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Urinary excretion of 8-oxo-7, 8-dihydro-2'-deoxyguanosine as a predictor of the development of diabetic nephropathy

Diabetologia, 2002-06, Vol.45 (6), p.877-882

2002

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Oxidative DNA damage in diabetes mellitus : its association with diabetic complications

Diabetologia, 1999-08, Vol.42 (8), p.995-998

1999

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Role of urotensin II gene in genetic susceptibility to Type 2 diabetes mellitus in Japanese subjects

Diabetologia, 2003-07, Vol.46 (7), p.972-976

2003

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Organization and partial sequence of the hepatocyte nuclear factor-4 alpha/MODY1 gene and identification of a missense mutation, R127W, in a Japanese family with MODY

Diabetes (New York, N.Y.), 1997-10, Vol.46 (10), p.1652-1657

1997

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The effects of coenzyme Q10 treatment on maternally inherited diabetes mellitus and deafness, and mitochondrial DNA 3243 (A to G) mutation

Diabetologia, 1998-05, Vol.41 (5), p.584-588

1998

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Tyrosine hydroxylase gene microsatellite polymorphism associated with insulin resistance in depressive disorder

Metabolism, clinical and experimental, 2000-09, Vol.49 (9), p.1145-1149

2000

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Genetic variation in the gene encoding calpain-10 is associated with type 2 diabetes mellitus

Nature genetics, 2000-10, Vol.26 (2), p.163-175

2000

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Group specific component protein genotype is associated with NIDDM in Japan

Diabetologia, 1998-06, Vol.41 (6), p.742-743

1998

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Diabetes associated with a novel 3264 mitochondrial tRNA(Leu)(UUR) mutation

Diabetes care, 1997-07, Vol.20 (7), p.1138

1997

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Urinary chiro-inositol excretion is an index marker of insulin sensitivity in Japanese type II diabetes

Diabetes care, 1994-12, Vol.17 (12), p.1465-1468

1994

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Mutation in hepatocyte nuclear factor-1β gene (TCF2) associated with MODY

Nature genetics, 1997-12, Vol.17 (4), p.384-385

1997

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Pancreatic beta-cell secretory defect associated with mitochondrial point mutation of the tRNA(LEU(UUR)) gene: a study in seven families with mitochondrial encephalomyopathy, lactic acidosis and stroke-like episodes (MELAS)

Diabetologia, 1994-08, Vol.37 (8), p.818-825

1994

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Secondary sulfonylurea failure: Comparison of period until insulin treatment between diabetic patients treated with gliclazide and glibenclamide

Diabetes research and clinical practice, 2005-12, Vol.70 (3), p.291-297

2005

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Beta-cell transcription factors and diabetes: no evidence for diabetes-associated mutations in the hepatocyte nuclear factor-3beta gene (HNF3B) in Japanese patients with maturity-onset diabetes of the young

Diabetes (New York, N.Y.), 2000-02, Vol.49 (2), p.302-305

2000

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Genetic variations at urotensin II and urotensin II receptor genes and risk of type 2 diabetes mellitus in Japanese

Peptides (New York, N.Y. : 1980), 2004-10, Vol.25 (10), p.1803-1808

2004

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Variations in vitamin D-binding protein (group-specific component protein) are associated with fasting plasma insulin levels in Japanese with normal glucose tolerance

The journal of clinical endocrinology and metabolism, 2000-05, Vol.85 (5), p.1951-1953

2000

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Mutations in the genes for hepatocyte nuclear factor (HNF)-1alpha, -4alpha, -1beta, and -3beta; the dimerization cofactor of HNF-1; and insulin promoter factor 1 are not common causes of early-onset type 2 diabetes in Pima Indians

Diabetes care, 2000-03, Vol.23 (3), p.302-304

2000

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Mutations in the hepatocyte nuclear factor-1alpha/MODY3 gene in Japanese subjects with early- and late-onset NIDDM

Diabetes (New York, N.Y.), 1997-09, Vol.46 (9), p.1504-1508

1997

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Oxidative damage to mitochondrial DNA and its relationship to diabetic complications

Diabetes research and clinical practice, 1999-09, Vol.45 (2), p.161-168

1999

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Genetic variation in the hepatocyte nuclear factor-3beta gene (HNF3B) does not contribute to maturity-onset diabetes of the young in French Caucasians

Diabetes (New York, N.Y.), 2000-02, Vol.49 (2), p.306-308

2000

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WRN gene 1367 Arg allele protects against development of type 2 diabetes mellitus

Diabetes research and clinical practice, 2005-09, Vol.69 (3), p.287-292

2005

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Diabetes with mitochondrial gene tRNALYS mutation

Diabetes care, 1994-12, Vol.17 (12), p.1428-1432

1994

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Promoter polymorphism of SLC11A1 (formerly NRAMP1) confers susceptibility to autoimmune type 1 diabetes mellitus in Japanese

Tissue antigens, 2004-03, Vol.63 (3), p.231-236

2004

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Mitochondrial DNA 3394 Mutation in the NADH Dehydrogenase Subunit 1 Associated with Non-Insulin-Dependent Diabetes Mellitus

Biochemical and biophysical research communications, 1996-02, Vol.219 (3), p.951-955

1996

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β-cell transcription factors and diabetes ; No evidence for diabetes-associated mutations in the hepatocyte nuclear factor-3β gene (HNF3B) in Japanese patients with maturity-onset diabetes of the young

Diabetes (New York, N.Y.), 2000-02, Vol.49 (2), p.302-305

2000

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Urinary excretion of 8-oxo-7, 8-dihydro-2'-deoxyguanosine as a predictor of the development of diabetic nephropathy

Oxidative DNA damage in diabetes mellitus : its association with diabetic complications

Role of urotensin II gene in genetic susceptibility to Type 2 diabetes mellitus in Japanese subjects

Organization and partial sequence of the hepatocyte nuclear factor-4 alpha/MODY1 gene and identification of a missense mutation, R127W, in a Japanese family with MODY

The effects of coenzyme Q10 treatment on maternally inherited diabetes mellitus and deafness, and mitochondrial DNA 3243 (A to G) mutation

Tyrosine hydroxylase gene microsatellite polymorphism associated with insulin resistance in depressive disorder

Genetic variation in the gene encoding calpain-10 is associated with type 2 diabetes mellitus

Group specific component protein genotype is associated with NIDDM in Japan

Diabetes associated with a novel 3264 mitochondrial tRNA(Leu)(UUR) mutation

Urinary chiro-inositol excretion is an index marker of insulin sensitivity in Japanese type II diabetes

Mutation in hepatocyte nuclear factor-1β gene (TCF2) associated with MODY

Pancreatic beta-cell secretory defect associated with mitochondrial point mutation of the tRNA(LEU(UUR)) gene: a study in seven families with mitochondrial encephalomyopathy, lactic acidosis and stroke-like episodes (MELAS)

Secondary sulfonylurea failure: Comparison of period until insulin treatment between diabetic patients treated with gliclazide and glibenclamide

Beta-cell transcription factors and diabetes: no evidence for diabetes-associated mutations in the hepatocyte nuclear factor-3beta gene (HNF3B) in Japanese patients with maturity-onset diabetes of the young

Genetic variations at urotensin II and urotensin II receptor genes and risk of type 2 diabetes mellitus in Japanese

Variations in vitamin D-binding protein (group-specific component protein) are associated with fasting plasma insulin levels in Japanese with normal glucose tolerance

Mutations in the genes for hepatocyte nuclear factor (HNF)-1alpha, -4alpha, -1beta, and -3beta; the dimerization cofactor of HNF-1; and insulin promoter factor 1 are not common causes of early-onset type 2 diabetes in Pima Indians

Mutations in the hepatocyte nuclear factor-1alpha/MODY3 gene in Japanese subjects with early- and late-onset NIDDM

Oxidative damage to mitochondrial DNA and its relationship to diabetic complications

Genetic variation in the hepatocyte nuclear factor-3beta gene (HNF3B) does not contribute to maturity-onset diabetes of the young in French Caucasians

WRN gene 1367 Arg allele protects against development of type 2 diabetes mellitus

Diabetes with mitochondrial gene tRNALYS mutation

Promoter polymorphism of SLC11A1 (formerly NRAMP1) confers susceptibility to autoimmune type 1 diabetes mellitus in Japanese

Mitochondrial DNA 3394 Mutation in the NADH Dehydrogenase Subunit 1 Associated with Non-Insulin-Dependent Diabetes Mellitus

β-cell transcription factors and diabetes ; No evidence for diabetes-associated mutations in the hepatocyte nuclear factor-3β gene (HNF3B) in Japanese patients with maturity-onset diabetes of the young

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