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Functional and structural studies of CYP21A2 gene mutants in congenital adren...
Steroid 21-hydroxylase deficiency is the most common enzymatic defect causing congenita ladrenal hyperplasia. A large number of new mutations has been detected in the... -
Transparent aluminate glass-ceramics : crystallization mechanisms and structu...
This thesis concerns the crystallization and the structural study of different alumino-silicate glasses. This study has led to several completely crystallized and... -
Structural and functionnal studies of proteins involved in iron uptake in Gra...
Iron is essential for life because it has a key role in many biological processes. Despite its abundance in the earth's crust, iron is poorly bioavailable. To...
