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4. Genetic analysis of MRL-lpr mice: relationship of the Fas apoptosis gene to disease manifestations and renal disease-modifying loci. Watson ML; Rao JK; Gilkeson GS; Ruiz P; Eicher EM; Pisetsky DS; Matsuzawa A; Rochelle JM; Seldin MF J Exp Med; 1992 Dec; 176(6):1645-56. PubMed ID: 1460423 [TBL] [Abstract][Full Text] [Related]
5. Genetic dissection of vasculitis in MRL/lpr lupus mice: a novel susceptibility locus involving the CD72c allele. Qu WM; Miyazaki T; Terada M; Lu LM; Nishihara M; Yamada A; Mori S; Nakamura Y; Ogasawara H; Yazawa C; Nakatsuru S; Nose M Eur J Immunol; 2000 Jul; 30(7):2027-37. PubMed ID: 10940892 [TBL] [Abstract][Full Text] [Related]
6. Genetic analysis of autoimmune gld mice. I. Identification of a restriction fragment length polymorphism closely linked to the gld mutation within a conserved linkage group. Seldin MF; Morse HC; Reeves JP; Scribner CL; LeBoeuf RC; Steinberg AD J Exp Med; 1988 Feb; 167(2):688-93. PubMed ID: 2894402 [TBL] [Abstract][Full Text] [Related]
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9. Myc-1 is centromeric to the linkage group Ly-6--Sis--Gdc-1 on mouse chromosome 15. Huppi K; Duncan R; Potter M Immunogenetics; 1988; 27(3):215-9. PubMed ID: 2892786 [TBL] [Abstract][Full Text] [Related]
10. Mapping of the Hox-3.1 and Myc-1.2 genes on chromosome 15 of the mouse by restriction fragment length variations. Watanabe T; Ohno K; Shimizu A; Sakai Y; Takahashi M; Takahashi N Biochem Genet; 1990 Jun; 28(5-6):257-66. PubMed ID: 1975491 [TBL] [Abstract][Full Text] [Related]
11. Host modifier genes affect mouse autoimmunity induced by the lpr gene. Wang Y; Nose M; Kamoto T; Nishimura M; Hiai H Am J Pathol; 1997 Dec; 151(6):1791-8. PubMed ID: 9403730 [TBL] [Abstract][Full Text] [Related]
12. Analysis of granulomatous arteritis in MRL/Mp autoimmune disease mice bearing lymphoproliferative genes. The use of mouse genetics to dissociate the development of arteritis and glomerulonephritis. Nose M; Nishimura M; Kyogoku M Am J Pathol; 1989 Aug; 135(2):271-80. PubMed ID: 2782373 [TBL] [Abstract][Full Text] [Related]
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14. Restriction fragment length polymorphism and chromosome mapping of a mouse homeo box gene, Hox-2.1. Watanabe T; Masaki S; Takahashi N; Nishimura M; Kato H Biochem Genet; 1988 Dec; 26(11-12):805-13. PubMed ID: 2907403 [TBL] [Abstract][Full Text] [Related]
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17. Genetic dissociation of dacryoadenitis and sialadenitis in a Sjogren's syndrome mouse model with common and different susceptibility gene loci. Kamao T; Miyazaki T; Soga Y; Komori H; Terada M; Ohashi Y; Nose M Invest Ophthalmol Vis Sci; 2009 Jul; 50(7):3257-65. PubMed ID: 19218603 [TBL] [Abstract][Full Text] [Related]