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Results 1 - 20 of 205,800  for All Library Resources

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1
Tumor exosome-based nanoparticles are efficient drug carriers for chemotherapy
Tumor exosome-based nanoparticles are efficient drug carriers for chemotherapy
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Tumor exosome-based nanoparticles are efficient drug carriers for chemotherapy

Nature communications, 2019-08, Vol.10 (1), p.3838-16, Article 3838 [Peer Reviewed Journal]

2019. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;The Author(s) 2019 ;ISSN: 2041-1723 ;EISSN: 2041-1723 ;DOI: 10.1038/s41467-019-11718-4 ;PMID: 31444335

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2
Artificially cloaked viral nanovaccine for cancer immunotherapy
Artificially cloaked viral nanovaccine for cancer immunotherapy
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Artificially cloaked viral nanovaccine for cancer immunotherapy

Nature communications, 2019-12, Vol.10 (1), p.5747-13, Article 5747 [Peer Reviewed Journal]

2019. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;The Author(s) 2019 ;ISSN: 2041-1723 ;EISSN: 2041-1723 ;DOI: 10.1038/s41467-019-13744-8 ;PMID: 31848338

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3
Deep Learning in Label-free Cell Classification
Deep Learning in Label-free Cell Classification
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Deep Learning in Label-free Cell Classification

Scientific reports, 2016-03, Vol.6 (1), p.21471-21471, Article 21471 [Peer Reviewed Journal]

Copyright Nature Publishing Group Mar 2016 ;Copyright © 2016, Macmillan Publishers Limited 2016 Macmillan Publishers Limited ;ISSN: 2045-2322 ;EISSN: 2045-2322 ;DOI: 10.1038/srep21471 ;PMID: 26975219

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4
GAS5, a non-protein-coding RNA, controls apoptosis and is downregulated in breast cancer
GAS5, a non-protein-coding RNA, controls apoptosis and is downregulated in breast cancer
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GAS5, a non-protein-coding RNA, controls apoptosis and is downregulated in breast cancer

Oncogene, 2009-01, Vol.28 (2), p.195-208 [Peer Reviewed Journal]

COPYRIGHT 2009 Nature Publishing Group ;Copyright Nature Publishing Group Jan 15, 2009 ;ISSN: 0950-9232 ;EISSN: 1476-5594 ;DOI: 10.1038/onc.2008.373 ;PMID: 18836484 ;CODEN: ONCNES

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5
TGF-β induces miR-182 to sustain NF-κB activation in glioma subsets
TGF-β induces miR-182 to sustain NF-κB activation in glioma subsets
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TGF-β induces miR-182 to sustain NF-κB activation in glioma subsets

The Journal of clinical investigation, 2012-10, Vol.122 (10), p.3563-3578 [Peer Reviewed Journal]

Copyright © 2012, American Society for Clinical Investigation 2012 ;ISSN: 0021-9738 ;EISSN: 1558-8238 ;DOI: 10.1172/JCI62339 ;PMID: 23006329

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6
NOX4 Inhibition Potentiates Immunotherapy by Overcoming Cancer-Associated Fibroblast-Mediated CD8 T-cell Exclusion from Tumors
NOX4 Inhibition Potentiates Immunotherapy by Overcoming Cancer-Associated Fibroblast-Mediated CD8 T-cell Exclusion from Tumors
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NOX4 Inhibition Potentiates Immunotherapy by Overcoming Cancer-Associated Fibroblast-Mediated CD8 T-cell Exclusion from Tumors

Cancer research (Chicago, Ill.), 2020-05, Vol.80 (9), p.1846-1860 [Peer Reviewed Journal]

2020 American Association for Cancer Research. ;ISSN: 0008-5472 ;EISSN: 1538-7445 ;DOI: 10.1158/0008-5472.CAN-19-3158 ;PMID: 32122909

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7
A class of extracellular vesicles from breast cancer cells activates VEGF receptors and tumour angiogenesis
A class of extracellular vesicles from breast cancer cells activates VEGF receptors and tumour angiogenesis
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A class of extracellular vesicles from breast cancer cells activates VEGF receptors and tumour angiogenesis

Nature communications, 2017-02, Vol.8 (1), p.14450-14450, Article 14450 [Peer Reviewed Journal]

Copyright Nature Publishing Group Feb 2017 ;Copyright © 2017, The Author(s) 2017 The Author(s) ;ISSN: 2041-1723 ;EISSN: 2041-1723 ;DOI: 10.1038/ncomms14450 ;PMID: 28205552

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8
The Clinical Relevance of Cancer Cell Lines
The Clinical Relevance of Cancer Cell Lines
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The Clinical Relevance of Cancer Cell Lines

JNCI : Journal of the National Cancer Institute, 2013-04, Vol.105 (7), p.452-458 [Peer Reviewed Journal]

2014 INIST-CNRS ;Copyright Oxford Publishing Limited(England) Apr 3, 2013 ;Published by Oxford University Press. For Permissions, please e-mail: journals.permissions@oup.com. 2013 ;ISSN: 0027-8874 ;EISSN: 1460-2105 ;DOI: 10.1093/jnci/djt007 ;PMID: 23434901 ;CODEN: JNCIEQ

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9
Pre-treatment with chemotherapy can enhance the antigenicity and immunogenicity of tumours by promoting adaptive immune responses
Pre-treatment with chemotherapy can enhance the antigenicity and immunogenicity of tumours by promoting adaptive immune responses
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Pre-treatment with chemotherapy can enhance the antigenicity and immunogenicity of tumours by promoting adaptive immune responses

British journal of cancer, 2010-01, Vol.102 (1), p.115-123 [Peer Reviewed Journal]

2015 INIST-CNRS ;Copyright Nature Publishing Group Jan 5, 2010 ;Copyright © 2010 Cancer Research UK 2010 Cancer Research UK ;ISSN: 0007-0920 ;EISSN: 1532-1827 ;DOI: 10.1038/sj.bjc.6605465 ;PMID: 19997099 ;CODEN: BJCAAI

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10
Lung Cancer Cell Lines as Tools for Biomedical Discovery and Research
Lung Cancer Cell Lines as Tools for Biomedical Discovery and Research
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Lung Cancer Cell Lines as Tools for Biomedical Discovery and Research

JNCI : Journal of the National Cancer Institute, 2010-09, Vol.102 (17), p.1310-1321 [Peer Reviewed Journal]

2015 INIST-CNRS ;Copyright Oxford Publishing Limited(England) Sep 8, 2010 ;The Author 2010. Published by Oxford University Press. 2010 ;ISSN: 0027-8874 ;EISSN: 1460-2105 ;DOI: 10.1093/jnci/djq279 ;PMID: 20679594 ;CODEN: JNCIEQ

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11
Comprehensive comparison of molecular portraits between cell lines and tumors in breast cancer
Comprehensive comparison of molecular portraits between cell lines and tumors in breast cancer
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Comprehensive comparison of molecular portraits between cell lines and tumors in breast cancer

BMC genomics, 2016-08, Vol.17 Suppl 7 (Suppl 7), p.525-525, Article 525 [Peer Reviewed Journal]

COPYRIGHT 2016 BioMed Central Ltd. ;COPYRIGHT 2016 BioMed Central Ltd. ;The Author(s). 2016 ;ISSN: 1471-2164 ;EISSN: 1471-2164 ;DOI: 10.1186/s12864-016-2911-z ;PMID: 27556158

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12
Acquired Resistance to BET-PROTACs (Proteolysis-Targeting Chimeras) Caused by Genomic Alterations in Core Components of E3 Ligase Complexes
Acquired Resistance to BET-PROTACs (Proteolysis-Targeting Chimeras) Caused by Genomic Alterations in Core Components of E3 Ligase Complexes
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Acquired Resistance to BET-PROTACs (Proteolysis-Targeting Chimeras) Caused by Genomic Alterations in Core Components of E3 Ligase Complexes

Molecular cancer therapeutics, 2019-07, Vol.18 (7), p.1302-1311 [Peer Reviewed Journal]

2019 American Association for Cancer Research. ;ISSN: 1535-7163 ;EISSN: 1538-8514 ;DOI: 10.1158/1535-7163.mct-18-1129 ;PMID: 31064868

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13
role of fluctuations and stress on the effective viscosity of cell aggregates
role of fluctuations and stress on the effective viscosity of cell aggregates
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role of fluctuations and stress on the effective viscosity of cell aggregates

Proceedings of the National Academy of Sciences - PNAS, 2009-10, Vol.106 (41), p.17271-17275 [Peer Reviewed Journal]

Copyright National Academy of Sciences Oct 13, 2009 ;Distributed under a Creative Commons Attribution 4.0 International License ;ISSN: 0027-8424 ;EISSN: 1091-6490 ;DOI: 10.1073/pnas.0902085106 ;PMID: 19805170

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14
High-Resolution CRISPR Screens Reveal Fitness Genes and Genotype-Specific Cancer Liabilities
High-Resolution CRISPR Screens Reveal Fitness Genes and Genotype-Specific Cancer Liabilities
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High-Resolution CRISPR Screens Reveal Fitness Genes and Genotype-Specific Cancer Liabilities

Cell, 2015-12, Vol.163 (6), p.1515-1526 [Peer Reviewed Journal]

2015 Elsevier Inc. ;Copyright © 2015 Elsevier Inc. All rights reserved. ;ISSN: 0092-8674 ;ISSN: 1097-4172 ;EISSN: 1097-4172 ;DOI: 10.1016/j.cell.2015.11.015 ;PMID: 26627737

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15
Reassessment of Exosome Composition
Reassessment of Exosome Composition
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Reassessment of Exosome Composition

Cell, 2019-04, Vol.177 (2), p.428-445.e18 [Peer Reviewed Journal]

2019 Elsevier Inc. ;Copyright © 2019 Elsevier Inc. All rights reserved. ;ISSN: 0092-8674 ;EISSN: 1097-4172 ;DOI: 10.1016/j.cell.2019.02.029 ;PMID: 30951670

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16
Internalization of Exosomes through Receptor-Mediated Endocytosis
Internalization of Exosomes through Receptor-Mediated Endocytosis
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Internalization of Exosomes through Receptor-Mediated Endocytosis

Molecular cancer research, 2019-02, Vol.17 (2), p.337-347 [Peer Reviewed Journal]

2018 American Association for Cancer Research. ;ISSN: 1541-7786 ;EISSN: 1557-3125 ;DOI: 10.1158/1541-7786.mcr-18-0891 ;PMID: 30487244

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17
SIRT1 deacetylated and stabilized XRCC1 to promote chemoresistance in lung cancer
SIRT1 deacetylated and stabilized XRCC1 to promote chemoresistance in lung cancer
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SIRT1 deacetylated and stabilized XRCC1 to promote chemoresistance in lung cancer

Cell death & disease, 2019-05, Vol.10 (5), p.363, Article 363 [Peer Reviewed Journal]

The Author(s) 2019. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;The Author(s) 2019 ;ISSN: 2041-4889 ;EISSN: 2041-4889 ;DOI: 10.1038/s41419-019-1592-3 ;PMID: 31043584

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18
Molecular and Genetic Characterization of MHC Deficiency Identifies EZH2 as Therapeutic Target for Enhancing Immune Recognition
Molecular and Genetic Characterization of MHC Deficiency Identifies EZH2 as Therapeutic Target for Enhancing Immune Recognition
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Molecular and Genetic Characterization of MHC Deficiency Identifies EZH2 as Therapeutic Target for Enhancing Immune Recognition

Cancer discovery, 2019-04, Vol.9 (4), p.546-563

2019 American Association for Cancer Research. ;ISSN: 2159-8274 ;EISSN: 2159-8290 ;DOI: 10.1158/2159-8290.cd-18-1090 ;PMID: 30705065

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19
Cellular Uptake, Cytotoxicity, and Metabolic Profiling of Human Cancer Cells Treated with Ruthenium(II) Polypyridyl Complexes [Ru(bpy)2(NN)]Cl2 with NN=bpy, phen, dpq, dppz, and dppn
Cellular Uptake, Cytotoxicity, and Metabolic Profiling of Human Cancer Cells Treated with Ruthenium(II) Polypyridyl Complexes [Ru(bpy)2(NN)]Cl2 with NN=bpy, phen, dpq, dppz, and dppn
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Cellular Uptake, Cytotoxicity, and Metabolic Profiling of Human Cancer Cells Treated with Ruthenium(II) Polypyridyl Complexes [Ru(bpy)2(NN)]Cl2 with NN=bpy, phen, dpq, dppz, and dppn

ChemMedChem, 2008-07, Vol.3 (7), p.1104-1109 [Peer Reviewed Journal]

Copyright © 2008 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim ;ISSN: 1860-7179 ;EISSN: 1860-7187 ;DOI: 10.1002/cmdc.200800039 ;PMID: 18425738

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20
lncRNA MIR100HG-derived miR-100 and miR-125b mediate cetuximab resistance via Wnt/β-catenin signaling
lncRNA MIR100HG-derived miR-100 and miR-125b mediate cetuximab resistance via Wnt/β-catenin signaling
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lncRNA MIR100HG-derived miR-100 and miR-125b mediate cetuximab resistance via Wnt/β-catenin signaling

Nature medicine, 2017-11, Vol.23 (11), p.1331-1341 [Peer Reviewed Journal]

ISSN: 1078-8956 ;EISSN: 1546-170X ;DOI: 10.1038/nm.4424 ;PMID: 29035371

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