Fluorescence probes in oncology /:
A comprehensive description of fluorescence probes and the methodology for the study and diagnostics of oncology. The material is drawn directly from the work of pioneer researchers in cell biology and pathology, and offers a perspective of their crucial investigations and lifetime experiences; it a...
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| Format: | Elektronisch E-Book |
| Sprache: | English |
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London : River Edge, NJ :
Imperial College Press ; Distributed by World Scientific Pub.,
©2002.
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| Zusammenfassung: | A comprehensive description of fluorescence probes and the methodology for the study and diagnostics of oncology. The material is drawn directly from the work of pioneer researchers in cell biology and pathology, and offers a perspective of their crucial investigations and lifetime experiences; it also seeks to open new horizons on future developments in fundamental methods and diagnostics relevant to cellular physiopathology. Researchers in cell pathology have contributed a broad range of spectral and fluorescence images which supplement the information derived from Virchow style microscope slides (these still remain valid after more than 150 years, and a considerable body of knowledge and interpretation can be built around them). |
| Beschreibung: | 1 online resource (xxix, 704 pages) : illustrations (some color) |
| Bibliographie: | Includes bibliographical references and index. |
| ISBN: | 9781860947919 1860947913 1281866733 9781281866738 |
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| 100 | 1 | |a Kohen, Elli. | |
| 245 | 1 | 0 | |a Fluorescence probes in oncology / |c Elli Kohen, René Santus, Joseph G. Hirschberg. |
| 260 | |a London : |b Imperial College Press ; |a River Edge, NJ : |b Distributed by World Scientific Pub., |c ©2002. | ||
| 300 | |a 1 online resource (xxix, 704 pages) : |b illustrations (some color) | ||
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| 504 | |a Includes bibliographical references and index. | ||
| 588 | 0 | |a Print version record. | |
| 520 | |a A comprehensive description of fluorescence probes and the methodology for the study and diagnostics of oncology. The material is drawn directly from the work of pioneer researchers in cell biology and pathology, and offers a perspective of their crucial investigations and lifetime experiences; it also seeks to open new horizons on future developments in fundamental methods and diagnostics relevant to cellular physiopathology. Researchers in cell pathology have contributed a broad range of spectral and fluorescence images which supplement the information derived from Virchow style microscope slides (these still remain valid after more than 150 years, and a considerable body of knowledge and interpretation can be built around them). | ||
| 505 | 0 | |a Ch. I. The nature of light. 1.1. Origins. 1.2. Refraction. 1.3. Fermat's principle. 1.4. The speed of light. 1.5. The wave nature of light. 1.6. Diffraction and resolution limits. 1.7. The quantum theory and photons. 1.8. The production of light. 1.9. The Planck equation and photochemical reactions -- ch. II. Introduction to photophysics. 2.1. From atoms to molecules: the formation of chemical bonds. 2.2. Electronic transitions. 2.3. Excitation and deactivation of molecules. 2.4. Factors influencing the fluorescence quantum yield. 2.5. Quenching of the first excited singlet state by energy transfer -- ch. III. Basic approaches to the experimental study of chemical and biological luminescence. 3.1. Long-lifetime probes: metal-ligand complexes as a new class of long-lived fluorophores for protein hydrodynamics. 3.2. Chemiluminescence. 3.3. Bioluminescence. 3.4. Green fluorescent protein (GFP) -- ch. IV. Methods and instrumentation. 4.1. Spectrofluorometers and cell sorters. 4.2. Microspectrofluorometers. 4.3. Detectors used in fluorescence imaging. 4.4. Fluorescence imaging with CCD cameras. 4.5. Digital imaging. 4.6. Ratio fluorescence microscopy. 4.7. Multiparameter imaging. 4.8. Multiprobe approach to the study of intercellular communication. 4.9. Photodiode array fluorescence spectroscopy. 4.10. Confocal fluorescence microscopy. 4.11. Fluorescence lifetime imaging (FLIM). 4.12. Frequency-domain spectroscopy and tomography of tissues. 4.13. Fluorescence photobleaching recovery (FPR, also FRAP) and green fluorescent protein (GFP) chimeras. 4.14. Time-resolved fluorescence resonance energy transfer (FRET). 4.15. Fluorescence polarization in the microscope. 4.16. Polarization fluorescence photobleaching recovery (PFPR). 4.17. Picosecond fluorescence kinetics. 4.18. Raman fluorescence spectroscopy in single living cells. 4.19. Experimental time-resolved methods and photon migration in tissues studied by time-resolved spectroscopy. 4.20. Fourier transform spectroscopy in the infrared. 4.21. Secondary ion mass spectrometry (SIMS). | |
| 505 | 8 | |a Ch. V. New methods. Theoretical basis and potential applications to biology. 5.1. Total internal reflection fluorescence microscopy (TIRF) in cells. 5.2. Surface fluorescence detection by a microscope. 5.3. Intracellular sensing and optical imaging beyond the diffraction limit: scanning near-field optical microscopy (SNOM). 5.4. Optical forces, optical traps, optical tweezers in combination with microspectroscopy and fluorescent DNA intercalating dyes. 5.5. Fourier interferometric stimulation (FIS) and spectral image analysis. 5.6. Fourier transform multiplex spectroscopy and spectral imaging of protoporphyrin in single melanoma cells. 5.7. Fluorescence in situ hybridization (FISH). 5.8. Beyond FISH: multicolor spectral karyotyping of human chromosomes (SKY). 5.9. Combinatorial multi-fluor FISH. 5.10. Two-photon excitation induced fluorescence. 5.11. Three-photon induced fluorescence. 5.12. Light fluorescence quenching (LQ) and stimulate emission (SE). 5.13. Related topics: infrared imaging spectroscopy of breast -- ch. VI. Fluorescent probes. 6.1. Ion probes. 6.2. Membrane potential probes. 6.3. Cell organelle probes. 6.4. Probes of cell metabolism in the living cell, as a receptacle of smart probes. 6.5. Probes of cyclic Amp (cAMP) probing, signaling and oscillations. 6.6. Nucleic acid probes. 6.7. Probes of oxygenation and anoxia. 6.8. Fluorescent probes of reduced glutathione and thiol groups. 6.9. Merocyanines. 6.10. Caged substrates and photoactivated probes. 6.11. Optical thermometry in single living cells -- ch. VII. Applications of fluorescence techniques to study biological processes in normal and pathological cells. 7.1. Cell metabolism. 7.2. Signal transduction -- ch. VIII. Cell physiopathology. 8.1. Brain tumors. 8.2. Pituitary tumors. 8.3. Breast tumors. 8.4. Head and neck tumors. 8.5. Cancer of the cervix. 8.6. Lung and lung tumors. 8.7. Prostate cancer. 8.8. Cancer of the colon. 8.9. Sarcoma. 8.10. Immunoperoxidase studies of tumors. 8.11. Tumors with images of the characteristic immunoperoxidase reaction. 8.12. Viral pathology. 8.13. AIDS. | |
| 650 | 0 | |a Fluorescent probes. |0 http://id.loc.gov/authorities/subjects/sh93005286 | |
| 650 | 0 | |a Cell physiology |x Technique. |0 http://id.loc.gov/authorities/subjects/sh2020010014 | |
| 650 | 0 | |a Fluorescence microscopy. |0 http://id.loc.gov/authorities/subjects/sh85049410 | |
| 650 | 0 | |a Fluorescent probes |x Diagnostic use. | |
| 650 | 0 | |a Brain |x Tumors |x Diagnosis. |0 http://id.loc.gov/authorities/subjects/sh85016352 | |
| 650 | 0 | |a Oncology. |0 http://id.loc.gov/authorities/subjects/sh85094724 | |
| 650 | 0 | |a Cell physiology. |0 http://id.loc.gov/authorities/subjects/sh85021662 | |
| 650 | 1 | 2 | |a Fluorescent Dyes |0 https://id.nlm.nih.gov/mesh/D005456 |
| 650 | 2 | 2 | |a Brain Neoplasms |x diagnosis |
| 650 | 2 | 2 | |a Cell Physiological Phenomena |
| 650 | 2 | 2 | |a Microscopy, Fluorescence |
| 650 | 2 | |a Medical Oncology |0 https://id.nlm.nih.gov/mesh/D008495 | |
| 650 | 6 | |a Sondes fluorescentes. | |
| 650 | 6 | |a Microscopie de fluorescence. | |
| 650 | 6 | |a Sondes fluorescentes |x Utilisation diagnostique. | |
| 650 | 6 | |a Cancérologie. | |
| 650 | 6 | |a Cellules |x Physiologie. | |
| 650 | 7 | |a fluorescence microscopy. |2 aat | |
| 650 | 7 | |a SCIENCE |x Life Sciences |x Cell Biology. |2 bisacsh | |
| 650 | 7 | |a Cell physiology |2 fast | |
| 650 | 7 | |a Brain |x Tumors |x Diagnosis |2 fast | |
| 650 | 7 | |a Cell physiology |x Technique |2 fast | |
| 650 | 7 | |a Fluorescence microscopy |2 fast | |
| 650 | 7 | |a Fluorescent probes |2 fast | |
| 650 | 7 | |a Oncology |2 fast | |
| 650 | 7 | |a Oncologia. |2 larpcal | |
| 650 | 7 | |a Fluorescência. |2 larpcal | |
| 700 | 1 | |a Santus, René. | |
| 700 | 1 | |a Hirschberg, Joseph G. | |
| 776 | 0 | 8 | |i Print version: |a Kohen, Elli. |t Fluorescence probes in oncology. |d London : Imperial College Press ; River Edge, NJ : Distributed by World Scientific Pub., ©2002 |z 9781860941504 |w (OCoLC)50190958 |
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Datensatz im Suchindex
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| author | Kohen, Elli |
| author2 | Santus, René Hirschberg, Joseph G. |
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| author_facet | Kohen, Elli Santus, René Hirschberg, Joseph G. |
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| contents | Ch. I. The nature of light. 1.1. Origins. 1.2. Refraction. 1.3. Fermat's principle. 1.4. The speed of light. 1.5. The wave nature of light. 1.6. Diffraction and resolution limits. 1.7. The quantum theory and photons. 1.8. The production of light. 1.9. The Planck equation and photochemical reactions -- ch. II. Introduction to photophysics. 2.1. From atoms to molecules: the formation of chemical bonds. 2.2. Electronic transitions. 2.3. Excitation and deactivation of molecules. 2.4. Factors influencing the fluorescence quantum yield. 2.5. Quenching of the first excited singlet state by energy transfer -- ch. III. Basic approaches to the experimental study of chemical and biological luminescence. 3.1. Long-lifetime probes: metal-ligand complexes as a new class of long-lived fluorophores for protein hydrodynamics. 3.2. Chemiluminescence. 3.3. Bioluminescence. 3.4. Green fluorescent protein (GFP) -- ch. IV. Methods and instrumentation. 4.1. Spectrofluorometers and cell sorters. 4.2. Microspectrofluorometers. 4.3. Detectors used in fluorescence imaging. 4.4. Fluorescence imaging with CCD cameras. 4.5. Digital imaging. 4.6. Ratio fluorescence microscopy. 4.7. Multiparameter imaging. 4.8. Multiprobe approach to the study of intercellular communication. 4.9. Photodiode array fluorescence spectroscopy. 4.10. Confocal fluorescence microscopy. 4.11. Fluorescence lifetime imaging (FLIM). 4.12. Frequency-domain spectroscopy and tomography of tissues. 4.13. Fluorescence photobleaching recovery (FPR, also FRAP) and green fluorescent protein (GFP) chimeras. 4.14. Time-resolved fluorescence resonance energy transfer (FRET). 4.15. Fluorescence polarization in the microscope. 4.16. Polarization fluorescence photobleaching recovery (PFPR). 4.17. Picosecond fluorescence kinetics. 4.18. Raman fluorescence spectroscopy in single living cells. 4.19. Experimental time-resolved methods and photon migration in tissues studied by time-resolved spectroscopy. 4.20. Fourier transform spectroscopy in the infrared. 4.21. Secondary ion mass spectrometry (SIMS). Ch. V. New methods. Theoretical basis and potential applications to biology. 5.1. Total internal reflection fluorescence microscopy (TIRF) in cells. 5.2. Surface fluorescence detection by a microscope. 5.3. Intracellular sensing and optical imaging beyond the diffraction limit: scanning near-field optical microscopy (SNOM). 5.4. Optical forces, optical traps, optical tweezers in combination with microspectroscopy and fluorescent DNA intercalating dyes. 5.5. Fourier interferometric stimulation (FIS) and spectral image analysis. 5.6. Fourier transform multiplex spectroscopy and spectral imaging of protoporphyrin in single melanoma cells. 5.7. Fluorescence in situ hybridization (FISH). 5.8. Beyond FISH: multicolor spectral karyotyping of human chromosomes (SKY). 5.9. Combinatorial multi-fluor FISH. 5.10. Two-photon excitation induced fluorescence. 5.11. Three-photon induced fluorescence. 5.12. Light fluorescence quenching (LQ) and stimulate emission (SE). 5.13. Related topics: infrared imaging spectroscopy of breast -- ch. VI. Fluorescent probes. 6.1. Ion probes. 6.2. Membrane potential probes. 6.3. Cell organelle probes. 6.4. Probes of cell metabolism in the living cell, as a receptacle of smart probes. 6.5. Probes of cyclic Amp (cAMP) probing, signaling and oscillations. 6.6. Nucleic acid probes. 6.7. Probes of oxygenation and anoxia. 6.8. Fluorescent probes of reduced glutathione and thiol groups. 6.9. Merocyanines. 6.10. Caged substrates and photoactivated probes. 6.11. Optical thermometry in single living cells -- ch. VII. Applications of fluorescence techniques to study biological processes in normal and pathological cells. 7.1. Cell metabolism. 7.2. Signal transduction -- ch. VIII. Cell physiopathology. 8.1. Brain tumors. 8.2. Pituitary tumors. 8.3. Breast tumors. 8.4. Head and neck tumors. 8.5. Cancer of the cervix. 8.6. Lung and lung tumors. 8.7. Prostate cancer. 8.8. Cancer of the colon. 8.9. Sarcoma. 8.10. Immunoperoxidase studies of tumors. 8.11. Tumors with images of the characteristic immunoperoxidase reaction. 8.12. Viral pathology. 8.13. AIDS. |
| ctrlnum | (OCoLC)826660246 |
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The material is drawn directly from the work of pioneer researchers in cell biology and pathology, and offers a perspective of their crucial investigations and lifetime experiences; it also seeks to open new horizons on future developments in fundamental methods and diagnostics relevant to cellular physiopathology. Researchers in cell pathology have contributed a broad range of spectral and fluorescence images which supplement the information derived from Virchow style microscope slides (these still remain valid after more than 150 years, and a considerable body of knowledge and interpretation can be built around them).</subfield></datafield><datafield tag="505" ind1="0" ind2=" "><subfield code="a">Ch. I. The nature of light. 1.1. Origins. 1.2. Refraction. 1.3. Fermat's principle. 1.4. The speed of light. 1.5. The wave nature of light. 1.6. Diffraction and resolution limits. 1.7. The quantum theory and photons. 1.8. The production of light. 1.9. The Planck equation and photochemical reactions -- ch. II. Introduction to photophysics. 2.1. From atoms to molecules: the formation of chemical bonds. 2.2. Electronic transitions. 2.3. Excitation and deactivation of molecules. 2.4. Factors influencing the fluorescence quantum yield. 2.5. Quenching of the first excited singlet state by energy transfer -- ch. III. Basic approaches to the experimental study of chemical and biological luminescence. 3.1. Long-lifetime probes: metal-ligand complexes as a new class of long-lived fluorophores for protein hydrodynamics. 3.2. Chemiluminescence. 3.3. Bioluminescence. 3.4. Green fluorescent protein (GFP) -- ch. IV. Methods and instrumentation. 4.1. Spectrofluorometers and cell sorters. 4.2. Microspectrofluorometers. 4.3. Detectors used in fluorescence imaging. 4.4. Fluorescence imaging with CCD cameras. 4.5. Digital imaging. 4.6. Ratio fluorescence microscopy. 4.7. Multiparameter imaging. 4.8. Multiprobe approach to the study of intercellular communication. 4.9. Photodiode array fluorescence spectroscopy. 4.10. Confocal fluorescence microscopy. 4.11. Fluorescence lifetime imaging (FLIM). 4.12. Frequency-domain spectroscopy and tomography of tissues. 4.13. Fluorescence photobleaching recovery (FPR, also FRAP) and green fluorescent protein (GFP) chimeras. 4.14. Time-resolved fluorescence resonance energy transfer (FRET). 4.15. Fluorescence polarization in the microscope. 4.16. Polarization fluorescence photobleaching recovery (PFPR). 4.17. Picosecond fluorescence kinetics. 4.18. Raman fluorescence spectroscopy in single living cells. 4.19. Experimental time-resolved methods and photon migration in tissues studied by time-resolved spectroscopy. 4.20. Fourier transform spectroscopy in the infrared. 4.21. Secondary ion mass spectrometry (SIMS).</subfield></datafield><datafield tag="505" ind1="8" ind2=" "><subfield code="a">Ch. V. New methods. Theoretical basis and potential applications to biology. 5.1. Total internal reflection fluorescence microscopy (TIRF) in cells. 5.2. Surface fluorescence detection by a microscope. 5.3. Intracellular sensing and optical imaging beyond the diffraction limit: scanning near-field optical microscopy (SNOM). 5.4. Optical forces, optical traps, optical tweezers in combination with microspectroscopy and fluorescent DNA intercalating dyes. 5.5. Fourier interferometric stimulation (FIS) and spectral image analysis. 5.6. Fourier transform multiplex spectroscopy and spectral imaging of protoporphyrin in single melanoma cells. 5.7. Fluorescence in situ hybridization (FISH). 5.8. Beyond FISH: multicolor spectral karyotyping of human chromosomes (SKY). 5.9. Combinatorial multi-fluor FISH. 5.10. Two-photon excitation induced fluorescence. 5.11. Three-photon induced fluorescence. 5.12. Light fluorescence quenching (LQ) and stimulate emission (SE). 5.13. Related topics: infrared imaging spectroscopy of breast -- ch. VI. Fluorescent probes. 6.1. Ion probes. 6.2. Membrane potential probes. 6.3. Cell organelle probes. 6.4. Probes of cell metabolism in the living cell, as a receptacle of smart probes. 6.5. Probes of cyclic Amp (cAMP) probing, signaling and oscillations. 6.6. Nucleic acid probes. 6.7. Probes of oxygenation and anoxia. 6.8. Fluorescent probes of reduced glutathione and thiol groups. 6.9. Merocyanines. 6.10. Caged substrates and photoactivated probes. 6.11. Optical thermometry in single living cells -- ch. VII. Applications of fluorescence techniques to study biological processes in normal and pathological cells. 7.1. Cell metabolism. 7.2. Signal transduction -- ch. VIII. Cell physiopathology. 8.1. Brain tumors. 8.2. Pituitary tumors. 8.3. Breast tumors. 8.4. Head and neck tumors. 8.5. Cancer of the cervix. 8.6. Lung and lung tumors. 8.7. Prostate cancer. 8.8. Cancer of the colon. 8.9. Sarcoma. 8.10. Immunoperoxidase studies of tumors. 8.11. Tumors with images of the characteristic immunoperoxidase reaction. 8.12. Viral pathology. 8.13. 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| id | ZDB-4-EBA-ocn826660246 |
| illustrated | Illustrated |
| indexdate | 2024-11-27T13:25:10Z |
| institution | BVB |
| isbn | 9781860947919 1860947913 1281866733 9781281866738 |
| language | English |
| oclc_num | 826660246 |
| open_access_boolean | |
| owner | MAIN DE-863 DE-BY-FWS |
| owner_facet | MAIN DE-863 DE-BY-FWS |
| physical | 1 online resource (xxix, 704 pages) : illustrations (some color) |
| psigel | ZDB-4-EBA |
| publishDate | 2002 |
| publishDateSearch | 2002 |
| publishDateSort | 2002 |
| publisher | Imperial College Press ; Distributed by World Scientific Pub., |
| record_format | marc |
| spelling | Kohen, Elli. Fluorescence probes in oncology / Elli Kohen, René Santus, Joseph G. Hirschberg. London : Imperial College Press ; River Edge, NJ : Distributed by World Scientific Pub., ©2002. 1 online resource (xxix, 704 pages) : illustrations (some color) text txt rdacontent computer c rdamedia online resource cr rdacarrier Includes bibliographical references and index. Print version record. A comprehensive description of fluorescence probes and the methodology for the study and diagnostics of oncology. The material is drawn directly from the work of pioneer researchers in cell biology and pathology, and offers a perspective of their crucial investigations and lifetime experiences; it also seeks to open new horizons on future developments in fundamental methods and diagnostics relevant to cellular physiopathology. Researchers in cell pathology have contributed a broad range of spectral and fluorescence images which supplement the information derived from Virchow style microscope slides (these still remain valid after more than 150 years, and a considerable body of knowledge and interpretation can be built around them). Ch. I. The nature of light. 1.1. Origins. 1.2. Refraction. 1.3. Fermat's principle. 1.4. The speed of light. 1.5. The wave nature of light. 1.6. Diffraction and resolution limits. 1.7. The quantum theory and photons. 1.8. The production of light. 1.9. The Planck equation and photochemical reactions -- ch. II. Introduction to photophysics. 2.1. From atoms to molecules: the formation of chemical bonds. 2.2. Electronic transitions. 2.3. Excitation and deactivation of molecules. 2.4. Factors influencing the fluorescence quantum yield. 2.5. Quenching of the first excited singlet state by energy transfer -- ch. III. Basic approaches to the experimental study of chemical and biological luminescence. 3.1. Long-lifetime probes: metal-ligand complexes as a new class of long-lived fluorophores for protein hydrodynamics. 3.2. Chemiluminescence. 3.3. Bioluminescence. 3.4. Green fluorescent protein (GFP) -- ch. IV. Methods and instrumentation. 4.1. Spectrofluorometers and cell sorters. 4.2. Microspectrofluorometers. 4.3. Detectors used in fluorescence imaging. 4.4. Fluorescence imaging with CCD cameras. 4.5. Digital imaging. 4.6. Ratio fluorescence microscopy. 4.7. Multiparameter imaging. 4.8. Multiprobe approach to the study of intercellular communication. 4.9. Photodiode array fluorescence spectroscopy. 4.10. Confocal fluorescence microscopy. 4.11. Fluorescence lifetime imaging (FLIM). 4.12. Frequency-domain spectroscopy and tomography of tissues. 4.13. Fluorescence photobleaching recovery (FPR, also FRAP) and green fluorescent protein (GFP) chimeras. 4.14. Time-resolved fluorescence resonance energy transfer (FRET). 4.15. Fluorescence polarization in the microscope. 4.16. Polarization fluorescence photobleaching recovery (PFPR). 4.17. Picosecond fluorescence kinetics. 4.18. Raman fluorescence spectroscopy in single living cells. 4.19. Experimental time-resolved methods and photon migration in tissues studied by time-resolved spectroscopy. 4.20. Fourier transform spectroscopy in the infrared. 4.21. Secondary ion mass spectrometry (SIMS). Ch. V. New methods. Theoretical basis and potential applications to biology. 5.1. Total internal reflection fluorescence microscopy (TIRF) in cells. 5.2. Surface fluorescence detection by a microscope. 5.3. Intracellular sensing and optical imaging beyond the diffraction limit: scanning near-field optical microscopy (SNOM). 5.4. Optical forces, optical traps, optical tweezers in combination with microspectroscopy and fluorescent DNA intercalating dyes. 5.5. Fourier interferometric stimulation (FIS) and spectral image analysis. 5.6. Fourier transform multiplex spectroscopy and spectral imaging of protoporphyrin in single melanoma cells. 5.7. Fluorescence in situ hybridization (FISH). 5.8. Beyond FISH: multicolor spectral karyotyping of human chromosomes (SKY). 5.9. Combinatorial multi-fluor FISH. 5.10. Two-photon excitation induced fluorescence. 5.11. Three-photon induced fluorescence. 5.12. Light fluorescence quenching (LQ) and stimulate emission (SE). 5.13. Related topics: infrared imaging spectroscopy of breast -- ch. VI. Fluorescent probes. 6.1. Ion probes. 6.2. Membrane potential probes. 6.3. Cell organelle probes. 6.4. Probes of cell metabolism in the living cell, as a receptacle of smart probes. 6.5. Probes of cyclic Amp (cAMP) probing, signaling and oscillations. 6.6. Nucleic acid probes. 6.7. Probes of oxygenation and anoxia. 6.8. Fluorescent probes of reduced glutathione and thiol groups. 6.9. Merocyanines. 6.10. Caged substrates and photoactivated probes. 6.11. Optical thermometry in single living cells -- ch. VII. Applications of fluorescence techniques to study biological processes in normal and pathological cells. 7.1. Cell metabolism. 7.2. Signal transduction -- ch. VIII. Cell physiopathology. 8.1. Brain tumors. 8.2. Pituitary tumors. 8.3. Breast tumors. 8.4. Head and neck tumors. 8.5. Cancer of the cervix. 8.6. Lung and lung tumors. 8.7. Prostate cancer. 8.8. Cancer of the colon. 8.9. Sarcoma. 8.10. Immunoperoxidase studies of tumors. 8.11. Tumors with images of the characteristic immunoperoxidase reaction. 8.12. Viral pathology. 8.13. AIDS. Fluorescent probes. http://id.loc.gov/authorities/subjects/sh93005286 Cell physiology Technique. http://id.loc.gov/authorities/subjects/sh2020010014 Fluorescence microscopy. http://id.loc.gov/authorities/subjects/sh85049410 Fluorescent probes Diagnostic use. Brain Tumors Diagnosis. http://id.loc.gov/authorities/subjects/sh85016352 Oncology. http://id.loc.gov/authorities/subjects/sh85094724 Cell physiology. http://id.loc.gov/authorities/subjects/sh85021662 Fluorescent Dyes https://id.nlm.nih.gov/mesh/D005456 Brain Neoplasms diagnosis Cell Physiological Phenomena Microscopy, Fluorescence Medical Oncology https://id.nlm.nih.gov/mesh/D008495 Sondes fluorescentes. Microscopie de fluorescence. Sondes fluorescentes Utilisation diagnostique. Cancérologie. Cellules Physiologie. fluorescence microscopy. aat SCIENCE Life Sciences Cell Biology. bisacsh Cell physiology fast Brain Tumors Diagnosis fast Cell physiology Technique fast Fluorescence microscopy fast Fluorescent probes fast Oncology fast Oncologia. larpcal Fluorescência. larpcal Santus, René. Hirschberg, Joseph G. Print version: Kohen, Elli. Fluorescence probes in oncology. London : Imperial College Press ; River Edge, NJ : Distributed by World Scientific Pub., ©2002 9781860941504 (OCoLC)50190958 FWS01 ZDB-4-EBA FWS_PDA_EBA https://search.ebscohost.com/login.aspx?direct=true&scope=site&db=nlebk&AN=521290 Volltext |
| spellingShingle | Kohen, Elli Fluorescence probes in oncology / Ch. I. The nature of light. 1.1. Origins. 1.2. Refraction. 1.3. Fermat's principle. 1.4. The speed of light. 1.5. The wave nature of light. 1.6. Diffraction and resolution limits. 1.7. The quantum theory and photons. 1.8. The production of light. 1.9. The Planck equation and photochemical reactions -- ch. II. Introduction to photophysics. 2.1. From atoms to molecules: the formation of chemical bonds. 2.2. Electronic transitions. 2.3. Excitation and deactivation of molecules. 2.4. Factors influencing the fluorescence quantum yield. 2.5. Quenching of the first excited singlet state by energy transfer -- ch. III. Basic approaches to the experimental study of chemical and biological luminescence. 3.1. Long-lifetime probes: metal-ligand complexes as a new class of long-lived fluorophores for protein hydrodynamics. 3.2. Chemiluminescence. 3.3. Bioluminescence. 3.4. Green fluorescent protein (GFP) -- ch. IV. Methods and instrumentation. 4.1. Spectrofluorometers and cell sorters. 4.2. Microspectrofluorometers. 4.3. Detectors used in fluorescence imaging. 4.4. Fluorescence imaging with CCD cameras. 4.5. Digital imaging. 4.6. Ratio fluorescence microscopy. 4.7. Multiparameter imaging. 4.8. Multiprobe approach to the study of intercellular communication. 4.9. Photodiode array fluorescence spectroscopy. 4.10. Confocal fluorescence microscopy. 4.11. Fluorescence lifetime imaging (FLIM). 4.12. Frequency-domain spectroscopy and tomography of tissues. 4.13. Fluorescence photobleaching recovery (FPR, also FRAP) and green fluorescent protein (GFP) chimeras. 4.14. Time-resolved fluorescence resonance energy transfer (FRET). 4.15. Fluorescence polarization in the microscope. 4.16. Polarization fluorescence photobleaching recovery (PFPR). 4.17. Picosecond fluorescence kinetics. 4.18. Raman fluorescence spectroscopy in single living cells. 4.19. Experimental time-resolved methods and photon migration in tissues studied by time-resolved spectroscopy. 4.20. Fourier transform spectroscopy in the infrared. 4.21. Secondary ion mass spectrometry (SIMS). Ch. V. New methods. Theoretical basis and potential applications to biology. 5.1. Total internal reflection fluorescence microscopy (TIRF) in cells. 5.2. Surface fluorescence detection by a microscope. 5.3. Intracellular sensing and optical imaging beyond the diffraction limit: scanning near-field optical microscopy (SNOM). 5.4. Optical forces, optical traps, optical tweezers in combination with microspectroscopy and fluorescent DNA intercalating dyes. 5.5. Fourier interferometric stimulation (FIS) and spectral image analysis. 5.6. Fourier transform multiplex spectroscopy and spectral imaging of protoporphyrin in single melanoma cells. 5.7. Fluorescence in situ hybridization (FISH). 5.8. Beyond FISH: multicolor spectral karyotyping of human chromosomes (SKY). 5.9. Combinatorial multi-fluor FISH. 5.10. Two-photon excitation induced fluorescence. 5.11. Three-photon induced fluorescence. 5.12. Light fluorescence quenching (LQ) and stimulate emission (SE). 5.13. Related topics: infrared imaging spectroscopy of breast -- ch. VI. Fluorescent probes. 6.1. Ion probes. 6.2. Membrane potential probes. 6.3. Cell organelle probes. 6.4. Probes of cell metabolism in the living cell, as a receptacle of smart probes. 6.5. Probes of cyclic Amp (cAMP) probing, signaling and oscillations. 6.6. Nucleic acid probes. 6.7. Probes of oxygenation and anoxia. 6.8. Fluorescent probes of reduced glutathione and thiol groups. 6.9. Merocyanines. 6.10. Caged substrates and photoactivated probes. 6.11. Optical thermometry in single living cells -- ch. VII. Applications of fluorescence techniques to study biological processes in normal and pathological cells. 7.1. Cell metabolism. 7.2. Signal transduction -- ch. VIII. Cell physiopathology. 8.1. Brain tumors. 8.2. Pituitary tumors. 8.3. Breast tumors. 8.4. Head and neck tumors. 8.5. Cancer of the cervix. 8.6. Lung and lung tumors. 8.7. Prostate cancer. 8.8. Cancer of the colon. 8.9. Sarcoma. 8.10. Immunoperoxidase studies of tumors. 8.11. Tumors with images of the characteristic immunoperoxidase reaction. 8.12. Viral pathology. 8.13. AIDS. Fluorescent probes. http://id.loc.gov/authorities/subjects/sh93005286 Cell physiology Technique. http://id.loc.gov/authorities/subjects/sh2020010014 Fluorescence microscopy. http://id.loc.gov/authorities/subjects/sh85049410 Fluorescent probes Diagnostic use. Brain Tumors Diagnosis. http://id.loc.gov/authorities/subjects/sh85016352 Oncology. http://id.loc.gov/authorities/subjects/sh85094724 Cell physiology. http://id.loc.gov/authorities/subjects/sh85021662 Fluorescent Dyes https://id.nlm.nih.gov/mesh/D005456 Brain Neoplasms diagnosis Cell Physiological Phenomena Microscopy, Fluorescence Medical Oncology https://id.nlm.nih.gov/mesh/D008495 Sondes fluorescentes. Microscopie de fluorescence. Sondes fluorescentes Utilisation diagnostique. Cancérologie. Cellules Physiologie. fluorescence microscopy. aat SCIENCE Life Sciences Cell Biology. bisacsh Cell physiology fast Brain Tumors Diagnosis fast Cell physiology Technique fast Fluorescence microscopy fast Fluorescent probes fast Oncology fast Oncologia. larpcal Fluorescência. larpcal |
| subject_GND | http://id.loc.gov/authorities/subjects/sh93005286 http://id.loc.gov/authorities/subjects/sh2020010014 http://id.loc.gov/authorities/subjects/sh85049410 http://id.loc.gov/authorities/subjects/sh85016352 http://id.loc.gov/authorities/subjects/sh85094724 http://id.loc.gov/authorities/subjects/sh85021662 https://id.nlm.nih.gov/mesh/D005456 https://id.nlm.nih.gov/mesh/D008495 |
| title | Fluorescence probes in oncology / |
| title_auth | Fluorescence probes in oncology / |
| title_exact_search | Fluorescence probes in oncology / |
| title_full | Fluorescence probes in oncology / Elli Kohen, René Santus, Joseph G. Hirschberg. |
| title_fullStr | Fluorescence probes in oncology / Elli Kohen, René Santus, Joseph G. Hirschberg. |
| title_full_unstemmed | Fluorescence probes in oncology / Elli Kohen, René Santus, Joseph G. Hirschberg. |
| title_short | Fluorescence probes in oncology / |
| title_sort | fluorescence probes in oncology |
| topic | Fluorescent probes. http://id.loc.gov/authorities/subjects/sh93005286 Cell physiology Technique. http://id.loc.gov/authorities/subjects/sh2020010014 Fluorescence microscopy. http://id.loc.gov/authorities/subjects/sh85049410 Fluorescent probes Diagnostic use. Brain Tumors Diagnosis. http://id.loc.gov/authorities/subjects/sh85016352 Oncology. http://id.loc.gov/authorities/subjects/sh85094724 Cell physiology. http://id.loc.gov/authorities/subjects/sh85021662 Fluorescent Dyes https://id.nlm.nih.gov/mesh/D005456 Brain Neoplasms diagnosis Cell Physiological Phenomena Microscopy, Fluorescence Medical Oncology https://id.nlm.nih.gov/mesh/D008495 Sondes fluorescentes. Microscopie de fluorescence. Sondes fluorescentes Utilisation diagnostique. Cancérologie. Cellules Physiologie. fluorescence microscopy. aat SCIENCE Life Sciences Cell Biology. bisacsh Cell physiology fast Brain Tumors Diagnosis fast Cell physiology Technique fast Fluorescence microscopy fast Fluorescent probes fast Oncology fast Oncologia. larpcal Fluorescência. larpcal |
| topic_facet | Fluorescent probes. Cell physiology Technique. Fluorescence microscopy. Fluorescent probes Diagnostic use. Brain Tumors Diagnosis. Oncology. Cell physiology. Fluorescent Dyes Brain Neoplasms diagnosis Cell Physiological Phenomena Microscopy, Fluorescence Medical Oncology Sondes fluorescentes. Microscopie de fluorescence. Sondes fluorescentes Utilisation diagnostique. Cancérologie. Cellules Physiologie. fluorescence microscopy. SCIENCE Life Sciences Cell Biology. Cell physiology Brain Tumors Diagnosis Cell physiology Technique Fluorescence microscopy Fluorescent probes Oncology Oncologia. Fluorescência. |
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| work_keys_str_mv | AT kohenelli fluorescenceprobesinoncology AT santusrene fluorescenceprobesinoncology AT hirschbergjosephg fluorescenceprobesinoncology |