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Molecular Cell, ISSN 1097-2765, 1999, Volume 3, Issue 5, pp. 661 - 671
High-affinity histamine-binding proteins (HBPs) were discovered in the saliva of Rhipicephalus a ppendiculatusticks. Their ability to outcompete histamine... 
LARVAL FEEDING SITES | QUANTITIES | RHIPICEPHALUS-APPENDICULATUS | IMMUNE SERUM | CRYSTAL-STRUCTURE | BIOCHEMISTRY & MOLECULAR BIOLOGY | RESOLUTION | GLYCOPROTEINS | RESISTANCE | BACULOVIRUS EXPRESSION VECTORS | GUINEA-PIGS | CELL BIOLOGY | Receptors, Histamine H3 - chemistry | Receptors, Histamine H2 - chemistry | Ticks | Molecular Sequence Data | RNA, Messenger - analysis | Male | Crystallography | Histamine - metabolism | Receptors, Histamine H1 - metabolism | Gene Expression - physiology | Hemeproteins - chemistry | Receptors, Histamine - chemistry | Binding Sites - physiology | Cloning, Molecular | Receptors, Histamine H1 - genetics | Carrier Proteins - chemistry | Cysteine Proteinase Inhibitors - chemistry | Female | Platelet Aggregation Inhibitors - metabolism | Histamine Antagonists - chemistry | Receptors, Histamine H3 - metabolism | Insect Proteins - metabolism | Receptors, Histamine H1 - chemistry | Receptors, Histamine H2 - metabolism | Protein Structure, Tertiary | Lipocalin 1 | Protein Structure, Secondary | Receptors, Histamine H2 - genetics | Insect Proteins - genetics | Receptors, Histamine - genetics | Proteins - genetics | Sequence Homology, Amino Acid | Receptors, Histamine - metabolism | Animals | Insect Proteins - chemistry | Receptors, Histamine H3 - genetics | Platelet Aggregation Inhibitors - chemistry | Salivary Proteins and Peptides - chemistry | Proteins - chemistry | Index Medicus
Journal Article
Nature, ISSN 0028-0836, 05/2005, Volume 435, Issue 7041, pp. 441 - 445
The plant hormone auxin regulates diverse aspects of plant growth and development. Recent studies indicate that auxin acts by promoting the degradation of the... 
SCFTIR1 | COMPLEX | MULTIDISCIPLINARY SCIENCES | GROWTH | DEGRADATION | AUX/IAA PROTEINS | MECHANISMS | ARABIDOPSIS | SCF UBIQUITIN-LIGASE | EXPRESSION | BINDING | Transcription, Genetic - drug effects | Temperature | Molecular Sequence Data | Spodoptera | Arabidopsis Proteins - metabolism | DNA-Binding Proteins - metabolism | Protein Binding - drug effects | Carrier Proteins - chemistry | Receptors, Cell Surface - chemistry | Receptors, Cell Surface - isolation & purification | Repressor Proteins - metabolism | Amino Acid Sequence | Cell Line | Arabidopsis Proteins - genetics | Indoleacetic Acids - metabolism | Signal Transduction | F-Box Proteins - metabolism | F-Box Proteins - chemistry | Receptors, Cell Surface - metabolism | Nuclear Proteins - metabolism | SKP Cullin F-Box Protein Ligases - metabolism | SKP Cullin F-Box Protein Ligases - chemistry | Arabidopsis - metabolism | Arabidopsis - genetics | Arabidopsis Proteins - isolation & purification | Carrier Proteins - genetics | Gene Expression Regulation, Plant - drug effects | Animals | Carrier Proteins - metabolism | Arabidopsis Proteins - chemistry | Indoleacetic Acids - pharmacology | Carrier Proteins - isolation & purification | F-Box Proteins - isolation & purification | F-Box Proteins - genetics | Receptors, Cell Surface - genetics | Proteins | Hormones | Physical growth | Botany | Index Medicus | Space life sciences
Journal Article
Science, ISSN 0036-8075, 11/2002, Volume 298, Issue 5595, pp. 1039 - 1043
Polycomb group (PcG) proteins play important roles in maintaining the silent state of HOX genes. Recent studies have implicated histone methylation in... 
Polymerase chain reaction | Gels | Drosophila | Genes | Histones | Antibodies | Amino acids | Reports | Biochemistry | Repression | Methylation | BITHORAX COMPLEX | SITE | REPRESSION | DROSOPHILA-MELANOGASTER | GROUP GENE | MULTIDISCIPLINARY SCIENCES | GROUP PROTEINS | ENHANCER | HP1 | CHROMO DOMAIN | ZESTE | Protein Methyltransferases | Chromatin - metabolism | Temperature | Methyltransferases - isolation & purification | Humans | Methyltransferases - metabolism | Drosophila Proteins - metabolism | Proteins - isolation & purification | DNA-Binding Proteins - metabolism | Peptide Mapping | RNA Interference | Repressor Proteins - isolation & purification | Lysine - metabolism | Genes, Homeobox | Repressor Proteins - metabolism | Response Elements | Histone-Lysine N-Methyltransferase | Cell Cycle Proteins - metabolism | Gene Silencing | Nucleosomes - metabolism | Nuclear Proteins - metabolism | DNA-Binding Proteins - genetics | Enhancer of Zeste Homolog 2 Protein | Precipitin Tests | Polycomb Repressive Complex 2 | Animals | Carrier Proteins - metabolism | Histone Methyltransferases | Polycomb Repressive Complex 1 | Proteins - metabolism | Homeodomain Proteins | Carrier Proteins - isolation & purification | Transcription Factors | Drosophila Proteins - genetics | HeLa Cells | Histones - metabolism | Protein engineering | Research | Lysine | Proteins | Insects | Index Medicus
Journal Article
Journal Article
Methods in Enzymology, ISSN 0076-6879, 2018, Volume 600, pp. 25 - 66
Accurate repair of DNA double-strand breaks (DSBs) is carried out by homologous recombination. In order to repair DNA breaks by the recombination pathway, the... 
Helicase | Mre11 | Protein purification | Homologous recombination | Bloom | Biochemistry | Dna2 | Nuclease | DNA end resection | Werner | IRON-SULFUR CLUSTER | COMPLEX | STRAND BREAK REPAIR | RECQ HELICASES | BIOCHEMISTRY & MOLECULAR BIOLOGY | BIOCHEMICAL RESEARCH METHODS | SYNDROME HELICASE | FUNCTIONAL MRX | MRE11 NUCLEASE | SAE2 | WERNER-SYNDROME PROTEIN | ENDONUCLEASE ACTIVITY | Nuclear Proteins - isolation & purification | RecQ Helicases - isolation & purification | RecQ Helicases - metabolism | Humans | Baculoviridae - genetics | Cell Culture Techniques - methods | DNA Breaks, Double-Stranded | Spodoptera | DNA, Single-Stranded - genetics | DNA-Binding Proteins - metabolism | Recombinant Proteins - isolation & purification | Sf9 Cells | Transfection - methods | DNA Repair Enzymes - metabolism | Recombinant Proteins - metabolism | Cell Cycle Proteins - isolation & purification | Recombinational DNA Repair | DNA Repair Enzymes - isolation & purification | Cell Culture Techniques - instrumentation | DNA, Single-Stranded - metabolism | Cell Cycle Proteins - metabolism | Enzyme Assays - methods | Nuclear Proteins - metabolism | Replication Protein A - isolation & purification | Replication Protein A - metabolism | DNA Helicases - isolation & purification | DNA-Binding Proteins - isolation & purification | DNA Helicases - metabolism | Animals | Carrier Proteins - metabolism | Werner Syndrome Helicase - metabolism | Enzyme Assays - instrumentation | Carrier Proteins - isolation & purification | Werner Syndrome Helicase - isolation & purification | MRE11 Homologue Protein - metabolism | MRE11 Homologue Protein - isolation & purification | Index Medicus
Journal Article
Methods in Enzymology, ISSN 0076-6879, 2018, Volume 600, pp. 67 - 106
DNA end resection initiates the largely accurate repair of DNA double-strand breaks (DSBs) by homologous recombination. Specifically, recombination requires... 
Helicase | In vitro assay | Mre11 | Homologous recombination | Bloom | Biochemistry | Dna2 | Nuclease | DNA end resection | Werner | PROMOTES 5 | COMPLEX | REPAIR | ENDONUCLEASE | RECQ HELICASES | MECHANISM | REPLICATION PROTEIN-A | BIOCHEMISTRY & MOLECULAR BIOLOGY | BIOCHEMICAL RESEARCH METHODS | DOUBLE-STRAND BREAKS | MRE11 NUCLEASE | SAE2 | Nuclear Proteins - isolation & purification | RecQ Helicases - isolation & purification | RecQ Helicases - metabolism | Humans | Baculoviridae - genetics | Electrophoresis, Polyacrylamide Gel - instrumentation | Cell Culture Techniques - methods | DNA Breaks, Double-Stranded | Spodoptera | DNA, Single-Stranded - genetics | DNA-Binding Proteins - metabolism | Recombinant Proteins - isolation & purification | Sf9 Cells | Transfection - methods | DNA Repair Enzymes - metabolism | Buffers | Recombinant Proteins - metabolism | Cell Cycle Proteins - isolation & purification | Recombinational DNA Repair | DNA Repair Enzymes - isolation & purification | Cell Culture Techniques - instrumentation | DNA, Single-Stranded - metabolism | Cell Cycle Proteins - metabolism | Enzyme Assays - methods | Nuclear Proteins - metabolism | Replication Protein A - isolation & purification | Replication Protein A - metabolism | DNA Helicases - isolation & purification | DNA-Binding Proteins - isolation & purification | Electrophoresis, Polyacrylamide Gel - methods | DNA Helicases - metabolism | Oligonucleotides - metabolism | Animals | Carrier Proteins - metabolism | Werner Syndrome Helicase - metabolism | Enzyme Assays - instrumentation | Carrier Proteins - isolation & purification | Werner Syndrome Helicase - isolation & purification | MRE11 Homologue Protein - metabolism | MRE11 Homologue Protein - isolation & purification | Index Medicus
Journal Article
Science, ISSN 0036-8075, 2/2009, Volume 323, Issue 5917, pp. 1057 - 1060
Journal Article
PLoS ONE, ISSN 1932-6203, 03/2016, Volume 11, Issue 3, pp. e0150239 - e0150239
Proximity-dependent trans-biotinylation by the Escherichia coli biotin ligase BirA mutant R118G (BirA*) allows stringent streptavidin affinity purification of... 
CAENORHABDITIS-ELEGANS | NONSENSE-MEDIATED DECAY | SMG5-SMG7 HETERODIMER | MULTIDISCIPLINARY SCIENCES | TRANSLATION INITIATION | ENDOPLASMIC-RETICULUM | UPF1 PHOSPHORYLATION | INTERACTION NETWORKS | MESSENGER-RNA DECAY | EXON JUNCTION COMPLEX | MAMMALIAN-CELLS | Recombinant Fusion Proteins - isolation & purification | Humans | Trans-Activators - isolation & purification | RNA, Messenger - metabolism | Carbon-Nitrogen Ligases - isolation & purification | Recombinant Fusion Proteins - metabolism | Carbon-Nitrogen Ligases - genetics | Protein Interaction Maps | Tandem Mass Spectrometry | Cloning, Molecular | Escherichia coli - metabolism | Trans-Activators - genetics | Chromatography, Liquid | Repressor Proteins - isolation & purification | Repressor Proteins - metabolism | Cell Line | Biotinylation | Carbon-Nitrogen Ligases - metabolism | Immunoprecipitation - methods | Repressor Proteins - genetics | Escherichia coli Proteins - metabolism | Transcription Factors - genetics | Escherichia coli Proteins - isolation & purification | Nonsense Mediated mRNA Decay | Transcription Factors - metabolism | Carrier Proteins - genetics | Protein Interaction Mapping - methods | Carrier Proteins - metabolism | Escherichia coli - genetics | Carrier Proteins - isolation & purification | Escherichia coli Proteins - genetics | Recombinant Fusion Proteins - genetics | Trans-Activators - metabolism | Transcription Factors - isolation & purification | HeLa Cells | Usage | Biotin | Liquid chromatography | Research | Protein-protein interactions | Post-transcription | Phosphorylation | Immunoprecipitation | Peptides | Protein purification | mRNA turnover | Escherichia coli | Mass spectroscopy | Biochemistry | Nonsense-mediated mRNA decay | Kinases | Machinery | Proteins | Chemistry | Streptavidin | Scientific imaging | Protein interaction | Mass spectrometry | Index Medicus
Journal Article
PLoS ONE, ISSN 1932-6203, 12/2013, Volume 8, Issue 12, pp. e84112 - e84112
The avian eggshell membranes are essential elements in the fabrication of the calcified shell as a defense against bacterial penetration. Ovocalyxin-36... 
GRAM-POSITIVE BACTERIA | PSEUDOMONAS-AERUGINOSA INFECTION | LIPOPOLYSACCHARIDE-BINDING PROTEIN | MULTIDISCIPLINARY SCIENCES | NEGATIVE BACTERIA | FUNCTIONAL VARIANT | TERMINAL FRAGMENT | PROTEOMIC ANALYSIS | BACTERICIDAL/PERMEABILITY-INCREASING PROTEIN | HEN EGG-WHITE | STATISTICAL-MODEL | Egg Proteins - metabolism | Anti-Infective Agents - isolation & purification | Membrane Glycoproteins - metabolism | Anti-Infective Agents - metabolism | Lipopolysaccharides - metabolism | Acute-Phase Proteins - genetics | Antimicrobial Cationic Peptides - metabolism | Blood Proteins - metabolism | Tandem Mass Spectrometry | Blood Proteins - genetics | Blood Proteins - isolation & purification | Teichoic Acids - metabolism | Chromatography, Liquid | Cell Membrane - metabolism | Acute-Phase Proteins - isolation & purification | Antimicrobial Cationic Peptides - genetics | Bacterial Infections - microbiology | Membrane Glycoproteins - isolation & purification | Enzyme-Linked Immunosorbent Assay | Acute-Phase Proteins - metabolism | Blotting, Western | Membrane Glycoproteins - genetics | Carrier Proteins - genetics | Bacterial Infections - prevention & control | Animals | Antimicrobial Cationic Peptides - isolation & purification | Carrier Proteins - metabolism | Carrier Proteins - isolation & purification | Chickens | Polymorphism, Single Nucleotide - genetics | Bacteria - pathogenicity | Egg Proteins - isolation & purification | Egg Proteins - genetics | Bacterial Infections - metabolism | Single nucleotide polymorphisms | Chromosomes | Mitogens | Escherichia coli | Organic acids | Protein binding | Membranes | Egg shells | Protein purification | Serine | Lung | Lipoteichoic acid | Membrane permeability | Proline | Homology | Single-nucleotide polymorphism | Phosphatase | Eggs | Molecular weight | Lipopolysaccharides | Proteins | Fabrication | Anion exchange | Reproduction | Breeding success | Bacteria | Product safety | Lipopolysaccharide-binding protein | Amino acid sequence | Cation exchanging | Pattern recognition | Permeability | Mammals | Epithelium | Membrane proteins | Anion exchanging | Calcification | Sepsis | BPI protein | Palate | Food safety | Index Medicus
Journal Article