Mutation - Page 8

Periplasmic Cu,Zn superoxide dismutase and cytoplasmic Dps concur in protecting Salmonella enterica serovar Typhimurium from extracellular reactive oxygen species

Biological Sciences / Mutation / Bacterial resistance / Reactive Oxygen Species / Mice / Animals / Salmonella Typhimurium / Physical sciences / Detoxification / Superoxide Dismutase / NADPH oxidase / Hydrogen Peroxide / Antioxidant enzyme / Phagocytosis / Oxidative Damage / Cytoplasm / DNA binding proteins / Superoxides / Respiratory Burst / Biochemistry and cell biology / Animals / Salmonella Typhimurium / Physical sciences / Detoxification / Superoxide Dismutase / NADPH oxidase / Hydrogen Peroxide / Antioxidant enzyme / Phagocytosis / Oxidative Damage / Cytoplasm / DNA binding proteins / Superoxides / Respiratory Burst / Biochemistry and cell biology

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High efficiency recombineering in lactic acid bacteria

Genetic Engineering / Biological Sciences / Vancomycin / Environmental Sciences / Mutation / Lactobacillus / Nucleic Acids / Phenotype / Anti-Bacterial Agents / Homologous Recombination / Lactococcus lactis / Lactobacillus / Nucleic Acids / Phenotype / Anti-Bacterial Agents / Homologous Recombination / Lactococcus lactis

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A pmrA Constitutive Mutant Sensitizes Escherichia coli to Deoxycholic Acid

Bacteriology / Sequence Analysis / Biological Sciences / Lipopolysaccharide / Mutation / Escherichia coli / Zinc / Iron / Gram-negative bacteria / Chemical Composition / Lipid A / Escherichia coli / Zinc / Iron / Gram-negative bacteria / Chemical Composition / Lipid A

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Genetic Characterization of Human Immunodeficiency Virus Type 1 in Elite Controllers: Lack of Gross Genetic Defects or Common Amino Acid Changes

Genetics / Microbiology / Immunology / Polymorphism / Molecular Evolution / Medical Microbiology / Virology / Mozambique / Adolescent / HIV / Genetic Diversity / Biological Sciences / Phylogeny / Pregnancy / Humans / Child / Sequence alignment / Mutation / Microbes / Female / Blood / Drug Resistance / Blood sampling / Male / Sexual Behavior / Polymerase Chain Reaction / Infant / AIDS / Clinical Sciences / Vagina / Middle Aged / Molecular cloning / Human immunodeficiency virus / Adult / Time Factors / Highly Active Antiretroviral Therapy / Hiv seropositivity / Amino Acid Profile / Semen / Amino Acid Sequence / Base Sequence / Lymphocytes / Reverse Transcriptase / Binding Site / Viral Load / Medical Microbiology / Virology / Mozambique / Adolescent / HIV / Genetic Diversity / Biological Sciences / Phylogeny / Pregnancy / Humans / Child / Sequence alignment / Mutation / Microbes / Female / Blood / Drug Resistance / Blood sampling / Male / Sexual Behavior / Polymerase Chain Reaction / Infant / AIDS / Clinical Sciences / Vagina / Middle Aged / Molecular cloning / Human immunodeficiency virus / Adult / Time Factors / Highly Active Antiretroviral Therapy / Hiv seropositivity / Amino Acid Profile / Semen / Amino Acid Sequence / Base Sequence / Lymphocytes / Reverse Transcriptase / Binding Site / Viral Load

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ALX4 dysfunction disrupts craniofacial and epidermal development

Web Design / Web Technologies / Web Development / Transcription Factors / Biological Sciences / Web / Humans / Child / Mutation / Male / Human Molecular Genetics / Infant / Epidermis / WEB DEVELOPMENT / Facial Bones / DNA binding proteins / E Commerce / Craniofacial Dysostosis / Web / Humans / Child / Mutation / Male / Human Molecular Genetics / Infant / Epidermis / WEB DEVELOPMENT / Facial Bones / DNA binding proteins / E Commerce / Craniofacial Dysostosis

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New Efficient Recombinant Expression System To Engineer Candida antarctica Lipase B

Gene expression / Multidisciplinary / Genetic Engineering / Mutation / Applied / Applied Environmental Microbiology / Yarrowia / Lipase / Applied Environmental Microbiology / Yarrowia / Lipase

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Combinatorial Engineering of Dextransucrase Specificity

Catalysis / Magnetic Resonance Spectroscopy / Multidisciplinary / Protein Engineering / Mutation / Glucans / PLoS one / Substrate Specificity / Glycosyltransferases / Amino Acid Sequence / Structure activity Relationship / Site-directed Mutagenesis / Leuconostoc / Glucans / PLoS one / Substrate Specificity / Glycosyltransferases / Amino Acid Sequence / Structure activity Relationship / Site-directed Mutagenesis / Leuconostoc

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Triosephosphate isomerase deficiency: a neurodegenerative misfolding disease

Protein Folding / Kinetics / Humans / Mutation / Male / Microtubules / Glycolysis / Triosephosphate Isomerase / Biochemistry and cell biology / Pentose Phosphate Pathway / Microtubules / Glycolysis / Triosephosphate Isomerase / Biochemistry and cell biology / Pentose Phosphate Pathway

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acr-23 Encodes a Monepantel-Sensitive Channel in Caenorhabditis elegans

Microbiology / Immunology / Caenorhabditis elegans / Medical Microbiology / Ion Channels / Mutation / Animals / Drug Resistance / Xenopus laevis / Aminoacetonitrile / Gene Expression Regulation / Mutation / Animals / Drug Resistance / Xenopus laevis / Aminoacetonitrile / Gene Expression Regulation

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A population genetic approach to mapping neurological disorder genes using deep resequencing

Genetics / Schizophrenia / Population Genetics / Humans / Child / Mutation / Female / Male / Sample Size / Autism Spectrum Disorder / Human Genome / Analytical Method / Population Model / PLoS Genetics / Cohort Studies / Mutation / Female / Male / Sample Size / Autism Spectrum Disorder / Human Genome / Analytical Method / Population Model / PLoS Genetics / Cohort Studies

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Ultra-Deep Pyrosequencing (UDPS) Data Treatment to Study Amplicon HCV Minor Variants

Multidisciplinary / Humans / Mutation / Polymerase Chain Reaction / PLoS one / Molecular cloning / Reproducibility of Results / Genetic variation / Molecular cloning / Reproducibility of Results / Genetic variation

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Triosephosphate isomerase deficiency: a neurodegenerative misfolding disease

Protein Folding / Kinetics / Humans / Mutation / Male / Microtubules / Glycolysis / Triosephosphate Isomerase / Biochemistry and cell biology / Pentose Phosphate Pathway / Microtubules / Glycolysis / Triosephosphate Isomerase / Biochemistry and cell biology / Pentose Phosphate Pathway

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DNA repair efficiency in transgenic mice over expressing ribosomal protein S3

Oxidative Stress / DNA damage / DNA repair / Transgenic Mice / Protein synthesis / Humans / Mutation / Mice / Female / Animals / Male / Ribosomal proteins / Oxidative Damage / In Vitro Studies / Oxidative Dna Damage / Ribosomal Protein / Binding affinity / Humans / Mutation / Mice / Female / Animals / Male / Ribosomal proteins / Oxidative Damage / In Vitro Studies / Oxidative Dna Damage / Ribosomal Protein / Binding affinity

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Comprehensive genomic characterization defines human glioblastoma genes and core pathways

Genomics / Cancer / Adolescent / DNA repair / Gene expression / Multidisciplinary / Nature / Signal Transduction / Humans / Mutation / Glioblastoma / Female / Male / DNA methylation / Gene Dosage / Aged / Middle Aged / Human Genome / Adult / Retrospective Studies / Large Scale / DNA Copy Number / Multi Dimensional / Pilot project / Brain Neoplasms / Multidisciplinary / Nature / Signal Transduction / Humans / Mutation / Glioblastoma / Female / Male / DNA methylation / Gene Dosage / Aged / Middle Aged / Human Genome / Adult / Retrospective Studies / Large Scale / DNA Copy Number / Multi Dimensional / Pilot project / Brain Neoplasms

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N-terminal amphipathic helix as a trigger of hemolytic activity in antimicrobial peptides: A case study in latarcins

Biochemistry / Microbiology / Immunology / Molecular Biology / Computational Biology / Protein Engineering / Molecular modeling / Mutation / EC / Case Study / Animals / Antimicrobial Peptide / AMPs / Antimicrobial Cationic Peptides / Protein Secondary Structure Prediction / Cytotoxic Activity / Ec / Amino Acid Sequence / In Silico / Biochemistry and cell biology / Hemolysis / Proof of Concept / Protein Engineering / Molecular modeling / Mutation / EC / Case Study / Animals / Antimicrobial Peptide / AMPs / Antimicrobial Cationic Peptides / Protein Secondary Structure Prediction / Cytotoxic Activity / Ec / Amino Acid Sequence / In Silico / Biochemistry and cell biology / Hemolysis / Proof of Concept

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HAX1 deficiency causes autosomal recessive severe congenital neutropenia (Kostmann disease)

Adolescent / Apoptosis / Nature / Biological Sciences / Humans / Child / Genetic Testing / Mutation / Female / Male / Infant / Proteins / Pedigree / Adult / Autosomal Recessive / Myeloid Cells / Syndrome / Child / Genetic Testing / Mutation / Female / Male / Infant / Proteins / Pedigree / Adult / Autosomal Recessive / Myeloid Cells / Syndrome

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