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Journal of Immunology (Baltimore, Md. : 1950)|March 11, 1999
Genome-wide linkage analysis of chronic relapsing experimental autoimmune encephalomyelitis in the rat identifies a major susceptibility locus on chromosome 9I Dahlman, L Jacobsson, A Glaser, et al.
Diabetes|February 1, 1994
Impact of diabetic inheritance on glucose tolerance and insulin secretion in spontaneously diabetic GK-Wistar ratsS M Abdel-Halim, A Guenifi, H Luthman, et al.
The Journal of Biological Chemistry|April 16, 1998
Naturally occurring mutants of human steroid 21-hydroxylase (P450c21) pinpoint residues important for enzyme activity and stabilityA Nikoshkov, S Lajic, A Vlamis-Gardikas, et al.
Journal of Neuroimmunology|December 31, 1997
Genetic analysis of inflammation, cytokine mRNA expression and disease course of relapsing experimental autoimmune encephalomyelitis in DA ratsJ C Lorentzen, M Andersson, S Issazadeh, et al.
Human Molecular Genetics|March 7, 2001
Rats made congenic for Oia3 on chromosome 10 become susceptible to squalene-induced arthritisB C Holm, H W Xu, L Jacobsson, et al.
Bone|February 19, 2008
Genetic variation in the PTH pathway and bone phenotypes in elderly women: evaluation of PTH, PTHLH, PTHR1 and PTHR2 genesM Tenne, F McGuigan, L Jansson, et al.
British Journal of Cancer|August 1, 1992
Quantitative determination of mdr1 gene expression in leukaemic cells from patients with acute leukaemiaA Gruber, S Vitols, S Norgren, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 30, 1998
Identification of rat susceptibility loci for adjuvant-oil-induced arthritisJ C Lorentzen, A Glaser, L Jacobsson, et al.
Acta Dermato-Venereologica|July 6, 2000
Characterization by phenotype of families with atopic dermatitisM Bradley, I Kockum, C Söderhäll, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|September 27, 2001
Identification of a new mutation in the alpha4(IV) collagen gene in a family with autosomal dominant Alport syndrome and hypercholesterolaemiaM Ciccarese, D Casu, F Ki Wong, et al.
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