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You searched for subject:(paracrine factors). Showing records 1 – 8 of 8 total matches.

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Temple University

1. Duran, Jason Mathew. Bone-derived stem cells repair the heart after myocardial infarction through transdifferentiation and paracrine signaling mechanisms.

Degree: PhD, 2015, Temple University

Physiology

Rationale: Autologous bone marrow- or cardiac-derived stem cell therapy for heart disease has demonstrated safety and efficacy in clinical trials but has only offered… (more)

Subjects/Keywords: Physiology; myocardial infarction; paracrine factors; regeneration; stem cells; transdifferentiation

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APA (6th Edition):

Duran, J. M. (2015). Bone-derived stem cells repair the heart after myocardial infarction through transdifferentiation and paracrine signaling mechanisms. (Doctoral Dissertation). Temple University. Retrieved from http://digital.library.temple.edu/u?/p245801coll10,253042

Chicago Manual of Style (16th Edition):

Duran, Jason Mathew. “Bone-derived stem cells repair the heart after myocardial infarction through transdifferentiation and paracrine signaling mechanisms.” 2015. Doctoral Dissertation, Temple University. Accessed August 12, 2020. http://digital.library.temple.edu/u?/p245801coll10,253042.

MLA Handbook (7th Edition):

Duran, Jason Mathew. “Bone-derived stem cells repair the heart after myocardial infarction through transdifferentiation and paracrine signaling mechanisms.” 2015. Web. 12 Aug 2020.

Vancouver:

Duran JM. Bone-derived stem cells repair the heart after myocardial infarction through transdifferentiation and paracrine signaling mechanisms. [Internet] [Doctoral dissertation]. Temple University; 2015. [cited 2020 Aug 12]. Available from: http://digital.library.temple.edu/u?/p245801coll10,253042.

Council of Science Editors:

Duran JM. Bone-derived stem cells repair the heart after myocardial infarction through transdifferentiation and paracrine signaling mechanisms. [Doctoral Dissertation]. Temple University; 2015. Available from: http://digital.library.temple.edu/u?/p245801coll10,253042


University of Toronto

2. Silberberg, Amanda. Evaluating the Impact of Novel Bone Marrow Cell-secreted Factors, C19orf10 and C1orf54, on Immunomodulation, Lung Cell Proliferation, and Resistance to Injury.

Degree: 2017, University of Toronto

Bone marrow-derived mesenchymal stem cells possess significant immunomodulatory and tissue-reparative capacity, and have been shown to promote recovery from lung injury, predominantly through their secretion… (more)

Subjects/Keywords: Acute lung injury; Bone marrow; Paracrine factors; 0379

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APA (6th Edition):

Silberberg, A. (2017). Evaluating the Impact of Novel Bone Marrow Cell-secreted Factors, C19orf10 and C1orf54, on Immunomodulation, Lung Cell Proliferation, and Resistance to Injury. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/76668

Chicago Manual of Style (16th Edition):

Silberberg, Amanda. “Evaluating the Impact of Novel Bone Marrow Cell-secreted Factors, C19orf10 and C1orf54, on Immunomodulation, Lung Cell Proliferation, and Resistance to Injury.” 2017. Masters Thesis, University of Toronto. Accessed August 12, 2020. http://hdl.handle.net/1807/76668.

MLA Handbook (7th Edition):

Silberberg, Amanda. “Evaluating the Impact of Novel Bone Marrow Cell-secreted Factors, C19orf10 and C1orf54, on Immunomodulation, Lung Cell Proliferation, and Resistance to Injury.” 2017. Web. 12 Aug 2020.

Vancouver:

Silberberg A. Evaluating the Impact of Novel Bone Marrow Cell-secreted Factors, C19orf10 and C1orf54, on Immunomodulation, Lung Cell Proliferation, and Resistance to Injury. [Internet] [Masters thesis]. University of Toronto; 2017. [cited 2020 Aug 12]. Available from: http://hdl.handle.net/1807/76668.

Council of Science Editors:

Silberberg A. Evaluating the Impact of Novel Bone Marrow Cell-secreted Factors, C19orf10 and C1orf54, on Immunomodulation, Lung Cell Proliferation, and Resistance to Injury. [Masters Thesis]. University of Toronto; 2017. Available from: http://hdl.handle.net/1807/76668


Universitat de Valencia

3. López Pérez, Nuria. Identification of Specific Somatic Stem Cell Markers in the Human Endometrium and Mechanisms of the Bone Marrow for Endometrial Regeneration .

Degree: 2018, Universitat de Valencia

 INTRODUCTION The endometrium is a unique tissue with a high reconstitution potential during the menstrual cycle throughout the women’s reproductive life. This high regenerative potential… (more)

Subjects/Keywords: Stem cells; Endometrium; Reproductive medicine; Stem cell markers; Niche; ICAM1; W5C5; Side Population; Paracrine Factors

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APA (6th Edition):

López Pérez, N. (2018). Identification of Specific Somatic Stem Cell Markers in the Human Endometrium and Mechanisms of the Bone Marrow for Endometrial Regeneration . (Doctoral Dissertation). Universitat de Valencia. Retrieved from http://hdl.handle.net/10550/67255

Chicago Manual of Style (16th Edition):

López Pérez, Nuria. “Identification of Specific Somatic Stem Cell Markers in the Human Endometrium and Mechanisms of the Bone Marrow for Endometrial Regeneration .” 2018. Doctoral Dissertation, Universitat de Valencia. Accessed August 12, 2020. http://hdl.handle.net/10550/67255.

MLA Handbook (7th Edition):

López Pérez, Nuria. “Identification of Specific Somatic Stem Cell Markers in the Human Endometrium and Mechanisms of the Bone Marrow for Endometrial Regeneration .” 2018. Web. 12 Aug 2020.

Vancouver:

López Pérez N. Identification of Specific Somatic Stem Cell Markers in the Human Endometrium and Mechanisms of the Bone Marrow for Endometrial Regeneration . [Internet] [Doctoral dissertation]. Universitat de Valencia; 2018. [cited 2020 Aug 12]. Available from: http://hdl.handle.net/10550/67255.

Council of Science Editors:

López Pérez N. Identification of Specific Somatic Stem Cell Markers in the Human Endometrium and Mechanisms of the Bone Marrow for Endometrial Regeneration . [Doctoral Dissertation]. Universitat de Valencia; 2018. Available from: http://hdl.handle.net/10550/67255

4. Vrijsen, K.R. Exosomes in cardiac injury and repair.

Degree: 2013, University Utrecht

 Stem cell therapy has been proposed as a strategy to regenerate the damaged myocardium after myocardial infarction. The differentiation capacity of many different stem cells… (more)

Subjects/Keywords: Regenerative medicine; stem cells; paracrine factors; microvesicles; exosomes; angiogenesis; immune modulation; miRNA-1

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APA (6th Edition):

Vrijsen, K. R. (2013). Exosomes in cardiac injury and repair. (Doctoral Dissertation). University Utrecht. Retrieved from http://dspace.library.uu.nl/handle/1874/274315 ; URN:NBN:NL:UI:10-1874-274315 ; urn:isbn:978-90-8891-601-4 ; URN:NBN:NL:UI:10-1874-274315 ; http://dspace.library.uu.nl/handle/1874/274315

Chicago Manual of Style (16th Edition):

Vrijsen, K R. “Exosomes in cardiac injury and repair.” 2013. Doctoral Dissertation, University Utrecht. Accessed August 12, 2020. http://dspace.library.uu.nl/handle/1874/274315 ; URN:NBN:NL:UI:10-1874-274315 ; urn:isbn:978-90-8891-601-4 ; URN:NBN:NL:UI:10-1874-274315 ; http://dspace.library.uu.nl/handle/1874/274315.

MLA Handbook (7th Edition):

Vrijsen, K R. “Exosomes in cardiac injury and repair.” 2013. Web. 12 Aug 2020.

Vancouver:

Vrijsen KR. Exosomes in cardiac injury and repair. [Internet] [Doctoral dissertation]. University Utrecht; 2013. [cited 2020 Aug 12]. Available from: http://dspace.library.uu.nl/handle/1874/274315 ; URN:NBN:NL:UI:10-1874-274315 ; urn:isbn:978-90-8891-601-4 ; URN:NBN:NL:UI:10-1874-274315 ; http://dspace.library.uu.nl/handle/1874/274315.

Council of Science Editors:

Vrijsen KR. Exosomes in cardiac injury and repair. [Doctoral Dissertation]. University Utrecht; 2013. Available from: http://dspace.library.uu.nl/handle/1874/274315 ; URN:NBN:NL:UI:10-1874-274315 ; urn:isbn:978-90-8891-601-4 ; URN:NBN:NL:UI:10-1874-274315 ; http://dspace.library.uu.nl/handle/1874/274315

5. Vrijsen, K.R. Exosomes in cardiac injury and repair.

Degree: 2013, University Utrecht

 Stem cell therapy has been proposed as a strategy to regenerate the damaged myocardium after myocardial infarction. The differentiation capacity of many different stem cells… (more)

Subjects/Keywords: Regenerative medicine; stem cells; paracrine factors; microvesicles; exosomes; angiogenesis; immune modulation; miRNA-1

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

APA (6th Edition):

Vrijsen, K. R. (2013). Exosomes in cardiac injury and repair. (Doctoral Dissertation). University Utrecht. Retrieved from https://dspace.library.uu.nl/handle/1874/274315 ; URN:NBN:NL:UI:10-1874-274315 ; urn:isbn:978-90-8891-601-4 ; URN:NBN:NL:UI:10-1874-274315 ; https://dspace.library.uu.nl/handle/1874/274315

Chicago Manual of Style (16th Edition):

Vrijsen, K R. “Exosomes in cardiac injury and repair.” 2013. Doctoral Dissertation, University Utrecht. Accessed August 12, 2020. https://dspace.library.uu.nl/handle/1874/274315 ; URN:NBN:NL:UI:10-1874-274315 ; urn:isbn:978-90-8891-601-4 ; URN:NBN:NL:UI:10-1874-274315 ; https://dspace.library.uu.nl/handle/1874/274315.

MLA Handbook (7th Edition):

Vrijsen, K R. “Exosomes in cardiac injury and repair.” 2013. Web. 12 Aug 2020.

Vancouver:

Vrijsen KR. Exosomes in cardiac injury and repair. [Internet] [Doctoral dissertation]. University Utrecht; 2013. [cited 2020 Aug 12]. Available from: https://dspace.library.uu.nl/handle/1874/274315 ; URN:NBN:NL:UI:10-1874-274315 ; urn:isbn:978-90-8891-601-4 ; URN:NBN:NL:UI:10-1874-274315 ; https://dspace.library.uu.nl/handle/1874/274315.

Council of Science Editors:

Vrijsen KR. Exosomes in cardiac injury and repair. [Doctoral Dissertation]. University Utrecht; 2013. Available from: https://dspace.library.uu.nl/handle/1874/274315 ; URN:NBN:NL:UI:10-1874-274315 ; urn:isbn:978-90-8891-601-4 ; URN:NBN:NL:UI:10-1874-274315 ; https://dspace.library.uu.nl/handle/1874/274315


University of Adelaide

6. Robertson, Sarah Anne. Granulocyte-macrophage colony stimulating factor (GM-CSF) : a paracrine regulator in the pre-implantation mouse uterus / Sarah A. Robertson.

Degree: 1993, University of Adelaide

Investigates whether cytokines influence the development of the embryo prior to implantation. Advisors/Committee Members: Dept. of Obstetrics and Gynaecology (school), Dept. of Microbiology and Immunology (school).

Subjects/Keywords: 591/.03/3 20; Granulocyte-macrophage colony-stimulating factor.; Cytokines Pathophysiology.; Growth factors Physiological effect.; Embryology.; Ovum implantation.; Paracrine mechanisms.

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APA (6th Edition):

Robertson, S. A. (1993). Granulocyte-macrophage colony stimulating factor (GM-CSF) : a paracrine regulator in the pre-implantation mouse uterus / Sarah A. Robertson. (Thesis). University of Adelaide. Retrieved from http://hdl.handle.net/2440/20966

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):

Robertson, Sarah Anne. “Granulocyte-macrophage colony stimulating factor (GM-CSF) : a paracrine regulator in the pre-implantation mouse uterus / Sarah A. Robertson.” 1993. Thesis, University of Adelaide. Accessed August 12, 2020. http://hdl.handle.net/2440/20966.

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

MLA Handbook (7th Edition):

Robertson, Sarah Anne. “Granulocyte-macrophage colony stimulating factor (GM-CSF) : a paracrine regulator in the pre-implantation mouse uterus / Sarah A. Robertson.” 1993. Web. 12 Aug 2020.

Vancouver:

Robertson SA. Granulocyte-macrophage colony stimulating factor (GM-CSF) : a paracrine regulator in the pre-implantation mouse uterus / Sarah A. Robertson. [Internet] [Thesis]. University of Adelaide; 1993. [cited 2020 Aug 12]. Available from: http://hdl.handle.net/2440/20966.

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

Council of Science Editors:

Robertson SA. Granulocyte-macrophage colony stimulating factor (GM-CSF) : a paracrine regulator in the pre-implantation mouse uterus / Sarah A. Robertson. [Thesis]. University of Adelaide; 1993. Available from: http://hdl.handle.net/2440/20966

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

7. Lee, Christopher S. D. Directing the paracrine actions of adipose stem cells for cartilage regeneration.

Degree: PhD, Biomedical Engineering, 2012, Georgia Tech

 Current cartilage repair methods are ineffective in restoring the mechanical and biological functions of native hyaline cartilage. Therefore, using the paracrine actions of stem cell… (more)

Subjects/Keywords: Stem cells; Cartilage; Paracrine factors; Connective tissues; Connective tissues Growth; Chondrogenesis

…of ASC Paracrine Signaling and Secreted Factors on Chondrocyte Gene Expression 130 Effect… …cartilage development and may elucidate the paracrine factors needed for cartilage regeneration… …paracrine factors that can promote cartilage regeneration. ASCs produce a wide array of growth… …use stem cell paracrine factors for regenerate cartilage. 7 SIGNALING MOLECUES REGULATING… …Effect of Ascorbic Acid-2-Phodphate, Dexamethasone, and Growth Factors in MSC Growth… 

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APA (6th Edition):

Lee, C. S. D. (2012). Directing the paracrine actions of adipose stem cells for cartilage regeneration. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/44713

Chicago Manual of Style (16th Edition):

Lee, Christopher S D. “Directing the paracrine actions of adipose stem cells for cartilage regeneration.” 2012. Doctoral Dissertation, Georgia Tech. Accessed August 12, 2020. http://hdl.handle.net/1853/44713.

MLA Handbook (7th Edition):

Lee, Christopher S D. “Directing the paracrine actions of adipose stem cells for cartilage regeneration.” 2012. Web. 12 Aug 2020.

Vancouver:

Lee CSD. Directing the paracrine actions of adipose stem cells for cartilage regeneration. [Internet] [Doctoral dissertation]. Georgia Tech; 2012. [cited 2020 Aug 12]. Available from: http://hdl.handle.net/1853/44713.

Council of Science Editors:

Lee CSD. Directing the paracrine actions of adipose stem cells for cartilage regeneration. [Doctoral Dissertation]. Georgia Tech; 2012. Available from: http://hdl.handle.net/1853/44713

8. Karan, Priyanka. Embryonic stem cells alter cardiomyocyte electrophysiological properties.

Degree: MS, Computer Science, 2008, Georgia Tech

 Embryonic stem cells (ESCs) are being considered as a cell source for cardiac regeneration because of their potency and availability. We studied the electrophysiological implications… (more)

Subjects/Keywords: Paracrine factors; Microelectrode arrays; Arrhythmias; Embryonic stem cells; Cardiomyoplasty; Embryonic stem cells; Electrophysiology

…vehicles aimed at modifying the local myocardial environment by secreting paracrine factors.26 8… …myoblast/cardiomyocyte co-cultures may be related to myoblast secreted paracrine factors. More… …ESCs were having direct or paracrine effects on NRVMs. viii Media conditioned by 3x106… …factors secreted by ESCs and resulted, in part, from reduced Na+ channel and Cx43 levels. These… …factors designed to encourage cardiac cell growth and differentiation. The effects of various… 

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APA (6th Edition):

Karan, P. (2008). Embryonic stem cells alter cardiomyocyte electrophysiological properties. (Masters Thesis). Georgia Tech. Retrieved from http://hdl.handle.net/1853/24691

Chicago Manual of Style (16th Edition):

Karan, Priyanka. “Embryonic stem cells alter cardiomyocyte electrophysiological properties.” 2008. Masters Thesis, Georgia Tech. Accessed August 12, 2020. http://hdl.handle.net/1853/24691.

MLA Handbook (7th Edition):

Karan, Priyanka. “Embryonic stem cells alter cardiomyocyte electrophysiological properties.” 2008. Web. 12 Aug 2020.

Vancouver:

Karan P. Embryonic stem cells alter cardiomyocyte electrophysiological properties. [Internet] [Masters thesis]. Georgia Tech; 2008. [cited 2020 Aug 12]. Available from: http://hdl.handle.net/1853/24691.

Council of Science Editors:

Karan P. Embryonic stem cells alter cardiomyocyte electrophysiological properties. [Masters Thesis]. Georgia Tech; 2008. Available from: http://hdl.handle.net/1853/24691

.