Phenotype - Page 8

Complementary antioxidant defense by cytoplasmic and mitochondrial peroxiredoxins in Leishmania infantum

Free Radicals / RNA / Fluorescence Microscopy / Oxidative Stress / Mitochondria / Western blotting / Free Radical / DNA / Antioxidants / Phylogeny / Peroxidase / Animals / Detoxification / Phenotype / Enzyme / Subcellular Localization / Hydrogen Peroxide / Peroxidases / Transfection / Protozoan Proteins / Leishmania infantum / Amino Acid Sequence / Gene Family / Cytoplasm / Oxidation-Reduction / Biochemistry and cell biology / Peroxiredoxins / Western blotting / Free Radical / DNA / Antioxidants / Phylogeny / Peroxidase / Animals / Detoxification / Phenotype / Enzyme / Subcellular Localization / Hydrogen Peroxide / Peroxidases / Transfection / Protozoan Proteins / Leishmania infantum / Amino Acid Sequence / Gene Family / Cytoplasm / Oxidation-Reduction / Biochemistry and cell biology / Peroxiredoxins

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Complementary antioxidant defense by cytoplasmic and mitochondrial peroxiredoxins in Leishmania infantum

Free Radicals / RNA / Fluorescence Microscopy / Oxidative Stress / Mitochondria / Western blotting / Free Radical / DNA / Antioxidants / Phylogeny / Peroxidase / Animals / Detoxification / Phenotype / Enzyme / Subcellular Localization / Hydrogen Peroxide / Peroxidases / Transfection / Protozoan Proteins / Leishmania infantum / Amino Acid Sequence / Gene Family / Cytoplasm / Oxidation-Reduction / Biochemistry and cell biology / Peroxiredoxins / Western blotting / Free Radical / DNA / Antioxidants / Phylogeny / Peroxidase / Animals / Detoxification / Phenotype / Enzyme / Subcellular Localization / Hydrogen Peroxide / Peroxidases / Transfection / Protozoan Proteins / Leishmania infantum / Amino Acid Sequence / Gene Family / Cytoplasm / Oxidation-Reduction / Biochemistry and cell biology / Peroxiredoxins

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Bile acid-CoA ligase deficiency—a new inborn error of bile acid metabolism

Pakistan / Humans / Female / Inborn errors of metabolism / Phenotype / Clinical Sciences / Genotype / Consanguinity / Gas Chromatography/mass Spectrometry / Clinical Sciences / Genotype / Consanguinity / Gas Chromatography/mass Spectrometry

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Bile acid-CoA ligase deficiency—a new inborn error of bile acid metabolism

Pakistan / Humans / Female / Inborn errors of metabolism / Phenotype / Clinical Sciences / Genotype / Consanguinity / Gas Chromatography/mass Spectrometry / Clinical Sciences / Genotype / Consanguinity / Gas Chromatography/mass Spectrometry

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Arterial and renal consequences of partial genetic deficiency in tissue kallikrein activity in humans

Genetics / Diet / Humans / Kidney / Mice / Aldosterone / Animals / Clinical / Male / Potassium / Phenotype / Mechanical Stress / Adult / Sodium / Vasodilation / Clinical Investigation / Cross-Over Studies / Atrial Natriuretic Factor / Brachial artery / Aldosterone / Animals / Clinical / Male / Potassium / Phenotype / Mechanical Stress / Adult / Sodium / Vasodilation / Clinical Investigation / Cross-Over Studies / Atrial Natriuretic Factor / Brachial artery

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Arterial and renal consequences of partial genetic deficiency in tissue kallikrein activity in humans

Genetics / Diet / Humans / Kidney / Mice / Aldosterone / Animals / Clinical / Male / Potassium / Phenotype / Mechanical Stress / Adult / Sodium / Vasodilation / Clinical Investigation / Cross-Over Studies / Atrial Natriuretic Factor / Brachial artery / Aldosterone / Animals / Clinical / Male / Potassium / Phenotype / Mechanical Stress / Adult / Sodium / Vasodilation / Clinical Investigation / Cross-Over Studies / Atrial Natriuretic Factor / Brachial artery

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Você conhece esta síndrome?

Adolescent / Biopsy / Macular Degeneration / Insulin Resistance / Humans / Child / Hypotrichosis / Female / Male / Infant / Differential Diagnosis / Skin / Immunoglobulin E / Phenotype / Deafness / Skin Diseases / Clinical Sciences / Middle Aged / Darier Disease / Adult / Mouth mucosa / Tuberous sclerosis / Hyperpigmentation / Noonan syndrome / Syndrome / Keratitis / Skin Neoplasms / Hypertriglyceridemia / Child / Hypotrichosis / Female / Male / Infant / Differential Diagnosis / Skin / Immunoglobulin E / Phenotype / Deafness / Skin Diseases / Clinical Sciences / Middle Aged / Darier Disease / Adult / Mouth mucosa / Tuberous sclerosis / Hyperpigmentation / Noonan syndrome / Syndrome / Keratitis / Skin Neoplasms / Hypertriglyceridemia

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Prolyl 3-hydroxylase 1 deficiency causes a recessive metabolic bone disorder resembling lethal/severe osteogenesis imperfecta

Mass Spectrometry / Biological Sciences / Humans / Mutation / Osteogenesis Imperfecta / Female / Male / Phenotype / Proteoglycans / Time Factors / Deficiency / Deficit / Female / Male / Phenotype / Proteoglycans / Time Factors / Deficiency / Deficit

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Long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency: Identification of a new inborn error of mitochondrial fatty acidβ-oxidation

Nursing / Pediatrics / Treatment Outcome / Mitochondria / Pediatric nursing / Adolescent / Liver diseases / High Frequency / Heart Failure / Pregnancy / Humans / Child / Liver Cirrhosis / Liver / Mutation / Female / Male / Hypoglycemia / Fatty Acid Oxidation / Infant / Follow-up studies / Netherlands / Differential Diagnosis / HELLP Syndrome / Phenotype / Clinical Sciences / Newborn Infant / L-carnitine / Questionnaires / Optometry and Ophthalmology / Public health systems and services research / Survival Rate / Fatty Acid / Health surveys / Multienzyme complexes / Cardiomyopathies / Status Epilepticus / Base Sequence / Human Fibroblasts / Clinical Presentation / Clinical Signs / Antiepileptic Drug / Archivos Argentinos De Pediatria / Brain Damage / Age of Onset / Adolescent / Liver diseases / High Frequency / Heart Failure / Pregnancy / Humans / Child / Liver Cirrhosis / Liver / Mutation / Female / Male / Hypoglycemia / Fatty Acid Oxidation / Infant / Follow-up studies / Netherlands / Differential Diagnosis / HELLP Syndrome / Phenotype / Clinical Sciences / Newborn Infant / L-carnitine / Questionnaires / Optometry and Ophthalmology / Public health systems and services research / Survival Rate / Fatty Acid / Health surveys / Multienzyme complexes / Cardiomyopathies / Status Epilepticus / Base Sequence / Human Fibroblasts / Clinical Presentation / Clinical Signs / Antiepileptic Drug / Archivos Argentinos De Pediatria / Brain Damage / Age of Onset

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PLoS Computational Biology conference postcards from ISMB 2010

Computational Biology / Ecology / Biological Sciences / Software / Humans / Mathematical Sciences / Animals / Quantitative Microscopy / Phenotype / Protein Abundance / Genotype / Individualized Medicine / Mathematical Sciences / Animals / Quantitative Microscopy / Phenotype / Protein Abundance / Genotype / Individualized Medicine

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PLoS Computational Biology Conference Postcards from ISMB/ECCB 2011

Computational Biology / Ecology / Biological Sciences / Software / Humans / Mathematical Sciences / Animals / Quantitative Microscopy / Phenotype / Protein Abundance / Genotype / Individualized Medicine / Mathematical Sciences / Animals / Quantitative Microscopy / Phenotype / Protein Abundance / Genotype / Individualized Medicine

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Human Pulmonary Valve Progenitor Cells Exhibit Endothelial/Mesenchymal Plasticity in Response to Vascular Endothelial Growth FactorA and Transforming Growth Factor2

Tissue Engineering / Stem Cells / Cell separation / Cell Culture / Cell Differentiation / Humans / Endothelial Cells / Female / Vascular endothelium / Phenotype / Clinical Sciences / Middle Aged / Heart valves / Endothelial cell / Circulation / Transforming Growth Factor Beta / Biological markers / Fetus / Heart Valve / Vascular Endothelial Growth Factor / Transforming Growth Factor / Humans / Endothelial Cells / Female / Vascular endothelium / Phenotype / Clinical Sciences / Middle Aged / Heart valves / Endothelial cell / Circulation / Transforming Growth Factor Beta / Biological markers / Fetus / Heart Valve / Vascular Endothelial Growth Factor / Transforming Growth Factor

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Culture on electrospun polyurethane scaffolds decreases atrial natriuretic peptide expression by cardiomyocytes in vitro

Biomaterials / Tissue Engineering / Flow Cytometry / Multidisciplinary / Cell separation / Tissue culture / Animals / Polymerase Chain Reaction / Phenotype / Steady state / Rats / Molecular Marker / Polyurethanes / Cell Shape / High Density Concrete / Cell Survival / Gene Expression Regulation / Electrical Coupling / Atrial Natriuretic Factor / Tissue culture / Animals / Polymerase Chain Reaction / Phenotype / Steady state / Rats / Molecular Marker / Polyurethanes / Cell Shape / High Density Concrete / Cell Survival / Gene Expression Regulation / Electrical Coupling / Atrial Natriuretic Factor

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Noncompensation in peptide/receptor gene expression and distinct behavioral phenotypes in VIP- and PACAP-deficient mice

Animal Behavior / Aging / Neurochemistry / Gene expression / Brain / Mice / Female / Animals / Male / Phenotype / Vasoactive Intestinal Peptide / Time Factors / Neurosciences / Mice / Female / Animals / Male / Phenotype / Vasoactive Intestinal Peptide / Time Factors / Neurosciences

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Você conhece esta síndrome?

Adolescent / Biopsy / Macular Degeneration / Insulin Resistance / Humans / Child / Hypotrichosis / Female / Male / Infant / Differential Diagnosis / Skin / Immunoglobulin E / Phenotype / Deafness / Skin Diseases / Clinical Sciences / Middle Aged / Darier Disease / Adult / Mouth mucosa / Tuberous sclerosis / Hyperpigmentation / Noonan syndrome / Syndrome / Keratitis / Skin Neoplasms / Hypertriglyceridemia / Child / Hypotrichosis / Female / Male / Infant / Differential Diagnosis / Skin / Immunoglobulin E / Phenotype / Deafness / Skin Diseases / Clinical Sciences / Middle Aged / Darier Disease / Adult / Mouth mucosa / Tuberous sclerosis / Hyperpigmentation / Noonan syndrome / Syndrome / Keratitis / Skin Neoplasms / Hypertriglyceridemia

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Transgenic complementation of MeCP2 deficiency: phenotypic rescue of Mecp2-null mice by isoform-specific transgenes

Genetics / Animal Behavior / Gene expression / Longevity / Mutation / Mice / Animals / Male / Cytomegalovirus / Alternative splicing / Neurons / Phenotype / European / Rett syndrome / Mouse Model / Age Factors / X chromosome / Alternative Splicing / Protein isoforms / Protein Binding / Transgene Expression / Weight Gain / Mice / Animals / Male / Cytomegalovirus / Alternative splicing / Neurons / Phenotype / European / Rett syndrome / Mouse Model / Age Factors / X chromosome / Alternative Splicing / Protein isoforms / Protein Binding / Transgene Expression / Weight Gain

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