Concepedia

Single nucleotide polymorphisms in the Trx2/TXNIP and TrxR2 genes of the mitochondrial thioredoxin antioxidant system and the risk of diabetic retinopathy in patients with Type 2 diabetes mellitus

Ines Cilenšek, Mojca Globočnik Petrovič, Miroslav Souček, Peter Kružliak, Daniel Petrovič

Journal of Diabetes and its Complications · 2015 · 26 citations · 48 references

Concepts

MedicineGeneticsMolecular GeneticsDiabetologyMedical GeneticsMitochondrial GeneticsDiabetes MellitusDiabetic RetinopathyDiabetic Retinopathy EpidemiologyMitochondrial DysfunctionThioredoxin SystemDiabetic Retinopathy IncidenceDiabetic Retinopathy ProgressionMitochondrial Genetic SusceptibilityMitochondrial Thioredoxin SystemSingle-nucleotide PolymorphismsType 2 Diabetes Retinopathy Epidemiology

References

48

Intensive blood-glucose control with sulphonylureas or insulin compared with conventional treatment and risk of complications in patients with type 2 diabetes (UKPDS 33)

The Lancet · 1998 · 20.1K citations

Medicine, Endocrinology, Pharmacotherapy +13

Diagnosis and Classification of Diabetes Mellitus

Diabetes Care · 2010 · 14K citations · Full text

Medicine, Endocrinology, Internal Medicine +11

Intensive blood-glucose control with sulphonylureas or insulin compared with conventional treatment and risk of complications in patients with type 2 diabetes (UKPDS 33). UK Prospective Diabetes Study (UKPDS) Group.

R. C. Turner, Charles Fox, Matthews et al. · The Lancet · 1998 · 8.4K citations

Medicine, Endocrinology, Pharmacotherapy +15

Diagnosis and Classification of Diabetes Mellitus

Diabetes Care · 2013 · 6K citations · Full text

Medicine, Endocrinology, Internal Medicine +11

A novel MHC class I–like gene is mutated in patients with hereditary haemochromatosis

John N. Feder, Andreas Gnirke, Zenta Tsuchihashi et al. · Nature Genetics · 1996 · 3.7K citations

Life Sciences, Genetics, Molecular Genetics +12