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Bell, Graeme
One or more keywords matched the following items that are connected to Bell, Graeme
Item TypeName
Concept Adenosine Deaminase
Concept Haplorhini
Concept Abnormalities, Multiple
Concept Cyclic AMP
Concept Adenosine Triphosphate
Concept Cholecystokinin
Concept Chromosome Banding
Concept Chromosomes, Human, Pair 11
Concept Chromosomes, Human, Pair 2
Concept Chromosomes, Human, Pair 6
Concept Analysis of Variance
Concept Chromosomes, Human, Pair 8
Concept Cell Differentiation
Concept Bangladesh
Concept Autoradiography
Concept Cattle
Concept Ischemic Attack, Transient
Concept Chromosomes, Human, Pair 1
Concept Chromosomes, Human, Pair 21
Concept Chromosomes, Human, Pair 3
Concept Cerebellum
Concept Chromosomes, Human, Pair 12
Concept Chromosomes, Human, Pair 14
Concept Colonic Neoplasms
Concept Chromosome Deletion
Concept Chromosomes, Human, Pair 13
Concept Chromosomes, Human, Pair 22
Concept Chromosomes, Human, Pair 4
Concept Codon
Concept Chromosomes, Human, Pair 5
Concept Chromosomes, Human, Pair 7
Concept Cricetulus
Concept Chromosomes, Human, Pair 20
Concept Coronary Artery Disease
Concept Dextrorphan
Concept Indians, North American
Concept Dogs
Concept Gluconeogenesis
Concept Electrophysiology
Concept Chromosomes, Human, Pair 10
Concept Chromosomes, Human, Pair 17
Concept Chromosomes, Human, Pair 19
Concept Chromosomes, Human, Pair 9
Concept Exons
Concept Family
Concept Fathers
Concept Macaca fascicularis
Concept Cost-Benefit Analysis
Concept Drosophila melanogaster
Concept DNA, Satellite
Concept Introns
Concept Histocytochemistry
Concept Environmental Microbiology
Concept Genetics, Population
Concept Mesencephalon
Concept Microcephaly
Concept Mammals
Concept Naltrexone
Concept Mice, Transgenic
Concept Potassium Chloride
Concept Immunohistochemistry
Concept Monosaccharide Transport Proteins
Concept NADP
Concept Mice, Inbred BALB C
Concept Mice, Inbred C57BL
Concept Molecular Biology
Concept Cricetinae
Concept Rodentia
Concept Naloxone
Concept Nuclear Family
Concept Fetal Blood
Concept Primates
Concept Hybridization, Genetic
Concept Rats, Zucker
Concept Salmonella
Concept Xenopus
Concept Potassium Channels
Concept Serotyping
Concept Polycystic Kidney Diseases
Concept Thyroxine-Binding Proteins
Concept Humans
Concept Trisomy
Concept Xenopus laevis
Concept Calcium Channels
Concept Bacterial Typing Techniques
Concept Chorionic Villi Sampling
Concept Levorphanol
Concept RNA Splice Sites
Concept Water Microbiology
Concept Transcription Initiation Site
Concept Deoxyribonucleases, Type II Site-Specific
Concept Morphine
Concept Rats, Sprague-Dawley
Concept Rats, Wistar
Concept Methionine
Concept Ecosystem
Concept Mice, Obese
Concept RNA-Binding Proteins
Concept Mice, Knockout
Concept Dinucleotide Repeats
Concept ras Proteins
Concept Craniofacial Abnormalities
Concept Glucose Transporter Type 2
Concept Amino Acid Transport Systems, Neutral
Concept Multidrug Resistance-Associated Proteins
Concept CpG Islands
Concept Receptors, Dopamine D1
Concept Protein Folding
Concept Ryanodine Receptor Calcium Release Channel
Concept Potassium Channels, Inwardly Rectifying
Concept Amino Acid Transport Systems
Concept Peromyscus
Concept Animals, Genetically Modified
Concept Precipitin Tests
Concept Promoter Regions, Genetic
Concept Mice
Concept Receptors, Dopamine
Concept Inositol 1,4,5-Trisphosphate Receptors
Concept Ryanodine
Concept Threonine
Concept Glucose Transporter Type 1
Concept Rats
Concept Tooth Abnormalities
Concept Finches
Concept Vanadates
Concept Adaptor Proteins, Signal Transducing
Concept Insulin-Secreting Cells
Concept Regulatory Elements, Transcriptional
Concept Chloramphenicol O-Acetyltransferase
Concept Multivariate Analysis
Concept Hominidae
Concept Patient Satisfaction
Concept Antisense Elements (Genetics)
Concept ATP-Binding Cassette Transporters
Concept GTP-Binding Proteins
Concept Untranslated Regions
Concept Smegmamorpha
Concept Glycine Plasma Membrane Transport Proteins
Concept p300-CBP Transcription Factors
Concept KCNQ1 Potassium Channel
Concept KATP Channels
Concept Insulin Receptor Substrate Proteins
Concept RNA, Small Interfering
Concept Receptors, CCR6
Concept Calcium-Binding Proteins
Concept Chickens
Concept Chromosomes, Human
Concept Chromosomes, Human, Pair 16
Concept Chromosomes, Human, Pair 18
Concept Electrophoresis, Agar Gel
Concept Enhancer Elements, Genetic
Concept Membrane Potentials
Concept Mice, Mutant Strains
Concept Mothers
Concept Rats, Mutant Strains
Concept Superior Colliculi
Concept Oligonucleotides, Antisense
Concept Mice, SCID
Concept Mice, Inbred NOD
Concept Cyclic AMP-Dependent Protein Kinases
Concept Genomics
Concept Glucose Transporter Type 4
Concept Glucose Transporter Type 5
Academic Article Sequence and functional characterization of a third inositol trisphosphate receptor subtype, IP3R-3, expressed in pancreatic islets, kidney, gastrointestinal tract, and other tissues.
Academic Article Human glucagon-like peptide-1 receptor gene. Localization to chromosome band 6p21 by fluorescence in situ hybridization and linkage of a highly polymorphic simple tandem repeat DNA polymorphism to other markers on chromosome 6.
Academic Article Pharmacological properties of two cloned somatostatin receptors.
Academic Article Cloning and functional comparison of kappa and delta opioid receptors from mouse brain.
Academic Article Hormonal/metabolic regulation of the human GLUT4/muscle-fat facilitative glucose transporter gene in transgenic mice.
Academic Article Assignment of human potassium channel gene KCNA4 (Kv1.4, PCN2) to chromosome 11q13.4-->q14.1.
Academic Article Human insulin receptor substrate-1 gene (IRS1): chromosomal localization to 2q35-q36.1 and identification of a simple tandem repeat DNA polymorphism.
Academic Article cDNA sequence and localization of polymorphic human cytosolic phosphoenolpyruvate carboxykinase gene (PCK1) to chromosome 20, band q13.31: PCK1 is not tightly linked to maturity-onset diabetes of the young.
Academic Article Identification of a simple tandem repeat DNA polymorphism in the human glycogen synthase gene and linkage to five markers on chromosome 19q.
Academic Article Assignment of the gene encoding glycogen synthase (GYS) to human chromosome 19, band q13.3.
Academic Article Human GLUT4/muscle-fat glucose-transporter gene. Characterization and genetic variation.
Academic Article Linkage and association studies in insulin-dependent diabetes with a new dinucleotide repeat polymorphism at the GAD65 locus.
Academic Article Sequence of human hexokinase III cDNA and assignment of the human hexokinase III gene (HK3) to chromosome band 5q35.2 by fluorescence in situ hybridization.
Academic Article The aggregation of the 5' insulin gene polymorphism in insulin dependent (type I) diabetes mellitus families.
Academic Article Chromosomal assignment and tissue distribution of novel expressed sequence tags from a human pancreatic islet cDNA library.
Academic Article Characterization of a third simple tandem repeat polymorphism in the human glucokinase gene.
Academic Article Human somatostatin receptor genes: localization to human chromosomes 14, 17, and 22 and identification of simple tandem repeat polymorphisms.
Academic Article JAK/STAT eats the fat.
Academic Article Exclusion of epidermal growth factor and high-resolution physical mapping across the Rieger syndrome locus.
Academic Article Mutations in the hepatocyte nuclear factor-1alpha gene in maturity-onset diabetes of the young (MODY3)
Academic Article Detection of a polymorphism within the pepsinogen C gene with PCR: construction of a linkage map around PGC from 6p11-6p21.3.
Academic Article Hepatic function in a family with a nonsense mutation (R154X) in the hepatocyte nuclear factor-4alpha/MODY1 gene.
Academic Article Molecular analysis of the fructose transporter gene (GLUT5) in isolated fructose malabsorption.
Academic Article MODY: a model for the study of the molecular genetics of NIDDM.
Academic Article Human Oct3 gene family: cDNA sequences, alternative splicing, gene organization, chromosomal location, and expression at low levels in adult tissues.
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 Mutations in the hepatocyte nuclear factor-1alpha/MODY3 gene in Japanese subjects with early- and late-onset NIDDM.
Academic Article Genetic variation in the hepatocyte nuclear factor-1 alpha gene in Danish Caucasians with late-onset NIDDM.
Academic Article Maturity onset diabetes of the young (MODY).
Academic Article Nonsense mutation in the glucokinase gene causes early-onset non-insulin-dependent diabetes mellitus.
Academic Article Genetic variation in the gene encoding calpain-10 is associated with type 2 diabetes mellitus.
Academic Article Expression and regulation of the human GLUT4/muscle-fat facilitative glucose transporter gene in transgenic mice.
Academic Article Molecular mechanisms and clinical pathophysiology of maturity-onset diabetes of the young.
Academic Article Neonatal diabetes mellitus due to complete glucokinase deficiency.
Academic Article Diabetes mellitus and genetically programmed defects in beta-cell function.
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 Control of pancreas and liver gene expression by HNF transcription factors.
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 RyR2 and calpain-10 delineate a novel apoptosis pathway in pancreatic islets.
Academic Article Mapping genes influencing type 2 diabetes risk and BMI in Japanese subjects.
Academic Article Epilepsy in the United Kingdom: seizure frequency and severity, anti-epileptic drug utilization and impact on life in 1652 people with epilepsy.
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 Dual promoter structure of ZFP106: regulation by myogenin and nuclear respiratory factor-1.
Academic Article Imaging Beta cell development in real-time using pancreatic explants from mice with green fluorescent protein-labeled pancreatic Beta cells.
Academic Article Anti-diabetic effect of ginsenoside Re in ob/ob mice.
Academic Article Gene symbol: IPF1. Disease: MODY 4.
Academic Article Calpain system regulates muscle mass and glucose transporter GLUT4 turnover.
Academic Article Permanent neonatal diabetes due to mutations in KCNJ11 encoding Kir6.2: patient characteristics and initial response to sulfonylurea therapy.
Academic Article Confirmed locus on chromosome 11p and candidate loci on 6q and 8p for the triglyceride and cholesterol traits of combined hyperlipidemia.
Academic Article Insulin gene mutations as a cause of permanent neonatal diabetes.
Academic Article Genetic variants in the calpain-10 gene and the development of type 2 diabetes in the Japanese population.
Academic Article Subcellular recruitment by TSG118 and TSPYL implicates a role for zinc finger protein 106 in a novel developmental pathway.
Academic Article Association of the (AU)AT-rich element polymorphism in PPP1R3 with hormonal and metabolic features of polycystic ovary syndrome.
Academic Article Update in neonatal diabetes.
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 Calpain-10 is a component of the obesity-related quantitative trait locus Adip1.
Academic Article Mutant proinsulin proteins associated with neonatal diabetes are retained in the endoplasmic reticulum and not efficiently secreted.
Academic Article Dinucleotide repeat polymorphism at D9S328E (EST hbc220).
Academic Article Human G-protein-coupled inwardly rectifying potassium channel (GIRK1) gene (KCNJ3): localization to chromosome 2 and identification of a simple tandem repeat polymorphism.
Academic Article Localization of the kappa opioid receptor gene to human chromosome band 8q11.2.
Academic Article Human hexokinase II: localization of the polymorphic gene to chromosome 2.
Academic Article Assignment of the gastric inhibitory polypeptide receptor gene (GIPR) to chromosome bands 19q13.2-q13.3 by fluorescence in situ hybridization.
Academic Article Human type I pituitary adenylate cyclase activating polypeptide receptor (ADCYAP1R): localization to chromosome band 7p14 and integration into the cytogenetic, physical, and genetic map of chromosome 7.
Academic Article Gi alpha 3 and G(o) alpha selectively associate with the cloned somatostatin receptor subtype SSTR2.
Academic Article Human fructose-1,6-bisphosphatase gene (FBP1): exon-intron organization, localization to chromosome bands 9q22.2-q22.3, and mutation screening in subjects with fructose-1,6-bisphosphatase deficiency.
Academic Article Localization of the gene encoding a neutral amino acid transporter-like protein to human chromosome band 19q13.3 and characterization of a simple sequence repeat DNA polymorphism.
Academic Article Localization of the genes encoding two transcription factors, LMX1 and CDX3, regulating insulin gene expression to human chromosomes 1 and 13.
Academic Article Inositol 1,4,5-trisphosphate receptors, secretory granules and secretion in endocrine and neuroendocrine cells.
Academic Article Stimulation of tyrosine phosphatase and inhibition of cell proliferation by somatostatin analogues: mediation by human somatostatin receptor subtypes SSTR1 and SSTR2.
Academic Article Dinucleotide repeat polymorphism in the NEC2 gene.
Academic Article Structure and function of ASP, the human homolog of the mouse agouti gene.
Academic Article Linkage of Rieger syndrome to the region of the epidermal growth factor gene on chromosome 4.
Academic Article Assignment of the gene encoding the alpha 1 subunit of the neuroendocrine/brain-type calcium channel (CACNL1A2) to human chromosome 3, band p14.3.
Academic Article Alternative splicing of human inwardly rectifying K+ channel ROMK1 mRNA.
Academic Article Somatostatin receptors, an expanding gene family: cloning and functional characterization of human SSTR3, a protein coupled to adenylyl cyclase.
Academic Article Repression of the insulin-like growth factor II gene by the Wilms tumor suppressor WT1.
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 Localization of human homeodomain transcription factor insulin promoter factor 1 (IPF1) to chromosome band 13q12.1.
Academic Article The 31-cM region of chromosome 11 including the obesity gene tubby and ATP-sensitive potassium channel genes, SUR1 and Kir6.2, does not contain a major susceptibility locus for NIDDM in 127 non-Hispanic white affected sibships.
Academic Article Missense glucokinase mutation in maturity-onset diabetes of the young and mutation screening in late-onset diabetes.
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 Abnormal insulin secretion, not insulin resistance, is the genetic or primary defect of MODY in the RW pedigree.
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 Three Strikes and You're Cured.
Academic Article Linkage and association between insulin-dependent diabetes mellitus (IDDM) susceptibility and markers near the glucokinase gene on chromosome 7.
Academic Article Altered insulin secretory responses to glucose in subjects with a mutation in the MODY1 gene on chromosome 20.
Academic Article Cloning of a novel somatostatin receptor, SSTR3, coupled to adenylylcyclase.
Academic Article Dinucleotide repeat polymorphism in the human thyroid hormone receptor alpha gene (THRA1) on chromosome 17.
Academic Article Microsatellite polymorphism in the human platelet glycoprotein IIIa gene (GP3A) on chromosome 17.
Academic Article Human pancreatic beta-cell glucokinase: cDNA sequence and localization of the polymorphic gene to chromosome 7, band p 13.
Academic Article Dinucleotide repeat polymorphism at the human ribophorin II locus (RPN2) on chromosome 20q.
Academic Article Localization of the glucagon receptor gene to human chromosome band 17q25.
Academic Article Molecular mechanisms of agonist-induced desensitization of the cloned mouse kappa opioid receptor.
Academic Article Inhibition of cell proliferation by the somatostatin analogue RC-160 is mediated by somatostatin receptor subtypes SSTR2 and SSTR5 through different mechanisms.
Academic Article Assignment of SLC6A9 to human chromosome band 1p33 by in situ hybridization.
Academic Article Structure and function of mammalian facilitative sugar transporters.
Academic Article Molecular genetics of myeloid leukemia: identification of the commonly deleted segment of chromosome 20.
Academic Article Activation of human somatostatin receptor type 2 causes inhibition of cell growth in transfected HEK293 but not in transfected CHO cells.
Academic Article Apparent confined placental mosaicism of trisomy 16 and multiple fetal anomalies: case report.
Academic Article Examination of trisomy 13, 18 and 21 foetal tissues at different gestational ages using FISH.
Academic Article The oligogenic view of adaptation.
Academic Article Localization of human somatostatin receptor 5 gene (SSTR5) to chromosome band 16p13.3 by fluorescence in situ hybridization.
Academic Article Human somatostatin receptor genes: localization of SSTR5 to human chromosome 20p11.2.
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 Genetics and pathophysiology of neonatal diabetes mellitus.
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 Sex and the spread of retrotransposon Ty3 in experimental populations of Saccharomyces cerevisiae.
Academic Article Remifentanil vs fentanyl/morphine for pain and stress control during pediatric cardiac surgery.
Academic Article Beyond type 2 diabetes, obesity and hypertension: an axis including sleep apnea, left ventricular hypertrophy, endothelial dysfunction, and aortic stiffness among Mexican Americans in Starr County, Texas.
Academic Article Resting beta-cells - A functional reserve?
Academic Article Transancestral fine-mapping of four type 2 diabetes susceptibility loci highlights potential causal regulatory mechanisms.
Academic Article Femtosecond laser desorption ionization mass spectrometry imaging and multivariate analysis of lipids in pancreatic tissue.
Academic Article Deep tubewell microbial water quality and access in arsenic mitigation programs in rural Bangladesh.
Concept Perilipin-1
Concept Sulfonylurea Receptors
Grant GENES FOR NON-INSULIN-DEPENDENT DIABETES MELLITUS
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