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You searched for subject:(fluorine 18). Showing records 1 – 30 of 38 total matches.

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University of Melbourne

1. HASKALI, MOHAMMAD. Synthesis and [18F] fluorine-radiolabelling of peptides for positron emission tomography imaging of cancer.

Degree: 2014, University of Melbourne

 Positron Emission Tomography (PET) is a molecular imaging technique, requiring biologically active molecules that are radiolabelled with positron emitting radionuclides. [18F]Fluorine is considered an ideal… (more)

Subjects/Keywords: radiochemistry; PET imaging; radiolabelling; 18-fluorine; peptides

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APA (6th Edition):

HASKALI, M. (2014). Synthesis and [18F] fluorine-radiolabelling of peptides for positron emission tomography imaging of cancer. (Doctoral Dissertation). University of Melbourne. Retrieved from http://hdl.handle.net/11343/52367

Chicago Manual of Style (16th Edition):

HASKALI, MOHAMMAD. “Synthesis and [18F] fluorine-radiolabelling of peptides for positron emission tomography imaging of cancer.” 2014. Doctoral Dissertation, University of Melbourne. Accessed September 19, 2019. http://hdl.handle.net/11343/52367.

MLA Handbook (7th Edition):

HASKALI, MOHAMMAD. “Synthesis and [18F] fluorine-radiolabelling of peptides for positron emission tomography imaging of cancer.” 2014. Web. 19 Sep 2019.

Vancouver:

HASKALI M. Synthesis and [18F] fluorine-radiolabelling of peptides for positron emission tomography imaging of cancer. [Internet] [Doctoral dissertation]. University of Melbourne; 2014. [cited 2019 Sep 19]. Available from: http://hdl.handle.net/11343/52367.

Council of Science Editors:

HASKALI M. Synthesis and [18F] fluorine-radiolabelling of peptides for positron emission tomography imaging of cancer. [Doctoral Dissertation]. University of Melbourne; 2014. Available from: http://hdl.handle.net/11343/52367


Texas A&M University

2. Chansaenpak, Kantapat. Organoboranes as 18F Fluoride Anion Captors.

Degree: 2015, Texas A&M University

Fluorine-18 (18F) is the most frequently used radionuclide in positron emission tomography (PET). This is, in part, due to the fact that fluorine is the… (more)

Subjects/Keywords: Fluoride captor; Organoborane; Fluorine-18; Positron Emission Tomography

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APA (6th Edition):

Chansaenpak, K. (2015). Organoboranes as 18F Fluoride Anion Captors. (Thesis). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/155557

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Chansaenpak, Kantapat. “Organoboranes as 18F Fluoride Anion Captors.” 2015. Thesis, Texas A&M University. Accessed September 19, 2019. http://hdl.handle.net/1969.1/155557.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Chansaenpak, Kantapat. “Organoboranes as 18F Fluoride Anion Captors.” 2015. Web. 19 Sep 2019.

Vancouver:

Chansaenpak K. Organoboranes as 18F Fluoride Anion Captors. [Internet] [Thesis]. Texas A&M University; 2015. [cited 2019 Sep 19]. Available from: http://hdl.handle.net/1969.1/155557.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Chansaenpak K. Organoboranes as 18F Fluoride Anion Captors. [Thesis]. Texas A&M University; 2015. Available from: http://hdl.handle.net/1969.1/155557

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of Manchester

3. Fairclough, Michael Edward. PET Radiochemistry for the Investigation of the biology of pain and inflammation.

Degree: 2015, University of Manchester

 Positron emission tomography (PET) is an important and powerful nuclear imaging modality and is essential in a range of medical fields. A suitable radiotracer must… (more)

Subjects/Keywords: PET; Radiochemistry; Carbon-11; Fluorine-18; Zirconium-89; Inflammation Imaging; Opioids

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APA (6th Edition):

Fairclough, M. E. (2015). PET Radiochemistry for the Investigation of the biology of pain and inflammation. (Doctoral Dissertation). University of Manchester. Retrieved from http://www.manchester.ac.uk/escholar/uk-ac-man-scw:271063

Chicago Manual of Style (16th Edition):

Fairclough, Michael Edward. “PET Radiochemistry for the Investigation of the biology of pain and inflammation.” 2015. Doctoral Dissertation, University of Manchester. Accessed September 19, 2019. http://www.manchester.ac.uk/escholar/uk-ac-man-scw:271063.

MLA Handbook (7th Edition):

Fairclough, Michael Edward. “PET Radiochemistry for the Investigation of the biology of pain and inflammation.” 2015. Web. 19 Sep 2019.

Vancouver:

Fairclough ME. PET Radiochemistry for the Investigation of the biology of pain and inflammation. [Internet] [Doctoral dissertation]. University of Manchester; 2015. [cited 2019 Sep 19]. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:271063.

Council of Science Editors:

Fairclough ME. PET Radiochemistry for the Investigation of the biology of pain and inflammation. [Doctoral Dissertation]. University of Manchester; 2015. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:271063


University of Illinois – Urbana-Champaign

4. Yasui, Norio. I. Facile preparation of ortho-fluorophenols from non-aromatic precursors and investigation of applications to fluorine-18 labeling II. Resin-supported silyl ester precursors for kit-like radiolabeling with fluorine-18.

Degree: PhD, Chemistry, 2015, University of Illinois – Urbana-Champaign

 Molecular imaging is a technique that can be used to visualize complex biochemical processes without perturbing living organisms, and it has been playing increasingly important… (more)

Subjects/Keywords: fluorine-18; radiochemistry; fluorination; diazoketone; silyl ester; resin-supported

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APA (6th Edition):

Yasui, N. (2015). I. Facile preparation of ortho-fluorophenols from non-aromatic precursors and investigation of applications to fluorine-18 labeling II. Resin-supported silyl ester precursors for kit-like radiolabeling with fluorine-18. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/88254

Chicago Manual of Style (16th Edition):

Yasui, Norio. “I. Facile preparation of ortho-fluorophenols from non-aromatic precursors and investigation of applications to fluorine-18 labeling II. Resin-supported silyl ester precursors for kit-like radiolabeling with fluorine-18.” 2015. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed September 19, 2019. http://hdl.handle.net/2142/88254.

MLA Handbook (7th Edition):

Yasui, Norio. “I. Facile preparation of ortho-fluorophenols from non-aromatic precursors and investigation of applications to fluorine-18 labeling II. Resin-supported silyl ester precursors for kit-like radiolabeling with fluorine-18.” 2015. Web. 19 Sep 2019.

Vancouver:

Yasui N. I. Facile preparation of ortho-fluorophenols from non-aromatic precursors and investigation of applications to fluorine-18 labeling II. Resin-supported silyl ester precursors for kit-like radiolabeling with fluorine-18. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2015. [cited 2019 Sep 19]. Available from: http://hdl.handle.net/2142/88254.

Council of Science Editors:

Yasui N. I. Facile preparation of ortho-fluorophenols from non-aromatic precursors and investigation of applications to fluorine-18 labeling II. Resin-supported silyl ester precursors for kit-like radiolabeling with fluorine-18. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2015. Available from: http://hdl.handle.net/2142/88254


University of Illinois – Urbana-Champaign

5. Carroll, Vincent. I. Development of novel silicon precursors for rapid and efficient radiofluorination reactions: synthesis and biological evaluation of a 18f-labelled estrogen dendrimer conjugate II. Other studies on 18f-labelled estrogens.

Degree: PhD, Chemistry, 2012, University of Illinois – Urbana-Champaign

 Molecular imaging (MI) has revolutionized the visualization of complex biochemical processes in normal physiology and diseased states. Although still in its infancy, the data generated… (more)

Subjects/Keywords: 2-fluoroestradiol; estrogen dendrimer conjugate; estrogen receptor; fluorine-18

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APA (6th Edition):

Carroll, V. (2012). I. Development of novel silicon precursors for rapid and efficient radiofluorination reactions: synthesis and biological evaluation of a 18f-labelled estrogen dendrimer conjugate II. Other studies on 18f-labelled estrogens. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/95662

Chicago Manual of Style (16th Edition):

Carroll, Vincent. “I. Development of novel silicon precursors for rapid and efficient radiofluorination reactions: synthesis and biological evaluation of a 18f-labelled estrogen dendrimer conjugate II. Other studies on 18f-labelled estrogens.” 2012. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed September 19, 2019. http://hdl.handle.net/2142/95662.

MLA Handbook (7th Edition):

Carroll, Vincent. “I. Development of novel silicon precursors for rapid and efficient radiofluorination reactions: synthesis and biological evaluation of a 18f-labelled estrogen dendrimer conjugate II. Other studies on 18f-labelled estrogens.” 2012. Web. 19 Sep 2019.

Vancouver:

Carroll V. I. Development of novel silicon precursors for rapid and efficient radiofluorination reactions: synthesis and biological evaluation of a 18f-labelled estrogen dendrimer conjugate II. Other studies on 18f-labelled estrogens. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2012. [cited 2019 Sep 19]. Available from: http://hdl.handle.net/2142/95662.

Council of Science Editors:

Carroll V. I. Development of novel silicon precursors for rapid and efficient radiofluorination reactions: synthesis and biological evaluation of a 18f-labelled estrogen dendrimer conjugate II. Other studies on 18f-labelled estrogens. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2012. Available from: http://hdl.handle.net/2142/95662


University of Oxford

6. Calderwood, Samuel. Novel methods for 18F-radiolabelling.

Degree: PhD, 2016, University of Oxford

 The expansion of [18F]-radiolabelling methodologies is vital for the advancement of Positron Emission Tomography (PET) as a medical imaging tool. Novel protocols will simplify access… (more)

Subjects/Keywords: 541; Radiochemistry; Radiofluorination; Fluorine-18; Organic Chemistry; Positron Emission Tomography

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APA (6th Edition):

Calderwood, S. (2016). Novel methods for 18F-radiolabelling. (Doctoral Dissertation). University of Oxford. Retrieved from https://ora.ox.ac.uk/objects/uuid:9cd31311-0825-4f10-bd84-8568191175f7 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.730136

Chicago Manual of Style (16th Edition):

Calderwood, Samuel. “Novel methods for 18F-radiolabelling.” 2016. Doctoral Dissertation, University of Oxford. Accessed September 19, 2019. https://ora.ox.ac.uk/objects/uuid:9cd31311-0825-4f10-bd84-8568191175f7 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.730136.

MLA Handbook (7th Edition):

Calderwood, Samuel. “Novel methods for 18F-radiolabelling.” 2016. Web. 19 Sep 2019.

Vancouver:

Calderwood S. Novel methods for 18F-radiolabelling. [Internet] [Doctoral dissertation]. University of Oxford; 2016. [cited 2019 Sep 19]. Available from: https://ora.ox.ac.uk/objects/uuid:9cd31311-0825-4f10-bd84-8568191175f7 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.730136.

Council of Science Editors:

Calderwood S. Novel methods for 18F-radiolabelling. [Doctoral Dissertation]. University of Oxford; 2016. Available from: https://ora.ox.ac.uk/objects/uuid:9cd31311-0825-4f10-bd84-8568191175f7 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.730136


North Carolina State University

7. Roberts, Amy Nicole. Thermosyphon Targets Designed for the Production of 18F for use in Positron Emission Tomography.

Degree: MS, Nuclear Engineering, 2002, North Carolina State University

 ¹⁸F is a radioisotope commonly used in Positron Emission Tomography. One way to produce ¹⁸F is to bombard ¹⁸O enriched water with protons, generated by… (more)

Subjects/Keywords: Fluorodeoxyglucose; Fluorine 18; F-18; FDG; Positron Emission Tomography; thermosyphon; Fluorine-18

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APA (6th Edition):

Roberts, A. N. (2002). Thermosyphon Targets Designed for the Production of 18F for use in Positron Emission Tomography. (Thesis). North Carolina State University. Retrieved from http://www.lib.ncsu.edu/resolver/1840.16/2333

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Roberts, Amy Nicole. “Thermosyphon Targets Designed for the Production of 18F for use in Positron Emission Tomography.” 2002. Thesis, North Carolina State University. Accessed September 19, 2019. http://www.lib.ncsu.edu/resolver/1840.16/2333.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Roberts, Amy Nicole. “Thermosyphon Targets Designed for the Production of 18F for use in Positron Emission Tomography.” 2002. Web. 19 Sep 2019.

Vancouver:

Roberts AN. Thermosyphon Targets Designed for the Production of 18F for use in Positron Emission Tomography. [Internet] [Thesis]. North Carolina State University; 2002. [cited 2019 Sep 19]. Available from: http://www.lib.ncsu.edu/resolver/1840.16/2333.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Roberts AN. Thermosyphon Targets Designed for the Production of 18F for use in Positron Emission Tomography. [Thesis]. North Carolina State University; 2002. Available from: http://www.lib.ncsu.edu/resolver/1840.16/2333

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


Université Paris-Sud – Paris XI

8. Médran-Navarrete, Vincent. Synthèse de nouvelles sondes moléculaires marquées au fluor-18 pour l’imagerie de la neuroinflammation par Tomographie par Emission de Positons : Synthesis of new molecular probes radiolabelled with fluorine-18 for imaging neuroinflammation with Positon Emission Tomography.

Degree: Docteur es, Chimie, 2014, Université Paris-Sud – Paris XI

Les travaux présentés dans ce manuscrit ont pour objectifs la synthèse chimique de nouveaux ligands de la protéine de translocation 18 kDa (TSPO), leur évaluation… (more)

Subjects/Keywords: Chimie médicinale; Radiochimie; Fluor-18; Imagerie moléculaire; Tomographie par Emission de Positons; Neuroinflammation; TSPO 18 kDa; Medicinal chemistry; Radiochemistry; Fluorine-18; Molecular Imaging; Positron Emission Tomography; Neuroinflammation; TSPO 18 kDa

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APA (6th Edition):

Médran-Navarrete, V. (2014). Synthèse de nouvelles sondes moléculaires marquées au fluor-18 pour l’imagerie de la neuroinflammation par Tomographie par Emission de Positons : Synthesis of new molecular probes radiolabelled with fluorine-18 for imaging neuroinflammation with Positon Emission Tomography. (Doctoral Dissertation). Université Paris-Sud – Paris XI. Retrieved from http://www.theses.fr/2014PA112097

Chicago Manual of Style (16th Edition):

Médran-Navarrete, Vincent. “Synthèse de nouvelles sondes moléculaires marquées au fluor-18 pour l’imagerie de la neuroinflammation par Tomographie par Emission de Positons : Synthesis of new molecular probes radiolabelled with fluorine-18 for imaging neuroinflammation with Positon Emission Tomography.” 2014. Doctoral Dissertation, Université Paris-Sud – Paris XI. Accessed September 19, 2019. http://www.theses.fr/2014PA112097.

MLA Handbook (7th Edition):

Médran-Navarrete, Vincent. “Synthèse de nouvelles sondes moléculaires marquées au fluor-18 pour l’imagerie de la neuroinflammation par Tomographie par Emission de Positons : Synthesis of new molecular probes radiolabelled with fluorine-18 for imaging neuroinflammation with Positon Emission Tomography.” 2014. Web. 19 Sep 2019.

Vancouver:

Médran-Navarrete V. Synthèse de nouvelles sondes moléculaires marquées au fluor-18 pour l’imagerie de la neuroinflammation par Tomographie par Emission de Positons : Synthesis of new molecular probes radiolabelled with fluorine-18 for imaging neuroinflammation with Positon Emission Tomography. [Internet] [Doctoral dissertation]. Université Paris-Sud – Paris XI; 2014. [cited 2019 Sep 19]. Available from: http://www.theses.fr/2014PA112097.

Council of Science Editors:

Médran-Navarrete V. Synthèse de nouvelles sondes moléculaires marquées au fluor-18 pour l’imagerie de la neuroinflammation par Tomographie par Emission de Positons : Synthesis of new molecular probes radiolabelled with fluorine-18 for imaging neuroinflammation with Positon Emission Tomography. [Doctoral Dissertation]. Université Paris-Sud – Paris XI; 2014. Available from: http://www.theses.fr/2014PA112097

9. Joyard, Yoann. Synthèse de nouveaux radiomarqueurs potentiels de l’hypoxie tumorale : Développement d’une nouvelle méthodologie de fluoration nucléophile et son application vers la synthèse du 2-[18F]Fluoro-2-désoxy-D-glucose : Synthesis of new potential radiotracers for imaging tumor hypoxia : Development of a new nucleophilic fluorination strategy applied to the synthesis of [18F]Fluorodeoxyglucose.

Degree: Docteur es, Chimie, 2013, Rouen, INSA

L’hypoxie est connue pour être responsable d’une propagation tumorale accrue. En conséquence, les tumeurs hypoxiques nécessitent un diagnostic rapide et précis. L’accès à toutes les… (more)

Subjects/Keywords: Radiochimie; Technétium 99m; Fluor 18; TEMP; TEP; Hypoxie; Radiochemistry; 99m-Technetium; 18-Fluorine; SPECT; PET; Hypoxia

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APA (6th Edition):

Joyard, Y. (2013). Synthèse de nouveaux radiomarqueurs potentiels de l’hypoxie tumorale : Développement d’une nouvelle méthodologie de fluoration nucléophile et son application vers la synthèse du 2-[18F]Fluoro-2-désoxy-D-glucose : Synthesis of new potential radiotracers for imaging tumor hypoxia : Development of a new nucleophilic fluorination strategy applied to the synthesis of [18F]Fluorodeoxyglucose. (Doctoral Dissertation). Rouen, INSA. Retrieved from http://www.theses.fr/2013ISAM0018

Chicago Manual of Style (16th Edition):

Joyard, Yoann. “Synthèse de nouveaux radiomarqueurs potentiels de l’hypoxie tumorale : Développement d’une nouvelle méthodologie de fluoration nucléophile et son application vers la synthèse du 2-[18F]Fluoro-2-désoxy-D-glucose : Synthesis of new potential radiotracers for imaging tumor hypoxia : Development of a new nucleophilic fluorination strategy applied to the synthesis of [18F]Fluorodeoxyglucose.” 2013. Doctoral Dissertation, Rouen, INSA. Accessed September 19, 2019. http://www.theses.fr/2013ISAM0018.

MLA Handbook (7th Edition):

Joyard, Yoann. “Synthèse de nouveaux radiomarqueurs potentiels de l’hypoxie tumorale : Développement d’une nouvelle méthodologie de fluoration nucléophile et son application vers la synthèse du 2-[18F]Fluoro-2-désoxy-D-glucose : Synthesis of new potential radiotracers for imaging tumor hypoxia : Development of a new nucleophilic fluorination strategy applied to the synthesis of [18F]Fluorodeoxyglucose.” 2013. Web. 19 Sep 2019.

Vancouver:

Joyard Y. Synthèse de nouveaux radiomarqueurs potentiels de l’hypoxie tumorale : Développement d’une nouvelle méthodologie de fluoration nucléophile et son application vers la synthèse du 2-[18F]Fluoro-2-désoxy-D-glucose : Synthesis of new potential radiotracers for imaging tumor hypoxia : Development of a new nucleophilic fluorination strategy applied to the synthesis of [18F]Fluorodeoxyglucose. [Internet] [Doctoral dissertation]. Rouen, INSA; 2013. [cited 2019 Sep 19]. Available from: http://www.theses.fr/2013ISAM0018.

Council of Science Editors:

Joyard Y. Synthèse de nouveaux radiomarqueurs potentiels de l’hypoxie tumorale : Développement d’une nouvelle méthodologie de fluoration nucléophile et son application vers la synthèse du 2-[18F]Fluoro-2-désoxy-D-glucose : Synthesis of new potential radiotracers for imaging tumor hypoxia : Development of a new nucleophilic fluorination strategy applied to the synthesis of [18F]Fluorodeoxyglucose. [Doctoral Dissertation]. Rouen, INSA; 2013. Available from: http://www.theses.fr/2013ISAM0018

10. Morlot, Marine. Développement de la radiosynthèse de la [¹¹C] sulfasalazine et du radiomarquage au fluor-18 d'aminoesters via un aziridinium pour l'imagerie TEP : Development of radiolabelling method with fluoride-18 of fluoroaminoesters via aziridinium intermediate and radiosynthesis of [11C]sulfasalazine for PET imaging.

Degree: Docteur es, Chimie, 2017, Normandie

Les transporteurs d’acides aminés sont très souvent surexprimés au niveau des cellules tumorales et représentent une cible moléculaire privilégiée pour l’imagerie TEP (Tomographie par Emission… (more)

Subjects/Keywords: TEP; Carbone-11; Fluor-18; Aziridinium; Transporteurs Xc-; PET; Radiochemistry; Carbon-11; Fluorine-18; Fluoroaminoesters; Xc- transporters; Radioresistance

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APA (6th Edition):

Morlot, M. (2017). Développement de la radiosynthèse de la [¹¹C] sulfasalazine et du radiomarquage au fluor-18 d'aminoesters via un aziridinium pour l'imagerie TEP : Development of radiolabelling method with fluoride-18 of fluoroaminoesters via aziridinium intermediate and radiosynthesis of [11C]sulfasalazine for PET imaging. (Doctoral Dissertation). Normandie. Retrieved from http://www.theses.fr/2017NORMC253

Chicago Manual of Style (16th Edition):

Morlot, Marine. “Développement de la radiosynthèse de la [¹¹C] sulfasalazine et du radiomarquage au fluor-18 d'aminoesters via un aziridinium pour l'imagerie TEP : Development of radiolabelling method with fluoride-18 of fluoroaminoesters via aziridinium intermediate and radiosynthesis of [11C]sulfasalazine for PET imaging.” 2017. Doctoral Dissertation, Normandie. Accessed September 19, 2019. http://www.theses.fr/2017NORMC253.

MLA Handbook (7th Edition):

Morlot, Marine. “Développement de la radiosynthèse de la [¹¹C] sulfasalazine et du radiomarquage au fluor-18 d'aminoesters via un aziridinium pour l'imagerie TEP : Development of radiolabelling method with fluoride-18 of fluoroaminoesters via aziridinium intermediate and radiosynthesis of [11C]sulfasalazine for PET imaging.” 2017. Web. 19 Sep 2019.

Vancouver:

Morlot M. Développement de la radiosynthèse de la [¹¹C] sulfasalazine et du radiomarquage au fluor-18 d'aminoesters via un aziridinium pour l'imagerie TEP : Development of radiolabelling method with fluoride-18 of fluoroaminoesters via aziridinium intermediate and radiosynthesis of [11C]sulfasalazine for PET imaging. [Internet] [Doctoral dissertation]. Normandie; 2017. [cited 2019 Sep 19]. Available from: http://www.theses.fr/2017NORMC253.

Council of Science Editors:

Morlot M. Développement de la radiosynthèse de la [¹¹C] sulfasalazine et du radiomarquage au fluor-18 d'aminoesters via un aziridinium pour l'imagerie TEP : Development of radiolabelling method with fluoride-18 of fluoroaminoesters via aziridinium intermediate and radiosynthesis of [11C]sulfasalazine for PET imaging. [Doctoral Dissertation]. Normandie; 2017. Available from: http://www.theses.fr/2017NORMC253

11. Leonardo Tafas Constantino do Nascimento. Síntese, controle de qualidade e ensaios de eficácia e toxicidade in vitro do radiofármaco 18F Fluortimidina (18FLT) .

Degree: Master, 2014, Centro de Desenvolvimento da Tecnologia Nuclear

3-Desoxi-3-[18F]Fluor-Timidina (18FLT) é um análogo radioativo do nucleosídeo timidina usado desde 1998 em exames de tomografia por emissão de pósitrons (PET) para diagnóstico de vários… (more)

Subjects/Keywords: Radiofármacos; Medicina nuclear; Qualidade; Fluor 18; In vitro; Timidina; Sinterização; Radiopharmaceuticals; Nuclear medicine; Quality; Fluorine 18; In vitro; Thymidine; Sintering; FARMACIA

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APA (6th Edition):

Nascimento, L. T. C. d. (2014). Síntese, controle de qualidade e ensaios de eficácia e toxicidade in vitro do radiofármaco 18F Fluortimidina (18FLT) . (Masters Thesis). Centro de Desenvolvimento da Tecnologia Nuclear. Retrieved from http://www.bdtd.cdtn.br//tde_busca/arquivo.php?codArquivo=338 ;

Chicago Manual of Style (16th Edition):

Nascimento, Leonardo Tafas Constantino do. “Síntese, controle de qualidade e ensaios de eficácia e toxicidade in vitro do radiofármaco 18F Fluortimidina (18FLT) .” 2014. Masters Thesis, Centro de Desenvolvimento da Tecnologia Nuclear. Accessed September 19, 2019. http://www.bdtd.cdtn.br//tde_busca/arquivo.php?codArquivo=338 ;.

MLA Handbook (7th Edition):

Nascimento, Leonardo Tafas Constantino do. “Síntese, controle de qualidade e ensaios de eficácia e toxicidade in vitro do radiofármaco 18F Fluortimidina (18FLT) .” 2014. Web. 19 Sep 2019.

Vancouver:

Nascimento LTCd. Síntese, controle de qualidade e ensaios de eficácia e toxicidade in vitro do radiofármaco 18F Fluortimidina (18FLT) . [Internet] [Masters thesis]. Centro de Desenvolvimento da Tecnologia Nuclear; 2014. [cited 2019 Sep 19]. Available from: http://www.bdtd.cdtn.br//tde_busca/arquivo.php?codArquivo=338 ;.

Council of Science Editors:

Nascimento LTCd. Síntese, controle de qualidade e ensaios de eficácia e toxicidade in vitro do radiofármaco 18F Fluortimidina (18FLT) . [Masters Thesis]. Centro de Desenvolvimento da Tecnologia Nuclear; 2014. Available from: http://www.bdtd.cdtn.br//tde_busca/arquivo.php?codArquivo=338 ;


Johannes Gutenberg Universität Mainz

12. Beyerlein, Friederike. Synthese und Evaluierung von [18 F]-Fluormethyltosylat als prosthetische Gruppe für die 18 F-Fluormethylierung von ZNS-Liganden für die PET.

Degree: 2012, Johannes Gutenberg Universität Mainz

Die 11C-Methylierung von Radioliganden ist eine weit verbreitete Markierungsstrategie für PET-Liganden. Aber die kurze Halbwertszeit des Kohlenstoff-11 von 20,3 Minuten limitiert seinen Nutzen. Daher ist… (more)

Subjects/Keywords: Positronen-Emissions-Tomographie; Fluor-18; Fluormethylierung; ZNS; positron emission tomography; fluorine-18; fluoromethylation; CNS; Chemistry and allied sciences

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Beyerlein, F. (2012). Synthese und Evaluierung von [18 F]-Fluormethyltosylat als prosthetische Gruppe für die 18 F-Fluormethylierung von ZNS-Liganden für die PET. (Doctoral Dissertation). Johannes Gutenberg Universität Mainz. Retrieved from http://ubm.opus.hbz-nrw.de/volltexte/2012/3147/

Chicago Manual of Style (16th Edition):

Beyerlein, Friederike. “Synthese und Evaluierung von [18 F]-Fluormethyltosylat als prosthetische Gruppe für die 18 F-Fluormethylierung von ZNS-Liganden für die PET.” 2012. Doctoral Dissertation, Johannes Gutenberg Universität Mainz. Accessed September 19, 2019. http://ubm.opus.hbz-nrw.de/volltexte/2012/3147/.

MLA Handbook (7th Edition):

Beyerlein, Friederike. “Synthese und Evaluierung von [18 F]-Fluormethyltosylat als prosthetische Gruppe für die 18 F-Fluormethylierung von ZNS-Liganden für die PET.” 2012. Web. 19 Sep 2019.

Vancouver:

Beyerlein F. Synthese und Evaluierung von [18 F]-Fluormethyltosylat als prosthetische Gruppe für die 18 F-Fluormethylierung von ZNS-Liganden für die PET. [Internet] [Doctoral dissertation]. Johannes Gutenberg Universität Mainz; 2012. [cited 2019 Sep 19]. Available from: http://ubm.opus.hbz-nrw.de/volltexte/2012/3147/.

Council of Science Editors:

Beyerlein F. Synthese und Evaluierung von [18 F]-Fluormethyltosylat als prosthetische Gruppe für die 18 F-Fluormethylierung von ZNS-Liganden für die PET. [Doctoral Dissertation]. Johannes Gutenberg Universität Mainz; 2012. Available from: http://ubm.opus.hbz-nrw.de/volltexte/2012/3147/

13. Collet, Charlotte. Élaboration de nouveaux radiotraceurs pour le diagnostic de la Maladie d'Alzheimer : Preparation of new radiotracers for the diagnosis of Alzheimer's Disease.

Degree: Docteur es, Chimie, 2011, Université Henri Poincaré – Nancy I

La synthèse de nouveaux radiotraceurs permettant un diagnostic précoce de la maladie d'Alzheimer par imagerie par tomographie de Positron (TEP) est en plein essor. Des… (more)

Subjects/Keywords: Radiotraceurs; Inositol; Fluor-18; Tep; Radiochimie; Maladie d'Alzheimer; Radiotracers; Inositol; Fluorine-18; PET; Radiochemistry; Alzheimer's disease; 541.38; 616.83

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APA (6th Edition):

Collet, C. (2011). Élaboration de nouveaux radiotraceurs pour le diagnostic de la Maladie d'Alzheimer : Preparation of new radiotracers for the diagnosis of Alzheimer's Disease. (Doctoral Dissertation). Université Henri Poincaré – Nancy I. Retrieved from http://www.theses.fr/2011NAN10150

Chicago Manual of Style (16th Edition):

Collet, Charlotte. “Élaboration de nouveaux radiotraceurs pour le diagnostic de la Maladie d'Alzheimer : Preparation of new radiotracers for the diagnosis of Alzheimer's Disease.” 2011. Doctoral Dissertation, Université Henri Poincaré – Nancy I. Accessed September 19, 2019. http://www.theses.fr/2011NAN10150.

MLA Handbook (7th Edition):

Collet, Charlotte. “Élaboration de nouveaux radiotraceurs pour le diagnostic de la Maladie d'Alzheimer : Preparation of new radiotracers for the diagnosis of Alzheimer's Disease.” 2011. Web. 19 Sep 2019.

Vancouver:

Collet C. Élaboration de nouveaux radiotraceurs pour le diagnostic de la Maladie d'Alzheimer : Preparation of new radiotracers for the diagnosis of Alzheimer's Disease. [Internet] [Doctoral dissertation]. Université Henri Poincaré – Nancy I; 2011. [cited 2019 Sep 19]. Available from: http://www.theses.fr/2011NAN10150.

Council of Science Editors:

Collet C. Élaboration de nouveaux radiotraceurs pour le diagnostic de la Maladie d'Alzheimer : Preparation of new radiotracers for the diagnosis of Alzheimer's Disease. [Doctoral Dissertation]. Université Henri Poincaré – Nancy I; 2011. Available from: http://www.theses.fr/2011NAN10150

14. Roche, Mélanie. Stratégies innovantes pour le radiomarquage de macro-biomolécules au fluor-18 pour des applications en imagerie moléculaire in vivo : Development of novel strategies for the radiolabeling of biologics with fluorine-18 for in vivo molecular imaging applications.

Degree: Docteur es, Chimie, 2018, Paris Saclay

Le radiomarquage des macro-biomolécules au fluor-18 représente un défi majeur en radiochimie vu leur importance en imagerie moléculaire. Les macro-biomolécules et en particulier les peptides… (more)

Subjects/Keywords: Macromolécules; Chimie click; Pyridines; SNAP-Tag; Fluor‑18; TEP; Biologics; Click chemistry; Pyridines; SNAP-Tag; Fluorine-18; PET

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APA (6th Edition):

Roche, M. (2018). Stratégies innovantes pour le radiomarquage de macro-biomolécules au fluor-18 pour des applications en imagerie moléculaire in vivo : Development of novel strategies for the radiolabeling of biologics with fluorine-18 for in vivo molecular imaging applications. (Doctoral Dissertation). Paris Saclay. Retrieved from http://www.theses.fr/2018SACLS031

Chicago Manual of Style (16th Edition):

Roche, Mélanie. “Stratégies innovantes pour le radiomarquage de macro-biomolécules au fluor-18 pour des applications en imagerie moléculaire in vivo : Development of novel strategies for the radiolabeling of biologics with fluorine-18 for in vivo molecular imaging applications.” 2018. Doctoral Dissertation, Paris Saclay. Accessed September 19, 2019. http://www.theses.fr/2018SACLS031.

MLA Handbook (7th Edition):

Roche, Mélanie. “Stratégies innovantes pour le radiomarquage de macro-biomolécules au fluor-18 pour des applications en imagerie moléculaire in vivo : Development of novel strategies for the radiolabeling of biologics with fluorine-18 for in vivo molecular imaging applications.” 2018. Web. 19 Sep 2019.

Vancouver:

Roche M. Stratégies innovantes pour le radiomarquage de macro-biomolécules au fluor-18 pour des applications en imagerie moléculaire in vivo : Development of novel strategies for the radiolabeling of biologics with fluorine-18 for in vivo molecular imaging applications. [Internet] [Doctoral dissertation]. Paris Saclay; 2018. [cited 2019 Sep 19]. Available from: http://www.theses.fr/2018SACLS031.

Council of Science Editors:

Roche M. Stratégies innovantes pour le radiomarquage de macro-biomolécules au fluor-18 pour des applications en imagerie moléculaire in vivo : Development of novel strategies for the radiolabeling of biologics with fluorine-18 for in vivo molecular imaging applications. [Doctoral Dissertation]. Paris Saclay; 2018. Available from: http://www.theses.fr/2018SACLS031

15. Cacheux, Fanny. Synthèse de nouveaux ligands pour l'imagerie de la neuroinflammation par tomographie par émission de positons : Synthesis of novel ligands for neuroinflammation imaging using Positron Emission Tomography.

Degree: Docteur es, Chimie, 2016, Paris Saclay

La neuroinflammation joue un rôle important dans de nombreuses maladies neurodégénératives telles que la maladie d’Alzheimer, Parkinson, ou encore la sclérose en plaques. De récents… (more)

Subjects/Keywords: Neuroinflammation; Imagerie moléculaire; Tomographie par Emission de Positon; Fluor-18; Tspo; Neuroinflammation; Molecular imaging; Positron Emission Tomography; Fluorine-18; Tspo

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Cacheux, F. (2016). Synthèse de nouveaux ligands pour l'imagerie de la neuroinflammation par tomographie par émission de positons : Synthesis of novel ligands for neuroinflammation imaging using Positron Emission Tomography. (Doctoral Dissertation). Paris Saclay. Retrieved from http://www.theses.fr/2016SACLS342

Chicago Manual of Style (16th Edition):

Cacheux, Fanny. “Synthèse de nouveaux ligands pour l'imagerie de la neuroinflammation par tomographie par émission de positons : Synthesis of novel ligands for neuroinflammation imaging using Positron Emission Tomography.” 2016. Doctoral Dissertation, Paris Saclay. Accessed September 19, 2019. http://www.theses.fr/2016SACLS342.

MLA Handbook (7th Edition):

Cacheux, Fanny. “Synthèse de nouveaux ligands pour l'imagerie de la neuroinflammation par tomographie par émission de positons : Synthesis of novel ligands for neuroinflammation imaging using Positron Emission Tomography.” 2016. Web. 19 Sep 2019.

Vancouver:

Cacheux F. Synthèse de nouveaux ligands pour l'imagerie de la neuroinflammation par tomographie par émission de positons : Synthesis of novel ligands for neuroinflammation imaging using Positron Emission Tomography. [Internet] [Doctoral dissertation]. Paris Saclay; 2016. [cited 2019 Sep 19]. Available from: http://www.theses.fr/2016SACLS342.

Council of Science Editors:

Cacheux F. Synthèse de nouveaux ligands pour l'imagerie de la neuroinflammation par tomographie par émission de positons : Synthesis of novel ligands for neuroinflammation imaging using Positron Emission Tomography. [Doctoral Dissertation]. Paris Saclay; 2016. Available from: http://www.theses.fr/2016SACLS342

16. Pauton, Mathilde. Radiosynthèse de 3/5-[18F]-fluoropyridines à partir de précurseurs iodoniums : Radiosynthesis of 3/5-[18F]fluoropyridines by using iodoniums as precursors.

Degree: Docteur es, Chimie, 2018, Normandie

Le motif fluoropyridine est très fréquent dans les molécules d’intérêt thérapeutique et diagnostique pour l’imagerie par tomographie par émission de positons. Bien que les 3/5-[18F]fluoropyridines… (more)

Subjects/Keywords: 3/5-[18F]fluoropyridines; Fluor-18; Radiochemistry; Radiofluorination; Fluorine-18; Iodonium salts; 3/5-[18F]fluoropyridines; TEMPO

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APA (6th Edition):

Pauton, M. (2018). Radiosynthèse de 3/5-[18F]-fluoropyridines à partir de précurseurs iodoniums : Radiosynthesis of 3/5-[18F]fluoropyridines by using iodoniums as precursors. (Doctoral Dissertation). Normandie. Retrieved from http://www.theses.fr/2018NORMC280

Chicago Manual of Style (16th Edition):

Pauton, Mathilde. “Radiosynthèse de 3/5-[18F]-fluoropyridines à partir de précurseurs iodoniums : Radiosynthesis of 3/5-[18F]fluoropyridines by using iodoniums as precursors.” 2018. Doctoral Dissertation, Normandie. Accessed September 19, 2019. http://www.theses.fr/2018NORMC280.

MLA Handbook (7th Edition):

Pauton, Mathilde. “Radiosynthèse de 3/5-[18F]-fluoropyridines à partir de précurseurs iodoniums : Radiosynthesis of 3/5-[18F]fluoropyridines by using iodoniums as precursors.” 2018. Web. 19 Sep 2019.

Vancouver:

Pauton M. Radiosynthèse de 3/5-[18F]-fluoropyridines à partir de précurseurs iodoniums : Radiosynthesis of 3/5-[18F]fluoropyridines by using iodoniums as precursors. [Internet] [Doctoral dissertation]. Normandie; 2018. [cited 2019 Sep 19]. Available from: http://www.theses.fr/2018NORMC280.

Council of Science Editors:

Pauton M. Radiosynthèse de 3/5-[18F]-fluoropyridines à partir de précurseurs iodoniums : Radiosynthesis of 3/5-[18F]fluoropyridines by using iodoniums as precursors. [Doctoral Dissertation]. Normandie; 2018. Available from: http://www.theses.fr/2018NORMC280

17. Fairclough, Michael Edward. PET radiochemistry for the investigation of the biology of pain and inflammation.

Degree: PhD, 2015, University of Manchester

 Positron emission tomography (PET) is an important and powerful nuclear imaging modality and is essential in a range of medical fields. A suitable radiotracer must… (more)

Subjects/Keywords: 616.07; PET; Radiochemistry; Carbon-11; Fluorine-18; Zirconium-89; Inflammation Imaging; Opioids

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APA (6th Edition):

Fairclough, M. E. (2015). PET radiochemistry for the investigation of the biology of pain and inflammation. (Doctoral Dissertation). University of Manchester. Retrieved from https://www.research.manchester.ac.uk/portal/en/theses/pet-radiochemistry-for-the-investigation-of-the-biology-of-pain-and-inflammation(19893fb0-59b1-4324-81f4-6124e6e0490b).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.666870

Chicago Manual of Style (16th Edition):

Fairclough, Michael Edward. “PET radiochemistry for the investigation of the biology of pain and inflammation.” 2015. Doctoral Dissertation, University of Manchester. Accessed September 19, 2019. https://www.research.manchester.ac.uk/portal/en/theses/pet-radiochemistry-for-the-investigation-of-the-biology-of-pain-and-inflammation(19893fb0-59b1-4324-81f4-6124e6e0490b).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.666870.

MLA Handbook (7th Edition):

Fairclough, Michael Edward. “PET radiochemistry for the investigation of the biology of pain and inflammation.” 2015. Web. 19 Sep 2019.

Vancouver:

Fairclough ME. PET radiochemistry for the investigation of the biology of pain and inflammation. [Internet] [Doctoral dissertation]. University of Manchester; 2015. [cited 2019 Sep 19]. Available from: https://www.research.manchester.ac.uk/portal/en/theses/pet-radiochemistry-for-the-investigation-of-the-biology-of-pain-and-inflammation(19893fb0-59b1-4324-81f4-6124e6e0490b).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.666870.

Council of Science Editors:

Fairclough ME. PET radiochemistry for the investigation of the biology of pain and inflammation. [Doctoral Dissertation]. University of Manchester; 2015. Available from: https://www.research.manchester.ac.uk/portal/en/theses/pet-radiochemistry-for-the-investigation-of-the-biology-of-pain-and-inflammation(19893fb0-59b1-4324-81f4-6124e6e0490b).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.666870


UCLA

18. Lazari, Mark Saul. Thinking inside the “box”: Development and implementation of a novel automated radiosynthesizer for 18F-labeled positron emission tomography tracers.

Degree: Biomedical Engineering, 2015, UCLA

 Since the industrial revolution, automation has proven to be a vital component in the growth of any major industry. For positron emission tomography (PET), automation… (more)

Subjects/Keywords: Biomedical engineering; Robotics; Pharmaceutical sciences; Automation; Characterization; Fluorine-18; Optimization; PET; Radiochemistry

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APA (6th Edition):

Lazari, M. S. (2015). Thinking inside the “box”: Development and implementation of a novel automated radiosynthesizer for 18F-labeled positron emission tomography tracers. (Thesis). UCLA. Retrieved from http://www.escholarship.org/uc/item/51c575zh

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Lazari, Mark Saul. “Thinking inside the “box”: Development and implementation of a novel automated radiosynthesizer for 18F-labeled positron emission tomography tracers.” 2015. Thesis, UCLA. Accessed September 19, 2019. http://www.escholarship.org/uc/item/51c575zh.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Lazari, Mark Saul. “Thinking inside the “box”: Development and implementation of a novel automated radiosynthesizer for 18F-labeled positron emission tomography tracers.” 2015. Web. 19 Sep 2019.

Vancouver:

Lazari MS. Thinking inside the “box”: Development and implementation of a novel automated radiosynthesizer for 18F-labeled positron emission tomography tracers. [Internet] [Thesis]. UCLA; 2015. [cited 2019 Sep 19]. Available from: http://www.escholarship.org/uc/item/51c575zh.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Lazari MS. Thinking inside the “box”: Development and implementation of a novel automated radiosynthesizer for 18F-labeled positron emission tomography tracers. [Thesis]. UCLA; 2015. Available from: http://www.escholarship.org/uc/item/51c575zh

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of Michigan

19. Sowa, Alexandra. Synthesis and Evaluation of GAT-1 Selective PET Probes.

Degree: PhD, Medicinal Chemistry, 2018, University of Michigan

 Positron emission tomography (PET) is a high resolution, non-invasive functional imaging technique used for observation of biochemical processes in vivo. This thesis describes work towards… (more)

Subjects/Keywords: GABA; transporter; medicinal chemistry; fluorine-18; positron emission tomography; neuroimaging; Chemistry; Science

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APA (6th Edition):

Sowa, A. (2018). Synthesis and Evaluation of GAT-1 Selective PET Probes. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/147548

Chicago Manual of Style (16th Edition):

Sowa, Alexandra. “Synthesis and Evaluation of GAT-1 Selective PET Probes.” 2018. Doctoral Dissertation, University of Michigan. Accessed September 19, 2019. http://hdl.handle.net/2027.42/147548.

MLA Handbook (7th Edition):

Sowa, Alexandra. “Synthesis and Evaluation of GAT-1 Selective PET Probes.” 2018. Web. 19 Sep 2019.

Vancouver:

Sowa A. Synthesis and Evaluation of GAT-1 Selective PET Probes. [Internet] [Doctoral dissertation]. University of Michigan; 2018. [cited 2019 Sep 19]. Available from: http://hdl.handle.net/2027.42/147548.

Council of Science Editors:

Sowa A. Synthesis and Evaluation of GAT-1 Selective PET Probes. [Doctoral Dissertation]. University of Michigan; 2018. Available from: http://hdl.handle.net/2027.42/147548


University of Michigan

20. Stewart, Megan. Positron Emission Tomography Radiochemistry: Improved Methodology and a Novel PET Imaging Agent for the Dopamine D3 Receptor.

Degree: PhD, Medicinal Chemistry, 2017, University of Michigan

 Positron Emission Tomography (PET) imaging is a powerful non-invasive imaging modality used to quantify biochemical processes in vivo. The work described in this thesis encompasses… (more)

Subjects/Keywords: Positron Emission Tomography; Radiochemistry; Fluorine-18; Dopamine Receptors; D3 Receptors; Green Chemistry; Chemistry; Science

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APA (6th Edition):

Stewart, M. (2017). Positron Emission Tomography Radiochemistry: Improved Methodology and a Novel PET Imaging Agent for the Dopamine D3 Receptor. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/144039

Chicago Manual of Style (16th Edition):

Stewart, Megan. “Positron Emission Tomography Radiochemistry: Improved Methodology and a Novel PET Imaging Agent for the Dopamine D3 Receptor.” 2017. Doctoral Dissertation, University of Michigan. Accessed September 19, 2019. http://hdl.handle.net/2027.42/144039.

MLA Handbook (7th Edition):

Stewart, Megan. “Positron Emission Tomography Radiochemistry: Improved Methodology and a Novel PET Imaging Agent for the Dopamine D3 Receptor.” 2017. Web. 19 Sep 2019.

Vancouver:

Stewart M. Positron Emission Tomography Radiochemistry: Improved Methodology and a Novel PET Imaging Agent for the Dopamine D3 Receptor. [Internet] [Doctoral dissertation]. University of Michigan; 2017. [cited 2019 Sep 19]. Available from: http://hdl.handle.net/2027.42/144039.

Council of Science Editors:

Stewart M. Positron Emission Tomography Radiochemistry: Improved Methodology and a Novel PET Imaging Agent for the Dopamine D3 Receptor. [Doctoral Dissertation]. University of Michigan; 2017. Available from: http://hdl.handle.net/2027.42/144039


University of Western Ontario

21. Murrell, Emily M. Incorporation of Fluorine into Peptides and One-Bead One-Compound Libraries through Copper-free Click Chemistry for the Discovery of Radiopharmaceuticals.

Degree: 2019, University of Western Ontario

 Molecular imaging is making possible the understanding of intricate biological processes in real-time in both healthy and diseased tissues. The ability to non-invasively locate biomarkers… (more)

Subjects/Keywords: Molecular Imaging; OBOC; Peptides; Fluorine-18; Click Chemistry; CXCR4; Medicinal-Pharmaceutical Chemistry

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APA (6th Edition):

Murrell, E. M. (2019). Incorporation of Fluorine into Peptides and One-Bead One-Compound Libraries through Copper-free Click Chemistry for the Discovery of Radiopharmaceuticals. (Thesis). University of Western Ontario. Retrieved from https://ir.lib.uwo.ca/etd/6351

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Murrell, Emily M. “Incorporation of Fluorine into Peptides and One-Bead One-Compound Libraries through Copper-free Click Chemistry for the Discovery of Radiopharmaceuticals.” 2019. Thesis, University of Western Ontario. Accessed September 19, 2019. https://ir.lib.uwo.ca/etd/6351.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Murrell, Emily M. “Incorporation of Fluorine into Peptides and One-Bead One-Compound Libraries through Copper-free Click Chemistry for the Discovery of Radiopharmaceuticals.” 2019. Web. 19 Sep 2019.

Vancouver:

Murrell EM. Incorporation of Fluorine into Peptides and One-Bead One-Compound Libraries through Copper-free Click Chemistry for the Discovery of Radiopharmaceuticals. [Internet] [Thesis]. University of Western Ontario; 2019. [cited 2019 Sep 19]. Available from: https://ir.lib.uwo.ca/etd/6351.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Murrell EM. Incorporation of Fluorine into Peptides and One-Bead One-Compound Libraries through Copper-free Click Chemistry for the Discovery of Radiopharmaceuticals. [Thesis]. University of Western Ontario; 2019. Available from: https://ir.lib.uwo.ca/etd/6351

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


Université de Montréal

22. Lee, Yanick. Radiosynthesis of hexadecyl-4-[18F]fluorobenzoate for labeling exosomes and chitosan hydrogels .

Degree: 2017, Université de Montréal

 La tomographie par émission de positons (TEP) est une modalité d’imagerie nucléaire puissante, permettant des mesures fonctionnelles non-invasive dans les cellules, les animaux et les… (more)

Subjects/Keywords: F-18; Fluor-18; Radiosynthèse; automatisé; exosome; nanovésicule; biomatériaux; hydrogels; chitosan; marquage; tomographie par émission de positons; TEP; Fluorine-18; automated; Radiosynthesis; nanovesicle; biomaterials; radiolabeling; Positron emission tomography; PET

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APA (6th Edition):

Lee, Y. (2017). Radiosynthesis of hexadecyl-4-[18F]fluorobenzoate for labeling exosomes and chitosan hydrogels . (Thesis). Université de Montréal. Retrieved from http://hdl.handle.net/1866/19446

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Lee, Yanick. “Radiosynthesis of hexadecyl-4-[18F]fluorobenzoate for labeling exosomes and chitosan hydrogels .” 2017. Thesis, Université de Montréal. Accessed September 19, 2019. http://hdl.handle.net/1866/19446.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Lee, Yanick. “Radiosynthesis of hexadecyl-4-[18F]fluorobenzoate for labeling exosomes and chitosan hydrogels .” 2017. Web. 19 Sep 2019.

Vancouver:

Lee Y. Radiosynthesis of hexadecyl-4-[18F]fluorobenzoate for labeling exosomes and chitosan hydrogels . [Internet] [Thesis]. Université de Montréal; 2017. [cited 2019 Sep 19]. Available from: http://hdl.handle.net/1866/19446.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Lee Y. Radiosynthesis of hexadecyl-4-[18F]fluorobenzoate for labeling exosomes and chitosan hydrogels . [Thesis]. Université de Montréal; 2017. Available from: http://hdl.handle.net/1866/19446

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

23. Roberts, Andrew D. Fluorine-18 Production for PET and an Investigation of the Fluorine-18(p,alpha)Oxygen-15 Reaction with a Radioactive Beam.

Degree: 1995, Minnesota State University – Mankato

 Improved methods for the production of 18F have been developed. The isotope, a beta+ emitter with a 110 min half-life, serves a vital role in… (more)

Subjects/Keywords: fluorine; fluorine 18; F18; oxygen 15; 15O; radioactive isotopes; radioactive ion beams; Nuclear

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APA (6th Edition):

Roberts, A. D. (1995). Fluorine-18 Production for PET and an Investigation of the Fluorine-18(p,alpha)Oxygen-15 Reaction with a Radioactive Beam. (Thesis). Minnesota State University – Mankato. Retrieved from https://cornerstone.lib.mnsu.edu/phys_ast_fac_pubs/153

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Roberts, Andrew D. “Fluorine-18 Production for PET and an Investigation of the Fluorine-18(p,alpha)Oxygen-15 Reaction with a Radioactive Beam.” 1995. Thesis, Minnesota State University – Mankato. Accessed September 19, 2019. https://cornerstone.lib.mnsu.edu/phys_ast_fac_pubs/153.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Roberts, Andrew D. “Fluorine-18 Production for PET and an Investigation of the Fluorine-18(p,alpha)Oxygen-15 Reaction with a Radioactive Beam.” 1995. Web. 19 Sep 2019.

Vancouver:

Roberts AD. Fluorine-18 Production for PET and an Investigation of the Fluorine-18(p,alpha)Oxygen-15 Reaction with a Radioactive Beam. [Internet] [Thesis]. Minnesota State University – Mankato; 1995. [cited 2019 Sep 19]. Available from: https://cornerstone.lib.mnsu.edu/phys_ast_fac_pubs/153.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Roberts AD. Fluorine-18 Production for PET and an Investigation of the Fluorine-18(p,alpha)Oxygen-15 Reaction with a Radioactive Beam. [Thesis]. Minnesota State University – Mankato; 1995. Available from: https://cornerstone.lib.mnsu.edu/phys_ast_fac_pubs/153

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


Case Western Reserve University

24. Zheng, Lei. Synthesis and evaluation of a beta-adrenergic receptor ligand: Fluorine-18 labeled fluorocarazolol.

Degree: PhD, Chemistry, 1994, Case Western Reserve University

 Fluorocarazolol was synthesized, labeled with fluorine-18, and investigated as a potential radiopharmaceutical for use in positron tomography (PET). S-Fluorocarazolol was found to have a high… (more)

Subjects/Keywords: Chemistry, Organic; Fluorocarazolol; Fluorine-18; Beta-adrenergic receptor

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APA (6th Edition):

Zheng, L. (1994). Synthesis and evaluation of a beta-adrenergic receptor ligand: Fluorine-18 labeled fluorocarazolol. (Doctoral Dissertation). Case Western Reserve University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=case1061219721

Chicago Manual of Style (16th Edition):

Zheng, Lei. “Synthesis and evaluation of a beta-adrenergic receptor ligand: Fluorine-18 labeled fluorocarazolol.” 1994. Doctoral Dissertation, Case Western Reserve University. Accessed September 19, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=case1061219721.

MLA Handbook (7th Edition):

Zheng, Lei. “Synthesis and evaluation of a beta-adrenergic receptor ligand: Fluorine-18 labeled fluorocarazolol.” 1994. Web. 19 Sep 2019.

Vancouver:

Zheng L. Synthesis and evaluation of a beta-adrenergic receptor ligand: Fluorine-18 labeled fluorocarazolol. [Internet] [Doctoral dissertation]. Case Western Reserve University; 1994. [cited 2019 Sep 19]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=case1061219721.

Council of Science Editors:

Zheng L. Synthesis and evaluation of a beta-adrenergic receptor ligand: Fluorine-18 labeled fluorocarazolol. [Doctoral Dissertation]. Case Western Reserve University; 1994. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=case1061219721

25. Provost, Claire. Comparaison de radiotraceurs marqués au gallium-68 et au fluor-18 pour l’imagerie TEP de modèles précliniques de neuroblastome, de glioblastome ou de cancer bronchopulmonaire. : Comparison of gallium-68 and fluor-18 labelled radiotracers for PET imaging of preclinical models of neuroblastoma, glioblastoma or bronchopulmonary cancer.

Degree: Docteur es, Sciences de la vie et de la santé, 2018, Paris Saclay

La Tomographie par Emission de Positons (TEP) est une modalité d’imagerie médicale en pleine expansion depuis une quinzaine d’années. En oncologie, la TEP au 18F-fluorodésoxyglucose… (more)

Subjects/Keywords: Fluor-18; Gallium-68; Tep; Édotréotide; Peptides RGD; Oncologie; Fluorine; Gallium-68; Tep; Edotreotide; RGD peptides; Oncology

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APA (6th Edition):

Provost, C. (2018). Comparaison de radiotraceurs marqués au gallium-68 et au fluor-18 pour l’imagerie TEP de modèles précliniques de neuroblastome, de glioblastome ou de cancer bronchopulmonaire. : Comparison of gallium-68 and fluor-18 labelled radiotracers for PET imaging of preclinical models of neuroblastoma, glioblastoma or bronchopulmonary cancer. (Doctoral Dissertation). Paris Saclay. Retrieved from http://www.theses.fr/2018SACLS052

Chicago Manual of Style (16th Edition):

Provost, Claire. “Comparaison de radiotraceurs marqués au gallium-68 et au fluor-18 pour l’imagerie TEP de modèles précliniques de neuroblastome, de glioblastome ou de cancer bronchopulmonaire. : Comparison of gallium-68 and fluor-18 labelled radiotracers for PET imaging of preclinical models of neuroblastoma, glioblastoma or bronchopulmonary cancer.” 2018. Doctoral Dissertation, Paris Saclay. Accessed September 19, 2019. http://www.theses.fr/2018SACLS052.

MLA Handbook (7th Edition):

Provost, Claire. “Comparaison de radiotraceurs marqués au gallium-68 et au fluor-18 pour l’imagerie TEP de modèles précliniques de neuroblastome, de glioblastome ou de cancer bronchopulmonaire. : Comparison of gallium-68 and fluor-18 labelled radiotracers for PET imaging of preclinical models of neuroblastoma, glioblastoma or bronchopulmonary cancer.” 2018. Web. 19 Sep 2019.

Vancouver:

Provost C. Comparaison de radiotraceurs marqués au gallium-68 et au fluor-18 pour l’imagerie TEP de modèles précliniques de neuroblastome, de glioblastome ou de cancer bronchopulmonaire. : Comparison of gallium-68 and fluor-18 labelled radiotracers for PET imaging of preclinical models of neuroblastoma, glioblastoma or bronchopulmonary cancer. [Internet] [Doctoral dissertation]. Paris Saclay; 2018. [cited 2019 Sep 19]. Available from: http://www.theses.fr/2018SACLS052.

Council of Science Editors:

Provost C. Comparaison de radiotraceurs marqués au gallium-68 et au fluor-18 pour l’imagerie TEP de modèles précliniques de neuroblastome, de glioblastome ou de cancer bronchopulmonaire. : Comparison of gallium-68 and fluor-18 labelled radiotracers for PET imaging of preclinical models of neuroblastoma, glioblastoma or bronchopulmonary cancer. [Doctoral Dissertation]. Paris Saclay; 2018. Available from: http://www.theses.fr/2018SACLS052

26. Kennel, Sybille. Synthèse de traceurs bimodaux utilisables en imagerie médicale TEP/IRM : Bimodal tracers synthesis for medical imaging PET/MRI.

Degree: Docteur es, Interface Chimie-Biologie, 2015, Bordeaux

Aujourd’hui les médecins disposent de nombreuses techniques d’imagerie médicale afin d’établir des diagnostics précis et précoces. Cependant, chacune de ces techniques possède ses propres avantages… (more)

Subjects/Keywords: Traceurs bimodaux; IRM; TEP; DO3A; Gadolinium; Gallium 68; Fluor 18; Chimie «click» catalysée au ruthénium; Bimodal Tracer; MRI; PET; DO3A; Gadolinium; Gallium 68; Fluorine 18; Ruthenium catalyzed « click » chemistry

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APA (6th Edition):

Kennel, S. (2015). Synthèse de traceurs bimodaux utilisables en imagerie médicale TEP/IRM : Bimodal tracers synthesis for medical imaging PET/MRI. (Doctoral Dissertation). Bordeaux. Retrieved from http://www.theses.fr/2015BORD0190

Chicago Manual of Style (16th Edition):

Kennel, Sybille. “Synthèse de traceurs bimodaux utilisables en imagerie médicale TEP/IRM : Bimodal tracers synthesis for medical imaging PET/MRI.” 2015. Doctoral Dissertation, Bordeaux. Accessed September 19, 2019. http://www.theses.fr/2015BORD0190.

MLA Handbook (7th Edition):

Kennel, Sybille. “Synthèse de traceurs bimodaux utilisables en imagerie médicale TEP/IRM : Bimodal tracers synthesis for medical imaging PET/MRI.” 2015. Web. 19 Sep 2019.

Vancouver:

Kennel S. Synthèse de traceurs bimodaux utilisables en imagerie médicale TEP/IRM : Bimodal tracers synthesis for medical imaging PET/MRI. [Internet] [Doctoral dissertation]. Bordeaux; 2015. [cited 2019 Sep 19]. Available from: http://www.theses.fr/2015BORD0190.

Council of Science Editors:

Kennel S. Synthèse de traceurs bimodaux utilisables en imagerie médicale TEP/IRM : Bimodal tracers synthesis for medical imaging PET/MRI. [Doctoral Dissertation]. Bordeaux; 2015. Available from: http://www.theses.fr/2015BORD0190

27. Flávia Mesquita Costa. Produção de 18F-Fluorocolina no Centro de Desenvolvimento da Tecnologia Nuclear: síntese e estudos de citotoxicidade in vitro.

Degree: Master, 2014, Centro de Desenvolvimento da Tecnologia Nuclear

 A 18FCH é um biomarcador promissor para imagem de tumores usando a tecnologia PET, sendo eficaz no diagnóstico de tumores metastáticos e específico para tumores… (more)

Subjects/Keywords: MEDICINA; Fluor 18; Radiofármacos; Medicina nuclear; Neoplasmas; Diagnóstico; Controle de qualidade; PET; Radiopharmaceuticals; Neoplasms; Nuclear medicine; Fluorine 18; Diagnosis; Choline; PET; Quality control

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APA (6th Edition):

Costa, F. M. (2014). Produção de 18F-Fluorocolina no Centro de Desenvolvimento da Tecnologia Nuclear: síntese e estudos de citotoxicidade in vitro. (Masters Thesis). Centro de Desenvolvimento da Tecnologia Nuclear. Retrieved from http://www.bdtd.cdtn.br//tde_busca/arquivo.php?codArquivo=336 ;

Chicago Manual of Style (16th Edition):

Costa, Flávia Mesquita. “Produção de 18F-Fluorocolina no Centro de Desenvolvimento da Tecnologia Nuclear: síntese e estudos de citotoxicidade in vitro.” 2014. Masters Thesis, Centro de Desenvolvimento da Tecnologia Nuclear. Accessed September 19, 2019. http://www.bdtd.cdtn.br//tde_busca/arquivo.php?codArquivo=336 ;.

MLA Handbook (7th Edition):

Costa, Flávia Mesquita. “Produção de 18F-Fluorocolina no Centro de Desenvolvimento da Tecnologia Nuclear: síntese e estudos de citotoxicidade in vitro.” 2014. Web. 19 Sep 2019.

Vancouver:

Costa FM. Produção de 18F-Fluorocolina no Centro de Desenvolvimento da Tecnologia Nuclear: síntese e estudos de citotoxicidade in vitro. [Internet] [Masters thesis]. Centro de Desenvolvimento da Tecnologia Nuclear; 2014. [cited 2019 Sep 19]. Available from: http://www.bdtd.cdtn.br//tde_busca/arquivo.php?codArquivo=336 ;.

Council of Science Editors:

Costa FM. Produção de 18F-Fluorocolina no Centro de Desenvolvimento da Tecnologia Nuclear: síntese e estudos de citotoxicidade in vitro. [Masters Thesis]. Centro de Desenvolvimento da Tecnologia Nuclear; 2014. Available from: http://www.bdtd.cdtn.br//tde_busca/arquivo.php?codArquivo=336 ;


Johannes Gutenberg Universität Mainz

28. Stark, Daniela. Synthese und 18 F-Fluorierung von Aromataseinhibitoren.

Degree: 2007, Johannes Gutenberg Universität Mainz

 ZusammenfassungrnrnrnZwei 18F-markierte Derivate des Aromataseinhibitors Letrozol 5, [18F]FML 17 und [18F]FEL 18, sowie die benötigten Markierungsvorläufer sollten im Rahmen dieser Arbeit hergestellt werden. Die Referenzverbindungen… (more)

Subjects/Keywords: Fluor-18; Aromataseinhibitoren; Fluorine-18; Aromatase inhibitors; Chemistry and allied sciences

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APA (6th Edition):

Stark, D. (2007). Synthese und 18 F-Fluorierung von Aromataseinhibitoren. (Doctoral Dissertation). Johannes Gutenberg Universität Mainz. Retrieved from http://ubm.opus.hbz-nrw.de/volltexte/2010/2155/

Chicago Manual of Style (16th Edition):

Stark, Daniela. “Synthese und 18 F-Fluorierung von Aromataseinhibitoren.” 2007. Doctoral Dissertation, Johannes Gutenberg Universität Mainz. Accessed September 19, 2019. http://ubm.opus.hbz-nrw.de/volltexte/2010/2155/.

MLA Handbook (7th Edition):

Stark, Daniela. “Synthese und 18 F-Fluorierung von Aromataseinhibitoren.” 2007. Web. 19 Sep 2019.

Vancouver:

Stark D. Synthese und 18 F-Fluorierung von Aromataseinhibitoren. [Internet] [Doctoral dissertation]. Johannes Gutenberg Universität Mainz; 2007. [cited 2019 Sep 19]. Available from: http://ubm.opus.hbz-nrw.de/volltexte/2010/2155/.

Council of Science Editors:

Stark D. Synthese und 18 F-Fluorierung von Aromataseinhibitoren. [Doctoral Dissertation]. Johannes Gutenberg Universität Mainz; 2007. Available from: http://ubm.opus.hbz-nrw.de/volltexte/2010/2155/

29. Colomb, Julie. Synthèse et radiomarquage de ligands des récepteurs sérotoninergiques 5-HT6 et 5-HT7 pour la tomographie par émission de positons : Synthesis and radiolabeling of 5-HT6 and 5-HT7 serotoninergic receptor ligands for Positron Emission Tomography.

Degree: Docteur es, Chimie, 2013, Université Claude Bernard – Lyon I

Le développement de radiotraceurs (18F) des récepteurs de la sérotonine 5-HT6 et 5-HT7 pour l'imagerie TEP (tomographie par émission de positons) permettrait d'étudier la fonction… (more)

Subjects/Keywords: Tomographie par émission de positon; Synthèse organique; Quinoline; Pyrrolidine; Radiomarquage; Fluor 18; Sérotonine; 5-HT6; Positron emission tomography; Organic synthesis; Quinoline; Pyrrolidine; Radiolabeling; Fluorine 18; Serotonin; 5-HT6; 547

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APA (6th Edition):

Colomb, J. (2013). Synthèse et radiomarquage de ligands des récepteurs sérotoninergiques 5-HT6 et 5-HT7 pour la tomographie par émission de positons : Synthesis and radiolabeling of 5-HT6 and 5-HT7 serotoninergic receptor ligands for Positron Emission Tomography. (Doctoral Dissertation). Université Claude Bernard – Lyon I. Retrieved from http://www.theses.fr/2013LYO10173

Chicago Manual of Style (16th Edition):

Colomb, Julie. “Synthèse et radiomarquage de ligands des récepteurs sérotoninergiques 5-HT6 et 5-HT7 pour la tomographie par émission de positons : Synthesis and radiolabeling of 5-HT6 and 5-HT7 serotoninergic receptor ligands for Positron Emission Tomography.” 2013. Doctoral Dissertation, Université Claude Bernard – Lyon I. Accessed September 19, 2019. http://www.theses.fr/2013LYO10173.

MLA Handbook (7th Edition):

Colomb, Julie. “Synthèse et radiomarquage de ligands des récepteurs sérotoninergiques 5-HT6 et 5-HT7 pour la tomographie par émission de positons : Synthesis and radiolabeling of 5-HT6 and 5-HT7 serotoninergic receptor ligands for Positron Emission Tomography.” 2013. Web. 19 Sep 2019.

Vancouver:

Colomb J. Synthèse et radiomarquage de ligands des récepteurs sérotoninergiques 5-HT6 et 5-HT7 pour la tomographie par émission de positons : Synthesis and radiolabeling of 5-HT6 and 5-HT7 serotoninergic receptor ligands for Positron Emission Tomography. [Internet] [Doctoral dissertation]. Université Claude Bernard – Lyon I; 2013. [cited 2019 Sep 19]. Available from: http://www.theses.fr/2013LYO10173.

Council of Science Editors:

Colomb J. Synthèse et radiomarquage de ligands des récepteurs sérotoninergiques 5-HT6 et 5-HT7 pour la tomographie par émission de positons : Synthesis and radiolabeling of 5-HT6 and 5-HT7 serotoninergic receptor ligands for Positron Emission Tomography. [Doctoral Dissertation]. Université Claude Bernard – Lyon I; 2013. Available from: http://www.theses.fr/2013LYO10173


University of Vienna

30. Klag, Irene. Entwicklung einer enzymatischen Methode für die in-vitro Umsetzung von 6-[18F]Fluoro-L-DOPA zu 6-[18F]Fluoro-Dopamin mit Aufreinigung über Festphasenextraktion und anschließender HPLC-Qualitätskontrolle.

Degree: 2016, University of Vienna

Ziel: Ziel dieser Arbeit war es ein Enzym zu finden, das eine rasche und möglichst quantitative Decarboxylierung von 6-[18F]Fluoro-L-DOPA zu 6-[18F]Fluoro-Dopamin katalysieren kann. Methoden: Es… (more)

Subjects/Keywords: 30.03 Methoden und Techniken in den Naturwissenschaften; 44.40 Pharmazie, Pharmazeutika; 35.15 Radiochemie; Enzym / Decarboxylase / Dopamin / Fluor-18; Enzyme / Decarboxylase / Dopamine / Fluorine-18

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APA (6th Edition):

Klag, I. (2016). Entwicklung einer enzymatischen Methode für die in-vitro Umsetzung von 6-[18F]Fluoro-L-DOPA zu 6-[18F]Fluoro-Dopamin mit Aufreinigung über Festphasenextraktion und anschließender HPLC-Qualitätskontrolle. (Thesis). University of Vienna. Retrieved from http://othes.univie.ac.at/46520/

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Klag, Irene. “Entwicklung einer enzymatischen Methode für die in-vitro Umsetzung von 6-[18F]Fluoro-L-DOPA zu 6-[18F]Fluoro-Dopamin mit Aufreinigung über Festphasenextraktion und anschließender HPLC-Qualitätskontrolle.” 2016. Thesis, University of Vienna. Accessed September 19, 2019. http://othes.univie.ac.at/46520/.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Klag, Irene. “Entwicklung einer enzymatischen Methode für die in-vitro Umsetzung von 6-[18F]Fluoro-L-DOPA zu 6-[18F]Fluoro-Dopamin mit Aufreinigung über Festphasenextraktion und anschließender HPLC-Qualitätskontrolle.” 2016. Web. 19 Sep 2019.

Vancouver:

Klag I. Entwicklung einer enzymatischen Methode für die in-vitro Umsetzung von 6-[18F]Fluoro-L-DOPA zu 6-[18F]Fluoro-Dopamin mit Aufreinigung über Festphasenextraktion und anschließender HPLC-Qualitätskontrolle. [Internet] [Thesis]. University of Vienna; 2016. [cited 2019 Sep 19]. Available from: http://othes.univie.ac.at/46520/.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Klag I. Entwicklung einer enzymatischen Methode für die in-vitro Umsetzung von 6-[18F]Fluoro-L-DOPA zu 6-[18F]Fluoro-Dopamin mit Aufreinigung über Festphasenextraktion und anschließender HPLC-Qualitätskontrolle. [Thesis]. University of Vienna; 2016. Available from: http://othes.univie.ac.at/46520/

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

[1] [2]

.