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You searched for +publisher:"Penn State University" +contributor:("Jong Kak Yun, Committee Member"). Showing records 1 – 21 of 21 total matches.

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Penn State University

1. Ali-rahmani, Fatima Ghazanfar. HFE GENE VARIANTS AND DYSREGULATION OF CHOLESTEROL AND IRON METABOLISM IN ALZHEIMER DISEASE AND CANCER.

Degree: 2012, Penn State University

 Cholesterol and iron are essential for a number of cellular processes. Disruption of both cholesterol and iron metabolism have been independently reported to contribute to… (more)

Subjects/Keywords: Iron; HFE; Cholesterol; Alzheimer disease; Cancer; mouse model

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APA (6th Edition):

Ali-rahmani, F. G. (2012). HFE GENE VARIANTS AND DYSREGULATION OF CHOLESTEROL AND IRON METABOLISM IN ALZHEIMER DISEASE AND CANCER. (Thesis). Penn State University. Retrieved from https://submit-etda.libraries.psu.edu/catalog/16178

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):

Ali-rahmani, Fatima Ghazanfar. “HFE GENE VARIANTS AND DYSREGULATION OF CHOLESTEROL AND IRON METABOLISM IN ALZHEIMER DISEASE AND CANCER.” 2012. Thesis, Penn State University. Accessed April 16, 2021. https://submit-etda.libraries.psu.edu/catalog/16178.

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

MLA Handbook (7th Edition):

Ali-rahmani, Fatima Ghazanfar. “HFE GENE VARIANTS AND DYSREGULATION OF CHOLESTEROL AND IRON METABOLISM IN ALZHEIMER DISEASE AND CANCER.” 2012. Web. 16 Apr 2021.

Vancouver:

Ali-rahmani FG. HFE GENE VARIANTS AND DYSREGULATION OF CHOLESTEROL AND IRON METABOLISM IN ALZHEIMER DISEASE AND CANCER. [Internet] [Thesis]. Penn State University; 2012. [cited 2021 Apr 16]. Available from: https://submit-etda.libraries.psu.edu/catalog/16178.

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

Council of Science Editors:

Ali-rahmani FG. HFE GENE VARIANTS AND DYSREGULATION OF CHOLESTEROL AND IRON METABOLISM IN ALZHEIMER DISEASE AND CANCER. [Thesis]. Penn State University; 2012. Available from: https://submit-etda.libraries.psu.edu/catalog/16178

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


Penn State University

2. Karelia, Deepkamal Nilkamal. DISCOVERY OF NOVEL Se-ASPIRIN MOLECULES AS POTENTIAL THERAPEUTICS FOR GASTROINTESTINAL CANCERS.

Degree: 2016, Penn State University

 In today’s era there have been a lot of advances in cancer screening, surgery, and chemotherapy, however, gastrointestinal (GI) cancer remains the second leading cause… (more)

Subjects/Keywords: Pancreatic cancer; colorectal cancer; small molecule; NSAIDs; apoptotsis; inflammatory pathways; selenium; aspirin; cell cycle; MTT; EMSA; Panc-1

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APA (6th Edition):

Karelia, D. N. (2016). DISCOVERY OF NOVEL Se-ASPIRIN MOLECULES AS POTENTIAL THERAPEUTICS FOR GASTROINTESTINAL CANCERS. (Thesis). Penn State University. Retrieved from https://submit-etda.libraries.psu.edu/catalog/z603qx40z

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):

Karelia, Deepkamal Nilkamal. “DISCOVERY OF NOVEL Se-ASPIRIN MOLECULES AS POTENTIAL THERAPEUTICS FOR GASTROINTESTINAL CANCERS.” 2016. Thesis, Penn State University. Accessed April 16, 2021. https://submit-etda.libraries.psu.edu/catalog/z603qx40z.

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

MLA Handbook (7th Edition):

Karelia, Deepkamal Nilkamal. “DISCOVERY OF NOVEL Se-ASPIRIN MOLECULES AS POTENTIAL THERAPEUTICS FOR GASTROINTESTINAL CANCERS.” 2016. Web. 16 Apr 2021.

Vancouver:

Karelia DN. DISCOVERY OF NOVEL Se-ASPIRIN MOLECULES AS POTENTIAL THERAPEUTICS FOR GASTROINTESTINAL CANCERS. [Internet] [Thesis]. Penn State University; 2016. [cited 2021 Apr 16]. Available from: https://submit-etda.libraries.psu.edu/catalog/z603qx40z.

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

Council of Science Editors:

Karelia DN. DISCOVERY OF NOVEL Se-ASPIRIN MOLECULES AS POTENTIAL THERAPEUTICS FOR GASTROINTESTINAL CANCERS. [Thesis]. Penn State University; 2016. Available from: https://submit-etda.libraries.psu.edu/catalog/z603qx40z

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


Penn State University

3. Steffens, Sadie Lynne. Mechanism of Drug Action of the Specific Ck2 Inhibitor Cx-4945 in Acute Myeloid Leukemia.

Degree: 2015, Penn State University

 Acute myeloid leukemia (AML) is a malignant disease of the myeloid line of blood cells and is characterized by the rapid growth of abnormal white… (more)

Subjects/Keywords: Ikaros; CK2; AML; drug resistance; BCL2A1; MTHFR; CDA; DLX1; DLX2; cytarabine; methotrexate; doxorubicin

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APA (6th Edition):

Steffens, S. L. (2015). Mechanism of Drug Action of the Specific Ck2 Inhibitor Cx-4945 in Acute Myeloid Leukemia. (Thesis). Penn State University. Retrieved from https://submit-etda.libraries.psu.edu/catalog/27412

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):

Steffens, Sadie Lynne. “Mechanism of Drug Action of the Specific Ck2 Inhibitor Cx-4945 in Acute Myeloid Leukemia.” 2015. Thesis, Penn State University. Accessed April 16, 2021. https://submit-etda.libraries.psu.edu/catalog/27412.

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

MLA Handbook (7th Edition):

Steffens, Sadie Lynne. “Mechanism of Drug Action of the Specific Ck2 Inhibitor Cx-4945 in Acute Myeloid Leukemia.” 2015. Web. 16 Apr 2021.

Vancouver:

Steffens SL. Mechanism of Drug Action of the Specific Ck2 Inhibitor Cx-4945 in Acute Myeloid Leukemia. [Internet] [Thesis]. Penn State University; 2015. [cited 2021 Apr 16]. Available from: https://submit-etda.libraries.psu.edu/catalog/27412.

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

Council of Science Editors:

Steffens SL. Mechanism of Drug Action of the Specific Ck2 Inhibitor Cx-4945 in Acute Myeloid Leukemia. [Thesis]. Penn State University; 2015. Available from: https://submit-etda.libraries.psu.edu/catalog/27412

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


Penn State University

4. Mrowczynski, Oliver D. Exosomes and their Implications in Glioblastoma.

Degree: 2018, Penn State University

 Exosomes are 20-100 nm cellular derived vesicles that when discovered, were initially thought to be a form of cellular recycling of intracellular contents. More recently,… (more)

Subjects/Keywords: exosomes; glioblastoma; radiation; glioma stem cell; neuroblastoma; HFE

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APA (6th Edition):

Mrowczynski, O. D. (2018). Exosomes and their Implications in Glioblastoma. (Thesis). Penn State University. Retrieved from https://submit-etda.libraries.psu.edu/catalog/14783odm102

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):

Mrowczynski, Oliver D. “Exosomes and their Implications in Glioblastoma.” 2018. Thesis, Penn State University. Accessed April 16, 2021. https://submit-etda.libraries.psu.edu/catalog/14783odm102.

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

MLA Handbook (7th Edition):

Mrowczynski, Oliver D. “Exosomes and their Implications in Glioblastoma.” 2018. Web. 16 Apr 2021.

Vancouver:

Mrowczynski OD. Exosomes and their Implications in Glioblastoma. [Internet] [Thesis]. Penn State University; 2018. [cited 2021 Apr 16]. Available from: https://submit-etda.libraries.psu.edu/catalog/14783odm102.

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

Council of Science Editors:

Mrowczynski OD. Exosomes and their Implications in Glioblastoma. [Thesis]. Penn State University; 2018. Available from: https://submit-etda.libraries.psu.edu/catalog/14783odm102

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


Penn State University

5. Weinberg, Rebecca Bronwyn. INFLAMMATORY CYTOKINE RESPONSES TO MALARIA PARASITE GLYCOSYLPHOSPHATIDYLINOSITOLS.

Degree: 2011, Penn State University

 Inflammatory cytokine responses play an important role in the pathogenesis of malaria. Glycosylphosphatidylinositols (GPIs) of Plasmodium falciparum are a key component in the recognition of… (more)

Subjects/Keywords: malaria; innate immunity; cytokines; signal transduction; macrophages

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APA (6th Edition):

Weinberg, R. B. (2011). INFLAMMATORY CYTOKINE RESPONSES TO MALARIA PARASITE GLYCOSYLPHOSPHATIDYLINOSITOLS. (Thesis). Penn State University. Retrieved from https://submit-etda.libraries.psu.edu/catalog/12166

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):

Weinberg, Rebecca Bronwyn. “INFLAMMATORY CYTOKINE RESPONSES TO MALARIA PARASITE GLYCOSYLPHOSPHATIDYLINOSITOLS.” 2011. Thesis, Penn State University. Accessed April 16, 2021. https://submit-etda.libraries.psu.edu/catalog/12166.

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

MLA Handbook (7th Edition):

Weinberg, Rebecca Bronwyn. “INFLAMMATORY CYTOKINE RESPONSES TO MALARIA PARASITE GLYCOSYLPHOSPHATIDYLINOSITOLS.” 2011. Web. 16 Apr 2021.

Vancouver:

Weinberg RB. INFLAMMATORY CYTOKINE RESPONSES TO MALARIA PARASITE GLYCOSYLPHOSPHATIDYLINOSITOLS. [Internet] [Thesis]. Penn State University; 2011. [cited 2021 Apr 16]. Available from: https://submit-etda.libraries.psu.edu/catalog/12166.

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

Council of Science Editors:

Weinberg RB. INFLAMMATORY CYTOKINE RESPONSES TO MALARIA PARASITE GLYCOSYLPHOSPHATIDYLINOSITOLS. [Thesis]. Penn State University; 2011. Available from: https://submit-etda.libraries.psu.edu/catalog/12166

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


Penn State University

6. Jones, Nathan Richard. Expression of uridinediphosphate glucuronosyltransferase genes: focus on alternative splicing and transcriptional regulatory mechanisms that contribute to interindividual differences in drug and carcinogen metabolism.

Degree: 2012, Penn State University

 There is a complex interplay between genetic and environmental factors that determine inter-individual differences in disease disposition and therapeutic response. Drug metabolism pathways have been… (more)

Subjects/Keywords: UDP-glucuronosyltransferase; expression; transcriptional regulation; alternative splicing; pharmacogenetics

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APA (6th Edition):

Jones, N. R. (2012). Expression of uridinediphosphate glucuronosyltransferase genes: focus on alternative splicing and transcriptional regulatory mechanisms that contribute to interindividual differences in drug and carcinogen metabolism. (Thesis). Penn State University. Retrieved from https://submit-etda.libraries.psu.edu/catalog/13184

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):

Jones, Nathan Richard. “Expression of uridinediphosphate glucuronosyltransferase genes: focus on alternative splicing and transcriptional regulatory mechanisms that contribute to interindividual differences in drug and carcinogen metabolism.” 2012. Thesis, Penn State University. Accessed April 16, 2021. https://submit-etda.libraries.psu.edu/catalog/13184.

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

MLA Handbook (7th Edition):

Jones, Nathan Richard. “Expression of uridinediphosphate glucuronosyltransferase genes: focus on alternative splicing and transcriptional regulatory mechanisms that contribute to interindividual differences in drug and carcinogen metabolism.” 2012. Web. 16 Apr 2021.

Vancouver:

Jones NR. Expression of uridinediphosphate glucuronosyltransferase genes: focus on alternative splicing and transcriptional regulatory mechanisms that contribute to interindividual differences in drug and carcinogen metabolism. [Internet] [Thesis]. Penn State University; 2012. [cited 2021 Apr 16]. Available from: https://submit-etda.libraries.psu.edu/catalog/13184.

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

Council of Science Editors:

Jones NR. Expression of uridinediphosphate glucuronosyltransferase genes: focus on alternative splicing and transcriptional regulatory mechanisms that contribute to interindividual differences in drug and carcinogen metabolism. [Thesis]. Penn State University; 2012. Available from: https://submit-etda.libraries.psu.edu/catalog/13184

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


Penn State University

7. Lee, Brian D. Development and Characterization of P-glycoprotein specific Multidrug Resistance Modulators.

Degree: 2008, Penn State University

 Multidrug resistance (MDR) is a phenomenon by which tumor cells develop reduced sensitivity to anticancer drugs, which often leads to the failure of cancer chemotherapy.… (more)

Subjects/Keywords: P-glycoprotein; multidrug resistance; in vivo tumor model; actinomycin D transport

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APA (6th Edition):

Lee, B. D. (2008). Development and Characterization of P-glycoprotein specific Multidrug Resistance Modulators. (Thesis). Penn State University. Retrieved from https://submit-etda.libraries.psu.edu/catalog/6151

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, Brian D. “Development and Characterization of P-glycoprotein specific Multidrug Resistance Modulators.” 2008. Thesis, Penn State University. Accessed April 16, 2021. https://submit-etda.libraries.psu.edu/catalog/6151.

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

MLA Handbook (7th Edition):

Lee, Brian D. “Development and Characterization of P-glycoprotein specific Multidrug Resistance Modulators.” 2008. Web. 16 Apr 2021.

Vancouver:

Lee BD. Development and Characterization of P-glycoprotein specific Multidrug Resistance Modulators. [Internet] [Thesis]. Penn State University; 2008. [cited 2021 Apr 16]. Available from: https://submit-etda.libraries.psu.edu/catalog/6151.

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

Council of Science Editors:

Lee BD. Development and Characterization of P-glycoprotein specific Multidrug Resistance Modulators. [Thesis]. Penn State University; 2008. Available from: https://submit-etda.libraries.psu.edu/catalog/6151

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


Penn State University

8. Stover, Thomas Christopher. THE DEVELOPMENT AND EVALUATION OF SYSTEMIC DRUG DELIVERY SYSTEMS FOR C6-CERAMIDE AS A BREAST CANCER CHEMOTHERAPEUTIC AGENT .

Degree: 2008, Penn State University

 Ceramide is a bioactive sphingolipid-derived second messenger that has been demonstrated to induce apoptosis and cell cycle arrest in various cancer cell culture systems. An… (more)

Subjects/Keywords: tumor; breast cancer; dendrimers; liposomes; drug delivery; Ceramide; pharmacokinetics

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APA (6th Edition):

Stover, T. C. (2008). THE DEVELOPMENT AND EVALUATION OF SYSTEMIC DRUG DELIVERY SYSTEMS FOR C6-CERAMIDE AS A BREAST CANCER CHEMOTHERAPEUTIC AGENT . (Thesis). Penn State University. Retrieved from https://submit-etda.libraries.psu.edu/catalog/6509

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):

Stover, Thomas Christopher. “THE DEVELOPMENT AND EVALUATION OF SYSTEMIC DRUG DELIVERY SYSTEMS FOR C6-CERAMIDE AS A BREAST CANCER CHEMOTHERAPEUTIC AGENT .” 2008. Thesis, Penn State University. Accessed April 16, 2021. https://submit-etda.libraries.psu.edu/catalog/6509.

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

MLA Handbook (7th Edition):

Stover, Thomas Christopher. “THE DEVELOPMENT AND EVALUATION OF SYSTEMIC DRUG DELIVERY SYSTEMS FOR C6-CERAMIDE AS A BREAST CANCER CHEMOTHERAPEUTIC AGENT .” 2008. Web. 16 Apr 2021.

Vancouver:

Stover TC. THE DEVELOPMENT AND EVALUATION OF SYSTEMIC DRUG DELIVERY SYSTEMS FOR C6-CERAMIDE AS A BREAST CANCER CHEMOTHERAPEUTIC AGENT . [Internet] [Thesis]. Penn State University; 2008. [cited 2021 Apr 16]. Available from: https://submit-etda.libraries.psu.edu/catalog/6509.

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

Council of Science Editors:

Stover TC. THE DEVELOPMENT AND EVALUATION OF SYSTEMIC DRUG DELIVERY SYSTEMS FOR C6-CERAMIDE AS A BREAST CANCER CHEMOTHERAPEUTIC AGENT . [Thesis]. Penn State University; 2008. Available from: https://submit-etda.libraries.psu.edu/catalog/6509

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


Penn State University

9. Petro, Kimberly Anna. ROLES OF LIPID RAFTS IN BOTULINUM NEUROTOXIN SEROTYPE A ACTIVITY AND DIFFERENTIATION OF NEUROBLASTOMA CELLS .

Degree: 2008, Penn State University

 Botulinum neurotoxin serotype A (BoNT/A), one of seven serotypes of botulinum neurotoxin, is taken up by neurons of the peripheral nervous system. Within the neurons… (more)

Subjects/Keywords: differentiation; gangliosides; botulinum neurotoxin; membrane rafts; lipid rafts

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APA (6th Edition):

Petro, K. A. (2008). ROLES OF LIPID RAFTS IN BOTULINUM NEUROTOXIN SEROTYPE A ACTIVITY AND DIFFERENTIATION OF NEUROBLASTOMA CELLS . (Thesis). Penn State University. Retrieved from https://submit-etda.libraries.psu.edu/catalog/8197

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):

Petro, Kimberly Anna. “ROLES OF LIPID RAFTS IN BOTULINUM NEUROTOXIN SEROTYPE A ACTIVITY AND DIFFERENTIATION OF NEUROBLASTOMA CELLS .” 2008. Thesis, Penn State University. Accessed April 16, 2021. https://submit-etda.libraries.psu.edu/catalog/8197.

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

MLA Handbook (7th Edition):

Petro, Kimberly Anna. “ROLES OF LIPID RAFTS IN BOTULINUM NEUROTOXIN SEROTYPE A ACTIVITY AND DIFFERENTIATION OF NEUROBLASTOMA CELLS .” 2008. Web. 16 Apr 2021.

Vancouver:

Petro KA. ROLES OF LIPID RAFTS IN BOTULINUM NEUROTOXIN SEROTYPE A ACTIVITY AND DIFFERENTIATION OF NEUROBLASTOMA CELLS . [Internet] [Thesis]. Penn State University; 2008. [cited 2021 Apr 16]. Available from: https://submit-etda.libraries.psu.edu/catalog/8197.

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

Council of Science Editors:

Petro KA. ROLES OF LIPID RAFTS IN BOTULINUM NEUROTOXIN SEROTYPE A ACTIVITY AND DIFFERENTIATION OF NEUROBLASTOMA CELLS . [Thesis]. Penn State University; 2008. Available from: https://submit-etda.libraries.psu.edu/catalog/8197

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


Penn State University

10. Houck, Kristy Lee. SPHINGOLIPID AND PHOSPHOLIPID METABOLITES REGULATE THE PHENOTYPE OF VASCULAR SMOOTH MUSCLE CELLS .

Degree: 2008, Penn State University

 Cardiovascular disease, particularly atherosclerosis, is a major cause of concern as it is the primary cause of death today. Atherosclerosis is an inflammatory disease that… (more)

Subjects/Keywords: toll-like receptor; diglycerides; ceramide-1-phosphate; vascular smooth muscle; signaling cascades; cytokine

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APA (6th Edition):

Houck, K. L. (2008). SPHINGOLIPID AND PHOSPHOLIPID METABOLITES REGULATE THE PHENOTYPE OF VASCULAR SMOOTH MUSCLE CELLS . (Thesis). Penn State University. Retrieved from https://submit-etda.libraries.psu.edu/catalog/8344

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):

Houck, Kristy Lee. “SPHINGOLIPID AND PHOSPHOLIPID METABOLITES REGULATE THE PHENOTYPE OF VASCULAR SMOOTH MUSCLE CELLS .” 2008. Thesis, Penn State University. Accessed April 16, 2021. https://submit-etda.libraries.psu.edu/catalog/8344.

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

MLA Handbook (7th Edition):

Houck, Kristy Lee. “SPHINGOLIPID AND PHOSPHOLIPID METABOLITES REGULATE THE PHENOTYPE OF VASCULAR SMOOTH MUSCLE CELLS .” 2008. Web. 16 Apr 2021.

Vancouver:

Houck KL. SPHINGOLIPID AND PHOSPHOLIPID METABOLITES REGULATE THE PHENOTYPE OF VASCULAR SMOOTH MUSCLE CELLS . [Internet] [Thesis]. Penn State University; 2008. [cited 2021 Apr 16]. Available from: https://submit-etda.libraries.psu.edu/catalog/8344.

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

Council of Science Editors:

Houck KL. SPHINGOLIPID AND PHOSPHOLIPID METABOLITES REGULATE THE PHENOTYPE OF VASCULAR SMOOTH MUSCLE CELLS . [Thesis]. Penn State University; 2008. Available from: https://submit-etda.libraries.psu.edu/catalog/8344

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


Penn State University

11. Chang, Mikyoung. SIGNALING FUNCTIONS OF THE NFkappaB1 GENE PRODUCTS IN MACROPHAGES AND T CELLS .

Degree: 2008, Penn State University

 The NF-kappaB family of transcription factors plays a pivotal role in the regulation of genes involved in diverse biological processes, including immune responses, inflammation, apoptosis,… (more)

Subjects/Keywords: T cells; inflammation; macrophage; p105; IkappaBgamma; NFkappaB

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APA (6th Edition):

Chang, M. (2008). SIGNALING FUNCTIONS OF THE NFkappaB1 GENE PRODUCTS IN MACROPHAGES AND T CELLS . (Thesis). Penn State University. Retrieved from https://submit-etda.libraries.psu.edu/catalog/8219

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):

Chang, Mikyoung. “SIGNALING FUNCTIONS OF THE NFkappaB1 GENE PRODUCTS IN MACROPHAGES AND T CELLS .” 2008. Thesis, Penn State University. Accessed April 16, 2021. https://submit-etda.libraries.psu.edu/catalog/8219.

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

MLA Handbook (7th Edition):

Chang, Mikyoung. “SIGNALING FUNCTIONS OF THE NFkappaB1 GENE PRODUCTS IN MACROPHAGES AND T CELLS .” 2008. Web. 16 Apr 2021.

Vancouver:

Chang M. SIGNALING FUNCTIONS OF THE NFkappaB1 GENE PRODUCTS IN MACROPHAGES AND T CELLS . [Internet] [Thesis]. Penn State University; 2008. [cited 2021 Apr 16]. Available from: https://submit-etda.libraries.psu.edu/catalog/8219.

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

Council of Science Editors:

Chang M. SIGNALING FUNCTIONS OF THE NFkappaB1 GENE PRODUCTS IN MACROPHAGES AND T CELLS . [Thesis]. Penn State University; 2008. Available from: https://submit-etda.libraries.psu.edu/catalog/8219

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


Penn State University

12. Nelson, Amanda Marie. Insights into the Mechanism of Action of 13-cis Retinoic Acid in Suppressing Sebaceous Gland Function .

Degree: 2008, Penn State University

 Nearly 40-50 million people of all races and ages in the United States have acne, making it the most common skin disease. Although acne is… (more)

Subjects/Keywords: skin; retinoin; acne

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APA (6th Edition):

Nelson, A. M. (2008). Insights into the Mechanism of Action of 13-cis Retinoic Acid in Suppressing Sebaceous Gland Function . (Thesis). Penn State University. Retrieved from https://submit-etda.libraries.psu.edu/catalog/7530

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):

Nelson, Amanda Marie. “Insights into the Mechanism of Action of 13-cis Retinoic Acid in Suppressing Sebaceous Gland Function .” 2008. Thesis, Penn State University. Accessed April 16, 2021. https://submit-etda.libraries.psu.edu/catalog/7530.

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

MLA Handbook (7th Edition):

Nelson, Amanda Marie. “Insights into the Mechanism of Action of 13-cis Retinoic Acid in Suppressing Sebaceous Gland Function .” 2008. Web. 16 Apr 2021.

Vancouver:

Nelson AM. Insights into the Mechanism of Action of 13-cis Retinoic Acid in Suppressing Sebaceous Gland Function . [Internet] [Thesis]. Penn State University; 2008. [cited 2021 Apr 16]. Available from: https://submit-etda.libraries.psu.edu/catalog/7530.

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

Council of Science Editors:

Nelson AM. Insights into the Mechanism of Action of 13-cis Retinoic Acid in Suppressing Sebaceous Gland Function . [Thesis]. Penn State University; 2008. Available from: https://submit-etda.libraries.psu.edu/catalog/7530

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


Penn State University

13. Draper, Jeremiah Michael. Identification of Human DHHC20 as a Transforming Palmitoyl Acyltransferase .

Degree: 2008, Penn State University

 Many important signaling proteins require the post-translational addition of fatty acid chains for their proper subcellular localization and function. One such modification is the addition… (more)

Subjects/Keywords: localization; transformation; Palmitoyl acyltransferase; drug target

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APA (6th Edition):

Draper, J. M. (2008). Identification of Human DHHC20 as a Transforming Palmitoyl Acyltransferase . (Thesis). Penn State University. Retrieved from https://submit-etda.libraries.psu.edu/catalog/8983

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):

Draper, Jeremiah Michael. “Identification of Human DHHC20 as a Transforming Palmitoyl Acyltransferase .” 2008. Thesis, Penn State University. Accessed April 16, 2021. https://submit-etda.libraries.psu.edu/catalog/8983.

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

MLA Handbook (7th Edition):

Draper, Jeremiah Michael. “Identification of Human DHHC20 as a Transforming Palmitoyl Acyltransferase .” 2008. Web. 16 Apr 2021.

Vancouver:

Draper JM. Identification of Human DHHC20 as a Transforming Palmitoyl Acyltransferase . [Internet] [Thesis]. Penn State University; 2008. [cited 2021 Apr 16]. Available from: https://submit-etda.libraries.psu.edu/catalog/8983.

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

Council of Science Editors:

Draper JM. Identification of Human DHHC20 as a Transforming Palmitoyl Acyltransferase . [Thesis]. Penn State University; 2008. Available from: https://submit-etda.libraries.psu.edu/catalog/8983

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


Penn State University

14. Kuntz-Melcavage, Kara Lynn. Incubation of heroin-seeking behavior and accompanying molecular changes.

Degree: 2009, Penn State University

 The field of neuroscience provides an opportunity to combine psychological and biological studies with the ultimate goal of gaining a better understanding of physiological systems.… (more)

Subjects/Keywords: addiction; drug relapse; heroin; opiate

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APA (6th Edition):

Kuntz-Melcavage, K. L. (2009). Incubation of heroin-seeking behavior and accompanying molecular changes. (Thesis). Penn State University. Retrieved from https://submit-etda.libraries.psu.edu/catalog/9237

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):

Kuntz-Melcavage, Kara Lynn. “Incubation of heroin-seeking behavior and accompanying molecular changes.” 2009. Thesis, Penn State University. Accessed April 16, 2021. https://submit-etda.libraries.psu.edu/catalog/9237.

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

MLA Handbook (7th Edition):

Kuntz-Melcavage, Kara Lynn. “Incubation of heroin-seeking behavior and accompanying molecular changes.” 2009. Web. 16 Apr 2021.

Vancouver:

Kuntz-Melcavage KL. Incubation of heroin-seeking behavior and accompanying molecular changes. [Internet] [Thesis]. Penn State University; 2009. [cited 2021 Apr 16]. Available from: https://submit-etda.libraries.psu.edu/catalog/9237.

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

Council of Science Editors:

Kuntz-Melcavage KL. Incubation of heroin-seeking behavior and accompanying molecular changes. [Thesis]. Penn State University; 2009. Available from: https://submit-etda.libraries.psu.edu/catalog/9237

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


Penn State University

15. O'Neill, Sean Michael. INSIGHTS INTO HUMAN NEUTRAL CERAMIDASE TRANSCRIPTION AND THE ROLE OF CERAMIDE METABOLISM IN THE DEVELOPMENT OF AN INHIBITOR OF RESTENOSIS .

Degree: 2009, Penn State University

 Atherosclerosis is the predominant underlying cause of cardiovascular disease (CVD). CVD is the leading cause of death in the United States and much of Europe,… (more)

Subjects/Keywords: ceramidase; restenosis; atherosclerosis; transcription; Ceramide; sphingolipid

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APA (6th Edition):

O'Neill, S. M. (2009). INSIGHTS INTO HUMAN NEUTRAL CERAMIDASE TRANSCRIPTION AND THE ROLE OF CERAMIDE METABOLISM IN THE DEVELOPMENT OF AN INHIBITOR OF RESTENOSIS . (Thesis). Penn State University. Retrieved from https://submit-etda.libraries.psu.edu/catalog/9488

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):

O'Neill, Sean Michael. “INSIGHTS INTO HUMAN NEUTRAL CERAMIDASE TRANSCRIPTION AND THE ROLE OF CERAMIDE METABOLISM IN THE DEVELOPMENT OF AN INHIBITOR OF RESTENOSIS .” 2009. Thesis, Penn State University. Accessed April 16, 2021. https://submit-etda.libraries.psu.edu/catalog/9488.

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

MLA Handbook (7th Edition):

O'Neill, Sean Michael. “INSIGHTS INTO HUMAN NEUTRAL CERAMIDASE TRANSCRIPTION AND THE ROLE OF CERAMIDE METABOLISM IN THE DEVELOPMENT OF AN INHIBITOR OF RESTENOSIS .” 2009. Web. 16 Apr 2021.

Vancouver:

O'Neill SM. INSIGHTS INTO HUMAN NEUTRAL CERAMIDASE TRANSCRIPTION AND THE ROLE OF CERAMIDE METABOLISM IN THE DEVELOPMENT OF AN INHIBITOR OF RESTENOSIS . [Internet] [Thesis]. Penn State University; 2009. [cited 2021 Apr 16]. Available from: https://submit-etda.libraries.psu.edu/catalog/9488.

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

Council of Science Editors:

O'Neill SM. INSIGHTS INTO HUMAN NEUTRAL CERAMIDASE TRANSCRIPTION AND THE ROLE OF CERAMIDE METABOLISM IN THE DEVELOPMENT OF AN INHIBITOR OF RESTENOSIS . [Thesis]. Penn State University; 2009. Available from: https://submit-etda.libraries.psu.edu/catalog/9488

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


Penn State University

16. Gramling, Sarah Jean Byers. Genomic Instability-Indicated Mechanisms of Early Carcinogenesis Following Hepatocarcinogen Treatment .

Degree: 2009, Penn State University

 Carcinogenicity testing is perhaps one of the most challenging aspects in drug development. Carcinogenicity tests not only provide the basis for human risk assessment and… (more)

Subjects/Keywords: Transgenic Mice; NMuLi cells; Reporter Models; Repeat Sequences; Microsatellites

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APA (6th Edition):

Gramling, S. J. B. (2009). Genomic Instability-Indicated Mechanisms of Early Carcinogenesis Following Hepatocarcinogen Treatment . (Thesis). Penn State University. Retrieved from https://submit-etda.libraries.psu.edu/catalog/8935

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):

Gramling, Sarah Jean Byers. “Genomic Instability-Indicated Mechanisms of Early Carcinogenesis Following Hepatocarcinogen Treatment .” 2009. Thesis, Penn State University. Accessed April 16, 2021. https://submit-etda.libraries.psu.edu/catalog/8935.

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

MLA Handbook (7th Edition):

Gramling, Sarah Jean Byers. “Genomic Instability-Indicated Mechanisms of Early Carcinogenesis Following Hepatocarcinogen Treatment .” 2009. Web. 16 Apr 2021.

Vancouver:

Gramling SJB. Genomic Instability-Indicated Mechanisms of Early Carcinogenesis Following Hepatocarcinogen Treatment . [Internet] [Thesis]. Penn State University; 2009. [cited 2021 Apr 16]. Available from: https://submit-etda.libraries.psu.edu/catalog/8935.

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

Council of Science Editors:

Gramling SJB. Genomic Instability-Indicated Mechanisms of Early Carcinogenesis Following Hepatocarcinogen Treatment . [Thesis]. Penn State University; 2009. Available from: https://submit-etda.libraries.psu.edu/catalog/8935

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


Penn State University

17. Heakal, Yasser M. IDENTIFICATION OF NOVEL PHARMACOLOGICAL APPROACHES TO INHIBIT NEUROTENSIN RECEPTOR-1 MITOGENIC SIGNALING IN BREAST CANCER CELLS .

Degree: 2009, Penn State University

 G protein coupled receptors (GPCRs) represent the largest family of cell surface receptors and serve as the primary pharmacological targets for more than thirty percent… (more)

Subjects/Keywords: Breast Cancer; Neurotensin; Ceramide; GPCR

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APA (6th Edition):

Heakal, Y. M. (2009). IDENTIFICATION OF NOVEL PHARMACOLOGICAL APPROACHES TO INHIBIT NEUROTENSIN RECEPTOR-1 MITOGENIC SIGNALING IN BREAST CANCER CELLS . (Thesis). Penn State University. Retrieved from https://submit-etda.libraries.psu.edu/catalog/10222

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):

Heakal, Yasser M. “IDENTIFICATION OF NOVEL PHARMACOLOGICAL APPROACHES TO INHIBIT NEUROTENSIN RECEPTOR-1 MITOGENIC SIGNALING IN BREAST CANCER CELLS .” 2009. Thesis, Penn State University. Accessed April 16, 2021. https://submit-etda.libraries.psu.edu/catalog/10222.

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

MLA Handbook (7th Edition):

Heakal, Yasser M. “IDENTIFICATION OF NOVEL PHARMACOLOGICAL APPROACHES TO INHIBIT NEUROTENSIN RECEPTOR-1 MITOGENIC SIGNALING IN BREAST CANCER CELLS .” 2009. Web. 16 Apr 2021.

Vancouver:

Heakal YM. IDENTIFICATION OF NOVEL PHARMACOLOGICAL APPROACHES TO INHIBIT NEUROTENSIN RECEPTOR-1 MITOGENIC SIGNALING IN BREAST CANCER CELLS . [Internet] [Thesis]. Penn State University; 2009. [cited 2021 Apr 16]. Available from: https://submit-etda.libraries.psu.edu/catalog/10222.

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

Council of Science Editors:

Heakal YM. IDENTIFICATION OF NOVEL PHARMACOLOGICAL APPROACHES TO INHIBIT NEUROTENSIN RECEPTOR-1 MITOGENIC SIGNALING IN BREAST CANCER CELLS . [Thesis]. Penn State University; 2009. Available from: https://submit-etda.libraries.psu.edu/catalog/10222

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


Penn State University

18. Miller, Joshua Christopher. ADENYLOSUCCINATE SYNTHETASE 1: A NOVEL TARGET OF DELETION IN LUNG ADENOCARCINOMA WITH IMPLICATIONS FOR METABOLIC STRESS TOLERANCE .

Degree: 2010, Penn State University

 Tobacco smoke consists of numerous carcinogens whose effect on lung tumor development includes the induction of mutations in key metabolic genes as well as the… (more)

Subjects/Keywords: lung cancer; lung adenocarcinoma; metabolic reprogramming; adenylosuccinate synthetase; , novel deletion

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APA (6th Edition):

Miller, J. C. (2010). ADENYLOSUCCINATE SYNTHETASE 1: A NOVEL TARGET OF DELETION IN LUNG ADENOCARCINOMA WITH IMPLICATIONS FOR METABOLIC STRESS TOLERANCE . (Thesis). Penn State University. Retrieved from https://submit-etda.libraries.psu.edu/catalog/11282

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):

Miller, Joshua Christopher. “ADENYLOSUCCINATE SYNTHETASE 1: A NOVEL TARGET OF DELETION IN LUNG ADENOCARCINOMA WITH IMPLICATIONS FOR METABOLIC STRESS TOLERANCE .” 2010. Thesis, Penn State University. Accessed April 16, 2021. https://submit-etda.libraries.psu.edu/catalog/11282.

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

MLA Handbook (7th Edition):

Miller, Joshua Christopher. “ADENYLOSUCCINATE SYNTHETASE 1: A NOVEL TARGET OF DELETION IN LUNG ADENOCARCINOMA WITH IMPLICATIONS FOR METABOLIC STRESS TOLERANCE .” 2010. Web. 16 Apr 2021.

Vancouver:

Miller JC. ADENYLOSUCCINATE SYNTHETASE 1: A NOVEL TARGET OF DELETION IN LUNG ADENOCARCINOMA WITH IMPLICATIONS FOR METABOLIC STRESS TOLERANCE . [Internet] [Thesis]. Penn State University; 2010. [cited 2021 Apr 16]. Available from: https://submit-etda.libraries.psu.edu/catalog/11282.

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

Council of Science Editors:

Miller JC. ADENYLOSUCCINATE SYNTHETASE 1: A NOVEL TARGET OF DELETION IN LUNG ADENOCARCINOMA WITH IMPLICATIONS FOR METABOLIC STRESS TOLERANCE . [Thesis]. Penn State University; 2010. Available from: https://submit-etda.libraries.psu.edu/catalog/11282

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


Penn State University

19. Keasey, Nikki R. AMINO ACID PERMEASE INVOLVEMENT IN THE VOLATILE ANESTHETIC RESPONSE OF SACCHAROMYCES CEREVISIAE.

Degree: 2008, Penn State University

 Despite the clinical importance of volatile anesthetics, their mechanisms of action remain unknown. Understanding how anesthetics produce their numerous cellular effects will facilitate the design… (more)

Subjects/Keywords: yeast; volatile anesthetics; nutrient transport

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APA (6th Edition):

Keasey, N. R. (2008). AMINO ACID PERMEASE INVOLVEMENT IN THE VOLATILE ANESTHETIC RESPONSE OF SACCHAROMYCES CEREVISIAE. (Thesis). Penn State University. Retrieved from https://submit-etda.libraries.psu.edu/catalog/8350

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):

Keasey, Nikki R. “AMINO ACID PERMEASE INVOLVEMENT IN THE VOLATILE ANESTHETIC RESPONSE OF SACCHAROMYCES CEREVISIAE.” 2008. Thesis, Penn State University. Accessed April 16, 2021. https://submit-etda.libraries.psu.edu/catalog/8350.

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

MLA Handbook (7th Edition):

Keasey, Nikki R. “AMINO ACID PERMEASE INVOLVEMENT IN THE VOLATILE ANESTHETIC RESPONSE OF SACCHAROMYCES CEREVISIAE.” 2008. Web. 16 Apr 2021.

Vancouver:

Keasey NR. AMINO ACID PERMEASE INVOLVEMENT IN THE VOLATILE ANESTHETIC RESPONSE OF SACCHAROMYCES CEREVISIAE. [Internet] [Thesis]. Penn State University; 2008. [cited 2021 Apr 16]. Available from: https://submit-etda.libraries.psu.edu/catalog/8350.

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

Council of Science Editors:

Keasey NR. AMINO ACID PERMEASE INVOLVEMENT IN THE VOLATILE ANESTHETIC RESPONSE OF SACCHAROMYCES CEREVISIAE. [Thesis]. Penn State University; 2008. Available from: https://submit-etda.libraries.psu.edu/catalog/8350

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


Penn State University

20. Henderson, Rebecca Jane. The Development of an Iron Responsive Element (IRE)-Driven Fluorescent Reporter Construct.

Degree: 2008, Penn State University

 A wide variety of debilitating illnesses have been directly connected with an imbalance of iron regulation within the body or indirectly through the occurrence of… (more)

Subjects/Keywords: iron; ferritin; hereditary hemochromatosis; beta-amyloid; iron regulation

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APA (6th Edition):

Henderson, R. J. (2008). The Development of an Iron Responsive Element (IRE)-Driven Fluorescent Reporter Construct. (Thesis). Penn State University. Retrieved from https://submit-etda.libraries.psu.edu/catalog/6415

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):

Henderson, Rebecca Jane. “The Development of an Iron Responsive Element (IRE)-Driven Fluorescent Reporter Construct.” 2008. Thesis, Penn State University. Accessed April 16, 2021. https://submit-etda.libraries.psu.edu/catalog/6415.

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

MLA Handbook (7th Edition):

Henderson, Rebecca Jane. “The Development of an Iron Responsive Element (IRE)-Driven Fluorescent Reporter Construct.” 2008. Web. 16 Apr 2021.

Vancouver:

Henderson RJ. The Development of an Iron Responsive Element (IRE)-Driven Fluorescent Reporter Construct. [Internet] [Thesis]. Penn State University; 2008. [cited 2021 Apr 16]. Available from: https://submit-etda.libraries.psu.edu/catalog/6415.

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

Council of Science Editors:

Henderson RJ. The Development of an Iron Responsive Element (IRE)-Driven Fluorescent Reporter Construct. [Thesis]. Penn State University; 2008. Available from: https://submit-etda.libraries.psu.edu/catalog/6415

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


Penn State University

21. MIN, JUNGSOO. Mechanisms of IGF-1 regulation of S and G2/M cell cycle phases in oligodendrocyte progenitor (OP) cells .

Degree: 2009, Penn State University

 Oligodendrocytes are macroglial cells in the central nervous system (CNS), which myelinate and provide electric insulation for the axons of nerve cells. Oligodendrocyte progenitor (OP)… (more)

Subjects/Keywords: IGF-1; oligodendrocyte; cell cycle

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APA (6th Edition):

MIN, J. (2009). Mechanisms of IGF-1 regulation of S and G2/M cell cycle phases in oligodendrocyte progenitor (OP) cells . (Thesis). Penn State University. Retrieved from https://submit-etda.libraries.psu.edu/catalog/10077

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):

MIN, JUNGSOO. “Mechanisms of IGF-1 regulation of S and G2/M cell cycle phases in oligodendrocyte progenitor (OP) cells .” 2009. Thesis, Penn State University. Accessed April 16, 2021. https://submit-etda.libraries.psu.edu/catalog/10077.

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

MLA Handbook (7th Edition):

MIN, JUNGSOO. “Mechanisms of IGF-1 regulation of S and G2/M cell cycle phases in oligodendrocyte progenitor (OP) cells .” 2009. Web. 16 Apr 2021.

Vancouver:

MIN J. Mechanisms of IGF-1 regulation of S and G2/M cell cycle phases in oligodendrocyte progenitor (OP) cells . [Internet] [Thesis]. Penn State University; 2009. [cited 2021 Apr 16]. Available from: https://submit-etda.libraries.psu.edu/catalog/10077.

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

Council of Science Editors:

MIN J. Mechanisms of IGF-1 regulation of S and G2/M cell cycle phases in oligodendrocyte progenitor (OP) cells . [Thesis]. Penn State University; 2009. Available from: https://submit-etda.libraries.psu.edu/catalog/10077

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

.