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Titlebook: Apoptosis, Cell Signaling, and Human Diseases; Molecular Mechanisms Rakesh Srivastava Book 2007 Humana Press 2007 DNA.HIV.gene expression.g

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發(fā)表于 2025-3-21 17:58:14 | 只看該作者 |倒序?yàn)g覽 |閱讀模式
期刊全稱Apoptosis, Cell Signaling, and Human Diseases
期刊簡(jiǎn)稱Molecular Mechanisms
影響因子2023Rakesh Srivastava
視頻videohttp://file.papertrans.cn/160/159014/159014.mp4
發(fā)行地址Includes supplementary material:
圖書(shū)封面Titlebook: Apoptosis, Cell Signaling, and Human Diseases; Molecular Mechanisms Rakesh Srivastava Book 2007 Humana Press 2007 DNA.HIV.gene expression.g
影響因子.Apoptosis, Cell Signaling, and Human Diseases: Molecular Mechanisms, Volumes 1 & 2, present a concise synthesis of recent developments in the understanding of both cell survival and apoptotic pathways. Particular attention is given to apoptosis in human diseases, such as different forms of cancer and neurodegenerative diseases. These comprehensive volumes integrate the most innovative and current findings from several related disciplines of scientific research, including pathology, genetics, virology, cell biology, immunology, and molecular biology...Volume 1 is divided into two sections: "Malignant Transformation and Metastasis" and "Molecular Basis of Disease Therapy." Volume 2 follows a similar structure and is divided into sections entitled "Kinases and Phosphate" and "Molecular Basis of Cell Death." All of the contributors are at the forefront of scientific discovery, and the reviews they present systemically examine the most exciting and innovative aspects of their particular areas of expertise. Researchers will find these volumes of major benefit as they search for novel and more effective treatments for human diseases..
Pindex Book 2007
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Protein Kinase C and Apoptosisproliferation and survival and their expression or activity is altered in some human diseases, particularly cancer. The development and utilization of PKC isoform specific tools, including dominant inhibitory kinases, mouse models in which specific PKC isoforms have been disrupted, and PKC isoform s
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MAPK Signaling in Human Diseasesng cell proliferation, differentiation, motility, and survival. Three subfamilies of MAPK have been extensively studied: extracellular signal-regulated kinases (ERK), p38-MAPK, and c-Jun N-terminal kinase (JNK). The ERKs play roles in cell proliferation, survival, and motility, and inhibitors of thi
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Serine/Threonine Protein Phosphatases in Apoptosis, myosin light chain, lamin B, some caspases and their inhibitors, as well as transcriptions factors like CREB and NF-kB/I-kB. Most is known about the protein phosphatases (PPs) PP1, PP2A, PP2B/calcineurin, PP4/PPX, and PP5. With the possible exception of PP5, which so far appears to mainly promote
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Urokinase/Urokinase Receptor-Mediated Signaling in Cancerits receptor (uPAR), and its major inhibitor plasminogen activator inhibtor-1 (PAI-1) or -2 (PAI-2) are activated by common signaling mechanisms. In tumor cells of mesenchymal or epithelial origin uPA, uPAR, and PAIs or metallo-proteinases (MMPs) are overexpressed and these molecules are implicated
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發(fā)表于 2025-3-23 03:40:53 | 只看該作者
Signaling Pathways That Protect the Heart Against Apoptosis Induced by Ischemia and Reperfusionly regulated. Two mechanisms of apoptosis involve the extrinsic death receptor pathway and the intrinsic mitochondrial pathway. Both pathways lead to the activation of effector caspases, resulting in cell death. The mitochondrial pathway plays a key role in initiating apoptosis after ischemia and re
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