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Titlebook: Heparanase; From Basic Research Israel Vlodavsky,Ralph D. Sanderson,Neta Ilan Book 2020 The Editor(s) (if applicable) and The Author(s), u

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發(fā)表于 2025-3-21 20:05:43 | 只看該作者 |倒序?yàn)g覽 |閱讀模式
書(shū)目名稱(chēng)Heparanase
副標(biāo)題From Basic Research
編輯Israel Vlodavsky,Ralph D. Sanderson,Neta Ilan
視頻videohttp://file.papertrans.cn/426/425682/425682.mp4
概述Features a comprehensive and detailed discussion of the biology of heparanase and heparanase-2 and its role and function in aggressive cancer phenotypes.The book‘s 8 chapters are written by internatio
叢書(shū)名稱(chēng)Advances in Experimental Medicine and Biology
圖書(shū)封面Titlebook: Heparanase; From Basic Research  Israel Vlodavsky,Ralph D. Sanderson,Neta Ilan Book 2020 The Editor(s) (if applicable) and The Author(s), u
描述.Written by internationally recognized leaders in Heparanase biology, the book’s eight chapters offer an opportunity for scientists, clinicians and advanced students in cell biology, tumor biology and oncology to obtain a comprehensive understanding of Heparanase’s multifaceted activities in cancer, inflammation, diabetes and other diseases, as well as its related clinical applications.?.Proteases and their involvement in cancer progression have been well addressed and documented; however, the emerging premise presented within this book is that Heparanase is a master regulator of aggressive cancer phenotypes and crosstalk with the tumor microenvironment. This endoglycosidase contributes to tumor-mediated remodeling of the extracellular matrix and cell surfaces, augmenting the bioavailability of pro-tumorigenic and pro-inflammatory growth factors and cytokines that are bound to Heparan sulfate. Compelling evidence ties Heparanase with all steps of tumor progression including tumor initiation, growth, angiogenesis, metastasis, and chemoresistance, supporting the notion that Heparanase is an important contributor to the poor outcome of cancer patients and a validated target for therap
出版日期Book 2020
關(guān)鍵詞heparanase; carcinoma; sarcoma; cell microenvironment; metastasis; angiogenesis; hematological malignancie
版次1
doihttps://doi.org/10.1007/978-3-030-34521-1
isbn_softcover978-3-030-34523-5
isbn_ebook978-3-030-34521-1Series ISSN 0065-2598 Series E-ISSN 2214-8019
issn_series 0065-2598
copyrightThe Editor(s) (if applicable) and The Author(s), under exclusive license to Springer Nature Switzerl
The information of publication is updating

書(shū)目名稱(chēng)Heparanase影響因子(影響力)




書(shū)目名稱(chēng)Heparanase影響因子(影響力)學(xué)科排名




書(shū)目名稱(chēng)Heparanase網(wǎng)絡(luò)公開(kāi)度




書(shū)目名稱(chēng)Heparanase網(wǎng)絡(luò)公開(kāi)度學(xué)科排名




書(shū)目名稱(chēng)Heparanase被引頻次




書(shū)目名稱(chēng)Heparanase被引頻次學(xué)科排名




書(shū)目名稱(chēng)Heparanase年度引用




書(shū)目名稱(chēng)Heparanase年度引用學(xué)科排名




書(shū)目名稱(chēng)Heparanase讀者反饋




書(shū)目名稱(chēng)Heparanase讀者反饋學(xué)科排名




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Mayank Khanna,Christopher R. Parisho serve as a guide for addressing various open problems in accelerating analytics workloads, e.g., new architectural features for supporting analytics workloads978-3-031-00621-0978-3-031-01749-0Series ISSN 1935-3235 Series E-ISSN 1935-3243
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Forty Years of Basic and Translational Heparanase Researchinvestigating its biological activities and significance in cancer and other pathologies. Studies performed during the first area are briefly introduced in a layman style followed by the relevant abstracts presented chronologically, essentially as appears in PubMed. The second era started in 1999 wh
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An Overview of the Structure, Mechanism and Specificity of Human Heparanaseinteraction with HS substrates of varying sulfation states. We also examine HPSE in a wider context against related β-D-glucuronidases from other species, highlighting the structural features that control ./. ? glycosidase selectivity in this family of enzymes.
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Mechanism of HPSE Gene SNPs Function: From Normal Processes to Inflammation, Cancerogenesis and Tumoregion. Instead of heparanase, the helicase-like transcription factor (HLTF) binds to the regulatory region. These and subsequent studies will elucidate how modification in the HPSE enhancer region could be applied to develop new approaches for cancer treatment.
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