Item Type | Name |
Concept
|
Actins
|
Concept
|
Age Factors
|
Concept
|
Amyloid
|
Concept
|
Adenosine Deaminase
|
Concept
|
Antigens, Neoplasm
|
Concept
|
Apolipoproteins
|
Concept
|
Arcuate Nucleus of Hypothalamus
|
Concept
|
Arsenic
|
Concept
|
Animals, Domestic
|
Concept
|
Haplorhini
|
Concept
|
Abortion, Induced
|
Concept
|
Adenylyl Cyclases
|
Concept
|
Cyclic AMP
|
Concept
|
Adenosine Triphosphatases
|
Concept
|
3-Pyridinecarboxylic acid, 1,4-dihydro-2,6-dimethyl-5-nitro-4-(2-(trifluoromethyl)phenyl)-, Methyl ester
|
Concept
|
Africa
|
Concept
|
Analgesics, Opioid
|
Concept
|
alpha-MSH
|
Concept
|
Amino Acid Sequence
|
Concept
|
Anticonvulsants
|
Concept
|
Cerebral Cortex
|
Concept
|
Analgesics
|
Concept
|
Animals
|
Concept
|
Animals, Newborn
|
Concept
|
Aorta
|
Concept
|
Calpain
|
Concept
|
Animals, Wild
|
Concept
|
Cholecystokinin
|
Concept
|
Chromatography, Affinity
|
Concept
|
Chromosome Banding
|
Concept
|
Chromosomes, Human, Pair 11
|
Concept
|
Chromosomes, Human, Pair 2
|
Concept
|
Chromosomes, Human, Pair 6
|
Concept
|
Epitopes
|
Concept
|
Analysis of Variance
|
Concept
|
Chromosomes, Human, Pair 8
|
Concept
|
Arizona
|
Concept
|
Arginine
|
Concept
|
Cytoplasmic Granules
|
Concept
|
Antigens, Bacterial
|
Concept
|
Base Sequence
|
Concept
|
Cell Count
|
Concept
|
Cell Nucleus
|
Concept
|
Diabetes Mellitus, Experimental
|
Concept
|
Aspartic Acid
|
Concept
|
Dipeptides
|
Concept
|
Bacterial Outer Membrane Proteins
|
Concept
|
China
|
Concept
|
Autoantibodies
|
Concept
|
Binding Sites
|
Concept
|
Birth Weight
|
Concept
|
Blood Glucose
|
Concept
|
Biometry
|
Concept
|
Biopsy
|
Concept
|
Body Weight
|
Concept
|
England
|
Concept
|
Cattle
|
Concept
|
Cell Division
|
Concept
|
Cell Separation
|
Concept
|
Brain Mapping
|
Concept
|
Biological Evolution
|
Concept
|
Exocytosis
|
Concept
|
Chromosomes, Human, Pair 1
|
Concept
|
Chromosomes, Human, Pair 21
|
Concept
|
Chromosomes, Human, Pair 3
|
Concept
|
Cerebellum
|
Concept
|
Cerebral Angiography
|
Concept
|
Cholic Acids
|
Concept
|
Chromosomes, Human, Pair 12
|
Concept
|
Chromosomes, Human, Pair 14
|
Concept
|
Colonic Neoplasms
|
Concept
|
Chemotaxis
|
Concept
|
Chicago
|
Concept
|
Chromosome Deletion
|
Concept
|
Chromosomes, Human, Pair 13
|
Concept
|
Chromosomes, Human, Pair 22
|
Concept
|
Chromosomes, Human, Pair 4
|
Concept
|
Codon
|
Concept
|
Cognition
|
Concept
|
Chromosomes, Human, Pair 5
|
Concept
|
Chromosomes, Human, Pair 7
|
Concept
|
C-Peptide
|
Concept
|
Glutamate Decarboxylase
|
Concept
|
United Kingdom
|
Concept
|
Cricetulus
|
Concept
|
Cosmids
|
Concept
|
Cholesterol
|
Concept
|
Chromosomes, Human, Pair 20
|
Concept
|
Coronary Artery Disease
|
Concept
|
Cytosol
|
Concept
|
Diabetes Mellitus, Type 1
|
Concept
|
Diabetes Mellitus, Type 2
|
Concept
|
Cytochalasin B
|
Concept
|
Denmark
|
Concept
|
DNA Transposable Elements
|
Concept
|
Dexamethasone
|
Concept
|
Diabetic Angiopathies
|
Concept
|
Drug Synergism
|
Concept
|
Detergents
|
Concept
|
Dextrorphan
|
Concept
|
Diabetic Nephropathies
|
Concept
|
Immunosuppressive Agents
|
Concept
|
Indians, North American
|
Concept
|
Insulin
|
Concept
|
Endothelium, Vascular
|
Concept
|
Epilepsy
|
Concept
|
Decision Support Techniques
|
Concept
|
DNA, Bacterial
|
Concept
|
Child, Preschool
|
Concept
|
DNA, Recombinant
|
Concept
|
Dogs
|
Concept
|
Electrophoresis, Polyacrylamide Gel
|
Concept
|
Europe
|
Concept
|
Fructose Intolerance
|
Concept
|
Genes, Regulator
|
Concept
|
Germany
|
Concept
|
Gluconeogenesis
|
Concept
|
Glycogen Synthase
|
Concept
|
Growth Inhibitors
|
Concept
|
Heparitin Sulfate
|
Concept
|
Electrophysiology
|
Concept
|
Enkephalins
|
Concept
|
Endoplasmic Reticulum
|
Concept
|
Estradiol
|
Concept
|
London
|
Concept
|
Chromosomes, Human, Pair 10
|
Concept
|
Chromosomes, Human, Pair 17
|
Concept
|
Chromosomes, Human, Pair 19
|
Concept
|
Chromosomes, Human, Pair 9
|
Concept
|
Chronic Disease
|
Concept
|
Fathers
|
Concept
|
Finland
|
Concept
|
Macaca fascicularis
|
Concept
|
Cross-Sectional Studies
|
Concept
|
Dantrolene
|
Concept
|
Disease Susceptibility
|
Concept
|
DNA
|
Concept
|
Drosophila melanogaster
|
Concept
|
Drug Utilization
|
Concept
|
DNA, Satellite
|
Concept
|
Colforsin
|
Concept
|
Fetal Growth Retardation
|
Concept
|
Fetal Macrosomia
|
Concept
|
Indicators and Reagents
|
Concept
|
Infant, Newborn
|
Concept
|
Insulin-Like Growth Factor II
|
Concept
|
Insulinoma
|
Concept
|
Introns
|
Concept
|
Electric Conductivity
|
Concept
|
Glucagon-Like Peptides
|
Concept
|
Fluorescence
|
Concept
|
Fructose
|
Concept
|
Decision Making
|
Concept
|
Multienzyme Complexes
|
Concept
|
Genes, Dominant
|
Concept
|
Glaucoma
|
Concept
|
Glucagon
|
Concept
|
Fasting
|
Concept
|
Terminology as Topic
|
Concept
|
Karyotyping
|
Concept
|
Kidney Diseases
|
Concept
|
Gonorrhea
|
Concept
|
Guanosine Triphosphate
|
Concept
|
Health Services Needs and Demand
|
Concept
|
Genetic Complementation Test
|
Concept
|
Obesity
|
Concept
|
Histocytochemistry
|
Concept
|
Electric Stimulation Therapy
|
Concept
|
Dose-Response Relationship, Drug
|
Concept
|
Hyperlipoproteinemia Type II
|
Concept
|
Hyperlipidemia, Familial Combined
|
Concept
|
Hypoglycemic Agents
|
Concept
|
Liver Neoplasms
|
Concept
|
Endocrine Glands
|
Concept
|
Environmental Monitoring
|
Concept
|
Enkephalin, Leucine
|
Concept
|
Environmental Microbiology
|
Concept
|
Hospitalization
|
Concept
|
Fibrosarcoma
|
Concept
|
Flow Cytometry
|
Concept
|
Inflammation
|
Concept
|
Infusions, Intravenous
|
Concept
|
Forms and Records Control
|
Concept
|
Guanylate Cyclase
|
Concept
|
Leucine
|
Concept
|
Health Services Accessibility
|
Concept
|
Luminescent Measurements
|
Concept
|
HLA-DQ Antigens
|
Concept
|
Hyperlipoproteinemias
|
Concept
|
Microcephaly
|
Concept
|
Models, Molecular
|
Concept
|
Mosaicism
|
Concept
|
Phosphatidylcholines
|
Concept
|
Mammals
|
Concept
|
Myometrium
|
Concept
|
Naltrexone
|
Concept
|
Narcotics
|
Concept
|
Mice, Transgenic
|
Concept
|
Michigan
|
Concept
|
Models, Genetic
|
Concept
|
Models, Theoretical
|
Concept
|
Nephrons
|
Concept
|
Potassium Chloride
|
Concept
|
Primary Health Care
|
Concept
|
Illinois
|
Concept
|
Immunohistochemistry
|
Concept
|
Organ Size
|
Concept
|
Molecular Sequence Data
|
Concept
|
Molecular Weight
|
Concept
|
Monosaccharide Transport Proteins
|
Concept
|
Pain
|
Concept
|
Pancreatic Neoplasms
|
Concept
|
Mice, Inbred BALB C
|
Concept
|
Mice, Inbred C57BL
|
Concept
|
Repetitive Sequences, Nucleic Acid
|
Concept
|
Molecular Biology
|
Concept
|
Cricetinae
|
Concept
|
Heat-Shock Proteins
|
Concept
|
HeLa Cells
|
Concept
|
Patient Admission
|
Concept
|
Patient Education as Topic
|
Concept
|
RNA, Transfer, Leu
|
Concept
|
Wilms Tumor
|
Concept
|
Nitric Oxide
|
Concept
|
Synaptic Transmission
|
Concept
|
Norway
|
Concept
|
Ovary
|
Concept
|
Pain, Postoperative
|
Concept
|
Ligands
|
Concept
|
Cholesterol, HDL
|
Concept
|
Luciferases
|
Concept
|
Major Histocompatibility Complex
|
Concept
|
Rodentia
|
Concept
|
Oocytes
|
Concept
|
Muscle Proteins
|
Concept
|
Naloxone
|
Concept
|
Neisseria gonorrhoeae
|
Concept
|
Neuropeptide Y
|
Concept
|
Nose
|
Concept
|
Nuclear Family
|
Concept
|
Paraplegia
|
Concept
|
Patient Care Team
|
Concept
|
Feeding Behavior
|
Concept
|
Probability
|
Concept
|
Proinsulin
|
Concept
|
Pituitary Gland
|
Concept
|
Primates
|
Concept
|
Protein Conformation
|
Concept
|
Pseudomonas fluorescens
|
Concept
|
Hyperinsulinism
|
Concept
|
Glyburide
|
Concept
|
Hypoglycemia
|
Concept
|
Regression Analysis
|
Concept
|
Hair Color
|
Concept
|
Rats, Zucker
|
Concept
|
Receptors, Cell Surface
|
Concept
|
Receptors, Gastrointestinal Hormone
|
Concept
|
Receptor, Insulin
|
Concept
|
Referral and Consultation
|
Concept
|
Registries
|
Concept
|
Risk Factors
|
Concept
|
Quadriplegia
|
Concept
|
Salmonella
|
Concept
|
Sequence Homology, Nucleic Acid
|
Concept
|
Receptors, Pituitary Hormone
|
Concept
|
Xenopus
|
Concept
|
Insulin Resistance
|
Concept
|
Intestine, Small
|
Concept
|
Somatostatin
|
Concept
|
Potassium Channels
|
Concept
|
Cohort Studies
|
Concept
|
RNA Probes
|
Concept
|
Genes, ras
|
Concept
|
Regulatory Sequences, Nucleic Acid
|
Concept
|
Polymorphism, Restriction Fragment Length
|
Concept
|
Ribonucleosides
|
Concept
|
Sodium
|
Concept
|
Salmonella Infections
|
Concept
|
Scandinavian and Nordic Countries
|
Concept
|
Seasons
|
Concept
|
Serotyping
|
Concept
|
Japan
|
Concept
|
Polycystic Kidney Diseases
|
Concept
|
State Medicine
|
Concept
|
Subarachnoid Hemorrhage
|
Concept
|
Risk
|
Concept
|
RNA
|
Concept
|
RNA Polymerase II
|
Concept
|
Sensitivity and Specificity
|
Concept
|
Sleep, REM
|
Concept
|
Starvation
|
Concept
|
Sulfonylurea Compounds
|
Concept
|
Sweetening Agents
|
Concept
|
Texas
|
Concept
|
Heterochromatin
|
Concept
|
Homeostasis
|
Concept
|
Hong Kong
|
Concept
|
Humans
|
Concept
|
Body Mass Index
|
Concept
|
Incidence
|
Concept
|
Cluster Analysis
|
Concept
|
Staphylococcal Infections
|
Concept
|
Synapses
|
Concept
|
Tritium
|
Concept
|
Intracellular Membranes
|
Concept
|
CHO Cells
|
Concept
|
Diabetes, Gestational
|
Concept
|
United States
|
Concept
|
Syndrome
|
Concept
|
Trisomy
|
Concept
|
Umbilicus
|
Concept
|
Receptors, Opioid, mu
|
Concept
|
Receptors, Opioid, kappa
|
Concept
|
Water Supply
|
Concept
|
Testis
|
Concept
|
Xenopus laevis
|
Concept
|
Calcium Channels
|
Concept
|
Islets of Langerhans
|
Concept
|
Receptors, Purinergic P2
|
Concept
|
Octreotide
|
Concept
|
Oligonucleotide Probes
|
Concept
|
Chorionic Villi Sampling
|
Concept
|
Sulfotransferases
|
Concept
|
Leukemia, Myeloid
|
Concept
|
Levorphanol
|
Concept
|
Cholesterol, LDL
|
Concept
|
Lung
|
Concept
|
Risk Assessment
|
Concept
|
Retroelements
|
Concept
|
Muscle Fibers, Fast-Twitch
|
Concept
|
Glutamic Acid
|
Concept
|
Cell Culture Techniques
|
Concept
|
3,4-Dichloro-N-methyl-N-(2-(1-pyrrolidinyl)-cyclohexyl)-benzeneacetamide, (trans)-Isomer
|
Concept
|
Caspases
|
Concept
|
Sleep Apnea, Obstructive
|
Concept
|
Multifactorial Inheritance
|
Concept
|
Weaning
|
Concept
|
RNA Splice Sites
|
Concept
|
Water Microbiology
|
Concept
|
Guanosine 5'-O-(3-Thiotriphosphate)
|
Concept
|
Electrophoretic Mobility Shift Assay
|
Concept
|
Prevalence
|
Concept
|
Genes, Tumor Suppressor
|
Concept
|
Genes, Wilms Tumor
|
Concept
|
Contact Tracing
|
Concept
|
Mexico
|
Concept
|
Ion Channel Gating
|
Concept
|
Mitochondria
|
Concept
|
Morphine
|
Concept
|
Fructose-1,6-Diphosphatase Deficiency
|
Concept
|
Molecular Probes
|
Concept
|
DNA Probes
|
Concept
|
Cysteine Proteinase Inhibitors
|
Concept
|
Chi-Square Distribution
|
Concept
|
Genomic Library
|
Concept
|
Rats, Sprague-Dawley
|
Concept
|
Rats, Wistar
|
Concept
|
Mutagenesis, Site-Directed
|
Concept
|
Tacrolimus
|
Concept
|
Myocardium
|
Concept
|
Case-Control Studies
|
Concept
|
In Situ Hybridization
|
Concept
|
Protein Structure, Tertiary
|
Concept
|
Receptors, Endothelin
|
Concept
|
Methionine
|
Concept
|
Ecosystem
|
Concept
|
Genes, Reporter
|
Concept
|
Mice, Obese
|
Concept
|
Oligodeoxyribonucleotides
|
Concept
|
Consensus Sequence
|
Concept
|
Point Mutation
|
Concept
|
Hypertrophy, Left Ventricular
|
Concept
|
Gene Deletion
|
Concept
|
Sequence Deletion
|
Concept
|
Hepatoblastoma
|
Concept
|
Mice, Knockout
|
Concept
|
Receptors, Somatostatin
|
Concept
|
MyoD Protein
|
Concept
|
Patch-Clamp Techniques
|
Concept
|
Myogenin
|
Concept
|
DNA, Complementary
|
Concept
|
Cell Proliferation
|
Concept
|
HSP70 Heat-Shock Proteins
|
Concept
|
Dinucleotide Repeats
|
Concept
|
Chemokines
|
Concept
|
Thrombomodulin
|
Concept
|
Sample Size
|
Concept
|
Disease Progression
|
Concept
|
Evolution, Molecular
|
Concept
|
Muscle, Skeletal
|
Concept
|
ras Proteins
|
Concept
|
Muscle Fibers, Slow-Twitch
|
Concept
|
Phosphatidylethanolamine N-Methyltransferase
|
Concept
|
Apoptosis Regulatory Proteins
|
Concept
|
Glucose Intolerance
|
Concept
|
Helix-Loop-Helix Motifs
|
Concept
|
Blindness, Cortical
|
Concept
|
Receptors, Pituitary Adenylate Cyclase-Activating Polypeptide
|
Concept
|
Glucose Transporter Type 2
|
Concept
|
Hepatocyte Nuclear Factor 1-alpha
|
Concept
|
Caspase 3
|
Concept
|
Chemokines, CC
|
Concept
|
eIF-2 Kinase
|
Concept
|
Hepatocytes
|
Concept
|
Mutation, Missense
|
Concept
|
Base Pair Mismatch
|
Concept
|
Metabolic Syndrome
|
Concept
|
Amino Acid Transport Systems, Neutral
|
Concept
|
Multidrug Resistance-Associated Proteins
|
Concept
|
Drosophila Proteins
|
Concept
|
CpG Islands
|
Concept
|
Myosin Heavy Chains
|
Concept
|
Metabolome
|
Concept
|
In Situ Hybridization, Fluorescence
|
Concept
|
Protein Structure, Secondary
|
Concept
|
Receptors, Dopamine D1
|
Concept
|
Receptors, Opioid, delta
|
Concept
|
AT Rich Sequence
|
Concept
|
Fatal Outcome
|
Concept
|
Endoplasmic Reticulum Stress
|
Concept
|
Intercellular Signaling Peptides and Proteins
|
Concept
|
Pertussis Toxin
|
Concept
|
Adenylate Cyclase Toxin
|
Concept
|
Benzeneacetamides
|
Concept
|
Proprotein Convertase 2
|
Concept
|
Green Fluorescent Proteins
|
Concept
|
History, 21st Century
|
Concept
|
Inheritance Patterns
|
Concept
|
NIH 3T3 Cells
|
Concept
|
Chromatin Assembly and Disassembly
|
Concept
|
HSC70 Heat-Shock Proteins
|
Concept
|
Hepatocyte Nuclear Factor 1
|
Concept
|
Imidazolines
|
Concept
|
COS Cells
|
Concept
|
Genomic Imprinting
|
Concept
|
Microscopy, Confocal
|
Concept
|
Ryanodine Receptor Calcium Release Channel
|
Concept
|
Proto-Oncogene Proteins c-raf
|
Concept
|
Cyclin-Dependent Kinase Inhibitor p16
|
Concept
|
Amino Acid Substitution
|
Concept
|
Trinucleotide Repeats
|
Concept
|
Pancreatic Polypeptide
|
Concept
|
Oligonucleotide Array Sequence Analysis
|
Concept
|
Quality-Adjusted Life Years
|
Concept
|
Fluorescent Antibody Technique, Direct
|
Concept
|
Leptin
|
Concept
|
Potassium Channels, Inwardly Rectifying
|
Concept
|
Cytoprotection
|
Concept
|
Amino Acid Transport Systems
|
Concept
|
Sirolimus
|
Concept
|
Peromyscus
|
Concept
|
Phosphoenolpyruvate Carboxykinase (GTP)
|
Concept
|
Polycystic Ovary Syndrome
|
Concept
|
Animals, Genetically Modified
|
Concept
|
Precipitin Tests
|
Concept
|
Promoter Regions, Genetic
|
Concept
|
Mice
|
Concept
|
beta-Adrenergic Receptor Kinases
|
Concept
|
Receptors, Dopamine
|
Concept
|
Receptors, Glucocorticoid
|
Concept
|
Receptors, Muscarinic
|
Concept
|
Inositol 1,4,5-Trisphosphate Receptors
|
Concept
|
Surveys and Questionnaires
|
Concept
|
tRNA Methyltransferases
|
Concept
|
Ryanodine
|
Concept
|
Salmonella Infections, Animal
|
Concept
|
Severity of Illness Index
|
Concept
|
RNA, Messenger
|
Concept
|
Glycogen Synthase Kinase 3
|
Concept
|
Sleep Apnea Syndromes
|
Concept
|
Receptors, Leptin
|
Concept
|
Congenital Hyperinsulinism
|
Concept
|
Glycemic Index
|
Concept
|
Receptor, Muscarinic M3
|
Concept
|
Luciferases, Firefly
|
Concept
|
Receptors, Pituitary Adenylate Cyclase-Activating Polypeptide, Type I
|
Concept
|
Nuclear Respiratory Factor 1
|
Concept
|
Glucose Transporter Type 1
|
Concept
|
Rats
|
Concept
|
Basic Helix-Loop-Helix Leucine Zipper Transcription Factors
|
Concept
|
Sterol Regulatory Element Binding Protein 1
|
Concept
|
TCF Transcription Factors
|
Concept
|
Finches
|
Concept
|
Sex Factors
|
Concept
|
Growth Hormone
|
Concept
|
Spleen
|
Concept
|
Staphylococcus aureus
|
Concept
|
Streptozocin
|
Concept
|
Vanadates
|
Concept
|
Water Pollution, Chemical
|
Concept
|
Adaptor Proteins, Signal Transducing
|
Concept
|
Insulin-Secreting Cells
|
Concept
|
Immunoblotting
|
Concept
|
Blotting, Western
|
Concept
|
Chloramphenicol O-Acetyltransferase
|
Concept
|
Inositol 1,4,5-Trisphosphate
|
Concept
|
Multivariate Analysis
|
Concept
|
Survival Analysis
|
Concept
|
Lentivirus
|
Concept
|
Tetradecanoylphorbol Acetate
|
Concept
|
Frameshift Mutation
|
Concept
|
Islets of Langerhans Transplantation
|
Concept
|
Sex-Determining Region Y Protein
|
Concept
|
Blotting, Southern
|
Concept
|
Blotting, Northern
|
Concept
|
Hominidae
|
Concept
|
Reproducibility of Results
|
Concept
|
Patient Satisfaction
|
Concept
|
Genetic Therapy
|
Concept
|
Confidence Intervals
|
Concept
|
Receptors, Glucagon
|
Concept
|
Codon, Nonsense
|
Concept
|
Odds Ratio
|
Concept
|
Polymerase Chain Reaction
|
Concept
|
Zinc Fingers
|
Concept
|
Antisense Elements (Genetics)
|
Concept
|
ATP-Binding Cassette Transporters
|
Concept
|
Genes, src
|
Concept
|
GTP-Binding Proteins
|
Concept
|
Metabolic Networks and Pathways
|
Concept
|
Receptors, Chemokine
|
Concept
|
Gene Knockdown Techniques
|
Concept
|
Homeodomain Proteins
|
Concept
|
Muscle Fibers, Skeletal
|
Concept
|
HSP90 Heat-Shock Proteins
|
Concept
|
Microsatellite Repeats
|
Concept
|
Nitric Oxide Synthase
|
Concept
|
Macrophage Inflammatory Proteins
|
Concept
|
Untranslated Regions
|
Concept
|
Ginsenosides
|
Concept
|
Receptor, Endothelin B
|
Concept
|
RNA, Untranslated
|
Concept
|
Smegmamorpha
|
Concept
|
Abdominal Fat
|
Concept
|
Glycine Plasma Membrane Transport Proteins
|
Concept
|
Transcription Factor 7-Like 2 Protein
|
Concept
|
p300-CBP Transcription Factors
|
Concept
|
Hepatocyte Nuclear Factor 1-beta
|
Concept
|
Hepatocyte Nuclear Factor 6
|
Concept
|
KCNQ1 Potassium Channel
|
Concept
|
KATP Channels
|
Concept
|
Agouti Signaling Protein
|
Concept
|
Genome-Wide Association Study
|
Concept
|
AMP-Activated Protein Kinases
|
Concept
|
Insulin Receptor Substrate Proteins
|
Concept
|
Precision Medicine
|
Concept
|
Water Quality
|
Concept
|
RNA, Small Interfering
|
Concept
|
Control Groups
|
Concept
|
LIM-Homeodomain Proteins
|
Concept
|
Water Wells
|
Concept
|
Lipid Metabolism
|
Concept
|
Octamer Transcription Factor-3
|
Concept
|
Receptors, CCR6
|
Concept
|
Incretins
|
Concept
|
Islet Amyloid Polypeptide
|
Concept
|
HLA-DQ alpha-Chains
|
Concept
|
Antibodies
|
Concept
|
Binding, Competitive
|
Concept
|
Bone Development
|
Concept
|
Calcium
|
Concept
|
Cell Nucleolus
|
Concept
|
Chickens
|
Concept
|
Chromosomes, Human
|
Concept
|
Chromosomes, Human, Pair 16
|
Concept
|
Chromosomes, Human, Pair 18
|
Concept
|
Data Interpretation, Statistical
|
Concept
|
Diabetes Mellitus
|
Concept
|
Disease Models, Animal
|
Concept
|
DNA, Single-Stranded
|
Concept
|
Dynorphins
|
Concept
|
Electrophoresis, Agar Gel
|
Concept
|
Enhancer Elements, Genetic
|
Concept
|
Enzyme Stability
|
Concept
|
Epidermal Growth Factor
|
Concept
|
Epilepsy, Generalized
|
Concept
|
Eye
|
Concept
|
Family Health
|
Concept
|
Fat Emulsions, Intravenous
|
Concept
|
Follow-Up Studies
|
Concept
|
Genes, Fungal
|
Concept
|
Genetic Testing
|
Concept
|
Gestational Age
|
Concept
|
Glucose
|
Concept
|
Phosphorylases
|
Concept
|
Health Services Research
|
Concept
|
Heart Rate
|
Concept
|
Hernia, Diaphragmatic
|
Concept
|
Hyperglycemia
|
Concept
|
Ireland
|
Concept
|
Longitudinal Studies
|
Concept
|
Lymphocyte Activation
|
Concept
|
Lymphocytes
|
Concept
|
Lysine
|
Concept
|
Membrane Potentials
|
Concept
|
Metabolism, Inborn Errors
|
Concept
|
Mice, Mutant Strains
|
Concept
|
Microscopy, Fluorescence
|
Concept
|
Models, Biological
|
Concept
|
Mothers
|
Concept
|
Movement
|
Concept
|
Neurologic Manifestations
|
Concept
|
Niacin
|
Concept
|
Platelet Membrane Glycoproteins
|
Concept
|
Pregnancy, Animal
|
Concept
|
Prospective Studies
|
Concept
|
Rats, Mutant Strains
|
Concept
|
Receptors, Opioid
|
Concept
|
Retrospective Studies
|
Concept
|
RNA, Ribosomal
|
Concept
|
Spermatozoa
|
Concept
|
Tolbutamide
|
Concept
|
Translocation, Genetic
|
Concept
|
Tropomyosin
|
Concept
|
Hypertriglyceridemia
|
Concept
|
Databases, Factual
|
Concept
|
Oligonucleotides, Antisense
|
Concept
|
Mice, SCID
|
Concept
|
Mice, Inbred NOD
|
Concept
|
Mexican Americans
|
Concept
|
Conserved Sequence
|
Concept
|
Age of Onset
|
Concept
|
Cyclic AMP-Dependent Protein Kinases
|
Concept
|
DNA Primers
|
Concept
|
Receptors, Neurotransmitter
|
Concept
|
Directed Molecular Evolution
|
Concept
|
Quantitative Trait, Heritable
|
Concept
|
Genetic Predisposition to Disease
|
Concept
|
Polymorphism, Single Nucleotide
|
Concept
|
Protein Array Analysis
|
Concept
|
Luminescent Agents
|
Concept
|
Cyclin-Dependent Kinase Inhibitor p18
|
Concept
|
Proto-Oncogene Proteins c-akt
|
Concept
|
Glucose Transporter Type 4
|
Concept
|
Glucose Transporter Type 5
|
Concept
|
Chemokine CCL20
|
Concept
|
Insulin, Regular, Human
|
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
|
Leptin, the obese gene product, rapidly modulates synaptic transmission in the hypothalamus.
|
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
|
Glucokinase mutations, insulin secretion, and diabetes mellitus.
|
Academic Article
|
The aggregation of the 5' insulin gene polymorphism in insulin dependent (type I) diabetes mellitus families.
|
Academic Article
|
Novel MODY3 mutations in the hepatocyte nuclear factor-1alpha gene: evidence for a hyperexcitability of pancreatic beta-cells to intravenous secretagogues in a glucose-tolerant carrier of a P447L mutation.
|
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
|
NIDDM is associated with loss of pancreatic beta-cell L-type Ca2+ channel activity.
|
Academic Article
|
Human somatostatin receptor genes: localization to human chromosomes 14, 17, and 22 and identification of simple tandem repeat polymorphisms.
|
Academic Article
|
Rat inwardly rectifying potassium channel Kir6.2: cloning electrophysiological characterization, and decreased expression in pancreatic islets of male Zucker diabetic fatty rats.
|
Academic Article
|
Mammalian facilitative glucose transporters: evidence for similar substrate recognition sites in functionally monomeric proteins.
|
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
|
Identification of microsatellite markers near the human genes encoding the beta-cell ATP-sensitive K+ channel and linkage studies with NIDDM in Japanese.
|
Academic Article
|
Mutations in the hepatocyte nuclear factor-4alpha gene in maturity-onset diabetes of the young (MODY1)
|
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
|
Mutations in the hepatocyte nuclear factor-1alpha gene in MODY and early-onset NIDDM: evidence for a mutational hotspot in exon 4.
|
Academic Article
|
Changes in pancreatic islet glucokinase and hexokinase activities with increasing age, obesity, and the onset of diabetes.
|
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
|
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
|
Increase in serum leptin and uterine leptin receptor messenger RNA levels during pregnancy in rats.
|
Academic Article
|
Mutations in the hepatocyte nuclear factor-1alpha/MODY3 gene in Japanese subjects with early- and late-onset NIDDM.
|
Academic Article
|
Identification of nine novel mutations in the hepatocyte nuclear factor 1 alpha gene associated with maturity-onset diabetes of the young (MODY3).
|
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
|
An approach for identifying simple sequence repeat DNA polymorphisms near cloned cDNAs and genes. Linkage studies of the islet amyloid polypeptide/amylin and liver glycogen synthase genes and NIDDM.
|
Academic Article
|
Activation of a protein tyrosine phosphatase and inactivation of Raf-1 by somatostatin.
|
Academic Article
|
Nonsense mutation in the glucokinase gene causes early-onset non-insulin-dependent diabetes mellitus.
|
Academic Article
|
Nature or nurture: an insightful illustration from a Chinese family with hepatocyte nuclear factor-1 alpha diabetes (MODY3)
|
Academic Article
|
Genetic variation in the gene encoding calpain-10 is associated with type 2 diabetes mellitus.
|
Academic Article
|
Studies of association between the gene for calpain-10 and type 2 diabetes mellitus in the United Kingdom.
|
Academic Article
|
Evidence that insulin is imprinted in the human yolk sac.
|
Academic Article
|
Mutations in the coding region of the neurogenin 3 gene (NEUROG3) are not a common cause of maturity-onset diabetes of the young in Japanese subjects.
|
Academic Article
|
Abnormal nephron development associated with a frameshift mutation in the transcription factor hepatocyte nuclear factor-1 beta.
|
Academic Article
|
Linkage analysis of maturity-onset diabetes of the young with microsatellite polymorphisms. No linkage to ADA or GLUT2 genes in two families.
|
Academic Article
|
beta-cell transcription factors and diabetes: no evidence for diabetes-associated mutations in the gene encoding the basic helix-loop-helix transcription factor neurogenic differentiation 4 (NEUROD4) in Japanese patients with MODY.
|
Academic Article
|
A simple test for the high-frequency P291fsinsC mutation in the HNF1 alpha/MODY3 gene.
|
Academic Article
|
Relationship of insulin receptor substrate-1 and -2 genotypes to phenotypic features of polycystic ovary syndrome.
|
Academic Article
|
Reduced pancreatic polypeptide response to hypoglycemia and amylin response to arginine in subjects with a mutation in the HNF-4alpha/MODY1 gene.
|
Academic Article
|
Functional properties of the R154X HNF-4alpha protein generated by a mutation associated with maturity-onset diabetes of the young, type 1.
|
Academic Article
|
Identification of three missense mutations in the peroxisome proliferator-activated receptor alpha gene in Japanese subjects with maturity-onset diabetes of the young.
|
Academic Article
|
Beta-cell transcription factors and diabetes: no evidence for diabetes-associated mutations in the hepatocyte nuclear factor-3beta gene (HNF3B) in Japanese patients with maturity-onset diabetes of the young.
|
Academic Article
|
Calpains play a role in insulin secretion and action.
|
Academic Article
|
No diabetes-associated mutations in the coding region of the hepatocyte nuclear factor-4gamma gene (HNF4G) in Japanese patients with MODY.
|
Academic Article
|
Improved glucose tolerance and insulin sensitivity after electrical stimulation-assisted cycling in people with spinal cord injury.
|
Academic Article
|
Diabetes mellitus and genetically programmed defects in beta-cell function.
|
Academic Article
|
NHS services for epilepsy from the patient's perspective: a survey of primary, secondary and tertiary care access throughout the UK.
|
Academic Article
|
Nuclear translocation of SHP and visualization of interaction with HNF-4alpha in living cells.
|
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
|
A 48-hour exposure of pancreatic islets to calpain inhibitors impairs mitochondrial fuel metabolism and the exocytosis of insulin.
|
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
|
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
|
Optical imaging of pancreatic beta cells in living mice expressing a mouse insulin I promoter-firefly luciferase transgene.
|
Academic Article
|
Gene symbol: IPF1. Disease: MODY 4.
|
Academic Article
|
Patterns of linkage disequilibrium in the type 2 diabetes gene calpain-10.
|
Academic Article
|
Phenotypic heterogeneity between different mutations of MODY subtypes and within MODY pedigrees.
|
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
|
Noninvasive monitoring of changes in pancreatic beta-cell mass by bioluminescent imaging in MIP-luc transgenic mice.
|
Academic Article
|
Macrosomia and neonatal hypoglycaemia in RW pedigree subjects with a mutation (Q268X) in the gene encoding hepatocyte nuclear factor 4alpha (HNF4A).
|
Academic Article
|
Diagnosis and treatment of neonatal diabetes: a United States experience.
|
Academic Article
|
Insulin mutation screening in 1,044 patients with diabetes: mutations in the INS gene are a common cause of neonatal diabetes but a rare cause of diabetes diagnosed in childhood or adulthood.
|
Academic Article
|
Genetic variants in the calpain-10 gene and the development of type 2 diabetes in the Japanese population.
|
Academic Article
|
Update in neonatal diabetes.
|
Academic Article
|
The linkage and association of the gene encoding upstream stimulatory factor 1 with type 2 diabetes and metabolic syndrome in the Chinese population.
|
Academic Article
|
From clinicogenetic studies of maturity-onset diabetes of the young to unraveling complex mechanisms of glucokinase regulation.
|
Academic Article
|
Kir6.2 variant E23K increases ATP-sensitive K+ channel activity and is associated with impaired insulin release and enhanced insulin sensitivity in adults with normal glucose tolerance.
|
Academic Article
|
Common polymorphisms of calpain-10 are associated with abdominal obesity in subjects at high risk of type 2 diabetes.
|
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
|
Neonatal diabetes mellitus: a model for personalized medicine.
|
Academic Article
|
TCF7L2 variant rs7903146 affects the risk of type 2 diabetes by modulating incretin action.
|
Academic Article
|
Neonatal diabetes: an expanding list of genes allows for improved diagnosis and treatment.
|
Academic Article
|
Identification of microsatellite markers near the human ob gene and linkage studies in NIDDM-affected sib pairs.
|
Academic Article
|
Splice variant of the somatostatin receptor 2 subtype, somatostatin receptor 2B, couples to adenylyl cyclase.
|
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
|
Compensation in pancreatic beta-cell function in subjects with glucokinase mutations.
|
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
|
Localization of inositol trisphosphate receptor subtype 3 to insulin and somatostatin secretory granules and regulation of expression in islets and insulinoma cells.
|
Academic Article
|
Mutation of an aspartate at residue 89 in somatostatin receptor subtype 2 prevents Na+ regulation of agonist binding but does not alter receptor-G protein association.
|
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
|
Evolution of beta-cell dysfunction in the male Zucker diabetic fatty rat.
|
Academic Article
|
No evidence for mutations in a putative beta-cell ATP-sensitive K+ channel subunit in MODY, NIDDM, or GDM.
|
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
|
G protein-activated inwardly rectifying potassium channel (GIRK1/KGA) mRNA in adult rat heart and brain by in situ hybridization histochemistry.
|
Academic Article
|
Inositol 1,4,5-trisphosphate receptors, secretory granules and secretion in endocrine and neuroendocrine cells.
|
Academic Article
|
Pharmacological characterization of the cloned kappa-, delta-, and mu-opioid receptors.
|
Academic Article
|
Agonists and antagonists bind to different domains of the cloned kappa opioid receptor.
|
Academic Article
|
Immunological detection of isoforms of the somatostatin receptor subtype, SSTR2.
|
Academic Article
|
Dinucleotide repeat polymorphism in the NEC2 gene.
|
Academic Article
|
Expression of calcium channel mRNAs in rat pancreatic islets and downregulation after glucose infusion.
|
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
|
The population association of glucokinase gene with type 2 (noninsulin-dependent) diabetes mellitus in Chinese.
|
Academic Article
|
Maturity-onset diabetes of the young.
|
Academic Article
|
Repression of the insulin-like growth factor II gene by the Wilms tumor suppressor WT1.
|
Academic Article
|
Organization of the human GLUT2 (pancreatic beta-cell and hepatocyte) glucose transporter gene.
|
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
|
Identification of 14 new glucokinase mutations and description of the clinical profile of 42 MODY-2 families.
|
Academic Article
|
Mutations in the hepatocyte nuclear factor-1alpha gene are a common cause of maturity-onset diabetes of the young in the U.K.
|
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
|
Mapping diabetes-susceptibility genes. Lessons learned from search for DNA marker for maturity-onset diabetes of the young.
|
Academic Article
|
Patients' perspectives on services for epilepsy: a survey of patient satisfaction, preferences and information provision in 2394 people with epilepsy.
|
Academic Article
|
Variation in the calpain-10 gene affects blood glucose levels in the British population.
|
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
|
Organ alchemy: producing insulin in the liver.
|
Academic Article
|
Linkage of calpain 10 to type 2 diabetes: the biological rationale.
|
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
|
Identification of type 2 diabetes genes in Mexican Americans through genome-wide association studies.
|
Academic Article
|
Mutations in the insulin gene can cause MODY and autoantibody-negative type 1 diabetes.
|
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
|
Altered insulin secretory responses to glucose in subjects with a mutation in the MODY1 gene on chromosome 20.
|
Academic Article
|
Creation of an inositol 1,4,5-trisphosphate-sensitive Ca2+ store in secretory granules of insulin-producing cells.
|
Academic Article
|
Molecular model of human beta-cell glucokinase built by analogy to the crystal structure of yeast hexokinase B.
|
Academic Article
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Type 2 (non-insulin-dependent) diabetes mellitus associated with a mutation of the glucokinase gene in a Japanese family.
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Dinucleotide repeat polymorphism in the human thyroid hormone receptor alpha gene (THRA1) on chromosome 17.
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Microsatellite polymorphism in the human platelet glycoprotein IIIa gene (GP3A) on chromosome 17.
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Human pancreatic beta-cell glucokinase: cDNA sequence and localization of the polymorphic gene to chromosome 7, band p 13.
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Dinucleotide repeat polymorphism at the human ribophorin II locus (RPN2) on chromosome 20q.
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Molecular biology of opioid receptors.
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The cloned kappa opioid receptor couples to an N-type calcium current in undifferentiated PC-12 cells.
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Localization of the glucagon receptor gene to human chromosome band 17q25.
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Molecular mechanisms of agonist-induced desensitization of the cloned mouse kappa opioid receptor.
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Differential expression of messenger RNAs for somatostatin receptor subtypes SSTR1, SSTR2 and SSTR3 in adult rat brain: analysis by RNA blotting and in situ hybridization histochemistry.
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Assignment of SLC6A9 to human chromosome band 1p33 by in situ hybridization.
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Expression of inositol 1,4,5-trisphosphate receptors changes the Ca2+ signal of Xenopus oocytes.
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Characterization of cloned somatostatin receptors SSTR4 and SSTR5.
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Cloned somatostatin receptors: identification of subtype-selective peptides and demonstration of high affinity binding of linear peptides.
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Molecular genetics of myeloid leukemia: identification of the commonly deleted segment of chromosome 20.
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Evolution of simple sequence repeats.
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Changes in endothelial nitric oxide synthase mRNA during vasospasm after subarachnoid hemorrhage in monkeys.
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Apparent confined placental mosaicism of trisomy 16 and multiple fetal anomalies: case report.
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Gi alpha 1 selectively couples somatostatin receptor subtype 3 to adenylyl cyclase: identification of the functional domains of this alpha subunit necessary for mediating the inhibition by somatostatin of cAMP formation.
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Sexual partner networks in the transmission of sexually transmitted diseases. An analysis of gonorrhea cases in Sheffield, UK.
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The length distribution of perfect dimer repetitive DNA is consistent with its evolution by an unbiased single-step mutation process.
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The advantage of sex in evolving yeast populations.
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Persistence of two genotypes of Neisseria gonorrhoeae during transmission.
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Identification of gestationally regulated genes in rat myometrium by use of messenger ribonucleic acid differential display.
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Examination of trisomy 13, 18 and 21 foetal tissues at different gestational ages using FISH.
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Intrapancreatic delivery of human umbilical cord blood aldehyde dehydrogenase-producing cells promotes islet regeneration.
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The oligogenic view of adaptation.
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In vitro scan for enhancers at the TCF7L2 locus.
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Localization of human somatostatin receptor 5 gene (SSTR5) to chromosome band 16p13.3 by fluorescence in situ hybridization.
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Human somatostatin receptor genes: localization of SSTR5 to human chromosome 20p11.2.
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Molecular biology of somatostatin receptors.
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Role of BH3-only molecules Bim and Puma in ß-cell death in Pdx1 deficiency.
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Evidence of non-pancreatic beta cell-dependent roles of Tcf7l2 in the regulation of glucose metabolism in mice.
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Effect of genetic variation in a Drosophila model of diabetes-associated misfolded human proinsulin.
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Genetic complexity in a Drosophila model of diabetes-associated misfolded human proinsulin.
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Localization of hepatocyte nuclear factor-4a in the nucleolus and nucleus is regulated by its C-terminus.
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Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility.
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Continued lessons from the INS gene: an intronic mutation causing diabetes through a novel mechanism.
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Resting beta-cells - A functional reserve?
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The genetic architecture of type 2 diabetes.
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Disturbance and diversity in experimental microcosms.
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Diversity peaks at intermediate productivity in a laboratory microcosm.
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Multiethnic Meta-Analysis Identifies RAI1 as a Possible Obstructive Sleep Apnea-related Quantitative Trait Locus in Men.
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Exome sequencing of 20,791 cases of type 2 diabetes and 24,440 controls.
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In celebration of a century with insulin - Update of insulin gene mutations in diabetes.
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Concept
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Glucagon-Like Peptide-1 Receptor
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Concept
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Perilipin-1
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Concept
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Glycogen Synthase Kinase 3 beta
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Concept
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Bcl-2-Like Protein 11
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Concept
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One Health
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Concept
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RNA, Long Noncoding
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Concept
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Sulfonylurea Receptors
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Concept
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Betacellulin
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Concept
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In Vitro Techniques
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