Showing 1,121 - 1,140 results of 2,988 for search '"Mutation"', query time: 0.07s Refine Results
  1. 1121

    Bilocation - Dislocation - Xlocation : The Apocalypse of Place in Eamonn Wall’s Poetry by Pascale Guibert

    Published 2020-05-01
    “…Contemporary Irish-American poet Eamonn Wall, commuting between continents, has experienced a new form of exile, made of impermanence and mutation. His poetry, which shows this new relation to places, has had to find a language capable of expressing the continuous transformations of landscape as his multiple journeys have led him to apprehend it: no longer stable and delimited. …”
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  2. 1122

    Enhanced growth of short stature in Ellis-van Creveld syndrome: A case report of a Saudi child by Essam Al Ageeli

    Published 2024-12-01
    “…Diagnosis was confirmed through genetic testing, revealing a nonsense homozygous mutation in the EVC2 gene. Remarkably, the absence of cardiac abnormalities allowed for the successful administration of growth hormone (GH) therapy, which led to a notable increase in height over 2 years, from 108 cm at age 12 to 122 cm at age 14. …”
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  3. 1123

    Eye of the Tiger Sign in Pantothenate Kinase-Associated Neurodegeneration by S. Choayb, H. Adil, Daoud Ali Mohamed, N. Allali, L. Chat, S. El Haddad

    Published 2021-01-01
    “…Pantothenate kinase-associated neurodegeneration (PKAN) is a rare disorder associated with brain iron accumulation caused by a recessive mutation in pantothenate kinase 2 gene (PANK2). We present a case of an 11 year-old boy presenting extrapyramidal signs and developmental regression. …”
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  4. 1124

    Mitochondrial DNA Damage and Animal Longevity: Insights from Comparative Studies by Reinald Pamplona

    Published 2011-01-01
    “…ROS can modify mtDNA directly at the sugar-phosphate backbone or at the bases, producing many different oxidatively modified purines and pyrimidines, as well as single and double strand breaks and DNA mutations. In this scenario, natural selection tends to decrease the mitochondrial ROS generation, the oxidative damage to mtDNA, and the mitochondrial mutation rate in long-lived species, in agreement with the mitochondrial oxidative stress theory of aging.…”
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  5. 1125

    Noonan's Syndrome. Case Report by Mirsa Rosas Hernández, Elba Daisy Rivas Rodríguez, Raúl E. Silva Silva

    Published 2015-04-01
    “…Noonan's syndrome is a genetic, little-known disease, produced for a mutation in the 12q22 chromosome. Few data on this affection exists in Cuba; since studies with a significant sample have not been conducted that demonstrate the real frequency of the affection. …”
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  6. 1126

    Les agglomérations du Centre-Est de la Gaule : quel devenir durant l’Antiquité tardive ? by Pierre Nouvel, Stéphane Venault

    Published 2017-12-01
    “…The reality of urban retraction, the abandonment or mutation of public places, the changes of use within these evolutions can now be discussed on a more solid basis. …”
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  7. 1127

    The influence of salt iodisation on the incidence of thyroid cancer by Karolina P. Sas, Kamila Tokarczyk, Damian Zieliński, Janusz Strzelczyk

    Published 2024-09-01
    “…Additionally, the analysis shows a correlation between the BRAF mutation and an increase in the incidence of papillary cancer, especially in areas with excessive iodine intake. …”
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  8. 1128

    Evolutionary dynamics of prey-predator systems with Holling type II functional response by Jian Zu, Wendi Wang, Bo Zu

    Published 2007-01-01
    “…The evolutionarydynamics is constructed from a stochastic process of mutation andselection. We investigate the ecological and evolutionary conditionsthat allow for continuously stable strategy and evolutionarybranching. …”
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  9. 1129

    An Alternate Iterative Differential Evolution Algorithm for Parameter Identification of Chaotic Systems by Wanli Xiang, Xuelei Meng, Meiqing An

    Published 2015-01-01
    “…Then through integrating two differential mutation strategies, an improved greedy selection mechanism and a population diversity balance scheme, an alternate iterative differential algorithm, called AIDE, is presented to solve the problem in this paper. …”
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  10. 1130

    Retinoid Therapy in a Case of Harlequin Ichthyosis with a Short Literature Review by Emad Bahashwan, Jaber Alfaifi, Sahar Elmaghawri Mohamed Moursi, Youssef Elbayoumi Soliman

    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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  11. 1131

    HFE-Associated Hereditary Haemochromatosis by Emmeke J Eijkelkamp, Thomas R Yapp, Lawrie W Powell

    Published 2000-01-01
    “…Feder et al identified the hereditary hemochromatosis gene (HFE) in 1996 and two candidate mutations; the C282Y mutation has been shown to be responsible for the majority of the hereditary hemochromatosis cases worldwide. …”
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  12. 1132

    IDH Mutant Cholangiocarcinoma: Pathogenesis, Management, and Future Therapies by Alexander Bray, Vaibhav Sahai

    Published 2025-01-01
    “…Mutations in isocitrate dehydrogenase (IDH) genes are among the most frequently encountered molecular alterations in cholangiocarcinoma (CCA). …”
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  13. 1133

    Improving Strawberry Varieties by Somaclonal Variation by Cheol-Min Yoo, Cheryl Dalid, Catalina Moyer, Vance Whitaker, Seonghee Lee

    Published 2022-10-01
    “…This offers an alternative to mutation breeding for the introduction of new genetic variations in existing strawberry varieties. …”
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  14. 1134

    STUDY OF THE THERMAL STABILITY OF BARNASE PROTEIN MUTANTS WITH MOLKERN SOFTWARE by E. S. Fomin, N. A. Alemasov

    Published 2014-12-01
    “…The results obtained for the R72G mutation show a better agreement with experimental values than the results of other authors.…”
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  15. 1135

    Williams-Beuren Syndrome and Congenital Lobar Emphysema: Uncommon Association with Common Pathology? by Timothy Andrew Walsh, Krishna Revanna Gopagondanahalli, Atul Malhotra

    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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  16. 1136

    Enhancing Ikeda Time Delay System by Breaking the Symmetry of Sine Nonlinearity by Xiaojing Gao

    Published 2019-01-01
    “…In the present contribution, an asymmetric central contraction mutation (ACCM) model is proposed to enhance the Ikeda time delay system. …”
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  17. 1137

    An UAV-Assisted Edge Computing Resource Allocation Strategy for 5G Communication in IoT Environment by Hao Liu

    Published 2022-01-01
    “…Then, the genetic algorithm is improved by introducing a penalty function to solve this problem, in which selection, crossover, and mutation operations are iterated to obtain the optimal allocation strategy for computational resources. …”
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  18. 1138

    Analyse interprétative du discours du Landscape Urbanism et impact sur le développement des pratiques des paysagistes dans le contexte français by Anaïs Leger-Smith

    Published 2013-12-01
    “…Will Landscape Urbanism, in the long term, acquire the status of critical theory, capable of provoking a mutation of the profession towards more innovative practices?…”
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  19. 1139

    "The Truth lies in Black and White." The Language of Truth and the Search for Coloured Identity in Zoe Wicomb’s David’s Story by Fiona Mc Cann

    Published 2007-05-01
    “…Ancré dans l’Afrique du Sud peu après la chute de l’apartheid, ce roman reflète les difficultés intrinsèques à un pays en pleine mutation et soulève des questions importantes quant à la (re)construction de l’identité. …”
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  20. 1140

    Genetics and Epigenetics of Parkinson's Disease by Fabio Coppedè

    Published 2012-01-01
    “…In 1997 a mutation in the a-synuclein (SNCA) gene was associated with familial autosomal dominant Parkinson’s disease (PD). …”
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