FGB gene

Known as: FGB, FIBRINOGEN, B BETA POLYPEPTIDE, FIBRINOGEN--BETA POLYPEPTIDE CHAIN 
 

Topic mentions per year

Topic mentions per year

2000-2017
012320002017

Papers overview

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2016
2016
Afibrinogenemia represents the rarest form of fibrinogen deficiency. Causative missense mutations occur rarely and may improve… (More)
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2013
2013
Justice This report was financed by and prepared for the use of the European Commission, Directorate General for Justice; Unit D2… (More)
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2013
2013
Congenital afibrinogenaemia is a rare autosomal recessive disorder caused by various mutations within the fibrinogen genes FGA… (More)
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2010
2010
OBJECTIVES It is well established that patients with a unilateral posterior crossbite, when chewing on the affected side, show an… (More)
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2009
2009
The frequencies of alleles and genotypes for ten functionally significant single-nucleotide polymorphisms were determined in the… (More)
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2009
2009
Carriage frequencies of alleles and genotypes of 10 functionally important single nucleotide polymorphisms that are located in… (More)
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2007
2007
This study was conducted to evaluate the effects of different barley processing techniques on the glycaemic and insulinaemic… (More)
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2007
2007
The aim of this work was to test the effects of the Function Generator Bite (FGB) on the masticatory muscles of temporomandibular… (More)
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2007
2007
A case of a 5.2 years-old child, with a left unilateral posterior cross-bite, from the canine to the second deciduous molar… (More)
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2006
2006
Inflammatory markers have consistently been associated with vascular disease. Evidence of genetic polymorphisms in inflammatory… (More)
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