Analyze Diet

Animal genetics.

Periodical
Genetics
Zoology
Animals
Publisher:
Published by Blackwell Scientific Publications for the International Society for Animal Blood Group Research,. Oxford, England : Wiley-Blackwell
Frequency: Bimonthly,
Country: England
Language: English
Author(s):
International Society for Animal Blood Group Research., International Society for Animal Genetics.
Start Year:1986 -
ISSN:
0268-9146 (Print)
1365-2052 (Electronic)
0268-9146 (Linking)
Impact Factor
2.4
2022
NLM ID:8605704
(DNLM):SR0056566(s)
(OCoLC):13459823
Coden:ANGEE3
LCCN:sf 93095318
Classification:W1 AN228P
Joint report of the Third International Workshop on Lymphocyte Alloantigens of the Horse, Kennett Square, Pennsylvania, 25-27 April 1984.
Animal genetics    January 1, 1986   Volume 17, Issue 4 363-373 doi: 10.1111/j.1365-2052.1986.tb00730.x
Antczak DF, Bailey E, Barger B, Guerin G, Lazary S, McClure J, Mottironi VD, Symons R, Templeton J, Varewyck H.The Third International Workshop on Lymphocyte Alloantigens of the Horse was held on 25-27 April 1984 in Kennett Square, Pennsylvania. Twelve laboratories from five countries participated. The principal purpose of this Workshop was to determine the phenotypic and gene frequencies of the 10 equine lymphocyte antigens (ELA) and a non-ELA lymphocyte antigen, ELY-2.1, in several breeds of horse. A total of 86 alloantisera characterized in previous workshops were tested against lymphocytes from 1179 horses. In addition, several experimental antisera were also tested against the same panel of lympho...
Genetic linkage between loci for a red cell alloantigen (U) and serum protease inhibitor (Pi) in the horse.
Animal genetics    January 1, 1986   Volume 17, Issue 3 217-223 doi: 10.1111/j.1365-2052.1986.tb03193.x
Bowling AT.Preliminary evidence for the fifth autosomal linkage group in the horse, comprised of the loci for a red cell alloantigen (U) and serum protease inhibitor (Pi), was demonstrated by means of paternal half-sib groups in thoroughbred, standardbred and Arabian breeds. Recombination frequency in males was estimated to be 0.125 +/- 0.019.
Electrophoretic polymorphism and molecular structure of equine C3.
Animal genetics    January 1, 1986   Volume 17, Issue 3 209-215 doi: 10.1111/j.1365-2052.1986.tb03192.x
Kay PH, Dawkins RL, Bowling AT, Bernoco D.Plasma or serum samples from 12 Arabian and 181 standardbred horses have been typed using an immunofixation technique to determine electrophoretic polymorphism of equine third complement component (C3). Six distinctly different electrophoretic patterns of equine C3 have been recognized thus far. SDS PAGE analysis of equine C3/anti C3 complexes revealed that the submolecular structure comprised an alpha chain and beta chain of molecular weights approximately 118,000 and 63,000 daltons respectively. The molecular weights of the alpha and beta chains were similar in all electrophoretic variants t...
Polymorphic restriction sites in the horse beta-globin gene cluster.
Animal genetics    January 1, 1986   Volume 17, Issue 3 245-253 doi: 10.1111/j.1365-2052.1986.tb03196.x
Rando A, Di Gregorio P, Masina P.Horse DNA samples digested with PstI and probed with the rabbit beta 1 globin gene show three phenotypes determined by one fragment of variable length (about 5.1 or 3.3 kb). Family data demonstrate that these fragments segregate as Mendelian alleles. The frequencies of the two alleles are 0.66 for the 3.3-kb fragment and 0.34 for the 5.1-kb one. Another polymorphism has been detected with BamHI. Again three phenotypes determined by two alleles (fragments of 7.5 and 3.8 kb) have been observed. Allelic frequencies of the 7.5- and 3.8-kb fragments are 0.24 and 0.76 respectively. The two polymorph...
DNA polymorphism in the major histocompatibility complex of man and various farm animals.
Animal genetics    January 1, 1986   Volume 17, Issue 2 113-133 doi: 10.1111/j.1365-2052.1986.tb00732.x
Vaiman M, Chardon P, Cohen D.In the past few years it has been possible by combining enzymatic cleavage of genomic DNA and the Southern blot hybridization technique to explore the endonuclease recognition site polymorphism of the MHC. HLA class I and DR and DQ alpha and beta class II specific probes as well as human C4 and Bf class III probes were used. All these probes were shown to cross-hybridize with DNA from pigs, cattle, sheep and horses. Hybridization of human genomic DNA with a class I probe showed 15-25 bands per genome depending on the enzyme used. Distinct endonucleases generated clusters of restriction fragmen...
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