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You searched for +publisher:"Harvard University" +contributor:("Denkin, Steven"). Showing records 1 – 30 of 33 total matches.

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Harvard University

1. Barnett, Hillary F. A Point-of-Care Device for Measuring Glucose,ketones,hemoglobin, and Glycated Hemoglobin From Whole Blood.

Degree: ALM, Bioengineering and Nanotechnology, 2016, Harvard University

 Point of care blood glucose meters and test strips are utilized by millions of individuals multiple times daily. Unlike clinical laboratories which analyze plasma samples… (more)

Subjects/Keywords: Engineering; Biomedical

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APA (6th Edition):

Barnett, H. F. (2016). A Point-of-Care Device for Measuring Glucose,ketones,hemoglobin, and Glycated Hemoglobin From Whole Blood. (Masters Thesis). Harvard University. Retrieved from http://nrs.harvard.edu/urn-3:HUL.InstRepos:33797351

Chicago Manual of Style (16th Edition):

Barnett, Hillary F. “A Point-of-Care Device for Measuring Glucose,ketones,hemoglobin, and Glycated Hemoglobin From Whole Blood.” 2016. Masters Thesis, Harvard University. Accessed October 16, 2018. http://nrs.harvard.edu/urn-3:HUL.InstRepos:33797351.

MLA Handbook (7th Edition):

Barnett, Hillary F. “A Point-of-Care Device for Measuring Glucose,ketones,hemoglobin, and Glycated Hemoglobin From Whole Blood.” 2016. Web. 16 Oct 2018.

Vancouver:

Barnett HF. A Point-of-Care Device for Measuring Glucose,ketones,hemoglobin, and Glycated Hemoglobin From Whole Blood. [Internet] [Masters thesis]. Harvard University; 2016. [cited 2018 Oct 16]. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:33797351.

Council of Science Editors:

Barnett HF. A Point-of-Care Device for Measuring Glucose,ketones,hemoglobin, and Glycated Hemoglobin From Whole Blood. [Masters Thesis]. Harvard University; 2016. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:33797351


Harvard University

2. Gutierrez, Bryan J. Financial Analysis of Biosimilar Development Candidates: A Case Study on the US Biosimilar Business.

Degree: ALM, Biotechnology Management, 2015, Harvard University

 This case study investigates the US biosimilar business and the approach that should be implemented when financially analyzing biosimilar development candidates. To challenge the theory… (more)

Subjects/Keywords: Business Administration, General; Health Sciences, General; Biology, General

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APA (6th Edition):

Gutierrez, B. J. (2015). Financial Analysis of Biosimilar Development Candidates: A Case Study on the US Biosimilar Business. (Masters Thesis). Harvard University. Retrieved from http://nrs.harvard.edu/urn-3:HUL.InstRepos:24078352

Chicago Manual of Style (16th Edition):

Gutierrez, Bryan J. “Financial Analysis of Biosimilar Development Candidates: A Case Study on the US Biosimilar Business.” 2015. Masters Thesis, Harvard University. Accessed October 16, 2018. http://nrs.harvard.edu/urn-3:HUL.InstRepos:24078352.

MLA Handbook (7th Edition):

Gutierrez, Bryan J. “Financial Analysis of Biosimilar Development Candidates: A Case Study on the US Biosimilar Business.” 2015. Web. 16 Oct 2018.

Vancouver:

Gutierrez BJ. Financial Analysis of Biosimilar Development Candidates: A Case Study on the US Biosimilar Business. [Internet] [Masters thesis]. Harvard University; 2015. [cited 2018 Oct 16]. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:24078352.

Council of Science Editors:

Gutierrez BJ. Financial Analysis of Biosimilar Development Candidates: A Case Study on the US Biosimilar Business. [Masters Thesis]. Harvard University; 2015. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:24078352


Harvard University

3. Schweber, Jessica Tobias Pinkham. Partial Depletion of Pth Increases Susceptibility to Macrolide Drug Treatment in M. Tuberculosis.

Degree: ALM, Biotechnology Life Sciences, 2016, Harvard University

 The goal of this work was to investigate whether a ubiquitous bacterial protein, peptidyl-tRNA hydrolase (Pth), would be an appropriate candidate for target-based drug discovery… (more)

Subjects/Keywords: Biology; Microbiology

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APA (6th Edition):

Schweber, J. T. P. (2016). Partial Depletion of Pth Increases Susceptibility to Macrolide Drug Treatment in M. Tuberculosis. (Masters Thesis). Harvard University. Retrieved from http://nrs.harvard.edu/urn-3:HUL.InstRepos:33797262

Chicago Manual of Style (16th Edition):

Schweber, Jessica Tobias Pinkham. “Partial Depletion of Pth Increases Susceptibility to Macrolide Drug Treatment in M. Tuberculosis.” 2016. Masters Thesis, Harvard University. Accessed October 16, 2018. http://nrs.harvard.edu/urn-3:HUL.InstRepos:33797262.

MLA Handbook (7th Edition):

Schweber, Jessica Tobias Pinkham. “Partial Depletion of Pth Increases Susceptibility to Macrolide Drug Treatment in M. Tuberculosis.” 2016. Web. 16 Oct 2018.

Vancouver:

Schweber JTP. Partial Depletion of Pth Increases Susceptibility to Macrolide Drug Treatment in M. Tuberculosis. [Internet] [Masters thesis]. Harvard University; 2016. [cited 2018 Oct 16]. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:33797262.

Council of Science Editors:

Schweber JTP. Partial Depletion of Pth Increases Susceptibility to Macrolide Drug Treatment in M. Tuberculosis. [Masters Thesis]. Harvard University; 2016. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:33797262


Harvard University

4. Hahn, SaraBeth. Key Business Strategy Tools to Survive a Patent Cliff in the Biopharmaceutical Industry.

Degree: ALM, 2016, Harvard University

 This case study presents the research gathered in seeking to identify a number of key business strategy tools that biopharmaceutical companies have used to revitalize… (more)

Subjects/Keywords: Health Sciences; General

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APA (6th Edition):

Hahn, S. (2016). Key Business Strategy Tools to Survive a Patent Cliff in the Biopharmaceutical Industry. (Masters Thesis). Harvard University. Retrieved from http://nrs.harvard.edu/urn-3:HUL.InstRepos:33797271

Chicago Manual of Style (16th Edition):

Hahn, SaraBeth. “Key Business Strategy Tools to Survive a Patent Cliff in the Biopharmaceutical Industry.” 2016. Masters Thesis, Harvard University. Accessed October 16, 2018. http://nrs.harvard.edu/urn-3:HUL.InstRepos:33797271.

MLA Handbook (7th Edition):

Hahn, SaraBeth. “Key Business Strategy Tools to Survive a Patent Cliff in the Biopharmaceutical Industry.” 2016. Web. 16 Oct 2018.

Vancouver:

Hahn S. Key Business Strategy Tools to Survive a Patent Cliff in the Biopharmaceutical Industry. [Internet] [Masters thesis]. Harvard University; 2016. [cited 2018 Oct 16]. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:33797271.

Council of Science Editors:

Hahn S. Key Business Strategy Tools to Survive a Patent Cliff in the Biopharmaceutical Industry. [Masters Thesis]. Harvard University; 2016. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:33797271


Harvard University

5. Beeks, Andrea O. Creatine Assay for Use on Bench Top Chemistry Analyzer: Quick Analysis of Creatine in Human Serum Smaples.

Degree: ALM, 2016, Harvard University

 Creatine (Cr) was initially discovered in the 1830s by a Frenchman named Chevreul. In subsequent years, it was discovered that creatine was utilized by the… (more)

Subjects/Keywords: Biology, General; Chemistry, Analytical

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APA (6th Edition):

Beeks, A. O. (2016). Creatine Assay for Use on Bench Top Chemistry Analyzer: Quick Analysis of Creatine in Human Serum Smaples. (Masters Thesis). Harvard University. Retrieved from http://nrs.harvard.edu/urn-3:HUL.InstRepos:33797310

Chicago Manual of Style (16th Edition):

Beeks, Andrea O. “Creatine Assay for Use on Bench Top Chemistry Analyzer: Quick Analysis of Creatine in Human Serum Smaples.” 2016. Masters Thesis, Harvard University. Accessed October 16, 2018. http://nrs.harvard.edu/urn-3:HUL.InstRepos:33797310.

MLA Handbook (7th Edition):

Beeks, Andrea O. “Creatine Assay for Use on Bench Top Chemistry Analyzer: Quick Analysis of Creatine in Human Serum Smaples.” 2016. Web. 16 Oct 2018.

Vancouver:

Beeks AO. Creatine Assay for Use on Bench Top Chemistry Analyzer: Quick Analysis of Creatine in Human Serum Smaples. [Internet] [Masters thesis]. Harvard University; 2016. [cited 2018 Oct 16]. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:33797310.

Council of Science Editors:

Beeks AO. Creatine Assay for Use on Bench Top Chemistry Analyzer: Quick Analysis of Creatine in Human Serum Smaples. [Masters Thesis]. Harvard University; 2016. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:33797310


Harvard University

6. Merluzzo, Angela M. A Novel Diagnostic Approach to Screen for Chemotherapy Drug Response in Non-Small Cell Lung Cancer Using Sortase Technology.

Degree: ALM, Biotechnology, 2016, Harvard University

 Drug resistance is the most significant barrier to improving long-term outcomes for patients with non-small cell lung cancer (NSCLC). Recent advances in the understanding of… (more)

Subjects/Keywords: Biology, Cell; Biology, Molecular; Health Sciences, Oncology

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APA (6th Edition):

Merluzzo, A. M. (2016). A Novel Diagnostic Approach to Screen for Chemotherapy Drug Response in Non-Small Cell Lung Cancer Using Sortase Technology. (Masters Thesis). Harvard University. Retrieved from http://nrs.harvard.edu/urn-3:HUL.InstRepos:33797314

Chicago Manual of Style (16th Edition):

Merluzzo, Angela M. “A Novel Diagnostic Approach to Screen for Chemotherapy Drug Response in Non-Small Cell Lung Cancer Using Sortase Technology.” 2016. Masters Thesis, Harvard University. Accessed October 16, 2018. http://nrs.harvard.edu/urn-3:HUL.InstRepos:33797314.

MLA Handbook (7th Edition):

Merluzzo, Angela M. “A Novel Diagnostic Approach to Screen for Chemotherapy Drug Response in Non-Small Cell Lung Cancer Using Sortase Technology.” 2016. Web. 16 Oct 2018.

Vancouver:

Merluzzo AM. A Novel Diagnostic Approach to Screen for Chemotherapy Drug Response in Non-Small Cell Lung Cancer Using Sortase Technology. [Internet] [Masters thesis]. Harvard University; 2016. [cited 2018 Oct 16]. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:33797314.

Council of Science Editors:

Merluzzo AM. A Novel Diagnostic Approach to Screen for Chemotherapy Drug Response in Non-Small Cell Lung Cancer Using Sortase Technology. [Masters Thesis]. Harvard University; 2016. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:33797314


Harvard University

7. Greene-Colozzi, April. Using the CRISPR/Cas9 System to Derive an Isogenic BRCA1 Mutant (187delAG) Strain From a Wild Type BRCA1 Mammary Epithelial Strain.

Degree: ALM, Life Sciences, 2016, Harvard University

 A powerful new genomic engineering technique, the Clustered RegularInterspersed Short Palindromic Repeats (CRISPR), was co-opted from the immunesystem of bacteria and archaea, and uses specific… (more)

Subjects/Keywords: Health Sciences, Oncology; Biology, Molecular; Engineering, Biomedical

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APA (6th Edition):

Greene-Colozzi, A. (2016). Using the CRISPR/Cas9 System to Derive an Isogenic BRCA1 Mutant (187delAG) Strain From a Wild Type BRCA1 Mammary Epithelial Strain. (Masters Thesis). Harvard University. Retrieved from http://nrs.harvard.edu/urn-3:HUL.InstRepos:33797319

Chicago Manual of Style (16th Edition):

Greene-Colozzi, April. “Using the CRISPR/Cas9 System to Derive an Isogenic BRCA1 Mutant (187delAG) Strain From a Wild Type BRCA1 Mammary Epithelial Strain.” 2016. Masters Thesis, Harvard University. Accessed October 16, 2018. http://nrs.harvard.edu/urn-3:HUL.InstRepos:33797319.

MLA Handbook (7th Edition):

Greene-Colozzi, April. “Using the CRISPR/Cas9 System to Derive an Isogenic BRCA1 Mutant (187delAG) Strain From a Wild Type BRCA1 Mammary Epithelial Strain.” 2016. Web. 16 Oct 2018.

Vancouver:

Greene-Colozzi A. Using the CRISPR/Cas9 System to Derive an Isogenic BRCA1 Mutant (187delAG) Strain From a Wild Type BRCA1 Mammary Epithelial Strain. [Internet] [Masters thesis]. Harvard University; 2016. [cited 2018 Oct 16]. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:33797319.

Council of Science Editors:

Greene-Colozzi A. Using the CRISPR/Cas9 System to Derive an Isogenic BRCA1 Mutant (187delAG) Strain From a Wild Type BRCA1 Mammary Epithelial Strain. [Masters Thesis]. Harvard University; 2016. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:33797319


Harvard University

8. Friedsam, Claudia. Development of a New Uniform File Format for Neuroscience Data Across the Globe.

Degree: ALM, 2016, Harvard University

 With about 1011 neurons and about 1015 synaptic connections the human brain is among the most complex biologic systems ever observed (Rautenberg, Sobolev et al.… (more)

Subjects/Keywords: Biology, Neuroscience; Computer Science

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APA (6th Edition):

Friedsam, C. (2016). Development of a New Uniform File Format for Neuroscience Data Across the Globe. (Masters Thesis). Harvard University. Retrieved from http://nrs.harvard.edu/urn-3:HUL.InstRepos:33797333

Chicago Manual of Style (16th Edition):

Friedsam, Claudia. “Development of a New Uniform File Format for Neuroscience Data Across the Globe.” 2016. Masters Thesis, Harvard University. Accessed October 16, 2018. http://nrs.harvard.edu/urn-3:HUL.InstRepos:33797333.

MLA Handbook (7th Edition):

Friedsam, Claudia. “Development of a New Uniform File Format for Neuroscience Data Across the Globe.” 2016. Web. 16 Oct 2018.

Vancouver:

Friedsam C. Development of a New Uniform File Format for Neuroscience Data Across the Globe. [Internet] [Masters thesis]. Harvard University; 2016. [cited 2018 Oct 16]. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:33797333.

Council of Science Editors:

Friedsam C. Development of a New Uniform File Format for Neuroscience Data Across the Globe. [Masters Thesis]. Harvard University; 2016. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:33797333


Harvard University

9. Benso, Lia. Differential Function of in Vitro Generated Macrophages From Systemic Lupus Erythematosus and Non-Diseased Peripheral Blood Mononuclear Cells.

Degree: ALM, Biotechnology, 2016, Harvard University

 Macrophages are a major type of tissue resident phagocytic cell that help orchestrate the innate immune response (through recognition to highly conserved pathogens) as well… (more)

Subjects/Keywords: Biology; Cell

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APA (6th Edition):

Benso, L. (2016). Differential Function of in Vitro Generated Macrophages From Systemic Lupus Erythematosus and Non-Diseased Peripheral Blood Mononuclear Cells. (Masters Thesis). Harvard University. Retrieved from http://nrs.harvard.edu/urn-3:HUL.InstRepos:33797337

Chicago Manual of Style (16th Edition):

Benso, Lia. “Differential Function of in Vitro Generated Macrophages From Systemic Lupus Erythematosus and Non-Diseased Peripheral Blood Mononuclear Cells.” 2016. Masters Thesis, Harvard University. Accessed October 16, 2018. http://nrs.harvard.edu/urn-3:HUL.InstRepos:33797337.

MLA Handbook (7th Edition):

Benso, Lia. “Differential Function of in Vitro Generated Macrophages From Systemic Lupus Erythematosus and Non-Diseased Peripheral Blood Mononuclear Cells.” 2016. Web. 16 Oct 2018.

Vancouver:

Benso L. Differential Function of in Vitro Generated Macrophages From Systemic Lupus Erythematosus and Non-Diseased Peripheral Blood Mononuclear Cells. [Internet] [Masters thesis]. Harvard University; 2016. [cited 2018 Oct 16]. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:33797337.

Council of Science Editors:

Benso L. Differential Function of in Vitro Generated Macrophages From Systemic Lupus Erythematosus and Non-Diseased Peripheral Blood Mononuclear Cells. [Masters Thesis]. Harvard University; 2016. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:33797337


Harvard University

10. Powers, Elisabeth H. Determining the Feasibility of a Liposomal Prototype Formulation for GC-C Agonist Peptide Drug Delivery.

Degree: ALM, Biotechnology, Bioengineering and nanotechnology, 2016, Harvard University

 The purpose of this study was to determine the feasibility of using a liposomal formulation for the systemic delivery of a GC-C agonist peptide drug.… (more)

Subjects/Keywords: Chemistry, Pharmaceutical; Biology, General; Chemistry, Analytical

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APA (6th Edition):

Powers, E. H. (2016). Determining the Feasibility of a Liposomal Prototype Formulation for GC-C Agonist Peptide Drug Delivery. (Masters Thesis). Harvard University. Retrieved from http://nrs.harvard.edu/urn-3:HUL.InstRepos:33797338

Chicago Manual of Style (16th Edition):

Powers, Elisabeth H. “Determining the Feasibility of a Liposomal Prototype Formulation for GC-C Agonist Peptide Drug Delivery.” 2016. Masters Thesis, Harvard University. Accessed October 16, 2018. http://nrs.harvard.edu/urn-3:HUL.InstRepos:33797338.

MLA Handbook (7th Edition):

Powers, Elisabeth H. “Determining the Feasibility of a Liposomal Prototype Formulation for GC-C Agonist Peptide Drug Delivery.” 2016. Web. 16 Oct 2018.

Vancouver:

Powers EH. Determining the Feasibility of a Liposomal Prototype Formulation for GC-C Agonist Peptide Drug Delivery. [Internet] [Masters thesis]. Harvard University; 2016. [cited 2018 Oct 16]. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:33797338.

Council of Science Editors:

Powers EH. Determining the Feasibility of a Liposomal Prototype Formulation for GC-C Agonist Peptide Drug Delivery. [Masters Thesis]. Harvard University; 2016. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:33797338


Harvard University

11. O'Mara, Patrick. EpiProt: A Java Application Combining Protein Information With Epitope Prediction Software.

Degree: ALM, Bioinformatics, 2016, Harvard University

 EpiProt is a bioinformatics suite designed to help users determine antigenic regions within proteins for the production of antibodies. It combines seven epitope prediction programs… (more)

Subjects/Keywords: Biology, Bioinformatics; Computer Science; Biology, Molecular

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APA (6th Edition):

O'Mara, P. (2016). EpiProt: A Java Application Combining Protein Information With Epitope Prediction Software. (Masters Thesis). Harvard University. Retrieved from http://nrs.harvard.edu/urn-3:HUL.InstRepos:33797405

Chicago Manual of Style (16th Edition):

O'Mara, Patrick. “EpiProt: A Java Application Combining Protein Information With Epitope Prediction Software.” 2016. Masters Thesis, Harvard University. Accessed October 16, 2018. http://nrs.harvard.edu/urn-3:HUL.InstRepos:33797405.

MLA Handbook (7th Edition):

O'Mara, Patrick. “EpiProt: A Java Application Combining Protein Information With Epitope Prediction Software.” 2016. Web. 16 Oct 2018.

Vancouver:

O'Mara P. EpiProt: A Java Application Combining Protein Information With Epitope Prediction Software. [Internet] [Masters thesis]. Harvard University; 2016. [cited 2018 Oct 16]. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:33797405.

Council of Science Editors:

O'Mara P. EpiProt: A Java Application Combining Protein Information With Epitope Prediction Software. [Masters Thesis]. Harvard University; 2016. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:33797405


Harvard University

12. Sykes, Sean M. Genomic Analysis of the Population Structure and Virulence of the Human Pathogen, Cryptococcus Neoformans Var. Grubii.

Degree: ALM, 2017, Harvard University

 This study examined a large cohort of clinical and environmental strains of Cryptococcus neoformans var. grubii to better understand its population structure and identify potential… (more)

Subjects/Keywords: Biology; Bioinformatics

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APA (6th Edition):

Sykes, S. M. (2017). Genomic Analysis of the Population Structure and Virulence of the Human Pathogen, Cryptococcus Neoformans Var. Grubii. (Masters Thesis). Harvard University. Retrieved from http://nrs.harvard.edu/urn-3:HUL.InstRepos:33813402

Chicago Manual of Style (16th Edition):

Sykes, Sean M. “Genomic Analysis of the Population Structure and Virulence of the Human Pathogen, Cryptococcus Neoformans Var. Grubii.” 2017. Masters Thesis, Harvard University. Accessed October 16, 2018. http://nrs.harvard.edu/urn-3:HUL.InstRepos:33813402.

MLA Handbook (7th Edition):

Sykes, Sean M. “Genomic Analysis of the Population Structure and Virulence of the Human Pathogen, Cryptococcus Neoformans Var. Grubii.” 2017. Web. 16 Oct 2018.

Vancouver:

Sykes SM. Genomic Analysis of the Population Structure and Virulence of the Human Pathogen, Cryptococcus Neoformans Var. Grubii. [Internet] [Masters thesis]. Harvard University; 2017. [cited 2018 Oct 16]. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:33813402.

Council of Science Editors:

Sykes SM. Genomic Analysis of the Population Structure and Virulence of the Human Pathogen, Cryptococcus Neoformans Var. Grubii. [Masters Thesis]. Harvard University; 2017. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:33813402

13. Williams, Miguel. A Skin Substitute Reepithelialization Calculator for Natural, Synthetic, and Composite Skin Cell Scaffolds.

Degree: ALM, 2017, Harvard University

 Tissue engineering is a rapidly advancing field. Researchers around the globe have been working on novel ways to replicate the natural properties of tissues and… (more)

Subjects/Keywords: Engineering; Materials Science

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APA (6th Edition):

Williams, M. (2017). A Skin Substitute Reepithelialization Calculator for Natural, Synthetic, and Composite Skin Cell Scaffolds. (Masters Thesis). Harvard University. Retrieved from http://nrs.harvard.edu/urn-3:HUL.InstRepos:33813409

Chicago Manual of Style (16th Edition):

Williams, Miguel. “A Skin Substitute Reepithelialization Calculator for Natural, Synthetic, and Composite Skin Cell Scaffolds.” 2017. Masters Thesis, Harvard University. Accessed October 16, 2018. http://nrs.harvard.edu/urn-3:HUL.InstRepos:33813409.

MLA Handbook (7th Edition):

Williams, Miguel. “A Skin Substitute Reepithelialization Calculator for Natural, Synthetic, and Composite Skin Cell Scaffolds.” 2017. Web. 16 Oct 2018.

Vancouver:

Williams M. A Skin Substitute Reepithelialization Calculator for Natural, Synthetic, and Composite Skin Cell Scaffolds. [Internet] [Masters thesis]. Harvard University; 2017. [cited 2018 Oct 16]. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:33813409.

Council of Science Editors:

Williams M. A Skin Substitute Reepithelialization Calculator for Natural, Synthetic, and Composite Skin Cell Scaffolds. [Masters Thesis]. Harvard University; 2017. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:33813409


Harvard University

14. Bigdeli, Ashkan. Annow: BLAST Based Analytical Sequence Annotation Software.

Degree: ALM, 2017, Harvard University

 As gene sequencing becomes more common the annotations that give meaning to biological data change. The large quantity of –omics data generated by these projects… (more)

Subjects/Keywords: Biology; Bioinformatics

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APA (6th Edition):

Bigdeli, A. (2017). Annow: BLAST Based Analytical Sequence Annotation Software. (Masters Thesis). Harvard University. Retrieved from http://nrs.harvard.edu/urn-3:HUL.InstRepos:33825849

Chicago Manual of Style (16th Edition):

Bigdeli, Ashkan. “Annow: BLAST Based Analytical Sequence Annotation Software.” 2017. Masters Thesis, Harvard University. Accessed October 16, 2018. http://nrs.harvard.edu/urn-3:HUL.InstRepos:33825849.

MLA Handbook (7th Edition):

Bigdeli, Ashkan. “Annow: BLAST Based Analytical Sequence Annotation Software.” 2017. Web. 16 Oct 2018.

Vancouver:

Bigdeli A. Annow: BLAST Based Analytical Sequence Annotation Software. [Internet] [Masters thesis]. Harvard University; 2017. [cited 2018 Oct 16]. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:33825849.

Council of Science Editors:

Bigdeli A. Annow: BLAST Based Analytical Sequence Annotation Software. [Masters Thesis]. Harvard University; 2017. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:33825849


Harvard University

15. Taylor, Bradley Ryan. An Analytical Method for Inferring Library Identity From Illumina NGS Read Groups.

Degree: ALM, 2017, Harvard University

 When working with genetic sequence data, it is important to know the individual, sample, and sequencing library from which the data derives. While multiple software… (more)

Subjects/Keywords: Biology, Bioinformatics; Biology, Genetics

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APA (6th Edition):

Taylor, B. R. (2017). An Analytical Method for Inferring Library Identity From Illumina NGS Read Groups. (Masters Thesis). Harvard University. Retrieved from http://nrs.harvard.edu/urn-3:HUL.InstRepos:33826059

Chicago Manual of Style (16th Edition):

Taylor, Bradley Ryan. “An Analytical Method for Inferring Library Identity From Illumina NGS Read Groups.” 2017. Masters Thesis, Harvard University. Accessed October 16, 2018. http://nrs.harvard.edu/urn-3:HUL.InstRepos:33826059.

MLA Handbook (7th Edition):

Taylor, Bradley Ryan. “An Analytical Method for Inferring Library Identity From Illumina NGS Read Groups.” 2017. Web. 16 Oct 2018.

Vancouver:

Taylor BR. An Analytical Method for Inferring Library Identity From Illumina NGS Read Groups. [Internet] [Masters thesis]. Harvard University; 2017. [cited 2018 Oct 16]. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:33826059.

Council of Science Editors:

Taylor BR. An Analytical Method for Inferring Library Identity From Illumina NGS Read Groups. [Masters Thesis]. Harvard University; 2017. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:33826059


Harvard University

16. Mota, Cassandra. Detection of Intracellular Cytokeratin 20 in CD14dim Monocytes: A Potential Tool for the Screening of Colorectal Adenocarcinoma in Peripheral Blood.

Degree: ALM, 2017, Harvard University

 Cancer is among the leading causes of death worldwide. Early and accurate detection is essential as it can effectively attenuate the dismal prognosis of this… (more)

Subjects/Keywords: Biology, Cell; Health Sciences, Immunology; Health Sciences, Medicine and Surgery

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APA (6th Edition):

Mota, C. (2017). Detection of Intracellular Cytokeratin 20 in CD14dim Monocytes: A Potential Tool for the Screening of Colorectal Adenocarcinoma in Peripheral Blood. (Masters Thesis). Harvard University. Retrieved from http://nrs.harvard.edu/urn-3:HUL.InstRepos:33826081

Chicago Manual of Style (16th Edition):

Mota, Cassandra. “Detection of Intracellular Cytokeratin 20 in CD14dim Monocytes: A Potential Tool for the Screening of Colorectal Adenocarcinoma in Peripheral Blood.” 2017. Masters Thesis, Harvard University. Accessed October 16, 2018. http://nrs.harvard.edu/urn-3:HUL.InstRepos:33826081.

MLA Handbook (7th Edition):

Mota, Cassandra. “Detection of Intracellular Cytokeratin 20 in CD14dim Monocytes: A Potential Tool for the Screening of Colorectal Adenocarcinoma in Peripheral Blood.” 2017. Web. 16 Oct 2018.

Vancouver:

Mota C. Detection of Intracellular Cytokeratin 20 in CD14dim Monocytes: A Potential Tool for the Screening of Colorectal Adenocarcinoma in Peripheral Blood. [Internet] [Masters thesis]. Harvard University; 2017. [cited 2018 Oct 16]. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:33826081.

Council of Science Editors:

Mota C. Detection of Intracellular Cytokeratin 20 in CD14dim Monocytes: A Potential Tool for the Screening of Colorectal Adenocarcinoma in Peripheral Blood. [Masters Thesis]. Harvard University; 2017. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:33826081


Harvard University

17. Srinivasan, Sharanya. High-Throughput Mapping of Diverse Functional Genomic Elements Governing BRCA2 Expression.

Degree: ALM, 2017, Harvard University

 The goal of this work is to develop a high-throughput approach to quantify the functional impact of the regulatory genome on target gene expression, and… (more)

Subjects/Keywords: Biology; Genetics

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APA (6th Edition):

Srinivasan, S. (2017). High-Throughput Mapping of Diverse Functional Genomic Elements Governing BRCA2 Expression. (Masters Thesis). Harvard University. Retrieved from http://nrs.harvard.edu/urn-3:HUL.InstRepos:33826163

Chicago Manual of Style (16th Edition):

Srinivasan, Sharanya. “High-Throughput Mapping of Diverse Functional Genomic Elements Governing BRCA2 Expression.” 2017. Masters Thesis, Harvard University. Accessed October 16, 2018. http://nrs.harvard.edu/urn-3:HUL.InstRepos:33826163.

MLA Handbook (7th Edition):

Srinivasan, Sharanya. “High-Throughput Mapping of Diverse Functional Genomic Elements Governing BRCA2 Expression.” 2017. Web. 16 Oct 2018.

Vancouver:

Srinivasan S. High-Throughput Mapping of Diverse Functional Genomic Elements Governing BRCA2 Expression. [Internet] [Masters thesis]. Harvard University; 2017. [cited 2018 Oct 16]. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:33826163.

Council of Science Editors:

Srinivasan S. High-Throughput Mapping of Diverse Functional Genomic Elements Governing BRCA2 Expression. [Masters Thesis]. Harvard University; 2017. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:33826163


Harvard University

18. Njenga, Moses. Design and Characterization of a Stealth Immunoliposome Encapsulating a Large Molecule Biotherapeutic (Antibody).

Degree: ALM, 2017, Harvard University

 This thesis project will endeavor to solve the obstacles around synthesis of Immunoliposomes loaded with an antibody therapeutic. Most steps in the preparation of liposomes… (more)

Subjects/Keywords: Biology, General; Biology, General

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APA (6th Edition):

Njenga, M. (2017). Design and Characterization of a Stealth Immunoliposome Encapsulating a Large Molecule Biotherapeutic (Antibody). (Masters Thesis). Harvard University. Retrieved from http://nrs.harvard.edu/urn-3:HUL.InstRepos:33826206

Chicago Manual of Style (16th Edition):

Njenga, Moses. “Design and Characterization of a Stealth Immunoliposome Encapsulating a Large Molecule Biotherapeutic (Antibody).” 2017. Masters Thesis, Harvard University. Accessed October 16, 2018. http://nrs.harvard.edu/urn-3:HUL.InstRepos:33826206.

MLA Handbook (7th Edition):

Njenga, Moses. “Design and Characterization of a Stealth Immunoliposome Encapsulating a Large Molecule Biotherapeutic (Antibody).” 2017. Web. 16 Oct 2018.

Vancouver:

Njenga M. Design and Characterization of a Stealth Immunoliposome Encapsulating a Large Molecule Biotherapeutic (Antibody). [Internet] [Masters thesis]. Harvard University; 2017. [cited 2018 Oct 16]. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:33826206.

Council of Science Editors:

Njenga M. Design and Characterization of a Stealth Immunoliposome Encapsulating a Large Molecule Biotherapeutic (Antibody). [Masters Thesis]. Harvard University; 2017. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:33826206


Harvard University

19. Wilk, Katarzyna. Differential Gene Expression and Pathway Analysis of Prx1-Expressing Cells in Calvarial Sutures and Long Bone Periosteum.

Degree: ALM, 2017, Harvard University

 The Pair-related homeobox transcription factor (Prx1) is required for normal development of the cranium and axial skeleton. Prx1-expressing cells are found in the suture of… (more)

Subjects/Keywords: Biology, Molecular; Biology, Bioinformatics

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APA (6th Edition):

Wilk, K. (2017). Differential Gene Expression and Pathway Analysis of Prx1-Expressing Cells in Calvarial Sutures and Long Bone Periosteum. (Masters Thesis). Harvard University. Retrieved from http://nrs.harvard.edu/urn-3:HUL.InstRepos:33826387

Chicago Manual of Style (16th Edition):

Wilk, Katarzyna. “Differential Gene Expression and Pathway Analysis of Prx1-Expressing Cells in Calvarial Sutures and Long Bone Periosteum.” 2017. Masters Thesis, Harvard University. Accessed October 16, 2018. http://nrs.harvard.edu/urn-3:HUL.InstRepos:33826387.

MLA Handbook (7th Edition):

Wilk, Katarzyna. “Differential Gene Expression and Pathway Analysis of Prx1-Expressing Cells in Calvarial Sutures and Long Bone Periosteum.” 2017. Web. 16 Oct 2018.

Vancouver:

Wilk K. Differential Gene Expression and Pathway Analysis of Prx1-Expressing Cells in Calvarial Sutures and Long Bone Periosteum. [Internet] [Masters thesis]. Harvard University; 2017. [cited 2018 Oct 16]. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:33826387.

Council of Science Editors:

Wilk K. Differential Gene Expression and Pathway Analysis of Prx1-Expressing Cells in Calvarial Sutures and Long Bone Periosteum. [Masters Thesis]. Harvard University; 2017. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:33826387


Harvard University

20. Wright, Quentin George. Role of Microbiota in Strengthening Ocular Mucosal Barrier Function Through Secretory IgA.

Degree: ALM, 2017, Harvard University

 Unlike other mucosal sites, the ocular mucosal surfaces are paucibacterial, which suggests that effective cellular and molecular mechanisms ensure limited commensal presence. Given that secretory… (more)

Subjects/Keywords: Health Sciences, Immunology; Biology, General; Health Sciences, Ophthalmology

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APA (6th Edition):

Wright, Q. G. (2017). Role of Microbiota in Strengthening Ocular Mucosal Barrier Function Through Secretory IgA. (Masters Thesis). Harvard University. Retrieved from http://nrs.harvard.edu/urn-3:HUL.InstRepos:33826852

Chicago Manual of Style (16th Edition):

Wright, Quentin George. “Role of Microbiota in Strengthening Ocular Mucosal Barrier Function Through Secretory IgA.” 2017. Masters Thesis, Harvard University. Accessed October 16, 2018. http://nrs.harvard.edu/urn-3:HUL.InstRepos:33826852.

MLA Handbook (7th Edition):

Wright, Quentin George. “Role of Microbiota in Strengthening Ocular Mucosal Barrier Function Through Secretory IgA.” 2017. Web. 16 Oct 2018.

Vancouver:

Wright QG. Role of Microbiota in Strengthening Ocular Mucosal Barrier Function Through Secretory IgA. [Internet] [Masters thesis]. Harvard University; 2017. [cited 2018 Oct 16]. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:33826852.

Council of Science Editors:

Wright QG. Role of Microbiota in Strengthening Ocular Mucosal Barrier Function Through Secretory IgA. [Masters Thesis]. Harvard University; 2017. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:33826852


Harvard University

21. López, John Emilio William. Genetic Diversity in Urban and Rural Indigenous Mexico.

Degree: ALM, Biotechnology, 2016, Harvard University

 The goal of this study was to examine the genetic diversity of indigenous (and semi-indigenous) populations in Mexico and determine if any genetic variation correlated… (more)

Subjects/Keywords: Biology, Genetics; Anthropology, Medical and Forensic; Sociology, Ethnic and Racial Studies

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APA (6th Edition):

López, J. E. W. (2016). Genetic Diversity in Urban and Rural Indigenous Mexico. (Masters Thesis). Harvard University. Retrieved from http://nrs.harvard.edu/urn-3:HUL.InstRepos:33797263

Chicago Manual of Style (16th Edition):

López, John Emilio William. “Genetic Diversity in Urban and Rural Indigenous Mexico.” 2016. Masters Thesis, Harvard University. Accessed October 16, 2018. http://nrs.harvard.edu/urn-3:HUL.InstRepos:33797263.

MLA Handbook (7th Edition):

López, John Emilio William. “Genetic Diversity in Urban and Rural Indigenous Mexico.” 2016. Web. 16 Oct 2018.

Vancouver:

López JEW. Genetic Diversity in Urban and Rural Indigenous Mexico. [Internet] [Masters thesis]. Harvard University; 2016. [cited 2018 Oct 16]. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:33797263.

Council of Science Editors:

López JEW. Genetic Diversity in Urban and Rural Indigenous Mexico. [Masters Thesis]. Harvard University; 2016. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:33797263


Harvard University

22. Khromykh, Alina. Cost-Effectiveness and Utility of Preemptive Pharmacogenomic Testing in Infants.

Degree: ALM, 2017, Harvard University

 The goal of this work is to investigate whether preemptive pharmacogenetic testing offered in early childhood displays cost-efficiency and is an economically advantageous screening option… (more)

Subjects/Keywords: Health Sciences, Health Care Management; Health Sciences, Pharmacology; Health Sciences, General

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APA (6th Edition):

Khromykh, A. (2017). Cost-Effectiveness and Utility of Preemptive Pharmacogenomic Testing in Infants. (Masters Thesis). Harvard University. Retrieved from http://nrs.harvard.edu/urn-3:HUL.InstRepos:33825891

Chicago Manual of Style (16th Edition):

Khromykh, Alina. “Cost-Effectiveness and Utility of Preemptive Pharmacogenomic Testing in Infants.” 2017. Masters Thesis, Harvard University. Accessed October 16, 2018. http://nrs.harvard.edu/urn-3:HUL.InstRepos:33825891.

MLA Handbook (7th Edition):

Khromykh, Alina. “Cost-Effectiveness and Utility of Preemptive Pharmacogenomic Testing in Infants.” 2017. Web. 16 Oct 2018.

Vancouver:

Khromykh A. Cost-Effectiveness and Utility of Preemptive Pharmacogenomic Testing in Infants. [Internet] [Masters thesis]. Harvard University; 2017. [cited 2018 Oct 16]. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:33825891.

Council of Science Editors:

Khromykh A. Cost-Effectiveness and Utility of Preemptive Pharmacogenomic Testing in Infants. [Masters Thesis]. Harvard University; 2017. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:33825891


Harvard University

23. Mayo, Tara C. Innovative Pricing Models Potentially Drive Payer Coverage: A Market Access Case Study for RNAi Therapeutics.

Degree: ALM, 2017, Harvard University

 The objective of this thesis is to establish a strong understanding of the US payer landscape and key influencers in the orphan disease space. This… (more)

Subjects/Keywords: Health Sciences; Health Care Management

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APA (6th Edition):

Mayo, T. C. (2017). Innovative Pricing Models Potentially Drive Payer Coverage: A Market Access Case Study for RNAi Therapeutics. (Masters Thesis). Harvard University. Retrieved from http://nrs.harvard.edu/urn-3:HUL.InstRepos:33813400

Chicago Manual of Style (16th Edition):

Mayo, Tara C. “Innovative Pricing Models Potentially Drive Payer Coverage: A Market Access Case Study for RNAi Therapeutics.” 2017. Masters Thesis, Harvard University. Accessed October 16, 2018. http://nrs.harvard.edu/urn-3:HUL.InstRepos:33813400.

MLA Handbook (7th Edition):

Mayo, Tara C. “Innovative Pricing Models Potentially Drive Payer Coverage: A Market Access Case Study for RNAi Therapeutics.” 2017. Web. 16 Oct 2018.

Vancouver:

Mayo TC. Innovative Pricing Models Potentially Drive Payer Coverage: A Market Access Case Study for RNAi Therapeutics. [Internet] [Masters thesis]. Harvard University; 2017. [cited 2018 Oct 16]. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:33813400.

Council of Science Editors:

Mayo TC. Innovative Pricing Models Potentially Drive Payer Coverage: A Market Access Case Study for RNAi Therapeutics. [Masters Thesis]. Harvard University; 2017. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:33813400


Harvard University

24. Salmon, Wendy C. Methods for Measuring Ciliary Calcium Dynamics: Potential Role for the Ciliary Inversin Compartment.

Degree: ALM, 2017, Harvard University

 The primary cilium is a cellular organelle at the nexus of many human disease syndromes that include polycystic kidney disease (PKD), embryonic developmental defects and… (more)

Subjects/Keywords: Biology; Cell

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APA (6th Edition):

Salmon, W. C. (2017). Methods for Measuring Ciliary Calcium Dynamics: Potential Role for the Ciliary Inversin Compartment. (Masters Thesis). Harvard University. Retrieved from http://nrs.harvard.edu/urn-3:HUL.InstRepos:33825975

Chicago Manual of Style (16th Edition):

Salmon, Wendy C. “Methods for Measuring Ciliary Calcium Dynamics: Potential Role for the Ciliary Inversin Compartment.” 2017. Masters Thesis, Harvard University. Accessed October 16, 2018. http://nrs.harvard.edu/urn-3:HUL.InstRepos:33825975.

MLA Handbook (7th Edition):

Salmon, Wendy C. “Methods for Measuring Ciliary Calcium Dynamics: Potential Role for the Ciliary Inversin Compartment.” 2017. Web. 16 Oct 2018.

Vancouver:

Salmon WC. Methods for Measuring Ciliary Calcium Dynamics: Potential Role for the Ciliary Inversin Compartment. [Internet] [Masters thesis]. Harvard University; 2017. [cited 2018 Oct 16]. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:33825975.

Council of Science Editors:

Salmon WC. Methods for Measuring Ciliary Calcium Dynamics: Potential Role for the Ciliary Inversin Compartment. [Masters Thesis]. Harvard University; 2017. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:33825975


Harvard University

25. Valerio, Manuel. An Analysis of the SmartCells Business Model and Its General Applicability Toward Building Successful Early-Stage Ventures in the Pharmaceutical Industry.

Degree: ALM, 2017, Harvard University

 SmartCells developed a technology that would re-engineer the existing pharmaceutical, insulin, to perform in a way that was safer and more efficacious than the original… (more)

Subjects/Keywords: Biology, General; Engineering, Biomedical; Business Administration, Management

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APA (6th Edition):

Valerio, M. (2017). An Analysis of the SmartCells Business Model and Its General Applicability Toward Building Successful Early-Stage Ventures in the Pharmaceutical Industry. (Masters Thesis). Harvard University. Retrieved from http://nrs.harvard.edu/urn-3:HUL.InstRepos:33826000

Chicago Manual of Style (16th Edition):

Valerio, Manuel. “An Analysis of the SmartCells Business Model and Its General Applicability Toward Building Successful Early-Stage Ventures in the Pharmaceutical Industry.” 2017. Masters Thesis, Harvard University. Accessed October 16, 2018. http://nrs.harvard.edu/urn-3:HUL.InstRepos:33826000.

MLA Handbook (7th Edition):

Valerio, Manuel. “An Analysis of the SmartCells Business Model and Its General Applicability Toward Building Successful Early-Stage Ventures in the Pharmaceutical Industry.” 2017. Web. 16 Oct 2018.

Vancouver:

Valerio M. An Analysis of the SmartCells Business Model and Its General Applicability Toward Building Successful Early-Stage Ventures in the Pharmaceutical Industry. [Internet] [Masters thesis]. Harvard University; 2017. [cited 2018 Oct 16]. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:33826000.

Council of Science Editors:

Valerio M. An Analysis of the SmartCells Business Model and Its General Applicability Toward Building Successful Early-Stage Ventures in the Pharmaceutical Industry. [Masters Thesis]. Harvard University; 2017. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:33826000


Harvard University

26. Sarno, Renee T. Expression of Soluble Guanylate Cyclase in Rat and Human Hepatocytes.

Degree: ALM, 2017, Harvard University

 Soluble Guanylate Cyclase (sGC) is a key enzyme in the nitric oxide (NO) signaling pathway. sGC binds NO to produce cyclic guanosine-3’,5’-monophosphate (cGMP). The NO-sGC-cGMP… (more)

Subjects/Keywords: Biology, Cell; Biology, Molecular

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APA (6th Edition):

Sarno, R. T. (2017). Expression of Soluble Guanylate Cyclase in Rat and Human Hepatocytes. (Masters Thesis). Harvard University. Retrieved from http://nrs.harvard.edu/urn-3:HUL.InstRepos:33826016

Chicago Manual of Style (16th Edition):

Sarno, Renee T. “Expression of Soluble Guanylate Cyclase in Rat and Human Hepatocytes.” 2017. Masters Thesis, Harvard University. Accessed October 16, 2018. http://nrs.harvard.edu/urn-3:HUL.InstRepos:33826016.

MLA Handbook (7th Edition):

Sarno, Renee T. “Expression of Soluble Guanylate Cyclase in Rat and Human Hepatocytes.” 2017. Web. 16 Oct 2018.

Vancouver:

Sarno RT. Expression of Soluble Guanylate Cyclase in Rat and Human Hepatocytes. [Internet] [Masters thesis]. Harvard University; 2017. [cited 2018 Oct 16]. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:33826016.

Council of Science Editors:

Sarno RT. Expression of Soluble Guanylate Cyclase in Rat and Human Hepatocytes. [Masters Thesis]. Harvard University; 2017. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:33826016

27. Tonini, Matthew. Examining the Anti-Inflammatory Characteristics of Translocator Protein Through IL-10 Modulation.

Degree: ALM, Biotechnology, 2015, Harvard University

 Several central nervous system related diseases involve various cellular inflammation related components. Among others these components include increases in complement activation and synthesis of inflammatory… (more)

Subjects/Keywords: Biology, Cell; Biology, Neuroscience; Biology, Microbiology

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APA (6th Edition):

Tonini, M. (2015). Examining the Anti-Inflammatory Characteristics of Translocator Protein Through IL-10 Modulation. (Masters Thesis). Harvard University. Retrieved from http://nrs.harvard.edu/urn-3:HUL.InstRepos:24078348

Chicago Manual of Style (16th Edition):

Tonini, Matthew. “Examining the Anti-Inflammatory Characteristics of Translocator Protein Through IL-10 Modulation.” 2015. Masters Thesis, Harvard University. Accessed October 16, 2018. http://nrs.harvard.edu/urn-3:HUL.InstRepos:24078348.

MLA Handbook (7th Edition):

Tonini, Matthew. “Examining the Anti-Inflammatory Characteristics of Translocator Protein Through IL-10 Modulation.” 2015. Web. 16 Oct 2018.

Vancouver:

Tonini M. Examining the Anti-Inflammatory Characteristics of Translocator Protein Through IL-10 Modulation. [Internet] [Masters thesis]. Harvard University; 2015. [cited 2018 Oct 16]. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:24078348.

Council of Science Editors:

Tonini M. Examining the Anti-Inflammatory Characteristics of Translocator Protein Through IL-10 Modulation. [Masters Thesis]. Harvard University; 2015. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:24078348

28. Koch, Tyree J. Aggregation Propensity: Characterization of Monoclonal Antibody Stability.

Degree: ALM, Biotechnology, 2015, Harvard University

 The study of aggregation propensity of a monoclonal antibody (mAb) and its sensitivity to applied stresses is believed to correlate with the overall stability of… (more)

Subjects/Keywords: Chemistry; Biochemistry

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APA (6th Edition):

Koch, T. J. (2015). Aggregation Propensity: Characterization of Monoclonal Antibody Stability. (Masters Thesis). Harvard University. Retrieved from http://nrs.harvard.edu/urn-3:HUL.InstRepos:24078351

Chicago Manual of Style (16th Edition):

Koch, Tyree J. “Aggregation Propensity: Characterization of Monoclonal Antibody Stability.” 2015. Masters Thesis, Harvard University. Accessed October 16, 2018. http://nrs.harvard.edu/urn-3:HUL.InstRepos:24078351.

MLA Handbook (7th Edition):

Koch, Tyree J. “Aggregation Propensity: Characterization of Monoclonal Antibody Stability.” 2015. Web. 16 Oct 2018.

Vancouver:

Koch TJ. Aggregation Propensity: Characterization of Monoclonal Antibody Stability. [Internet] [Masters thesis]. Harvard University; 2015. [cited 2018 Oct 16]. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:24078351.

Council of Science Editors:

Koch TJ. Aggregation Propensity: Characterization of Monoclonal Antibody Stability. [Masters Thesis]. Harvard University; 2015. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:24078351

29. Brewer, Judy. Metabolic Modeling of Inborn Errors of Metabolism: Carnitine Palmitoyltransferase II Deficiency and Respiratory Chain Complex I Deficiency.

Degree: ALM, Biotechnology, 2015, Harvard University

 The research goal was to assess the current capabilities of a metabolic modeling environment to support exploration of inborn errors of metabolism (IEMs); and to… (more)

Subjects/Keywords: Biology, Bioinformatics; Computer Science; Biology, Genetics

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APA (6th Edition):

Brewer, J. (2015). Metabolic Modeling of Inborn Errors of Metabolism: Carnitine Palmitoyltransferase II Deficiency and Respiratory Chain Complex I Deficiency. (Masters Thesis). Harvard University. Retrieved from http://nrs.harvard.edu/urn-3:HUL.InstRepos:24078365

Chicago Manual of Style (16th Edition):

Brewer, Judy. “Metabolic Modeling of Inborn Errors of Metabolism: Carnitine Palmitoyltransferase II Deficiency and Respiratory Chain Complex I Deficiency.” 2015. Masters Thesis, Harvard University. Accessed October 16, 2018. http://nrs.harvard.edu/urn-3:HUL.InstRepos:24078365.

MLA Handbook (7th Edition):

Brewer, Judy. “Metabolic Modeling of Inborn Errors of Metabolism: Carnitine Palmitoyltransferase II Deficiency and Respiratory Chain Complex I Deficiency.” 2015. Web. 16 Oct 2018.

Vancouver:

Brewer J. Metabolic Modeling of Inborn Errors of Metabolism: Carnitine Palmitoyltransferase II Deficiency and Respiratory Chain Complex I Deficiency. [Internet] [Masters thesis]. Harvard University; 2015. [cited 2018 Oct 16]. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:24078365.

Council of Science Editors:

Brewer J. Metabolic Modeling of Inborn Errors of Metabolism: Carnitine Palmitoyltransferase II Deficiency and Respiratory Chain Complex I Deficiency. [Masters Thesis]. Harvard University; 2015. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:24078365

30. So, Kathy. Pooled shRNA Library Screening to Identify Enhancers of Lysosomal Exocytosis.

Degree: ALM, Biotechnology, 2016, Harvard University

 Lysosomal exocytosis results in the removal of the lysosomal content by fusion of the lysosome with the plasma membrane, simultaneously relocating the lysosomal marker LAMP1… (more)

Subjects/Keywords: Biology; Cell

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APA (6th Edition):

So, K. (2016). Pooled shRNA Library Screening to Identify Enhancers of Lysosomal Exocytosis. (Masters Thesis). Harvard University. Retrieved from http://nrs.harvard.edu/urn-3:HUL.InstRepos:33797320

Chicago Manual of Style (16th Edition):

So, Kathy. “Pooled shRNA Library Screening to Identify Enhancers of Lysosomal Exocytosis.” 2016. Masters Thesis, Harvard University. Accessed October 16, 2018. http://nrs.harvard.edu/urn-3:HUL.InstRepos:33797320.

MLA Handbook (7th Edition):

So, Kathy. “Pooled shRNA Library Screening to Identify Enhancers of Lysosomal Exocytosis.” 2016. Web. 16 Oct 2018.

Vancouver:

So K. Pooled shRNA Library Screening to Identify Enhancers of Lysosomal Exocytosis. [Internet] [Masters thesis]. Harvard University; 2016. [cited 2018 Oct 16]. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:33797320.

Council of Science Editors:

So K. Pooled shRNA Library Screening to Identify Enhancers of Lysosomal Exocytosis. [Masters Thesis]. Harvard University; 2016. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:33797320

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