Item Type | Name |
Concept
|
Air
|
Concept
|
Acclimatization
|
Concept
|
Adenosine Deaminase
|
Concept
|
Adenosine Diphosphate
|
Concept
|
Haplorhini
|
Concept
|
Bird Diseases
|
Concept
|
Birds
|
Concept
|
Adenosine Triphosphate
|
Concept
|
Catheterization
|
Concept
|
Cats
|
Concept
|
Chromosome Banding
|
Concept
|
Chromosomes, Human, Pair 11
|
Concept
|
Chromosomes, Human, Pair 2
|
Concept
|
Chromosomes, Human, Pair 6
|
Concept
|
Analysis of Variance
|
Concept
|
Antarctic Regions
|
Concept
|
Chromosomes, Human, Pair 8
|
Concept
|
Cytogenetics
|
Concept
|
Cell Differentiation
|
Concept
|
Attention Deficit Disorder with Hyperactivity
|
Concept
|
Bayes Theorem
|
Concept
|
Autoradiography
|
Concept
|
Ethics, Medical
|
Concept
|
Ferrets
|
Concept
|
Chromosomes, Human, Pair 1
|
Concept
|
Chromosomes, Human, Pair 15
|
Concept
|
Chromosomes, Human, Pair 21
|
Concept
|
Chromosomes, Human, Pair 3
|
Concept
|
Cerebellum
|
Concept
|
Chromosomes, Human, Pair 12
|
Concept
|
Chromosomes, Human, Pair 13
|
Concept
|
Chromosomes, Human, Pair 22
|
Concept
|
Codon
|
Concept
|
Chromosomes, Human, Pair 5
|
Concept
|
Chromosomes, Human, Pair 7
|
Concept
|
Cold Temperature
|
Concept
|
Chromosomes, Human, Pair 20
|
Concept
|
Coronary Artery Disease
|
Concept
|
Indians, North American
|
Concept
|
Congenital Hypothyroidism
|
Concept
|
Dogs
|
Concept
|
Ducks
|
Concept
|
Chromosomes, Human, Pair 10
|
Concept
|
Chromosomes, Human, Pair 19
|
Concept
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Chromosomes, Human, Pair 9
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Concept
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Exons
|
Concept
|
Family
|
Concept
|
Health Expenditures
|
Concept
|
Cost-Benefit Analysis
|
Concept
|
DNA, Satellite
|
Concept
|
Influenza in Birds
|
Concept
|
Introns
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Concept
|
Mice, Inbred C3H
|
Concept
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Geese
|
Concept
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Genetics, Behavioral
|
Concept
|
Dyslexia
|
Concept
|
Genetics, Medical
|
Concept
|
Genetics, Population
|
Concept
|
Iodides
|
Concept
|
Language Development Disorders
|
Concept
|
Pharmacogenetics
|
Concept
|
Mice, Transgenic
|
Concept
|
Poultry
|
Concept
|
Monosaccharide Transport Proteins
|
Concept
|
NADP
|
Concept
|
Mice, Inbred BALB C
|
Concept
|
Mice, Inbred C57BL
|
Concept
|
Cricetinae
|
Concept
|
Nuclear Family
|
Concept
|
Poultry Diseases
|
Concept
|
Primates
|
Concept
|
Rabbits
|
Concept
|
Quail
|
Concept
|
Virology
|
Concept
|
Reye Syndrome
|
Concept
|
Potassium Channels
|
Concept
|
Receptors, GABA-A
|
Concept
|
Health Knowledge, Attitudes, Practice
|
Concept
|
Speech Disorders
|
Concept
|
Swine
|
Concept
|
Humans
|
Concept
|
Warfarin
|
Concept
|
Tamoxifen
|
Concept
|
Marriage
|
Concept
|
Gangliosidosis, GM1
|
Concept
|
Deoxyribonucleases, Type II Site-Specific
|
Concept
|
Bias
|
Concept
|
Campylobacter jejuni
|
Concept
|
Postmenopause
|
Concept
|
Mice, Obese
|
Concept
|
Mites
|
Concept
|
Gallstones
|
Concept
|
RNA-Binding Proteins
|
Concept
|
Health Care Costs
|
Concept
|
TNF Receptor-Associated Factor 6
|
Concept
|
Mice, Knockout
|
Concept
|
Receptors, AMPA
|
Concept
|
Serotonin Plasma Membrane Transport Proteins
|
Concept
|
Telomerase
|
Concept
|
Antineoplastic Agents, Alkylating
|
Concept
|
Multidrug Resistance-Associated Proteins
|
Concept
|
Protein Folding
|
Concept
|
Systems Biology
|
Concept
|
Proteomics
|
Concept
|
Parents
|
Concept
|
3' Untranslated Regions
|
Concept
|
Potassium Channels, Inwardly Rectifying
|
Concept
|
Promoter Regions, Genetic
|
Concept
|
Mice
|
Concept
|
Adiposity
|
Concept
|
Rats
|
Concept
|
Adaptor Proteins, Signal Transducing
|
Concept
|
Insulin-Secreting Cells
|
Concept
|
Temperature
|
Concept
|
Multivariate Analysis
|
Concept
|
ATP-Binding Cassette Transporters
|
Concept
|
Coronary Angiography
|
Concept
|
GTP-Binding Proteins
|
Concept
|
Molecular Epidemiology
|
Concept
|
CD4 Lymphocyte Count
|
Concept
|
Untranslated Regions
|
Concept
|
Metabolomics
|
Concept
|
Insulin Receptor Substrate Proteins
|
Concept
|
RNA, Small Interfering
|
Concept
|
Siblings
|
Concept
|
Drug Discovery
|
Concept
|
Chickens
|
Concept
|
Chromosomes, Human
|
Concept
|
Chromosomes, Human, Pair 16
|
Concept
|
DNA Restriction Enzymes
|
Concept
|
Electrophoresis, Agar Gel
|
Concept
|
Hemagglutinins
|
Concept
|
Mothers
|
Concept
|
Patient Compliance
|
Concept
|
Stuttering
|
Concept
|
Cost of Illness
|
Concept
|
Computational Biology
|
Concept
|
Genomics
|
Concept
|
Membrane Transport Proteins
|
Concept
|
MicroRNAs
|
Concept
|
Chromosomes, Human, X
|
Concept
|
Dopamine Plasma Membrane Transport Proteins
|
Concept
|
Excitatory Amino Acid Transporter 3
|
Concept
|
HapMap Project
|
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
|
Mutations in the hepatocyte nuclear factor-1alpha gene in maturity-onset diabetes of the young (MODY3)
|
Academic Article
|
The gene responsible for autosomal dominant Doyne's honeycomb retinal dystrophy (DHRD) maps to chromosome 2p16.
|
Academic Article
|
Genome-wide search for asthma susceptibility loci in a founder population. The Collaborative Study on the Genetics of Asthma.
|
Academic Article
|
Allele-sharing models: LOD scores and accurate linkage tests.
|
Academic Article
|
Human influenza A (H1N2) viruses isolated from China.
|
Academic Article
|
Genetic variation in the gene encoding calpain-10 is associated with type 2 diabetes mellitus.
|
Academic Article
|
Linkage-disequilibrium mapping of autistic disorder, with 15q11-13 markers.
|
Academic Article
|
Loci on chromosomes 2 (NIDDM1) and 15 interact to increase susceptibility to diabetes in Mexican Americans.
|
Academic Article
|
Genetic characterization of the pathogenic influenza A/Goose/Guangdong/1/96 (H5N1) virus: similarity of its hemagglutinin gene to those of H5N1 viruses from the 1997 outbreaks in Hong Kong.
|
Academic Article
|
Variation in the interleukin 4-receptor alpha gene confers susceptibility to asthma and atopy in ethnically diverse populations.
|
Academic Article
|
Role of calpain-10 gene variants in familial type 2 diabetes in Caucasians.
|
Academic Article
|
Risk of influenza A (H5N1) infection among poultry workers, Hong Kong, 1997-1998.
|
Academic Article
|
Genomewide screen and identification of gene-gene interactions for asthma-susceptibility loci in three U.S. populations: collaborative study on the genetics of asthma.
|
Academic Article
|
Infection of a child in Hong Kong by an influenza A H3N2 virus closely related to viruses circulating in European pigs.
|
Academic Article
|
Seven regions of the genome show evidence of linkage to type 1 diabetes in a consensus analysis of 767 multiplex families.
|
Academic Article
|
Methods for analysis and visualization of SNP genotype data for complex diseases.
|
Academic Article
|
Lack of evidence for human-to-human transmission of avian influenza A (H9N2) viruses in Hong Kong, China 1999.
|
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
|
Genome scan for loci linked to mite sensitivity: the Collaborative Study on the Genetics of Asthma (CSGA).
|
Academic Article
|
Geographic and haplotype structure of candidate type 2 diabetes susceptibility variants at the calpain-10 locus.
|
Academic Article
|
Findings in an independent sample support an association between bipolar affective disorder and the G72/G30 locus on chromosome 13q33.
|
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
|
Loci on chromosomes 6q and 6p interact to increase susceptibility to bipolar affective disorder in the national institute of mental health genetics initiative pedigrees.
|
Academic Article
|
Polymorphisms of GLUT2 and GLUT4 genes. Use in evaluation of genetic susceptibility to NIDDM in blacks.
|
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
|
Gene for non-insulin-dependent diabetes mellitus (maturity-onset diabetes of the young subtype) is linked to DNA polymorphism on human chromosome 20q.
|
Academic Article
|
Haplotype structure and phylogenetic shadowing of a hypervariable region in the CAPN10 gene.
|
Academic Article
|
Genetic epidemiology of diabetes.
|
Academic Article
|
Combined analysis of three whole genome linkage scans for Ankylosing Spondylitis.
|
Academic Article
|
Relationship of EGFR mutations, expression, amplification, and polymorphisms to epidermal growth factor receptor inhibitors in the NCI60 cell lines.
|
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
|
Gene-based SNP mapping of a psychotic bipolar affective disorder linkage region on 22q12.3: association with HMG2L1 and TOM1.
|
Academic Article
|
Prevention and control of influenza: recommendations of the Advisory Committee on Immunization Practices (ACIP).
|
Academic Article
|
Quality of life in paediatric lupus.
|
Academic Article
|
Insulin gene mutations as a cause of permanent neonatal diabetes.
|
Academic Article
|
Polygenic virulence factors involved in pathogenesis of 1997 Hong Kong H5N1 influenza viruses in mice.
|
Academic Article
|
Evidence for a susceptibility locus on chromosome 10p15 in early-onset obsessive-compulsive disorder.
|
Academic Article
|
Evaluation of genetic variation contributing to differences in gene expression between populations.
|
Academic Article
|
Population-specific GSTM1 copy number variation.
|
Academic Article
|
Prevention and control of influenza: recommendations of the Advisory Committee on Immunization Practices (ACIP).
|
Academic Article
|
Genetic variants in the calpain-10 gene and the development of type 2 diabetes in the Japanese population.
|
Academic Article
|
Genomewide significant linkage to stuttering on chromosome 12.
|
Academic Article
|
Human genetics: an expression of interest.
|
Academic Article
|
No bias in linkage analysis.
|
Academic Article
|
Rational inferences about departures from Hardy-Weinberg equilibrium.
|
Academic Article
|
Genomewide linkage scan of 409 European-ancestry and African American families with schizophrenia: suggestive evidence of linkage at 8p23.3-p21.2 and 11p13.1-q14.1 in the combined sample.
|
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
|
Fine mapping and positional candidate studies on chromosome 5p13 identify multiple asthma susceptibility loci.
|
Academic Article
|
SCAN: SNP and copy number annotation.
|
Academic Article
|
Are genome-wide association studies all that we need to dissect the genetic component of complex human diseases?
|
Academic Article
|
Genetic variations in GRIA1 on chromosome 5q33 related to asparaginase hypersensitivity.
|
Academic Article
|
Genetic bases of the temperature-sensitive phenotype of a master donor virus used in live attenuated influenza vaccines: A/Leningrad/134/17/57 (H2N2).
|
Academic Article
|
A German genome-wide linkage scan for type 2 diabetes supports the existence of a metabolic syndrome locus on chromosome 1p36.13 and a type 2 diabetes locus on chromosome 16p12.2.
|
Academic Article
|
The missing association: sequencing-based discovery of novel SNPs in VKORC1 and CYP2C9 that affect warfarin dose in African Americans.
|
Academic Article
|
Platinum sensitivity-related germline polymorphism discovered via a cell-based approach and analysis of its association with outcome in ovarian cancer patients.
|
Academic Article
|
Lack of association between common single nucleotide polymorphisms in the TERT-CLPTM1L locus and breast cancer in women of African ancestry.
|
Academic Article
|
Genome-wide meta-analysis for severe diabetic retinopathy.
|
Academic Article
|
Meta-analysis of 23 type 2 diabetes linkage studies from the International Type 2 Diabetes Linkage Analysis Consortium.
|
Academic Article
|
Genome-wide ancestry association testing identifies a common European variant on 6q14.1 as a risk factor for asthma in African American subjects.
|
Academic Article
|
Bgl II RFLP at the human erythrocyte/HepG2-type glucose transporter (GLUT) locus on chromosome 1.
|
Academic Article
|
Linkage disequilibrium in the human insulin/insulin-like growth factor II region of human chromosome II.
|
Academic Article
|
Maternal transmission of a rare GABRB3 signal peptide variant is associated with autism.
|
Academic Article
|
Multiple Taq I RFLPs at the human manganese superoxide dismutase (S0D2) locus on chromosome 6.
|
Academic Article
|
Genetic architecture of transcript-level variation in humans.
|
Academic Article
|
Prolonged shedding of amantadine-resistant influenzae A viruses by immunodeficient patients: detection by polymerase chain reaction-restriction analysis.
|
Academic Article
|
Interaction of prenatal exposure to cigarettes and MAOA genotype in pathways to youth antisocial behavior.
|
Academic Article
|
Restriction fragment polymorphisms of the HLA-DR, HLA-DQ, and insulin gene regions in IDDM: the GAW5 data.
|
Academic Article
|
Comprehensive evaluation of the contribution of X chromosome genes to platinum sensitivity.
|
Academic Article
|
Parent-of-origin effects of the serotonin transporter gene associated with autism.
|
Academic Article
|
Lack of significant person-to-person spread of swine influenza-like virus following fatal infection in an immunocompromised child.
|
Academic Article
|
Nucleotide sequences of the neuraminidase genes of influenza A/Leningrad/134/57 (H2N2) virus and two of its live, attenuated, cold-adapted variants.
|
Academic Article
|
Isolation of a cDNA clone encoding a KATP channel-like protein expressed in insulin-secreting cells, localization of the human gene to chromosome band 21q22.1, and linkage studies with NIDDM.
|
Academic Article
|
Apa I and Sst I RFLPs at the insulin-like growth factor II (IGF2) locus on chromosome 11.
|
Academic Article
|
Influenza A virus haemagglutinin polymorphism: pleiotropic antigenic variants of A/Shanghai/11/87 (H3N2) virus selected as high yield reassortants.
|
Academic Article
|
Genetic stability of cold-adapted A/Leningrad/134/47/57 (H2N2) influenza virus: sequence analysis of live cold-adapted reassortant vaccine strains before and after replication in children.
|
Academic Article
|
Stuttering: a complex behavioral disorder for our times?
|
Academic Article
|
Recombinant mapping of the familial hyperinsulinism gene to an 0.8 cM region on chromosome 11p15.1 and demonstration of a founder effect in Ashkenazi Jews.
|
Academic Article
|
FstSNP-HapMap3: a database of SNPs with high population differentiation for HapMap3.
|
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 novel germline polymorphisms governing capecitabine sensitivity.
|
Academic Article
|
Inheritance of human platelet thermolabile phenol sulfotransferase (TL PST) activity.
|
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
|
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
|
Fine mapping and positional candidate studies identify HLA-G as an asthma susceptibility gene on chromosome 6p21.
|
Academic Article
|
GEL: a novel genotype calling algorithm using empirical likelihood.
|
Academic Article
|
Genetic studies of stuttering in a founder population.
|
Academic Article
|
Transmission disequilibrium testing of the chromosome 15q11-q13 region in autism.
|
Academic Article
|
Reconstructability analysis as a tool for identifying gene-gene interactions in studies of human diseases.
|
Academic Article
|
Germline polymorphisms discovered via a cell-based, genome-wide approach predict platinum response in head and neck cancers.
|
Academic Article
|
Genome-wide association study identifies germline polymorphisms associated with relapse of childhood acute lymphoblastic leukemia.
|
Academic Article
|
Can recovery from stuttering be considered a genetically milder subtype of stuttering?
|
Academic Article
|
Localization of MODY3 to a 5-cM region of human chromosome 12.
|
Academic Article
|
Avian-to-human transmission of H9N2 subtype influenza A viruses: relationship between H9N2 and H5N1 human isolates.
|
Academic Article
|
Influenza-associated deaths among children in the United States, 2003-2004.
|
Academic Article
|
Integration of cell line and clinical trial genome-wide analyses supports a polygenic architecture of Paclitaxel-induced sensory peripheral neuropathy.
|
Academic Article
|
In vitro evolution of H5N1 avian influenza virus toward human-type receptor specificity.
|
Academic Article
|
Fine mapping of breast cancer genome-wide association studies loci in women of African ancestry identifies novel susceptibility markers.
|
Academic Article
|
Genome-wide association study of Tourette's syndrome.
|
Academic Article
|
Influenza-associated hospitalizations in the United States.
|
Academic Article
|
Genome-wide meta-analysis identifies variants associated with platinating agent susceptibility across populations.
|
Academic Article
|
A genome-wide association study of breast cancer in women of African ancestry.
|
Academic Article
|
National Institutes of Health State-of-the-Science Conference statement: preventing alzheimer disease and cognitive decline.
|
Academic Article
|
Effect of receptor binding domain mutations on receptor binding and transmissibility of avian influenza H5N1 viruses.
|
Academic Article
|
Influenza A(H1N1)pdm09 virus among healthy show pigs, United States.
|
Academic Article
|
A genome-wide integrative study of microRNAs in human liver.
|
Academic Article
|
Genetic analysis of avian influenza A viruses isolated from domestic waterfowl in live-bird markets of Hanoi, Vietnam, preceding fatal H5N1 human infections in 2004.
|
Academic Article
|
Quantification of immunoreactive viral influenza proteins by immunoaffinity capture and isotope-dilution liquid chromatography-tandem mass spectrometry.
|
Academic Article
|
Genome-wide interrogation of longitudinal FEV1 in children with asthma.
|
Academic Article
|
Poly-omic prediction of complex traits: OmicKriging.
|
Academic Article
|
Integrative analyses of genetic variation, epigenetic regulation, and the transcriptome to elucidate the biology of platinum sensitivity.
|
Academic Article
|
Clinical drug response can be predicted using baseline gene expression levels and in vitro drug sensitivity in cell lines.
|
Academic Article
|
A nondegenerate code of deleterious variants in Mendelian loci contributes to complex disease risk.
|
Academic Article
|
Immunogenicity and reactogenicity of 1 versus 2 doses of trivalent inactivated influenza vaccine in vaccine-naive 5-8-year-old children.
|
Academic Article
|
Genetic analysis of human H2N2 and early H3N2 influenza viruses, 1957-1972: evidence for genetic divergence and multiple reassortment events.
|
Academic Article
|
Influenza A virus neuraminidase protein enhances cell survival through interaction with carcinoembryonic antigen-related cell adhesion molecule 6 (CEACAM6) protein.
|
Academic Article
|
The chromosome 3q25 genomic region is associated with measures of adiposity in newborns in a multi-ethnic genome-wide association study.
|
Academic Article
|
Surveillance of resistance to adamantanes among influenza A(H3N2) and A(H1N1) viruses isolated worldwide.
|
Academic Article
|
Institutional Profile: University of Chicago Center for Personalized Therapeutics: research, education and implementation science.
|
Academic Article
|
Anti-ganglioside antibody induction by swine (A/NJ/1976/H1N1) and other influenza vaccines: insights into vaccine-associated Guillain-Barré syndrome.
|
Academic Article
|
Comparative immunogenicity and cross-clade protective efficacy of mammalian cell-grown inactivated and live attenuated H5N1 reassortant vaccines in ferrets.
|
Concept
|
Sequestosome-1 Protein
|
Concept
|
Perilipin-1
|
Concept
|
Sulfonylurea Receptors
|