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Toplam kayıt 3, listelenen: 1-3
Functional characterisation of the type 1 von Willebrand disease candidate VWF gene variants: p. M771I, p. L881R and p. P1413L
(SIMTI Servizi, 2017)
Background. Abnormalities in the biosynthetic pathway or increased clearance of plasma von Willebrand factor (VWF) are likely to contribute to decreased plasma VWF levels in inherited type 1 von Willebrand disease (VWD). ...
De novo 8p23.1 deletion in a patient with absence epilepsy
(John Libbey Eurotext, 2017)
The 8p23.1 deletion syndrome is a rare multisystem disorder with high penetrance and a variable phenotypic spectrum that includes congenital heart disease (CHD), intellectual disability, behavioural problems, microcephalia, ...
Effect of Plant Oil-Based Crosslinker on Drug Release Behaviour of Hydrogels
(IEEE, 2017)
Thermoresponsive hydrogels have great potential in biomedical applications such as drug delivery systems and tissue engineering. Synthesis of hydrogels from renewable resources attracts attention day by day. In this study ...