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Haplotypes
Haplotypes
Co-amplification of mitochondrial pseudogenes in Calomys musculinus (Rodentia, Cricetidae): a source of error in phylogeographic studies
Genetics / Geography / Agricultural Biotechnology / Phylogeny / Sequence alignment / Haplotypes / Animals / Polymerase Chain Reaction / Genome / Arvicolinae / Amino Acid Sequence / Pseudogenes / Haplotypes / Animals / Polymerase Chain Reaction / Genome / Arvicolinae / Amino Acid Sequence / Pseudogenes
Genetic diversity and connectivity remain high in Holothuria polii (Delle Chiaje 1823) across a coastal lagoon-open sea environmental gradient
Genetics / Gene Flow / Population Genetics / Genetic Diversity / Mitochondrial DNA / Genetica / Haplotypes / Genetic Structure / Animals / Coastal lagoon / Selection / Population Growth / Generalized Additive Model / Environmental Gradient / Genetic Differentiation / Ecosystem / Environmental Conditions / Genetic Divergence / Population Genetic Structure / Genetic variation / Genetic Markers / Mutation Rate / Oceans and Seas / Cytochrome Oxidase I / Genetica / Haplotypes / Genetic Structure / Animals / Coastal lagoon / Selection / Population Growth / Generalized Additive Model / Environmental Gradient / Genetic Differentiation / Ecosystem / Environmental Conditions / Genetic Divergence / Population Genetic Structure / Genetic variation / Genetic Markers / Mutation Rate / Oceans and Seas / Cytochrome Oxidase I
Morphometric and molecular evidence of intraspecific biogeographical differentiation of Rhodnius pallescens (HEMIPTERA: REDUVIIDAE: RHODNIINI) from Colombia and Panama
Genetics / Colombia / Molecular Evolution / Panama / Phylogeny / Haplotypes / Animals / Male / Analysis of Variance / Genetic variation / Insect Vectors / Wing / Haplotypes / Animals / Male / Analysis of Variance / Genetic variation / Insect Vectors / Wing
Recomendaciones de buenas prácticas para el diagnóstico genético de la distrofia miotónica
Benchmarking / Software Design / Pregnancy / Humans / Genetic Testing / Mutation / Haplotypes / Female / Male / Polymerase Chain Reaction / Myotonic Dystrophy / Duchenne Muscular Dystrophy / Preimplantation genetic diagnosis / RNA-binding proteins / Prenatal Diagnosis / Molecular Diagnostic Techniques / Dystrophin / Medicina Clinica / Early Diagnosis / Genetic Markers / Mutation / Haplotypes / Female / Male / Polymerase Chain Reaction / Myotonic Dystrophy / Duchenne Muscular Dystrophy / Preimplantation genetic diagnosis / RNA-binding proteins / Prenatal Diagnosis / Molecular Diagnostic Techniques / Dystrophin / Medicina Clinica / Early Diagnosis / Genetic Markers
Recomendaciones de buenas prácticas para el diagnóstico genético de la distrofia miotónica
Benchmarking / Software Design / Pregnancy / Humans / Genetic Testing / Mutation / Haplotypes / Female / Male / Polymerase Chain Reaction / Myotonic Dystrophy / Duchenne Muscular Dystrophy / Preimplantation genetic diagnosis / RNA-binding proteins / Prenatal Diagnosis / Molecular Diagnostic Techniques / Dystrophin / Medicina Clinica / Early Diagnosis / Genetic Markers / Mutation / Haplotypes / Female / Male / Polymerase Chain Reaction / Myotonic Dystrophy / Duchenne Muscular Dystrophy / Preimplantation genetic diagnosis / RNA-binding proteins / Prenatal Diagnosis / Molecular Diagnostic Techniques / Dystrophin / Medicina Clinica / Early Diagnosis / Genetic Markers
X‐linked vacuolar myopathies: Two separate loci and refined genetic mapping
Adolescent / Humans / Haplotypes / Female / Male / Genetic Map / Pedigree / Genetic linkage analysis / Clinical Sciences / Adult / X chromosome / Neurosciences / Vacuoles / Genetic Map / Pedigree / Genetic linkage analysis / Clinical Sciences / Adult / X chromosome / Neurosciences / Vacuoles
Simplifying genetic locus assignment of HLA-DRB genes
Immunology / Gene expression / Humans / Haplotypes
Mitochondrial DNA recombination in a free-ranging Australian lizard
Geography / Australia / Biological Sciences / Phylogeny / Mitochondrial DNA / Haplotypes / Lizards / Animals / Genetic Recombination / Base Sequence / Haplotypes / Lizards / Animals / Genetic Recombination / Base Sequence
Progranulin genetic variability contributes to amyotrophic lateral sclerosis
Cognitive Science / Neurology / Dementia / Belgium / Amyotrophic Lateral Sclerosis / Humans / Genetic Testing / Mutation / Haplotypes / Female / Male / Netherlands / Clinical Sciences / Aged / Middle Aged / Genotype / Adult / Survival Rate / Genetic variation / Genetic Variability / Genetic Markers / Neurosciences / Age of Onset / Humans / Genetic Testing / Mutation / Haplotypes / Female / Male / Netherlands / Clinical Sciences / Aged / Middle Aged / Genotype / Adult / Survival Rate / Genetic variation / Genetic Variability / Genetic Markers / Neurosciences / Age of Onset
Intraspecific Patterns of Mitochondrial Variation in Natural Population Fragments of a Localized Desert Dung Beetle Species, Pachysoma gariepinum (Coleoptera: Scarabaeidae)
Genetics / Southern Africa / Mitochondria / Heredity / TIME / Phylogeny / Mitochondrial DNA / Haplotypes / Animals / Biological evolution / Beetles / Genetic variation / Time / Conservation of Natural Resources / Phylogeny / Mitochondrial DNA / Haplotypes / Animals / Biological evolution / Beetles / Genetic variation / Time / Conservation of Natural Resources
Frontotemporal dementia–amyotrophic lateral sclerosis syndrome locus on chromosome 16p12.1–q12.2: genetic, clinical and neuropathological analysis
Cognitive Science / Magnetic Resonance Imaging / Positron Emission Tomography / Amyotrophic Lateral Sclerosis / Brain / Humans / Haplotypes / Female / Male / Iron / Differential Diagnosis / Electromyography / Phosphorylation / Pedigree / Genetic linkage analysis / Clinical Sciences / Aged / Middle Aged / Frontotemporal Dementia / DNA binding proteins / Neurosciences / Humans / Haplotypes / Female / Male / Iron / Differential Diagnosis / Electromyography / Phosphorylation / Pedigree / Genetic linkage analysis / Clinical Sciences / Aged / Middle Aged / Frontotemporal Dementia / DNA binding proteins / Neurosciences
N-Acetyltransferase Polymorphism Among Northern Sudanese
Genetics / Geography / Polymorphism / Drug metabolism / Adolescent / Low Frequency / Sudan / Human Biology / Humans / Child / Haplotypes / Female / Male / Polymerase Chain Reaction / Phenotype / Enzyme / Arylamine N-acetyltransferase / Middle Aged / Genotype / Adult / Single Nucleotide Polymorphism / Adverse Drug Reaction / Molecular Computers / Drug Toxicity / Computational Method / Allele Frequency / Low Frequency / Sudan / Human Biology / Humans / Child / Haplotypes / Female / Male / Polymerase Chain Reaction / Phenotype / Enzyme / Arylamine N-acetyltransferase / Middle Aged / Genotype / Adult / Single Nucleotide Polymorphism / Adverse Drug Reaction / Molecular Computers / Drug Toxicity / Computational Method / Allele Frequency
Phenylalanine hydroxylase deficiency: Molecular epidemiology and predictable BH4-responsiveness in South Portugal PKU patients
Polymorphism / Molecular Genetics / Molecular Epidemiology / Portugal / Humans / Haplotypes / Phenylketonuria / Genetic Association Studies / Phenotype / Clinical Sciences / Spectrum / Genomic DNA / Molecular Characterization / Phenylalanine hydroxylase / Haplotypes / Phenylketonuria / Genetic Association Studies / Phenotype / Clinical Sciences / Spectrum / Genomic DNA / Molecular Characterization / Phenylalanine hydroxylase
Phenylalanine hydroxylase deficiency: Molecular epidemiology and predictable BH4-responsiveness in South Portugal PKU patients
Polymorphism / Molecular Genetics / Molecular Epidemiology / Portugal / Humans / Haplotypes / Phenylketonuria / Genetic Association Studies / Phenotype / Clinical Sciences / Spectrum / Genomic DNA / Molecular Characterization / Phenylalanine hydroxylase / Haplotypes / Phenylketonuria / Genetic Association Studies / Phenotype / Clinical Sciences / Spectrum / Genomic DNA / Molecular Characterization / Phenylalanine hydroxylase
LADA and T1D in Estonian population — Two different genetic risk profiles
Genetics / Population Genetics / Molecular Evolution / Risk / Transcription Factors / Humans / Insulin / Estonia / Haplotypes / Female / Male / Young Adult / Gene / Phenotype / Middle Aged / Snp / Adult / VNTR / European Continental Ancestry Group / Type 2 Diabetes Mellitus / Age of Onset / Humans / Insulin / Estonia / Haplotypes / Female / Male / Young Adult / Gene / Phenotype / Middle Aged / Snp / Adult / VNTR / European Continental Ancestry Group / Type 2 Diabetes Mellitus / Age of Onset
Competition Between Mitochondrial Haplotypes in Distinct Nuclear Genetic Environments: Drosophilu pseudoobscura vs. D. persirnilis
Genetics / Fertility / Drosophila / Mitochondrial DNA / Haplotypes / Female / Animals / Male / Mitochondrial Genome / Cell nucleus / Analysis of Variance / Sibling Species / Species Specificity / Female Fertility / General Population / Female / Animals / Male / Mitochondrial Genome / Cell nucleus / Analysis of Variance / Sibling Species / Species Specificity / Female Fertility / General Population
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