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Published by VDM Verlag Dr. Müller, 2008
ISBN 10: 3836490013 ISBN 13: 9783836490016
Language: English
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Published by VDM Verlag Dr. Müller, 2008
ISBN 10: 3836490013 ISBN 13: 9783836490016
Language: English
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Published by VDM Verlag Dr. Müller, 2008
ISBN 10: 3836490013 ISBN 13: 9783836490016
Language: English
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Published by VDM Verlag Dr. Müller, 2008
ISBN 10: 3836490013 ISBN 13: 9783836490016
Language: English
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Published by VDM Verlag Dr. M�ller 2008-04-08, 2008
ISBN 10: 3836490013 ISBN 13: 9783836490016
Language: English
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Published by GRIN Verlag, GRIN Verlag Jul 2020, 2020
ISBN 10: 3346206017 ISBN 13: 9783346206015
Language: English
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Add to basketTaschenbuch. Condition: Neu. Neuware -Academic Paper from the year 2020 in the subject Biology - Genetics / Gene Technology, grade: 9.0, , course: Cell Biology and Genetics, language: English, abstract: Nucleic acids have proven to be viable targets for small molecule drugs. While many examples of such drugs are detailed in the literature, only a select few have found practical use in a clinical setting. These currently employed nucleic acid targeting therapies suffer from either debilitating off-target side effects or succumb to a resistance mechanism of the target. The need for new small molecules that target nucleic acids is evident.However, designing a novel drug to bind to DNA or RNA requires a detailed understanding of exactly what binding environments each nucleic acid presents. In an effort to broaden this knowledge, the work presented in this thesis details the binding location and affinity of known and novel nucleic acid binding small molecules with targets ranging from simple RNA secondary structure all the way to the complex structure of ribosomal RNA. Specifically, it is shown that the anthracycline classes of antineoplastics prefer to bind at or near mismatch base pairs in both physiologically relevant iron responsive element RNA hairpin constructs as well as DNA hairpin constructs presenting mismatched base pairs.Also characterized in this thesis is a novel class of topoisomerase II / histone deacetylase inhibitor conjugates that display a unique affinity for DNA over RNA. Finally, the novel class of macrolide-peptide conjugates, known as peptolides, is shown to retain potent translation inhibition of the prokaryotic ribosome and identification of a novel binding site for the anthracycline class of drugs and the characterization of the two novel drug designs presented in this thesis will undoubtedly aid in the effort to design and discover new molecules that aim for nucleic acid targets.Books on Demand GmbH, Überseering 33, 22297 Hamburg 32 pp. Englisch.
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Add to basketTaschenbuch. Condition: Neu. Druck auf Anfrage Neuware - Printed after ordering - Academic Paper from the year 2020 in the subject Biology - Genetics / Gene Technology, grade: 9.0, , course: Cell Biology and Genetics, language: English, abstract: Nucleic acids have proven to be viable targets for small molecule drugs. While many examples of such drugs are detailed in the literature, only a select few have found practical use in a clinical setting. These currently employed nucleic acid targeting therapies suffer from either debilitating off-target side effects or succumb to a resistance mechanism of the target. The need for new small molecules that target nucleic acids is evident.However, designing a novel drug to bind to DNA or RNA requires a detailed understanding of exactly what binding environments each nucleic acid presents. In an effort to broaden this knowledge, the work presented in this thesis details the binding location and affinity of known and novel nucleic acid binding small molecules with targets ranging from simple RNA secondary structure all the way to the complex structure of ribosomal RNA. Specifically, it is shown that the anthracycline classes of antineoplastics prefer to bind at or near mismatch base pairs in both physiologically relevant iron responsive element RNA hairpin constructs as well as DNA hairpin constructs presenting mismatched base pairs.Also characterized in this thesis is a novel class of topoisomerase II / histone deacetylase inhibitor conjugates that display a unique affinity for DNA over RNA. Finally, the novel class of macrolide-peptide conjugates, known as peptolides, is shown to retain potent translation inhibition of the prokaryotic ribosome and identification of a novel binding site for the anthracycline class of drugs and the characterization of the two novel drug designs presented in this thesis will undoubtedly aid in the effort to design and discover new molecules that aim for nucleic acid targets.
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Add to basketTaschenbuch. Condition: Neu. Effect of Small Molecules on Nucleic Acid Stability and Improvements to RNA Structure Prediction | Kehinde Sowunmi | Taschenbuch | 32 S. | Englisch | 2020 | GRIN Verlag | EAN 9783346206015 | Verantwortliche Person für die EU: BoD - Books on Demand, In de Tarpen 42, 22848 Norderstedt, info[at]bod[dot]de | Anbieter: preigu.
Published by Walter de Gruyter, Berlin, 2013
ISBN 10: 3110284596 ISBN 13: 9783110284591
Language: English
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Seller: Ria Christie Collections, Uxbridge, United Kingdom
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Published by Springer-Verlag New York Inc., New York, NY, 2024
ISBN 10: 1071627708 ISBN 13: 9781071627709
Language: English
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Paperback. Condition: new. Paperback. This book explores recent progress in RNA secondary, tertiary structure prediction, and its application from an expansive point of view. Because of advancements in experimental protocols and devices, the integration of new types of data as well as new analysis techniques is necessary, and this volume discusses additional topics that are closely related to RNA structure prediction, such as the detection of structure-disrupting mutations, high-throughput structure analysis, and 3D structure design. Written for the highly successful Methods in Molecular Biology series, chapters feature the kind of detailed implementation advice that leads to quality research results. Authoritative and practical, RNA Structure Prediction serves as a valuable guide for both experimental and computational RNA researchers. Shipping may be from multiple locations in the US or from the UK, depending on stock availability.
Published by Springer-Verlag Berlin and Heidelberg GmbH & Co. KG, Berlin, 2014
ISBN 10: 3642445691 ISBN 13: 9783642445699
Language: English
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Paperback. Condition: new. Paperback. With the dramatic increase in RNA 3D structure determination in recent years, we now know that RNA molecules are highly structured. Moreover, knowledge of RNA 3D structures has proven crucial for understanding in atomic detail how they carry out their biological functions. Because of the huge number of potentially important RNA molecules in biology, many more than can be studied experimentally, we need theoretical approaches for predicting 3D structures on the basis of sequences alone. This volume provides a comprehensive overview of current progress in the field by leading practitioners employing a variety of methods to model RNA 3D structures by homology, by fragment assembly, and by de novo energy and knowledge-based approaches. With the dramatic increase in RNA 3D structure determination in recent years, we now know that RNA molecules are highly structured. Shipping may be from multiple locations in the US or from the UK, depending on stock availability.
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Published by Springer-Verlag Berlin and Heidelberg GmbH & Co. KG, Berlin, 2012
ISBN 10: 3642257399 ISBN 13: 9783642257391
Language: English
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Hardcover. Condition: new. Hardcover. With the dramatic increase in RNA 3D structure determination in recent years, we now know that RNA molecules are highly structured. Moreover, knowledge of RNA 3D structures has proven crucial for understanding in atomic detail how they carry out their biological functions. Because of the huge number of potentially important RNA molecules in biology, many more than can be studied experimentally, we need theoretical approaches for predicting 3D structures on the basis of sequences alone. This volume provides a comprehensive overview of current progress in the field by leading practitioners employing a variety of methods to model RNA 3D structures by homology, by fragment assembly, and by de novo energy and knowledge-based approaches. With the dramatic increase in RNA 3D structure determination in recent years, we now know that RNA molecules are highly structured. Shipping may be from multiple locations in the US or from the UK, depending on stock availability.
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Add to basketpaperback. Condition: New. Language:Chinese.Paperback. Pub Date: 2024-02 Pages: 244 Publisher: Science Press This book introduces the structural characteristics of RNA. especially the characteristics of RNA tertiary structure. conformational sampling representation model. Rosetta framework. cell deconvolution algorithm. transcription factor binding site prediction algorithm. specific site prediction algorithm. etc.; studies the RNA tertiary structure prediction algorithm and complexity. the construction of conformation.
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Condition: New. pp. 412.