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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.
Microheterogeneity in ferritin molecules.
Biochimica et biophysica acta    April 28, 1970   Volume 207, Issue 1 256-258 doi: 10.1016/0005-2795(70)90158-3
Drysdale JW.No abstract available
N-Terminal sequences of equine and human immunoglobulin heavy chains.
Biochimica et biophysica acta    February 17, 1970   Volume 200, Issue 2 258-266 doi: 10.1016/0005-2795(70)90169-8
Montgomery PC, Bello AC, Rockey JH.N-terminal tetrapeptides from heavy chains of equine γGab- and γT-globulins, and of human γG and γA myeloma proteins and a γM macroglobulin, have been studied. The equine and human heavy chains lacked free α-amino-terminal groups. After mild alkaline hydrolysis, glutamic acid was identified as the terminal amino acid by reaction with dimethylaminonaphthalenesulfonyl chloride, tentatively identifying pyrrolid-2-one-5-carboxylic acid (PCA) as the unreactive terminal residue of each heavy chain. Peptides lacking a free α-amino group were isolated from subtilisin and pronase digests of the ...
A comparison of fingerprints of tryptic digests of human, horse and rat apoferritins.
Comparative biochemistry and physiology    February 1, 1970   Volume 32, Issue 3 451-458 doi: 10.1016/0010-406x(70)90462-7
Richter GW, Moppert GA, Lee JC.1. Fingerprints of tryptic digests of apoferritins from a human liver, horse spleens and ACI rat livers were made by means of electrophoresis and chromatography on microcrystalline cellulose, and were compared. 2. All tryptic peptides also present in apoferritins from the human liver and the horse spleens were also present in apoferritin from the rat livers. 3. In the digests of horse and of rat apoferritin there was a peptide that was not present in the digests of human apoferritin. Another peptide was obtained from human and from rat apoferritin, but not from horse apoferritin. 4. T...
Gene expression in an interspecific hybrid: analysis of hemoglobins in donkey, horse, and mule by peptide mapping.
Biochemical genetics    February 1, 1970   Volume 4, Issue 1 73-85 doi: 10.1007/BF00484019
Isaacs WA.No abstract available
Physicochemical studies of equine infectious anemia virus. IV. Determination of the nucleic acid type in the virus.
Archiv fur die gesamte Virusforschung    January 1, 1970   Volume 31, Issue 3 273-280 doi: 10.1007/BF01253762
Nakajima H, Tanaka S, Ushimi C.No abstract available
Structural comparison of the hemoglobins of the genus Equus with those of ruminants.
The Journal of biological chemistry    December 10, 1969   Volume 244, Issue 23 6533-6542 
Kitchen H, Easley CW.No abstract available
[Covalent structure of horse myoglobin].
European journal of biochemistry    December 1, 1969   Volume 11, Issue 2 267-277 doi: 10.1111/j.1432-1033.1969.tb00769.x
Dautrevaux M, Boulanger Y, Han K, Biserte G.No abstract available
Studies on the structure of ferritin and apoferritin from horse spleen. I. Tryptic digestion of ferritin and apoferritin.
Biochimica et biophysica acta    November 11, 1969   Volume 194, Issue 1 34-42 doi: 10.1016/0005-2795(69)90176-7
Crichton RR.No abstract available
Interaction of coenzyme with differently prepared zinc-free (apo) horse liver alcohol dehydrogenases.
The Journal of biological chemistry    November 10, 1969   Volume 244, Issue 21 5967-5971 
Hoagstrom CW, Iweibo I, Weiner H.No abstract available
Heterogeneity of erythrocyte catalase. Correlations between sulfhydryl group content, chromatographic and electrophoretic properties.
European journal of biochemistry    November 1, 1969   Volume 11, Issue 1 49-57 doi: 10.1111/j.1432-1033.1969.tb00737.x
Mörikofer-Zwez S, Cantz M, Kaufmann H, von Wartburg JP, Aebi H.No abstract available
Zinc isotope exchange in horse liver alcohol dehydrogenase.
Biochemistry    September 1, 1969   Volume 8, Issue 9 3792-3797 doi: 10.1021/bi00837a045
Drum DE, Li TK, Vallee BL.No abstract available
Occurrence and nature of equine and bovine myoglobin dimers.
European journal of biochemistry    August 1, 1969   Volume 10, Issue 1 140-145 doi: 10.1111/j.1432-1033.1969.tb00665.x
Van den Oord AH, Wesdorp JJ, Van Dam AF, Verheij JA.In commercial samples of equine myoglobin and samples of equine and bovine myoglobin prepared in the laboratory, a small amount of the protein was present as an aggregate. The presence of the myoglobin aggregate could be demonstrated by gel filtration on Sephadex G-100 Superfine, which also provided a means of isolating it. Gel filtration on Sephadex G-100 showed the molecular weights of the equine and bovine moyglobin aggregates to be about 35000 and 34000 respectively, thus supporting the hypothesis that they are dimers. This was confirmed for the equine myoglobin by ultracentrifugation meas...
[Middle peptide sequence obtained by cleaving horse myoglobin with cyanogen bromide].
Bulletin de la Societe de chimie biologique    July 25, 1969   Volume 51, Issue 3 439-455 
Han K, Boulanger Y, Dautrevaux M, Biserte G.No abstract available
Optical rotatory dispersion and circular dichroism of horse myoglobin and its derivatives.
Journal of biochemistry    May 1, 1969   Volume 65, Issue 5 759-766 doi: 10.1093/oxfordjournals.jbchem.a129075
Samejima T, Kita M.No abstract available
[Corecipitation: methods for analysing monovalent antibody fragments. I. Equine antidiphtheria system: hyperimmune sera].
Annales de l'Institut Pasteur    May 1, 1969   Volume 116, Issue 5 657-685 
Iscaki S, Raynaud M.No abstract available
Measurement of ligand-induced conformational changes in hemoglobin by circular dichroism.
Proceedings of the National Academy of Sciences of the United States of America    May 1, 1969   Volume 63, Issue 1 205-212 doi: 10.1073/pnas.63.1.205
Simon SR, Cantor CR.The UV circular-dichroism spectra of human and horse hemoglobins have been determined at various degrees of partial saturation with oxygen. Spectra of the two native hemoglobins were compared with spectra of the corresponding proteins modified with a reagent known to eliminate the conformational rearrangement normally associated with cooperativity. Such comparison indicates that one region, around 260 mmu, is sensitive chiefly to the state of the hemes; changes in another region, around 285 mmu, may be correlated with the conformational transformation linked to cooperative interactions. All ci...
Horse muscle acyl phosphatase: purification and some properties.
Archives of biochemistry and biophysics    March 1, 1969   Volume 130, Issue 1 362-369 doi: 10.1016/0003-9861(69)90045-9
Ramponi G, Guerritore A, Treves C, Nassi P, Baccari V.No abstract available
Binding of long chain alkyl sulphates to equine ferric myoglobin.
European journal of biochemistry    March 1, 1969   Volume 8, Issue 2 263-272 doi: 10.1111/j.1432-1033.1969.tb00523.x
van den Oord AH, Wesdorp JJ.When ferric myoglobin reacts with alkyl sulphates, its absorption spectrum changes into one characteristic of a haemichrome or parahaematin. The reaction equilibrium was studied over a range of protein concentrations using dodecyl sulphate and other alkyl sulphates with different chain lengths. The results obtained from spectrophotometric measurements and equilibrium dialysis experiments are not in agreement with those of other authors who, from an analysis of spectral changes only, supported the hypothesis of an all-or-none type of reaction whereby 18 detergent anions were bound to one molecu...
Studies on tissue culture of equine ovarian cell types: pathways of steroidogenesis.
The Journal of endocrinology    March 1, 1969   Volume 43, Issue 3 403-414 doi: 10.1677/joe.0.0430403
Channing CP.No abstract available
Studies on tissue culture of equine ovarian cell types: steroidogenesis.
The Journal of endocrinology    March 1, 1969   Volume 43, Issue 3 391-402 doi: 10.1677/joe.0.0430391
Channing CP, Grieves SA.No abstract available
Equine antihapten antibody. The molecular weights of the subunits of equine immunoglobulins.
Biochemistry    March 1, 1969   Volume 8, Issue 3 1247-1258 doi: 10.1021/bi00831a060
Montgomery PC, Dorrington KJ, Rockey JH.Three independent methods have been used to determine the molecular weights of the heavyand light-polypeptide chain subunits of equine yGab-, yGc-, and yT-immunoglobulins. Extensively reduced and alkylated proteins were filtered through standard columns of Sephadex G-100 or G-200 in 8 M urea405 M propionic acid. Subunit molecular weights were obtained from the linear elution volume, V,, us. logarithm molecular weight relationship defined for each column with rabbit yG-globulin heavy and light chains and horse heart cytochrome c. Molecular weights also were determined by equilibrium se...
The nucleic acid content of skeletal muscle and liver in mammals of different body size.
Comparative biochemistry and physiology    February 1, 1969   Volume 28, Issue 2 897-905 doi: 10.1016/0010-406x(69)92123-9
Munro HN, Gray JA.No abstract available
Granular localization of corticotropin-releasing activity in horse hypophysial stalk homogenate.
Endocrinologia japonica    February 1, 1969   Volume 16, Issue 1 171-177 doi: 10.1507/endocrj1954.16.171
Ishii S, Iwata T, Kobayashi H.No abstract available
[Structure of peptides isolated from chymotrypsin hydrolysates of horse myoglobin].
Bulletin de la Societe de chimie biologique    January 30, 1969   Volume 50, Issue 10 1651-1669 
Boulanger Y, Dautrevaux M, Han K, Biserte G.No abstract available
Equine immunoglobulins: a comparison of molecular properties.
Acta biochimica Polonica    January 1, 1969   Volume 16, Issue 3 279-296 
Buchowicz I, Goch H, Zakrzewski K.No abstract available
Cleavage of horse immunoglobulin by cyanogen bromide.
Immunochemistry    November 1, 1968   Volume 5, Issue 6 513-524 doi: 10.1016/0019-2791(68)90088-8
Ernst ML, Arnon R, Sela M.No abstract available
Succinylcholine analogs as substrates and inhibitors of pseudocholinesterase.
Journal of medicinal chemistry    November 1, 1968   Volume 11, Issue 6 1126-1128 doi: 10.1021/jm00312a005
Beckett AH, Vaughan CL, Mitchard M.No abstract available
The binding of plutonium to serum proteins in vitro.
Radiation research    October 1, 1968   Volume 36, Issue 1 22-30 
Turner GA, Taylor DM.The interactions between tetravalent plutonium and horse serum proteins were studied in vitro by electrophoresis on cellulose acetate and by gel filtration. The results show that in horse serum, as in other mammalian sera, the plutonium is associated principally with the transferrin component of the beta1-globulins. The formation of the plutonium-transferrin complex requires the presence of HCO3-, and plutonium is displaced from the complex by excess iron, thus indicating that similar binding sites may be involved in the complexing of iron and plutonium. The plutonium complex is considered to ...
Action of horse urinary kallikrein on synthetic derivatives of bradykinin.
Biochemical pharmacology    October 1, 1968   Volume 17, Issue 10 2232-2234 doi: 10.1016/0006-2952(68)90200-1
Babel I, Stella RC, Prado ES.Previous experiments indicated that horse urinary kallikrein (UK) hydrolyzes salminei- e and polyarginine, a but not polylysine. This paper reports the action of UK on bradykinyl-serine, methionyllysyl-bradykinin and lysyllysyl-bradykinin.
Comparison of protein structure in the crystal and in solution. V. Solubility of horse methemoglobin and azide binding.
Journal of molecular biology    August 14, 1968   Volume 35, Issue 3 477-481 doi: 10.1016/s0022-2836(68)80007-5
Rupley JA, Gates V.No abstract available