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You searched for +publisher:"University of Colorado" +contributor:("Rui Yi"). Showing records 1 – 19 of 19 total matches.

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University of Colorado

1. Brown, Tobin Elliott. Dynamic Hydrogels to Investigate Cell-Matrix Interactions.

Degree: PhD, 2018, University of Colorado

 Mammalian cells reside in contact with an extracellular matrix (ECM) with which they are inextricably linked. Native ECMs are instructive, and cells are able to… (more)

Subjects/Keywords: hydrogel; photodegradation; stem cells; photochemical; thioester; Chemical Engineering; Materials Science and Engineering

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APA (6th Edition):

Brown, T. E. (2018). Dynamic Hydrogels to Investigate Cell-Matrix Interactions. (Doctoral Dissertation). University of Colorado. Retrieved from https://scholar.colorado.edu/chbe_gradetds/116

Chicago Manual of Style (16th Edition):

Brown, Tobin Elliott. “Dynamic Hydrogels to Investigate Cell-Matrix Interactions.” 2018. Doctoral Dissertation, University of Colorado. Accessed April 08, 2020. https://scholar.colorado.edu/chbe_gradetds/116.

MLA Handbook (7th Edition):

Brown, Tobin Elliott. “Dynamic Hydrogels to Investigate Cell-Matrix Interactions.” 2018. Web. 08 Apr 2020.

Vancouver:

Brown TE. Dynamic Hydrogels to Investigate Cell-Matrix Interactions. [Internet] [Doctoral dissertation]. University of Colorado; 2018. [cited 2020 Apr 08]. Available from: https://scholar.colorado.edu/chbe_gradetds/116.

Council of Science Editors:

Brown TE. Dynamic Hydrogels to Investigate Cell-Matrix Interactions. [Doctoral Dissertation]. University of Colorado; 2018. Available from: https://scholar.colorado.edu/chbe_gradetds/116


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 April 08, 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. 08 Apr 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 Apr 08]. 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. Zhang, Zhaojie. Genomic Analysis of microRNAs in Mouse Skin: Quantification, Biogenesis, Target Recognition and Regulatory Functions.

Degree: PhD, 2013, University of Colorado

  MiRNAs are a class of small RNAs, approximately 20~22 nucleotides in length. These broadly conserved molecules represent a novel layer of gene regulation that… (more)

Subjects/Keywords: Argonaute; miR-203; miRNA; NGS; Developmental Biology; Molecular Biology

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APA (6th Edition):

Zhang, Z. (2013). Genomic Analysis of microRNAs in Mouse Skin: Quantification, Biogenesis, Target Recognition and Regulatory Functions. (Doctoral Dissertation). University of Colorado. Retrieved from https://scholar.colorado.edu/mcdb_gradetds/23

Chicago Manual of Style (16th Edition):

Zhang, Zhaojie. “Genomic Analysis of microRNAs in Mouse Skin: Quantification, Biogenesis, Target Recognition and Regulatory Functions.” 2013. Doctoral Dissertation, University of Colorado. Accessed April 08, 2020. https://scholar.colorado.edu/mcdb_gradetds/23.

MLA Handbook (7th Edition):

Zhang, Zhaojie. “Genomic Analysis of microRNAs in Mouse Skin: Quantification, Biogenesis, Target Recognition and Regulatory Functions.” 2013. Web. 08 Apr 2020.

Vancouver:

Zhang Z. Genomic Analysis of microRNAs in Mouse Skin: Quantification, Biogenesis, Target Recognition and Regulatory Functions. [Internet] [Doctoral dissertation]. University of Colorado; 2013. [cited 2020 Apr 08]. Available from: https://scholar.colorado.edu/mcdb_gradetds/23.

Council of Science Editors:

Zhang Z. Genomic Analysis of microRNAs in Mouse Skin: Quantification, Biogenesis, Target Recognition and Regulatory Functions. [Doctoral Dissertation]. University of Colorado; 2013. Available from: https://scholar.colorado.edu/mcdb_gradetds/23


University of Colorado

4. Read, Timothy. Identification and Characterization of Functional Regulatory Variants in S. cerevisiae.

Degree: PhD, 2015, University of Colorado

  Most genetic variants associated with disease occur within regulatory regions of the genome, underscoring the need to define the mechanisms that control differences in… (more)

Subjects/Keywords: disease; gene regulation; genomics; saccharomyces cerevisiae; expression profiling; RIM101 allele; Genomics; Pathogenic Microbiology

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APA (6th Edition):

Read, T. (2015). Identification and Characterization of Functional Regulatory Variants in S. cerevisiae. (Doctoral Dissertation). University of Colorado. Retrieved from https://scholar.colorado.edu/mcdb_gradetds/39

Chicago Manual of Style (16th Edition):

Read, Timothy. “Identification and Characterization of Functional Regulatory Variants in S. cerevisiae.” 2015. Doctoral Dissertation, University of Colorado. Accessed April 08, 2020. https://scholar.colorado.edu/mcdb_gradetds/39.

MLA Handbook (7th Edition):

Read, Timothy. “Identification and Characterization of Functional Regulatory Variants in S. cerevisiae.” 2015. Web. 08 Apr 2020.

Vancouver:

Read T. Identification and Characterization of Functional Regulatory Variants in S. cerevisiae. [Internet] [Doctoral dissertation]. University of Colorado; 2015. [cited 2020 Apr 08]. Available from: https://scholar.colorado.edu/mcdb_gradetds/39.

Council of Science Editors:

Read T. Identification and Characterization of Functional Regulatory Variants in S. cerevisiae. [Doctoral Dissertation]. University of Colorado; 2015. Available from: https://scholar.colorado.edu/mcdb_gradetds/39


University of Colorado

5. Bennett, Christopher. Investigating the molecular mechanisms and functions of the Musashi-2 RNA-binding protein.

Degree: PhD, 2016, University of Colorado

  The Musashi (Msi) family of RNA-binding proteins is post-transcriptional regulators of gene expression. They were discovered in 1994 as being required for Drosophila sensory… (more)

Subjects/Keywords: HITS-CLIP; Musashi; Ribosome Profiling; RNA -seq; Cell Biology; Molecular Biology

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APA (6th Edition):

Bennett, C. (2016). Investigating the molecular mechanisms and functions of the Musashi-2 RNA-binding protein. (Doctoral Dissertation). University of Colorado. Retrieved from https://scholar.colorado.edu/mcdb_gradetds/42

Chicago Manual of Style (16th Edition):

Bennett, Christopher. “Investigating the molecular mechanisms and functions of the Musashi-2 RNA-binding protein.” 2016. Doctoral Dissertation, University of Colorado. Accessed April 08, 2020. https://scholar.colorado.edu/mcdb_gradetds/42.

MLA Handbook (7th Edition):

Bennett, Christopher. “Investigating the molecular mechanisms and functions of the Musashi-2 RNA-binding protein.” 2016. Web. 08 Apr 2020.

Vancouver:

Bennett C. Investigating the molecular mechanisms and functions of the Musashi-2 RNA-binding protein. [Internet] [Doctoral dissertation]. University of Colorado; 2016. [cited 2020 Apr 08]. Available from: https://scholar.colorado.edu/mcdb_gradetds/42.

Council of Science Editors:

Bennett C. Investigating the molecular mechanisms and functions of the Musashi-2 RNA-binding protein. [Doctoral Dissertation]. University of Colorado; 2016. Available from: https://scholar.colorado.edu/mcdb_gradetds/42


University of Colorado

6. Shukla, Siddharth. Investigation of RNA Quality Control Pathways in RNP Hypo-Assembly Diseases.

Degree: PhD, Chemistry & Biochemistry, 2016, University of Colorado

  A key aspect of cellular function is the proper assembly and utilization of ribonucleoproteins (RNPs). Defects in the formation of RNPs lead to "RNP… (more)

Subjects/Keywords: human telomerase RNA; PARN; RNA quality control; RNP hypo-assembly; snRNA; Biochemistry

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APA (6th Edition):

Shukla, S. (2016). Investigation of RNA Quality Control Pathways in RNP Hypo-Assembly Diseases. (Doctoral Dissertation). University of Colorado. Retrieved from https://scholar.colorado.edu/chem_gradetds/199

Chicago Manual of Style (16th Edition):

Shukla, Siddharth. “Investigation of RNA Quality Control Pathways in RNP Hypo-Assembly Diseases.” 2016. Doctoral Dissertation, University of Colorado. Accessed April 08, 2020. https://scholar.colorado.edu/chem_gradetds/199.

MLA Handbook (7th Edition):

Shukla, Siddharth. “Investigation of RNA Quality Control Pathways in RNP Hypo-Assembly Diseases.” 2016. Web. 08 Apr 2020.

Vancouver:

Shukla S. Investigation of RNA Quality Control Pathways in RNP Hypo-Assembly Diseases. [Internet] [Doctoral dissertation]. University of Colorado; 2016. [cited 2020 Apr 08]. Available from: https://scholar.colorado.edu/chem_gradetds/199.

Council of Science Editors:

Shukla S. Investigation of RNA Quality Control Pathways in RNP Hypo-Assembly Diseases. [Doctoral Dissertation]. University of Colorado; 2016. Available from: https://scholar.colorado.edu/chem_gradetds/199


University of Colorado

7. Bernet, Jennifer Delaney. Dysregulated FGF and P38 MAPK Signaling Underlies Loss of Stem Cell Self-Renewal in Aging Skeletal Muscle.

Degree: PhD, 2013, University of Colorado

  Sarcopenia is a geriatric syndrome characterized by loss of skeletal muscle mass, skeletal muscle function and decreased regenerative capacity. A number of skeletal muscle-specific… (more)

Subjects/Keywords: adult stem cells; aging; hydrogels; regenerative medicine; skeletal muscle; stem cell niche; Cell Biology; Geriatrics; Molecular Biology

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APA (6th Edition):

Bernet, J. D. (2013). Dysregulated FGF and P38 MAPK Signaling Underlies Loss of Stem Cell Self-Renewal in Aging Skeletal Muscle. (Doctoral Dissertation). University of Colorado. Retrieved from https://scholar.colorado.edu/mcdb_gradetds/56

Chicago Manual of Style (16th Edition):

Bernet, Jennifer Delaney. “Dysregulated FGF and P38 MAPK Signaling Underlies Loss of Stem Cell Self-Renewal in Aging Skeletal Muscle.” 2013. Doctoral Dissertation, University of Colorado. Accessed April 08, 2020. https://scholar.colorado.edu/mcdb_gradetds/56.

MLA Handbook (7th Edition):

Bernet, Jennifer Delaney. “Dysregulated FGF and P38 MAPK Signaling Underlies Loss of Stem Cell Self-Renewal in Aging Skeletal Muscle.” 2013. Web. 08 Apr 2020.

Vancouver:

Bernet JD. Dysregulated FGF and P38 MAPK Signaling Underlies Loss of Stem Cell Self-Renewal in Aging Skeletal Muscle. [Internet] [Doctoral dissertation]. University of Colorado; 2013. [cited 2020 Apr 08]. Available from: https://scholar.colorado.edu/mcdb_gradetds/56.

Council of Science Editors:

Bernet JD. Dysregulated FGF and P38 MAPK Signaling Underlies Loss of Stem Cell Self-Renewal in Aging Skeletal Muscle. [Doctoral Dissertation]. University of Colorado; 2013. Available from: https://scholar.colorado.edu/mcdb_gradetds/56


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 April 08, 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. 08 Apr 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 Apr 08]. 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. Zabinsky, Rebecca A. miRNAs Collaborate with a Conserved RNA Binding Protein to Ensure Development and Stress Response in C. elegans.

Degree: PhD, 2015, University of Colorado

  miRNAs play critical roles in development and other cellular processes in C. elegans even though most individual miRNAs are not essential for development or… (more)

Subjects/Keywords: miRNA; development; C. elegans; stress conditions; gene regulation; developmental robustness; Vigilin; Developmental Biology; Genetics; Molecular Biology

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APA (6th Edition):

Zabinsky, R. A. (2015). miRNAs Collaborate with a Conserved RNA Binding Protein to Ensure Development and Stress Response in C. elegans. (Doctoral Dissertation). University of Colorado. Retrieved from https://scholar.colorado.edu/mcdb_gradetds/37

Chicago Manual of Style (16th Edition):

Zabinsky, Rebecca A. “miRNAs Collaborate with a Conserved RNA Binding Protein to Ensure Development and Stress Response in C. elegans.” 2015. Doctoral Dissertation, University of Colorado. Accessed April 08, 2020. https://scholar.colorado.edu/mcdb_gradetds/37.

MLA Handbook (7th Edition):

Zabinsky, Rebecca A. “miRNAs Collaborate with a Conserved RNA Binding Protein to Ensure Development and Stress Response in C. elegans.” 2015. Web. 08 Apr 2020.

Vancouver:

Zabinsky RA. miRNAs Collaborate with a Conserved RNA Binding Protein to Ensure Development and Stress Response in C. elegans. [Internet] [Doctoral dissertation]. University of Colorado; 2015. [cited 2020 Apr 08]. Available from: https://scholar.colorado.edu/mcdb_gradetds/37.

Council of Science Editors:

Zabinsky RA. miRNAs Collaborate with a Conserved RNA Binding Protein to Ensure Development and Stress Response in C. elegans. [Doctoral Dissertation]. University of Colorado; 2015. Available from: https://scholar.colorado.edu/mcdb_gradetds/37


University of Colorado

10. Wang, Li. Cell-intrinsic mechanisms governing stem cell quiescence and regulating cancer progression in mammalian skin.

Degree: PhD, 2015, University of Colorado

  Self-renewal of quiescent stem cells requires reentry of the cell cycle and activates cell division machinery. Molecular mechanisms that govern quiescence or promote self-renewal… (more)

Subjects/Keywords: cell self-renewal; multipotency; Bioinformatics; Biology; Developmental Biology

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APA (6th Edition):

Wang, L. (2015). Cell-intrinsic mechanisms governing stem cell quiescence and regulating cancer progression in mammalian skin. (Doctoral Dissertation). University of Colorado. Retrieved from https://scholar.colorado.edu/mcdb_gradetds/38

Chicago Manual of Style (16th Edition):

Wang, Li. “Cell-intrinsic mechanisms governing stem cell quiescence and regulating cancer progression in mammalian skin.” 2015. Doctoral Dissertation, University of Colorado. Accessed April 08, 2020. https://scholar.colorado.edu/mcdb_gradetds/38.

MLA Handbook (7th Edition):

Wang, Li. “Cell-intrinsic mechanisms governing stem cell quiescence and regulating cancer progression in mammalian skin.” 2015. Web. 08 Apr 2020.

Vancouver:

Wang L. Cell-intrinsic mechanisms governing stem cell quiescence and regulating cancer progression in mammalian skin. [Internet] [Doctoral dissertation]. University of Colorado; 2015. [cited 2020 Apr 08]. Available from: https://scholar.colorado.edu/mcdb_gradetds/38.

Council of Science Editors:

Wang L. Cell-intrinsic mechanisms governing stem cell quiescence and regulating cancer progression in mammalian skin. [Doctoral Dissertation]. University of Colorado; 2015. Available from: https://scholar.colorado.edu/mcdb_gradetds/38


University of Colorado

11. Burke, Russell Thomas. Understanding Exportin-1 as an Anti-Cancer Target.

Degree: PhD, 2018, University of Colorado

 Exportin-1 is a promising new anti-cancer target for selective inhibitors of nuclear export (SINE) molecules. Selinexor is a first-in-class SINE molecule in clinical trials for… (more)

Subjects/Keywords: cancer biology; cell biology; exportin-1; microscopy; nucleolus; targeted therapy; Cellular and Molecular Physiology; Molecular Biology

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APA (6th Edition):

Burke, R. T. (2018). Understanding Exportin-1 as an Anti-Cancer Target. (Doctoral Dissertation). University of Colorado. Retrieved from https://scholar.colorado.edu/mcdb_gradetds/83

Chicago Manual of Style (16th Edition):

Burke, Russell Thomas. “Understanding Exportin-1 as an Anti-Cancer Target.” 2018. Doctoral Dissertation, University of Colorado. Accessed April 08, 2020. https://scholar.colorado.edu/mcdb_gradetds/83.

MLA Handbook (7th Edition):

Burke, Russell Thomas. “Understanding Exportin-1 as an Anti-Cancer Target.” 2018. Web. 08 Apr 2020.

Vancouver:

Burke RT. Understanding Exportin-1 as an Anti-Cancer Target. [Internet] [Doctoral dissertation]. University of Colorado; 2018. [cited 2020 Apr 08]. Available from: https://scholar.colorado.edu/mcdb_gradetds/83.

Council of Science Editors:

Burke RT. Understanding Exportin-1 as an Anti-Cancer Target. [Doctoral Dissertation]. University of Colorado; 2018. Available from: https://scholar.colorado.edu/mcdb_gradetds/83


University of Colorado

12. Wang, Xueyin. The Molecular Basis of RNA Recognition and Transcriptional Regulation by FUS and PRC2.

Degree: PhD, 2018, University of Colorado

  RNA and protein interact with each other in the cell nucleus to form RNP (ribonucleoprotein) complexes. These RNPs play key roles in various steps… (more)

Subjects/Keywords: rna; protein; fused in sarcoma; polycomb repressive complex 2; methyltransferase; Biochemistry; Molecular Biology

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APA (6th Edition):

Wang, X. (2018). The Molecular Basis of RNA Recognition and Transcriptional Regulation by FUS and PRC2. (Doctoral Dissertation). University of Colorado. Retrieved from https://scholar.colorado.edu/chem_gradetds/271

Chicago Manual of Style (16th Edition):

Wang, Xueyin. “The Molecular Basis of RNA Recognition and Transcriptional Regulation by FUS and PRC2.” 2018. Doctoral Dissertation, University of Colorado. Accessed April 08, 2020. https://scholar.colorado.edu/chem_gradetds/271.

MLA Handbook (7th Edition):

Wang, Xueyin. “The Molecular Basis of RNA Recognition and Transcriptional Regulation by FUS and PRC2.” 2018. Web. 08 Apr 2020.

Vancouver:

Wang X. The Molecular Basis of RNA Recognition and Transcriptional Regulation by FUS and PRC2. [Internet] [Doctoral dissertation]. University of Colorado; 2018. [cited 2020 Apr 08]. Available from: https://scholar.colorado.edu/chem_gradetds/271.

Council of Science Editors:

Wang X. The Molecular Basis of RNA Recognition and Transcriptional Regulation by FUS and PRC2. [Doctoral Dissertation]. University of Colorado; 2018. Available from: https://scholar.colorado.edu/chem_gradetds/271


University of Colorado

13. Wang, Huan. Signaling from Matrix Elasticity and TGF-beta1 to Cells of the Cardiac Valve.

Degree: PhD, 2013, University of Colorado

  Coordinated movement of cardiac valves controls unidirectional flow of the blood with every heart beat. Cardiac valves are composed of thin, pliable leaflets that… (more)

Subjects/Keywords: cadherin; Hydrogel elasticity; Mechanosensing; PI3K signaling; TGF-beta1 signaling; Valvular myofibroblasts; Biology

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APA (6th Edition):

Wang, H. (2013). Signaling from Matrix Elasticity and TGF-beta1 to Cells of the Cardiac Valve. (Doctoral Dissertation). University of Colorado. Retrieved from https://scholar.colorado.edu/mcdb_gradetds/16

Chicago Manual of Style (16th Edition):

Wang, Huan. “Signaling from Matrix Elasticity and TGF-beta1 to Cells of the Cardiac Valve.” 2013. Doctoral Dissertation, University of Colorado. Accessed April 08, 2020. https://scholar.colorado.edu/mcdb_gradetds/16.

MLA Handbook (7th Edition):

Wang, Huan. “Signaling from Matrix Elasticity and TGF-beta1 to Cells of the Cardiac Valve.” 2013. Web. 08 Apr 2020.

Vancouver:

Wang H. Signaling from Matrix Elasticity and TGF-beta1 to Cells of the Cardiac Valve. [Internet] [Doctoral dissertation]. University of Colorado; 2013. [cited 2020 Apr 08]. Available from: https://scholar.colorado.edu/mcdb_gradetds/16.

Council of Science Editors:

Wang H. Signaling from Matrix Elasticity and TGF-beta1 to Cells of the Cardiac Valve. [Doctoral Dissertation]. University of Colorado; 2013. Available from: https://scholar.colorado.edu/mcdb_gradetds/16


University of Colorado

14. Troy, Andrew A. An Asymmetric Jam2/Par Complex Renews Muscle Stem Cells by Localized p38alpha/beta MAPK Signaling.

Degree: PhD, 2011, University of Colorado

  Skeletal muscle is maintained and repaired by satellite cells. Satellite cells are quiescent in uninjured muscle but activate, proliferate and repair the muscle after… (more)

Subjects/Keywords: asymmetric division; regeneration; satellite cell; skeletal muscle; stem cell; Bioinformatics; Cell Biology; Molecular Biology

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APA (6th Edition):

Troy, A. A. (2011). An Asymmetric Jam2/Par Complex Renews Muscle Stem Cells by Localized p38alpha/beta MAPK Signaling. (Doctoral Dissertation). University of Colorado. Retrieved from https://scholar.colorado.edu/mcdb_gradetds/44

Chicago Manual of Style (16th Edition):

Troy, Andrew A. “An Asymmetric Jam2/Par Complex Renews Muscle Stem Cells by Localized p38alpha/beta MAPK Signaling.” 2011. Doctoral Dissertation, University of Colorado. Accessed April 08, 2020. https://scholar.colorado.edu/mcdb_gradetds/44.

MLA Handbook (7th Edition):

Troy, Andrew A. “An Asymmetric Jam2/Par Complex Renews Muscle Stem Cells by Localized p38alpha/beta MAPK Signaling.” 2011. Web. 08 Apr 2020.

Vancouver:

Troy AA. An Asymmetric Jam2/Par Complex Renews Muscle Stem Cells by Localized p38alpha/beta MAPK Signaling. [Internet] [Doctoral dissertation]. University of Colorado; 2011. [cited 2020 Apr 08]. Available from: https://scholar.colorado.edu/mcdb_gradetds/44.

Council of Science Editors:

Troy AA. An Asymmetric Jam2/Par Complex Renews Muscle Stem Cells by Localized p38alpha/beta MAPK Signaling. [Doctoral Dissertation]. University of Colorado; 2011. Available from: https://scholar.colorado.edu/mcdb_gradetds/44


University of Colorado

15. Heimiller, Joseph Karl. Genome-Wide Analysis of Splicing Requirements and Function through mRNA Profiling.

Degree: PhD, 2013, University of Colorado

  The RNA-binding proteins U2AF and PTB play important roles in gene expression in many eukaryotic species. Although U2AF and PTB have been well-studied, their… (more)

Subjects/Keywords: bioinformatics; nucleotide composition; PTB; RNA splicing; splicing modeling; U2AF; Bioinformatics; Biology; Molecular Biology

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APA (6th Edition):

Heimiller, J. K. (2013). Genome-Wide Analysis of Splicing Requirements and Function through mRNA Profiling. (Doctoral Dissertation). University of Colorado. Retrieved from https://scholar.colorado.edu/mcdb_gradetds/57

Chicago Manual of Style (16th Edition):

Heimiller, Joseph Karl. “Genome-Wide Analysis of Splicing Requirements and Function through mRNA Profiling.” 2013. Doctoral Dissertation, University of Colorado. Accessed April 08, 2020. https://scholar.colorado.edu/mcdb_gradetds/57.

MLA Handbook (7th Edition):

Heimiller, Joseph Karl. “Genome-Wide Analysis of Splicing Requirements and Function through mRNA Profiling.” 2013. Web. 08 Apr 2020.

Vancouver:

Heimiller JK. Genome-Wide Analysis of Splicing Requirements and Function through mRNA Profiling. [Internet] [Doctoral dissertation]. University of Colorado; 2013. [cited 2020 Apr 08]. Available from: https://scholar.colorado.edu/mcdb_gradetds/57.

Council of Science Editors:

Heimiller JK. Genome-Wide Analysis of Splicing Requirements and Function through mRNA Profiling. [Doctoral Dissertation]. University of Colorado; 2013. Available from: https://scholar.colorado.edu/mcdb_gradetds/57


University of Colorado

16. Riemondy, Kent Augustus, Jr. Identification of Novel MicroRNA Targets and Tumor Suppressive Functions of miR-203 in Murine Skin.

Degree: PhD, 2015, University of Colorado

  miRNAs are small non-coding RNAs, approximately 22 nucleotide in length, that mediate post-transcriptional repression of target mRNAs. Since their discovery in mammals in the… (more)

Subjects/Keywords: RNA; gene expression; cancer; Bioinformatics; Cell Biology; Molecular Biology

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APA (6th Edition):

Riemondy, Kent Augustus, J. (2015). Identification of Novel MicroRNA Targets and Tumor Suppressive Functions of miR-203 in Murine Skin. (Doctoral Dissertation). University of Colorado. Retrieved from https://scholar.colorado.edu/mcdb_gradetds/48

Chicago Manual of Style (16th Edition):

Riemondy, Kent Augustus, Jr. “Identification of Novel MicroRNA Targets and Tumor Suppressive Functions of miR-203 in Murine Skin.” 2015. Doctoral Dissertation, University of Colorado. Accessed April 08, 2020. https://scholar.colorado.edu/mcdb_gradetds/48.

MLA Handbook (7th Edition):

Riemondy, Kent Augustus, Jr. “Identification of Novel MicroRNA Targets and Tumor Suppressive Functions of miR-203 in Murine Skin.” 2015. Web. 08 Apr 2020.

Vancouver:

Riemondy, Kent Augustus J. Identification of Novel MicroRNA Targets and Tumor Suppressive Functions of miR-203 in Murine Skin. [Internet] [Doctoral dissertation]. University of Colorado; 2015. [cited 2020 Apr 08]. Available from: https://scholar.colorado.edu/mcdb_gradetds/48.

Council of Science Editors:

Riemondy, Kent Augustus J. Identification of Novel MicroRNA Targets and Tumor Suppressive Functions of miR-203 in Murine Skin. [Doctoral Dissertation]. University of Colorado; 2015. Available from: https://scholar.colorado.edu/mcdb_gradetds/48


University of Colorado

17. Wang, Xueyin. The Molecular Basis of RNA Recognition and Transcriptional Regulation by FUS and PRC2.

Degree: PhD, Chemistry & Biochemistry, 2017, University of Colorado

  RNA and protein interact with each other in the cell nucleus to form RNP (ribonucleoprotein) complexes. These RNPs play key roles in various steps… (more)

Subjects/Keywords: incRNA; chromatin-modifiers; polycomb repressive complex; guanines; Biochemistry

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APA (6th Edition):

Wang, X. (2017). The Molecular Basis of RNA Recognition and Transcriptional Regulation by FUS and PRC2. (Doctoral Dissertation). University of Colorado. Retrieved from https://scholar.colorado.edu/chem_gradetds/217

Chicago Manual of Style (16th Edition):

Wang, Xueyin. “The Molecular Basis of RNA Recognition and Transcriptional Regulation by FUS and PRC2.” 2017. Doctoral Dissertation, University of Colorado. Accessed April 08, 2020. https://scholar.colorado.edu/chem_gradetds/217.

MLA Handbook (7th Edition):

Wang, Xueyin. “The Molecular Basis of RNA Recognition and Transcriptional Regulation by FUS and PRC2.” 2017. Web. 08 Apr 2020.

Vancouver:

Wang X. The Molecular Basis of RNA Recognition and Transcriptional Regulation by FUS and PRC2. [Internet] [Doctoral dissertation]. University of Colorado; 2017. [cited 2020 Apr 08]. Available from: https://scholar.colorado.edu/chem_gradetds/217.

Council of Science Editors:

Wang X. The Molecular Basis of RNA Recognition and Transcriptional Regulation by FUS and PRC2. [Doctoral Dissertation]. University of Colorado; 2017. Available from: https://scholar.colorado.edu/chem_gradetds/217


University of Colorado

18. Hoefert, Jaimee Elizabeth. Targets and Functions of the Microrna-200 Family in the Developing Skin and Hair Follicle.

Degree: PhD, Microbiology, Molecular Biology and Biochemistry, 2018, University of Colorado

  The microRNA-200 (miR-200) family is well known for preventing epithelial-to-mesenchymal transition in cancer. However, the targets and functions of this family in normal epithelial… (more)

Subjects/Keywords: hair follicle development; microRNA; miR-200; skin; Cell Biology; Developmental Biology; Molecular Biology

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

APA (6th Edition):

Hoefert, J. E. (2018). Targets and Functions of the Microrna-200 Family in the Developing Skin and Hair Follicle. (Doctoral Dissertation). University of Colorado. Retrieved from https://scholar.colorado.edu/mcdb_gradetds/78

Chicago Manual of Style (16th Edition):

Hoefert, Jaimee Elizabeth. “Targets and Functions of the Microrna-200 Family in the Developing Skin and Hair Follicle.” 2018. Doctoral Dissertation, University of Colorado. Accessed April 08, 2020. https://scholar.colorado.edu/mcdb_gradetds/78.

MLA Handbook (7th Edition):

Hoefert, Jaimee Elizabeth. “Targets and Functions of the Microrna-200 Family in the Developing Skin and Hair Follicle.” 2018. Web. 08 Apr 2020.

Vancouver:

Hoefert JE. Targets and Functions of the Microrna-200 Family in the Developing Skin and Hair Follicle. [Internet] [Doctoral dissertation]. University of Colorado; 2018. [cited 2020 Apr 08]. Available from: https://scholar.colorado.edu/mcdb_gradetds/78.

Council of Science Editors:

Hoefert JE. Targets and Functions of the Microrna-200 Family in the Developing Skin and Hair Follicle. [Doctoral Dissertation]. University of Colorado; 2018. Available from: https://scholar.colorado.edu/mcdb_gradetds/78


University of Colorado

19. Guess, Martin G. Characterization of microRNA Function During Skeletal Myogenesis.

Degree: PhD, 2014, University of Colorado

  Skeletal muscle is a remarkable organ system that is required for almost all animal life. In vertebrates, skeletal muscle can alter its functional and… (more)

Subjects/Keywords: Deep sequencing; Genetics; In vivo imaging; microRNA; Muscle Disease; Muscular Dystrophy; Cell Biology; Developmental Biology; Molecular Biology

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

APA (6th Edition):

Guess, M. G. (2014). Characterization of microRNA Function During Skeletal Myogenesis. (Doctoral Dissertation). University of Colorado. Retrieved from https://scholar.colorado.edu/mcdb_gradetds/28

Chicago Manual of Style (16th Edition):

Guess, Martin G. “Characterization of microRNA Function During Skeletal Myogenesis.” 2014. Doctoral Dissertation, University of Colorado. Accessed April 08, 2020. https://scholar.colorado.edu/mcdb_gradetds/28.

MLA Handbook (7th Edition):

Guess, Martin G. “Characterization of microRNA Function During Skeletal Myogenesis.” 2014. Web. 08 Apr 2020.

Vancouver:

Guess MG. Characterization of microRNA Function During Skeletal Myogenesis. [Internet] [Doctoral dissertation]. University of Colorado; 2014. [cited 2020 Apr 08]. Available from: https://scholar.colorado.edu/mcdb_gradetds/28.

Council of Science Editors:

Guess MG. Characterization of microRNA Function During Skeletal Myogenesis. [Doctoral Dissertation]. University of Colorado; 2014. Available from: https://scholar.colorado.edu/mcdb_gradetds/28

.