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You searched for +publisher:"Rutgers University" +contributor:("Chen, Suzie"). Showing records 1 – 29 of 29 total matches.

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Rutgers University

1. Wahler, Gabriella, 1988-. Nitrogen mustard induces early changes in skin protein expression: potential targets for therapeutic intervention.

Degree: PhD, Toxicology, 2020, Rutgers University

Exposure to mustard gas is a current issue. Recently there has been resurgence in chemical warfare attacks, specifically in the Middle East. In August 2015,… (more)

Subjects/Keywords: Vesicating agents; Mustard gas  – Toxicology

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APA (6th Edition):

Wahler, Gabriella, 1. (2020). Nitrogen mustard induces early changes in skin protein expression: potential targets for therapeutic intervention. (Doctoral Dissertation). Rutgers University. Retrieved from https://rucore.libraries.rutgers.edu/rutgers-lib/63137/

Chicago Manual of Style (16th Edition):

Wahler, Gabriella, 1988-. “Nitrogen mustard induces early changes in skin protein expression: potential targets for therapeutic intervention.” 2020. Doctoral Dissertation, Rutgers University. Accessed May 08, 2021. https://rucore.libraries.rutgers.edu/rutgers-lib/63137/.

MLA Handbook (7th Edition):

Wahler, Gabriella, 1988-. “Nitrogen mustard induces early changes in skin protein expression: potential targets for therapeutic intervention.” 2020. Web. 08 May 2021.

Vancouver:

Wahler, Gabriella 1. Nitrogen mustard induces early changes in skin protein expression: potential targets for therapeutic intervention. [Internet] [Doctoral dissertation]. Rutgers University; 2020. [cited 2021 May 08]. Available from: https://rucore.libraries.rutgers.edu/rutgers-lib/63137/.

Council of Science Editors:

Wahler, Gabriella 1. Nitrogen mustard induces early changes in skin protein expression: potential targets for therapeutic intervention. [Doctoral Dissertation]. Rutgers University; 2020. Available from: https://rucore.libraries.rutgers.edu/rutgers-lib/63137/


Rutgers University

2. Chen, Ho-Chung, 1991-. Expression of mutated BRAF (V600E) in melanocytes activates metabotropic glutamate receptor 1 expression.

Degree: MS, Chemical and Biochemical Engineering, 2016, Rutgers University

 Melanoma is the most aggressive form of skin cancer, which is caused by the neoplastic transformation of melanocytes. The precise genetic aberrations that initiate the… (more)

Subjects/Keywords: Melanoma

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APA (6th Edition):

Chen, Ho-Chung, 1. (2016). Expression of mutated BRAF (V600E) in melanocytes activates metabotropic glutamate receptor 1 expression. (Masters Thesis). Rutgers University. Retrieved from https://rucore.libraries.rutgers.edu/rutgers-lib/51246/

Chicago Manual of Style (16th Edition):

Chen, Ho-Chung, 1991-. “Expression of mutated BRAF (V600E) in melanocytes activates metabotropic glutamate receptor 1 expression.” 2016. Masters Thesis, Rutgers University. Accessed May 08, 2021. https://rucore.libraries.rutgers.edu/rutgers-lib/51246/.

MLA Handbook (7th Edition):

Chen, Ho-Chung, 1991-. “Expression of mutated BRAF (V600E) in melanocytes activates metabotropic glutamate receptor 1 expression.” 2016. Web. 08 May 2021.

Vancouver:

Chen, Ho-Chung 1. Expression of mutated BRAF (V600E) in melanocytes activates metabotropic glutamate receptor 1 expression. [Internet] [Masters thesis]. Rutgers University; 2016. [cited 2021 May 08]. Available from: https://rucore.libraries.rutgers.edu/rutgers-lib/51246/.

Council of Science Editors:

Chen, Ho-Chung 1. Expression of mutated BRAF (V600E) in melanocytes activates metabotropic glutamate receptor 1 expression. [Masters Thesis]. Rutgers University; 2016. Available from: https://rucore.libraries.rutgers.edu/rutgers-lib/51246/


Rutgers University

3. Sierra, Jairo L., 1987-. Activation of Grm1 expression by inducible mutated B-RAF in vitro and in vivo.

Degree: MS, Cell and Developmental Biology, 2015, Rutgers University

 Melanoma is a form of skin cancer that arises from the neoplastic transformation of melanocytes. Constitutive activation of the MAPK pathway due to mutations in… (more)

Subjects/Keywords: Melanoma

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APA (6th Edition):

Sierra, Jairo L., 1. (2015). Activation of Grm1 expression by inducible mutated B-RAF in vitro and in vivo. (Masters Thesis). Rutgers University. Retrieved from https://rucore.libraries.rutgers.edu/rutgers-lib/48659/

Chicago Manual of Style (16th Edition):

Sierra, Jairo L., 1987-. “Activation of Grm1 expression by inducible mutated B-RAF in vitro and in vivo.” 2015. Masters Thesis, Rutgers University. Accessed May 08, 2021. https://rucore.libraries.rutgers.edu/rutgers-lib/48659/.

MLA Handbook (7th Edition):

Sierra, Jairo L., 1987-. “Activation of Grm1 expression by inducible mutated B-RAF in vitro and in vivo.” 2015. Web. 08 May 2021.

Vancouver:

Sierra, Jairo L. 1. Activation of Grm1 expression by inducible mutated B-RAF in vitro and in vivo. [Internet] [Masters thesis]. Rutgers University; 2015. [cited 2021 May 08]. Available from: https://rucore.libraries.rutgers.edu/rutgers-lib/48659/.

Council of Science Editors:

Sierra, Jairo L. 1. Activation of Grm1 expression by inducible mutated B-RAF in vitro and in vivo. [Masters Thesis]. Rutgers University; 2015. Available from: https://rucore.libraries.rutgers.edu/rutgers-lib/48659/


Rutgers University

4. Patrizii, Michele. Post-translational modifications on the K2 domain modulate SOX9 transcriptional activity in lung cancer.

Degree: PhD, Pharmacology, Cellular and Molecular, 2019, Rutgers University

Lung cancer is the deadliest cancer type, accounting for about 25% of all cancer-related deaths. Despite impressive advancements in the molecular characterization of lung cancer,… (more)

Subjects/Keywords: Lungs  – Cancer  – Molecular aspects

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APA (6th Edition):

Patrizii, M. (2019). Post-translational modifications on the K2 domain modulate SOX9 transcriptional activity in lung cancer. (Doctoral Dissertation). Rutgers University. Retrieved from https://rucore.libraries.rutgers.edu/rutgers-lib/61905/

Chicago Manual of Style (16th Edition):

Patrizii, Michele. “Post-translational modifications on the K2 domain modulate SOX9 transcriptional activity in lung cancer.” 2019. Doctoral Dissertation, Rutgers University. Accessed May 08, 2021. https://rucore.libraries.rutgers.edu/rutgers-lib/61905/.

MLA Handbook (7th Edition):

Patrizii, Michele. “Post-translational modifications on the K2 domain modulate SOX9 transcriptional activity in lung cancer.” 2019. Web. 08 May 2021.

Vancouver:

Patrizii M. Post-translational modifications on the K2 domain modulate SOX9 transcriptional activity in lung cancer. [Internet] [Doctoral dissertation]. Rutgers University; 2019. [cited 2021 May 08]. Available from: https://rucore.libraries.rutgers.edu/rutgers-lib/61905/.

Council of Science Editors:

Patrizii M. Post-translational modifications on the K2 domain modulate SOX9 transcriptional activity in lung cancer. [Doctoral Dissertation]. Rutgers University; 2019. Available from: https://rucore.libraries.rutgers.edu/rutgers-lib/61905/

5. Yang, Yuqing. Targeting epigenetics and Nrf2-pathway by dietary phytochemicals: promising cancer prevention approach.

Degree: PhD, Pharmaceutical Science, 2017, Rutgers University

The induction of nuclear factor (erythroid-derived 2)-like 2 (Nrf2)- antioxidant response elements (ARE)-mediated antioxidant enzymes provides a cellular defense against oxidative stress, a major drive… (more)

Subjects/Keywords: Epigenetics

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APA (6th Edition):

Yang, Y. (2017). Targeting epigenetics and Nrf2-pathway by dietary phytochemicals: promising cancer prevention approach. (Doctoral Dissertation). Rutgers University. Retrieved from https://rucore.libraries.rutgers.edu/rutgers-lib/55783/

Chicago Manual of Style (16th Edition):

Yang, Yuqing. “Targeting epigenetics and Nrf2-pathway by dietary phytochemicals: promising cancer prevention approach.” 2017. Doctoral Dissertation, Rutgers University. Accessed May 08, 2021. https://rucore.libraries.rutgers.edu/rutgers-lib/55783/.

MLA Handbook (7th Edition):

Yang, Yuqing. “Targeting epigenetics and Nrf2-pathway by dietary phytochemicals: promising cancer prevention approach.” 2017. Web. 08 May 2021.

Vancouver:

Yang Y. Targeting epigenetics and Nrf2-pathway by dietary phytochemicals: promising cancer prevention approach. [Internet] [Doctoral dissertation]. Rutgers University; 2017. [cited 2021 May 08]. Available from: https://rucore.libraries.rutgers.edu/rutgers-lib/55783/.

Council of Science Editors:

Yang Y. Targeting epigenetics and Nrf2-pathway by dietary phytochemicals: promising cancer prevention approach. [Doctoral Dissertation]. Rutgers University; 2017. Available from: https://rucore.libraries.rutgers.edu/rutgers-lib/55783/


Rutgers University

6. Wahler, Joseph, 1987-. Inhibition of breast cancer progression with Vitamin D compounds.

Degree: PhD, Pharmacology, Cellular and Molecular, 2015, Rutgers University

Early epidemiological studies have shown an inverse correlation of increased vitamin D3 to breast cancer. Since this discovery, many studies have linked 1,25-dihydroxyvitamin D3, the… (more)

Subjects/Keywords: Breast – Cancer – Treatment; Vitamin D

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APA (6th Edition):

Wahler, Joseph, 1. (2015). Inhibition of breast cancer progression with Vitamin D compounds. (Doctoral Dissertation). Rutgers University. Retrieved from https://rucore.libraries.rutgers.edu/rutgers-lib/48709/

Chicago Manual of Style (16th Edition):

Wahler, Joseph, 1987-. “Inhibition of breast cancer progression with Vitamin D compounds.” 2015. Doctoral Dissertation, Rutgers University. Accessed May 08, 2021. https://rucore.libraries.rutgers.edu/rutgers-lib/48709/.

MLA Handbook (7th Edition):

Wahler, Joseph, 1987-. “Inhibition of breast cancer progression with Vitamin D compounds.” 2015. Web. 08 May 2021.

Vancouver:

Wahler, Joseph 1. Inhibition of breast cancer progression with Vitamin D compounds. [Internet] [Doctoral dissertation]. Rutgers University; 2015. [cited 2021 May 08]. Available from: https://rucore.libraries.rutgers.edu/rutgers-lib/48709/.

Council of Science Editors:

Wahler, Joseph 1. Inhibition of breast cancer progression with Vitamin D compounds. [Doctoral Dissertation]. Rutgers University; 2015. Available from: https://rucore.libraries.rutgers.edu/rutgers-lib/48709/


Rutgers University

7. Sheleg, Michal, 1983-. Regulation of mouse behavior by ephrin-a5.

Degree: PhD, Toxicology, 2015, Rutgers University

Social behaviors in mammals are regulated by core neural circuits that respond to stimuli from the environment. These circuits are formed by guidance molecules and… (more)

Subjects/Keywords: Receptor-ligand complexes; Protein-tyrosine kinase

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APA (6th Edition):

Sheleg, Michal, 1. (2015). Regulation of mouse behavior by ephrin-a5. (Doctoral Dissertation). Rutgers University. Retrieved from https://rucore.libraries.rutgers.edu/rutgers-lib/46436/

Chicago Manual of Style (16th Edition):

Sheleg, Michal, 1983-. “Regulation of mouse behavior by ephrin-a5.” 2015. Doctoral Dissertation, Rutgers University. Accessed May 08, 2021. https://rucore.libraries.rutgers.edu/rutgers-lib/46436/.

MLA Handbook (7th Edition):

Sheleg, Michal, 1983-. “Regulation of mouse behavior by ephrin-a5.” 2015. Web. 08 May 2021.

Vancouver:

Sheleg, Michal 1. Regulation of mouse behavior by ephrin-a5. [Internet] [Doctoral dissertation]. Rutgers University; 2015. [cited 2021 May 08]. Available from: https://rucore.libraries.rutgers.edu/rutgers-lib/46436/.

Council of Science Editors:

Sheleg, Michal 1. Regulation of mouse behavior by ephrin-a5. [Doctoral Dissertation]. Rutgers University; 2015. Available from: https://rucore.libraries.rutgers.edu/rutgers-lib/46436/


Rutgers University

8. Shan, Naing Lin, 1985-. Understanding the role of cancer stemness in breast tumorigenesis.

Degree: PhD, Breast cancer, 2020, Rutgers University

Breast cancer is a heterogeneous disease; its high degrees of intra- and inter-tumoral diversity are attributable to the presence of a subset of tumor-initiating cells… (more)

Subjects/Keywords: Microbiology and Molecular Genetics

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APA (6th Edition):

Shan, Naing Lin, 1. (2020). Understanding the role of cancer stemness in breast tumorigenesis. (Doctoral Dissertation). Rutgers University. Retrieved from https://rucore.libraries.rutgers.edu/rutgers-lib/64927/

Chicago Manual of Style (16th Edition):

Shan, Naing Lin, 1985-. “Understanding the role of cancer stemness in breast tumorigenesis.” 2020. Doctoral Dissertation, Rutgers University. Accessed May 08, 2021. https://rucore.libraries.rutgers.edu/rutgers-lib/64927/.

MLA Handbook (7th Edition):

Shan, Naing Lin, 1985-. “Understanding the role of cancer stemness in breast tumorigenesis.” 2020. Web. 08 May 2021.

Vancouver:

Shan, Naing Lin 1. Understanding the role of cancer stemness in breast tumorigenesis. [Internet] [Doctoral dissertation]. Rutgers University; 2020. [cited 2021 May 08]. Available from: https://rucore.libraries.rutgers.edu/rutgers-lib/64927/.

Council of Science Editors:

Shan, Naing Lin 1. Understanding the role of cancer stemness in breast tumorigenesis. [Doctoral Dissertation]. Rutgers University; 2020. Available from: https://rucore.libraries.rutgers.edu/rutgers-lib/64927/


Rutgers University

9. Isola, Allison L. Role of GRM1 in exosome production and melanoma metastasis.

Degree: PhD, Toxicology, 2017, Rutgers University

Exosomes are naturally occurring membrane-bound nanovesicles generated constitutively and released by various cell types, and often in higher quantities by tumor cells. Exosomes have been… (more)

Subjects/Keywords: Melanoma

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APA (6th Edition):

Isola, A. L. (2017). Role of GRM1 in exosome production and melanoma metastasis. (Doctoral Dissertation). Rutgers University. Retrieved from https://rucore.libraries.rutgers.edu/rutgers-lib/55510/

Chicago Manual of Style (16th Edition):

Isola, Allison L. “Role of GRM1 in exosome production and melanoma metastasis.” 2017. Doctoral Dissertation, Rutgers University. Accessed May 08, 2021. https://rucore.libraries.rutgers.edu/rutgers-lib/55510/.

MLA Handbook (7th Edition):

Isola, Allison L. “Role of GRM1 in exosome production and melanoma metastasis.” 2017. Web. 08 May 2021.

Vancouver:

Isola AL. Role of GRM1 in exosome production and melanoma metastasis. [Internet] [Doctoral dissertation]. Rutgers University; 2017. [cited 2021 May 08]. Available from: https://rucore.libraries.rutgers.edu/rutgers-lib/55510/.

Council of Science Editors:

Isola AL. Role of GRM1 in exosome production and melanoma metastasis. [Doctoral Dissertation]. Rutgers University; 2017. Available from: https://rucore.libraries.rutgers.edu/rutgers-lib/55510/


Rutgers University

10. Saitta, Kyle S., 1989-. The role of the group I metabotropic glutamate receptor agonist, CHPG, in oligodendrocyte regeneration and repair following a cuprizone-induced lesion.

Degree: PhD, BDNF, 2020, Rutgers University

Demyelinating diseases or demyelination in response to toxic agents can be debilitating to patients and can greatly impair the quality of life. Therefore, new therapeutic… (more)

Subjects/Keywords: Toxicology

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APA (6th Edition):

Saitta, Kyle S., 1. (2020). The role of the group I metabotropic glutamate receptor agonist, CHPG, in oligodendrocyte regeneration and repair following a cuprizone-induced lesion. (Doctoral Dissertation). Rutgers University. Retrieved from https://rucore.libraries.rutgers.edu/rutgers-lib/64381/

Chicago Manual of Style (16th Edition):

Saitta, Kyle S., 1989-. “The role of the group I metabotropic glutamate receptor agonist, CHPG, in oligodendrocyte regeneration and repair following a cuprizone-induced lesion.” 2020. Doctoral Dissertation, Rutgers University. Accessed May 08, 2021. https://rucore.libraries.rutgers.edu/rutgers-lib/64381/.

MLA Handbook (7th Edition):

Saitta, Kyle S., 1989-. “The role of the group I metabotropic glutamate receptor agonist, CHPG, in oligodendrocyte regeneration and repair following a cuprizone-induced lesion.” 2020. Web. 08 May 2021.

Vancouver:

Saitta, Kyle S. 1. The role of the group I metabotropic glutamate receptor agonist, CHPG, in oligodendrocyte regeneration and repair following a cuprizone-induced lesion. [Internet] [Doctoral dissertation]. Rutgers University; 2020. [cited 2021 May 08]. Available from: https://rucore.libraries.rutgers.edu/rutgers-lib/64381/.

Council of Science Editors:

Saitta, Kyle S. 1. The role of the group I metabotropic glutamate receptor agonist, CHPG, in oligodendrocyte regeneration and repair following a cuprizone-induced lesion. [Doctoral Dissertation]. Rutgers University; 2020. Available from: https://rucore.libraries.rutgers.edu/rutgers-lib/64381/


Rutgers University

11. Shah, Raj D. Role of GRM1 in altering glutamate metabolism and bioavailability.

Degree: PhD, Glutamate, 2020, Rutgers University

 Altered metabolic activity has been implicated in several types of cancer including malignant melanoma. Previously, we have illustrated the role of a neuronal receptor, metabotropic… (more)

Subjects/Keywords: Toxicology

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APA (6th Edition):

Shah, R. D. (2020). Role of GRM1 in altering glutamate metabolism and bioavailability. (Doctoral Dissertation). Rutgers University. Retrieved from https://rucore.libraries.rutgers.edu/rutgers-lib/64382/

Chicago Manual of Style (16th Edition):

Shah, Raj D. “Role of GRM1 in altering glutamate metabolism and bioavailability.” 2020. Doctoral Dissertation, Rutgers University. Accessed May 08, 2021. https://rucore.libraries.rutgers.edu/rutgers-lib/64382/.

MLA Handbook (7th Edition):

Shah, Raj D. “Role of GRM1 in altering glutamate metabolism and bioavailability.” 2020. Web. 08 May 2021.

Vancouver:

Shah RD. Role of GRM1 in altering glutamate metabolism and bioavailability. [Internet] [Doctoral dissertation]. Rutgers University; 2020. [cited 2021 May 08]. Available from: https://rucore.libraries.rutgers.edu/rutgers-lib/64382/.

Council of Science Editors:

Shah RD. Role of GRM1 in altering glutamate metabolism and bioavailability. [Doctoral Dissertation]. Rutgers University; 2020. Available from: https://rucore.libraries.rutgers.edu/rutgers-lib/64382/

12. Robinson, Ann K., 1991-. Treating melanoma in an experimental system by targeting glutamatergic signaling and PD-1 inhibition.

Degree: MS, Microbiology and Molecular Genetics, 2017, Rutgers University

 Melanoma is the most dangerous type of skin cancer due to the frequency of metastasis and resistance to therapies, including radiation, traditional chemotherapies, and targeted… (more)

Subjects/Keywords: Melanoma – Treatment

…Committee at Rutgers University. For this study, we used fifty-four female, immunocompetent C57BL… 

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APA (6th Edition):

Robinson, Ann K., 1. (2017). Treating melanoma in an experimental system by targeting glutamatergic signaling and PD-1 inhibition. (Masters Thesis). Rutgers University. Retrieved from https://rucore.libraries.rutgers.edu/rutgers-lib/55673/

Chicago Manual of Style (16th Edition):

Robinson, Ann K., 1991-. “Treating melanoma in an experimental system by targeting glutamatergic signaling and PD-1 inhibition.” 2017. Masters Thesis, Rutgers University. Accessed May 08, 2021. https://rucore.libraries.rutgers.edu/rutgers-lib/55673/.

MLA Handbook (7th Edition):

Robinson, Ann K., 1991-. “Treating melanoma in an experimental system by targeting glutamatergic signaling and PD-1 inhibition.” 2017. Web. 08 May 2021.

Vancouver:

Robinson, Ann K. 1. Treating melanoma in an experimental system by targeting glutamatergic signaling and PD-1 inhibition. [Internet] [Masters thesis]. Rutgers University; 2017. [cited 2021 May 08]. Available from: https://rucore.libraries.rutgers.edu/rutgers-lib/55673/.

Council of Science Editors:

Robinson, Ann K. 1. Treating melanoma in an experimental system by targeting glutamatergic signaling and PD-1 inhibition. [Masters Thesis]. Rutgers University; 2017. Available from: https://rucore.libraries.rutgers.edu/rutgers-lib/55673/

13. Cerchio, Robert M. Riluzole induces DNA double strand breaks in mGluR1 expressing human melanoma cells.

Degree: MS, Toxicology, 2018, Rutgers University

 Melanoma is the most aggressive form of skin cancer; in 2018 about 90,000 new cases and 9,000 deaths are expected in the United States. Our… (more)

Subjects/Keywords: Drugs—Toxicology

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APA (6th Edition):

Cerchio, R. M. (2018). Riluzole induces DNA double strand breaks in mGluR1 expressing human melanoma cells. (Masters Thesis). Rutgers University. Retrieved from https://rucore.libraries.rutgers.edu/rutgers-lib/58945/

Chicago Manual of Style (16th Edition):

Cerchio, Robert M. “Riluzole induces DNA double strand breaks in mGluR1 expressing human melanoma cells.” 2018. Masters Thesis, Rutgers University. Accessed May 08, 2021. https://rucore.libraries.rutgers.edu/rutgers-lib/58945/.

MLA Handbook (7th Edition):

Cerchio, Robert M. “Riluzole induces DNA double strand breaks in mGluR1 expressing human melanoma cells.” 2018. Web. 08 May 2021.

Vancouver:

Cerchio RM. Riluzole induces DNA double strand breaks in mGluR1 expressing human melanoma cells. [Internet] [Masters thesis]. Rutgers University; 2018. [cited 2021 May 08]. Available from: https://rucore.libraries.rutgers.edu/rutgers-lib/58945/.

Council of Science Editors:

Cerchio RM. Riluzole induces DNA double strand breaks in mGluR1 expressing human melanoma cells. [Masters Thesis]. Rutgers University; 2018. Available from: https://rucore.libraries.rutgers.edu/rutgers-lib/58945/

14. Zhang, Chengyue, 1986-. Emerging epigenetics in cancer chemoprevention by dietary phytochemicals.

Degree: PhD, Pharmaceutical Science, 2017, Rutgers University

 Cancer chemoprevention is defined as the strategy to block or slow the onset of premalignant tumors and using relatively nontoxic chemical substance. Recently, accumulating experimental… (more)

Subjects/Keywords: Cancer – Chemoprevention; Phytochemicals

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APA (6th Edition):

Zhang, Chengyue, 1. (2017). Emerging epigenetics in cancer chemoprevention by dietary phytochemicals. (Doctoral Dissertation). Rutgers University. Retrieved from https://rucore.libraries.rutgers.edu/rutgers-lib/52287/

Chicago Manual of Style (16th Edition):

Zhang, Chengyue, 1986-. “Emerging epigenetics in cancer chemoprevention by dietary phytochemicals.” 2017. Doctoral Dissertation, Rutgers University. Accessed May 08, 2021. https://rucore.libraries.rutgers.edu/rutgers-lib/52287/.

MLA Handbook (7th Edition):

Zhang, Chengyue, 1986-. “Emerging epigenetics in cancer chemoprevention by dietary phytochemicals.” 2017. Web. 08 May 2021.

Vancouver:

Zhang, Chengyue 1. Emerging epigenetics in cancer chemoprevention by dietary phytochemicals. [Internet] [Doctoral dissertation]. Rutgers University; 2017. [cited 2021 May 08]. Available from: https://rucore.libraries.rutgers.edu/rutgers-lib/52287/.

Council of Science Editors:

Zhang, Chengyue 1. Emerging epigenetics in cancer chemoprevention by dietary phytochemicals. [Doctoral Dissertation]. Rutgers University; 2017. Available from: https://rucore.libraries.rutgers.edu/rutgers-lib/52287/

15. Kim, Jung-Hwan. Investigation of novel NRF2 partners, RAC3 and IQGAP1.

Degree: PhD, Pharmaceutical Science, 2009, Rutgers University

Nuclear factor-erythroid-related factor 2 (Nrf2) is essential for the antioxidant responsive element (ARE)-mediated expression of a group of detoxifying and antioxidant genes, which detoxify carcinogens… (more)

Subjects/Keywords: Transcription factors; Cell receptors; Nuclear receptors (Biochemistry)

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APA (6th Edition):

Kim, J. (2009). Investigation of novel NRF2 partners, RAC3 and IQGAP1. (Doctoral Dissertation). Rutgers University. Retrieved from http://hdl.rutgers.edu/1782.2/rucore10001600001.ETD.000052254

Chicago Manual of Style (16th Edition):

Kim, Jung-Hwan. “Investigation of novel NRF2 partners, RAC3 and IQGAP1.” 2009. Doctoral Dissertation, Rutgers University. Accessed May 08, 2021. http://hdl.rutgers.edu/1782.2/rucore10001600001.ETD.000052254.

MLA Handbook (7th Edition):

Kim, Jung-Hwan. “Investigation of novel NRF2 partners, RAC3 and IQGAP1.” 2009. Web. 08 May 2021.

Vancouver:

Kim J. Investigation of novel NRF2 partners, RAC3 and IQGAP1. [Internet] [Doctoral dissertation]. Rutgers University; 2009. [cited 2021 May 08]. Available from: http://hdl.rutgers.edu/1782.2/rucore10001600001.ETD.000052254.

Council of Science Editors:

Kim J. Investigation of novel NRF2 partners, RAC3 and IQGAP1. [Doctoral Dissertation]. Rutgers University; 2009. Available from: http://hdl.rutgers.edu/1782.2/rucore10001600001.ETD.000052254

16. Smolarek, Amanda Kathryn, 1985-. Chemopreventive activity of tocopherols in mammary tumorigenesis.

Degree: Toxicology, 2013, Rutgers University

Subjects/Keywords: Breast – Cancer – Chemoprevention; Vitamin E; Apoptosis; Breast – Cancer – Animal models

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APA (6th Edition):

Smolarek, Amanda Kathryn, 1. (2013). Chemopreventive activity of tocopherols in mammary tumorigenesis. (Thesis). Rutgers University. Retrieved from http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000067844

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):

Smolarek, Amanda Kathryn, 1985-. “Chemopreventive activity of tocopherols in mammary tumorigenesis.” 2013. Thesis, Rutgers University. Accessed May 08, 2021. http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000067844.

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

MLA Handbook (7th Edition):

Smolarek, Amanda Kathryn, 1985-. “Chemopreventive activity of tocopherols in mammary tumorigenesis.” 2013. Web. 08 May 2021.

Vancouver:

Smolarek, Amanda Kathryn 1. Chemopreventive activity of tocopherols in mammary tumorigenesis. [Internet] [Thesis]. Rutgers University; 2013. [cited 2021 May 08]. Available from: http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000067844.

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

Council of Science Editors:

Smolarek, Amanda Kathryn 1. Chemopreventive activity of tocopherols in mammary tumorigenesis. [Thesis]. Rutgers University; 2013. Available from: http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000067844

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

17. Son, Alexander I., 1983-. The role of ephrin-A5 in lens maintenance and vitreous humor development.

Degree: Neuroscience, 2013, Rutgers University

Subjects/Keywords: Protein-tyrosine kinase – Receptors; Vitreous body – Diseases; Vitreous humor

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

APA (6th Edition):

Son, Alexander I., 1. (2013). The role of ephrin-A5 in lens maintenance and vitreous humor development. (Thesis). Rutgers University. Retrieved from http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000067846

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):

Son, Alexander I., 1983-. “The role of ephrin-A5 in lens maintenance and vitreous humor development.” 2013. Thesis, Rutgers University. Accessed May 08, 2021. http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000067846.

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

MLA Handbook (7th Edition):

Son, Alexander I., 1983-. “The role of ephrin-A5 in lens maintenance and vitreous humor development.” 2013. Web. 08 May 2021.

Vancouver:

Son, Alexander I. 1. The role of ephrin-A5 in lens maintenance and vitreous humor development. [Internet] [Thesis]. Rutgers University; 2013. [cited 2021 May 08]. Available from: http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000067846.

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

Council of Science Editors:

Son, Alexander I. 1. The role of ephrin-A5 in lens maintenance and vitreous humor development. [Thesis]. Rutgers University; 2013. Available from: http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000067846

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

18. Wall, Brian A., 1978-. GRM1, a potential target for human melanoma.

Degree: Toxicology, 2013, Rutgers University

Subjects/Keywords: Melanoma – Research; Melanoma – Treatment; DNA ligases

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

APA (6th Edition):

Wall, Brian A., 1. (2013). GRM1, a potential target for human melanoma. (Thesis). Rutgers University. Retrieved from http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000067885

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):

Wall, Brian A., 1978-. “GRM1, a potential target for human melanoma.” 2013. Thesis, Rutgers University. Accessed May 08, 2021. http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000067885.

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

MLA Handbook (7th Edition):

Wall, Brian A., 1978-. “GRM1, a potential target for human melanoma.” 2013. Web. 08 May 2021.

Vancouver:

Wall, Brian A. 1. GRM1, a potential target for human melanoma. [Internet] [Thesis]. Rutgers University; 2013. [cited 2021 May 08]. Available from: http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000067885.

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

Council of Science Editors:

Wall, Brian A. 1. GRM1, a potential target for human melanoma. [Thesis]. Rutgers University; 2013. Available from: http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000067885

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

19. Naczynski, Dominik Jan, 1984-. Developing a multifunctional nanocomposite using albumin-encapsulated rare-earth doped nanoparticles for tumor targeting.

Degree: Chemical and Biochemical Engineering, 2012, Rutgers University

Subjects/Keywords: Nanoparticles; Cancer – Imaging; Albumins

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APA (6th Edition):

Naczynski, Dominik Jan, 1. (2012). Developing a multifunctional nanocomposite using albumin-encapsulated rare-earth doped nanoparticles for tumor targeting. (Thesis). Rutgers University. Retrieved from http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000066924

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):

Naczynski, Dominik Jan, 1984-. “Developing a multifunctional nanocomposite using albumin-encapsulated rare-earth doped nanoparticles for tumor targeting.” 2012. Thesis, Rutgers University. Accessed May 08, 2021. http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000066924.

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

MLA Handbook (7th Edition):

Naczynski, Dominik Jan, 1984-. “Developing a multifunctional nanocomposite using albumin-encapsulated rare-earth doped nanoparticles for tumor targeting.” 2012. Web. 08 May 2021.

Vancouver:

Naczynski, Dominik Jan 1. Developing a multifunctional nanocomposite using albumin-encapsulated rare-earth doped nanoparticles for tumor targeting. [Internet] [Thesis]. Rutgers University; 2012. [cited 2021 May 08]. Available from: http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000066924.

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

Council of Science Editors:

Naczynski, Dominik Jan 1. Developing a multifunctional nanocomposite using albumin-encapsulated rare-earth doped nanoparticles for tumor targeting. [Thesis]. Rutgers University; 2012. Available from: http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000066924

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

20. Wu, Tien-Yuan. Novel perspectives in cancer chemoprevention via Nrf2 pathway: from pharmacogenomics to pharmacoepigenetics.

Degree: Pharmaceutical Science, 2012, Rutgers University

Subjects/Keywords: Cancer – Chemoprevention; Phytochemicals; Pharmacogenomics

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APA (6th Edition):

Wu, T. (2012). Novel perspectives in cancer chemoprevention via Nrf2 pathway: from pharmacogenomics to pharmacoepigenetics. (Thesis). Rutgers University. Retrieved from http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000067028

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):

Wu, Tien-Yuan. “Novel perspectives in cancer chemoprevention via Nrf2 pathway: from pharmacogenomics to pharmacoepigenetics.” 2012. Thesis, Rutgers University. Accessed May 08, 2021. http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000067028.

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

MLA Handbook (7th Edition):

Wu, Tien-Yuan. “Novel perspectives in cancer chemoprevention via Nrf2 pathway: from pharmacogenomics to pharmacoepigenetics.” 2012. Web. 08 May 2021.

Vancouver:

Wu T. Novel perspectives in cancer chemoprevention via Nrf2 pathway: from pharmacogenomics to pharmacoepigenetics. [Internet] [Thesis]. Rutgers University; 2012. [cited 2021 May 08]. Available from: http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000067028.

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

Council of Science Editors:

Wu T. Novel perspectives in cancer chemoprevention via Nrf2 pathway: from pharmacogenomics to pharmacoepigenetics. [Thesis]. Rutgers University; 2012. Available from: http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000067028

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


Rutgers University

21. Namkoong, Jin. Metabotropic glutamate receptor 1 and glutamate signaling in human melanoma.

Degree: PhD, Microbiology and Molecular Genetics, 2007, Rutgers University

Melanoma is the most malignant form of skin cancers that originated from melanocytes, the pigment cells in the skin. Early detection is the key for… (more)

Subjects/Keywords: Melanoma; Cancer; Skin

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APA (6th Edition):

Namkoong, J. (2007). Metabotropic glutamate receptor 1 and glutamate signaling in human melanoma. (Doctoral Dissertation). Rutgers University. Retrieved from http://hdl.rutgers.edu/1782.2/rucore10001600001.ETD.13495

Chicago Manual of Style (16th Edition):

Namkoong, Jin. “Metabotropic glutamate receptor 1 and glutamate signaling in human melanoma.” 2007. Doctoral Dissertation, Rutgers University. Accessed May 08, 2021. http://hdl.rutgers.edu/1782.2/rucore10001600001.ETD.13495.

MLA Handbook (7th Edition):

Namkoong, Jin. “Metabotropic glutamate receptor 1 and glutamate signaling in human melanoma.” 2007. Web. 08 May 2021.

Vancouver:

Namkoong J. Metabotropic glutamate receptor 1 and glutamate signaling in human melanoma. [Internet] [Doctoral dissertation]. Rutgers University; 2007. [cited 2021 May 08]. Available from: http://hdl.rutgers.edu/1782.2/rucore10001600001.ETD.13495.

Council of Science Editors:

Namkoong J. Metabotropic glutamate receptor 1 and glutamate signaling in human melanoma. [Doctoral Dissertation]. Rutgers University; 2007. Available from: http://hdl.rutgers.edu/1782.2/rucore10001600001.ETD.13495


Rutgers University

22. Wilimczyk, Barbara J. Continuous expression of metabotropic glutamate receptor 1 is required for maintenance of tumorigenesis in GRM1 transformed mouse kidney epithelial cells.

Degree: MS, Microbiology and Molecular Genetics, 2009, Rutgers University

 Within the United States, skin cancer has become a predominant form of cancer that occurs across all age groups, racial backgrounds, and to both genders… (more)

Subjects/Keywords: Cancer cells – Proliferation; Carcinogenesis; Cancer – Treatment

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APA (6th Edition):

Wilimczyk, B. J. (2009). Continuous expression of metabotropic glutamate receptor 1 is required for maintenance of tumorigenesis in GRM1 transformed mouse kidney epithelial cells. (Masters Thesis). Rutgers University. Retrieved from http://hdl.rutgers.edu/1782.2/rucore10001600001.ETD.000051419

Chicago Manual of Style (16th Edition):

Wilimczyk, Barbara J. “Continuous expression of metabotropic glutamate receptor 1 is required for maintenance of tumorigenesis in GRM1 transformed mouse kidney epithelial cells.” 2009. Masters Thesis, Rutgers University. Accessed May 08, 2021. http://hdl.rutgers.edu/1782.2/rucore10001600001.ETD.000051419.

MLA Handbook (7th Edition):

Wilimczyk, Barbara J. “Continuous expression of metabotropic glutamate receptor 1 is required for maintenance of tumorigenesis in GRM1 transformed mouse kidney epithelial cells.” 2009. Web. 08 May 2021.

Vancouver:

Wilimczyk BJ. Continuous expression of metabotropic glutamate receptor 1 is required for maintenance of tumorigenesis in GRM1 transformed mouse kidney epithelial cells. [Internet] [Masters thesis]. Rutgers University; 2009. [cited 2021 May 08]. Available from: http://hdl.rutgers.edu/1782.2/rucore10001600001.ETD.000051419.

Council of Science Editors:

Wilimczyk BJ. Continuous expression of metabotropic glutamate receptor 1 is required for maintenance of tumorigenesis in GRM1 transformed mouse kidney epithelial cells. [Masters Thesis]. Rutgers University; 2009. Available from: http://hdl.rutgers.edu/1782.2/rucore10001600001.ETD.000051419


Rutgers University

23. Teh, Jessica, 1984-. Metabotropic glutamate receptor 1 in human malignancies.

Degree: Cell and Developmental Biology, 2013, Rutgers University

Subjects/Keywords: Glutamic acid; Cancer cells; Cancer – Research

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APA (6th Edition):

Teh, Jessica, 1. (2013). Metabotropic glutamate receptor 1 in human malignancies. (Thesis). Rutgers University. Retrieved from https://rucore.libraries.rutgers.edu/rutgers-lib/41934/

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):

Teh, Jessica, 1984-. “Metabotropic glutamate receptor 1 in human malignancies.” 2013. Thesis, Rutgers University. Accessed May 08, 2021. https://rucore.libraries.rutgers.edu/rutgers-lib/41934/.

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

MLA Handbook (7th Edition):

Teh, Jessica, 1984-. “Metabotropic glutamate receptor 1 in human malignancies.” 2013. Web. 08 May 2021.

Vancouver:

Teh, Jessica 1. Metabotropic glutamate receptor 1 in human malignancies. [Internet] [Thesis]. Rutgers University; 2013. [cited 2021 May 08]. Available from: https://rucore.libraries.rutgers.edu/rutgers-lib/41934/.

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

Council of Science Editors:

Teh, Jessica 1. Metabotropic glutamate receptor 1 in human malignancies. [Thesis]. Rutgers University; 2013. Available from: https://rucore.libraries.rutgers.edu/rutgers-lib/41934/

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


Rutgers University

24. Park, Hye-Jin. Identification of phosphorylation sites of TOPORS and a role for phosphorylated residues in the regulation of ubiquitin and SUMO E3 ligase activity:.

Degree: PhD, Pharmaceutical Science, 2008, Rutgers University

TOPORS is the first example of a protein that possesses both ubiquitin and SUMO E3 ligase activity. The ubiquitination activity maps to a conserved RING… (more)

Subjects/Keywords: DNA topoisomerases; Phosphorylation; Ubiquitin; Ligases

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APA (6th Edition):

Park, H. (2008). Identification of phosphorylation sites of TOPORS and a role for phosphorylated residues in the regulation of ubiquitin and SUMO E3 ligase activity:. (Doctoral Dissertation). Rutgers University. Retrieved from http://hdl.rutgers.edu/1782.2/rucore10001600001.ETD.000051763

Chicago Manual of Style (16th Edition):

Park, Hye-Jin. “Identification of phosphorylation sites of TOPORS and a role for phosphorylated residues in the regulation of ubiquitin and SUMO E3 ligase activity:.” 2008. Doctoral Dissertation, Rutgers University. Accessed May 08, 2021. http://hdl.rutgers.edu/1782.2/rucore10001600001.ETD.000051763.

MLA Handbook (7th Edition):

Park, Hye-Jin. “Identification of phosphorylation sites of TOPORS and a role for phosphorylated residues in the regulation of ubiquitin and SUMO E3 ligase activity:.” 2008. Web. 08 May 2021.

Vancouver:

Park H. Identification of phosphorylation sites of TOPORS and a role for phosphorylated residues in the regulation of ubiquitin and SUMO E3 ligase activity:. [Internet] [Doctoral dissertation]. Rutgers University; 2008. [cited 2021 May 08]. Available from: http://hdl.rutgers.edu/1782.2/rucore10001600001.ETD.000051763.

Council of Science Editors:

Park H. Identification of phosphorylation sites of TOPORS and a role for phosphorylated residues in the regulation of ubiquitin and SUMO E3 ligase activity:. [Doctoral Dissertation]. Rutgers University; 2008. Available from: http://hdl.rutgers.edu/1782.2/rucore10001600001.ETD.000051763


Rutgers University

25. Lee, Hangnoh, 1979-. Regulation of differentiation-specific genes by the Drosophila RB, E2F, and Myb-interacting proteins complex (dREAM).

Degree: Cell and Developmental Biology, 2011, Rutgers University

Subjects/Keywords: Cell cycle—Regulation

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APA (6th Edition):

Lee, Hangnoh, 1. (2011). Regulation of differentiation-specific genes by the Drosophila RB, E2F, and Myb-interacting proteins complex (dREAM). (Thesis). Rutgers University. Retrieved from http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000063512

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

Chicago Manual of Style (16th Edition):

Lee, Hangnoh, 1979-. “Regulation of differentiation-specific genes by the Drosophila RB, E2F, and Myb-interacting proteins complex (dREAM).” 2011. Thesis, Rutgers University. Accessed May 08, 2021. http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000063512.

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

MLA Handbook (7th Edition):

Lee, Hangnoh, 1979-. “Regulation of differentiation-specific genes by the Drosophila RB, E2F, and Myb-interacting proteins complex (dREAM).” 2011. Web. 08 May 2021.

Vancouver:

Lee, Hangnoh 1. Regulation of differentiation-specific genes by the Drosophila RB, E2F, and Myb-interacting proteins complex (dREAM). [Internet] [Thesis]. Rutgers University; 2011. [cited 2021 May 08]. Available from: http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000063512.

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

Council of Science Editors:

Lee, Hangnoh 1. Regulation of differentiation-specific genes by the Drosophila RB, E2F, and Myb-interacting proteins complex (dREAM). [Thesis]. Rutgers University; 2011. Available from: http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000063512

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


Rutgers University

26. Liu, Yingying. The role of Pak4 in tumorigenesis in vivo.

Degree: PhD, Pharmacology, Cellular and Molecular, 2010, Rutgers University

The Pak4 (P21 activated kinase) serine/threonine kinase is an important effector of Rho GTPases and has been implicated in the regulation of cell morphology and… (more)

Subjects/Keywords: Carcinogenesis; Cells – Morphology; Nude mouse – Research

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APA (6th Edition):

Liu, Y. (2010). The role of Pak4 in tumorigenesis in vivo. (Doctoral Dissertation). Rutgers University. Retrieved from http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000056516

Chicago Manual of Style (16th Edition):

Liu, Yingying. “The role of Pak4 in tumorigenesis in vivo.” 2010. Doctoral Dissertation, Rutgers University. Accessed May 08, 2021. http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000056516.

MLA Handbook (7th Edition):

Liu, Yingying. “The role of Pak4 in tumorigenesis in vivo.” 2010. Web. 08 May 2021.

Vancouver:

Liu Y. The role of Pak4 in tumorigenesis in vivo. [Internet] [Doctoral dissertation]. Rutgers University; 2010. [cited 2021 May 08]. Available from: http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000056516.

Council of Science Editors:

Liu Y. The role of Pak4 in tumorigenesis in vivo. [Doctoral Dissertation]. Rutgers University; 2010. Available from: http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000056516


Rutgers University

27. Lee, Hong Jin. Vitamin D-mediated suppression of mammary tumorigenesis and mechanism of action:.

Degree: PhD, Food Science, 2008, Rutgers University

Numerous preclinical, epidemiological and clinical studies with vitamin D and analogs have suggested the benefits of vitamin D and analogs for prevention and treatment of… (more)

Subjects/Keywords: Breast – Cancer – Treatment; Breast – Cancer – Prevention; Vitamin D – Therapeutic use

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

APA (6th Edition):

Lee, H. J. (2008). Vitamin D-mediated suppression of mammary tumorigenesis and mechanism of action:. (Doctoral Dissertation). Rutgers University. Retrieved from http://hdl.rutgers.edu/1782.2/rucore10001600001.ETD.000051764

Chicago Manual of Style (16th Edition):

Lee, Hong Jin. “Vitamin D-mediated suppression of mammary tumorigenesis and mechanism of action:.” 2008. Doctoral Dissertation, Rutgers University. Accessed May 08, 2021. http://hdl.rutgers.edu/1782.2/rucore10001600001.ETD.000051764.

MLA Handbook (7th Edition):

Lee, Hong Jin. “Vitamin D-mediated suppression of mammary tumorigenesis and mechanism of action:.” 2008. Web. 08 May 2021.

Vancouver:

Lee HJ. Vitamin D-mediated suppression of mammary tumorigenesis and mechanism of action:. [Internet] [Doctoral dissertation]. Rutgers University; 2008. [cited 2021 May 08]. Available from: http://hdl.rutgers.edu/1782.2/rucore10001600001.ETD.000051764.

Council of Science Editors:

Lee HJ. Vitamin D-mediated suppression of mammary tumorigenesis and mechanism of action:. [Doctoral Dissertation]. Rutgers University; 2008. Available from: http://hdl.rutgers.edu/1782.2/rucore10001600001.ETD.000051764


Rutgers University

28. Cheung, Ka Lung. NRF2 and chemoprevention: signaling, epigenetics and role in intestinal carcinogensis.

Degree: PhD, Pharmaceutical Science, 2011, Rutgers University

Prevention is better than cure. The carcinogenesis could take as long as 20 to 30 years to develop from initiated cells to malignant tumor, therefore… (more)

Subjects/Keywords: Cancer – Chemoprevention

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APA (6th Edition):

Cheung, K. L. (2011). NRF2 and chemoprevention: signaling, epigenetics and role in intestinal carcinogensis. (Doctoral Dissertation). Rutgers University. Retrieved from http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000061171

Chicago Manual of Style (16th Edition):

Cheung, Ka Lung. “NRF2 and chemoprevention: signaling, epigenetics and role in intestinal carcinogensis.” 2011. Doctoral Dissertation, Rutgers University. Accessed May 08, 2021. http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000061171.

MLA Handbook (7th Edition):

Cheung, Ka Lung. “NRF2 and chemoprevention: signaling, epigenetics and role in intestinal carcinogensis.” 2011. Web. 08 May 2021.

Vancouver:

Cheung KL. NRF2 and chemoprevention: signaling, epigenetics and role in intestinal carcinogensis. [Internet] [Doctoral dissertation]. Rutgers University; 2011. [cited 2021 May 08]. Available from: http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000061171.

Council of Science Editors:

Cheung KL. NRF2 and chemoprevention: signaling, epigenetics and role in intestinal carcinogensis. [Doctoral Dissertation]. Rutgers University; 2011. Available from: http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000061171


Rutgers University

29. Rodrigues, Andrea DeSantis, 1982-. Countermeasures against vesicant-induced epithelial de-adhesion in the cornea.

Degree: Toxicology, 2011, Rutgers University

Subjects/Keywords: Mustard gas; Cornea—Ulcers; Cornea—Diseases – Treatment

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APA (6th Edition):

Rodrigues, Andrea DeSantis, 1. (2011). Countermeasures against vesicant-induced epithelial de-adhesion in the cornea. (Thesis). Rutgers University. Retrieved from http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000063583

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):

Rodrigues, Andrea DeSantis, 1982-. “Countermeasures against vesicant-induced epithelial de-adhesion in the cornea.” 2011. Thesis, Rutgers University. Accessed May 08, 2021. http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000063583.

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

MLA Handbook (7th Edition):

Rodrigues, Andrea DeSantis, 1982-. “Countermeasures against vesicant-induced epithelial de-adhesion in the cornea.” 2011. Web. 08 May 2021.

Vancouver:

Rodrigues, Andrea DeSantis 1. Countermeasures against vesicant-induced epithelial de-adhesion in the cornea. [Internet] [Thesis]. Rutgers University; 2011. [cited 2021 May 08]. Available from: http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000063583.

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

Council of Science Editors:

Rodrigues, Andrea DeSantis 1. Countermeasures against vesicant-induced epithelial de-adhesion in the cornea. [Thesis]. Rutgers University; 2011. Available from: http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000063583

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

.