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

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Penn State University

1. D'cruz, Travis Savio. Molecular Mechanisms of Retinal Synaptophysin Loss in Experimental Diabetes.

Degree: 2013, Penn State University

 Diabetic retinopathy (DR) is a complication of diabetes that compromises the structure and function of the retina causing deficits in vision. It is the leading… (more)

Subjects/Keywords: Diabetic Retinopathy; N-glycosylation; Synaptophysin; Mannosylation; Alpha-Mannosidase

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APA (6th Edition):

D'cruz, T. S. (2013). Molecular Mechanisms of Retinal Synaptophysin Loss in Experimental Diabetes. (Thesis). Penn State University. Retrieved from https://submit-etda.libraries.psu.edu/catalog/18303

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):

D'cruz, Travis Savio. “Molecular Mechanisms of Retinal Synaptophysin Loss in Experimental Diabetes.” 2013. Thesis, Penn State University. Accessed March 03, 2021. https://submit-etda.libraries.psu.edu/catalog/18303.

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

MLA Handbook (7th Edition):

D'cruz, Travis Savio. “Molecular Mechanisms of Retinal Synaptophysin Loss in Experimental Diabetes.” 2013. Web. 03 Mar 2021.

Vancouver:

D'cruz TS. Molecular Mechanisms of Retinal Synaptophysin Loss in Experimental Diabetes. [Internet] [Thesis]. Penn State University; 2013. [cited 2021 Mar 03]. Available from: https://submit-etda.libraries.psu.edu/catalog/18303.

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

Council of Science Editors:

D'cruz TS. Molecular Mechanisms of Retinal Synaptophysin Loss in Experimental Diabetes. [Thesis]. Penn State University; 2013. Available from: https://submit-etda.libraries.psu.edu/catalog/18303

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


Penn State University

2. Qi, Ji. Connecting the miRNA network to the lung transcriptional program.

Degree: 2012, Penn State University

 MicroRNAs (miRNAs) are small RNA regulators of gene expression. Owing to their ability to target multiple genes and pathways simultaneously, miRNAs, which are about 22-nt… (more)

Subjects/Keywords: microRNA; lung cancer; TTF-1; NKX2-8; miR-365

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APA (6th Edition):

Qi, J. (2012). Connecting the miRNA network to the lung transcriptional program. (Thesis). Penn State University. Retrieved from https://submit-etda.libraries.psu.edu/catalog/15124

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):

Qi, Ji. “Connecting the miRNA network to the lung transcriptional program.” 2012. Thesis, Penn State University. Accessed March 03, 2021. https://submit-etda.libraries.psu.edu/catalog/15124.

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

MLA Handbook (7th Edition):

Qi, Ji. “Connecting the miRNA network to the lung transcriptional program.” 2012. Web. 03 Mar 2021.

Vancouver:

Qi J. Connecting the miRNA network to the lung transcriptional program. [Internet] [Thesis]. Penn State University; 2012. [cited 2021 Mar 03]. Available from: https://submit-etda.libraries.psu.edu/catalog/15124.

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

Council of Science Editors:

Qi J. Connecting the miRNA network to the lung transcriptional program. [Thesis]. Penn State University; 2012. Available from: https://submit-etda.libraries.psu.edu/catalog/15124

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


Penn State University

3. Hornick, Jacob. Analysis of Naturally Occurring Genetic Variants in the Sphingosine-1-Phosphate Receptor Family.

Degree: 2019, Penn State University

 The field of personalized medicine has significantly expanded with the advent of gene sequencing and the decreasing cost and increasing availability of whole genome sequencing… (more)

Subjects/Keywords: Personalized medicine; GPCR; S1P; RRMS; G protein; Genetic variation; yeast

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APA (6th Edition):

Hornick, J. (2019). Analysis of Naturally Occurring Genetic Variants in the Sphingosine-1-Phosphate Receptor Family. (Thesis). Penn State University. Retrieved from https://submit-etda.libraries.psu.edu/catalog/16283jth5217

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):

Hornick, Jacob. “Analysis of Naturally Occurring Genetic Variants in the Sphingosine-1-Phosphate Receptor Family.” 2019. Thesis, Penn State University. Accessed March 03, 2021. https://submit-etda.libraries.psu.edu/catalog/16283jth5217.

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

MLA Handbook (7th Edition):

Hornick, Jacob. “Analysis of Naturally Occurring Genetic Variants in the Sphingosine-1-Phosphate Receptor Family.” 2019. Web. 03 Mar 2021.

Vancouver:

Hornick J. Analysis of Naturally Occurring Genetic Variants in the Sphingosine-1-Phosphate Receptor Family. [Internet] [Thesis]. Penn State University; 2019. [cited 2021 Mar 03]. Available from: https://submit-etda.libraries.psu.edu/catalog/16283jth5217.

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

Council of Science Editors:

Hornick J. Analysis of Naturally Occurring Genetic Variants in the Sphingosine-1-Phosphate Receptor Family. [Thesis]. Penn State University; 2019. Available from: https://submit-etda.libraries.psu.edu/catalog/16283jth5217

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


Penn State University

4. Bharatula, Vasudha. REGULATION OF STRESS INDUCED GENE EXPRESSION IN SACCHAROMYCES CEREVISIAE.

Degree: 2019, Penn State University

 Transcription initiation is complex process involving transcription factors (TF), co-activators, nucleosome remodelers and the pre-initiation complex (PIC); general transcription factors (GTF) and RNA polymerase II… (more)

Subjects/Keywords: Msn2; yeast; Stress

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APA (6th Edition):

Bharatula, V. (2019). REGULATION OF STRESS INDUCED GENE EXPRESSION IN SACCHAROMYCES CEREVISIAE. (Thesis). Penn State University. Retrieved from https://submit-etda.libraries.psu.edu/catalog/15778vxb158

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):

Bharatula, Vasudha. “REGULATION OF STRESS INDUCED GENE EXPRESSION IN SACCHAROMYCES CEREVISIAE.” 2019. Thesis, Penn State University. Accessed March 03, 2021. https://submit-etda.libraries.psu.edu/catalog/15778vxb158.

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

MLA Handbook (7th Edition):

Bharatula, Vasudha. “REGULATION OF STRESS INDUCED GENE EXPRESSION IN SACCHAROMYCES CEREVISIAE.” 2019. Web. 03 Mar 2021.

Vancouver:

Bharatula V. REGULATION OF STRESS INDUCED GENE EXPRESSION IN SACCHAROMYCES CEREVISIAE. [Internet] [Thesis]. Penn State University; 2019. [cited 2021 Mar 03]. Available from: https://submit-etda.libraries.psu.edu/catalog/15778vxb158.

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

Council of Science Editors:

Bharatula V. REGULATION OF STRESS INDUCED GENE EXPRESSION IN SACCHAROMYCES CEREVISIAE. [Thesis]. Penn State University; 2019. Available from: https://submit-etda.libraries.psu.edu/catalog/15778vxb158

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


Penn State University

5. Choe, Katherine Naeun. HUWE1 Interacts with PCNA to Alleviate Replication Stress.

Degree: 2016, Penn State University

 The integrity of the genome relies on the accurate and faithful duplication of genetic information from a parental cell to its progeny during each cellular… (more)

Subjects/Keywords: DNA replication; Genomic instability; H2AX; DNA Damage; HUWE1; PCNA; Replication stress

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APA (6th Edition):

Choe, K. N. (2016). HUWE1 Interacts with PCNA to Alleviate Replication Stress. (Thesis). Penn State University. Retrieved from https://submit-etda.libraries.psu.edu/catalog/13492kzc152

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):

Choe, Katherine Naeun. “HUWE1 Interacts with PCNA to Alleviate Replication Stress.” 2016. Thesis, Penn State University. Accessed March 03, 2021. https://submit-etda.libraries.psu.edu/catalog/13492kzc152.

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

MLA Handbook (7th Edition):

Choe, Katherine Naeun. “HUWE1 Interacts with PCNA to Alleviate Replication Stress.” 2016. Web. 03 Mar 2021.

Vancouver:

Choe KN. HUWE1 Interacts with PCNA to Alleviate Replication Stress. [Internet] [Thesis]. Penn State University; 2016. [cited 2021 Mar 03]. Available from: https://submit-etda.libraries.psu.edu/catalog/13492kzc152.

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

Council of Science Editors:

Choe KN. HUWE1 Interacts with PCNA to Alleviate Replication Stress. [Thesis]. Penn State University; 2016. Available from: https://submit-etda.libraries.psu.edu/catalog/13492kzc152

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


Penn State University

6. Chakraborty, Sangita Abid. Construction and characterization of a minichromosome reporter system to study structure-function relationship between gene silencing and chromatin boundaries in Saccharomyces cerevisiae.

Degree: 2012, Penn State University

 In the eukaryotic cell nucleus, DNA is packed into arrays of nucleosomes, the repeating structural units of chromatin. Each nucleosome contains ~150 bp of DNA… (more)

Subjects/Keywords: Chromatin; Heterochromatin; Boundary; Barrier; anti-silencer; gene silencing; URA3; 601 nucleosome; Minichromosome; Yeast

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APA (6th Edition):

Chakraborty, S. A. (2012). Construction and characterization of a minichromosome reporter system to study structure-function relationship between gene silencing and chromatin boundaries in Saccharomyces cerevisiae. (Thesis). Penn State University. Retrieved from https://submit-etda.libraries.psu.edu/catalog/14589

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):

Chakraborty, Sangita Abid. “Construction and characterization of a minichromosome reporter system to study structure-function relationship between gene silencing and chromatin boundaries in Saccharomyces cerevisiae.” 2012. Thesis, Penn State University. Accessed March 03, 2021. https://submit-etda.libraries.psu.edu/catalog/14589.

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

MLA Handbook (7th Edition):

Chakraborty, Sangita Abid. “Construction and characterization of a minichromosome reporter system to study structure-function relationship between gene silencing and chromatin boundaries in Saccharomyces cerevisiae.” 2012. Web. 03 Mar 2021.

Vancouver:

Chakraborty SA. Construction and characterization of a minichromosome reporter system to study structure-function relationship between gene silencing and chromatin boundaries in Saccharomyces cerevisiae. [Internet] [Thesis]. Penn State University; 2012. [cited 2021 Mar 03]. Available from: https://submit-etda.libraries.psu.edu/catalog/14589.

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

Council of Science Editors:

Chakraborty SA. Construction and characterization of a minichromosome reporter system to study structure-function relationship between gene silencing and chromatin boundaries in Saccharomyces cerevisiae. [Thesis]. Penn State University; 2012. Available from: https://submit-etda.libraries.psu.edu/catalog/14589

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


Penn State University

7. Winter, Jeremiah Nathanael. The Regulation of mTORC1 Signaling Through Multiple Simultaneous Stimulatory Inputs To The TSC1/2 Complex .

Degree: 2011, Penn State University

 The mammalian target of rapamycin (mTOR) protein kinase exists in two distinct complexes, mTOR complex 1 (mTORC1) and mTOR complex 2 (mTORC2). The mTORC1 signaling… (more)

Subjects/Keywords: lysophosphatidic acid; TSC; ERK; Akt; protein kinase B; leucine; phosphatidic acid; PLD; mTORC1; LPAAT; PLA; Rag proteins

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APA (6th Edition):

Winter, J. N. (2011). The Regulation of mTORC1 Signaling Through Multiple Simultaneous Stimulatory Inputs To The TSC1/2 Complex . (Thesis). Penn State University. Retrieved from https://submit-etda.libraries.psu.edu/catalog/11094

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):

Winter, Jeremiah Nathanael. “The Regulation of mTORC1 Signaling Through Multiple Simultaneous Stimulatory Inputs To The TSC1/2 Complex .” 2011. Thesis, Penn State University. Accessed March 03, 2021. https://submit-etda.libraries.psu.edu/catalog/11094.

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

MLA Handbook (7th Edition):

Winter, Jeremiah Nathanael. “The Regulation of mTORC1 Signaling Through Multiple Simultaneous Stimulatory Inputs To The TSC1/2 Complex .” 2011. Web. 03 Mar 2021.

Vancouver:

Winter JN. The Regulation of mTORC1 Signaling Through Multiple Simultaneous Stimulatory Inputs To The TSC1/2 Complex . [Internet] [Thesis]. Penn State University; 2011. [cited 2021 Mar 03]. Available from: https://submit-etda.libraries.psu.edu/catalog/11094.

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

Council of Science Editors:

Winter JN. The Regulation of mTORC1 Signaling Through Multiple Simultaneous Stimulatory Inputs To The TSC1/2 Complex . [Thesis]. Penn State University; 2011. Available from: https://submit-etda.libraries.psu.edu/catalog/11094

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


Penn State University

8. Chin-quee, Karis P. Breast cancer cell secretions promote a pre-metastatic niche in bone; an in vitro look .

Degree: 2013, Penn State University

 ABSTRACT Successful metastasis requires some degree of hospitality from the host organ that is metastasized. In recent years, evidence has been mounting that the primary… (more)

Subjects/Keywords: breast cancer metastasis; pre-metastatic niche; bone; collagen fragments; collagenase

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APA (6th Edition):

Chin-quee, K. P. (2013). Breast cancer cell secretions promote a pre-metastatic niche in bone; an in vitro look . (Thesis). Penn State University. Retrieved from https://submit-etda.libraries.psu.edu/catalog/17496

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):

Chin-quee, Karis P. “Breast cancer cell secretions promote a pre-metastatic niche in bone; an in vitro look .” 2013. Thesis, Penn State University. Accessed March 03, 2021. https://submit-etda.libraries.psu.edu/catalog/17496.

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

MLA Handbook (7th Edition):

Chin-quee, Karis P. “Breast cancer cell secretions promote a pre-metastatic niche in bone; an in vitro look .” 2013. Web. 03 Mar 2021.

Vancouver:

Chin-quee KP. Breast cancer cell secretions promote a pre-metastatic niche in bone; an in vitro look . [Internet] [Thesis]. Penn State University; 2013. [cited 2021 Mar 03]. Available from: https://submit-etda.libraries.psu.edu/catalog/17496.

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

Council of Science Editors:

Chin-quee KP. Breast cancer cell secretions promote a pre-metastatic niche in bone; an in vitro look . [Thesis]. Penn State University; 2013. Available from: https://submit-etda.libraries.psu.edu/catalog/17496

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


Penn State University

9. Woll, Nicole Leanor. Understanding Osteogenic Nodule Formation From Single Embryonic Stem Cell-Derived Progenitors .

Degree: 2008, Penn State University

 The process of bone formation can be observed in vitro in the form of a mineralized nodule. Mesenchymal stem cells (MSCs), the immediate precursors to… (more)

Subjects/Keywords: embryonic stem cells; osteoblasts; bone; differentiation

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APA (6th Edition):

Woll, N. L. (2008). Understanding Osteogenic Nodule Formation From Single Embryonic Stem Cell-Derived Progenitors . (Thesis). Penn State University. Retrieved from https://submit-etda.libraries.psu.edu/catalog/7484

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):

Woll, Nicole Leanor. “Understanding Osteogenic Nodule Formation From Single Embryonic Stem Cell-Derived Progenitors .” 2008. Thesis, Penn State University. Accessed March 03, 2021. https://submit-etda.libraries.psu.edu/catalog/7484.

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

MLA Handbook (7th Edition):

Woll, Nicole Leanor. “Understanding Osteogenic Nodule Formation From Single Embryonic Stem Cell-Derived Progenitors .” 2008. Web. 03 Mar 2021.

Vancouver:

Woll NL. Understanding Osteogenic Nodule Formation From Single Embryonic Stem Cell-Derived Progenitors . [Internet] [Thesis]. Penn State University; 2008. [cited 2021 Mar 03]. Available from: https://submit-etda.libraries.psu.edu/catalog/7484.

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

Council of Science Editors:

Woll NL. Understanding Osteogenic Nodule Formation From Single Embryonic Stem Cell-Derived Progenitors . [Thesis]. Penn State University; 2008. Available from: https://submit-etda.libraries.psu.edu/catalog/7484

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


Penn State University

10. Nguyen, David H. INHIBITION OF HEPATITIS B VIRUS REPLICATION BY THE APOBEC3 PROTEINS .

Degree: 2008, Penn State University

 Hepatitis B virus (HBV) is a major cause of acute and chronic viral hepatitis. In the United States, there are approximately 250,000 to 300,000 new… (more)

Subjects/Keywords: A3G; HBV; APOBEC3; Reverse transcription; Intrinsic immunity

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APA (6th Edition):

Nguyen, D. H. (2008). INHIBITION OF HEPATITIS B VIRUS REPLICATION BY THE APOBEC3 PROTEINS . (Thesis). Penn State University. Retrieved from https://submit-etda.libraries.psu.edu/catalog/8560

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):

Nguyen, David H. “INHIBITION OF HEPATITIS B VIRUS REPLICATION BY THE APOBEC3 PROTEINS .” 2008. Thesis, Penn State University. Accessed March 03, 2021. https://submit-etda.libraries.psu.edu/catalog/8560.

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

MLA Handbook (7th Edition):

Nguyen, David H. “INHIBITION OF HEPATITIS B VIRUS REPLICATION BY THE APOBEC3 PROTEINS .” 2008. Web. 03 Mar 2021.

Vancouver:

Nguyen DH. INHIBITION OF HEPATITIS B VIRUS REPLICATION BY THE APOBEC3 PROTEINS . [Internet] [Thesis]. Penn State University; 2008. [cited 2021 Mar 03]. Available from: https://submit-etda.libraries.psu.edu/catalog/8560.

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

Council of Science Editors:

Nguyen DH. INHIBITION OF HEPATITIS B VIRUS REPLICATION BY THE APOBEC3 PROTEINS . [Thesis]. Penn State University; 2008. Available from: https://submit-etda.libraries.psu.edu/catalog/8560

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


Penn State University

11. Zahwa, Hassan. MODULATION OF THE NEONATAL T CELL-MEDIATED IMMUNE RESPONSE BY MATERNALLY DERIVED STRESS HORMONES.

Degree: 2008, Penn State University

 A simple National Library of Medicine title search for the term “psychological stress” returns over 1400 titles, the majority of which address the impact of… (more)

Subjects/Keywords: stress; neonatal immune; T cell adaptive immunity; Herpes Simplex Virus; maternal stress

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APA (6th Edition):

Zahwa, H. (2008). MODULATION OF THE NEONATAL T CELL-MEDIATED IMMUNE RESPONSE BY MATERNALLY DERIVED STRESS HORMONES. (Thesis). Penn State University. Retrieved from https://submit-etda.libraries.psu.edu/catalog/8480

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):

Zahwa, Hassan. “MODULATION OF THE NEONATAL T CELL-MEDIATED IMMUNE RESPONSE BY MATERNALLY DERIVED STRESS HORMONES.” 2008. Thesis, Penn State University. Accessed March 03, 2021. https://submit-etda.libraries.psu.edu/catalog/8480.

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

MLA Handbook (7th Edition):

Zahwa, Hassan. “MODULATION OF THE NEONATAL T CELL-MEDIATED IMMUNE RESPONSE BY MATERNALLY DERIVED STRESS HORMONES.” 2008. Web. 03 Mar 2021.

Vancouver:

Zahwa H. MODULATION OF THE NEONATAL T CELL-MEDIATED IMMUNE RESPONSE BY MATERNALLY DERIVED STRESS HORMONES. [Internet] [Thesis]. Penn State University; 2008. [cited 2021 Mar 03]. Available from: https://submit-etda.libraries.psu.edu/catalog/8480.

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

Council of Science Editors:

Zahwa H. MODULATION OF THE NEONATAL T CELL-MEDIATED IMMUNE RESPONSE BY MATERNALLY DERIVED STRESS HORMONES. [Thesis]. Penn State University; 2008. Available from: https://submit-etda.libraries.psu.edu/catalog/8480

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


Penn State University

12. Murthi, Athulaprabha. TARGETING PROTEINS TO THE NUCLEAR MEMBRANE: A GENOMIC STUDY IN SACCHAROMYCES CEREVISIAE USING Trm1 AS A REPORTER .

Degree: 2008, Penn State University

 Appropriate nuclear membrane structure is important for all eukaryotic organisms as evidenced by the numerous human diseases and alterations in gene expression caused by inappropriate… (more)

Subjects/Keywords: protein targetng; protein modification; N-acetylation; Inner nuclear membrane; Membrane biogenesis; Ice2

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APA (6th Edition):

Murthi, A. (2008). TARGETING PROTEINS TO THE NUCLEAR MEMBRANE: A GENOMIC STUDY IN SACCHAROMYCES CEREVISIAE USING Trm1 AS A REPORTER . (Thesis). Penn State University. Retrieved from https://submit-etda.libraries.psu.edu/catalog/7053

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):

Murthi, Athulaprabha. “TARGETING PROTEINS TO THE NUCLEAR MEMBRANE: A GENOMIC STUDY IN SACCHAROMYCES CEREVISIAE USING Trm1 AS A REPORTER .” 2008. Thesis, Penn State University. Accessed March 03, 2021. https://submit-etda.libraries.psu.edu/catalog/7053.

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

MLA Handbook (7th Edition):

Murthi, Athulaprabha. “TARGETING PROTEINS TO THE NUCLEAR MEMBRANE: A GENOMIC STUDY IN SACCHAROMYCES CEREVISIAE USING Trm1 AS A REPORTER .” 2008. Web. 03 Mar 2021.

Vancouver:

Murthi A. TARGETING PROTEINS TO THE NUCLEAR MEMBRANE: A GENOMIC STUDY IN SACCHAROMYCES CEREVISIAE USING Trm1 AS A REPORTER . [Internet] [Thesis]. Penn State University; 2008. [cited 2021 Mar 03]. Available from: https://submit-etda.libraries.psu.edu/catalog/7053.

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

Council of Science Editors:

Murthi A. TARGETING PROTEINS TO THE NUCLEAR MEMBRANE: A GENOMIC STUDY IN SACCHAROMYCES CEREVISIAE USING Trm1 AS A REPORTER . [Thesis]. Penn State University; 2008. Available from: https://submit-etda.libraries.psu.edu/catalog/7053

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


Penn State University

13. Hannan, Meredith A. IDENTIFICATION OF NOVEL PROTEIN CONSTITUENTS OF THE DOPAMINE D2 RECEPTOR SIGNALPLEX: A STUDY OF TRPC1/D2R INTERACTION AND ITS ROLE IN SIGNALPLEX TRAFFICKING .

Degree: 2008, Penn State University

 Dopamine exerts its effects through the activation of a family of dopamine receptors (DRs) and their subsequent coupling to downstream effector molecules. Dysfunction of dopaminergic… (more)

Subjects/Keywords: Signalplex; Transient Receptor Potential; Dopamine D2 Receptor; Schizophrenia

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

APA (6th Edition):

Hannan, M. A. (2008). IDENTIFICATION OF NOVEL PROTEIN CONSTITUENTS OF THE DOPAMINE D2 RECEPTOR SIGNALPLEX: A STUDY OF TRPC1/D2R INTERACTION AND ITS ROLE IN SIGNALPLEX TRAFFICKING . (Thesis). Penn State University. Retrieved from https://submit-etda.libraries.psu.edu/catalog/7869

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):

Hannan, Meredith A. “IDENTIFICATION OF NOVEL PROTEIN CONSTITUENTS OF THE DOPAMINE D2 RECEPTOR SIGNALPLEX: A STUDY OF TRPC1/D2R INTERACTION AND ITS ROLE IN SIGNALPLEX TRAFFICKING .” 2008. Thesis, Penn State University. Accessed March 03, 2021. https://submit-etda.libraries.psu.edu/catalog/7869.

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

MLA Handbook (7th Edition):

Hannan, Meredith A. “IDENTIFICATION OF NOVEL PROTEIN CONSTITUENTS OF THE DOPAMINE D2 RECEPTOR SIGNALPLEX: A STUDY OF TRPC1/D2R INTERACTION AND ITS ROLE IN SIGNALPLEX TRAFFICKING .” 2008. Web. 03 Mar 2021.

Vancouver:

Hannan MA. IDENTIFICATION OF NOVEL PROTEIN CONSTITUENTS OF THE DOPAMINE D2 RECEPTOR SIGNALPLEX: A STUDY OF TRPC1/D2R INTERACTION AND ITS ROLE IN SIGNALPLEX TRAFFICKING . [Internet] [Thesis]. Penn State University; 2008. [cited 2021 Mar 03]. Available from: https://submit-etda.libraries.psu.edu/catalog/7869.

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

Council of Science Editors:

Hannan MA. IDENTIFICATION OF NOVEL PROTEIN CONSTITUENTS OF THE DOPAMINE D2 RECEPTOR SIGNALPLEX: A STUDY OF TRPC1/D2R INTERACTION AND ITS ROLE IN SIGNALPLEX TRAFFICKING . [Thesis]. Penn State University; 2008. Available from: https://submit-etda.libraries.psu.edu/catalog/7869

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


Penn State University

14. Dang Do, An Ngoc. The eIF2 alpha Kinases GCN2 and PERK Regulate Phosphorylation of TOR Target Proteins and Differential Translation of mRNAs .

Degree: 2008, Penn State University

 In eukaryotes, regulation of mRNA translation enables a fast, localized and finely tuned expression of gene products. Within the translation process, the first stage of… (more)

Subjects/Keywords: 2; cycloheximide; 4-di-tert-butylhydroquinone; translation initiation; translation elongation; eIF2; eIF2B; 4E-BP1; GCN2; p70S6K1; PERK; TOR; methionine deprivation; leucine deprivation; polysome; microarray; QRT-PCR; histidinol; leucinol; sucrose gradient; atf4; atf5; slc3a2; slc3a3; trfr; ldlr; stch; hspa5; igfbp-2

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APA (6th Edition):

Dang Do, A. N. (2008). The eIF2 alpha Kinases GCN2 and PERK Regulate Phosphorylation of TOR Target Proteins and Differential Translation of mRNAs . (Thesis). Penn State University. Retrieved from https://submit-etda.libraries.psu.edu/catalog/8191

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):

Dang Do, An Ngoc. “The eIF2 alpha Kinases GCN2 and PERK Regulate Phosphorylation of TOR Target Proteins and Differential Translation of mRNAs .” 2008. Thesis, Penn State University. Accessed March 03, 2021. https://submit-etda.libraries.psu.edu/catalog/8191.

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

MLA Handbook (7th Edition):

Dang Do, An Ngoc. “The eIF2 alpha Kinases GCN2 and PERK Regulate Phosphorylation of TOR Target Proteins and Differential Translation of mRNAs .” 2008. Web. 03 Mar 2021.

Vancouver:

Dang Do AN. The eIF2 alpha Kinases GCN2 and PERK Regulate Phosphorylation of TOR Target Proteins and Differential Translation of mRNAs . [Internet] [Thesis]. Penn State University; 2008. [cited 2021 Mar 03]. Available from: https://submit-etda.libraries.psu.edu/catalog/8191.

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

Council of Science Editors:

Dang Do AN. The eIF2 alpha Kinases GCN2 and PERK Regulate Phosphorylation of TOR Target Proteins and Differential Translation of mRNAs . [Thesis]. Penn State University; 2008. Available from: https://submit-etda.libraries.psu.edu/catalog/8191

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


Penn State University

15. Eisaman, Duane. LOS1P INDEPENDENT NUCLEAR TRNA EXPORT IN SACCHAROMYCES CEREVISIAE A ROLE FOR NUCLEAR TRNA AMINOACYLATION AND EXPORT .

Degree: 2008, Penn State University

 Proper movement of macromolecules between the nucleus and the cytoplasm is essential for life. The transport of molecules is an energy-dependent and receptor-mediated process. All… (more)

Subjects/Keywords: tRNA; yeast; RNAi; Export; cerevisiae; Sol1

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

APA (6th Edition):

Eisaman, D. (2008). LOS1P INDEPENDENT NUCLEAR TRNA EXPORT IN SACCHAROMYCES CEREVISIAE A ROLE FOR NUCLEAR TRNA AMINOACYLATION AND EXPORT . (Thesis). Penn State University. Retrieved from https://submit-etda.libraries.psu.edu/catalog/7494

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):

Eisaman, Duane. “LOS1P INDEPENDENT NUCLEAR TRNA EXPORT IN SACCHAROMYCES CEREVISIAE A ROLE FOR NUCLEAR TRNA AMINOACYLATION AND EXPORT .” 2008. Thesis, Penn State University. Accessed March 03, 2021. https://submit-etda.libraries.psu.edu/catalog/7494.

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

MLA Handbook (7th Edition):

Eisaman, Duane. “LOS1P INDEPENDENT NUCLEAR TRNA EXPORT IN SACCHAROMYCES CEREVISIAE A ROLE FOR NUCLEAR TRNA AMINOACYLATION AND EXPORT .” 2008. Web. 03 Mar 2021.

Vancouver:

Eisaman D. LOS1P INDEPENDENT NUCLEAR TRNA EXPORT IN SACCHAROMYCES CEREVISIAE A ROLE FOR NUCLEAR TRNA AMINOACYLATION AND EXPORT . [Internet] [Thesis]. Penn State University; 2008. [cited 2021 Mar 03]. Available from: https://submit-etda.libraries.psu.edu/catalog/7494.

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

Council of Science Editors:

Eisaman D. LOS1P INDEPENDENT NUCLEAR TRNA EXPORT IN SACCHAROMYCES CEREVISIAE A ROLE FOR NUCLEAR TRNA AMINOACYLATION AND EXPORT . [Thesis]. Penn State University; 2008. Available from: https://submit-etda.libraries.psu.edu/catalog/7494

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


Penn State University

16. Hurto, Rebecca Lee. UNCOVERING ENVIRONMENTAL AND GENETIC FACTORS INFLUENCING THE NUCLEUS-CYTOSOL DISTRIBUTION OF TRANSFER RNAS .

Degree: 2008, Penn State University

 The goals of my research were to identify proteins involved in regulating tRNA nucleus-cytosol distribution in order to further define tRNA nucleus-cytosol trafficking and to… (more)

Subjects/Keywords: nucleus-cytosol distribution; yeast; phosphate; tRNA

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

APA (6th Edition):

Hurto, R. L. (2008). UNCOVERING ENVIRONMENTAL AND GENETIC FACTORS INFLUENCING THE NUCLEUS-CYTOSOL DISTRIBUTION OF TRANSFER RNAS . (Thesis). Penn State University. Retrieved from https://submit-etda.libraries.psu.edu/catalog/7136

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):

Hurto, Rebecca Lee. “UNCOVERING ENVIRONMENTAL AND GENETIC FACTORS INFLUENCING THE NUCLEUS-CYTOSOL DISTRIBUTION OF TRANSFER RNAS .” 2008. Thesis, Penn State University. Accessed March 03, 2021. https://submit-etda.libraries.psu.edu/catalog/7136.

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

MLA Handbook (7th Edition):

Hurto, Rebecca Lee. “UNCOVERING ENVIRONMENTAL AND GENETIC FACTORS INFLUENCING THE NUCLEUS-CYTOSOL DISTRIBUTION OF TRANSFER RNAS .” 2008. Web. 03 Mar 2021.

Vancouver:

Hurto RL. UNCOVERING ENVIRONMENTAL AND GENETIC FACTORS INFLUENCING THE NUCLEUS-CYTOSOL DISTRIBUTION OF TRANSFER RNAS . [Internet] [Thesis]. Penn State University; 2008. [cited 2021 Mar 03]. Available from: https://submit-etda.libraries.psu.edu/catalog/7136.

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

Council of Science Editors:

Hurto RL. UNCOVERING ENVIRONMENTAL AND GENETIC FACTORS INFLUENCING THE NUCLEUS-CYTOSOL DISTRIBUTION OF TRANSFER RNAS . [Thesis]. Penn State University; 2008. Available from: https://submit-etda.libraries.psu.edu/catalog/7136

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


Penn State University

17. Tewalt , Eric Franklin. Antigen Processing and Presentation: Contributions of the Cross-Presentation Pathway in Eliciting CD8+ T cell Responses In Vivo .

Degree: 2009, Penn State University

 CD8+ T cells (TCD8+) are activated by peptide-MHC (pMHC) Class I complexes presented on the surface of professional antigen presenting cells (pAPC). Antigenic pMHC-I can… (more)

Subjects/Keywords: Scavenger Receptor; Cross-presentation; Vaccinia Virus; T cells; gp96; Dendritic Cell

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

APA (6th Edition):

Tewalt , E. F. (2009). Antigen Processing and Presentation: Contributions of the Cross-Presentation Pathway in Eliciting CD8+ T cell Responses In Vivo . (Thesis). Penn State University. Retrieved from https://submit-etda.libraries.psu.edu/catalog/8980

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):

Tewalt , Eric Franklin. “Antigen Processing and Presentation: Contributions of the Cross-Presentation Pathway in Eliciting CD8+ T cell Responses In Vivo .” 2009. Thesis, Penn State University. Accessed March 03, 2021. https://submit-etda.libraries.psu.edu/catalog/8980.

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

MLA Handbook (7th Edition):

Tewalt , Eric Franklin. “Antigen Processing and Presentation: Contributions of the Cross-Presentation Pathway in Eliciting CD8+ T cell Responses In Vivo .” 2009. Web. 03 Mar 2021.

Vancouver:

Tewalt EF. Antigen Processing and Presentation: Contributions of the Cross-Presentation Pathway in Eliciting CD8+ T cell Responses In Vivo . [Internet] [Thesis]. Penn State University; 2009. [cited 2021 Mar 03]. Available from: https://submit-etda.libraries.psu.edu/catalog/8980.

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

Council of Science Editors:

Tewalt EF. Antigen Processing and Presentation: Contributions of the Cross-Presentation Pathway in Eliciting CD8+ T cell Responses In Vivo . [Thesis]. Penn State University; 2009. Available from: https://submit-etda.libraries.psu.edu/catalog/8980

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


Penn State University

18. Snyder, Amanda Marie. The Impact of Ferritins in the Nigrostriatal System: Animal Models and Neurological Disease .

Degree: 2009, Penn State University

 Iron status is higher in the substantia nigra than in other brain regions but can fluctuate as function of diet, genetics, and disease. Because iron… (more)

Subjects/Keywords: H-ferritin; mitochondrial ferritin; iron

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APA (6th Edition):

Snyder, A. M. (2009). The Impact of Ferritins in the Nigrostriatal System: Animal Models and Neurological Disease . (Thesis). Penn State University. Retrieved from https://submit-etda.libraries.psu.edu/catalog/10153

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):

Snyder, Amanda Marie. “The Impact of Ferritins in the Nigrostriatal System: Animal Models and Neurological Disease .” 2009. Thesis, Penn State University. Accessed March 03, 2021. https://submit-etda.libraries.psu.edu/catalog/10153.

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

MLA Handbook (7th Edition):

Snyder, Amanda Marie. “The Impact of Ferritins in the Nigrostriatal System: Animal Models and Neurological Disease .” 2009. Web. 03 Mar 2021.

Vancouver:

Snyder AM. The Impact of Ferritins in the Nigrostriatal System: Animal Models and Neurological Disease . [Internet] [Thesis]. Penn State University; 2009. [cited 2021 Mar 03]. Available from: https://submit-etda.libraries.psu.edu/catalog/10153.

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

Council of Science Editors:

Snyder AM. The Impact of Ferritins in the Nigrostriatal System: Animal Models and Neurological Disease . [Thesis]. Penn State University; 2009. Available from: https://submit-etda.libraries.psu.edu/catalog/10153

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


Penn State University

19. Jacob, Kimberly Dawn. The Role of Non-Replicative DNA Polymerases in Microsatellite Mutagenesis.

Degree: 2009, Penn State University

 Microsatellites, or short tandem repeats (STR), are sequences of 1-6 base pairs per unit repeat and are found throughout the human genome. Mutations in these… (more)

Subjects/Keywords: mutagenesis; poymerae beta; polymerase IV; DNA replication

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APA (6th Edition):

Jacob, K. D. (2009). The Role of Non-Replicative DNA Polymerases in Microsatellite Mutagenesis. (Thesis). Penn State University. Retrieved from https://submit-etda.libraries.psu.edu/catalog/10186

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):

Jacob, Kimberly Dawn. “The Role of Non-Replicative DNA Polymerases in Microsatellite Mutagenesis.” 2009. Thesis, Penn State University. Accessed March 03, 2021. https://submit-etda.libraries.psu.edu/catalog/10186.

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

MLA Handbook (7th Edition):

Jacob, Kimberly Dawn. “The Role of Non-Replicative DNA Polymerases in Microsatellite Mutagenesis.” 2009. Web. 03 Mar 2021.

Vancouver:

Jacob KD. The Role of Non-Replicative DNA Polymerases in Microsatellite Mutagenesis. [Internet] [Thesis]. Penn State University; 2009. [cited 2021 Mar 03]. Available from: https://submit-etda.libraries.psu.edu/catalog/10186.

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

Council of Science Editors:

Jacob KD. The Role of Non-Replicative DNA Polymerases in Microsatellite Mutagenesis. [Thesis]. Penn State University; 2009. Available from: https://submit-etda.libraries.psu.edu/catalog/10186

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


Penn State University

20. Gudleski, Nicole. SUBCELLULAR TRAFFICKING AND EARLY ASSEMBLY OF THE RETROVIRAL GAG POLYPROTEIN .

Degree: 2010, Penn State University

 Abstract The Gag polyprotein, the main structural protein of all retroviruses, is both necessary and sufficient for virus particle assembly. This assembly process occurs in… (more)

Subjects/Keywords: subcellular trafficking; assembly; Retrovirus; Gag polyprotein

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APA (6th Edition):

Gudleski, N. (2010). SUBCELLULAR TRAFFICKING AND EARLY ASSEMBLY OF THE RETROVIRAL GAG POLYPROTEIN . (Thesis). Penn State University. Retrieved from https://submit-etda.libraries.psu.edu/catalog/10516

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):

Gudleski, Nicole. “SUBCELLULAR TRAFFICKING AND EARLY ASSEMBLY OF THE RETROVIRAL GAG POLYPROTEIN .” 2010. Thesis, Penn State University. Accessed March 03, 2021. https://submit-etda.libraries.psu.edu/catalog/10516.

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

MLA Handbook (7th Edition):

Gudleski, Nicole. “SUBCELLULAR TRAFFICKING AND EARLY ASSEMBLY OF THE RETROVIRAL GAG POLYPROTEIN .” 2010. Web. 03 Mar 2021.

Vancouver:

Gudleski N. SUBCELLULAR TRAFFICKING AND EARLY ASSEMBLY OF THE RETROVIRAL GAG POLYPROTEIN . [Internet] [Thesis]. Penn State University; 2010. [cited 2021 Mar 03]. Available from: https://submit-etda.libraries.psu.edu/catalog/10516.

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

Council of Science Editors:

Gudleski N. SUBCELLULAR TRAFFICKING AND EARLY ASSEMBLY OF THE RETROVIRAL GAG POLYPROTEIN . [Thesis]. Penn State University; 2010. Available from: https://submit-etda.libraries.psu.edu/catalog/10516

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


Penn State University

21. Lokhandwala, Parvez Mubasshir. ROLE OF PROTEIN CONFORMATION AND CHARGE-SHIELDING IN RETROVIRAL CAPSID MATURATION .

Degree: 2010, Penn State University

 Currently there is no cure available for an HIV-infected individual. The current anti-retroviral regimen that requires treating a patient indefinitely with multiple medications suffers from… (more)

Subjects/Keywords: MHR; maturation; capsid; CA; Retrovirus; Rous sarcoma virus

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

APA (6th Edition):

Lokhandwala, P. M. (2010). ROLE OF PROTEIN CONFORMATION AND CHARGE-SHIELDING IN RETROVIRAL CAPSID MATURATION . (Thesis). Penn State University. Retrieved from https://submit-etda.libraries.psu.edu/catalog/11243

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):

Lokhandwala, Parvez Mubasshir. “ROLE OF PROTEIN CONFORMATION AND CHARGE-SHIELDING IN RETROVIRAL CAPSID MATURATION .” 2010. Thesis, Penn State University. Accessed March 03, 2021. https://submit-etda.libraries.psu.edu/catalog/11243.

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

MLA Handbook (7th Edition):

Lokhandwala, Parvez Mubasshir. “ROLE OF PROTEIN CONFORMATION AND CHARGE-SHIELDING IN RETROVIRAL CAPSID MATURATION .” 2010. Web. 03 Mar 2021.

Vancouver:

Lokhandwala PM. ROLE OF PROTEIN CONFORMATION AND CHARGE-SHIELDING IN RETROVIRAL CAPSID MATURATION . [Internet] [Thesis]. Penn State University; 2010. [cited 2021 Mar 03]. Available from: https://submit-etda.libraries.psu.edu/catalog/11243.

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

Council of Science Editors:

Lokhandwala PM. ROLE OF PROTEIN CONFORMATION AND CHARGE-SHIELDING IN RETROVIRAL CAPSID MATURATION . [Thesis]. Penn State University; 2010. Available from: https://submit-etda.libraries.psu.edu/catalog/11243

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

.