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Florida Agricultural and Mechanical University. Basic Pharmaceutical Sciences. degree granting institution.

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The University of Manchester (United Kingdom). degree granting institution.

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Yale University. Yale School of Medicine. degree granting institution.

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Abraham, Pranav Samuel, author.

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Adunlin, Georges, author.

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Agarwal, Pranay, author.

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Algan, Ozer, author.

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Almabadi, Huda Muslih, author.

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Amer, Mostafa, author.

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Anderson, Julie Elizabeth, author.

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Barrett, Sophie Victoria, author.

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Bjersand, Kathrine, author.

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Brigham Young University. Physiology and Developmental Biology. degree granting institution.

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Burke, Daniel, author.

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Conev, Nikolay, author.

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El-Mahdi, Alya Faysal, author.

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Erler, Janine, author.

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Florida Agricultural and Mechanical University. Economic, Social, and Administrative Pharmacy. degree granting institution.

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Gary, Cyril Sergei, author.

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Groves, Thomas, author.

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Halliburton, Gray Halliburton, author.

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Henderson, Elizabeth D., author.

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Illinois Institute of Technology. Biology. degree granting institution.

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Kandar, Bojidar M., author.

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Kent State University. College of Arts and Sciences / Department of Computer Science. degree granting institution.

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Krishnamurthy, Nishanth, author.

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Lederer, Nirosha Mahendraratnam, author.

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Liu, Shuai, author.

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Mackay, Amy Dee, author.

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Mai, Wilson Xuan, author.

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Manas Nunez, Adriana, author.

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Massachusetts College of Pharmacy and Health Sciences. Pharmaceutical Economics and Policy. degree granting institution.

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McCabe-Lankford, Eleanor, author.

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Medical University of Varna (Bulgaria). degree granting institution.

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Miles, Jana S., author.

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Poku, Rosemary A., author.

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Purdue University. Chemistry. degree granting institution.

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Reilly, Nicole M., author.

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Roy, Jyoti, author.

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Shubbar, Safa, author.

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Sojourner, Samantha J., author.

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Solitro, Abigail Rae, author.

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State University of New York at Buffalo. Roswell Park . Biophysics. degree granting institution.

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Stocke, Nathanael A., author.

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Stojanovic, Lora, author.

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The Ohio State University. Biomedical Engineering. degree granting institution.

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The University of Arizona. Biomedical Engineering. degree granting institution.

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The University of Edinburgh (United Kingdom). degree granting institution.

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The University of Manchester (United Kingdom). School of Biological Sciences. degree granting institution.

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The University of Memphis. Biomedical Engineering. degree granting institution.

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The University of North Carolina at Chapel Hill. Pharmaceutical Sciences. degree granting institution.

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The University of Oklahoma Health Sciences Center. Clinical and Translational Science. degree granting institution.

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Thomson, Angela B., author.

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Tufts University. Biomedical Engineering. degree granting institution.

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Tulane University School of Science and Engineering. Biomedical Engineering. degree granting institution.

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Uddin, Mohammad Burhan, author.

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University of Arkansas for Medical Sciences. Neurobiology and Developmental Science. degree granting institution.

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University of Arkansas for Medical Sciences. Pharmaceutical Sciences. degree granting institution.

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University of California, Los Angeles. Molecular and Medical Pharmacology. degree granting institution.

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University of Glasgow (United Kingdom). Department not provided. degree granting institution.

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University of Kentucky. Chemical and Materials Engineering. degree granting institution.

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University of London, King's College (United Kingdom). degree granting institution.

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University of Louisiana at Monroe. Pharmacy. degree granting institution.

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University of Maryland, Baltimore. Molecular Medicine. degree granting institution.

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University of Massachusetts Boston. Chemistry/Organic Chemistry (PhD). degree granting institution.

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University of South Carolina. Pharmaceutical Science. degree granting institution.

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Uppsala Universitet (Sweden). degree granting institution.

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Van Andel Research Institute. Biomedical. degree granting institution.

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Wake Forest University. Molecular Medicine and Translational Science. degree granting institution.

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Watson, Jeffrey R., author.

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Whitmore, Aurellia M., author.

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Zhu, Rebecca, author.

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Cover image for Effects of Breast Cancer Chemotherapy on Hippocampal Physiology and Cognitive Function in Female Mice

Effects of Breast Cancer Chemotherapy on Hippocampal Physiology and Cognitive Function in Female Mice

1.

Effects of Breast Cancer Chemotherapy on Hippocampal Physiology and Cognitive Function in Female Mice

by

Anderson, Julie Elizabeth, author.

http://gateway.proquest.com/openurl?url_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:dissertation&res_dat=xri:pqm&rft_dat=xri:pqdiss:10844475

Format:

Excerpt:

Effects of Breast Cancer Chemotherapy on Hippocampal Physiology and Cognitive Function in Female

Cover image for Adverse events associated with chemotherapy in a cancer centre in a developing country

Adverse events associated with chemotherapy in a cancer centre in a developing country

2.

Adverse events associated with chemotherapy in a cancer centre in a developing country

by

El-Mahdi, Alya Faysal, author.

http://gateway.proquest.com/openurl?url_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:dissertation&res_dat=xri:pqm&rft_dat=xri:pqdiss:13873290

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Excerpt:

Adverse events associated with chemotherapy in a cancer centre in a developing country / El-Mahdi

Cover image for Serum Expression Levels of Mir-17, Mir-21, Mir-29a and Mir-92 as Potential Biomarkers for Recurrence after Adjuvant Chemotherapy in Colon Cancer Patients = Микрорибонуклеинови киселини miR-17, miR-21, miR-29a и miR-92 като потенциални маркери за оценка на риск от рецидив след адювантна химиотерапия при пациенти с карцином на колона

Serum Expression Levels of Mir-17, Mir-21, Mir-29a and Mir-92 as Potential Biomarkers for Recurrence after Adjuvant Chemotherapy in Colon Cancer Patients = Микрорибонуклеинови киселини miR-17, miR-21, miR-29a и miR-92 като потенциални маркери за оценка на риск от рецидив след адювантна химиотерапия при пациенти с карцином на колона

3.

Serum Expression Levels of Mir-17, Mir-21, Mir-29a and Mir-92 as Potential Biomarkers for Recurrence after Adjuvant Chemotherapy in Colon Cancer Patients = Микрорибонуклеинови киселини miR-17, miR-21, miR-29a и miR-92 като потенциални маркери за оценка на риск от рецидив след адювантна химиотерапия при пациенти с карцином на колона

by

Conev, Nikolay, author.

http://gateway.proquest.com/openurl?url_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:dissertation&res_dat=xri:pqm&rft_dat=xri:pqdiss:10680178

Format:

Excerpt:

Recurrence after Adjuvant Chemotherapy in Colon Cancer Patients = Микрорибонуклеинови киселини miR-17, miR-21

Cover image for Ultrasound Medical Imaging Systems Using Telemedicine and Blockchain for Remote Monitoring of Responses to Neoadjuvant Chemotherapy in Women's Breast Cancer: Concept and Implementation

Ultrasound Medical Imaging Systems Using Telemedicine and Blockchain for Remote Monitoring of Responses to Neoadjuvant Chemotherapy in Women's Breast Cancer: Concept and Implementation

4.

Ultrasound Medical Imaging Systems Using Telemedicine and Blockchain for Remote Monitoring of Responses to Neoadjuvant Chemotherapy in Women's Breast Cancer: Concept and Implementation

by

Shubbar, Safa, author.

http://gateway.proquest.com/openurl?url_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:dissertation&res_dat=xri:pqm&rft_dat=xri:pqdiss:10891755

Format:

Excerpt:

Responses to Neoadjuvant Chemotherapy in Women's Breast Cancer: Concept and Implementation / Shubbar, Safa

Cover image for Synergistic Enhancement of Thermally Triggered Chemotherapy for Liver Cancer by HIFU: Evidence from in vitro and in vivo Studies

Synergistic Enhancement of Thermally Triggered Chemotherapy for Liver Cancer by HIFU: Evidence from in vitro and in vivo Studies

5.

Synergistic Enhancement of Thermally Triggered Chemotherapy for Liver Cancer by HIFU: Evidence from in vitro and in vivo Studies

by

Halliburton, Gray Halliburton, author.

http://gateway.proquest.com/openurl?url_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:dissertation&res_dat=xri:pqm&rft_dat=xri:pqdiss:10608337

Format:

Excerpt:

Synergistic Enhancement of Thermally Triggered Chemotherapy for Liver Cancer by HIFU: Evidence from

Cover image for Comprehensive Characterization of the Apoptotic Machinery in Glioblastoma Identifies New Therapeutic Strategies

Comprehensive Characterization of the Apoptotic Machinery in Glioblastoma Identifies New Therapeutic Strategies

6.

Comprehensive Characterization of the Apoptotic Machinery in Glioblastoma Identifies New Therapeutic Strategies

by

Mai, Wilson Xuan, author.

http://gateway.proquest.com/openurl?url_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:dissertation&res_dat=xri:pqm&rft_dat=xri:pqdiss:10809335

Format:

Excerpt:

results in tumor survival and resistance. Glioblastoma (GBM), the deadliest form of brain cancer, has poor

Cover image for DNA Methyltransferase Inhibitors in Combination with PARP inhibitors Generate Synthetic Lethality in BRCA-proficient Ovarian Cancer

DNA Methyltransferase Inhibitors in Combination with PARP inhibitors Generate Synthetic Lethality in BRCA-proficient Ovarian Cancer

7.

DNA Methyltransferase Inhibitors in Combination with PARP inhibitors Generate Synthetic Lethality in BRCA-proficient Ovarian Cancer

by

Stojanovic, Lora, author.

http://gateway.proquest.com/openurl?url_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:dissertation&res_dat=xri:pqm&rft_dat=xri:pqdiss:10815850

Format:

Excerpt:

therapy for EOC patients is platinum-based chemotherapy which often leads to resistance to this treatment

Cover image for Evaluation of the Role of Human DNAJAs in the Response to Cytotoxic Agents in a Yeast Model System

Evaluation of the Role of Human DNAJAs in the Response to Cytotoxic Agents in a Yeast Model System

8.

Evaluation of the Role of Human DNAJAs in the Response to Cytotoxic Agents in a Yeast Model System

by

Whitmore, Aurellia M., author.

http://gateway.proquest.com/openurl?url_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:dissertation&res_dat=xri:pqm&rft_dat=xri:pqdiss:10812926

Format:

Excerpt:

contributing to cancer cell survival. Cytotoxic chemotherapy continues to play an important role in the

Cover image for Targeted Polymer Nanoparticles for the Detection and Treatment of Disseminated Colorectal Cancer In Vivo

Targeted Polymer Nanoparticles for the Detection and Treatment of Disseminated Colorectal Cancer In Vivo

9.

Targeted Polymer Nanoparticles for the Detection and Treatment of Disseminated Colorectal Cancer In Vivo

by

McCabe-Lankford, Eleanor, author.

http://gateway.proquest.com/openurl?url_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:dissertation&res_dat=xri:pqm&rft_dat=xri:pqdiss:10813569

Format:

Excerpt:

Colorectal cancer (CRC) is the second leading cause of cancer-related deaths and the fourth most

Cover image for Multi-Tissue Examination of Exercise or Metformin on the Consequences of Doxorubicin Treatment

Multi-Tissue Examination of Exercise or Metformin on the Consequences of Doxorubicin Treatment

10.

Multi-Tissue Examination of Exercise or Metformin on the Consequences of Doxorubicin Treatment

by

Mackay, Amy Dee, author.

http://gateway.proquest.com/openurl?url_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:dissertation&res_dat=xri:pqm&rft_dat=xri:pqdiss:10790295

Format:

Excerpt:

cancer treatments, addressing the long-term side effects of chemotherapy treatment becomes critical. In

Cover image for Autophagy Inhibition in Non-small Cell Lung Cancer

Autophagy Inhibition in Non-small Cell Lung Cancer

11.

Autophagy Inhibition in Non-small Cell Lung Cancer

by

Solitro, Abigail Rae, author.

http://gateway.proquest.com/openurl?url_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:dissertation&res_dat=xri:pqm&rft_dat=xri:pqdiss:10829750

Format:

Excerpt:

autophagy to fuel hyperproliferation and resist cytotoxic chemotherapy. As a result, autophagy inhibition is

Cover image for Toll-like Receptor-5 Agonist Entolimod Broadens the Therapeutic Window of 5-Fluorouracil by Reducing Its Toxicity to Normal Tissues in Mice

Toll-like Receptor-5 Agonist Entolimod Broadens the Therapeutic Window of 5-Fluorouracil by Reducing Its Toxicity to Normal Tissues in Mice

12.

Toll-like Receptor-5 Agonist Entolimod Broadens the Therapeutic Window of 5-Fluorouracil by Reducing Its Toxicity to Normal Tissues in Mice

by

Kandar, Bojidar M., author.

http://gateway.proquest.com/openurl?url_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:dissertation&res_dat=xri:pqm&rft_dat=xri:pqdiss:10746366

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Excerpt:

radiation. Here, using 5-Fluorouracil (5-FU) treated mice as a model of chemotherapy-induced side effects; I

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