| Item Type | Name |
|
Concept
|
Fetal Diseases
|
|
Concept
|
Communicable Disease Control
|
|
Concept
|
Coronary Artery Disease
|
|
Concept
|
Chronic Disease
|
|
Concept
|
Disease Susceptibility
|
|
Concept
|
Multienzyme Complexes
|
|
Concept
|
Kidney Diseases
|
|
Concept
|
Major Histocompatibility Complex
|
|
Concept
|
Polycystic Kidney Diseases
|
|
Concept
|
Disease Transmission, Infectious
|
|
Concept
|
Disease Progression
|
|
Concept
|
Genetic Diseases, Inborn
|
|
Concept
|
Male Urogenital Diseases
|
|
Concept
|
Disease Models, Animal
|
|
Concept
|
Infant, Newborn, Diseases
|
|
Concept
|
Pancreatic Diseases
|
|
Concept
|
Genetic Predisposition to Disease
|
|
Academic Article
|
The aggregation of the 5' insulin gene polymorphism in insulin dependent (type I) diabetes mellitus families.
|
|
Academic Article
|
Searching for NIDDM susceptibility genes: studies of genes with triplet repeats expressed in skeletal muscle.
|
|
Academic Article
|
Altered insulin secretory responses to glucose in diabetic and nondiabetic subjects with mutations in the diabetes susceptibility gene MODY3 on chromosome 12.
|
|
Academic Article
|
Genetic variation in the gene encoding calpain-10 is associated with type 2 diabetes mellitus.
|
|
Academic Article
|
Abnormal nephron development associated with a frameshift mutation in the transcription factor hepatocyte nuclear factor-1 beta.
|
|
Academic Article
|
Relationship of insulin receptor substrate-1 and -2 genotypes to phenotypic features of polycystic ovary syndrome.
|
|
Academic Article
|
Relationship of calpain-10 genotype to phenotypic features of polycystic ovary syndrome.
|
|
Academic Article
|
Variation within the type 2 diabetes susceptibility gene calpain-10 and polycystic ovary syndrome.
|
|
Academic Article
|
Variants within the calpain-10 gene on chromosome 2q37 (NIDDM1) and relationships to type 2 diabetes, insulin resistance, and impaired acute insulin secretion among Scandinavian Caucasians.
|
|
Academic Article
|
Genetic variants of hepatocyte nuclear factor-1beta in Chinese young-onset diabetic patients with nephropathy.
|
|
Academic Article
|
Geographic and haplotype structure of candidate type 2 diabetes susceptibility variants at the calpain-10 locus.
|
|
Academic Article
|
Genome-wide scan for metabolic syndrome and related quantitative traits in Hong Kong Chinese and confirmation of a susceptibility locus on chromosome 1q21-q25.
|
|
Academic Article
|
Mapping genes influencing type 2 diabetes risk and BMI in Japanese subjects.
|
|
Academic Article
|
Genome-wide scan for type 2 diabetes loci in Hong Kong Chinese and confirmation of a susceptibility locus on chromosome 1q21-q25.
|
|
Academic Article
|
Meta-analysis and a large association study confirm a role for calpain-10 variation in type 2 diabetes susceptibility.
|
|
Academic Article
|
Gene symbol: IPF1. Disease: MODY 4.
|
|
Academic Article
|
From clinicogenetic studies of maturity-onset diabetes of the young to unraveling complex mechanisms of glucokinase regulation.
|
|
Academic Article
|
Common polymorphisms of calpain-10 are associated with abdominal obesity in subjects at high risk of type 2 diabetes.
|
|
Academic Article
|
Obesity and hyperinsulinemia in a family with pancreatic agenesis and MODY caused by the IPF1 mutation Pro63fsX60.
|
|
Academic Article
|
Mutant proinsulin proteins associated with neonatal diabetes are retained in the endoplasmic reticulum and not efficiently secreted.
|
|
Academic Article
|
Seeing is believing: how the MIP-luc mouse can advance the field of islet transplantation and ß-cell regeneration.
|
|
Academic Article
|
Neonatal diabetes: an expanding list of genes allows for improved diagnosis and treatment.
|
|
Academic Article
|
An in vivo cis-regulatory screen at the type 2 diabetes associated TCF7L2 locus identifies multiple tissue-specific enhancers.
|
|
Academic Article
|
Identification of microsatellite markers near the human ob gene and linkage studies in NIDDM-affected sib pairs.
|
|
Academic Article
|
Glucokinase: structural analysis of a protein involved in susceptibility to diabetes.
|
|
Academic Article
|
In vitro processing and secretion of mutant insulin proteins that cause permanent neonatal diabetes.
|
|
Academic Article
|
A yeast artificial chromosome-based map of the region of chromosome 20 containing the diabetes-susceptibility gene, MODY1, and a myeloid leukemia related gene.
|
|
Academic Article
|
A genome-wide search for human non-insulin-dependent (type 2) diabetes genes reveals a major susceptibility locus on chromosome 2.
|
|
Academic Article
|
Clinical and molecular genetics of neonatal diabetes due to mutations in the insulin gene.
|
|
Academic Article
|
Alterations in TCF7L2 expression define its role as a key regulator of glucose metabolism.
|
|
Academic Article
|
Genetic contribution of polymorphism of the GLUT1 and GLUT4 genes to the susceptibility to type 2 (non-insulin-dependent) diabetes mellitus in different populations.
|
|
Academic Article
|
Mapping diabetes-susceptibility genes. Lessons learned from search for DNA marker for maturity-onset diabetes of the young.
|
|
Academic Article
|
Locus on chromosome 6p linked to elevated HDL cholesterol serum levels and to protection against premature atherosclerosis in a kindred with familial hypercholesterolemia.
|
|
Academic Article
|
Linkage of calpain 10 to type 2 diabetes: the biological rationale.
|
|
Academic Article
|
5-amino-imidazole carboxamide riboside acutely potentiates glucose-stimulated insulin secretion from mouse pancreatic islets by KATP channel-dependent and -independent pathways.
|
|
Academic Article
|
Genome-wide association and meta-analysis in populations from Starr County, Texas, and Mexico City identify type 2 diabetes susceptibility loci and enrichment for expression quantitative trait loci in top signals.
|
|
Academic Article
|
Linkage and association between insulin-dependent diabetes mellitus (IDDM) susceptibility and markers near the glucokinase gene on chromosome 7.
|
|
Academic Article
|
Evolution of simple sequence repeats.
|
|
Academic Article
|
Sexual partner networks in the transmission of sexually transmitted diseases. An analysis of gonorrhea cases in Sheffield, UK.
|
|
Academic Article
|
Examination of trisomy 13, 18 and 21 foetal tissues at different gestational ages using FISH.
|
|
Academic Article
|
In vitro scan for enhancers at the TCF7L2 locus.
|
|
Academic Article
|
Microcephaly, epilepsy, and neonatal diabetes due to compound heterozygous mutations in IER3IP1: insights into the natural history of a rare disorder.
|
|
Academic Article
|
GSK-3ß function in bone regulates skeletal development, whole-body metabolism, and male life span.
|
|
Academic Article
|
Evidence of non-pancreatic beta cell-dependent roles of Tcf7l2 in the regulation of glucose metabolism in mice.
|
|
Academic Article
|
Effect of genetic variation in a Drosophila model of diabetes-associated misfolded human proinsulin.
|
|
Academic Article
|
Genetic complexity in a Drosophila model of diabetes-associated misfolded human proinsulin.
|
|
Academic Article
|
Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility.
|
|
Academic Article
|
The genetic architecture of type 2 diabetes.
|
|
Academic Article
|
Transancestral fine-mapping of four type 2 diabetes susceptibility loci highlights potential causal regulatory mechanisms.
|
|
Academic Article
|
A Low-Frequency Inactivating AKT2 Variant Enriched in the Finnish Population Is Associated With Fasting Insulin Levels and Type 2 Diabetes Risk.
|
|
Academic Article
|
Evaluating the contribution of rare variants to type 2 diabetes and related traits using pedigrees.
|
|
Academic Article
|
A One Health investigation of Salmonella enterica serovar Wangata in north-eastern New South Wales, Australia, 2016-2017.
|
|
Grant
|
A Fly Model of Complex Protein Misfolding Disease
|
|
Grant
|
Functional follow-up of the association between TCF7L2 and T2D
|