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You searched for +publisher:"Penn State University" +contributor:("Jin Ming Yang, Committee Member"). Showing records 1 – 9 of 9 total matches.

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Penn State University

1. Kardos, Gregory Robert. Therapeutic utility of targeting protein synthetic machinery in melanoma.

Degree: 2014, Penn State University

 Malignant melanoma is a cancer with few treatment options and thus, a very poor prognosis. Targeted therapies directed at commonly over-activated signaling pathways in melanoma… (more)

Subjects/Keywords: melanoma; RPL13; ALDH18A1; ribosome; proline; nanoliposome; protein synthesis; P5CS; GCN2; eIF2alpha

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

APA (6th Edition):

Kardos, G. R. (2014). Therapeutic utility of targeting protein synthetic machinery in melanoma. (Thesis). Penn State University. Retrieved from https://submit-etda.libraries.psu.edu/catalog/23537

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):

Kardos, Gregory Robert. “Therapeutic utility of targeting protein synthetic machinery in melanoma.” 2014. Thesis, Penn State University. Accessed April 16, 2021. https://submit-etda.libraries.psu.edu/catalog/23537.

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

MLA Handbook (7th Edition):

Kardos, Gregory Robert. “Therapeutic utility of targeting protein synthetic machinery in melanoma.” 2014. Web. 16 Apr 2021.

Vancouver:

Kardos GR. Therapeutic utility of targeting protein synthetic machinery in melanoma. [Internet] [Thesis]. Penn State University; 2014. [cited 2021 Apr 16]. Available from: https://submit-etda.libraries.psu.edu/catalog/23537.

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

Council of Science Editors:

Kardos GR. Therapeutic utility of targeting protein synthetic machinery in melanoma. [Thesis]. Penn State University; 2014. Available from: https://submit-etda.libraries.psu.edu/catalog/23537

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


Penn State University

2. Kuzu, Omer Faruk. Lysosomotropic Cholesterol Transport Inhibitors as Potential Chemotherapeutic Agents .

Degree: 2014, Penn State University

 According to American Cancer Society’s 2014 Cancer Facts report, cancer is the second leading cause of death in United States and over half million people… (more)

Subjects/Keywords: Melanoma; tricyclic antidepressant; antipsychotic; FIASMA; lysosomotropic; intracellular cholesterol transport inhibitor

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APA (6th Edition):

Kuzu, O. F. (2014). Lysosomotropic Cholesterol Transport Inhibitors as Potential Chemotherapeutic Agents . (Thesis). Penn State University. Retrieved from https://submit-etda.libraries.psu.edu/catalog/23545

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):

Kuzu, Omer Faruk. “Lysosomotropic Cholesterol Transport Inhibitors as Potential Chemotherapeutic Agents .” 2014. Thesis, Penn State University. Accessed April 16, 2021. https://submit-etda.libraries.psu.edu/catalog/23545.

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

MLA Handbook (7th Edition):

Kuzu, Omer Faruk. “Lysosomotropic Cholesterol Transport Inhibitors as Potential Chemotherapeutic Agents .” 2014. Web. 16 Apr 2021.

Vancouver:

Kuzu OF. Lysosomotropic Cholesterol Transport Inhibitors as Potential Chemotherapeutic Agents . [Internet] [Thesis]. Penn State University; 2014. [cited 2021 Apr 16]. Available from: https://submit-etda.libraries.psu.edu/catalog/23545.

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

Council of Science Editors:

Kuzu OF. Lysosomotropic Cholesterol Transport Inhibitors as Potential Chemotherapeutic Agents . [Thesis]. Penn State University; 2014. Available from: https://submit-etda.libraries.psu.edu/catalog/23545

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


Penn State University

3. Lulla, Amriti R. miRNAs AS THERAPEUTICS TO TARGET CELL CYCLE PROGRESSION AND PROMOTE CELL DEATH IN CANCER CELLS.

Degree: 2018, Penn State University

 Mature MicroRNAs (miRNAs) are ~22 nt endogenous, non-coding RNA sequences that bind to the 3’UTR of target genes and inhibit their translation. miRNA expression is… (more)

Subjects/Keywords: miRNA therapeutics CDK4 cell cycle apoptosis TRAIL High-throughput screening

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APA (6th Edition):

Lulla, A. R. (2018). miRNAs AS THERAPEUTICS TO TARGET CELL CYCLE PROGRESSION AND PROMOTE CELL DEATH IN CANCER CELLS. (Thesis). Penn State University. Retrieved from https://submit-etda.libraries.psu.edu/catalog/15216arl189

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):

Lulla, Amriti R. “miRNAs AS THERAPEUTICS TO TARGET CELL CYCLE PROGRESSION AND PROMOTE CELL DEATH IN CANCER CELLS.” 2018. Thesis, Penn State University. Accessed April 16, 2021. https://submit-etda.libraries.psu.edu/catalog/15216arl189.

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

MLA Handbook (7th Edition):

Lulla, Amriti R. “miRNAs AS THERAPEUTICS TO TARGET CELL CYCLE PROGRESSION AND PROMOTE CELL DEATH IN CANCER CELLS.” 2018. Web. 16 Apr 2021.

Vancouver:

Lulla AR. miRNAs AS THERAPEUTICS TO TARGET CELL CYCLE PROGRESSION AND PROMOTE CELL DEATH IN CANCER CELLS. [Internet] [Thesis]. Penn State University; 2018. [cited 2021 Apr 16]. Available from: https://submit-etda.libraries.psu.edu/catalog/15216arl189.

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

Council of Science Editors:

Lulla AR. miRNAs AS THERAPEUTICS TO TARGET CELL CYCLE PROGRESSION AND PROMOTE CELL DEATH IN CANCER CELLS. [Thesis]. Penn State University; 2018. Available from: https://submit-etda.libraries.psu.edu/catalog/15216arl189

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


Penn State University

4. Gokare, Prashanth Ravishankar. Differential p53 signaling in response to 5-FU and Etoposide in modulating toxicity via DPYD and Chk2 in cancer therapy.

Degree: 2017, Penn State University

 Tp53 is a major transcription factor that controls a multitude of processes involved in the response to cellular stress. It plays a critical role in… (more)

Subjects/Keywords: DPYD; p53; 5-FU; chemotherapeutic; toxicity; DNA damage; Chk2; etoposide; metabolism

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APA (6th Edition):

Gokare, P. R. (2017). Differential p53 signaling in response to 5-FU and Etoposide in modulating toxicity via DPYD and Chk2 in cancer therapy. (Thesis). Penn State University. Retrieved from https://submit-etda.libraries.psu.edu/catalog/14233pug125

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):

Gokare, Prashanth Ravishankar. “Differential p53 signaling in response to 5-FU and Etoposide in modulating toxicity via DPYD and Chk2 in cancer therapy.” 2017. Thesis, Penn State University. Accessed April 16, 2021. https://submit-etda.libraries.psu.edu/catalog/14233pug125.

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

MLA Handbook (7th Edition):

Gokare, Prashanth Ravishankar. “Differential p53 signaling in response to 5-FU and Etoposide in modulating toxicity via DPYD and Chk2 in cancer therapy.” 2017. Web. 16 Apr 2021.

Vancouver:

Gokare PR. Differential p53 signaling in response to 5-FU and Etoposide in modulating toxicity via DPYD and Chk2 in cancer therapy. [Internet] [Thesis]. Penn State University; 2017. [cited 2021 Apr 16]. Available from: https://submit-etda.libraries.psu.edu/catalog/14233pug125.

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

Council of Science Editors:

Gokare PR. Differential p53 signaling in response to 5-FU and Etoposide in modulating toxicity via DPYD and Chk2 in cancer therapy. [Thesis]. Penn State University; 2017. Available from: https://submit-etda.libraries.psu.edu/catalog/14233pug125

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


Penn State University

5. Ryland, Lindsay Kate. DIFFERENTIAL MECHANISMS OF CELL DEATH INDUCTION VIA DELIVERY OF THERAPEUTIC NANOLIPOSOMAL CERAMIDE IN LEUKEMIAS .

Degree: 2011, Penn State University

 Large granular lymphocyte (LGL) leukemia is a rare lymphoproliferative malignancy that involves blood, bone marrow and spleen infiltration. Clinically, LGL leukemia can manifest as a… (more)

Subjects/Keywords: sphingolipid; ceramide; nanoliposome; chronic lymphocytic leukemia

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APA (6th Edition):

Ryland, L. K. (2011). DIFFERENTIAL MECHANISMS OF CELL DEATH INDUCTION VIA DELIVERY OF THERAPEUTIC NANOLIPOSOMAL CERAMIDE IN LEUKEMIAS . (Thesis). Penn State University. Retrieved from https://submit-etda.libraries.psu.edu/catalog/12511

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):

Ryland, Lindsay Kate. “DIFFERENTIAL MECHANISMS OF CELL DEATH INDUCTION VIA DELIVERY OF THERAPEUTIC NANOLIPOSOMAL CERAMIDE IN LEUKEMIAS .” 2011. Thesis, Penn State University. Accessed April 16, 2021. https://submit-etda.libraries.psu.edu/catalog/12511.

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

MLA Handbook (7th Edition):

Ryland, Lindsay Kate. “DIFFERENTIAL MECHANISMS OF CELL DEATH INDUCTION VIA DELIVERY OF THERAPEUTIC NANOLIPOSOMAL CERAMIDE IN LEUKEMIAS .” 2011. Web. 16 Apr 2021.

Vancouver:

Ryland LK. DIFFERENTIAL MECHANISMS OF CELL DEATH INDUCTION VIA DELIVERY OF THERAPEUTIC NANOLIPOSOMAL CERAMIDE IN LEUKEMIAS . [Internet] [Thesis]. Penn State University; 2011. [cited 2021 Apr 16]. Available from: https://submit-etda.libraries.psu.edu/catalog/12511.

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

Council of Science Editors:

Ryland LK. DIFFERENTIAL MECHANISMS OF CELL DEATH INDUCTION VIA DELIVERY OF THERAPEUTIC NANOLIPOSOMAL CERAMIDE IN LEUKEMIAS . [Thesis]. Penn State University; 2011. Available from: https://submit-etda.libraries.psu.edu/catalog/12511

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


Penn State University

6. Young, Megan Marie. The Role Of Sphingosine Kinase In The Crosstalk Between Apoptosis, Autophagy And Endocytosis.

Degree: 2015, Penn State University

 Autophagy is a catabolic process in which cytoplasmic components are sequestered within double-membrane vesicles called autophagosomes and delivered to lysosomes for degradation and recycling. Autophagy… (more)

Subjects/Keywords: autophagy; apoptosis; endocytosis; iDISC; sphingosine kinase; sphingosine; sphingolipid; SK1i; SKI-I; late endosome

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APA (6th Edition):

Young, M. M. (2015). The Role Of Sphingosine Kinase In The Crosstalk Between Apoptosis, Autophagy And Endocytosis. (Thesis). Penn State University. Retrieved from https://submit-etda.libraries.psu.edu/catalog/27408

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):

Young, Megan Marie. “The Role Of Sphingosine Kinase In The Crosstalk Between Apoptosis, Autophagy And Endocytosis.” 2015. Thesis, Penn State University. Accessed April 16, 2021. https://submit-etda.libraries.psu.edu/catalog/27408.

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

MLA Handbook (7th Edition):

Young, Megan Marie. “The Role Of Sphingosine Kinase In The Crosstalk Between Apoptosis, Autophagy And Endocytosis.” 2015. Web. 16 Apr 2021.

Vancouver:

Young MM. The Role Of Sphingosine Kinase In The Crosstalk Between Apoptosis, Autophagy And Endocytosis. [Internet] [Thesis]. Penn State University; 2015. [cited 2021 Apr 16]. Available from: https://submit-etda.libraries.psu.edu/catalog/27408.

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

Council of Science Editors:

Young MM. The Role Of Sphingosine Kinase In The Crosstalk Between Apoptosis, Autophagy And Endocytosis. [Thesis]. Penn State University; 2015. Available from: https://submit-etda.libraries.psu.edu/catalog/27408

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


Penn State University

7. Alibhoy, Abbas Abizar. Characterization of the Functions of VID30 and VPS34 in the Vacuole Import and Degradation Pathway.

Degree: 2012, Penn State University

 Glucose deprivation induces the synthesis of gluconeogenic enzymes such as fructose-1,6-bisphosphatase (FBPase), malate dehydrogenase (MDH2), phosphoenolpyruvate carboxykinase (Pck1p) and isocitrate lyase (Icl1p) in Saccharomyces cerevisiae.… (more)

Subjects/Keywords: Autophagy; Gluconeogenesis; Vacuole Import and Degradation; Actin; VPS34; VID30

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APA (6th Edition):

Alibhoy, A. A. (2012). Characterization of the Functions of VID30 and VPS34 in the Vacuole Import and Degradation Pathway. (Thesis). Penn State University. Retrieved from https://submit-etda.libraries.psu.edu/catalog/15233

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):

Alibhoy, Abbas Abizar. “Characterization of the Functions of VID30 and VPS34 in the Vacuole Import and Degradation Pathway.” 2012. Thesis, Penn State University. Accessed April 16, 2021. https://submit-etda.libraries.psu.edu/catalog/15233.

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

MLA Handbook (7th Edition):

Alibhoy, Abbas Abizar. “Characterization of the Functions of VID30 and VPS34 in the Vacuole Import and Degradation Pathway.” 2012. Web. 16 Apr 2021.

Vancouver:

Alibhoy AA. Characterization of the Functions of VID30 and VPS34 in the Vacuole Import and Degradation Pathway. [Internet] [Thesis]. Penn State University; 2012. [cited 2021 Apr 16]. Available from: https://submit-etda.libraries.psu.edu/catalog/15233.

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

Council of Science Editors:

Alibhoy AA. Characterization of the Functions of VID30 and VPS34 in the Vacuole Import and Degradation Pathway. [Thesis]. Penn State University; 2012. Available from: https://submit-etda.libraries.psu.edu/catalog/15233

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


Penn State University

8. Runkle, Kristin Beth. Bif-1 Regulates EGFR Endocytosis and Chemotactic Cell Migration in Breast Cancer.

Degree: 2012, Penn State University

 Epidermal growth factor receptor (EGFR) expression and perpetual signaling are well documented as contributing factors to disease progression and metastasis in several types of cancer… (more)

Subjects/Keywords: EGFR; Endocytosis; Cell Migration; Breast Cancer; Bif-1; Rab7

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APA (6th Edition):

Runkle, K. B. (2012). Bif-1 Regulates EGFR Endocytosis and Chemotactic Cell Migration in Breast Cancer. (Thesis). Penn State University. Retrieved from https://submit-etda.libraries.psu.edu/catalog/15551

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):

Runkle, Kristin Beth. “Bif-1 Regulates EGFR Endocytosis and Chemotactic Cell Migration in Breast Cancer.” 2012. Thesis, Penn State University. Accessed April 16, 2021. https://submit-etda.libraries.psu.edu/catalog/15551.

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

MLA Handbook (7th Edition):

Runkle, Kristin Beth. “Bif-1 Regulates EGFR Endocytosis and Chemotactic Cell Migration in Breast Cancer.” 2012. Web. 16 Apr 2021.

Vancouver:

Runkle KB. Bif-1 Regulates EGFR Endocytosis and Chemotactic Cell Migration in Breast Cancer. [Internet] [Thesis]. Penn State University; 2012. [cited 2021 Apr 16]. Available from: https://submit-etda.libraries.psu.edu/catalog/15551.

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

Council of Science Editors:

Runkle KB. Bif-1 Regulates EGFR Endocytosis and Chemotactic Cell Migration in Breast Cancer. [Thesis]. Penn State University; 2012. Available from: https://submit-etda.libraries.psu.edu/catalog/15551

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


Penn State University

9. Tan, Su-fern. Role of Acid Ceramidase in Regulating Survival and Drug Resistance in Acute Myeloid Leukemia.

Degree: 2013, Penn State University

 Acute myeloid leukemia (AML) is a heterogeneous disease that affects the differentiation of myeloid precursors. In normal hematopoiesis, hematopoietic stem cells committed to the myeloid… (more)

Subjects/Keywords: AML; Acid Ceramidase; Mcl-1; P-glycoprotein; NF-kB; sphingolipids

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

APA (6th Edition):

Tan, S. (2013). Role of Acid Ceramidase in Regulating Survival and Drug Resistance in Acute Myeloid Leukemia. (Thesis). Penn State University. Retrieved from https://submit-etda.libraries.psu.edu/catalog/19626

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):

Tan, Su-fern. “Role of Acid Ceramidase in Regulating Survival and Drug Resistance in Acute Myeloid Leukemia.” 2013. Thesis, Penn State University. Accessed April 16, 2021. https://submit-etda.libraries.psu.edu/catalog/19626.

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

MLA Handbook (7th Edition):

Tan, Su-fern. “Role of Acid Ceramidase in Regulating Survival and Drug Resistance in Acute Myeloid Leukemia.” 2013. Web. 16 Apr 2021.

Vancouver:

Tan S. Role of Acid Ceramidase in Regulating Survival and Drug Resistance in Acute Myeloid Leukemia. [Internet] [Thesis]. Penn State University; 2013. [cited 2021 Apr 16]. Available from: https://submit-etda.libraries.psu.edu/catalog/19626.

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

Council of Science Editors:

Tan S. Role of Acid Ceramidase in Regulating Survival and Drug Resistance in Acute Myeloid Leukemia. [Thesis]. Penn State University; 2013. Available from: https://submit-etda.libraries.psu.edu/catalog/19626

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

.