Suggested Topics within your search.
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1281
Atrial Fibrillation and Long QT Syndrome Presenting in a 12-Year-Old Girl
Published 2012-01-01“…Mutations in KCNQ1 are the most common cause of LQTS. …”
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1282
Discrete and Continuous Optimization Based on Hierarchical Artificial Bee Colony Optimizer
Published 2014-01-01“…At the same time, the comprehensive learning method with crossover and mutation operator is applied to enhance the global search ability between species. …”
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1283
Genetic and Biochemical Alterations in Non-Small Cell Lung Cancer
Published 2012-01-01“…This paper describes these molecular targets in NSCLC, and describes the biological significance of each mutation and their potential to act as a therapeutic target.…”
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1284
Cognitive Impairment Involving Social Cognition in SPG4 Hereditary Spastic Paraplegia
Published 2016-01-01“…We reported a series of nine patients with SPG4 mutation with an extensive neuropsychological examination including social cognition assessment. …”
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1285
Hereditary Hyperferritinemia-Cataract Syndrome in 3 Generations of a Family in East Tennessee
Published 2020-01-01“…While investigators have dissected the gene where several responsible mutations reside, it remains a relatively unknown genetic disorder to clinicians. …”
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1286
Interstitial Lung Disease in Werner Syndrome: A Case Report of a 55-Year-Old Male Patient
Published 2015-01-01“…Although telomere length, with or without germline mutation, is known to be associated with interstitial lung disease, the latter is not associated with WS. …”
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1287
Disordered and Multiple Destinations Path Planning Methods for Mobile Robot in Dynamic Environment
Published 2016-01-01“…It can calculate the crossover probability and mutation probability adaptively changing with environment at any time. …”
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1288
A Rheological Model of Sandstones considering Response to Thermal Treatment
Published 2019-01-01“…As a consequence, the heterogeneous deformation occurs, and macrocracks are present, leading to the irregular fluctuation and mutation in strain over time. A higher temperature contributes to a more severe structure damage and in turn reduces the intactness of sandstones and elevates the rheological response. …”
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1289
A Pleural Solitary Fibrous Tumor, Multiple Gastrointestinal Stromal Tumors, Moyamoya Disease, and Hyperparathyroidism in a Patient Associated with NF1
Published 2015-01-01“…Loss of the gene function, due to a point mutation, leads to an increase in cell proliferation and the development of several tumors. …”
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1290
Design of SVC Controller Based on Improved Biogeography-Based Optimization Algorithm
Published 2014-01-01“…Considering that common subsynchronous resonance controllers cannot adapt to the characteristics of the time-varying and nonlinear behavior of a power system, the cosine migration model, the improved migration operator, and the mutative scale of chaos and Cauchy mutation strategy are introduced into an improved biogeography-based optimization (IBBO) algorithm in order to design an optimal subsynchronous damping controller based on the mechanism of suppressing SSR by static var compensator (SVC). …”
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1291
Characteristics and Treatment Results of 5 Patients with Fibrous Dysplasia and Review of the Literature
Published 2015-01-01“…Fibrous dysplasia is a rare bone disease caused by missense mutation leading to abnormal fibroblast and osteoblast proliferation and increased bone resorption. …”
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1292
The enigmatic SLC26A6 multifunctional anion transporter: recent advances in structure-function relationship, pathophysiological significance and novel pharmacological inhibitors
Published 2025-01-01“…How does this finding fit with previous genetic studies in mice and humans of SLC26A6 gene mutations? Thirdly, progress has been made in identifying specific inhibitors for SLC26A6. …”
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1293
Hyperparathyroidism Jaw Tumor Syndrome Presenting as Recurrent Femur Fractures in a Young Woman; a Rare Presentation of a Rare Disease
Published 2020-01-01“…Based on the associated clinical manifestations, hyperparathyroidism jaw tumor syndrome was suspected, and genetic studies reported a positive CDC73 mutation with a whole-gene deletion of exon 1–17. Conclusion. …”
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1294
Freeman–Sheldon Syndrome: First Molecularly Confirmed Case from Sub-Saharan Africa
Published 2017-01-01“…Diagnosis was based on the distinctive clinical characteristics of the syndrome and confirmed by genetic analysis that showed a de novo missense mutation c.2015G>A (p.Arg672His) of the MYH3 gene. …”
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1295
Recombinant human growth hormone treatment of Floating-Harbor syndrome: a case report and literature review
Published 2025-02-01“…The genetic characteristic is a heterozygous nonsense mutation of the SRCAP gene. rhGH treatment is an effective treatment method for FHS.…”
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1296
A Novel Maximum Power Point Tracking Algorithm Based on Glowworm Swarm Optimization for Photovoltaic Systems
Published 2016-01-01“…The simulation results demonstrate that the tracking capability of the GSO algorithm is superior to that of the traditional P&O algorithm, particularly under low radiance and sudden mutation irradiance conditions.…”
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1297
Comparative analysis of regression algorithms for drug response prediction using GDSC dataset
Published 2025-01-01“…However, integration of mutation and copy number variation information did not contribute to the prediction. …”
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1298
Forecasting Renewable energy and electricity consumption using evolutionary hyperheuristic algorithm
Published 2025-01-01“…Additionally, the crossover and mutation rates of GA evolve over iteration time and fitness value space, further enhancing its adaptability. …”
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1299
Progress on the prevention of poultry Salmonella with natural medicines
Published 2025-01-01“…However, the current abuse of antibiotics has accelerated the mutation of pathogenic bacteria to generate antibiotic-resistant strains. …”
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1300
GENETIC AND MOLECULAR ANALYSIS OF COMPLEMENTATION OF THE FLAMENCO AND PIWI LOCI IN DROSOPHILA MELANOGASTER
Published 2015-01-01“…Piwi is the primary component of the RNA interference machinery. Mutations in piwi and flamenco have the same phenotype – an enhanced transcription and frequency of transposition of the retrotransposon/retrovirus gypsy. …”
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