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  • 1975-1979  (6)
  • 1978  (3)
  • 1977  (3)
  • 1
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Journal of neurochemistry 29 (1977), S. 0 
    ISSN: 1471-4159
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Notes: Abstract— Non-histone chromosomal proteins (NHCP) from mouse brain at different stages of development and from adult liver and kidney of strain related mice were analyzed by SDS-polyacrylamide gel electrophoresis and were compared with the mouse teratoma, OTT-6050. The fetal, neonatal and adult brains were qualitatively similar in their NHCP profiles but had quantitative differences. The NHCP composition of the adult brain was clearly distinct from that of the liver and kidney and was dissimilar from that of the teratoma.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1471-4159
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Journal of neurochemistry 30 (1978), S. 0 
    ISSN: 1471-4159
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Notes: Abstract— The effects of altered osmolarity on respiration and fine structure were compared in isolated rat cerebral versus liver mitochondria.Polarographic study of cerebral mitochondria in hypo-osmolar media showed inhibition of State 3 (ADP-dependent) respiration which was not reversed by dinitrophenol. In hyperosmolar media, State 3 respiration was transiently inhibited and State 4 (ADP-independent) respiration increased with the NAD-linked substrate pair, glutamate and malate. With succinate as substrate, respiration was not affected by moderate hyperosmolarity. In the most hyperosmolar medium, State 3 respiration was inhibited with both substrates.In contrast to the results with cerebral mitochondria, State 4 respiration was increased in hypo-osmolar media and State 3 respiration was persistently inhibited in hyperosmolar media in liver mitochondria with both substrates.In both cerebral and liver mitochondria, cytochrome c oxidase (EC 1.9.3.1.) activity was mildly inhibited in hypo-osmolar media and increased in hyperosmolar media.Electron microscopy showed that liver mitochondria were swollen in hypo-osmolar media and condensed in hyperosmolar media. Cerebral mitochondria showed mild rarefaction in hypo-osmolar media and, in hyperosmolar media, more than half the mitochondria showed either no or minimal changes in fine structure.Our results suggest that there are differences in metabolic control and structure between mitochondria from different cell types, which may be important in the cellular metabolic response to pathologic changes in water or osmolarity.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Acta neuropathologica 39 (1977), S. 281-287 
    ISSN: 1432-0533
    Keywords: Neuroepithelial differentiation ; Microcomplement fixation ; Indirect immunofluorescence
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Mouse neonatal brain cell fractions enriched for surface membranes were used as immunogens to produce a heterologous immune serum. Following absorption to remove non-neural anti-mouse activity, this serum demonstrated by microcomplement fixation an anti-brain activity that was completely removed by absorption with neonatal mouse brain or with solid tumors of the mouse transplantable teratoma OTT-6050. Indirect immunofluorescence applied to living monolayer cultures of differentiating teratoma embryoid bodies showed the absorbed serum's reaction with neural cell surfaces only. In material studied with frozen sections, the absorbed serum recognized antigenic sites in all examined areas of both neonatal and adult mouse brain, and only within neuroepithelial cell populations of solid transplants of the teratoma.
    Type of Medium: Electronic Resource
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  • 5
    ISSN: 0021-9541
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: The metabolic flow of trace amounts of D-[14C]-galactose was followed in cultures of transformed and untransformed hamster cells over a period ranging from five minutes to two hours. The results of chromatographic and enzymatic analyses of the soluble pools are described. Non-glycolytic cells (previously deprived of sugar for periods of up to 24 hours) convert D-galactose to galactose-1-phosphate and uridine diphosphoglucuronic acid in 10 to 20 minutes. In the same short assay time, glycolytic cells which have been maintained for 24 hours in media containing glucose or galactose convert D-galactose to uridine diphosphogalactose and uridine diphosphoglucose (ratio 1.4:1). Longterm deprivation of sugar also results in 3- to 4-fold increases in the uptake of galactose. In addition, the incorporation of galactose label into chloroform-methanol soluble material appears to be influenced by the culture conditions of the untransformed cells while incorporation in the transformed cells appears unaffected. When cycloheximide is included in the maintenance medium for extended periods, the non-glycolytic cells also show increases in galactose uptake rates but the glucose-fed, glycolytic cells lose uptake ability. UDPhexose is the main galactose metabolic peak in the soluble pools of the cycloheximide-treated, glycolytic and the cycloheximide-treated, non-glycolytic cells. The results of these experiments suggest that uptake of galactose and its subsequent metabolism are under separate control.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Cellular Physiology 96 (1978), S. 23-29 
    ISSN: 0021-9541
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: Administration of radioactively labeled galactose to cultured mammalian cells brings about an accumulation of metabolic products the pattern of which seems to be governed by a variety of vectors in the intracellular milieu. By manipulation of culture conditions some of these vectors appear to be a function of glycolysis. In the non-glycolytic culture, label from a galactose probe appears as Galactose-1-phosphate (Gal-1-P) and UDPglucuronic acid (UDPGlcUA). Conversely, glycolytic culture conditions seem not to permit the formation to UDPGlcUA since the only labeled accumulation product formed was UDPHex. A suggestion is made that the difference in metabolic activity of glucose-fed and glucose-starved cultures may be related to the effect of NADH on the in situ activity of UDPG dehydrogenase (UDPglucose:NAD oxidoreductase, E.C. 1.1.1.22) (abbreviation, UDPG-DH). This prompted an investigation of the effects of NAD and NADH on the activity of partially purified UDPG-DH. The results of these experiments strongly suggest that the activity of UDPG-DH (in situ) is negatively controlled by increased levels of NADH; the latter condition is known to exist in glycolytically active cells (Schwartz and Johnson, 1976). Added to this is a second control mechanism which is characterized by a transient inhibition of uridylyltransferase (UDP glucose:α-D-galactose-1-phosphate uridylyltransferase, E.C. 2.7.7.12). Since it is known that there is little, if any, effect on galactokinase (ATP:D-galactose-1-phosphotransferase, E.C. 2.7.1.6) activity as a result of sugar starvation (Christopher et al., 1976), the low in vivo activity of uridylyltransferase contributes not only to the increased accumulation of Gal-1-P but also to a drastic decrease of labeled UDPhexoses, although the pre-existing pool of UDPhexose was found to decrease only moderately under the condition of glucose starvation (30% still persisted). The benefit of this type of control is not clear.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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