Bennegadi N, Gidenne T, Licois D. 2001. Impact of fibre deficiency and sanitary status on non-specific enteropathy of the growing rabbit. Anim Res 50:401–414.
Rochambeau HDe, Licois D, Gidenne T, Verdelhan S, Coudert P, Elsen JM. 2006. Genetic variability of the resistance for three types of enteropathy in the growing rabbit. Livest Sci 101:110–115.
Dewrée R, Meulemans L, Lassence C, Desmecht D, Ducatelle R, Mast J, Licois D. 2007. Experimentally induced epizootic rabbit enteropathy: clinical, histopathological, ultrastructural, bacteriological and haematological findings. World Rabbit Sci 15:91–102.
Hayashi K. 1991. PCR-SSCP: a simple and sensitive method for detection of mutations in the genomic DNA. Genome Res 1:34–38.
Hayashi K. 1992. PCR-SSCP: a method for detection of mutations. Genet. Anal.: Biomol Eng 9:73–79.
Hugot JP, Chamaillard M, Zouali H, Lesage S, Cézard JP, Belaiche J, Almer S, Tysk C, O’Morain CA, Gassull M. 2001. Association of NOD2 leucine-rich repeat variants with susceptibility to Crohn’s disease. Nature 411:599–603.
Jéru I, Le Borgne G, Cochet E, Hayrapetyan H, Duquesnoy P, Grateau G, Morali A, Sarkisian T, Amselem S. 2011. Identification and functional consequences of a recurrent NLRP12 missense mutation in periodic fever syndromes. Arthritis Rheum 63:1459–1464.
Janeway CA, Medzhitov R. 2002. Innate immune recognition. Annu Rev Immunol 20:197–216.
Lich JD, Williams KL, Moore CB, Arthur JC, Davis BK, Taxman DJ, Ting JPY. 2007. Cutting edge: Monarch-1 suppresses non-canonical NF-κB activation and p52-dependent chemokine expression in monocytes. J Immunol 178:1256–1260.
Licois D. 2004. Domestic rabbit enteropathies. Proceedings of the eighth world rabbit congress. 385–403.
Livak KJ, Schmittgen TD. 2001. Analysis of relative gene expression data using real-time quantitative PCR and the 2
−ΔΔCT method. Methods 25:402–408.
Macaluso F, Nothnagel M, Parwez Q, Petrasch-Parwez E, Bechara FG, Epplen JT, Hoffjan S. 2007. Polymorphisms in NACHT LRR (NLR) genes in atopic dermatitis. Exp Dermatol 16:692–698.
Ogura Y, Bonen DK, Inohara N, Nicolae DL, Chen FF, Ramos R, Britton H, Moran T, Karaliuskas R, Duerr RH. 2001. A frameshift mutation in
NOD2 associated with susceptibility to Crohn's disease. Nature 411:603–606.
Richards N, Schaner P, Diaz A, Stuckey J, Shelden E, Wadhwa A, Gumucio DL. 2001. Interaction between pyrin and the apoptotic speck protein (ASC) modulates ASC-induced apoptosis. J Biol Chem 276:39320–39329.
Solé X, Guinó E, Valls J, Iniesta R, Moreno V. 2006. SNPStats: a web tool for the analysis of association studies. Bioinformatics 22:1928–1929.
Tang H, Quertermous T, Rodriguez B, Kardia SLR, Zhu X, Brown A, Pankow JS, Province MA, Hunt SC, Boerwinkle E. 2005. Genetic structure, self-identified race/ethnicity, and confounding in case-control association studies. Am J Hum Genet 76:268–275.
Wang L, Manji GA, Grenier JM, Al-Garawi A, Merriam S, Lora JM, Geddes BJ, Briskin M, DiStefano PS, Bertin J. 2002. PYPAF7, a novel PYRIN-containing Apaf1-like protein that regulates activation of NF-κB and caspase-1-dependent cytokine processing. J Biol Chem 277:29874–29880.
Williams KL, Lich JD, Duncan JA, Reed W, Rallabhandi P, Moore C, Kurtz S, Coffield VMN, Accavitti-Loper MA, Su L. 2005. The CATERPILLER protein Monarch-1 is an antagonist of Toll-like receptor-, tumor necrosis factor α-, and
Mycobacterium tuberculosis-induced pro-inflammatory signals. J Biol Chem 280:39914–39924.
Williams KL, Taxman DJ, Linhoff MW, Reed W, Ting JPY. 2003. Cutting edge: Monarch-1: a pyrin/nucleotide-binding domain/leucine-rich repeat protein that controls classical and nonclassical MHC class I genes. J Immunol 170:5354–5358.
Ye Z, Ting JPY. 2008. NLR, the nucleotide-binding domain leucine-rich repeat containing gene family. Curr Opin Immunol 20:3–9.
Zhang GW, Wang HZ, Chen SY, Li ZC, Zhang WX, Lai SJ. 2011. A reduced incidence of digestive disorders in rabbits is associated with allelic diversity at the TLR4 locus. Vet Immunol Immunopathol 144:482–486.
Zhang WX, Zhang GW, Peng J, Zhang JL, Yang Y, Lai SJ. 2013. A synonymous mutation in NOD2 gene was significantly associated with non-specific digestive disorder in rabbit. Gene 516:193–197.