Analyze Diet

Topic:Bioinformatics

Bioinformatics in horses involves the application of computational tools and techniques to analyze and interpret biological data related to equine species. This interdisciplinary field integrates biology, computer science, and information technology to study genetic, genomic, and proteomic information in horses. Bioinformatics can be used to investigate genetic variations, understand disease mechanisms, and assist in the development of targeted therapies and breeding programs. Key areas of focus include genome sequencing, gene expression analysis, and the identification of genetic markers associated with specific traits or conditions. This page compiles peer-reviewed research studies and scholarly articles that explore the application and impact of bioinformatics on equine genetics, health, and breeding.
A screening test to differentiate cattle meat from horse, donkey, kangaroo, pig and sheep meats.
Australian veterinary journal    August 1, 1982   Volume 59, Issue 2 59 doi: 10.1111/j.1751-0813.1982.tb02720.x
Johnston LA, Tracey-Patte P, Donaldson RA, Parkinson B.No abstract available
Identification of a transforming retrovirus from cultured equine dermal fibrosarcoma.
Virology    July 30, 1982   Volume 120, Issue 2 490-494 doi: 10.1016/0042-6822(82)90050-2
Fatemi-Nainie S, Anderson LW, Cheevers WP.No abstract available
Positional distribution of fatty acids in triglycerides from milk of several species of mammals.
Lipids    June 1, 1982   Volume 17, Issue 6 437-442 doi: 10.1007/BF02535223
Parodi PW.Milk triglycerides from the echidna, koala, Tammar wallaby, guinea pig, dog, cat, Weddell seal, horse, pig and cow were subjected to fatty acid and stereospecific analysis to determine the positional distribution of the fatty acids in the triglycerides. The samples presented a wide range of fatty acids, most of which varied in content among species. The compositions of the acids at the 3 positions also varied among species, reflecting the content of these acids in the triglycerides. However, there was a general similarity in fatty acid positional distribution patterns for all the species with ...
Pancreatic colipase: crystallographic and biochemical aspects.
European journal of biochemistry    April 1, 1982   Volume 123, Issue 2 347-354 doi: 10.1111/j.1432-1033.1982.tb19774.x
Pierrot M, Astier JP, Astier M, Charles M, Drenth J.A detailed study of the crystallization of hog and horse colipases has been undertaken. Several crystallographic varieties have been obtained and a 0.3-nm resolution structure determination is actually in progress. The sequence of the A form of horse colipase (one methionine) is given. From spectrophotometric experiments and sequence comparisons, the involvement of the aromatic residue in position 52 in the micelle binding site has been demonstrated.
Investigation of intermediates and transition states in the catalytic mechanisms of active site substituted cobalt(II), nickel(II), zinc(II), and cadmium(II) horse liver alcohol dehydrogenase.
Biochemistry    January 19, 1982   Volume 21, Issue 2 354-363 doi: 10.1021/bi00531a024
Dunn MF, Dietrich H, MacGibbon AK, Koerber SC, Zeppezauer M.No abstract available
The karyotype of the primitive East Carpathian horse (Equus caballus gmelini Ant.), as revealed by G- and C-banding techniques.
Folia biologica    January 1, 1982   Volume 30, Issue 3-4 139-142 
Rudek Z.No abstract available
Limited trypsinolysis of porcine and equine colipases. Spectroscopic and kinetic studies.
Biochimica et biophysica acta    December 29, 1981   Volume 671, Issue 2 155-163 doi: 10.1016/0005-2795(81)90129-x
Rathelot J, Canioni P, Bosc-Bierne I, Sarda L, Kamoun A, Kaptein R, Cozzone PJ.Porcine and equine colipases have been submitted to mild tryptic digestion. Proteolysis occurs at the Arg5-Gly6 bond with the loss of the N-terminal pentapeptide. Studies of native and trypsin-treated colipases by circular dichroism and laser chemically induced dynamic nuclear polarization indicate that proteolysis induces conformational changes in the region of the tyrosine cluster. Experiments in the presence of phospholipid provide further evidence showing that these residues are in or close to the region of the protein interacting with aggregated lipids. Kinetic studies of the reaction of ...
Circular dichroism study of horse colipase interaction with bile salt.
Biochimica et biophysica acta    October 28, 1981   Volume 670, Issue 3 305-311 doi: 10.1016/0005-2795(81)90101-x
Canioni P, Julien R, Romanetti R, Cozzone P, Sarda L.No abstract available
Amino acid sequence of horse spleen apoferritin.
FEBS letters    July 6, 1981   Volume 129, Issue 2 322-327 doi: 10.1016/0014-5793(81)80193-7
Heusterspreute M, Crichton RR.No abstract available
Nucleic acid-protein interactions. Degradation of double-stranded RNA by glycosylated ribonucleases.
Biochimica et biophysica acta    June 26, 1981   Volume 654, Issue 1 77-85 doi: 10.1016/0005-2787(81)90138-6
Carsana A, Furia A, Gallo A, Beintema JJ, Libonati M.1. Extensively glycosylated ribonucleases, like the enzymes from pig and horse pancreas, show a much higher activity on double-stranded RNAs than similarly charged, carbohydrate-free RNAases under stranded assay conditions (relatively high salt concentrations). Glycosylated pig and horse pancreas RNAases also show a larger destabilizing effect on double-stranded poly[d(A-T)] X poly[d(A-T)], than that displayed by bovine RNAase A under these conditions. Both activities show a similar dependence on the ionic strength of the medium. 2. A partial enzymic removal of the heterosaccharide side chains...
[Investigations on the individual-region distribution of adipocyte diameters by means of advanced statistical methods].
Bollettino della Societa italiana di biologia sperimentale    May 30, 1981   Volume 57, Issue 10 1047-1053 
Strigazzi A, Bianchi M.The dimensional distributions of the adipocytes in Equus caballus in many subjects and in many regions have been studied: such distributions turn out to be in good approximation galtonian ones. Furthermore, all the logarithm populations of the cell diameters have significantly the same variance. The used statistical methods (ANOVA two way with replications, and TUKEY -test) indicate an extremely significant different among the various regions (the smallest cells are in the supra-orbital fossa, the greatest ones are in the abdominal subserous floor).
Rapid-scanning spectral evidence for catalytically nonequivalent but interconvertible forms of equine liver alcohol dehydrogenase.
Biochimie    February 1, 1981   Volume 63, Issue 2 97-102 doi: 10.1016/s0300-9084(81)80171-x
Koerber SC, Dunn MF.These rapid-scanning stopped-flow kinetic studies of the equine liver alcohol dehydrogenase-catalyzed reduction of p-nitrobenzaldehyde by NADH and (4R)-4-deuterio NADH (NADD) under single turnover conditions establish : (1) The reaction is biphasic using NADD as coenzyme, k1 approximately 200 sec-1, k2 = 0.5 sec-1 and the amplitude ratio (A1)/(A1 + A2) approximately equal to 0.5. (2) Each phase of the reaction involves the oxidation of enzyme-bound reduced coenzyme. (3) The recycling of sites in the presence of 20 mM pyrazole is negligible. (4) The rates of E(NAD-pyrazole) complex formation at...
Alcohol dehydrogenase from Leuconostoc mesenteroides: molecular properties in comparison with the yeast and horse liver enzyme.
The International journal of biochemistry    January 1, 1981   Volume 13, Issue 12 1215-1224 doi: 10.1016/0020-711x(81)90067-7
Schneider-Bernlöhr H, Fiedler H, Gerber M, Weber C, Zeppezauer M.No abstract available
Predicted secondary structure of horse muscle acylphosphatase. Comparison with circular dichroism measurements.
Physiological chemistry and physics    January 1, 1981   Volume 13, Issue 3 267-273 
Camici G, Manao G, Cappugi G, Ramponi G.We have predicted the secondary structure of horse muscle acylphosphatase by the statistical method of Chou and Fasman. In addition, we have studied the circular dichroism spectra of the enzyme, obtaining values for comparison to the predicted results. Discrepancies were found for the alpha-helix content estimated by the two methods.
Biochemical properties of equine chorionic gonadotrophin from two different pools of pregnant mare sera.
Biology of reproduction    October 1, 1980   Volume 23, Issue 3 570-576 doi: 10.1095/biolreprod23.3.570
Aggarwal BB, Farmer SW, Papkoff H, Seidel GE.No abstract available
Horse erythrocyte gangliosides: preparation of the major hematoside NeuNG1-Lac-Cer.
Lipids    September 1, 1980   Volume 15, Issue 9 682-685 doi: 10.1007/BF02534019
Maget-Dana R, Michalski JC.A simple method for the isolation of hematoside NeuNG1-Lac-Cer from horse erythrocytes is described. An aliquot of the crude ganglioside fraction was labeled by tritiated sodium borohydride after mild periodate oxidation. The compounds obtained were used as radioactive tracers in column chromatography. Gangliosides were applied onto a silicic acid column and eluted stepwise by solvents of steadily increasing polarity. The major ganglioside, NeuNG1-Lac-Cer, was eluted in a high yield by the solvent mixture chloroform/methanol/water (60:35:8, v/v/v).
Assembly of intra- and interspecies hybrid apoferritins.
The Journal of biological chemistry    July 10, 1980   Volume 255, Issue 13 6234-6237 
Otsuka S, Listowsky I, Niitsu Y, Urushizaki I.An intraspecies hybrid apoferritin was assembled by mixing subunits of horse heart ferritin, which consists mainly of H-type subunits, and horse spleen ferritin, in which L-type subunits predominate. Interspecies hybrid apoferritins were reconstituted from subunits of human liver-horse spleen ferritins and from rat liver-horse spleen ferritins. All the hybrid ferritins migrated as single zones with electrophoretic mobilities intermediate between those of the parent ferritins. Isoelectric focusing data and immunological patterns were consistent with the view that the reassembled apoferritins we...
A biologically active, three-fragment complex of horse heart cytochrome c.
The Journal of biological chemistry    February 10, 1980   Volume 255, Issue 3 845-853 
Juillerat M, Parr GR, Taniuchi H.No abstract available
Identification and genetics of horse lymphocyte alloantigens.
Immunogenetics    January 1, 1980   Volume 11, Issue 5 499-506 doi: 10.1007/BF01567818
Bailey E.Six hundred horses were tested with lymphocytotoxic antisera derived from 550 parous mares and 58 antisera produced by alloimmunization with horse blood cells. Seven equine lymphocyte specificities were identified using correlation analysis of the test data, absorption analysis and lysostripping. These specificities are expressed on lymphocytes and platelets, but not on red blood cells (RBC). Therefore, these specificities do not appear to be products of any of the eight known blood group systems of the horse. The distribution of these specificities in 113 Thoroughbred horses and 57 Arabian ho...
Insensitivity of the ferritin iron core to heat treatment.
Experientia    March 15, 1979   Volume 35, Issue 3 300-301 doi: 10.1007/BF01964311
Bertrand ML, Harris DC.To test whether the reactivity of ferritin iron is affected by the heat treatment used in ferritin isolation, we prepared ferritin from the same horse spleen with or without heating. Both samples exhibited similar reactivity upon reduction or chelation of iron.
The amino acid sequence of equine metallothioneins.
Experientia. Supplementum    January 1, 1979   Volume 34 153-161 doi: 10.1007/978-3-0348-6493-0_6
Kojima Y, Berger C, Kägi JH.No abstract available
A detection tube for cholinesterase inhibiting compounds.
International journal of environmental analytical chemistry    January 1, 1979   Volume 6, Issue 2 89-94 doi: 10.1080/03067317908071163
Barendsz AW.The enzyme butyrylcholinesterase from horse serum catalyses the hydrolysis of certain esters. The orange-red 2,6-dichloroindophenyl acetate will be converted by the enzyme into a deep blue alcohol. The colour transformation does not occur when the enzyme is inactivated. By making use of this biochemical reaction a cheap and simple, but very sensitive and specific detection tube could bedeveloped. The tube comprises a breakable ampoule with an aqueous buffer solution, a freeze-dried preparation of the chromogenic ester with a filler promoting its dissolution, a freeze-dried preparation of butyr...
Biochemical changes in horses during endurance rides.
The Veterinary record    May 27, 1978   Volume 102, Issue 21 469 doi: 10.1136/vr.102.21.469
Orton RG.No abstract available
Ferritin: structure, biosynthesis, and role in iron metabolism.
Physiological reviews    April 1, 1978   Volume 58, Issue 2 317-396 doi: 10.1152/physrev.1978.58.2.317
Munro HN, Linder MC.No abstract available
Enzymes in organic synthesis. Influence of substrate structure on rates of horse liver alcohol dehydrogenase-catalysed oxidoreductions.
Journal of the Chemical Society. Perkin transactions 1    January 1, 1978   Volume 12 1636-1642 doi: 10.1039/p19780001636
Irwin AJ, Lok KP, Huang KW, Jones JB.No abstract available
Methods for quantifying mammalian spermatogenesis: a review.
Journal of animal science    May 1, 1977   Volume 44, Issue 5 818-833 doi: 10.2527/jas1977.445818x
Berndtson WE.No abstract available
Amino acid composition of casein isolated from the milks of different species.
Canadian journal of zoology    January 1, 1977   Volume 55, Issue 1 231-236 doi: 10.1139/z77-026
Lauer BH, Baker BE.Casein was isolated from the milks of the following species: cow, horse, pig, reindeer, caribou, moose, harp seal, musk-ox, polar bear, dall sheep, and fin whale. The caseins were subjected to acid hydrolysis, the resultant amino acids were converted to their n-butyl-N-trifluoroacetyl esters, and the amino acid composition of the caseins was determined by gas chromatographic analysis of these esters. Notable among the results was the close similarity, with respect to amino acid composition, of reindeer and caribou caseins. The results of the amino acid analyses of the other caseins are present...
[Distribution of surface electric potentials in the horse heart].
Veterinarni medicina    October 1, 1976   Volume 21, Issue 10 623-631 
Chvátal O, Hanák J.Surface electric potentials of the heart of four horses were measured by use of unipolar leak with the so called central Wilson's clip; the measurements were performed on 95 precisely fixed places of the equine body. Potentials found out in this way were re-measured with bipolar leaks: the negative electrode was fixed in the place of the highest negative potentials, the positive electrode was gradually attached to places with the highest values of positive potentials. The largest potential differences when the negative electrode was placed in the region of the heart were obtained from the regi...
[Study of hydrolysis of aminoalcohol ethers, phenol and choline under the action of horse blood serum cholinesterase].
Biokhimiia (Moscow, Russia)    October 1, 1976   Volume 41, Issue 10 1773-1777 
Kundriutskova LA, Kruglikova RI.Hydrolysis of ethers of saturated and unsaturated alcohols and ethers, e.g. phenol and choline, under the action of horse blood serum cholinesterase, was studied. The reactivity towards enzymatic hydrolysis is decreased due to a greater length of the chain in the alcohol residue of the benzoic acid aminoethers; at nCH2 = 4 the compound is a poor substrate. An increase in nydrophobicity of the acyl residue of the ether molecule also leads to a decrease in the Vmax and Km values. In case of cholinesterase substrates, an increase in the molecule hydrophobicity results in an increase of its non-pr...
Catalytic iodination of proteins by horse myeloperoxidase in solid state.
Analytical biochemistry    May 7, 1976   Volume 72 372-379 doi: 10.1016/0003-2697(76)90544-3
Dubin A, Silberring J.No abstract available