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You searched for +publisher:"University of Colorado" +contributor:("Leslie A. Leinwand"). Showing records 1 – 13 of 13 total matches.

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University of Colorado

1. LaNasa, Stephanie Marie. Development and Characterization of Porous and Patterned Hydrogel Scaffolds for Cardiac Muscle Tissue Engineering.

Degree: PhD, Chemical & Biochemical Engineering, 2010, University of Colorado

  Coronary heart disease has become increasingly prevalent in the U.S. and worldwide, and now affects over one million Americans annually. The damaged tissue that… (more)

Subjects/Keywords: Cardiomyocyte; Channels; Gene Expression; Hydrogel; Mechanical Properties; Biomedical Engineering and Bioengineering; Chemical Engineering

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APA (6th Edition):

LaNasa, S. M. (2010). Development and Characterization of Porous and Patterned Hydrogel Scaffolds for Cardiac Muscle Tissue Engineering. (Doctoral Dissertation). University of Colorado. Retrieved from https://scholar.colorado.edu/chbe_gradetds/4

Chicago Manual of Style (16th Edition):

LaNasa, Stephanie Marie. “Development and Characterization of Porous and Patterned Hydrogel Scaffolds for Cardiac Muscle Tissue Engineering.” 2010. Doctoral Dissertation, University of Colorado. Accessed January 19, 2020. https://scholar.colorado.edu/chbe_gradetds/4.

MLA Handbook (7th Edition):

LaNasa, Stephanie Marie. “Development and Characterization of Porous and Patterned Hydrogel Scaffolds for Cardiac Muscle Tissue Engineering.” 2010. Web. 19 Jan 2020.

Vancouver:

LaNasa SM. Development and Characterization of Porous and Patterned Hydrogel Scaffolds for Cardiac Muscle Tissue Engineering. [Internet] [Doctoral dissertation]. University of Colorado; 2010. [cited 2020 Jan 19]. Available from: https://scholar.colorado.edu/chbe_gradetds/4.

Council of Science Editors:

LaNasa SM. Development and Characterization of Porous and Patterned Hydrogel Scaffolds for Cardiac Muscle Tissue Engineering. [Doctoral Dissertation]. University of Colorado; 2010. Available from: https://scholar.colorado.edu/chbe_gradetds/4


University of Colorado

2. Hausburg, Melissa Ann. Tristetraprolin Regulation of MyoD mRNA Stability Commits Quiescent Adult Muscle Stem Cells to Myogenesis.

Degree: PhD, 2010, University of Colorado

  In animals, tissue maintenance, plasticity and repair rely on adult stem cells which have been identified in nearly all tissues. Many adult stem cells… (more)

Subjects/Keywords: MyoD; RNA decay; satellite cell; skeletal muscle; stem cell; Tristetraprolin; Other Cell and Developmental Biology

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APA (6th Edition):

Hausburg, M. A. (2010). Tristetraprolin Regulation of MyoD mRNA Stability Commits Quiescent Adult Muscle Stem Cells to Myogenesis. (Doctoral Dissertation). University of Colorado. Retrieved from https://scholar.colorado.edu/mcdb_gradetds/3

Chicago Manual of Style (16th Edition):

Hausburg, Melissa Ann. “Tristetraprolin Regulation of MyoD mRNA Stability Commits Quiescent Adult Muscle Stem Cells to Myogenesis.” 2010. Doctoral Dissertation, University of Colorado. Accessed January 19, 2020. https://scholar.colorado.edu/mcdb_gradetds/3.

MLA Handbook (7th Edition):

Hausburg, Melissa Ann. “Tristetraprolin Regulation of MyoD mRNA Stability Commits Quiescent Adult Muscle Stem Cells to Myogenesis.” 2010. Web. 19 Jan 2020.

Vancouver:

Hausburg MA. Tristetraprolin Regulation of MyoD mRNA Stability Commits Quiescent Adult Muscle Stem Cells to Myogenesis. [Internet] [Doctoral dissertation]. University of Colorado; 2010. [cited 2020 Jan 19]. Available from: https://scholar.colorado.edu/mcdb_gradetds/3.

Council of Science Editors:

Hausburg MA. Tristetraprolin Regulation of MyoD mRNA Stability Commits Quiescent Adult Muscle Stem Cells to Myogenesis. [Doctoral Dissertation]. University of Colorado; 2010. Available from: https://scholar.colorado.edu/mcdb_gradetds/3


University of Colorado

3. Vera, Carlos D. Functional Characterization of Disease-Causing Mutations in Human Myosin Heavy Chain Genes.

Degree: PhD, 2018, University of Colorado

 Biophysical and biochemical imbalance of mechanisms relevant to muscle function, can result in morphological changes to the tissue. While the purpose of activities involving exercise… (more)

Subjects/Keywords: cardiomyopathy; muscle; myosin; embryonic myosin; atpase cycle parameters; Biochemistry; Biophysics; Molecular Biology

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APA (6th Edition):

Vera, C. D. (2018). Functional Characterization of Disease-Causing Mutations in Human Myosin Heavy Chain Genes. (Doctoral Dissertation). University of Colorado. Retrieved from https://scholar.colorado.edu/mcdb_gradetds/94

Chicago Manual of Style (16th Edition):

Vera, Carlos D. “Functional Characterization of Disease-Causing Mutations in Human Myosin Heavy Chain Genes.” 2018. Doctoral Dissertation, University of Colorado. Accessed January 19, 2020. https://scholar.colorado.edu/mcdb_gradetds/94.

MLA Handbook (7th Edition):

Vera, Carlos D. “Functional Characterization of Disease-Causing Mutations in Human Myosin Heavy Chain Genes.” 2018. Web. 19 Jan 2020.

Vancouver:

Vera CD. Functional Characterization of Disease-Causing Mutations in Human Myosin Heavy Chain Genes. [Internet] [Doctoral dissertation]. University of Colorado; 2018. [cited 2020 Jan 19]. Available from: https://scholar.colorado.edu/mcdb_gradetds/94.

Council of Science Editors:

Vera CD. Functional Characterization of Disease-Causing Mutations in Human Myosin Heavy Chain Genes. [Doctoral Dissertation]. University of Colorado; 2018. Available from: https://scholar.colorado.edu/mcdb_gradetds/94


University of Colorado

4. Cosper, Pippa Froukje. Cardiac Atrophy Due to Cancer: Characterization, Mechanisms, and Sex Differences.

Degree: PhD, 2011, University of Colorado

  Approximately one-third of cancer deaths are caused by cachexia, a severe form of skeletal muscle and adipose tissue wasting that affects men more than… (more)

Subjects/Keywords: atrophy; cachexia; cancer; heart; muscle; myosin; Cell Biology; Molecular Biology

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APA (6th Edition):

Cosper, P. F. (2011). Cardiac Atrophy Due to Cancer: Characterization, Mechanisms, and Sex Differences. (Doctoral Dissertation). University of Colorado. Retrieved from https://scholar.colorado.edu/mcdb_gradetds/60

Chicago Manual of Style (16th Edition):

Cosper, Pippa Froukje. “Cardiac Atrophy Due to Cancer: Characterization, Mechanisms, and Sex Differences.” 2011. Doctoral Dissertation, University of Colorado. Accessed January 19, 2020. https://scholar.colorado.edu/mcdb_gradetds/60.

MLA Handbook (7th Edition):

Cosper, Pippa Froukje. “Cardiac Atrophy Due to Cancer: Characterization, Mechanisms, and Sex Differences.” 2011. Web. 19 Jan 2020.

Vancouver:

Cosper PF. Cardiac Atrophy Due to Cancer: Characterization, Mechanisms, and Sex Differences. [Internet] [Doctoral dissertation]. University of Colorado; 2011. [cited 2020 Jan 19]. Available from: https://scholar.colorado.edu/mcdb_gradetds/60.

Council of Science Editors:

Cosper PF. Cardiac Atrophy Due to Cancer: Characterization, Mechanisms, and Sex Differences. [Doctoral Dissertation]. University of Colorado; 2011. Available from: https://scholar.colorado.edu/mcdb_gradetds/60


University of Colorado

5. Mehan, Ryan Scott. The Role of Matrix Metalloproteinase-9 in Remodeling of Skeletal Muscle Connective Tissue in Mice.

Degree: PhD, Integrative Physiology, 2012, University of Colorado

  The basal lamina of skeletal muscle is a specialized region of extracellular matrix (ECM) comprised primarily of type IV collagen. Remodeling of the basal… (more)

Subjects/Keywords: Aging; Extracellular Matrix; Injury; Matrix Metalloproteinase; Mice; Skeletal Muscle; Biology; Physiology

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APA (6th Edition):

Mehan, R. S. (2012). The Role of Matrix Metalloproteinase-9 in Remodeling of Skeletal Muscle Connective Tissue in Mice. (Doctoral Dissertation). University of Colorado. Retrieved from https://scholar.colorado.edu/iphy_gradetds/17

Chicago Manual of Style (16th Edition):

Mehan, Ryan Scott. “The Role of Matrix Metalloproteinase-9 in Remodeling of Skeletal Muscle Connective Tissue in Mice.” 2012. Doctoral Dissertation, University of Colorado. Accessed January 19, 2020. https://scholar.colorado.edu/iphy_gradetds/17.

MLA Handbook (7th Edition):

Mehan, Ryan Scott. “The Role of Matrix Metalloproteinase-9 in Remodeling of Skeletal Muscle Connective Tissue in Mice.” 2012. Web. 19 Jan 2020.

Vancouver:

Mehan RS. The Role of Matrix Metalloproteinase-9 in Remodeling of Skeletal Muscle Connective Tissue in Mice. [Internet] [Doctoral dissertation]. University of Colorado; 2012. [cited 2020 Jan 19]. Available from: https://scholar.colorado.edu/iphy_gradetds/17.

Council of Science Editors:

Mehan RS. The Role of Matrix Metalloproteinase-9 in Remodeling of Skeletal Muscle Connective Tissue in Mice. [Doctoral Dissertation]. University of Colorado; 2012. Available from: https://scholar.colorado.edu/iphy_gradetds/17


University of Colorado

6. 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 January 19, 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. 19 Jan 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 Jan 19]. 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

7. 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 January 19, 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. 19 Jan 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 Jan 19]. 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

8. 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 January 19, 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. 19 Jan 2020.

Vancouver:

Heimiller JK. Genome-Wide Analysis of Splicing Requirements and Function through mRNA Profiling. [Internet] [Doctoral dissertation]. University of Colorado; 2013. [cited 2020 Jan 19]. 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

9. Dengler, Veronica L. Transcriptional Regulation in Cancer-Driven Cellular Stress and Functional Specialization of a Myosin Heavy Chain Protein, MYH7B.

Degree: PhD, 2017, University of Colorado

  Cancer is a disease of dysregulated gene expression in which many developmental programs are hijacked. One such program is the cellular response to hypoxia,… (more)

Subjects/Keywords: cancer; HIF; heavy chain proteins; Biochemistry; Molecular Biology

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APA (6th Edition):

Dengler, V. L. (2017). Transcriptional Regulation in Cancer-Driven Cellular Stress and Functional Specialization of a Myosin Heavy Chain Protein, MYH7B. (Doctoral Dissertation). University of Colorado. Retrieved from https://scholar.colorado.edu/mcdb_gradetds/69

Chicago Manual of Style (16th Edition):

Dengler, Veronica L. “Transcriptional Regulation in Cancer-Driven Cellular Stress and Functional Specialization of a Myosin Heavy Chain Protein, MYH7B.” 2017. Doctoral Dissertation, University of Colorado. Accessed January 19, 2020. https://scholar.colorado.edu/mcdb_gradetds/69.

MLA Handbook (7th Edition):

Dengler, Veronica L. “Transcriptional Regulation in Cancer-Driven Cellular Stress and Functional Specialization of a Myosin Heavy Chain Protein, MYH7B.” 2017. Web. 19 Jan 2020.

Vancouver:

Dengler VL. Transcriptional Regulation in Cancer-Driven Cellular Stress and Functional Specialization of a Myosin Heavy Chain Protein, MYH7B. [Internet] [Doctoral dissertation]. University of Colorado; 2017. [cited 2020 Jan 19]. Available from: https://scholar.colorado.edu/mcdb_gradetds/69.

Council of Science Editors:

Dengler VL. Transcriptional Regulation in Cancer-Driven Cellular Stress and Functional Specialization of a Myosin Heavy Chain Protein, MYH7B. [Doctoral Dissertation]. University of Colorado; 2017. Available from: https://scholar.colorado.edu/mcdb_gradetds/69


University of Colorado

10. Carter, Kyle Pierce. Engineering and Evaluating Fluorescent Tools for Endoplasmic Reticulum Zinc.

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

 Zinc (Zn2+) is an essential micronutrient for human health. However, excess Zn2+ is toxic and Zn2+ deficiency can be fatal, so the concentration of this… (more)

Subjects/Keywords: Biosensors; Endoplasmic reticulum; Fluorescence microscopy; FRET; Protein engineering; Zinc; Biochemistry; Biophysics; Cell Biology

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APA (6th Edition):

Carter, K. P. (2017). Engineering and Evaluating Fluorescent Tools for Endoplasmic Reticulum Zinc. (Doctoral Dissertation). University of Colorado. Retrieved from https://scholar.colorado.edu/chem_gradetds/223

Chicago Manual of Style (16th Edition):

Carter, Kyle Pierce. “Engineering and Evaluating Fluorescent Tools for Endoplasmic Reticulum Zinc.” 2017. Doctoral Dissertation, University of Colorado. Accessed January 19, 2020. https://scholar.colorado.edu/chem_gradetds/223.

MLA Handbook (7th Edition):

Carter, Kyle Pierce. “Engineering and Evaluating Fluorescent Tools for Endoplasmic Reticulum Zinc.” 2017. Web. 19 Jan 2020.

Vancouver:

Carter KP. Engineering and Evaluating Fluorescent Tools for Endoplasmic Reticulum Zinc. [Internet] [Doctoral dissertation]. University of Colorado; 2017. [cited 2020 Jan 19]. Available from: https://scholar.colorado.edu/chem_gradetds/223.

Council of Science Editors:

Carter KP. Engineering and Evaluating Fluorescent Tools for Endoplasmic Reticulum Zinc. [Doctoral Dissertation]. University of Colorado; 2017. Available from: https://scholar.colorado.edu/chem_gradetds/223


University of Colorado

11. 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 (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 January 19, 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. 19 Jan 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 Jan 19]. 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

12. 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 (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 January 19, 2020. https://scholar.colorado.edu/mcdb_gradetds/28.

MLA Handbook (7th Edition):

Guess, Martin G. “Characterization of microRNA Function During Skeletal Myogenesis.” 2014. Web. 19 Jan 2020.

Vancouver:

Guess MG. Characterization of microRNA Function During Skeletal Myogenesis. [Internet] [Doctoral dissertation]. University of Colorado; 2014. [cited 2020 Jan 19]. 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


University of Colorado

13. Welsh, Molly Catherine. Plasma and Skeletal Muscle Matrix Metalloproteinase-9 Response to Eccentric Exercise-Induced Injury in Humans.

Degree: PhD, Integrative Physiology, 2014, University of Colorado

  Exercise induced muscle injury is a phenomenon that most adults have experienced when beginning a new or novel exercise program. It is perceived as… (more)

Subjects/Keywords: connective tissue; eccentric exercise; exercise-induced muscle injury; extracellular matrix; matrix metalloproteinase-9; muscle soreness; Exercise Physiology; Integrative Biology; Physiology

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APA (6th Edition):

Welsh, M. C. (2014). Plasma and Skeletal Muscle Matrix Metalloproteinase-9 Response to Eccentric Exercise-Induced Injury in Humans. (Doctoral Dissertation). University of Colorado. Retrieved from https://scholar.colorado.edu/iphy_gradetds/39

Chicago Manual of Style (16th Edition):

Welsh, Molly Catherine. “Plasma and Skeletal Muscle Matrix Metalloproteinase-9 Response to Eccentric Exercise-Induced Injury in Humans.” 2014. Doctoral Dissertation, University of Colorado. Accessed January 19, 2020. https://scholar.colorado.edu/iphy_gradetds/39.

MLA Handbook (7th Edition):

Welsh, Molly Catherine. “Plasma and Skeletal Muscle Matrix Metalloproteinase-9 Response to Eccentric Exercise-Induced Injury in Humans.” 2014. Web. 19 Jan 2020.

Vancouver:

Welsh MC. Plasma and Skeletal Muscle Matrix Metalloproteinase-9 Response to Eccentric Exercise-Induced Injury in Humans. [Internet] [Doctoral dissertation]. University of Colorado; 2014. [cited 2020 Jan 19]. Available from: https://scholar.colorado.edu/iphy_gradetds/39.

Council of Science Editors:

Welsh MC. Plasma and Skeletal Muscle Matrix Metalloproteinase-9 Response to Eccentric Exercise-Induced Injury in Humans. [Doctoral Dissertation]. University of Colorado; 2014. Available from: https://scholar.colorado.edu/iphy_gradetds/39

.