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You searched for subject:(healthspan). Showing records 1 – 16 of 16 total matches.

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Deakin University

1. Masaldan, Shashank. Investigating metal aberrations in cellular senescence.

Degree: School of Life and Environmental Sciences, 2017, Deakin University

 This study explored perturbations in iron and copper homeostasis in senescent cells that contribute to age-associated disease and dysfunction. Altered metal regulation was associated with… (more)

Subjects/Keywords: ageing; autophagy; healthspan; senescence; ferritin; ferritinophagy; ferroptosis

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APA (6th Edition):

Masaldan, S. (2017). Investigating metal aberrations in cellular senescence. (Thesis). Deakin University. Retrieved from http://hdl.handle.net/10536/DRO/DU:30103501

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):

Masaldan, Shashank. “Investigating metal aberrations in cellular senescence.” 2017. Thesis, Deakin University. Accessed January 26, 2020. http://hdl.handle.net/10536/DRO/DU:30103501.

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

MLA Handbook (7th Edition):

Masaldan, Shashank. “Investigating metal aberrations in cellular senescence.” 2017. Web. 26 Jan 2020.

Vancouver:

Masaldan S. Investigating metal aberrations in cellular senescence. [Internet] [Thesis]. Deakin University; 2017. [cited 2020 Jan 26]. Available from: http://hdl.handle.net/10536/DRO/DU:30103501.

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

Council of Science Editors:

Masaldan S. Investigating metal aberrations in cellular senescence. [Thesis]. Deakin University; 2017. Available from: http://hdl.handle.net/10536/DRO/DU:30103501

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


Colorado State University

2. Reid, Justin. Novel insights into protein synthesis rates in the brain following two lifespan-extending treatments.

Degree: MS(M.S.), Health and Exercise Science, 2018, Colorado State University

 The number of individuals 65 years or older is rapidly increasing. Aging is the predominant risk factor for chronic disease and disability. Dramatic increases in… (more)

Subjects/Keywords: Healthspan; Rapamycin; Brain; Slowed Aging; Metformin

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APA (6th Edition):

Reid, J. (2018). Novel insights into protein synthesis rates in the brain following two lifespan-extending treatments. (Masters Thesis). Colorado State University. Retrieved from http://hdl.handle.net/10217/191325

Chicago Manual of Style (16th Edition):

Reid, Justin. “Novel insights into protein synthesis rates in the brain following two lifespan-extending treatments.” 2018. Masters Thesis, Colorado State University. Accessed January 26, 2020. http://hdl.handle.net/10217/191325.

MLA Handbook (7th Edition):

Reid, Justin. “Novel insights into protein synthesis rates in the brain following two lifespan-extending treatments.” 2018. Web. 26 Jan 2020.

Vancouver:

Reid J. Novel insights into protein synthesis rates in the brain following two lifespan-extending treatments. [Internet] [Masters thesis]. Colorado State University; 2018. [cited 2020 Jan 26]. Available from: http://hdl.handle.net/10217/191325.

Council of Science Editors:

Reid J. Novel insights into protein synthesis rates in the brain following two lifespan-extending treatments. [Masters Thesis]. Colorado State University; 2018. Available from: http://hdl.handle.net/10217/191325


University of California – Irvine

3. Lopez, Terry Enriquez. The effect of green tea polyphenols on Drosophila melanogaster lifespan and healthspan.

Degree: Pharmacological Sciences with a concentration in Pharmaceutical Sciences Ph, 2016, University of California – Irvine

 Green tea is a popular beverage believed to have many health benefits including reducing the risks of neurodegenerative disorders, cardiovascular disease, and some cancers. As… (more)

Subjects/Keywords: Pharmaceutical sciences; Pharmacology; Drosophila; fertility; green tea; healthspan; iron; lifespan

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APA (6th Edition):

Lopez, T. E. (2016). The effect of green tea polyphenols on Drosophila melanogaster lifespan and healthspan. (Thesis). University of California – Irvine. Retrieved from http://www.escholarship.org/uc/item/17b2p728

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):

Lopez, Terry Enriquez. “The effect of green tea polyphenols on Drosophila melanogaster lifespan and healthspan.” 2016. Thesis, University of California – Irvine. Accessed January 26, 2020. http://www.escholarship.org/uc/item/17b2p728.

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

MLA Handbook (7th Edition):

Lopez, Terry Enriquez. “The effect of green tea polyphenols on Drosophila melanogaster lifespan and healthspan.” 2016. Web. 26 Jan 2020.

Vancouver:

Lopez TE. The effect of green tea polyphenols on Drosophila melanogaster lifespan and healthspan. [Internet] [Thesis]. University of California – Irvine; 2016. [cited 2020 Jan 26]. Available from: http://www.escholarship.org/uc/item/17b2p728.

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

Council of Science Editors:

Lopez TE. The effect of green tea polyphenols on Drosophila melanogaster lifespan and healthspan. [Thesis]. University of California – Irvine; 2016. Available from: http://www.escholarship.org/uc/item/17b2p728

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


University of Colorado

4. Newell-Stamper, Breanne L. From Cells to Mice: Mutations Conferring Oxidative Stress-Resistance on Longevity Phenotypes in the Mouse.

Degree: PhD, 2018, University of Colorado

  Oxidative stress is one of the drivers of the aging process and resistance to oxidative stress is a common characteristic of long-lived organisms. For… (more)

Subjects/Keywords: oxidative stress resistance; genetic; healthspan; lifespan; mice; Genetics; Physiology

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APA (6th Edition):

Newell-Stamper, B. L. (2018). From Cells to Mice: Mutations Conferring Oxidative Stress-Resistance on Longevity Phenotypes in the Mouse. (Doctoral Dissertation). University of Colorado. Retrieved from https://scholar.colorado.edu/iphy_gradetds/69

Chicago Manual of Style (16th Edition):

Newell-Stamper, Breanne L. “From Cells to Mice: Mutations Conferring Oxidative Stress-Resistance on Longevity Phenotypes in the Mouse.” 2018. Doctoral Dissertation, University of Colorado. Accessed January 26, 2020. https://scholar.colorado.edu/iphy_gradetds/69.

MLA Handbook (7th Edition):

Newell-Stamper, Breanne L. “From Cells to Mice: Mutations Conferring Oxidative Stress-Resistance on Longevity Phenotypes in the Mouse.” 2018. Web. 26 Jan 2020.

Vancouver:

Newell-Stamper BL. From Cells to Mice: Mutations Conferring Oxidative Stress-Resistance on Longevity Phenotypes in the Mouse. [Internet] [Doctoral dissertation]. University of Colorado; 2018. [cited 2020 Jan 26]. Available from: https://scholar.colorado.edu/iphy_gradetds/69.

Council of Science Editors:

Newell-Stamper BL. From Cells to Mice: Mutations Conferring Oxidative Stress-Resistance on Longevity Phenotypes in the Mouse. [Doctoral Dissertation]. University of Colorado; 2018. Available from: https://scholar.colorado.edu/iphy_gradetds/69


University of Arizona

5. Goldberg, Emily L. Lifespan Extension, Nutrient Sensing and Immune Competence .

Degree: 2014, University of Arizona

 Immune protection wanes during aging. This is evidenced by increased morbidity and mortality from infectious disease in aged individuals. As the aging population continues to… (more)

Subjects/Keywords: CD8 T cell; Healthspan; metabolism; nutrient sensing; Nutritional Sciences; Aging

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APA (6th Edition):

Goldberg, E. L. (2014). Lifespan Extension, Nutrient Sensing and Immune Competence . (Doctoral Dissertation). University of Arizona. Retrieved from http://hdl.handle.net/10150/321459

Chicago Manual of Style (16th Edition):

Goldberg, Emily L. “Lifespan Extension, Nutrient Sensing and Immune Competence .” 2014. Doctoral Dissertation, University of Arizona. Accessed January 26, 2020. http://hdl.handle.net/10150/321459.

MLA Handbook (7th Edition):

Goldberg, Emily L. “Lifespan Extension, Nutrient Sensing and Immune Competence .” 2014. Web. 26 Jan 2020.

Vancouver:

Goldberg EL. Lifespan Extension, Nutrient Sensing and Immune Competence . [Internet] [Doctoral dissertation]. University of Arizona; 2014. [cited 2020 Jan 26]. Available from: http://hdl.handle.net/10150/321459.

Council of Science Editors:

Goldberg EL. Lifespan Extension, Nutrient Sensing and Immune Competence . [Doctoral Dissertation]. University of Arizona; 2014. Available from: http://hdl.handle.net/10150/321459


Universitat de Valencia

6. Salvador Pascual, Andrea. Moderate overexpression of glucose-6-phosphate dehydrogenase improves healthspan in mice. Implications in skeletal muscle regeneration .

Degree: 2019, Universitat de Valencia

 An enormous increment in the average lifespan of diverse populations occurred worldwide in the 20th century. In the last 10–15 years, the importance has changed… (more)

Subjects/Keywords: healthspan; oxidative stress; g6pd; skeletal muscle; regeneration; aging

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APA (6th Edition):

Salvador Pascual, A. (2019). Moderate overexpression of glucose-6-phosphate dehydrogenase improves healthspan in mice. Implications in skeletal muscle regeneration . (Doctoral Dissertation). Universitat de Valencia. Retrieved from http://hdl.handle.net/10550/70756

Chicago Manual of Style (16th Edition):

Salvador Pascual, Andrea. “Moderate overexpression of glucose-6-phosphate dehydrogenase improves healthspan in mice. Implications in skeletal muscle regeneration .” 2019. Doctoral Dissertation, Universitat de Valencia. Accessed January 26, 2020. http://hdl.handle.net/10550/70756.

MLA Handbook (7th Edition):

Salvador Pascual, Andrea. “Moderate overexpression of glucose-6-phosphate dehydrogenase improves healthspan in mice. Implications in skeletal muscle regeneration .” 2019. Web. 26 Jan 2020.

Vancouver:

Salvador Pascual A. Moderate overexpression of glucose-6-phosphate dehydrogenase improves healthspan in mice. Implications in skeletal muscle regeneration . [Internet] [Doctoral dissertation]. Universitat de Valencia; 2019. [cited 2020 Jan 26]. Available from: http://hdl.handle.net/10550/70756.

Council of Science Editors:

Salvador Pascual A. Moderate overexpression of glucose-6-phosphate dehydrogenase improves healthspan in mice. Implications in skeletal muscle regeneration . [Doctoral Dissertation]. Universitat de Valencia; 2019. Available from: http://hdl.handle.net/10550/70756


Queen Mary, University of London

7. 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 January 26, 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. 26 Jan 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 Jan 26]. 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


Georgia Tech

8. Cho, YongMin. Automated microfluidic platforms for high-throughput in vivo functional imaging and individualized long-term health and longevity tracking of C. elegans.

Degree: PhD, Chemical and Biomolecular Engineering, 2017, Georgia Tech

 One of big questions in neuroscience is how animals modulate behavior in response to external stimuli and environmental cues, and how this changes with age.… (more)

Subjects/Keywords: Microfluidics; C. elegans; Mechanosensation; Multisensory integration; Aging; Healthspan; Lifespan

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APA (6th Edition):

Cho, Y. (2017). Automated microfluidic platforms for high-throughput in vivo functional imaging and individualized long-term health and longevity tracking of C. elegans. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/59770

Chicago Manual of Style (16th Edition):

Cho, YongMin. “Automated microfluidic platforms for high-throughput in vivo functional imaging and individualized long-term health and longevity tracking of C. elegans.” 2017. Doctoral Dissertation, Georgia Tech. Accessed January 26, 2020. http://hdl.handle.net/1853/59770.

MLA Handbook (7th Edition):

Cho, YongMin. “Automated microfluidic platforms for high-throughput in vivo functional imaging and individualized long-term health and longevity tracking of C. elegans.” 2017. Web. 26 Jan 2020.

Vancouver:

Cho Y. Automated microfluidic platforms for high-throughput in vivo functional imaging and individualized long-term health and longevity tracking of C. elegans. [Internet] [Doctoral dissertation]. Georgia Tech; 2017. [cited 2020 Jan 26]. Available from: http://hdl.handle.net/1853/59770.

Council of Science Editors:

Cho Y. Automated microfluidic platforms for high-throughput in vivo functional imaging and individualized long-term health and longevity tracking of C. elegans. [Doctoral Dissertation]. Georgia Tech; 2017. Available from: http://hdl.handle.net/1853/59770


University of Washington

9. Lee, Mitchell. The consequences of mutator-driven mutagenesis and analysis of lifespan extending compounds using outgrowth analysis and replicative lifespan in Saccharomyces cerevisiae.

Degree: PhD, 2018, University of Washington

 The hope of dramatically extending our lifespan has captivated humanity for millennia. Over the last two decades, the biology of aging has matured as a… (more)

Subjects/Keywords: Geroscience; Healthspan; Mutator; Genetics; Molecular biology; Gerontology; Pathology

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APA (6th Edition):

Lee, M. (2018). The consequences of mutator-driven mutagenesis and analysis of lifespan extending compounds using outgrowth analysis and replicative lifespan in Saccharomyces cerevisiae. (Doctoral Dissertation). University of Washington. Retrieved from http://hdl.handle.net/1773/43123

Chicago Manual of Style (16th Edition):

Lee, Mitchell. “The consequences of mutator-driven mutagenesis and analysis of lifespan extending compounds using outgrowth analysis and replicative lifespan in Saccharomyces cerevisiae.” 2018. Doctoral Dissertation, University of Washington. Accessed January 26, 2020. http://hdl.handle.net/1773/43123.

MLA Handbook (7th Edition):

Lee, Mitchell. “The consequences of mutator-driven mutagenesis and analysis of lifespan extending compounds using outgrowth analysis and replicative lifespan in Saccharomyces cerevisiae.” 2018. Web. 26 Jan 2020.

Vancouver:

Lee M. The consequences of mutator-driven mutagenesis and analysis of lifespan extending compounds using outgrowth analysis and replicative lifespan in Saccharomyces cerevisiae. [Internet] [Doctoral dissertation]. University of Washington; 2018. [cited 2020 Jan 26]. Available from: http://hdl.handle.net/1773/43123.

Council of Science Editors:

Lee M. The consequences of mutator-driven mutagenesis and analysis of lifespan extending compounds using outgrowth analysis and replicative lifespan in Saccharomyces cerevisiae. [Doctoral Dissertation]. University of Washington; 2018. Available from: http://hdl.handle.net/1773/43123


University of Colorado

10. Johnson, Lawrence Cody. Aging and the Plasma Metabolome: Relation to Physiological Function.

Degree: PhD, 2018, University of Colorado

  Advancing age is associated with declines across numerous physiological systems, leading to an increased risk of chronic disease and disability. Whereas aging itself is… (more)

Subjects/Keywords: aging; biological aging; healthspan; metabolomics; physiological function; Gerontology; Systems and Integrative Physiology

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APA (6th Edition):

Johnson, L. C. (2018). Aging and the Plasma Metabolome: Relation to Physiological Function. (Doctoral Dissertation). University of Colorado. Retrieved from https://scholar.colorado.edu/iphy_gradetds/85

Chicago Manual of Style (16th Edition):

Johnson, Lawrence Cody. “Aging and the Plasma Metabolome: Relation to Physiological Function.” 2018. Doctoral Dissertation, University of Colorado. Accessed January 26, 2020. https://scholar.colorado.edu/iphy_gradetds/85.

MLA Handbook (7th Edition):

Johnson, Lawrence Cody. “Aging and the Plasma Metabolome: Relation to Physiological Function.” 2018. Web. 26 Jan 2020.

Vancouver:

Johnson LC. Aging and the Plasma Metabolome: Relation to Physiological Function. [Internet] [Doctoral dissertation]. University of Colorado; 2018. [cited 2020 Jan 26]. Available from: https://scholar.colorado.edu/iphy_gradetds/85.

Council of Science Editors:

Johnson LC. Aging and the Plasma Metabolome: Relation to Physiological Function. [Doctoral Dissertation]. University of Colorado; 2018. Available from: https://scholar.colorado.edu/iphy_gradetds/85


University of Colorado

11. Johnson, Lawrence Cody. Aging and the Plasma Metabolome: Relation to Physiological Function.

Degree: PhD, Integrative Physiology, 2017, University of Colorado

  Advancing age is associated with declines across numerous physiological systems, leading to an increased risk of chronic disease and disability. Whereas aging itself is… (more)

Subjects/Keywords: Aging; Biological Aging; Healthspan; Metabolomics; Physiological Function; Biochemical Phenomena, Metabolism, and Nutrition; Gerontology

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APA (6th Edition):

Johnson, L. C. (2017). Aging and the Plasma Metabolome: Relation to Physiological Function. (Doctoral Dissertation). University of Colorado. Retrieved from https://scholar.colorado.edu/iphy_gradetds/60

Chicago Manual of Style (16th Edition):

Johnson, Lawrence Cody. “Aging and the Plasma Metabolome: Relation to Physiological Function.” 2017. Doctoral Dissertation, University of Colorado. Accessed January 26, 2020. https://scholar.colorado.edu/iphy_gradetds/60.

MLA Handbook (7th Edition):

Johnson, Lawrence Cody. “Aging and the Plasma Metabolome: Relation to Physiological Function.” 2017. Web. 26 Jan 2020.

Vancouver:

Johnson LC. Aging and the Plasma Metabolome: Relation to Physiological Function. [Internet] [Doctoral dissertation]. University of Colorado; 2017. [cited 2020 Jan 26]. Available from: https://scholar.colorado.edu/iphy_gradetds/60.

Council of Science Editors:

Johnson LC. Aging and the Plasma Metabolome: Relation to Physiological Function. [Doctoral Dissertation]. University of Colorado; 2017. Available from: https://scholar.colorado.edu/iphy_gradetds/60

12. TESFAHUN DESSALE ADMASU. DRUG SYNERGY, TARGETING EVOLUTIONARY CONSERVED LONGEVITY AND AGING NETWORKS TO EXTEND HEALTHY LIFESPAN.

Degree: 2018, National University of Singapore

Subjects/Keywords: Drug synergy; Transcriptomics; Lipidomics; Healthspan; Aging; Lifespan

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APA (6th Edition):

ADMASU, T. D. (2018). DRUG SYNERGY, TARGETING EVOLUTIONARY CONSERVED LONGEVITY AND AGING NETWORKS TO EXTEND HEALTHY LIFESPAN. (Thesis). National University of Singapore. Retrieved from http://scholarbank.nus.edu.sg/handle/10635/150884

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):

ADMASU, TESFAHUN DESSALE. “DRUG SYNERGY, TARGETING EVOLUTIONARY CONSERVED LONGEVITY AND AGING NETWORKS TO EXTEND HEALTHY LIFESPAN.” 2018. Thesis, National University of Singapore. Accessed January 26, 2020. http://scholarbank.nus.edu.sg/handle/10635/150884.

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

MLA Handbook (7th Edition):

ADMASU, TESFAHUN DESSALE. “DRUG SYNERGY, TARGETING EVOLUTIONARY CONSERVED LONGEVITY AND AGING NETWORKS TO EXTEND HEALTHY LIFESPAN.” 2018. Web. 26 Jan 2020.

Vancouver:

ADMASU TD. DRUG SYNERGY, TARGETING EVOLUTIONARY CONSERVED LONGEVITY AND AGING NETWORKS TO EXTEND HEALTHY LIFESPAN. [Internet] [Thesis]. National University of Singapore; 2018. [cited 2020 Jan 26]. Available from: http://scholarbank.nus.edu.sg/handle/10635/150884.

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

Council of Science Editors:

ADMASU TD. DRUG SYNERGY, TARGETING EVOLUTIONARY CONSERVED LONGEVITY AND AGING NETWORKS TO EXTEND HEALTHY LIFESPAN. [Thesis]. National University of Singapore; 2018. Available from: http://scholarbank.nus.edu.sg/handle/10635/150884

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

13. Berry, Alessandra. Oxidative stress, neuroendocrine function and behavior in an animal model of extended longevity.

Degree: 2010, Department of Neuropharmacology, Faculty of Medicine, Leiden University Medical Center (LUMC), Leiden University

 Stress and oxidative stress (OS) might act synergistically to exacerbate the neuronal decay associated with aging. Recent evidence has shown a redox regulation of the… (more)

Subjects/Keywords: p66Shc; Aging; Hypothalamic-pituitary-adrenal axis (HPA); Mice; Oxidative stress; Behaviour; Animal model; Lifespan; Healthspan; p66Shc; Aging; Hypothalamic-pituitary-adrenal axis (HPA); Mice; Oxidative stress; Behaviour; Animal model; Lifespan; Healthspan

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APA (6th Edition):

Berry, A. (2010). Oxidative stress, neuroendocrine function and behavior in an animal model of extended longevity. (Doctoral Dissertation). Department of Neuropharmacology, Faculty of Medicine, Leiden University Medical Center (LUMC), Leiden University. Retrieved from http://hdl.handle.net/1887/15280

Chicago Manual of Style (16th Edition):

Berry, Alessandra. “Oxidative stress, neuroendocrine function and behavior in an animal model of extended longevity.” 2010. Doctoral Dissertation, Department of Neuropharmacology, Faculty of Medicine, Leiden University Medical Center (LUMC), Leiden University. Accessed January 26, 2020. http://hdl.handle.net/1887/15280.

MLA Handbook (7th Edition):

Berry, Alessandra. “Oxidative stress, neuroendocrine function and behavior in an animal model of extended longevity.” 2010. Web. 26 Jan 2020.

Vancouver:

Berry A. Oxidative stress, neuroendocrine function and behavior in an animal model of extended longevity. [Internet] [Doctoral dissertation]. Department of Neuropharmacology, Faculty of Medicine, Leiden University Medical Center (LUMC), Leiden University; 2010. [cited 2020 Jan 26]. Available from: http://hdl.handle.net/1887/15280.

Council of Science Editors:

Berry A. Oxidative stress, neuroendocrine function and behavior in an animal model of extended longevity. [Doctoral Dissertation]. Department of Neuropharmacology, Faculty of Medicine, Leiden University Medical Center (LUMC), Leiden University; 2010. Available from: http://hdl.handle.net/1887/15280

14. Chao, Elizabeth. Optimizing Pharmacological Lifespan Extension: Testing Chemical Compounds for Additive Effects on Longevity.

Degree: MS, Biological Sciences, 2016, Dominican University of California

No abstract available Advisors/Committee Members: Gordon Lithgow, PhD, Maria Carranza, PhD.

Subjects/Keywords: Caenorhabditis elegans; lifespan; longevity; aging; healthspan; pharmacology; ALS; amyotrophic lateral sclerosis; neurodegenerative disease; Biochemistry, Biophysics, and Structural Biology; Biology; Nutrition; Pharmacology, Toxicology and Environmental Health

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APA (6th Edition):

Chao, E. (2016). Optimizing Pharmacological Lifespan Extension: Testing Chemical Compounds for Additive Effects on Longevity. (Masters Thesis). Dominican University of California. Retrieved from https://scholar.dominican.edu/masters-theses/222

Chicago Manual of Style (16th Edition):

Chao, Elizabeth. “Optimizing Pharmacological Lifespan Extension: Testing Chemical Compounds for Additive Effects on Longevity.” 2016. Masters Thesis, Dominican University of California. Accessed January 26, 2020. https://scholar.dominican.edu/masters-theses/222.

MLA Handbook (7th Edition):

Chao, Elizabeth. “Optimizing Pharmacological Lifespan Extension: Testing Chemical Compounds for Additive Effects on Longevity.” 2016. Web. 26 Jan 2020.

Vancouver:

Chao E. Optimizing Pharmacological Lifespan Extension: Testing Chemical Compounds for Additive Effects on Longevity. [Internet] [Masters thesis]. Dominican University of California; 2016. [cited 2020 Jan 26]. Available from: https://scholar.dominican.edu/masters-theses/222.

Council of Science Editors:

Chao E. Optimizing Pharmacological Lifespan Extension: Testing Chemical Compounds for Additive Effects on Longevity. [Masters Thesis]. Dominican University of California; 2016. Available from: https://scholar.dominican.edu/masters-theses/222

15. Churgin, Matthew Alexander. Longitudinal Studies Of Caenorhabditis Elegans Aging And Behavior Using A Microfabricated Multi-Well Device.

Degree: 2017, University of Pennsylvania

 The roundworm C. elegans is a powerful model organism for dissecting the genetics of behavior and aging. The central genetic pathways regulating lifespan, such as… (more)

Subjects/Keywords: Aging; Behavior; C. elegans; Genetics; Healthspan; Neural circuits; Biomedical; Family, Life Course, and Society; Social and Behavioral Sciences

…2 MEASURING AGING WITH LIFESPAN AND HEALTHSPAN… …Murphy (Murphy 2006). MEASURING AGING WITH LIFESPAN AND HEALTHSPAN A critical… …category of aging measurements is an organism's healthspan, or the amount of life spent in a… …x29;. Like lifespan, healthspan is a single number that defines an aspect of aging, namely… …the span of an individual's health. Healthspan is more difficult to define than… 

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

APA (6th Edition):

Churgin, M. A. (2017). Longitudinal Studies Of Caenorhabditis Elegans Aging And Behavior Using A Microfabricated Multi-Well Device. (Thesis). University of Pennsylvania. Retrieved from https://repository.upenn.edu/edissertations/2230

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):

Churgin, Matthew Alexander. “Longitudinal Studies Of Caenorhabditis Elegans Aging And Behavior Using A Microfabricated Multi-Well Device.” 2017. Thesis, University of Pennsylvania. Accessed January 26, 2020. https://repository.upenn.edu/edissertations/2230.

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

MLA Handbook (7th Edition):

Churgin, Matthew Alexander. “Longitudinal Studies Of Caenorhabditis Elegans Aging And Behavior Using A Microfabricated Multi-Well Device.” 2017. Web. 26 Jan 2020.

Vancouver:

Churgin MA. Longitudinal Studies Of Caenorhabditis Elegans Aging And Behavior Using A Microfabricated Multi-Well Device. [Internet] [Thesis]. University of Pennsylvania; 2017. [cited 2020 Jan 26]. Available from: https://repository.upenn.edu/edissertations/2230.

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

Council of Science Editors:

Churgin MA. Longitudinal Studies Of Caenorhabditis Elegans Aging And Behavior Using A Microfabricated Multi-Well Device. [Thesis]. University of Pennsylvania; 2017. Available from: https://repository.upenn.edu/edissertations/2230

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

16. Zhang, William. Mechanics of Phenotypic Aging Trajectories in C. elegans and Humans.

Degree: PhD, Biology & Biomedical Sciences (Computational & Systems Biology), 2019, Washington University in St. Louis

  Overall, my dissertation integrates longitudinal measurements of physiology to investigate the aging process. In the first half, I examine the surprising and largely unexplained… (more)

Subjects/Keywords: aging, biodemography, Caenorhabditis elegans, healthspan, inter-individual variation, rate of aging; Biostatistics; Family, Life Course, and Society; Gerontology; Physiology

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

APA (6th Edition):

Zhang, W. (2019). Mechanics of Phenotypic Aging Trajectories in C. elegans and Humans. (Doctoral Dissertation). Washington University in St. Louis. Retrieved from https://openscholarship.wustl.edu/art_sci_etds/1821

Chicago Manual of Style (16th Edition):

Zhang, William. “Mechanics of Phenotypic Aging Trajectories in C. elegans and Humans.” 2019. Doctoral Dissertation, Washington University in St. Louis. Accessed January 26, 2020. https://openscholarship.wustl.edu/art_sci_etds/1821.

MLA Handbook (7th Edition):

Zhang, William. “Mechanics of Phenotypic Aging Trajectories in C. elegans and Humans.” 2019. Web. 26 Jan 2020.

Vancouver:

Zhang W. Mechanics of Phenotypic Aging Trajectories in C. elegans and Humans. [Internet] [Doctoral dissertation]. Washington University in St. Louis; 2019. [cited 2020 Jan 26]. Available from: https://openscholarship.wustl.edu/art_sci_etds/1821.

Council of Science Editors:

Zhang W. Mechanics of Phenotypic Aging Trajectories in C. elegans and Humans. [Doctoral Dissertation]. Washington University in St. Louis; 2019. Available from: https://openscholarship.wustl.edu/art_sci_etds/1821

.