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You searched for +publisher:"Drexel University" +contributor:("College of Medicine"). Showing records 1 – 30 of 94 total matches.

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Drexel University

1. Huang, Yu-Hung. Role of HuR in Mediating Ovarian Cancer Treatment.

Degree: 2016, Drexel University

An mRNA-binding protein, HuR (Human antigen R, aka ELAVL1), is highly elevated in many cancers, and is a master regulator of gene expression. HuR-regulated genes… (more)

Subjects/Keywords: Molecular biology; Cytology; Genetics; Biochemical Phenomena; Genetic Phenomena; Genetic Processes

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

APA (6th Edition):

Huang, Y. (2016). Role of HuR in Mediating Ovarian Cancer Treatment. (Thesis). Drexel University. Retrieved from http://hdl.handle.net/1860/idea:7154

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):

Huang, Yu-Hung. “Role of HuR in Mediating Ovarian Cancer Treatment.” 2016. Thesis, Drexel University. Accessed April 11, 2021. http://hdl.handle.net/1860/idea:7154.

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

MLA Handbook (7th Edition):

Huang, Yu-Hung. “Role of HuR in Mediating Ovarian Cancer Treatment.” 2016. Web. 11 Apr 2021.

Vancouver:

Huang Y. Role of HuR in Mediating Ovarian Cancer Treatment. [Internet] [Thesis]. Drexel University; 2016. [cited 2021 Apr 11]. Available from: http://hdl.handle.net/1860/idea:7154.

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

Council of Science Editors:

Huang Y. Role of HuR in Mediating Ovarian Cancer Treatment. [Thesis]. Drexel University; 2016. Available from: http://hdl.handle.net/1860/idea:7154

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


Drexel University

2. Manners, Melissa Taft. Role of MeCP2 in Pain and its Regulation by miRNAs.

Degree: 2016, Drexel University

Nerve injury induces chronic pain and dysregulation of microRNAs in the dorsal root ganglia (DRG). Several downregulated microRNAs are predicted to target methyl-CpG-binding protein 2… (more)

Subjects/Keywords: Physiology; Pharmacology; Pharmacological and Toxicological Phenomena and Processes; Physiological Phemonena

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APA (6th Edition):

Manners, M. T. (2016). Role of MeCP2 in Pain and its Regulation by miRNAs. (Thesis). Drexel University. Retrieved from http://hdl.handle.net/1860/idea:7156

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):

Manners, Melissa Taft. “Role of MeCP2 in Pain and its Regulation by miRNAs.” 2016. Thesis, Drexel University. Accessed April 11, 2021. http://hdl.handle.net/1860/idea:7156.

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

MLA Handbook (7th Edition):

Manners, Melissa Taft. “Role of MeCP2 in Pain and its Regulation by miRNAs.” 2016. Web. 11 Apr 2021.

Vancouver:

Manners MT. Role of MeCP2 in Pain and its Regulation by miRNAs. [Internet] [Thesis]. Drexel University; 2016. [cited 2021 Apr 11]. Available from: http://hdl.handle.net/1860/idea:7156.

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

Council of Science Editors:

Manners MT. Role of MeCP2 in Pain and its Regulation by miRNAs. [Thesis]. Drexel University; 2016. Available from: http://hdl.handle.net/1860/idea:7156

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


Drexel University

3. Patra, Sayani. Development of RNAi-based genetic tools to silence MKP3 expression in a cell-specific manner.

Degree: 2016, Drexel University

Drug addiction is believed to occur, in part, as a result of maladaptive changes in dopaminergic pathways. The extracellular signal-regulated kinase 1/2 (ERK1/2) mitogen-activated protein… (more)

Subjects/Keywords: Biochemical Phenomena; Drug Design; Drug development

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APA (6th Edition):

Patra, S. (2016). Development of RNAi-based genetic tools to silence MKP3 expression in a cell-specific manner. (Thesis). Drexel University. Retrieved from http://hdl.handle.net/1860/idea:7168

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):

Patra, Sayani. “Development of RNAi-based genetic tools to silence MKP3 expression in a cell-specific manner.” 2016. Thesis, Drexel University. Accessed April 11, 2021. http://hdl.handle.net/1860/idea:7168.

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

MLA Handbook (7th Edition):

Patra, Sayani. “Development of RNAi-based genetic tools to silence MKP3 expression in a cell-specific manner.” 2016. Web. 11 Apr 2021.

Vancouver:

Patra S. Development of RNAi-based genetic tools to silence MKP3 expression in a cell-specific manner. [Internet] [Thesis]. Drexel University; 2016. [cited 2021 Apr 11]. Available from: http://hdl.handle.net/1860/idea:7168.

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

Council of Science Editors:

Patra S. Development of RNAi-based genetic tools to silence MKP3 expression in a cell-specific manner. [Thesis]. Drexel University; 2016. Available from: http://hdl.handle.net/1860/idea:7168

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


Drexel University

4. Leo, Lanfranco. Microtubule-severing proteins and their role in the development and degeneration of the central nervous system.

Degree: 2016, Drexel University

Neuronal cells are among the most morphologically elaborate cells in the human body. The creation, maintenance and modification of such high complexity are dependent on… (more)

Subjects/Keywords: Neurosciences; Neurobiology; Neurophysiology

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APA (6th Edition):

Leo, L. (2016). Microtubule-severing proteins and their role in the development and degeneration of the central nervous system. (Thesis). Drexel University. Retrieved from http://hdl.handle.net/1860/idea:7174

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):

Leo, Lanfranco. “Microtubule-severing proteins and their role in the development and degeneration of the central nervous system.” 2016. Thesis, Drexel University. Accessed April 11, 2021. http://hdl.handle.net/1860/idea:7174.

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

MLA Handbook (7th Edition):

Leo, Lanfranco. “Microtubule-severing proteins and their role in the development and degeneration of the central nervous system.” 2016. Web. 11 Apr 2021.

Vancouver:

Leo L. Microtubule-severing proteins and their role in the development and degeneration of the central nervous system. [Internet] [Thesis]. Drexel University; 2016. [cited 2021 Apr 11]. Available from: http://hdl.handle.net/1860/idea:7174.

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

Council of Science Editors:

Leo L. Microtubule-severing proteins and their role in the development and degeneration of the central nervous system. [Thesis]. Drexel University; 2016. Available from: http://hdl.handle.net/1860/idea:7174

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


Drexel University

5. Shahriari, Kristina S. Interleukin-1[beta] drives prostate cancer cell cooperation in the bone metastatic niche.

Degree: 2016, Drexel University

Advanced prostate cancer frequently leads to bone metastasis, a major cause of morbidity and mortality. In this study, we reveal a novel phenomenon in which… (more)

Subjects/Keywords: Pharmacology; Physiology; Pharmacological and Toxicological Phenomena and Processes; Physiological Phemonena

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

APA (6th Edition):

Shahriari, K. S. (2016). Interleukin-1[beta] drives prostate cancer cell cooperation in the bone metastatic niche. (Thesis). Drexel University. Retrieved from http://hdl.handle.net/1860/idea:7175

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):

Shahriari, Kristina S. “Interleukin-1[beta] drives prostate cancer cell cooperation in the bone metastatic niche.” 2016. Thesis, Drexel University. Accessed April 11, 2021. http://hdl.handle.net/1860/idea:7175.

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

MLA Handbook (7th Edition):

Shahriari, Kristina S. “Interleukin-1[beta] drives prostate cancer cell cooperation in the bone metastatic niche.” 2016. Web. 11 Apr 2021.

Vancouver:

Shahriari KS. Interleukin-1[beta] drives prostate cancer cell cooperation in the bone metastatic niche. [Internet] [Thesis]. Drexel University; 2016. [cited 2021 Apr 11]. Available from: http://hdl.handle.net/1860/idea:7175.

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

Council of Science Editors:

Shahriari KS. Interleukin-1[beta] drives prostate cancer cell cooperation in the bone metastatic niche. [Thesis]. Drexel University; 2016. Available from: http://hdl.handle.net/1860/idea:7175

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


Drexel University

6. Tuyishime, Marina. Investigation into the mechanism of a novel HIV-1 fusion inhibitor, SC12.

Degree: 2016, Drexel University

Due to the emergence of drug-resistant viruses and problems with drug side effects, new drugs and drug targets are constantly required in the battle against… (more)

Subjects/Keywords: Molecular biology; Cytology; Genetics; Biochemical Phenomena; Genetic Phenomena; Genetic Processes

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

APA (6th Edition):

Tuyishime, M. (2016). Investigation into the mechanism of a novel HIV-1 fusion inhibitor, SC12. (Thesis). Drexel University. Retrieved from http://hdl.handle.net/1860/idea:7177

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):

Tuyishime, Marina. “Investigation into the mechanism of a novel HIV-1 fusion inhibitor, SC12.” 2016. Thesis, Drexel University. Accessed April 11, 2021. http://hdl.handle.net/1860/idea:7177.

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

MLA Handbook (7th Edition):

Tuyishime, Marina. “Investigation into the mechanism of a novel HIV-1 fusion inhibitor, SC12.” 2016. Web. 11 Apr 2021.

Vancouver:

Tuyishime M. Investigation into the mechanism of a novel HIV-1 fusion inhibitor, SC12. [Internet] [Thesis]. Drexel University; 2016. [cited 2021 Apr 11]. Available from: http://hdl.handle.net/1860/idea:7177.

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

Council of Science Editors:

Tuyishime M. Investigation into the mechanism of a novel HIV-1 fusion inhibitor, SC12. [Thesis]. Drexel University; 2016. Available from: http://hdl.handle.net/1860/idea:7177

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


Drexel University

7. Donegan, William Edward. Targeting the DNA Damage Response for the Treatment of Oral Mucosal HSV-1 Infection.

Degree: 2016, Drexel University

Herpes simplex virus type 1 (HSV-1) is a highly prevalent pathogen that infects 67% of the world’s population. HSV-1 most commonly infects the oral mucosal… (more)

Subjects/Keywords: Molecular biology; Cytology; Genetics

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APA (6th Edition):

Donegan, W. E. (2016). Targeting the DNA Damage Response for the Treatment of Oral Mucosal HSV-1 Infection. (Thesis). Drexel University. Retrieved from http://hdl.handle.net/1860/idea:7171

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):

Donegan, William Edward. “Targeting the DNA Damage Response for the Treatment of Oral Mucosal HSV-1 Infection.” 2016. Thesis, Drexel University. Accessed April 11, 2021. http://hdl.handle.net/1860/idea:7171.

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

MLA Handbook (7th Edition):

Donegan, William Edward. “Targeting the DNA Damage Response for the Treatment of Oral Mucosal HSV-1 Infection.” 2016. Web. 11 Apr 2021.

Vancouver:

Donegan WE. Targeting the DNA Damage Response for the Treatment of Oral Mucosal HSV-1 Infection. [Internet] [Thesis]. Drexel University; 2016. [cited 2021 Apr 11]. Available from: http://hdl.handle.net/1860/idea:7171.

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

Council of Science Editors:

Donegan WE. Targeting the DNA Damage Response for the Treatment of Oral Mucosal HSV-1 Infection. [Thesis]. Drexel University; 2016. Available from: http://hdl.handle.net/1860/idea:7171

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


Drexel University

8. Feng, Yayi. Targeting Aurora A kinase (AURKA) and p21-activated kinase 1 (PAK1) in hormone receptor-positive breast cancer.

Degree: 2016, Drexel University

Estrogen receptor [alpha] (ER[alpha]) is a hormone-dependent nuclear and cytoplasmic receptor that regulates many physiological processes, such as reproduction, bone integrity, cardiovascular health, cognition, and… (more)

Subjects/Keywords: Cancer biology; Biology; Cancer; Biochemical Phenomena; Neoplasms

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APA (6th Edition):

Feng, Y. (2016). Targeting Aurora A kinase (AURKA) and p21-activated kinase 1 (PAK1) in hormone receptor-positive breast cancer. (Thesis). Drexel University. Retrieved from http://hdl.handle.net/1860/idea:7173

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):

Feng, Yayi. “Targeting Aurora A kinase (AURKA) and p21-activated kinase 1 (PAK1) in hormone receptor-positive breast cancer.” 2016. Thesis, Drexel University. Accessed April 11, 2021. http://hdl.handle.net/1860/idea:7173.

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

MLA Handbook (7th Edition):

Feng, Yayi. “Targeting Aurora A kinase (AURKA) and p21-activated kinase 1 (PAK1) in hormone receptor-positive breast cancer.” 2016. Web. 11 Apr 2021.

Vancouver:

Feng Y. Targeting Aurora A kinase (AURKA) and p21-activated kinase 1 (PAK1) in hormone receptor-positive breast cancer. [Internet] [Thesis]. Drexel University; 2016. [cited 2021 Apr 11]. Available from: http://hdl.handle.net/1860/idea:7173.

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

Council of Science Editors:

Feng Y. Targeting Aurora A kinase (AURKA) and p21-activated kinase 1 (PAK1) in hormone receptor-positive breast cancer. [Thesis]. Drexel University; 2016. Available from: http://hdl.handle.net/1860/idea:7173

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


Drexel University

9. Sodi, Valerie. Regulation of O-GlcNAc Transferase in breast cancer and its role in regulating lipid metabolism.

Degree: 2016, Drexel University

Cancer cells exhibit altered metabolism characterized by increased glucose and glutamine uptake. Altered utilization of these substrates directly contributes to O-linked-[beta]-N-acetylglucosamine (O-GlcNAc) modifications on intracellular… (more)

Subjects/Keywords: Molecular biology; Cytology; Genetics; Biochemical Phenomena; Genetic Phenomena; Genetic Processes

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

APA (6th Edition):

Sodi, V. (2016). Regulation of O-GlcNAc Transferase in breast cancer and its role in regulating lipid metabolism. (Thesis). Drexel University. Retrieved from http://hdl.handle.net/1860/idea:7176

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):

Sodi, Valerie. “Regulation of O-GlcNAc Transferase in breast cancer and its role in regulating lipid metabolism.” 2016. Thesis, Drexel University. Accessed April 11, 2021. http://hdl.handle.net/1860/idea:7176.

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

MLA Handbook (7th Edition):

Sodi, Valerie. “Regulation of O-GlcNAc Transferase in breast cancer and its role in regulating lipid metabolism.” 2016. Web. 11 Apr 2021.

Vancouver:

Sodi V. Regulation of O-GlcNAc Transferase in breast cancer and its role in regulating lipid metabolism. [Internet] [Thesis]. Drexel University; 2016. [cited 2021 Apr 11]. Available from: http://hdl.handle.net/1860/idea:7176.

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

Council of Science Editors:

Sodi V. Regulation of O-GlcNAc Transferase in breast cancer and its role in regulating lipid metabolism. [Thesis]. Drexel University; 2016. Available from: http://hdl.handle.net/1860/idea:7176

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


Drexel University

10. Sowash Molinari, Aislinn Rebecca. Transcription Factor Specificity Protein 1 (Sp1) Regulates the Centrochromatin Landscape and Centromeric Transcription During Mitosis.

Degree: 2016, Drexel University

Chromosomal instability (CIN) is a dynamic and continual gain or loss of whole chromosomes, or parts of chromosomes, during cell division. It is associated with… (more)

Subjects/Keywords: Molecular biology; Cytology; Genetics; Biochemical Phenomena; Genetic Phenomena; Genetic Processes

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

APA (6th Edition):

Sowash Molinari, A. R. (2016). Transcription Factor Specificity Protein 1 (Sp1) Regulates the Centrochromatin Landscape and Centromeric Transcription During Mitosis. (Thesis). Drexel University. Retrieved from http://hdl.handle.net/1860/idea:7146

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):

Sowash Molinari, Aislinn Rebecca. “Transcription Factor Specificity Protein 1 (Sp1) Regulates the Centrochromatin Landscape and Centromeric Transcription During Mitosis.” 2016. Thesis, Drexel University. Accessed April 11, 2021. http://hdl.handle.net/1860/idea:7146.

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

MLA Handbook (7th Edition):

Sowash Molinari, Aislinn Rebecca. “Transcription Factor Specificity Protein 1 (Sp1) Regulates the Centrochromatin Landscape and Centromeric Transcription During Mitosis.” 2016. Web. 11 Apr 2021.

Vancouver:

Sowash Molinari AR. Transcription Factor Specificity Protein 1 (Sp1) Regulates the Centrochromatin Landscape and Centromeric Transcription During Mitosis. [Internet] [Thesis]. Drexel University; 2016. [cited 2021 Apr 11]. Available from: http://hdl.handle.net/1860/idea:7146.

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

Council of Science Editors:

Sowash Molinari AR. Transcription Factor Specificity Protein 1 (Sp1) Regulates the Centrochromatin Landscape and Centromeric Transcription During Mitosis. [Thesis]. Drexel University; 2016. Available from: http://hdl.handle.net/1860/idea:7146

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


Drexel University

11. Eckert, Selina. Emotional and somatic disturbances following mild traumatic brain injury.

Degree: 2015, Drexel University

Two of the most common symptoms following mild traumatic brain injury (mTBI) are post-traumatic headache (PTH) and depression, yet these symptoms are understudied in preclinical… (more)

Subjects/Keywords: Neurobiology; Neurosciences; Nervous System Physiological Phenomena

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APA (6th Edition):

Eckert, S. (2015). Emotional and somatic disturbances following mild traumatic brain injury. (Thesis). Drexel University. Retrieved from http://hdl.handle.net/1860/idea:7163

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):

Eckert, Selina. “Emotional and somatic disturbances following mild traumatic brain injury.” 2015. Thesis, Drexel University. Accessed April 11, 2021. http://hdl.handle.net/1860/idea:7163.

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

MLA Handbook (7th Edition):

Eckert, Selina. “Emotional and somatic disturbances following mild traumatic brain injury.” 2015. Web. 11 Apr 2021.

Vancouver:

Eckert S. Emotional and somatic disturbances following mild traumatic brain injury. [Internet] [Thesis]. Drexel University; 2015. [cited 2021 Apr 11]. Available from: http://hdl.handle.net/1860/idea:7163.

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

Council of Science Editors:

Eckert S. Emotional and somatic disturbances following mild traumatic brain injury. [Thesis]. Drexel University; 2015. Available from: http://hdl.handle.net/1860/idea:7163

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


Drexel University

12. Rollins, Dustin. Netrin-G1 Enhances in Desmoplastic Fibroblasts Enhances Interactions with Pancreatic Cancer Cells.

Degree: 2016, Drexel University

Pancreatic Ductal Adenocarcinoma (PDAC) is amongst the most lethal forms of cancer encountered in patients. One of the defining characteristics of this neoplasia is a… (more)

Subjects/Keywords: Cancer biology; Cancer; Biochemical Phenomena; Neoplasms; Biology

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APA (6th Edition):

Rollins, D. (2016). Netrin-G1 Enhances in Desmoplastic Fibroblasts Enhances Interactions with Pancreatic Cancer Cells. (Thesis). Drexel University. Retrieved from http://hdl.handle.net/1860/idea:7164

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):

Rollins, Dustin. “Netrin-G1 Enhances in Desmoplastic Fibroblasts Enhances Interactions with Pancreatic Cancer Cells.” 2016. Thesis, Drexel University. Accessed April 11, 2021. http://hdl.handle.net/1860/idea:7164.

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

MLA Handbook (7th Edition):

Rollins, Dustin. “Netrin-G1 Enhances in Desmoplastic Fibroblasts Enhances Interactions with Pancreatic Cancer Cells.” 2016. Web. 11 Apr 2021.

Vancouver:

Rollins D. Netrin-G1 Enhances in Desmoplastic Fibroblasts Enhances Interactions with Pancreatic Cancer Cells. [Internet] [Thesis]. Drexel University; 2016. [cited 2021 Apr 11]. Available from: http://hdl.handle.net/1860/idea:7164.

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

Council of Science Editors:

Rollins D. Netrin-G1 Enhances in Desmoplastic Fibroblasts Enhances Interactions with Pancreatic Cancer Cells. [Thesis]. Drexel University; 2016. Available from: http://hdl.handle.net/1860/idea:7164

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


Drexel University

13. Falcucci, Romulo Martelli. Neuroprotective properties of novel positive allosteric modulators of EAAT2.

Degree: 2016, Drexel University

Excitatory amino acid transporters (EAATs) play a crucial role in the removal of synaptic glutamate to maintain extracellular concentrations below excitotoxic levels. Glutamate-mediated excitotoxicity has… (more)

Subjects/Keywords: Drug Design; Drug development; Biochemical Phenomena

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APA (6th Edition):

Falcucci, R. M. (2016). Neuroprotective properties of novel positive allosteric modulators of EAAT2. (Thesis). Drexel University. Retrieved from http://hdl.handle.net/1860/idea:7166

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):

Falcucci, Romulo Martelli. “Neuroprotective properties of novel positive allosteric modulators of EAAT2.” 2016. Thesis, Drexel University. Accessed April 11, 2021. http://hdl.handle.net/1860/idea:7166.

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

MLA Handbook (7th Edition):

Falcucci, Romulo Martelli. “Neuroprotective properties of novel positive allosteric modulators of EAAT2.” 2016. Web. 11 Apr 2021.

Vancouver:

Falcucci RM. Neuroprotective properties of novel positive allosteric modulators of EAAT2. [Internet] [Thesis]. Drexel University; 2016. [cited 2021 Apr 11]. Available from: http://hdl.handle.net/1860/idea:7166.

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

Council of Science Editors:

Falcucci RM. Neuroprotective properties of novel positive allosteric modulators of EAAT2. [Thesis]. Drexel University; 2016. Available from: http://hdl.handle.net/1860/idea:7166

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


Drexel University

14. Pershing, April M. Genetic exploration of the ATP synthase complex in Plasmodium falciparum.

Degree: 2016, Drexel University

During the blood stages of its life cycle, P. falciparum relies on glycolysis as its major source of ATP rather than oxidative phosphorylation. Yet, we… (more)

Subjects/Keywords: Molecular biology; Cytology; Genetics; Biochemical Phenomena; Genetic Phenomena; Genetic Processes

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APA (6th Edition):

Pershing, A. M. (2016). Genetic exploration of the ATP synthase complex in Plasmodium falciparum. (Thesis). Drexel University. Retrieved from http://hdl.handle.net/1860/idea:7148

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):

Pershing, April M. “Genetic exploration of the ATP synthase complex in Plasmodium falciparum.” 2016. Thesis, Drexel University. Accessed April 11, 2021. http://hdl.handle.net/1860/idea:7148.

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

MLA Handbook (7th Edition):

Pershing, April M. “Genetic exploration of the ATP synthase complex in Plasmodium falciparum.” 2016. Web. 11 Apr 2021.

Vancouver:

Pershing AM. Genetic exploration of the ATP synthase complex in Plasmodium falciparum. [Internet] [Thesis]. Drexel University; 2016. [cited 2021 Apr 11]. Available from: http://hdl.handle.net/1860/idea:7148.

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

Council of Science Editors:

Pershing AM. Genetic exploration of the ATP synthase complex in Plasmodium falciparum. [Thesis]. Drexel University; 2016. Available from: http://hdl.handle.net/1860/idea:7148

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


Drexel University

15. Lamontagne, Richard Jason. Global analysis of HBV-mediated changes to the primary hepatocyte transcriptome and metabolome.

Degree: 2015, Drexel University

Chronic infection with hepatitis B virus (HBV) remains a significant health concern, with between 350-500 million people chronically infected worldwide. Approximately 25% of chronically infected… (more)

Subjects/Keywords: Microbiology; Immunology; Allergy and Immunology

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APA (6th Edition):

Lamontagne, R. J. (2015). Global analysis of HBV-mediated changes to the primary hepatocyte transcriptome and metabolome. (Thesis). Drexel University. Retrieved from http://hdl.handle.net/1860/idea:7152

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):

Lamontagne, Richard Jason. “Global analysis of HBV-mediated changes to the primary hepatocyte transcriptome and metabolome.” 2015. Thesis, Drexel University. Accessed April 11, 2021. http://hdl.handle.net/1860/idea:7152.

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

MLA Handbook (7th Edition):

Lamontagne, Richard Jason. “Global analysis of HBV-mediated changes to the primary hepatocyte transcriptome and metabolome.” 2015. Web. 11 Apr 2021.

Vancouver:

Lamontagne RJ. Global analysis of HBV-mediated changes to the primary hepatocyte transcriptome and metabolome. [Internet] [Thesis]. Drexel University; 2015. [cited 2021 Apr 11]. Available from: http://hdl.handle.net/1860/idea:7152.

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

Council of Science Editors:

Lamontagne RJ. Global analysis of HBV-mediated changes to the primary hepatocyte transcriptome and metabolome. [Thesis]. Drexel University; 2015. Available from: http://hdl.handle.net/1860/idea:7152

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


Drexel University

16. Chen, Nan. Small Molecule Sigma1 Modulators Induce the Degradation of Androgen Receptor and Splice Variants in Castration Resistant Prostate Cancer Cells.

Degree: 2015, Drexel University

Androgen receptor (AR) signaling is the primary driver for prostate cancer progression. Androgen deprivation therapy (ADT) although initially effective, will eventually fail with the development… (more)

Subjects/Keywords: Drug development; Drug Design; Biochemical Phenomena

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APA (6th Edition):

Chen, N. (2015). Small Molecule Sigma1 Modulators Induce the Degradation of Androgen Receptor and Splice Variants in Castration Resistant Prostate Cancer Cells. (Thesis). Drexel University. Retrieved from http://hdl.handle.net/1860/idea:7165

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):

Chen, Nan. “Small Molecule Sigma1 Modulators Induce the Degradation of Androgen Receptor and Splice Variants in Castration Resistant Prostate Cancer Cells.” 2015. Thesis, Drexel University. Accessed April 11, 2021. http://hdl.handle.net/1860/idea:7165.

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

MLA Handbook (7th Edition):

Chen, Nan. “Small Molecule Sigma1 Modulators Induce the Degradation of Androgen Receptor and Splice Variants in Castration Resistant Prostate Cancer Cells.” 2015. Web. 11 Apr 2021.

Vancouver:

Chen N. Small Molecule Sigma1 Modulators Induce the Degradation of Androgen Receptor and Splice Variants in Castration Resistant Prostate Cancer Cells. [Internet] [Thesis]. Drexel University; 2015. [cited 2021 Apr 11]. Available from: http://hdl.handle.net/1860/idea:7165.

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

Council of Science Editors:

Chen N. Small Molecule Sigma1 Modulators Induce the Degradation of Androgen Receptor and Splice Variants in Castration Resistant Prostate Cancer Cells. [Thesis]. Drexel University; 2015. Available from: http://hdl.handle.net/1860/idea:7165

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


Drexel University

17. Karnay, Ashley M. Hippocampal Neuron Stimulation Promotes Intracellular Tip60 Dynamics with Concomitant Genome Reorganization and Synaptic Gene Activation.

Degree: 2018, Drexel University

Coordinated gene transcription within mammalian nuclei in response to external stimuli is a highly orchestrated process involving the interplay between epigenetics-mediated chromatin remodeling and RNA… (more)

Subjects/Keywords: Neurosciences

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APA (6th Edition):

Karnay, A. M. (2018). Hippocampal Neuron Stimulation Promotes Intracellular Tip60 Dynamics with Concomitant Genome Reorganization and Synaptic Gene Activation. (Thesis). Drexel University. Retrieved from https://idea.library.drexel.edu/islandora/object/idea%3A7962

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):

Karnay, Ashley M. “Hippocampal Neuron Stimulation Promotes Intracellular Tip60 Dynamics with Concomitant Genome Reorganization and Synaptic Gene Activation.” 2018. Thesis, Drexel University. Accessed April 11, 2021. https://idea.library.drexel.edu/islandora/object/idea%3A7962.

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

MLA Handbook (7th Edition):

Karnay, Ashley M. “Hippocampal Neuron Stimulation Promotes Intracellular Tip60 Dynamics with Concomitant Genome Reorganization and Synaptic Gene Activation.” 2018. Web. 11 Apr 2021.

Vancouver:

Karnay AM. Hippocampal Neuron Stimulation Promotes Intracellular Tip60 Dynamics with Concomitant Genome Reorganization and Synaptic Gene Activation. [Internet] [Thesis]. Drexel University; 2018. [cited 2021 Apr 11]. Available from: https://idea.library.drexel.edu/islandora/object/idea%3A7962.

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

Council of Science Editors:

Karnay AM. Hippocampal Neuron Stimulation Promotes Intracellular Tip60 Dynamics with Concomitant Genome Reorganization and Synaptic Gene Activation. [Thesis]. Drexel University; 2018. Available from: https://idea.library.drexel.edu/islandora/object/idea%3A7962

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


Drexel University

18. Anthony, Sajitha. Characterization of polymers of nucleotide biosynthetic enzymes.

Degree: 2017, Drexel University

Mammalian cells contain various proteins that assemble into filamentous structures. Examples include cytoskeletal proteins such as actin and even metabolic enzymes like acetyl-CoA carboxylase. Within… (more)

Subjects/Keywords: Molecular biology; Cytology; Genetics

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APA (6th Edition):

Anthony, S. (2017). Characterization of polymers of nucleotide biosynthetic enzymes. (Thesis). Drexel University. Retrieved from http://hdl.handle.net/1860/idea:7519

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):

Anthony, Sajitha. “Characterization of polymers of nucleotide biosynthetic enzymes.” 2017. Thesis, Drexel University. Accessed April 11, 2021. http://hdl.handle.net/1860/idea:7519.

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

MLA Handbook (7th Edition):

Anthony, Sajitha. “Characterization of polymers of nucleotide biosynthetic enzymes.” 2017. Web. 11 Apr 2021.

Vancouver:

Anthony S. Characterization of polymers of nucleotide biosynthetic enzymes. [Internet] [Thesis]. Drexel University; 2017. [cited 2021 Apr 11]. Available from: http://hdl.handle.net/1860/idea:7519.

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

Council of Science Editors:

Anthony S. Characterization of polymers of nucleotide biosynthetic enzymes. [Thesis]. Drexel University; 2017. Available from: http://hdl.handle.net/1860/idea:7519

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


Drexel University

19. Gulchina, Yelena. NMDA receptor dysfunction in the developing prefrontal cortex in two animal models for schizophrenia: expression profile, epigenetic mechanisms, and physiology.

Degree: 2017, Drexel University

Schizophrenia is a highly debilitating illness often diagnosed in late adolescence and early adulthood following the emergence of psychotic symptoms. In addition to psychosis, negative… (more)

Subjects/Keywords: Neurosciences

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APA (6th Edition):

Gulchina, Y. (2017). NMDA receptor dysfunction in the developing prefrontal cortex in two animal models for schizophrenia: expression profile, epigenetic mechanisms, and physiology. (Thesis). Drexel University. Retrieved from http://hdl.handle.net/1860/idea:7524

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):

Gulchina, Yelena. “NMDA receptor dysfunction in the developing prefrontal cortex in two animal models for schizophrenia: expression profile, epigenetic mechanisms, and physiology.” 2017. Thesis, Drexel University. Accessed April 11, 2021. http://hdl.handle.net/1860/idea:7524.

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

MLA Handbook (7th Edition):

Gulchina, Yelena. “NMDA receptor dysfunction in the developing prefrontal cortex in two animal models for schizophrenia: expression profile, epigenetic mechanisms, and physiology.” 2017. Web. 11 Apr 2021.

Vancouver:

Gulchina Y. NMDA receptor dysfunction in the developing prefrontal cortex in two animal models for schizophrenia: expression profile, epigenetic mechanisms, and physiology. [Internet] [Thesis]. Drexel University; 2017. [cited 2021 Apr 11]. Available from: http://hdl.handle.net/1860/idea:7524.

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

Council of Science Editors:

Gulchina Y. NMDA receptor dysfunction in the developing prefrontal cortex in two animal models for schizophrenia: expression profile, epigenetic mechanisms, and physiology. [Thesis]. Drexel University; 2017. Available from: http://hdl.handle.net/1860/idea:7524

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


Drexel University

20. Ramamurthi, Arjun. Plasmid DNA as a platform for the development of prophylactic and therapeutic vaccines against Clostridium difficile in aging models of disease.

Degree: 2017, Drexel University

 Clostridium difficile associated disease (CDAD) is a gastrointestinal disease whose symptoms range from mild diarrhea to pseudomembranous colitis and toxic megacolon. Statistically, it is among… (more)

Subjects/Keywords: Microbiology

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APA (6th Edition):

Ramamurthi, A. (2017). Plasmid DNA as a platform for the development of prophylactic and therapeutic vaccines against Clostridium difficile in aging models of disease. (Thesis). Drexel University. Retrieved from http://hdl.handle.net/1860/idea:7521

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):

Ramamurthi, Arjun. “Plasmid DNA as a platform for the development of prophylactic and therapeutic vaccines against Clostridium difficile in aging models of disease.” 2017. Thesis, Drexel University. Accessed April 11, 2021. http://hdl.handle.net/1860/idea:7521.

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

MLA Handbook (7th Edition):

Ramamurthi, Arjun. “Plasmid DNA as a platform for the development of prophylactic and therapeutic vaccines against Clostridium difficile in aging models of disease.” 2017. Web. 11 Apr 2021.

Vancouver:

Ramamurthi A. Plasmid DNA as a platform for the development of prophylactic and therapeutic vaccines against Clostridium difficile in aging models of disease. [Internet] [Thesis]. Drexel University; 2017. [cited 2021 Apr 11]. Available from: http://hdl.handle.net/1860/idea:7521.

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

Council of Science Editors:

Ramamurthi A. Plasmid DNA as a platform for the development of prophylactic and therapeutic vaccines against Clostridium difficile in aging models of disease. [Thesis]. Drexel University; 2017. Available from: http://hdl.handle.net/1860/idea:7521

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


Drexel University

21. Goyal, Nadish. Role of N-terminal domain of RAD54 in Branch Migration of Holliday Junctions.

Degree: 2017, Drexel University

Homologous recombination plays an important role in repairing the most harmful types of DNA damage, including DNA double-strand breaks and interstrand cross-links, in promoting faithful… (more)

Subjects/Keywords: Biochemistry

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APA (6th Edition):

Goyal, N. (2017). Role of N-terminal domain of RAD54 in Branch Migration of Holliday Junctions. (Thesis). Drexel University. Retrieved from http://hdl.handle.net/1860/idea:7520

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):

Goyal, Nadish. “Role of N-terminal domain of RAD54 in Branch Migration of Holliday Junctions.” 2017. Thesis, Drexel University. Accessed April 11, 2021. http://hdl.handle.net/1860/idea:7520.

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

MLA Handbook (7th Edition):

Goyal, Nadish. “Role of N-terminal domain of RAD54 in Branch Migration of Holliday Junctions.” 2017. Web. 11 Apr 2021.

Vancouver:

Goyal N. Role of N-terminal domain of RAD54 in Branch Migration of Holliday Junctions. [Internet] [Thesis]. Drexel University; 2017. [cited 2021 Apr 11]. Available from: http://hdl.handle.net/1860/idea:7520.

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

Council of Science Editors:

Goyal N. Role of N-terminal domain of RAD54 in Branch Migration of Holliday Junctions. [Thesis]. Drexel University; 2017. Available from: http://hdl.handle.net/1860/idea:7520

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


Drexel University

22. Theriault, Amber. Investigating the Role of Timeless in Acetaldehyde-Mediated DNA Damage Response and Repair.

Degree: 2017, Drexel University

Esophageal squamous cell carcinoma (ESCC) is highly associated with chronic alcohol consumption. Acetaldehyde, the intermediate metabolite in alcohol metabolism, is considered to be a carcinogenic… (more)

Subjects/Keywords: Biochemistry

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APA (6th Edition):

Theriault, A. (2017). Investigating the Role of Timeless in Acetaldehyde-Mediated DNA Damage Response and Repair. (Thesis). Drexel University. Retrieved from http://hdl.handle.net/1860/idea:7531

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):

Theriault, Amber. “Investigating the Role of Timeless in Acetaldehyde-Mediated DNA Damage Response and Repair.” 2017. Thesis, Drexel University. Accessed April 11, 2021. http://hdl.handle.net/1860/idea:7531.

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

MLA Handbook (7th Edition):

Theriault, Amber. “Investigating the Role of Timeless in Acetaldehyde-Mediated DNA Damage Response and Repair.” 2017. Web. 11 Apr 2021.

Vancouver:

Theriault A. Investigating the Role of Timeless in Acetaldehyde-Mediated DNA Damage Response and Repair. [Internet] [Thesis]. Drexel University; 2017. [cited 2021 Apr 11]. Available from: http://hdl.handle.net/1860/idea:7531.

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

Council of Science Editors:

Theriault A. Investigating the Role of Timeless in Acetaldehyde-Mediated DNA Damage Response and Repair. [Thesis]. Drexel University; 2017. Available from: http://hdl.handle.net/1860/idea:7531

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


Drexel University

23. Hanlon, Lauren A. Microglial reactivity and functional deficits following traumatic brain injury in the neonate rat.

Degree: 2017, Drexel University

Traumatic brain injury (TBI) is a leading cause of disability in young children as survivors face life-long physical and cognitive impairments. Inflammation, specifically microglia/macrophage activation,… (more)

Subjects/Keywords: Neurosciences

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APA (6th Edition):

Hanlon, L. A. (2017). Microglial reactivity and functional deficits following traumatic brain injury in the neonate rat. (Thesis). Drexel University. Retrieved from http://hdl.handle.net/1860/idea:7525

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):

Hanlon, Lauren A. “Microglial reactivity and functional deficits following traumatic brain injury in the neonate rat.” 2017. Thesis, Drexel University. Accessed April 11, 2021. http://hdl.handle.net/1860/idea:7525.

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

MLA Handbook (7th Edition):

Hanlon, Lauren A. “Microglial reactivity and functional deficits following traumatic brain injury in the neonate rat.” 2017. Web. 11 Apr 2021.

Vancouver:

Hanlon LA. Microglial reactivity and functional deficits following traumatic brain injury in the neonate rat. [Internet] [Thesis]. Drexel University; 2017. [cited 2021 Apr 11]. Available from: http://hdl.handle.net/1860/idea:7525.

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

Council of Science Editors:

Hanlon LA. Microglial reactivity and functional deficits following traumatic brain injury in the neonate rat. [Thesis]. Drexel University; 2017. Available from: http://hdl.handle.net/1860/idea:7525

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


Drexel University

24. Reesey, Emily. Characterization of the Mitochondrial DNA Polymerase in Plasmodium falciparum.

Degree: 2017, Drexel University

Several anti-malarials in clinical use and under development act on the mitochondrial electron transport chain (mtETC) of malaria parasites. The mtETC is an essential process… (more)

Subjects/Keywords: Microbiology

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APA (6th Edition):

Reesey, E. (2017). Characterization of the Mitochondrial DNA Polymerase in Plasmodium falciparum. (Thesis). Drexel University. Retrieved from http://hdl.handle.net/1860/idea:7529

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):

Reesey, Emily. “Characterization of the Mitochondrial DNA Polymerase in Plasmodium falciparum.” 2017. Thesis, Drexel University. Accessed April 11, 2021. http://hdl.handle.net/1860/idea:7529.

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

MLA Handbook (7th Edition):

Reesey, Emily. “Characterization of the Mitochondrial DNA Polymerase in Plasmodium falciparum.” 2017. Web. 11 Apr 2021.

Vancouver:

Reesey E. Characterization of the Mitochondrial DNA Polymerase in Plasmodium falciparum. [Internet] [Thesis]. Drexel University; 2017. [cited 2021 Apr 11]. Available from: http://hdl.handle.net/1860/idea:7529.

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

Council of Science Editors:

Reesey E. Characterization of the Mitochondrial DNA Polymerase in Plasmodium falciparum. [Thesis]. Drexel University; 2017. Available from: http://hdl.handle.net/1860/idea:7529

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


Drexel University

25. Shenoda, Botros. A Role for XIST in the Regulation of Inflammatory Response by Female Cells.

Degree: 2017, Drexel University

Biological sex influences inflammatory response [1]. There is a greater incidence of acute inflammation in men, and chronic inflammation in women. X-inactive specific transcript (XIST)… (more)

Subjects/Keywords: Pharmacology; Physiology; Inflammation

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APA (6th Edition):

Shenoda, B. (2017). A Role for XIST in the Regulation of Inflammatory Response by Female Cells. (Thesis). Drexel University. Retrieved from https://idea.library.drexel.edu/islandora/object/idea%3A9409

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):

Shenoda, Botros. “A Role for XIST in the Regulation of Inflammatory Response by Female Cells.” 2017. Thesis, Drexel University. Accessed April 11, 2021. https://idea.library.drexel.edu/islandora/object/idea%3A9409.

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

MLA Handbook (7th Edition):

Shenoda, Botros. “A Role for XIST in the Regulation of Inflammatory Response by Female Cells.” 2017. Web. 11 Apr 2021.

Vancouver:

Shenoda B. A Role for XIST in the Regulation of Inflammatory Response by Female Cells. [Internet] [Thesis]. Drexel University; 2017. [cited 2021 Apr 11]. Available from: https://idea.library.drexel.edu/islandora/object/idea%3A9409.

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

Council of Science Editors:

Shenoda B. A Role for XIST in the Regulation of Inflammatory Response by Female Cells. [Thesis]. Drexel University; 2017. Available from: https://idea.library.drexel.edu/islandora/object/idea%3A9409

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


Drexel University

26. Mironets, Eugene. sTNF[alpha] Signaling Mediates Autonomic Reflex Circuits Implicated in Cardiovascular and Immune Dysfunction After Spinal Cord Injury.

Degree: 2019, Drexel University

 The sympathetic nervous system is a critical regulator of cardiovascular and immune function. Sympathetic preganglionic neurons (SPN) reside in thoracolumbar cord and project peripherally to… (more)

Subjects/Keywords: Neurosciences; Immunology; Autonomic nervous system; Spinal cord – Wounds and injuries

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APA (6th Edition):

Mironets, E. (2019). sTNF[alpha] Signaling Mediates Autonomic Reflex Circuits Implicated in Cardiovascular and Immune Dysfunction After Spinal Cord Injury. (Thesis). Drexel University. Retrieved from https://idea.library.drexel.edu/islandora/object/idea%3A9432

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):

Mironets, Eugene. “sTNF[alpha] Signaling Mediates Autonomic Reflex Circuits Implicated in Cardiovascular and Immune Dysfunction After Spinal Cord Injury.” 2019. Thesis, Drexel University. Accessed April 11, 2021. https://idea.library.drexel.edu/islandora/object/idea%3A9432.

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

MLA Handbook (7th Edition):

Mironets, Eugene. “sTNF[alpha] Signaling Mediates Autonomic Reflex Circuits Implicated in Cardiovascular and Immune Dysfunction After Spinal Cord Injury.” 2019. Web. 11 Apr 2021.

Vancouver:

Mironets E. sTNF[alpha] Signaling Mediates Autonomic Reflex Circuits Implicated in Cardiovascular and Immune Dysfunction After Spinal Cord Injury. [Internet] [Thesis]. Drexel University; 2019. [cited 2021 Apr 11]. Available from: https://idea.library.drexel.edu/islandora/object/idea%3A9432.

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

Council of Science Editors:

Mironets E. sTNF[alpha] Signaling Mediates Autonomic Reflex Circuits Implicated in Cardiovascular and Immune Dysfunction After Spinal Cord Injury. [Thesis]. Drexel University; 2019. Available from: https://idea.library.drexel.edu/islandora/object/idea%3A9432

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


Drexel University

27. Jean-Toussaint, Renee. Exosome Mediated Neuro-immune Communication in Chronic Pain.

Degree: 2019, Drexel University

 Chronic pain, both inflammatory and neuropathic, is extremely difficult to treat. There is a need for investigating novel mechanisms underlying pain to identify new therapeutic… (more)

Subjects/Keywords: Pharmacology; Physiology; Neurosciences; Inflammation; MicroRNA; Chronic pain

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APA (6th Edition):

Jean-Toussaint, R. (2019). Exosome Mediated Neuro-immune Communication in Chronic Pain. (Thesis). Drexel University. Retrieved from https://idea.library.drexel.edu/islandora/object/idea%3A9434

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):

Jean-Toussaint, Renee. “Exosome Mediated Neuro-immune Communication in Chronic Pain.” 2019. Thesis, Drexel University. Accessed April 11, 2021. https://idea.library.drexel.edu/islandora/object/idea%3A9434.

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

MLA Handbook (7th Edition):

Jean-Toussaint, Renee. “Exosome Mediated Neuro-immune Communication in Chronic Pain.” 2019. Web. 11 Apr 2021.

Vancouver:

Jean-Toussaint R. Exosome Mediated Neuro-immune Communication in Chronic Pain. [Internet] [Thesis]. Drexel University; 2019. [cited 2021 Apr 11]. Available from: https://idea.library.drexel.edu/islandora/object/idea%3A9434.

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

Council of Science Editors:

Jean-Toussaint R. Exosome Mediated Neuro-immune Communication in Chronic Pain. [Thesis]. Drexel University; 2019. Available from: https://idea.library.drexel.edu/islandora/object/idea%3A9434

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


Drexel University

28. Stachowski, Nicholas James. The Role of Spino-Parabrachial Neurons in post-SCI Affective Pain.

Degree: 2018, Drexel University

Neuropathic pain develops in over 80% of spinal cord injury (SCI) patients. Negative affective disorders, such as anxiety and depression, are highly comorbid with neuropathic… (more)

Subjects/Keywords: Neurosciences; Spinal cord – Wounds and injuries; Pain; Pain – Physiological aspects

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

APA (6th Edition):

Stachowski, N. J. (2018). The Role of Spino-Parabrachial Neurons in post-SCI Affective Pain. (Thesis). Drexel University. Retrieved from https://idea.library.drexel.edu/islandora/object/idea%3A8156

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):

Stachowski, Nicholas James. “The Role of Spino-Parabrachial Neurons in post-SCI Affective Pain.” 2018. Thesis, Drexel University. Accessed April 11, 2021. https://idea.library.drexel.edu/islandora/object/idea%3A8156.

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

MLA Handbook (7th Edition):

Stachowski, Nicholas James. “The Role of Spino-Parabrachial Neurons in post-SCI Affective Pain.” 2018. Web. 11 Apr 2021.

Vancouver:

Stachowski NJ. The Role of Spino-Parabrachial Neurons in post-SCI Affective Pain. [Internet] [Thesis]. Drexel University; 2018. [cited 2021 Apr 11]. Available from: https://idea.library.drexel.edu/islandora/object/idea%3A8156.

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

Council of Science Editors:

Stachowski NJ. The Role of Spino-Parabrachial Neurons in post-SCI Affective Pain. [Thesis]. Drexel University; 2018. Available from: https://idea.library.drexel.edu/islandora/object/idea%3A8156

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


Drexel University

29. Mukhopadhyay, Dimpi. Role of Spastin in regulating glioblastoma cell survival.

Degree: 2017, Drexel University

Glioblastomas are the most aggressive form of brain tumors and the most abundant malignant glioma among adults. These are notoriously aggressive cancers with the median… (more)

Subjects/Keywords: Cytology; Oncology; Glioblastoma multiforme; Microtubules

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

APA (6th Edition):

Mukhopadhyay, D. (2017). Role of Spastin in regulating glioblastoma cell survival. (Thesis). Drexel University. Retrieved from http://hdl.handle.net/1860/idea:7749

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):

Mukhopadhyay, Dimpi. “Role of Spastin in regulating glioblastoma cell survival.” 2017. Thesis, Drexel University. Accessed April 11, 2021. http://hdl.handle.net/1860/idea:7749.

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

MLA Handbook (7th Edition):

Mukhopadhyay, Dimpi. “Role of Spastin in regulating glioblastoma cell survival.” 2017. Web. 11 Apr 2021.

Vancouver:

Mukhopadhyay D. Role of Spastin in regulating glioblastoma cell survival. [Internet] [Thesis]. Drexel University; 2017. [cited 2021 Apr 11]. Available from: http://hdl.handle.net/1860/idea:7749.

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

Council of Science Editors:

Mukhopadhyay D. Role of Spastin in regulating glioblastoma cell survival. [Thesis]. Drexel University; 2017. Available from: http://hdl.handle.net/1860/idea:7749

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


Drexel University

30. Cornell, Brett Thomas. 14-3-3 Proteins in Neuronal Migration and Neuromorphogenesis during Cortical Development and Neurodevelopmental Disorders.

Degree: 2017, Drexel University

The development of the human brain is a vastly complex process resulting in an elaborate network of over one hundred billion neurons, with each neuron… (more)

Subjects/Keywords: Autism spectrum disorders; Williams syndrome

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

APA (6th Edition):

Cornell, B. T. (2017). 14-3-3 Proteins in Neuronal Migration and Neuromorphogenesis during Cortical Development and Neurodevelopmental Disorders. (Thesis). Drexel University. Retrieved from http://hdl.handle.net/1860/idea:7420

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):

Cornell, Brett Thomas. “14-3-3 Proteins in Neuronal Migration and Neuromorphogenesis during Cortical Development and Neurodevelopmental Disorders.” 2017. Thesis, Drexel University. Accessed April 11, 2021. http://hdl.handle.net/1860/idea:7420.

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

MLA Handbook (7th Edition):

Cornell, Brett Thomas. “14-3-3 Proteins in Neuronal Migration and Neuromorphogenesis during Cortical Development and Neurodevelopmental Disorders.” 2017. Web. 11 Apr 2021.

Vancouver:

Cornell BT. 14-3-3 Proteins in Neuronal Migration and Neuromorphogenesis during Cortical Development and Neurodevelopmental Disorders. [Internet] [Thesis]. Drexel University; 2017. [cited 2021 Apr 11]. Available from: http://hdl.handle.net/1860/idea:7420.

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

Council of Science Editors:

Cornell BT. 14-3-3 Proteins in Neuronal Migration and Neuromorphogenesis during Cortical Development and Neurodevelopmental Disorders. [Thesis]. Drexel University; 2017. Available from: http://hdl.handle.net/1860/idea:7420

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

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