Found: 18
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Common coding variant in the TCF7L2 gene and study of the association with type 2 diabetes in Japanese subjects.
- Published in:
- Journal of Human Genetics, 2008, v. 53, n. 11/12, p. 972, doi. 10.1007/s10038-008-0339-2
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- Article
SNPs in the KCNJ11- ABCC8 gene locus are associated with type 2 diabetes and blood pressure levels in the Japanese population.
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- Journal of Human Genetics, 2007, v. 52, n. 10, p. 781, doi. 10.1007/s10038-007-0190-x
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- Article
Effect of +36T > C in intron 1 on the glutamine: fructose-6-phosphate amidotransferase 1 gene and its contribution to type 2 diabetes in different populations.
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- Journal of Human Genetics, 2006, v. 51, n. 12, p. 1100, doi. 10.1007/s10038-006-0072-7
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- Article
Autosomal Dominant Gnathodiaphyseal Dysplasia Maps to Chromosome 11p14.3-15.1.
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- Journal of Bone & Mineral Research, 2003, v. 18, n. 3, p. 413, doi. 10.1359/jbmr.2003.18.3.413
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- Article
Absence of Germ-Line Mutations of the Multiple Endocrine Neoplasia Type 1 (MEN1) Gene in Familial Pituitary Adenoma in Contrast to MEN1 in Japanese*.
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- Journal of Clinical Endocrinology & Metabolism, 1998, v. 83, n. 3, p. 960, doi. 10.1210/jcem.83.3.4653
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- Article
Association study on chromosome 20q11.21-13.13 locus and its contribution to type 2 diabetes susceptibility in Japanese.
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- Human Genetics, 2006, v. 120, n. 4, p. 527, doi. 10.1007/s00439-006-0231-0
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- Publication type:
- Article
Identification of monogenic gene mutations in Japanese subjects diagnosed with type 1B diabetes between > 5 and 15.1 years of age.
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- Journal of Pediatric Endocrinology & Metabolism, 2016, v. 29, n. 9, p. 1047, doi. 10.1515/jpem-2016-0030
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- Publication type:
- Article
Identification of Novel GCK and HNF4α Gene Variants in Japanese Pediatric Patients with Onset of Diabetes before 17 Years of Age.
- Published in:
- Journal of Diabetes Research, 2021, p. 1, doi. 10.1155/2021/7216339
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- Article
The Rate of Cell Growth Is Regulated by Purine Biosynthesis via ATP Production and G1 to S Phase Transition1.
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- Journal of Biochemistry, 2000, v. 128, n. 1, p. 57, doi. 10.1093/oxfordjournals.jbchem.a022730
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- Article
Bhlhe40, a potential diabetic modifier gene on locus, Dbm1 negatively controls myocyte fatty acid oxidation.
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- Genes & Genetic Systems, 2012, v. 87, n. 4, p. 253, doi. 10.1266/ggs.87.253
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- Article
Diabetic modifier QTL, Dbm4, affecting elevated fasting blood glucose concentrations in congenic mice.
- Published in:
- Genes & Genetic Systems, 2012, v. 87, n. 5, p. 341, doi. 10.1266/ggs.87.341
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- Publication type:
- Article
Diabetic modifier QTLs in F<sub>2</sub> intercrosses carrying homozygous transgene of TGF-β.
- Published in:
- Mammalian Genome, 2008, v. 19, n. 1, p. 15, doi. 10.1007/s00335-007-9080-y
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- Publication type:
- Article
Diabetic modifier QTLs identified in F<sub>2</sub> intercrosses between Akita and A/J mice.
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- Mammalian Genome, 2006, v. 17, n. 9, p. 927, doi. 10.1007/s00335-005-0130-z
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- Article
Identification of INS and KCNJ11 gene mutations in type 1B diabetes in Japanese children with onset of diabetes before 5 yr of age.
- Published in:
- Pediatric Diabetes, 2013, v. 14, n. 2, p. 112, doi. 10.1111/j.1399-5448.2012.00917.x
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- Article
A case of a Japanese patient with neonatal diabetes mellitus caused by a novel mutation in the ABCC8 gene and successfully controlled with oral glibenclamide.
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- 2015
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- Publication type:
- Case Study
Multidimensional genome scans identify the combinations of genetic loci linked to diabetes-related phenotypes in mice.
- Published in:
- Human Molecular Genetics, 2006, v. 15, n. 1, p. 113, doi. 10.1093/hmg/ddi433
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- Article
GENETIC DISORDERS - DEVELOPMENT Familial juvenile hyperuricemic nephropathy: Detection of mutations in the uromodulin gene in five Japanese families.
- Published in:
- Kidney International, 2004, v. 65, n. 5, p. 1589, doi. 10.1111/j.1523-1755.2004.00559.x
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- Article
Lack of association of genetic variation in chromosome region 15q14-22.1 with type 2 diabetes in a Japanese population.
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- BMC Medical Genetics, 2008, v. 9, p. 1, doi. 10.1186/1471-2350-9-22
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- Publication type:
- Article