Results 191 to 200 of about 15,899 (233)
Very high cycle fatigue of high-strength steels: Crack initiation by FGA formation investigated at artificial defects [PDF]
Procedia Structural Integrity, 2016 It is well known, that high-strength steels do not show a classical fatigue limit and failure occurs still after 107 cycles. The reason for this late failure is that the fatigue properties in the long life region are strongly affected by non-metallic ...
Daniel Spriestersbach +2 more
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Phenotypic forking genetic algorithm (p-fGA)
Proceedings of 1995 IEEE International Conference on Evolutionary Computation, 2002Proposes a new type of multi-population genetic algorithm, the p-fGA (phenotypic forking GA), an extension of the previously proposed g-fGA (genotype forking GA). Both the g-fGA and the p-fGA are designed to solve multi-modal problems which are difficult to solve by traditional GAs.
S. Tsutsui, Y. Fujimoto
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Allele Frequencies of D21S11, FGA, TH01, and VWA in Populations of the Balkans
Human Biology, 2004This study is part of an extensive investigation of the genetic relationship between Balkan populations, especially the Aromuns. Allele frequencies of four STRs (D21S11, FGA, TH01, VWA) from Macedonians (Skopje), Gramostian Aromuns from the Stip region (Macedonia), Moskopolian Aromuns from Krusevo (Macedonia), and Musequiar Aromuns from Dukasi (Albania)
W, Huckenbeck +4 more
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Identification of dual false indirect exclusions on the D5S818 and FGA loci
Legal Medicine, 2011Here, we present a case in which the result of a maternity test was obscured due to two false indirect exclusions that occurred in two out of 15 genetic loci through the use of the AmpFlSTR Identifiler PCR Amplification kit (Applied Biosystems, Foster City, CA).
Wenxiao, Jiang +3 more
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Mutation of the translation initiation codon in FGA causes congenital afibrinogenemia
Blood Coagulation & Fibrinolysis, 2012Congenital afibrinogenemia is characterized by the complete absence of fibrinogen, the precursor of the major protein constituent of the blood clot, fibrin. Extensive allelic heterogeneity has been found for this disorder and more than 40 mutations, the majority in FGA, have been identified in homozygosity or in compound heterozygosity.
Tirefort Yordanka +3 more
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A novel regulatory element between the human FGA and FGG genes
Thrombosis and Haemostasis, 2012SummaryHigh circulating fibrinogen levels correlate with cardiovascular disease (CVD) risk. Fibrinogen levels vary between people and also change in response to physiological and environmental stimuli. A modest proportion of the variation in fibrinogen levels can be explained by genotype, inferring that variation in genomic sequences that regulate the ...
Fish, Richard, Neerman Arbez, Marguerite
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[Identification of a rare allele of FGA-13].
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics, 2009To identify a rare allele in the FGA locus in a Hainan Li ethnic family.Short tandem repeat-PCR (STR-PCR) and DNA sequencing were used to detect the allele.A rare allele in the FGA locus was identified. It is FGA-13.This finding enriched the gene polymorphism database, and may improve the ability of individual identification.
Ying, Zhao, Lu, Zhong, Shengmiao, Fu
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Analysis of the photosite reset in FGA image sensors
IEEE Transactions on Electron Devices, 1990An analysis of the photosite reset mechanism in floating gate array image sensors is presented. The photosite elements in these devices consist of a JFET transistor with the gate capacitively coupled to an address line. The addressed cell is reset by forward biasing the gate-drain junction.
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