Matrix-isolation and ab initio study of HKrCCCl and HXeCCCl.
Helsinki, Finland. In J Chem Phys, Jan 2016
The assignments of the new noble-gas molecules are supported by deuteration experiments and quantum chemical calculations at the MP2(full) and CCSD(T) levels of theory with the def2-TZVPPD basis set.
Monogenic autoinflammatory diseases: Cytokinopathies.
Australia. In Cytokine, Aug 2015
These include syndromes where the production of IL-1 is increased by mutation of innate immune sensors such as NLRP3, upstream signalling molecules such as PSTPIP1 and receptors or downstream signalling molecules, such as IL-1Ra.
CT and MRI of congenital nasal lesions in syndromic conditions.
Chicago, United States. In Pediatr Radiol, Jul 2015
Congenital malformations of the nose can be associated with a variety of syndromes, including solitary median maxillary central incisor syndrome, CHARGE syndrome, Bosma syndrome, median cleft face syndrome, PHACES association, Bartsocas-Papas syndrome, Binder syndrome, duplication of the pituitary gland-plus syndrome and syndromic craniosynsotosis (e.g., Apert and Crouzon syndromes) among other craniofacial syndromes.
Dresden, Germany. In Curr Opin Rheumatol, 2011
PSTPIP1 is a cytoskeleton-associated adaptor protein that links PEST-type phosphatases to their substrates.