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1. |
Record Nr. |
UNINA9910465040903321 |
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Titolo |
Fundamentalism : perspectives on a contested history / / edited by Simon A. Wood and David Harrington Watt |
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Pubbl/distr/stampa |
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Columbia, South Carolina : , : The University of South Carolina Press, , 2014 |
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©2014 |
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ISBN |
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Descrizione fisica |
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1 online resource (295 p.) |
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Collana |
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Studies in Comparative Religion |
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Disciplina |
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Soggetti |
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Religious fundamentalism - History |
Electronic books. |
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Lingua di pubblicazione |
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Formato |
Materiale a stampa |
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Livello bibliografico |
Monografia |
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Note generali |
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Description based upon print version of record. |
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Nota di bibliografia |
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Includes bibliographical references and index. |
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Nota di contenuto |
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Cover; FUNDAMENTALISM; Title; Copyright; Contents; Series Editor's Preface; Acknowledgments; Introduction; Fundamentalists of the 1920's and 1930's; The Idea of Militancy in American Fundamentalism; Fundamentalism and Christianity; "America Is No Different," "America Is Different"-Is There an American Jewish Fundamentalism? Part I. American Habad; "America Is No Different," "America Is Different"-Is There an American Jewish Fundamentalism? Part II. American Satmar; The Jewish Settler Movement and the Concept of Fundamentalism; The Concept of Global Fundamentalism: A Short Critique |
Muslim "Fundamentalism," Salafism, Sufism, and Other Trends Fundamentalism and Shiism; Fundamentalism, Khomeinism, and the Islamic Republic of Iran; Fundamentalism Diluted: From Enclave to Globalism in Conservative Muslim Ecological Discourse; Islamic Education and the Limitations of Fundamentalism as an Analytical Category; Conclusion; Afterword; Selected Bibliography; Contributors; Index |
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Sommario/riassunto |
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Through a collection of essays, Fundamentalism: Perspectives on a Contested History explores the ways in which the concept of global fundamentalism does and does not illuminate developments in modern Christianity, Judaism, and Islam. At issue is whether, beyond the specific milieu of American Protestantism in the early decades of the |
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twentieth century, the word 'fundamentalism' captures something important on a global scale that is not captured-or not as well-by other words. Readers will quickly discover that in exploring this issue the book is "at war with itself."In Fundamentalism Simon A. W |
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2. |
Record Nr. |
UNINA9910838993703321 |
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Titolo |
Omodeo tra storicismo e storicismo / Fulvio Tessitore |
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Pubbl/distr/stampa |
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[Bologna], : Societa Editrice il Mulino, 1990? |
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Descrizione fisica |
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Locazione |
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Collocazione |
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Lingua di pubblicazione |
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Formato |
Materiale a stampa |
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Livello bibliografico |
Monografia |
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Note generali |
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Estratto da: Annali dell'Istituto Italiano per gli studi storici, 11(1989-1990) |
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3. |
Record Nr. |
UNINA9911019298203321 |
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Titolo |
Pseudo-peptides in drug discovery / / [edited by] Peter E. Neilsen |
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Pubbl/distr/stampa |
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Weinheim, : Wiley-VCH, c2004 |
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ISBN |
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9786610520695 |
9781280520693 |
1280520698 |
9783527605699 |
352760569X |
9783527601905 |
3527601902 |
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Descrizione fisica |
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1 online resource (258 p.) |
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Altri autori (Persone) |
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Disciplina |
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Soggetti |
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Peptide drugs - Design |
Peptides |
Amino acids - Synthesis |
Polyamides |
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Lingua di pubblicazione |
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Formato |
Materiale a stampa |
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Livello bibliografico |
Monografia |
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Note generali |
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Description based upon print version of record. |
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Nota di bibliografia |
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Includes bibliographical references and index. |
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Nota di contenuto |
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Pseudo-peptides in Drug Discovery; Contents; Preface; List of Contributors; 1 Versatile Oligo(N-Substituted) Glycines: The Many Roles of Peptoids in Drug Discovery; 1.1 Introduction; 1.2 Peptoid Synthesis; 1.2.1 Solid-Phase Synthesis; 1.2.2 Sub-monomer Solid-Phase Method; 1.2.3 Side Reactions; 1.2.4 Post-Synthetic Analysis; 1.3 Drug Discovery via Small-Molecule Peptoid Libraries; 1.3.1 Peptoid Drugs from Combinatorial Libraries; 1.3.2 Peptoid Inhibitors of RNA-Protein Interactions; 1.4 Peptoid-Based Drug Delivery and Molecular Transporters: Cellular Uptake |
1.4.1 Peptoid Mimics of HIV-Tat Protein1.4.2 Cellular Delivery of Nucleic Acids; 1.5 Peptoid Mimics of Peptide Ligands; 1.6 Peptoids with Folded Structure; 1.6.1 Restricting Conformational Space; 1.6.2 Peptoid Helices; 1.6.2.1 CD and NMR Studies of a Helical Peptoid Pentamer with α-Chiral Aromatic Side Chains; 1.6.2.2 CD Studies of Longer Peptoid |
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Helices Containing α-Chiral Aromatic Side Chains; 1.6.2.3 Structural Studies of Peptoids with Aliphatic Side Chains by CD, NMR, and X-ray Crystallography; 1.6.2.4 Summary; 1.6.3 Protein-mimetic Structures |
1.7 Biomimetic Peptoid Structures for Therapeutic Applications1.7.1 Peptoid Mimics of Antibacterial Peptides; 1.7.2 Peptoid-Based Mimics of Lung Surfactant Proteins; 1.7.3 Collagen-based Structures Containing Peptoid Residues; 1.8 Obstacles to the Development of Biomedically-useful Peptoids; 1.8.1 Enhance the Diversity of Secondary Structure in Peptoid Foldamers; 1.8.2 Improve Understanding of Peptoid Sequence/Structure Relationships; 1.8.3 Translate Bioactive Peptide Sequences into Bioactive Peptoid Sequences; 1.8.4 Develop Peptoids with Stable Tertiary Structure |
1.8.5 Develop Peptoid Shuttles for Intracellular Import of Xenobiotic Agents1.8.6 Optimize Pharmacological Profile of Oligopeptoids; 1.9 Conclusion; 1.10 References; 2 β-Peptides, γ-Peptides and Isosteric Backbones: New Scaffolds with Controlled Shapes for Mimicking Protein Secondary Structure Elements; 2.1 Introduction; 2.2 Molecular Organization in β-Peptide Oligomers; 2.2.1 Historical Background; 2.2.2 β-Amino Acids versus α-Amino Acids: An Enormous Increase in Chemical Diversity; 2.2.3 Helical Folds; 2.2.3.1 The 3(14)-Helix; 2.2.3.2 The 12/10- (10/12-) Helix; 2.2.3.3 The 2.5(12)-Helix |
2.2.3.4 The 2(8)-Helix2.2.4 Extended β-Peptide Strands, Turns and Formation of Sheet Structures; 2.3 Molecular Organization in γ-Peptide Oligomers; 2.3.1 Preparation of γ-Amino Acid Monomers for γ-Peptide Synthesis; 2.3.2 Helical Folds; 2.3.3 Turn and Sheet Structures; 2.4 Biological Activities of β- and γ-Peptides; 2.4.1 Biological Stability; 2.4.2 Bioactive Peptides Based on Helical Scaffolds; 2.4.3 Bioactive Peptides Based on Open-Chain β-Turn Mimetics; 2.4.4 Cell Penetrating β-Peptides; 2.5 Isosteres; 2.5.1 Example 1: Oligomers of α-Aminooxy Acids as β-Peptide Mimetics |
2.5.2 Example 2: N,N ́-Linked Oligoureas as γ-Peptide Mimetics |
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Sommario/riassunto |
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Peptides are among the most versatile bioactive molecules, yet the do not make good drugs, because they are quickly degraded or modified in the body.To overcome this problem, stable and at the same time biologically active pseudo-peptides have been developed. These novel compounds open up new perspectives in drug design by providing an entire range of highly specific and non-toxic pharmaceuticals.This is the first work devoted to the topic and draws together knowledge gained on different types of peptidomimetics and other pseudo-peptides with drug properties. As such, it includes pepto |
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