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Effect of exposure to non-esterified fatty acid on progressive deterioration of insulin secretion in patients with Type 2 diabetes: a long-term follow-up study

Diabetic medicine, 2012-08, Vol.29 (8), p.980-985

2012

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Podocalyxin expression in undifferentiated thyroid carcinomas

Journal of clinical pathology, 2008-11, Vol.61 (11), p.1228-1229

2008

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Missense mutation of amylin gene (S20G) in Japanese NIDDM patients

Diabetes (New York, N.Y.), 1996-09, Vol.45 (9), p.1279-1281

1996

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Nonsense mutation of islet-1 gene (Q310X) found in a type 2 diabetic patient with a strong family history

Diabetes (New York, N.Y.), 2000-09, Vol.49 (9), p.1597-1600

2000

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Single nucleotide polymorphism (D68D, T to C) in the syntaxin 1A gene correlates to age at onset and insulin requirement in Type II diabetic patients

Diabetologia, 2001-11, Vol.44 (11), p.2092-2097

2001

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Non-autoimmune fulminant type 1 diabetes

Rinsho byori. The Japanese journal of clinical pathology, 2001-12, Vol.49 (12), p.1185

Sanke, T

2001

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Functional Variants in the Glutathione Peroxidase-1 (GPx-1) Gene Are Associated With Increased Intima-Media Thickness of Carotid Arteries and Risk of Macrovascular Diseases in Japanese Type 2 Diabetic Patients

Diabetes (New York, N.Y.), 2004-09, Vol.53 (9), p.2455-2460

2004

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An islet amyloid peptide is derived from an 89-amino acid precursor by proteolytic processing

The Journal of biological chemistry, 1988-11, Vol.263 (33), p.17243-17246

1988

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Organization of the human carboxypeptidase E gene and molecular scanning for mutations in Japanese subjects with NIDDM or obesity

Diabetologia, 1998-06, Vol.41 (6), p.701-705

1998

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Development of prediction for NIDDM from a view point of genetics

Nihon rinshō, 1997-11, Vol.55 Suppl, p.362

Sanke, T

1997

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Enhanced in vitro production of amyloid-like fibrils from mutant (S20G) islet amyloid polypeptide

Amyloid, 2001, Vol.8 (4), p.242-249

2001

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Plasma islet amyloid polypeptide (Amylin) levels and their responses to oral glucose in type 2 (non-insulin-dependent) diabetic patients

Diabetologia, 1991-02, Vol.34 (2), p.129-132

1991

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A missense mutation of the muscle glycogen synthase gene (M416V) is associated with insulin resistance in the Japanese population

Diabetologia, 1997-08, Vol.40 (8), p.947-952

1997

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Lessons learned from molecular biology of insulin-gene mutations

Diabetes care, 1990-06, Vol.13 (6), p.600-609

1990

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Association of the prohormone convertase 2 gene (PCSK2) on chromosome 20 with NIDDM in Japanese subjects

Diabetes (New York, N.Y.), 1995-04, Vol.44 (4), p.389-393

1995

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Molecular scanning for mutations in the melanocortin-4 receptor gene in obese/diabetic Japanese

Annals of human genetics, 1999-11, Vol.63, p.483-487

1999

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Human prohormone convertase 3 gene: exon-intron organization and molecular scanning for mutations in Japanese subjects with NIDDM

Diabetes (New York, N.Y.), 1996-07, Vol.45 (7), p.897-901

1996

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Contrast-Enhanced Ultrasonography in the Diagnosis of Solid Renal Tumors

Journal of ultrasound in medicine, 2005-12, Vol.24 (12), p.1635-1640

2005

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Islet amyloid polypeptide amide causes peripheral insulin resistance in vivo in dogs

Diabetologia, 1990-02, Vol.33 (2), p.118-120

1990

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Molecular scanning for mutations in the melanocortin-4 receptor gene in obese/diabetic Japanese

Annals of human genetics, 1999-11, Vol.63 (6), p.483-487

1999

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Human prohormone convertase 3 gene: exon-intron organization and molecular scanning for mutations in Japanese subjects with NIDDM

Diabetes (New York, N.Y.), 1996-07, Vol.45 (7), p.897-901

1996

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Simple tandem repeat DNA polymorphism in the human glycogen synthase gene is associated with NIDDM in Japanese subjects

Diabetologia, 1994-05, Vol.37 (5), p.536-539

1994

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Cloning of mouse islet amyloid polypeptide gene and characterization of its promoter

Journal of molecular endocrinology, 1997-08, Vol.19 (1), p.79-86

1997

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S20G Mutant Amylin Exhibits Increased in Vitro Amyloidogenicity and Increased Intracellular Cytotoxicity Compared to Wild-Type Amylin

The American journal of pathology, 2000-12, Vol.157 (6), p.2101-2109

2000

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A Missense Mutation of Pax4 Gene (R121W) Is Associated With Type 2 Diabetes in Japanese

Diabetes (New York, N.Y.), 2001-12, Vol.50 (12), p.2864-2869

2001

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Effect of exposure to non-esterified fatty acid on progressive deterioration of insulin secretion in patients with Type 2 diabetes: a long-term follow-up study

Podocalyxin expression in undifferentiated thyroid carcinomas

Missense mutation of amylin gene (S20G) in Japanese NIDDM patients

Nonsense mutation of islet-1 gene (Q310X) found in a type 2 diabetic patient with a strong family history

Single nucleotide polymorphism (D68D, T to C) in the syntaxin 1A gene correlates to age at onset and insulin requirement in Type II diabetic patients

Non-autoimmune fulminant type 1 diabetes

Functional Variants in the Glutathione Peroxidase-1 (GPx-1) Gene Are Associated With Increased Intima-Media Thickness of Carotid Arteries and Risk of Macrovascular Diseases in Japanese Type 2 Diabetic Patients

An islet amyloid peptide is derived from an 89-amino acid precursor by proteolytic processing

Organization of the human carboxypeptidase E gene and molecular scanning for mutations in Japanese subjects with NIDDM or obesity

Development of prediction for NIDDM from a view point of genetics

Enhanced in vitro production of amyloid-like fibrils from mutant (S20G) islet amyloid polypeptide

Plasma islet amyloid polypeptide (Amylin) levels and their responses to oral glucose in type 2 (non-insulin-dependent) diabetic patients

A missense mutation of the muscle glycogen synthase gene (M416V) is associated with insulin resistance in the Japanese population

Lessons learned from molecular biology of insulin-gene mutations

Association of the prohormone convertase 2 gene (PCSK2) on chromosome 20 with NIDDM in Japanese subjects

Molecular scanning for mutations in the melanocortin-4 receptor gene in obese/diabetic Japanese

Human prohormone convertase 3 gene: exon-intron organization and molecular scanning for mutations in Japanese subjects with NIDDM

Contrast-Enhanced Ultrasonography in the Diagnosis of Solid Renal Tumors

Islet amyloid polypeptide amide causes peripheral insulin resistance in vivo in dogs

Molecular scanning for mutations in the melanocortin-4 receptor gene in obese/diabetic Japanese

Human prohormone convertase 3 gene: exon-intron organization and molecular scanning for mutations in Japanese subjects with NIDDM

Simple tandem repeat DNA polymorphism in the human glycogen synthase gene is associated with NIDDM in Japanese subjects

Cloning of mouse islet amyloid polypeptide gene and characterization of its promoter

S20G Mutant Amylin Exhibits Increased in Vitro Amyloidogenicity and Increased Intracellular Cytotoxicity Compared to Wild-Type Amylin

A Missense Mutation of Pax4 Gene (R121W) Is Associated With Type 2 Diabetes in Japanese

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