REFERENCES
Calvet, J. P. (1993). Polycystic kidney disease: Primary extracellular matrix abnormality or defective cellular differentiation? Kidney Int. 43: 101.
Guay-Woodford, L. M., Bryda, E., Christine, B., Lindsey, J., Collier, W., Avner, E., D'Eustachio, P., and Flaherty, L. (1996). Evidence that two phenotypically distinct mouse PKD mutations, bpk and jcpk, are allelic. Kidney Int. 50: 1158.
Hagg, P., Rehn, M., Huhtala, P., Vaisanen, T., Tamminen, M., and Pihlajaniemi, T. (1998). Type XIII collagen is identified as a plasma membrane protein. J.Biol.Chem. 273: 15590.
Iakoubova, O., Dushkin, H., and Beier, D. (1995). Localization of a murine recessive polycystic kidney disease mutation and modifying loci that affect disease severity. Genomics 26: 107.
Kelly, C. J., and Neilson, E. G. (1987). Contrasuppression in autoimmunity. Abnormal contrasuppression facilitates expression of nephritogenic effector T cells and interstitial nephritis in kdkd mice. J.Exp.Med. 165: 107.
Kelly, C. J., Korngold, R., Mann, R., Clayman, M., Haverty, T., and Neilson, E. G. (1986). Spontaneous interstitial nephritis in kdkd mice. II. Characterization of a tubular antigen-specific, H-2K-restricted Lyt-21 effector T cell that mediates destructive tubulointerstitial injury. J.Immunol. 136: 526.
Konrad, M., Saunier, S., Heidet, L., Silbermann, F., Benessy, F., Calado, J., LePaslier, D., Broyer, M., Gubler, M.-C., and Antignac, C. (1996). Large homozygous deletions of the 2q13 region are a major cause of juvenile nephronophthisis. Hum.Mol.Genet. 5: 367.
Lyon, M. F., and Hulse, E. V. (1971). An inherited kidney disease of mice resembling human nephronophthisis. J.Med.Genet. 8: 41.
Neilson, E. G., McCafferty, E., Feldman, A., Clayman, M. D., Zakheim, B., and Korngold, R. (1984). Spontaneous interstitial nephritis in kdkd mice. I. An experimental model of autoimmune renal disease. J.Immunol. 133: 2560.
Peltonen, S., Rehn, M., and Pihlajaniemi, T. (1997). Alternative splicing of mouse alpha1(XIII) collagen RNAs results in at least 17 different transcripts, predicting alpha1(XIII) collagen chains with length varying between 651 and 710 amino acid residues. DNA Cell Biol. 16: 227.
Pihlajaniemi, T., and Tamminen, M. (1990). The alpha 1 chain of type XIII collagen consists of three collagenous and four noncollagenous domains, and its primary transcript undergoes complex alternative splicing. J.Biol.Chem. 265: 16922.
Rowe, L. B., Nadeau, J. H., Turner, R., Frankel, W. N., Letts, V. A., Eppig, J. T., Ko, M. S., Thurston, S. J., and Birkenmeier, E. H. (1994). Maps from two interspecific backcross DNA panel available as a community genetic mapping resource. Mammal.Genome 5: 253.
Sibalic, V., Fan, X., and Wuthrich, R. P. (1997). Characterization of cellular infiltration and adhesion molecule expression in CBA/CaH-kdkd mice with tubulointerstitial renal disease. Histochem.Cell Biol. 108: 235.
Shows, T. B., Tikka, L., Byers, M. G., Eddy, R. L., Haley, L. L., Henry, W. M., Prockop, D. J., and Tryggvason, K. (1989). Assignment of the human collagen alpha-1(XIII) chain gene (COL13A1) to the q22 region of chromosome 10. Genomics 5: 128.
Smoyer, W. E., and Kelly, C. J. (1994). Inherited interstitial nephritis in kdkd mice. Int.Rev.Immunol. 11: 245.
Author information
Authors and Affiliations
Rights and permissions
About this article
Cite this article
Mrug, M., Stockwin, J., W¨uthrich, R.P. et al. Mapping of Mouse α1(XIII) Collagen to Chromosome 10 and Its Exclusion as a kd Candidate Gene. Biochem Genet 38, 337–340 (2000). https://doi.org/10.1023/A:1002013218535
Issue Date:
DOI: https://doi.org/10.1023/A:1002013218535