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You searched for subject:(Cell Aging mesh ). Showing records 1 – 30 of 42755 total matches.

[1] [2] [3] [4] [5] … [1426]

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University of Florida

1. Flanary, Barry Eric ( Dissertant ). Analysis of Rat Microglial Cellular Senescence as Determined by Measurements of Telomere Length and Telomerase Activity.

Degree: PhD, Department of Neuroscience, 2005, University of Florida

 Normal somatic cells have a finite replicative capacity, and with each cell division, telomeres (the physical ends of chromosomes) progressively shorten until they reach a… (more)

Subjects/Keywords: Astrocytes; Cells; Cellular senescence; Cerebellum; Cultured cells; In vitro fertilization; Microglia; Rats; Telomeres; Vitamin E; Aging ( mesh ); Astrocytes ( mesh ); Axotomy ( mesh ); Cell Proliferation ( mesh ); Microglia ( mesh ); Research ( mesh ); Telomerase ( mesh ); Tocopherols ( mesh ); Transduction, Genetic ( mesh )

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APA (6th Edition):

Flanary, B. E. (. D. ). (2005). Analysis of Rat Microglial Cellular Senescence as Determined by Measurements of Telomere Length and Telomerase Activity. (Doctoral Dissertation). University of Florida. Retrieved from https://ufdc.ufl.edu/UFE0009641

Chicago Manual of Style (16th Edition):

Flanary, Barry Eric ( Dissertant ). “Analysis of Rat Microglial Cellular Senescence as Determined by Measurements of Telomere Length and Telomerase Activity.” 2005. Doctoral Dissertation, University of Florida. Accessed December 05, 2020. https://ufdc.ufl.edu/UFE0009641.

MLA Handbook (7th Edition):

Flanary, Barry Eric ( Dissertant ). “Analysis of Rat Microglial Cellular Senescence as Determined by Measurements of Telomere Length and Telomerase Activity.” 2005. Web. 05 Dec 2020.

Vancouver:

Flanary BE(D). Analysis of Rat Microglial Cellular Senescence as Determined by Measurements of Telomere Length and Telomerase Activity. [Internet] [Doctoral dissertation]. University of Florida; 2005. [cited 2020 Dec 05]. Available from: https://ufdc.ufl.edu/UFE0009641.

Council of Science Editors:

Flanary BE(D). Analysis of Rat Microglial Cellular Senescence as Determined by Measurements of Telomere Length and Telomerase Activity. [Doctoral Dissertation]. University of Florida; 2005. Available from: https://ufdc.ufl.edu/UFE0009641


University of New South Wales

2. Siette, Joyce. Exercise and cell therapy: restorative mechanisms for reversing age-related memory decline.

Degree: Psychology, 2012, University of New South Wales

 Memory problems in late life are extraordinarily common, ranging from mild episode memory complaints to the more severe memory impairment associated with dementia and neurodegenerative… (more)

Subjects/Keywords: Exercise; Ageing; Memory; Cell transplant

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APA (6th Edition):

Siette, J. (2012). Exercise and cell therapy: restorative mechanisms for reversing age-related memory decline. (Doctoral Dissertation). University of New South Wales. Retrieved from http://handle.unsw.edu.au/1959.4/52513 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:11186/SOURCE1?view=true

Chicago Manual of Style (16th Edition):

Siette, Joyce. “Exercise and cell therapy: restorative mechanisms for reversing age-related memory decline.” 2012. Doctoral Dissertation, University of New South Wales. Accessed December 05, 2020. http://handle.unsw.edu.au/1959.4/52513 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:11186/SOURCE1?view=true.

MLA Handbook (7th Edition):

Siette, Joyce. “Exercise and cell therapy: restorative mechanisms for reversing age-related memory decline.” 2012. Web. 05 Dec 2020.

Vancouver:

Siette J. Exercise and cell therapy: restorative mechanisms for reversing age-related memory decline. [Internet] [Doctoral dissertation]. University of New South Wales; 2012. [cited 2020 Dec 05]. Available from: http://handle.unsw.edu.au/1959.4/52513 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:11186/SOURCE1?view=true.

Council of Science Editors:

Siette J. Exercise and cell therapy: restorative mechanisms for reversing age-related memory decline. [Doctoral Dissertation]. University of New South Wales; 2012. Available from: http://handle.unsw.edu.au/1959.4/52513 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:11186/SOURCE1?view=true


University of Florida

3. Eppler, Barbel, 1964-. Taurine and aging biosynthesis, antioxidation, and dietary manipulations.

Degree: 1998, University of Florida

Subjects/Keywords: Amino acids; Antioxidants; Biosynthesis; DNA damage; Enzymes; Kidneys; Liver; Oxidation; Quinones; Rats; Aging ( mesh ); Antioxidants ( mesh ); Cell Aging ( mesh ); Department of Pharmacodynamics thesis Ph.D ( mesh ); Diet ( mesh ); Rats, Inbred F344 ( mesh ); Rats, Sprague-Dawley ( mesh ); Research ( mesh ); Taurine ( mesh ); City of Gainesville ( local )

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APA (6th Edition):

Eppler, Barbel, 1. (1998). Taurine and aging biosynthesis, antioxidation, and dietary manipulations. (Thesis). University of Florida. Retrieved from https://ufdc.ufl.edu/AA00054290

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

Chicago Manual of Style (16th Edition):

Eppler, Barbel, 1964-. “Taurine and aging biosynthesis, antioxidation, and dietary manipulations.” 1998. Thesis, University of Florida. Accessed December 05, 2020. https://ufdc.ufl.edu/AA00054290.

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

MLA Handbook (7th Edition):

Eppler, Barbel, 1964-. “Taurine and aging biosynthesis, antioxidation, and dietary manipulations.” 1998. Web. 05 Dec 2020.

Vancouver:

Eppler, Barbel 1. Taurine and aging biosynthesis, antioxidation, and dietary manipulations. [Internet] [Thesis]. University of Florida; 1998. [cited 2020 Dec 05]. Available from: https://ufdc.ufl.edu/AA00054290.

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

Council of Science Editors:

Eppler, Barbel 1. Taurine and aging biosynthesis, antioxidation, and dietary manipulations. [Thesis]. University of Florida; 1998. Available from: https://ufdc.ufl.edu/AA00054290

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


University of Manchester

4. Ogden, Stephanie. An investigation of Langerhans' cell function in aged skin.

Degree: PhD, 2013, University of Manchester

 With increasing age, aspects of the innate and adaptive immune systems show functional decline. In the skin this is associated with an increased incidence of… (more)

Subjects/Keywords: 616.97; Langerhans' cell; Ageing; Interleukin-1

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APA (6th Edition):

Ogden, S. (2013). An investigation of Langerhans' cell function in aged skin. (Doctoral Dissertation). University of Manchester. Retrieved from https://www.research.manchester.ac.uk/portal/en/theses/an-investigation-of-langerhans-cell-function-in-aged-skin(a5d3967f-51bc-49fb-ab05-31e5aad4ae40).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.570266

Chicago Manual of Style (16th Edition):

Ogden, Stephanie. “An investigation of Langerhans' cell function in aged skin.” 2013. Doctoral Dissertation, University of Manchester. Accessed December 05, 2020. https://www.research.manchester.ac.uk/portal/en/theses/an-investigation-of-langerhans-cell-function-in-aged-skin(a5d3967f-51bc-49fb-ab05-31e5aad4ae40).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.570266.

MLA Handbook (7th Edition):

Ogden, Stephanie. “An investigation of Langerhans' cell function in aged skin.” 2013. Web. 05 Dec 2020.

Vancouver:

Ogden S. An investigation of Langerhans' cell function in aged skin. [Internet] [Doctoral dissertation]. University of Manchester; 2013. [cited 2020 Dec 05]. Available from: https://www.research.manchester.ac.uk/portal/en/theses/an-investigation-of-langerhans-cell-function-in-aged-skin(a5d3967f-51bc-49fb-ab05-31e5aad4ae40).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.570266.

Council of Science Editors:

Ogden S. An investigation of Langerhans' cell function in aged skin. [Doctoral Dissertation]. University of Manchester; 2013. Available from: https://www.research.manchester.ac.uk/portal/en/theses/an-investigation-of-langerhans-cell-function-in-aged-skin(a5d3967f-51bc-49fb-ab05-31e5aad4ae40).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.570266


University of Florida

5. Daniels, Kellye K., 1967-. Properties of high-affinity L-Glutamate transport in glial- and neuronal-enriched fractions from rat brain Kellye K. Daniels.

Degree: 1997, University of Florida

Subjects/Keywords: Brain; Enzymes; Neuroglia; Neurons; Phorbol esters; Phosphatases; Phosphorylation; Protein isoforms; Rats; Synaptosomes; Biological Transport  – physiology ( mesh ); Brain ( mesh ); Cell Aging ( mesh ); Department of Neuroscience thesis Ph.D ( mesh ); Glutamates  – metabolism ( mesh ); Glutamates  – physiology ( mesh ); Neuroglia ( mesh ); Neurons ( mesh ); Neurotransmitter Uptake Inhibitors  – pharmacokinetics ( mesh ); Phosphorylation ( mesh ); Protein Kinase C ( mesh ); Rats ( mesh ); Research ( mesh ); Subcellular Fractions  – analysis ( mesh ); Subcellular Fractions  – isolation &; purification ( mesh )

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APA (6th Edition):

Daniels, Kellye K., 1. (1997). Properties of high-affinity L-Glutamate transport in glial- and neuronal-enriched fractions from rat brain Kellye K. Daniels. (Thesis). University of Florida. Retrieved from https://ufdc.ufl.edu/AA00031499

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

Chicago Manual of Style (16th Edition):

Daniels, Kellye K., 1967-. “Properties of high-affinity L-Glutamate transport in glial- and neuronal-enriched fractions from rat brain Kellye K. Daniels.” 1997. Thesis, University of Florida. Accessed December 05, 2020. https://ufdc.ufl.edu/AA00031499.

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

MLA Handbook (7th Edition):

Daniels, Kellye K., 1967-. “Properties of high-affinity L-Glutamate transport in glial- and neuronal-enriched fractions from rat brain Kellye K. Daniels.” 1997. Web. 05 Dec 2020.

Vancouver:

Daniels, Kellye K. 1. Properties of high-affinity L-Glutamate transport in glial- and neuronal-enriched fractions from rat brain Kellye K. Daniels. [Internet] [Thesis]. University of Florida; 1997. [cited 2020 Dec 05]. Available from: https://ufdc.ufl.edu/AA00031499.

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

Council of Science Editors:

Daniels, Kellye K. 1. Properties of high-affinity L-Glutamate transport in glial- and neuronal-enriched fractions from rat brain Kellye K. Daniels. [Thesis]. University of Florida; 1997. Available from: https://ufdc.ufl.edu/AA00031499

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


University of Rochester

6. Li, Hongjie. Stem cell, compartmentalization, and microbiota in the aging Drosophila intestine.

Degree: PhD, 2016, University of Rochester

 The gastrointestinal (GI) tract of most metazoans, including humans, is lined by a series of epithelia that share common digestive function, but also have distinct… (more)

Subjects/Keywords: Aging; Drosophila; Microbiota; Stem cell

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APA (6th Edition):

Li, H. (2016). Stem cell, compartmentalization, and microbiota in the aging Drosophila intestine. (Doctoral Dissertation). University of Rochester. Retrieved from http://hdl.handle.net/1802/30603

Chicago Manual of Style (16th Edition):

Li, Hongjie. “Stem cell, compartmentalization, and microbiota in the aging Drosophila intestine.” 2016. Doctoral Dissertation, University of Rochester. Accessed December 05, 2020. http://hdl.handle.net/1802/30603.

MLA Handbook (7th Edition):

Li, Hongjie. “Stem cell, compartmentalization, and microbiota in the aging Drosophila intestine.” 2016. Web. 05 Dec 2020.

Vancouver:

Li H. Stem cell, compartmentalization, and microbiota in the aging Drosophila intestine. [Internet] [Doctoral dissertation]. University of Rochester; 2016. [cited 2020 Dec 05]. Available from: http://hdl.handle.net/1802/30603.

Council of Science Editors:

Li H. Stem cell, compartmentalization, and microbiota in the aging Drosophila intestine. [Doctoral Dissertation]. University of Rochester; 2016. Available from: http://hdl.handle.net/1802/30603


University of Otago

7. Chu, Hsiang I (Vivian). Regeneration Capacity of the Upper Esophageal Sphincter in Adult and Aging Rats .

Degree: 2010, University of Otago

 Swallowing difficulty is a common problem in the elderly. Dysfunction of the upper esophagus sphincter (UES) is one of the common causes. The UES regulates… (more)

Subjects/Keywords: UES; aging; myogenic stem cell

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APA (6th Edition):

Chu, H. I. (. (2010). Regeneration Capacity of the Upper Esophageal Sphincter in Adult and Aging Rats . (Masters Thesis). University of Otago. Retrieved from http://hdl.handle.net/10523/443

Chicago Manual of Style (16th Edition):

Chu, Hsiang I (Vivian). “Regeneration Capacity of the Upper Esophageal Sphincter in Adult and Aging Rats .” 2010. Masters Thesis, University of Otago. Accessed December 05, 2020. http://hdl.handle.net/10523/443.

MLA Handbook (7th Edition):

Chu, Hsiang I (Vivian). “Regeneration Capacity of the Upper Esophageal Sphincter in Adult and Aging Rats .” 2010. Web. 05 Dec 2020.

Vancouver:

Chu HI(. Regeneration Capacity of the Upper Esophageal Sphincter in Adult and Aging Rats . [Internet] [Masters thesis]. University of Otago; 2010. [cited 2020 Dec 05]. Available from: http://hdl.handle.net/10523/443.

Council of Science Editors:

Chu HI(. Regeneration Capacity of the Upper Esophageal Sphincter in Adult and Aging Rats . [Masters Thesis]. University of Otago; 2010. Available from: http://hdl.handle.net/10523/443


University of Florida

8. Mitchell, Josephine Jean, 1964-. Aging and N-methyl-D-aspartate receptors.

Degree: 1995, University of Florida

Subjects/Keywords: Age groups; Brain; Entorhinal cortex; Hippocampus; Memory; Messenger RNA; N methyl D aspartate receptors; Rats; Receptors; Septum of brain; Age Factors ( mesh ); Aging ( mesh ); Brain  – physiology ( mesh ); Brain Chemistry ( mesh ); Cell Aging ( mesh ); Department of Neuroscience thesis Ph.D ( mesh ); Glutamic Acid  – physiology ( mesh ); Neuronal Plasticity ( mesh ); Rats, Inbred F344 ( mesh ); Receptors, N-Methyl-D-Aspartate  – physiology ( mesh ); Receptors, N-Methyl-D-Aspartate  – ultrastructure ( mesh ); Research ( mesh )

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APA (6th Edition):

Mitchell, Josephine Jean, 1. (1995). Aging and N-methyl-D-aspartate receptors. (Thesis). University of Florida. Retrieved from https://ufdc.ufl.edu/AA00009034

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

Chicago Manual of Style (16th Edition):

Mitchell, Josephine Jean, 1964-. “Aging and N-methyl-D-aspartate receptors.” 1995. Thesis, University of Florida. Accessed December 05, 2020. https://ufdc.ufl.edu/AA00009034.

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

MLA Handbook (7th Edition):

Mitchell, Josephine Jean, 1964-. “Aging and N-methyl-D-aspartate receptors.” 1995. Web. 05 Dec 2020.

Vancouver:

Mitchell, Josephine Jean 1. Aging and N-methyl-D-aspartate receptors. [Internet] [Thesis]. University of Florida; 1995. [cited 2020 Dec 05]. Available from: https://ufdc.ufl.edu/AA00009034.

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

Council of Science Editors:

Mitchell, Josephine Jean 1. Aging and N-methyl-D-aspartate receptors. [Thesis]. University of Florida; 1995. Available from: https://ufdc.ufl.edu/AA00009034

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

9. Rocha, Ana Filipa Seixas Fonte da. Metabolomics of cell lines: a tool for aging research .

Degree: 2020, Universidade de Aveiro

 The world is aging and therefore it is essential to understand how the development of this process in organisms is, especially in human beings. Its… (more)

Subjects/Keywords: Aging; Aging biomarkers; Cell cultures for aging studies; Fibroblasts; FTIR; Metabolomics

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APA (6th Edition):

Rocha, A. F. S. F. d. (2020). Metabolomics of cell lines: a tool for aging research . (Thesis). Universidade de Aveiro. Retrieved from http://hdl.handle.net/10773/28961

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

Chicago Manual of Style (16th Edition):

Rocha, Ana Filipa Seixas Fonte da. “Metabolomics of cell lines: a tool for aging research .” 2020. Thesis, Universidade de Aveiro. Accessed December 05, 2020. http://hdl.handle.net/10773/28961.

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

MLA Handbook (7th Edition):

Rocha, Ana Filipa Seixas Fonte da. “Metabolomics of cell lines: a tool for aging research .” 2020. Web. 05 Dec 2020.

Vancouver:

Rocha AFSFd. Metabolomics of cell lines: a tool for aging research . [Internet] [Thesis]. Universidade de Aveiro; 2020. [cited 2020 Dec 05]. Available from: http://hdl.handle.net/10773/28961.

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

Council of Science Editors:

Rocha AFSFd. Metabolomics of cell lines: a tool for aging research . [Thesis]. Universidade de Aveiro; 2020. Available from: http://hdl.handle.net/10773/28961

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


University of Minnesota

10. Zhang, Chonglin. Adaptive mesh refinement and cut-cell algorithms for DSMC simulation of hypersonic flows.

Degree: MS, Aerospace Engineering and Mechanics, 2010, University of Minnesota

University of Minnesota M.S. thesis. May 2010. Major: Aerospace Engineering and Mechanics. Advisor: Dr. Thomas Schwartzentruber. 1 computer file (PDF); vii, 47 pages. Ill. (some… (more)

Subjects/Keywords: Cut-cell algorithms; Adaptive mesh refinement (AMR); Cartesian mesh; Flow field; Aerospace Engineering and Mechanics

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APA (6th Edition):

Zhang, C. (2010). Adaptive mesh refinement and cut-cell algorithms for DSMC simulation of hypersonic flows. (Masters Thesis). University of Minnesota. Retrieved from http://purl.umn.edu/93553

Chicago Manual of Style (16th Edition):

Zhang, Chonglin. “Adaptive mesh refinement and cut-cell algorithms for DSMC simulation of hypersonic flows.” 2010. Masters Thesis, University of Minnesota. Accessed December 05, 2020. http://purl.umn.edu/93553.

MLA Handbook (7th Edition):

Zhang, Chonglin. “Adaptive mesh refinement and cut-cell algorithms for DSMC simulation of hypersonic flows.” 2010. Web. 05 Dec 2020.

Vancouver:

Zhang C. Adaptive mesh refinement and cut-cell algorithms for DSMC simulation of hypersonic flows. [Internet] [Masters thesis]. University of Minnesota; 2010. [cited 2020 Dec 05]. Available from: http://purl.umn.edu/93553.

Council of Science Editors:

Zhang C. Adaptive mesh refinement and cut-cell algorithms for DSMC simulation of hypersonic flows. [Masters Thesis]. University of Minnesota; 2010. Available from: http://purl.umn.edu/93553


University of Georgia

11. Cao, Jing. In vitro study of synthetic prosthetic meshes for inguinal hernia repair.

Degree: 2014, University of Georgia

 Inguinal hernia is a protrusion of part of viscera through the abdominal wall. The prosthetic mesh is widely used in inguinal hernia repair, where it… (more)

Subjects/Keywords: Prosthetic hernia mesh; In vitro; Vital/avital composite mesh; Cell incorporation; Stiffness

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APA (6th Edition):

Cao, J. (2014). In vitro study of synthetic prosthetic meshes for inguinal hernia repair. (Thesis). University of Georgia. Retrieved from http://hdl.handle.net/10724/26587

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

Chicago Manual of Style (16th Edition):

Cao, Jing. “In vitro study of synthetic prosthetic meshes for inguinal hernia repair.” 2014. Thesis, University of Georgia. Accessed December 05, 2020. http://hdl.handle.net/10724/26587.

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

MLA Handbook (7th Edition):

Cao, Jing. “In vitro study of synthetic prosthetic meshes for inguinal hernia repair.” 2014. Web. 05 Dec 2020.

Vancouver:

Cao J. In vitro study of synthetic prosthetic meshes for inguinal hernia repair. [Internet] [Thesis]. University of Georgia; 2014. [cited 2020 Dec 05]. Available from: http://hdl.handle.net/10724/26587.

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

Council of Science Editors:

Cao J. In vitro study of synthetic prosthetic meshes for inguinal hernia repair. [Thesis]. University of Georgia; 2014. Available from: http://hdl.handle.net/10724/26587

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


University of California – San Francisco

12. Jeng, Mark Yungjie. Elucidating Molecular Changes in CD8+ T cells During Aging.

Degree: Biomedical Sciences, 2016, University of California – San Francisco

 One of the consequences of human aging is an overall decline in immune function. A hallmark of this aging process, termed immunosenescence, is the downregulation… (more)

Subjects/Keywords: Immunology; Aging; Cellular biology; Aging; CD8 T cell; FoxO1; Metabolism; SIRT1

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APA (6th Edition):

Jeng, M. Y. (2016). Elucidating Molecular Changes in CD8+ T cells During Aging. (Thesis). University of California – San Francisco. Retrieved from http://www.escholarship.org/uc/item/9m81j4k6

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

Chicago Manual of Style (16th Edition):

Jeng, Mark Yungjie. “Elucidating Molecular Changes in CD8+ T cells During Aging.” 2016. Thesis, University of California – San Francisco. Accessed December 05, 2020. http://www.escholarship.org/uc/item/9m81j4k6.

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

MLA Handbook (7th Edition):

Jeng, Mark Yungjie. “Elucidating Molecular Changes in CD8+ T cells During Aging.” 2016. Web. 05 Dec 2020.

Vancouver:

Jeng MY. Elucidating Molecular Changes in CD8+ T cells During Aging. [Internet] [Thesis]. University of California – San Francisco; 2016. [cited 2020 Dec 05]. Available from: http://www.escholarship.org/uc/item/9m81j4k6.

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

Council of Science Editors:

Jeng MY. Elucidating Molecular Changes in CD8+ T cells During Aging. [Thesis]. University of California – San Francisco; 2016. Available from: http://www.escholarship.org/uc/item/9m81j4k6

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


Columbia University

13. Pernice, Wolfgang Maximilian. Asymmetric Mitochondrial Inheritance and Retention in the Regulation of Aging in S. cerevisiae.

Degree: 2016, Columbia University

 Both an intuitive observation and maybe the most mysterious process of biology, aging describes the progressive deterioration of cellular functions with time. Asymmetric cell divisions… (more)

Subjects/Keywords: Cytology; Cell division; Mitochondria; Saccharomyces cerevisiae; Aging

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APA (6th Edition):

Pernice, W. M. (2016). Asymmetric Mitochondrial Inheritance and Retention in the Regulation of Aging in S. cerevisiae. (Doctoral Dissertation). Columbia University. Retrieved from https://doi.org/10.7916/D8N58MP3

Chicago Manual of Style (16th Edition):

Pernice, Wolfgang Maximilian. “Asymmetric Mitochondrial Inheritance and Retention in the Regulation of Aging in S. cerevisiae.” 2016. Doctoral Dissertation, Columbia University. Accessed December 05, 2020. https://doi.org/10.7916/D8N58MP3.

MLA Handbook (7th Edition):

Pernice, Wolfgang Maximilian. “Asymmetric Mitochondrial Inheritance and Retention in the Regulation of Aging in S. cerevisiae.” 2016. Web. 05 Dec 2020.

Vancouver:

Pernice WM. Asymmetric Mitochondrial Inheritance and Retention in the Regulation of Aging in S. cerevisiae. [Internet] [Doctoral dissertation]. Columbia University; 2016. [cited 2020 Dec 05]. Available from: https://doi.org/10.7916/D8N58MP3.

Council of Science Editors:

Pernice WM. Asymmetric Mitochondrial Inheritance and Retention in the Regulation of Aging in S. cerevisiae. [Doctoral Dissertation]. Columbia University; 2016. Available from: https://doi.org/10.7916/D8N58MP3


Boston University

14. Bu, Yi. Role of CCR3 in aging rhesus monkey brain.

Degree: MS, Anatomy & Neurobiology, 2019, Boston University

 Each year, aging and age-related deficits in cognitive function affect larger population worldwide. Research on aging has focused on changes in gray matter and white… (more)

Subjects/Keywords: Neurosciences; Aging; CCR3; Oligodendrocyte precursor cell

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APA (6th Edition):

Bu, Y. (2019). Role of CCR3 in aging rhesus monkey brain. (Masters Thesis). Boston University. Retrieved from http://hdl.handle.net/2144/38657

Chicago Manual of Style (16th Edition):

Bu, Yi. “Role of CCR3 in aging rhesus monkey brain.” 2019. Masters Thesis, Boston University. Accessed December 05, 2020. http://hdl.handle.net/2144/38657.

MLA Handbook (7th Edition):

Bu, Yi. “Role of CCR3 in aging rhesus monkey brain.” 2019. Web. 05 Dec 2020.

Vancouver:

Bu Y. Role of CCR3 in aging rhesus monkey brain. [Internet] [Masters thesis]. Boston University; 2019. [cited 2020 Dec 05]. Available from: http://hdl.handle.net/2144/38657.

Council of Science Editors:

Bu Y. Role of CCR3 in aging rhesus monkey brain. [Masters Thesis]. Boston University; 2019. Available from: http://hdl.handle.net/2144/38657


University of Arizona

15. Renkema, Kristin. Differential Maintenance, Function, and Transcriptional Profile of CD8⁺ T cells with Age .

Degree: 2013, University of Arizona

 Infectious diseases remain amongst leading causes of death in people aged 65 years and older; therefore, much research is focused on determining the immune components… (more)

Subjects/Keywords: CD8⁺ T cell; Homeostasis; Immunobiology; Aging

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

APA (6th Edition):

Renkema, K. (2013). Differential Maintenance, Function, and Transcriptional Profile of CD8⁺ T cells with Age . (Doctoral Dissertation). University of Arizona. Retrieved from http://hdl.handle.net/10150/293484

Chicago Manual of Style (16th Edition):

Renkema, Kristin. “Differential Maintenance, Function, and Transcriptional Profile of CD8⁺ T cells with Age .” 2013. Doctoral Dissertation, University of Arizona. Accessed December 05, 2020. http://hdl.handle.net/10150/293484.

MLA Handbook (7th Edition):

Renkema, Kristin. “Differential Maintenance, Function, and Transcriptional Profile of CD8⁺ T cells with Age .” 2013. Web. 05 Dec 2020.

Vancouver:

Renkema K. Differential Maintenance, Function, and Transcriptional Profile of CD8⁺ T cells with Age . [Internet] [Doctoral dissertation]. University of Arizona; 2013. [cited 2020 Dec 05]. Available from: http://hdl.handle.net/10150/293484.

Council of Science Editors:

Renkema K. Differential Maintenance, Function, and Transcriptional Profile of CD8⁺ T cells with Age . [Doctoral Dissertation]. University of Arizona; 2013. Available from: http://hdl.handle.net/10150/293484


Cranfield University

16. Lapenna, Antonio. T cells development in vitro : a minimalist approach.

Degree: PhD, 2012, Cranfield University

 T lymphocytes are considered an essential and advanced component of the immune system, since these cells are able to discriminate self from non-self, start up… (more)

Subjects/Keywords: T cell development; Notch signalling; Dll-4; HSC; stem cells ageing

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APA (6th Edition):

Lapenna, A. (2012). T cells development in vitro : a minimalist approach. (Doctoral Dissertation). Cranfield University. Retrieved from http://dspace.lib.cranfield.ac.uk/handle/1826/7797

Chicago Manual of Style (16th Edition):

Lapenna, Antonio. “T cells development in vitro : a minimalist approach.” 2012. Doctoral Dissertation, Cranfield University. Accessed December 05, 2020. http://dspace.lib.cranfield.ac.uk/handle/1826/7797.

MLA Handbook (7th Edition):

Lapenna, Antonio. “T cells development in vitro : a minimalist approach.” 2012. Web. 05 Dec 2020.

Vancouver:

Lapenna A. T cells development in vitro : a minimalist approach. [Internet] [Doctoral dissertation]. Cranfield University; 2012. [cited 2020 Dec 05]. Available from: http://dspace.lib.cranfield.ac.uk/handle/1826/7797.

Council of Science Editors:

Lapenna A. T cells development in vitro : a minimalist approach. [Doctoral Dissertation]. Cranfield University; 2012. Available from: http://dspace.lib.cranfield.ac.uk/handle/1826/7797


Queen Mary, University of London

17. Tyler, Eleanor. Understanding the molecular interplay between senescence, rejuvenation, and healthy ageing.

Degree: PhD, 2017, Queen Mary, University of London

 Senescence is classically defined as an irreversible cell cycle arrest. There is now convincing evidence that senescent cells accumulate during human ageing, potentially driving age-related… (more)

Subjects/Keywords: Cell Biology and Cutaneous Research; senescence; rejevenation; human ageing; healthspan

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APA (6th Edition):

Tyler, E. (2017). Understanding the molecular interplay between senescence, rejuvenation, and healthy ageing. (Doctoral Dissertation). Queen Mary, University of London. Retrieved from http://qmro.qmul.ac.uk/xmlui/handle/123456789/25981 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.765998

Chicago Manual of Style (16th Edition):

Tyler, Eleanor. “Understanding the molecular interplay between senescence, rejuvenation, and healthy ageing.” 2017. Doctoral Dissertation, Queen Mary, University of London. Accessed December 05, 2020. http://qmro.qmul.ac.uk/xmlui/handle/123456789/25981 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.765998.

MLA Handbook (7th Edition):

Tyler, Eleanor. “Understanding the molecular interplay between senescence, rejuvenation, and healthy ageing.” 2017. Web. 05 Dec 2020.

Vancouver:

Tyler E. Understanding the molecular interplay between senescence, rejuvenation, and healthy ageing. [Internet] [Doctoral dissertation]. Queen Mary, University of London; 2017. [cited 2020 Dec 05]. Available from: http://qmro.qmul.ac.uk/xmlui/handle/123456789/25981 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.765998.

Council of Science Editors:

Tyler E. Understanding the molecular interplay between senescence, rejuvenation, and healthy ageing. [Doctoral Dissertation]. Queen Mary, University of London; 2017. Available from: http://qmro.qmul.ac.uk/xmlui/handle/123456789/25981 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.765998


Cranfield University

18. Lapenna, Antonio. T cells development in vitro : a minimalist approach.

Degree: PhD, 2012, Cranfield University

 T lymphocytes are considered an essential and advanced component of the immune system, since these cells are able to discriminate self from non-self, start up… (more)

Subjects/Keywords: T cell development; Notch signalling; Dll-4; HSC; stem cells ageing

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

APA (6th Edition):

Lapenna, A. (2012). T cells development in vitro : a minimalist approach. (Doctoral Dissertation). Cranfield University. Retrieved from http://dspace.lib.cranfield.ac.uk/handle/1826/7797 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.566043

Chicago Manual of Style (16th Edition):

Lapenna, Antonio. “T cells development in vitro : a minimalist approach.” 2012. Doctoral Dissertation, Cranfield University. Accessed December 05, 2020. http://dspace.lib.cranfield.ac.uk/handle/1826/7797 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.566043.

MLA Handbook (7th Edition):

Lapenna, Antonio. “T cells development in vitro : a minimalist approach.” 2012. Web. 05 Dec 2020.

Vancouver:

Lapenna A. T cells development in vitro : a minimalist approach. [Internet] [Doctoral dissertation]. Cranfield University; 2012. [cited 2020 Dec 05]. Available from: http://dspace.lib.cranfield.ac.uk/handle/1826/7797 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.566043.

Council of Science Editors:

Lapenna A. T cells development in vitro : a minimalist approach. [Doctoral Dissertation]. Cranfield University; 2012. Available from: http://dspace.lib.cranfield.ac.uk/handle/1826/7797 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.566043


University of Manchester

19. Burrow, Kimberley Louise. The influence of donor age and in vitro expansion on the proliferation and differentiation properties of donor-matched bone marrow and adipose-derived mesenchymal stem cells : implications for musculoskeletal tissue engineering.

Degree: PhD, 2014, University of Manchester

 Introduction: Mesenchymal stem cells (MSC) offer a novel cell therapy within tissue engineering and regenerative medicine (TERM)-based strategies, and the prospect of MSC therapies are… (more)

Subjects/Keywords: 610.28; Mesenchymal stem cell; Senescence; Musculoskeletal tissue engineering; Ageing

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

APA (6th Edition):

Burrow, K. L. (2014). The influence of donor age and in vitro expansion on the proliferation and differentiation properties of donor-matched bone marrow and adipose-derived mesenchymal stem cells : implications for musculoskeletal tissue engineering. (Doctoral Dissertation). University of Manchester. Retrieved from https://www.research.manchester.ac.uk/portal/en/theses/the-influence-of-donor-age-and-in-vitro-expansion-on-the-proliferation-and-differentiation-properties-of-donormatched-bone-marrow-and-adiposederived-mesenchymal-stem-cells-implications-for-musculoskeletal-tissue-engineering(3c8f388c-8886-47b3-bcde-afe85787fd0c).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.632325

Chicago Manual of Style (16th Edition):

Burrow, Kimberley Louise. “The influence of donor age and in vitro expansion on the proliferation and differentiation properties of donor-matched bone marrow and adipose-derived mesenchymal stem cells : implications for musculoskeletal tissue engineering.” 2014. Doctoral Dissertation, University of Manchester. Accessed December 05, 2020. https://www.research.manchester.ac.uk/portal/en/theses/the-influence-of-donor-age-and-in-vitro-expansion-on-the-proliferation-and-differentiation-properties-of-donormatched-bone-marrow-and-adiposederived-mesenchymal-stem-cells-implications-for-musculoskeletal-tissue-engineering(3c8f388c-8886-47b3-bcde-afe85787fd0c).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.632325.

MLA Handbook (7th Edition):

Burrow, Kimberley Louise. “The influence of donor age and in vitro expansion on the proliferation and differentiation properties of donor-matched bone marrow and adipose-derived mesenchymal stem cells : implications for musculoskeletal tissue engineering.” 2014. Web. 05 Dec 2020.

Vancouver:

Burrow KL. The influence of donor age and in vitro expansion on the proliferation and differentiation properties of donor-matched bone marrow and adipose-derived mesenchymal stem cells : implications for musculoskeletal tissue engineering. [Internet] [Doctoral dissertation]. University of Manchester; 2014. [cited 2020 Dec 05]. Available from: https://www.research.manchester.ac.uk/portal/en/theses/the-influence-of-donor-age-and-in-vitro-expansion-on-the-proliferation-and-differentiation-properties-of-donormatched-bone-marrow-and-adiposederived-mesenchymal-stem-cells-implications-for-musculoskeletal-tissue-engineering(3c8f388c-8886-47b3-bcde-afe85787fd0c).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.632325.

Council of Science Editors:

Burrow KL. The influence of donor age and in vitro expansion on the proliferation and differentiation properties of donor-matched bone marrow and adipose-derived mesenchymal stem cells : implications for musculoskeletal tissue engineering. [Doctoral Dissertation]. University of Manchester; 2014. Available from: https://www.research.manchester.ac.uk/portal/en/theses/the-influence-of-donor-age-and-in-vitro-expansion-on-the-proliferation-and-differentiation-properties-of-donormatched-bone-marrow-and-adiposederived-mesenchymal-stem-cells-implications-for-musculoskeletal-tissue-engineering(3c8f388c-8886-47b3-bcde-afe85787fd0c).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.632325


University of Florida

20. Spearman, Marshall Edward, 1953-. The effects of aging on electrophile and epoxide metabolism by hepatic and pulmonary cytosolic glutathione S-transferases.

Degree: 1983, University of Florida

Subjects/Keywords: Aging ( mesh ); Biotransformation  – Aged ( mesh ); Glutathione Transferase ( mesh ); Metabolism  – Aged ( mesh ); Pharmacology and Therapeutics thesis Ph.D ( mesh )

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APA (6th Edition):

Spearman, Marshall Edward, 1. (1983). The effects of aging on electrophile and epoxide metabolism by hepatic and pulmonary cytosolic glutathione S-transferases. (Thesis). University of Florida. Retrieved from https://ufdc.ufl.edu/AA00009108

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

Chicago Manual of Style (16th Edition):

Spearman, Marshall Edward, 1953-. “The effects of aging on electrophile and epoxide metabolism by hepatic and pulmonary cytosolic glutathione S-transferases.” 1983. Thesis, University of Florida. Accessed December 05, 2020. https://ufdc.ufl.edu/AA00009108.

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

MLA Handbook (7th Edition):

Spearman, Marshall Edward, 1953-. “The effects of aging on electrophile and epoxide metabolism by hepatic and pulmonary cytosolic glutathione S-transferases.” 1983. Web. 05 Dec 2020.

Vancouver:

Spearman, Marshall Edward 1. The effects of aging on electrophile and epoxide metabolism by hepatic and pulmonary cytosolic glutathione S-transferases. [Internet] [Thesis]. University of Florida; 1983. [cited 2020 Dec 05]. Available from: https://ufdc.ufl.edu/AA00009108.

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

Council of Science Editors:

Spearman, Marshall Edward 1. The effects of aging on electrophile and epoxide metabolism by hepatic and pulmonary cytosolic glutathione S-transferases. [Thesis]. University of Florida; 1983. Available from: https://ufdc.ufl.edu/AA00009108

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


Jönköping University

21. Yousaf, Imran. MAC SCHEDULING IN INDUSTRIAL WIRELESS CELL-BASED MESH SENSOR NETWORKS.

Degree: Computer and Electrical Engineering, 2011, Jönköping University

  Undergoing developments for the adaptation of Wireless Sensor Networks (WSNs) in automation industry is creating several research questions. The usage of wireless technologies in… (more)

Subjects/Keywords: Cell-Based Mesh Networks; Industrial Wireless Sensor Networks

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APA (6th Edition):

Yousaf, I. (2011). MAC SCHEDULING IN INDUSTRIAL WIRELESS CELL-BASED MESH SENSOR NETWORKS. (Thesis). Jönköping University. Retrieved from http://urn.kb.se/resolve?urn=urn:nbn:se:hj:diva-19940

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

Chicago Manual of Style (16th Edition):

Yousaf, Imran. “MAC SCHEDULING IN INDUSTRIAL WIRELESS CELL-BASED MESH SENSOR NETWORKS.” 2011. Thesis, Jönköping University. Accessed December 05, 2020. http://urn.kb.se/resolve?urn=urn:nbn:se:hj:diva-19940.

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

MLA Handbook (7th Edition):

Yousaf, Imran. “MAC SCHEDULING IN INDUSTRIAL WIRELESS CELL-BASED MESH SENSOR NETWORKS.” 2011. Web. 05 Dec 2020.

Vancouver:

Yousaf I. MAC SCHEDULING IN INDUSTRIAL WIRELESS CELL-BASED MESH SENSOR NETWORKS. [Internet] [Thesis]. Jönköping University; 2011. [cited 2020 Dec 05]. Available from: http://urn.kb.se/resolve?urn=urn:nbn:se:hj:diva-19940.

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

Council of Science Editors:

Yousaf I. MAC SCHEDULING IN INDUSTRIAL WIRELESS CELL-BASED MESH SENSOR NETWORKS. [Thesis]. Jönköping University; 2011. Available from: http://urn.kb.se/resolve?urn=urn:nbn:se:hj:diva-19940

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


Clemson University

22. Stowe Gilmore, Jordan Anthony. Development and Fabrication of Novel Woven Meshes as Bone Graft Substitutes for Critical Sized Defects.

Degree: PhD, Bioengineering, 2015, Clemson University

  With more than $2.5 billion spent per year, and over 2.2 million procedures conducted annually worldwide, bone grafting continues to be a large part… (more)

Subjects/Keywords: Bone; Mesh; Scaffold; Stem Cell; Tissue Engineering; Woven

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APA (6th Edition):

Stowe Gilmore, J. A. (2015). Development and Fabrication of Novel Woven Meshes as Bone Graft Substitutes for Critical Sized Defects. (Doctoral Dissertation). Clemson University. Retrieved from https://tigerprints.clemson.edu/all_dissertations/1478

Chicago Manual of Style (16th Edition):

Stowe Gilmore, Jordan Anthony. “Development and Fabrication of Novel Woven Meshes as Bone Graft Substitutes for Critical Sized Defects.” 2015. Doctoral Dissertation, Clemson University. Accessed December 05, 2020. https://tigerprints.clemson.edu/all_dissertations/1478.

MLA Handbook (7th Edition):

Stowe Gilmore, Jordan Anthony. “Development and Fabrication of Novel Woven Meshes as Bone Graft Substitutes for Critical Sized Defects.” 2015. Web. 05 Dec 2020.

Vancouver:

Stowe Gilmore JA. Development and Fabrication of Novel Woven Meshes as Bone Graft Substitutes for Critical Sized Defects. [Internet] [Doctoral dissertation]. Clemson University; 2015. [cited 2020 Dec 05]. Available from: https://tigerprints.clemson.edu/all_dissertations/1478.

Council of Science Editors:

Stowe Gilmore JA. Development and Fabrication of Novel Woven Meshes as Bone Graft Substitutes for Critical Sized Defects. [Doctoral Dissertation]. Clemson University; 2015. Available from: https://tigerprints.clemson.edu/all_dissertations/1478


University of California – Riverside

23. Arora, Astha. Microwoven Meshes Used for Particle Separation and Capture.

Degree: Bioengineering, 2016, University of California – Riverside

Cell separation is a powerful technique, which is widely used in many strands of biological and biomedical research and in clinical therapy. The most common… (more)

Subjects/Keywords: Biomedical engineering; cell separation; cell sorting; Deterministic Lateral Displacement; microfluidics; microwoven mesh

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APA (6th Edition):

Arora, A. (2016). Microwoven Meshes Used for Particle Separation and Capture. (Thesis). University of California – Riverside. Retrieved from http://www.escholarship.org/uc/item/92m7v1d3

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

Chicago Manual of Style (16th Edition):

Arora, Astha. “Microwoven Meshes Used for Particle Separation and Capture.” 2016. Thesis, University of California – Riverside. Accessed December 05, 2020. http://www.escholarship.org/uc/item/92m7v1d3.

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

MLA Handbook (7th Edition):

Arora, Astha. “Microwoven Meshes Used for Particle Separation and Capture.” 2016. Web. 05 Dec 2020.

Vancouver:

Arora A. Microwoven Meshes Used for Particle Separation and Capture. [Internet] [Thesis]. University of California – Riverside; 2016. [cited 2020 Dec 05]. Available from: http://www.escholarship.org/uc/item/92m7v1d3.

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

Council of Science Editors:

Arora A. Microwoven Meshes Used for Particle Separation and Capture. [Thesis]. University of California – Riverside; 2016. Available from: http://www.escholarship.org/uc/item/92m7v1d3

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


Freie Universität Berlin

24. Zabel, Solveig. Bacterial ligation of CEACAM1 reduces Toll-like receptor2-triggered antibacterial responses of pulmonary epithelial cells.

Degree: 2010, Freie Universität Berlin

 Chronic obstructive pulmonary disease (COPD) is a major cause of chronic morbidity and mortality throughout the world. Modern drugs and therapies do not sufficiently influence… (more)

Subjects/Keywords: Moraxella catarrhalis; Bacterial Outer Membrane Proteins (MeSH); Respiratory Diseases; Respiratory Mucosa/immunology (MeSH); 1-Phosphatidylinositol 3-Kinase/metabolism (MeSH); Cell Adhesion Molecules (MeSH); Toll-Like Receptor 2 (MeSH); Signal Transduction (MeSH); 600 Technik, Medizin, angewandte Wissenschaften::630 Landwirtschaft

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APA (6th Edition):

Zabel, S. (2010). Bacterial ligation of CEACAM1 reduces Toll-like receptor2-triggered antibacterial responses of pulmonary epithelial cells. (Thesis). Freie Universität Berlin. Retrieved from http://dx.doi.org/10.17169/refubium-9409

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

Chicago Manual of Style (16th Edition):

Zabel, Solveig. “Bacterial ligation of CEACAM1 reduces Toll-like receptor2-triggered antibacterial responses of pulmonary epithelial cells.” 2010. Thesis, Freie Universität Berlin. Accessed December 05, 2020. http://dx.doi.org/10.17169/refubium-9409.

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

MLA Handbook (7th Edition):

Zabel, Solveig. “Bacterial ligation of CEACAM1 reduces Toll-like receptor2-triggered antibacterial responses of pulmonary epithelial cells.” 2010. Web. 05 Dec 2020.

Vancouver:

Zabel S. Bacterial ligation of CEACAM1 reduces Toll-like receptor2-triggered antibacterial responses of pulmonary epithelial cells. [Internet] [Thesis]. Freie Universität Berlin; 2010. [cited 2020 Dec 05]. Available from: http://dx.doi.org/10.17169/refubium-9409.

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

Council of Science Editors:

Zabel S. Bacterial ligation of CEACAM1 reduces Toll-like receptor2-triggered antibacterial responses of pulmonary epithelial cells. [Thesis]. Freie Universität Berlin; 2010. Available from: http://dx.doi.org/10.17169/refubium-9409

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


University of Florida

25. Klopp, Alan John. Characterization of DNA cleavage sites induced by topoisomerase II inhibitor drugs.

Degree: 1997, University of Florida

Subjects/Keywords: Research ( mesh ); DNA Topoisomerase (ATP-Hydrolysing) ( mesh ); Enzyme Inhibitors ( mesh ); Apoptosis ( mesh ); DNA Fragmentation ( mesh ); Telomere ( mesh ); Cytarabine ( mesh ); Tubulin ( mesh ); Mammals ( mesh ); Cell Line ( mesh ); Department of Pharmacology and Therapeutics thesis Ph.D ( mesh )

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APA (6th Edition):

Klopp, A. J. (1997). Characterization of DNA cleavage sites induced by topoisomerase II inhibitor drugs. (Thesis). University of Florida. Retrieved from https://ufdc.ufl.edu/AA00065818

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

Chicago Manual of Style (16th Edition):

Klopp, Alan John. “Characterization of DNA cleavage sites induced by topoisomerase II inhibitor drugs.” 1997. Thesis, University of Florida. Accessed December 05, 2020. https://ufdc.ufl.edu/AA00065818.

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

MLA Handbook (7th Edition):

Klopp, Alan John. “Characterization of DNA cleavage sites induced by topoisomerase II inhibitor drugs.” 1997. Web. 05 Dec 2020.

Vancouver:

Klopp AJ. Characterization of DNA cleavage sites induced by topoisomerase II inhibitor drugs. [Internet] [Thesis]. University of Florida; 1997. [cited 2020 Dec 05]. Available from: https://ufdc.ufl.edu/AA00065818.

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

Council of Science Editors:

Klopp AJ. Characterization of DNA cleavage sites induced by topoisomerase II inhibitor drugs. [Thesis]. University of Florida; 1997. Available from: https://ufdc.ufl.edu/AA00065818

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


University of California – San Diego

26. Benthuysen, Jacqueline. Regulation of pancreatic beta cell proliferation and aging.

Degree: Biomedical Sciences, 2016, University of California – San Diego

 The replicative capacity of insulin-producing pancreatic beta cells is dynamically regulated during development, maturation, and aging. Early in life, beta cells proliferate rapidly to expand… (more)

Subjects/Keywords: Molecular biology; Genetics; Beta cell; Beta cell aging; Beta cell proliferation; Glucose; MAPK; Nkx6.1

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APA (6th Edition):

Benthuysen, J. (2016). Regulation of pancreatic beta cell proliferation and aging. (Thesis). University of California – San Diego. Retrieved from http://www.escholarship.org/uc/item/1k9844q3

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

Chicago Manual of Style (16th Edition):

Benthuysen, Jacqueline. “Regulation of pancreatic beta cell proliferation and aging.” 2016. Thesis, University of California – San Diego. Accessed December 05, 2020. http://www.escholarship.org/uc/item/1k9844q3.

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

MLA Handbook (7th Edition):

Benthuysen, Jacqueline. “Regulation of pancreatic beta cell proliferation and aging.” 2016. Web. 05 Dec 2020.

Vancouver:

Benthuysen J. Regulation of pancreatic beta cell proliferation and aging. [Internet] [Thesis]. University of California – San Diego; 2016. [cited 2020 Dec 05]. Available from: http://www.escholarship.org/uc/item/1k9844q3.

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

Council of Science Editors:

Benthuysen J. Regulation of pancreatic beta cell proliferation and aging. [Thesis]. University of California – San Diego; 2016. Available from: http://www.escholarship.org/uc/item/1k9844q3

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


University of Minnesota

27. Smith, Michelle. Mechanisms of Thymic Involution and Therapies to Prevent or Treat the loss of Thymic Epithelial Cells.

Degree: PhD, Microbiology, Immunology and Cancer Biology, 2016, University of Minnesota

 The thymus has great importance to human health as naïve T cells cannot be generated in its absence. The composition and organization of its specialized… (more)

Subjects/Keywords: Aging; Cell Therapy; Hematopoietic Stem Cell Transplant; T cell differentiation; Thymic microenvironment; Thymus

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APA (6th Edition):

Smith, M. (2016). Mechanisms of Thymic Involution and Therapies to Prevent or Treat the loss of Thymic Epithelial Cells. (Doctoral Dissertation). University of Minnesota. Retrieved from http://hdl.handle.net/11299/191443

Chicago Manual of Style (16th Edition):

Smith, Michelle. “Mechanisms of Thymic Involution and Therapies to Prevent or Treat the loss of Thymic Epithelial Cells.” 2016. Doctoral Dissertation, University of Minnesota. Accessed December 05, 2020. http://hdl.handle.net/11299/191443.

MLA Handbook (7th Edition):

Smith, Michelle. “Mechanisms of Thymic Involution and Therapies to Prevent or Treat the loss of Thymic Epithelial Cells.” 2016. Web. 05 Dec 2020.

Vancouver:

Smith M. Mechanisms of Thymic Involution and Therapies to Prevent or Treat the loss of Thymic Epithelial Cells. [Internet] [Doctoral dissertation]. University of Minnesota; 2016. [cited 2020 Dec 05]. Available from: http://hdl.handle.net/11299/191443.

Council of Science Editors:

Smith M. Mechanisms of Thymic Involution and Therapies to Prevent or Treat the loss of Thymic Epithelial Cells. [Doctoral Dissertation]. University of Minnesota; 2016. Available from: http://hdl.handle.net/11299/191443


University of Florida

28. Mohamed, Sumia Sir-Elkhatim, 1958-. The Disposition of codeine in sickle cell patients compared to healthy controls.

Degree: 1991, University of Florida

Subjects/Keywords: Research ( mesh ); Codeine  – analysis ( mesh ); Codeine  – pharmacokinetics ( mesh ); Codeine  – metabolism ( mesh ); Protein Binding ( mesh ); Erythrocytes ( mesh ); Blood Proteins ( mesh ); Anemia, Sickle Cell ( mesh ); Chromatography, High Pressure Liquid  – methods ( mesh ); Department of Pharmaceutics thesis Ph.D ( mesh )

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

APA (6th Edition):

Mohamed, Sumia Sir-Elkhatim, 1. (1991). The Disposition of codeine in sickle cell patients compared to healthy controls. (Thesis). University of Florida. Retrieved from https://ufdc.ufl.edu/AA00065788

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

Chicago Manual of Style (16th Edition):

Mohamed, Sumia Sir-Elkhatim, 1958-. “The Disposition of codeine in sickle cell patients compared to healthy controls.” 1991. Thesis, University of Florida. Accessed December 05, 2020. https://ufdc.ufl.edu/AA00065788.

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

MLA Handbook (7th Edition):

Mohamed, Sumia Sir-Elkhatim, 1958-. “The Disposition of codeine in sickle cell patients compared to healthy controls.” 1991. Web. 05 Dec 2020.

Vancouver:

Mohamed, Sumia Sir-Elkhatim 1. The Disposition of codeine in sickle cell patients compared to healthy controls. [Internet] [Thesis]. University of Florida; 1991. [cited 2020 Dec 05]. Available from: https://ufdc.ufl.edu/AA00065788.

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

Council of Science Editors:

Mohamed, Sumia Sir-Elkhatim 1. The Disposition of codeine in sickle cell patients compared to healthy controls. [Thesis]. University of Florida; 1991. Available from: https://ufdc.ufl.edu/AA00065788

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


University of Florida

29. Cariappa, Rohit, 1962-. Biogenesis, domain localization, and targeting of the hepatic system A amino acid transporter.

Degree: 1991, University of Florida

Subjects/Keywords: Research ( mesh ); Amino Acids  – metabolism ( mesh ); Biological Transport ( mesh ); Carrier Proteins ( mesh ); Cell Membrane  – physiology ( mesh ); Golgi Apparatus  – physiology ( mesh ); Glucagon ( mesh ); Dexamethasone ( mesh ); Rats ( mesh ); Department of Biochemistry and Molecular Biology thesis Ph.D ( mesh )

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

APA (6th Edition):

Cariappa, Rohit, 1. (1991). Biogenesis, domain localization, and targeting of the hepatic system A amino acid transporter. (Thesis). University of Florida. Retrieved from https://ufdc.ufl.edu/AA00065775

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

Chicago Manual of Style (16th Edition):

Cariappa, Rohit, 1962-. “Biogenesis, domain localization, and targeting of the hepatic system A amino acid transporter.” 1991. Thesis, University of Florida. Accessed December 05, 2020. https://ufdc.ufl.edu/AA00065775.

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

MLA Handbook (7th Edition):

Cariappa, Rohit, 1962-. “Biogenesis, domain localization, and targeting of the hepatic system A amino acid transporter.” 1991. Web. 05 Dec 2020.

Vancouver:

Cariappa, Rohit 1. Biogenesis, domain localization, and targeting of the hepatic system A amino acid transporter. [Internet] [Thesis]. University of Florida; 1991. [cited 2020 Dec 05]. Available from: https://ufdc.ufl.edu/AA00065775.

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

Council of Science Editors:

Cariappa, Rohit 1. Biogenesis, domain localization, and targeting of the hepatic system A amino acid transporter. [Thesis]. University of Florida; 1991. Available from: https://ufdc.ufl.edu/AA00065775

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

30. Ogden, Stephanie. An Investigation of Langerhans' Cell Function in Aged Skin.

Degree: 2013, University of Manchester

 With increasing age, aspects of the innate and adaptive immune systems show functional decline. In the skin this is associated with an increased incidence of… (more)

Subjects/Keywords: Langerhans' cell; Ageing; Interleukin-1

…74 List of Figures Figure 1.1 Langerhans’ cell (LC) migration. Following… …x28;TNF-α) in Langerhans’ cell migration. (Keratinocyte, K, tan; LC, grey; antigen… …Langerhans’ cell migration upon exposure to a contact allergen. The pro-inflammatory cytokines, IL… …post(B) magnetic activated cell sorting (MACS). Green lines; CD14, pink… …80 Figure 3.2 Mean percentage CD14+ cells pre- and post- magnetic activated cell sorting… 

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

APA (6th Edition):

Ogden, S. (2013). An Investigation of Langerhans' Cell Function in Aged Skin. (Doctoral Dissertation). University of Manchester. Retrieved from http://www.manchester.ac.uk/escholar/uk-ac-man-scw:189982

Chicago Manual of Style (16th Edition):

Ogden, Stephanie. “An Investigation of Langerhans' Cell Function in Aged Skin.” 2013. Doctoral Dissertation, University of Manchester. Accessed December 05, 2020. http://www.manchester.ac.uk/escholar/uk-ac-man-scw:189982.

MLA Handbook (7th Edition):

Ogden, Stephanie. “An Investigation of Langerhans' Cell Function in Aged Skin.” 2013. Web. 05 Dec 2020.

Vancouver:

Ogden S. An Investigation of Langerhans' Cell Function in Aged Skin. [Internet] [Doctoral dissertation]. University of Manchester; 2013. [cited 2020 Dec 05]. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:189982.

Council of Science Editors:

Ogden S. An Investigation of Langerhans' Cell Function in Aged Skin. [Doctoral Dissertation]. University of Manchester; 2013. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:189982

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