Genotype

Congenital adrenal hyperplasia clinical characteristics and genotype in newborn, childhood and adolescence

Molecular Genetics / Adolescent / Genetic counseling / Humans / Child / Mutation / Medicina / Female / Male / Infant / Follow-up studies / Gene Conversion / Phenotype / Newborn Infant / Genotype / Congenital Adrenal Hyperplasia / Enzymatic Activity / Mutation / Medicina / Female / Male / Infant / Follow-up studies / Gene Conversion / Phenotype / Newborn Infant / Genotype / Congenital Adrenal Hyperplasia / Enzymatic Activity

Advantages of Using Mitochondrial 16S rDNA Sequences to Classify Clinical Isolates of Acanthamoeba

Mitochondria / Biological Sciences / Phylogeny / Animals / Genotype / Acanthamoeba / Acanthamoeba keratitis / Acanthamoeba / Acanthamoeba keratitis

Serotonin transporter, tryptophan hydroxylase, and monoamine oxidase A gene polymorphisms in premenstrual dysphoric disorder

Obstetrics / Polymorphism / Premenstrual Syndrome / Humans / Female / Serotonin Transporter / American / Mental Disorders / Middle Aged / Gene Polymorphism / Gynecology / Genotype / Adult / Tryptophan hydroxylase / Genetic Variability / Monoamine oxidase / Cohort Studies / Serotonin Transporter / American / Mental Disorders / Middle Aged / Gene Polymorphism / Gynecology / Genotype / Adult / Tryptophan hydroxylase / Genetic Variability / Monoamine oxidase / Cohort Studies

Serotonin transporter, tryptophan hydroxylase, and monoamine oxidase A gene polymorphisms in premenstrual dysphoric disorder

Obstetrics / Polymorphism / Premenstrual Syndrome / Humans / Female / Serotonin Transporter / American / Mental Disorders / Middle Aged / Gene Polymorphism / Gynecology / Genotype / Adult / Tryptophan hydroxylase / Genetic Variability / Monoamine oxidase / Cohort Studies / Serotonin Transporter / American / Mental Disorders / Middle Aged / Gene Polymorphism / Gynecology / Genotype / Adult / Tryptophan hydroxylase / Genetic Variability / Monoamine oxidase / Cohort Studies

A synthetic HIV-1 subtype C backbone generates comparable PR and RT resistance profiles to a subtype B backbone in a recombinant virus assay

Multidisciplinary / HIV / Mutation / PLoS one / Genotype

NR2E3 mutations in enhanced S-cone sensitivity syndrome (ESCS), Goldmann-Favre syndrome (GFS), clumped pigmentary retinal degeneration (CPRD), and retinitis pigmentosa (RP)

Genetics / Transcription / Humans / Mutation / Mice / Retinitis pigmentosa / Animals / Expression / Differential Diagnosis / Transcription Factor / Clinical Sciences / Genotype / Orphan Nuclear Receptors / Syndrome / Nuclear hormone receptor / Retinitis pigmentosa / Animals / Expression / Differential Diagnosis / Transcription Factor / Clinical Sciences / Genotype / Orphan Nuclear Receptors / Syndrome / Nuclear hormone receptor

Serotonin transporter-linked polymorphic region (5-HTTLPR) genotype and stressful life events interact to predict preschool-onset depression: a replication and developmental extension

Psychology / Cognitive Science / Depression / Child Development / Humans / Female / Male / Clinical Sciences / Longitudinal Studies / Genotype / Life Change Events / Female / Male / Clinical Sciences / Longitudinal Studies / Genotype / Life Change Events

Developmental consequences of in utero sodium arsenate exposure in mice with folate transport deficiencies

Reproduction / Arsenic / Folic acid / Transgenic Mice / Mice / Female / Animals / Male / Genetic modification / Detoxification / Membrane transport proteins / Genetically Modified / Genotype / Chimera / Reproductive Toxicity / Arsenates / Female / Animals / Male / Genetic modification / Detoxification / Membrane transport proteins / Genetically Modified / Genotype / Chimera / Reproductive Toxicity / Arsenates

Ubiquitin Carboxyl-Terminal Esterase L1 (UCHL1) S18Y Polymorphism In Patients With Cataracts

Ubiquitin / Humans / Female / Nucleic acid hybridization / Male / Polymerase Chain Reaction / Cataract / Aged / Middle Aged / Optometry and Ophthalmology / Genotype / OPHTHALMIC GENETICS / Polymerase Chain Reaction / Cataract / Aged / Middle Aged / Optometry and Ophthalmology / Genotype / OPHTHALMIC GENETICS

Calcium intake and ion transporter genetic polymorphisms interact in human colorectal neoplasia risk in a 2-phase study

Nutrition and Dietetics / Nutrition / Calcium / Animal Production / Humans / Risk factors / Aged / Middle Aged / Genotype / Adult / Odds ratio / Food Sciences / Risk Factors / Adenoma / Case Control Studies / Risk factors / Aged / Middle Aged / Genotype / Adult / Odds ratio / Food Sciences / Risk Factors / Adenoma / Case Control Studies

A 3-factor epistatic model predicts digital ulcers in Italian scleroderma patients

Cytokines / Italy / Humans / Systemic sclerosis / Female / Male / Clinical Sciences / Petri Net / European / Middle Aged / Genotype / Adult / Fingers / Male / Clinical Sciences / Petri Net / European / Middle Aged / Genotype / Adult / Fingers

Molecular evolution and phylogenetics of rodent malaria parasites

Evolutionary Biology / Genetics / Molecular Evolution / Malaria / Plasmodium / Rodentia / Phylogeny / Animals / Host-parasite interactions / Genotype / Time Factors / Genetic variation / Protozoan Proteins / Bayes Theorem / Plasmodium yoelii / Plasmodium berghei / Rodentia / Phylogeny / Animals / Host-parasite interactions / Genotype / Time Factors / Genetic variation / Protozoan Proteins / Bayes Theorem / Plasmodium yoelii / Plasmodium berghei

SOLiD sequencing of four Vibrio vulnificus genomes enables comparative genomic analysis and identification of candidate clade-specific virulence genes

Genomics / Comparative Genomics / Next generation sequencing / Biological Sciences / Virulence / Phylogeny / Mice / United States / Animals / Vibrio vulnificus / Animal Model / Comparative Analysis / Plasmids / Phenotype / Genome Comparison / Genomic DNA / Genotype / Single Nucleotide Polymorphism / Virulence factor / Genome sequence / Sialic Acid / Base Sequence / Phylogeny / Mice / United States / Animals / Vibrio vulnificus / Animal Model / Comparative Analysis / Plasmids / Phenotype / Genome Comparison / Genomic DNA / Genotype / Single Nucleotide Polymorphism / Virulence factor / Genome sequence / Sialic Acid / Base Sequence

DCUN1D1 is a risk factor for frontotemporal lobar degeneration

Dementia / Polymorphism / Humans / Female / Male / Risk factors / Genes / Clinical Sciences / European / Aged / Middle Aged / Risk Factor / Genotype / Single Nucleotide Polymorphism / Risk Factors / Genotypes / Neurosciences / Logistic Models / Risk factors / Genes / Clinical Sciences / European / Aged / Middle Aged / Risk Factor / Genotype / Single Nucleotide Polymorphism / Risk Factors / Genotypes / Neurosciences / Logistic Models

Chronic nonhemolytic unconjugated hyperbilirubinemia with glucuronyl transferase deficiency

Genetics / Adolescent / Humans / Liver / Female / Inborn errors of metabolism / Male / Jaundice / Bilirubin / Pedigree / Phenotype / Genotype / Adult / Phenobarbital / The American / Bile / Inborn errors of metabolism / Male / Jaundice / Bilirubin / Pedigree / Phenotype / Genotype / Adult / Phenobarbital / The American / Bile

Novel 3-N-Aminoglycoside Acetyltransferase Gene, aac(3)-Ic, from a Pseudomonas aeruginosa Integron

Microbiology / Medical Microbiology / In Vitro / Humans / Escherichia coli / Resistance / Bacteria / Gene / Pseudomonas aeruginosa / Molecular cloning / Integrons / Gen / Genotype / Pseudomonas Aeruginosa / Biological activity / Amino Acid Sequence / Beta Lactamases / Resistance / Bacteria / Gene / Pseudomonas aeruginosa / Molecular cloning / Integrons / Gen / Genotype / Pseudomonas Aeruginosa / Biological activity / Amino Acid Sequence / Beta Lactamases

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