Found: 14
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Vibration perception threshold for sight-threatening retinopathy screening in type 2 diabetic outpatients.
- Published in:
- Diabetes/Metabolism Research & Reviews, 2013, v. 29, n. 7, p. 525, doi. 10.1002/dmrr.2423
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- Publication type:
- Article
Mutations in KCNJ11 are associated with the development of autosomal dominant, early-onset type 2 diabetes.
- Published in:
- Diabetologia, 2013, v. 56, n. 12, p. 2609, doi. 10.1007/s00125-013-3031-9
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- Publication type:
- Article
Different effect of testosterone and oestrogen on urinary excretion of metformin via regulating OCTs and MATEs expression in the kidney of mice.
- Published in:
- Journal of Cellular & Molecular Medicine, 2016, v. 20, n. 12, p. 2309, doi. 10.1111/jcmm.12922
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- Publication type:
- Article
Polymorphism of Organic Cation Transporter 2 Improves Glucose-Lowering Effect of Metformin via Influencing Its Pharmacokinetics in Chinese Type 2 Diabetic Patients.
- Published in:
- Molecular Diagnosis & Therapy, 2015, v. 19, n. 1, p. 25, doi. 10.1007/s40291-014-0126-z
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- Publication type:
- Article
The angiotensin-I converting enzyme gene I/D variation contributes to end-stage renal disease risk in Chinese patients with type 2 diabetes receiving hemodialysis.
- Published in:
- Molecular & Cellular Biochemistry, 2016, v. 422, n. 1/2, p. 181, doi. 10.1007/s11010-016-2819-6
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- Publication type:
- Article
The E23K and A190A variations of the KCNJ11 gene are associated with early-onset type 2 diabetes and blood pressure in the Chinese population.
- Published in:
- Molecular & Cellular Biochemistry, 2015, v. 404, n. 1/2, p. 133, doi. 10.1007/s11010-015-2373-7
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- Publication type:
- Article
The Leu72Met polymorphism of the GHRL gene prevents the development of diabetic nephropathy in Chinese patients with type 2 diabetes mellitus.
- Published in:
- Molecular & Cellular Biochemistry, 2014, v. 387, n. 1/2, p. 19, doi. 10.1007/s11010-013-1865-6
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- Publication type:
- Article
Polymorphic variations in manganese superoxide dismutase (MnSOD), glutathione peroxidase-1 (GPX1), and catalase (CAT) contribute to elevated plasma triglyceride levels in Chinese patients with type 2 diabetes or diabetic cardiovascular disease.
- Published in:
- Molecular & Cellular Biochemistry, 2012, v. 363, n. 1/2, p. 85, doi. 10.1007/s11010-011-1160-3
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- Publication type:
- Article
The manganese superoxide dismutase Val16Ala polymorphism is associated with decreased risk of diabetic nephropathy in Chinese patients with type 2 diabetes.
- Published in:
- Molecular & Cellular Biochemistry, 2009, v. 322, n. 1/2, p. 87, doi. 10.1007/s11010-008-9943-x
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- Publication type:
- Article
A novel mutation, Ser159Pro in the NeuroD1/BETA2 gene contributes to the development of diabetes in a Chinese potential MODY family.
- Published in:
- Molecular & Cellular Biochemistry, 2007, v. 303, n. 1/2, p. 115, doi. 10.1007/s11010-007-9463-0
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- Publication type:
- Article
Pro1981eu of Gpx-1 Gene in the Development of Nephropathy and Coronary Heart Desease in Chinese Type 2 Diabetes Mellitus.
- Published in:
- Diabetes, 2007, v. 56, p. A199
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- Publication type:
- Article
Genome-wide search for type 2 diabetes/impaired glucose homeostasis susceptibility genes in the Chinese: significant linkage to chromosome 6q21-q23 and chromosome 1q21-q24.
- Published in:
- 2004
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- Publication type:
- journal article
Genome-Wide Search for Type 2 Diabetes/Impaired Glucose Homeostasis Susceptibility Genes in the Chinese.
- Published in:
- Diabetes, 2004, v. 53, n. 1, p. 228, doi. 10.2337/diabetes.53.1.228
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- Publication type:
- Article
Pro12Ala Polymorphism in the PPARG Gene Contributes to the Development of Diabetic Nephropathy in Chinese Type 2 Diabetic Patients.
- Published in:
- Diabetes Care, 2010, v. 33, n. 1, p. 144, doi. 10.2337/dc09-1258
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- Publication type:
- Article