genotypes with Vitamin D Metabolites
Published 2020-01-01“…Objective. Genetic studies have identified four Qatari genotypes: Q1 Arab, Bedouin; Q2 Asian/Persian; Q3 African; and a fourth admixed group not fitting into the previous 3 groups. …”
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8704
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8705
Cerebral Venous Thrombosis Revealing Primary Sjögren Syndrome: Report of 2 Cases
Published 2013-01-01“…We report two cases of primary SS in which the revealing symptom was cerebral venous thrombosis (CVT) in the absence of genetic or acquired thrombophilias.…”
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8706
Improved AC-GA based data association method for multi-target tracking
Published 2011-01-01“…An AC-GADA(ant colony-genetic algorithm data association) algorithm was proposed to deal with the data as-sociation problem for multi-target tracking.This algorithm designed difference pheromone for each ant and improved global pheromone increment model,and combined crossover and mutation strategy with fitness of population model in or-der to improve rate of convergence and avoid the appearance of local extremum.The comparison with ACDA(ant colony data association) and JPAD(joint pobabilistic data association) proved its efficiency and superiority.…”
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8707
Generation of induced pluripotent stem cell lines TRNDi037-A and TRNDi038-A from two patients with Alagille syndrome carrying heterozygous JAG1 mutations
Published 2025-02-01“…Human induced pluripotent stem cell (iPSC) lines TRNDi037-A and TRNDi038-A were generated from the lymphoblastoid cell lines (LCL) of two patients with different heterozygous JAG1 variants resulting in Alagille syndrome (ALGS). ALGS is a rare genetic disease of haploinsufficiency that affects the formation of the bile duct, in addition to other symptoms. …”
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8708
A case of CDKL5 deficiency disorder with a novel intragenic multi-exonic duplication
Published 2024-11-01“…This case highlights the importance of careful phenotyping and comprehensive genetic testing to detect rare structural variants in CDD patients.…”
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8709
Attempts to regulate the circulation of foreign currency in Russian Far East Anti–Bolshevik Power in 1919
Published 2024-02-01“…The theoretical basis of the research is such methods of historical research as historical-genetic, historical-comparative methods, as well as the method of content analysis. …”
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8710
Charge Scheduling of an Energy Storage System under Time-of-Use Pricing and a Demand Charge
Published 2014-01-01“…A real-coded genetic algorithm is used to schedule the charging of an energy storage system (ESS), operated in tandem with renewable power by an electricity consumer who is subject to time-of-use pricing and a demand charge. …”
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8711
Hierarchical Sliding Mode Algorithm for Athlete Robot Walking
Published 2017-01-01“…A new method based on hierarchical sliding mode for controlling postures is also introduced. Genetic algorithm is applied to design the oscillator for robot motion. …”
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8712
Path Planning Using a Hybrid Evolutionary Algorithm Based on Tree Structure Encoding
Published 2014-01-01“…To solve the problem of hybrid genetic algorithm and particle swarm optimization, the “dummy node” is added into the binary trees to deal with the different lengths of representations. …”
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8713
Problem ludzkiej wolności i adekwatnej interpretacji przyrody w świetle genocentryzmu
Published 2011-12-01“…In the article, the stance of genetic determinism, represented by Edward Wilson and Richard Dawkins on the grounds of sociobiology, has been presented and critically commented. …”
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8714
Lung Transplantation in a Patient with COPA Syndrome
Published 2020-01-01“…COPA syndrome is a newly discovered, rare genetic autoimmune disorder, which can affect the lungs, joints, and kidneys. …”
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8715
Molecular Targets for the Treatment of Juvenile Myelomonocytic Leukemia
Published 2012-01-01“…Significant advances in our understanding of the genetic defects and the pathogenesis of juvenile myelomonocytic leukemia (JMML) have been achieved in the last several years. …”
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8716
Growing Feijoa Fruit in Florida
Published 2021-12-01“…Its value as a potentially heavy producer of flavorful fruits (and flavorful flowers) is frequently overlooked due to issues in pollination and limited genetic improvement. This new 5-page publication of the UF/IFAS Horticultural Sciences Department describes the opportunity and limitations of feijoa as a horticultural crop. https://edis.ifas.ufl.edu/hs1424 …”
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8717
Congenital Defects in Neutrophil Dynamics
Published 2014-01-01“…Their high turnover rate, their fine-tuned killing machinery, and their arsenal of toxic vesicles leave them particularly vulnerable to various genetic deficiencies. The aim of this review is to highlight those congenital immunodeficiencies which impede the dynamics of neutrophils, such as migration, cytoskeletal rearrangements, vesicular trafficking, and secretion.…”
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8718
Non-Scarring Alopecia in Females: A Comprehensive Review
Published 2024-08-01“…Various aetiologic factors are implicated in non-scarring alopecia, including genetic predisposition, loss of immune privilege, oxidative damage, and hormonal fluctuations. …”
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8719
Antineoplastic Effects of 5-Aminosalicylates and Potential Cancer Preventive Role in Inflammatory Bowel Disease
Published 2004-01-01“…It was subsequently appreciated that the degree of risk depended on the population being studied and on both genetic and environmental factors (eg diet, drugs and prior surgical treatment). …”
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8720
Liver Failure with Marked Hyperferritinemia: ‘Ironing Out’ the Diagnosis
Published 2001-01-01“…Clinical recognition and diagnosis of HLH can be difficult but are crucial for appropriate therapy and genetic counselling. Liver transplantation is absolutely contraindicated for patients with HLH but may be the only life-saving treatment modality for patients with perinatal hemochromatosis.…”
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