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The challenges of antibiotic resistance in the development of new therapeutics.

Detalles Bibliográficos
Clasificación:Libro Electrónico
Autor principal: Manuela, Oliveira
Otros Autores: Serrano, Isa D.
Formato: Electrónico eBook
Idioma:Inglés
Publicado: Sharjah : Bentham Science Publishers, 2015.
Colección:Frontiers in Antimicrobial Agents.
Temas:
Acceso en línea:Texto completo

MARC

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100 1 |a Manuela, Oliveira. 
245 1 4 |a The challenges of antibiotic resistance in the development of new therapeutics. 
260 |a Sharjah :  |b Bentham Science Publishers,  |c 2015. 
300 |a 1 online resource (279 pages) 
336 |a text  |b txt  |2 rdacontent 
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490 1 |a Frontiers in Antimicrobial Agents ;  |v v. 1 
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505 0 |6 880-01  |a FOREWORD ; PREFACE ; List of Contributors ; Introduction ; INTRODUCTION; CONFLICT OF INTEREST; ACKNOWLEDGEMENTS; REFERENCES; Bacteriophages as Antibacterial Agents: Why are We Facing an Antibiotic Crisis and How Could Bacteriophages be of Help? ; 1. INTRODUCTION; 2. WHY ARE WE FACING AN ANTIBIOTIC (AB) CRISIS? ; 3. HOW TO RESOLVE THIS ANTIBIOTIC CRISIS? ; 4. BACTERIOPHAGES OR IN SHORT 'PHAGES'; 5. BACTERIOPHAGE THERAPY OR PHAGE THERAPY; 6. EXPERIMENTAL PHAGE THERAPY; 7. SAFETY ISSUES; 8. IN FACT WE LIVE IN AN "OCEAN" OF BACTERIOPHAGES; 9. SAFETY REQUIREMENTS FOR PHAGE THERAPY. 
505 8 |a 10. THE POTENTIAL ADVANTAGES OF PHAGE THERAPY VERSUS ANTIBIOTICS11. PHAGE THERAPY IN PUBLIC HEALTH; 12. WHY PHAGE THERAPY IS NOT YET IMPLEMENTED?; CONCLUSIONS AND PERSPECTIVES; CONFLICT OF INTEREST; ACKNOWLEDGEMENTS; REFERENCES; Antimicrobial Peptides ; INTRODUCTION; 1. WHAT ARE ANTIMICROBIAL PEPTIDES (AMPS); 1.1. Mode of Action; 1.2. Immune System; 1.3. Resistance; 2. CHRONOLOGY OF AMPS DISCOVERY -- A BRIEF HISTORY; 2.1. Classification of AMPs; 2.1.1. Biological Source; 2.1.2. Biological Functions; 2.1.3. Biosynthesis; 2.1.4. Molecular Properties; 2.1.5. Molecular Targets. 
505 8 |a 2.1.6. Three-Dimensional (3D) Structure2.2. Currently Active AMPs Databases; 3. THERAPEUTIC APPLICATIONS OF AMPS; 3.1. Anticancer AMPs; 3.2. Antiviral AMPs; 3.3. Anti-parasitic AMPs; 3.4. New Generation of AMPs; CONCLUDING REMARKS; CONFLICT OF INTEREST; ACKNOWLEDGEMENTS; REFERENCES; Probiotics: Ways of Action and Beneficial Effects ; 1. INTRODUCTION; 2. SELECTION OF PROBIOTICS; 3. COMMERCIALLY IMPORTANT PROBIOTICS; 4. MECHANISMS OF ACTION OF PROBIOTICS; 4.1. Immunomodulation; 4.2. Direct Effects on Other Microorganisms; 5. BENEFICIAL HEALTH EFFECTS OF PROBIOTICS. 
505 8 |a 5.1. Alleviation of Lactose Intolerance5.2. Effect on Helicobacter Pylori Eradication ; 5.3. Anti-carcinogenic Effect; 5.4. Cholesterol-lowering Effects; 5.5. Allergy and Atopic Dermatitis; 5.6. Inflammatory Diseases and Bowel Syndromes ; CONCLUSION; CONFLICT OF INTEREST; ACKNOWLEDGEMENTS; REFERENCES; Immunotherapy ; 1. BACTERIAL INFECTIVITY, IMMUNE RESPONSE AND MULTIRESISTANT INFECTIONS : NEW PERSPECTIVES; 1.1. Introduction; 1.2. Host Resistance; 1.3. Bacterial Strategies for Evading, Surviving Host Defense Systems and Create Infection; 2. IMMUNOTHERAPY; 2.1. Introduction. 
500 |a 2.10.2. Propionibacterium Acnes. 
504 |a Includes bibliographical references at the end of each chapters and index. 
590 |a ProQuest Ebook Central  |b Ebook Central Academic Complete 
650 0 |a Drug resistance in microorganisms. 
650 7 |a Drug resistance in microorganisms  |2 fast 
700 1 |a Serrano, Isa D. 
776 0 8 |i Print version:  |a Manuela, Oliveira.  |t Challenges of antibiotic resistance in the development of new therapeutics.  |d Sharjah : Bentham Science Publishers, ©2015  |z 9781681081410 
830 0 |a Frontiers in Antimicrobial Agents. 
856 4 0 |u https://ebookcentral.uam.elogim.com/lib/uam-ebooks/detail.action?docID=4412594  |z Texto completo 
880 4 |6 264-00/Zsym  |c �[2015] 
880 8 |6 505-01/(S  |a 2.2. Applications of Immunotherapy2.3. Passive Immunotherapy; 2.4. Passive Immunotherapy: Antibodies ; 2.5. Passive Immunotherapy: Adoptive T-cell Transfer; 2.6. Passive Immunotherapy: Immunomodulators; 2.7. Growth Factors; 2.7.1. Filgastrim ; 2.7.2. Sargramostim ; 2.7.3. Erythropoietin (EPO) ; 2.7.4. Insulin-like Growth Factor-1 (IGF-1); 2.8. Interleukins; 2.8.1. Interleukin 2; 2.8.2. Interleukin-8; 2.9. Interferons; 2.9.1. Human Interferon Alpha (HuIFN- α); 2.9.2. Recombinant-Feline Interferon Omega (rFeIFN- ω) ; 2.10. Nonspecific Immunostimulants; 2.10.1. Staphylococcal Protein A (SPA). 
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