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You searched for subject:(Native Chemical Ligation). Showing records 1 – 26 of 26 total matches.

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University of Sydney

1. Malins, Lara. Development and utility of novel peptide ligation methodologies .

Degree: 2013, University of Sydney

 The chemical synthesis of homogeneous peptides and proteins is crucial for application in detailed biological studies and the development of novel therapeutics. This thesis describes… (more)

Subjects/Keywords: Peptide ligation; Native chemical ligation

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

APA (6th Edition):

Malins, L. (2013). Development and utility of novel peptide ligation methodologies . (Thesis). University of Sydney. Retrieved from http://hdl.handle.net/2123/10442

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):

Malins, Lara. “Development and utility of novel peptide ligation methodologies .” 2013. Thesis, University of Sydney. Accessed June 16, 2019. http://hdl.handle.net/2123/10442.

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

MLA Handbook (7th Edition):

Malins, Lara. “Development and utility of novel peptide ligation methodologies .” 2013. Web. 16 Jun 2019.

Vancouver:

Malins L. Development and utility of novel peptide ligation methodologies . [Internet] [Thesis]. University of Sydney; 2013. [cited 2019 Jun 16]. Available from: http://hdl.handle.net/2123/10442.

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

Council of Science Editors:

Malins L. Development and utility of novel peptide ligation methodologies . [Thesis]. University of Sydney; 2013. Available from: http://hdl.handle.net/2123/10442

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


University of Vienna

2. Schrems, Maximilian. Synthesis of new generation PEGylated ligation auxiliaries for glycopeptide preparation.

Degree: 2017, University of Vienna

Die inhärente chemische Komplexität der Kohlenhydrate in Kombination mit aufwendigen zellulären Synthesewegen erlaubt bis dato lediglich ein eingeschränktes Verständnis der Funktion von Proteinglykosylierungen und bremst… (more)

Subjects/Keywords: 35.76 Aminosäuren, Peptide, Eiweiße; Ligationsauxiliar / Glykopeptid / Glykosylierung / PEG / lichtspaltbar / native chemische Ligation; ligation auxiliary / glycopeptide / glycosylation / PEG / photocleavable / native chemical ligation

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APA (6th Edition):

Schrems, M. (2017). Synthesis of new generation PEGylated ligation auxiliaries for glycopeptide preparation. (Thesis). University of Vienna. Retrieved from http://othes.univie.ac.at/48121/

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):

Schrems, Maximilian. “Synthesis of new generation PEGylated ligation auxiliaries for glycopeptide preparation.” 2017. Thesis, University of Vienna. Accessed June 16, 2019. http://othes.univie.ac.at/48121/.

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

MLA Handbook (7th Edition):

Schrems, Maximilian. “Synthesis of new generation PEGylated ligation auxiliaries for glycopeptide preparation.” 2017. Web. 16 Jun 2019.

Vancouver:

Schrems M. Synthesis of new generation PEGylated ligation auxiliaries for glycopeptide preparation. [Internet] [Thesis]. University of Vienna; 2017. [cited 2019 Jun 16]. Available from: http://othes.univie.ac.at/48121/.

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

Council of Science Editors:

Schrems M. Synthesis of new generation PEGylated ligation auxiliaries for glycopeptide preparation. [Thesis]. University of Vienna; 2017. Available from: http://othes.univie.ac.at/48121/

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


University of Washington

3. Weller, Caroline Elise. Development of auxiliary-mediated protein semisynthesis methods toward the study of histone SUMOylation.

Degree: PhD, 2017, University of Washington

 Eukaryotic DNA is packaged into chromatin, which consists of a fundamental repeating unit, the nucleosome, and its associated proteins. Nucleosomes are made up of histone… (more)

Subjects/Keywords: CoREST; HDAC1; ligation auxiliary; Native chemical ligation; SUMO; Ubiquitin; Biochemistry; Chemistry; Chemistry

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APA (6th Edition):

Weller, C. E. (2017). Development of auxiliary-mediated protein semisynthesis methods toward the study of histone SUMOylation. (Doctoral Dissertation). University of Washington. Retrieved from http://hdl.handle.net/1773/40520

Chicago Manual of Style (16th Edition):

Weller, Caroline Elise. “Development of auxiliary-mediated protein semisynthesis methods toward the study of histone SUMOylation.” 2017. Doctoral Dissertation, University of Washington. Accessed June 16, 2019. http://hdl.handle.net/1773/40520.

MLA Handbook (7th Edition):

Weller, Caroline Elise. “Development of auxiliary-mediated protein semisynthesis methods toward the study of histone SUMOylation.” 2017. Web. 16 Jun 2019.

Vancouver:

Weller CE. Development of auxiliary-mediated protein semisynthesis methods toward the study of histone SUMOylation. [Internet] [Doctoral dissertation]. University of Washington; 2017. [cited 2019 Jun 16]. Available from: http://hdl.handle.net/1773/40520.

Council of Science Editors:

Weller CE. Development of auxiliary-mediated protein semisynthesis methods toward the study of histone SUMOylation. [Doctoral Dissertation]. University of Washington; 2017. Available from: http://hdl.handle.net/1773/40520

4. Casas Mora, Alba. A catch-and-release purification method to simplify the synthesis of cysteine-rich peptides : Développement d’une méthode de purification non-chromatographique de peptides riches en cystéine par immobilisation temporaire.

Degree: Docteur es, Chimie, 2017, Université d'Orléans

Bien que la synthèse peptidique en phase solide (SPPS) soit maintenant une technique mature et très largement popularisée pour des peptides simples, certaines séquences restent… (more)

Subjects/Keywords: Synthèse peptidique; Ligation chimique native; Peptides riches en cystéines; Ligation chimique en phase solide; Synthetic methods; Native chemical ligation; Cysteine-rich peptides; Solid supported ligation; 547.7

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APA (6th Edition):

Casas Mora, A. (2017). A catch-and-release purification method to simplify the synthesis of cysteine-rich peptides : Développement d’une méthode de purification non-chromatographique de peptides riches en cystéine par immobilisation temporaire. (Doctoral Dissertation). Université d'Orléans. Retrieved from http://www.theses.fr/2017ORLE2050

Chicago Manual of Style (16th Edition):

Casas Mora, Alba. “A catch-and-release purification method to simplify the synthesis of cysteine-rich peptides : Développement d’une méthode de purification non-chromatographique de peptides riches en cystéine par immobilisation temporaire.” 2017. Doctoral Dissertation, Université d'Orléans. Accessed June 16, 2019. http://www.theses.fr/2017ORLE2050.

MLA Handbook (7th Edition):

Casas Mora, Alba. “A catch-and-release purification method to simplify the synthesis of cysteine-rich peptides : Développement d’une méthode de purification non-chromatographique de peptides riches en cystéine par immobilisation temporaire.” 2017. Web. 16 Jun 2019.

Vancouver:

Casas Mora A. A catch-and-release purification method to simplify the synthesis of cysteine-rich peptides : Développement d’une méthode de purification non-chromatographique de peptides riches en cystéine par immobilisation temporaire. [Internet] [Doctoral dissertation]. Université d'Orléans; 2017. [cited 2019 Jun 16]. Available from: http://www.theses.fr/2017ORLE2050.

Council of Science Editors:

Casas Mora A. A catch-and-release purification method to simplify the synthesis of cysteine-rich peptides : Développement d’une méthode de purification non-chromatographique de peptides riches en cystéine par immobilisation temporaire. [Doctoral Dissertation]. Université d'Orléans; 2017. Available from: http://www.theses.fr/2017ORLE2050

5. Garavini, Valentina. Native chemical ligation for the design of dynamic covalent peptides : Ligation chimique native réversible pour la conception de peptides covalents dynamiques.

Degree: Docteur es, Chimie, 2015, Université de Strasbourg

Utiliser la liaison peptidique dans des systèmes dynamiques covalents est très difficile en raison de sa stabilité intrinsèque. Dans ce travail, une nouvelle méthodologie pour… (more)

Subjects/Keywords: Peptides; Chimie combinatoire dynamique; Liaison réversible; Ligation chimique native; Peptides; Dynamic combinatorial chemistry; Reversible bond; Native chemical ligation; 547.7

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APA (6th Edition):

Garavini, V. (2015). Native chemical ligation for the design of dynamic covalent peptides : Ligation chimique native réversible pour la conception de peptides covalents dynamiques. (Doctoral Dissertation). Université de Strasbourg. Retrieved from http://www.theses.fr/2015STRAF053

Chicago Manual of Style (16th Edition):

Garavini, Valentina. “Native chemical ligation for the design of dynamic covalent peptides : Ligation chimique native réversible pour la conception de peptides covalents dynamiques.” 2015. Doctoral Dissertation, Université de Strasbourg. Accessed June 16, 2019. http://www.theses.fr/2015STRAF053.

MLA Handbook (7th Edition):

Garavini, Valentina. “Native chemical ligation for the design of dynamic covalent peptides : Ligation chimique native réversible pour la conception de peptides covalents dynamiques.” 2015. Web. 16 Jun 2019.

Vancouver:

Garavini V. Native chemical ligation for the design of dynamic covalent peptides : Ligation chimique native réversible pour la conception de peptides covalents dynamiques. [Internet] [Doctoral dissertation]. Université de Strasbourg; 2015. [cited 2019 Jun 16]. Available from: http://www.theses.fr/2015STRAF053.

Council of Science Editors:

Garavini V. Native chemical ligation for the design of dynamic covalent peptides : Ligation chimique native réversible pour la conception de peptides covalents dynamiques. [Doctoral Dissertation]. Université de Strasbourg; 2015. Available from: http://www.theses.fr/2015STRAF053


Texas A&M University

6. Ma, Zhen. Physicochemical Characterization of the Bacterial Cu(I) Sensor CsoR.

Degree: 2011, Texas A&M University

 M. tuberculosis copper-sensitive operon repressor (Mtb CsoR) is the founding member of a new metalloregulatory protein family in prokaryotes that regulates the transcription of the… (more)

Subjects/Keywords: CsoR; Cu(I) sensor; allosteric regulation; native chemical ligation

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APA (6th Edition):

Ma, Z. (2011). Physicochemical Characterization of the Bacterial Cu(I) Sensor CsoR. (Thesis). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/ETD-TAMU-2009-12-7351

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):

Ma, Zhen. “Physicochemical Characterization of the Bacterial Cu(I) Sensor CsoR.” 2011. Thesis, Texas A&M University. Accessed June 16, 2019. http://hdl.handle.net/1969.1/ETD-TAMU-2009-12-7351.

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

MLA Handbook (7th Edition):

Ma, Zhen. “Physicochemical Characterization of the Bacterial Cu(I) Sensor CsoR.” 2011. Web. 16 Jun 2019.

Vancouver:

Ma Z. Physicochemical Characterization of the Bacterial Cu(I) Sensor CsoR. [Internet] [Thesis]. Texas A&M University; 2011. [cited 2019 Jun 16]. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-2009-12-7351.

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

Council of Science Editors:

Ma Z. Physicochemical Characterization of the Bacterial Cu(I) Sensor CsoR. [Thesis]. Texas A&M University; 2011. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-2009-12-7351

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


University of Hawaii – Manoa

7. Thapa, Parashar. Peptide Toxin Bioengineering: Exploring the Potential of Cyclized Conotoxins as Oral Drugs, Fluorescent Probes and Phyla - Selective Peptides.

Degree: 2017, University of Hawaii – Manoa

Ph.D. University of Hawaii at Manoa 2015.

Studies into N- to C-terminal cyclic peptide backbone structures have provided for the lateral transition of important principles… (more)

Subjects/Keywords: Peptides; Conotoxins; Native Chemical Ligation; Cyclization; Trifluoromethanesulfonic Acid; Huwentoxin and Bioengineering

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APA (6th Edition):

Thapa, P. (2017). Peptide Toxin Bioengineering: Exploring the Potential of Cyclized Conotoxins as Oral Drugs, Fluorescent Probes and Phyla - Selective Peptides. (Thesis). University of Hawaii – Manoa. Retrieved from http://hdl.handle.net/10125/51234

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):

Thapa, Parashar. “Peptide Toxin Bioengineering: Exploring the Potential of Cyclized Conotoxins as Oral Drugs, Fluorescent Probes and Phyla - Selective Peptides.” 2017. Thesis, University of Hawaii – Manoa. Accessed June 16, 2019. http://hdl.handle.net/10125/51234.

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

MLA Handbook (7th Edition):

Thapa, Parashar. “Peptide Toxin Bioengineering: Exploring the Potential of Cyclized Conotoxins as Oral Drugs, Fluorescent Probes and Phyla - Selective Peptides.” 2017. Web. 16 Jun 2019.

Vancouver:

Thapa P. Peptide Toxin Bioengineering: Exploring the Potential of Cyclized Conotoxins as Oral Drugs, Fluorescent Probes and Phyla - Selective Peptides. [Internet] [Thesis]. University of Hawaii – Manoa; 2017. [cited 2019 Jun 16]. Available from: http://hdl.handle.net/10125/51234.

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

Council of Science Editors:

Thapa P. Peptide Toxin Bioengineering: Exploring the Potential of Cyclized Conotoxins as Oral Drugs, Fluorescent Probes and Phyla - Selective Peptides. [Thesis]. University of Hawaii – Manoa; 2017. Available from: http://hdl.handle.net/10125/51234

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


Queensland University of Technology

8. Fernandes, Wren Austin. Synthesis of an erodible biomimetic hydrogel for drug delivery using native chemical ligation.

Degree: 2012, Queensland University of Technology

 Hydrogels are hydrophilic, three dimensional polymers that imbibe large quantities of water while remaining insoluble in aqueous solutions due to chemical or physical cross-linking. The… (more)

Subjects/Keywords: hydrogel; biomimetic; polyethylene glycol; native chemical ligation; controlled drug delivery

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APA (6th Edition):

Fernandes, W. A. (2012). Synthesis of an erodible biomimetic hydrogel for drug delivery using native chemical ligation. (Thesis). Queensland University of Technology. Retrieved from https://eprints.qut.edu.au/59502/

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):

Fernandes, Wren Austin. “Synthesis of an erodible biomimetic hydrogel for drug delivery using native chemical ligation.” 2012. Thesis, Queensland University of Technology. Accessed June 16, 2019. https://eprints.qut.edu.au/59502/.

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

MLA Handbook (7th Edition):

Fernandes, Wren Austin. “Synthesis of an erodible biomimetic hydrogel for drug delivery using native chemical ligation.” 2012. Web. 16 Jun 2019.

Vancouver:

Fernandes WA. Synthesis of an erodible biomimetic hydrogel for drug delivery using native chemical ligation. [Internet] [Thesis]. Queensland University of Technology; 2012. [cited 2019 Jun 16]. Available from: https://eprints.qut.edu.au/59502/.

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

Council of Science Editors:

Fernandes WA. Synthesis of an erodible biomimetic hydrogel for drug delivery using native chemical ligation. [Thesis]. Queensland University of Technology; 2012. Available from: https://eprints.qut.edu.au/59502/

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


NSYSU

9. Huang, Kai-jin. Synthesis of Linear and Cyclic Oligopeptides via Histidine-Promoted Native Peptide Ligation.

Degree: Master, Chemistry, 2017, NSYSU

 In recent years, it has been found that the histidine-containing peptide sequence has a very good effect on the chelation of cupric ion. It has… (more)

Subjects/Keywords: acyl transfer catalyst; Cupric ion chelating; histidine; peptides; acyl migration; native chemical ligation

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APA (6th Edition):

Huang, K. (2017). Synthesis of Linear and Cyclic Oligopeptides via Histidine-Promoted Native Peptide Ligation. (Thesis). NSYSU. Retrieved from http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0708117-122112

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):

Huang, Kai-jin. “Synthesis of Linear and Cyclic Oligopeptides via Histidine-Promoted Native Peptide Ligation.” 2017. Thesis, NSYSU. Accessed June 16, 2019. http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0708117-122112.

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

MLA Handbook (7th Edition):

Huang, Kai-jin. “Synthesis of Linear and Cyclic Oligopeptides via Histidine-Promoted Native Peptide Ligation.” 2017. Web. 16 Jun 2019.

Vancouver:

Huang K. Synthesis of Linear and Cyclic Oligopeptides via Histidine-Promoted Native Peptide Ligation. [Internet] [Thesis]. NSYSU; 2017. [cited 2019 Jun 16]. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0708117-122112.

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

Council of Science Editors:

Huang K. Synthesis of Linear and Cyclic Oligopeptides via Histidine-Promoted Native Peptide Ligation. [Thesis]. NSYSU; 2017. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0708117-122112

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


NSYSU

10. Liao, Jia-Shiang. Chemical ligation at methionine via acyl transfer of homocysteine thiolactone.

Degree: Master, Chemistry, 2016, NSYSU

 Peptide synthesis had been developed for more than 30 years. For the moment, there have been many methods for peptide synthesis. During the development of… (more)

Subjects/Keywords: acyl transfer; peptide synthesis; ring-opening reaction; peptide coupling; native chemical ligation

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APA (6th Edition):

Liao, J. (2016). Chemical ligation at methionine via acyl transfer of homocysteine thiolactone. (Thesis). NSYSU. Retrieved from http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0708116-113037

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):

Liao, Jia-Shiang. “Chemical ligation at methionine via acyl transfer of homocysteine thiolactone.” 2016. Thesis, NSYSU. Accessed June 16, 2019. http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0708116-113037.

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

MLA Handbook (7th Edition):

Liao, Jia-Shiang. “Chemical ligation at methionine via acyl transfer of homocysteine thiolactone.” 2016. Web. 16 Jun 2019.

Vancouver:

Liao J. Chemical ligation at methionine via acyl transfer of homocysteine thiolactone. [Internet] [Thesis]. NSYSU; 2016. [cited 2019 Jun 16]. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0708116-113037.

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

Council of Science Editors:

Liao J. Chemical ligation at methionine via acyl transfer of homocysteine thiolactone. [Thesis]. NSYSU; 2016. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0708116-113037

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


University of Manchester

11. Weissenborn, Martin. Development and application of peptide- and glycoarrays.

Degree: PhD, 2012, University of Manchester

 Microarrays enable high throughput analysis with minute amounts of analyte. They are widely used in the ’omics’ fields both as diagnostic and analytical tools. Their… (more)

Subjects/Keywords: 547; Glycoarray; Peptidearray; Native Chemical Ligation; non conductive; aluminium foil; MALDI on glass

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APA (6th Edition):

Weissenborn, M. (2012). Development and application of peptide- and glycoarrays. (Doctoral Dissertation). University of Manchester. Retrieved from https://www.research.manchester.ac.uk/portal/en/theses/development-and-application-of-peptide-and-glycoarrays(dfe37ee9-85be-4751-b491-de7b1eb759f2).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.566539

Chicago Manual of Style (16th Edition):

Weissenborn, Martin. “Development and application of peptide- and glycoarrays.” 2012. Doctoral Dissertation, University of Manchester. Accessed June 16, 2019. https://www.research.manchester.ac.uk/portal/en/theses/development-and-application-of-peptide-and-glycoarrays(dfe37ee9-85be-4751-b491-de7b1eb759f2).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.566539.

MLA Handbook (7th Edition):

Weissenborn, Martin. “Development and application of peptide- and glycoarrays.” 2012. Web. 16 Jun 2019.

Vancouver:

Weissenborn M. Development and application of peptide- and glycoarrays. [Internet] [Doctoral dissertation]. University of Manchester; 2012. [cited 2019 Jun 16]. Available from: https://www.research.manchester.ac.uk/portal/en/theses/development-and-application-of-peptide-and-glycoarrays(dfe37ee9-85be-4751-b491-de7b1eb759f2).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.566539.

Council of Science Editors:

Weissenborn M. Development and application of peptide- and glycoarrays. [Doctoral Dissertation]. University of Manchester; 2012. Available from: https://www.research.manchester.ac.uk/portal/en/theses/development-and-application-of-peptide-and-glycoarrays(dfe37ee9-85be-4751-b491-de7b1eb759f2).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.566539


University of Manchester

12. Camarillo Lopez, Raul Horacio. Applying Native Chemical Ligation to the Development of Magnetically-responsive Drug Delivery Platforms for Biomedical Applications.

Degree: 2017, University of Manchester

 The potential of magnetic nanoparticle-vesicle assemblies (MNP-V) as remote controlled drug delivery platforms capable of inducing cellular responses under magnetic stimuli has been previously demonstrated… (more)

Subjects/Keywords: Native Chemical Ligation; Magnetic Nanoparticles; Drug Delivery Systems; Nanotechnology; Thiol-thioester exchange

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APA (6th Edition):

Camarillo Lopez, R. H. (2017). Applying Native Chemical Ligation to the Development of Magnetically-responsive Drug Delivery Platforms for Biomedical Applications. (Doctoral Dissertation). University of Manchester. Retrieved from http://www.manchester.ac.uk/escholar/uk-ac-man-scw:307668

Chicago Manual of Style (16th Edition):

Camarillo Lopez, Raul Horacio. “Applying Native Chemical Ligation to the Development of Magnetically-responsive Drug Delivery Platforms for Biomedical Applications.” 2017. Doctoral Dissertation, University of Manchester. Accessed June 16, 2019. http://www.manchester.ac.uk/escholar/uk-ac-man-scw:307668.

MLA Handbook (7th Edition):

Camarillo Lopez, Raul Horacio. “Applying Native Chemical Ligation to the Development of Magnetically-responsive Drug Delivery Platforms for Biomedical Applications.” 2017. Web. 16 Jun 2019.

Vancouver:

Camarillo Lopez RH. Applying Native Chemical Ligation to the Development of Magnetically-responsive Drug Delivery Platforms for Biomedical Applications. [Internet] [Doctoral dissertation]. University of Manchester; 2017. [cited 2019 Jun 16]. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:307668.

Council of Science Editors:

Camarillo Lopez RH. Applying Native Chemical Ligation to the Development of Magnetically-responsive Drug Delivery Platforms for Biomedical Applications. [Doctoral Dissertation]. University of Manchester; 2017. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:307668

13. Cargoët, Marine. Nouvelles méthodologies pour la synthèse totale de protéines : New methodologies for total protein synthesis.

Degree: Docteur es, Chimie organique, 2017, Université Lille II – Droit et Santé

Les protéines jouent un rôle essentiel dans le fonctionnement des organismes vivants et sont au cœur de nombreux mécanismes biologiques. La synthèse totale chimique des… (more)

Subjects/Keywords: Ligation SEA; Synthèse en phase solide; Ligations chimiques natives; Biosynthèse des protéines; Catalyseurs; Granulysine; Sélénoester; Synthesis of proteins; Native Chemical Ligation; SEA ligation

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APA (6th Edition):

Cargoët, M. (2017). Nouvelles méthodologies pour la synthèse totale de protéines : New methodologies for total protein synthesis. (Doctoral Dissertation). Université Lille II – Droit et Santé. Retrieved from http://www.theses.fr/2017LIL2S025

Chicago Manual of Style (16th Edition):

Cargoët, Marine. “Nouvelles méthodologies pour la synthèse totale de protéines : New methodologies for total protein synthesis.” 2017. Doctoral Dissertation, Université Lille II – Droit et Santé. Accessed June 16, 2019. http://www.theses.fr/2017LIL2S025.

MLA Handbook (7th Edition):

Cargoët, Marine. “Nouvelles méthodologies pour la synthèse totale de protéines : New methodologies for total protein synthesis.” 2017. Web. 16 Jun 2019.

Vancouver:

Cargoët M. Nouvelles méthodologies pour la synthèse totale de protéines : New methodologies for total protein synthesis. [Internet] [Doctoral dissertation]. Université Lille II – Droit et Santé 2017. [cited 2019 Jun 16]. Available from: http://www.theses.fr/2017LIL2S025.

Council of Science Editors:

Cargoët M. Nouvelles méthodologies pour la synthèse totale de protéines : New methodologies for total protein synthesis. [Doctoral Dissertation]. Université Lille II – Droit et Santé 2017. Available from: http://www.theses.fr/2017LIL2S025

14. Amoura, Mehdi. Conception et étude de nouveaux peptides vecteurs cycliques : Design and study of new cyclic cell-penetrating peptides.

Degree: Docteur es, Chimie, 2015, Université Pierre et Marie Curie – Paris VI

Les peptides vecteurs ou CPP sont de petits peptides, en général de taille inférieure à 30 acides aminés. Parmi les nombreux CPP décrits dans la… (more)

Subjects/Keywords: Peptides vecteurs (CPP); Lipopeptides; Ligation chimique native; Peptides thioester; Alpha-méthyle cystéine; Spectrométrie de masse MALDI-TOF; Cell-penetrating peptides (CPPs); Native chemical ligation; MALDI-TOF mass spectrometry; 572.65

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APA (6th Edition):

Amoura, M. (2015). Conception et étude de nouveaux peptides vecteurs cycliques : Design and study of new cyclic cell-penetrating peptides. (Doctoral Dissertation). Université Pierre et Marie Curie – Paris VI. Retrieved from http://www.theses.fr/2015PA066635

Chicago Manual of Style (16th Edition):

Amoura, Mehdi. “Conception et étude de nouveaux peptides vecteurs cycliques : Design and study of new cyclic cell-penetrating peptides.” 2015. Doctoral Dissertation, Université Pierre et Marie Curie – Paris VI. Accessed June 16, 2019. http://www.theses.fr/2015PA066635.

MLA Handbook (7th Edition):

Amoura, Mehdi. “Conception et étude de nouveaux peptides vecteurs cycliques : Design and study of new cyclic cell-penetrating peptides.” 2015. Web. 16 Jun 2019.

Vancouver:

Amoura M. Conception et étude de nouveaux peptides vecteurs cycliques : Design and study of new cyclic cell-penetrating peptides. [Internet] [Doctoral dissertation]. Université Pierre et Marie Curie – Paris VI; 2015. [cited 2019 Jun 16]. Available from: http://www.theses.fr/2015PA066635.

Council of Science Editors:

Amoura M. Conception et étude de nouveaux peptides vecteurs cycliques : Design and study of new cyclic cell-penetrating peptides. [Doctoral Dissertation]. Université Pierre et Marie Curie – Paris VI; 2015. Available from: http://www.theses.fr/2015PA066635


University of Florida

15. Kayaleh, Roger. A novel approach to the synthesis of biologically active peptides.

Degree: 2014, University of Florida

 Tryptophan plays a significant role in a living organism. Tryptophan and its derivatives are involved in the formation of peptides, regulation of the immune system,… (more)

Subjects/Keywords: Amino acids; Chemicals; Cyclic amino acids; Hydrochlorides; Ions; Ligation; Microwaves; Molecules; Neutral amino acids; Proteins; Long Range Acyl Migration; N-acyl Migration; Native Chemical Ligation; Organic Synthesis; Tryptophan

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APA (6th Edition):

Kayaleh, R. (2014). A novel approach to the synthesis of biologically active peptides. (Thesis). University of Florida. Retrieved from http://ufdc.ufl.edu/AA00027020

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):

Kayaleh, Roger. “A novel approach to the synthesis of biologically active peptides.” 2014. Thesis, University of Florida. Accessed June 16, 2019. http://ufdc.ufl.edu/AA00027020.

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

MLA Handbook (7th Edition):

Kayaleh, Roger. “A novel approach to the synthesis of biologically active peptides.” 2014. Web. 16 Jun 2019.

Vancouver:

Kayaleh R. A novel approach to the synthesis of biologically active peptides. [Internet] [Thesis]. University of Florida; 2014. [cited 2019 Jun 16]. Available from: http://ufdc.ufl.edu/AA00027020.

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

Council of Science Editors:

Kayaleh R. A novel approach to the synthesis of biologically active peptides. [Thesis]. University of Florida; 2014. Available from: http://ufdc.ufl.edu/AA00027020

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

16. 粟飯原, 圭佑. Synthetic studies of cyclic/stapled peptides for potential cancer therapeutic agents : 創薬展開を指向した環状・架橋ペプチドの合成研究.

Degree: 博士(薬科学), 2017, Tokushima University / 徳島大学

Subjects/Keywords: cyclic peptide; stapled peptide; native chemical ligation; olefin metathesis

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APA (6th Edition):

粟飯原, . (2017). Synthetic studies of cyclic/stapled peptides for potential cancer therapeutic agents : 創薬展開を指向した環状・架橋ペプチドの合成研究. (Thesis). Tokushima University / 徳島大学. Retrieved from http://repo.lib.tokushima-u.ac.jp/110128

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):

粟飯原, 圭佑. “Synthetic studies of cyclic/stapled peptides for potential cancer therapeutic agents : 創薬展開を指向した環状・架橋ペプチドの合成研究.” 2017. Thesis, Tokushima University / 徳島大学. Accessed June 16, 2019. http://repo.lib.tokushima-u.ac.jp/110128.

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

MLA Handbook (7th Edition):

粟飯原, 圭佑. “Synthetic studies of cyclic/stapled peptides for potential cancer therapeutic agents : 創薬展開を指向した環状・架橋ペプチドの合成研究.” 2017. Web. 16 Jun 2019.

Vancouver:

粟飯原 . Synthetic studies of cyclic/stapled peptides for potential cancer therapeutic agents : 創薬展開を指向した環状・架橋ペプチドの合成研究. [Internet] [Thesis]. Tokushima University / 徳島大学; 2017. [cited 2019 Jun 16]. Available from: http://repo.lib.tokushima-u.ac.jp/110128.

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

Council of Science Editors:

粟飯原 . Synthetic studies of cyclic/stapled peptides for potential cancer therapeutic agents : 創薬展開を指向した環状・架橋ペプチドの合成研究. [Thesis]. Tokushima University / 徳島大学; 2017. Available from: http://repo.lib.tokushima-u.ac.jp/110128

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

17. Tsuda, Shugo. Development of synthetic procedures using novel thioester derivatives for chemical synthesis of proteins : タンパク質の化学合成を目指した新規チオエステル誘導体の開発研究.

Degree: 博士(薬科学), 2016, Tokushima University / 徳島大学

Subjects/Keywords: peptide synthesis; native chemical ligation; cysteine; peptide thioester; thiol-additive

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APA (6th Edition):

Tsuda, S. (2016). Development of synthetic procedures using novel thioester derivatives for chemical synthesis of proteins : タンパク質の化学合成を目指した新規チオエステル誘導体の開発研究. (Thesis). Tokushima University / 徳島大学. Retrieved from http://repo.lib.tokushima-u.ac.jp/109895

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):

Tsuda, Shugo. “Development of synthetic procedures using novel thioester derivatives for chemical synthesis of proteins : タンパク質の化学合成を目指した新規チオエステル誘導体の開発研究.” 2016. Thesis, Tokushima University / 徳島大学. Accessed June 16, 2019. http://repo.lib.tokushima-u.ac.jp/109895.

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

MLA Handbook (7th Edition):

Tsuda, Shugo. “Development of synthetic procedures using novel thioester derivatives for chemical synthesis of proteins : タンパク質の化学合成を目指した新規チオエステル誘導体の開発研究.” 2016. Web. 16 Jun 2019.

Vancouver:

Tsuda S. Development of synthetic procedures using novel thioester derivatives for chemical synthesis of proteins : タンパク質の化学合成を目指した新規チオエステル誘導体の開発研究. [Internet] [Thesis]. Tokushima University / 徳島大学; 2016. [cited 2019 Jun 16]. Available from: http://repo.lib.tokushima-u.ac.jp/109895.

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

Council of Science Editors:

Tsuda S. Development of synthetic procedures using novel thioester derivatives for chemical synthesis of proteins : タンパク質の化学合成を目指した新規チオエステル誘導体の開発研究. [Thesis]. Tokushima University / 徳島大学; 2016. Available from: http://repo.lib.tokushima-u.ac.jp/109895

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


The Ohio State University

18. Li, Xin. Development and Application of Chemical and Structural Biology Approaches to Probe Protein Function.

Degree: PhD, Biophysics, 2011, The Ohio State University

  My research in The Ohio State University is focused on the development and application of structural and chemical biology approaches to probe protein function.… (more)

Subjects/Keywords: Biochemistry; Biophysics; membrane protein; crystallography; Rh protein; Rhesus; channel; CO2; ammonium; carbonic anhydrase; pyrrolysine; nonnatural amino acid; genetic code expansion; intein; click chemistry; ubiquitin; ubiquitination; native chemical ligation; semisynthesis

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APA (6th Edition):

Li, X. (2011). Development and Application of Chemical and Structural Biology Approaches to Probe Protein Function. (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1306439016

Chicago Manual of Style (16th Edition):

Li, Xin. “Development and Application of Chemical and Structural Biology Approaches to Probe Protein Function.” 2011. Doctoral Dissertation, The Ohio State University. Accessed June 16, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=osu1306439016.

MLA Handbook (7th Edition):

Li, Xin. “Development and Application of Chemical and Structural Biology Approaches to Probe Protein Function.” 2011. Web. 16 Jun 2019.

Vancouver:

Li X. Development and Application of Chemical and Structural Biology Approaches to Probe Protein Function. [Internet] [Doctoral dissertation]. The Ohio State University; 2011. [cited 2019 Jun 16]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1306439016.

Council of Science Editors:

Li X. Development and Application of Chemical and Structural Biology Approaches to Probe Protein Function. [Doctoral Dissertation]. The Ohio State University; 2011. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1306439016

19. YEO SU-YIN, DAWN. Intein-mediated generation of N-terminal cysteine proteins and their applications in live cell bioimaging and protein microarray.

Degree: 2004, National University of Singapore

Subjects/Keywords: Inteins; Native chemical ligation; In vivo protein labeling; Protein microarray; Bioimaging; Fluorescence

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APA (6th Edition):

YEO SU-YIN, D. (2004). Intein-mediated generation of N-terminal cysteine proteins and their applications in live cell bioimaging and protein microarray. (Thesis). National University of Singapore. Retrieved from http://scholarbank.nus.edu.sg/handle/10635/14338

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):

YEO SU-YIN, DAWN. “Intein-mediated generation of N-terminal cysteine proteins and their applications in live cell bioimaging and protein microarray.” 2004. Thesis, National University of Singapore. Accessed June 16, 2019. http://scholarbank.nus.edu.sg/handle/10635/14338.

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

MLA Handbook (7th Edition):

YEO SU-YIN, DAWN. “Intein-mediated generation of N-terminal cysteine proteins and their applications in live cell bioimaging and protein microarray.” 2004. Web. 16 Jun 2019.

Vancouver:

YEO SU-YIN D. Intein-mediated generation of N-terminal cysteine proteins and their applications in live cell bioimaging and protein microarray. [Internet] [Thesis]. National University of Singapore; 2004. [cited 2019 Jun 16]. Available from: http://scholarbank.nus.edu.sg/handle/10635/14338.

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

Council of Science Editors:

YEO SU-YIN D. Intein-mediated generation of N-terminal cysteine proteins and their applications in live cell bioimaging and protein microarray. [Thesis]. National University of Singapore; 2004. Available from: http://scholarbank.nus.edu.sg/handle/10635/14338

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


EPFL

20. Hejjaoui, Mirva. Elucidating the role of post-translational modifications of alpha-synuclein using semisynthesis: phosphorylation at Tyrosine 125 and monoubiquitination at Lysine 6.

Degree: 2012, EPFL

 Alpha-synuclein (α-syn) is a natively unfolded protein that is closely linked to Parkinson’s disease (PD) by genetic, neuropathologic and biochemical evidence. Aggregated and fibrillar forms… (more)

Subjects/Keywords: Parkinson’s disease (PD); alphα-synuclein (α-syn); Lewy Bodies (LB); Aggregation; Amyloid; Oligomers; Dopamine (DA); Solid-phase peptide synthesis (SPPS); Native Chemical Ligation (NCL); Expressed Protein Ligation (EPL); Intein; Circular Dichroism (CD); Nuclear Magnetic Resonance (NMR); Transmission Electron Microscopy (TEM); Microinjection; Immunocytochemistry; Fluorescent Microscopy; Nanobodies; Isothermal Titration Calorimetry (ITC)

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APA (6th Edition):

Hejjaoui, M. (2012). Elucidating the role of post-translational modifications of alpha-synuclein using semisynthesis: phosphorylation at Tyrosine 125 and monoubiquitination at Lysine 6. (Thesis). EPFL. Retrieved from http://infoscience.epfl.ch/record/181225

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):

Hejjaoui, Mirva. “Elucidating the role of post-translational modifications of alpha-synuclein using semisynthesis: phosphorylation at Tyrosine 125 and monoubiquitination at Lysine 6.” 2012. Thesis, EPFL. Accessed June 16, 2019. http://infoscience.epfl.ch/record/181225.

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

MLA Handbook (7th Edition):

Hejjaoui, Mirva. “Elucidating the role of post-translational modifications of alpha-synuclein using semisynthesis: phosphorylation at Tyrosine 125 and monoubiquitination at Lysine 6.” 2012. Web. 16 Jun 2019.

Vancouver:

Hejjaoui M. Elucidating the role of post-translational modifications of alpha-synuclein using semisynthesis: phosphorylation at Tyrosine 125 and monoubiquitination at Lysine 6. [Internet] [Thesis]. EPFL; 2012. [cited 2019 Jun 16]. Available from: http://infoscience.epfl.ch/record/181225.

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

Council of Science Editors:

Hejjaoui M. Elucidating the role of post-translational modifications of alpha-synuclein using semisynthesis: phosphorylation at Tyrosine 125 and monoubiquitination at Lysine 6. [Thesis]. EPFL; 2012. Available from: http://infoscience.epfl.ch/record/181225

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

21. Shimko, John C. Synthetic Tools for the Preparation of Modified Histones.

Degree: PhD, Biochemistry Program, Ohio State, 2011, The Ohio State University

  The eukaryotic genome is organized into nucleosomes consisting of 146 bp of DNA wrapped around an octamer of histone proteins, two copies each of… (more)

Subjects/Keywords: Biochemistry; histone; post-translational modification; peptide synthesis; native chemical ligation; total synthesis

…9 Peptide Synthesis and Native Chemical Ligation… …9 Figure 5. Native chemical ligation scheme… …size of the synthetic unit. Native chemical ligation (NCL) is the chemoselective… …biological relevant species. Figure 5. Native chemical ligation scheme 14 EPL has been of… …mercaptophenylacetic acid MS Mass spectrometry Nbz N-acyl-benzimidazolinone xxi NCL Native chemical… 

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APA (6th Edition):

Shimko, J. C. (2011). Synthetic Tools for the Preparation of Modified Histones. (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1322664987

Chicago Manual of Style (16th Edition):

Shimko, John C. “Synthetic Tools for the Preparation of Modified Histones.” 2011. Doctoral Dissertation, The Ohio State University. Accessed June 16, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=osu1322664987.

MLA Handbook (7th Edition):

Shimko, John C. “Synthetic Tools for the Preparation of Modified Histones.” 2011. Web. 16 Jun 2019.

Vancouver:

Shimko JC. Synthetic Tools for the Preparation of Modified Histones. [Internet] [Doctoral dissertation]. The Ohio State University; 2011. [cited 2019 Jun 16]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1322664987.

Council of Science Editors:

Shimko JC. Synthetic Tools for the Preparation of Modified Histones. [Doctoral Dissertation]. The Ohio State University; 2011. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1322664987

22. Γούλας, Σπυρίδων. Μεθοδολογία σύνθεσης πρωτεϊνών: σύνθεση ιρουδίνης.

Degree: 2003, University of Patras; Πανεπιστήμιο Πατρών

The number of peptides and small proteins that is used as pharmaceutical products has increased in the last years. These peptides were produced with techniques… (more)

Subjects/Keywords: Σύνθεση πρωτεϊνών; Τμηματική συμπύκνωση; Ορθογωνική σύνδεση μέσω θειοεστέρα; Protein synthesis; Fragment condensation; Native chemical ligation

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APA (6th Edition):

Γούλας, . . (2003). Μεθοδολογία σύνθεσης πρωτεϊνών: σύνθεση ιρουδίνης. (Thesis). University of Patras; Πανεπιστήμιο Πατρών. Retrieved from http://hdl.handle.net/10442/hedi/14228

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):

Γούλας, Σπυρίδων. “Μεθοδολογία σύνθεσης πρωτεϊνών: σύνθεση ιρουδίνης.” 2003. Thesis, University of Patras; Πανεπιστήμιο Πατρών. Accessed June 16, 2019. http://hdl.handle.net/10442/hedi/14228.

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

MLA Handbook (7th Edition):

Γούλας, Σπυρίδων. “Μεθοδολογία σύνθεσης πρωτεϊνών: σύνθεση ιρουδίνης.” 2003. Web. 16 Jun 2019.

Vancouver:

Γούλας . Μεθοδολογία σύνθεσης πρωτεϊνών: σύνθεση ιρουδίνης. [Internet] [Thesis]. University of Patras; Πανεπιστήμιο Πατρών; 2003. [cited 2019 Jun 16]. Available from: http://hdl.handle.net/10442/hedi/14228.

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

Council of Science Editors:

Γούλας . Μεθοδολογία σύνθεσης πρωτεϊνών: σύνθεση ιρουδίνης. [Thesis]. University of Patras; Πανεπιστήμιο Πατρών; 2003. Available from: http://hdl.handle.net/10442/hedi/14228

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

23. Sinha, Divya. Investigating higher-order chromatin structure and SAGA cooperativity using existing and modified in vitro chromatin systems.

Degree: 2013, Iowa State University

 The organization of genomic DNA with histones and other proteins ensures the proper storage, utilization and segregation of DNA's encoded information in a healthy eukaryotic… (more)

Subjects/Keywords: chromatin system; higher-order chromatin structure; native chemical ligation; Nucleosome; Biochemistry; Molecular Biology

…templates for nucleosome assembly and have improved our native chemical ligation technique for… …x28;2004) Creating designer histones by native chemical ligation. Methods in enzymology 375… …native peptide ligation strategy for deciphering nucleosomal histone modifications. The Journal… …histones generated by the modified histone ligation method were successfully used for the study… …identification of the hereditary units as genes and their chemical nature that of DNA (1)… 

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APA (6th Edition):

Sinha, D. (2013). Investigating higher-order chromatin structure and SAGA cooperativity using existing and modified in vitro chromatin systems. (Thesis). Iowa State University. Retrieved from https://lib.dr.iastate.edu/etd/13455

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):

Sinha, Divya. “Investigating higher-order chromatin structure and SAGA cooperativity using existing and modified in vitro chromatin systems.” 2013. Thesis, Iowa State University. Accessed June 16, 2019. https://lib.dr.iastate.edu/etd/13455.

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

MLA Handbook (7th Edition):

Sinha, Divya. “Investigating higher-order chromatin structure and SAGA cooperativity using existing and modified in vitro chromatin systems.” 2013. Web. 16 Jun 2019.

Vancouver:

Sinha D. Investigating higher-order chromatin structure and SAGA cooperativity using existing and modified in vitro chromatin systems. [Internet] [Thesis]. Iowa State University; 2013. [cited 2019 Jun 16]. Available from: https://lib.dr.iastate.edu/etd/13455.

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

Council of Science Editors:

Sinha D. Investigating higher-order chromatin structure and SAGA cooperativity using existing and modified in vitro chromatin systems. [Thesis]. Iowa State University; 2013. Available from: https://lib.dr.iastate.edu/etd/13455

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

24. Jung, Jangwook Philip. Engineering Modular Self-Assembling Biomaterials for Multifunctionality.

Degree: PhD, Engineering and Applied Science: Biomedical Engineering, 2010, University of Cincinnati

 The objective of this thesis was to design self-assembling biomaterials whose physical and biological properties can be systematically adjusted to modulate cell growth and differentiation.… (more)

Subjects/Keywords: Biomedical Research; modular biomaterials; ECM; self-assembly; Design of Experiments; native chemical ligation; nitric oxide

…describes the covalent crosslinking via native chemical ligation to increase the stiffness of self… …x28;4sulfophenyl)-2H-tetrazolium NCL: native chemical ligation NO: nitric oxide NOS: nitric oxide… …mechanics via chemoselective ligation..34 2.6.3 Release of a soluble factor, nitric oxide… …replicate the complexity and functionality of native BMs, requiring the development of new… …crosslinking functional groups in order to utilize a chemoselective ligation approach for modulating… 

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APA (6th Edition):

Jung, J. P. (2010). Engineering Modular Self-Assembling Biomaterials for Multifunctionality. (Doctoral Dissertation). University of Cincinnati. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=ucin1291150805

Chicago Manual of Style (16th Edition):

Jung, Jangwook Philip. “Engineering Modular Self-Assembling Biomaterials for Multifunctionality.” 2010. Doctoral Dissertation, University of Cincinnati. Accessed June 16, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1291150805.

MLA Handbook (7th Edition):

Jung, Jangwook Philip. “Engineering Modular Self-Assembling Biomaterials for Multifunctionality.” 2010. Web. 16 Jun 2019.

Vancouver:

Jung JP. Engineering Modular Self-Assembling Biomaterials for Multifunctionality. [Internet] [Doctoral dissertation]. University of Cincinnati; 2010. [cited 2019 Jun 16]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ucin1291150805.

Council of Science Editors:

Jung JP. Engineering Modular Self-Assembling Biomaterials for Multifunctionality. [Doctoral Dissertation]. University of Cincinnati; 2010. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ucin1291150805

25. Weissenborn, Martin. DEVELOPMENT AND APPLICATION OF PEPTIDE- AND GLYCOARRAYS.

Degree: 2012, University of Manchester

 Microarrays enable high throughput analysis with minute amounts of analyte. They arewidely used in the ’omics’ fields both as diagnostic and analytical tools. Their abilityto… (more)

Subjects/Keywords: Glycoarray; Peptidearray; Native Chemical Ligation; non conductive; aluminium foil; MALDI on glass

…solely with synthetic ligands. A modified native chemical ligation (NCL) strategy, in… …native chemical ligation. 47 Maleimides are used to covalently link thiols to the SAM and… …SOLID-SUPPORT This invited review for Chemical Society Reviews is ready for submission… …[email protected] ‡ These authors contributed equally to this work that chemical and… …stereoselective and can catalyse reactions under mild biocompatible conditions. Solid-phase chemical… 

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

APA (6th Edition):

Weissenborn, M. (2012). DEVELOPMENT AND APPLICATION OF PEPTIDE- AND GLYCOARRAYS. (Doctoral Dissertation). University of Manchester. Retrieved from http://www.manchester.ac.uk/escholar/uk-ac-man-scw:182989

Chicago Manual of Style (16th Edition):

Weissenborn, Martin. “DEVELOPMENT AND APPLICATION OF PEPTIDE- AND GLYCOARRAYS.” 2012. Doctoral Dissertation, University of Manchester. Accessed June 16, 2019. http://www.manchester.ac.uk/escholar/uk-ac-man-scw:182989.

MLA Handbook (7th Edition):

Weissenborn, Martin. “DEVELOPMENT AND APPLICATION OF PEPTIDE- AND GLYCOARRAYS.” 2012. Web. 16 Jun 2019.

Vancouver:

Weissenborn M. DEVELOPMENT AND APPLICATION OF PEPTIDE- AND GLYCOARRAYS. [Internet] [Doctoral dissertation]. University of Manchester; 2012. [cited 2019 Jun 16]. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:182989.

Council of Science Editors:

Weissenborn M. DEVELOPMENT AND APPLICATION OF PEPTIDE- AND GLYCOARRAYS. [Doctoral Dissertation]. University of Manchester; 2012. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:182989

26. Camarillo López, Raúl Horacio. Applying native chemical ligation to the development of magnetically-responsive drug delivery platforms for biomedical applications.

Degree: PhD, 2017, University of Manchester

 The potential of magnetic nanoparticle-vesicle assemblies (MNP-V) as remote controlled drug delivery platforms capable of inducing cellular responses under magnetic stimuli has been previously demonstrated… (more)

Subjects/Keywords: 547; Thiol-thioester exchange; Nanotechnology; Native Chemical Ligation; Magnetic Nanoparticles; Drug Delivery Systems

…MRI magnetic resonance imaging 11 MS mass spectrometry NCL native chemical ligation… …Aldrich) 13 Applying Native Chemical Ligation to the development of… …exploration of the potential of thiol-thioester exchange reactions (leading to native chemical… …Figure 4.4 Chemical structure of Rh-DHPE. 137 Figure 4.5 Fluorescence micrographs of MNP-Vs… …ligation, NCL) to create magnetoresponsive materials, which potentially have applications in… 

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

APA (6th Edition):

Camarillo López, R. H. (2017). Applying native chemical ligation to the development of magnetically-responsive drug delivery platforms for biomedical applications. (Doctoral Dissertation). University of Manchester. Retrieved from https://www.research.manchester.ac.uk/portal/en/theses/applying-native-chemical-ligation-to-the-development-of-magneticallyresponsive-drug-delivery-platforms-for-biomedical-applications(fb997ce4-c359-4d3a-8ddc-170c4efb1c53).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.728218

Chicago Manual of Style (16th Edition):

Camarillo López, Raúl Horacio. “Applying native chemical ligation to the development of magnetically-responsive drug delivery platforms for biomedical applications.” 2017. Doctoral Dissertation, University of Manchester. Accessed June 16, 2019. https://www.research.manchester.ac.uk/portal/en/theses/applying-native-chemical-ligation-to-the-development-of-magneticallyresponsive-drug-delivery-platforms-for-biomedical-applications(fb997ce4-c359-4d3a-8ddc-170c4efb1c53).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.728218.

MLA Handbook (7th Edition):

Camarillo López, Raúl Horacio. “Applying native chemical ligation to the development of magnetically-responsive drug delivery platforms for biomedical applications.” 2017. Web. 16 Jun 2019.

Vancouver:

Camarillo López RH. Applying native chemical ligation to the development of magnetically-responsive drug delivery platforms for biomedical applications. [Internet] [Doctoral dissertation]. University of Manchester; 2017. [cited 2019 Jun 16]. Available from: https://www.research.manchester.ac.uk/portal/en/theses/applying-native-chemical-ligation-to-the-development-of-magneticallyresponsive-drug-delivery-platforms-for-biomedical-applications(fb997ce4-c359-4d3a-8ddc-170c4efb1c53).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.728218.

Council of Science Editors:

Camarillo López RH. Applying native chemical ligation to the development of magnetically-responsive drug delivery platforms for biomedical applications. [Doctoral Dissertation]. University of Manchester; 2017. Available from: https://www.research.manchester.ac.uk/portal/en/theses/applying-native-chemical-ligation-to-the-development-of-magneticallyresponsive-drug-delivery-platforms-for-biomedical-applications(fb997ce4-c359-4d3a-8ddc-170c4efb1c53).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.728218

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