Showing 1,101 - 1,120 results of 2,988 for search '"Mutation"', query time: 0.04s Refine Results
  1. 1101

    Mexican Pointy Boots and the Tribal Scene: Global Appropriations of Local Cultural Practices in the Virtual Age by Helena Simonett, César Burgos Dávila

    Published 2016-01-01
    “…In this essay, we examine music and its performative power by engaging in issues such as the localization of global cultural practices, the embracing of cultural practices based on a shared sense of marginalization and peripheralization, as well as the appropriation and resignification of “odd” cultural practices for global consumption, resulting in a cultural mutation of such practices and their objects from “low” to “art.” …”
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  2. 1102

    Design and Construction of Hybrid Music Recommendation System Integrating Music Gene by Xuelin Zhao

    Published 2022-01-01
    “…Moreover, this study verifies it through the running time of the simulation experiment, using the growth method as the way of mutation. In addition, while adopting the optimal individual retention strategy, this study makes the eigenvalues of the input matrix IX all fall within the unit circle or unit circumference and makes the maximum fitness value of the individuals in the population equal to the global optimal fitness value. …”
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  3. 1103

    Fuzzy Logic Controller Based on Genetic Algorithm for Electric Drive of Crane Trolley by S. E. Alavi, I. N. Petrenko

    Published 2009-04-01
    “…Using a specific structure of  a chromosome, a special mutation operation and an adequate fitness function  the proposed methodology makes it possible to select a fuzzy rule base, to minimize a number of rules, rationally to place input sets of fuzzy functions and corresponding arrangement of output singletons in the form of single-element sets. …”
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  4. 1104
  5. 1105

    Familial Hypercholesterolemia: Genetics, Symptoms, Diagnosis and Treatment - A Literature Overview by Maciej Rutkiewicz, Sabina Przygodzka, Katarzyna Gadżała, Karolina Garbino, Katarzyna Brudniak, Antoni Szuścik, Magdalena Czyczerska

    Published 2025-02-01
    “…People who are affected by mutation have around thirteen times higher risk of coronary artery disease (CAD) and, in order to that, premature death. …”
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  6. 1106

    Proximal bronchiolar adenoma with malignant transformation to invasive mucinous adenocarcinoma with 4 years follow-up: a case report and literature review by Yuan-Hui Yang, Ke Yin, Jia-Qi Xu, Xiao-Ying Xu, Jun-Lei Zhang, Ji-Xuan Liu, Xin-Zhi Feng, Xiao-Yan Lin, Xiao-Yan Lin

    Published 2025-01-01
    “…However, due to the high mutation frequency of the driver gene, there is still debate as to whether BA has the potential for malignant transformation. …”
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  7. 1107
  8. 1108

    Diversity in Adaptive Evolution of Methicillin-Resistant Staphylococcus aureus Clinical Isolates Under Exposure to Continuous Linezolid Stress in vitro by Han T, Jia T, Wang J

    Published 2025-02-01
    “…Except G2576T mutations in 23S rRNA gene, the distribution of other mutations (A2451T, T2504A, C2404T, T2500A, G2447T) exhibited obvious strain heterogeneity. …”
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  9. 1109

    The hypertrophic cardiomyopathy-associated A331P actin variant enhances basal contractile activity and elicits resting muscle dysfunction by Matthew H. Doran, Michael J. Rynkiewicz, Evan Despond, Meera C. Viswanathan, Aditi Madan, Kripa Chitre, Axel J. Fenwick, Duncan Sousa, William Lehman, John F. Dawson, Anthony Cammarato

    Published 2025-02-01
    “…Summary: Previous studies aimed at defining the mechanistic basis of hypertrophic cardiomyopathy caused by A331P cardiac actin have reported conflicting results. The mutation is located along an actin surface strand, proximal to residues that interact with tropomyosin. …”
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  10. 1110

    Microsatellite instability and somatic gene variant profile in solid organ tumors by Ibrahim Halil Erdogdu, Seda Orenay-Boyacioglu, Olcay Boyacioglu, Nesibe Kahraman-Cetin, Habibe Guler, Merve Turan, Ibrahim Meteoglu

    Published 2024-05-01
    “…Conclusions Our study covers not only colorectal cancer patients but also other solid tumor types, providing the first data from the Turkish population on the MSI-H/dMMR status and somatic mutation profile in the presence of this condition.…”
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  11. 1111

    Optimal parameter identification of photovoltaic systems based on enhanced differential evolution optimization technique by Shubhranshu Mohan Parida, Vivekananda Pattanaik, Subhasis Panda, Pravat Kumar Rout, Binod Kumar Sahu, Mohit Bajaj, Vojtech Blazek, Lukas Prokop

    Published 2025-01-01
    “…With the above motivation, this article suggests a stage-specific mutation strategy for the proposed enhanced differential evolution (EDE) that adopts a better search process to arrive at optimal solutions by adaptively varying the mutation factor and crossover rate at different search stages. …”
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  12. 1112

    A Case Report and Literature Review of Pseudo-TORCH Syndrome Type 2 (PTORCH2) by Rami A. Misk, Lama Qawasme, Fawzy M. Abunejma, Bahaa Ibrahim Abu Rahma, Ehab Mohammad Abuawwad, Raja Imad Abu Iram, Abdulrahman Hussein Karaki, Tareq Z. Alzughayyar, Jihad Samer Zalloum

    Published 2022-01-01
    “…We present a 4-day-old female patient with jaundice, abnormal movement, and convulsions who was found to be homozygous for the missense USP18 gene mutation that causes pseudo-TORCH syndrome 2 (PTORCH2). …”
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  13. 1113

    Pattern Synthesis of Linear Antenna Arrays Using Enhanced Flower Pollination Algorithm by Urvinder Singh, Rohit Salgotra

    Published 2017-01-01
    “…The proposed algorithm uses the concept of Cauchy mutation in global pollination and enhanced local search to improve the exploration and exploitation tendencies of FPA. …”
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  14. 1114

    Congenital Tufting Enteropathy, a Rare Cause of Diarrhea and Malnourishment in Arab Child with Genetic and Histopathology Investigations by Shooq Alkhalifa, Aysha Darwish, Mohamed Awadh, Salman M. Alkhalifa, Abdulla Darwish

    Published 2023-01-01
    “…Congenital tufting enteropathy (CTE), also known as intestinal epithelial dysplasia (IED), is a rare autosomal recessive disorder due to EPCAM gene mutation. It is a rare congenital enteropathy that presents in early infancy as an intractable diarrhea that is independent of breast formula feeding that requires life-long total parental nutrition (TPN) to acquire adequate calories and fluid intake or small bowel transplantation in severe cases. …”
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  15. 1115

    Optimization on Production-Inventory Problem with Multistage and Varying Demand by Duan Gang, Chen Li, Li Yin-Zhen, Song Jie-Yan, Akhtar Tanweer

    Published 2012-01-01
    “…At last the combination of crossover probability and mutation probability is tested for all problems and a law is found for large size.…”
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  16. 1116

    Squamous Cell Carcinoma of the Lung with Metastasis to the GI Tract Associated with EGFR Exon 19 Deletion by Glen J. Weiss, Agnes K. Liman, Jeffrey Allen, Philip Y. Cheung, Rajesh N. Kukunoor

    Published 2013-01-01
    “…Consideration of EGFR exon 19 mutation testing in SCC of the lung, particularly for those with GI tract metastasis, may identify this potentially drug-targetable entity.…”
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  17. 1117

    Control Design of the Wave Compensation System Based on the Genetic PID Algorithm by Mingjian Zhou, Yuqin Wang, Haibing Wu

    Published 2019-01-01
    “…The control block diagram of the wave compensation system based on the genetic PID control algorithm is established, and the optimal index and PID parameters are optimized by the crossover and mutation operators of the genetic particle swarm optimization algorithm. …”
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  18. 1118

    An Optimization to Schedule Train Operations with Phase-Regular Framework for Intercity Rail Lines by Huimin Niu, Minghui Zhang

    Published 2012-01-01
    “…A hybrid genetic algorithm associated with the layered crossover and mutation operation is carefully designed to solve the proposed model. …”
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  19. 1119

    Clinical and Genetic Review of Hereditary Acral Reticulate Pigmentary Disorders by H. Alshaikh, F. Alsaif, S. Aldukhi

    Published 2017-01-01
    “…However, each of these hereditary conditions possesses a unique genetic mutation, and genetic analysis is thus more useful in the diagnosis of these conditions. …”
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  20. 1120

    Concurrent B Cell Acute Lymphoblastic Lymphoma/Leukemia and Monoclonal B Cell Lymphocytosis: A Case Report with Extensive Molecular Analysis by Maryam Mehdipour Dalivand, Parastou Tizro, Julie Partain, Anita Aggarwal, Jack Lichy, Francisco Mot Ara, Victor E. Nava

    Published 2022-01-01
    “…Detailed molecular characterization revealed an unusual MPL (T487I) point mutation and unmutated VH4-39. After nonstandard chemotherapy, the patient remains in morphologic remission. …”
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