Identification of microsatellite markers near the human genes encoding the β-cell ATP-sensitive K+ channel and linkage studies with NIDDM in Japanese

Diabetes

Volumn 45, Issue 2, 1996, Pages 267-269

  Iwasaki, Naoko ^a,b   Kawamura, Makiko ^a   Yamagata, Kazuya ^c   Cox, Nancy J ^c   Karibe, Sachiyo ^a   Ohgawara, Hisako ^a   Inagaki, Nobuya ^a,b   Seino, Susumu ^b   Bell, Graeme I ^c   Omori, Yasue ^a  

^a TOKYO WOMEN'S MEDICAL UNIVERSITY   (Japan)

^b CHIBA UNIVERSITY SCHOOL OF MEDICINE   (Japan)

^c UNIVERSITY OF CHICAGO   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ADENOSINE TRIPHOSPHATE; GLUCOSE; HEMOGLOBIN A1C; INSULIN; MICROSATELLITE DNA; ORAL ANTIDIABETIC AGENT; POTASSIUM; POTASSIUM CHANNEL; RECEPTOR SUBUNIT; SULFONYLUREA;

ADULT; AGED; ARTICLE; CHROMOSOME 11; DIET THERAPY; DNA POLYMORPHISM; FEMALE; GENETIC LINKAGE; GENETIC SUSCEPTIBILITY; HUMAN; HUMAN CELL; INSULIN RELEASE; JAPAN; MAJOR CLINICAL STUDY; MALE; NON INSULIN DEPENDENT DIABETES MELLITUS; ORAL DRUG ADMINISTRATION; PANCREAS ISLET BETA CELL; PRIORITY JOURNAL; SIBLING; YEAST ARTIFICIAL CHROMOSOME;

EID: 13344259308     PISSN: 00121797     EISSN: None     Source Type: Journal    
DOI: 10.2337/diab.45.2.267     Document Type: Article

References (20)

1. Ashcroft FM, Rorsman P: Electrophysiology of pancreatic islet cells. In The Electrophysiology of Neuroendocrine Cells. Scherübl H, Hescheler H, Eds. Boca Raton, FL, CRC Press, 1995, p. 207-243
2. Ashcroft SJH, Ashcroft FM: The sulfonylurea receptor. Biochem Biophys Acta 1175:45-59, 1992
3. KTAP. an inward rectifier subunit plus the sulfonylurea receptor. Science 270:1166-1170, 1995
4. Aguilar-Bryan L, Nichols CG, Wechsler SW, Clement JP IV, Boyd AE III, González G, Herrera-Sosa H, Nguy K, Bryan J, Nelson DA: Cloning of the β-cell high-affinity sulfonylurea receptor: a regulator of insulin secretion. Science 268:423-426, 1995
5. Thomas PM, Cote GJ, Wohllk N, Haddad B, Mathew PM, Rabl W, Aguilar-Bryan, L, Gagel RF, Bryan J: Mutations in the sulphonylurea receptor gene in familial persistent hyperinsulinemic hypoglycemia of infancy. Science 268:426-428, 1995
6. Glaser B, Chiu KC, Anker R, Nestrowicz A, Landau H, Ben-Bassat H, Shlomai Z, Kaiser N, Thornton PS, Stanley CA, Spielman RS, Gogolin-Ewens K, Cerasi E, Baker L, Rice J, Donis-Keller H, Permutt MA: Familial hyperinsulinism maps to chromosome 11p14-15.1, 30 cM centromeric to the insulin gene. Nature Genet 7:185-188, 1994
7. Thomas PM, Cote GJ, Hallman DM, Mathew PM: Homozygosity mapping, to chromosome 11p, of the gene for familial persistent hyperinsulinemic hypoglycemia of infancy. Am J Hum Genet 56:416-421, 1995
8. Glaser B, Chiu KC, Liu L, Anker R, Nestorowicz A, Cox NJ, Landau H, Kaiser N, Thornton PS, Stanley CA, Cerasi E, Baker L, Donis-Keller H, Permutt MA: Recombinant mapping of the familial hyperinsulinism gene to an 0.8 cM on chromosome 11p15 1 and demonstration of a founder effect in Ashkenzai Jews. Hum Mol Genet 4:879-886, 1995
9. World Health Organization: Diabetes Mellitus: Report of a WHO Study Group. Geneva, World Health Org., 1985 (Tech. Rep. Ser., no. 727)
10. ATP-channel-like 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, 1995
11. Stirling B, Cox NJ, Bell GI, Hanis CL, Spielman RS, Concannon P: Identification of microsatellite markers near the human ob gene and linkage studies in NIDDM-affected sib pairs. Diabetes 44.999-1001, 1995
12. Bishop DT, Williamson JA: The power of identity-by-state methods for linkage analysis. Am J Hum Genet 46:254-265, 1990
13. Holmans P: Asymptotic properties of affected-sib-pair linkage analysis. Am J Hum Genet 52:362-374, 1993
14. Warram JH, Rich SS, Krolewski AS: Epidemiology and genetics of diabetes mellitus. In Joslin's Diabetes Mellitus 13th ed. Kahn CR, Weir GC, Eds. Philadelphia, Lea and Febiger, 1994, p. 201-215
15. Rotter JI, Vadheim CM, Rimoin DL: Genetics of diabetes mellitus. In Diabetes Mellitus, Theory and Practice. 4th ed. Rifkin H, Porte D, Eds. New York, Elsevier, 1990, p. 378-413
16. Vaxillaire M, Boccio V, Philippi A, Vigouroux C, Terwilliger J, Passa P, Beckmann JS, Velho G, Lathrop GM, Froguel P: A gene for maturity onset diabetes of the young (MODY) maps to chromosome 12q. Nature Genet 9.418-423, 1995
17. DeFronzo RA, Bonadonna RC, Ferrannini E Pathogenesis of NIDDM: a balanced overview. Diabetes Care 15:318-368, 1992
18. + channel subunit in MODY, NIDDM, or GDM. Diabetes 44:597-600, 1995
19. Yasuda K, Sakura H, Mori Y, Iwamoto K, Shimokawa K, Kadowaki H, Hagura R, Akanuma Y, Adelman JP, Yazaki Y, Ashcroft FM, Kadowaki T: No evidence for mutations in a putative subunit of the beta-cell ATP-sensitive potassium channel (K-ATP channel) in Japanese NIDDM patients Biochem Biophys Res Com 211:1036-1040, 1995
20. Cohen D, Chumakov I, Weissenbach J: A first-generation physical map of the human genome Nature 366:698-701, 1993