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Histone Deacetylase Inhibitors in Combinatorial Anticancer Therapy, Ganai Shabir Ahmad


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Цена: 20962.00р.
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Автор: Ganai Shabir Ahmad
Название:  Histone Deacetylase Inhibitors in Combinatorial Anticancer Therapy
ISBN: 9789811581816
Издательство: Springer
Классификация:



ISBN-10: 9811581819
Обложка/Формат: Paperback
Страницы: 278
Вес: 0.39 кг.
Дата издания: 08.12.2021
Язык: English
Издание: 1st ed. 2020
Иллюстрации: 13 illustrations, color; 14 illustrations, black and white; xvii, 258 p. 27 illus., 13 illus. in color.
Размер: 23.39 x 15.60 x 1.47 cm
Читательская аудитория: Professional & vocational
Ссылка на Издательство: Link
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Поставляется из: Германии
Описание: This book reviews the latest developments in the design, synthesis, and molecular mechanism of action of Histone Deacetylase (HDAC) inhibitors in the context of potential cancer therapy.


Histone Deacetylases

Автор: Eric Verdin
Название: Histone Deacetylases
ISBN: 1617376027 ISBN-13(EAN): 9781617376023
Издательство: Springer
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Цена: 34799.00 р.
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Описание: A panel of leading investigators summarizes and synthesizes the new discoveries in the rapidly evolving field of histone acetylation as a key regulatory mechanism for gene expression.

PARP Inhibitors for Cancer Therapy

Автор: Nicola J. Curtin; Ricky A. Sharma
Название: PARP Inhibitors for Cancer Therapy
ISBN: 3319141503 ISBN-13(EAN): 9783319141503
Издательство: Springer
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Цена: 23757.00 р.
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Описание: PARP Inhibitors for Cancer Therapy provides a comprehensive overview of the role of PARP in cancer therapy. PARP plays a pivotal role in DNA repair and may contribute to the therapeutic resistance to DNA damaging agents used to treat cancer.

Parp Inhibitors for Cancer Therapy

Автор: Curtin Nicola J., Sharma Ricky A.
Название: Parp Inhibitors for Cancer Therapy
ISBN: 3319344897 ISBN-13(EAN): 9783319344898
Издательство: Springer
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Цена: 20962.00 р.
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Описание: PARP Inhibitors for Cancer Therapy provides a comprehensive overview of the role of PARP in cancer therapy. The volume covers the history of the discovery of PARP (poly ADP ribose polymerase) and its role in DNA repair. In addition, a description of discovery of the PARP family, and other DNA maintenance-associated PARPs will also be discussed. The volume also features a section on accessible chemistry behind the development of inhibitors. PARP inhibitors are a group of pharmacological inhibitors that are a particularly good target for cancer therapy. PARP plays a pivotal role in DNA repair and may contribute to the therapeutic resistance to DNA damaging agents used to treat cancer. Researchers have learned a tremendous amount about the biology of PARP and how tumour-specific defects in DNA repair can be exploited by PARPi. The “synthetic lethality” of PARPi is an exciting concept for cancer therapy and has led to a heightened activity in this area.

Histone Deacetylase Inhibitors in Combinatorial Anticancer Therapy

Автор: Ganai Shabir Ahmad
Название: Histone Deacetylase Inhibitors in Combinatorial Anticancer Therapy
ISBN: 9811581789 ISBN-13(EAN): 9789811581786
Издательство: Springer
Цена: 20962.00 р.
Наличие на складе: Есть у поставщика Поставка под заказ.

Описание: This book reviews the latest developments in the design, synthesis, and molecular mechanism of action of Histone Deacetylase (HDAC) inhibitors in the context of potential cancer therapy.

Histone Deacetylase Inhibitors — Epidrugs for Neurological Disorders

Автор: Shabir Ahmad Ganai
Название: Histone Deacetylase Inhibitors — Epidrugs for Neurological Disorders
ISBN: 981138018X ISBN-13(EAN): 9789811380181
Издательство: Springer
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Цена: 19564.00 р.
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Описание: This book provides an outline of epigenetics as a whole, while also specifically examining a range of epigenetic players, including histone acetyl transferases (HATs) and histone deacetylases (HDACs). It chiefly focuses on the emerging targets of HDACs and their implications for various neurological disorders, while also discussing the drawbacks of current therapeutic strategies, the classification of HDAC inhibitors, and their promising effects in connection with specific neurological disorders. The book explores the potential use of these inhibitors as novel therapeutic agents, considers the current challenges involved in using them to tackle neurological complications, and offers a novel solution by designing isoform-selective inhibitors and employing combinatorial therapeutic strategies. Its final section, which explores future directions, elaborates on the possibility of enhancing HDAC inhibitors’ therapeutic efficacy against various neurological complications.

Histone Deacetylases: the Biology and Clinical Implication

Автор: Tso-Pang Yao; Edward Seto
Название: Histone Deacetylases: the Biology and Clinical Implication
ISBN: 3642270859 ISBN-13(EAN): 9783642270857
Издательство: Springer
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Цена: 41925.00 р.
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Описание: The book highlights work from many different labs that taught us abnormal HDACs potentially contribute to the development or progression of many human diseases including immune dysfunctions, heart disease, cancer, memory impairment, aging, and metabolic disorders.

Farnesyltransferase Inhibitors in Cancer Therapy

Автор: Sa?d M. Sebti; Andrew D. Hamilton
Название: Farnesyltransferase Inhibitors in Cancer Therapy
ISBN: 1468496069 ISBN-13(EAN): 9781468496062
Издательство: Springer
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Цена: 20962.00 р.
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Cell Cycle Inhibitors in Cancer Therapy

Автор: Antonio Giordano; Kenneth J. Soprano
Название: Cell Cycle Inhibitors in Cancer Therapy
ISBN: 1617372579 ISBN-13(EAN): 9781617372575
Издательство: Springer
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Цена: 32004.00 р.
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Описание: Leading clinicians and investigators review in a comprehensible and user-friendly style all the latest information about the molecular biology of cell cycle control and demonstrate its clinical relevance to understanding neoplastic diseases.

mTOR Pathway and mTOR Inhibitors in Cancer Therapy

Автор: Vitaly A. Polunovsky; Peter J. Houghton
Название: mTOR Pathway and mTOR Inhibitors in Cancer Therapy
ISBN: 1617796948 ISBN-13(EAN): 9781617796944
Издательство: Springer
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Цена: 28732.00 р.
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Описание: The target of rapamycin (TOR) was rst identi ed in Saccharomyces cerevisiae and subsequently in mammals (mTOR) as a conserved atypical serine/threonine kinase. Rapamycin was isolated as a product of the soil bacteria Streptomyces hygroscopicus, identi ed in a soil sample taken from the island of Rapa Nui (Easter Island).


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