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Genetics of Craniosynostosis.
Valterová, Simona ; Křepelová, Anna (advisor) ; Baxová, Alice (referee)
Craniosynostoses are premature fusions of one or more cranial sutures. They affect all cranial sutures and are the main symptom of many genetic syndromes. Syndromes connected with craniosynostosis are serious disorders associated with skeleton abnormalities, limb malformations or mental disability. These syndroms are caused by different mutations in FGFR1, FGFR2, FGFR3, TWIST1, EFNB1, RECQL4, and RAB23 genes. The aim of this review was to summarize contemporary knowledge of phenotype and genetic basis of these diseases.
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Pevnostní a ekonomické parametry strojově šitých švů v současné čalounické výrobě
Falátek, Adam
This thesis dealt with strength and economic parameters of machine-sewn seams in current upholstery production. It is focused on the determination of the tensile strength of the bound seams and the influence of the decorative seams and the various types of lining on it. In the economic part of the test, material and time consumption is measured. The result is the evaluation of the different types of seams and lining and taxation in connection with the consumption of time, materials and their cost.
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Vývoj čalounické technologie od historie po 30. léta 20. století
Falátek, Adam
This thesis deals with the historical development of conventional technologies in upholstery. Its aim was to analyze the procedures of upholstery in different historical periods, to notify important milestones and factors that influenced the classical technology. The result was a summary of the issues within conventional technology of upholstery.
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Genetics of Craniosynostosis.
Valterová, Simona ; Křepelová, Anna (advisor) ; Baxová, Alice (referee)
Craniosynostoses are premature fusions of one or more cranial sutures. They affect all cranial sutures and are the main symptom of many genetic syndromes. Syndromes connected with craniosynostosis are serious disorders associated with skeleton abnormalities, limb malformations or mental disability. These syndroms are caused by different mutations in FGFR1, FGFR2, FGFR3, TWIST1, EFNB1, RECQL4, and RAB23 genes. The aim of this review was to summarize contemporary knowledge of phenotype and genetic basis of these diseases.
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