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Mapping NIDDM susceptibility loci in French families: studies with markers in the region of NIDDM1 on chromosome 2q.
- Published in:
- 1997
- By:
- Publication type:
- journal article
Diagnostic heterogeneity of diabetes in lean young adults: classification based on immunological and genetic parameters.
- Published in:
- 1997
- By:
- Publication type:
- journal article
Transmission of Type 2 diabetes to sons and daughters: the D.E.S.I.R. cohort.
- Published in:
- Diabetic Medicine, 2017, v. 34, n. 11, p. 1615, doi. 10.1111/dme.13446
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- Publication type:
- Article
beta-cell genes and diabetes: quantitative and qualitative differences in the pathophysiology of hepatic nuclear factor-1alpha and glucokinase mutations.
- Published in:
- 2001
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- Publication type:
- journal 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
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:
- 2000
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- Publication type:
- journal article
A sib-pair analysis study of 15 candidate genes in French families with morbid obesity: indication for linkage with islet 1 locus on chromosome 5q.
- 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 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
Genetics of NIDDM in France: studies with 19 candidate genes in affected sib pairs.
- Published in:
- 1997
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- Publication type:
- journal 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
Identification of trinucleotide repeat-containing genes in human pancreatic islets.
- Published in:
- 1996
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- 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
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- Publication type:
- journal article
Compensation in pancreatic beta-cell function in subjects with glucokinase mutations.
- Published in:
- 1994
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- Publication type:
- journal article
Higher maternal than paternal inheritance of diabetes in GK rats.
- Published in:
- 1994
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- Publication type:
- journal article
In vitro and in vivo stability of electrode potentials in needle-type glucose sensors. Influence of needle material.
- Published in:
- 1989
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- Publication type:
- journal article
Alcohol consumption and risk of type 2 diabetes in European men and women: influence of beverage type and body size The EPIC-InterAct study.
- Published in:
- 2012
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- Publication type:
- journal article
Alcohol consumption and risk of type 2 diabetes in European men and women: influence of beverage type and body sizeThe EPIC-InterAct study.
- Published in:
- Journal of Internal Medicine, 2012, v. 272, n. 4, p. 358, doi. 10.1111/j.1365-2796.2012.02532.x
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- Publication type:
- Article
The EIF2AK3 gene region and type I diabetes in subjects from South India.
- Published in:
- Genes & Immunity, 2004, v. 5, n. 8, p. 648, doi. 10.1038/sj.gene.6364139
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- Publication type:
- Article
Effects of genetic susceptibility for type 2 diabetes on the evolution of glucose homeostasis traits before and after diabetes diagnosis: data from the D.E.S.I.R. Study.
- Published in:
- 2011
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- Publication type:
- journal article
Prevalence of loss-of-function FTO mutations in lean and obese individuals.
- Published in:
- 2010
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- Publication type:
- journal article
A rare mutation in ABCC8/SUR1 leading to altered ATP-sensitive K+ channel activity and beta-cell glucose sensing is associated with type 2 diabetes in adults.
- Published in:
- 2008
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- Publication type:
- journal article
Common variation in the LMNA gene (encoding lamin A/C) and type 2 diabetes: association analyses in 9,518 subjects.
- Published in:
- 2007
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- Publication type:
- journal article
TCF7L2 Variation Predicts Hyperglycemia Incidence in a French General Population: The Data From an Epidemiological Study on the Insulin Resistance Syndrome (DESIR) Study.
- Published in:
- 2006
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- Publication type:
- Journal Article
Transcription Factor TCF7L2 Genetic Study in the French Population: Expression in Human {beta}-Cells and Adipose Tissue and Strong Association With Type 2 Diabetes.
- Published in:
- 2006
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- Publication type:
- Journal Article
Hepatocyte nuclear factor-4alpha P2 promoter haplotypes are associated with type 2 diabetes in the Japanese population.
- Published in:
- 2006
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- Publication type:
- journal article
The PPARG Pro12Ala polymorphism is associated with a decreased risk of developing hyperglycemia over 6 years and combines with the effect of the APM1 G-11391A single nucleotide polymorphism: the Data From an Epidemiological Study on the Insulin Resistance Syndrome (DESIR) study.
- Published in:
- 2006
- By:
- Publication type:
- journal article
A synonymous coding polymorphism in the alpha2-Heremans-schmid glycoprotein gene is associated with type 2 diabetes in French Caucasians.
- Published in:
- 2005
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- Publication type:
- journal article
The adiponectin gene SNP+45 is associated with coronary artery disease in Type 2 (non-insulin-dependent) diabetes mellitus.
- Published in:
- 2004
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- Publication type:
- Journal Article
Macrophage Gene Expression in Adipose Tissue is Associated with Insulin Sensitivity and Serum Lipid Levels Independent of Obesity.
- Published in:
- Obesity (19307381), 2013, v. 21, n. 12, p. E571, doi. 10.1002/oby.20443
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- Publication type:
- Article
A Genetic Study of the Ghrelin and Growth Hormone Secretagogue Receptor ( GHSR) Genes and Stature.
- Published in:
- Annals of Human Genetics, 2009, v. 73, n. 1, p. 1, doi. 10.1111/j.1469-1809.2008.00484.x
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- Publication type:
- Article
Epistasis Between Type 2 Diabetes Susceptibility Loci on Chromosomes 1q21-25 and 10q23-26 in Northern Europeans.
- Published in:
- Annals of Human Genetics, 2006, v. 70, n. 6, p. 726, doi. 10.1111/j.1469-1809.2006.00289.x
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- Publication type:
- Article
Genetic and clinical characterisation of maturity-onset diabetes of the young in Spanish families.
- Published in:
- European Journal of Endocrinology, 2000, v. 142, n. 4, p. 380, doi. 10.1530/eje.0.1420380
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- Publication type:
- Article
Islet-brain 1/c-Jun N-terminal kinase interacting protein-1 (IB1/JIP-1) promoter variant is associated with Alzheimer's disease.
- Published in:
- Molecular Psychiatry, 2003, v. 8, n. 4, p. 363, doi. 10.1038/sj.mp.4001342
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- Publication type:
- Article
Islet-brain1/C-Jun N-terminal kinase interacting protein-1 (IB1/JIP-1) promoter variant is associated with Alzheimer's disease.
- Published in:
- Molecular Psychiatry, 2003, v. 8, n. 4, p. 413, doi. 10.1038/sj.mp.4001344
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- Publication type:
- Article
Mutation screening of the urocortin gene: identification of new single nucleotide polymorphisms and association studies with obesity in French Caucasians.
- Published in:
- 2002
- By:
- Publication type:
- journal article
Diabetes complications in NIDDM kindreds linked to the MODY3 locus on chromosome 12q.
- Published in:
- 1996
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- Publication type:
- journal article
Arginine-induced insulin release in glucokinase-deficient subjects.
- Published in:
- 1994
- By:
- Publication type:
- journal article
Lipoprotein(a) in diabetic patients and normoglycemic relatives in familial NIDDM.
- Published in:
- 1993
- By:
- Publication type:
- journal article
Adipose tissue resting energy expenditure and expression of genes involved in mitochondrial function are higher in women than in men.
- Published in:
- 2013
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- Publication type:
- journal article
Multiple functional polymorphisms in the G6PC2 gene contribute to the association with higher fasting plasma glucose levels.
- Published in:
- Diabetologia, 2013, v. 56, n. 6, p. 1306, doi. 10.1007/s00125-013-2875-3
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- Publication type:
- Article
Reassessment of the putative role of BLK-p.A71T loss-of-function mutation in MODY and type 2 diabetes.
- Published in:
- Diabetologia, 2013, v. 56, n. 3, p. 492, doi. 10.1007/s00125-012-2794-8
- By:
- Publication type:
- Article
GATA6 inactivating mutations are associated with heart defects and, inconsistently, with pancreatic agenesis and diabetes.
- Published in:
- 2012
- By:
- Publication type:
- Letter