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PLoS ONE, ISSN 1932-6203, 06/2016, Volume 11, Issue 6, p. e0157620
We have recently described sustained clinical recovery associated with dampened neuroinflammation and remyelination following transplantation of neural... 
RECOVERY | DEMYELINATION | CONVERSION | MULTIDISCIPLINARY SCIENCES | DISEASE | NERVOUS-SYSTEM INFLAMMATION | DIFFERENTIATION | CORONAVIRUS | RAT MODEL | AUTOIMMUNE ENCEPHALOMYELITIS | NEUROPROTECTION | Forkhead Transcription Factors - immunology | Cell- and Tissue-Based Therapy - methods | Human Embryonic Stem Cells - cytology | Humans | Male | Murine hepatitis virus - growth & development | Neural Stem Cells - cytology | T-Lymphocytes, Regulatory - pathology | T-Lymphocytes, Regulatory - immunology | Neural Stem Cells - immunology | Embryoid Bodies - cytology | Human Embryonic Stem Cells - immunology | Neural Stem Cells - transplantation | Cell Differentiation | Hepatitis, Viral, Animal - virology | Hepatitis, Viral, Animal - therapy | CD4 Antigens - genetics | Disease Models, Animal | Biomarkers - metabolism | Hepatitis, Viral, Animal - immunology | Hepatitis, Viral, Animal - pathology | CD4 Antigens - immunology | Gene Expression | Myelin Sheath - immunology | Lymphocyte Activation | Mice, Inbred C57BL | Forkhead Transcription Factors - genetics | Murine hepatitis virus - pathogenicity | Organ Specificity | Coronavirus Infections - immunology | Multiple Sclerosis - therapy | Animals | Coronavirus Infections - virology | Coronavirus Infections - therapy | Coronavirus Infections - pathology | Multiple Sclerosis - immunology | Multiple Sclerosis - pathology | Mice | Embryoid Bodies - immunology | Cell culture | Multiple sclerosis | Spinal cord | Transplants & implants | Embryo cells | Central nervous system | Stem cell transplantation | Viruses | Nervous system | Transplantation | Lymphocytes T | Biochemistry | Recovery | Hepatitis | Immunology | Demyelination | Lymphocytes | Precursors | Rodents | Neural cell transplants | Cell cycle | Foxp3 protein | Physiology | Immunoregulation | Inflammation | Gene expression | CD4 antigen | Medicine | Myelination | Brain research | Stem cells | Molecular biology | Differentiation | Pluripotency
Journal Article
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 9/2011, Volume 108, Issue 38, pp. 15978 - 15983
Antiviral compounds that increase the resistance of host tissues represent an attractive class of therapeutic. Here, we show that squalamine, a compound... 
Hepatocytes | Liver | Humans | Antivirals | Viruses | Lipids | Infections | Cell membranes | Endothelial cells | P branes | Innate immunity | Hepatitis B virus | Dengue virus | Eastern equine encephalitis virus | Yellow fever virus | FEVER VIRUS-INFECTION | MURINE CYTOMEGALOVIRUS-INFECTION | hepatitis B virus | MULTIDISCIPLINARY SCIENCES | dengue virus | HAMSTER MESOCRICETUS-AURATUS | MATRIX DOMAIN | YELLOW-FEVER | GAG MEMBRANE-BINDING | VACCINE CANDIDATES | yellow fever virus | innate immunity | eastern equine encephalitis virus | EASTERN EQUINE ENCEPHALITIS | ANGIOGENESIS INHIBITOR | Hepatitis B virus - growth & development | Male | Virus Diseases - virology | Cell Membrane - chemistry | Cholestanols - chemistry | Virus Diseases - drug therapy | Antiviral Agents - chemistry | X-Ray Diffraction | Anti-Bacterial Agents - chemistry | Mesocricetus | Female | Hepatitis Delta Virus - drug effects | Molecular Structure | rac1 GTP-Binding Protein - chemistry | Cell Membrane - drug effects | Hepatocytes - drug effects | Cell Line | Virus Replication - drug effects | Antiviral Agents - pharmacology | Cricetinae | Hepatitis Delta Virus - growth & development | Cells, Cultured | Scattering, Small Angle | Muromegalovirus - growth & development | Muromegalovirus - drug effects | Cholestanols - pharmacology | Hepatitis B virus - drug effects | Animals | Hepatocytes - virology | Anti-Bacterial Agents - pharmacology | Mice | Mice, Inbred BALB C | Antiviral agents | Research | Health aspects | Biological Sciences
Journal Article
Journal of Applied Microbiology, ISSN 1364-5072, 04/2018, Volume 124, Issue 4, pp. 965 - 976
Aim To assess the potential of a viability dye and an enzymatic reverse transcription quantitative PCR (RT‐qPCR) pretreatment to discriminate between... 
viruses | enzymatic PCR | infectivity | heat inactivation | viability PCR | public health | LISTERIA-MONOCYTOGENES | ETHIDIUM MONOAZIDE TREATMENT | FRESH-CUT VEGETABLES | QUANTITATIVE PCR | MICROBIOLOGY | REAL-TIME PCR | ENTERIC VIRUSES | REVERSE-TRANSCRIPTION-PCR | BIOTECHNOLOGY & APPLIED MICROBIOLOGY | MICROBIAL INDICATORS | MURINE NOROVIRUS-1 | PROPIDIUM MONOAZIDE | Norovirus - chemistry | Norovirus - physiology | Caliciviridae Infections - virology | Ribonucleases - chemistry | Hepatitis A virus - genetics | Humans | Real-Time Polymerase Chain Reaction - methods | Enterovirus - isolation & purification | Hot Temperature | Reverse Transcriptase Polymerase Chain Reaction | Hepatitis A virus - physiology | Enterovirus - chemistry | Enterovirus - genetics | Enterovirus Infections - virology | Norovirus - growth & development | Enterovirus - growth & development | Hepatitis A - virology | Hepatitis A virus - growth & development | Hepatitis A virus - chemistry | Virus Inactivation | Norovirus - genetics | Hepatitis A virus | Surface active agents | Risk assessment | Diagnosis | Ribonuclease | Health aspects | Hepatitis A | Public health | Cell culture | Dyes | Deactivation | Triton | Health risks | Reverse transcription | Viruses | Surfactants | Inactivation | Assaying | Hepatitis | Enteroviruses | Ribonuclease IV | Infectious diseases | Infectivity | Plaque assay | Pretreatment | Pollutants | Health risk assessment | Viability
Journal Article