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You searched for subject:(Post translational modifications). Showing records 1 – 30 of 169 total matches.

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University of Manitoba

1. Sikarwar, Anurag Singh. Post-translational modifications of thromboxane receptor G-protein alpha q complex in hypoxic PPHN.

Degree: Physiology and Pathophysiology, 2014, University of Manitoba

 Introduction: Persistent pulmonary hypertension of the newborn (PPHN) is associated with an elevated thromboxane to prostacyclin ratio, pulmonary artery (PA) hyperreactivity and hypersensitivity. Thromboxane receptor… (more)

Subjects/Keywords: PPHN; post-translational modifications

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APA (6th Edition):

Sikarwar, A. S. (2014). Post-translational modifications of thromboxane receptor G-protein alpha q complex in hypoxic PPHN. (Thesis). University of Manitoba. Retrieved from http://hdl.handle.net/1993/31664

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):

Sikarwar, Anurag Singh. “Post-translational modifications of thromboxane receptor G-protein alpha q complex in hypoxic PPHN.” 2014. Thesis, University of Manitoba. Accessed January 16, 2021. http://hdl.handle.net/1993/31664.

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

MLA Handbook (7th Edition):

Sikarwar, Anurag Singh. “Post-translational modifications of thromboxane receptor G-protein alpha q complex in hypoxic PPHN.” 2014. Web. 16 Jan 2021.

Vancouver:

Sikarwar AS. Post-translational modifications of thromboxane receptor G-protein alpha q complex in hypoxic PPHN. [Internet] [Thesis]. University of Manitoba; 2014. [cited 2021 Jan 16]. Available from: http://hdl.handle.net/1993/31664.

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

Council of Science Editors:

Sikarwar AS. Post-translational modifications of thromboxane receptor G-protein alpha q complex in hypoxic PPHN. [Thesis]. University of Manitoba; 2014. Available from: http://hdl.handle.net/1993/31664

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

2. Parameswaran Kalaivani, Nithyha. Understanding the mechanisms of histone modifications in vivo : Comprendre les mécanismes de nouvelles modifications des histones in vivo.

Degree: Docteur es, Aspects moléculaires et cellulaires de la biologie, 2016, Université de Strasbourg

Les modifications post-traductionnelles (MPTs) d’histones sont apparues comme un acteur majeur de la régulation de l’expression des gènes. Cependant peu de choses sont connues sur… (more)

Subjects/Keywords: Epigénétiques; Histones; Modifications post-traductionnelles; Epigenetics; Histones; Post translational modifications; 572.8

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APA (6th Edition):

Parameswaran Kalaivani, N. (2016). Understanding the mechanisms of histone modifications in vivo : Comprendre les mécanismes de nouvelles modifications des histones in vivo. (Doctoral Dissertation). Université de Strasbourg. Retrieved from http://www.theses.fr/2016STRAJ097

Chicago Manual of Style (16th Edition):

Parameswaran Kalaivani, Nithyha. “Understanding the mechanisms of histone modifications in vivo : Comprendre les mécanismes de nouvelles modifications des histones in vivo.” 2016. Doctoral Dissertation, Université de Strasbourg. Accessed January 16, 2021. http://www.theses.fr/2016STRAJ097.

MLA Handbook (7th Edition):

Parameswaran Kalaivani, Nithyha. “Understanding the mechanisms of histone modifications in vivo : Comprendre les mécanismes de nouvelles modifications des histones in vivo.” 2016. Web. 16 Jan 2021.

Vancouver:

Parameswaran Kalaivani N. Understanding the mechanisms of histone modifications in vivo : Comprendre les mécanismes de nouvelles modifications des histones in vivo. [Internet] [Doctoral dissertation]. Université de Strasbourg; 2016. [cited 2021 Jan 16]. Available from: http://www.theses.fr/2016STRAJ097.

Council of Science Editors:

Parameswaran Kalaivani N. Understanding the mechanisms of histone modifications in vivo : Comprendre les mécanismes de nouvelles modifications des histones in vivo. [Doctoral Dissertation]. Université de Strasbourg; 2016. Available from: http://www.theses.fr/2016STRAJ097


University of Manchester

3. Fowler, Nicholas. Investigating the role of electrostatic interactions in modulating protein function.

Degree: 2018, University of Manchester

 The work in this thesis centres on understanding how electrostatic interactions modulate the function of proteins. A computational method is presented to predict the reduction… (more)

Subjects/Keywords: Protein electrostatics; Copper proteins; Post-translational modifications

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APA (6th Edition):

Fowler, N. (2018). Investigating the role of electrostatic interactions in modulating protein function. (Doctoral Dissertation). University of Manchester. Retrieved from http://www.manchester.ac.uk/escholar/uk-ac-man-scw:316046

Chicago Manual of Style (16th Edition):

Fowler, Nicholas. “Investigating the role of electrostatic interactions in modulating protein function.” 2018. Doctoral Dissertation, University of Manchester. Accessed January 16, 2021. http://www.manchester.ac.uk/escholar/uk-ac-man-scw:316046.

MLA Handbook (7th Edition):

Fowler, Nicholas. “Investigating the role of electrostatic interactions in modulating protein function.” 2018. Web. 16 Jan 2021.

Vancouver:

Fowler N. Investigating the role of electrostatic interactions in modulating protein function. [Internet] [Doctoral dissertation]. University of Manchester; 2018. [cited 2021 Jan 16]. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:316046.

Council of Science Editors:

Fowler N. Investigating the role of electrostatic interactions in modulating protein function. [Doctoral Dissertation]. University of Manchester; 2018. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:316046


Princeton University

4. Britton, Laura-Mae. Serine, Threonine and Tyrosine O-Acetylation in the Chromatin Landscape .

Degree: PhD, 2014, Princeton University

 Histone post translational modifications (PTMs) are a key component of the dynamic and responsive nucleoprotein structure that is chromatin. Assorted physiological processes such as transcription… (more)

Subjects/Keywords: histone post translational modifications; mass spectrometry

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APA (6th Edition):

Britton, L. (2014). Serine, Threonine and Tyrosine O-Acetylation in the Chromatin Landscape . (Doctoral Dissertation). Princeton University. Retrieved from http://arks.princeton.edu/ark:/88435/dsp016969z300m

Chicago Manual of Style (16th Edition):

Britton, Laura-Mae. “Serine, Threonine and Tyrosine O-Acetylation in the Chromatin Landscape .” 2014. Doctoral Dissertation, Princeton University. Accessed January 16, 2021. http://arks.princeton.edu/ark:/88435/dsp016969z300m.

MLA Handbook (7th Edition):

Britton, Laura-Mae. “Serine, Threonine and Tyrosine O-Acetylation in the Chromatin Landscape .” 2014. Web. 16 Jan 2021.

Vancouver:

Britton L. Serine, Threonine and Tyrosine O-Acetylation in the Chromatin Landscape . [Internet] [Doctoral dissertation]. Princeton University; 2014. [cited 2021 Jan 16]. Available from: http://arks.princeton.edu/ark:/88435/dsp016969z300m.

Council of Science Editors:

Britton L. Serine, Threonine and Tyrosine O-Acetylation in the Chromatin Landscape . [Doctoral Dissertation]. Princeton University; 2014. Available from: http://arks.princeton.edu/ark:/88435/dsp016969z300m


University of Manchester

5. Salmi-Leshem, Rotem. Molecular functions of multi-SUMO-binding protein complexes.

Degree: PhD, 2019, University of Manchester

 Gene expression is regulated in many ways, one of which is SUMOylation of transcription factors and associated complexes. This covalent modification by small ubiquitin-like modifier… (more)

Subjects/Keywords: SUMO2/3; 5FMC complex; Post-Translational Modifications

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APA (6th Edition):

Salmi-Leshem, R. (2019). Molecular functions of multi-SUMO-binding protein complexes. (Doctoral Dissertation). University of Manchester. Retrieved from https://www.research.manchester.ac.uk/portal/en/theses/molecular-functions-of-multisumobinding-protein-complexes(88e07f70-8262-49e5-a8e2-407623fd8664).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.820079

Chicago Manual of Style (16th Edition):

Salmi-Leshem, Rotem. “Molecular functions of multi-SUMO-binding protein complexes.” 2019. Doctoral Dissertation, University of Manchester. Accessed January 16, 2021. https://www.research.manchester.ac.uk/portal/en/theses/molecular-functions-of-multisumobinding-protein-complexes(88e07f70-8262-49e5-a8e2-407623fd8664).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.820079.

MLA Handbook (7th Edition):

Salmi-Leshem, Rotem. “Molecular functions of multi-SUMO-binding protein complexes.” 2019. Web. 16 Jan 2021.

Vancouver:

Salmi-Leshem R. Molecular functions of multi-SUMO-binding protein complexes. [Internet] [Doctoral dissertation]. University of Manchester; 2019. [cited 2021 Jan 16]. Available from: https://www.research.manchester.ac.uk/portal/en/theses/molecular-functions-of-multisumobinding-protein-complexes(88e07f70-8262-49e5-a8e2-407623fd8664).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.820079.

Council of Science Editors:

Salmi-Leshem R. Molecular functions of multi-SUMO-binding protein complexes. [Doctoral Dissertation]. University of Manchester; 2019. Available from: https://www.research.manchester.ac.uk/portal/en/theses/molecular-functions-of-multisumobinding-protein-complexes(88e07f70-8262-49e5-a8e2-407623fd8664).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.820079


University of Southern California

6. Reilly-Rhoten, Heather Noelle. Identification and characterization of post-translational modifications on histones: an on-line top-down mass spectrometry workflow for analysis using ProSight PTM.

Degree: MS, Biochemistry and Molecular Biology, 2012, University of Southern California

 The importance of histones for DNA management cannot be understated. From rearrangement to regulation of expression, histones act as the principle effectors of DNA availability… (more)

Subjects/Keywords: mass spectrometry; histones; post-translational modifications

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APA (6th Edition):

Reilly-Rhoten, H. N. (2012). Identification and characterization of post-translational modifications on histones: an on-line top-down mass spectrometry workflow for analysis using ProSight PTM. (Masters Thesis). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/8330/rec/3314

Chicago Manual of Style (16th Edition):

Reilly-Rhoten, Heather Noelle. “Identification and characterization of post-translational modifications on histones: an on-line top-down mass spectrometry workflow for analysis using ProSight PTM.” 2012. Masters Thesis, University of Southern California. Accessed January 16, 2021. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/8330/rec/3314.

MLA Handbook (7th Edition):

Reilly-Rhoten, Heather Noelle. “Identification and characterization of post-translational modifications on histones: an on-line top-down mass spectrometry workflow for analysis using ProSight PTM.” 2012. Web. 16 Jan 2021.

Vancouver:

Reilly-Rhoten HN. Identification and characterization of post-translational modifications on histones: an on-line top-down mass spectrometry workflow for analysis using ProSight PTM. [Internet] [Masters thesis]. University of Southern California; 2012. [cited 2021 Jan 16]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/8330/rec/3314.

Council of Science Editors:

Reilly-Rhoten HN. Identification and characterization of post-translational modifications on histones: an on-line top-down mass spectrometry workflow for analysis using ProSight PTM. [Masters Thesis]. University of Southern California; 2012. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/8330/rec/3314


University of Manchester

7. Salmi-Leshem, Rotem. Molecular Functions of Multi-SUMO-Binding Protein Complexes.

Degree: 2019, University of Manchester

 Gene expression is regulated in many ways, one of which is SUMOylation of transcription factors and associated complexes. This covalent modification by small ubiquitin-like modifier… (more)

Subjects/Keywords: Post-Translational Modifications; SUMO2/3; 5FMC complex

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APA (6th Edition):

Salmi-Leshem, R. (2019). Molecular Functions of Multi-SUMO-Binding Protein Complexes. (Doctoral Dissertation). University of Manchester. Retrieved from http://www.manchester.ac.uk/escholar/uk-ac-man-scw:322492

Chicago Manual of Style (16th Edition):

Salmi-Leshem, Rotem. “Molecular Functions of Multi-SUMO-Binding Protein Complexes.” 2019. Doctoral Dissertation, University of Manchester. Accessed January 16, 2021. http://www.manchester.ac.uk/escholar/uk-ac-man-scw:322492.

MLA Handbook (7th Edition):

Salmi-Leshem, Rotem. “Molecular Functions of Multi-SUMO-Binding Protein Complexes.” 2019. Web. 16 Jan 2021.

Vancouver:

Salmi-Leshem R. Molecular Functions of Multi-SUMO-Binding Protein Complexes. [Internet] [Doctoral dissertation]. University of Manchester; 2019. [cited 2021 Jan 16]. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:322492.

Council of Science Editors:

Salmi-Leshem R. Molecular Functions of Multi-SUMO-Binding Protein Complexes. [Doctoral Dissertation]. University of Manchester; 2019. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:322492


Universiteit Utrecht

8. Hollman, D.A.A. Transactivation versus transrepression in FXR: lessons learned from other Nuclear Receptors.

Degree: 2011, Universiteit Utrecht

 Farnesoid X Receptor (FXR) is an important player in the upregulation of genes (transactivation) in bile acid homeostasis and fat and glucose metabolism. Recently, it… (more)

Subjects/Keywords: Nuclear Receptors; Farnesoid X Receptor; Transactivation; Transrepression; Post-translational modifications

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APA (6th Edition):

Hollman, D. A. A. (2011). Transactivation versus transrepression in FXR: lessons learned from other Nuclear Receptors. (Masters Thesis). Universiteit Utrecht. Retrieved from http://dspace.library.uu.nl:8080/handle/1874/208274

Chicago Manual of Style (16th Edition):

Hollman, D A A. “Transactivation versus transrepression in FXR: lessons learned from other Nuclear Receptors.” 2011. Masters Thesis, Universiteit Utrecht. Accessed January 16, 2021. http://dspace.library.uu.nl:8080/handle/1874/208274.

MLA Handbook (7th Edition):

Hollman, D A A. “Transactivation versus transrepression in FXR: lessons learned from other Nuclear Receptors.” 2011. Web. 16 Jan 2021.

Vancouver:

Hollman DAA. Transactivation versus transrepression in FXR: lessons learned from other Nuclear Receptors. [Internet] [Masters thesis]. Universiteit Utrecht; 2011. [cited 2021 Jan 16]. Available from: http://dspace.library.uu.nl:8080/handle/1874/208274.

Council of Science Editors:

Hollman DAA. Transactivation versus transrepression in FXR: lessons learned from other Nuclear Receptors. [Masters Thesis]. Universiteit Utrecht; 2011. Available from: http://dspace.library.uu.nl:8080/handle/1874/208274


Vanderbilt University

9. Wenke, Jamie Lyn. Spatially-Resolved Proteomics of the Human Lens: Mapping Age- and Development-Related Lens Protein Modifications.

Degree: PhD, Biochemistry, 2016, Vanderbilt University

 The ocular lens is a transparent optical element that focuses light onto the retina for clear vision. The bulk of the lens is composed of… (more)

Subjects/Keywords: aging; proteomics; human lens; mass spectrometry; post-translational modifications

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APA (6th Edition):

Wenke, J. L. (2016). Spatially-Resolved Proteomics of the Human Lens: Mapping Age- and Development-Related Lens Protein Modifications. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://hdl.handle.net/1803/10430

Chicago Manual of Style (16th Edition):

Wenke, Jamie Lyn. “Spatially-Resolved Proteomics of the Human Lens: Mapping Age- and Development-Related Lens Protein Modifications.” 2016. Doctoral Dissertation, Vanderbilt University. Accessed January 16, 2021. http://hdl.handle.net/1803/10430.

MLA Handbook (7th Edition):

Wenke, Jamie Lyn. “Spatially-Resolved Proteomics of the Human Lens: Mapping Age- and Development-Related Lens Protein Modifications.” 2016. Web. 16 Jan 2021.

Vancouver:

Wenke JL. Spatially-Resolved Proteomics of the Human Lens: Mapping Age- and Development-Related Lens Protein Modifications. [Internet] [Doctoral dissertation]. Vanderbilt University; 2016. [cited 2021 Jan 16]. Available from: http://hdl.handle.net/1803/10430.

Council of Science Editors:

Wenke JL. Spatially-Resolved Proteomics of the Human Lens: Mapping Age- and Development-Related Lens Protein Modifications. [Doctoral Dissertation]. Vanderbilt University; 2016. Available from: http://hdl.handle.net/1803/10430

10. M. Restelli. ANALYSIS OF THE UPSTREAM SIGNALLING PATHWAY CONTROLLING DELTANP63ALPHA PROTEIN STABILITY AND FUNCTION.

Degree: 2014, Università degli Studi di Milano

 1. Abstract The p63 transcription factor, homolog to the p53 tumor suppressor, plays a crucial role in epidermal and limb development. Dominant mutations in the… (more)

Subjects/Keywords: p63; limb development; post-translational modifications; Settore BIO/11 - Biologia Molecolare

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APA (6th Edition):

Restelli, M. (2014). ANALYSIS OF THE UPSTREAM SIGNALLING PATHWAY CONTROLLING DELTANP63ALPHA PROTEIN STABILITY AND FUNCTION. (Thesis). Università degli Studi di Milano. Retrieved from http://hdl.handle.net/2434/238008

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):

Restelli, M.. “ANALYSIS OF THE UPSTREAM SIGNALLING PATHWAY CONTROLLING DELTANP63ALPHA PROTEIN STABILITY AND FUNCTION.” 2014. Thesis, Università degli Studi di Milano. Accessed January 16, 2021. http://hdl.handle.net/2434/238008.

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

MLA Handbook (7th Edition):

Restelli, M.. “ANALYSIS OF THE UPSTREAM SIGNALLING PATHWAY CONTROLLING DELTANP63ALPHA PROTEIN STABILITY AND FUNCTION.” 2014. Web. 16 Jan 2021.

Vancouver:

Restelli M. ANALYSIS OF THE UPSTREAM SIGNALLING PATHWAY CONTROLLING DELTANP63ALPHA PROTEIN STABILITY AND FUNCTION. [Internet] [Thesis]. Università degli Studi di Milano; 2014. [cited 2021 Jan 16]. Available from: http://hdl.handle.net/2434/238008.

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

Council of Science Editors:

Restelli M. ANALYSIS OF THE UPSTREAM SIGNALLING PATHWAY CONTROLLING DELTANP63ALPHA PROTEIN STABILITY AND FUNCTION. [Thesis]. Università degli Studi di Milano; 2014. Available from: http://hdl.handle.net/2434/238008

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


University of Guelph

11. Ahmed, Zaheer. The Regulation of Starch Biosynthesis in Barley (Hordeum vulgare).

Degree: PhD, Department of Molecular and Cellular Biology, 2014, University of Guelph

 Starch has enormous uses in the food and non-food industries in different forms. An important form of starch in the food industry is resistant starch… (more)

Subjects/Keywords: Starch; Resistant starch; Biosynthesis; Barley; Regulation; Post-translational modifications

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APA (6th Edition):

Ahmed, Z. (2014). The Regulation of Starch Biosynthesis in Barley (Hordeum vulgare). (Doctoral Dissertation). University of Guelph. Retrieved from https://atrium.lib.uoguelph.ca/xmlui/handle/10214/7789

Chicago Manual of Style (16th Edition):

Ahmed, Zaheer. “The Regulation of Starch Biosynthesis in Barley (Hordeum vulgare).” 2014. Doctoral Dissertation, University of Guelph. Accessed January 16, 2021. https://atrium.lib.uoguelph.ca/xmlui/handle/10214/7789.

MLA Handbook (7th Edition):

Ahmed, Zaheer. “The Regulation of Starch Biosynthesis in Barley (Hordeum vulgare).” 2014. Web. 16 Jan 2021.

Vancouver:

Ahmed Z. The Regulation of Starch Biosynthesis in Barley (Hordeum vulgare). [Internet] [Doctoral dissertation]. University of Guelph; 2014. [cited 2021 Jan 16]. Available from: https://atrium.lib.uoguelph.ca/xmlui/handle/10214/7789.

Council of Science Editors:

Ahmed Z. The Regulation of Starch Biosynthesis in Barley (Hordeum vulgare). [Doctoral Dissertation]. University of Guelph; 2014. Available from: https://atrium.lib.uoguelph.ca/xmlui/handle/10214/7789


Northeastern University

12. Ni, Wenqin. Advances in protein post-translational modifications (PTMS) using liquid chromatography-mass spectrometry.

Degree: PhD, Department of Chemistry and Chemical Biology, 2013, Northeastern University

 Protein post-translational modifications (PTMs) play significant roles in affecting the physical, chemical, and biological properties of proteins. PTMs can regulate protein functions by modulating protein… (more)

Subjects/Keywords: Protein post-translational modifications; Liquid chromatography; mass spectrometry; Chemistry

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APA (6th Edition):

Ni, W. (2013). Advances in protein post-translational modifications (PTMS) using liquid chromatography-mass spectrometry. (Doctoral Dissertation). Northeastern University. Retrieved from http://hdl.handle.net/2047/d20003037

Chicago Manual of Style (16th Edition):

Ni, Wenqin. “Advances in protein post-translational modifications (PTMS) using liquid chromatography-mass spectrometry.” 2013. Doctoral Dissertation, Northeastern University. Accessed January 16, 2021. http://hdl.handle.net/2047/d20003037.

MLA Handbook (7th Edition):

Ni, Wenqin. “Advances in protein post-translational modifications (PTMS) using liquid chromatography-mass spectrometry.” 2013. Web. 16 Jan 2021.

Vancouver:

Ni W. Advances in protein post-translational modifications (PTMS) using liquid chromatography-mass spectrometry. [Internet] [Doctoral dissertation]. Northeastern University; 2013. [cited 2021 Jan 16]. Available from: http://hdl.handle.net/2047/d20003037.

Council of Science Editors:

Ni W. Advances in protein post-translational modifications (PTMS) using liquid chromatography-mass spectrometry. [Doctoral Dissertation]. Northeastern University; 2013. Available from: http://hdl.handle.net/2047/d20003037


University of Washington

13. Shelton, Patrick Michael McPhee. Chemical Approaches to Investigate the Biochemical Crosstalk Between Histone Sumoylation, Methylation and Acetylation.

Degree: PhD, 2020, University of Washington

 Histone post-translational modifications (PTM) within chromatin control many DNA-templated cellular processes, from DNA damage repair pathways to gene transcription. In order to understand the influence… (more)

Subjects/Keywords: Chromatin; Enzymology; Post-translational modifications; Semisynthesis; Thioesterification; Chemistry; Chemistry

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APA (6th Edition):

Shelton, P. M. M. (2020). Chemical Approaches to Investigate the Biochemical Crosstalk Between Histone Sumoylation, Methylation and Acetylation. (Doctoral Dissertation). University of Washington. Retrieved from http://hdl.handle.net/1773/45137

Chicago Manual of Style (16th Edition):

Shelton, Patrick Michael McPhee. “Chemical Approaches to Investigate the Biochemical Crosstalk Between Histone Sumoylation, Methylation and Acetylation.” 2020. Doctoral Dissertation, University of Washington. Accessed January 16, 2021. http://hdl.handle.net/1773/45137.

MLA Handbook (7th Edition):

Shelton, Patrick Michael McPhee. “Chemical Approaches to Investigate the Biochemical Crosstalk Between Histone Sumoylation, Methylation and Acetylation.” 2020. Web. 16 Jan 2021.

Vancouver:

Shelton PMM. Chemical Approaches to Investigate the Biochemical Crosstalk Between Histone Sumoylation, Methylation and Acetylation. [Internet] [Doctoral dissertation]. University of Washington; 2020. [cited 2021 Jan 16]. Available from: http://hdl.handle.net/1773/45137.

Council of Science Editors:

Shelton PMM. Chemical Approaches to Investigate the Biochemical Crosstalk Between Histone Sumoylation, Methylation and Acetylation. [Doctoral Dissertation]. University of Washington; 2020. Available from: http://hdl.handle.net/1773/45137


Princeton University

14. Dann, Geoffrey Paul. Diverse Regulation of ISWI Family ATP-dependent Chromatin Remodeling Enzymes by Nucleosome Modifications .

Degree: PhD, 2017, Princeton University

 ATP-dependent chromatin remodelers regulate access to genetic information by controlling nucleosome positions in vivo. However, the mechanism by which remodelers discriminate between different nucleosome substrates… (more)

Subjects/Keywords: Chemical Biology; Chromatin Biology; Chromatin Remodeling; Epigenetics; Histones; Post-translational modifications

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APA (6th Edition):

Dann, G. P. (2017). Diverse Regulation of ISWI Family ATP-dependent Chromatin Remodeling Enzymes by Nucleosome Modifications . (Doctoral Dissertation). Princeton University. Retrieved from http://arks.princeton.edu/ark:/88435/dsp01j9602327k

Chicago Manual of Style (16th Edition):

Dann, Geoffrey Paul. “Diverse Regulation of ISWI Family ATP-dependent Chromatin Remodeling Enzymes by Nucleosome Modifications .” 2017. Doctoral Dissertation, Princeton University. Accessed January 16, 2021. http://arks.princeton.edu/ark:/88435/dsp01j9602327k.

MLA Handbook (7th Edition):

Dann, Geoffrey Paul. “Diverse Regulation of ISWI Family ATP-dependent Chromatin Remodeling Enzymes by Nucleosome Modifications .” 2017. Web. 16 Jan 2021.

Vancouver:

Dann GP. Diverse Regulation of ISWI Family ATP-dependent Chromatin Remodeling Enzymes by Nucleosome Modifications . [Internet] [Doctoral dissertation]. Princeton University; 2017. [cited 2021 Jan 16]. Available from: http://arks.princeton.edu/ark:/88435/dsp01j9602327k.

Council of Science Editors:

Dann GP. Diverse Regulation of ISWI Family ATP-dependent Chromatin Remodeling Enzymes by Nucleosome Modifications . [Doctoral Dissertation]. Princeton University; 2017. Available from: http://arks.princeton.edu/ark:/88435/dsp01j9602327k


University of Toronto

15. Kalkat, Manpreet. Characterizing Novel Regulators of MYC-dependent Tumorigenesis.

Degree: PhD, 2017, University of Toronto

The MYC oncogene has been the subject of intense study for over 30 years due its important role in tumorigenesis. MYC is a nuclear transcription… (more)

Subjects/Keywords: cancer; c-MYC; interactome; post-translational modifications; 0306

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APA (6th Edition):

Kalkat, M. (2017). Characterizing Novel Regulators of MYC-dependent Tumorigenesis. (Doctoral Dissertation). University of Toronto. Retrieved from http://hdl.handle.net/1807/91235

Chicago Manual of Style (16th Edition):

Kalkat, Manpreet. “Characterizing Novel Regulators of MYC-dependent Tumorigenesis.” 2017. Doctoral Dissertation, University of Toronto. Accessed January 16, 2021. http://hdl.handle.net/1807/91235.

MLA Handbook (7th Edition):

Kalkat, Manpreet. “Characterizing Novel Regulators of MYC-dependent Tumorigenesis.” 2017. Web. 16 Jan 2021.

Vancouver:

Kalkat M. Characterizing Novel Regulators of MYC-dependent Tumorigenesis. [Internet] [Doctoral dissertation]. University of Toronto; 2017. [cited 2021 Jan 16]. Available from: http://hdl.handle.net/1807/91235.

Council of Science Editors:

Kalkat M. Characterizing Novel Regulators of MYC-dependent Tumorigenesis. [Doctoral Dissertation]. University of Toronto; 2017. Available from: http://hdl.handle.net/1807/91235


University of Southern California

16. Zaro, Balyn Wood. Optimization of chemical reporters of O-GlcNAc for improved specificity and metabolic mapping.

Degree: PhD, Chemistry, 2014, University of Southern California

Post-translational modifications (PTMs) are ancillary decorations that are transferred onto fully-synthesized proteins. These modifications have been shown to significantly alter the fate and function of… (more)

Subjects/Keywords: O-GlcNAc; carbohydrates; chemical reporters; click chemistry; acetylation; post-translational modifications

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APA (6th Edition):

Zaro, B. W. (2014). Optimization of chemical reporters of O-GlcNAc for improved specificity and metabolic mapping. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/476825/rec/4611

Chicago Manual of Style (16th Edition):

Zaro, Balyn Wood. “Optimization of chemical reporters of O-GlcNAc for improved specificity and metabolic mapping.” 2014. Doctoral Dissertation, University of Southern California. Accessed January 16, 2021. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/476825/rec/4611.

MLA Handbook (7th Edition):

Zaro, Balyn Wood. “Optimization of chemical reporters of O-GlcNAc for improved specificity and metabolic mapping.” 2014. Web. 16 Jan 2021.

Vancouver:

Zaro BW. Optimization of chemical reporters of O-GlcNAc for improved specificity and metabolic mapping. [Internet] [Doctoral dissertation]. University of Southern California; 2014. [cited 2021 Jan 16]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/476825/rec/4611.

Council of Science Editors:

Zaro BW. Optimization of chemical reporters of O-GlcNAc for improved specificity and metabolic mapping. [Doctoral Dissertation]. University of Southern California; 2014. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/476825/rec/4611


Brigham Young University

17. Bursey, Devan. Ribosomally Synthesized and Post-Translationally Modified Peptides as Potential Scaffolds for Peptide Engineering.

Degree: MS, 2019, Brigham Young University

  Peptides are small proteins that are crucial in many biological pathways such as antimicrobial defense, hormone signaling, and virulence. They often exhibit tight specificity… (more)

Subjects/Keywords: peptide engineering; post-translational modifications; thiazole; lasso peptides; thiopeptides

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APA (6th Edition):

Bursey, D. (2019). Ribosomally Synthesized and Post-Translationally Modified Peptides as Potential Scaffolds for Peptide Engineering. (Masters Thesis). Brigham Young University. Retrieved from https://scholarsarchive.byu.edu/cgi/viewcontent.cgi?article=9124&context=etd

Chicago Manual of Style (16th Edition):

Bursey, Devan. “Ribosomally Synthesized and Post-Translationally Modified Peptides as Potential Scaffolds for Peptide Engineering.” 2019. Masters Thesis, Brigham Young University. Accessed January 16, 2021. https://scholarsarchive.byu.edu/cgi/viewcontent.cgi?article=9124&context=etd.

MLA Handbook (7th Edition):

Bursey, Devan. “Ribosomally Synthesized and Post-Translationally Modified Peptides as Potential Scaffolds for Peptide Engineering.” 2019. Web. 16 Jan 2021.

Vancouver:

Bursey D. Ribosomally Synthesized and Post-Translationally Modified Peptides as Potential Scaffolds for Peptide Engineering. [Internet] [Masters thesis]. Brigham Young University; 2019. [cited 2021 Jan 16]. Available from: https://scholarsarchive.byu.edu/cgi/viewcontent.cgi?article=9124&context=etd.

Council of Science Editors:

Bursey D. Ribosomally Synthesized and Post-Translationally Modified Peptides as Potential Scaffolds for Peptide Engineering. [Masters Thesis]. Brigham Young University; 2019. Available from: https://scholarsarchive.byu.edu/cgi/viewcontent.cgi?article=9124&context=etd


University of Manchester

18. Fowler, Nicholas. Investigating the role of electrostatic interactions in modulating protein function.

Degree: PhD, 2018, University of Manchester

 The work in this thesis centres on understanding how electrostatic interactions modulate the function of proteins. A computational method is presented to predict the reduction… (more)

Subjects/Keywords: 540; Protein electrostatics; Copper proteins; Post-translational modifications

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APA (6th Edition):

Fowler, N. (2018). Investigating the role of electrostatic interactions in modulating protein function. (Doctoral Dissertation). University of Manchester. Retrieved from https://www.research.manchester.ac.uk/portal/en/theses/investigating-the-role-of-electrostatic-interactions-in-modulating-protein-function(fef940ff-46f3-46cc-82d9-2fcab7704479).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.791145

Chicago Manual of Style (16th Edition):

Fowler, Nicholas. “Investigating the role of electrostatic interactions in modulating protein function.” 2018. Doctoral Dissertation, University of Manchester. Accessed January 16, 2021. https://www.research.manchester.ac.uk/portal/en/theses/investigating-the-role-of-electrostatic-interactions-in-modulating-protein-function(fef940ff-46f3-46cc-82d9-2fcab7704479).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.791145.

MLA Handbook (7th Edition):

Fowler, Nicholas. “Investigating the role of electrostatic interactions in modulating protein function.” 2018. Web. 16 Jan 2021.

Vancouver:

Fowler N. Investigating the role of electrostatic interactions in modulating protein function. [Internet] [Doctoral dissertation]. University of Manchester; 2018. [cited 2021 Jan 16]. Available from: https://www.research.manchester.ac.uk/portal/en/theses/investigating-the-role-of-electrostatic-interactions-in-modulating-protein-function(fef940ff-46f3-46cc-82d9-2fcab7704479).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.791145.

Council of Science Editors:

Fowler N. Investigating the role of electrostatic interactions in modulating protein function. [Doctoral Dissertation]. University of Manchester; 2018. Available from: https://www.research.manchester.ac.uk/portal/en/theses/investigating-the-role-of-electrostatic-interactions-in-modulating-protein-function(fef940ff-46f3-46cc-82d9-2fcab7704479).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.791145


University of Georgia

19. Stuart, Ryan Patrick. Establishing genotype-phenotype relationships in POMGnT1 associated with congenital muscular dystrophy.

Degree: 2014, University of Georgia

 Protein O-linked-mannose beta-1,2-N-acetylglucosaminyltransferase1 (POMGnT1) is an influential glycosyltransferase required for modifying α-dystroglycan. Mutations in POMGnT1, removing GlcNAc modifications, have been associated with muscle-eye-brain (MEB) disease,… (more)

Subjects/Keywords: POMGnT1; post-translational modifications; α-DG; congenital muscular dystrophy

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APA (6th Edition):

Stuart, R. P. (2014). Establishing genotype-phenotype relationships in POMGnT1 associated with congenital muscular dystrophy. (Thesis). University of Georgia. Retrieved from http://hdl.handle.net/10724/29661

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):

Stuart, Ryan Patrick. “Establishing genotype-phenotype relationships in POMGnT1 associated with congenital muscular dystrophy.” 2014. Thesis, University of Georgia. Accessed January 16, 2021. http://hdl.handle.net/10724/29661.

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

MLA Handbook (7th Edition):

Stuart, Ryan Patrick. “Establishing genotype-phenotype relationships in POMGnT1 associated with congenital muscular dystrophy.” 2014. Web. 16 Jan 2021.

Vancouver:

Stuart RP. Establishing genotype-phenotype relationships in POMGnT1 associated with congenital muscular dystrophy. [Internet] [Thesis]. University of Georgia; 2014. [cited 2021 Jan 16]. Available from: http://hdl.handle.net/10724/29661.

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

Council of Science Editors:

Stuart RP. Establishing genotype-phenotype relationships in POMGnT1 associated with congenital muscular dystrophy. [Thesis]. University of Georgia; 2014. Available from: http://hdl.handle.net/10724/29661

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


University of Sydney

20. Hsieh, Yves Shang-Yi. Chemical Synthesis of Peptides & Proteins with Post-Translational Modifications .

Degree: 2013, University of Sydney

 This thesis describes efforts aimed at the synthesis of peptides and proteins bearing homogeneous carbohydrate and sulfate modifications for interrogation of the structural and functional… (more)

Subjects/Keywords: protein; peptide; post-translational modifications; glycosylation; sulfation; solid-phase peptide synthesis

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APA (6th Edition):

Hsieh, Y. S. (2013). Chemical Synthesis of Peptides & Proteins with Post-Translational Modifications . (Thesis). University of Sydney. Retrieved from http://hdl.handle.net/2123/9422

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):

Hsieh, Yves Shang-Yi. “Chemical Synthesis of Peptides & Proteins with Post-Translational Modifications .” 2013. Thesis, University of Sydney. Accessed January 16, 2021. http://hdl.handle.net/2123/9422.

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

MLA Handbook (7th Edition):

Hsieh, Yves Shang-Yi. “Chemical Synthesis of Peptides & Proteins with Post-Translational Modifications .” 2013. Web. 16 Jan 2021.

Vancouver:

Hsieh YS. Chemical Synthesis of Peptides & Proteins with Post-Translational Modifications . [Internet] [Thesis]. University of Sydney; 2013. [cited 2021 Jan 16]. Available from: http://hdl.handle.net/2123/9422.

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

Council of Science Editors:

Hsieh YS. Chemical Synthesis of Peptides & Proteins with Post-Translational Modifications . [Thesis]. University of Sydney; 2013. Available from: http://hdl.handle.net/2123/9422

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


University of New South Wales

21. Winter, Daniel. From top to bottom: the methylproteome at the systems and molecular levels.

Degree: Biotechnology & Biomolecular Sciences, 2018, University of New South Wales

 In recent years, research into the methylproteome (the subset of the proteome that is post-translationally methylated) has gained traction, with the report of novel protein… (more)

Subjects/Keywords: Mass spectrometry; Proteomics; Methylation; FAIMS; Post-translational modifications

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APA (6th Edition):

Winter, D. (2018). From top to bottom: the methylproteome at the systems and molecular levels. (Doctoral Dissertation). University of New South Wales. Retrieved from http://handle.unsw.edu.au/1959.4/60225 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:51258/SOURCE2?view=true

Chicago Manual of Style (16th Edition):

Winter, Daniel. “From top to bottom: the methylproteome at the systems and molecular levels.” 2018. Doctoral Dissertation, University of New South Wales. Accessed January 16, 2021. http://handle.unsw.edu.au/1959.4/60225 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:51258/SOURCE2?view=true.

MLA Handbook (7th Edition):

Winter, Daniel. “From top to bottom: the methylproteome at the systems and molecular levels.” 2018. Web. 16 Jan 2021.

Vancouver:

Winter D. From top to bottom: the methylproteome at the systems and molecular levels. [Internet] [Doctoral dissertation]. University of New South Wales; 2018. [cited 2021 Jan 16]. Available from: http://handle.unsw.edu.au/1959.4/60225 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:51258/SOURCE2?view=true.

Council of Science Editors:

Winter D. From top to bottom: the methylproteome at the systems and molecular levels. [Doctoral Dissertation]. University of New South Wales; 2018. Available from: http://handle.unsw.edu.au/1959.4/60225 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:51258/SOURCE2?view=true


The Ohio State University

22. Beasley, Miranda L. Developing a Model System to Probe Biological Mechanisms of Post-Translational Modifications that Destabilize the Nucleosome.

Degree: MS, Biochemistry, 2014, The Ohio State University

 To develop a model system to probe biological cellular processes, we synthesized histones with four modifications along the histone-DNA interface: acetylation of lysines 115 and… (more)

Subjects/Keywords: Biochemistry; Histones; post-translational modifications; nucleosomes; retrovrial integration; prototype foamy virus

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APA (6th Edition):

Beasley, M. L. (2014). Developing a Model System to Probe Biological Mechanisms of Post-Translational Modifications that Destabilize the Nucleosome. (Masters Thesis). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1408961013

Chicago Manual of Style (16th Edition):

Beasley, Miranda L. “Developing a Model System to Probe Biological Mechanisms of Post-Translational Modifications that Destabilize the Nucleosome.” 2014. Masters Thesis, The Ohio State University. Accessed January 16, 2021. http://rave.ohiolink.edu/etdc/view?acc_num=osu1408961013.

MLA Handbook (7th Edition):

Beasley, Miranda L. “Developing a Model System to Probe Biological Mechanisms of Post-Translational Modifications that Destabilize the Nucleosome.” 2014. Web. 16 Jan 2021.

Vancouver:

Beasley ML. Developing a Model System to Probe Biological Mechanisms of Post-Translational Modifications that Destabilize the Nucleosome. [Internet] [Masters thesis]. The Ohio State University; 2014. [cited 2021 Jan 16]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1408961013.

Council of Science Editors:

Beasley ML. Developing a Model System to Probe Biological Mechanisms of Post-Translational Modifications that Destabilize the Nucleosome. [Masters Thesis]. The Ohio State University; 2014. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1408961013

23. Sebti, Salwa. Rôle de la protéine BAT3 dans la signalisation cellulaire de l'autophagie : Role of BAT3 in autophagy signaling.

Degree: Docteur es, Biologie Santé, 2013, Université Montpellier I

L'autophagie est un processus d'autodigestion qui se produit dans toutes les cellules eucaryotes et conduit à la dégradation d'éléments du cytoplasme (organites, macromolécules) par le… (more)

Subjects/Keywords: Autophagie; Régulation post-traductionnelle; Signalisation cellulaire; Cancer; Autophagy; Post-translational modifications; Signaling pathways; Cancer

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APA (6th Edition):

Sebti, S. (2013). Rôle de la protéine BAT3 dans la signalisation cellulaire de l'autophagie : Role of BAT3 in autophagy signaling. (Doctoral Dissertation). Université Montpellier I. Retrieved from http://www.theses.fr/2013MON1T028

Chicago Manual of Style (16th Edition):

Sebti, Salwa. “Rôle de la protéine BAT3 dans la signalisation cellulaire de l'autophagie : Role of BAT3 in autophagy signaling.” 2013. Doctoral Dissertation, Université Montpellier I. Accessed January 16, 2021. http://www.theses.fr/2013MON1T028.

MLA Handbook (7th Edition):

Sebti, Salwa. “Rôle de la protéine BAT3 dans la signalisation cellulaire de l'autophagie : Role of BAT3 in autophagy signaling.” 2013. Web. 16 Jan 2021.

Vancouver:

Sebti S. Rôle de la protéine BAT3 dans la signalisation cellulaire de l'autophagie : Role of BAT3 in autophagy signaling. [Internet] [Doctoral dissertation]. Université Montpellier I; 2013. [cited 2021 Jan 16]. Available from: http://www.theses.fr/2013MON1T028.

Council of Science Editors:

Sebti S. Rôle de la protéine BAT3 dans la signalisation cellulaire de l'autophagie : Role of BAT3 in autophagy signaling. [Doctoral Dissertation]. Université Montpellier I; 2013. Available from: http://www.theses.fr/2013MON1T028


Universitat Pompeu Fabra

24. Martínez Cebrián, Gerard, 1992-. Identification of novel histone marks required for the transcriptional stress response.

Degree: Departament de Ciències Experimentals i de la Salut, 2019, Universitat Pompeu Fabra

 Durant estressos ambientals, com ara fluctuacions de temperatura o augment de l'osmolaritat, el llevat Saccharomyces cerevisiae indueix una reprogramació transcripcional per sobreviure i adaptar-se a… (more)

Subjects/Keywords: Histones; Transcription; Stress; Kinases; Histones; Transcripció; Estrès; Modificacions post-traduccionals; Post-translational modifications; Quinases; 577

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APA (6th Edition):

Martínez Cebrián, Gerard, 1. (2019). Identification of novel histone marks required for the transcriptional stress response. (Thesis). Universitat Pompeu Fabra. Retrieved from http://hdl.handle.net/10803/668153

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):

Martínez Cebrián, Gerard, 1992-. “Identification of novel histone marks required for the transcriptional stress response.” 2019. Thesis, Universitat Pompeu Fabra. Accessed January 16, 2021. http://hdl.handle.net/10803/668153.

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

MLA Handbook (7th Edition):

Martínez Cebrián, Gerard, 1992-. “Identification of novel histone marks required for the transcriptional stress response.” 2019. Web. 16 Jan 2021.

Vancouver:

Martínez Cebrián, Gerard 1. Identification of novel histone marks required for the transcriptional stress response. [Internet] [Thesis]. Universitat Pompeu Fabra; 2019. [cited 2021 Jan 16]. Available from: http://hdl.handle.net/10803/668153.

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

Council of Science Editors:

Martínez Cebrián, Gerard 1. Identification of novel histone marks required for the transcriptional stress response. [Thesis]. Universitat Pompeu Fabra; 2019. Available from: http://hdl.handle.net/10803/668153

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


Université Paris-Sud – Paris XI

25. Laligné, Chloé. Étude de la fonction de la protéine Bug22p dans différents organismes : Study of Bug22p protein in different organisms.

Degree: Docteur es, Biologie cellulaire et moléculaire, 2011, Université Paris-Sud – Paris XI

 Les cils sont des organites très conservés au cours de l’évolution des eucaryotes et présents à la surface de presque tous les types cellulaires. Ils… (more)

Subjects/Keywords: Cils; Battement ciliaire; Modifications post-traductionnelles; GTL3; Bug22; Cilia; Ciliary beating; Post-translational modifications; GTL3; Bug22

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APA (6th Edition):

Laligné, C. (2011). Étude de la fonction de la protéine Bug22p dans différents organismes : Study of Bug22p protein in different organisms. (Doctoral Dissertation). Université Paris-Sud – Paris XI. Retrieved from http://www.theses.fr/2011PA112170

Chicago Manual of Style (16th Edition):

Laligné, Chloé. “Étude de la fonction de la protéine Bug22p dans différents organismes : Study of Bug22p protein in different organisms.” 2011. Doctoral Dissertation, Université Paris-Sud – Paris XI. Accessed January 16, 2021. http://www.theses.fr/2011PA112170.

MLA Handbook (7th Edition):

Laligné, Chloé. “Étude de la fonction de la protéine Bug22p dans différents organismes : Study of Bug22p protein in different organisms.” 2011. Web. 16 Jan 2021.

Vancouver:

Laligné C. Étude de la fonction de la protéine Bug22p dans différents organismes : Study of Bug22p protein in different organisms. [Internet] [Doctoral dissertation]. Université Paris-Sud – Paris XI; 2011. [cited 2021 Jan 16]. Available from: http://www.theses.fr/2011PA112170.

Council of Science Editors:

Laligné C. Étude de la fonction de la protéine Bug22p dans différents organismes : Study of Bug22p protein in different organisms. [Doctoral Dissertation]. Université Paris-Sud – Paris XI; 2011. Available from: http://www.theses.fr/2011PA112170


Université de Lorraine

26. Wilhelm, Dafné. Utilisation du modèle cellulaire ATDC5 pour la caractérisation des mécanismes de maturation des procollagènes et de leurs relations avec le processus de minéralisation matricielle : Use of the ATDC5 cellular model for the characterization of the mechanisms of procollagen maturation and their relationship with the matrix mineralization process.

Degree: Docteur es, Sciences de la vie et de la santé, 2019, Université de Lorraine

L'ossification endochondrale est le mécanisme par lequel les os longs se développent chez les Vertébrés. Elle nécessite la formation d'un patron cartilagineux primaire par chondrogenèse,… (more)

Subjects/Keywords: ATDC5; Modifications post-traductionnelles; Procollagènes; Spectrométrie de masse; ATModificationsDC5; Post-translational modifications; Procollagens; Mass spectrometry; 573.76

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APA (6th Edition):

Wilhelm, D. (2019). Utilisation du modèle cellulaire ATDC5 pour la caractérisation des mécanismes de maturation des procollagènes et de leurs relations avec le processus de minéralisation matricielle : Use of the ATDC5 cellular model for the characterization of the mechanisms of procollagen maturation and their relationship with the matrix mineralization process. (Doctoral Dissertation). Université de Lorraine. Retrieved from http://www.theses.fr/2019LORR0286

Chicago Manual of Style (16th Edition):

Wilhelm, Dafné. “Utilisation du modèle cellulaire ATDC5 pour la caractérisation des mécanismes de maturation des procollagènes et de leurs relations avec le processus de minéralisation matricielle : Use of the ATDC5 cellular model for the characterization of the mechanisms of procollagen maturation and their relationship with the matrix mineralization process.” 2019. Doctoral Dissertation, Université de Lorraine. Accessed January 16, 2021. http://www.theses.fr/2019LORR0286.

MLA Handbook (7th Edition):

Wilhelm, Dafné. “Utilisation du modèle cellulaire ATDC5 pour la caractérisation des mécanismes de maturation des procollagènes et de leurs relations avec le processus de minéralisation matricielle : Use of the ATDC5 cellular model for the characterization of the mechanisms of procollagen maturation and their relationship with the matrix mineralization process.” 2019. Web. 16 Jan 2021.

Vancouver:

Wilhelm D. Utilisation du modèle cellulaire ATDC5 pour la caractérisation des mécanismes de maturation des procollagènes et de leurs relations avec le processus de minéralisation matricielle : Use of the ATDC5 cellular model for the characterization of the mechanisms of procollagen maturation and their relationship with the matrix mineralization process. [Internet] [Doctoral dissertation]. Université de Lorraine; 2019. [cited 2021 Jan 16]. Available from: http://www.theses.fr/2019LORR0286.

Council of Science Editors:

Wilhelm D. Utilisation du modèle cellulaire ATDC5 pour la caractérisation des mécanismes de maturation des procollagènes et de leurs relations avec le processus de minéralisation matricielle : Use of the ATDC5 cellular model for the characterization of the mechanisms of procollagen maturation and their relationship with the matrix mineralization process. [Doctoral Dissertation]. Université de Lorraine; 2019. Available from: http://www.theses.fr/2019LORR0286

27. Rentier, Cédric. Maladies auto-immunes : conception, synthèse et screening immunologique de peptides porteurs de modifications post-traductionnelles pour la caractérisation d'autoanticorps dans les sérums de patients : Autoimmune diseases : design, synthesis and immunological screening of post-translationally modified peptides to characterize autoantibodies in patients' sera.

Degree: Docteur es, Chimie - Cergy, 2015, Cergy-Pontoise; Università degli studi (Florence, Italie)

Ces travaux de recherche visent à mettre au point par une nouvelle « Approche Chimique Inverse » des antigènes synthétiques pour le diagnostic de maladies… (more)

Subjects/Keywords: Maladies auto-immunes; Modifications post-Traductionnelles; Autoanticorps; Proteines; Peptides; Autoimmune diseases; Post-Translational modifications; Autoantibodies; Proteins; Peptides

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APA (6th Edition):

Rentier, C. (2015). Maladies auto-immunes : conception, synthèse et screening immunologique de peptides porteurs de modifications post-traductionnelles pour la caractérisation d'autoanticorps dans les sérums de patients : Autoimmune diseases : design, synthesis and immunological screening of post-translationally modified peptides to characterize autoantibodies in patients' sera. (Doctoral Dissertation). Cergy-Pontoise; Università degli studi (Florence, Italie). Retrieved from http://www.theses.fr/2015CERG0746

Chicago Manual of Style (16th Edition):

Rentier, Cédric. “Maladies auto-immunes : conception, synthèse et screening immunologique de peptides porteurs de modifications post-traductionnelles pour la caractérisation d'autoanticorps dans les sérums de patients : Autoimmune diseases : design, synthesis and immunological screening of post-translationally modified peptides to characterize autoantibodies in patients' sera.” 2015. Doctoral Dissertation, Cergy-Pontoise; Università degli studi (Florence, Italie). Accessed January 16, 2021. http://www.theses.fr/2015CERG0746.

MLA Handbook (7th Edition):

Rentier, Cédric. “Maladies auto-immunes : conception, synthèse et screening immunologique de peptides porteurs de modifications post-traductionnelles pour la caractérisation d'autoanticorps dans les sérums de patients : Autoimmune diseases : design, synthesis and immunological screening of post-translationally modified peptides to characterize autoantibodies in patients' sera.” 2015. Web. 16 Jan 2021.

Vancouver:

Rentier C. Maladies auto-immunes : conception, synthèse et screening immunologique de peptides porteurs de modifications post-traductionnelles pour la caractérisation d'autoanticorps dans les sérums de patients : Autoimmune diseases : design, synthesis and immunological screening of post-translationally modified peptides to characterize autoantibodies in patients' sera. [Internet] [Doctoral dissertation]. Cergy-Pontoise; Università degli studi (Florence, Italie); 2015. [cited 2021 Jan 16]. Available from: http://www.theses.fr/2015CERG0746.

Council of Science Editors:

Rentier C. Maladies auto-immunes : conception, synthèse et screening immunologique de peptides porteurs de modifications post-traductionnelles pour la caractérisation d'autoanticorps dans les sérums de patients : Autoimmune diseases : design, synthesis and immunological screening of post-translationally modified peptides to characterize autoantibodies in patients' sera. [Doctoral Dissertation]. Cergy-Pontoise; Università degli studi (Florence, Italie); 2015. Available from: http://www.theses.fr/2015CERG0746

28. Gaviard, Charlotte. L'Effet " Modifications Post-Traductionnelles" : petits groupements chimiques, grandes conséquences? Caractérisation de protéines modifiées chez Pseudomonas aeruginosa PA14 par analyse protéomique. : "Post-translational modifications" effect : small chemical groups, influencial consequences? Characterization of modified proteins in Pseudomonas aeruginosa PA14 by proteomic analysis.

Degree: Docteur es, Chimie, 2018, Normandie

Pseudomonas aeruginosa PA14 est une bactérie pathogène très résistante aux antibiotiques et impliquée dans de nombreuses infections nosocomiales. Toutefois, la disponibilité d'agents antibactériens efficaces contre… (more)

Subjects/Keywords: Pseudomonas aeruginosa; Modifications post-traductionnelles; Protéomique; Acylation de la lysine; Phosphorylation; Pseudomonas aeruginosa; Post-translational modifications; Proteomic; Lysine acylation; Phosphorylation; 572.6

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

APA (6th Edition):

Gaviard, C. (2018). L'Effet " Modifications Post-Traductionnelles" : petits groupements chimiques, grandes conséquences? Caractérisation de protéines modifiées chez Pseudomonas aeruginosa PA14 par analyse protéomique. : "Post-translational modifications" effect : small chemical groups, influencial consequences? Characterization of modified proteins in Pseudomonas aeruginosa PA14 by proteomic analysis. (Doctoral Dissertation). Normandie. Retrieved from http://www.theses.fr/2018NORMR094

Chicago Manual of Style (16th Edition):

Gaviard, Charlotte. “L'Effet " Modifications Post-Traductionnelles" : petits groupements chimiques, grandes conséquences? Caractérisation de protéines modifiées chez Pseudomonas aeruginosa PA14 par analyse protéomique. : "Post-translational modifications" effect : small chemical groups, influencial consequences? Characterization of modified proteins in Pseudomonas aeruginosa PA14 by proteomic analysis.” 2018. Doctoral Dissertation, Normandie. Accessed January 16, 2021. http://www.theses.fr/2018NORMR094.

MLA Handbook (7th Edition):

Gaviard, Charlotte. “L'Effet " Modifications Post-Traductionnelles" : petits groupements chimiques, grandes conséquences? Caractérisation de protéines modifiées chez Pseudomonas aeruginosa PA14 par analyse protéomique. : "Post-translational modifications" effect : small chemical groups, influencial consequences? Characterization of modified proteins in Pseudomonas aeruginosa PA14 by proteomic analysis.” 2018. Web. 16 Jan 2021.

Vancouver:

Gaviard C. L'Effet " Modifications Post-Traductionnelles" : petits groupements chimiques, grandes conséquences? Caractérisation de protéines modifiées chez Pseudomonas aeruginosa PA14 par analyse protéomique. : "Post-translational modifications" effect : small chemical groups, influencial consequences? Characterization of modified proteins in Pseudomonas aeruginosa PA14 by proteomic analysis. [Internet] [Doctoral dissertation]. Normandie; 2018. [cited 2021 Jan 16]. Available from: http://www.theses.fr/2018NORMR094.

Council of Science Editors:

Gaviard C. L'Effet " Modifications Post-Traductionnelles" : petits groupements chimiques, grandes conséquences? Caractérisation de protéines modifiées chez Pseudomonas aeruginosa PA14 par analyse protéomique. : "Post-translational modifications" effect : small chemical groups, influencial consequences? Characterization of modified proteins in Pseudomonas aeruginosa PA14 by proteomic analysis. [Doctoral Dissertation]. Normandie; 2018. Available from: http://www.theses.fr/2018NORMR094


UCLA

29. Dzialo, Maria Charlene. Found in Translation: The Search for Functional Roles of Translation Elongation Factor Methylation and the Discovery of a Novel Type of Protein Methylation.

Degree: Biochemistry & Molecular Biology, 2015, UCLA

 Methylation has emerged as an essential modification of small molecules, lipids, nucleic acids, and proteins. Given the variety of potential substrates, the effects the addition… (more)

Subjects/Keywords: Biochemistry; Molecular biology; Lysine methylation; Methylation; Methyltransferases; Post-translational modifications; Protein; Saccharomyces cerevisiae

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

APA (6th Edition):

Dzialo, M. C. (2015). Found in Translation: The Search for Functional Roles of Translation Elongation Factor Methylation and the Discovery of a Novel Type of Protein Methylation. (Thesis). UCLA. Retrieved from http://www.escholarship.org/uc/item/0w7998h0

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):

Dzialo, Maria Charlene. “Found in Translation: The Search for Functional Roles of Translation Elongation Factor Methylation and the Discovery of a Novel Type of Protein Methylation.” 2015. Thesis, UCLA. Accessed January 16, 2021. http://www.escholarship.org/uc/item/0w7998h0.

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

MLA Handbook (7th Edition):

Dzialo, Maria Charlene. “Found in Translation: The Search for Functional Roles of Translation Elongation Factor Methylation and the Discovery of a Novel Type of Protein Methylation.” 2015. Web. 16 Jan 2021.

Vancouver:

Dzialo MC. Found in Translation: The Search for Functional Roles of Translation Elongation Factor Methylation and the Discovery of a Novel Type of Protein Methylation. [Internet] [Thesis]. UCLA; 2015. [cited 2021 Jan 16]. Available from: http://www.escholarship.org/uc/item/0w7998h0.

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

Council of Science Editors:

Dzialo MC. Found in Translation: The Search for Functional Roles of Translation Elongation Factor Methylation and the Discovery of a Novel Type of Protein Methylation. [Thesis]. UCLA; 2015. Available from: http://www.escholarship.org/uc/item/0w7998h0

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


Cornell University

30. Negron Abril, Yashira Liz. TUMOR PROMOTING FUNCTIONS FOR THE METABOLIC REGULATOR SIRT5.

Degree: PhD, Chemistry and Chemical Biology, 2018, Cornell University

 Cancer is among the leading causes of death worldwide, highlighting the urgent need for identification of new targets and the development of new strategies to… (more)

Subjects/Keywords: Mice; Post-translational modifications; SIRT5; Sirtuins; Small molecules; Biology; Molecular biology; Chemistry; cancer

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

APA (6th Edition):

Negron Abril, Y. L. (2018). TUMOR PROMOTING FUNCTIONS FOR THE METABOLIC REGULATOR SIRT5. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/59440

Chicago Manual of Style (16th Edition):

Negron Abril, Yashira Liz. “TUMOR PROMOTING FUNCTIONS FOR THE METABOLIC REGULATOR SIRT5.” 2018. Doctoral Dissertation, Cornell University. Accessed January 16, 2021. http://hdl.handle.net/1813/59440.

MLA Handbook (7th Edition):

Negron Abril, Yashira Liz. “TUMOR PROMOTING FUNCTIONS FOR THE METABOLIC REGULATOR SIRT5.” 2018. Web. 16 Jan 2021.

Vancouver:

Negron Abril YL. TUMOR PROMOTING FUNCTIONS FOR THE METABOLIC REGULATOR SIRT5. [Internet] [Doctoral dissertation]. Cornell University; 2018. [cited 2021 Jan 16]. Available from: http://hdl.handle.net/1813/59440.

Council of Science Editors:

Negron Abril YL. TUMOR PROMOTING FUNCTIONS FOR THE METABOLIC REGULATOR SIRT5. [Doctoral Dissertation]. Cornell University; 2018. Available from: http://hdl.handle.net/1813/59440

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