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You searched for +publisher:"University of Colorado" +contributor:("Leslie Leinwand"). Showing records 1 – 10 of 10 total matches.

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University of Colorado

1. Geng, Xin. Characterization of caspase regulation and Hepatitis B Virus induced cell death in the nematode Caenorhabditis elegans.

Degree: PhD, 2011, University of Colorado

  The nematode Caenorhabditis elegans has become a successful animal model for biomedical research, particularly in studying mechanisms of cell death and human disease. The… (more)

Subjects/Keywords: caspase; C.elegans; HBx; Cell Biology; Genetics

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APA (6th Edition):

Geng, X. (2011). Characterization of caspase regulation and Hepatitis B Virus induced cell death in the nematode Caenorhabditis elegans. (Doctoral Dissertation). University of Colorado. Retrieved from https://scholar.colorado.edu/mcdb_gradetds/2

Chicago Manual of Style (16th Edition):

Geng, Xin. “Characterization of caspase regulation and Hepatitis B Virus induced cell death in the nematode Caenorhabditis elegans.” 2011. Doctoral Dissertation, University of Colorado. Accessed March 30, 2020. https://scholar.colorado.edu/mcdb_gradetds/2.

MLA Handbook (7th Edition):

Geng, Xin. “Characterization of caspase regulation and Hepatitis B Virus induced cell death in the nematode Caenorhabditis elegans.” 2011. Web. 30 Mar 2020.

Vancouver:

Geng X. Characterization of caspase regulation and Hepatitis B Virus induced cell death in the nematode Caenorhabditis elegans. [Internet] [Doctoral dissertation]. University of Colorado; 2011. [cited 2020 Mar 30]. Available from: https://scholar.colorado.edu/mcdb_gradetds/2.

Council of Science Editors:

Geng X. Characterization of caspase regulation and Hepatitis B Virus induced cell death in the nematode Caenorhabditis elegans. [Doctoral Dissertation]. University of Colorado; 2011. Available from: https://scholar.colorado.edu/mcdb_gradetds/2


University of Colorado

2. Bilak, Amber. The Drosophila Receptor Tyrosine Kinase Tie Instructs Function of the bantam MicroRNA in the Response to Ionizing Radiation.

Degree: PhD, 2012, University of Colorado

  Life or death choices of cells in Drosophila depend on the accumulation of critical levels of pro-apoptotic factors such as hid. Ionizing radiation (IR)… (more)

Subjects/Keywords: apoptosis; bantam; Drosophila melanogaster; ionizing radiation; miRNA; tie; Cell Biology; Developmental Biology; Genetics

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APA (6th Edition):

Bilak, A. (2012). The Drosophila Receptor Tyrosine Kinase Tie Instructs Function of the bantam MicroRNA in the Response to Ionizing Radiation. (Doctoral Dissertation). University of Colorado. Retrieved from https://scholar.colorado.edu/mcdb_gradetds/10

Chicago Manual of Style (16th Edition):

Bilak, Amber. “The Drosophila Receptor Tyrosine Kinase Tie Instructs Function of the bantam MicroRNA in the Response to Ionizing Radiation.” 2012. Doctoral Dissertation, University of Colorado. Accessed March 30, 2020. https://scholar.colorado.edu/mcdb_gradetds/10.

MLA Handbook (7th Edition):

Bilak, Amber. “The Drosophila Receptor Tyrosine Kinase Tie Instructs Function of the bantam MicroRNA in the Response to Ionizing Radiation.” 2012. Web. 30 Mar 2020.

Vancouver:

Bilak A. The Drosophila Receptor Tyrosine Kinase Tie Instructs Function of the bantam MicroRNA in the Response to Ionizing Radiation. [Internet] [Doctoral dissertation]. University of Colorado; 2012. [cited 2020 Mar 30]. Available from: https://scholar.colorado.edu/mcdb_gradetds/10.

Council of Science Editors:

Bilak A. The Drosophila Receptor Tyrosine Kinase Tie Instructs Function of the bantam MicroRNA in the Response to Ionizing Radiation. [Doctoral Dissertation]. University of Colorado; 2012. Available from: https://scholar.colorado.edu/mcdb_gradetds/10


University of Colorado

3. Deacon, John C. Fast kinetics of human myosin heavy chain contraction in health and disease.

Degree: PhD, 2012, University of Colorado

  The myosin heavy chain composition of human heart and skeletal muscles is dynamic in health and disease and is known to define the maximum… (more)

Subjects/Keywords: Kinetics; Muscle; Myosin; Biochemistry; Biophysics; Molecular Biology

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APA (6th Edition):

Deacon, J. C. (2012). Fast kinetics of human myosin heavy chain contraction in health and disease. (Doctoral Dissertation). University of Colorado. Retrieved from https://scholar.colorado.edu/mcdb_gradetds/11

Chicago Manual of Style (16th Edition):

Deacon, John C. “Fast kinetics of human myosin heavy chain contraction in health and disease.” 2012. Doctoral Dissertation, University of Colorado. Accessed March 30, 2020. https://scholar.colorado.edu/mcdb_gradetds/11.

MLA Handbook (7th Edition):

Deacon, John C. “Fast kinetics of human myosin heavy chain contraction in health and disease.” 2012. Web. 30 Mar 2020.

Vancouver:

Deacon JC. Fast kinetics of human myosin heavy chain contraction in health and disease. [Internet] [Doctoral dissertation]. University of Colorado; 2012. [cited 2020 Mar 30]. Available from: https://scholar.colorado.edu/mcdb_gradetds/11.

Council of Science Editors:

Deacon JC. Fast kinetics of human myosin heavy chain contraction in health and disease. [Doctoral Dissertation]. University of Colorado; 2012. Available from: https://scholar.colorado.edu/mcdb_gradetds/11


University of Colorado

4. Gould, Sarah Trexler. Integrin Binding Peptide-Functionalized Poly(Ethylene Glycol) Hydrogels for Understanding the Role of Matricellular Effects on VIC Phenotype and Tissue Deposition.

Degree: PhD, Chemical & Biochemical Engineering, 2013, University of Colorado

  Aortic valve stenosis (AS) results in almost 100,000 valve replacement surgeries per year in the United States. These replacements are generally made of synthetic… (more)

Subjects/Keywords: Aortic Valve Stenosis; ECM; Hydrogels; Myofibroblasts; PEG; VICs; Biomedical Engineering and Bioengineering; Chemical Engineering

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APA (6th Edition):

Gould, S. T. (2013). Integrin Binding Peptide-Functionalized Poly(Ethylene Glycol) Hydrogels for Understanding the Role of Matricellular Effects on VIC Phenotype and Tissue Deposition. (Doctoral Dissertation). University of Colorado. Retrieved from https://scholar.colorado.edu/chbe_gradetds/51

Chicago Manual of Style (16th Edition):

Gould, Sarah Trexler. “Integrin Binding Peptide-Functionalized Poly(Ethylene Glycol) Hydrogels for Understanding the Role of Matricellular Effects on VIC Phenotype and Tissue Deposition.” 2013. Doctoral Dissertation, University of Colorado. Accessed March 30, 2020. https://scholar.colorado.edu/chbe_gradetds/51.

MLA Handbook (7th Edition):

Gould, Sarah Trexler. “Integrin Binding Peptide-Functionalized Poly(Ethylene Glycol) Hydrogels for Understanding the Role of Matricellular Effects on VIC Phenotype and Tissue Deposition.” 2013. Web. 30 Mar 2020.

Vancouver:

Gould ST. Integrin Binding Peptide-Functionalized Poly(Ethylene Glycol) Hydrogels for Understanding the Role of Matricellular Effects on VIC Phenotype and Tissue Deposition. [Internet] [Doctoral dissertation]. University of Colorado; 2013. [cited 2020 Mar 30]. Available from: https://scholar.colorado.edu/chbe_gradetds/51.

Council of Science Editors:

Gould ST. Integrin Binding Peptide-Functionalized Poly(Ethylene Glycol) Hydrogels for Understanding the Role of Matricellular Effects on VIC Phenotype and Tissue Deposition. [Doctoral Dissertation]. University of Colorado; 2013. Available from: https://scholar.colorado.edu/chbe_gradetds/51


University of Colorado

5. Wemmer, Megan Anne. Regulation of ESCRT-III Assembly and Membrane Scission Activity in the Budding Yeast Saccharomyces cerevisiae.

Degree: PhD, 2011, University of Colorado

  The sequential recruitment and assembly of endosomal sorting complexes required for transport (ESCRTs) at the endosomal membrane mediate the selection and clustering of cargoes… (more)

Subjects/Keywords: electron microscopy; electron tomography; endosome; ESCRT; multivesicular body; Biology; Cell Biology; Molecular Biology

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APA (6th Edition):

Wemmer, M. A. (2011). Regulation of ESCRT-III Assembly and Membrane Scission Activity in the Budding Yeast Saccharomyces cerevisiae. (Doctoral Dissertation). University of Colorado. Retrieved from https://scholar.colorado.edu/mcdb_gradetds/45

Chicago Manual of Style (16th Edition):

Wemmer, Megan Anne. “Regulation of ESCRT-III Assembly and Membrane Scission Activity in the Budding Yeast Saccharomyces cerevisiae.” 2011. Doctoral Dissertation, University of Colorado. Accessed March 30, 2020. https://scholar.colorado.edu/mcdb_gradetds/45.

MLA Handbook (7th Edition):

Wemmer, Megan Anne. “Regulation of ESCRT-III Assembly and Membrane Scission Activity in the Budding Yeast Saccharomyces cerevisiae.” 2011. Web. 30 Mar 2020.

Vancouver:

Wemmer MA. Regulation of ESCRT-III Assembly and Membrane Scission Activity in the Budding Yeast Saccharomyces cerevisiae. [Internet] [Doctoral dissertation]. University of Colorado; 2011. [cited 2020 Mar 30]. Available from: https://scholar.colorado.edu/mcdb_gradetds/45.

Council of Science Editors:

Wemmer MA. Regulation of ESCRT-III Assembly and Membrane Scission Activity in the Budding Yeast Saccharomyces cerevisiae. [Doctoral Dissertation]. University of Colorado; 2011. Available from: https://scholar.colorado.edu/mcdb_gradetds/45


University of Colorado

6. O'Hara, Samantha D. Polyomavirus Interactions with Host Cell Surface Receptors Mediate Important Steps in Virus Infection: from Signaling to Pathogenesis.

Degree: PhD, 2016, University of Colorado

  Virus binding to the cell surface triggers an array of host responses important for infection. Gangliosides are the cell surface receptors for Polyomavirus (PyV)… (more)

Subjects/Keywords: Gangliosides; Host-pathogen interactions; Virus entry; Virus-receptor interactions; Virus Signaling; Cell Biology; Molecular Biology; Virology

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APA (6th Edition):

O'Hara, S. D. (2016). Polyomavirus Interactions with Host Cell Surface Receptors Mediate Important Steps in Virus Infection: from Signaling to Pathogenesis. (Doctoral Dissertation). University of Colorado. Retrieved from https://scholar.colorado.edu/mcdb_gradetds/63

Chicago Manual of Style (16th Edition):

O'Hara, Samantha D. “Polyomavirus Interactions with Host Cell Surface Receptors Mediate Important Steps in Virus Infection: from Signaling to Pathogenesis.” 2016. Doctoral Dissertation, University of Colorado. Accessed March 30, 2020. https://scholar.colorado.edu/mcdb_gradetds/63.

MLA Handbook (7th Edition):

O'Hara, Samantha D. “Polyomavirus Interactions with Host Cell Surface Receptors Mediate Important Steps in Virus Infection: from Signaling to Pathogenesis.” 2016. Web. 30 Mar 2020.

Vancouver:

O'Hara SD. Polyomavirus Interactions with Host Cell Surface Receptors Mediate Important Steps in Virus Infection: from Signaling to Pathogenesis. [Internet] [Doctoral dissertation]. University of Colorado; 2016. [cited 2020 Mar 30]. Available from: https://scholar.colorado.edu/mcdb_gradetds/63.

Council of Science Editors:

O'Hara SD. Polyomavirus Interactions with Host Cell Surface Receptors Mediate Important Steps in Virus Infection: from Signaling to Pathogenesis. [Doctoral Dissertation]. University of Colorado; 2016. Available from: https://scholar.colorado.edu/mcdb_gradetds/63


University of Colorado

7. Busha, David. A Novel Selection Technology for the Discovery of High-Affinity Human Proteins.

Degree: PhD, 2014, University of Colorado

  Proteins that bind with high-affinity to cellular targets can be useful therapeutic treatments. High-throughput affinity screening of large protein libraries is often more successful… (more)

Subjects/Keywords: Affinity Selection; Directed Evolution; Display; HSV-1; Mammalian proteins; Proteins; Biomedical Engineering and Bioengineering; Molecular Biology; Virology

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APA (6th Edition):

Busha, D. (2014). A Novel Selection Technology for the Discovery of High-Affinity Human Proteins. (Doctoral Dissertation). University of Colorado. Retrieved from https://scholar.colorado.edu/mcdb_gradetds/29

Chicago Manual of Style (16th Edition):

Busha, David. “A Novel Selection Technology for the Discovery of High-Affinity Human Proteins.” 2014. Doctoral Dissertation, University of Colorado. Accessed March 30, 2020. https://scholar.colorado.edu/mcdb_gradetds/29.

MLA Handbook (7th Edition):

Busha, David. “A Novel Selection Technology for the Discovery of High-Affinity Human Proteins.” 2014. Web. 30 Mar 2020.

Vancouver:

Busha D. A Novel Selection Technology for the Discovery of High-Affinity Human Proteins. [Internet] [Doctoral dissertation]. University of Colorado; 2014. [cited 2020 Mar 30]. Available from: https://scholar.colorado.edu/mcdb_gradetds/29.

Council of Science Editors:

Busha D. A Novel Selection Technology for the Discovery of High-Affinity Human Proteins. [Doctoral Dissertation]. University of Colorado; 2014. Available from: https://scholar.colorado.edu/mcdb_gradetds/29


University of Colorado

8. Pulliam, Crystal Dawn. Examining Post-Transcriptional Regulation of Skeletal Muscle Satellite Cell Homeostasis, Activation and Fate Determination.

Degree: PhD, 2014, University of Colorado

  Skeletal muscle is essential for respiration, mobility, reproduction and metabolism. Deficits in muscle function due to disease, injury or age reduce both quality of… (more)

Subjects/Keywords: Aging; Homeostasis; Injury; Post-Transcriptional Regulation; Satellite Cell; Skeletal Muscle; Bioinformatics; Cell Biology; Molecular Biology

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APA (6th Edition):

Pulliam, C. D. (2014). Examining Post-Transcriptional Regulation of Skeletal Muscle Satellite Cell Homeostasis, Activation and Fate Determination. (Doctoral Dissertation). University of Colorado. Retrieved from https://scholar.colorado.edu/mcdb_gradetds/31

Chicago Manual of Style (16th Edition):

Pulliam, Crystal Dawn. “Examining Post-Transcriptional Regulation of Skeletal Muscle Satellite Cell Homeostasis, Activation and Fate Determination.” 2014. Doctoral Dissertation, University of Colorado. Accessed March 30, 2020. https://scholar.colorado.edu/mcdb_gradetds/31.

MLA Handbook (7th Edition):

Pulliam, Crystal Dawn. “Examining Post-Transcriptional Regulation of Skeletal Muscle Satellite Cell Homeostasis, Activation and Fate Determination.” 2014. Web. 30 Mar 2020.

Vancouver:

Pulliam CD. Examining Post-Transcriptional Regulation of Skeletal Muscle Satellite Cell Homeostasis, Activation and Fate Determination. [Internet] [Doctoral dissertation]. University of Colorado; 2014. [cited 2020 Mar 30]. Available from: https://scholar.colorado.edu/mcdb_gradetds/31.

Council of Science Editors:

Pulliam CD. Examining Post-Transcriptional Regulation of Skeletal Muscle Satellite Cell Homeostasis, Activation and Fate Determination. [Doctoral Dissertation]. University of Colorado; 2014. Available from: https://scholar.colorado.edu/mcdb_gradetds/31


University of Colorado

9. Pugach, Emily K. Sexually dimorphic cardiac adaptation is mediated by Cre expression, independent of estrogen-receptor-α expression.

Degree: PhD, Biology, 2015, University of Colorado

  The mammalian heart is a remarkably adaptable organ. In particular, the contractile cells of the heart, the cardiac myocytes can respond to dramatic changes… (more)

Subjects/Keywords: Transgenic; Bioinformatics; Biology; Cell Biology; Molecular Biology

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APA (6th Edition):

Pugach, E. K. (2015). Sexually dimorphic cardiac adaptation is mediated by Cre expression, independent of estrogen-receptor-α expression. (Doctoral Dissertation). University of Colorado. Retrieved from https://scholar.colorado.edu/mcdb_gradetds/34

Chicago Manual of Style (16th Edition):

Pugach, Emily K. “Sexually dimorphic cardiac adaptation is mediated by Cre expression, independent of estrogen-receptor-α expression.” 2015. Doctoral Dissertation, University of Colorado. Accessed March 30, 2020. https://scholar.colorado.edu/mcdb_gradetds/34.

MLA Handbook (7th Edition):

Pugach, Emily K. “Sexually dimorphic cardiac adaptation is mediated by Cre expression, independent of estrogen-receptor-α expression.” 2015. Web. 30 Mar 2020.

Vancouver:

Pugach EK. Sexually dimorphic cardiac adaptation is mediated by Cre expression, independent of estrogen-receptor-α expression. [Internet] [Doctoral dissertation]. University of Colorado; 2015. [cited 2020 Mar 30]. Available from: https://scholar.colorado.edu/mcdb_gradetds/34.

Council of Science Editors:

Pugach EK. Sexually dimorphic cardiac adaptation is mediated by Cre expression, independent of estrogen-receptor-α expression. [Doctoral Dissertation]. University of Colorado; 2015. Available from: https://scholar.colorado.edu/mcdb_gradetds/34


University of Colorado

10. Mabry, Kelly Marie Pollock. The Role of Matrix Properties in Directing Valvular Interstitial Cell Phenotype.

Degree: PhD, Chemical & Biochemical Engineering, 2015, University of Colorado

  This thesis presents the development of hydrogel platforms to study the fibroblast-to-myofibroblast transition in valvular interstitial cells (VICs). These systems were used to characterize… (more)

Subjects/Keywords: aortic stenosis; biomaterials; valves; Biomedical Engineering and Bioengineering; Cell Biology; Chemical Engineering

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APA (6th Edition):

Mabry, K. M. P. (2015). The Role of Matrix Properties in Directing Valvular Interstitial Cell Phenotype. (Doctoral Dissertation). University of Colorado. Retrieved from https://scholar.colorado.edu/chbe_gradetds/92

Chicago Manual of Style (16th Edition):

Mabry, Kelly Marie Pollock. “The Role of Matrix Properties in Directing Valvular Interstitial Cell Phenotype.” 2015. Doctoral Dissertation, University of Colorado. Accessed March 30, 2020. https://scholar.colorado.edu/chbe_gradetds/92.

MLA Handbook (7th Edition):

Mabry, Kelly Marie Pollock. “The Role of Matrix Properties in Directing Valvular Interstitial Cell Phenotype.” 2015. Web. 30 Mar 2020.

Vancouver:

Mabry KMP. The Role of Matrix Properties in Directing Valvular Interstitial Cell Phenotype. [Internet] [Doctoral dissertation]. University of Colorado; 2015. [cited 2020 Mar 30]. Available from: https://scholar.colorado.edu/chbe_gradetds/92.

Council of Science Editors:

Mabry KMP. The Role of Matrix Properties in Directing Valvular Interstitial Cell Phenotype. [Doctoral Dissertation]. University of Colorado; 2015. Available from: https://scholar.colorado.edu/chbe_gradetds/92

.