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Haplotype Combinations of Calpain 10 Gene Polymorphisms Associate With Increased Risk of Impaired Glucose Tolerance and Type 2 Diabetes in South Indians

Diabetes (New York, N.Y.), 2002-05, Vol.51 (5), p.1622-1628

2002

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Adults with RRM2B-related mitochondrial disease have distinct clinical and molecular characteristics

Brain (London, England : 1878), 2012-11, Vol.135 (Pt 11), p.3392-3403

2012

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Variation in the Calpain-10 Gene Affects Blood Glucose Levels in the British Population

Diabetes (New York, N.Y.), 2002-01, Vol.51 (1), p.247-250

2002

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NTNG1 mutations are a rare cause of Rett syndrome

American journal of medical genetics. Part A, 2006-04, Vol.140A (7), p.691-694

2006

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beta-cell genes and diabetes: molecular and clinical characterization of mutations in transcription factors

Diabetes (New York, N.Y.), 2001-02, Vol.50 (suppl 1), p.S94-S100

2001

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Early onset seizures and Rett-like features associated with mutations in CDKL5

European journal of human genetics : EJHG, 2005-10, Vol.13 (10), p.1113-1120

2005

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Apolipoprotein-E Influences Aspects of Intellectual Ability in Type 1 Diabetes

Diabetes (New York, N.Y.), 2003-01, Vol.52 (1), p.145-148

2003

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Family-Based Analysis Using a Dense Single-Nucleotide Polymorphism–Based Map Defines Genetic Variation at PSORS1, the Major Psoriasis-Susceptibility Locus

American journal of human genetics, 2002-09, Vol.71 (3), p.554-564

2002

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Missense mutations in the insulin promoter factor-1 gene predispose to type 2 diabetes

The Journal of clinical investigation, 1999-11, Vol.104 (9), p.R33-R39

1999

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Variation within the Type 2 Diabetes Susceptibility Gene Calpain-10 and Polycystic Ovary Syndrome

The journal of clinical endocrinology and metabolism, 2002-06, Vol.87 (6), p.2606-2610

2002

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Variation in exon 1 coding region and promoter of MECP2 in Rett syndrome and controls

European journal of human genetics : EJHG, 2005-01, Vol.13 (1), p.124-126

2005

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Retrospective natural history of thymidine kinase 2 deficiency

Journal of medical genetics, 2018-08, Vol.55 (8), p.515

2018

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Parent-offspring trios: a resource to facilitate the identification of type 2 diabetes genes

Diabetes (New York, N.Y.), 1999-12, Vol.48 (12), p.2475

1999

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A Genome-Wide Scan in Families With Maturity-Onset Diabetes of the Young

Diabetes (New York, N.Y.), 2003-03, Vol.52 (3), p.872-881

2003

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Studies of Association between the Gene for Calpain-10 and Type 2 Diabetes Mellitus in the United Kingdom

American journal of human genetics, 2001-09, Vol.69 (3), p.544-552

2001

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Variation within the type 2 diabetes susceptibility gene calpain-10 and polycystic ovary syndrome

The journal of clinical endocrinology and metabolism, 2002-06, Vol.87 (6), p.2606-2610

2002

Volltextzugriff (PDF)

Variation in the caplain-10 gene affects blood glucose levels in the British population

Diabetes (New York, N.Y.), 2002-01, Vol.51 (1), p.247

2002

Volltextzugriff (PDF)

Haplotype combinations of calpain 10 gene polymorphisms assiciate with increased risk of impaired glucose tolerance and type 2 diabetes in South Indians

Diabetes (New York, N.Y.), 2002-05, Vol.51 (5), p.1622

2002

Volltextzugriff (PDF)

(Beta)-cell genes and diabetes: Molecular and clinical characterization of mutations in transcription factors

Diabetes (New York, N.Y.), 2001-02, Vol.50, p.S94

2001

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Variation in the Calpain 10 Gene Is Associated with Glucose Tolerance in Non-Diabetic European Caucasians

Diabetes (New York, N.Y.), 2000-05, Vol.49 (5), p.A198

2000

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Transmission Disequilibruim at the Calpain10/NIDDDM1 Gene in UK Caucasian Type 2 Diabetes Parent-Offspring Trios

Diabetes (New York, N.Y.), 2000-05, Vol.49 (5), p.A8

2000

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[Beta]-Cell Genes and Diabetes

Diabetes (New York, N.Y.), 2001-02, Vol.50 (2), p.S94

2001

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Β-Cell Genes and Diabetes

Diabetes (New York, N.Y.), 2001-02, Vol.50 (2), p.S94

2001

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Haplotype Combinations of Calpain 10 Gene Polymorphisms Associate With Increased Risk of Impaired Glucose Tolerance and Type 2 Diabetes in South Indians

Adults with RRM2B-related mitochondrial disease have distinct clinical and molecular characteristics

Variation in the Calpain-10 Gene Affects Blood Glucose Levels in the British Population

NTNG1 mutations are a rare cause of Rett syndrome

beta-cell genes and diabetes: molecular and clinical characterization of mutations in transcription factors

Early onset seizures and Rett-like features associated with mutations in CDKL5

Apolipoprotein-E Influences Aspects of Intellectual Ability in Type 1 Diabetes

Family-Based Analysis Using a Dense Single-Nucleotide Polymorphism–Based Map Defines Genetic Variation at PSORS1, the Major Psoriasis-Susceptibility Locus

Missense mutations in the insulin promoter factor-1 gene predispose to type 2 diabetes

Association of the calpain-10 gene with type 2 diabetes in Europeans: Results of pooled and meta-analyses

Variation within the Type 2 Diabetes Susceptibility Gene Calpain-10 and Polycystic Ovary Syndrome

A genome-wide scan in families with maturity-onset diabetes of the young: Evidence for further genetic heterogeneity

Variation in exon 1 coding region and promoter of MECP2 in Rett syndrome and controls

Retrospective natural history of thymidine kinase 2 deficiency

Parent-offspring trios: a resource to facilitate the identification of type 2 diabetes genes

A Genome-Wide Scan in Families With Maturity-Onset Diabetes of the Young

Studies of Association between the Gene for Calpain-10 and Type 2 Diabetes Mellitus in the United Kingdom

Variation within the type 2 diabetes susceptibility gene calpain-10 and polycystic ovary syndrome

Variation in the caplain-10 gene affects blood glucose levels in the British population

Haplotype combinations of calpain 10 gene polymorphisms assiciate with increased risk of impaired glucose tolerance and type 2 diabetes in South Indians

(Beta)-cell genes and diabetes: Molecular and clinical characterization of mutations in transcription factors

Variation in the Calpain 10 Gene Is Associated with Glucose Tolerance in Non-Diabetic European Caucasians

Transmission Disequilibruim at the Calpain10/NIDDDM1 Gene in UK Caucasian Type 2 Diabetes Parent-Offspring Trios

[Beta]-Cell Genes and Diabetes

Β-Cell Genes and Diabetes

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