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You searched for +publisher:"Temple University" +contributor:("Ramirez, Servio;"). Showing records 1 – 10 of 10 total matches.

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Temple University

1. Yuan, Ke. THE CHARACTERIZATION OF HSA-MIR148A IN HEPATOCARCINOGENESIS.

Degree: PhD, 2011, Temple University

Biology

Chronic Hepatitis B Virus (HBV) infection is a global health problem because of its connection to acute and chronic liver diseases as well as… (more)

Subjects/Keywords: Virology; Biochemistry; Cellular Biology; AKT; hepatitis B x antigen; hepatocellular carcinoma; miR148a; PTEN; URG11

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

APA (6th Edition):

Yuan, K. (2011). THE CHARACTERIZATION OF HSA-MIR148A IN HEPATOCARCINOGENESIS. (Doctoral Dissertation). Temple University. Retrieved from http://digital.library.temple.edu/u?/p245801coll10,154268

Chicago Manual of Style (16th Edition):

Yuan, Ke. “THE CHARACTERIZATION OF HSA-MIR148A IN HEPATOCARCINOGENESIS.” 2011. Doctoral Dissertation, Temple University. Accessed September 20, 2020. http://digital.library.temple.edu/u?/p245801coll10,154268.

MLA Handbook (7th Edition):

Yuan, Ke. “THE CHARACTERIZATION OF HSA-MIR148A IN HEPATOCARCINOGENESIS.” 2011. Web. 20 Sep 2020.

Vancouver:

Yuan K. THE CHARACTERIZATION OF HSA-MIR148A IN HEPATOCARCINOGENESIS. [Internet] [Doctoral dissertation]. Temple University; 2011. [cited 2020 Sep 20]. Available from: http://digital.library.temple.edu/u?/p245801coll10,154268.

Council of Science Editors:

Yuan K. THE CHARACTERIZATION OF HSA-MIR148A IN HEPATOCARCINOGENESIS. [Doctoral Dissertation]. Temple University; 2011. Available from: http://digital.library.temple.edu/u?/p245801coll10,154268


Temple University

2. Zhou, Yu. HCV, Heroin Use, and MicroRNAs.

Degree: PhD, 2014, Temple University

Pathology

Hepatitis C virus (HCV) infection is common among injection drug users (IDUs). There is accumulating evidence that circulating microRNAs (miRNAs) are related to HCV… (more)

Subjects/Keywords: Biology; Microbiology; Immunology;

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APA (6th Edition):

Zhou, Y. (2014). HCV, Heroin Use, and MicroRNAs. (Doctoral Dissertation). Temple University. Retrieved from http://digital.library.temple.edu/u?/p245801coll10,309425

Chicago Manual of Style (16th Edition):

Zhou, Yu. “HCV, Heroin Use, and MicroRNAs.” 2014. Doctoral Dissertation, Temple University. Accessed September 20, 2020. http://digital.library.temple.edu/u?/p245801coll10,309425.

MLA Handbook (7th Edition):

Zhou, Yu. “HCV, Heroin Use, and MicroRNAs.” 2014. Web. 20 Sep 2020.

Vancouver:

Zhou Y. HCV, Heroin Use, and MicroRNAs. [Internet] [Doctoral dissertation]. Temple University; 2014. [cited 2020 Sep 20]. Available from: http://digital.library.temple.edu/u?/p245801coll10,309425.

Council of Science Editors:

Zhou Y. HCV, Heroin Use, and MicroRNAs. [Doctoral Dissertation]. Temple University; 2014. Available from: http://digital.library.temple.edu/u?/p245801coll10,309425


Temple University

3. Gofman, Larisa. Role of Purinergic Receptor (P2X4) in EtOH-Mediated Microglial Immune Responses.

Degree: PhD, 2015, Temple University

Pathology

Ethanol (EtOH) abuse is the third leading cause of preventable death in the United States. Mounting evidence indicates that EtOH-induced neuropathology may result from… (more)

Subjects/Keywords: Neurosciences;

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APA (6th Edition):

Gofman, L. (2015). Role of Purinergic Receptor (P2X4) in EtOH-Mediated Microglial Immune Responses. (Doctoral Dissertation). Temple University. Retrieved from http://digital.library.temple.edu/u?/p245801coll10,315641

Chicago Manual of Style (16th Edition):

Gofman, Larisa. “Role of Purinergic Receptor (P2X4) in EtOH-Mediated Microglial Immune Responses.” 2015. Doctoral Dissertation, Temple University. Accessed September 20, 2020. http://digital.library.temple.edu/u?/p245801coll10,315641.

MLA Handbook (7th Edition):

Gofman, Larisa. “Role of Purinergic Receptor (P2X4) in EtOH-Mediated Microglial Immune Responses.” 2015. Web. 20 Sep 2020.

Vancouver:

Gofman L. Role of Purinergic Receptor (P2X4) in EtOH-Mediated Microglial Immune Responses. [Internet] [Doctoral dissertation]. Temple University; 2015. [cited 2020 Sep 20]. Available from: http://digital.library.temple.edu/u?/p245801coll10,315641.

Council of Science Editors:

Gofman L. Role of Purinergic Receptor (P2X4) in EtOH-Mediated Microglial Immune Responses. [Doctoral Dissertation]. Temple University; 2015. Available from: http://digital.library.temple.edu/u?/p245801coll10,315641


Temple University

4. Daswani, Varsha. Fluorescence and aggregation properties of the anti-cancer drug, CA4P, in archaeal liposomes.

Degree: PhD, 2015, Temple University

Biomedical Sciences

Combretastatin A4 phosphate (CA4P) is a potent vascular disrupting agent utilized in the treatment of cancer. The observed rapid vascular shutdown post administration… (more)

Subjects/Keywords: Biochemistry; Biophysics; Chemistry;

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APA (6th Edition):

Daswani, V. (2015). Fluorescence and aggregation properties of the anti-cancer drug, CA4P, in archaeal liposomes. (Doctoral Dissertation). Temple University. Retrieved from http://digital.library.temple.edu/u?/p245801coll10,334013

Chicago Manual of Style (16th Edition):

Daswani, Varsha. “Fluorescence and aggregation properties of the anti-cancer drug, CA4P, in archaeal liposomes.” 2015. Doctoral Dissertation, Temple University. Accessed September 20, 2020. http://digital.library.temple.edu/u?/p245801coll10,334013.

MLA Handbook (7th Edition):

Daswani, Varsha. “Fluorescence and aggregation properties of the anti-cancer drug, CA4P, in archaeal liposomes.” 2015. Web. 20 Sep 2020.

Vancouver:

Daswani V. Fluorescence and aggregation properties of the anti-cancer drug, CA4P, in archaeal liposomes. [Internet] [Doctoral dissertation]. Temple University; 2015. [cited 2020 Sep 20]. Available from: http://digital.library.temple.edu/u?/p245801coll10,334013.

Council of Science Editors:

Daswani V. Fluorescence and aggregation properties of the anti-cancer drug, CA4P, in archaeal liposomes. [Doctoral Dissertation]. Temple University; 2015. Available from: http://digital.library.temple.edu/u?/p245801coll10,334013


Temple University

5. Ayesa, Umme. CHARACTERIZATION OF THERMOSENSITIVE HYBRID ARCHAEOSOMES AND DPA-CY3[22,22]/POPC LIPOSOMES AND IN VITRO EVALUATION OF THEIR POTENTIAL USEFULNESS IN TARGETED DELIVERY AND CONTROLLED RELEASE.

Degree: PhD, 2016, Temple University

Biochemistry

One of earlier challenges in treating cancer was utilizing drugs that are powerful yet do not cause severe toxicity to patients. Although the use… (more)

Subjects/Keywords: Biophysics

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

APA (6th Edition):

Ayesa, U. (2016). CHARACTERIZATION OF THERMOSENSITIVE HYBRID ARCHAEOSOMES AND DPA-CY3[22,22]/POPC LIPOSOMES AND IN VITRO EVALUATION OF THEIR POTENTIAL USEFULNESS IN TARGETED DELIVERY AND CONTROLLED RELEASE. (Doctoral Dissertation). Temple University. Retrieved from http://digital.library.temple.edu/u?/p245801coll10,368614

Chicago Manual of Style (16th Edition):

Ayesa, Umme. “CHARACTERIZATION OF THERMOSENSITIVE HYBRID ARCHAEOSOMES AND DPA-CY3[22,22]/POPC LIPOSOMES AND IN VITRO EVALUATION OF THEIR POTENTIAL USEFULNESS IN TARGETED DELIVERY AND CONTROLLED RELEASE.” 2016. Doctoral Dissertation, Temple University. Accessed September 20, 2020. http://digital.library.temple.edu/u?/p245801coll10,368614.

MLA Handbook (7th Edition):

Ayesa, Umme. “CHARACTERIZATION OF THERMOSENSITIVE HYBRID ARCHAEOSOMES AND DPA-CY3[22,22]/POPC LIPOSOMES AND IN VITRO EVALUATION OF THEIR POTENTIAL USEFULNESS IN TARGETED DELIVERY AND CONTROLLED RELEASE.” 2016. Web. 20 Sep 2020.

Vancouver:

Ayesa U. CHARACTERIZATION OF THERMOSENSITIVE HYBRID ARCHAEOSOMES AND DPA-CY3[22,22]/POPC LIPOSOMES AND IN VITRO EVALUATION OF THEIR POTENTIAL USEFULNESS IN TARGETED DELIVERY AND CONTROLLED RELEASE. [Internet] [Doctoral dissertation]. Temple University; 2016. [cited 2020 Sep 20]. Available from: http://digital.library.temple.edu/u?/p245801coll10,368614.

Council of Science Editors:

Ayesa U. CHARACTERIZATION OF THERMOSENSITIVE HYBRID ARCHAEOSOMES AND DPA-CY3[22,22]/POPC LIPOSOMES AND IN VITRO EVALUATION OF THEIR POTENTIAL USEFULNESS IN TARGETED DELIVERY AND CONTROLLED RELEASE. [Doctoral Dissertation]. Temple University; 2016. Available from: http://digital.library.temple.edu/u?/p245801coll10,368614


Temple University

6. Collura, Kaitlin Marie. Palmitoylation-Dependent Regulation of the DLK/JNK/cJun and the GP130/JAK/STAT Retrograde Signaling Pathways.

Degree: PhD, 2015, Temple University

Biomedical Sciences

Palmitoylation is the post-translational addition of the 16-carbon fatty acid palmitate to protein cysteine residues. This process is best known for its roles… (more)

Subjects/Keywords: Neurosciences

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APA (6th Edition):

Collura, K. M. (2015). Palmitoylation-Dependent Regulation of the DLK/JNK/cJun and the GP130/JAK/STAT Retrograde Signaling Pathways. (Doctoral Dissertation). Temple University. Retrieved from http://digital.library.temple.edu/u?/p245801coll10,426710

Chicago Manual of Style (16th Edition):

Collura, Kaitlin Marie. “Palmitoylation-Dependent Regulation of the DLK/JNK/cJun and the GP130/JAK/STAT Retrograde Signaling Pathways.” 2015. Doctoral Dissertation, Temple University. Accessed September 20, 2020. http://digital.library.temple.edu/u?/p245801coll10,426710.

MLA Handbook (7th Edition):

Collura, Kaitlin Marie. “Palmitoylation-Dependent Regulation of the DLK/JNK/cJun and the GP130/JAK/STAT Retrograde Signaling Pathways.” 2015. Web. 20 Sep 2020.

Vancouver:

Collura KM. Palmitoylation-Dependent Regulation of the DLK/JNK/cJun and the GP130/JAK/STAT Retrograde Signaling Pathways. [Internet] [Doctoral dissertation]. Temple University; 2015. [cited 2020 Sep 20]. Available from: http://digital.library.temple.edu/u?/p245801coll10,426710.

Council of Science Editors:

Collura KM. Palmitoylation-Dependent Regulation of the DLK/JNK/cJun and the GP130/JAK/STAT Retrograde Signaling Pathways. [Doctoral Dissertation]. Temple University; 2015. Available from: http://digital.library.temple.edu/u?/p245801coll10,426710


Temple University

7. Merkel, Steven Franklin. Effects of Traumatic Brain Injury on Addiction-Like Behavior and Their Neuropathological Correlates.

Degree: PhD, 2017, Temple University

Pathology

Recent clinical and preclinical reports have identified traumatic brain injury (TBI) as an important risk factor affecting the development of substance use disorders (SUDs).… (more)

Subjects/Keywords: Medicine; Pathology; Neurosciences;

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APA (6th Edition):

Merkel, S. F. (2017). Effects of Traumatic Brain Injury on Addiction-Like Behavior and Their Neuropathological Correlates. (Doctoral Dissertation). Temple University. Retrieved from http://digital.library.temple.edu/u?/p245801coll10,450997

Chicago Manual of Style (16th Edition):

Merkel, Steven Franklin. “Effects of Traumatic Brain Injury on Addiction-Like Behavior and Their Neuropathological Correlates.” 2017. Doctoral Dissertation, Temple University. Accessed September 20, 2020. http://digital.library.temple.edu/u?/p245801coll10,450997.

MLA Handbook (7th Edition):

Merkel, Steven Franklin. “Effects of Traumatic Brain Injury on Addiction-Like Behavior and Their Neuropathological Correlates.” 2017. Web. 20 Sep 2020.

Vancouver:

Merkel SF. Effects of Traumatic Brain Injury on Addiction-Like Behavior and Their Neuropathological Correlates. [Internet] [Doctoral dissertation]. Temple University; 2017. [cited 2020 Sep 20]. Available from: http://digital.library.temple.edu/u?/p245801coll10,450997.

Council of Science Editors:

Merkel SF. Effects of Traumatic Brain Injury on Addiction-Like Behavior and Their Neuropathological Correlates. [Doctoral Dissertation]. Temple University; 2017. Available from: http://digital.library.temple.edu/u?/p245801coll10,450997


Temple University

8. Putatunda, Raj. HIV-1 INFECTION OF NEURAL STEM CELLS RESULTS IN COGNITIVE DEFICITS THROUGH ADULT NEUROGENIC MODULATION.

Degree: PhD, 2018, Temple University

Biomedical Sciences

While antiretroviral therapy (ART) regimens have significantly decreased the mortality rate in patients with HIV-1 infection and subsequent opportunistic infections, the co-morbidities continue… (more)

Subjects/Keywords: Neurosciences; Virology; Cellular biology;

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APA (6th Edition):

Putatunda, R. (2018). HIV-1 INFECTION OF NEURAL STEM CELLS RESULTS IN COGNITIVE DEFICITS THROUGH ADULT NEUROGENIC MODULATION. (Doctoral Dissertation). Temple University. Retrieved from http://digital.library.temple.edu/u?/p245801coll10,514815

Chicago Manual of Style (16th Edition):

Putatunda, Raj. “HIV-1 INFECTION OF NEURAL STEM CELLS RESULTS IN COGNITIVE DEFICITS THROUGH ADULT NEUROGENIC MODULATION.” 2018. Doctoral Dissertation, Temple University. Accessed September 20, 2020. http://digital.library.temple.edu/u?/p245801coll10,514815.

MLA Handbook (7th Edition):

Putatunda, Raj. “HIV-1 INFECTION OF NEURAL STEM CELLS RESULTS IN COGNITIVE DEFICITS THROUGH ADULT NEUROGENIC MODULATION.” 2018. Web. 20 Sep 2020.

Vancouver:

Putatunda R. HIV-1 INFECTION OF NEURAL STEM CELLS RESULTS IN COGNITIVE DEFICITS THROUGH ADULT NEUROGENIC MODULATION. [Internet] [Doctoral dissertation]. Temple University; 2018. [cited 2020 Sep 20]. Available from: http://digital.library.temple.edu/u?/p245801coll10,514815.

Council of Science Editors:

Putatunda R. HIV-1 INFECTION OF NEURAL STEM CELLS RESULTS IN COGNITIVE DEFICITS THROUGH ADULT NEUROGENIC MODULATION. [Doctoral Dissertation]. Temple University; 2018. Available from: http://digital.library.temple.edu/u?/p245801coll10,514815


Temple University

9. Skuba, Andrew. In vivo imaging analysis of the regeneration failure of dorsal root axons in adult mice.

Degree: PhD, 2014, Temple University

Cell Biology

After injury, dorsal root (DR) axons regenerate in the peripheral nervous system (PNS), but turn around or stop at the dorsal root entry… (more)

Subjects/Keywords: Cellular biology; Neurosciences;

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APA (6th Edition):

Skuba, A. (2014). In vivo imaging analysis of the regeneration failure of dorsal root axons in adult mice. (Doctoral Dissertation). Temple University. Retrieved from http://digital.library.temple.edu/u?/p245801coll10,292900

Chicago Manual of Style (16th Edition):

Skuba, Andrew. “In vivo imaging analysis of the regeneration failure of dorsal root axons in adult mice.” 2014. Doctoral Dissertation, Temple University. Accessed September 20, 2020. http://digital.library.temple.edu/u?/p245801coll10,292900.

MLA Handbook (7th Edition):

Skuba, Andrew. “In vivo imaging analysis of the regeneration failure of dorsal root axons in adult mice.” 2014. Web. 20 Sep 2020.

Vancouver:

Skuba A. In vivo imaging analysis of the regeneration failure of dorsal root axons in adult mice. [Internet] [Doctoral dissertation]. Temple University; 2014. [cited 2020 Sep 20]. Available from: http://digital.library.temple.edu/u?/p245801coll10,292900.

Council of Science Editors:

Skuba A. In vivo imaging analysis of the regeneration failure of dorsal root axons in adult mice. [Doctoral Dissertation]. Temple University; 2014. Available from: http://digital.library.temple.edu/u?/p245801coll10,292900


Temple University

10. Kim, Jae Kyun. CXCL12/CXCR4 signaling in mesocorticolimbic reward pathways: relevance to cocaine reinforcement and relapse.

Degree: PhD, 2016, Temple University

Pharmacology

The role of chemokines as chemotactic cytokines and their functions in the immune system and related pathologies are well defined. Recently, strong evidence supporting… (more)

Subjects/Keywords: Pharmacology;

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

APA (6th Edition):

Kim, J. K. (2016). CXCL12/CXCR4 signaling in mesocorticolimbic reward pathways: relevance to cocaine reinforcement and relapse. (Doctoral Dissertation). Temple University. Retrieved from http://digital.library.temple.edu/u?/p245801coll10,399036

Chicago Manual of Style (16th Edition):

Kim, Jae Kyun. “CXCL12/CXCR4 signaling in mesocorticolimbic reward pathways: relevance to cocaine reinforcement and relapse.” 2016. Doctoral Dissertation, Temple University. Accessed September 20, 2020. http://digital.library.temple.edu/u?/p245801coll10,399036.

MLA Handbook (7th Edition):

Kim, Jae Kyun. “CXCL12/CXCR4 signaling in mesocorticolimbic reward pathways: relevance to cocaine reinforcement and relapse.” 2016. Web. 20 Sep 2020.

Vancouver:

Kim JK. CXCL12/CXCR4 signaling in mesocorticolimbic reward pathways: relevance to cocaine reinforcement and relapse. [Internet] [Doctoral dissertation]. Temple University; 2016. [cited 2020 Sep 20]. Available from: http://digital.library.temple.edu/u?/p245801coll10,399036.

Council of Science Editors:

Kim JK. CXCL12/CXCR4 signaling in mesocorticolimbic reward pathways: relevance to cocaine reinforcement and relapse. [Doctoral Dissertation]. Temple University; 2016. Available from: http://digital.library.temple.edu/u?/p245801coll10,399036

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