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Genotype
Genotype
Genetic study on frontotemporal lobar degeneration in India
Cognitive Science / India / Humans / Haplotypes / Clinical Sciences / Genotype / Frontotemporal Dementia / Genotype / Frontotemporal Dementia
A Comprehensive Linkage Analysis of Chromosome 21q22 Supports Prior Evidence for a Putative Bipolar Affective Disorder Locus
Genetics / Bipolar Disorder / Biological Sciences / Humans / Cost effectiveness / Genetic linkage analysis / Genotype / Bipolar Affective Disorder / Genetic Markers / Affective Disorder / Linkage Analysis / The American / Genetic linkage analysis / Genotype / Bipolar Affective Disorder / Genetic Markers / Affective Disorder / Linkage Analysis / The American
Lactase Persistence in Central Asia: Phenotype, Genotype, and Evolution
Genetics / Polymorphism / Molecular Evolution / Life Style / Low Frequency / Natural Selection / Human / Human Biology / Humans / Blood Glucose / Lactose intolerance / Pastoralism / Phenotype / Ethnic Groups / Questionnaires / Genotype / Ethnic Group / Genetic variation / Statistics as Topic / Natural Selection / Human / Human Biology / Humans / Blood Glucose / Lactose intolerance / Pastoralism / Phenotype / Ethnic Groups / Questionnaires / Genotype / Ethnic Group / Genetic variation / Statistics as Topic
Genetic influences on bipolar EEG power spectra
Genetics / Algorithms / Psychophysiology / Electrophysiology / Electroencephalography / Adolescent / Power / Humans / Child / Alcoholism / Female / Male / Siblings / Heritability / Genetic determinism / Genotype / Adult / Adolescent / Power / Humans / Child / Alcoholism / Female / Male / Siblings / Heritability / Genetic determinism / Genotype / Adult
Frecuencias alélicas, genotípicas y haplotípicas HLA-A, HLA-B, HLA-DRB1 en donantes fallecidos, Medellín, Colombia
Haplotypes / Genotype / Biomedica
Cholesteryl Ester Transfer Protein I405V Polymorphism Influences Apolipoprotein A-I Response to a Change in Dietary Fatty Acid Composition
Enzymology / Polymorphism / Adolescent / Humans / Fatty acids / Female / Male / Young Adult / apolipoprotein A-I / Clinical Sciences / Genotype / Case Control Studies / Dietary fats / Female / Male / Young Adult / apolipoprotein A-I / Clinical Sciences / Genotype / Case Control Studies / Dietary fats
Evidence for a link between local and seasonal cycles in gene frequencies and latitudinal gene clines in a cyclic parthenogen
Genetics / Polymorphism / Canada / Population structure / Seasonality / Parthenogenesis / Genetica / United States / Animals / Aphids / Ornamental plants / Climatic Factor / Clines / Genotype / Seasons / Large Scale / Genetic Variability / Seasonal change / Aphid / Parthenogenesis / Genetica / United States / Animals / Aphids / Ornamental plants / Climatic Factor / Clines / Genotype / Seasons / Large Scale / Genetic Variability / Seasonal change / Aphid
TaqIB polymorphism in cholesterol ester transfer protein (CETP) gene predicts future cardiovascular death in patients experiencing an acute coronary syndrome
Cognitive Science / Polymorphism / Survival Analysis / Clinical Chemistry / Gene Prediction / Prospective studies / Humans / Female / Male / Clinical Sciences / Aged / Middle Aged / Acute Coronary Syndrome / Genotype / Predictive value of tests / Cohort Studies / Prospective studies / Humans / Female / Male / Clinical Sciences / Aged / Middle Aged / Acute Coronary Syndrome / Genotype / Predictive value of tests / Cohort Studies
Bicaudal C1 promotes pancreatic NEUROG3+ endocrine progenitor differentiation and ductal morphogenesis
Stem Cells / Development / Western blotting / Biological Sciences / Mice / Animals / Fluorescent Antibody Technique / Genotype / RNA-binding proteins / Animals / Fluorescent Antibody Technique / Genotype / RNA-binding proteins
Comprehensive Mu-Opioid-Receptor Genotyping by Pyrosequencing
Biochemistry / Clinical Chemistry / Humans / Mutation / Medical Biotechnology / Clinical / Mu Opioid Receptor / Polymerase Chain Reaction / Clinical Sciences / Genotype / DNA mutational analysis / Clinical / Mu Opioid Receptor / Polymerase Chain Reaction / Clinical Sciences / Genotype / DNA mutational analysis
A complex bilateral polysyndactyly disease locus maps to chromosome 7q36
Biological Sciences / Humans / Female / Male / Pedigree / Genetic linkage analysis / Polydactyly / Genotype / Base Sequence / Genetic Markers / Syndactyly / Molecular Sequence Data / Genetic linkage analysis / Polydactyly / Genotype / Base Sequence / Genetic Markers / Syndactyly / Molecular Sequence Data
Common paraoxonase gene variants, mortality risk and fatal cardiovascular events in elderly subjects
Polymorphism / Atherosclerosis / Survival Analysis / Risk assessment / Cardiovascular disease / Prospective studies / Humans / Female / Male / Population based study / Statistical Significance / Confidence intervals / Netherlands / Enzyme / Clinical Sciences / Aged / Genotype / Adult / Cross Section / Survival Rate / Linkage Disequilibrium / Cardiovascular Diseases / Risk Assessment / Esterases / Coronary Artery Disease / Cross Sectional Studies / Proportional Hazards Models / Mortality Risk / Cohort Studies / Prospective studies / Humans / Female / Male / Population based study / Statistical Significance / Confidence intervals / Netherlands / Enzyme / Clinical Sciences / Aged / Genotype / Adult / Cross Section / Survival Rate / Linkage Disequilibrium / Cardiovascular Diseases / Risk Assessment / Esterases / Coronary Artery Disease / Cross Sectional Studies / Proportional Hazards Models / Mortality Risk / Cohort Studies
Congenital adrenal hyperplasia due to steroid 21-hydroxylase deficiency
Endocrinology / Nutrition / Molecular Biology / Treatment / Pregnancy / Humans / Mutation / Female / Hormones / Male / Genetic determinism / Etiology / Phenotype / Clinical Sciences / Newborn Infant / Genotype / Congenital Adrenal Hyperplasia / Deficiency / Prenatal Diagnosis / Clinical Endocrinology / Deficit / Humans / Mutation / Female / Hormones / Male / Genetic determinism / Etiology / Phenotype / Clinical Sciences / Newborn Infant / Genotype / Congenital Adrenal Hyperplasia / Deficiency / Prenatal Diagnosis / Clinical Endocrinology / Deficit
Predictive power of individual genetic and environmental factor scores
Genetics / Cognitive Science / Skeletal muscle biology / Prediction / Forecasting / Adolescent / Multivariate Analysis / Humans / Strength Training / Male / Confidence intervals / Weight Lifting / Phenotype / Clinical Sciences / Elbow Joint / Genotype / Adult / Analysis of Variance / Odds ratio / Muscle contraction / Physiological Stress Markers / Sensitivity and Specificity / Environment / Genetic Markers / Twin / Isometric Contraction / Adolescent / Multivariate Analysis / Humans / Strength Training / Male / Confidence intervals / Weight Lifting / Phenotype / Clinical Sciences / Elbow Joint / Genotype / Adult / Analysis of Variance / Odds ratio / Muscle contraction / Physiological Stress Markers / Sensitivity and Specificity / Environment / Genetic Markers / Twin / Isometric Contraction
Foetal macrosomia and erythrocyte acid phosphatase (ACP1) polymorphism in diabetic and normal pregnancy
Cognitive Science / Polymorphism / Pregnancy / Humans / Female / Phenotype / Clinical Sciences / Newborn Infant / Early human dispersal / Genotype / Adult / Type 2 Diabetes Mellitus / Erythrocytes / Phenotype / Clinical Sciences / Newborn Infant / Early human dispersal / Genotype / Adult / Type 2 Diabetes Mellitus / Erythrocytes
Análisis del polimorfismo rs20541 (R130Q) del gen de la IL-13 en pacientes con enfermedades inflamatorias crónicas asociadas al envejecimiento
Rheumatoid Arthritis / Humans / Female / Male / Aged / Middle Aged / Genotype / Age Factors / Biological markers / Polymyalgia Rheumatica / Giant Cell Arteritis / Genetic Markers / Case Control Studies / Interleukin / Middle Aged / Genotype / Age Factors / Biological markers / Polymyalgia Rheumatica / Giant Cell Arteritis / Genetic Markers / Case Control Studies / Interleukin
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