Records |
Author |
Jallon, J.M.; Risler, Y.; Iwatsubo, M. |
Title |
Beef liver L-Glutamate dehydrogenase mechanism: presteady state study of the catalytic reduction of 2.oxoglutarate by NADPH |
Type |
Journal Article |
Year |
1975 |
Publication |
Biochemical and biophysical research communications |
Abbreviated Journal ![sorted by Abbreviated Journal field, descending order (down)](img/sort_desc.gif) |
Biochem Biophys Res Commun |
Volume |
67 |
Issue |
4 |
Pages |
1527-1536 |
Keywords |
Animals; Cattle; Glutamate Dehydrogenase/*metabolism; Ketoglutaric Acids; Kinetics; Liver/*enzymology; Nadp; Oxidation-Reduction; Spectrometry, Fluorescence; Spectrophotometry, Ultraviolet |
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0006-291X |
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PMID:1038 |
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Call Number |
Admin @ knut @ |
Serial |
21 |
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Author |
Bayley, P.; Martin, S.; Anson, M. |
Title |
Temperature-jump circular dichroism: observation of chiroptical relaxation processes at millisecond time resolution |
Type |
Journal Article |
Year |
1975 |
Publication |
Biochemical and Biophysical Research Communications |
Abbreviated Journal ![sorted by Abbreviated Journal field, descending order (down)](img/sort_desc.gif) |
Biochem Biophys Res Commun |
Volume |
66 |
Issue |
1 |
Pages |
303-308 |
Keywords |
*Alcohol Oxidoreductases/metabolism; Animals; Circular Dichroism; Horses; Kinetics; Liver/enzymology; Mathematics; Protein Conformation; Temperature; Time Factors |
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0006-291X |
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PMID:1172440 |
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Equine Behaviour @ team @ |
Serial |
3816 |
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Author |
Bergmann, H.H.; Klaus, S.; Muller, F.; Wiesner, J. |
Title |
[Individuality and type specificity in the songs of a population of hazel grouse (Bonasa bonasia bonasia L., Tetraoninae, Phasianidae)] |
Type |
Journal Article |
Year |
1975 |
Publication |
Behaviour |
Abbreviated Journal ![sorted by Abbreviated Journal field, descending order (down)](img/sort_desc.gif) |
Behaviour |
Volume |
55 |
Issue |
1-2 |
Pages |
94-114 |
Keywords |
Animals; *Birds; Female; *Individuality; Male; Time Factors; *Vocalization, Animal |
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German |
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Individualitat und Artspezifitat in den Gesangsstrophen einer Population des Haselhuhns (Bonasa bonasia bonasia L., Tetraoninae, Phasianidae) |
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0005-7959 |
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PMID:1191217 |
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no |
Call Number |
Equine Behaviour @ team @ |
Serial |
4152 |
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Author |
Jensen, G.D.; Gordon, B.N.; Wolfheim, J. |
Title |
Nursing behavior in infant monkeys: a sequence analysis |
Type |
Journal Article |
Year |
1975 |
Publication |
Behaviour |
Abbreviated Journal ![sorted by Abbreviated Journal field, descending order (down)](img/sort_desc.gif) |
Behaviour |
Volume |
55 |
Issue |
1-2 |
Pages |
115-127 |
Keywords |
Animals; Dependency (Psychology); *Feeding Behavior; Female; *Macaca; Male; Sensory Deprivation; Social Behavior; Spatial Behavior |
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0005-7959 |
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PMID:1191212 |
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no |
Call Number |
Equine Behaviour @ team @ |
Serial |
4153 |
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Author |
FRASER AF et al, |
Title |
An exploratory ultrasonic study on quntitative foetal kinesis in the horse |
Type |
Journal Article |
Year |
1975 |
Publication |
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Abbreviated Journal ![sorted by Abbreviated Journal field, descending order (down)](img/sort_desc.gif) |
Appl Anim Ethol |
Volume |
1 |
Issue |
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Pages |
395-404 |
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Notes |
from Professor Hans Klingels Equine Reference List |
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no |
Call Number |
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Serial |
1093 |
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Author |
Ruckebusch Y, |
Title |
The hypnogram as an index of adaptation of farm animals to changes in their environment |
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Journal Article |
Year |
1975 |
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App Anim Ethol |
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2 |
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Pages |
3-18 |
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Notes |
from Professor Hans Klingels Equine Reference List |
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no |
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Serial |
1531 |
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Author |
Syme, G.J.; Syme, L.A. |
Title |
The concept of spatial leadership in farm animals: An experiment with sheep |
Type |
Journal Article |
Year |
1975 |
Publication |
Animal Behaviour. |
Abbreviated Journal ![sorted by Abbreviated Journal field, descending order (down)](img/sort_desc.gif) |
Anim. Behav. |
Volume |
23 |
Issue |
Part 4 |
Pages |
921-925 |
Keywords |
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Abstract |
The concept of spatial leadership as applied to farm animals is discussed with particular emphasis on methodological problems. Using three experimental procedures forced spatial leadership orders were measured in a group of Romney ewes. Comparisons between orders showed the effects of both the different experimental tasks and the social context on leadership structure. Both these variables were found to affect the orders obtained. The results are interpreted in terms of the utility of the concept of spatial leadership in domestic animals and the necessity for more systematic procedural investigations in this area. |
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no |
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Serial |
2039 |
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Author |
Scherer, W.F.; Madalengoitia, J.; Flores, W.; Acosta, M. |
Title |
Ecologic studies of Venezuelan encephalitis virus in Peru during 1970-1971 |
Type |
Journal Article |
Year |
1975 |
Publication |
American Journal of Epidemiology |
Abbreviated Journal ![sorted by Abbreviated Journal field, descending order (down)](img/sort_desc.gif) |
Am J Epidemiol |
Volume |
101 |
Issue |
4 |
Pages |
347-355 |
Keywords |
Animals; Antibodies, Viral; Cricetinae/immunology; Culicidae/microbiology; *Disease Vectors; Ecology; *Encephalitis Virus, Venezuelan Equine/immunology/isolation & purification; Encephalomyelitis, Equine/immunology/microbiology/transmission; Female; Hemagglutination Inhibition Tests; Horses/immunology; Humans; Neutralization Tests; Peru |
Abstract |
Venezuelan encephalitis (VE) virus has intermittently produced epidemics and equine epizootics on the dry Pacific coastal plain of Peru since at least the 1930's. However, evidence that the virus exists in the Amazon region of Peru to the east of the Andes mountains was not obtained until antibodies were found in human sera collected in 1965, and 10 strains of the virus were isolated in a forest near the city of Iquitos, Peru during February and March 1971. Eight strains came from mosquitoes and two from dead sentinel hamsters. Three hamsters exposed in forests near Iquitos developed VE virus antibodies suggesting that hamster-benign strains also exist there. Antibody tests of equine sera revealed no evidence that VE virus was actively cycling during the late 1950's or 1960's in southern coastal Peru, where equine epizootics had occurred in the 1930's and 1940's. In northern coastal Peru bordering Ecuador, antibodies were present in equine sera, presumably residual from the 1969 outbreak caused by subtype I virus, since neutralizing antibody titers were higher to subtype I virus than to subtypes III or IV. No VE virus was detected in this northern region during the dry season of 1970 by use of sentinel hamsters. The possibility is considered that VE epidemics and equine epizootics on the Pacific coast of Peru are caused by movements of virus in infected vertebrates traversing Andean passes or in infected vertebrates or mosquitoes carried in airplanes from the Amazon region. |
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0002-9262 |
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Notes |
PMID:235838 |
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no |
Call Number |
Equine Behaviour @ team @ |
Serial |
2705 |
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Author |
Sudia, W.D.; Fernandez, L.; Newhouse, V.F.; Sanz, R.; Calisher, C.H. |
Title |
Arbovirus vector ecology studies in Mexico during the 1972 Venezuelan equine encephalitis outbreak |
Type |
Journal Article |
Year |
1975 |
Publication |
American Journal of Epidemiology |
Abbreviated Journal ![sorted by Abbreviated Journal field, descending order (down)](img/sort_desc.gif) |
Am J Epidemiol |
Volume |
101 |
Issue |
1 |
Pages |
51-58 |
Keywords |
Animals; Arboviruses/isolation & purification; Culicidae/microbiology; Disease Vectors/*microbiology; Ecology; Encephalitis Virus, St. Louis/isolation & purification; Encephalitis Virus, Venezuelan Equine/*isolation & purification; Encephalitis Virus, Western Equine/isolation & purification; Encephalomyelitis, Equine/epidemiology/*transmission/veterinary; Horse Diseases/epidemiology/*transmission; Horses; Insect Vectors/microbiology; Mexico |
Abstract |
Virus vector studies were conducted in the States of Durango, Chihuahua, and Tamaulipas, Mexico, in June and July 1972. Apparently only a low level of Venzuelan equine encephalitis (VEE) virus transmission to equines occured at the time of the study, and the infection was restricted to areas which had not experienced overt activity during the preceding year. The low level of infection was associated with a scarcity of mosquitoes. The IB (epidemic) strain of VEE virus was isolated from two pools of Anopheles pseudopunctipennis (Theo.) and the blood of one symptomatic equine. The low mosquito population, the relatively few equine cases observed, and the absence of reports of VEE human disease from the outbreak area suggested VEE virus persistence through a low-level mosquito-equine transmission cycle. Other studies have already indicated that wild vertebrates play no more than a minor role in outbreaks of epidemic VEE. Mosquito collections made in areas of the states of Durango, Chihuahua, and Tamaulipas, where considerable epidemic activity of VEE had occurred in 1971, failed to reveal evidence of VEE virus persistence. Twenty-nine ioslations of other arboviruses were also made in these studies: including 22 of St. Louis encephalitis virus (SLE), 2 of Flanders virus, 1 of Turlock virus, 1 of Trivittatus virus of the California Group, 1 of western equine encephalitis virus (VEE), and 2 (from Santa Rose) which possibly represent a hitherto unknown virus in the Bunyamwera Group. These are the first reports of SLE virus isolations from mosquitoes in Mexico, and the first demonstration of Trivittatus, VEE Turlock and Flanders viruses in Mexico from any source. |
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0002-9262 |
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PMID:235213 |
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Equine Behaviour @ team @ |
Serial |
2706 |
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Author |
Czerlinski, G.H.; Wagner, M.; Erickson, J.O.; Theorell, H. |
Title |
Chemical relaxation studies on the system liver alcohol dehydrogenase, NADH and imidazole |
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Journal Article |
Year |
1975 |
Publication |
Acta Chemica Scandinavica. Series B: Organic Chemistry and Biochemistry |
Abbreviated Journal ![sorted by Abbreviated Journal field, descending order (down)](img/sort_desc.gif) |
Acta Chem Scand B |
Volume |
29 |
Issue |
8 |
Pages |
797-810 |
Keywords |
Alcohol Oxidoreductases/*metabolism; Animals; Computers; Hydrogen-Ion Concentration; Imidazoles/*metabolism; Kinetics; Liver/enzymology/*metabolism; Mathematics; Models, Chemical; NAD/*metabolism; Time Factors |
Abstract |
Several years ago, Theorell and Czerlinski conducted experiments on the system of horse liver alcohol dehydrogenase, reduced nicotinamide adenine dinucleotide and imidazole, using the first version of the temperature jump apparatus with detection of changes in fluorescence. These early experiments were repeated with improved instrumentation and confirmed the early experiments in general terms. However, the improved detection system allowed to measure a slight concentration dependence of the relaxation time of around 3 ms. Furthermore, the chemical relaxation time was smaller than the one determined earlier (by factor 2). The data were evaluated much more rigorously than before, allowing an appropriate interpretation of the results. The observed relaxation time is largely due to rate constants in an interconversion of ternary complexes, which are faster than three (of the four) dissociation rate constants, determined previously by Theorell and McKinley-McKee.1,2 This fact contributed to earlier difficulties of finding any concentration dependence. However, the binding of imidazole to the binary enzyme-coenzyme complex can be made to couple kinetically into the interconversion rate of the two ternary complexes. The observed signal derives largely from the ternary complex(es). A substantial fluorescence signal change is associated with the observed relaxation process, suggesting a relocation of the imidazole in reference to the nicotinamide moiety of the bound coenzyme. Nine models are considered with two types of coupling of pre-equilibria (none-all). Quantitative evaluations favor the model with two ternary complexes connected by an interconversion outside the four-step (bimolecular) cycle. The ternary complex outside the cycle has much higher fluorescence yield than the one inside. The interconversion equilibrium is near unity for imidazole. If it would be shifted very much to the side of the “dead-end” complex (as in isobutyramide?!), stimulating action could not take place. |
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0302-4369 |
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PMID:882 |
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refbase @ user @ |
Serial |
3887 |
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