Advanced search options

Advanced Search Options 🞨

Browse by author name (“Author name starts with…”).

Find ETDs with:

in
/  
in
/  
in
/  
in

Written in Published in Earliest date Latest date

Sorted by

Results per page:

Sorted by: relevance · author · university · dateNew search

You searched for subject:(post translational modification). Showing records 1 – 30 of 207 total matches.

[1] [2] [3] [4] [5] [6] [7]

Search Limiters

Last 2 Years | English Only

Degrees

Levels

Languages

Country

▼ Search Limiters


University of Georgia

1. Tucker, Alex Clayton. Reversible lysine acetylation in Streptomyces lividans and Salmonella enterica.

Degree: 2014, University of Georgia

 Lysine acetylation is a post-translational modification conserved in all domains of life. Lysine acetylation occurs lysine side chains and affects functions of proteins involved in… (more)

Subjects/Keywords: post-translational modification; acetylation; bacteria; Salmonella; Streptomyces

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Tucker, A. C. (2014). Reversible lysine acetylation in Streptomyces lividans and Salmonella enterica. (Thesis). University of Georgia. Retrieved from http://hdl.handle.net/10724/30038

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):

Tucker, Alex Clayton. “Reversible lysine acetylation in Streptomyces lividans and Salmonella enterica.” 2014. Thesis, University of Georgia. Accessed March 03, 2021. http://hdl.handle.net/10724/30038.

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

MLA Handbook (7th Edition):

Tucker, Alex Clayton. “Reversible lysine acetylation in Streptomyces lividans and Salmonella enterica.” 2014. Web. 03 Mar 2021.

Vancouver:

Tucker AC. Reversible lysine acetylation in Streptomyces lividans and Salmonella enterica. [Internet] [Thesis]. University of Georgia; 2014. [cited 2021 Mar 03]. Available from: http://hdl.handle.net/10724/30038.

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

Council of Science Editors:

Tucker AC. Reversible lysine acetylation in Streptomyces lividans and Salmonella enterica. [Thesis]. University of Georgia; 2014. Available from: http://hdl.handle.net/10724/30038

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

2. Hernandez, Patricia. Peptide identification by tandem mass spectrometry: a tag-oriented open-modification search method.

Degree: 2005, Université de Genève

 Dans la majorité des projets de recherche en protéomique, il faut, à un moment ou un autre, déterminer l'identité des protéines présentes dans l'échantillon biologique… (more)

Subjects/Keywords: post-translational modification

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Hernandez, P. (2005). Peptide identification by tandem mass spectrometry: a tag-oriented open-modification search method. (Thesis). Université de Genève. Retrieved from http://doc.rero.ch/record/5535

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):

Hernandez, Patricia. “Peptide identification by tandem mass spectrometry: a tag-oriented open-modification search method.” 2005. Thesis, Université de Genève. Accessed March 03, 2021. http://doc.rero.ch/record/5535.

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

MLA Handbook (7th Edition):

Hernandez, Patricia. “Peptide identification by tandem mass spectrometry: a tag-oriented open-modification search method.” 2005. Web. 03 Mar 2021.

Vancouver:

Hernandez P. Peptide identification by tandem mass spectrometry: a tag-oriented open-modification search method. [Internet] [Thesis]. Université de Genève; 2005. [cited 2021 Mar 03]. Available from: http://doc.rero.ch/record/5535.

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

Council of Science Editors:

Hernandez P. Peptide identification by tandem mass spectrometry: a tag-oriented open-modification search method. [Thesis]. Université de Genève; 2005. Available from: http://doc.rero.ch/record/5535

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


University of Aberdeen

3. Zenko, Dmitry. The role of ubiquitination in the post-endocytic trafficking of M2 muscarinic cholinergic receptor.

Degree: PhD, 2019, University of Aberdeen

 Prolonged agonist stimulation of mAChRs promotes their down-regulation which has been implicated in a number of disease states such as bipolar disorder and cognitive impairment… (more)

Subjects/Keywords: Muscarinic receptors; Acetylcholine; Post-translational modification; Ubiquitin

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Zenko, D. (2019). The role of ubiquitination in the post-endocytic trafficking of M2 muscarinic cholinergic receptor. (Doctoral Dissertation). University of Aberdeen. Retrieved from https://abdn.alma.exlibrisgroup.com/view/delivery/44ABE_INST/12152886030005941 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.774060

Chicago Manual of Style (16th Edition):

Zenko, Dmitry. “The role of ubiquitination in the post-endocytic trafficking of M2 muscarinic cholinergic receptor.” 2019. Doctoral Dissertation, University of Aberdeen. Accessed March 03, 2021. https://abdn.alma.exlibrisgroup.com/view/delivery/44ABE_INST/12152886030005941 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.774060.

MLA Handbook (7th Edition):

Zenko, Dmitry. “The role of ubiquitination in the post-endocytic trafficking of M2 muscarinic cholinergic receptor.” 2019. Web. 03 Mar 2021.

Vancouver:

Zenko D. The role of ubiquitination in the post-endocytic trafficking of M2 muscarinic cholinergic receptor. [Internet] [Doctoral dissertation]. University of Aberdeen; 2019. [cited 2021 Mar 03]. Available from: https://abdn.alma.exlibrisgroup.com/view/delivery/44ABE_INST/12152886030005941 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.774060.

Council of Science Editors:

Zenko D. The role of ubiquitination in the post-endocytic trafficking of M2 muscarinic cholinergic receptor. [Doctoral Dissertation]. University of Aberdeen; 2019. Available from: https://abdn.alma.exlibrisgroup.com/view/delivery/44ABE_INST/12152886030005941 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.774060


University of Lethbridge

4. Naziga, Emmanuel B. Computational studies of protein posttranslational modification : glycosylation of oligoproline and collagen peptides .

Degree: 2013, University of Lethbridge

 Glycosylation is the most complex posttranslational modification of proteins and has consequences on protein structure and function. In particular, the hydroxyproline (Hyp) rich glycoproteins (HRGPs)… (more)

Subjects/Keywords: Post-translational modification  – Computer simulation; Post-translational modification  – Research; Glycosylation  – Research; Glycoproteins  – Research

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Naziga, E. B. (2013). Computational studies of protein posttranslational modification : glycosylation of oligoproline and collagen peptides . (Thesis). University of Lethbridge. Retrieved from http://hdl.handle.net/10133/3474

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):

Naziga, Emmanuel B. “Computational studies of protein posttranslational modification : glycosylation of oligoproline and collagen peptides .” 2013. Thesis, University of Lethbridge. Accessed March 03, 2021. http://hdl.handle.net/10133/3474.

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

MLA Handbook (7th Edition):

Naziga, Emmanuel B. “Computational studies of protein posttranslational modification : glycosylation of oligoproline and collagen peptides .” 2013. Web. 03 Mar 2021.

Vancouver:

Naziga EB. Computational studies of protein posttranslational modification : glycosylation of oligoproline and collagen peptides . [Internet] [Thesis]. University of Lethbridge; 2013. [cited 2021 Mar 03]. Available from: http://hdl.handle.net/10133/3474.

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

Council of Science Editors:

Naziga EB. Computational studies of protein posttranslational modification : glycosylation of oligoproline and collagen peptides . [Thesis]. University of Lethbridge; 2013. Available from: http://hdl.handle.net/10133/3474

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

5. Schorova, Lenka. Étude des mécanismes de régulation synaptique de la balance sumoylation/désumoylation : Investigating the molecular pathways driving the sumoylation/desumoylation balance in rat hippocampal synapses.

Degree: Docteur es, Interactions moléculaires et cellulaires, 2018, Université Côte d'Azur (ComUE)

La SUMOylation est une modification post-traductionnelle essentielle pour toutes les cellules eucaryotes. C’est un processus enzymatique qui permet la liaison covalente du polypeptide SUMO sur… (more)

Subjects/Keywords: Synapse; Modification post-traductionnelle; Sumoylation; SENP1; Synapse; Post-translational modification; Sumoylation; SENP1

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Schorova, L. (2018). Étude des mécanismes de régulation synaptique de la balance sumoylation/désumoylation : Investigating the molecular pathways driving the sumoylation/desumoylation balance in rat hippocampal synapses. (Doctoral Dissertation). Université Côte d'Azur (ComUE). Retrieved from http://www.theses.fr/2018AZUR4021

Chicago Manual of Style (16th Edition):

Schorova, Lenka. “Étude des mécanismes de régulation synaptique de la balance sumoylation/désumoylation : Investigating the molecular pathways driving the sumoylation/desumoylation balance in rat hippocampal synapses.” 2018. Doctoral Dissertation, Université Côte d'Azur (ComUE). Accessed March 03, 2021. http://www.theses.fr/2018AZUR4021.

MLA Handbook (7th Edition):

Schorova, Lenka. “Étude des mécanismes de régulation synaptique de la balance sumoylation/désumoylation : Investigating the molecular pathways driving the sumoylation/desumoylation balance in rat hippocampal synapses.” 2018. Web. 03 Mar 2021.

Vancouver:

Schorova L. Étude des mécanismes de régulation synaptique de la balance sumoylation/désumoylation : Investigating the molecular pathways driving the sumoylation/desumoylation balance in rat hippocampal synapses. [Internet] [Doctoral dissertation]. Université Côte d'Azur (ComUE); 2018. [cited 2021 Mar 03]. Available from: http://www.theses.fr/2018AZUR4021.

Council of Science Editors:

Schorova L. Étude des mécanismes de régulation synaptique de la balance sumoylation/désumoylation : Investigating the molecular pathways driving the sumoylation/desumoylation balance in rat hippocampal synapses. [Doctoral Dissertation]. Université Côte d'Azur (ComUE); 2018. Available from: http://www.theses.fr/2018AZUR4021


University of Oxford

6. Feng, Tianshu. Characterisation of 2-oxoglutarate- and fe(II)-dependent oxygenases targeting the protein synthesis apparatus.

Degree: PhD, 2014, University of Oxford

 Members of the 2-oxoglutarate (2OG)- and Fe(II)-dependent oxygenase (2OG oxygenase) superfamily catalyse a wide range of oxidative reactions in biology. 2OG oxygenases require Fe(II) and… (more)

Subjects/Keywords: 572; Biochemistry; Cell Biology; oxygen sensing; protein synthesis; translational termination; ribosome; post-translational modification

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Feng, T. (2014). Characterisation of 2-oxoglutarate- and fe(II)-dependent oxygenases targeting the protein synthesis apparatus. (Doctoral Dissertation). University of Oxford. Retrieved from http://ora.ox.ac.uk/objects/uuid:406a311b-dae6-48c6-9785-1e2f0b889e45 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.655026

Chicago Manual of Style (16th Edition):

Feng, Tianshu. “Characterisation of 2-oxoglutarate- and fe(II)-dependent oxygenases targeting the protein synthesis apparatus.” 2014. Doctoral Dissertation, University of Oxford. Accessed March 03, 2021. http://ora.ox.ac.uk/objects/uuid:406a311b-dae6-48c6-9785-1e2f0b889e45 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.655026.

MLA Handbook (7th Edition):

Feng, Tianshu. “Characterisation of 2-oxoglutarate- and fe(II)-dependent oxygenases targeting the protein synthesis apparatus.” 2014. Web. 03 Mar 2021.

Vancouver:

Feng T. Characterisation of 2-oxoglutarate- and fe(II)-dependent oxygenases targeting the protein synthesis apparatus. [Internet] [Doctoral dissertation]. University of Oxford; 2014. [cited 2021 Mar 03]. Available from: http://ora.ox.ac.uk/objects/uuid:406a311b-dae6-48c6-9785-1e2f0b889e45 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.655026.

Council of Science Editors:

Feng T. Characterisation of 2-oxoglutarate- and fe(II)-dependent oxygenases targeting the protein synthesis apparatus. [Doctoral Dissertation]. University of Oxford; 2014. Available from: http://ora.ox.ac.uk/objects/uuid:406a311b-dae6-48c6-9785-1e2f0b889e45 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.655026


University of Utah

7. Kowalak, Jeffrey A. Determination of posttranscriptional modification in RNA by mass spectrometry;.

Degree: PhD, Biochemistry;, 1994, University of Utah

 Substantial biochemical and genetic evidence exists that implicates ribosomal RNA as a functional component of the translational apparatus. The nucleotide sequences in functionally important regions… (more)

Subjects/Keywords: Post-translational Modification; Genetics

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Kowalak, J. A. (1994). Determination of posttranscriptional modification in RNA by mass spectrometry;. (Doctoral Dissertation). University of Utah. Retrieved from http://content.lib.utah.edu/cdm/singleitem/collection/etd1/id/1391/rec/300

Chicago Manual of Style (16th Edition):

Kowalak, Jeffrey A. “Determination of posttranscriptional modification in RNA by mass spectrometry;.” 1994. Doctoral Dissertation, University of Utah. Accessed March 03, 2021. http://content.lib.utah.edu/cdm/singleitem/collection/etd1/id/1391/rec/300.

MLA Handbook (7th Edition):

Kowalak, Jeffrey A. “Determination of posttranscriptional modification in RNA by mass spectrometry;.” 1994. Web. 03 Mar 2021.

Vancouver:

Kowalak JA. Determination of posttranscriptional modification in RNA by mass spectrometry;. [Internet] [Doctoral dissertation]. University of Utah; 1994. [cited 2021 Mar 03]. Available from: http://content.lib.utah.edu/cdm/singleitem/collection/etd1/id/1391/rec/300.

Council of Science Editors:

Kowalak JA. Determination of posttranscriptional modification in RNA by mass spectrometry;. [Doctoral Dissertation]. University of Utah; 1994. Available from: http://content.lib.utah.edu/cdm/singleitem/collection/etd1/id/1391/rec/300


University of California – Riverside

8. Kung, Raphael Chih-Chung. Quantitative FRET (qFRET) Technology for Determination of Protein Interaction Dissociation Constant in the Presence of Other Proteins and Development of Microfluidic Device.

Degree: Bioengineering, 2015, University of California – Riverside

Post-translational modification is one of the most vital functions at the cellular level in the human body. Ubiquitin and the Ubiquitin-like modifiers (Ubl's) are one… (more)

Subjects/Keywords: Biomedical engineering; Förster Resonance Energy Transfer; Microfluidics; Post-Translational Modification; SUMOylation

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Kung, R. C. (2015). Quantitative FRET (qFRET) Technology for Determination of Protein Interaction Dissociation Constant in the Presence of Other Proteins and Development of Microfluidic Device. (Thesis). University of California – Riverside. Retrieved from http://www.escholarship.org/uc/item/3832v90w

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):

Kung, Raphael Chih-Chung. “Quantitative FRET (qFRET) Technology for Determination of Protein Interaction Dissociation Constant in the Presence of Other Proteins and Development of Microfluidic Device.” 2015. Thesis, University of California – Riverside. Accessed March 03, 2021. http://www.escholarship.org/uc/item/3832v90w.

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

MLA Handbook (7th Edition):

Kung, Raphael Chih-Chung. “Quantitative FRET (qFRET) Technology for Determination of Protein Interaction Dissociation Constant in the Presence of Other Proteins and Development of Microfluidic Device.” 2015. Web. 03 Mar 2021.

Vancouver:

Kung RC. Quantitative FRET (qFRET) Technology for Determination of Protein Interaction Dissociation Constant in the Presence of Other Proteins and Development of Microfluidic Device. [Internet] [Thesis]. University of California – Riverside; 2015. [cited 2021 Mar 03]. Available from: http://www.escholarship.org/uc/item/3832v90w.

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

Council of Science Editors:

Kung RC. Quantitative FRET (qFRET) Technology for Determination of Protein Interaction Dissociation Constant in the Presence of Other Proteins and Development of Microfluidic Device. [Thesis]. University of California – Riverside; 2015. Available from: http://www.escholarship.org/uc/item/3832v90w

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


Ryerson University

9. Padgett, Jill Marie Anderson. Adaptive time-stepping in the numerical solution of the reaction-diffusion master equation.

Degree: 2015, Ryerson University

 Stochastic modeling and simulation are essential tools for studying cellular processes. The dynamics of spatially heterogeneous biochemical systems with species in low amounts is governed… (more)

Subjects/Keywords: Cytology; Cells  – Growth; Post-translational modification; Reaction  – diffusion equations

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Padgett, J. M. A. (2015). Adaptive time-stepping in the numerical solution of the reaction-diffusion master equation. (Thesis). Ryerson University. Retrieved from https://digital.library.ryerson.ca/islandora/object/RULA%3A4369

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):

Padgett, Jill Marie Anderson. “Adaptive time-stepping in the numerical solution of the reaction-diffusion master equation.” 2015. Thesis, Ryerson University. Accessed March 03, 2021. https://digital.library.ryerson.ca/islandora/object/RULA%3A4369.

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

MLA Handbook (7th Edition):

Padgett, Jill Marie Anderson. “Adaptive time-stepping in the numerical solution of the reaction-diffusion master equation.” 2015. Web. 03 Mar 2021.

Vancouver:

Padgett JMA. Adaptive time-stepping in the numerical solution of the reaction-diffusion master equation. [Internet] [Thesis]. Ryerson University; 2015. [cited 2021 Mar 03]. Available from: https://digital.library.ryerson.ca/islandora/object/RULA%3A4369.

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

Council of Science Editors:

Padgett JMA. Adaptive time-stepping in the numerical solution of the reaction-diffusion master equation. [Thesis]. Ryerson University; 2015. Available from: https://digital.library.ryerson.ca/islandora/object/RULA%3A4369

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

10. Hersman, Elisabeth. Sensitive and Specific Proteomic Identification and Quantitation of Murine Cytochrome P450 Enzymes and Histone Post-Translational Modifications using Mass Spectrometry.

Degree: 2014, Johns Hopkins University

 Mouse models are widely used in pharmacology, yet the expression profile of the murine drug metabolizing enzymes has only begun to be characterized at the… (more)

Subjects/Keywords: Mass spectrometry; histone; post-translational modification; efavirenz; cytochrome P450

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Hersman, E. (2014). Sensitive and Specific Proteomic Identification and Quantitation of Murine Cytochrome P450 Enzymes and Histone Post-Translational Modifications using Mass Spectrometry. (Thesis). Johns Hopkins University. Retrieved from http://jhir.library.jhu.edu/handle/1774.2/36977

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):

Hersman, Elisabeth. “Sensitive and Specific Proteomic Identification and Quantitation of Murine Cytochrome P450 Enzymes and Histone Post-Translational Modifications using Mass Spectrometry.” 2014. Thesis, Johns Hopkins University. Accessed March 03, 2021. http://jhir.library.jhu.edu/handle/1774.2/36977.

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

MLA Handbook (7th Edition):

Hersman, Elisabeth. “Sensitive and Specific Proteomic Identification and Quantitation of Murine Cytochrome P450 Enzymes and Histone Post-Translational Modifications using Mass Spectrometry.” 2014. Web. 03 Mar 2021.

Vancouver:

Hersman E. Sensitive and Specific Proteomic Identification and Quantitation of Murine Cytochrome P450 Enzymes and Histone Post-Translational Modifications using Mass Spectrometry. [Internet] [Thesis]. Johns Hopkins University; 2014. [cited 2021 Mar 03]. Available from: http://jhir.library.jhu.edu/handle/1774.2/36977.

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

Council of Science Editors:

Hersman E. Sensitive and Specific Proteomic Identification and Quantitation of Murine Cytochrome P450 Enzymes and Histone Post-Translational Modifications using Mass Spectrometry. [Thesis]. Johns Hopkins University; 2014. Available from: http://jhir.library.jhu.edu/handle/1774.2/36977

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


Vanderbilt University

11. Lu, Xinyuan. LZAP and PPM phosphatases: reciprocal regulation and shared mechanisms altering tumor behavior.

Degree: PhD, Cancer Biology, 2013, Vanderbilt University

 LZAP (Cdk5rap3, C53) is a putative tumor suppressor lost in 30% of human head and neck squamous cell carcinoma. LZAP depletion enhances cell invasion, xenograft… (more)

Subjects/Keywords: post-translational modification; phosphatase; tumor suppressor; NF kappa B; metastasis; PPM1A

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Lu, X. (2013). LZAP and PPM phosphatases: reciprocal regulation and shared mechanisms altering tumor behavior. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://hdl.handle.net/1803/12947

Chicago Manual of Style (16th Edition):

Lu, Xinyuan. “LZAP and PPM phosphatases: reciprocal regulation and shared mechanisms altering tumor behavior.” 2013. Doctoral Dissertation, Vanderbilt University. Accessed March 03, 2021. http://hdl.handle.net/1803/12947.

MLA Handbook (7th Edition):

Lu, Xinyuan. “LZAP and PPM phosphatases: reciprocal regulation and shared mechanisms altering tumor behavior.” 2013. Web. 03 Mar 2021.

Vancouver:

Lu X. LZAP and PPM phosphatases: reciprocal regulation and shared mechanisms altering tumor behavior. [Internet] [Doctoral dissertation]. Vanderbilt University; 2013. [cited 2021 Mar 03]. Available from: http://hdl.handle.net/1803/12947.

Council of Science Editors:

Lu X. LZAP and PPM phosphatases: reciprocal regulation and shared mechanisms altering tumor behavior. [Doctoral Dissertation]. Vanderbilt University; 2013. Available from: http://hdl.handle.net/1803/12947


Texas A&M University

12. Wang, Zhipeng. The Chemical Synthetic Investigation of Proteins with Sitespecific Lysine Post-Translational Modifications.

Degree: PhD, Chemistry, 2018, Texas A&M University

 In the recent decade, an increasing amount of protein post-translational modifications (PTMs) have been discovered, which are important epigenetic markers widespread on nucleic and cytoplasmic… (more)

Subjects/Keywords: Protein chemical biology; Post-translational modification; Lysine; noncanonical amino acids

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Wang, Z. (2018). The Chemical Synthetic Investigation of Proteins with Sitespecific Lysine Post-Translational Modifications. (Doctoral Dissertation). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/173444

Chicago Manual of Style (16th Edition):

Wang, Zhipeng. “The Chemical Synthetic Investigation of Proteins with Sitespecific Lysine Post-Translational Modifications.” 2018. Doctoral Dissertation, Texas A&M University. Accessed March 03, 2021. http://hdl.handle.net/1969.1/173444.

MLA Handbook (7th Edition):

Wang, Zhipeng. “The Chemical Synthetic Investigation of Proteins with Sitespecific Lysine Post-Translational Modifications.” 2018. Web. 03 Mar 2021.

Vancouver:

Wang Z. The Chemical Synthetic Investigation of Proteins with Sitespecific Lysine Post-Translational Modifications. [Internet] [Doctoral dissertation]. Texas A&M University; 2018. [cited 2021 Mar 03]. Available from: http://hdl.handle.net/1969.1/173444.

Council of Science Editors:

Wang Z. The Chemical Synthetic Investigation of Proteins with Sitespecific Lysine Post-Translational Modifications. [Doctoral Dissertation]. Texas A&M University; 2018. Available from: http://hdl.handle.net/1969.1/173444


Penn State University

13. Sun, Dengyun. The roles of post-translational modification of PIV5 P protein in viral gene expression .

Degree: 2011, Penn State University

 Paramyxovirus RNA synthesis requires the large (L) protein and the phosphoprotein (P). It was initially thought that phosphorylation of the P protein was important for… (more)

Subjects/Keywords: Kinase; Virus; Post-translational modification; Gene expression; Apoptosis; Immune response

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Sun, D. (2011). The roles of post-translational modification of PIV5 P protein in viral gene expression . (Thesis). Penn State University. Retrieved from https://submit-etda.libraries.psu.edu/catalog/11702

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):

Sun, Dengyun. “The roles of post-translational modification of PIV5 P protein in viral gene expression .” 2011. Thesis, Penn State University. Accessed March 03, 2021. https://submit-etda.libraries.psu.edu/catalog/11702.

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

MLA Handbook (7th Edition):

Sun, Dengyun. “The roles of post-translational modification of PIV5 P protein in viral gene expression .” 2011. Web. 03 Mar 2021.

Vancouver:

Sun D. The roles of post-translational modification of PIV5 P protein in viral gene expression . [Internet] [Thesis]. Penn State University; 2011. [cited 2021 Mar 03]. Available from: https://submit-etda.libraries.psu.edu/catalog/11702.

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

Council of Science Editors:

Sun D. The roles of post-translational modification of PIV5 P protein in viral gene expression . [Thesis]. Penn State University; 2011. Available from: https://submit-etda.libraries.psu.edu/catalog/11702

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


Boston University

14. Ji, Yuhuan. Mass spectrometry analysis of protein/peptide S-palmitoylation.

Degree: PhD, Biochemistry, 2015, Boston University

 The dynamic S-palmitoylation regulates many intracellular events, including protein trafficking, anchoring, targeting, and protein-protein interactions. Direct detection of S-palmitoylation by conventional liquid chromatography-mass spectrometry (LC-MS)… (more)

Subjects/Keywords: Biochemistry; High-performance liquid chromatography; Mass spectrometry; Palmitoylation; Post-translational modification

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Ji, Y. (2015). Mass spectrometry analysis of protein/peptide S-palmitoylation. (Doctoral Dissertation). Boston University. Retrieved from http://hdl.handle.net/2144/15657

Chicago Manual of Style (16th Edition):

Ji, Yuhuan. “Mass spectrometry analysis of protein/peptide S-palmitoylation.” 2015. Doctoral Dissertation, Boston University. Accessed March 03, 2021. http://hdl.handle.net/2144/15657.

MLA Handbook (7th Edition):

Ji, Yuhuan. “Mass spectrometry analysis of protein/peptide S-palmitoylation.” 2015. Web. 03 Mar 2021.

Vancouver:

Ji Y. Mass spectrometry analysis of protein/peptide S-palmitoylation. [Internet] [Doctoral dissertation]. Boston University; 2015. [cited 2021 Mar 03]. Available from: http://hdl.handle.net/2144/15657.

Council of Science Editors:

Ji Y. Mass spectrometry analysis of protein/peptide S-palmitoylation. [Doctoral Dissertation]. Boston University; 2015. Available from: http://hdl.handle.net/2144/15657


Texas Medical Center

15. Manshouri, Roxsan. POST-TRANSLATIONAL REGULATION OF ZEB1 CONTRIBUTES TO TGFβ-MEDIATED EMT.

Degree: MS, 2015, Texas Medical Center

  Non-small cell lung cancer (NSCLC) is the leading cause of cancer-related death in the United States due in part to the affinity of tumors… (more)

Subjects/Keywords: ZEB1; EMT; TGF-beta; post-translational modification; Medicine and Health Sciences

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Manshouri, R. (2015). POST-TRANSLATIONAL REGULATION OF ZEB1 CONTRIBUTES TO TGFβ-MEDIATED EMT. (Thesis). Texas Medical Center. Retrieved from https://digitalcommons.library.tmc.edu/utgsbs_dissertations/591

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):

Manshouri, Roxsan. “POST-TRANSLATIONAL REGULATION OF ZEB1 CONTRIBUTES TO TGFβ-MEDIATED EMT.” 2015. Thesis, Texas Medical Center. Accessed March 03, 2021. https://digitalcommons.library.tmc.edu/utgsbs_dissertations/591.

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

MLA Handbook (7th Edition):

Manshouri, Roxsan. “POST-TRANSLATIONAL REGULATION OF ZEB1 CONTRIBUTES TO TGFβ-MEDIATED EMT.” 2015. Web. 03 Mar 2021.

Vancouver:

Manshouri R. POST-TRANSLATIONAL REGULATION OF ZEB1 CONTRIBUTES TO TGFβ-MEDIATED EMT. [Internet] [Thesis]. Texas Medical Center; 2015. [cited 2021 Mar 03]. Available from: https://digitalcommons.library.tmc.edu/utgsbs_dissertations/591.

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

Council of Science Editors:

Manshouri R. POST-TRANSLATIONAL REGULATION OF ZEB1 CONTRIBUTES TO TGFβ-MEDIATED EMT. [Thesis]. Texas Medical Center; 2015. Available from: https://digitalcommons.library.tmc.edu/utgsbs_dissertations/591

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


University of Toronto

16. Chandrakumar, Arun A. Characterization of Novel Substrates of the Tankyrase and RNF146 Destruction Complex and Mechanisms of its Regulation.

Degree: PhD, 2020, University of Toronto

 Poly-ADP-ribose is a post-translational modification that was first described over 50 years ago as a polymer derived from nicotinamide adenine dinucleotide or NAD. Since then,… (more)

Subjects/Keywords: ADP-Ribosylation; Poly-ADP-Ribose Polymerases; post-translational modification; Tankyrase; 0379

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Chandrakumar, A. A. (2020). Characterization of Novel Substrates of the Tankyrase and RNF146 Destruction Complex and Mechanisms of its Regulation. (Doctoral Dissertation). University of Toronto. Retrieved from http://hdl.handle.net/1807/101171

Chicago Manual of Style (16th Edition):

Chandrakumar, Arun A. “Characterization of Novel Substrates of the Tankyrase and RNF146 Destruction Complex and Mechanisms of its Regulation.” 2020. Doctoral Dissertation, University of Toronto. Accessed March 03, 2021. http://hdl.handle.net/1807/101171.

MLA Handbook (7th Edition):

Chandrakumar, Arun A. “Characterization of Novel Substrates of the Tankyrase and RNF146 Destruction Complex and Mechanisms of its Regulation.” 2020. Web. 03 Mar 2021.

Vancouver:

Chandrakumar AA. Characterization of Novel Substrates of the Tankyrase and RNF146 Destruction Complex and Mechanisms of its Regulation. [Internet] [Doctoral dissertation]. University of Toronto; 2020. [cited 2021 Mar 03]. Available from: http://hdl.handle.net/1807/101171.

Council of Science Editors:

Chandrakumar AA. Characterization of Novel Substrates of the Tankyrase and RNF146 Destruction Complex and Mechanisms of its Regulation. [Doctoral Dissertation]. University of Toronto; 2020. Available from: http://hdl.handle.net/1807/101171


University of Adelaide

17. Lisy, Karolina. Investigating potential post-translational modification of factor-inhibiting HIF (FIH-1.

Degree: 2011, University of Adelaide

 The Hypoxia Inducible Factors (HIFs) are widely expressed transcription factors critical for altering gene expression in hypoxic cells and enabling cellular adaptation to conditions of… (more)

Subjects/Keywords: FIH-1; hypoxia; post-translational modification; two-dimensional electrophoresis

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Lisy, K. (2011). Investigating potential post-translational modification of factor-inhibiting HIF (FIH-1. (Thesis). University of Adelaide. Retrieved from http://hdl.handle.net/2440/80233

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):

Lisy, Karolina. “Investigating potential post-translational modification of factor-inhibiting HIF (FIH-1.” 2011. Thesis, University of Adelaide. Accessed March 03, 2021. http://hdl.handle.net/2440/80233.

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

MLA Handbook (7th Edition):

Lisy, Karolina. “Investigating potential post-translational modification of factor-inhibiting HIF (FIH-1.” 2011. Web. 03 Mar 2021.

Vancouver:

Lisy K. Investigating potential post-translational modification of factor-inhibiting HIF (FIH-1. [Internet] [Thesis]. University of Adelaide; 2011. [cited 2021 Mar 03]. Available from: http://hdl.handle.net/2440/80233.

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

Council of Science Editors:

Lisy K. Investigating potential post-translational modification of factor-inhibiting HIF (FIH-1. [Thesis]. University of Adelaide; 2011. Available from: http://hdl.handle.net/2440/80233

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


University of Ottawa

18. Liu, Serena E. B. Kinome-wide RNAi Screening to Identify Kinases Involved in Post-translational Modification of FUS .

Degree: 2016, University of Ottawa

 Amyotrophic lateral sclerosis (ALS) is a devastating adult onset neurodegenerative disorder characterized by the selective degeneration of upper and lower motor neurons. Patients typically die… (more)

Subjects/Keywords: FUS; ALS; Kinome-wide RNAI Screen; Post-translational Modification

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Liu, S. E. B. (2016). Kinome-wide RNAi Screening to Identify Kinases Involved in Post-translational Modification of FUS . (Thesis). University of Ottawa. Retrieved from http://hdl.handle.net/10393/34199

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):

Liu, Serena E B. “Kinome-wide RNAi Screening to Identify Kinases Involved in Post-translational Modification of FUS .” 2016. Thesis, University of Ottawa. Accessed March 03, 2021. http://hdl.handle.net/10393/34199.

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

MLA Handbook (7th Edition):

Liu, Serena E B. “Kinome-wide RNAi Screening to Identify Kinases Involved in Post-translational Modification of FUS .” 2016. Web. 03 Mar 2021.

Vancouver:

Liu SEB. Kinome-wide RNAi Screening to Identify Kinases Involved in Post-translational Modification of FUS . [Internet] [Thesis]. University of Ottawa; 2016. [cited 2021 Mar 03]. Available from: http://hdl.handle.net/10393/34199.

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

Council of Science Editors:

Liu SEB. Kinome-wide RNAi Screening to Identify Kinases Involved in Post-translational Modification of FUS . [Thesis]. University of Ottawa; 2016. Available from: http://hdl.handle.net/10393/34199

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


University of Ottawa

19. Pourhanifeh-Lemeri, Roghayeh. Identification of Non-histone Acetylation Targets in Saccharomyces cerevisiae .

Degree: 2012, University of Ottawa

 Lysine acetylation is a conserved post-translational modification (PTM) which was traditionally believed to be limited to histones and the regulation of gene expression. However, recent… (more)

Subjects/Keywords: Lysine acetylation; KAT; Post-translational modification; NuA4; Eaf1; Epl1

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Pourhanifeh-Lemeri, R. (2012). Identification of Non-histone Acetylation Targets in Saccharomyces cerevisiae . (Thesis). University of Ottawa. Retrieved from http://hdl.handle.net/10393/22885

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):

Pourhanifeh-Lemeri, Roghayeh. “Identification of Non-histone Acetylation Targets in Saccharomyces cerevisiae .” 2012. Thesis, University of Ottawa. Accessed March 03, 2021. http://hdl.handle.net/10393/22885.

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

MLA Handbook (7th Edition):

Pourhanifeh-Lemeri, Roghayeh. “Identification of Non-histone Acetylation Targets in Saccharomyces cerevisiae .” 2012. Web. 03 Mar 2021.

Vancouver:

Pourhanifeh-Lemeri R. Identification of Non-histone Acetylation Targets in Saccharomyces cerevisiae . [Internet] [Thesis]. University of Ottawa; 2012. [cited 2021 Mar 03]. Available from: http://hdl.handle.net/10393/22885.

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

Council of Science Editors:

Pourhanifeh-Lemeri R. Identification of Non-histone Acetylation Targets in Saccharomyces cerevisiae . [Thesis]. University of Ottawa; 2012. Available from: http://hdl.handle.net/10393/22885

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


University of Dundee

20. Trapannone, Riccardo. Function and inhibition of the mitochondrial O-GlcNAc transferase isoform.

Degree: PhD, 2015, University of Dundee

 The O-linked N-acetylglucosamine post-translational modification (O-GlcNAcylation) is the dynamic and reversible attachment of N-acetylglucosamine to serine and threonine residues of target proteins. It is abundant… (more)

Subjects/Keywords: 579; Protein post-translational modification; O-GlcNAc; OGT; Mitochondria

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Trapannone, R. (2015). Function and inhibition of the mitochondrial O-GlcNAc transferase isoform. (Doctoral Dissertation). University of Dundee. Retrieved from https://discovery.dundee.ac.uk/en/studentTheses/e8d62f76-313d-4ec4-b149-212afb910188 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.681466

Chicago Manual of Style (16th Edition):

Trapannone, Riccardo. “Function and inhibition of the mitochondrial O-GlcNAc transferase isoform.” 2015. Doctoral Dissertation, University of Dundee. Accessed March 03, 2021. https://discovery.dundee.ac.uk/en/studentTheses/e8d62f76-313d-4ec4-b149-212afb910188 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.681466.

MLA Handbook (7th Edition):

Trapannone, Riccardo. “Function and inhibition of the mitochondrial O-GlcNAc transferase isoform.” 2015. Web. 03 Mar 2021.

Vancouver:

Trapannone R. Function and inhibition of the mitochondrial O-GlcNAc transferase isoform. [Internet] [Doctoral dissertation]. University of Dundee; 2015. [cited 2021 Mar 03]. Available from: https://discovery.dundee.ac.uk/en/studentTheses/e8d62f76-313d-4ec4-b149-212afb910188 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.681466.

Council of Science Editors:

Trapannone R. Function and inhibition of the mitochondrial O-GlcNAc transferase isoform. [Doctoral Dissertation]. University of Dundee; 2015. Available from: https://discovery.dundee.ac.uk/en/studentTheses/e8d62f76-313d-4ec4-b149-212afb910188 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.681466


Hong Kong University of Science and Technology

21. Hu, Qin. Technology and methodology to manipulate proteins and study protein post-translation modifications.

Degree: 2014, Hong Kong University of Science and Technology

 Plants have intrinsic ROS/RNS metabolism and subsequent signaling to maintain the redox homeostasis. Redox post-translation modifications (PTMs) are mainly focus on the revisable cysteine modification(more)

Subjects/Keywords: Post-translational modification ; Protein-protein interactions ; Oxidation-reduction reaction ; Cysteine proteinases

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Hu, Q. (2014). Technology and methodology to manipulate proteins and study protein post-translation modifications. (Thesis). Hong Kong University of Science and Technology. Retrieved from http://repository.ust.hk/ir/Record/1783.1-71652 ; https://doi.org/10.14711/thesis-b1334221 ; http://repository.ust.hk/ir/bitstream/1783.1-71652/1/th_redirect.html

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):

Hu, Qin. “Technology and methodology to manipulate proteins and study protein post-translation modifications.” 2014. Thesis, Hong Kong University of Science and Technology. Accessed March 03, 2021. http://repository.ust.hk/ir/Record/1783.1-71652 ; https://doi.org/10.14711/thesis-b1334221 ; http://repository.ust.hk/ir/bitstream/1783.1-71652/1/th_redirect.html.

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

MLA Handbook (7th Edition):

Hu, Qin. “Technology and methodology to manipulate proteins and study protein post-translation modifications.” 2014. Web. 03 Mar 2021.

Vancouver:

Hu Q. Technology and methodology to manipulate proteins and study protein post-translation modifications. [Internet] [Thesis]. Hong Kong University of Science and Technology; 2014. [cited 2021 Mar 03]. Available from: http://repository.ust.hk/ir/Record/1783.1-71652 ; https://doi.org/10.14711/thesis-b1334221 ; http://repository.ust.hk/ir/bitstream/1783.1-71652/1/th_redirect.html.

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

Council of Science Editors:

Hu Q. Technology and methodology to manipulate proteins and study protein post-translation modifications. [Thesis]. Hong Kong University of Science and Technology; 2014. Available from: http://repository.ust.hk/ir/Record/1783.1-71652 ; https://doi.org/10.14711/thesis-b1334221 ; http://repository.ust.hk/ir/bitstream/1783.1-71652/1/th_redirect.html

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


Hong Kong University of Science and Technology

22. Hu, Yingwei. Building and searching predicted spectral libraries for identification of protein post-translational modifications.

Degree: 2015, Hong Kong University of Science and Technology

Post-translational modification (PTM) is a key step in protein biosynthesis, critical for the correct trafficking and function of the protein. However, the high-throughput identification of… (more)

Subjects/Keywords: Post-translational modification ; Data processing ; Proteins ; Synthesis ; Analysis ; Mass spectrometry

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Hu, Y. (2015). Building and searching predicted spectral libraries for identification of protein post-translational modifications. (Thesis). Hong Kong University of Science and Technology. Retrieved from http://repository.ust.hk/ir/Record/1783.1-83610 ; https://doi.org/10.14711/thesis-b1451938 ; http://repository.ust.hk/ir/bitstream/1783.1-83610/1/th_redirect.html

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):

Hu, Yingwei. “Building and searching predicted spectral libraries for identification of protein post-translational modifications.” 2015. Thesis, Hong Kong University of Science and Technology. Accessed March 03, 2021. http://repository.ust.hk/ir/Record/1783.1-83610 ; https://doi.org/10.14711/thesis-b1451938 ; http://repository.ust.hk/ir/bitstream/1783.1-83610/1/th_redirect.html.

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

MLA Handbook (7th Edition):

Hu, Yingwei. “Building and searching predicted spectral libraries for identification of protein post-translational modifications.” 2015. Web. 03 Mar 2021.

Vancouver:

Hu Y. Building and searching predicted spectral libraries for identification of protein post-translational modifications. [Internet] [Thesis]. Hong Kong University of Science and Technology; 2015. [cited 2021 Mar 03]. Available from: http://repository.ust.hk/ir/Record/1783.1-83610 ; https://doi.org/10.14711/thesis-b1451938 ; http://repository.ust.hk/ir/bitstream/1783.1-83610/1/th_redirect.html.

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

Council of Science Editors:

Hu Y. Building and searching predicted spectral libraries for identification of protein post-translational modifications. [Thesis]. Hong Kong University of Science and Technology; 2015. Available from: http://repository.ust.hk/ir/Record/1783.1-83610 ; https://doi.org/10.14711/thesis-b1451938 ; http://repository.ust.hk/ir/bitstream/1783.1-83610/1/th_redirect.html

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


Hong Kong University of Science and Technology

23. Yu, Fengchao. Beyond conventional peptide identification-cross-linked peptides identification and unlimited post-translational modification identification.

Degree: 2017, Hong Kong University of Science and Technology

 Liquid chromatography–mass spectrometry (LC-MS) based proteomics has achieved great success in recent years, and is becoming one of the major approaches to studying biological problems.… (more)

Subjects/Keywords: Peptides ; Identification ; Post-translational modification ; Proteomics ; Crosslinking (Polymerization)

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Yu, F. (2017). Beyond conventional peptide identification-cross-linked peptides identification and unlimited post-translational modification identification. (Thesis). Hong Kong University of Science and Technology. Retrieved from http://repository.ust.hk/ir/Record/1783.1-88452 ; https://doi.org/10.14711/thesis-991012535962603412 ; http://repository.ust.hk/ir/bitstream/1783.1-88452/1/th_redirect.html

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):

Yu, Fengchao. “Beyond conventional peptide identification-cross-linked peptides identification and unlimited post-translational modification identification.” 2017. Thesis, Hong Kong University of Science and Technology. Accessed March 03, 2021. http://repository.ust.hk/ir/Record/1783.1-88452 ; https://doi.org/10.14711/thesis-991012535962603412 ; http://repository.ust.hk/ir/bitstream/1783.1-88452/1/th_redirect.html.

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

MLA Handbook (7th Edition):

Yu, Fengchao. “Beyond conventional peptide identification-cross-linked peptides identification and unlimited post-translational modification identification.” 2017. Web. 03 Mar 2021.

Vancouver:

Yu F. Beyond conventional peptide identification-cross-linked peptides identification and unlimited post-translational modification identification. [Internet] [Thesis]. Hong Kong University of Science and Technology; 2017. [cited 2021 Mar 03]. Available from: http://repository.ust.hk/ir/Record/1783.1-88452 ; https://doi.org/10.14711/thesis-991012535962603412 ; http://repository.ust.hk/ir/bitstream/1783.1-88452/1/th_redirect.html.

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

Council of Science Editors:

Yu F. Beyond conventional peptide identification-cross-linked peptides identification and unlimited post-translational modification identification. [Thesis]. Hong Kong University of Science and Technology; 2017. Available from: http://repository.ust.hk/ir/Record/1783.1-88452 ; https://doi.org/10.14711/thesis-991012535962603412 ; http://repository.ust.hk/ir/bitstream/1783.1-88452/1/th_redirect.html

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

24. Hasin, Naushaba. Functional significance of Hsp70 post-translational modification in prion propagation and cellular function.

Degree: 2012, RIAN

 The term prion (proteinaceous infectious particles) was first coined by Stanley Prusiner while naming the causative agent responsible for a group of invariably fatal neurodegenerative… (more)

Subjects/Keywords: Biology; Hsp70 post-translational modification; prion propagation; cellular function

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Hasin, N. (2012). Functional significance of Hsp70 post-translational modification in prion propagation and cellular function. (Thesis). RIAN. Retrieved from http://eprints.maynoothuniversity.ie/4077/

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):

Hasin, Naushaba. “Functional significance of Hsp70 post-translational modification in prion propagation and cellular function.” 2012. Thesis, RIAN. Accessed March 03, 2021. http://eprints.maynoothuniversity.ie/4077/.

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

MLA Handbook (7th Edition):

Hasin, Naushaba. “Functional significance of Hsp70 post-translational modification in prion propagation and cellular function.” 2012. Web. 03 Mar 2021.

Vancouver:

Hasin N. Functional significance of Hsp70 post-translational modification in prion propagation and cellular function. [Internet] [Thesis]. RIAN; 2012. [cited 2021 Mar 03]. Available from: http://eprints.maynoothuniversity.ie/4077/.

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

Council of Science Editors:

Hasin N. Functional significance of Hsp70 post-translational modification in prion propagation and cellular function. [Thesis]. RIAN; 2012. Available from: http://eprints.maynoothuniversity.ie/4077/

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


Australian National University

25. Ray, Nicholas John. The Effects of Age-Related Modifications on the Stability and Function of Human Eye Lens Crystallins .

Degree: 2015, Australian National University

 The crystallins are the primary proteins of the eye lens and are largely responsible for its high transparency, high refractive index and long-term stability. While… (more)

Subjects/Keywords: Crystallin; Cataract; Aging; Post-translational modification; Protein; Deamidation; Eye; Eye lens

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Ray, N. J. (2015). The Effects of Age-Related Modifications on the Stability and Function of Human Eye Lens Crystallins . (Thesis). Australian National University. Retrieved from http://hdl.handle.net/1885/104582

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):

Ray, Nicholas John. “The Effects of Age-Related Modifications on the Stability and Function of Human Eye Lens Crystallins .” 2015. Thesis, Australian National University. Accessed March 03, 2021. http://hdl.handle.net/1885/104582.

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

MLA Handbook (7th Edition):

Ray, Nicholas John. “The Effects of Age-Related Modifications on the Stability and Function of Human Eye Lens Crystallins .” 2015. Web. 03 Mar 2021.

Vancouver:

Ray NJ. The Effects of Age-Related Modifications on the Stability and Function of Human Eye Lens Crystallins . [Internet] [Thesis]. Australian National University; 2015. [cited 2021 Mar 03]. Available from: http://hdl.handle.net/1885/104582.

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

Council of Science Editors:

Ray NJ. The Effects of Age-Related Modifications on the Stability and Function of Human Eye Lens Crystallins . [Thesis]. Australian National University; 2015. Available from: http://hdl.handle.net/1885/104582

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


University of Technology, Sydney

26. Tacchi, JL. Proteomic investigation of the genome-reduced pathogen, Mycoplasma hyopneumoniae.

Degree: 2015, University of Technology, Sydney

 Mycoplasma hyopneumoniae is a genome-reduced bacterium and an economically significant pathogen that chronically infects the respiratory tract of swine. This infection often leads to pneumonia… (more)

Subjects/Keywords: Microbiology.; Proteolysis.; Post-translational modification.; Global proteome.; Adhesins.

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Tacchi, J. (2015). Proteomic investigation of the genome-reduced pathogen, Mycoplasma hyopneumoniae. (Thesis). University of Technology, Sydney. Retrieved from http://hdl.handle.net/10453/37143

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):

Tacchi, JL. “Proteomic investigation of the genome-reduced pathogen, Mycoplasma hyopneumoniae.” 2015. Thesis, University of Technology, Sydney. Accessed March 03, 2021. http://hdl.handle.net/10453/37143.

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

MLA Handbook (7th Edition):

Tacchi, JL. “Proteomic investigation of the genome-reduced pathogen, Mycoplasma hyopneumoniae.” 2015. Web. 03 Mar 2021.

Vancouver:

Tacchi J. Proteomic investigation of the genome-reduced pathogen, Mycoplasma hyopneumoniae. [Internet] [Thesis]. University of Technology, Sydney; 2015. [cited 2021 Mar 03]. Available from: http://hdl.handle.net/10453/37143.

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

Council of Science Editors:

Tacchi J. Proteomic investigation of the genome-reduced pathogen, Mycoplasma hyopneumoniae. [Thesis]. University of Technology, Sydney; 2015. Available from: http://hdl.handle.net/10453/37143

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


University of Western Ontario

27. Singh, Randeep K. Regulation of E2F1 in Keratinocytes During UV-Damage and Differentiation.

Degree: 2016, University of Western Ontario

 The E2F1 transcription factor regulates the expression of key genes involved in cell proliferation and differentiation to maintain skin homeostasis. The expression of E2F1 is… (more)

Subjects/Keywords: Keratinocytes; E2F; post-translational modification; hHR23; DNA photodamage; Cdh1.; Cancer Biology

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Singh, R. K. (2016). Regulation of E2F1 in Keratinocytes During UV-Damage and Differentiation. (Thesis). University of Western Ontario. Retrieved from https://ir.lib.uwo.ca/etd/4202

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):

Singh, Randeep K. “Regulation of E2F1 in Keratinocytes During UV-Damage and Differentiation.” 2016. Thesis, University of Western Ontario. Accessed March 03, 2021. https://ir.lib.uwo.ca/etd/4202.

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

MLA Handbook (7th Edition):

Singh, Randeep K. “Regulation of E2F1 in Keratinocytes During UV-Damage and Differentiation.” 2016. Web. 03 Mar 2021.

Vancouver:

Singh RK. Regulation of E2F1 in Keratinocytes During UV-Damage and Differentiation. [Internet] [Thesis]. University of Western Ontario; 2016. [cited 2021 Mar 03]. Available from: https://ir.lib.uwo.ca/etd/4202.

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

Council of Science Editors:

Singh RK. Regulation of E2F1 in Keratinocytes During UV-Damage and Differentiation. [Thesis]. University of Western Ontario; 2016. Available from: https://ir.lib.uwo.ca/etd/4202

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

28. Jouette, Julie. Phosphoinositides et contrôle de la polarité cellulaire : régulations croisées entre la PIP5K Skittles et les protéines de polarité PAR1 et PAR3 : Phosphoinositides and cell polarity control : interplay between the PIP5K Skittles and the polarity proteins PAR1 and PAR3.

Degree: Docteur es, Physiologie et biologie des organismes, populations, interactions. Génomes, épigénomes, destin cellulaire, 2017, Sorbonne Paris Cité

La polarité cellulaire est un processus fondamental qui contrôle les spécificités fonctionnelle et physiologique de la plupart des cellules eucaryotes. Cette asymétrie intracellulaire repose sur… (more)

Subjects/Keywords: Protéines PAR; Trafic vésiculaire; PAR proteins; Vésicular trafic; Post-translational modification

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Jouette, J. (2017). Phosphoinositides et contrôle de la polarité cellulaire : régulations croisées entre la PIP5K Skittles et les protéines de polarité PAR1 et PAR3 : Phosphoinositides and cell polarity control : interplay between the PIP5K Skittles and the polarity proteins PAR1 and PAR3. (Doctoral Dissertation). Sorbonne Paris Cité. Retrieved from http://www.theses.fr/2017USPCC118

Chicago Manual of Style (16th Edition):

Jouette, Julie. “Phosphoinositides et contrôle de la polarité cellulaire : régulations croisées entre la PIP5K Skittles et les protéines de polarité PAR1 et PAR3 : Phosphoinositides and cell polarity control : interplay between the PIP5K Skittles and the polarity proteins PAR1 and PAR3.” 2017. Doctoral Dissertation, Sorbonne Paris Cité. Accessed March 03, 2021. http://www.theses.fr/2017USPCC118.

MLA Handbook (7th Edition):

Jouette, Julie. “Phosphoinositides et contrôle de la polarité cellulaire : régulations croisées entre la PIP5K Skittles et les protéines de polarité PAR1 et PAR3 : Phosphoinositides and cell polarity control : interplay between the PIP5K Skittles and the polarity proteins PAR1 and PAR3.” 2017. Web. 03 Mar 2021.

Vancouver:

Jouette J. Phosphoinositides et contrôle de la polarité cellulaire : régulations croisées entre la PIP5K Skittles et les protéines de polarité PAR1 et PAR3 : Phosphoinositides and cell polarity control : interplay between the PIP5K Skittles and the polarity proteins PAR1 and PAR3. [Internet] [Doctoral dissertation]. Sorbonne Paris Cité; 2017. [cited 2021 Mar 03]. Available from: http://www.theses.fr/2017USPCC118.

Council of Science Editors:

Jouette J. Phosphoinositides et contrôle de la polarité cellulaire : régulations croisées entre la PIP5K Skittles et les protéines de polarité PAR1 et PAR3 : Phosphoinositides and cell polarity control : interplay between the PIP5K Skittles and the polarity proteins PAR1 and PAR3. [Doctoral Dissertation]. Sorbonne Paris Cité; 2017. Available from: http://www.theses.fr/2017USPCC118

29. Hasin, Naushaba. Functional significance of Hsp70 post-translational modification in prion propagation and cellular function.

Degree: 2012, RIAN

 The term prion (proteinaceous infectious particles) was first coined by Stanley Prusiner while naming the causative agent responsible for a group of invariably fatal neurodegenerative… (more)

Subjects/Keywords: Biology; Hsp70 post-translational modification; prion propagation; cellular function

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Hasin, N. (2012). Functional significance of Hsp70 post-translational modification in prion propagation and cellular function. (Thesis). RIAN. Retrieved from http://mural.maynoothuniversity.ie/4077/

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):

Hasin, Naushaba. “Functional significance of Hsp70 post-translational modification in prion propagation and cellular function.” 2012. Thesis, RIAN. Accessed March 03, 2021. http://mural.maynoothuniversity.ie/4077/.

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

MLA Handbook (7th Edition):

Hasin, Naushaba. “Functional significance of Hsp70 post-translational modification in prion propagation and cellular function.” 2012. Web. 03 Mar 2021.

Vancouver:

Hasin N. Functional significance of Hsp70 post-translational modification in prion propagation and cellular function. [Internet] [Thesis]. RIAN; 2012. [cited 2021 Mar 03]. Available from: http://mural.maynoothuniversity.ie/4077/.

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

Council of Science Editors:

Hasin N. Functional significance of Hsp70 post-translational modification in prion propagation and cellular function. [Thesis]. RIAN; 2012. Available from: http://mural.maynoothuniversity.ie/4077/

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


University of Hong Kong

30. Xiong, Ying. Development of chemical reporters for glutarylation and HMGylation.

Degree: 2014, University of Hong Kong

 Protein post-translational modifications (PTMs) are covalent chemical modifications that occur after protein translation. As such, PTMs have greatly expanded the diversity and complexity of proteomes.… (more)

Subjects/Keywords: Post-translational modification; Proteomics

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Xiong, Y. (2014). Development of chemical reporters for glutarylation and HMGylation. (Thesis). University of Hong Kong. Retrieved from http://hdl.handle.net/10722/216261

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):

Xiong, Ying. “Development of chemical reporters for glutarylation and HMGylation.” 2014. Thesis, University of Hong Kong. Accessed March 03, 2021. http://hdl.handle.net/10722/216261.

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

MLA Handbook (7th Edition):

Xiong, Ying. “Development of chemical reporters for glutarylation and HMGylation.” 2014. Web. 03 Mar 2021.

Vancouver:

Xiong Y. Development of chemical reporters for glutarylation and HMGylation. [Internet] [Thesis]. University of Hong Kong; 2014. [cited 2021 Mar 03]. Available from: http://hdl.handle.net/10722/216261.

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

Council of Science Editors:

Xiong Y. Development of chemical reporters for glutarylation and HMGylation. [Thesis]. University of Hong Kong; 2014. Available from: http://hdl.handle.net/10722/216261

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

[1] [2] [3] [4] [5] [6] [7]

.