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351.
K W Alt 《Anthropologischer Anzeiger; Bericht über die biologisch-anthropologische Literatur》1991,49(3):261-272
This paper draws attention to problems of assessment and interpretation of frequencies of the retention/displacement of teeth (impacted teeth and germ impaction), presents diagnostic criteria, comments on the incidence and frequency of retention/displacement and other disturbances in recent probands, lists the order in which teeth are affected, and discusses the causes of these disturbances. Reasons for the existing lack of anthropological data on the subject are suggested, and the potential usefulness of representative surveys of large samples of prehistoric populations is stressed. 相似文献
352.
353.
Jeremy A Alt Ferenc Obal T R Traynor Janos Gardi Jeannine A Majde James M Krueger 《Journal of applied physiology》2003,95(2):460-468
Viral infections induce excess non-rapid eye movement sleep (NREMS) in mice. Growth hormone-releasing hormone receptor (GHRH receptor) was previously identified as a candidate gene responsible for NREMS responses to influenza challenge in mice. The dwarf lit/lit mouse with a nonfunctional GHRH receptor was used to assess the role of the GHRH receptor in viral-induced NREMS. After influenza A virus infection the duration and intensity [electroencephalogram (EEG) delta power] of NREMS increased in heterozygous mice with the normal phenotype, whereas NREMS and EEG delta power decreased in homozygous lit/lit mice. Lit/lit mice developed a pathological state with EEG slow waves and enhanced muscle tone. Other influenza-induced responses (decreases in rapid eye movement sleep, changes in the EEG high-frequency bands during the various stages of vigilance, hypothermia, and decreased motor activity) did not differ between the heterozygous and lit/lit mice. GH replacement failed to normalize the NREMS responses in the lit/lit mice after influenza inoculation. Decreases in NREMS paralleled hypothermia in the lit/lit mice. Lung virus levels were similar in the two mouse strains. Lit/lit mice had a higher death rate after influenza challenge than the heterozygotes. In conclusion, GHRH signaling is involved in the NREMS response to influenza infection. 相似文献