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LIBRIS Formathandbok  (Information om MARC21)
FältnamnIndikatorerMetadata
00006984naa a2200733 4500
001oai:DiVA.org:kth-300767
003SwePub
008210909s2020 | |||||||||||000 ||eng|
024a https://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-3007672 URI
024a https://doi.org/10.1021/acs.jproteome.0c000212 DOI
040 a (SwePub)kth
041 a engb eng
042 9 SwePub
072 7a ref2 swepub-contenttype
072 7a art2 swepub-publicationtype
100a Kagan, Jacobu NCI, Canc Biomarkers Res Grp, Div Canc Prevent, Bethesda, MD 20892 USA.4 aut
2451 0a National Cancer Institute Think-Tank Meeting Report on Proteomic Cartography and Biomarkers at the Single-Cell Level :b Interrogation of Premalignant Lesions
264 c 2020-03-12
264 1b American Chemical Society (ACS),c 2020
338 a print2 rdacarrier
500 a QC 20210909
520 a A Think-Tank Meeting was convened by the National Cancer Institute (NCI) to solicit experts' opinion on the development and application of multiomic single-cell analyses, and especially single-cell proteomics, to improve the development of a new generation of biomarkers for cancer risk, early detection, diagnosis, and prognosis as well as to discuss the discovery of new targets for prevention and therapy. It is anticipated that such markers and targets will be based on cellular, subcellular, molecular, and functional aberrations within the lesion and within individual cells. Single-cell proteomic data will be essential for the establishment of new tools with searchable and scalable features that indude spatial and temporal cartographies of premalignant and malignant lesions. Challenges and potential solutions that were discussed included (i) The best way/s to analyze single-cells from fresh and preserved tissue; (ii) Detection and analysis of secreted molecules and from single cells, especially from a tissue slice; (iii) Detection of new, previously undocumented cell type/s in the premalignant and early stage cancer tissue microenvironment; (iv) Multiomic integration of data to support and inform proteomic measurements; (v) Subcellular organelles-identifying abnormal structure, function, distribution, and location within individual premalignant and malignant cells; (vi) How to improve the dynamic range of single-cell proteomic measurements for discovery of differentially expressed proteins and their post-translational modifications (PTM); (vii) The depth of coverage measured concurrently using single-cell techniques; (viii) Quantitation - absolute or semiquantitative? (ix) Single methodology or multiplexed combinations? (x) Application of analytical methods for identification of biologically significant subsets; (xi) Data visualization of N-dimensional data sets; (xii) How to construct intercellular signaling networks in individual cells within premalignant tumor microenvironments (TME); (xiii) Associations between intrinsic cellular processes and extrinsic stimuli; (xiv) How to predict cellular responses to stress-inducing stimuli; (xv) Identification of new markers for prediction of progression from precursor, benign, and localized lesions to invasive cancer, based on spatial and temporal changes within individual cells; (xvi) Identification of new targets for immunoprevention or immunotherapy-identification of neoantigens and surfactome of individual cells within a lesion.
650 7a MEDICIN OCH HÄLSOVETENSKAPx Klinisk medicinx Cancer och onkologi0 (SwePub)302032 hsv//swe
650 7a MEDICAL AND HEALTH SCIENCESx Clinical Medicinex Cancer and Oncology0 (SwePub)302032 hsv//eng
650 7a MEDICIN OCH HÄLSOVETENSKAPx Medicinsk bioteknologi0 (SwePub)3042 hsv//swe
650 7a MEDICAL AND HEALTH SCIENCESx Medical Biotechnology0 (SwePub)3042 hsv//eng
653 a single-cell proteomics
653 a single-cell mass spectrometry
653 a targeted proteomics
653 a precursor lesion
653 a precancer
653 a tumorigenic lesion
653 a lesion's heterogeneity
653 a clonal evolution
653 a spatial and temporal cartography
653 a biomarkers
653 a early detection
653 a targets for prevention and therapy
700a Moritz, Robert L.u Inst Syst Biol, Seattle, WA 98109 USA.4 aut
700a Mazurchuk, Richardu NCI, Canc Biomarkers Res Grp, Div Canc Prevent, Bethesda, MD 20892 USA.4 aut
700a Lee, Je Hyuku Cold Spring Harbor Lab, POB 100, Cold Spring Harbor, NY 11724 USA.4 aut
700a Kharchenko, Peter Vasiliu Harvard Med Sch, Blavatn Inst Biomed Informat, Boston, MA 02115 USA.4 aut
700a Rozenblatt-Rosen, Oritu Broad Inst, Klarman Cell Observ, Boston, MA USA.4 aut
700a Ruppin, Eytanu NCI, Canc Data Sci Lab, Ctr Canc Res, Bethesda, MD 20892 USA.4 aut
700a Edfors, Fredriku KTH,Science for Life Laboratory, SciLifeLab,Systembiologi4 aut0 (Swepub:kth)u149ml0e
700a Ginty, Fionau GE Global Res Ctr, Life Sci & Mol Diagnost Lab, Niskayuna, NY USA.4 aut
700a Goltsev, Yuryu Stanford Univ, Stanford Med Sch, Dept Microbiol & Immunol, Baxter Lab Stem Cell Biol, Stanford, CA 94305 USA.4 aut
700a Wells, James A.u Univ Calif San Francisco, Dept Pharmaceut Sci, San Francisco, CA 94143 USA.4 aut
700a LaCava, Johnu Rockefeller Univ, Lab Cellular & Struct Biol, 1230 York Ave, New York, NY 10021 USA.4 aut
700a Riesterer, Jessica L.u Oregon Hlth & Sci Univ, Ctr Spatial Syst Biomed, Portland, OR 97201 USA.4 aut
700a Germain, Ronald N.u NIAID, Lab Immune Syst Biol, NIH, 9000 Rockville Pike, Bethesda, MD 20892 USA.4 aut
700a Shi, Tujinu Pacific Northwest Natl Lab, Biol Sci Div, Richland, WA 99352 USA.4 aut
700a Chee, Mark S.u Encodia Inc, San Diego, CA USA.4 aut
700a Budnik, Bogdan A.u Harvard Univ, Fac Arts & Sci, Div Sci, Boston, MA 02115 USA.4 aut
700a Yates, John R., IIIu Scripps Res Inst, Dept Mol Med, La Jolla, CA USA.4 aut
700a Chait, Brian T.u Rockefeller Univ, Lab Mass Spectrometry & Gaseous Ion Chem, 1230 York Ave, New York, NY 10021 USA.4 aut
700a Moffitt, Jeffery R.u Boston Childrens Hosp, Boston, MA USA.;Harvard Univ, Med Sch, Boston, MA 02115 USA.4 aut
700a Smith, Richard D.u Pacific Northwest Natl Lab, Biol Sci Div, Richland, WA 99352 USA.4 aut
700a Srivastava, Sudhiru NCI, Canc Biomarkers Res Grp, Div Canc Prevent, Bethesda, MD 20892 USA.4 aut
710a NCI, Canc Biomarkers Res Grp, Div Canc Prevent, Bethesda, MD 20892 USA.b Inst Syst Biol, Seattle, WA 98109 USA.4 org
773t Journal of Proteome Researchd : American Chemical Society (ACS)g 19:5, s. 1900-1912q 19:5<1900-1912x 1535-3893x 1535-3907
856u https://www.osti.gov/biblio/1639039
8564 8u https://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-300767
8564 8u https://doi.org/10.1021/acs.jproteome.0c00021

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