Item #:
238650422
Fetal Hemoglobin: The Panacea for Major ?-hemoglobinopathies
Item #:
238650422
XCD 1045
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This book brings together a selection of chapters dedicated to fetal hemoglobin -- its physiological role, regulation, methodologies to manipulate and future strategies.
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- Intricate processes involved in perpetuating the multitude of physiological phenomena in the human body often encounter aberrations and omissions in the genetic code of life. While such errors often lead to lethal diseases, at other times they provide distinctive survival advantages and thus unscramble cues to unconventional therapeutic strategies for life-threatening conditions. Hereditary Persistence of Fetal Hemoglobin (HPFH) is one such condition wherein the typically inactivated fetal form of hemoglobin (HbF) remains overexpressed even in adult stages of the bearer's life. Strikingly, this condition is known to ameliorate pathological manifestations in patients with aberrant adult hemoglobin synthesis (e.g. β-hemoglobinopathies like β-thalassemia, sickle cell disease etc.). Early researchers in the field expected such patients to suffer from clinical challenges owing to HbF's high affinity to oxygen and consequent difficulty in its release to cells and tissues. Surprisingly, these patients are known to lead a physiologically normal life. Modern-day hematologists and clinical researchers have looked-up to the concept of HbF reactivation as a potential curative strategy for patients suffering from β-hemoglobinopathies like β-thalassemia and sickle cell disease. As a result, several drugs like hydroxyurea, 5-azacytidine, cytosine arabinoside, natural products etc. have been tried in clinics to elevate HbF levels in such patients with limited success and poor understanding on the mechanisms of their action. Associated side-effects and complications of using cytotoxic agents like these restrict their use in most instances. Fortunately, with the advent of newer molecular tools and techniques, researchers are focusing their attention to reengineer the molecular machinery and thus reactivate the gamma-globin gene. This book brings together a selection of chapters dedicated to fetal hemoglobin -- its physiological role, regulation, methodologies to manipulate and future strategies. Researchers and scientists interested in the topic will have a comprehensive understanding of the current concepts on fetal hemoglobin modulation and therefore will serve as a launching pad for their research ideas.
| Publisher | Nova Science Pub Inc |
| Publication date | August 23, 2020 |
| Language | English |
| Print length | 355 pages |
| ISBN-10 | 1536179558 |
| ISBN-13 | 978-1536179552 |
| Item Weight | 612 g |
Product Description
Fetal Hemoglobin: The Panacea for Major ?-hemoglobinopathies
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Who is this book for?
Answer: It is intended for researchers and scientists interested in fetal hemoglobin and related therapies. -
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What does the book cover?
Answer: It covers the physiological role, regulation, manipulative methodologies, and future strategies of fetal hemoglobin. -
Question:
How can this book help in research?
Answer: It provides a comprehensive understanding of fetal hemoglobin which can inspire new research ideas and strategies.
English Edition Nishant Chakravorty (Editor) Format: Editorial Review
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Features & Benefits
- Comprehensive guide on fetal hemoglobin's role and regulation.
- Focuses on methodologies to manipulate fetal hemoglobin levels.
- Explores future strategies for treating hemoglobinopathies.
- Provides insights for researchers and clinical practitioners.
- Facilitates understanding of current concepts in hemoglobin modulation.
- Serves as a launching pad for innovative research ideas in the field.
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