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941.
942.
Zusammenfassung Die zelluläre Reaktion an traumatischen, mechanisch gesetzten Läsionen in der Gehirnrinde wurde an neugeborenen und erwachsenen Hunden sowie an Mäusen untersucht. Die Heilung der Läsionen in Neugeborenen war so, dass das Gehirngewebe makroskopisch normal aussah; histologisch waren die durchtrennten Elemente durch die Heilungsprozesse unter minimaler glialer Reaktion wieder gut reorganisiert. 相似文献
943.
Ferreri C Kratzsch S Landi L Brede O 《Cellular and molecular life sciences : CMLS》2005,62(7-8):834-847
Thiyl radicals are intermediates of enzyme- and radical-driven biochemical processes, and their potential as reactive species in the biological environment has been somehow underestimated. From organic chemistry, however, it is known that thiyl radicals isomerize the double bonds of unsaturated fatty acids to a mixture with very dominating trans isomers. Recently, this reaction has been particularly studied for biosystems, focusing on the effect of thiyl radicals on the natural all-cis double bonds of unsaturated phospholipids, which undergo a conversion to the unnatural trans form. In this paper we report briefly the role of thiyl radicals in biosystems, describe the main features of the radical-induced cis-trans isomerization process under both in vitro and in vivo conditions, and reflect on some consequences for membrane structures, lipid metabolism and enzymatic reactions.Received 29 October 2004; received after revision 3 December 2004; accepted 4 January 2005 相似文献
944.
Summary After hatching, young individuals of the Mexican blind characinAnoptichthys jordani Hubbs and Innes possess small, movable eyes. In the course of growth, the eyes are overlapped by skinfolds and tend to sink into the depth of the orbital cavity. Lens and pupilar opening may disappear and degeneration is to be found in the retina.Even very young blind characins seem to have no vision of movements, while they are able to perceive light. The lower limit is about 0.12 Lux of light intensity. Experiments concerning the localisation of this perception of light are in progress. 相似文献
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949.
Spink5-deficient mice mimic Netherton syndrome through degradation of desmoglein 1 by epidermal protease hyperactivity 总被引:10,自引:0,他引:10
Descargues P Deraison C Bonnart C Kreft M Kishibe M Ishida-Yamamoto A Elias P Barrandon Y Zambruno G Sonnenberg A Hovnanian A 《Nature genetics》2005,37(1):56-65
Mutations in SPINK5, encoding the serine protease inhibitor LEKTI, cause Netherton syndrome, a severe autosomal recessive genodermatosis. Spink5(-/-) mice faithfully replicate key features of Netherton syndrome, including altered desquamation, impaired keratinization, hair malformation and a skin barrier defect. LEKTI deficiency causes abnormal desmosome cleavage in the upper granular layer through degradation of desmoglein 1 due to stratum corneum tryptic enzyme and stratum corneum chymotryptic enzyme-like hyperactivity. This leads to defective stratum corneum adhesion and resultant loss of skin barrier function. Profilaggrin processing is increased and implicates LEKTI in the cornification process. This work identifies LEKTI as a key regulator of epidermal protease activity and degradation of desmoglein 1 as the primary pathogenic event in Netherton syndrome. 相似文献
950.
Epimutation of the telomeric imprinting center region on chromosome 11p15 in Silver-Russell syndrome
Gicquel C Rossignol S Cabrol S Houang M Steunou V Barbu V Danton F Thibaud N Le Merrer M Burglen L Bertrand AM Netchine I Le Bouc Y 《Nature genetics》2005,37(9):1003-1007
Silver-Russell syndrome (SRS, OMIM 180860) is a congenital disorder characterized by severe intrauterine and postnatal growth retardation, dysmorphic facial features and body asymmetry. SRS is genetically heterogenous with maternal uniparental disomy with respect to chromosome 7 occurring in approximately 10% of affected individuals. Given the crucial role of the 11p15 imprinted region in the control of fetal growth, we hypothesized that dysregulation of genes at 11p15 might be involved in syndromic intrauterine growth retardation. We identified an epimutation (demethylation) in the telomeric imprinting center region ICR1 of the 11p15 region in several individuals with clinically typical SRS. This epigenetic defect is associated with, and probably responsible for, relaxation of imprinting and biallelic expression of H19 and downregulation of IGF2. These findings provide new insight into the pathogenesis of SRS and strongly suggest that the 11p15 imprinted region, in addition to those of 7p11.2-p13 and 7q31-qter, is involved in SRS. 相似文献