|
|
|
|
LEADER |
00000cam a2200000 i 4500 |
001 |
SCIDIR_on1007309836 |
003 |
OCoLC |
005 |
20231120010226.0 |
006 |
m o d |
007 |
cr |n||||||||| |
008 |
171025s2017 maua ob 000 0 eng d |
040 |
|
|
|a YDX
|b eng
|e rda
|e pn
|c YDX
|d N$T
|d IDEBK
|d N$T
|d EBLCP
|d OPELS
|d UPM
|d OCLCF
|d OHS
|d OCLCO
|d MEU
|d D6H
|d AU@
|d YDX
|d INT
|d OCLCQ
|d OCLCA
|d OCLCQ
|d BRX
|d OCLCQ
|d S2H
|d OCLCQ
|d OCLCO
|d DKU
|d OCLCO
|d OCLCQ
|d OCLCO
|d OCLCQ
|d OCLCO
|
066 |
|
|
|c (S
|
019 |
|
|
|a 1007130083
|a 1028923634
|a 1029499755
|a 1030777752
|a 1032678883
|a 1034690310
|a 1038775124
|a 1039473152
|a 1084543079
|a 1264975396
|
020 |
|
|
|a 9780128126394
|q (electronic book)
|
020 |
|
|
|a 0128126396
|q (electronic book)
|
020 |
|
|
|z 9780128126387
|
020 |
|
|
|z 0128126388
|
035 |
|
|
|a (OCoLC)1007309836
|z (OCoLC)1007130083
|z (OCoLC)1028923634
|z (OCoLC)1029499755
|z (OCoLC)1030777752
|z (OCoLC)1032678883
|z (OCoLC)1034690310
|z (OCoLC)1038775124
|z (OCoLC)1039473152
|z (OCoLC)1084543079
|z (OCoLC)1264975396
|
050 |
|
4 |
|a QP552.P4
|b P478 2017
|
055 |
1 |
3 |
|a QP601.
|b E522 1970 v.42eb
|
072 |
|
7 |
|a SCI
|x 008000
|2 bisacsh
|
082 |
0 |
4 |
|a 572/.65
|2 23
|
082 |
0 |
4 |
|a 574.19/2456
|2 23
|
245 |
0 |
0 |
|a Peptidomics of cancer-derived enzyme products /
|c edited by Tony Y. Hu, Fuyuhiko Tamanoi.
|
250 |
|
|
|a First edition.
|
264 |
|
1 |
|a Cambridge, MA :
|b Academic Press,
|c 2017.
|
300 |
|
|
|a 1 online resource (xvi, 172 pages) :
|b illustrations
|
336 |
|
|
|a text
|b txt
|2 rdacontent
|
337 |
|
|
|a computer
|b c
|2 rdamedia
|
338 |
|
|
|a online resource
|b cr
|2 rdacarrier
|
490 |
1 |
|
|a The enzymes ;
|v volume forty two
|
546 |
|
|
|a Text in English.
|
504 |
|
|
|a Includes bibliographical references.
|
505 |
0 |
|
|6 880-01
|a Front Cover -- Peptidomics of Cancer-Derived Enzyme Products -- Copyright -- Contents -- Contributors -- Preface -- Overview -- 1. Molecular Changes in Cancer -- 2. Peptidomes and Advance in Mass Spectrometry -- 3. Nanotechnology and Nanodevices -- 4. Future Perspective -- Chapter One: Circulating Peptidome and Tumor-Resident Proteolysis -- 1. Introduction -- 1.1. Intracellular Proteases -- 1.1.1. Caspases (Cysteine Protease) -- 1.1.2. Deubiquitinases (Cysteine and Zinc Proteases) -- 1.1.3. Autophagins (Cysteine Proteases) -- 1.2. Extracellular Proteases
|
505 |
8 |
|
|a 1.2.1. Matrix Metalloproteinases1.2.2. Cysteine Cathepsins -- 1.2.3. Kallikreins -- 2. Organism and Cancer Degradomes -- 3. Tumor-Associated Peptidomics -- 4. Tumor Proteases Relative Peptide in Cancer Detection -- 5. Conclusion -- References -- Chapter Two: The Peptidome Comes of Age: Mass Spectrometry-Based Characterization of the Circulating Cancer Peptidome -- 1. Introduction -- 2. Biological Role of Peptides -- 3. Peptidomics: The Study of Physiological Peptides -- 4. Mass Spectrometry and Top/Middle-Down Proteomics
|
505 |
8 |
|
|a 4.1. Mass Spectrometry Technology Developments for Peptidomics4.2. Top-Top-Down or Native Mass Spectrometry -- 4.3. Top-Down-Based Mass Spectrometric Imaging -- 5. Strategies to Enrich the Peptidome -- 5.1. Selective Precipitation -- 5.2. Centrifugal Ultrafiltration -- 5.3. Capillary Ultrafiltration -- 5.4. Surface-Derivatised Magnetic Beads -- 5.5. Nanoporous Substrates -- 6. Application of Peptidomics in Cancer Biomarker Discovery -- 6.1. Role of Peptidomics as in Cancer Biomarker Discovery -- 6.2. Peptidomics and Cancer Diagnosis
|
505 |
8 |
|
|a 6.3. Plasma Protein/Peptide Profiling6.4. The Plasma Interactome -- 6.5. Endoproteolytic Cleavage -- 6.6. Exoproteolytic Cleavage -- 7. Data Processing and Informatics for Peptidome Analyses -- 7.1. Sequence Databases -- 7.2. Data Analyses -- 7.3. Data Repository -- 8. Emerging Technologies -- 9. Future Perspectives -- Acknowledgments -- References -- Chapter Three: Peptide Hormones as Tumor Markers in Clinical Practice -- 1. Introduction -- 2. Selected Peptide Hormones as Tumor Markers -- 2.1. Calcitonin -- 2.1.1. Biosynthesis From Prohormone
|
505 |
8 |
|
|a 2.1.2. Clinical Significance as Tumor Marker2.2. Alpha- and Beta-hCG -- 2.2.1. Processing of hCG -- 2.2.2. Clinical Applications as Tumor Markers -- 2.3. Insulin and C-Peptide -- 2.3.1. Biosynthesis From Prohormone -- 2.3.2. Clinical Significance as Tumor Marker -- 2.4. PTHrp -- 2.4.1. Biosynthesis From Prohormone -- 2.4.2. Clinical Significance as Tumor Marker -- 2.5. Gastrin -- 2.5.1. Biosynthesis From Prohormone -- 2.5.2. Clinical Significance as Tumor Marker -- 2.6. VIP -- 2.6.1. Biosynthesis From Prohormone
|
588 |
0 |
|
|a Online resource; title from digital title page (viewed on June 11, 2018).
|
650 |
|
0 |
|a Peptides
|x Analysis.
|
650 |
|
2 |
|a Peptides
|x analysis
|0 (DNLM)D010455Q000032
|
650 |
|
6 |
|a Peptides
|0 (CaQQLa)201-0006528
|x Analyse.
|0 (CaQQLa)201-0374819
|
650 |
|
7 |
|a SCIENCE
|x Life Sciences
|x Biology.
|2 bisacsh
|
650 |
|
7 |
|a Peptides
|x Analysis
|2 fast
|0 (OCoLC)fst01057565
|
700 |
1 |
|
|a Hu, Xiaohua,
|d 1960-
|e editor.
|
700 |
1 |
|
|a Tamanoi, Fuyuhiko,
|e editor.
|
773 |
0 |
|
|t Enzymes.
|
773 |
0 |
|
|t Elsevier.
|
776 |
0 |
8 |
|i Print version:
|t Peptidomics of cancer-derived enzyme products.
|b First edition.
|d Cambridge, MA : Academic Press, 2017
|z 9780128126387
|z 0128126388
|w (OCoLC)985078856
|
830 |
|
0 |
|a Enzymes ;
|v v. 42.
|
856 |
4 |
0 |
|u https://sciencedirect.uam.elogim.com/science/bookseries/18746047/42
|z Texto completo
|
880 |
0 |
0 |
|6 505-01/(S
|g Machine generated contents note:
|g 1.
|t Circulating Peptidome and Tumor-Resident Proteolysis /
|r Tony Y. Hu --
|g 1.
|t Introduction --
|g 2.
|t Organism and Cancer Degradomes --
|g 3.
|t Tumor-Associated Peptidomics --
|g 4.
|t Tumor Proteases Relative Peptide in Cancer Detection --
|g 5.
|t Conclusion --
|t References --
|g 2.
|t Peptidome Comes of Age: Mass Spectrometry-Based Characterization of the Circulating Cancer Peptidome /
|r Richard J. Simpson --
|g 1.
|t Introduction --
|g 2.
|t Biological Role of Peptides --
|g 3.
|t Peptidomics: The Study of Physiological Peptides --
|g 4.
|t Mass Spectrometry and Top/Middle-Down Proteomics --
|g 5.
|t Strategies to Enrich the Peptidome --
|g 6.
|t Application of Peptidomics in Cancer Biomarker Discovery --
|g 7.
|t Data Processing and Informatics for Peptidome Analyses --
|g 8.
|t Emerging Technologies --
|g 9.
|t Future Perspectives --
|t Acknowledgments --
|t References --
|g 3.
|t Peptide Hormones as Tumor Markers in Clinical Practice /
|r Zhen Zhao --
|g 1.
|t Introduction --
|g 2.
|t Selected Peptide Hormones as Tumor Markers --
|g 3.
|t Conclusion --
|t Acknowledgement --
|t References --
|g 4.
|t Insights on the HLA-Binding Peptidome in Cancer /
|r Douglas F. Lake --
|g 1.
|t Introduction --
|g 2.
|t Proteolysis of Proteins to Peptide Loading onto MHC --
|g 3.
|t Dysregulation of Antigen Processing in Cancer --
|g 4.
|t Tumor-Derived Defective Ribosomal Products --
|g 5.
|t Noncoding RNA Peptides --
|g 6.
|t Outlook --
|t References --
|g 5.
|t Strategies for Characterization of Low-Abundant Intact or Truncated Low-Molecular-Weight Proteins From Human Plasma /
|r Fuquan Yang --
|g 1.
|t Introduction --
|g 2.
|t Strategies for the Prefractionation or Enrichment of Small Intact or Truncated Proteins From the Human Plasma --
|g 3.
|t Characterization of LMW Proteins Based on MS --
|g 4.
|t Future Perspectives and Concluding Remarks --
|t Acknowledgments --
|t References --
|g 6.
|t Saliva-Exosomics in Cancer: Molecular Characterization of Cancer-Derived Exosomes in Saliva /
|r David T.W. Wong --
|g 1.
|t Introduction --
|g 2.
|t Salivaomics in Cancer --
|g 3.
|t Saliva-Exosomics: Next-Generation Salivaomics --
|g 4.
|t Salivary Exosomes as Potential Biomarkers for Cancer --
|g 5.
|t Future Perspective --
|t Acknowledgments --
|t Disclosure Statement --
|t References --
|g 7.
|t Exploiting Enzyme Alterations in Cancer for Drug Activation, Drug Delivery, and Nanotherapy /
|r Fuyuhiko Tamanoi --
|g 1.
|t Introduction --
|g 2.
|t Overview of Enzymes Used --
|g 3.
|t Protease Activatable Systems --
|g 4.
|t Hyaluronidase Activatable System --
|g 5.
|t Protein Kinase Cα Activatable System --
|g 6.
|t Esterase Activatable System --
|g 7.
|t Enzyme-Activated Nanovalves and Controlled Release of Anticancer Drugs --
|g 8.
|t Multistage Delivery Strategy --
|g 9.
|t Azoreductase and Colon-Specific Delivery --
|g 10.
|t Future Perspectives.
|