-
1
-
-
0342819254
-
-
Online Mendelian Inheritance in Man, OMIM (TM), Center for Medical Genetics, Johns Hopkins University (Baltimore, MD) and National Center for Biotechnology Information, National Library of Medicine (Bethesda, MD)
-
Online Mendelian Inheritance in Man, OMIM (TM), Center for Medical Genetics, Johns Hopkins University (Baltimore, MD) and National Center for Biotechnology Information, National Library of Medicine (Bethesda, MD), 1999: http://www.ncbi.nlm.nih.gov/ omim/
-
(1999)
-
-
-
2
-
-
3643062429
-
Evidence that the age at diagnosis of IDDM is genetically determined
-
Fava D, Gardner S, Pyke D, Leslie RD: Evidence that the age at diagnosis of IDDM is genetically determined. Diabetes Care 1998; 21: 925-929.
-
(1998)
Diabetes Care
, vol.21
, pp. 925-929
-
-
Fava, D.1
Gardner, S.2
Pyke, D.3
Leslie, R.D.4
-
3
-
-
0027172544
-
Polygenic control of autoimmune diabetes in nonobese diabetic mice
-
Ghosh S, Palmer SM, Rodrigues NR et al: Polygenic control of autoimmune diabetes in nonobese diabetic mice. Nat Genet 1993; 4: 404-409.
-
(1993)
Nat Genet
, vol.4
, pp. 404-409
-
-
Ghosh, S.1
Palmer, S.M.2
Rodrigues, N.R.3
-
5
-
-
0027933734
-
A genome-wide search for human type 1 diabetes susceptibility genes
-
Davies JL, Kawaguchi Y, Bennett ST et al: A genome-wide search for human type 1 diabetes susceptibility genes. Nature 1994; 371: 130-136.
-
(1994)
Nature
, vol.371
, pp. 130-136
-
-
Davies, J.L.1
Kawaguchi, Y.2
Bennett, S.T.3
-
6
-
-
17144452354
-
A search for type 1 diabetes susceptibility genes in families from the United Kingdom
-
Mein CA, Esposito L, Dunn MG et al: A search for type 1 diabetes susceptibility genes in families from the United Kingdom. Nat Genet 1998; 19: 297-300.
-
(1998)
Nat Genet
, vol.19
, pp. 297-300
-
-
Mein, C.A.1
Esposito, L.2
Dunn, M.G.3
-
7
-
-
0029046177
-
Complete multipoint sib-pair analysis of qualitative and quantitative traits
-
Kruglyak L, Lander ES: Complete multipoint sib-pair analysis of qualitative and quantitative traits. Am J Hum Genet 1995; 57: 439-454.
-
(1995)
Am J Hum Genet
, vol.57
, pp. 439-454
-
-
Kruglyak, L.1
Lander, E.S.2
-
8
-
-
8544270861
-
Evidence for a type 1 diabetes susceptibility locus (IDDM10) on human chromosome 10p11- Q11
-
Reed P, Cucca F, Jenkins S et al: Evidence for a type 1 diabetes susceptibility locus (IDDM10) on human chromosome 10p11- q11. Hum Mol Genet 1997; 6: 1011-1016.
-
(1997)
Hum Mol Genet
, vol.6
, pp. 1011-1016
-
-
Reed, P.1
Cucca, F.2
Jenkins, S.3
-
10
-
-
0029988255
-
A metric map of humans: 23,500 loci in 850 bands
-
Collins A, Frezal J, Teague J, Morton NE: A metric map of humans: 23,500 loci in 850 bands. Proc Natl Acad Sci USA 1996; 93. 14771-14775; http://cedar.genetics.soton.ac.uk/public - html/
-
(1996)
Proc Natl Acad Sci USA
, vol.93
, pp. 14771-14775
-
-
Collins, A.1
Frezal, J.2
Teague, J.3
Morton, N.E.4
-
11
-
-
0015521813
-
Increased frequency of diabetes mellitus in patients with Huntington's chorea
-
Podolsky S, Leopold NA, Sax DS: Increased frequency of diabetes mellitus in patients with Huntington's chorea. Lancet 1972; 1: 1356-1358.
-
(1972)
Lancet
, vol.1
, pp. 1356-1358
-
-
Podolsky, S.1
Leopold, N.A.2
Sax, D.S.3
-
12
-
-
0017369458
-
Abnormal glucose tolerance and arginine tolerance tests in Huntington's disease
-
Podolsky S, Leopold NA: Abnormal glucose tolerance and arginine tolerance tests in Huntington's disease. Gerontology 1977; 23: 55-63.
-
(1977)
Gerontology
, vol.23
, pp. 55-63
-
-
Podolsky, S.1
Leopold, N.A.2
-
13
-
-
0021927818
-
Diabetes mellitus in Huntington disease
-
Farrer LA: Diabetes mellitus in Huntington disease. Clin Genet 1985; 27: 62-67.
-
(1985)
Clin Genet
, vol.27
, pp. 62-67
-
-
Farrer, L.A.1
-
14
-
-
0033009587
-
Mice transgenic for an expanded CAG repeat in the Huntington's disease gene develop diabetes
-
Hurlbert MS, Zhou W, Wasmeier C, Kaddis FG, Hutton JC, Freed CR: Mice transgenic for an expanded CAG repeat in the Huntington's disease gene develop diabetes. Diabetes 1999; 48: 649-651.
-
(1999)
Diabetes
, vol.48
, pp. 649-651
-
-
Hurlbert, M.S.1
Zhou, W.2
Wasmeier, C.3
Kaddis, F.G.4
Hutton, J.C.5
Freed, C.R.6
-
15
-
-
0032919205
-
Formation of polyglutamine inclusions in non-CNS tissue
-
Sathasivam K, Hobbs C, Turmaine M et al: Formation of polyglutamine inclusions in non-CNS tissue. Hum Mol Genet 1999; 8: 813-22.
-
(1999)
Hum Mol Genet
, vol.8
, pp. 813-822
-
-
Sathasivam, K.1
Hobbs, C.2
Turmaine, M.3
-
16
-
-
0030739440
-
The solution structure of the N-terminal domain of alpha2- macroglobulin receptor-associated protein
-
Nielsen PR, Ellgaard L, Etzerodt M, Thogersen HC, Poulsen FM: The solution structure of the N-terminal domain of alpha2- macroglobulin receptor-associated protein. Proc Natl Acad Sci USA 1997; 94: 7521-7525.
-
(1997)
Proc Natl Acad Sci USA
, vol.94
, pp. 7521-7525
-
-
Nielsen, P.R.1
Ellgaard, L.2
Etzerodt, M.3
Thogersen, H.C.4
Poulsen, F.M.5
-
17
-
-
0029904111
-
Induction of passive Heymann nephritis with antibodies specific for a synthetic peptide derived from the receptor-associated protein
-
Kerjaschki D, Ullrich R, Exner M, Orlando RA, Farquhar MG: Induction of passive Heymann nephritis with antibodies specific for a synthetic peptide derived from the receptor-associated protein. J Exp Med 1996; 183: 2007-2015.
-
(1996)
J Exp Med
, vol.183
, pp. 2007-2015
-
-
Kerjaschki, D.1
Ullrich, R.2
Exner, M.3
Orlando, R.A.4
Farquhar, M.G.5
-
18
-
-
0017645098
-
Diabetes mellitus, diabetes insipidus, and optic atrophy. An autosomal recessive syndrome?
-
Fraser FC, Gunn T: Diabetes mellitus, diabetes insipidus, and optic atrophy. An autosomal recessive syndrome? J Med Genet 1977; 14: 190-193.
-
(1977)
J Med Genet
, vol.14
, pp. 190-193
-
-
Fraser, F.C.1
Gunn, T.2
-
19
-
-
0028808309
-
Neurodegeneration and diabetes: UK nationwide study of Wolfram (DIDMOAD) syndrome
-
Barrett TG, Bundey SE, Macleod AF: Neurodegeneration and diabetes: UK nationwide study of Wolfram (DIDMOAD) syndrome. Lancet 1995; 346: 1458-1463.
-
(1995)
Lancet
, vol.346
, pp. 1458-1463
-
-
Barrett, T.G.1
Bundey, S.E.2
Macleod, A.F.3
-
20
-
-
17344362695
-
A gene encoding a transmembrane protein is mutated in patients with diabetes mellitus and optic atrophy (Wolfram syndrome)
-
Inoue H, Tanizawa Y, Wasson J at al: A gene encoding a transmembrane protein is mutated in patients with diabetes mellitus and optic atrophy (Wolfram syndrome). Nat Genet 1998;20: 143-148.
-
(1998)
Nat Genet
, vol.20
, pp. 143-148
-
-
Inoue, H.1
Tanizawa, Y.2
Wasson, J.3
-
21
-
-
0031761895
-
Diabetes insipidus, diabetes mellitus, optic atrophy and deafness (DIDMOAD) caused by mutations in a novel gene (wolframin) coding for a predicted transmembrane protein
-
Strom TM, Hortnagel K, Hofmann S et al: Diabetes insipidus, diabetes mellitus, optic atrophy and deafness (DIDMOAD) caused by mutations in a novel gene (wolframin) coding for a predicted transmembrane protein. Hum Mol Genet 1998; 7: 2021-2028.
-
(1998)
Hum Mol Genet
, vol.7
, pp. 2021-2028
-
-
Strom, T.M.1
Hortnagel, K.2
Hofmann, S.3
-
22
-
-
17344372511
-
A second- Generation screen of the human genome for susceptibility to insulin-dependent diabetes mellitus
-
Concannon P, Gogolin-Ewens KJ, Hinds DA et al: A second- generation screen of the human genome for susceptibility to insulin-dependent diabetes mellitus. Nat Genet 1998; 19: 292-296.
-
(1998)
Nat Genet
, vol.19
, pp. 292-296
-
-
Concannon, P.1
Gogolin-Ewens, K.J.2
Hinds, D.A.3
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