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1. Full Text Antiviral drug resistance in herpesviruses other than cytomegalovirus
by Piret, Jocelyne and Boivin, Guy
Reviews in medical virology, ISSN 1052-9276, 05/2014, Volume 24, Issue 3, pp. 186 - 218
Life Sciences & Biomedicine | Science & Technology | Virology | Cytosine - analogs & derivatives | Acyclovir - therapeutic use | Humans | Herpesvirus 2, Human - metabolism | Herpesvirus 2, Human - genetics | Herpesvirus 3, Human - drug effects | Herpesvirus 3, Human - metabolism | Ganciclovir - therapeutic use | Cytosine - therapeutic use | Herpesvirus 2, Human - drug effects | Herpesvirus 6, Human - drug effects | Cytomegalovirus - genetics | Herpesvirus 1, Human - metabolism | Herpesvirus 6, Human - metabolism | Organophosphonates - therapeutic use | Antiviral Agents - therapeutic use | Cytomegalovirus - metabolism | Herpesvirus 6, Human - genetics | Herpesviridae Infections - virology | Herpesviridae Infections - drug therapy | Herpesvirus 3, Human - genetics | Herpesvirus 1, Human - drug effects | Drug Resistance, Viral - genetics | Herpesvirus 1, Human - genetics | Foscarnet - therapeutic use | Immunocompromised Host | Cytomegalovirus - drug effects | Herpesviridae Infections - immunology | Antiviral agents | Herpesviruses | Drug resistance | Drug therapy | Index Medicus
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2. Full Text CDK9 inhibitor FIT-039 prevents replication of multiple DNA viruses
by Yamamoto, Makoto and Onogi, Hiroshi and Kii, Isao and Yoshida, Suguru and Iida, Kei and Sakai, Hiroyuki and Abe, Minako and Tsubota, Toshiaki and Ito, Nobutoshi and Hosoya, Takamitsu and Hagiwara, Masatoshi
The Journal of clinical investigation, ISSN 0021-9738, 08/2014, Volume 124, Issue 8, pp. 3479 - 3488
Life Sciences & Biomedicine | Medicine, Research & Experimental | Science & Technology | Research & Experimental Medicine | Transcription, Genetic - drug effects | Rats, Wistar | Antiviral Agents - toxicity | Pyridines - chemistry | Humans | Drug Resistance, Viral | Host-Pathogen Interactions - drug effects | DNA Viruses - genetics | Herpes Simplex - drug therapy | Herpesvirus 1, Human - physiology | Protein Kinase Inhibitors - chemistry | Piperidines - pharmacology | Antiviral Agents - chemistry | HEK293 Cells | Flavonoids - pharmacology | DNA Viruses - physiology | Cytomegalovirus - physiology | Herpesvirus 2, Human - drug effects | Disease Models, Animal | Virus Replication - drug effects | Antiviral Agents - pharmacology | Acyclovir - pharmacology | Adenoviruses, Human - physiology | Rats | Cyclin-Dependent Kinase 9 - antagonists & inhibitors | Transcriptome - drug effects | Mice, Inbred ICR | Herpesvirus 1, Human - drug effects | Herpes Simplex - virology | Animals | Host-Pathogen Interactions - genetics | Pyridines - toxicity | Herpes Simplex - pathology | Adenoviruses, Human - drug effects | Protein Kinase Inhibitors - toxicity | Herpesvirus 2, Human - physiology | Mice | Protein Kinase Inhibitors - pharmacology | Pyridines - pharmacology | HeLa Cells | DNA Viruses - drug effects | Cytomegalovirus - drug effects | Physiological aspects | Research | DNA viruses | Health aspects | Protein kinases | Medical research | Drug resistance | Kinases | Cell cycle | Index Medicus | Abridged Index Medicus
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3. Full Text Curcumin Inhibits Proliferation of Epstein–Barr Virus-Associated Human Nasopharyngeal Carcinoma Cells by Inhibiting EBV Nuclear Antigen 1 Expression
by Liu, Limei and Yang, Jiaomin and Ji, Wuguang and Wang, Chao
BioMed research international, ISSN 2314-6133, 10/2019, Volume 2019, pp. 8592921 - 10
Life Sciences & Biomedicine | Biotechnology & Applied Microbiology | Medicine, Research & Experimental | Science & Technology | Research & Experimental Medicine | Virus Replication - drug effects | Nasopharyngeal Neoplasms - metabolism | Apoptosis - drug effects | Humans | Curcumin - pharmacology | Nasopharyngeal Neoplasms - virology | Ubiquitin - metabolism | Nasopharyngeal Carcinoma - metabolism | Mitochondria - metabolism | Mitochondria - drug effects | RNA, Messenger - metabolism | Nasopharyngeal Carcinoma - virology | Proteasome Endopeptidase Complex - drug effects | Signal Transduction - drug effects | Mitochondria - virology | Cell Line, Tumor | Nasopharyngeal Carcinoma - drug therapy | Cell Proliferation - drug effects | Herpesvirus 4, Human - pathogenicity | HeLa Cells | Nasopharyngeal Neoplasms - drug therapy | Proteasome Endopeptidase Complex - metabolism | Cell Cycle - drug effects | Epstein-Barr Virus Nuclear Antigens - metabolism | Antigens | Carcinoma | RNA | Analysis | Epstein-Barr virus | Cancer | Apoptosis | Cell proliferation | Ubiquitin | Flow cytometry | Transcription | Viruses | Cell viability | Infections | Gene expression | Lymphoma | Western blotting | Anticancer properties | Nanoparticles | Proteins | Nasopharyngeal carcinoma | Mitochondria | Cell growth | Cell cycle | Antitumor activity | Curcumin | Inhibition | Cholecystokinin | Index Medicus
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4. Full Text β-Amyloid peptides display protective activity against the human Alzheimer’s disease-associated herpes simplex virus-1
by Bourgade, Karine and Bourgade, Karine and Garneau, Hugo and Garneau, Hugo and Giroux, Geneviève and Giroux, Geneviève and Le Page, Aurélie Y and Le Page, Aurélie Y and Bocti, Christian and Bocti, Christian and Dupuis, Gilles and Dupuis, Gilles and Frost, Eric H and Frost, Eric H and Fülöp Jr, Tamàs and Fülöp Jr, Tamàs
Biogerontology (Dordrecht), ISSN 1389-5729, 2/2015, Volume 16, Issue 1, pp. 85 - 98
Life Sciences | Alzheimer’s disease | Geriatrics/Gerontology | Human adenovirus type 5 | Antimicrobial peptides | Viral replication inhibition | Developmental Biology | Beta-amyloid peptides | Herpes simplex virus-1 | Cell Biology | Life Sciences & Biomedicine | Geriatrics & Gerontology | Science & Technology | Fibroblasts - virology | Cell Line | Virus Replication - drug effects | Neuroglia - pathology | Amyloid beta-Peptides - pharmacology | Epithelial Cells - drug effects | Humans | Risk Factors | Epithelial Cells - pathology | Peptide Fragments - pharmacology | Fibroblasts - pathology | Herpesvirus 1, Human - drug effects | Neuroglia - drug effects | Alzheimer Disease - virology | Herpesvirus 1, Human - physiology | Amyloid beta-Peptides - therapeutic use | Epithelial Cells - virology | Fibroblasts - drug effects | Cell Line, Tumor | Plaque, Amyloid - virology | Alzheimer Disease - epidemiology | Herpes Simplex - prevention & control | Peptide Fragments - therapeutic use | Neuroglia - virology | Index Medicus
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5. Full Text Standard-dose and high-dose daily antiviral therapy for short episodes of genital HSV-2 reactivation: three randomised, open-label, cross-over trials
by Johnston, Christine, Dr and Saracino, Misty, PhD and Kuntz, Steve, PA-C and Magaret, Amalia, PhD and Selke, Stacy, MS and Huang, Meei-li, PhD and Schiffer, Joshua T, MD and Koelle, David M, Prof and Corey, Lawrence, Prof and Wald, Anna, Prof
The Lancet (British edition), ISSN 0140-6736, 2012, Volume 379, Issue 9816, pp. 641 - 647
Internal Medicine | Medicine, General & Internal | Life Sciences & Biomedicine | General & Internal Medicine | Science & Technology | Antiviral agents | General aspects | Infectious diseases | Pharmacology. Drug treatments | Viral diseases | Biological and medical sciences | Medical sciences | Antibiotics. Antiinfectious agents. Antiparasitic agents | Herpesvirus 2, Human - isolation & purification | Recurrence | Humans | Middle Aged | DNA, Viral - isolation & purification | Acyclovir - adverse effects | Male | Valine - administration & dosage | Herpes Genitalis - drug therapy | Herpesvirus 2, Human - genetics | Polymerase Chain Reaction | Adult | Female | Herpesvirus 2, Human - drug effects | Acute Disease | DNA, Viral - drug effects | Drug Administration Schedule | Acyclovir - analogs & derivatives | Valine - analogs & derivatives | Treatment Outcome | Antiviral Agents - administration & dosage | Cross-Over Studies | Antiviral Agents - adverse effects | Herpes Genitalis - virology | Valine - adverse effects | Acyclovir - administration & dosage | Physiological aspects | Complications and side effects | Dosage and administration | Herpes simplex virus | Studies | Design | Laboratories | Herpes viruses | Mathematical models | Drug therapy | Drug dosages | Deoxyribonucleic acid--DNA | Human subjects | Manuscripts | Index Medicus | Abridged Index Medicus
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6. Full Text Inhibitors of dual-specificity tyrosine phosphorylation-regulated kinases (DYRK) exert a strong anti-herpesviral activity
by Hutterer, Corina and Milbradt, Jens and Hamilton, Stuart and Zaja, Mirko and Leban, Johann and Henry, Christophe and Vitt, Daniel and Steingruber, Mirjam and Sonntag, Eric and Zeitträger, Isabel and Bahsi, Hanife and Stamminger, Thomas and Rawlinson, William and Strobl, Stefan and Marschall, Manfred
Antiviral research, ISSN 0166-3542, 07/2017, Volume 143, pp. 113 - 121
Virus-induced upregulation of DYRK1A and DYRK1B | Antiviral therapy | Broad anti-herpesviral activity | Antiviral drug target | DYRK inhibitors | Human cytomegalovirus | Pharmacology & Pharmacy | Life Sciences & Biomedicine | Science & Technology | Virology | Phosphorylation | Humans | Cercopithecus aethiops | Antiviral Agents - antagonists & inhibitors | Drug Delivery Systems | Gene Knockdown Techniques | Harmine - antagonists & inhibitors | Microbial Sensitivity Tests | Macaca mulatta - virology | Herpesvirus 3, Human - drug effects | Protein-Tyrosine Kinases - genetics | Sensitivity and Specificity | Protein-Tyrosine Kinases - drug effects | Vero Cells | Fibroblasts - virology | Cell Line | Cell Survival - drug effects | Virus Replication - drug effects | Ganciclovir - antagonists & inhibitors | Herpesviridae - drug effects | Protein-Serine-Threonine Kinases - genetics | Drug Discovery | Herpesvirus 1, Human - drug effects | Animals | Signal Transduction - drug effects | Cell Differentiation - drug effects | Protein-Serine-Threonine Kinases - drug effects | Cell Proliferation - drug effects | Cell Cycle - drug effects | Cytomegalovirus - drug effects | Tyrosine | Phenols | Antiviral agents | Gene expression | Health aspects | Analysis | Index Medicus
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7. Full Text Calcium spirulan derived from Spirulina platensis inhibits herpes simplex virus 1 attachment to human keratinocytes and protects against herpes labialis
by Mader, Julia, MEd and Gallo, Antonio, PhD and Schommartz, Tim, MSc and Handke, Wiebke, PhD and Nagel, Claus-Henning, PhD and Günther, Patrick, RPh and Brune, Wolfram, MD and Reich, Kristian, MD, PhD
Journal of allergy and clinical immunology, ISSN 0091-6749, 2015, Volume 137, Issue 1, pp. 197 - 203.e3
Allergy and Immunology | Herpes simplex virus 1 | Kaposi sarcoma | Spirulina microalgae | calcium spirulan | Kaposi sarcoma–associated herpesvirus/human herpes virus 8 | keratinocytes | herpes labialis | Kaposi sarcoma-associated herpesvirus/human herpes virus 8 | Allergy | Immunology | Life Sciences & Biomedicine | Science & Technology | Herpesvirus 8, Human - drug effects | Keratinocytes - virology | Epithelial Cells - drug effects | Humans | Middle Aged | Cercopithecus aethiops | Young Adult | Herpesvirus 1, Human - physiology | Herpesvirus 8, Human - pathogenicity | Adult | Cosmetics | Female | Vero Cells | Herpesvirus 8, Human - physiology | Polysaccharides - therapeutic use | Cell Line | Antiviral Agents - pharmacology | Antiviral Agents - therapeutic use | Herpes Labialis - prevention & control | Polysaccharides - pharmacology | Herpesvirus 1, Human - drug effects | Virus Attachment - drug effects | Spirulina | Animals | Keratinocytes - drug effects | Epithelial Cells - virology | Aged | Herpesvirus 1, Human - pathogenicity | Herpes simplex | Pharmaceutical industry | Health aspects | Herpes simplex virus | Antiviral agents | Sarcoma | Analysis | Epstein-Barr virus | Sulfates | Cold sores | Infections | Calcium | Algae | Herpes viruses | Methods | Viral infections | Index Medicus | Abridged Index Medicus
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