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You searched for subject:(protein arginine methyltransferase). Showing records 1 – 18 of 18 total matches.

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1. Stouth, Derek W. Protein Arginine Methyltransferase Expression, Localization, and Activity During Disuse-induced Skeletal Muscle Plasticity.

Degree: MSc, 2016, McMaster University

PRMT biology during skeletal muscle disuse.

Protein arginine methyltransferase 1 (PRMT1), PRMT4 (also known as co-activator-associated arginine methyltransferase 1; CARM1), and PRMT5 are critical components… (more)

Subjects/Keywords: PRMT; skeletal muscle plasticity; atrophy; Protein Arginine Methyltransferase; disuse

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APA (6th Edition):

Stouth, D. W. (2016). Protein Arginine Methyltransferase Expression, Localization, and Activity During Disuse-induced Skeletal Muscle Plasticity. (Masters Thesis). McMaster University. Retrieved from http://hdl.handle.net/11375/20740

Chicago Manual of Style (16th Edition):

Stouth, Derek W. “Protein Arginine Methyltransferase Expression, Localization, and Activity During Disuse-induced Skeletal Muscle Plasticity.” 2016. Masters Thesis, McMaster University. Accessed January 26, 2020. http://hdl.handle.net/11375/20740.

MLA Handbook (7th Edition):

Stouth, Derek W. “Protein Arginine Methyltransferase Expression, Localization, and Activity During Disuse-induced Skeletal Muscle Plasticity.” 2016. Web. 26 Jan 2020.

Vancouver:

Stouth DW. Protein Arginine Methyltransferase Expression, Localization, and Activity During Disuse-induced Skeletal Muscle Plasticity. [Internet] [Masters thesis]. McMaster University; 2016. [cited 2020 Jan 26]. Available from: http://hdl.handle.net/11375/20740.

Council of Science Editors:

Stouth DW. Protein Arginine Methyltransferase Expression, Localization, and Activity During Disuse-induced Skeletal Muscle Plasticity. [Masters Thesis]. McMaster University; 2016. Available from: http://hdl.handle.net/11375/20740


McMaster University

2. Shen, Nicole. CHARACTERIZING PROTEIN ARGININE METHYLTRANSFERASE EXPRESSION AND ACTIVITY DURING MYOGENESIS.

Degree: MSc, 2017, McMaster University

Despite the emerging importance of protein arginine methyltransferases (PRMTs) in regulating skeletal muscle plasticity, the biology of these enzymes during muscle development remains poorly understood.… (more)

Subjects/Keywords: Protein arginine methyltransferase; skeletal muscle; myogenesis; PGC-1α; mitochondria

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APA (6th Edition):

Shen, N. (2017). CHARACTERIZING PROTEIN ARGININE METHYLTRANSFERASE EXPRESSION AND ACTIVITY DURING MYOGENESIS. (Masters Thesis). McMaster University. Retrieved from http://hdl.handle.net/11375/22267

Chicago Manual of Style (16th Edition):

Shen, Nicole. “CHARACTERIZING PROTEIN ARGININE METHYLTRANSFERASE EXPRESSION AND ACTIVITY DURING MYOGENESIS.” 2017. Masters Thesis, McMaster University. Accessed January 26, 2020. http://hdl.handle.net/11375/22267.

MLA Handbook (7th Edition):

Shen, Nicole. “CHARACTERIZING PROTEIN ARGININE METHYLTRANSFERASE EXPRESSION AND ACTIVITY DURING MYOGENESIS.” 2017. Web. 26 Jan 2020.

Vancouver:

Shen N. CHARACTERIZING PROTEIN ARGININE METHYLTRANSFERASE EXPRESSION AND ACTIVITY DURING MYOGENESIS. [Internet] [Masters thesis]. McMaster University; 2017. [cited 2020 Jan 26]. Available from: http://hdl.handle.net/11375/22267.

Council of Science Editors:

Shen N. CHARACTERIZING PROTEIN ARGININE METHYLTRANSFERASE EXPRESSION AND ACTIVITY DURING MYOGENESIS. [Masters Thesis]. McMaster University; 2017. Available from: http://hdl.handle.net/11375/22267


McMaster University

3. vanLieshout, Tiffany. PRMT Biology During Acute Exercise.

Degree: MSc, 2017, McMaster University

Protein arginine methyltransferase 1 (PRMT1), -4 (also known as coactivator-associated arginine methyltransferase 1; CARM1), and -5 catalyze the methylation of arginine residues on target proteins.… (more)

Subjects/Keywords: Protein arginine methyltransferase; Exercise; Skeletal muscle; Fiber types; PGC-1alpha

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APA (6th Edition):

vanLieshout, T. (2017). PRMT Biology During Acute Exercise. (Masters Thesis). McMaster University. Retrieved from http://hdl.handle.net/11375/22264

Chicago Manual of Style (16th Edition):

vanLieshout, Tiffany. “PRMT Biology During Acute Exercise.” 2017. Masters Thesis, McMaster University. Accessed January 26, 2020. http://hdl.handle.net/11375/22264.

MLA Handbook (7th Edition):

vanLieshout, Tiffany. “PRMT Biology During Acute Exercise.” 2017. Web. 26 Jan 2020.

Vancouver:

vanLieshout T. PRMT Biology During Acute Exercise. [Internet] [Masters thesis]. McMaster University; 2017. [cited 2020 Jan 26]. Available from: http://hdl.handle.net/11375/22264.

Council of Science Editors:

vanLieshout T. PRMT Biology During Acute Exercise. [Masters Thesis]. McMaster University; 2017. Available from: http://hdl.handle.net/11375/22264


University of New South Wales

4. Zhang, Lelin. Discovery and characterization of novel protein methyltransferases in Saccharomyces cerevisiae.

Degree: Biotechnology & Biomolecular Sciences, 2014, University of New South Wales

Protein methylation is emerging as the fourth most prevalent post-translational modification in eukaryotes. Arginine and lysine methylation are implicated in a myriad of biological processes,… (more)

Subjects/Keywords: Yeast; Methylation; Proteome; Lysine; Arginine; Methyltransferase; Protein; Post-translational modification

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APA (6th Edition):

Zhang, L. (2014). Discovery and characterization of novel protein methyltransferases in Saccharomyces cerevisiae. (Doctoral Dissertation). University of New South Wales. Retrieved from http://handle.unsw.edu.au/1959.4/53490 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:12185/SOURCE02?view=true

Chicago Manual of Style (16th Edition):

Zhang, Lelin. “Discovery and characterization of novel protein methyltransferases in Saccharomyces cerevisiae.” 2014. Doctoral Dissertation, University of New South Wales. Accessed January 26, 2020. http://handle.unsw.edu.au/1959.4/53490 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:12185/SOURCE02?view=true.

MLA Handbook (7th Edition):

Zhang, Lelin. “Discovery and characterization of novel protein methyltransferases in Saccharomyces cerevisiae.” 2014. Web. 26 Jan 2020.

Vancouver:

Zhang L. Discovery and characterization of novel protein methyltransferases in Saccharomyces cerevisiae. [Internet] [Doctoral dissertation]. University of New South Wales; 2014. [cited 2020 Jan 26]. Available from: http://handle.unsw.edu.au/1959.4/53490 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:12185/SOURCE02?view=true.

Council of Science Editors:

Zhang L. Discovery and characterization of novel protein methyltransferases in Saccharomyces cerevisiae. [Doctoral Dissertation]. University of New South Wales; 2014. Available from: http://handle.unsw.edu.au/1959.4/53490 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:12185/SOURCE02?view=true


Utah State University

5. Suh-Lailam, Brenda Bienka. Development of Novel Methods and their Utilization in the Analysis of the Effect of the N-terminus of Human Protein Arginine Methyltransferase 1 Variant 1 on Enzymatic Activity, Protein-protein Interactions, and Substrate Specificity.

Degree: PhD, Chemistry and Biochemistry, 2010, Utah State University

Protein arginine methyltransferases (PRMTs) are enzymes that catalyze the methylation of protein arginine residues, resulting in the formation of monomethylarginine, and/or asymmetric or symmetric… (more)

Subjects/Keywords: enzyme activity measurement; Methylation; PROTEIN ARGININE METHYLTRANSFERASEs (PRMTs); protein-protein interactions; S-adenosyl-L-methionine-dependent methyltransferase; substrate specificity; Biochemistry

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APA (6th Edition):

Suh-Lailam, B. B. (2010). Development of Novel Methods and their Utilization in the Analysis of the Effect of the N-terminus of Human Protein Arginine Methyltransferase 1 Variant 1 on Enzymatic Activity, Protein-protein Interactions, and Substrate Specificity. (Doctoral Dissertation). Utah State University. Retrieved from https://digitalcommons.usu.edu/etd/863

Chicago Manual of Style (16th Edition):

Suh-Lailam, Brenda Bienka. “Development of Novel Methods and their Utilization in the Analysis of the Effect of the N-terminus of Human Protein Arginine Methyltransferase 1 Variant 1 on Enzymatic Activity, Protein-protein Interactions, and Substrate Specificity.” 2010. Doctoral Dissertation, Utah State University. Accessed January 26, 2020. https://digitalcommons.usu.edu/etd/863.

MLA Handbook (7th Edition):

Suh-Lailam, Brenda Bienka. “Development of Novel Methods and their Utilization in the Analysis of the Effect of the N-terminus of Human Protein Arginine Methyltransferase 1 Variant 1 on Enzymatic Activity, Protein-protein Interactions, and Substrate Specificity.” 2010. Web. 26 Jan 2020.

Vancouver:

Suh-Lailam BB. Development of Novel Methods and their Utilization in the Analysis of the Effect of the N-terminus of Human Protein Arginine Methyltransferase 1 Variant 1 on Enzymatic Activity, Protein-protein Interactions, and Substrate Specificity. [Internet] [Doctoral dissertation]. Utah State University; 2010. [cited 2020 Jan 26]. Available from: https://digitalcommons.usu.edu/etd/863.

Council of Science Editors:

Suh-Lailam BB. Development of Novel Methods and their Utilization in the Analysis of the Effect of the N-terminus of Human Protein Arginine Methyltransferase 1 Variant 1 on Enzymatic Activity, Protein-protein Interactions, and Substrate Specificity. [Doctoral Dissertation]. Utah State University; 2010. Available from: https://digitalcommons.usu.edu/etd/863


University of Illinois – Urbana-Champaign

6. Kanamaluru, Deepthi. Modulation of the activity of a key metabolic regulator Small Heterodimer Partner by post-translational modifications.

Degree: PhD, 0318, 2011, University of Illinois – Urbana-Champaign

 Small Heterodimer Partner (SHP, NR0B2), a member of the nuclear receptor superfamily, is an orphan receptor that lacks a DNA binding domain but contains a… (more)

Subjects/Keywords: Small Heterodimer Partner (SHP); Protein Arinine Methyltransferase 5 (PRMT5); arginine methylation; phosphorylation; protein kinase C zeta (PKC zeta); obesity and diabetes

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APA (6th Edition):

Kanamaluru, D. (2011). Modulation of the activity of a key metabolic regulator Small Heterodimer Partner by post-translational modifications. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/24491

Chicago Manual of Style (16th Edition):

Kanamaluru, Deepthi. “Modulation of the activity of a key metabolic regulator Small Heterodimer Partner by post-translational modifications.” 2011. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed January 26, 2020. http://hdl.handle.net/2142/24491.

MLA Handbook (7th Edition):

Kanamaluru, Deepthi. “Modulation of the activity of a key metabolic regulator Small Heterodimer Partner by post-translational modifications.” 2011. Web. 26 Jan 2020.

Vancouver:

Kanamaluru D. Modulation of the activity of a key metabolic regulator Small Heterodimer Partner by post-translational modifications. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2011. [cited 2020 Jan 26]. Available from: http://hdl.handle.net/2142/24491.

Council of Science Editors:

Kanamaluru D. Modulation of the activity of a key metabolic regulator Small Heterodimer Partner by post-translational modifications. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2011. Available from: http://hdl.handle.net/2142/24491

7. Ajebbar, Samira. Synthèse de ligands à la proteine CARM1 pour l'étude de son activité enzymatique et la synthèse d'inhibiteurs sélectifs : Insights into CARM1 methylation : design of selective inhibitors and peptide mimics : a structure based approach.

Degree: Docteur es, Chimie, 2012, Université de Strasbourg

Les protéines arginine méthyl transférases ("PRMTs") sont impliquées dans de nombreux processus cellulaires essentiels. La protéine CARMI ("Coactivator-associated arginine methyltransferase 1", appelée aussi "PRMT4") a… (more)

Subjects/Keywords: Coactivor-associated arginine methyltransferase 1; PRMT4; Protéines arginines méthyltransférases; Analogues de la S-Adénosyl-L-méthionine; Histone; Modifications épigénétiques; Coactivor-associated arginine methyltransferase 1; PRMT4; SAM analogues; Protein arginine methyltransferases; Histone; 572.8; 547.7

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APA (6th Edition):

Ajebbar, S. (2012). Synthèse de ligands à la proteine CARM1 pour l'étude de son activité enzymatique et la synthèse d'inhibiteurs sélectifs : Insights into CARM1 methylation : design of selective inhibitors and peptide mimics : a structure based approach. (Doctoral Dissertation). Université de Strasbourg. Retrieved from http://www.theses.fr/2012STRAF002

Chicago Manual of Style (16th Edition):

Ajebbar, Samira. “Synthèse de ligands à la proteine CARM1 pour l'étude de son activité enzymatique et la synthèse d'inhibiteurs sélectifs : Insights into CARM1 methylation : design of selective inhibitors and peptide mimics : a structure based approach.” 2012. Doctoral Dissertation, Université de Strasbourg. Accessed January 26, 2020. http://www.theses.fr/2012STRAF002.

MLA Handbook (7th Edition):

Ajebbar, Samira. “Synthèse de ligands à la proteine CARM1 pour l'étude de son activité enzymatique et la synthèse d'inhibiteurs sélectifs : Insights into CARM1 methylation : design of selective inhibitors and peptide mimics : a structure based approach.” 2012. Web. 26 Jan 2020.

Vancouver:

Ajebbar S. Synthèse de ligands à la proteine CARM1 pour l'étude de son activité enzymatique et la synthèse d'inhibiteurs sélectifs : Insights into CARM1 methylation : design of selective inhibitors and peptide mimics : a structure based approach. [Internet] [Doctoral dissertation]. Université de Strasbourg; 2012. [cited 2020 Jan 26]. Available from: http://www.theses.fr/2012STRAF002.

Council of Science Editors:

Ajebbar S. Synthèse de ligands à la proteine CARM1 pour l'étude de son activité enzymatique et la synthèse d'inhibiteurs sélectifs : Insights into CARM1 methylation : design of selective inhibitors and peptide mimics : a structure based approach. [Doctoral Dissertation]. Université de Strasbourg; 2012. Available from: http://www.theses.fr/2012STRAF002


Purdue University

8. Chen, Meng-Chieh. New Strategies To Reveal Protein Candidates In Protein-Protein Interactome Study.

Degree: MS, Biochemistry, 2014, Purdue University

  Comprehensive protein-protein interaction network analysis can help reveal protein functions in a system-wide manner. A reliable knowledgebase of interaction networks is not only important… (more)

Subjects/Keywords: Pure sciences; Biological sciences; Phosphoproteome; Polo-like kinase 1; Protein arginine methyltransferase 5; Protein-protein interaction; Sindbis virus; Virus-host interaction; Analytical Chemistry; Biochemistry; Molecular Biology

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APA (6th Edition):

Chen, M. (2014). New Strategies To Reveal Protein Candidates In Protein-Protein Interactome Study. (Thesis). Purdue University. Retrieved from http://docs.lib.purdue.edu/open_access_theses/310

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):

Chen, Meng-Chieh. “New Strategies To Reveal Protein Candidates In Protein-Protein Interactome Study.” 2014. Thesis, Purdue University. Accessed January 26, 2020. http://docs.lib.purdue.edu/open_access_theses/310.

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

MLA Handbook (7th Edition):

Chen, Meng-Chieh. “New Strategies To Reveal Protein Candidates In Protein-Protein Interactome Study.” 2014. Web. 26 Jan 2020.

Vancouver:

Chen M. New Strategies To Reveal Protein Candidates In Protein-Protein Interactome Study. [Internet] [Thesis]. Purdue University; 2014. [cited 2020 Jan 26]. Available from: http://docs.lib.purdue.edu/open_access_theses/310.

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

Council of Science Editors:

Chen M. New Strategies To Reveal Protein Candidates In Protein-Protein Interactome Study. [Thesis]. Purdue University; 2014. Available from: http://docs.lib.purdue.edu/open_access_theses/310

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


Utah State University

9. May, Kyle M. Investigation of Protein Dynamics and Communication in Adomet-Dependent Methyltransferases: Non-Ribosomal Peptide Synthetase and Protein Arginine Methyltransferase.

Degree: MS, Chemistry and Biochemistry, 2019, Utah State University

  For many enzymes to function correctly they must have the freedom to display a level of dynamics or communication during their catalytic cycle. The… (more)

Subjects/Keywords: Protein dynamics; protein communication; adomet-dependent methyltransferases; SAM-dependent; methyltrasferases; adomet; SAM; methyltransferase; non-ribosomal petide synthetase; NRPS protein arginine methyltrasferase; PRMT; Biochemistry

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APA (6th Edition):

May, K. M. (2019). Investigation of Protein Dynamics and Communication in Adomet-Dependent Methyltransferases: Non-Ribosomal Peptide Synthetase and Protein Arginine Methyltransferase. (Masters Thesis). Utah State University. Retrieved from https://digitalcommons.usu.edu/etd/7550

Chicago Manual of Style (16th Edition):

May, Kyle M. “Investigation of Protein Dynamics and Communication in Adomet-Dependent Methyltransferases: Non-Ribosomal Peptide Synthetase and Protein Arginine Methyltransferase.” 2019. Masters Thesis, Utah State University. Accessed January 26, 2020. https://digitalcommons.usu.edu/etd/7550.

MLA Handbook (7th Edition):

May, Kyle M. “Investigation of Protein Dynamics and Communication in Adomet-Dependent Methyltransferases: Non-Ribosomal Peptide Synthetase and Protein Arginine Methyltransferase.” 2019. Web. 26 Jan 2020.

Vancouver:

May KM. Investigation of Protein Dynamics and Communication in Adomet-Dependent Methyltransferases: Non-Ribosomal Peptide Synthetase and Protein Arginine Methyltransferase. [Internet] [Masters thesis]. Utah State University; 2019. [cited 2020 Jan 26]. Available from: https://digitalcommons.usu.edu/etd/7550.

Council of Science Editors:

May KM. Investigation of Protein Dynamics and Communication in Adomet-Dependent Methyltransferases: Non-Ribosomal Peptide Synthetase and Protein Arginine Methyltransferase. [Masters Thesis]. Utah State University; 2019. Available from: https://digitalcommons.usu.edu/etd/7550


University of Arkansas

10. Dhamad, Ahmed Edan. Molecular and Biochemical Studies of Several Novel Estrogen Receptor Alpha-Interacting Proteins in Breast Cancer Cells.

Degree: PhD, 2017, University of Arkansas

  Breast cancer is the second leading cause of cancer-related death in women, and approximately 70% of incidences are estrogen receptor (ER)-positive breast cancer. ERα… (more)

Subjects/Keywords: Breast Cancer; Chromatin Target of PRMT1 (CHTOP); Estrogen Receptor Alpha; Heat Shock Protein (Hsp); Histone Acetyltransferase (HAT); Protein Arginine Methyltransferase 5 (PRMT5); Biochemistry; Cancer Biology; Molecular Biology

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APA (6th Edition):

Dhamad, A. E. (2017). Molecular and Biochemical Studies of Several Novel Estrogen Receptor Alpha-Interacting Proteins in Breast Cancer Cells. (Doctoral Dissertation). University of Arkansas. Retrieved from https://scholarworks.uark.edu/etd/2403

Chicago Manual of Style (16th Edition):

Dhamad, Ahmed Edan. “Molecular and Biochemical Studies of Several Novel Estrogen Receptor Alpha-Interacting Proteins in Breast Cancer Cells.” 2017. Doctoral Dissertation, University of Arkansas. Accessed January 26, 2020. https://scholarworks.uark.edu/etd/2403.

MLA Handbook (7th Edition):

Dhamad, Ahmed Edan. “Molecular and Biochemical Studies of Several Novel Estrogen Receptor Alpha-Interacting Proteins in Breast Cancer Cells.” 2017. Web. 26 Jan 2020.

Vancouver:

Dhamad AE. Molecular and Biochemical Studies of Several Novel Estrogen Receptor Alpha-Interacting Proteins in Breast Cancer Cells. [Internet] [Doctoral dissertation]. University of Arkansas; 2017. [cited 2020 Jan 26]. Available from: https://scholarworks.uark.edu/etd/2403.

Council of Science Editors:

Dhamad AE. Molecular and Biochemical Studies of Several Novel Estrogen Receptor Alpha-Interacting Proteins in Breast Cancer Cells. [Doctoral Dissertation]. University of Arkansas; 2017. Available from: https://scholarworks.uark.edu/etd/2403

11. LEE KIA MING PATRICK. CHARACTERISATION OF STRUCTURAL PLASTICITY OF THE VISUAL CORTEX IN PRMT8 NULL MICE?.

Degree: 2016, National University of Singapore

Subjects/Keywords: neuroepigenetics; perineuronal nets; protein arginine methyltransferase; proteomics; tenascin-r; visual cortex

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APA (6th Edition):

PATRICK, L. K. M. (2016). CHARACTERISATION OF STRUCTURAL PLASTICITY OF THE VISUAL CORTEX IN PRMT8 NULL MICE?. (Thesis). National University of Singapore. Retrieved from http://scholarbank.nus.edu.sg/handle/10635/135183

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):

PATRICK, LEE KIA MING. “CHARACTERISATION OF STRUCTURAL PLASTICITY OF THE VISUAL CORTEX IN PRMT8 NULL MICE?.” 2016. Thesis, National University of Singapore. Accessed January 26, 2020. http://scholarbank.nus.edu.sg/handle/10635/135183.

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

MLA Handbook (7th Edition):

PATRICK, LEE KIA MING. “CHARACTERISATION OF STRUCTURAL PLASTICITY OF THE VISUAL CORTEX IN PRMT8 NULL MICE?.” 2016. Web. 26 Jan 2020.

Vancouver:

PATRICK LKM. CHARACTERISATION OF STRUCTURAL PLASTICITY OF THE VISUAL CORTEX IN PRMT8 NULL MICE?. [Internet] [Thesis]. National University of Singapore; 2016. [cited 2020 Jan 26]. Available from: http://scholarbank.nus.edu.sg/handle/10635/135183.

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

Council of Science Editors:

PATRICK LKM. CHARACTERISATION OF STRUCTURAL PLASTICITY OF THE VISUAL CORTEX IN PRMT8 NULL MICE?. [Thesis]. National University of Singapore; 2016. Available from: http://scholarbank.nus.edu.sg/handle/10635/135183

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

12. Canup, Brandon S. Discovery of Novel Cross-Talk between Protein Arginine Methyltransferase Isoforms and Design of Dimerization Inhibitors.

Degree: MS, Chemistry, 2013, Georgia State University

Protein arginine methyltransferase, PRMT, is a family of epigenetic enzymes that methylate arginine residues on histone and nonhistone substrates which result in a monomethylation,… (more)

Subjects/Keywords: Protein arginine methyltransferase (PRMT); peptide synthesis; histone; dimerization; methylation

…1 1.3 Protein arginine methyltransferase… …25 xiii LIST OF ABBREVIATIONS Protein arginine methyltransferase (PRMT) S… …Protein arginine methyltransferase Protein arginine methyltransferases (PRMTs) are a… …2 Figure 1.2- Protein arginine methylation mediated by PRMTs… …x5B;17] 4 Figure 1.2- Protein arginine methylation mediated by PRMTs PRMT1 and… 

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APA (6th Edition):

Canup, B. S. (2013). Discovery of Novel Cross-Talk between Protein Arginine Methyltransferase Isoforms and Design of Dimerization Inhibitors. (Thesis). Georgia State University. Retrieved from https://scholarworks.gsu.edu/chemistry_theses/58

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):

Canup, Brandon S. “Discovery of Novel Cross-Talk between Protein Arginine Methyltransferase Isoforms and Design of Dimerization Inhibitors.” 2013. Thesis, Georgia State University. Accessed January 26, 2020. https://scholarworks.gsu.edu/chemistry_theses/58.

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

MLA Handbook (7th Edition):

Canup, Brandon S. “Discovery of Novel Cross-Talk between Protein Arginine Methyltransferase Isoforms and Design of Dimerization Inhibitors.” 2013. Web. 26 Jan 2020.

Vancouver:

Canup BS. Discovery of Novel Cross-Talk between Protein Arginine Methyltransferase Isoforms and Design of Dimerization Inhibitors. [Internet] [Thesis]. Georgia State University; 2013. [cited 2020 Jan 26]. Available from: https://scholarworks.gsu.edu/chemistry_theses/58.

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

Council of Science Editors:

Canup BS. Discovery of Novel Cross-Talk between Protein Arginine Methyltransferase Isoforms and Design of Dimerization Inhibitors. [Thesis]. Georgia State University; 2013. Available from: https://scholarworks.gsu.edu/chemistry_theses/58

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

13. Dacwag, Caroline S. Analysis of Protein Arginine Methyltransferase Function during Myogenic Gene Transcription: A Dissertation.

Degree: Cell Biology, Biochemistry and Molecular Pharmacology, 2008, U of Massachusetts : Med

  Skeletal muscle differentiation requires synergy between tissue-specific transcription factors, chromatin remodeling enzymes and the general transcription machinery. Here we demonstrate that two distinct protein(more)

Subjects/Keywords: Protein-Arginine N-Methyltransferase; Myogenic Regulatory Factors; Muscle Development; Muscle; Skeletal; Amino Acids, Peptides, and Proteins; Genetic Phenomena; Musculoskeletal System

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APA (6th Edition):

Dacwag, C. S. (2008). Analysis of Protein Arginine Methyltransferase Function during Myogenic Gene Transcription: A Dissertation. (Doctoral Dissertation). U of Massachusetts : Med. Retrieved from https://escholarship.umassmed.edu/gsbs_diss/402

Chicago Manual of Style (16th Edition):

Dacwag, Caroline S. “Analysis of Protein Arginine Methyltransferase Function during Myogenic Gene Transcription: A Dissertation.” 2008. Doctoral Dissertation, U of Massachusetts : Med. Accessed January 26, 2020. https://escholarship.umassmed.edu/gsbs_diss/402.

MLA Handbook (7th Edition):

Dacwag, Caroline S. “Analysis of Protein Arginine Methyltransferase Function during Myogenic Gene Transcription: A Dissertation.” 2008. Web. 26 Jan 2020.

Vancouver:

Dacwag CS. Analysis of Protein Arginine Methyltransferase Function during Myogenic Gene Transcription: A Dissertation. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 2008. [cited 2020 Jan 26]. Available from: https://escholarship.umassmed.edu/gsbs_diss/402.

Council of Science Editors:

Dacwag CS. Analysis of Protein Arginine Methyltransferase Function during Myogenic Gene Transcription: A Dissertation. [Doctoral Dissertation]. U of Massachusetts : Med; 2008. Available from: https://escholarship.umassmed.edu/gsbs_diss/402

14. TAN QIANCHENG DARREN. THE ROLE OF PROTEIN ARGININE METHYLTRANSFERASE 5 IN HEMATOPOIESIS.

Degree: 2018, National University of Singapore

Subjects/Keywords: Protein arginine methyltransferase 5; hematopoietic stem cells; RNA; splicing; DNA damage; genomic integrity; proteostasis

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

APA (6th Edition):

DARREN, T. Q. (2018). THE ROLE OF PROTEIN ARGININE METHYLTRANSFERASE 5 IN HEMATOPOIESIS. (Thesis). National University of Singapore. Retrieved from http://scholarbank.nus.edu.sg/handle/10635/150483

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):

DARREN, TAN QIANCHENG. “THE ROLE OF PROTEIN ARGININE METHYLTRANSFERASE 5 IN HEMATOPOIESIS.” 2018. Thesis, National University of Singapore. Accessed January 26, 2020. http://scholarbank.nus.edu.sg/handle/10635/150483.

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

MLA Handbook (7th Edition):

DARREN, TAN QIANCHENG. “THE ROLE OF PROTEIN ARGININE METHYLTRANSFERASE 5 IN HEMATOPOIESIS.” 2018. Web. 26 Jan 2020.

Vancouver:

DARREN TQ. THE ROLE OF PROTEIN ARGININE METHYLTRANSFERASE 5 IN HEMATOPOIESIS. [Internet] [Thesis]. National University of Singapore; 2018. [cited 2020 Jan 26]. Available from: http://scholarbank.nus.edu.sg/handle/10635/150483.

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

Council of Science Editors:

DARREN TQ. THE ROLE OF PROTEIN ARGININE METHYLTRANSFERASE 5 IN HEMATOPOIESIS. [Thesis]. National University of Singapore; 2018. Available from: http://scholarbank.nus.edu.sg/handle/10635/150483

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

15. van Haren, M.J. Transition state mimics as inhibitors of methyltransferase enzymes.

Degree: 2017, University Utrecht

 The work described in this thesis focuses on the development of inhibitors against two distinct methyltransferase enzymes; the protein arginine N-methyltransferases (PRMTs) and nicotinamide N-methyltransferase(more)

Subjects/Keywords: PRMT; NNMT; protein arginine N-methyltransferase; nicotinamide N-methyltrasnferase; inhibitor; transition state mimic; bisubstrate; S-adenosyl-L-methionine; AdoMet; SAM

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APA (6th Edition):

van Haren, M. J. (2017). Transition state mimics as inhibitors of methyltransferase enzymes. (Doctoral Dissertation). University Utrecht. Retrieved from http://dspace.library.uu.nl/handle/1874/356093 ; URN:NBN:NL:UI:10-1874-356093 ; urn:isbn:978-90-393-6873-2 ; URN:NBN:NL:UI:10-1874-356093 ; http://dspace.library.uu.nl/handle/1874/356093

Chicago Manual of Style (16th Edition):

van Haren, M J. “Transition state mimics as inhibitors of methyltransferase enzymes.” 2017. Doctoral Dissertation, University Utrecht. Accessed January 26, 2020. http://dspace.library.uu.nl/handle/1874/356093 ; URN:NBN:NL:UI:10-1874-356093 ; urn:isbn:978-90-393-6873-2 ; URN:NBN:NL:UI:10-1874-356093 ; http://dspace.library.uu.nl/handle/1874/356093.

MLA Handbook (7th Edition):

van Haren, M J. “Transition state mimics as inhibitors of methyltransferase enzymes.” 2017. Web. 26 Jan 2020.

Vancouver:

van Haren MJ. Transition state mimics as inhibitors of methyltransferase enzymes. [Internet] [Doctoral dissertation]. University Utrecht; 2017. [cited 2020 Jan 26]. Available from: http://dspace.library.uu.nl/handle/1874/356093 ; URN:NBN:NL:UI:10-1874-356093 ; urn:isbn:978-90-393-6873-2 ; URN:NBN:NL:UI:10-1874-356093 ; http://dspace.library.uu.nl/handle/1874/356093.

Council of Science Editors:

van Haren MJ. Transition state mimics as inhibitors of methyltransferase enzymes. [Doctoral Dissertation]. University Utrecht; 2017. Available from: http://dspace.library.uu.nl/handle/1874/356093 ; URN:NBN:NL:UI:10-1874-356093 ; urn:isbn:978-90-393-6873-2 ; URN:NBN:NL:UI:10-1874-356093 ; http://dspace.library.uu.nl/handle/1874/356093

16. Goulet, Isabelle. New Roles for Arginine Methylation in RNA Metabolism and Cancer .

Degree: 2011, University of Ottawa

 Because it can expand the range of a protein’s interactions or modulate its activity, post-translational methylation of arginine residues in proteins must be duly coordinated… (more)

Subjects/Keywords: Arginine methylation; Protein arginine methyltransferases; Protein arginine methyltransferase 1; Tudor domain-containing proteins; TDRD3; PRMT1; Breast cancer; RNA metabolism; Stress granules; RNA processing; Tudor domain-containing protein 3; Tudor domain

…yields protein arginine methyltransferase 1 isoforms with distinct activity, substrate… …methyltransferases. 30 Figure 1-2. The mammalian protein arginine methyltransferase family. 32 Figure… …precursor messenger ribonucleic acid PRMT1-11 protein arginine methyltransferase 1 to 11 xx… …protein arginine methyltransferase 1, and the methyl-binding Tudor domains. Chapter 2 is a… …enzymatic activity/specificity of the protein arginine methyltransferases (PRMTs) and… 

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APA (6th Edition):

Goulet, I. (2011). New Roles for Arginine Methylation in RNA Metabolism and Cancer . (Thesis). University of Ottawa. Retrieved from http://hdl.handle.net/10393/20293

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):

Goulet, Isabelle. “New Roles for Arginine Methylation in RNA Metabolism and Cancer .” 2011. Thesis, University of Ottawa. Accessed January 26, 2020. http://hdl.handle.net/10393/20293.

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

MLA Handbook (7th Edition):

Goulet, Isabelle. “New Roles for Arginine Methylation in RNA Metabolism and Cancer .” 2011. Web. 26 Jan 2020.

Vancouver:

Goulet I. New Roles for Arginine Methylation in RNA Metabolism and Cancer . [Internet] [Thesis]. University of Ottawa; 2011. [cited 2020 Jan 26]. Available from: http://hdl.handle.net/10393/20293.

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

Council of Science Editors:

Goulet I. New Roles for Arginine Methylation in RNA Metabolism and Cancer . [Thesis]. University of Ottawa; 2011. Available from: http://hdl.handle.net/10393/20293

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


McGill University

17. Chénard, Carol Anne. Ribonucleoprotein complexes and protein arginine methylation : a role in diseases of the central nervous sytem.

Degree: PhD, Department of Microbiology and Immunology., 2008, McGill University

For the past 45 years, QKI has been studied for its role in the processes of development and central nervous system myelination using the qkv… (more)

Subjects/Keywords: RNA-Binding Proteins  – physiology.; Oligodendroglia  – cytology.; Heterogeneous-Nuclear Ribonucleoprotein K  – metabolism.; Protein-Arginine N-Methyltransferase  – metabolism.; Methylation.; Poly(A)-Binding Proteins  – metabolism.; Myelin Basic Proteins  – metabolism.; Mice.; Mice, Quaking.

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

APA (6th Edition):

Chénard, C. A. (2008). Ribonucleoprotein complexes and protein arginine methylation : a role in diseases of the central nervous sytem. (Doctoral Dissertation). McGill University. Retrieved from http://digitool.library.mcgill.ca/thesisfile115894.pdf

Chicago Manual of Style (16th Edition):

Chénard, Carol Anne. “Ribonucleoprotein complexes and protein arginine methylation : a role in diseases of the central nervous sytem.” 2008. Doctoral Dissertation, McGill University. Accessed January 26, 2020. http://digitool.library.mcgill.ca/thesisfile115894.pdf.

MLA Handbook (7th Edition):

Chénard, Carol Anne. “Ribonucleoprotein complexes and protein arginine methylation : a role in diseases of the central nervous sytem.” 2008. Web. 26 Jan 2020.

Vancouver:

Chénard CA. Ribonucleoprotein complexes and protein arginine methylation : a role in diseases of the central nervous sytem. [Internet] [Doctoral dissertation]. McGill University; 2008. [cited 2020 Jan 26]. Available from: http://digitool.library.mcgill.ca/thesisfile115894.pdf.

Council of Science Editors:

Chénard CA. Ribonucleoprotein complexes and protein arginine methylation : a role in diseases of the central nervous sytem. [Doctoral Dissertation]. McGill University; 2008. Available from: http://digitool.library.mcgill.ca/thesisfile115894.pdf

18. Smith, Porsha L. Protein Arginine Methyltransferase 5 as a Driver of Lymphomagenesis.

Degree: PhD, Biomedical Sciences, 2016, The Ohio State University

 Over the past decade, it has become clear that oncogenesis is a process driven by a wide variety of triggers including gene mutations, gene amplifications,… (more)

Subjects/Keywords: Molecular Biology; Biology; Biomedical Research; Cellular Biology; Experiments; Health Sciences; protein arginine methyltransferase 5; PRMT5; epigenetics; transgenic; cancer; lymphomagenesis; cancer driver; lymphoma; lymphoma mouse model

…Li C, Baiocchi RA. “Selective inhibition of protein arginine methyltransferase 5 blocks… …S, Kaur B, Baiocchi RA. “Genetic Validation of the Protein Arginine Methyltransferase… …Pileri S, Denis GV, Baiocchi RA, Sif S. “Protein arginine methyltransferase 5 (PRMT5)… …protein arginine methyltransferase 5 (PRMT5) enzyme, first discovered to contribute… …silencing [21]. Additionally H4R3me2 produced by protein arginine methyltransferase 5… 

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

APA (6th Edition):

Smith, P. L. (2016). Protein Arginine Methyltransferase 5 as a Driver of Lymphomagenesis. (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1468975682

Chicago Manual of Style (16th Edition):

Smith, Porsha L. “Protein Arginine Methyltransferase 5 as a Driver of Lymphomagenesis.” 2016. Doctoral Dissertation, The Ohio State University. Accessed January 26, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=osu1468975682.

MLA Handbook (7th Edition):

Smith, Porsha L. “Protein Arginine Methyltransferase 5 as a Driver of Lymphomagenesis.” 2016. Web. 26 Jan 2020.

Vancouver:

Smith PL. Protein Arginine Methyltransferase 5 as a Driver of Lymphomagenesis. [Internet] [Doctoral dissertation]. The Ohio State University; 2016. [cited 2020 Jan 26]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1468975682.

Council of Science Editors:

Smith PL. Protein Arginine Methyltransferase 5 as a Driver of Lymphomagenesis. [Doctoral Dissertation]. The Ohio State University; 2016. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1468975682

.