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Titlebook: Cystogenesis; Jong Hoon Park,Curie Ahn Book 2016 The Editor(s) (if applicable) and The Author(s), under exclusive license to Springer Natu

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發(fā)表于 2025-3-21 17:25:09 | 只看該作者 |倒序?yàn)g覽 |閱讀模式
書(shū)目名稱(chēng)Cystogenesis
編輯Jong Hoon Park,Curie Ahn
視頻videohttp://file.papertrans.cn/243/242603/242603.mp4
概述Presents key challenges in the study of Autosomal dominant polycystic kidney disease (ADPKD).Covers basic cellular mechanisms and clinical trials in ADPKD research.Opens the door for the development o
叢書(shū)名稱(chēng)Advances in Experimental Medicine and Biology
圖書(shū)封面Titlebook: Cystogenesis;  Jong Hoon Park,Curie Ahn Book 2016 The Editor(s) (if applicable) and The Author(s), under exclusive license to Springer Natu
描述Autosomal Dominant Polycystic Kidney Disease (ADPKD) is a highly prevalent hereditary renal disorder in which fluid-filled cysts are appeared in both kidneys. Main causative genes of ADPKD are PKD1 and PKD2, encoding for polycystin-1 (PC1) and polycystin-2 (PC2) respectively. Those proteins are localized on primary cilia and function as mechanosensor in response to the fluid flow, translating mechanistic stimuli into calcium signaling. With mutations either of PKD1 or PKD2, hyper-activated renal tubular epithelial cell proliferation is observed, followed by disrupted calcium homeostasis and aberrant intracellular cyclic AMP (cAMP) accumulation. Increased cell proliferation with fluid secretion leads to the development of thousands of epithelial-lined, fluid-filled cysts in kidneys. It is also accompanied by interstitial inflammation, fibrosis, and finally reaching end-stage renal disease (ESRD). In human ADPKD, the age at which renal failure typically occurs is later in life, however no specific targeted medications are available to cure ADPKD. Recently, potential therapeutic targets or surrogate diagnostic biomarkers for ADPKD are proposed with the advances in the understanding of
出版日期Book 2016
關(guān)鍵詞Autosomal Dominant Polycystic Kidney Disease (ADPKD); Cyst; End-stage Renal Disease (ESRD); Genetic mec
版次1
doihttps://doi.org/10.1007/978-981-10-2041-4
isbn_softcover978-981-10-9511-5
isbn_ebook978-981-10-2041-4Series 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 Singapor
The information of publication is updating

書(shū)目名稱(chēng)Cystogenesis影響因子(影響力)




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




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




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




書(shū)目名稱(chēng)Cystogenesis被引頻次




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




書(shū)目名稱(chēng)Cystogenesis年度引用




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




書(shū)目名稱(chēng)Cystogenesis讀者反饋




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




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沙發(fā)
發(fā)表于 2025-3-21 23:03:17 | 只看該作者
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發(fā)表于 2025-3-22 04:26:22 | 只看該作者
Cell Proliferation and Apoptosis in ADPKDisruption of either . or ., the main causative genes of ADPKD, intracellular calcium homeostasis and cAMP accumulation are disrupted, which in turn leads to altered signaling in the pathways that regulate cell proliferation. These dysregulations finally stimulate the development of fluid-filled cyst
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發(fā)表于 2025-3-22 07:37:03 | 只看該作者
Inflammation and Fibrosis in ADPKDtant pathway related to this disease. However, studies on the interactions of inflammation and fibrosis with polycystic kidney disease have been limited. Inflammation is one of the protective systems involved in the response to foreign molecules. In PKD, it was reported that the activity of signalin
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發(fā)表于 2025-3-22 10:36:09 | 只看該作者
Functional Study of the Primary Cilia in ADPKDays such as Wnt, PDGFRα, Hh, and mechanosignaling are localized to the membrane of the primary cilium. In the kidney, primary cilia extend from the cell membrane to the lumen of renal tubules to respond to fluidic stress. Recent studies have indicated that the disruption of ciliary proteins includin
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發(fā)表于 2025-3-22 13:43:42 | 只看該作者
Epigenetic Regulation in Cystogenesismodification, and gene regulation by microRNAs are well-known epigenetic modulations that are closely associated with several cellular processes and diverse disease states, such as cancers, even under precancerous conditions. More recently, several studies have indicated that epigenetic changes may
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發(fā)表于 2025-3-23 00:01:59 | 只看該作者
Diagnostic Evaluation as a Biomarker in Patients with ADPKD declines over a long period of time, the evaluation of treatment effects in ADPKD has been very difficult. Therefore, there has been a great interest to find out the “better” surrogate marker or biomarker which reflects disease progression. Biomarkers in ADPKD should have three clinical implication
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發(fā)表于 2025-3-23 03:50:05 | 只看該作者
Clinical Trials and a View Toward the Future of ADPKDies, autosomal dominant polycystic kidney disease (ADPKD) is the most common hereditary disease, and is characterized by the progressive enlargement of bilateral renal cysts, resulting in end-stage kidney failure. Progress in genetics and molecular pathobiology has enabled the development of therape
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發(fā)表于 2025-3-23 05:32:57 | 只看該作者
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