Phenotype

Human Haemato-Endothelial Precursors: Cord Blood CD34+ Cells Produce Haemogenic Endothelium

Cell Adhesion / Multidisciplinary / Hematopoiesis / Cell Differentiation / Humans / Mice / Animals / Phenotype / PLoS one / Newborn Infant / Hepatocytes / Cell Shape / Immunophenotyping / Mice / Animals / Phenotype / PLoS one / Newborn Infant / Hepatocytes / Cell Shape / Immunophenotyping

Adenine Phosphoribosyltransferase Deficiency

Kidney diseases / Enzyme Inhibitors / Adolescent / Humans / Child / Female / Animals / Inborn errors of metabolism / Male / Young Adult / Infant / Pediatric Nephrology / Pediatric / Phenotype / Recurrence / Clinical Sciences / Urolithiasis / Retrospective Studies / Prognosis / Biological markers / Disease Progression / Adenine / Allopurinol / Predictive value of tests / Female / Animals / Inborn errors of metabolism / Male / Young Adult / Infant / Pediatric Nephrology / Pediatric / Phenotype / Recurrence / Clinical Sciences / Urolithiasis / Retrospective Studies / Prognosis / Biological markers / Disease Progression / Adenine / Allopurinol / Predictive value of tests

Adenine phosphoribosyltransferase deficiency in children

Kidney diseases / Enzyme Inhibitors / Adolescent / Humans / Child / Female / Animals / Inborn errors of metabolism / Male / Young Adult / Infant / Pediatric Nephrology / Pediatric / Phenotype / Recurrence / Clinical Sciences / Urolithiasis / Retrospective Studies / Prognosis / Biological markers / Disease Progression / Adenine / Allopurinol / Predictive value of tests / Female / Animals / Inborn errors of metabolism / Male / Young Adult / Infant / Pediatric Nephrology / Pediatric / Phenotype / Recurrence / Clinical Sciences / Urolithiasis / Retrospective Studies / Prognosis / Biological markers / Disease Progression / Adenine / Allopurinol / Predictive value of tests

TOXIC HYDROGEN SULFIDE AND DARK CAVES: PHENOTYPIC AND GENETIC DIVERGENCE ACROSS TWO ABIOTIC ENVIRONMENTAL GRADIENTS IN POECILIA MEXICANA

Evolutionary Biology / Geography / Gene Flow / Population Genetics / Evolution / Quantitative Genetics / Molecular Genetics / Developmental Plasticity / Ecological Speciation / Female / Animals / Male / Spatial Scale / Biological evolution / Phenotype / Environmental Gradient / Divergent Selection / Poecilia / Genetic Differentiation / Reproductive Isolation / Local adaptation / Environmental Conditions / Gills / Hydrogen Sulfide / Genetic Divergence / Cytochrome B Gene / Phenotypic variation / Environment / Genetic Markers / Environmental Exposure / Extremophile / Quantitative Genetics / Molecular Genetics / Developmental Plasticity / Ecological Speciation / Female / Animals / Male / Spatial Scale / Biological evolution / Phenotype / Environmental Gradient / Divergent Selection / Poecilia / Genetic Differentiation / Reproductive Isolation / Local adaptation / Environmental Conditions / Gills / Hydrogen Sulfide / Genetic Divergence / Cytochrome B Gene / Phenotypic variation / Environment / Genetic Markers / Environmental Exposure / Extremophile

Interleukin-10 polymorphisms in Spanish IgA deficiency patients: a case-control and family study

Genetics / Polymorphism / Spain / Humans / Primary Immunodeficiency / Female / Male / Phenotype / Clinical Sciences / Single Nucleotide Polymorphism / European Continental Ancestry Group / Family Study / Immunoglobulin / Inheritance Patterns / Case Control Studies / Interleukin / Female / Male / Phenotype / Clinical Sciences / Single Nucleotide Polymorphism / European Continental Ancestry Group / Family Study / Immunoglobulin / Inheritance Patterns / Case Control Studies / Interleukin

Facioscapulohumeral muscular dystrophy (FSHD): an enigma unravelled?

Genetics / Cognitive Science / Neurology / Human Genetics / Complementary and Alternative Medicine / Skeletal muscle biology / Immunohistochemistry / Oxidative Stress / Stem Cell / Gene expression / Extracellular Matrix / Cell Culture / Biopsy / Western blotting / Cell line / Humans / Muscle / Mice / Muscular Dystrophy / Female / Muscular Dystrophies / Animals / Male / Muscles / Disease Control / Medical Physiology / Differentiation / Phenotype / Clinical Sciences / Middle Aged / Cell nucleus / Skeletal Muscle / Adult / Neuromuscular Disorders / HeLa cells / In Vitro Studies / Cell Cycle Arrest / Global Gene Expression / Expression analysis / Neuromuscular / Myofibrils / Neurosciences / Biochemistry and cell biology / Gene expression profiling / Extracellular Matrix Proteins / Case Control Studies / Myoblasts / Skeletal muscle biology / Immunohistochemistry / Oxidative Stress / Stem Cell / Gene expression / Extracellular Matrix / Cell Culture / Biopsy / Western blotting / Cell line / Humans / Muscle / Mice / Muscular Dystrophy / Female / Muscular Dystrophies / Animals / Male / Muscles / Disease Control / Medical Physiology / Differentiation / Phenotype / Clinical Sciences / Middle Aged / Cell nucleus / Skeletal Muscle / Adult / Neuromuscular Disorders / HeLa cells / In Vitro Studies / Cell Cycle Arrest / Global Gene Expression / Expression analysis / Neuromuscular / Myofibrils / Neurosciences / Biochemistry and cell biology / Gene expression profiling / Extracellular Matrix Proteins / Case Control Studies / Myoblasts

Linking Antley–Bixler syndrome and congenital adrenal hyperplasia: A novel case of P450 oxidoreductase deficiency

Genetics / STEROIDS / Pregnancy / Humans / Mutation / Female / Male / Infant / Phenotype / Clinical Sciences / Newborn Infant / Synostosis / Adult / Deficiency / Genitalia / Deficit / Syndrome / Female / Male / Infant / Phenotype / Clinical Sciences / Newborn Infant / Synostosis / Adult / Deficiency / Genitalia / Deficit / Syndrome

Pubertal Presentation in Seven Patients with Congenital Adrenal Hyperplasia due to P450 Oxidoreductase Deficiency

Endocrinology / Menstruation / Adolescent / STEROIDS / Biological Sciences / Humans / Puberty / Female / Clinical / Male / Androgens / Young Adult / Karyotyping / Phenotype / Clinical Sciences / Newborn Infant / Genitalia / Ovarian cysts / Ovary / Hormone Replacement Therapy / Biochemistry and cell biology / Cohort Studies / Humans / Puberty / Female / Clinical / Male / Androgens / Young Adult / Karyotyping / Phenotype / Clinical Sciences / Newborn Infant / Genitalia / Ovarian cysts / Ovary / Hormone Replacement Therapy / Biochemistry and cell biology / Cohort Studies

Identification of a Putative Mexican Strain of Serratia entomophila Pathogenic against Root-Damaging Larvae of Scarabaeidae (Coleoptera)

Bioengineering / Biochemistry / Bioinformatics / Genetics / Microbiology / Immunology / Molecular Biology / Animal Behavior / Genomics / Computational Biology / Biotechnology / Biology / Biological Control / Integrated Pest Management / Multidisciplinary / Mexico / Numerical Taxonomy / Applied / Animals / Applied Environmental Microbiology / Plant Roots / Feeding Behavior / Phenotype / Beetles / Larva / MEXICO / Serratia / Pathogenic Bacteria / Immunology / Molecular Biology / Animal Behavior / Genomics / Computational Biology / Biotechnology / Biology / Biological Control / Integrated Pest Management / Multidisciplinary / Mexico / Numerical Taxonomy / Applied / Animals / Applied Environmental Microbiology / Plant Roots / Feeding Behavior / Phenotype / Beetles / Larva / MEXICO / Serratia / Pathogenic Bacteria

Interactome: gateway into systems biology

Computational Biology / Systems Biology / Proteomics / System Biology / Biological Sciences / Humans / Animals / Human Molecular Genetics / Phenotype / Gene expression profiling / Humans / Animals / Human Molecular Genetics / Phenotype / Gene expression profiling

Proximal femoral focal deficiency (PFFD) and fibular a/hypoplasia (FA/H): A model of a developmental field defect

Genetics / Humans / Child / Fibula / Tibia / Femur / Female / Male / Infant / American / Phenotype / Clinical Sciences / Middle Aged / Medical / Femur / Female / Male / Infant / American / Phenotype / Clinical Sciences / Middle Aged / Medical

Low Carbamoyl Phosphate Pools May Drive Lactobacillus plantarum CO2Dependent Growth Phenotype

Technology / Carbon Dioxide / Biological Sciences / Lactic Acid Bacteria / Mutation / Phenotype / Functional Group / Lactobacillus Plantarum / Arginine / Amino Acid Sequence / Inorganic Carbon System / Nucleotides / Phenotype / Functional Group / Lactobacillus Plantarum / Arginine / Amino Acid Sequence / Inorganic Carbon System / Nucleotides

C-kit+ cardiac progenitors exhibit mesenchymal markers and preferential cardiovascular commitment

Cardiovascular / Flow Cytometry / Immunohistochemistry / Cell separation / Cell Differentiation / Humans / Endothelial Cells / Phenotype / Myocardium / Adipocytes / Biological markers / Cell Proliferation / Osteoblasts / Human Fibroblasts / Mesenchymal Stromal Cells / Humans / Endothelial Cells / Phenotype / Myocardium / Adipocytes / Biological markers / Cell Proliferation / Osteoblasts / Human Fibroblasts / Mesenchymal Stromal Cells

Glutaredoxin deficiency exacerbates neurodegeneration in C. elegans models of Parkinson\'s disease

Caenorhabditis elegans / Molecular Evolution / Oxidative Stress / Alpha Synuclein / Biological Sciences / Humans / Animals / Human Molecular Genetics / Phenotype / Homeostasis / Cysteine / Cell Survival / Dopaminergic Neurons / Parkinson Disease / Gene Expression Regulation / Humans / Animals / Human Molecular Genetics / Phenotype / Homeostasis / Cysteine / Cell Survival / Dopaminergic Neurons / Parkinson Disease / Gene Expression Regulation

Comparison between familial and sporadic cutaneous melanoma in Valencia, Spain

Spain / Humans / Female / Melanoma / Male / Regression Analysis / Risk factors / Phenotype / Clinical Sciences / Middle Aged / Adult / Risk Factors / Skin Neoplasms / Regression Analysis / Risk factors / Phenotype / Clinical Sciences / Middle Aged / Adult / Risk Factors / Skin Neoplasms

Facioscapulohumeral muscular dystrophy (FSHD): an enigma unravelled?

Genetics / Cognitive Science / Neurology / Human Genetics / Complementary and Alternative Medicine / Skeletal muscle biology / Immunohistochemistry / Oxidative Stress / Stem Cell / Gene expression / Extracellular Matrix / Cell Culture / Biopsy / Western blotting / Cell line / Humans / Muscle / Mice / Muscular Dystrophy / Female / Muscular Dystrophies / Animals / Male / Muscles / Disease Control / Medical Physiology / Differentiation / Phenotype / Clinical Sciences / Middle Aged / Cell nucleus / Skeletal Muscle / Adult / Neuromuscular Disorders / HeLa cells / In Vitro Studies / Cell Cycle Arrest / Global Gene Expression / Expression analysis / Neuromuscular / Myofibrils / Neurosciences / Biochemistry and cell biology / Gene expression profiling / Extracellular Matrix Proteins / Case Control Studies / Myoblasts / Skeletal muscle biology / Immunohistochemistry / Oxidative Stress / Stem Cell / Gene expression / Extracellular Matrix / Cell Culture / Biopsy / Western blotting / Cell line / Humans / Muscle / Mice / Muscular Dystrophy / Female / Muscular Dystrophies / Animals / Male / Muscles / Disease Control / Medical Physiology / Differentiation / Phenotype / Clinical Sciences / Middle Aged / Cell nucleus / Skeletal Muscle / Adult / Neuromuscular Disorders / HeLa cells / In Vitro Studies / Cell Cycle Arrest / Global Gene Expression / Expression analysis / Neuromuscular / Myofibrils / Neurosciences / Biochemistry and cell biology / Gene expression profiling / Extracellular Matrix Proteins / Case Control Studies / Myoblasts
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