Results 211 to 220 of about 19,595 (274)
Mutation of the translation initiation codon in FGA causes congenital afibrinogenemia
Blood Coagulation & Fibrinolysis, 2012 Congenital 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
semanticscholar +5 more sources
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 ...
D Spriestersbach +2 more
exaly +3 more sources
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Allele frequency data for the FGA locus in eight populations
International Journal of Legal Medicine, 1997Allele frequency data of the FGA locus were determined in eight population samples. No significant deviations from the Hardy Weinberg equilibrium were observed. The heterozygosity and mean exclusion chance ranged from 82 to 93% and 70 to 75% respectively.
B Rolf
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An isolated exclusion in the FGA system
International Congress Series, 2004Abstract In a paternity test with 35 short tandem repeats (STRs), an isolated exclusion for the FGA system was observed (probability of paternity >99.999%). Different mechanisms suitable to explain this finding like polymerase slippage, primer mismatch, a deletion of the FGA locus or gene conversion after formation of the zygote are discussed.
M Kleiber +2 more
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Variation in fibrinogen FGG and FGA genes and risk of stroke
Thrombosis and Haemostasis, 2008 SummaryHaplotypes of the fibrinogen gamma and alpha (FGG and FGA) genes are associated with the structure of the fibrin network and may therefore influence the risk of stroke. We investigated the relationship between common variation in these genes with ischemic and haemorrhagic stroke.
Cheung, Yee +6 more
openaire +3 more sources
FGA Controls VEGFA Secretion to Promote Angiogenesis by Activating the VEGFR2-FAK Signalling Pathway
Frontiers in Endocrinology, 2022 Background Our previous work revealed the high expression of fibrinogen alpha chain (FGA) in patients with endometriosis (EM) and that it could promote the migration and invasion of endometrial stromal cells.
E Cai, Xue Ye, Xiaohong Chang
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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).
Peter Hu
exaly +3 more sources
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
openaire +4 more sources
Fatigue and Fracture of Engineering Materials and Structures, 2018
F Ritz, C Stäcker, T Beck
exaly +2 more sources
F Ritz, C Stäcker, T Beck
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