Phenotype

Epigenetic influences may explain dental differences in monozygotic twin pairs

Genetics / Dentistry / Adolescent / Humans / Child / Female / Male / Phenotype / Clinical Sciences / Middle Aged / Genotype / Odontogenesis / Adult / Public health systems and services research / Incisor / Australian / Anodontia / Female / Male / Phenotype / Clinical Sciences / Middle Aged / Genotype / Odontogenesis / Adult / Public health systems and services research / Incisor / Australian / Anodontia

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 / Reactive Oxygen Species / Mice / Animals / Muscles / Beta-Catenin / Phenotype / Gene Expression Regulation / Gene expression profiling

Tissue transglutaminase expression promotes castration-resistant phenotype and transcriptional repression of androgen receptor

Epithelial-Mesenchymal Transition / Humans / Male / NF-kappa B / Phenotype / Transfection / Gtp Binding Proteins / Transglutaminases / Transfection / Gtp Binding Proteins / Transglutaminases

Enterocyte-specific A20 deficiency sensitizes to tumor necrosis factor-induced toxicity and experimental colitis

Cell Biology / Apoptosis / Disease susceptibility / Biological Sciences / Humans / Intestinal Mucosa / Mice / Animals / Bacteria / The / Cytoprotection / Phenotype / Colitis / Tumor necrosis factor-alpha / Experimental Medicine / Cysteine endopeptidases / Tumor Necrosis Factor–α (TNF) / Enterocytes / Intestinal Mucosa / Mice / Animals / Bacteria / The / Cytoprotection / Phenotype / Colitis / Tumor necrosis factor-alpha / Experimental Medicine / Cysteine endopeptidases / Tumor Necrosis Factor–α (TNF) / Enterocytes

Case Report

Genetics / Case Report / Humans / Mutation / Male / Alkaline phosphatase / Phenotype / Clinical Sciences / alkaline phosphatase activity (APA) / Genotype / Adult / Alkaline phosphatase / Phenotype / Clinical Sciences / alkaline phosphatase activity (APA) / Genotype / Adult

A SIRT1-LSD1 Corepressor Complex Regulates Notch Target Gene Expression and Development

Drosophila melanogaster / Gene expression / Cell and Molecular Biology / Biological Sciences / Geriatric Nursing / Mutation / Animals / Phenotype / Immunoprecipitation / Histones / Sirtuin / Mutation / Animals / Phenotype / Immunoprecipitation / Histones / Sirtuin

The adenovirus E1B 55 kD protein influences mRNA transport via an intranuclear effect on RNA metabolism

Biological Sciences / Cell line / Mutation / Cell Fractionation / Temperature / Phenotype / Cell nucleus / Time Factors / Autoradiography / Cytoplasm / Phenotype / Cell nucleus / Time Factors / Autoradiography / Cytoplasm

Cyclophilin A peptidyl-prolyl isomerase activity promotes ZPR1 nuclear export

Biological Sciences / Saccharomyces cerevisiae / Molecular and cellular biology / Mutagenesis / C2H2 zinc fingers / Plasmids / Phenotype / Cell nucleus / Zinc Finger / Plasmids / Phenotype / Cell nucleus / Zinc Finger

Congenital CataractsFacial DysmorphismNeuropathy syndrome

Genetics / Magnetic Resonance Imaging / Bulgaria / Electroencephalography / Face / Adolescent / Electrocardiography / Developmental Coordination Disorder / Gene Mapping / Brain / Humans / Child / Female / Male / Infant / Gypsies / Cataract / Pedigree / Phenotype / Clinical Sciences / European / Adult / Linkage Disequilibrium / Nervous System / Annals / Syndrome / Neurosciences / Nervous System Diseases / Founder Effect / Adolescent / Electrocardiography / Developmental Coordination Disorder / Gene Mapping / Brain / Humans / Child / Female / Male / Infant / Gypsies / Cataract / Pedigree / Phenotype / Clinical Sciences / European / Adult / Linkage Disequilibrium / Nervous System / Annals / Syndrome / Neurosciences / Nervous System Diseases / Founder Effect

WNT4 deficiency--a clinical phenotype distinct from the classic Mayer-Rokitansky-Kuster-Hauser syndrome: A Case Report

Adolescent / Case Report / Humans / Child / Sequence alignment / Kidney / Female / Infant / Sex Determination / Phenotype / Human reproduction / Adult / Amino Acid Sequence / Ovary / Amino Acid Substitution Rates / Sexual Differentiation / Uterus / Syndrome / Kidney / Female / Infant / Sex Determination / Phenotype / Human reproduction / Adult / Amino Acid Sequence / Ovary / Amino Acid Substitution Rates / Sexual Differentiation / Uterus / Syndrome

Untreated congenital adrenal hyperplasia due to 21-hydroxylase deficiency

Cortisol / Metabolic Bone Disease / Humans / Child / Mutation / Female / Phenotype / Medical Care / Enzyme / Congenital Adrenal Hyperplasia / Public health systems and services research / Sexual Maturation / Glucocorticoids / Medical Treatment / Female / Phenotype / Medical Care / Enzyme / Congenital Adrenal Hyperplasia / Public health systems and services research / Sexual Maturation / Glucocorticoids / Medical Treatment

Precise Excision of the Large Pathogenicity Island, SPI7, in Salmonella enterica Serovar Typhi

Bacteriology / Biological Sciences / Cell line / Humans / Phenotype / MDR Salmonella typhi / Genetic Recombination / Base Sequence / MDR Salmonella typhi / Genetic Recombination / Base Sequence

Synaptic vesicle transporter expression regulates vesicle phenotype and quantal size

Electrochemistry / Dopamine / Neuropeptides / Mice / Animals / The / Synaptic Transmission / Synaptic Vesicle Recycling / Microelectrodes / Neurons / Phenotype / Membrane transport proteins / Rats / Exocytosis / Transfection / Poisson Distribution / Axons / The / Synaptic Transmission / Synaptic Vesicle Recycling / Microelectrodes / Neurons / Phenotype / Membrane transport proteins / Rats / Exocytosis / Transfection / Poisson Distribution / Axons

Endoplasmic reticulum resident protein 44 (ERp44) deficiency in mice and zebrafish leads to cardiac developmental and functional defects

Membrane Proteins / Endoplasmic Reticulum Stress / Morphogenesis / Apoptosis / Molecular chaperones / Congenital Heart Defects / Reactive Oxygen Species / Animals / Endoplasmic Reticulum / Calcium Signaling / Embryonic Stem Cells / Phenotype / Time Factors / Zebrafish / Congenital Heart Defects / Reactive Oxygen Species / Animals / Endoplasmic Reticulum / Calcium Signaling / Embryonic Stem Cells / Phenotype / Time Factors / Zebrafish

EMMPRIN/CD147 deficiency disturbs ameloblast–odontoblast cross-talk and delays enamel mineralization

Engineering / Biological Sciences / Basement Membrane / Bone / Animals / Mandible / Phenotype / Incisor / Matrix Metalloproteinases / Dentin / Dental Enamel / X Ray Microtomography / Tooth Calcification / Mandible / Phenotype / Incisor / Matrix Metalloproteinases / Dentin / Dental Enamel / X Ray Microtomography / Tooth Calcification

Genes as gerontological variables: uniform genotypes☆

Genetics / Animal Behavior / Aging / Life Sciences / Diet / Mice / Female / Animals / Male / Animal Model / Phenotype / Genes / Clinical Sciences / Research Purpose / Spectrum / Longitudinal Studies / Genotype / Neurobiology of Aging / Cross Sectional Studies / Neurosciences / Mice / Female / Animals / Male / Animal Model / Phenotype / Genes / Clinical Sciences / Research Purpose / Spectrum / Longitudinal Studies / Genotype / Neurobiology of Aging / Cross Sectional Studies / Neurosciences

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