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You searched for subject:(Peptide Release). Showing records 1 – 19 of 19 total matches.

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Universiteit Utrecht

1. Shirangi, M. Chemical instability of pharmaceutical peptides in polymeric controlled release systems.

Degree: 2015, Universiteit Utrecht

Peptide and protein drugs are presently an important class of pharmaceuticals due to their favorable properties, i.e. high and selective activity. However, peptides and proteins… (more)

Subjects/Keywords: Peptide; Polyesters; PLGA; acylation; methyleneation; controlled release; polymer; chemical stability; integrity

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APA (6th Edition):

Shirangi, M. (2015). Chemical instability of pharmaceutical peptides in polymeric controlled release systems. (Doctoral Dissertation). Universiteit Utrecht. Retrieved from http://dspace.library.uu.nl:8080/handle/1874/327656

Chicago Manual of Style (16th Edition):

Shirangi, M. “Chemical instability of pharmaceutical peptides in polymeric controlled release systems.” 2015. Doctoral Dissertation, Universiteit Utrecht. Accessed April 13, 2021. http://dspace.library.uu.nl:8080/handle/1874/327656.

MLA Handbook (7th Edition):

Shirangi, M. “Chemical instability of pharmaceutical peptides in polymeric controlled release systems.” 2015. Web. 13 Apr 2021.

Vancouver:

Shirangi M. Chemical instability of pharmaceutical peptides in polymeric controlled release systems. [Internet] [Doctoral dissertation]. Universiteit Utrecht; 2015. [cited 2021 Apr 13]. Available from: http://dspace.library.uu.nl:8080/handle/1874/327656.

Council of Science Editors:

Shirangi M. Chemical instability of pharmaceutical peptides in polymeric controlled release systems. [Doctoral Dissertation]. Universiteit Utrecht; 2015. Available from: http://dspace.library.uu.nl:8080/handle/1874/327656


University of Rochester

2. Van Hove, Amy H. (1987 - ). Enzymatically-responsive poly(ethylene glycol) hydrogels for the controlled delivery of therapeutic peptides.

Degree: PhD, 2015, University of Rochester

 Therapeutic angiogenesis holds great potential for treatment of ischemic tissues and in tissue engineering, where insufficient vascularization limits construct size, complexity, and anastomosis with host… (more)

Subjects/Keywords: Controlled release; Drug delivery; Hydrogel; Peptide; Poly(ethylene glycol); Stimuli-responsive

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APA (6th Edition):

Van Hove, A. H. (. -. ). (2015). Enzymatically-responsive poly(ethylene glycol) hydrogels for the controlled delivery of therapeutic peptides. (Doctoral Dissertation). University of Rochester. Retrieved from http://hdl.handle.net/1802/29655

Chicago Manual of Style (16th Edition):

Van Hove, Amy H (1987 - ). “Enzymatically-responsive poly(ethylene glycol) hydrogels for the controlled delivery of therapeutic peptides.” 2015. Doctoral Dissertation, University of Rochester. Accessed April 13, 2021. http://hdl.handle.net/1802/29655.

MLA Handbook (7th Edition):

Van Hove, Amy H (1987 - ). “Enzymatically-responsive poly(ethylene glycol) hydrogels for the controlled delivery of therapeutic peptides.” 2015. Web. 13 Apr 2021.

Vancouver:

Van Hove AH(-). Enzymatically-responsive poly(ethylene glycol) hydrogels for the controlled delivery of therapeutic peptides. [Internet] [Doctoral dissertation]. University of Rochester; 2015. [cited 2021 Apr 13]. Available from: http://hdl.handle.net/1802/29655.

Council of Science Editors:

Van Hove AH(-). Enzymatically-responsive poly(ethylene glycol) hydrogels for the controlled delivery of therapeutic peptides. [Doctoral Dissertation]. University of Rochester; 2015. Available from: http://hdl.handle.net/1802/29655


Australian National University

3. Bruggeman, Kiara Anaya Fay. Novel Growth Factor Delivery Systems from Self-Assembling Peptide (SAP) Hydrogels .

Degree: 2016, Australian National University

 Growth factors are important signalling molecules in regenerative medicine and tissue engineering, but their inherent instability, lasting only minute to hours in vivo, presents an… (more)

Subjects/Keywords: self-assembling peptide; drug delivery; tissue engineering; regenerative medicine; growth factor; controlled release

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APA (6th Edition):

Bruggeman, K. A. F. (2016). Novel Growth Factor Delivery Systems from Self-Assembling Peptide (SAP) Hydrogels . (Thesis). Australian National University. Retrieved from http://hdl.handle.net/1885/117065

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):

Bruggeman, Kiara Anaya Fay. “Novel Growth Factor Delivery Systems from Self-Assembling Peptide (SAP) Hydrogels .” 2016. Thesis, Australian National University. Accessed April 13, 2021. http://hdl.handle.net/1885/117065.

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

MLA Handbook (7th Edition):

Bruggeman, Kiara Anaya Fay. “Novel Growth Factor Delivery Systems from Self-Assembling Peptide (SAP) Hydrogels .” 2016. Web. 13 Apr 2021.

Vancouver:

Bruggeman KAF. Novel Growth Factor Delivery Systems from Self-Assembling Peptide (SAP) Hydrogels . [Internet] [Thesis]. Australian National University; 2016. [cited 2021 Apr 13]. Available from: http://hdl.handle.net/1885/117065.

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

Council of Science Editors:

Bruggeman KAF. Novel Growth Factor Delivery Systems from Self-Assembling Peptide (SAP) Hydrogels . [Thesis]. Australian National University; 2016. Available from: http://hdl.handle.net/1885/117065

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


University of Adelaide

4. Valizadeh Kiamahalleh, Meisam. Nanoporous layered graphene hydrogel for controlled drug delivery.

Degree: 2015, University of Adelaide

 Graphene-related materials with tuneable pore sizes in the nanoscale range offer the potential to address significant challenges in biomolecule separation, controlled delivery of drugs, selective… (more)

Subjects/Keywords: graphene; peptide; self-assembly; hydrogel; nanoporous; adsorption; drug delivery; controlled release; anticancer; iocompatibility; cytotoxicity

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APA (6th Edition):

Valizadeh Kiamahalleh, M. (2015). Nanoporous layered graphene hydrogel for controlled drug delivery. (Thesis). University of Adelaide. Retrieved from http://hdl.handle.net/2440/106439

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):

Valizadeh Kiamahalleh, Meisam. “Nanoporous layered graphene hydrogel for controlled drug delivery.” 2015. Thesis, University of Adelaide. Accessed April 13, 2021. http://hdl.handle.net/2440/106439.

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

MLA Handbook (7th Edition):

Valizadeh Kiamahalleh, Meisam. “Nanoporous layered graphene hydrogel for controlled drug delivery.” 2015. Web. 13 Apr 2021.

Vancouver:

Valizadeh Kiamahalleh M. Nanoporous layered graphene hydrogel for controlled drug delivery. [Internet] [Thesis]. University of Adelaide; 2015. [cited 2021 Apr 13]. Available from: http://hdl.handle.net/2440/106439.

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

Council of Science Editors:

Valizadeh Kiamahalleh M. Nanoporous layered graphene hydrogel for controlled drug delivery. [Thesis]. University of Adelaide; 2015. Available from: http://hdl.handle.net/2440/106439

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


Duke University

5. Luginbuhl, Kelli Michelle. Recombinantly Engineered Polypeptides for Drug Delivery .

Degree: 2017, Duke University

  Novel drug delivery methods aims to improve the therapeutic efficacy by enhancing the molecule’s pharmacokinetic profile as well as increasing its accumulation at the… (more)

Subjects/Keywords: Biomedical engineering; Materials Science; Controlled release; Drug delivery; Drug depot; Glucagon-like peptide-1

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APA (6th Edition):

Luginbuhl, K. M. (2017). Recombinantly Engineered Polypeptides for Drug Delivery . (Thesis). Duke University. Retrieved from http://hdl.handle.net/10161/16310

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):

Luginbuhl, Kelli Michelle. “Recombinantly Engineered Polypeptides for Drug Delivery .” 2017. Thesis, Duke University. Accessed April 13, 2021. http://hdl.handle.net/10161/16310.

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

MLA Handbook (7th Edition):

Luginbuhl, Kelli Michelle. “Recombinantly Engineered Polypeptides for Drug Delivery .” 2017. Web. 13 Apr 2021.

Vancouver:

Luginbuhl KM. Recombinantly Engineered Polypeptides for Drug Delivery . [Internet] [Thesis]. Duke University; 2017. [cited 2021 Apr 13]. Available from: http://hdl.handle.net/10161/16310.

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

Council of Science Editors:

Luginbuhl KM. Recombinantly Engineered Polypeptides for Drug Delivery . [Thesis]. Duke University; 2017. Available from: http://hdl.handle.net/10161/16310

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

6. Geoghan, Allison F. New chemical linkage systems to address biological problems.

Degree: PhD, Chemistry and Biochemistry, 2018, Georgia Tech

 The research reported in this thesis explored and developed the formation of reversible and irreversible chemical linkages for use in biological systems. Through the synthesis… (more)

Subjects/Keywords: Click chemistry; CuAAC; Peptide; Linkers; Drug release; Antimicrobial; Surface modification; PVC; Medical tubing

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APA (6th Edition):

Geoghan, A. F. (2018). New chemical linkage systems to address biological problems. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/61149

Chicago Manual of Style (16th Edition):

Geoghan, Allison F. “New chemical linkage systems to address biological problems.” 2018. Doctoral Dissertation, Georgia Tech. Accessed April 13, 2021. http://hdl.handle.net/1853/61149.

MLA Handbook (7th Edition):

Geoghan, Allison F. “New chemical linkage systems to address biological problems.” 2018. Web. 13 Apr 2021.

Vancouver:

Geoghan AF. New chemical linkage systems to address biological problems. [Internet] [Doctoral dissertation]. Georgia Tech; 2018. [cited 2021 Apr 13]. Available from: http://hdl.handle.net/1853/61149.

Council of Science Editors:

Geoghan AF. New chemical linkage systems to address biological problems. [Doctoral Dissertation]. Georgia Tech; 2018. Available from: http://hdl.handle.net/1853/61149


University of New South Wales

7. Hassan, Md Musfizur. Controlled drug delivery from self-assembled hydrogels.

Degree: Chemistry, 2017, University of New South Wales

Peptide gelators are useful building blocks for creating diverse self- assembled nanostructures, including novel drug delivery systems. The aim of this Thesis is to understand… (more)

Subjects/Keywords: Elastin; Drug delivery; Anticancer drugs; Cell culture; Macromolecular; Self-assembled hydrogels; Drug release; Peptide

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APA (6th Edition):

Hassan, M. M. (2017). Controlled drug delivery from self-assembled hydrogels. (Doctoral Dissertation). University of New South Wales. Retrieved from http://handle.unsw.edu.au/1959.4/59145 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:48528/SOURCE02?view=true

Chicago Manual of Style (16th Edition):

Hassan, Md Musfizur. “Controlled drug delivery from self-assembled hydrogels.” 2017. Doctoral Dissertation, University of New South Wales. Accessed April 13, 2021. http://handle.unsw.edu.au/1959.4/59145 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:48528/SOURCE02?view=true.

MLA Handbook (7th Edition):

Hassan, Md Musfizur. “Controlled drug delivery from self-assembled hydrogels.” 2017. Web. 13 Apr 2021.

Vancouver:

Hassan MM. Controlled drug delivery from self-assembled hydrogels. [Internet] [Doctoral dissertation]. University of New South Wales; 2017. [cited 2021 Apr 13]. Available from: http://handle.unsw.edu.au/1959.4/59145 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:48528/SOURCE02?view=true.

Council of Science Editors:

Hassan MM. Controlled drug delivery from self-assembled hydrogels. [Doctoral Dissertation]. University of New South Wales; 2017. Available from: http://handle.unsw.edu.au/1959.4/59145 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:48528/SOURCE02?view=true


Virginia Tech

8. Qian, Yun. Self-assembled Peptide Hydrogels for Therapeutic H2S Delivery.

Degree: PhD, Macromolecular Science and Engineering, 2019, Virginia Tech

 Hydrogen sulfide (H2S) is a gasotransmitter that is produced endogenously and freely permeates cell membranes. It plays important roles in many physiological pathways, and by… (more)

Subjects/Keywords: Self-assembled peptide hydrogels; hydrogen sulfide (H2S); controllable release; anti-infection; wound treatment

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APA (6th Edition):

Qian, Y. (2019). Self-assembled Peptide Hydrogels for Therapeutic H2S Delivery. (Doctoral Dissertation). Virginia Tech. Retrieved from http://hdl.handle.net/10919/101094

Chicago Manual of Style (16th Edition):

Qian, Yun. “Self-assembled Peptide Hydrogels for Therapeutic H2S Delivery.” 2019. Doctoral Dissertation, Virginia Tech. Accessed April 13, 2021. http://hdl.handle.net/10919/101094.

MLA Handbook (7th Edition):

Qian, Yun. “Self-assembled Peptide Hydrogels for Therapeutic H2S Delivery.” 2019. Web. 13 Apr 2021.

Vancouver:

Qian Y. Self-assembled Peptide Hydrogels for Therapeutic H2S Delivery. [Internet] [Doctoral dissertation]. Virginia Tech; 2019. [cited 2021 Apr 13]. Available from: http://hdl.handle.net/10919/101094.

Council of Science Editors:

Qian Y. Self-assembled Peptide Hydrogels for Therapeutic H2S Delivery. [Doctoral Dissertation]. Virginia Tech; 2019. Available from: http://hdl.handle.net/10919/101094

9. Barros, Natan Roberto de [UNESP]. Estudo da incorporação e liberação de peptídeos hormonais utilizando membranas de látex natural como carreador.

Degree: 2016, Universidade Estadual Paulista (UNESP)

Submitted by NATAN ROBERTO DE BARROS null ([email protected]) on 2016-03-17T22:54:17Z No. of bitstreams: 1 DISSERTACAO FINAL - NATAN BARROS.pdf: 2287500 bytes, checksum: 5687ecdf1e7aabf2b962b2fed752c410 (MD5)

Approved… (more)

Subjects/Keywords: Látex natural; Peptídeo; Liberação sustentada; Biomaterial; Natural rubber latex; Peptide; Controlled release; Biomaterial

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APA (6th Edition):

Barros, N. R. d. [. (2016). Estudo da incorporação e liberação de peptídeos hormonais utilizando membranas de látex natural como carreador. (Masters Thesis). Universidade Estadual Paulista (UNESP). Retrieved from http://hdl.handle.net/11449/136323

Chicago Manual of Style (16th Edition):

Barros, Natan Roberto de [UNESP]. “Estudo da incorporação e liberação de peptídeos hormonais utilizando membranas de látex natural como carreador.” 2016. Masters Thesis, Universidade Estadual Paulista (UNESP). Accessed April 13, 2021. http://hdl.handle.net/11449/136323.

MLA Handbook (7th Edition):

Barros, Natan Roberto de [UNESP]. “Estudo da incorporação e liberação de peptídeos hormonais utilizando membranas de látex natural como carreador.” 2016. Web. 13 Apr 2021.

Vancouver:

Barros NRd[. Estudo da incorporação e liberação de peptídeos hormonais utilizando membranas de látex natural como carreador. [Internet] [Masters thesis]. Universidade Estadual Paulista (UNESP); 2016. [cited 2021 Apr 13]. Available from: http://hdl.handle.net/11449/136323.

Council of Science Editors:

Barros NRd[. Estudo da incorporação e liberação de peptídeos hormonais utilizando membranas de látex natural como carreador. [Masters Thesis]. Universidade Estadual Paulista (UNESP); 2016. Available from: http://hdl.handle.net/11449/136323


Clemson University

10. Blichmann, Paul. ORAL DELIVERY OF PEPTIDE DRUGS FOR MITIGATION OF CROHN'S DISEASE.

Degree: MS, Bioengineering, 2012, Clemson University

  Protein drugs are typically administered intravenously, but this practice has clear disadvantages such as widespread circulation and swift clearance from the body. Orally delivered… (more)

Subjects/Keywords: colon targeting; controlled release; Inflammatory Bowel Disease; MUC1 targeting; oral drug delivery; peptide drugs; Biomedical Engineering and Bioengineering

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APA (6th Edition):

Blichmann, P. (2012). ORAL DELIVERY OF PEPTIDE DRUGS FOR MITIGATION OF CROHN'S DISEASE. (Masters Thesis). Clemson University. Retrieved from https://tigerprints.clemson.edu/all_theses/1486

Chicago Manual of Style (16th Edition):

Blichmann, Paul. “ORAL DELIVERY OF PEPTIDE DRUGS FOR MITIGATION OF CROHN'S DISEASE.” 2012. Masters Thesis, Clemson University. Accessed April 13, 2021. https://tigerprints.clemson.edu/all_theses/1486.

MLA Handbook (7th Edition):

Blichmann, Paul. “ORAL DELIVERY OF PEPTIDE DRUGS FOR MITIGATION OF CROHN'S DISEASE.” 2012. Web. 13 Apr 2021.

Vancouver:

Blichmann P. ORAL DELIVERY OF PEPTIDE DRUGS FOR MITIGATION OF CROHN'S DISEASE. [Internet] [Masters thesis]. Clemson University; 2012. [cited 2021 Apr 13]. Available from: https://tigerprints.clemson.edu/all_theses/1486.

Council of Science Editors:

Blichmann P. ORAL DELIVERY OF PEPTIDE DRUGS FOR MITIGATION OF CROHN'S DISEASE. [Masters Thesis]. Clemson University; 2012. Available from: https://tigerprints.clemson.edu/all_theses/1486


Duke University

11. Gilroy, Caslin Anne. Controlled Release Systems for Treating Type 2 Diabetes and Their Application Toward Multi-Agonist Combination Therapies .

Degree: 2019, Duke University

  Over 30 million people in the United States suffer from type 2 diabetes (T2D), and this figure is rapidly increasing. Currently available glucose-lowering drugs… (more)

Subjects/Keywords: Biomedical engineering; Endocrinology; Controlled release; Drug delivery; Elastin-like polypeptides; Fibroblast growth factor 21; Glucagon-like peptide-1; Type 2 diabetes

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APA (6th Edition):

Gilroy, C. A. (2019). Controlled Release Systems for Treating Type 2 Diabetes and Their Application Toward Multi-Agonist Combination Therapies . (Thesis). Duke University. Retrieved from http://hdl.handle.net/10161/19873

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):

Gilroy, Caslin Anne. “Controlled Release Systems for Treating Type 2 Diabetes and Their Application Toward Multi-Agonist Combination Therapies .” 2019. Thesis, Duke University. Accessed April 13, 2021. http://hdl.handle.net/10161/19873.

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

MLA Handbook (7th Edition):

Gilroy, Caslin Anne. “Controlled Release Systems for Treating Type 2 Diabetes and Their Application Toward Multi-Agonist Combination Therapies .” 2019. Web. 13 Apr 2021.

Vancouver:

Gilroy CA. Controlled Release Systems for Treating Type 2 Diabetes and Their Application Toward Multi-Agonist Combination Therapies . [Internet] [Thesis]. Duke University; 2019. [cited 2021 Apr 13]. Available from: http://hdl.handle.net/10161/19873.

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

Council of Science Editors:

Gilroy CA. Controlled Release Systems for Treating Type 2 Diabetes and Their Application Toward Multi-Agonist Combination Therapies . [Thesis]. Duke University; 2019. Available from: http://hdl.handle.net/10161/19873

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


University of Illinois – Urbana-Champaign

12. Maki, Agatha. Analyzing peptide release using mass spectrometry.

Degree: PhD, 0323, 2014, University of Illinois – Urbana-Champaign

 Neuropeptides are cell-to-cell signaling molecules that act as neurotransmitters, neuromodulators and hormones that impact a large variety of neuronal processes. The term neuropeptide refers to… (more)

Subjects/Keywords: Peptides; Neuropeptides; Peptide Release; Mass Spectrometry; Fragile X Syndrome; Synaptoneurosomes; Brain Slices; Rab3A; Dense-Core Vesicles; Morphine; In Vivo Microdialysis; Hippocampus; Fibrinogen; Fibrinogen-α Chain Peptides; Fibrinopeptide A.

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APA (6th Edition):

Maki, A. (2014). Analyzing peptide release using mass spectrometry. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/49662

Chicago Manual of Style (16th Edition):

Maki, Agatha. “Analyzing peptide release using mass spectrometry.” 2014. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed April 13, 2021. http://hdl.handle.net/2142/49662.

MLA Handbook (7th Edition):

Maki, Agatha. “Analyzing peptide release using mass spectrometry.” 2014. Web. 13 Apr 2021.

Vancouver:

Maki A. Analyzing peptide release using mass spectrometry. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2014. [cited 2021 Apr 13]. Available from: http://hdl.handle.net/2142/49662.

Council of Science Editors:

Maki A. Analyzing peptide release using mass spectrometry. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2014. Available from: http://hdl.handle.net/2142/49662

13. Shirangi, M. Chemical instability of pharmaceutical peptides in polymeric controlled release systems.

Degree: 2015, University Utrecht

Peptide and protein drugs are presently an important class of pharmaceuticals due to their favorable properties, i.e. high and selective activity. However, peptides and proteins… (more)

Subjects/Keywords: Peptide; Polyesters; PLGA; acylation; methyleneation; controlled release; polymer; chemical stability; integrity

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

APA (6th Edition):

Shirangi, M. (2015). Chemical instability of pharmaceutical peptides in polymeric controlled release systems. (Doctoral Dissertation). University Utrecht. Retrieved from https://dspace.library.uu.nl/handle/1874/327656 ; URN:NBN:NL:UI:10-1874-327656 ; 1874/327656 ; URN:NBN:NL:UI:10-1874-327656 ; https://dspace.library.uu.nl/handle/1874/327656

Chicago Manual of Style (16th Edition):

Shirangi, M. “Chemical instability of pharmaceutical peptides in polymeric controlled release systems.” 2015. Doctoral Dissertation, University Utrecht. Accessed April 13, 2021. https://dspace.library.uu.nl/handle/1874/327656 ; URN:NBN:NL:UI:10-1874-327656 ; 1874/327656 ; URN:NBN:NL:UI:10-1874-327656 ; https://dspace.library.uu.nl/handle/1874/327656.

MLA Handbook (7th Edition):

Shirangi, M. “Chemical instability of pharmaceutical peptides in polymeric controlled release systems.” 2015. Web. 13 Apr 2021.

Vancouver:

Shirangi M. Chemical instability of pharmaceutical peptides in polymeric controlled release systems. [Internet] [Doctoral dissertation]. University Utrecht; 2015. [cited 2021 Apr 13]. Available from: https://dspace.library.uu.nl/handle/1874/327656 ; URN:NBN:NL:UI:10-1874-327656 ; 1874/327656 ; URN:NBN:NL:UI:10-1874-327656 ; https://dspace.library.uu.nl/handle/1874/327656.

Council of Science Editors:

Shirangi M. Chemical instability of pharmaceutical peptides in polymeric controlled release systems. [Doctoral Dissertation]. University Utrecht; 2015. Available from: https://dspace.library.uu.nl/handle/1874/327656 ; URN:NBN:NL:UI:10-1874-327656 ; 1874/327656 ; URN:NBN:NL:UI:10-1874-327656 ; https://dspace.library.uu.nl/handle/1874/327656


Vrije Universiteit Amsterdam

14. Stallmann, H.P. Antimicrobial peptides : Experimental prevention of osteomyelitis .

Degree: 2007, Vrije Universiteit Amsterdam

 The first chapter introduces the main concepts of this manuscript: osteomyelitis (bone infection), bacterial resistance and antimicrobial peptides (AMPs). As part of a solution to… (more)

Subjects/Keywords: Preventie van osteomyelitis met antimicrobieel peptide HLF 1-11; osteomyelitis; infection; resistance; antimicrobial peptide; rabbit; drug release

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APA (6th Edition):

Stallmann, H. P. (2007). Antimicrobial peptides : Experimental prevention of osteomyelitis . (Doctoral Dissertation). Vrije Universiteit Amsterdam. Retrieved from http://hdl.handle.net/1871/11059

Chicago Manual of Style (16th Edition):

Stallmann, H P. “Antimicrobial peptides : Experimental prevention of osteomyelitis .” 2007. Doctoral Dissertation, Vrije Universiteit Amsterdam. Accessed April 13, 2021. http://hdl.handle.net/1871/11059.

MLA Handbook (7th Edition):

Stallmann, H P. “Antimicrobial peptides : Experimental prevention of osteomyelitis .” 2007. Web. 13 Apr 2021.

Vancouver:

Stallmann HP. Antimicrobial peptides : Experimental prevention of osteomyelitis . [Internet] [Doctoral dissertation]. Vrije Universiteit Amsterdam; 2007. [cited 2021 Apr 13]. Available from: http://hdl.handle.net/1871/11059.

Council of Science Editors:

Stallmann HP. Antimicrobial peptides : Experimental prevention of osteomyelitis . [Doctoral Dissertation]. Vrije Universiteit Amsterdam; 2007. Available from: http://hdl.handle.net/1871/11059

15. Arnal Pastor, María Pilar. New scaffolding materials for the regeneration of infarcted myocardium .

Degree: 2015, Universitat Politècnica de València

 There is growing interest in the development of biomimetic matrices that are simultaneously cell-friendly, allow rapid vascularization, exhibit enough mechanical integrity to be comfortably handled… (more)

Subjects/Keywords: Scaffold; hyaluronic acid/Hyaluronan; poly(ethyl acrylate); self-assembling peptide gel; controlled release; cell seeding

…composite material would also be useful as a controlled release system because of the gel’s… …peptide, RAD16-I. HA is ubiquitously present in the body and its degradation products have been… …release device was based on the possibility of incorporating active soluble molecules in the… …hydrogel within the pores. A release study of bovine serum albumin (BSA), intended as a… …release drugs or are biodegradable or not, etc. [27, 30]. 29F These therapies restore… 

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

APA (6th Edition):

Arnal Pastor, M. P. (2015). New scaffolding materials for the regeneration of infarcted myocardium . (Doctoral Dissertation). Universitat Politècnica de València. Retrieved from http://hdl.handle.net/10251/46129

Chicago Manual of Style (16th Edition):

Arnal Pastor, María Pilar. “New scaffolding materials for the regeneration of infarcted myocardium .” 2015. Doctoral Dissertation, Universitat Politècnica de València. Accessed April 13, 2021. http://hdl.handle.net/10251/46129.

MLA Handbook (7th Edition):

Arnal Pastor, María Pilar. “New scaffolding materials for the regeneration of infarcted myocardium .” 2015. Web. 13 Apr 2021.

Vancouver:

Arnal Pastor MP. New scaffolding materials for the regeneration of infarcted myocardium . [Internet] [Doctoral dissertation]. Universitat Politècnica de València; 2015. [cited 2021 Apr 13]. Available from: http://hdl.handle.net/10251/46129.

Council of Science Editors:

Arnal Pastor MP. New scaffolding materials for the regeneration of infarcted myocardium . [Doctoral Dissertation]. Universitat Politècnica de València; 2015. Available from: http://hdl.handle.net/10251/46129


University of Queensland

16. Varasteh Moradi, Shayli. Improving the bioavailability and stability of luteinizing hormone-releasing hormone (LHRH) analogues.

Degree: School of Chemistry and Molecular Biosciences, 2015, University of Queensland

Subjects/Keywords: LHRH; Glycosylation; Peptide; Oral delivery; Prostate cancer; Glucose transporters; Efflux pump systems; Bioavailability; LH and FSH release; 0304 Medicinal and Biomolecular Chemistry; 1115 Pharmacology and Pharmaceutical Sciences

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

APA (6th Edition):

Varasteh Moradi, S. (2015). Improving the bioavailability and stability of luteinizing hormone-releasing hormone (LHRH) analogues. (Thesis). University of Queensland. Retrieved from http://espace.library.uq.edu.au/view/UQ:370230

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):

Varasteh Moradi, Shayli. “Improving the bioavailability and stability of luteinizing hormone-releasing hormone (LHRH) analogues.” 2015. Thesis, University of Queensland. Accessed April 13, 2021. http://espace.library.uq.edu.au/view/UQ:370230.

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

MLA Handbook (7th Edition):

Varasteh Moradi, Shayli. “Improving the bioavailability and stability of luteinizing hormone-releasing hormone (LHRH) analogues.” 2015. Web. 13 Apr 2021.

Vancouver:

Varasteh Moradi S. Improving the bioavailability and stability of luteinizing hormone-releasing hormone (LHRH) analogues. [Internet] [Thesis]. University of Queensland; 2015. [cited 2021 Apr 13]. Available from: http://espace.library.uq.edu.au/view/UQ:370230.

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

Council of Science Editors:

Varasteh Moradi S. Improving the bioavailability and stability of luteinizing hormone-releasing hormone (LHRH) analogues. [Thesis]. University of Queensland; 2015. Available from: http://espace.library.uq.edu.au/view/UQ:370230

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


University of Vienna

17. Juère, Estelle. Confinement of therapeutic agents into mesoporous silica nanoparticles for oral delivery applications.

Degree: 2020, University of Vienna

Unter den verschiedenen Wegen der Arzneimittelverabreichung bleibt der orale Weg für die Patienten der beliebteste auch wenn er aus pharmazeutischer Sicht recht her-ausfordernd ist. Die… (more)

Subjects/Keywords: 35.40 Anorganische Chemie: Allgemeines; 35.76 Aminosäuren, Peptide, Eiweiße; 42.15 Zellbiologie; 35.23 Analytische Chemie: Allgemeines; Dendritische mesoporöse Silica-Nanopartikel / Succinyliertes beta-Lactoglobulin / pH-abhängige Tabletten / Insulinfreisetzung / In vitro-Zytotoxizität / in vitro Stoffwechselaktivität; Dendritic mesoporous silica nanoparticles / Succinylated beta-lactoglobulin / pH-responsive tablets / Insulin release / In vitro mitochondrial activity / In vitro cytotoxicity

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

APA (6th Edition):

Juère, E. (2020). Confinement of therapeutic agents into mesoporous silica nanoparticles for oral delivery applications. (Thesis). University of Vienna. Retrieved from http://othes.univie.ac.at/63668/

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):

Juère, Estelle. “Confinement of therapeutic agents into mesoporous silica nanoparticles for oral delivery applications.” 2020. Thesis, University of Vienna. Accessed April 13, 2021. http://othes.univie.ac.at/63668/.

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

MLA Handbook (7th Edition):

Juère, Estelle. “Confinement of therapeutic agents into mesoporous silica nanoparticles for oral delivery applications.” 2020. Web. 13 Apr 2021.

Vancouver:

Juère E. Confinement of therapeutic agents into mesoporous silica nanoparticles for oral delivery applications. [Internet] [Thesis]. University of Vienna; 2020. [cited 2021 Apr 13]. Available from: http://othes.univie.ac.at/63668/.

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

Council of Science Editors:

Juère E. Confinement of therapeutic agents into mesoporous silica nanoparticles for oral delivery applications. [Thesis]. University of Vienna; 2020. Available from: http://othes.univie.ac.at/63668/

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

18. Wielen, van der, N. Intestinal nutrient sensing : a gut feeling for food.

Degree: 2016, Wageningen University

  The alarming increase in obesity rates creates an urgent need for effective prevention and treatment strategies. The most effective treatment for obesity today is… (more)

Subjects/Keywords: obesitas; hormonen; darmen; maagdarmhormonen; pancreozymine; vasoactief intestinaal peptide; aftasten; in vivo experimenten; diermodellen; in vitro; buik bypass; voedsel; gewichtsvermindering; stevia rebaudiana; vrijgeven; Voedingsfysiologie van de mens; obesity; hormones; intestines; gastrointestinal hormones; pancreozymin; vasoactive intestinal peptide; sensing; in vivo experimentation; animal models; in vitro; gastric bypass; food; weight reduction; stevia rebaudiana; release; Human Nutrition Physiology

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

APA (6th Edition):

Wielen, van der, N. (2016). Intestinal nutrient sensing : a gut feeling for food. (Doctoral Dissertation). Wageningen University. Retrieved from http://library.wur.nl/WebQuery/wurpubs/499589 ; urn:nbn:nl:ui:32-499589 ; urn:nbn:nl:ui:32-499589 ; http://library.wur.nl/WebQuery/wurpubs/499589

Chicago Manual of Style (16th Edition):

Wielen, van der, N. “Intestinal nutrient sensing : a gut feeling for food.” 2016. Doctoral Dissertation, Wageningen University. Accessed April 13, 2021. http://library.wur.nl/WebQuery/wurpubs/499589 ; urn:nbn:nl:ui:32-499589 ; urn:nbn:nl:ui:32-499589 ; http://library.wur.nl/WebQuery/wurpubs/499589.

MLA Handbook (7th Edition):

Wielen, van der, N. “Intestinal nutrient sensing : a gut feeling for food.” 2016. Web. 13 Apr 2021.

Vancouver:

Wielen, van der N. Intestinal nutrient sensing : a gut feeling for food. [Internet] [Doctoral dissertation]. Wageningen University; 2016. [cited 2021 Apr 13]. Available from: http://library.wur.nl/WebQuery/wurpubs/499589 ; urn:nbn:nl:ui:32-499589 ; urn:nbn:nl:ui:32-499589 ; http://library.wur.nl/WebQuery/wurpubs/499589.

Council of Science Editors:

Wielen, van der N. Intestinal nutrient sensing : a gut feeling for food. [Doctoral Dissertation]. Wageningen University; 2016. Available from: http://library.wur.nl/WebQuery/wurpubs/499589 ; urn:nbn:nl:ui:32-499589 ; urn:nbn:nl:ui:32-499589 ; http://library.wur.nl/WebQuery/wurpubs/499589

19. Zhao, Ruogang. The Development and Application of Tools to Study the Multiscale Biomechanics of the Aortic Valve.

Degree: 2012, University of Toronto

Calcific aortic valve disease (CAVD) is one of the most common causes of cardiovascular disease in North America. Mechanical factors have been closely linked to… (more)

Subjects/Keywords: biomechanics; aortic valve; valve interstitial cell; viscoelastic material property; micropipette aspiration; valve tissue mechanics; fibrosa and ventricularis; finite element model; digital image correlation; texture correlation; intracellular strain transfer; apoptosis and anoikis; hyperelastic material; RGD peptide; tension-release; loss of adhesion; valve calcification; multilayer tissue; gelatin gel; inverse finite element method; cell stretching; exponential strain energy function; 0541

…100 6.2.2 VIC tension release experiment… …105 6.2.5 Strain measurement under tension release… …mechanical tension release system ....................... 113 Figure 6-3 Tension-release system… …focal adhesions (a, c) before and (b, d) after tension release. Scale bar… …before and (b) after tension release… 

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

APA (6th Edition):

Zhao, R. (2012). The Development and Application of Tools to Study the Multiscale Biomechanics of the Aortic Valve. (Doctoral Dissertation). University of Toronto. Retrieved from http://hdl.handle.net/1807/33866

Chicago Manual of Style (16th Edition):

Zhao, Ruogang. “The Development and Application of Tools to Study the Multiscale Biomechanics of the Aortic Valve.” 2012. Doctoral Dissertation, University of Toronto. Accessed April 13, 2021. http://hdl.handle.net/1807/33866.

MLA Handbook (7th Edition):

Zhao, Ruogang. “The Development and Application of Tools to Study the Multiscale Biomechanics of the Aortic Valve.” 2012. Web. 13 Apr 2021.

Vancouver:

Zhao R. The Development and Application of Tools to Study the Multiscale Biomechanics of the Aortic Valve. [Internet] [Doctoral dissertation]. University of Toronto; 2012. [cited 2021 Apr 13]. Available from: http://hdl.handle.net/1807/33866.

Council of Science Editors:

Zhao R. The Development and Application of Tools to Study the Multiscale Biomechanics of the Aortic Valve. [Doctoral Dissertation]. University of Toronto; 2012. Available from: http://hdl.handle.net/1807/33866

.