Sib-pair Analysis of Japanese NIDDM Patients

Journal of the Japan Diabetes Society

Volumn 39, Issue 6, 1996, Pages 409-416

  Iwasaki, Naoko ^a   Kawamura, Makiko ^a   Ohgawara, Hisako ^a   Karibe, Sachiyo ^a   Cox, Nancy J ^b   Bell, Graeme I ^b   Omori, Yasue ^a  

^a TOKYO WOMEN'S MEDICAL UNIVERSITY   (Japan)

^b UNIVERSITY OF CHICAGO   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

EID: 10544248510     PISSN: 0021437X     EISSN: None     Source Type: Journal    
DOI: 10.11213/tonyobyo1958.39.409     Document Type: Article

References (33)

1. Bell, G. I., Xiang, K. S., Newman, M. V., Wu, S. H., Wright, L. G., Fajans, S. S., Spielman, R. S., Cox, N. J., (1991) Gene for non-insulin dependent diabetes mellitus (maturity-onset diabetes of the young subtype) is linked to DNA polymorphism on human chromosome 20q. Proc. Natl. Acad. Sci. USA 88 : 1484–1488.
2. Froguel, P., Vaxillaire, M., Sun, F., Velho, G., Zouali, H., Butel MO. Lesage, S., Vionnet, N., Clement, K., Fougerousse, F., Tanizawa, Y., Weissenbach, J., Beckmann, J. S., Lathrop, G. M., Passa, P., Permutt, M. A., Cohen, D., (1992) Close linkage of glucokinase-locus on chromosome 7p to early-onset non-insulin dependent diabetes mellitus. Nature 356 : 162–164.
3. Vaxillaire, M., Boccio, V., Philippi, A., Vigouroux, C., Terwilliger, J., Passa, P., Beckmann, J. S., Velho, G., Lathrop, G. M., Froguel, P., (1995) A gene for maturity onset diabetes of the young (MODY) maps to chromosome 12q. Nature Genet. 9 : 418–423.
4. Jeunemaitre, X., Soubrier, F., Kotelevtsev, Y. V., Lifton, R. P., Williams, C. S., Charru, A., Hunt, S. C., Hopkins, P. N., Williams, R. R., Lalouel, J. M., Corvol, P., (1992) Molecular basis of human hypertension : Role of an-giotensinogen. Cell 71 : 169–180.
5. Shah, S., Green, J. R., (1994) Disease susceptibility genes and the sib-pair method : a review of recent methodology. Am. Hum. Genet. 58 : 384–395.
6. Weeks, D. E., Lange, K., (1988) The affected-pedigree -member method of linkage analysis. Am. J. Hum. Genet. 42 : 315–326.
7. Davies, J. L., Kawaguchi, Y., Bennett, S. T., Copeman, J. B., Cordell, H. J., Pritchard, L. E., Reed, P. W., Gough, S. C. L., Jenkins, S. C., Palmer, S. M., Balfour, K. M., Rowe, B. R., Farrall, M., Barnett, A. H., Bain, C. S., Todd, J. A., (1994) A genome-wide search for human type 1 diabetes susceptiblity genes. Nature 371 : 130–135.
8. Hashimoto, L., Habita, C., Beressi, J. P., Lelepine, M., Besse, C., Cambon-Thomsen, A., Deschamps, I., Rotter, J. I., Djoulah, S., James, M. R., Froguel, P., Weissenbach, J., Lathrop, G. M., Julier, C., (1994) Genetic mapping a susceptibility locus for insulin-dependent diabetes mellitus on chromosome 11q. Nature 371 : 161–164.
9. WHO expert committee on diabetes mellitus (1980) WHO Tech. Rep. Ser. 646 : 1–80.
10. Stoffel, M., Bell, G. I., (1993) Characterization of a third simple tandem repeat polymorphism in the human glucokinase gene. Diabetologia 36 : 170–171.
11. Polymeropoulos, M. H., Xiao, H., Rath, D. S., Merril, C. R., (1991) Tetranucleotide repeat polymorphism at the human tyrosine hydroxylase gene (TH). Nucl. Acids Res. 19 : 3753.
12. Xiang, K. S., Granqvist, M., Seino, M., Seino, S., Bell, G. I., (1991) Microsatellite polymorphism in human insulin receptor gene (INSR) on chromosome 19. Nucl. Acids Res. 19 : 5094.
13. Froguel, P., Zouali, H., Sun F., Velho, G., Fukumoto, H., Passa, P., Cohen, D., (1991) CA repeat polymorphism in the glucose transporter GLUT2 gene. Nucl. Acids Res. 19 : 3754.
14. Seo, T. S., Hanabusa, T., Ohagi, S., Steiner, D. F., Bell, G. I., (1993) Dinucleotide repeat polymorphism in the NEC2 gene. Hum. Mol. Genet. 2 : 1983.
15. Tsaar, M. L., Menzel, S., Lai, F. P., Espinosa III R., Concannon, P., Spielman, R. S., Hanis, C. L., Cox, N. J., Le Beau, M. M., German, M. S., Jan, L. Y., Bell, G. I., Stoffel, M., (1995) Isolation of a cDNA clone encoding a KATP channellike protein expressed in insulin-secreting cells, localization of the human gene to chromosome band 21q22.1, and linkage studies with NIDDM, Diabetes 44 : 592–596.
16. Polymeropoulos, M. H., Rath, D. S., Xiao, H., Merril, C. R., (1990) Trinucleotide repeat polymorphism at human intestinal fatty acid binding protein gene (FABP2). Nucl. Acids Res. 18 : 7198.
17. Elbein, S. C., Hoffman, M., Ridinger, D., Otterud, B., Leppert, M., (1994) Description of a second microsatellite marker and linkage analysis of the muscle glycogen synthase locus in familial NIDDM. Diabetes 43 : 1061–1065.
18. Bishop, D. T., Williamson, J. A., (1990) The power of identity-by-state methods for linkage analysis. Am. J. Hum. Genet. 46 : 254–265.
19. Holmans, P., (1993) Asymptotic properties of affected-sib-pair linkage analysis. Am. J. Hum. Genet. 52 : 362–374.
20. Botstein, D., White, R. L., Skolnic, M., Davis, R. W., (1980) Construction of a genetic linkage map in man using restriction fragment length polymorphisms. Am. J. Hum. Genet. 32 : 314–331.
21. Baroni, M. G., Alcolado, J. C., Needham, E. W. A., Pozzilli, P., Stocks, J., Galton, D. J., (1992) Sib-pair analysis of adenosine deaminase locus in NIDDM. Diabetes 41 : 1640–1643.
22. Froguel, P., Zouali, H., Vionnet, N., Velho, G., Vaxillaire, M., Sun, F., Lesage, S., Stoffel, M., Takeda, J., Passa, P., Permutt, M. A., Beckmann, J. S., Bell, G. I., Cohen, D., (1993) Familial hyperglycemia due to mutations in glucokinase : definition of a subtype of diabetes mellitus. N. Engl. J. Med. 328 : 697–702.
23. Iwanishi, M., Haruta, T., Takata, Y., Ishibashi, O., Sasaoka, T., Egawa, K., Imamura, T., Naito, K., Itazu, T., Kobayashi, M., (1993) A mutation (Trp 1193-Leu 1193) in the kinase domain of the insulin receptor associated with Type A synrdrome of insulin resistance. Diabetologia 36 : 414–422.
24. Shimada, F., Makino, H., Iwaoka, H., Miyamoto, S., Hashimoto, N., Kanatsuka, A., Bell, G. I., Yoshida, S., (1995) Identification of two novel amino acid polymorphisms in beta-cell/liver (GLUT2) glucose transporter in Japanese subjects. Diabetologia 38 : 211–215.
25. Yoshida, H., Ohagi, S., Sanke, T., Furuta, H., Furuta, M., Nanjo, K., (1995) Association of the prohormone convertase 2 gene (PCSK2) on chromosome 20 with NIDDM in Japanese. Diabetes 44 : 389–393.
26. Prochazka, M., Lillioja, S., Tait, J. F., Knowler, W. C., Mott, D. M., Spraul, M., Bennett, P. H., Bogardus, C., (1993) Linkage of chromosomal markers on 4q with a putative gene determining maximal insulin action in Pima Indians. Diabetes 42 : 514–519.
27. Baire, L. J., Sacchettini, J. C., Knowler, W. C., Eads, J., Paolisso, G., Tataranni, P. A., Mochizuki, H., Benett, P. H., Bogardus, C., Prochazka, M., (1995) An amino acid substitution in the human intestinal fatty acid binding protein is associated with increased fatty acid binding, increased fat oxidation, and insulin resistance. J. Clin. Invest. 95 : 1281–1287.
28. Groop, L. C., Kankuri, M., Schalin-Jant, C., Ekstrand, A., Nikula-Ijas, P., Widen, E., Kuismanen, E., Eriksson, J., Franssila-Kallunki, A., Saloranta, C., Koskimies, S., (1993) Association between polymorphism of the glycogen synthase gene and non-insulin-dependent diabetes mellitus. N. Engl. J. Med. 328 : 10–14.
29. Iwasaki, N., Ohgawara, H., Nagahara, H., Kawamura, M., Bell, G. I., Omori, Y., (1995) Characterization of Japanese families with early-onset type 2 (non-insulin dependent) diabetes mellitus and screening for mutations in the glucokinase and mitochondrial tRNALeu(UUR) genes. Acta. Diabetol. 32 : 17–22.
30. Noda, K., Matsutani, A., Tanizawa, Y., Neuman, R., Kaneko, T., Permutt, M. A., Kaku, K., (1993) Polymorphic microsatellite repeat markers at the glucokinase gene locus are positively associated with NIDDM in Japanese. Diabetes 42 : 1147–1152.
31. Eto, K., Sakura, H., Shimokawa, K., Kadowaki, H., Hagura, R., Akanuma, Y., Yazaki, Y., Kadawaki, T., (1993) Sequence variations of the glucokinase gene in Japanese subjects with NIDDM. Diabetes 42 : 1133–1137.
32. Nishi, S., Hinata, S., Matsukage, T., Takeda, J., Ichiyama, A., Bell, G. I., Yoshimi, T., (1994) Glucokinase mutations are not a major cause of lateonset Type 2 diabetes mellitus in Japanese subjects. Diabetic Med. 11 : 193–197.
33. Ott, J., (1991) Methods of linkage analysis ; nonparametric approach. In Analysis of Human Genetic Linkage. Johns Hopkins Univ. Press. New York pp : 77–80.