Genetic Testing in Breast Cancer: Innovations in Diagnosis and Treatment
暫譯: 乳癌基因檢測:診斷與治療的創新
Mir, Manzoor Ahmad
- 出版商: Academic Press
- 出版日期: 2025-12-08
- 售價: $5,990
- 貴賓價: 9.5 折 $5,691
- 語言: 英文
- 頁數: 462
- 裝訂: Quality Paper - also called trade paper
- ISBN: 0443278016
- ISBN-13: 9780443278013
-
相關分類:
生物資訊 Bioinformatics
海外代購書籍(需單獨結帳)
相關主題
商品描述
Genetic Testing in Breast Cancer: Innovations in Diagnosis and Treatment addresses the urgent need for novel, minimally invasive diagnostic techniques to accurately identify breast cancer early and monitor treatment efficacy, focusing particularly on triple-negative breast cancer (TNBC). This comprehensive volume analyzes the latest research and developments in genetic testing, covering strategies like next-generation sequencing and the Sanger method. It highlights their potential to revolutionize early diagnosis and personalized treatment plans. The book also discusses challenges and opportunities, providing insights into hereditary mutations, genetic counseling, and clinical practice integration.
Serving as a valuable resource for students, researchers, oncologists, pharmacologists, and healthcare professionals, it includes preclinical and clinical case studies that illustrate the practical applications of genetic testing for various breast cancer subtypes, including TNBC and HER2-positive breast cancer. The editors aim to advance treatment and improve patient outcomes through cutting-edge genetic testing techniques.
Serving as a valuable resource for students, researchers, oncologists, pharmacologists, and healthcare professionals, it includes preclinical and clinical case studies that illustrate the practical applications of genetic testing for various breast cancer subtypes, including TNBC and HER2-positive breast cancer. The editors aim to advance treatment and improve patient outcomes through cutting-edge genetic testing techniques.
商品描述(中文翻譯)
《乳腺癌中的基因檢測:診斷與治療的創新》針對迫切需要新穎、微創的診斷技術,以準確早期識別乳腺癌並監測治療效果,特別聚焦於三陰性乳腺癌(TNBC)。這本綜合性著作分析了基因檢測的最新研究和發展,涵蓋了如下一代測序(next-generation sequencing)和桑格法(Sanger method)等策略。它突顯了這些技術在早期診斷和個性化治療計劃中的革命性潛力。書中還討論了挑戰與機會,提供了對遺傳突變、基因諮詢和臨床實踐整合的見解。
本書作為學生、研究人員、腫瘤科醫生、藥理學家和醫療專業人員的寶貴資源,包含了臨床前和臨床案例研究,展示了基因檢測在各種乳腺癌亞型(包括TNBC和HER2陽性乳腺癌)中的實際應用。編輯們旨在通過尖端的基因檢測技術推進治療並改善患者的治療結果。