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Pathogenic monoallelic variants in GLIS3 increase type 2 diabetes risk and identify a subgroup of patients sensitive to sulfonylureas.
- Published in:
- Diabetologia, 2024, v. 67, n. 2, p. 327, doi. 10.1007/s00125-023-06035-x
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- Publication type:
- Article
Fostering improved human islet research: a European perspective.
- Published in:
- 2019
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- Publication type:
- Letter
Early metabolic markers identify potential targets for the prevention of type 2 diabetes.
- Published in:
- Diabetologia, 2017, v. 60, n. 9, p. 1740, doi. 10.1007/s00125-017-4325-0
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- Publication type:
- Article
The case for too little melatonin signalling in increased diabetes risk.
- Published in:
- 2017
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- Publication type:
- Editorial
Management of pregnancy in a patient with congenital hyperinsulinism treated with association of diazoxide/calcium channel blocker.
- Published in:
- Acta Diabetologica, 2022, v. 59, n. 8, p. 1117, doi. 10.1007/s00592-022-01898-9
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- Publication type:
- Article
Lack of association between the Pro<sub>12</sub>Ala polymorphism of the PPAR-γ2 gene and type 2 diabetes mellitus in the Qatari consanguineous population.
- Published in:
- Acta Diabetologica, 2008, v. 45, n. 1, p. 15, doi. 10.1007/s00592-007-0013-8
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- Publication type:
- Article
Identification of susceptibility genes for complex diseases using pooling-based genome-wide association scans.
- Published in:
- Human Genetics, 2009, v. 125, n. 3, p. 305, doi. 10.1007/s00439-009-0626-9
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- Publication type:
- Article
Identification of a locus for nongoitrous congenital hypothyroidism on chromosome 15q25.3-26.1.
- Published in:
- Human Genetics, 2005, v. 118, n. 3/4, p. 348, doi. 10.1007/s00439-005-0036-6
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- Publication type:
- Article
Knocking Down CDKN2A in 3D hiPSC-Derived Brown Adipose Progenitors Potentiates Differentiation, Oxidative Metabolism and Browning Process.
- Published in:
- Cells (2073-4409), 2023, v. 12, n. 6, p. 870, doi. 10.3390/cells12060870
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- Publication type:
- Article
High-Throughput Quantitative Screening of Glucose-Stimulated Insulin Secretion and Insulin Content Using Automated MALDI-TOF Mass Spectrometry.
- Published in:
- Cells (2073-4409), 2023, v. 12, n. 6, p. 849, doi. 10.3390/cells12060849
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- Publication type:
- Article
Glucose Regulates m 6 A Methylation of RNA in Pancreatic Islets.
- Published in:
- Cells (2073-4409), 2022, v. 11, n. 2, p. 291, doi. 10.3390/cells11020291
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- Publication type:
- Article
Control of human pancreatic beta cell kinome by glucagon‐like peptide‐1 receptor biased agonism.
- Published in:
- Diabetes, Obesity & Metabolism, 2023, v. 25, n. 8, p. 2105, doi. 10.1111/dom.15083
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- Publication type:
- Article
Next-generation sequencing for identifying new genes in rare genetic diseases: many challenges and a pinch of luck.
- Published in:
- Genome Biology, 2013, v. 14, n. 7, p. 309, doi. 10.1186/gb-2013-14-7-309
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- Publication type:
- Article
Distinct virulence ranges for infection of mice by Bordetella pertussis revealed by engineering of the sensor-kinase BvgS.
- Published in:
- PLoS ONE, 2018, v. 13, n. 10, p. 1, doi. 10.1371/journal.pone.0204861
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- Publication type:
- Article
Multiple genetic variants at the SLC30A8 locus affect local super-enhancer activity and influence pancreatic ß-cell survival and function.
- Published in:
- FASEB Journal, 2024, v. 38, n. 8, p. 1, doi. 10.1096/fj.202301700RR
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- Publication type:
- Article
Genetics of the APM1 locus and its contribution to type 2 diabetes susceptibility in French Caucasians.
- Published in:
- 2004
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- Publication type:
- journal article
Kir6.2 Mutations Are a Common Cause of Permanent NeonatalDiabetes in a Large Cohort of French Patients.
- Published in:
- Diabetes, 2004, v. 53, n. 10, p. 2719, doi. 10.2337/diabetes.53.10.2719
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- Publication type:
- Article
Polymorphisms in the amino acid transporter solute carrier family 6 (neurotransmitter transporter) member 14 gene contribute to polygenic obesity in French Caucasians.
- Published in:
- 2004
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- Publication type:
- journal article
SREBF-1 gene polymorphisms are associated with obesity and type 2 diabetes in French obese and diabetic cohorts.
- Published in:
- 2004
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- Publication type:
- journal article
Genome-wide linkage analysis for severe obesity in french caucasians finds significant susceptibility locus on chromosome 19q.
- Published in:
- 2004
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- Publication type:
- journal article
Adiponectin gene polymorphisms and adiponectin levels are independently associated with the development of hyperglycemia during a 3-year period: the epidemiologic data on the insulin resistance syndrome prospective study.
- Published in:
- 2004
- By:
- Publication type:
- journal article
A Genome-Wide Scan for Childhood Obesity-Associated Traits in French Families Shows Significant Linkage on Chromosome 6q22.31-q23.2.
- Published in:
- Diabetes, 2004, v. 53, n. 3, p. 803, doi. 10.2337/diabetes.53.3.803
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- Publication type:
- Article
A quantitative trait locus influencing type 2 diabetes susceptibility maps to a region on 5q in an extended French family.
- Published in:
- 2002
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- Publication type:
- journal article
Positional candidate gene analysis of Lim domain homeobox gene (Isl-1) on chromosome 5q11-q13 in a French morbidly obese population suggests indication for association with type 2 diabetes.
- Published in:
- 2002
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- Publication type:
- journal article
No Evidence for Linkage or for Diabetes-Associated Mutations in the Activin Type 2B Receptor Gene (ACVR2B) in French Patients With Mature-Onset Diabetes of the Young or Type 2 Diabetes.
- Published in:
- Diabetes, 2001, v. 50, n. 5, p. 1219, doi. 10.2337/diabetes.50.5.1219
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- Publication type:
- Article
Promoter polymorphism T(-107)C of the paraoxonase PON1 gene is a risk factor for coronary heart disease in type 2 diabetic patients.
- Published in:
- 2000
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- Publication type:
- journal article
Soluble leptin receptor in serum of subjects with complete resistance to leptin: relation to fat mass.
- Published in:
- 2000
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- Publication type:
- journal article
Brief Genetics Report: Genetic variation in the hepatocyte nuclear factor-3beta gene (HNF3B) does not contribute to maturity-onset diabetes of the young in french Caucasians.
- Published in:
- Diabetes, 2000, v. 49, n. 2, p. 306, doi. 10.2337/diabetes.49.2.306
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- Publication type:
- Article
A sib-pair analysis study of 15 candidate genes in French families morbid obesity.
- Published in:
- Diabetes, 1999, v. 48, n. 2, p. 398, doi. 10.2337/diabetes.48.2.398
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- Publication type:
- Article
Mutation screening and association studies of the human uncoupling protein 3 gene in normoglycemic and diabetic morbidly obese patients.
- Published in:
- 1999
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- Publication type:
- journal article
No association between the Friedreich's ataxia gene and NIDDM in the French population.
- Published in:
- 1998
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- Publication type:
- journal article
Glucose utilization and production in patients with maturity-onset diabetes of the young caused by a mutation of the hepatocyte nuclear factor-1alpha gene.
- Published in:
- 1998
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- Publication type:
- journal article
Insulin promoter factor 1 gene is not a major cause of maturity-onset diabetes of the young in...
- Published in:
- Diabetes, 1998, v. 47, n. 5, p. 843, doi. 10.2337/diabetes.47.5.843
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- Publication type:
- Article
Mutation screening of the human UCP 2 gene in normoglycemic and NIDDM morbidly obese patients: lack of association between new UCP 2 polymorphisms and obesity in French Caucasians.
- Published in:
- 1998
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- Publication type:
- journal article
An automated fluorescent single-strand conformation polymorphism technique for screening mutations in the hepatocyte nuclear factor-1alpha gene (maturity-onset diabetes of the young).
- Published in:
- 1997
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- Publication type:
- journal article
Mapping NIDDM Susceptibility Loci in French Families.
- Published in:
- Diabetes, 1997, v. 46, n. 7, p. 1225, doi. 10.2337/diab.46.7.1225
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- Publication type:
- Article
Genetics of NIDDM in France.
- Published in:
- Diabetes, 1997, v. 46, n. 6, p. 1062, doi. 10.2337/diab.46.6.1062
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- Publication type:
- Article
Genetic studies of the sulfonylurea receptor gene locus in NIDDM and in morbid obesity among French Caucasians.
- Published in:
- 1997
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- Publication type:
- journal article
Diagnostic Heterogeneity of Diabetes in Lean Young Adults.
- Published in:
- Diabetes, 1997, v. 46, n. 4, p. 622, doi. 10.2337/diab.46.4.622
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- Publication type:
- Article
The Gly40Ser mutation in the human glucagon receptor gene associated with NIDDM results in a receptor with reduced sensitivity to glucagon.
- Published in:
- 1996
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- Publication type:
- journal article
Indication for Linkage of the Human OB Gene Region With Extreme Obesity.
- Published in:
- Diabetes, 1996, v. 45, n. 5, p. 687, doi. 10.2337/diab.45.5.687
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- Publication type:
- Article
Clinical phenotypes, insulin secretion, and insulin sensitivity in kindreds with maternally inherited diabetes and deafness due to mitochondrial tRNALeu(UUR) gene mutation.
- Published in:
- 1996
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- Publication type:
- journal article
Identification of trinucleotide repeat-containing genes in human pancreatic islets.
- Published in:
- 1996
- By:
- Publication type:
- journal article
Linkage analyses of the MODY3 locus on chromosome 12q with late-onset NIDDM.
- Published in:
- 1995
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- Publication type:
- journal article
Cloning, functional expression, and chromosomal localization of the human pancreatic islet glucose-dependent insulinotropic polypeptide receptor.
- Published in:
- 1995
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- Publication type:
- journal article
Characterization of the LIM/homeodomain gene islet-1 and single nucleotide screening in NIDDM.
- Published in:
- 1995
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- Publication type:
- journal article
Isolation of the human LIM/homeodomain gene islet-1 and identification of a simple sequence repeat polymorphism [corrected].
- Published in:
- 1994
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- Publication type:
- journal article
Maternally inherited diabetes and deafness is a distinct subtype of diabetes and associates with a single point mutation in the mitochondrial tRNA(Leu(UUR)) gene.
- Published in:
- 1994
- By:
- Publication type:
- journal article
Six mutations in the glucokinase gene identified in MODY by using a nonradioactive sensitive screening technique.
- Published in:
- 1994
- By:
- Publication type:
- journal article
Compensation in Pancreatic β-Cell Function in Subjects With Glucokinase Mutations.
- Published in:
- Diabetes, 1994, v. 43, n. 5, p. 718, doi. 10.2337/diab.43.5.718
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- Publication type:
- Article