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A genome-wide linkage scan for genes controlling variation in urinary albumin excretion in type II diabetes

Kidney international, 2006-01, Vol.69 (1), p.129-136

2006

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Glycosylated Hemoglobin and the Risk of Microalbuminuria in Patients with Insulin-Dependent Diabetes Mellitus

The New England journal of medicine, 1995-05, Vol.332 (19), p.1251-1255

1995

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Mutations in NEUROD1 are associated with the development of type 2 diabetes mellitus

Nature genetics, 1999-11, Vol.23 (3), p.323-328

1999

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Genetics of diabetic nephropathy: Evidence for major and minor gene effects

Kidney international, 1999-04, Vol.55 (4), p.1582-1596

Krolewski, Andrzej S.

1999

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Role of glucose and insulin resistance in development of type 2 diabetes mellitus: results of a 25-year follow-up study

The Lancet (British edition), 1992-10, Vol.340 (8825), p.925-929

1992

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Risk of advanced diabetic nephropathy in type 1 diabetes is associated with endothelial nitric oxide synthase gene polymorphism

Kidney international, 2000-02, Vol.57 (2), p.405-413

2000

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Risk of diabetes in siblings of index cases with Type 2 diabetes: implications for genetic studies

Diabetic medicine, 2002-01, Vol.19 (1), p.41-50

2002

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Familial factors determine the development of diabetic nephropathy in patients with IDDM

Diabetologia, 1996-08, Vol.39 (8), p.940-945

1996

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Major susceptibility locus for nephropathy in type 1 diabetes on chromosome 3q: results of novel discordant sib-pair analysis

Diabetes (New York, N.Y.), 1998-07, Vol.47 (7), p.1164

1998

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Physical activity and incidence of non-insulin-dependent diabetes mellitus in women

The Lancet (British edition), 1991-09, Vol.338 (8770), p.774-778

1991

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Effect of duration of type I diabetes on the prevalence of stages of diabetic nephropathy defined by urinary albumin/creatinine ratio

Journal of the American Society of Nephrology, 1996-06, Vol.7 (6), p.930-937

1996

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Aldose reductase gene polymorphisms and susceptibility to diabetic nephropathy in Type 1 diabetes mellitus

Diabetic medicine, 2000-02, Vol.17 (2), p.111-118

2000

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Segregation analysis of urinary albumin excretion in families with type 2 diabetes

Diabetes (New York, N.Y.), 2000-06, Vol.49 (6), p.1057-1063

2000

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Further evidence for a susceptibility locus for type 2 diabetes on chromosome 20q13.1-q13.2

Diabetes (New York, N.Y.), 2000-12, Vol.49 (12), p.2212-2216

2000

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Urinary albumin excretion in families with type 2 diabetes is heritable and genetically correlated to blood pressure

Kidney international, 2000-01, Vol.57 (1), p.250-257

2000

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APOE polymorphisms and the development of diabetic nephropathy in type 1 diabetes: results of case-control and family-based studies

Diabetes (New York, N.Y.), 2000-12, Vol.49 (12), p.2190-2195

2000

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Slow glucose removal rate and hyperinsulinemia precede the development of type II diabetes in the offspring of diabetic parents

Annals of internal medicine, 1990-12, Vol.113 (12), p.909

1990

Volltextzugriff (PDF)

Synergistic effect of angiotensin II type 1 receptor genotype and poor glycaemic control on risk of nephropathy in IDDM

Diabetologia, 1997-11, Vol.40 (11), p.1293-1299

1997

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Lack of association between polymorphisms in the gene encoding protein tyrosine phosphatase 1B (PTPN1) and risk of Type 2 diabetes

Diabetic medicine, 2007-06, Vol.24 (6), p.650-655

2007

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Examination of PPP1R3B as a candidate gene for the type 2 diabetes and MODY loci on chromosome 8p23

Annals of human genetics, 2006-09, Vol.70 (5), p.587-593

2006

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Progression of microalbuminuria to proteinuria in type 1 diabetes: nonlinear relationship with hyperglycemia

Diabetes (New York, N.Y.), 2000-01, Vol.49 (1), p.94-100

2000

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Evidence of a novel type 2 diabetes locus 50 cM centromeric to NIDDM2 on chromosome 12q

Diabetes (New York, N.Y.), 1999-11, Vol.48 (11), p.2246

1999

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Streszczenie diariusza wojennego Kazimierza Dłużewskiego z lat 1683–1696

Zeszyty naukowe Uniwersytetu Jagiellońskiego. Prace historyczne, 2019, Vol.146 (1), p.279-296

Hundert, Zbigniew

2019

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Polymorphisms of human paraoxonase 1 gene (PON1) and susceptibility to diabetic nephropathy in Type I diabetes mellitus

Diabetologia, 2000-12, Vol.43 (12), p.1540-1543

2000

Volltextzugriff (PDF)

A newly identified mutation in an IPF1 binding site of the insulin gene promoter may predispose to type 2 diabetes mellitus

Diabetologia, 2006-08, Vol.49 (8), p.1985-1987

2006

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A genome-wide linkage scan for genes controlling variation in urinary albumin excretion in type II diabetes

Glycosylated Hemoglobin and the Risk of Microalbuminuria in Patients with Insulin-Dependent Diabetes Mellitus

Mutations in NEUROD1 are associated with the development of type 2 diabetes mellitus

Genetics of diabetic nephropathy: Evidence for major and minor gene effects

Role of glucose and insulin resistance in development of type 2 diabetes mellitus: results of a 25-year follow-up study

Risk of advanced diabetic nephropathy in type 1 diabetes is associated with endothelial nitric oxide synthase gene polymorphism

Risk of diabetes in siblings of index cases with Type 2 diabetes: implications for genetic studies

Familial factors determine the development of diabetic nephropathy in patients with IDDM

Major susceptibility locus for nephropathy in type 1 diabetes on chromosome 3q: results of novel discordant sib-pair analysis

Physical activity and incidence of non-insulin-dependent diabetes mellitus in women

Effect of duration of type I diabetes on the prevalence of stages of diabetic nephropathy defined by urinary albumin/creatinine ratio

Aldose reductase gene polymorphisms and susceptibility to diabetic nephropathy in Type 1 diabetes mellitus

Segregation analysis of urinary albumin excretion in families with type 2 diabetes

Further evidence for a susceptibility locus for type 2 diabetes on chromosome 20q13.1-q13.2

Urinary albumin excretion in families with type 2 diabetes is heritable and genetically correlated to blood pressure

APOE polymorphisms and the development of diabetic nephropathy in type 1 diabetes: results of case-control and family-based studies

Slow glucose removal rate and hyperinsulinemia precede the development of type II diabetes in the offspring of diabetic parents

Synergistic effect of angiotensin II type 1 receptor genotype and poor glycaemic control on risk of nephropathy in IDDM

Lack of association between polymorphisms in the gene encoding protein tyrosine phosphatase 1B (PTPN1) and risk of Type 2 diabetes

Examination of PPP1R3B as a candidate gene for the type 2 diabetes and MODY loci on chromosome 8p23

Progression of microalbuminuria to proteinuria in type 1 diabetes: nonlinear relationship with hyperglycemia

Evidence of a novel type 2 diabetes locus 50 cM centromeric to NIDDM2 on chromosome 12q

Streszczenie diariusza wojennego Kazimierza Dłużewskiego z lat 1683–1696

Polymorphisms of human paraoxonase 1 gene (PON1) and susceptibility to diabetic nephropathy in Type I diabetes mellitus

A newly identified mutation in an IPF1 binding site of the insulin gene promoter may predispose to type 2 diabetes mellitus

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