Phenotype - Page 4

Lectura interpretada del antibiograma de bacilos gramnegativos no fermentadores

Medical Microbiology / Resistance / Microbial genetic and drug resistance / Phenotype / Pseudomonas aeruginosa / Anti-Bacterial Agents / Microbial Sensitivity Tests / Efflux Pumps / Pseudomonas Aeruginosa / Acinetobacter baumannii / S / P / A / Stenotrophomonas maltophilia / Anti-Bacterial Agents / Microbial Sensitivity Tests / Efflux Pumps / Pseudomonas Aeruginosa / Acinetobacter baumannii / S / P / A / Stenotrophomonas maltophilia

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Multivariate intralocus sexual conflict in seed beetles

Evolutionary Biology / Zoology / Metabolism / Molecular Evolution / Evolution / Sexual dimorphism / Female / Animals / Male / Sex chromosomes / Phenotype / Beetles / Pleiotropy / Sexual dimorphism / Female / Animals / Male / Sex chromosomes / Phenotype / Beetles / Pleiotropy

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Association between Archaeal Prolyl- and Leucyl-tRNA Synthetases Enhances tRNAPro Aminoacylation

Chromatography / Kinetics / Biological Chemistry / Biological Sciences / Escherichia coli / Biological / Temperature / Sodium Dodecyl Sulfate-Polyacrylamide Gel Electrophoresis / Phenotype / CHEMICAL SCIENCES / Protein Binding / Histidine / Protein Biosynthesis / Biological / Temperature / Sodium Dodecyl Sulfate-Polyacrylamide Gel Electrophoresis / Phenotype / CHEMICAL SCIENCES / Protein Binding / Histidine / Protein Biosynthesis

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A Pseudo-tRNA Modulates Antibiotic Resistance in Bacillus cereus

Biofilms / Oxidative Stress / Multidisciplinary / Nitric oxide / Microbial genetic and drug resistance / Iron / Phenotype / PLoS one / Bacillus Cereus / Iron / Phenotype / PLoS one / Bacillus Cereus

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Differential gene expression in umbilical cord blood and maternal peripheral blood

Pregnancy / Humans / Female / Cluster Analysis / Mothers / Phenotype / Umbilical Cord Blood / Newborn Infant / European / Immune system / Umbilical Cord / Pregnancy Outcome / Differential Gene Expression / Gene Expression Regulation / Gene expression profiling / Phenotype / Umbilical Cord Blood / Newborn Infant / European / Immune system / Umbilical Cord / Pregnancy Outcome / Differential Gene Expression / Gene Expression Regulation / Gene expression profiling

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Sensibilidad en el Reconocimiento de Emociones Faciales Como Endofenotipo de Esquizofrenia/ Sensitivity in the Recognition of Facial Emotions as an Endophenotype for Schizophrenia/ Sensibilidade no Reconhecimento de Emoções Faciais Como Endofenótipo de Esquizofrenia

Genetics / Schizophrenia / Facial expressions / Genetica / Facial Expressions and Emotions / Phenotype / Cognitive impairment / Reconocimiento de expresiones faciales / Esquizofrenia / Fenotipo / Deterioro Cognitivo / Phenotype / Cognitive impairment / Reconocimiento de expresiones faciales / Esquizofrenia / Fenotipo / Deterioro Cognitivo

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Parkin disease: a phenotypic study of a large case series

Brain / Humans / Mutation / Female / Male / Polymerase Chain Reaction / Mental Disorders / Pedigree / Levodopa / Dystonia / Phenotype / Aged / Middle Aged / Adult / Age of Onset / Polymerase Chain Reaction / Mental Disorders / Pedigree / Levodopa / Dystonia / Phenotype / Aged / Middle Aged / Adult / Age of Onset

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Genetic data on Alghero population (Sardinia): Contrast between biological and cultural evidence

Evolutionary Biology / Genetics / Archaeology / Anthropology / Population Genetics / Language / Spain / American Journal of Physical Anthropology / Italy / Humans / Female / Male / American / Phenotype / Genetic variation / Likelihood Functions / Genetic Markers / Language / Spain / American Journal of Physical Anthropology / Italy / Humans / Female / Male / American / Phenotype / Genetic variation / Likelihood Functions / Genetic Markers

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β-catenin is central to DUX4-driven network rewiring in facioscapulohumeral muscular dystrophy

Algorithms / Multidisciplinary / Biopsy / Signal Transduction / Humans / Reactive Oxygen Species / Mice / Animals / Muscles / Beta-Catenin / Phenotype / Gene Expression Regulation / Gene expression profiling / Myoblasts / Reactive Oxygen Species / Mice / Animals / Muscles / Beta-Catenin / Phenotype / Gene Expression Regulation / Gene expression profiling / Myoblasts

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Common variable immunodeficiency disorders: division into distinct clinical phenotypes

Autoimmunity / Humans / Blood / Registries / Phenotype / Clinical Sciences / Prognosis / Survival Time / Immunoglobulin / Age of Onset / Cohort Studies / Age at Onset / Clinical Sciences / Prognosis / Survival Time / Immunoglobulin / Age of Onset / Cohort Studies / Age at Onset

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Acute myeloblastic leukemia with minimal myeloid differentiation: phenotypical and ultrastructural characteristics

Leukemia / Peroxidase / Acute Myeloid Leukemia / Cell Differentiation / Humans / Case Study / Female / Male / Karyotyping / Phenotype / Clinical Sciences / Aged / Middle Aged / Adult / Immunophenotyping / Monoclonal Antibody / Myeloperoxidase / Case Study / Female / Male / Karyotyping / Phenotype / Clinical Sciences / Aged / Middle Aged / Adult / Immunophenotyping / Monoclonal Antibody / Myeloperoxidase

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Congenital adrenal hyperplasia due to steroid 21-hydroxylase deficiency

Algorithms / Molecular Biology / Evidence Based Practice / Treatment / Comorbidity / Pregnancy / Humans / Mutation / Female / Clinical / Hormones / Male / Genetic determinism / Etiology / Phenotype / Clinical Sciences / Newborn Infant / Genotype / Deficiency / Prenatal Diagnosis / Clinical Endocrinology / Deficit / Pregnancy / Humans / Mutation / Female / Clinical / Hormones / Male / Genetic determinism / Etiology / Phenotype / Clinical Sciences / Newborn Infant / Genotype / Deficiency / Prenatal Diagnosis / Clinical Endocrinology / Deficit

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Clinical features of facioscapulohumeral muscular dystrophy 2

Cognitive Science / Neurology / Adolescent / Humans / Child / Muscular Dystrophy / Female / Male / Gender Difference / DNA methylation / Young Adult / Infant / Disease Severity / Phenotype / Chromatin structure / Clinical Sciences / Newborn Infant / Middle Aged / Family Health / Genotype / Adult / Clinical Assessment / Cross sectional Study / Clinical Presentation / Cross Sectional Studies / Neurosciences / Clinical evaluation / Cohort Studies / Muscular Dystrophy / Female / Male / Gender Difference / DNA methylation / Young Adult / Infant / Disease Severity / Phenotype / Chromatin structure / Clinical Sciences / Newborn Infant / Middle Aged / Family Health / Genotype / Adult / Clinical Assessment / Cross sectional Study / Clinical Presentation / Cross Sectional Studies / Neurosciences / Clinical evaluation / Cohort Studies

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Comparison of clinical characteristics of familial and sporadic acquired accommodative esotropia

Adolescent / Family history / Visual acuity / India / Humans / OCD treatment / Female / Male / Obsessive Compulsive Disorder / Statistical Significance / Young Adult / American / Pedigree / Phenotype / Clinical Sciences / Middle Aged / Adult / Control Group / OCD treatment / Female / Male / Obsessive Compulsive Disorder / Statistical Significance / Young Adult / American / Pedigree / Phenotype / Clinical Sciences / Middle Aged / Adult / Control Group

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Disease expression and molecular genotype in congenital adrenal hyperplasia due to 21-hydroxylase deficiency

Humans / Mutation / Clinical / Pedigree / Phenotype / Congenital Adrenal Hyperplasia / Base Sequence / Clinical Investigation / Congenital Adrenal Hyperplasia / Base Sequence / Clinical Investigation

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Congenital Adrenal Hyperplasia due to 21Hydroxylase Deficiency

Physiology / Nursing / Kinetics / Quality of life / Pediatric nursing / Adolescent / Multidisciplinary / Screening / Cortisol / Pregnancy / Humans / Child / Mutation / Puberty / Female / Male / Disorders of sex development / Mutation Detection / Gene Conversion / Phenotype / Enzyme / Clinical Sciences / Newborn Infant / Optometry and Ophthalmology / Genotype / Adult / Congenital Adrenal Hyperplasia / Public health systems and services research / Prenatal Diagnosis / Amino Acid Sequence / Base Sequence / Structure activity Relationship / Enzymatic Activity / Glucocorticoids / Biochemistry and cell biology / Adolescent / Multidisciplinary / Screening / Cortisol / Pregnancy / Humans / Child / Mutation / Puberty / Female / Male / Disorders of sex development / Mutation Detection / Gene Conversion / Phenotype / Enzyme / Clinical Sciences / Newborn Infant / Optometry and Ophthalmology / Genotype / Adult / Congenital Adrenal Hyperplasia / Public health systems and services research / Prenatal Diagnosis / Amino Acid Sequence / Base Sequence / Structure activity Relationship / Enzymatic Activity / Glucocorticoids / Biochemistry and cell biology

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