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Vet. Res.
Volume 39, Number 6, November-December 2008
Number of page(s) 16
DOI http://dx.doi.org/10.1051/vetres:2008035
Published online 22 August 2008
How to cite this article Vet. Res. (2008) 39:58
References of  Vet. Res. (2008) 39:58
  1. Balic A., Bowles V.M., Meeusen E.N., The immunobiology of gastrointestinal nematode infections in ruminants, Adv. Parasitol. (2000) 45:181–241 [PubMed].
  2. Batycka M., Inglis N.F., Cook K., Adam A., Fraser-Pitt D., Smith D.G., et al., Ultra-fast tandem mass spectrometry scanning combined with monolithic column liquid chromatography increases throughput in proteomic analysis, Rapid Commun. Mass Spectrom. (2006) 20:2074–2080 [CrossRef] [PubMed].
  3. Dunphy J.L., Balic A., Barcham G.J., Horvath A.J., Nash A.D., Meeusen E.N., Isolation and characterization of a novel inducible mammalian galectin, J. Biol. Chem. (2000) 275:32106–32113 [CrossRef] [PubMed].
  4. Dziva F., Mahajan A., Cameron P., Currie C., Mc-endrick I.J.,WallisT.S., et al.,EspP, aTypeV-secreted serine protease of enterohaemorrhagic Escherichia coli O157:H7, influences intestinal colonization of calves and adherence to bovine primary intestinal epithelial cells, FEMS Microbiol. Lett. (2007) 271:258–264 [CrossRef] [PubMed].
  5. French A.T., Bethune J.A., Knight P.A., McNeilly T.N., Wattegedera S., Rhind S., et al., The expression of intelectin in sheep goblet cells and upregulation by interleukin-4, Vet. Immunol. Immunopathol. (2007) 120:41–46 [CrossRef] [PubMed].
  6. French A.T., Knight P.A., Smith W.D., Brown J.K., Craig N.M., Pate J.A., et al., Up-regulation of intelectin in sheep after infection with Teladorsagia circumcincta, Int. J. Parasitol. (2008) 38:467–475 [CrossRef] [PubMed].
  7. Gibson A., Lewis A.P., Affleck K., Aitken A.J., Meldrum E., Thompson N., hCLCA1 and mCLCA3 are secreted non-integral membrane proteins and therefore are not ion channels, J. Biol. Chem. (2005) 280:27205–27212 [CrossRef] [PubMed].
  8. González L., Anderson I., Deane D., Summers C., Buxton D., Detection of immune system cells in paraffin wax-embedded ovine tissues, J. Comp. Pathol. (2001) 125:41–47 [CrossRef] [PubMed].
  9. Halliday A.M., Routledge C.M., Smith S.K., Matthews J.B., SmithW.D., Parasite loss and inhibited development of Teladorsagia circumcincta in relation to the kinetics of the local IgA response in sheep, Parasite Immunol. (2007) 29:425–434 [CrossRef] [PubMed].
  10. Hughes V., Smith S., Garcia-Sanchez A., Sales J., Stevenson K., Proteomic comparison of Mycobacterium avium subspecies paratuberculosis grown in vitro and isolated from clinical cases of ovine paratuberculosis, Microbiology (2007) 153:196–205 [CrossRef] [PubMed].
  11. Huntley J.F., Gibson S., Brown D., Smith W.D., Jackson F., Miller H.R., Systemic release of a mast cell proteinase following nematode infections in sheep, Parasite Immunol. (1987) 9:603–614 [CrossRef] [PubMed].
  12. Huntley J.F., Haig D.M., Irvine J., Inglis L., MacDonald A., Rance A., Moqbel R., Characterisation of ovine mast cells derived from in vitro culture of haemopoietic tissue, Vet. Immunol. Immunopathol. (1992) 32:47–64 [CrossRef] [PubMed].
  13. Jackson F., Greer A.W., Huntley J., McAnulty R.W., Bartley D.J., Stanley A., et al., Studies using Teladorsagia circumcincta in an in vitro direct challenge method using abomasal tissue explants, Vet. Parasitol. (2004) 124:73–89 [CrossRef] [PubMed].
  14. Knight P.A., Wright S.H., Lawrence C.E., Paterson Y.Y., Miller H.R., Delayed expulsion of the nematode Trichinella spiralis in mice lacking the mucosal mast cell specific granule chymase, mouse mast cell protease 1, J. Exp. Med. (2000) 192:1849–2856 [CrossRef] [PubMed].
  15. Komiya T., Tanigawa Y., Hirohashi S., Cloning of the novel gene intelectin, which is expressed in intestinal paneth cells in mice, Biochem. Biophys. Res. Commun. (1998) 251:759–762 [CrossRef] [PubMed].
  16. Loewen M.E., Forsyth G.W., Structure and function of CLCA proteins, Physiol. Rev. (2005) 85:1061–1092 [CrossRef] [PubMed].
  17. McClure S. J., Emery D.L., Wagland B.M., Jones W.O., A serial study of rejection of Trichostrongylus colubriformis by immune sheep, Int. J. Parasitol. (1992) 22:227–234 [CrossRef] [PubMed].
  18. Meeusen E.N., Balic A., Do eosinophils have a role in the killing of helminth parasites?, Parasitol. Today (2000) 16: 95–101.
  19. Miller H.R., Huntley J.F., Protection against nematodes by intestinal mucus, Adv. Exp. Med. Biol. (1982) 144:243–245 [PubMed].
  20. Miller H.R., Jackson F., Newlands G., Appleyard W.T., Immune exclusion, a mechanism of protection against the ovine nematode Haemonchus contortus, Res. Vet. Sci. (1983) 35:357–363 [PubMed].
  21. Miller H.R., The protective mucosal response against gastrointestinal nematodes in ruminants and laboratory animals, Vet. Immunol. Immunopathol. (1984) 6:167–259 [CrossRef] [PubMed].
  22. Miyake K., Tanaka T., McNeil P.L., Disruptioninduced mucus secretion: repair and protection, PLoS Biol. (2006) 4:e276.
  23. Mundhenk L., Alfalah M., Elble R.C., Pauli B.U., Naim H.Y., Gruber A.D., Both cleavage products of the mCLCA3 protein are secreted soluble proteins, J. Biol. Chem. (2006) 281:30072–30080 [CrossRef] [PubMed].
  24. Pemberton A.D., McAleese S.M., Huntley J.F., Collie D.D., Scudamore C.L., McEuen A.R., et al., cDNA sequence of two sheep mast cell tryptases and the differential expression of tryptase and sheep mast cell proteinase-1 in lung, dermis and gastrointestinal tract, Clin. Exp. Allergy (2000) 30:818–832 [CrossRef] [PubMed].
  25. Pemberton A.D., Knight P.A., Wright S.H., Miller H.R.P., Proteomic analysis of mouse jejunal epithelium and its response to infection with the intestinal nematode, Trichinella spiralis, Proteomics (2004) 4:1101–1108 [CrossRef] [PubMed].
  26. Sabo-Attwood T., Ramos-Nino M., Bond J., Butnor K.J., Heintz N., Gruber A.D., et al., Gene expression profiles reveal increased mClca3 (Gob5) expression and mucin production in a murine model of asbestos-induced fibrogenesis, Am. J. Pathol. (2005) 167:1243–1256 [PubMed].
  27. Seaton D.S., Jackson F., Smith W.D., Angus K.W., Development of immunity to incoming radiolabelled larvae in lambs continuously infected with Ostertagia circumcincta, Res. Vet. Sci. (1989) 46:241–246 [PubMed]
  28. Stear M.J., Strain S., Bishop S.C., How lambs control infection with Ostertagia circumcincta, Vet. Immunol. Immunopathol. (1999) 72:213–218 [CrossRef] [PubMed].
  29. Taylor G.K., Goodlett D.R., Rules governing protein identification by mass spectrometry, Rapid Commun. Mass Spectrom. (2005) 19:3420 [CrossRef] [PubMed].
  30. Thévenod F., Ion channels in secretory granules of the pancreas and their role in exocytosis and release of secretory proteins, Am. J. Physiol. Cell Physiol. (2002) 283:C651–C672 [PubMed].
  31. Toda M., Tulic M.K., Levitt R.C., Hamid Q., A calcium activated chloride channel (HCLCA1) is strongly related to IL-9 expression and mucus production in bronchial epithelium of patients with asthma, J. Allergy Clin. Immunol. (2002) 109:246–250 [CrossRef] [PubMed].
  32. Wu C.C., MacCoss M.J., Shotgun proteomics: tools for the analysis of complex biological systems, Curr. Opin. Mol. Ther. (2002) 4:242–250 [PubMed].
  33. Yasuo M., Fujimoto K., Tanabe T., Yaegashi H., Tsushima K., Takasuna K., et al., Relationship between calcium-activated chloride channel 1 and MUC5AC in goblet cell hyperplasia induced by Interleuhin-13 in human bronchial epithelial cells, Respiration (2006) 73:347–359 [CrossRef] [PubMed].
  34. Zhou Y., Dong Q., Louahed J., Dragwa C., Savio D., Huang M., et al., Characterization of a calcium-activated chloride channel as a shared target of Th2 cytokine pathways and its potential involvement in asthma, Am. J. Respir. Cell Mol. Biol. (2001) 25:486–491 [PubMed].