Exact(4)
They have been experimentally characterised in two operating modes in order to determine how evaporative cooling improves heat recovery in each case, focussing on the influence of modifying the constructive characteristics.
Participatory practice research in general and participatory futures research in particular are always characterised in two ways: as a theory-based far-sighted study of future and innovative practice on the one hand and practice-oriented (accompanying) research which claims to be far-sighted on the other.
An identical, nonsense mutation, W129X, was characterised in two unrelated patients.
Delirium was characterised in two different ways: (1) as a binary variable (never vs ever delirious), and (2) as a categorical variable (0 3 days of delirium).
Similar(56)
This paper investigates the evolution of the gene tra, which was characterised in twelve tephritid species belonging to the less extensively analysed genus Anastrepha.
Three missense mutations were characterised in three cases of NHL after screening exons 5-8 of p53 of all the tumours with single-strand conformation polymorphism (SSCP) analysis.
Baseline morbidity was characterised in three ways: (1) history for each of cancer, large vessel disease, renal failure and visual deterioration; (2) the number of primary care contacts in the year prior to the index date; and (3) Charlson comorbidity index.
Abnormal sensory experience is characterised in three ways: (1) hypersensory sensation triggered by stimuli that is sub-threshold for triggering that sensation, (2) pesthesia altered sensory experience, and (3) allodynia sensation triggered by stimuli that do not normally trigger those sensations.
Furthermore the expression profile of these genes was characterised in-vitro in both monolayer and three dimensional (3D) cultures of tendon fibroblasts to identify whether such models fully recapitulate the tendon phenotype.
In this study, we have established and characterised in vitro two low-dose IFN- γ-producing NB cell lines, which differ in their genetic and phenotypic features.
To date, p16 INK4a germline mutations were characterised in only two out of 55 MM patients less than 30 years, but that both had a history of familial melanoma (Whiteman et al, 1997; Tsao et al, 2000).
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