| Records |
| Author |
Alexander, F.; Benzie, D. |
| Title |
A radiological study of the digestive tract of the foal |
Type |
Journal Article |
| Year |
1951 |
Publication |
Quarterly journal of experimental physiology and cognate medical sciences |
Abbreviated Journal |
Q J Exp Physiol Cogn Med Sci |
| Volume |
36 |
Issue |
4 |
Pages |
213-217 |
| Keywords |
Gastrointestinal Tract/*radiography; *Horses; *GASTROINTESTINAL SYSTEM/radiography; *Horses; *MYOCARDITIS/etiology and pathogenesis |
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English |
Summary Language |
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Abbreviated Series Title |
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Edition |
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| ISSN |
0033-5541 |
ISBN |
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| Notes |
PMID:14892238 |
Approved |
no |
| Call Number |
refbase @ user @ |
Serial |
129 |
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| Author |
Branchi, I.; Bichler, Z.; Berger-Sweeney, J.; Ricceri, L. |
| Title |
Animal models of mental retardation: from gene to cognitive function |
Type |
Journal Article |
| Year |
2003 |
Publication |
Neuroscience and Biobehavioral Reviews |
Abbreviated Journal |
Neurosci Biobehav Rev |
| Volume |
27 |
Issue |
1-2 |
Pages |
141-153 |
| Keywords |
Animals; Animals, Genetically Modified/growth & development; Behavior/physiology; Behavior, Animal; Brain/*growth & development; Cognition/*physiology; *Disease Models, Animal; Environment; Genes; Genetic Diseases, Inborn/physiopathology; Humans; Mental Retardation/classification/*genetics/*physiopathology |
| Abstract |
About 2-3% of all children are affected by mental retardation, and genetic conditions rank among the leading causes of mental retardation. Alterations in the information encoded by genes that regulate critical steps of brain development can disrupt the normal course of development, and have profound consequences on mental processes. Genetically modified mouse models have helped to elucidate the contribution of specific gene alterations and gene-environment interactions to the phenotype of several forms of mental retardation. Mouse models of several neurodevelopmental pathologies, such as Down and Rett syndromes and X-linked forms of mental retardation, have been developed. Because behavior is the ultimate output of brain, behavioral phenotyping of these models provides functional information that may not be detectable using molecular, cellular or histological evaluations. In particular, the study of ontogeny of behavior is recommended in mouse models of disorders having a developmental onset. Identifying the role of specific genes in neuropathologies provides a framework in which to understand key stages of human brain development, and provides a target for potential therapeutic intervention. |
| Address |
Section of Behavioural Pathophysiology, Laboratorio di Fisiopatologia di Organo e di Sistema, Istituto Superiore di Sanita, Viale Regina Elena 299, 00161 Roma, Italy. branchi@iss.it |
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English |
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Series Issue |
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Edition |
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| ISSN |
0149-7634 |
ISBN |
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Medium |
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Expedition |
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Conference |
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| Notes |
PMID:12732230 |
Approved |
no |
| Call Number |
Equine Behaviour @ team @ |
Serial |
2805 |
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| Author |
Czeh, B.; Muller-Keuker, J.I.H.; Rygula, R.; Abumaria, N.; Hiemke, C.; Domenici, E.; Fuchs, E. |
| Title |
Chronic Social Stress Inhibits Cell Proliferation in the Adult Medial Prefrontal Cortex: Hemispheric Asymmetry and Reversal by Fluoxetine Treatment |
Type |
Journal Article |
| Year |
2006 |
Publication |
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Abbreviated Journal |
Neuropsychopharmacology |
| Volume |
32 |
Issue |
7 |
Pages |
1490-1503 |
| Keywords |
neurogenesis, stereology, cell number, glia, NG2, hippocampus |
| Abstract |
Profound neuroplastic changes have been demonstrated in various limbic structures after chronic stress exposure and antidepressant treatment in animal models of mood disorders. Here, we examined in rats the effect of chronic social stress and concomitant antidepressant treatment on cell proliferation in the medial prefrontal cortex (mPFC). We also examined possible hemispheric differences. Animals were subjected to 5 weeks of daily social defeat by an aggressive conspecific and received concomitant, daily, oral fluoxetine (10 mg/kg) during the last 4 weeks. Bromodeoxyuridine (BrdU) labeling and quantitative stereological techniques were used to evaluate the treatment effects on proliferation and survival of newborn cells in limbic structures such as the mPFC and the hippocampal dentate gyrus, in comparison with nonlimbic structures such as the primary motor cortex and the subventricular zone. Phenotypic analysis showed that neurogenesis dominated the dentate gyrus, whereas in the mPFC most newborn cells were glia, with smaller numbers of endothelial cells. Chronic stress significantly suppressed cytogenesis in the mPFC and neurogenesis in the dentate gyrus, but had minor effect in nonlimbic structures. Fluoxetine treatment counteracted the inhibitory effect of stress. Hemispheric comparison revealed that the rate of cytogenesis was significantly higher in the left mPFC of control animals, whereas stress inverted this asymmetry, yielding a significantly higher incidence of newborn cells in the right mPFC. Fluoxetine treatment abolished hemispheric asymmetry in both control and stressed animals. These pronounced changes in gliogenesis after chronic stress exposure may relate to the abnormalities of glial cell numbers reported in the frontolimbic areas of depressed patients. |
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Series Title |
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Abbreviated Series Title |
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Series Issue |
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Edition |
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| ISSN |
0893-133x |
ISBN |
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Medium |
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Approved |
no |
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Equine Behaviour @ team @ |
Serial |
5785 |
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| Author |
Danchin, E.; Giraldeau, L.-A.; Valone, T.J.; Wagner, R.H. |
| Title |
Public information: from nosy neighbors to cultural evolution |
Type |
Journal Article |
| Year |
2004 |
Publication |
Science (New York, N.Y.) |
Abbreviated Journal |
Science |
| Volume |
305 |
Issue |
5683 |
Pages |
487-491 |
| Keywords |
Animals; *Behavior, Animal; Cues; *Cultural Evolution; *Decision Making; Environment; Evolution; Feeding Behavior; Female; Genes; Humans; Male; Reproduction; Sexual Behavior, Animal |
| Abstract |
Psychologists, economists, and advertising moguls have long known that human decision-making is strongly influenced by the behavior of others. A rapidly accumulating body of evidence suggests that the same is true in animals. Individuals can use information arising from cues inadvertently produced by the behavior of other individuals with similar requirements. Many of these cues provide public information about the quality of alternatives. The use of public information is taxonomically widespread and can enhance fitness. Public information can lead to cultural evolution, which we suggest may then affect biological evolution. |
| Address |
U.P.M.C. CNRS-UMR7625, Bat A-7e etage-Case 237, 7 quai Saint Bernard, 75252 Paris Cedex 05, France. edanchin@snv.jussieu.fr |
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English |
Summary Language |
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Abbreviated Series Title |
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Series Issue |
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Edition |
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| ISSN |
1095-9203 |
ISBN |
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Medium |
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Expedition |
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Conference |
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| Notes |
PMID:15273386 |
Approved |
no |
| Call Number |
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Serial |
2131 |
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| Author |
Hoshaw, B.A.; Evans, J.C.; Mueller, B.; Valentino, R.J.; Lucki, I. |
| Title |
Social competition in rats: Cell proliferation and behavior |
Type |
Journal Article |
| Year |
2006 |
Publication |
Behavioural Brain Research |
Abbreviated Journal |
Behav. Brain. Res. |
| Volume |
175 |
Issue |
2 |
Pages |
343-351 |
| Keywords |
Social stress; Depression; Forced swim test; Neurogenesis |
| Abstract |
Behavioral and physiological changes were studied following prolonged exposure to social competition in pairs of non-food-deprived rats competing daily for a limited supply of graham cracker crumbs. Stable dominant-subordinate relationships developed in most pairs, as measured by feeding time, which were maintained over a 5-6-week study period. In other behavioral tests, subordinates demonstrated a decreased latency to immobility in the forced swim test compared with dominants, but no difference in locomotor activity. Subordinates had increased bladder size, decreased adrenal gland size, and a 35% reduction of hippocampus cell proliferation compared with the dominant member. Therefore, prolonged social competition, based on restricted access to palatable substances, produced hierarchies among individuals that were associated with differences in behavior, physiology and hippocampal cell proliferation. |
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no |
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refbase @ user @ |
Serial |
802 |
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| Author |
Hostikka, S.L.; Eddy, R.L.; Byers, M.G.; Hoyhtya, M.; Shows, T.B.; Tryggvason, K. |
| Title |
Identification of a distinct type IV collagen alpha chain with restricted kidney distribution and assignment of its gene to the locus of X chromosome-linked Alport syndrome |
Type |
Journal Article |
| Year |
1990 |
Publication |
Proceedings of the National Academy of Sciences of the United States of America |
Abbreviated Journal |
Proc. Natl. Acad. Sci. U.S.A. |
| Volume |
87 |
Issue |
4 |
Pages |
1606-1610 |
| Keywords |
Amino Acid Sequence; Base Sequence; Chromosome Mapping; Cloning, Molecular; Collagen/*genetics; Epitopes/analysis; Female; Fluorescent Antibody Technique; Gene Library; *Genes; Humans; Immunoblotting; Kidney/cytology/*metabolism; Macromolecular Substances; Molecular Sequence Data; Nephritis, Hereditary/*genetics; Oligopeptides/chemical synthesis/immunology; Placenta/metabolism; Pregnancy; Restriction Mapping; Sequence Homology, Nucleic Acid; *X Chromosome |
| Abstract |
We have identified and extensively characterized a type IV collagen alpha chain, referred to as alpha 5(IV). Four overlapping cDNA clones isolated contain an open reading frame for 543 amino acid residues of the carboxyl-terminal end of a collagenous domain, a 229-residue carboxyl-terminal noncollagenous domain, and 1201 base pairs coding for a 3' untranslated region. The collagenous Gly-Xaa-Yaa repeat sequence has five imperfections that coincide with those in the corresponding region of the alpha 1(IV) chain. The noncollagenous domain has 12 conserved cysteine residues and 83% and 63% sequence identity with the noncollagenous domains of the alpha 1(IV) and alpha 2(IV) chains, respectively. The alpha 5(IV) chain has less sequence identity with the putative bovine alpha 3(IV) and alpha 4(IV) chains. Antiserum against an alpha 5(IV) synthetic peptide stained a polypeptide chain of about 185 kDa by immunoblot analysis and immunolocalization of the chain in human kidney was almost completely restricted to the glomerulus. The gene was assigned to the Xq22 locus by somatic cell hybrids and in situ hybridization. This may be identical or close to the locus of the X chromosome-linked Alport syndrome that is believed to be a type IV collagen disease. |
| Address |
Biocenter, University of Oulu, Finland |
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English |
Summary Language |
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Edition |
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0027-8424 |
ISBN |
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| Notes |
PMID:1689491 |
Approved |
no |
| Call Number |
Equine Behaviour @ team @ |
Serial |
5291 |
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| Author |
Penzhorn, B. L.; van der Merwe, N. J. |
| Title |
Testis size and onset of spermatogenesis in Cape mountain zebras (Equus zebra zebra) |
Type |
Journal Article |
| Year |
1988 |
Publication |
Journal of Reproduction and Fertility |
Abbreviated Journal |
J Reprod Fert |
| Volume |
83 |
Issue |
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Pages |
371-375 |
| Keywords |
mountain zebra; testis size; spermatogenesis |
| Abstract |
Testis mass of adult Cape mountain zebra stallions (mean 70·0 g) was appreciably less than that of other zebra species and domestic horses. The histological appearance of the testes of 11-, 24- and 29-month-old colts was typically prepubertal. Spermatogenic activity of a 4-year-old stallion obtained at the end of summer was at a very low level, while a 4·5-year-old stallion obtained 6 weeks after the winter solstice showed a marked increase in spermatogenesis compared with the 4-year-old. Stallions 6·5-19 years of age collected in different seasons all showed active spermatogenesis. |
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| Notes |
from Professor Hans Klingels Equine Reference List |
Approved |
yes |
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Serial |
1463 |
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| Author |
Thiruvenkadan, A.K.; Kandasamy, N.; Panneerselvam, S. |
| Title |
Coat colour inheritance in horses |
Type |
Journal Article |
| Year |
2008 |
Publication |
Livestock Science |
Abbreviated Journal |
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| Volume |
117 |
Issue |
2-3 |
Pages |
109-129 |
| Keywords |
Horse; Coat colour; Melanogenesis; Genetic control; Molecular genetics |
| Abstract |
The colours of the horses have long been a subject of interest to owners and breeders of horses as well as to scientists. Though, the colour of horses has little to do with its performance, it is a primary means of identification and also the first indicator of questionable parentage. Probably the ancestral colour of the horse was a black-based pattern that provided camouflage protection against predators. Horse colours are mostly controlled by genes at 12 different loci. The three basic colours of horses are black, bay and chestnut. The genetic control of the basic colours of horses resides at two genetic loci, namely Extension (E) and Agouti (A) loci. Among the basic colours bay is dominant to black and both are epistatic to chestnut. Dilution of basic colours of horses as a result of four colour dilution genes such as cream dilution, dun, silver dapple and champagne resulted in extensive array of possible colours of horses. The most widespread and familiar of the horse colour dilution gene is the one that produces the golden body colour and are called as palomino or buckskin based on the colour of the points. The grey coat colour is due to the presence of dominant gene (G) at the grey locus. Grey is epistatic to all coat colour genes except white and a grey horse must have at least one grey parent. Roan is due to a dominant gene (Rn) at roan locus and this combines with any base colour to produce the various shades of roan pattern. White coat is due to a single dominant gene (W) and it is epistatic to the genes controlling all other colours. White marking in the face and legs are due to genetic and non-genetic factors. Several genes are involved in producing white markings. During recent years, comparative genomics and whole genome scanning have been used to develop DNA tests for different variety of horse colours. Molecular genetic studies on coat colour in horses helped in identification of the genes and mutation responsible for coat colour variants. In future, this will be applied to breeding programmes to reduce the incidence of diseases and to increase the efficiency of race horse population. |
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Edition |
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| ISSN |
1871-1413 |
ISBN |
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Approved |
no |
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Equine Behaviour @ team @ |
Serial |
4776 |
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| Author |
Tumova, B. |
| Title |
Equine influenza--a segment in influenza virus ecology |
Type |
Journal Article |
| Year |
1980 |
Publication |
Comparative Immunology, Microbiology and Infectious Diseases |
Abbreviated Journal |
Comp Immunol Microbiol Infect Dis |
| Volume |
3 |
Issue |
1-2 |
Pages |
45-59 |
| Keywords |
Animals; Antigens, Viral; Genes, Viral; Horse Diseases/*microbiology; Horses; Influenza A virus/immunology/pathogenicity/*physiology; Orthomyxoviridae Infections/microbiology/*veterinary; Viral Proteins/analysis |
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English |
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Series Title |
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Abbreviated Series Title |
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Series Issue |
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Edition |
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| ISSN |
0147-9571 |
ISBN |
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| Notes |
PMID:6258849 |
Approved |
no |
| Call Number |
Equine Behaviour @ team @ |
Serial |
2691 |
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| Author |
Ulloa, A.; Gonzalez-Ceron, L.; Rodriguez, M.H. |
| Title |
Host selection and gonotrophic cycle length of Anopheles punctimacula in southern Mexico |
Type |
Journal Article |
| Year |
2006 |
Publication |
Journal of the American Mosquito Control Association |
Abbreviated Journal |
J Am Mosq Control Assoc |
| Volume |
22 |
Issue |
4 |
Pages |
648-653 |
| Keywords |
Animals; Anopheles/*physiology; Appetitive Behavior/*physiology; Cattle; Female; Horses; Humans; Insect Vectors/*physiology; Malaria/transmission; Mexico; Oviparity/*physiology; Seasons; Time Factors; Vitellogenesis/physiology |
| Abstract |
The host preference, survival rates, and length of the gonotrophic cycle of Anopheles punctimacula was investigated in southern Mexico. Mosquitoes were collected in 15-day separate experiments during the rainy and dry seasons. Daily changes in the parous-nulliparous ratio were recorded and the gonotrophic cycle length was estimated by a time series analysis. Anopheles punctimacula was most abundant during the dry season and preferred animals to humans. The daily survival rate in mosquitoes collected in animal traps was 0.96 (parity rate = 0.86; gonotrophic cycle = 4 days). The length of gonotrophic cycle of 4 days was estimated on the base of a high correlation coefficient value appearing every 4 days. The minimum time estimated for developing mature eggs after blood feeding was 72 h. The proportion of mosquitoes living enough to transmit Plasmodium vivax malaria during the dry season was 0.35. |
| Address |
Centro de Investigacion de Paludismo, Instituto Nacional de Salud Publica, Apartado Postal 537, Tapachula, Chiapas 30700, Mexico |
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English |
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Abbreviated Series Title |
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Series Issue |
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Edition |
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8756-971X |
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Conference |
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| Notes |
PMID:17304932 |
Approved |
no |
| Call Number |
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Serial |
1830 |
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