Relevant bibliographies by topics / Point accepted mutation

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Academic literature on the topic 'Point accepted mutation'

Author: Grafiati
Published: 3 June 2025
Last updated: 31 July 2025

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Journal articles on the topic "Point accepted mutation"

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Jyotshna, Dongardive, and Abraham Siby. "BRAIN Journal - Secondary Structure Prediction of Protein using Resilient Back Propagation Learning Algorithm." BRAIN - Broad Research in Artificial Intelligence and Neuroscience 6, no. 1-2 (2015): 22–29. https://doi.org/10.5281/zenodo.1044169.

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ABSTRACT The paper proposes a neural network based approach to predict secondary structure of protein. It uses Multilayer Feed Forward Network (MLFN) with resilient back propagation as the learning algorithm. Point Accepted Mutation (PAM) is adopted as the encoding scheme and CB396 data set is used for the training and testing of the network. Overall accuracy of the network has been experimentally calculated with different window sizes for the sliding window scheme and by varying the number of units in the hidden layer. The best results were obtained with eleven as the window size and seven as
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Aoki, Yoshinao, Maki Hashimoto, and Shunji Suzuki. "Emergence of Single Point Mutation in PvCesA3, Conferring Resistance to CAA Fungicides, in Plasmopara viticola Populations in Japan." Plant Health Progress 14, no. 1 (2013): 51. http://dx.doi.org/10.1094/php-2013-0729-01-br.

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As far as we know, there is no report of fungicide-resistant Plasmopara viticola in Japan. In the present study, we detected a single point mutation in the PvCesA3 of P. viticola sampled from a Japanese vineyard, which conferred resistance to mandipropamid. The emergence of the mandipropamid-resistant PvCesA3 allele may lead to the spread of mandipropamid-resistant P. viticola in vineyards all over Japan in the near future. Accepted for publication 23 April 2012. Published 29 July 2013.
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Yu, Yongfeng, Rongrong Chen, Jun Zhao, Xin Yi, and Shun Lu. "Analysis of canonical and noncanonical splicing site mutation of MET that causes exon 14 skipping." Journal of Clinical Oncology 38, no. 15_suppl (2020): e21513-e21513. http://dx.doi.org/10.1200/jco.2020.38.15_suppl.e21513.

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e21513 Background: The hepatocyte growth factor receptor gene ( MET) exon 14 skipping ( METex14) has been wildly accepted as a driver alteration in lung cancer targetable by tyrosine kinase inhibitors (TKIs) such as crizotinib. While it is easy to interpret canonical splicing site mutations, it is more controversial to interpret noncanonical splicing site mutations. Methods: Hybrid capture–based next generation sequencing of 59-1021 genes including MET was performed at the request of individual treating physicians. The mutation profiling of MET were retrospectively analyzed. Results: Of 3500 l
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Zheng, Weijie, Mingfeng Li, Renzhong Deng, and Benjamin Doerr. "How to Use the Metropolis Algorithm for Multi-Objective Optimization?" Proceedings of the AAAI Conference on Artificial Intelligence 38, no. 18 (2024): 20883–91. http://dx.doi.org/10.1609/aaai.v38i18.30078.

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The Metropolis algorithm can cope with local optima by accepting inferior solutions with suitably small probability. That this can work well was not only observed in empirical research, but also via mathematical runtime analyses on single-objective benchmarks. This paper takes several steps towards understanding, again via theoretical means, whether such advantages can also be obtained in multi-objective optimization. The original Metropolis algorithm has two components, one-bit mutation and the acceptance strategy, which allows accepting inferior solutions. When adjusting the acceptance strat
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McGlennen, Ronald C., and Nigel S. Key. "Clinical and Laboratory Management of the Prothrombin G20210A Mutation." Archives of Pathology & Laboratory Medicine 126, no. 11 (2002): 1319–25. http://dx.doi.org/10.5858/2002-126-1319-calmot.

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Abstract Objective.—To make recommendations regarding the appropriate evaluation for the prothrombin G20210A mutation, as reflected by published evidence and the consensus opinion of recognized experts in the field. Data Sources.—Review of the medical literature, primarily since 1996. Data Extraction and Synthesis.—After an initial assessment of the literature, key points defining the condition, and review of the clinical study design, a draft manuscript was prepared and circulated to every participant in the College of American Pathologists Conference on Diagnostic Issues in Thrombophilia bef
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Mah, Jean K., Kathryn Selby, Craig Campbell, et al. "A Population-Based Study of Dystrophin Mutations in Canada." Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques 38, no. 3 (2011): 465–74. http://dx.doi.org/10.1017/s0317167100011896.

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AbstractIntroduction:We carried out a population-based study of dystrophin mutations in patients followed by members of the Canadian Paediatric Neuromuscular Group (CPNG) over a ten-year period.Objectives:We aimed to describe the changes in diagnostic testing for dystrophinopathy and to determine the frequency of dystrophin mutations from 2000 to 2009.Methods:De-identified data containing the clinical phenotypes, diagnostic methods, and mutational reports from dystrophinopathy patients followed by CPNG centres from January 2000 to December 2009 were analyzed using descriptive statistics.Result
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Nikolova, D., A. Yordanov, V. Damyanova, A. Radinov, and D. Toncheva. "Janus kinase V617F mutation detection in patients with myelofibrosis." Balkan Journal of Medical Genetics 22, no. 1 (2019): 57–60. http://dx.doi.org/10.2478/bjmg-2019-0007.

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AbstractMyelofibrosis (MF) is characterized by a presence of an extra fibrous tissue in the bone marrow and additional hematopoiesis. The somatic mutation in the Janus kinase 2 (JAK2) gene (V617F) occurs gradually and is detected in about 50.0% of myelofibrosis or essential thrombo-cytopenia (ET) patients. Our aim was to determine the genotype status according to the carriers of the V617F mutation in patients with MF at the Hematology Ward of the University Hospital "Ivan Rilski" in Sofia, Bulgaria. DNA samples were isolated from venous blood of patients with various hematological disorders. D
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KREBS, WERNER G., and PHILIP E. BOURNE. "STATISTICAL AND VISUAL MORPH MOVIE ANALYSIS OF CRYSTALLOGRAPHIC MUTANT SELECTION BIAS IN PROTEIN MUTATION RESOURCE DATA." Journal of Bioinformatics and Computational Biology 02, no. 01 (2004): 61–75. http://dx.doi.org/10.1142/s0219720004000478.

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Structural studies of the effects of non-silent mutations on protein conformational change are an important key in deciphering the language that relates protein amino acid primary structure to tertiary structure. Elsewhere, we presented the Protein Mutant Resource (PMR) database, a set of online tools that systematically identified groups of related mutant structures in the Protein DataBank (PDB), accurately inferred mutant classifications in the Gene Ontology using an innovative, statistically rigorous data-mining algorithm with more general applicability, and illustrated the relationship of
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Dahlbäck, B. "Early days of APC resistance and FV Leiden." Hämostaseologie 28, no. 03 (2008): 103–9. http://dx.doi.org/10.1055/s-0037-1617167.

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SummaryVenous thrombosis is a major medical problem annually affecting millions of individuals worldwide. It is a typical multifactorial disease, the pathogenesis involving both environmental and genetic risk factors. A single point mutation in the gene of coagulation factor V (FV), which results in the replacement of Arg506 with a Gln (FV Leiden) is the most common genetic risk factor known to date. The anti - coagulant activated protein C (APC) regulates the activity of FVa by cleaving several sites in FVa, and the Arg506 is one of them. APC resistance, which is the consequence of the FV Arg
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Morin, Ryan D., Maria Mendez-Lago, Andrew J. Mungall, et al. "Identification of Genes Frequently Mutated In FL and DLBCL with Transcriptome, Genome and Exome Sequencing." Blood 116, no. 21 (2010): 804. http://dx.doi.org/10.1182/blood.v116.21.804.804.

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Abstract Abstract 804 Introduction: Follicular lymphoma (FL) and diffuse large B cell lymphoma (DLBCL) are the two most common types of non Hodgkin lymphoma (NHL). It is widely accepted that DLBCL can be divided into two major subtypes using gene expression profiling: germinal center B-cell (GCB) and activated B-cell (ABC). Both FL and the GCB subtype of DLBCL derive from germinal center B cells and have been found to share some common mutational events such as translocations leading to the deregulation of the BCL2 oncogene and mutations affecting a single tyrosine (Y641) in the histone methyl
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Books on the topic "Point accepted mutation"

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Minelli, Alessandro. Evolvability and Its Evolvability. Oxford University Press, 2017. http://dx.doi.org/10.1093/oso/9780199377176.003.0007.

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No universally accepted notion of evolvability is available, focus being alternatively put onto either genetic or phenotypic change. The heuristic power of this concept is best found when considering the intricacies of the genotype→phenotype map, which is not necessarily predictable, expression of variation depending on the structure of gene networks and especially on the modularity and robustness of developmental systems. We can hardly ignore evolvability whenever studying the role of cryptic variation in evolution, the often pervious boundary between phenotypic plasticity and the expression
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Book chapters on the topic "Point accepted mutation"

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Buiatti, Marcello, and Patrizia Bogani. "The Living State of Matter: Between Noise and Homeorrhetic Constraints." In Nonextensive Entropy. Oxford University Press, 2004. http://dx.doi.org/10.1093/oso/9780195159769.003.0018.

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The living state of matter, while obviously obeying physical and chemical laws, does exhibit some peculiar features which, taken altogether, distinguish it from the rest of the natural world. As discussed at length elsewhere [16, 18], these include, among others, hierarchical organization, individuality, invention, and homeostasis. One key category which was introduced by Waddington [94] is homeorrhesis. Homeorrhesis is the dynamical version of homeostasis and it may be defined as the capacity of living systems to maintain their harmonic dynamical networks through continuous change in response
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Conference papers on the topic "Point accepted mutation"

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Cuellar, Adriana, and Marcel Sanchez Prieto. "A River Runs Through It: Territory of Opportunistic Coexistence." In 2016 ACSA International Conference. ACSA Press, 2016. http://dx.doi.org/10.35483/acsa.intl.2016.53.

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In order to understand urban development in Latin America we must study the actions of an opportunistic environment that enables social progress. Usually, urban adaptations react to the pressures of a contested territory, that if seen as survival tactics, they amplify urban regeneration, where illicit acts of urbanism become primary sites of innovation. Such is the example of the international border between San Diego, and Tijuana. This region is no exception of witnessing the territorial conflicts and crime scenes that are typical characteristics of border regions. In particular this border e
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Tsurkas, Andrew, and Gang Bao. "Molecular Beacons for Sensitive Gene Detection in Living Cells." In ASME 2003 International Mechanical Engineering Congress and Exposition. ASMEDC, 2003. http://dx.doi.org/10.1115/imece2003-42959.

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Real-time imaging of gene expression in living cells has the potential to significantly impact clinical and laboratory studies of cancer, including cancer diagnosis and analysis. Molecular beacons (MBs) provide a simple and promising tool for the detection of target mRNA as tumor markers due to their high signal-to-background ratio, and their improved specificity in detecting point mutations. However, the harsh intracellular environment does limit the sensitivity of MB-based gene detection. Specifically, MBs bound to target mRNAs cannot be distinguished from those degraded by nucleases, or ope
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