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You searched for subject:(doxorubicin). Showing records 1 – 30 of 325 total matches.

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Laurentian University

1. Chenard, Pamela. A comparison of doxorubicin and doxorubicinol in rat heart and liver tissue following anthracycline administration .

Degree: 2015, Laurentian University

 This study examined the pharmacokinetic profile of the chemotherapeutic drug doxorubicin (DOX), and of its main metabolite doxorubicinol (DOXOL) in male Sprague-Dawley rats. HPLC was… (more)

Subjects/Keywords: Doxorubicin pharmacokinetics; Doxorubicin; Doxorubicinol; Chromatography

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

APA (6th Edition):

Chenard, P. (2015). A comparison of doxorubicin and doxorubicinol in rat heart and liver tissue following anthracycline administration . (Thesis). Laurentian University. Retrieved from https://zone.biblio.laurentian.ca/dspace/handle/10219/2423

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):

Chenard, Pamela. “A comparison of doxorubicin and doxorubicinol in rat heart and liver tissue following anthracycline administration .” 2015. Thesis, Laurentian University. Accessed September 19, 2020. https://zone.biblio.laurentian.ca/dspace/handle/10219/2423.

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

MLA Handbook (7th Edition):

Chenard, Pamela. “A comparison of doxorubicin and doxorubicinol in rat heart and liver tissue following anthracycline administration .” 2015. Web. 19 Sep 2020.

Vancouver:

Chenard P. A comparison of doxorubicin and doxorubicinol in rat heart and liver tissue following anthracycline administration . [Internet] [Thesis]. Laurentian University; 2015. [cited 2020 Sep 19]. Available from: https://zone.biblio.laurentian.ca/dspace/handle/10219/2423.

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

Council of Science Editors:

Chenard P. A comparison of doxorubicin and doxorubicinol in rat heart and liver tissue following anthracycline administration . [Thesis]. Laurentian University; 2015. Available from: https://zone.biblio.laurentian.ca/dspace/handle/10219/2423

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


University of Illinois – Chicago

2. Morrison, Joseph D. Transarterial Chemoembolization with Doxorubicin; Drug Delivery and Pharmacokinetics.

Degree: 2018, University of Illinois – Chicago

 ABSTRACT Purpose Ethiodized oil (Lipiodol; Guerbet, Villepente France) is the standard drug delivery vehicle for conventional transarterial chemoembolization (c-TACE) and represents the benchmark for comparative… (more)

Subjects/Keywords: Doxorubicin; TACE

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APA (6th Edition):

Morrison, J. D. (2018). Transarterial Chemoembolization with Doxorubicin; Drug Delivery and Pharmacokinetics. (Thesis). University of Illinois – Chicago. Retrieved from http://hdl.handle.net/10027/23057

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):

Morrison, Joseph D. “Transarterial Chemoembolization with Doxorubicin; Drug Delivery and Pharmacokinetics.” 2018. Thesis, University of Illinois – Chicago. Accessed September 19, 2020. http://hdl.handle.net/10027/23057.

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

MLA Handbook (7th Edition):

Morrison, Joseph D. “Transarterial Chemoembolization with Doxorubicin; Drug Delivery and Pharmacokinetics.” 2018. Web. 19 Sep 2020.

Vancouver:

Morrison JD. Transarterial Chemoembolization with Doxorubicin; Drug Delivery and Pharmacokinetics. [Internet] [Thesis]. University of Illinois – Chicago; 2018. [cited 2020 Sep 19]. Available from: http://hdl.handle.net/10027/23057.

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

Council of Science Editors:

Morrison JD. Transarterial Chemoembolization with Doxorubicin; Drug Delivery and Pharmacokinetics. [Thesis]. University of Illinois – Chicago; 2018. Available from: http://hdl.handle.net/10027/23057

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


Stellenbosch University

3. Scott, Kirsten Lee. The potential toxic effects of chronic doxorubicin treatment on the rat pancreas and the role of ghrelin in this context.

Degree: MSc, Physiological Sciences, 2018, Stellenbosch University

 ENGLISH ABSTRACT: Introduction: Doxorubicin (DOX), is a chemotherapeutic drug that has potent anti-neoplastic actions. It is for this reason that it remains one of the… (more)

Subjects/Keywords: Doxorubicin treatment  – Effectiveness; Doxorubicin  – Physiological effect; Ghrelin  – Physiological effect; Doxorubicin  – Effects on pancreas; UCTD

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APA (6th Edition):

Scott, K. L. (2018). The potential toxic effects of chronic doxorubicin treatment on the rat pancreas and the role of ghrelin in this context. (Masters Thesis). Stellenbosch University. Retrieved from http://hdl.handle.net/10019.1/103408

Chicago Manual of Style (16th Edition):

Scott, Kirsten Lee. “The potential toxic effects of chronic doxorubicin treatment on the rat pancreas and the role of ghrelin in this context.” 2018. Masters Thesis, Stellenbosch University. Accessed September 19, 2020. http://hdl.handle.net/10019.1/103408.

MLA Handbook (7th Edition):

Scott, Kirsten Lee. “The potential toxic effects of chronic doxorubicin treatment on the rat pancreas and the role of ghrelin in this context.” 2018. Web. 19 Sep 2020.

Vancouver:

Scott KL. The potential toxic effects of chronic doxorubicin treatment on the rat pancreas and the role of ghrelin in this context. [Internet] [Masters thesis]. Stellenbosch University; 2018. [cited 2020 Sep 19]. Available from: http://hdl.handle.net/10019.1/103408.

Council of Science Editors:

Scott KL. The potential toxic effects of chronic doxorubicin treatment on the rat pancreas and the role of ghrelin in this context. [Masters Thesis]. Stellenbosch University; 2018. Available from: http://hdl.handle.net/10019.1/103408

4. Τροχούτσου, Αικατερίνη. Διερεύνηση της σχέσης απόπτωσης και γενετικών αλλαγών που επάγονται από την αντικαρκινική ένωση δοξορουβικίνη στην κυτταρική σειρά ποντικού C2C12.

Degree: 2008, University of Patras

 Η δοξορουβικίνη αποτελεί μια ευρέως χρησιμοποιούμενη αντικαρκινική ένωση σε διάφορους τύπους νεοπλασιών και ανήκει στην οικογένεια των ανθρακυκλινών. Για την κυτταροστατική της δράση έχουν προταθεί… (more)

Subjects/Keywords: Δοξορουβικίνη; Μικροπυρήνες; 571.936; Doxorubicin; Micronuclei

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APA (6th Edition):

Τροχούτσου, . (2008). Διερεύνηση της σχέσης απόπτωσης και γενετικών αλλαγών που επάγονται από την αντικαρκινική ένωση δοξορουβικίνη στην κυτταρική σειρά ποντικού C2C12. (Masters Thesis). University of Patras. Retrieved from http://nemertes.lis.upatras.gr/jspui/handle/10889/1071

Chicago Manual of Style (16th Edition):

Τροχούτσου, Αικατερίνη. “Διερεύνηση της σχέσης απόπτωσης και γενετικών αλλαγών που επάγονται από την αντικαρκινική ένωση δοξορουβικίνη στην κυτταρική σειρά ποντικού C2C12.” 2008. Masters Thesis, University of Patras. Accessed September 19, 2020. http://nemertes.lis.upatras.gr/jspui/handle/10889/1071.

MLA Handbook (7th Edition):

Τροχούτσου, Αικατερίνη. “Διερεύνηση της σχέσης απόπτωσης και γενετικών αλλαγών που επάγονται από την αντικαρκινική ένωση δοξορουβικίνη στην κυτταρική σειρά ποντικού C2C12.” 2008. Web. 19 Sep 2020.

Vancouver:

Τροχούτσου . Διερεύνηση της σχέσης απόπτωσης και γενετικών αλλαγών που επάγονται από την αντικαρκινική ένωση δοξορουβικίνη στην κυτταρική σειρά ποντικού C2C12. [Internet] [Masters thesis]. University of Patras; 2008. [cited 2020 Sep 19]. Available from: http://nemertes.lis.upatras.gr/jspui/handle/10889/1071.

Council of Science Editors:

Τροχούτσου . Διερεύνηση της σχέσης απόπτωσης και γενετικών αλλαγών που επάγονται από την αντικαρκινική ένωση δοξορουβικίνη στην κυτταρική σειρά ποντικού C2C12. [Masters Thesis]. University of Patras; 2008. Available from: http://nemertes.lis.upatras.gr/jspui/handle/10889/1071


Ruhr Universität Bochum

5. Harati, Kamran. Apoptoseinduktion und Proliferationshemmung durch Doxorubicin, Trabectedin und Mafosfamid in Kombination mit TRAIL und Taurolidin in humanen HT1080 Fibrosarkomzellen.

Degree: 2013, Ruhr Universität Bochum

 Einleitung: In dieser Studie wurde untersucht, inwieweit die Wirkung etablierter und neuerer Chemotherapeutika durch das Antiseptikum Taurolidin (TRD) und das körpereigene Protein TRAIL (TNF related… (more)

Subjects/Keywords: Weichteilsarkom; Fibrosarkom; Apoptosis; Nekrose; Doxorubicin

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APA (6th Edition):

Harati, K. (2013). Apoptoseinduktion und Proliferationshemmung durch Doxorubicin, Trabectedin und Mafosfamid in Kombination mit TRAIL und Taurolidin in humanen HT1080 Fibrosarkomzellen. (Thesis). Ruhr Universität Bochum. Retrieved from http://nbn-resolving.de/urn/resolver.pl?urn=urn:nbn:de:hbz:294-37662

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):

Harati, Kamran. “Apoptoseinduktion und Proliferationshemmung durch Doxorubicin, Trabectedin und Mafosfamid in Kombination mit TRAIL und Taurolidin in humanen HT1080 Fibrosarkomzellen.” 2013. Thesis, Ruhr Universität Bochum. Accessed September 19, 2020. http://nbn-resolving.de/urn/resolver.pl?urn=urn:nbn:de:hbz:294-37662.

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

MLA Handbook (7th Edition):

Harati, Kamran. “Apoptoseinduktion und Proliferationshemmung durch Doxorubicin, Trabectedin und Mafosfamid in Kombination mit TRAIL und Taurolidin in humanen HT1080 Fibrosarkomzellen.” 2013. Web. 19 Sep 2020.

Vancouver:

Harati K. Apoptoseinduktion und Proliferationshemmung durch Doxorubicin, Trabectedin und Mafosfamid in Kombination mit TRAIL und Taurolidin in humanen HT1080 Fibrosarkomzellen. [Internet] [Thesis]. Ruhr Universität Bochum; 2013. [cited 2020 Sep 19]. Available from: http://nbn-resolving.de/urn/resolver.pl?urn=urn:nbn:de:hbz:294-37662.

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

Council of Science Editors:

Harati K. Apoptoseinduktion und Proliferationshemmung durch Doxorubicin, Trabectedin und Mafosfamid in Kombination mit TRAIL und Taurolidin in humanen HT1080 Fibrosarkomzellen. [Thesis]. Ruhr Universität Bochum; 2013. Available from: http://nbn-resolving.de/urn/resolver.pl?urn=urn:nbn:de:hbz:294-37662

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

6. 김, 은영. Regulation of Senescence Phenotypes by TIS21 gene in Huh7 Human Liver Cancer Cells.

Degree: 2011, Ajou University

일반적으로 Cellular senescence란 시간이 지나면 자연적으로 세포 증식이 억제되고 세포내 항상성 유지가 어렵게 되는 것을 말한다. 이러한 cellular senescence는 tumour cell에서도 일어나는데 tumour cell에서의 senescence는… (more)

Subjects/Keywords: TIS21; doxorubicin; 세포노화유도; Huh7; shRNA

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APA (6th Edition):

김, . (2011). Regulation of Senescence Phenotypes by TIS21 gene in Huh7 Human Liver Cancer Cells. (Thesis). Ajou University. Retrieved from http://repository.ajou.ac.kr/handle/201003/4405 ; http://dcoll.ajou.ac.kr:9080/dcollection/jsp/common/DcLoOrgPer.jsp?sItemId=000000011837

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):

김, 은영. “Regulation of Senescence Phenotypes by TIS21 gene in Huh7 Human Liver Cancer Cells.” 2011. Thesis, Ajou University. Accessed September 19, 2020. http://repository.ajou.ac.kr/handle/201003/4405 ; http://dcoll.ajou.ac.kr:9080/dcollection/jsp/common/DcLoOrgPer.jsp?sItemId=000000011837.

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

MLA Handbook (7th Edition):

김, 은영. “Regulation of Senescence Phenotypes by TIS21 gene in Huh7 Human Liver Cancer Cells.” 2011. Web. 19 Sep 2020.

Vancouver:

김 . Regulation of Senescence Phenotypes by TIS21 gene in Huh7 Human Liver Cancer Cells. [Internet] [Thesis]. Ajou University; 2011. [cited 2020 Sep 19]. Available from: http://repository.ajou.ac.kr/handle/201003/4405 ; http://dcoll.ajou.ac.kr:9080/dcollection/jsp/common/DcLoOrgPer.jsp?sItemId=000000011837.

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

Council of Science Editors:

김 . Regulation of Senescence Phenotypes by TIS21 gene in Huh7 Human Liver Cancer Cells. [Thesis]. Ajou University; 2011. Available from: http://repository.ajou.ac.kr/handle/201003/4405 ; http://dcoll.ajou.ac.kr:9080/dcollection/jsp/common/DcLoOrgPer.jsp?sItemId=000000011837

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


University of Minnesota

7. Anderson, Katie. Melanoma displays an evolutionarily conserved resistance to modulation of phagocytic signals.

Degree: PhD, Comparative and Molecular Biosciences, 2017, University of Minnesota

 Therapeutic activation of macrophage phagocytosis has the ability to restrain tumor growth through phagocytic clearance of tumor cells and activation of the adaptive immune response.… (more)

Subjects/Keywords: CD47; doxorubicin; macrophage; melanoma; phagocytosis

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APA (6th Edition):

Anderson, K. (2017). Melanoma displays an evolutionarily conserved resistance to modulation of phagocytic signals. (Doctoral Dissertation). University of Minnesota. Retrieved from http://hdl.handle.net/11299/191409

Chicago Manual of Style (16th Edition):

Anderson, Katie. “Melanoma displays an evolutionarily conserved resistance to modulation of phagocytic signals.” 2017. Doctoral Dissertation, University of Minnesota. Accessed September 19, 2020. http://hdl.handle.net/11299/191409.

MLA Handbook (7th Edition):

Anderson, Katie. “Melanoma displays an evolutionarily conserved resistance to modulation of phagocytic signals.” 2017. Web. 19 Sep 2020.

Vancouver:

Anderson K. Melanoma displays an evolutionarily conserved resistance to modulation of phagocytic signals. [Internet] [Doctoral dissertation]. University of Minnesota; 2017. [cited 2020 Sep 19]. Available from: http://hdl.handle.net/11299/191409.

Council of Science Editors:

Anderson K. Melanoma displays an evolutionarily conserved resistance to modulation of phagocytic signals. [Doctoral Dissertation]. University of Minnesota; 2017. Available from: http://hdl.handle.net/11299/191409


Brno University of Technology

8. Krausová, Kateřina. Studium exprese transferinových receptorů a využití v nanomedicíně: Study of expression of transferrin receptors (TfR1) and their utilization in nanomedicine.

Degree: 2019, Brno University of Technology

 Bachelor thesis deals with the expression of the transferrin receptor (TfR1) and its use in nanomedicine. During the last decade, nanotechnology emerged as one of… (more)

Subjects/Keywords: Nádorová onemocnění; nanomedicína; apoferritin; doxorubicin; Cancer; nanomedicine; apoferritin; doxorubicin

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APA (6th Edition):

Krausová, K. (2019). Studium exprese transferinových receptorů a využití v nanomedicíně: Study of expression of transferrin receptors (TfR1) and their utilization in nanomedicine. (Thesis). Brno University of Technology. Retrieved from http://hdl.handle.net/11012/68141

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):

Krausová, Kateřina. “Studium exprese transferinových receptorů a využití v nanomedicíně: Study of expression of transferrin receptors (TfR1) and their utilization in nanomedicine.” 2019. Thesis, Brno University of Technology. Accessed September 19, 2020. http://hdl.handle.net/11012/68141.

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

MLA Handbook (7th Edition):

Krausová, Kateřina. “Studium exprese transferinových receptorů a využití v nanomedicíně: Study of expression of transferrin receptors (TfR1) and their utilization in nanomedicine.” 2019. Web. 19 Sep 2020.

Vancouver:

Krausová K. Studium exprese transferinových receptorů a využití v nanomedicíně: Study of expression of transferrin receptors (TfR1) and their utilization in nanomedicine. [Internet] [Thesis]. Brno University of Technology; 2019. [cited 2020 Sep 19]. Available from: http://hdl.handle.net/11012/68141.

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

Council of Science Editors:

Krausová K. Studium exprese transferinových receptorů a využití v nanomedicíně: Study of expression of transferrin receptors (TfR1) and their utilization in nanomedicine. [Thesis]. Brno University of Technology; 2019. Available from: http://hdl.handle.net/11012/68141

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


The Ohio State University

9. Narasimhan, S. Lakshmi. Part I: A synthesis of 3-acetyl-6-bromo-3-hydroxy-1,5,8-trimethoxy-1,2,3,4-tetrahydronaphthalene. Part II: Synthesis of monothioacetals, ketones, and vinyl sulfides .

Degree: PhD, Graduate School, 1979, The Ohio State University

Subjects/Keywords: Chemistry; Doxorubicin; Daunomycin

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APA (6th Edition):

Narasimhan, S. L. (1979). Part I: A synthesis of 3-acetyl-6-bromo-3-hydroxy-1,5,8-trimethoxy-1,2,3,4-tetrahydronaphthalene. Part II: Synthesis of monothioacetals, ketones, and vinyl sulfides . (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1487085764396831

Chicago Manual of Style (16th Edition):

Narasimhan, S Lakshmi. “Part I: A synthesis of 3-acetyl-6-bromo-3-hydroxy-1,5,8-trimethoxy-1,2,3,4-tetrahydronaphthalene. Part II: Synthesis of monothioacetals, ketones, and vinyl sulfides .” 1979. Doctoral Dissertation, The Ohio State University. Accessed September 19, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=osu1487085764396831.

MLA Handbook (7th Edition):

Narasimhan, S Lakshmi. “Part I: A synthesis of 3-acetyl-6-bromo-3-hydroxy-1,5,8-trimethoxy-1,2,3,4-tetrahydronaphthalene. Part II: Synthesis of monothioacetals, ketones, and vinyl sulfides .” 1979. Web. 19 Sep 2020.

Vancouver:

Narasimhan SL. Part I: A synthesis of 3-acetyl-6-bromo-3-hydroxy-1,5,8-trimethoxy-1,2,3,4-tetrahydronaphthalene. Part II: Synthesis of monothioacetals, ketones, and vinyl sulfides . [Internet] [Doctoral dissertation]. The Ohio State University; 1979. [cited 2020 Sep 19]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1487085764396831.

Council of Science Editors:

Narasimhan SL. Part I: A synthesis of 3-acetyl-6-bromo-3-hydroxy-1,5,8-trimethoxy-1,2,3,4-tetrahydronaphthalene. Part II: Synthesis of monothioacetals, ketones, and vinyl sulfides . [Doctoral Dissertation]. The Ohio State University; 1979. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1487085764396831


Universidade do Rio Grande do Sul

10. Antonow, Michelli Barcelos. Desenvolvimento e caracterização físico-química de nanocápsulas multiparedes complexadas com zinco e funcionalizadas com RGD para reconhecimento por integrinas ανβ3 presentes em células tumorais.

Degree: 2016, Universidade do Rio Grande do Sul

A funcionalização de superfície nas nanocápsulas contendo doxorrubicina com o peptídeo RGD é uma estratégia promissora devido a ligação preferencial na integrina αvβ3 expressa em… (more)

Subjects/Keywords: RGD; Farmácia; Nanocapsules; Doxorubicin; αvβ3 integrin

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APA (6th Edition):

Antonow, M. B. (2016). Desenvolvimento e caracterização físico-química de nanocápsulas multiparedes complexadas com zinco e funcionalizadas com RGD para reconhecimento por integrinas ανβ3 presentes em células tumorais. (Thesis). Universidade do Rio Grande do Sul. Retrieved from http://hdl.handle.net/10183/149502

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):

Antonow, Michelli Barcelos. “Desenvolvimento e caracterização físico-química de nanocápsulas multiparedes complexadas com zinco e funcionalizadas com RGD para reconhecimento por integrinas ανβ3 presentes em células tumorais.” 2016. Thesis, Universidade do Rio Grande do Sul. Accessed September 19, 2020. http://hdl.handle.net/10183/149502.

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

MLA Handbook (7th Edition):

Antonow, Michelli Barcelos. “Desenvolvimento e caracterização físico-química de nanocápsulas multiparedes complexadas com zinco e funcionalizadas com RGD para reconhecimento por integrinas ανβ3 presentes em células tumorais.” 2016. Web. 19 Sep 2020.

Vancouver:

Antonow MB. Desenvolvimento e caracterização físico-química de nanocápsulas multiparedes complexadas com zinco e funcionalizadas com RGD para reconhecimento por integrinas ανβ3 presentes em células tumorais. [Internet] [Thesis]. Universidade do Rio Grande do Sul; 2016. [cited 2020 Sep 19]. Available from: http://hdl.handle.net/10183/149502.

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

Council of Science Editors:

Antonow MB. Desenvolvimento e caracterização físico-química de nanocápsulas multiparedes complexadas com zinco e funcionalizadas com RGD para reconhecimento por integrinas ανβ3 presentes em células tumorais. [Thesis]. Universidade do Rio Grande do Sul; 2016. Available from: http://hdl.handle.net/10183/149502

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


Vanderbilt University

11. McKenna, Matthew Thomas. Development and Validation of a Predictive Model of Chemotherapy in Triple Negative Breast Cancer.

Degree: PhD, Biomedical Engineering, 2017, Vanderbilt University

 Precision medicine is the concept of incorporating patient-specific variability into prevention and treatment strategies. Precision medicine initiatives in oncology have primarily focused on the use… (more)

Subjects/Keywords: doxorubicin; pharmacology; mathematical modeling; computational oncology

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APA (6th Edition):

McKenna, M. T. (2017). Development and Validation of a Predictive Model of Chemotherapy in Triple Negative Breast Cancer. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://hdl.handle.net/1803/14399

Chicago Manual of Style (16th Edition):

McKenna, Matthew Thomas. “Development and Validation of a Predictive Model of Chemotherapy in Triple Negative Breast Cancer.” 2017. Doctoral Dissertation, Vanderbilt University. Accessed September 19, 2020. http://hdl.handle.net/1803/14399.

MLA Handbook (7th Edition):

McKenna, Matthew Thomas. “Development and Validation of a Predictive Model of Chemotherapy in Triple Negative Breast Cancer.” 2017. Web. 19 Sep 2020.

Vancouver:

McKenna MT. Development and Validation of a Predictive Model of Chemotherapy in Triple Negative Breast Cancer. [Internet] [Doctoral dissertation]. Vanderbilt University; 2017. [cited 2020 Sep 19]. Available from: http://hdl.handle.net/1803/14399.

Council of Science Editors:

McKenna MT. Development and Validation of a Predictive Model of Chemotherapy in Triple Negative Breast Cancer. [Doctoral Dissertation]. Vanderbilt University; 2017. Available from: http://hdl.handle.net/1803/14399


Stellenbosch University

12. Chabaesele, Itumeleng. Does cardioprotection by autophagy go beyond acute cardiotoxicity?.

Degree: MSc, Physiological Sciences, 2016, Stellenbosch University

ENGLISH ABSTRACT: Introduction and Aim The discovery of Doxorubicin (DOX) in the 1960s has drastically improved the survival rates of cancer patients; however, its success… (more)

Subjects/Keywords: Cardiotoxicity; Doxorubicin (DOX); Cardioprotection; Autophagy induction; UCTD

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

APA (6th Edition):

Chabaesele, I. (2016). Does cardioprotection by autophagy go beyond acute cardiotoxicity?. (Masters Thesis). Stellenbosch University. Retrieved from http://hdl.handle.net/10019.1/98577

Chicago Manual of Style (16th Edition):

Chabaesele, Itumeleng. “Does cardioprotection by autophagy go beyond acute cardiotoxicity?.” 2016. Masters Thesis, Stellenbosch University. Accessed September 19, 2020. http://hdl.handle.net/10019.1/98577.

MLA Handbook (7th Edition):

Chabaesele, Itumeleng. “Does cardioprotection by autophagy go beyond acute cardiotoxicity?.” 2016. Web. 19 Sep 2020.

Vancouver:

Chabaesele I. Does cardioprotection by autophagy go beyond acute cardiotoxicity?. [Internet] [Masters thesis]. Stellenbosch University; 2016. [cited 2020 Sep 19]. Available from: http://hdl.handle.net/10019.1/98577.

Council of Science Editors:

Chabaesele I. Does cardioprotection by autophagy go beyond acute cardiotoxicity?. [Masters Thesis]. Stellenbosch University; 2016. Available from: http://hdl.handle.net/10019.1/98577


Stellenbosch University

13. Ilchev, Alexander. Amine end-functional poly(N-vinylpyrrolidone) as amMacroinitiator for L-lysine N-carboxyanhydride polymerization - towards the preparation of pH-responsive micelles for drug delivery.

Degree: PhD, Chemistry and Polymer Science, 2015, Stellenbosch University

 ENGLISH ABSTRACT: Cancer is a notorious affliction that knows no age, gender, ethnic, racial, or species bounds and is responsible for over 14% of annual… (more)

Subjects/Keywords: Cancer; Tumour; Phthalimidomethyl; RAFT; Doxorubicin; Polymerization; UCTD

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APA (6th Edition):

Ilchev, A. (2015). Amine end-functional poly(N-vinylpyrrolidone) as amMacroinitiator for L-lysine N-carboxyanhydride polymerization - towards the preparation of pH-responsive micelles for drug delivery. (Doctoral Dissertation). Stellenbosch University. Retrieved from http://hdl.handle.net/10019.1/96634

Chicago Manual of Style (16th Edition):

Ilchev, Alexander. “Amine end-functional poly(N-vinylpyrrolidone) as amMacroinitiator for L-lysine N-carboxyanhydride polymerization - towards the preparation of pH-responsive micelles for drug delivery.” 2015. Doctoral Dissertation, Stellenbosch University. Accessed September 19, 2020. http://hdl.handle.net/10019.1/96634.

MLA Handbook (7th Edition):

Ilchev, Alexander. “Amine end-functional poly(N-vinylpyrrolidone) as amMacroinitiator for L-lysine N-carboxyanhydride polymerization - towards the preparation of pH-responsive micelles for drug delivery.” 2015. Web. 19 Sep 2020.

Vancouver:

Ilchev A. Amine end-functional poly(N-vinylpyrrolidone) as amMacroinitiator for L-lysine N-carboxyanhydride polymerization - towards the preparation of pH-responsive micelles for drug delivery. [Internet] [Doctoral dissertation]. Stellenbosch University; 2015. [cited 2020 Sep 19]. Available from: http://hdl.handle.net/10019.1/96634.

Council of Science Editors:

Ilchev A. Amine end-functional poly(N-vinylpyrrolidone) as amMacroinitiator for L-lysine N-carboxyanhydride polymerization - towards the preparation of pH-responsive micelles for drug delivery. [Doctoral Dissertation]. Stellenbosch University; 2015. Available from: http://hdl.handle.net/10019.1/96634

14. Mazevet, Marianne. Etude de la cardiotoxicité induite par les traitements anticancéreux : Rôle d’Epac dans la cardiotoxicité induite par la Doxorubicine : DOXORUBICIN-INDUCED CARDIOTOXICITY : Role of EPAC signaling.

Degree: Docteur es, Physiologie, physiopathologie, 2015, Université Paris-Saclay (ComUE)

La doxorubicine induit un stress oxydant, des dommages à l’ADN conduisant aussi bien à la mort des cellules cancéreuses que des cardiomyocytes. De nos jours,… (more)

Subjects/Keywords: Cardiotoxicité; Doxorubicine; Epac; Cardiotoxicity; Doxorubicin; Epac

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APA (6th Edition):

Mazevet, M. (2015). Etude de la cardiotoxicité induite par les traitements anticancéreux : Rôle d’Epac dans la cardiotoxicité induite par la Doxorubicine : DOXORUBICIN-INDUCED CARDIOTOXICITY : Role of EPAC signaling. (Doctoral Dissertation). Université Paris-Saclay (ComUE). Retrieved from http://www.theses.fr/2015SACLS190

Chicago Manual of Style (16th Edition):

Mazevet, Marianne. “Etude de la cardiotoxicité induite par les traitements anticancéreux : Rôle d’Epac dans la cardiotoxicité induite par la Doxorubicine : DOXORUBICIN-INDUCED CARDIOTOXICITY : Role of EPAC signaling.” 2015. Doctoral Dissertation, Université Paris-Saclay (ComUE). Accessed September 19, 2020. http://www.theses.fr/2015SACLS190.

MLA Handbook (7th Edition):

Mazevet, Marianne. “Etude de la cardiotoxicité induite par les traitements anticancéreux : Rôle d’Epac dans la cardiotoxicité induite par la Doxorubicine : DOXORUBICIN-INDUCED CARDIOTOXICITY : Role of EPAC signaling.” 2015. Web. 19 Sep 2020.

Vancouver:

Mazevet M. Etude de la cardiotoxicité induite par les traitements anticancéreux : Rôle d’Epac dans la cardiotoxicité induite par la Doxorubicine : DOXORUBICIN-INDUCED CARDIOTOXICITY : Role of EPAC signaling. [Internet] [Doctoral dissertation]. Université Paris-Saclay (ComUE); 2015. [cited 2020 Sep 19]. Available from: http://www.theses.fr/2015SACLS190.

Council of Science Editors:

Mazevet M. Etude de la cardiotoxicité induite par les traitements anticancéreux : Rôle d’Epac dans la cardiotoxicité induite par la Doxorubicine : DOXORUBICIN-INDUCED CARDIOTOXICITY : Role of EPAC signaling. [Doctoral Dissertation]. Université Paris-Saclay (ComUE); 2015. Available from: http://www.theses.fr/2015SACLS190


University of Texas Southwestern Medical Center

15. Li, Dan. Doxorubicin Inhibits Cardiomyocyte Autophagic Flux by Suppressing Lysosomal Acidification.

Degree: 2015, University of Texas Southwestern Medical Center

 The clinical use of doxorubicin is limited by cardiotoxicity. Dysregulation of autophagy in the myocardium has been implicated in a variety of cardiovascular diseases. However,… (more)

Subjects/Keywords: Antibiotics, Antineoplastic; Autophagy; Doxorubicin; Lysosomes; Myocytes, Cardiac

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

APA (6th Edition):

Li, D. (2015). Doxorubicin Inhibits Cardiomyocyte Autophagic Flux by Suppressing Lysosomal Acidification. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/4128

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):

Li, Dan. “Doxorubicin Inhibits Cardiomyocyte Autophagic Flux by Suppressing Lysosomal Acidification.” 2015. Thesis, University of Texas Southwestern Medical Center. Accessed September 19, 2020. http://hdl.handle.net/2152.5/4128.

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

MLA Handbook (7th Edition):

Li, Dan. “Doxorubicin Inhibits Cardiomyocyte Autophagic Flux by Suppressing Lysosomal Acidification.” 2015. Web. 19 Sep 2020.

Vancouver:

Li D. Doxorubicin Inhibits Cardiomyocyte Autophagic Flux by Suppressing Lysosomal Acidification. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2015. [cited 2020 Sep 19]. Available from: http://hdl.handle.net/2152.5/4128.

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

Council of Science Editors:

Li D. Doxorubicin Inhibits Cardiomyocyte Autophagic Flux by Suppressing Lysosomal Acidification. [Thesis]. University of Texas Southwestern Medical Center; 2015. Available from: http://hdl.handle.net/2152.5/4128

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


Universidade Nova

16. Marques, Mara Lisa Miranda. Monotherapy and combined therapy of new potential antitumor compounds: antiproliferative activities and biological targets.

Degree: 2014, Universidade Nova

Review article Martins, P., Marques, M., Coito, L., Pombeiro, A.J.L., Baptista, P.V., Fernandes, A.R. 2014. Organometallic Compounds in Cancer Therapy: Past Lessons and Future Directions. Anti-cancer Agents in Medicinal Chemistry 14. PMID: 25173559 Advisors/Committee Members: Fernandes, Maria Alexandra.

Subjects/Keywords: Cancer; Cisplatin; Citotoxicity; Combined therapeutics; Doxorubicin; Rhenium

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APA (6th Edition):

Marques, M. L. M. (2014). Monotherapy and combined therapy of new potential antitumor compounds: antiproliferative activities and biological targets. (Thesis). Universidade Nova. Retrieved from http://www.rcaap.pt/detail.jsp?id=oai:run.unl.pt:10362/13912

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):

Marques, Mara Lisa Miranda. “Monotherapy and combined therapy of new potential antitumor compounds: antiproliferative activities and biological targets.” 2014. Thesis, Universidade Nova. Accessed September 19, 2020. http://www.rcaap.pt/detail.jsp?id=oai:run.unl.pt:10362/13912.

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

MLA Handbook (7th Edition):

Marques, Mara Lisa Miranda. “Monotherapy and combined therapy of new potential antitumor compounds: antiproliferative activities and biological targets.” 2014. Web. 19 Sep 2020.

Vancouver:

Marques MLM. Monotherapy and combined therapy of new potential antitumor compounds: antiproliferative activities and biological targets. [Internet] [Thesis]. Universidade Nova; 2014. [cited 2020 Sep 19]. Available from: http://www.rcaap.pt/detail.jsp?id=oai:run.unl.pt:10362/13912.

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

Council of Science Editors:

Marques MLM. Monotherapy and combined therapy of new potential antitumor compounds: antiproliferative activities and biological targets. [Thesis]. Universidade Nova; 2014. Available from: http://www.rcaap.pt/detail.jsp?id=oai:run.unl.pt:10362/13912

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


Virginia Tech

17. Xia, Long. Design and Synthesis of Doxorubicin Conjugated Gold Nanoparticles as Anticancer Drug Delivery System.

Degree: MS, Chemistry, 2016, Virginia Tech

Doxorubicin is one of the most widely used and effective anticancer agents to treat a wide spectrum of tumors. But its success in cancer therapy… (more)

Subjects/Keywords: Doxorubicin; Anticancer; Gold Nanoparticles; Drug Delivery

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APA (6th Edition):

Xia, L. (2016). Design and Synthesis of Doxorubicin Conjugated Gold Nanoparticles as Anticancer Drug Delivery System. (Masters Thesis). Virginia Tech. Retrieved from http://hdl.handle.net/10919/81256

Chicago Manual of Style (16th Edition):

Xia, Long. “Design and Synthesis of Doxorubicin Conjugated Gold Nanoparticles as Anticancer Drug Delivery System.” 2016. Masters Thesis, Virginia Tech. Accessed September 19, 2020. http://hdl.handle.net/10919/81256.

MLA Handbook (7th Edition):

Xia, Long. “Design and Synthesis of Doxorubicin Conjugated Gold Nanoparticles as Anticancer Drug Delivery System.” 2016. Web. 19 Sep 2020.

Vancouver:

Xia L. Design and Synthesis of Doxorubicin Conjugated Gold Nanoparticles as Anticancer Drug Delivery System. [Internet] [Masters thesis]. Virginia Tech; 2016. [cited 2020 Sep 19]. Available from: http://hdl.handle.net/10919/81256.

Council of Science Editors:

Xia L. Design and Synthesis of Doxorubicin Conjugated Gold Nanoparticles as Anticancer Drug Delivery System. [Masters Thesis]. Virginia Tech; 2016. Available from: http://hdl.handle.net/10919/81256


University of Guelph

18. Andrade, Adam. Evaluating the Role of TGFbeta and its Downstream Signaling Mediator TAZ in Canine Osteosarcoma Response to Doxorubicin.

Degree: MS, Department of Biomedical Sciences, 2016, University of Guelph

 Osteosarcoma (OSA) is the most common bone tumor in dogs. Metastatic canine OSA is resistant to chemotherapy and is responsible for patient mortality. OSA metastasis… (more)

Subjects/Keywords: Osteosarcoma; Doxorubicin; TGFbeta; TAZ; Canine; Chemoresistance

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APA (6th Edition):

Andrade, A. (2016). Evaluating the Role of TGFbeta and its Downstream Signaling Mediator TAZ in Canine Osteosarcoma Response to Doxorubicin. (Masters Thesis). University of Guelph. Retrieved from https://atrium.lib.uoguelph.ca/xmlui/handle/10214/10051

Chicago Manual of Style (16th Edition):

Andrade, Adam. “Evaluating the Role of TGFbeta and its Downstream Signaling Mediator TAZ in Canine Osteosarcoma Response to Doxorubicin.” 2016. Masters Thesis, University of Guelph. Accessed September 19, 2020. https://atrium.lib.uoguelph.ca/xmlui/handle/10214/10051.

MLA Handbook (7th Edition):

Andrade, Adam. “Evaluating the Role of TGFbeta and its Downstream Signaling Mediator TAZ in Canine Osteosarcoma Response to Doxorubicin.” 2016. Web. 19 Sep 2020.

Vancouver:

Andrade A. Evaluating the Role of TGFbeta and its Downstream Signaling Mediator TAZ in Canine Osteosarcoma Response to Doxorubicin. [Internet] [Masters thesis]. University of Guelph; 2016. [cited 2020 Sep 19]. Available from: https://atrium.lib.uoguelph.ca/xmlui/handle/10214/10051.

Council of Science Editors:

Andrade A. Evaluating the Role of TGFbeta and its Downstream Signaling Mediator TAZ in Canine Osteosarcoma Response to Doxorubicin. [Masters Thesis]. University of Guelph; 2016. Available from: https://atrium.lib.uoguelph.ca/xmlui/handle/10214/10051

19. 김, 빛나. Regulatio of actin cytoskeleton by TIS21 vi downregulating reactive oxygen species (ROS) in the doxorubicin-induced premature senescenc.

Degree: 2014, Ajou University

BTG2(B-cell translocation gene2)is a member of the BTG/Tob family of anti-proliferative genes and has been implicated in various cellular processes including cell cycle progression, differentiation… (more)

Subjects/Keywords: 세포노화; BTG2; TIS21; Doxorubicin; Stress induced senescence

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APA (6th Edition):

김, . (2014). Regulatio of actin cytoskeleton by TIS21 vi downregulating reactive oxygen species (ROS) in the doxorubicin-induced premature senescenc. (Thesis). Ajou University. Retrieved from http://repository.ajou.ac.kr/handle/201003/10848 ; http://dcoll.ajou.ac.kr:9080/dcollection/jsp/common/DcLoOrgPer.jsp?sItemId=000000016361

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):

김, 빛나. “Regulatio of actin cytoskeleton by TIS21 vi downregulating reactive oxygen species (ROS) in the doxorubicin-induced premature senescenc.” 2014. Thesis, Ajou University. Accessed September 19, 2020. http://repository.ajou.ac.kr/handle/201003/10848 ; http://dcoll.ajou.ac.kr:9080/dcollection/jsp/common/DcLoOrgPer.jsp?sItemId=000000016361.

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

MLA Handbook (7th Edition):

김, 빛나. “Regulatio of actin cytoskeleton by TIS21 vi downregulating reactive oxygen species (ROS) in the doxorubicin-induced premature senescenc.” 2014. Web. 19 Sep 2020.

Vancouver:

김 . Regulatio of actin cytoskeleton by TIS21 vi downregulating reactive oxygen species (ROS) in the doxorubicin-induced premature senescenc. [Internet] [Thesis]. Ajou University; 2014. [cited 2020 Sep 19]. Available from: http://repository.ajou.ac.kr/handle/201003/10848 ; http://dcoll.ajou.ac.kr:9080/dcollection/jsp/common/DcLoOrgPer.jsp?sItemId=000000016361.

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

Council of Science Editors:

김 . Regulatio of actin cytoskeleton by TIS21 vi downregulating reactive oxygen species (ROS) in the doxorubicin-induced premature senescenc. [Thesis]. Ajou University; 2014. Available from: http://repository.ajou.ac.kr/handle/201003/10848 ; http://dcoll.ajou.ac.kr:9080/dcollection/jsp/common/DcLoOrgPer.jsp?sItemId=000000016361

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

20. Akolkar, Gauri. Cardioprotective role of vitamin C in the mitigation of oxidative/nitrosative stress in doxorubicin-induced cardiotoxicity.

Degree: Physiology and Pathophysiology, 2017, University of Manitoba

Doxorubicin (Dox) cardiotoxicity is a serious concern in its use for the treatment of cancers. Oxidative stress (OS) and nitrosative stress (NS) are suggested to… (more)

Subjects/Keywords: oxidative stress; doxorubicin; antioxidant; cardiotoxicity; Vitamin C

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APA (6th Edition):

Akolkar, G. (2017). Cardioprotective role of vitamin C in the mitigation of oxidative/nitrosative stress in doxorubicin-induced cardiotoxicity. (Thesis). University of Manitoba. Retrieved from http://hdl.handle.net/1993/32366

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):

Akolkar, Gauri. “Cardioprotective role of vitamin C in the mitigation of oxidative/nitrosative stress in doxorubicin-induced cardiotoxicity.” 2017. Thesis, University of Manitoba. Accessed September 19, 2020. http://hdl.handle.net/1993/32366.

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

MLA Handbook (7th Edition):

Akolkar, Gauri. “Cardioprotective role of vitamin C in the mitigation of oxidative/nitrosative stress in doxorubicin-induced cardiotoxicity.” 2017. Web. 19 Sep 2020.

Vancouver:

Akolkar G. Cardioprotective role of vitamin C in the mitigation of oxidative/nitrosative stress in doxorubicin-induced cardiotoxicity. [Internet] [Thesis]. University of Manitoba; 2017. [cited 2020 Sep 19]. Available from: http://hdl.handle.net/1993/32366.

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

Council of Science Editors:

Akolkar G. Cardioprotective role of vitamin C in the mitigation of oxidative/nitrosative stress in doxorubicin-induced cardiotoxicity. [Thesis]. University of Manitoba; 2017. Available from: http://hdl.handle.net/1993/32366

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


University of Arizona

21. Bozak, Karen Aline, 1960-. ANTHRACYCLINE CARDIOTOXICITY MODELING USING INTRACELLULAR ATP LEVELS IN NEONATAL RAT HEART CELL CULTURES (CHEMOTHERAPY, DOXORUBICIN, MYOCYTES) .

Degree: 1986, University of Arizona

Subjects/Keywords: Anthracyclines.; Doxorubicin.; Antibiotics.

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APA (6th Edition):

Bozak, Karen Aline, 1. (1986). ANTHRACYCLINE CARDIOTOXICITY MODELING USING INTRACELLULAR ATP LEVELS IN NEONATAL RAT HEART CELL CULTURES (CHEMOTHERAPY, DOXORUBICIN, MYOCYTES) . (Masters Thesis). University of Arizona. Retrieved from http://hdl.handle.net/10150/276748

Chicago Manual of Style (16th Edition):

Bozak, Karen Aline, 1960-. “ANTHRACYCLINE CARDIOTOXICITY MODELING USING INTRACELLULAR ATP LEVELS IN NEONATAL RAT HEART CELL CULTURES (CHEMOTHERAPY, DOXORUBICIN, MYOCYTES) .” 1986. Masters Thesis, University of Arizona. Accessed September 19, 2020. http://hdl.handle.net/10150/276748.

MLA Handbook (7th Edition):

Bozak, Karen Aline, 1960-. “ANTHRACYCLINE CARDIOTOXICITY MODELING USING INTRACELLULAR ATP LEVELS IN NEONATAL RAT HEART CELL CULTURES (CHEMOTHERAPY, DOXORUBICIN, MYOCYTES) .” 1986. Web. 19 Sep 2020.

Vancouver:

Bozak, Karen Aline 1. ANTHRACYCLINE CARDIOTOXICITY MODELING USING INTRACELLULAR ATP LEVELS IN NEONATAL RAT HEART CELL CULTURES (CHEMOTHERAPY, DOXORUBICIN, MYOCYTES) . [Internet] [Masters thesis]. University of Arizona; 1986. [cited 2020 Sep 19]. Available from: http://hdl.handle.net/10150/276748.

Council of Science Editors:

Bozak, Karen Aline 1. ANTHRACYCLINE CARDIOTOXICITY MODELING USING INTRACELLULAR ATP LEVELS IN NEONATAL RAT HEART CELL CULTURES (CHEMOTHERAPY, DOXORUBICIN, MYOCYTES) . [Masters Thesis]. University of Arizona; 1986. Available from: http://hdl.handle.net/10150/276748


University of Toronto

22. Eetezadi, Sina. Nanomedicines and Combination Therapy of Doxorubicin and Olaparib for Treatment of Ovarian Cancer.

Degree: PhD, 2016, University of Toronto

 Ovarian cancer is the fourth leading cause of death in women of developed countries, with dismal survival improvements achieved in the past three decades. Specifically,… (more)

Subjects/Keywords: doxorubicin; nanomedicine; olaparib; ovarian cancer; 0572

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APA (6th Edition):

Eetezadi, S. (2016). Nanomedicines and Combination Therapy of Doxorubicin and Olaparib for Treatment of Ovarian Cancer. (Doctoral Dissertation). University of Toronto. Retrieved from http://hdl.handle.net/1807/71715

Chicago Manual of Style (16th Edition):

Eetezadi, Sina. “Nanomedicines and Combination Therapy of Doxorubicin and Olaparib for Treatment of Ovarian Cancer.” 2016. Doctoral Dissertation, University of Toronto. Accessed September 19, 2020. http://hdl.handle.net/1807/71715.

MLA Handbook (7th Edition):

Eetezadi, Sina. “Nanomedicines and Combination Therapy of Doxorubicin and Olaparib for Treatment of Ovarian Cancer.” 2016. Web. 19 Sep 2020.

Vancouver:

Eetezadi S. Nanomedicines and Combination Therapy of Doxorubicin and Olaparib for Treatment of Ovarian Cancer. [Internet] [Doctoral dissertation]. University of Toronto; 2016. [cited 2020 Sep 19]. Available from: http://hdl.handle.net/1807/71715.

Council of Science Editors:

Eetezadi S. Nanomedicines and Combination Therapy of Doxorubicin and Olaparib for Treatment of Ovarian Cancer. [Doctoral Dissertation]. University of Toronto; 2016. Available from: http://hdl.handle.net/1807/71715


University of Arizona

23. Knights-Mitchell, Shellie. Plasmon Resonant Liposomes as a Targeted, Controlled-Release Drug Delivery System .

Degree: 2018, University of Arizona

 For many types of cancers chemotherapy is the treatment of choice despite evidence that this treatment modality is contributing only about 2 % to the… (more)

Subjects/Keywords: Doxorubicin; Drug Delivery; Liposomes; Plasmon Resonance

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APA (6th Edition):

Knights-Mitchell, S. (2018). Plasmon Resonant Liposomes as a Targeted, Controlled-Release Drug Delivery System . (Doctoral Dissertation). University of Arizona. Retrieved from http://hdl.handle.net/10150/627719

Chicago Manual of Style (16th Edition):

Knights-Mitchell, Shellie. “Plasmon Resonant Liposomes as a Targeted, Controlled-Release Drug Delivery System .” 2018. Doctoral Dissertation, University of Arizona. Accessed September 19, 2020. http://hdl.handle.net/10150/627719.

MLA Handbook (7th Edition):

Knights-Mitchell, Shellie. “Plasmon Resonant Liposomes as a Targeted, Controlled-Release Drug Delivery System .” 2018. Web. 19 Sep 2020.

Vancouver:

Knights-Mitchell S. Plasmon Resonant Liposomes as a Targeted, Controlled-Release Drug Delivery System . [Internet] [Doctoral dissertation]. University of Arizona; 2018. [cited 2020 Sep 19]. Available from: http://hdl.handle.net/10150/627719.

Council of Science Editors:

Knights-Mitchell S. Plasmon Resonant Liposomes as a Targeted, Controlled-Release Drug Delivery System . [Doctoral Dissertation]. University of Arizona; 2018. Available from: http://hdl.handle.net/10150/627719


University of Western Ontario

24. Nalin, Nima. Nicotinamide mononucleotide imparts protection against Doxorubicin-induced cardiotoxicity by maintaining lysosomal acidification.

Degree: 2020, University of Western Ontario

Doxorubicin (DOX) blocks the autophagic flux in cardiomyocytes by inhibiting lysosome acidification. The acidic pH of lysosomes is maintained by the V-ATPase pump. NAD+ is… (more)

Subjects/Keywords: ATP6V0d1; cardiotoxicity; doxorubicin; lysosome; NAD+; NMN

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APA (6th Edition):

Nalin, N. (2020). Nicotinamide mononucleotide imparts protection against Doxorubicin-induced cardiotoxicity by maintaining lysosomal acidification. (Thesis). University of Western Ontario. Retrieved from https://ir.lib.uwo.ca/etd/7195

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):

Nalin, Nima. “Nicotinamide mononucleotide imparts protection against Doxorubicin-induced cardiotoxicity by maintaining lysosomal acidification.” 2020. Thesis, University of Western Ontario. Accessed September 19, 2020. https://ir.lib.uwo.ca/etd/7195.

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

MLA Handbook (7th Edition):

Nalin, Nima. “Nicotinamide mononucleotide imparts protection against Doxorubicin-induced cardiotoxicity by maintaining lysosomal acidification.” 2020. Web. 19 Sep 2020.

Vancouver:

Nalin N. Nicotinamide mononucleotide imparts protection against Doxorubicin-induced cardiotoxicity by maintaining lysosomal acidification. [Internet] [Thesis]. University of Western Ontario; 2020. [cited 2020 Sep 19]. Available from: https://ir.lib.uwo.ca/etd/7195.

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

Council of Science Editors:

Nalin N. Nicotinamide mononucleotide imparts protection against Doxorubicin-induced cardiotoxicity by maintaining lysosomal acidification. [Thesis]. University of Western Ontario; 2020. Available from: https://ir.lib.uwo.ca/etd/7195

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


Oklahoma State University

25. VanOsdol, Joshua Paul. Role of bubble-based nanosystems in chemo-immunotherapy of colon cancer.

Degree: Comparative Biomedical Sciences, 2020, Oklahoma State University

 Colorectal cancer is one of the most commonly diagnosed forms of cancer with over 4% of both men and women developing it sometime during their… (more)

Subjects/Keywords: colorectal cancer; doxorubicin; focused ultrasound; nanomedicine

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

APA (6th Edition):

VanOsdol, J. P. (2020). Role of bubble-based nanosystems in chemo-immunotherapy of colon cancer. (Thesis). Oklahoma State University. Retrieved from http://hdl.handle.net/11244/325404

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):

VanOsdol, Joshua Paul. “Role of bubble-based nanosystems in chemo-immunotherapy of colon cancer.” 2020. Thesis, Oklahoma State University. Accessed September 19, 2020. http://hdl.handle.net/11244/325404.

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

MLA Handbook (7th Edition):

VanOsdol, Joshua Paul. “Role of bubble-based nanosystems in chemo-immunotherapy of colon cancer.” 2020. Web. 19 Sep 2020.

Vancouver:

VanOsdol JP. Role of bubble-based nanosystems in chemo-immunotherapy of colon cancer. [Internet] [Thesis]. Oklahoma State University; 2020. [cited 2020 Sep 19]. Available from: http://hdl.handle.net/11244/325404.

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

Council of Science Editors:

VanOsdol JP. Role of bubble-based nanosystems in chemo-immunotherapy of colon cancer. [Thesis]. Oklahoma State University; 2020. Available from: http://hdl.handle.net/11244/325404

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


Johannes Gutenberg Universität Mainz

26. Henninger, Christian. Untersuchungen zum Einfluss des HMG-CoA-Reduktase-Inhibitors Lovastatin auf die Toxizität ionisierender Strahlung sowie des Anthrazyklinderivats Doxorubicin im Mausmodell.

Degree: 2012, Johannes Gutenberg Universität Mainz

 Hintergund: HMG-CoA-Reduktase-Inhibitoren (Statine) sind klinisch etablierte Cholesterinsenker. Über die Inhibition der intrinsischen Cholesterinbiosynthese hinaus zeigen sie sogenannte pleiotrope biologische Effekte. Ein Großteil dieser Wirkungen wird… (more)

Subjects/Keywords: Lovastatin, Doxorubicin, Normalgewebe, Toxizität, Rho; lovastatin, doxorubicin, normal tissue, toxicity, Rho; Life sciences

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

APA (6th Edition):

Henninger, C. (2012). Untersuchungen zum Einfluss des HMG-CoA-Reduktase-Inhibitors Lovastatin auf die Toxizität ionisierender Strahlung sowie des Anthrazyklinderivats Doxorubicin im Mausmodell. (Doctoral Dissertation). Johannes Gutenberg Universität Mainz. Retrieved from http://ubm.opus.hbz-nrw.de/volltexte/2013/3338/

Chicago Manual of Style (16th Edition):

Henninger, Christian. “Untersuchungen zum Einfluss des HMG-CoA-Reduktase-Inhibitors Lovastatin auf die Toxizität ionisierender Strahlung sowie des Anthrazyklinderivats Doxorubicin im Mausmodell.” 2012. Doctoral Dissertation, Johannes Gutenberg Universität Mainz. Accessed September 19, 2020. http://ubm.opus.hbz-nrw.de/volltexte/2013/3338/.

MLA Handbook (7th Edition):

Henninger, Christian. “Untersuchungen zum Einfluss des HMG-CoA-Reduktase-Inhibitors Lovastatin auf die Toxizität ionisierender Strahlung sowie des Anthrazyklinderivats Doxorubicin im Mausmodell.” 2012. Web. 19 Sep 2020.

Vancouver:

Henninger C. Untersuchungen zum Einfluss des HMG-CoA-Reduktase-Inhibitors Lovastatin auf die Toxizität ionisierender Strahlung sowie des Anthrazyklinderivats Doxorubicin im Mausmodell. [Internet] [Doctoral dissertation]. Johannes Gutenberg Universität Mainz; 2012. [cited 2020 Sep 19]. Available from: http://ubm.opus.hbz-nrw.de/volltexte/2013/3338/.

Council of Science Editors:

Henninger C. Untersuchungen zum Einfluss des HMG-CoA-Reduktase-Inhibitors Lovastatin auf die Toxizität ionisierender Strahlung sowie des Anthrazyklinderivats Doxorubicin im Mausmodell. [Doctoral Dissertation]. Johannes Gutenberg Universität Mainz; 2012. Available from: http://ubm.opus.hbz-nrw.de/volltexte/2013/3338/


Brno University of Technology

27. Přibyl, Jakub. Studium interakce DNA a doxorubicinu elektrochemickými metodami na nanostrukturovaných elektrodách: Study of DNA-doxorubicine interaction by electrochemical methods on nanostructured electrodes.

Degree: 2018, Brno University of Technology

 Cancer diseases are one of the leading causes of mortality worldwide, for this reason, great attention anticancer drugs. Doxorubicin falls into the category of the… (more)

Subjects/Keywords: Deoxyribonukleová kyselina; Doxorubicin; Impedance; Impedanční spektroskopie; Voltametrie; Deoxyribonucleic acid; Doxorubicin; Impedance; Impedance Spectroscopy; Voltammetry

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

APA (6th Edition):

Přibyl, J. (2018). Studium interakce DNA a doxorubicinu elektrochemickými metodami na nanostrukturovaných elektrodách: Study of DNA-doxorubicine interaction by electrochemical methods on nanostructured electrodes. (Thesis). Brno University of Technology. Retrieved from http://hdl.handle.net/11012/26176

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):

Přibyl, Jakub. “Studium interakce DNA a doxorubicinu elektrochemickými metodami na nanostrukturovaných elektrodách: Study of DNA-doxorubicine interaction by electrochemical methods on nanostructured electrodes.” 2018. Thesis, Brno University of Technology. Accessed September 19, 2020. http://hdl.handle.net/11012/26176.

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

MLA Handbook (7th Edition):

Přibyl, Jakub. “Studium interakce DNA a doxorubicinu elektrochemickými metodami na nanostrukturovaných elektrodách: Study of DNA-doxorubicine interaction by electrochemical methods on nanostructured electrodes.” 2018. Web. 19 Sep 2020.

Vancouver:

Přibyl J. Studium interakce DNA a doxorubicinu elektrochemickými metodami na nanostrukturovaných elektrodách: Study of DNA-doxorubicine interaction by electrochemical methods on nanostructured electrodes. [Internet] [Thesis]. Brno University of Technology; 2018. [cited 2020 Sep 19]. Available from: http://hdl.handle.net/11012/26176.

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

Council of Science Editors:

Přibyl J. Studium interakce DNA a doxorubicinu elektrochemickými metodami na nanostrukturovaných elektrodách: Study of DNA-doxorubicine interaction by electrochemical methods on nanostructured electrodes. [Thesis]. Brno University of Technology; 2018. Available from: http://hdl.handle.net/11012/26176

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


Johannes Gutenberg Universität Mainz

28. Lelle, Marco. Synthese und zytotoxische Eigenschaften neuartiger Doxorubicinderivate.

Degree: 2014, Johannes Gutenberg Universität Mainz

 Der Fokus dieser Arbeit lag auf der Darstellung modifizierter Doxorubicin-Moleküle, um die mit der therapeutischen Anwendung verbundenen Hindernisse wie DNA-Bindungsaffinität, Tumorselektivität, Zell- sowie Nukleusakkumulation, Arzneistoffaufnahme… (more)

Subjects/Keywords: Doxorubicin; Anthrazyklin; Peptidkonjugat; Tumortherapie; Vernetzer; Doxorubicin; anthracycline; peptide conjugate; tumor therapy; cross-linking reagent; Chemistry and allied sciences

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

APA (6th Edition):

Lelle, M. (2014). Synthese und zytotoxische Eigenschaften neuartiger Doxorubicinderivate. (Doctoral Dissertation). Johannes Gutenberg Universität Mainz. Retrieved from http://ubm.opus.hbz-nrw.de/volltexte/2014/3716/

Chicago Manual of Style (16th Edition):

Lelle, Marco. “Synthese und zytotoxische Eigenschaften neuartiger Doxorubicinderivate.” 2014. Doctoral Dissertation, Johannes Gutenberg Universität Mainz. Accessed September 19, 2020. http://ubm.opus.hbz-nrw.de/volltexte/2014/3716/.

MLA Handbook (7th Edition):

Lelle, Marco. “Synthese und zytotoxische Eigenschaften neuartiger Doxorubicinderivate.” 2014. Web. 19 Sep 2020.

Vancouver:

Lelle M. Synthese und zytotoxische Eigenschaften neuartiger Doxorubicinderivate. [Internet] [Doctoral dissertation]. Johannes Gutenberg Universität Mainz; 2014. [cited 2020 Sep 19]. Available from: http://ubm.opus.hbz-nrw.de/volltexte/2014/3716/.

Council of Science Editors:

Lelle M. Synthese und zytotoxische Eigenschaften neuartiger Doxorubicinderivate. [Doctoral Dissertation]. Johannes Gutenberg Universität Mainz; 2014. Available from: http://ubm.opus.hbz-nrw.de/volltexte/2014/3716/


Coventry University

29. Gharanei, A. M. Investigation into the cardiotoxic effects of doxorubicin and strategies for cardioprotection.

Degree: PhD, 2013, Coventry University

Doxorubicin is one of the most effective anti-cancer agents; however its use is associated with adverse cardiac effects, including cardiomyopathy and progressive heart failure. Mitochondrial… (more)

Subjects/Keywords: 616.99; doxorubicin, cancer drugs, side effects, cardiac, cardiotoxic effects; Doxorubicin; Cancer  – Treatment; Drugs  – Side effects; Heart

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

APA (6th Edition):

Gharanei, A. M. (2013). Investigation into the cardiotoxic effects of doxorubicin and strategies for cardioprotection. (Doctoral Dissertation). Coventry University. Retrieved from http://curve.coventry.ac.uk/open/items/ad712004-828e-4d9a-8ddb-17951146d414/1 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.629992

Chicago Manual of Style (16th Edition):

Gharanei, A M. “Investigation into the cardiotoxic effects of doxorubicin and strategies for cardioprotection.” 2013. Doctoral Dissertation, Coventry University. Accessed September 19, 2020. http://curve.coventry.ac.uk/open/items/ad712004-828e-4d9a-8ddb-17951146d414/1 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.629992.

MLA Handbook (7th Edition):

Gharanei, A M. “Investigation into the cardiotoxic effects of doxorubicin and strategies for cardioprotection.” 2013. Web. 19 Sep 2020.

Vancouver:

Gharanei AM. Investigation into the cardiotoxic effects of doxorubicin and strategies for cardioprotection. [Internet] [Doctoral dissertation]. Coventry University; 2013. [cited 2020 Sep 19]. Available from: http://curve.coventry.ac.uk/open/items/ad712004-828e-4d9a-8ddb-17951146d414/1 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.629992.

Council of Science Editors:

Gharanei AM. Investigation into the cardiotoxic effects of doxorubicin and strategies for cardioprotection. [Doctoral Dissertation]. Coventry University; 2013. Available from: http://curve.coventry.ac.uk/open/items/ad712004-828e-4d9a-8ddb-17951146d414/1 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.629992


Brno University of Technology

30. Krausová, Kateřina. Studium mechanismů disociace a reasociace feritinových proteinových klecí a jejich využití v nanomedicíně: Study of disassembly/reassembly mechanisms of ferritin protein cages and their utilization in nanomedicine.

Degree: 2019, Brno University of Technology

 Diploma thesis deals with the study of dissociation and reassociation of ferritin protein cages and their use in nanomedicine. Most studies that are focused on… (more)

Subjects/Keywords: Ferritin; disociace; reasociace; nativní PAGE; doxorubicin; karcinom prsu; Ferritin; dissociation; reassociation; native PAGE; doxorubicin; breast cancer

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

APA (6th Edition):

Krausová, K. (2019). Studium mechanismů disociace a reasociace feritinových proteinových klecí a jejich využití v nanomedicíně: Study of disassembly/reassembly mechanisms of ferritin protein cages and their utilization in nanomedicine. (Thesis). Brno University of Technology. Retrieved from http://hdl.handle.net/11012/177640

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):

Krausová, Kateřina. “Studium mechanismů disociace a reasociace feritinových proteinových klecí a jejich využití v nanomedicíně: Study of disassembly/reassembly mechanisms of ferritin protein cages and their utilization in nanomedicine.” 2019. Thesis, Brno University of Technology. Accessed September 19, 2020. http://hdl.handle.net/11012/177640.

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

MLA Handbook (7th Edition):

Krausová, Kateřina. “Studium mechanismů disociace a reasociace feritinových proteinových klecí a jejich využití v nanomedicíně: Study of disassembly/reassembly mechanisms of ferritin protein cages and their utilization in nanomedicine.” 2019. Web. 19 Sep 2020.

Vancouver:

Krausová K. Studium mechanismů disociace a reasociace feritinových proteinových klecí a jejich využití v nanomedicíně: Study of disassembly/reassembly mechanisms of ferritin protein cages and their utilization in nanomedicine. [Internet] [Thesis]. Brno University of Technology; 2019. [cited 2020 Sep 19]. Available from: http://hdl.handle.net/11012/177640.

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

Council of Science Editors:

Krausová K. Studium mechanismů disociace a reasociace feritinových proteinových klecí a jejich využití v nanomedicíně: Study of disassembly/reassembly mechanisms of ferritin protein cages and their utilization in nanomedicine. [Thesis]. Brno University of Technology; 2019. Available from: http://hdl.handle.net/11012/177640

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

[1] [2] [3] [4] [5] … [11]

.