Analyze Diet

Topic:Molecular biology

Molecular biology in horses involves the study of molecular processes and genetic mechanisms that underpin equine physiology and health. This field encompasses the analysis of DNA, RNA, proteins, and other biomolecules to understand gene expression, genetic variation, and cellular functions in horses. Techniques such as genomic sequencing, gene expression profiling, and molecular diagnostics are employed to explore topics like hereditary diseases, performance traits, and immune responses in equines. This page assembles peer-reviewed research studies and scholarly articles that investigate the molecular biology of horses, focusing on genetic research, molecular techniques, and their applications in equine science.
Characterization of an equine infectious anemia antigen extracted from infected horse spleen tissue.
Infection and immunity    November 1, 1971   Volume 4, Issue 5 528-531 doi: 10.1128/iai.4.5.528-531.1971
Norcross NL, Coggins L.The spleens of horses infected with equine infectious anemia contain an antigen that is useful for a diagnostic immunodiffusion test. This antigen was extracted from the spleen by homogenization of the tissue, centrifugation, and precipitation from the supernatant fluid at 50% saturation with (NH(4))(2)SO(4). The antigen was purified by subjecting it to two cycles of electrophoresis in a continuous free-flow electrophoresis cell and finally filtering through a column of Sephadex G-200 gel. The antigen was found to be a small protein with a molecular weight of 27,500 and sedimentation coefficie...
The complete enzymic hydrolysis of horse muscle acyl phosphatase.
Life sciences. Pt. 2: Biochemistry, general and molecular biology    September 8, 1971   Volume 10, Issue 17 983-988 doi: 10.1016/0024-3205(71)90101-9
Ramponi G, Cappugi G, Treves C, Nassi P.No abstract available
[Combined inhibition of horse serum cholinesterase by diphenylphosphinic and diphenylthiophosphinic esters].
Doklady Akademii nauk SSSR    September 1, 1971   Volume 200, Issue 1 103-106 
Brestkin AP, Brik IL, Volkova RI, Godovikov NN, Gurdaliev KhKh.No abstract available
[Characterization of horse spleen apoferritin by electrofocuing column fractionation].
Igaku to seibutsugaku. Medicine and biology    August 8, 1971   Volume 83, Issue 2 57-60 
Nitsu Y, Ishitani K, Urushizaki K.No abstract available
The binding of carbon dioxide by horse haemoglobin.
The Biochemical journal    August 1, 1971   Volume 124, Issue 1 31-45 doi: 10.1042/bj1240031
Kilmartin JV, Rossi-Bernardi L.1. Three modified horse haemoglobins have been prepared: (i) alpha(c) (2)beta(c) (2), in which both the alpha-amino groups of the alpha- and beta-chains have reacted with cyanate, (ii) alpha(c) (2)beta(2), in which the alpha-amino groups of the alpha-chains have reacted with cyanate, and (iii) alpha(2)beta(c) (2), in which the two alpha-amino groups of the beta-chain have reacted with cyanate. 2. The values of n (the Hill constant) for alpha(c) (2)beta(c) (2), alpha(2)beta(c) (2) and alpha(c) (2)beta(2) were (respectively) 2.5, 2.0 and 2.6, indicating the presence of co-operative interactions ...
The subunit structure of horse spleen apoferritin. I. The molecular weight of the subunit.
The Journal of biological chemistry    July 10, 1971   Volume 246, Issue 13 4198-4205 
Bryce CF, Crichton RR.No abstract available
Purification and properties of butyrylcholinesterase from horse serum.
Archives of biochemistry and biophysics    July 1, 1971   Volume 145, Issue 1 55-63 doi: 10.1016/0003-9861(71)90009-9
Lee JC, Harpst JA.No abstract available
Influence of chemical modifications of the reactive SH groups on the proton binding behaviour of human and horse hemoglobin.
Biochimica et biophysica acta    June 29, 1971   Volume 236, Issue 3 777-779 doi: 10.1016/0005-2795(71)90262-5
Janssen LH, de Bruin SH, van OS GA.No abstract available
Limited proteolysis of horse heart cytochrome c.
European journal of biochemistry    June 11, 1971   Volume 20, Issue 3 414-419 doi: 10.1111/j.1432-1033.1971.tb01407.x
Schejter A, Goldkorn T, Sokolovsky M.No abstract available
Structure and functional properties of chemically modified horse hemoglobin. I. Determination of the functional properties.
Journal of molecular biology    May 28, 1971   Volume 58, Issue 1 69-77 doi: 10.1016/0022-2836(71)90232-4
Simon SR, Arndt DJ, Konigsberg WH.No abstract available
Structure and functional properties of chemically modified horse hemoglobin. II. X-ray studies.
Journal of molecular biology    May 28, 1971   Volume 58, Issue 1 79-88 doi: 10.1016/0022-2836(71)90233-6
Moffat JK.No abstract available
Experimental variability of Venezuelan equine encephalomyelitis virus. I. Properties of mutants induced by alkylating compounds.
Soviet genetics    May 1, 1971   Volume 7, Issue 5 655-660 
Solyanik RG, Podoplekin VD, Fedorov YV.No abstract available
On the electron-transfer-coupled proton release of cytochrome c.
Biochimica et biophysica acta    April 6, 1971   Volume 234, Issue 1 57-61 doi: 10.1016/0005-2728(71)90129-0
Czerlinski GH, Dar K.No abstract available
[Comparative studies on the biochemical nature of myosin–smooth and skele- tal muscle myosin].
Seikagaku. The Journal of Japanese Biochemical Society    April 1, 1971   Volume 43, Issue 4 185-196 
Yamaguchi M.No abstract available
Chemical and immunochemical properties of two classes of globoside from equine organs.
The Japanese journal of experimental medicine    February 1, 1971   Volume 41, Issue 1 67-81 
Naiki M.No abstract available
Equine arteritis virus: ferritin-tagging and determination of ribonucleic acid core.
Archiv fur die gesamte Virusforschung    January 1, 1971   Volume 35, Issue 2 290-295 doi: 10.1007/BF01249721
Breese SS, McCollum WH.No abstract available
Occurrence of 19-oxoandrost-4-ene-3,17-dione in the course of oestrogen biosynthesis by equine testicular microsomes.
Acta endocrinologica    January 1, 1971   Volume 67, Issue 4 665-676 doi: 10.1530/acta.0.0670665
Oh R, Tamaoki B.No abstract available
Cholinesterase bonded to paper.
Canadian journal of biochemistry    December 1, 1970   Volume 48, Issue 12 1314-1317 doi: 10.1139/o70-204
Stasiw RO, Brown HD, Hasselberger FX.No abstract available
Three dimensional fourier synthesis of horse deoxyhaemoglobin at 2.8 Angstrom units resolution.
Nature    November 7, 1970   Volume 228, Issue 5271 551-552 doi: 10.1038/228551a0
Bolton W, Perutz MF.No abstract available
Horse haemoglobin polymorphism: evidence for two linked non-allelic alpha-chain genes.
Proceedings of the Royal Society of London. Series B, Biological sciences    November 3, 1970   Volume 176, Issue 1043 235-246 doi: 10.1098/rspb.1970.0041
Clegg JB.No abstract available
Equine antihapten antibody. Studies on the primary structure and conformation of equine immunoglobulins.
Biochemistry    October 27, 1970   Volume 9, Issue 22 4310-4321 doi: 10.1021/bi00824a011
Rockey JH, Montgomery PC, Dorrington KJ.No abstract available
Stabilization of horse globin by protoporphyrin IX and hemin.
The Journal of biological chemistry    October 25, 1970   Volume 245, Issue 20 5395-5403 
Sebring ED, Steinhardt J.No abstract available
Structure of dermatan sulfate. VII. The copolymeric structure of dermatan sulfate from horse aorta.
The Journal of biological chemistry    September 25, 1970   Volume 245, Issue 18 4770-4783 
Fransson LA, Havsmark B.The structure of dermatan sulfate-chondroitin sulfate copolymers, isolated from horse aorta, has been examined. It was found that a large proportion of the galactosaminoglycans of this tissue was obtained as a discrete polysaccharide fraction with an L-iduronic acid to D-glucuronic acid ratio of approximately 1: 2. This finding together with infrared data indicated that the polymer contained approximately equimolar proportions of the three repeating disaccharide units glucuronosyl-N-acetylgalactosamine 4-sulfate (A), iduronosyl-N-acetylgalactosamine 4-sulfate (B), and glucuronosyl-N-acet...
Ferritin and ferritin iron measurement in tissues by a quantitative immunoprecipitation technique.
Analytical biochemistry    September 1, 1970   Volume 37, Issue 1 64-72 doi: 10.1016/0003-2697(70)90258-7
Leslie AJ, Kaldor I.No abstract available
Preparation and properties of smooth muscle myosin from horse esophagus.
Biochimica et biophysica acta    September 1, 1970   Volume 216, Issue 2 411-421 doi: 10.1016/0005-2728(70)90233-1
Yamaguchi M, Miyazawa Y, Sekine T.Myosin was prepared from smooth muscle of horse esophagus in good yield (about 15 ° mg/Ioo g tissue) and was designated myosin S. Its properties were compared with those of myosin A from skeletal muscle. The ratio of the absorption of myosin S at 280 nm to that at 26o nm was about 1.8, and the amount of contaminating phosphorus was only o.91 g/io 5 g of myosin S, indicating that the latter is free of nucleic acid. The purity of this protein was examined by ultracentrifugation, gel filtration in the presence of 0.5 M KC1 and 6 M urea and chromatography on DEAE-cellulose columns. These e...
Molecular weight and amino acid composition of equine thrombin.
Journal of biochemistry    August 1, 1970   Volume 68, Issue 2 193-198 doi: 10.1093/oxfordjournals.jbchem.a129346
Inada Y, Matsushima A, Kotoku I, Hossain SA, Shibata K.No abstract available
Horse liver alcohol dehydrogenase. The primary structure of an N-terminal part of the protein chain of the ethanol-active isoenzyme.
European journal of biochemistry    July 1, 1970   Volume 14, Issue 3 521-534 doi: 10.1111/j.1432-1033.1970.tb00319.x
Jörnvall H.No abstract available
Comparative action of various kininogenases on crude horse plasma substrates.
Biochemical pharmacology    June 1, 1970   Volume 19, Issue 6 2083-2090 doi: 10.1016/0006-2952(70)90306-0
Budnitskaya P, Gapanhuk E, Henriques OB.The kininogenase activity of trypsin, plasmin, plasma kallikrein and heated Bothrops venom was compared, using fresh, heated and heat-acid-denatured horse plasma as source of kininogen. The venom kininogenase was found to have the highest activity on fresh horse plasma, followed by plasmin and trypsin which were equally active, and plasma kallikrein which was half as active as plasmin on these substrates. Plasmin and trypsin released more kinin from heat-treated than from fresh plasma whereas kallikrein released half as much as it liberates from fresh plasma. On heat-aciddenatured plasma equal...
Studies on equine immunoglobulins. I. The antigenic structure of horse IgG, its fragments and subunits.
Immunochemistry    May 1, 1970   Volume 7, Issue 5 401-412 doi: 10.1016/0019-2791(70)90222-3
Helms CM, Allen PZ.Immunodiffusion analysis of papain digestion products, heavy and light chains of horse IgG-globulins with several rabbit and anti-horse IgG sera, have permitted the demonstration of five antigenic specificities (Fc1, Fc2, L, Lsp and Fabsp) associated with these equine antigens. Reactivity with anti-Fc1 is shown by both F′c and Fc fragments, while anti-Fc2 reactivity is shown only by Fc fragment. Absorption of anti-Fab serum with L chain Fc fragment provides a reagent (anti-Fabsp) which precipitates only with Fab fragment, IgG-globulin or reduced and alkylated IgG. Upon exposure to deterge...
[Biosynthesis of N-acetyl-O-acetylneuraminic acids. I. Incorporation of (14C) acetate into sections of the submaxillary salivary gland of ox and horse].
Hoppe-Seyler's Zeitschrift fur physiologische Chemie    May 1, 1970   Volume 351, Issue 5 595-602 
Schauer R.No abstract available