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MeSH Review

Papio hamadryas

 
 
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High impact information on Papio hamadryas

  • The brains of four baboons (Papio hamadryas, 20-30 yr of age) were examined using the Gallyas silver technique for neurofibrillary changes and phosphorylation-dependent anti-tau antibodies (AT8, AT100, AT270, PHF-1, TG-3) [1].
  • We investigated dietary effects on pleiotropic relationships among 3 HDL cholesterol (C) subfractions (HDL1-C, HDL2-C, and HDL3-C; levels quantified by gradient gel electrophoresis) for 942 pedigreed baboons (Papio hamadryas) who were fed a basal (Chow) diet and a high cholesterol, saturated fat (HCSF) challenge diet [2].
  • Notably, males characterized by hamadryas admixture had significantly higher concentrations of HVA, 5-HIAA, and MHPG (p < .05, respectively), a result possibly driven by differences in serotonergic activity [3].
  • Comparison of AR DNA coding sequence from five primate species, Homo sapiens (human), Pan troglodytes (chimpanzee), Papio hamadryas (baboon), Macaca fascicularis (macaque), and Eulemur fulvus collaris (collared brown lemur), supports their phylogeny with complete conservation of the DNA and steroid binding domain protein sequence [4].
  • Pregnancy-specific glycoprotein (PSG) in baboon (Papio hamadryas): family size, domain structure, and prediction of a functional region in primate PSGs [5].
 

Biological context of Papio hamadryas

 

Associations of Papio hamadryas with chemical compounds

  • Low-dose nitro-L-arginine administration in baboon (Papio hamadryas) pregnancy [8].
  • 1. The haemodynamic effects of intravenous nitric oxide inhibitor, N-nitro-L-arginine (NOLA), were examined in four conscious non-restrained baboons (Papio hamadryas) [9].
  • The sequences of the fibrinopeptides A from the three baboons were identical: (sequence: see text) The fibrinopeptides B were composed of 9 residues and demonstrated the sequence: (sequence see text) where X3 = Arg in P. anubis, His in P. hamadryas, and Gly in Th. gelada [10].
  • Baboons (Papio hamadryas) were infused intravenously with a nonhypotensive dose (0.1 microgram X min-1 X kg-1) of synthetic human atriopeptin III (ANF) for 60 min [11].
 

Gene context of Papio hamadryas

References

  1. Filamentous tau pathology in nerve cells, astrocytes, and oligodendrocytes of aged baboons. Schultz, C., Dehghani, F., Hubbard, G.B., Thal, D.R., Struckhoff, G., Braak, E., Braak, H. J. Neuropathol. Exp. Neurol. (2000) [Pubmed]
  2. Pleiotropy and genotype by diet interaction in a baboon model for atherosclerosis: a multivariate quantitative genetic analysis of HDL subfractions in two dietary environments. Mahaney, M.C., Blangero, J., Rainwater, D.L., Mott, G.E., Comuzzie, A.G., MacCluer, J.W., VandeBerg, J.L. Arterioscler. Thromb. Vasc. Biol. (1999) [Pubmed]
  3. Cerebrospinal fluid monoaminergic metabolites differ in wild anubis and hybrid (Anubis hamadryas) baboons: possible relationships to life history and behavior. Kaplan, J.R., Phillips-Conroy, J., Fontenot, M.B., Jolly, C.J., Fairbanks, L.A., Mann, J.J. Neuropsychopharmacology (1999) [Pubmed]
  4. Evolution of the primate androgen receptor: a structural basis for disease. Choong, C.S., Kemppainen, J.A., Wilson, E.M. J. Mol. Evol. (1998) [Pubmed]
  5. Pregnancy-specific glycoprotein (PSG) in baboon (Papio hamadryas): family size, domain structure, and prediction of a functional region in primate PSGs. Zhou, G.Q., Hammarström, S. Biol. Reprod. (2001) [Pubmed]
  6. A non-human primate study (baboon; Papio hamadryas) to determine if a long-acting progestogen, levonorgestrel butanoate, combined with a long-acting androgen, testosterone buciclate, can suppress spermatogenesis: II. Efficacy study. Goncharov, N.P., Katzia, G.V., Butnev, V.U., Gorlushkin, V.M., Waites, G.M. Int. J. Androl. (1995) [Pubmed]
  7. Luteinizing hormone levels during the menstrual cycle of the baboon (Papio hamadryas). Goncharov, N., Antonichev, A.V., Gorluschkin, V.M., Chachundocova, L., Robertson, D.M., Diczfalusy, E. Acta Endocrinol. (1979) [Pubmed]
  8. Low-dose nitro-L-arginine administration in baboon (Papio hamadryas) pregnancy. Hennessy, A., Gillin, A.G., Duggin, G.G., Horvath, J.S., Tiller, D.J. Clin. Exp. Pharmacol. Physiol. (1999) [Pubmed]
  9. Haemodynamic actions of a nitric oxide (EDRF) synthesis inhibitor in conscious baboons (Papio hamadryas). Hennessy, A., Whitworth, J.A., Raymond, C.J., Phippard, A.F., Thompson, J.F., Horvath, J.S. Clin. Exp. Pharmacol. Physiol. (1994) [Pubmed]
  10. Fibrinopeptides A and B of baboons (Papio anubis, Papio hamadryas, and Theropithecus gelada): their amino acid sequences and evolutionary rates and a molecular phylogeny for the baboons. Nakamura, S., Takenaka, O., Takahashi, K. J. Biochem. (1983) [Pubmed]
  11. Renal effects of atrial natriuretic factor in primate. Bourgoignie, J.J., Gavellas, G., Hwang, K.H. Am. J. Physiol. (1986) [Pubmed]
  12. A primate model of monotypism in atherosclerotic lesions. Henkel, R.D., Sharp, R.M., Galindo, L.V., Aivaliotis, M.J., Carey, K.D., McGill, H.C., VandeBerg, J.L. Exp. Mol. Pathol. (1993) [Pubmed]
  13. Low Y chromosome variation in Saudi-Arabian hamadryas baboons (Papio hamadryas hamadryas). Lawson Handley, L.J., Hammond, R.L., Emaresi, G., Reber, A., Perrin, N. Heredity (2006) [Pubmed]
  14. Nuclear DNA polymorphisms in a wild population of yellow baboons (Papio hamadryas cynocephalus) from Mikumi National Park, Tanzania. Rogers, J., Kidd, K.K. Am. J. Phys. Anthropol. (1993) [Pubmed]
  15. Bone ALP and OC reference standards in adult baboons (Papio hamadryas) by sex and age. Havill, L.M., Hale, L.G., Newman, D.E., Witte, S.M., Mahaney, M.C. J. Med. Primatol. (2006) [Pubmed]
  16. Androgen effects on bioactive and immunoreactive gonadotrophin levels during puberty in male baboons. Crawford, B.A., Spaliviero, J., Simpson, J., Handelsman, D.J. Journal of pediatric endocrinology & metabolism : JPEM. (1997) [Pubmed]
 
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