Celecoxib treatment of fibrous dysplasia (FD) in a human FD cell line and FD-like lesions in mice with protein kinase A (PKA) defects
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چکیده
منابع مشابه
Akl(fd) { a Concurrent Language for Fd Programming Akl(fd) { a Concurrent Language for Fd Programming
We consider a complete implementation of an extension of the nite domain constraint system FD, including antimonotone constraints, and its integration in AKL, a deep-guard concurrent constraint language. We present the language AKL(FD), together with associated programming techniques. In particular, we show how powerful symbolic constraints can be deened as AKL(FD) programs, which is partly mad...
متن کاملAKL(FD) - A Concurrent Language for FD Programming
We consider a complete implementation of an extension of the nite domain constraint system FD, including antimonotone constraints, and its integration in AKL, a deep-guard concurrent constraint language. We present the language AKL(FD), together with associated programming techniques. In particular, we show how powerful symbolic constraints can be de ned as AKL(FD) programs, which is partly mad...
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In [1] we presented the language T OY(FD) that integrates the best features of existing functional and logic languages, as well as finite domain (FD) constraint solving. We believe that T OY(FD) is more flexible and expressive than the existing approaches of constraint logic programming on finite domain (CLP (FD) ) as it integrates FD constraint solving, lazy evaluation, higher order applicatio...
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Using a constrained superposition calculus and a disunification procedure, it is possible to employ superposition-based first-order reasoners for reasoning not only about all models of a first-order theory, but also about all models over a specific finite domain and often as well about the perfect models of the theory (or the unique minimal model in case of a Horn theory), both of which are sec...
متن کاملFamilial Dysautonomia (FD)
Familial dysautonomia (FD) is an autosomal recessive congenital neuropathy which results from poor development and progressive degeneration of the nervous system. The mutation responsible for FD was found at the 5�ss of intron 20 of the IKBKAP gene, encoding the I?B kinase complex-associated protein (IKAP...
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ژورنال
عنوان ژورنال: Molecular and Cellular Endocrinology
سال: 2017
ISSN: 0303-7207
DOI: 10.1016/j.mce.2016.08.004