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Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 11/2010, Volume 107, Issue 44, pp. 19002 - 19007
Extracellular vesicle production is a ubiquitous process in Gram-negative bacteria, but little is known about such process in Gram-positive bacteria. We report... 
Bacillus anthracis | Antigens | Anthrax | Toxicity | Gram positive bacteria | Antibodies | Toxins | Macrophages | Fatty acids | Gram negative bacteria | Passive immunity | Immunizations | Monoclonal antibody | OUTER-MEMBRANE | passive immunity | MULTIDISCIPLINARY SCIENCES | EUKARYOTIC CELLS | MONOCLONAL-ANTIBODY | SHIGELLA-FLEXNERI | GRAM-NEGATIVE BACTERIA | immunizations | PSEUDOMONAS-AERUGINOSA | CRYPTOCOCCUS-NEOFORMANS | STAPHYLOCOCCUS-AUREUS | POSITIVE BACTERIA | monoclonal antibody | ADENYLATE-CYCLASE | Membrane Glycoproteins - metabolism | Antigens, Bacterial - immunology | Antibodies, Bacterial - pharmacology | Cell Membrane Structures - immunology | Immunoglobulin M - immunology | Immunoglobulin M - metabolism | Bacillus anthracis - ultrastructure | Anthrax - prevention & control | Cell Membrane Structures - metabolism | Bacterial Proteins - immunology | Membrane Glycoproteins - immunology | Bacillus anthracis - genetics | Anthrax - pathology | Bacillus anthracis - metabolism | Antibodies, Monoclonal - immunology | Macrophages - immunology | Macrophages - microbiology | Cell Membrane Structures - genetics | Anthrax - immunology | Anthrax - epidemiology | Antibodies, Monoclonal - pharmacology | Bacterial Toxins - immunology | Bacterial Proteins - genetics | Anthrax - metabolism | Membrane Glycoproteins - genetics | Particle Size | Bacterial Toxins - metabolism | Cell Membrane Structures - ultrastructure | Macrophages - metabolism | Animals | Bacillus anthracis - immunology | Antibodies, Bacterial - immunology | Bacterial Proteins - metabolism | Mice | Mice, Inbred BALB C | Antigens, Bacterial - metabolism | Bacterial toxins | Monoclonal antibodies | Cellular immunity | Research | Properties | Health aspects | Biological Sciences
Journal Article
Cancer Cell, ISSN 1535-6108, 2010, Volume 17, Issue 6, pp. 574 - 583
Uptake of the anticancer drug cisplatin is mediated by the copper transporter CTR1 in cultured cells. Here we show in human ovarian tumors that low levels of... 
PROTEINS | CHEMBIO | CELLCYCLE | WILSON DISEASE GENE | CARBOPLATIN | GYNECOLOGIC-ONCOLOGY-GROUP | SQUAMOUS CARCINOGENESIS | ONCOLOGY | CERVICAL-CANCER | MECHANISMS | CELLULAR ACCUMULATION | TRANSPORTER CTR1 | CHEMOTHERAPY | TRANSGENIC MICE | CELL BIOLOGY | Neoplasms - metabolism | Adjuvants, Pharmaceutic - pharmacology | Copper-transporting ATPases | Gene Expression - genetics | Molybdenum - metabolism | Copper - blood | Humans | Middle Aged | Uterine Cervical Neoplasms - pathology | DNA Adducts - metabolism | Neovascularization, Pathologic - pathology | Carboplatin - therapeutic use | Uterine Cervical Neoplasms - metabolism | Cation Transport Proteins - metabolism | Copper - metabolism | Aged, 80 and over | Adult | Cation Transport Proteins - genetics | Female | Ovarian Neoplasms - metabolism | Ovarian Neoplasms - drug therapy | Disease Models, Animal | Cell Survival - drug effects | Animal Structures - drug effects | Molybdenum - therapeutic use | Treatment Outcome | Uterine Cervical Neoplasms - drug therapy | Molybdenum - pharmacology | Chelating Agents - pharmacology | Mice, Inbred Strains | Neoplasms - drug therapy | Cisplatin - metabolism | Disease-Free Survival | Animals | Cisplatin - therapeutic use | Neovascularization, Pathologic - drug therapy | Cell Line, Tumor | Adenosine Triphosphatases - genetics | Aged | Cell Proliferation - drug effects | Mice | Chelating Agents - metabolism | Animal Structures - metabolism | Chemotherapy | Messenger RNA | Analysis | Cervical cancer | Cisplatin | Tumors | Cancer
Journal Article
PLoS ONE, ISSN 1932-6203, 12/2011, Volume 6, Issue 12, p. e29690
Background: Cytoplasmic filamentous rods and rings (RR) structures were identified using human autoantibodies as probes. In the present study, the formation of... 
TARGET | AUTOANTIBODIES | PROTEIN | REPRESSION | AUTOANTIGENS | MULTIDISCIPLINARY SCIENCES | COMPONENTS | IDENTIFICATION | ANTITUMOR | MYCOPHENOLIC-ACID | DEHYDROGENASE | Neoplasms - metabolism | Cell Line | Embryonic Stem Cells - metabolism | Mammals - metabolism | Embryonic Stem Cells - cytology | Humans | Cytidine Triphosphate - metabolism | Enzyme Inhibitors - pharmacology | Guanosine Triphosphate - metabolism | Cytoplasmic Structures - drug effects | IMP Dehydrogenase - metabolism | Animals | Biosynthetic Pathways - drug effects | Embryonic Stem Cells - drug effects | IMP Dehydrogenase - antagonists & inhibitors | Time Factors | Mice | Cell Cycle - drug effects | Neoplasms - pathology | Cytoplasmic Structures - metabolism | Autoimmunity | Enzymes | Enzyme inhibitors | Autoantibodies | Embryonic stem cells | Tubulins | Muscle proteins | Intermediate filament proteins | Vimentin | Biotechnology | GTP | Norleucine | Laboratories | Embryo cells | Stem cell transplantation | Biology | Arthritis | Inosine monophosphate | Rods | Kinases | Ribavirin | Mammalian cells | Proteins | Hepatitis | Tubulin | Allografts | Immunology | Pathways | Actin | Cell cycle | Gangrene | Inhibition | Cytidine triphosphate--CTP | Localization | Antigens | Rheumatic diseases | Centrosomes | Tumor cell lines | Mammals | Medicine | Pathology | MicroRNAs | Cell lines | Stem cells | Immunofluorescence | Dismantling | Retinoic acid | Cancer | Apoptosis | Structure-function relationships | Cytidine triphosphate | CTP
Journal Article
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