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This paper reviews current psycholinguistic and neuroimaging evidence on language processing with particular focus on the relationship between production and comprehension. In the first part, different methods of psycholinguistic research are introduced and examples for psycholinguistic models (production: Levelt et al. 1999; comprehension: Friederici 2002) are sketched. In the second part, the neural correlates of semantic, phonological, and syntactic processing are reviewed. For semantics and phonology there seem to be different fronto-temporal networks which are shared in production and comprehension. The results for the processing of syntactic information are not entirely conclusive. Yet the data reveal that phonological strategies may be used in syntactic tasks. This finding opens the discussion of alternative, phonology-based strategies for language processing. Such strategies are accounted for by dual-route models featuring one direct and one indirect route which often involves phonological processing. This insight leads to some tentative conclusions about remediation strategies in dyslexics with selective (e.g., phonological) deficits.
EN
Analysis of relationships between the ageing cell phenotype and the age of cell donors is one of the ways towards understanding the link between cellular and organismal ageing. Cytogenetically, ageing is associated with a number of gross cellular changes, including altered size and morphology, genomic instability, and changes in expression and proliferation. Genomic instability can be easily assessed by analyzing the level of cytogenetic aberrations. In this review, we focus on the differences in the level and profile of cytogenetic aberrations observed in donors of different age and gender. Centenarians are a small fraction of the population at the extreme of human longevity. Their inclusion in such studies may shed light on one of the basic questions: whether genome stability is better maintained in successfully aged individuals compared to the rest of the population. At the same time, comparing the profile of age-related amount of chromosomal aberrations in men and women may help explaining the commonly observed gender differences in longevity.
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