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You searched for subject:(Arginine methylation). Showing records 1 – 30 of 41 total matches.

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University of Oxford

1. Lu, Yi-Chien. Arginine methylation on E2F1.

Degree: PhD, 2014, University of Oxford

 E2F1 is a transcription factor which paradoxically has major influence on both apoptosis and cell cycle progression. One of the most important questions in E2F1… (more)

Subjects/Keywords: Oncology; arginine methylation

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APA (6th Edition):

Lu, Y. (2014). Arginine methylation on E2F1. (Doctoral Dissertation). University of Oxford. Retrieved from http://ora.ox.ac.uk/objects/uuid:5e8cbf54-31d5-4b45-823c-52dbf82131d5 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.644704

Chicago Manual of Style (16th Edition):

Lu, Yi-Chien. “Arginine methylation on E2F1.” 2014. Doctoral Dissertation, University of Oxford. Accessed July 21, 2019. http://ora.ox.ac.uk/objects/uuid:5e8cbf54-31d5-4b45-823c-52dbf82131d5 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.644704.

MLA Handbook (7th Edition):

Lu, Yi-Chien. “Arginine methylation on E2F1.” 2014. Web. 21 Jul 2019.

Vancouver:

Lu Y. Arginine methylation on E2F1. [Internet] [Doctoral dissertation]. University of Oxford; 2014. [cited 2019 Jul 21]. Available from: http://ora.ox.ac.uk/objects/uuid:5e8cbf54-31d5-4b45-823c-52dbf82131d5 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.644704.

Council of Science Editors:

Lu Y. Arginine methylation on E2F1. [Doctoral Dissertation]. University of Oxford; 2014. Available from: http://ora.ox.ac.uk/objects/uuid:5e8cbf54-31d5-4b45-823c-52dbf82131d5 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.644704


University of Ottawa

2. Morettin, Alan James. Investigating the Role of Protein Arginine Methyltransferases in Breast Cancer Etiology .

Degree: 2015, University of Ottawa

 Breast cancer is the most commonly diagnosed cancer amongst Canadian women. Though numerous treatments are available, in many instances tumours become refractory or recur. Therefore,… (more)

Subjects/Keywords: Arginine Methylation; PRMTs; Breast Cancer

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APA (6th Edition):

Morettin, A. J. (2015). Investigating the Role of Protein Arginine Methyltransferases in Breast Cancer Etiology . (Thesis). University of Ottawa. Retrieved from http://hdl.handle.net/10393/31920

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):

Morettin, Alan James. “Investigating the Role of Protein Arginine Methyltransferases in Breast Cancer Etiology .” 2015. Thesis, University of Ottawa. Accessed July 21, 2019. http://hdl.handle.net/10393/31920.

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

MLA Handbook (7th Edition):

Morettin, Alan James. “Investigating the Role of Protein Arginine Methyltransferases in Breast Cancer Etiology .” 2015. Web. 21 Jul 2019.

Vancouver:

Morettin AJ. Investigating the Role of Protein Arginine Methyltransferases in Breast Cancer Etiology . [Internet] [Thesis]. University of Ottawa; 2015. [cited 2019 Jul 21]. Available from: http://hdl.handle.net/10393/31920.

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

Council of Science Editors:

Morettin AJ. Investigating the Role of Protein Arginine Methyltransferases in Breast Cancer Etiology . [Thesis]. University of Ottawa; 2015. Available from: http://hdl.handle.net/10393/31920

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


University of New South Wales

3. Low, Keng Kwang Jason. Proteome-wide analysis of arginine methylation in Saccharomyces cerevisiae.

Degree: Biotechnology & Biomolecular Sciences, 2012, University of New South Wales

Arginine methylation is a post-translational modification that has been implicated in a plethora of cellular processes. It is evolutionarily conserved and may play a role… (more)

Subjects/Keywords: Saccharomyces cerevisiae; Arginine methylation; Methylarginine

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APA (6th Edition):

Low, K. K. J. (2012). Proteome-wide analysis of arginine methylation in Saccharomyces cerevisiae. (Doctoral Dissertation). University of New South Wales. Retrieved from http://handle.unsw.edu.au/1959.4/52258 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:10930/SOURCE01?view=true

Chicago Manual of Style (16th Edition):

Low, Keng Kwang Jason. “Proteome-wide analysis of arginine methylation in Saccharomyces cerevisiae.” 2012. Doctoral Dissertation, University of New South Wales. Accessed July 21, 2019. http://handle.unsw.edu.au/1959.4/52258 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:10930/SOURCE01?view=true.

MLA Handbook (7th Edition):

Low, Keng Kwang Jason. “Proteome-wide analysis of arginine methylation in Saccharomyces cerevisiae.” 2012. Web. 21 Jul 2019.

Vancouver:

Low KKJ. Proteome-wide analysis of arginine methylation in Saccharomyces cerevisiae. [Internet] [Doctoral dissertation]. University of New South Wales; 2012. [cited 2019 Jul 21]. Available from: http://handle.unsw.edu.au/1959.4/52258 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:10930/SOURCE01?view=true.

Council of Science Editors:

Low KKJ. Proteome-wide analysis of arginine methylation in Saccharomyces cerevisiae. [Doctoral Dissertation]. University of New South Wales; 2012. Available from: http://handle.unsw.edu.au/1959.4/52258 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:10930/SOURCE01?view=true


University of Hong Kong

4. Liao, An, Anne. Characterization of arginine methylation of the RNA-binding protein Staufen in neurons.

Degree: Master of Medical Sciences, 2015, University of Hong Kong

The morphology and number of dendritic spines have been associated with learning and memory. Abnormality of spine morphogenesis has been found in patients suffering from… (more)

Subjects/Keywords: Arginine - Methylation; Neurons; RNA-protein interactions

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APA (6th Edition):

Liao, An, A. (2015). Characterization of arginine methylation of the RNA-binding protein Staufen in neurons. (Masters Thesis). University of Hong Kong. Retrieved from Liao, A. A. [廖安]. (2015). Characterization of arginine methylation of the RNA-binding protein Staufen in neurons. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5634738 ; http://hdl.handle.net/10722/221471

Chicago Manual of Style (16th Edition):

Liao, An, Anne. “Characterization of arginine methylation of the RNA-binding protein Staufen in neurons.” 2015. Masters Thesis, University of Hong Kong. Accessed July 21, 2019. Liao, A. A. [廖安]. (2015). Characterization of arginine methylation of the RNA-binding protein Staufen in neurons. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5634738 ; http://hdl.handle.net/10722/221471.

MLA Handbook (7th Edition):

Liao, An, Anne. “Characterization of arginine methylation of the RNA-binding protein Staufen in neurons.” 2015. Web. 21 Jul 2019.

Vancouver:

Liao, An A. Characterization of arginine methylation of the RNA-binding protein Staufen in neurons. [Internet] [Masters thesis]. University of Hong Kong; 2015. [cited 2019 Jul 21]. Available from: Liao, A. A. [廖安]. (2015). Characterization of arginine methylation of the RNA-binding protein Staufen in neurons. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5634738 ; http://hdl.handle.net/10722/221471.

Council of Science Editors:

Liao, An A. Characterization of arginine methylation of the RNA-binding protein Staufen in neurons. [Masters Thesis]. University of Hong Kong; 2015. Available from: Liao, A. A. [廖安]. (2015). Characterization of arginine methylation of the RNA-binding protein Staufen in neurons. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5634738 ; http://hdl.handle.net/10722/221471


University of Ottawa

5. Star, Alexandra. Enrichment and Identification of Methylation at the Proteome Level .

Degree: 2016, University of Ottawa

Methylation is a post-translational modification which occurs on lysine and arginine residues. Methylation is difficult to detect due to its low abundance and lack of… (more)

Subjects/Keywords: proteomics; methylation; biochemistry; lysine; arginine; mass spectrometry

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APA (6th Edition):

Star, A. (2016). Enrichment and Identification of Methylation at the Proteome Level . (Thesis). University of Ottawa. Retrieved from http://hdl.handle.net/10393/34178

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):

Star, Alexandra. “Enrichment and Identification of Methylation at the Proteome Level .” 2016. Thesis, University of Ottawa. Accessed July 21, 2019. http://hdl.handle.net/10393/34178.

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

MLA Handbook (7th Edition):

Star, Alexandra. “Enrichment and Identification of Methylation at the Proteome Level .” 2016. Web. 21 Jul 2019.

Vancouver:

Star A. Enrichment and Identification of Methylation at the Proteome Level . [Internet] [Thesis]. University of Ottawa; 2016. [cited 2019 Jul 21]. Available from: http://hdl.handle.net/10393/34178.

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

Council of Science Editors:

Star A. Enrichment and Identification of Methylation at the Proteome Level . [Thesis]. University of Ottawa; 2016. Available from: http://hdl.handle.net/10393/34178

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


Utah State University

6. Excell, Celeste. Pop2: A Potential Regulator of Hmt1-Catalyzed Arginine Methylation in Yeast.

Degree: MS, Chemistry and Biochemistry, 2014, Utah State University

  Protein arginine methylation is an important post-translational modification that is vital in regulating various cellular processes such as gene transcription, cell signaling, and RNA… (more)

Subjects/Keywords: arginine methylation; Hmt1; Pop2; PRMT; Biochemistry

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APA (6th Edition):

Excell, C. (2014). Pop2: A Potential Regulator of Hmt1-Catalyzed Arginine Methylation in Yeast. (Masters Thesis). Utah State University. Retrieved from https://digitalcommons.usu.edu/etd/2104

Chicago Manual of Style (16th Edition):

Excell, Celeste. “Pop2: A Potential Regulator of Hmt1-Catalyzed Arginine Methylation in Yeast.” 2014. Masters Thesis, Utah State University. Accessed July 21, 2019. https://digitalcommons.usu.edu/etd/2104.

MLA Handbook (7th Edition):

Excell, Celeste. “Pop2: A Potential Regulator of Hmt1-Catalyzed Arginine Methylation in Yeast.” 2014. Web. 21 Jul 2019.

Vancouver:

Excell C. Pop2: A Potential Regulator of Hmt1-Catalyzed Arginine Methylation in Yeast. [Internet] [Masters thesis]. Utah State University; 2014. [cited 2019 Jul 21]. Available from: https://digitalcommons.usu.edu/etd/2104.

Council of Science Editors:

Excell C. Pop2: A Potential Regulator of Hmt1-Catalyzed Arginine Methylation in Yeast. [Masters Thesis]. Utah State University; 2014. Available from: https://digitalcommons.usu.edu/etd/2104

7. LILING WU. BIOCHEMICAL STUDIES OF PROTEIN ARGININE AND LYSINE METHYLTRANSFERASES.

Degree: 2015, National University of Singapore

Subjects/Keywords: Arginine Lysine Methylation

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APA (6th Edition):

WU, L. (2015). BIOCHEMICAL STUDIES OF PROTEIN ARGININE AND LYSINE METHYLTRANSFERASES. (Thesis). National University of Singapore. Retrieved from http://scholarbank.nus.edu.sg/handle/10635/121882

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):

WU, LILING. “BIOCHEMICAL STUDIES OF PROTEIN ARGININE AND LYSINE METHYLTRANSFERASES.” 2015. Thesis, National University of Singapore. Accessed July 21, 2019. http://scholarbank.nus.edu.sg/handle/10635/121882.

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

MLA Handbook (7th Edition):

WU, LILING. “BIOCHEMICAL STUDIES OF PROTEIN ARGININE AND LYSINE METHYLTRANSFERASES.” 2015. Web. 21 Jul 2019.

Vancouver:

WU L. BIOCHEMICAL STUDIES OF PROTEIN ARGININE AND LYSINE METHYLTRANSFERASES. [Internet] [Thesis]. National University of Singapore; 2015. [cited 2019 Jul 21]. Available from: http://scholarbank.nus.edu.sg/handle/10635/121882.

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

Council of Science Editors:

WU L. BIOCHEMICAL STUDIES OF PROTEIN ARGININE AND LYSINE METHYLTRANSFERASES. [Thesis]. National University of Singapore; 2015. Available from: http://scholarbank.nus.edu.sg/handle/10635/121882

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


University of New South Wales

8. Chia, Samantha Zhiying. Transcriptomics-based study reveals a novel link between arginine methylation and phosphate regulation in Saccharomyces cerevisiae.

Degree: Biotechnology & Biomolecular Sciences, 2015, University of New South Wales

 Hmt1 is the predominant arginine methyltransferase in yeast, involved in biological processes such as transcription, transcriptional regulation, nucleocytoplasmic transport of proteins and mRNAs and RNA… (more)

Subjects/Keywords: Hmt1; Phosphate regulation; Arginine methylation; Polyphosphate

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APA (6th Edition):

Chia, S. Z. (2015). Transcriptomics-based study reveals a novel link between arginine methylation and phosphate regulation in Saccharomyces cerevisiae. (Doctoral Dissertation). University of New South Wales. Retrieved from http://handle.unsw.edu.au/1959.4/55695 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:38565/SOURCE02?view=true

Chicago Manual of Style (16th Edition):

Chia, Samantha Zhiying. “Transcriptomics-based study reveals a novel link between arginine methylation and phosphate regulation in Saccharomyces cerevisiae.” 2015. Doctoral Dissertation, University of New South Wales. Accessed July 21, 2019. http://handle.unsw.edu.au/1959.4/55695 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:38565/SOURCE02?view=true.

MLA Handbook (7th Edition):

Chia, Samantha Zhiying. “Transcriptomics-based study reveals a novel link between arginine methylation and phosphate regulation in Saccharomyces cerevisiae.” 2015. Web. 21 Jul 2019.

Vancouver:

Chia SZ. Transcriptomics-based study reveals a novel link between arginine methylation and phosphate regulation in Saccharomyces cerevisiae. [Internet] [Doctoral dissertation]. University of New South Wales; 2015. [cited 2019 Jul 21]. Available from: http://handle.unsw.edu.au/1959.4/55695 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:38565/SOURCE02?view=true.

Council of Science Editors:

Chia SZ. Transcriptomics-based study reveals a novel link between arginine methylation and phosphate regulation in Saccharomyces cerevisiae. [Doctoral Dissertation]. University of New South Wales; 2015. Available from: http://handle.unsw.edu.au/1959.4/55695 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:38565/SOURCE02?view=true


UCLA

9. Jain, Kanishk. Protein Arginine Methyltransferases: Catalytic Mechanisms and Crosstalk in Epigenetics.

Degree: Biochemistry & Molecular Biology, 2018, UCLA

 Over the last decade, protein arginine methyltransferases (PRMTs) have emerged as key regulators in epigenetic processes and have been shown to be crucial targets for… (more)

Subjects/Keywords: Biochemistry; Molecular biology; arginine methylation; epigenetics; histones; PRMT

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APA (6th Edition):

Jain, K. (2018). Protein Arginine Methyltransferases: Catalytic Mechanisms and Crosstalk in Epigenetics. (Thesis). UCLA. Retrieved from http://www.escholarship.org/uc/item/4ft92012

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):

Jain, Kanishk. “Protein Arginine Methyltransferases: Catalytic Mechanisms and Crosstalk in Epigenetics.” 2018. Thesis, UCLA. Accessed July 21, 2019. http://www.escholarship.org/uc/item/4ft92012.

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

MLA Handbook (7th Edition):

Jain, Kanishk. “Protein Arginine Methyltransferases: Catalytic Mechanisms and Crosstalk in Epigenetics.” 2018. Web. 21 Jul 2019.

Vancouver:

Jain K. Protein Arginine Methyltransferases: Catalytic Mechanisms and Crosstalk in Epigenetics. [Internet] [Thesis]. UCLA; 2018. [cited 2019 Jul 21]. Available from: http://www.escholarship.org/uc/item/4ft92012.

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

Council of Science Editors:

Jain K. Protein Arginine Methyltransferases: Catalytic Mechanisms and Crosstalk in Epigenetics. [Thesis]. UCLA; 2018. Available from: http://www.escholarship.org/uc/item/4ft92012

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


Texas Medical Center

10. Hsu, Jung-Mao. CROSSTALK BETWEEN R1175 METHYLATION AND Y1173 PHOSPHORYLATION NEGATIVELY MODULATES EGFR-MEDIATED ERK ACTIVATION.

Degree: PhD, 2011, Texas Medical Center

  Post-translational protein modifications are critical regulators of protein functions as they expand the signaling potentials of the modified proteins, leading to diverse physiological consequences.… (more)

Subjects/Keywords: EGFR; PRMT5; Protein Arginine Methylation; ERK; SHP1; Cancer Biology; Cell Biology

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APA (6th Edition):

Hsu, J. (2011). CROSSTALK BETWEEN R1175 METHYLATION AND Y1173 PHOSPHORYLATION NEGATIVELY MODULATES EGFR-MEDIATED ERK ACTIVATION. (Doctoral Dissertation). Texas Medical Center. Retrieved from http://digitalcommons.library.tmc.edu/utgsbs_dissertations/166

Chicago Manual of Style (16th Edition):

Hsu, Jung-Mao. “CROSSTALK BETWEEN R1175 METHYLATION AND Y1173 PHOSPHORYLATION NEGATIVELY MODULATES EGFR-MEDIATED ERK ACTIVATION.” 2011. Doctoral Dissertation, Texas Medical Center. Accessed July 21, 2019. http://digitalcommons.library.tmc.edu/utgsbs_dissertations/166.

MLA Handbook (7th Edition):

Hsu, Jung-Mao. “CROSSTALK BETWEEN R1175 METHYLATION AND Y1173 PHOSPHORYLATION NEGATIVELY MODULATES EGFR-MEDIATED ERK ACTIVATION.” 2011. Web. 21 Jul 2019.

Vancouver:

Hsu J. CROSSTALK BETWEEN R1175 METHYLATION AND Y1173 PHOSPHORYLATION NEGATIVELY MODULATES EGFR-MEDIATED ERK ACTIVATION. [Internet] [Doctoral dissertation]. Texas Medical Center; 2011. [cited 2019 Jul 21]. Available from: http://digitalcommons.library.tmc.edu/utgsbs_dissertations/166.

Council of Science Editors:

Hsu J. CROSSTALK BETWEEN R1175 METHYLATION AND Y1173 PHOSPHORYLATION NEGATIVELY MODULATES EGFR-MEDIATED ERK ACTIVATION. [Doctoral Dissertation]. Texas Medical Center; 2011. Available from: http://digitalcommons.library.tmc.edu/utgsbs_dissertations/166


Louisiana State University

11. Pellar, Gregory James. The post-translational methylation of arginine in the glycine arginine rich region of CHO nucleoin.

Degree: PhD, 2002, Louisiana State University

 Nucleolin is a nucleolar protein important for ribosome biogenesis. Nucleolin contains a conserved glycine arginine rich (GAR) domain near its carboxy terminus. GAR domains are… (more)

Subjects/Keywords: nucleolin; GAR domains; arginine methylation

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APA (6th Edition):

Pellar, G. J. (2002). The post-translational methylation of arginine in the glycine arginine rich region of CHO nucleoin. (Doctoral Dissertation). Louisiana State University. Retrieved from etd-0415102-111547 ; https://digitalcommons.lsu.edu/gradschool_dissertations/206

Chicago Manual of Style (16th Edition):

Pellar, Gregory James. “The post-translational methylation of arginine in the glycine arginine rich region of CHO nucleoin.” 2002. Doctoral Dissertation, Louisiana State University. Accessed July 21, 2019. etd-0415102-111547 ; https://digitalcommons.lsu.edu/gradschool_dissertations/206.

MLA Handbook (7th Edition):

Pellar, Gregory James. “The post-translational methylation of arginine in the glycine arginine rich region of CHO nucleoin.” 2002. Web. 21 Jul 2019.

Vancouver:

Pellar GJ. The post-translational methylation of arginine in the glycine arginine rich region of CHO nucleoin. [Internet] [Doctoral dissertation]. Louisiana State University; 2002. [cited 2019 Jul 21]. Available from: etd-0415102-111547 ; https://digitalcommons.lsu.edu/gradschool_dissertations/206.

Council of Science Editors:

Pellar GJ. The post-translational methylation of arginine in the glycine arginine rich region of CHO nucleoin. [Doctoral Dissertation]. Louisiana State University; 2002. Available from: etd-0415102-111547 ; https://digitalcommons.lsu.edu/gradschool_dissertations/206


University of Western Ontario

12. Coughlan, Niamh. The role of the arginine methyltransferase CARM1 in global transcriptional regulation.

Degree: 2014, University of Western Ontario

Arginine methylation is a prevalent post-translational modification that is found on many nuclear and cytoplasmic proteins, and has been implicated in the regulation of gene… (more)

Subjects/Keywords: Transcriptional regulation; arginine methylation; CARM1; p/CIP (SRC3); cancer; Biochemistry

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APA (6th Edition):

Coughlan, N. (2014). The role of the arginine methyltransferase CARM1 in global transcriptional regulation. (Thesis). University of Western Ontario. Retrieved from https://ir.lib.uwo.ca/etd/2013

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):

Coughlan, Niamh. “The role of the arginine methyltransferase CARM1 in global transcriptional regulation.” 2014. Thesis, University of Western Ontario. Accessed July 21, 2019. https://ir.lib.uwo.ca/etd/2013.

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

MLA Handbook (7th Edition):

Coughlan, Niamh. “The role of the arginine methyltransferase CARM1 in global transcriptional regulation.” 2014. Web. 21 Jul 2019.

Vancouver:

Coughlan N. The role of the arginine methyltransferase CARM1 in global transcriptional regulation. [Internet] [Thesis]. University of Western Ontario; 2014. [cited 2019 Jul 21]. Available from: https://ir.lib.uwo.ca/etd/2013.

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

Council of Science Editors:

Coughlan N. The role of the arginine methyltransferase CARM1 in global transcriptional regulation. [Thesis]. University of Western Ontario; 2014. Available from: https://ir.lib.uwo.ca/etd/2013

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


SUNY College at Brockport

13. Bumstead, Andrew R. Arginine Methylation and Enzymatic Activity of TbLpn, a Lipin Homologue from T. Brucei.

Degree: MS, Biology, 2016, SUNY College at Brockport

  Trypanosoma brucei is a flagellated protozoan parasite responsible for African Trypanosomiasis. T. brucei is a deadly immune-evasive parasite which circulates the bloodstream of mammalian… (more)

Subjects/Keywords: Trypanosoma brucei; protein arginine methylation; TbLpn; lipins; Biology

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APA (6th Edition):

Bumstead, A. R. (2016). Arginine Methylation and Enzymatic Activity of TbLpn, a Lipin Homologue from T. Brucei. (Thesis). SUNY College at Brockport. Retrieved from https://digitalcommons.brockport.edu/bio_theses/23

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):

Bumstead, Andrew R. “Arginine Methylation and Enzymatic Activity of TbLpn, a Lipin Homologue from T. Brucei.” 2016. Thesis, SUNY College at Brockport. Accessed July 21, 2019. https://digitalcommons.brockport.edu/bio_theses/23.

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

MLA Handbook (7th Edition):

Bumstead, Andrew R. “Arginine Methylation and Enzymatic Activity of TbLpn, a Lipin Homologue from T. Brucei.” 2016. Web. 21 Jul 2019.

Vancouver:

Bumstead AR. Arginine Methylation and Enzymatic Activity of TbLpn, a Lipin Homologue from T. Brucei. [Internet] [Thesis]. SUNY College at Brockport; 2016. [cited 2019 Jul 21]. Available from: https://digitalcommons.brockport.edu/bio_theses/23.

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

Council of Science Editors:

Bumstead AR. Arginine Methylation and Enzymatic Activity of TbLpn, a Lipin Homologue from T. Brucei. [Thesis]. SUNY College at Brockport; 2016. Available from: https://digitalcommons.brockport.edu/bio_theses/23

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


Utah State University

14. Gui, Shanying. Characterization of the Product Specificity and Kinetic Mechanism of Protein Arginine Methyltransferase 1.

Degree: PhD, Chemistry and Biochemistry, 2013, Utah State University

  Protein arginine methylation is an essential post-translational modification catalyzed by protein arginine methyltransferases (PRMTs). Type I PRMTs transfer the methyl group from S-adenosyl-L-methionine (AdoMet)… (more)

Subjects/Keywords: ADMA; arginine; kinetics; methylation; PRMT; product specificity; Biochemistry

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

APA (6th Edition):

Gui, S. (2013). Characterization of the Product Specificity and Kinetic Mechanism of Protein Arginine Methyltransferase 1. (Doctoral Dissertation). Utah State University. Retrieved from https://digitalcommons.usu.edu/etd/1980

Chicago Manual of Style (16th Edition):

Gui, Shanying. “Characterization of the Product Specificity and Kinetic Mechanism of Protein Arginine Methyltransferase 1.” 2013. Doctoral Dissertation, Utah State University. Accessed July 21, 2019. https://digitalcommons.usu.edu/etd/1980.

MLA Handbook (7th Edition):

Gui, Shanying. “Characterization of the Product Specificity and Kinetic Mechanism of Protein Arginine Methyltransferase 1.” 2013. Web. 21 Jul 2019.

Vancouver:

Gui S. Characterization of the Product Specificity and Kinetic Mechanism of Protein Arginine Methyltransferase 1. [Internet] [Doctoral dissertation]. Utah State University; 2013. [cited 2019 Jul 21]. Available from: https://digitalcommons.usu.edu/etd/1980.

Council of Science Editors:

Gui S. Characterization of the Product Specificity and Kinetic Mechanism of Protein Arginine Methyltransferase 1. [Doctoral Dissertation]. Utah State University; 2013. Available from: https://digitalcommons.usu.edu/etd/1980


University of New South Wales

15. 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 July 21, 2019. 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. 21 Jul 2019.

Vancouver:

Zhang L. Discovery and characterization of novel protein methyltransferases in Saccharomyces cerevisiae. [Internet] [Doctoral dissertation]. University of New South Wales; 2014. [cited 2019 Jul 21]. 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


University of Western Sydney

16. Jwad, Noor. Protein arginine methylation of CRMP and tubulin in mouse cortical neurons.

Degree: 2016, University of Western Sydney

 Protein arginine methylation is a common post-translational modification where methyl groups are added to the arginine residues of peptide chains. It is carried out by… (more)

Subjects/Keywords: arginine; methylation; proteins; tubulins; neurons; Thesis (Ph.D.) – Western Sydney University, 2016

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APA (6th Edition):

Jwad, N. (2016). Protein arginine methylation of CRMP and tubulin in mouse cortical neurons. (Thesis). University of Western Sydney. Retrieved from http://hdl.handle.net/1959.7/uws:38710

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):

Jwad, Noor. “Protein arginine methylation of CRMP and tubulin in mouse cortical neurons.” 2016. Thesis, University of Western Sydney. Accessed July 21, 2019. http://hdl.handle.net/1959.7/uws:38710.

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

MLA Handbook (7th Edition):

Jwad, Noor. “Protein arginine methylation of CRMP and tubulin in mouse cortical neurons.” 2016. Web. 21 Jul 2019.

Vancouver:

Jwad N. Protein arginine methylation of CRMP and tubulin in mouse cortical neurons. [Internet] [Thesis]. University of Western Sydney; 2016. [cited 2019 Jul 21]. Available from: http://hdl.handle.net/1959.7/uws:38710.

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

Council of Science Editors:

Jwad N. Protein arginine methylation of CRMP and tubulin in mouse cortical neurons. [Thesis]. University of Western Sydney; 2016. Available from: http://hdl.handle.net/1959.7/uws:38710

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


Texas Medical Center

17. Di Lorenzo, Alessandra. Gain-of-function Mouse Models to Investigate Biological Roles of PRMT6.

Degree: PhD, 2014, Texas Medical Center

  Gain-of-function Mouse Models to Investigate Biological Roles of PRMT6 Alessandra Di Lorenzo, Ph.D. Candidate Mentor: Dr. Mark T. Bedford Protein Arginine Methyltransferase 6 (PRMT6)… (more)

Subjects/Keywords: PRMT6; Arginine methylation; Transgenic mice; NF-kB; cancer; Biology; Laboratory and Basic Science Research

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

APA (6th Edition):

Di Lorenzo, A. (2014). Gain-of-function Mouse Models to Investigate Biological Roles of PRMT6. (Doctoral Dissertation). Texas Medical Center. Retrieved from http://digitalcommons.library.tmc.edu/utgsbs_dissertations/427

Chicago Manual of Style (16th Edition):

Di Lorenzo, Alessandra. “Gain-of-function Mouse Models to Investigate Biological Roles of PRMT6.” 2014. Doctoral Dissertation, Texas Medical Center. Accessed July 21, 2019. http://digitalcommons.library.tmc.edu/utgsbs_dissertations/427.

MLA Handbook (7th Edition):

Di Lorenzo, Alessandra. “Gain-of-function Mouse Models to Investigate Biological Roles of PRMT6.” 2014. Web. 21 Jul 2019.

Vancouver:

Di Lorenzo A. Gain-of-function Mouse Models to Investigate Biological Roles of PRMT6. [Internet] [Doctoral dissertation]. Texas Medical Center; 2014. [cited 2019 Jul 21]. Available from: http://digitalcommons.library.tmc.edu/utgsbs_dissertations/427.

Council of Science Editors:

Di Lorenzo A. Gain-of-function Mouse Models to Investigate Biological Roles of PRMT6. [Doctoral Dissertation]. Texas Medical Center; 2014. Available from: http://digitalcommons.library.tmc.edu/utgsbs_dissertations/427

18. V. Spadotto. THE ROLE OF ARGININE METHYLATION IN MIRNA BIOGENESIS INVESTIGATED BY MS-PROTEOMICS.

Degree: 2017, Università degli Studi di Milano

 MicroRNAs (miRNAs) are short, non-coding RNA molecules that fine tune gene expression at the post-transcriptional level. The efficient miRNA processing is fundamental to maintain their… (more)

Subjects/Keywords: Arginine methylation; PRMT1; proteomics; microRNAs; Large Drosha Complex; Settore BIO/10 - Biochimica

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

APA (6th Edition):

Spadotto, V. (2017). THE ROLE OF ARGININE METHYLATION IN MIRNA BIOGENESIS INVESTIGATED BY MS-PROTEOMICS. (Thesis). Università degli Studi di Milano. Retrieved from http://hdl.handle.net/2434/464940

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):

Spadotto, V.. “THE ROLE OF ARGININE METHYLATION IN MIRNA BIOGENESIS INVESTIGATED BY MS-PROTEOMICS.” 2017. Thesis, Università degli Studi di Milano. Accessed July 21, 2019. http://hdl.handle.net/2434/464940.

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

MLA Handbook (7th Edition):

Spadotto, V.. “THE ROLE OF ARGININE METHYLATION IN MIRNA BIOGENESIS INVESTIGATED BY MS-PROTEOMICS.” 2017. Web. 21 Jul 2019.

Vancouver:

Spadotto V. THE ROLE OF ARGININE METHYLATION IN MIRNA BIOGENESIS INVESTIGATED BY MS-PROTEOMICS. [Internet] [Thesis]. Università degli Studi di Milano; 2017. [cited 2019 Jul 21]. Available from: http://hdl.handle.net/2434/464940.

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

Council of Science Editors:

Spadotto V. THE ROLE OF ARGININE METHYLATION IN MIRNA BIOGENESIS INVESTIGATED BY MS-PROTEOMICS. [Thesis]. Università degli Studi di Milano; 2017. Available from: http://hdl.handle.net/2434/464940

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

19. MIGLIORI VALENTINA. The symmetric dimethylation of histone H3 arginine 2: A novel histone mark involved in Euchromatin maintenance.

Degree: 2012, National University of Singapore

Subjects/Keywords: histone; arginine methylation; epigenetics; chromatin; WDR5

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APA (6th Edition):

VALENTINA, M. (2012). The symmetric dimethylation of histone H3 arginine 2: A novel histone mark involved in Euchromatin maintenance. (Thesis). National University of Singapore. Retrieved from http://scholarbank.nus.edu.sg/handle/10635/34747

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):

VALENTINA, MIGLIORI. “The symmetric dimethylation of histone H3 arginine 2: A novel histone mark involved in Euchromatin maintenance.” 2012. Thesis, National University of Singapore. Accessed July 21, 2019. http://scholarbank.nus.edu.sg/handle/10635/34747.

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

MLA Handbook (7th Edition):

VALENTINA, MIGLIORI. “The symmetric dimethylation of histone H3 arginine 2: A novel histone mark involved in Euchromatin maintenance.” 2012. Web. 21 Jul 2019.

Vancouver:

VALENTINA M. The symmetric dimethylation of histone H3 arginine 2: A novel histone mark involved in Euchromatin maintenance. [Internet] [Thesis]. National University of Singapore; 2012. [cited 2019 Jul 21]. Available from: http://scholarbank.nus.edu.sg/handle/10635/34747.

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

Council of Science Editors:

VALENTINA M. The symmetric dimethylation of histone H3 arginine 2: A novel histone mark involved in Euchromatin maintenance. [Thesis]. National University of Singapore; 2012. Available from: http://scholarbank.nus.edu.sg/handle/10635/34747

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

20. MARCO BEZZI. Characterization of The Role of Protein Arginine Methyltransferase 5 (PRMT5) in Mammalian Development.

Degree: 2014, National University of Singapore

Subjects/Keywords: PRMT5; arginine; methylation; development; splicing; MDM4

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APA (6th Edition):

BEZZI, M. (2014). Characterization of The Role of Protein Arginine Methyltransferase 5 (PRMT5) in Mammalian Development. (Thesis). National University of Singapore. Retrieved from http://scholarbank.nus.edu.sg/handle/10635/77772

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):

BEZZI, MARCO. “Characterization of The Role of Protein Arginine Methyltransferase 5 (PRMT5) in Mammalian Development.” 2014. Thesis, National University of Singapore. Accessed July 21, 2019. http://scholarbank.nus.edu.sg/handle/10635/77772.

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

MLA Handbook (7th Edition):

BEZZI, MARCO. “Characterization of The Role of Protein Arginine Methyltransferase 5 (PRMT5) in Mammalian Development.” 2014. Web. 21 Jul 2019.

Vancouver:

BEZZI M. Characterization of The Role of Protein Arginine Methyltransferase 5 (PRMT5) in Mammalian Development. [Internet] [Thesis]. National University of Singapore; 2014. [cited 2019 Jul 21]. Available from: http://scholarbank.nus.edu.sg/handle/10635/77772.

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

Council of Science Editors:

BEZZI M. Characterization of The Role of Protein Arginine Methyltransferase 5 (PRMT5) in Mammalian Development. [Thesis]. National University of Singapore; 2014. Available from: http://scholarbank.nus.edu.sg/handle/10635/77772

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


University of Ottawa

21. Chitiprolu, Maneka. Novel Regulatory Mechanisms of Autophagy in Human Disease: Implications for the Development of Therapeutic Strategies .

Degree: 2018, University of Ottawa

 The dysfunction of autophagy pathways has been linked to the development and progression of numerous human diseases, in particular neurological disorders and cancer. Investigating these… (more)

Subjects/Keywords: Autophagy; RNA granules; ALS; Arginine methylation; Retrotransposon RNA; Tudor domain; Cancer; Exosomes

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APA (6th Edition):

Chitiprolu, M. (2018). Novel Regulatory Mechanisms of Autophagy in Human Disease: Implications for the Development of Therapeutic Strategies . (Thesis). University of Ottawa. Retrieved from http://hdl.handle.net/10393/38441

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):

Chitiprolu, Maneka. “Novel Regulatory Mechanisms of Autophagy in Human Disease: Implications for the Development of Therapeutic Strategies .” 2018. Thesis, University of Ottawa. Accessed July 21, 2019. http://hdl.handle.net/10393/38441.

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

MLA Handbook (7th Edition):

Chitiprolu, Maneka. “Novel Regulatory Mechanisms of Autophagy in Human Disease: Implications for the Development of Therapeutic Strategies .” 2018. Web. 21 Jul 2019.

Vancouver:

Chitiprolu M. Novel Regulatory Mechanisms of Autophagy in Human Disease: Implications for the Development of Therapeutic Strategies . [Internet] [Thesis]. University of Ottawa; 2018. [cited 2019 Jul 21]. Available from: http://hdl.handle.net/10393/38441.

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

Council of Science Editors:

Chitiprolu M. Novel Regulatory Mechanisms of Autophagy in Human Disease: Implications for the Development of Therapeutic Strategies . [Thesis]. University of Ottawa; 2018. Available from: http://hdl.handle.net/10393/38441

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


Texas Medical Center

22. Vemulapalli, Vidyasiri. Developing and using methyl-specific antibodies to study the biological roles of arginine methylation.

Degree: PhD, 2016, Texas Medical Center

Arginine residues can be modified in three different ways to produce asymmetric dimethylarginine (ADMA), symmetric dimethylarginine (SDMA), and monomethylarginine (MMA). These modifications are catalyzed… (more)

Subjects/Keywords: Arginine methylation; PRMT1; CARM1; MED12; ER; Monomethylation; asymmetric dimethylation; CARM1 substrates; Cell Biology; Medicine and Health Sciences; Molecular Biology

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APA (6th Edition):

Vemulapalli, V. (2016). Developing and using methyl-specific antibodies to study the biological roles of arginine methylation. (Doctoral Dissertation). Texas Medical Center. Retrieved from http://digitalcommons.library.tmc.edu/utgsbs_dissertations/648

Chicago Manual of Style (16th Edition):

Vemulapalli, Vidyasiri. “Developing and using methyl-specific antibodies to study the biological roles of arginine methylation.” 2016. Doctoral Dissertation, Texas Medical Center. Accessed July 21, 2019. http://digitalcommons.library.tmc.edu/utgsbs_dissertations/648.

MLA Handbook (7th Edition):

Vemulapalli, Vidyasiri. “Developing and using methyl-specific antibodies to study the biological roles of arginine methylation.” 2016. Web. 21 Jul 2019.

Vancouver:

Vemulapalli V. Developing and using methyl-specific antibodies to study the biological roles of arginine methylation. [Internet] [Doctoral dissertation]. Texas Medical Center; 2016. [cited 2019 Jul 21]. Available from: http://digitalcommons.library.tmc.edu/utgsbs_dissertations/648.

Council of Science Editors:

Vemulapalli V. Developing and using methyl-specific antibodies to study the biological roles of arginine methylation. [Doctoral Dissertation]. Texas Medical Center; 2016. Available from: http://digitalcommons.library.tmc.edu/utgsbs_dissertations/648


Texas Medical Center

23. Wang, Liang; and#60;pand#62;0000-0001-5038-694Xand#60;/pand#62. INVESTIGATING THE ROLE OF PRMT1 AND ARGININE METHYLATION OF HSP70 IN HUMAN PANCREATIC CANCER.

Degree: PhD, 2017, Texas Medical Center

  Protein arginine methyltransferase 1 (PRMT1) is the major arginine methyltransferase, which catalyzes the addition of one or two methyl groups to the arginine residues… (more)

Subjects/Keywords: pancreatic cancer; arginine methylation; PRMT1; protein-protein interaction; HSP70; drug resistance; Biochemistry; Cancer Biology; Medicine and Health Sciences; Molecular Biology

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APA (6th Edition):

Wang, L. a. (2017). INVESTIGATING THE ROLE OF PRMT1 AND ARGININE METHYLATION OF HSP70 IN HUMAN PANCREATIC CANCER. (Doctoral Dissertation). Texas Medical Center. Retrieved from http://digitalcommons.library.tmc.edu/utgsbs_dissertations/790

Chicago Manual of Style (16th Edition):

Wang, Liang; and#60;pand#62;0000-0001-5038-694Xand#60;/pand#62. “INVESTIGATING THE ROLE OF PRMT1 AND ARGININE METHYLATION OF HSP70 IN HUMAN PANCREATIC CANCER.” 2017. Doctoral Dissertation, Texas Medical Center. Accessed July 21, 2019. http://digitalcommons.library.tmc.edu/utgsbs_dissertations/790.

MLA Handbook (7th Edition):

Wang, Liang; and#60;pand#62;0000-0001-5038-694Xand#60;/pand#62. “INVESTIGATING THE ROLE OF PRMT1 AND ARGININE METHYLATION OF HSP70 IN HUMAN PANCREATIC CANCER.” 2017. Web. 21 Jul 2019.

Vancouver:

Wang La. INVESTIGATING THE ROLE OF PRMT1 AND ARGININE METHYLATION OF HSP70 IN HUMAN PANCREATIC CANCER. [Internet] [Doctoral dissertation]. Texas Medical Center; 2017. [cited 2019 Jul 21]. Available from: http://digitalcommons.library.tmc.edu/utgsbs_dissertations/790.

Council of Science Editors:

Wang La. INVESTIGATING THE ROLE OF PRMT1 AND ARGININE METHYLATION OF HSP70 IN HUMAN PANCREATIC CANCER. [Doctoral Dissertation]. Texas Medical Center; 2017. Available from: http://digitalcommons.library.tmc.edu/utgsbs_dissertations/790


Utah State University

24. 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 July 21, 2019. 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. 21 Jul 2019.

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 2019 Jul 21]. 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

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

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 July 21, 2019. 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. 21 Jul 2019.

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 2019 Jul 21]. 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

26. Lattouf, Hanine. Crosstalk entre la kinase LKB1 et l'arginine methyltransferase PRMT5 dans le cancer du sein : Crosstalk between the kinase LKB1 and the arginine methyltransferase PRMT5 in breast cancer.

Degree: Docteur es, Cancérologie, 2017, Lyon; École Doctorale des Sciences et de Technologie (Beyrouth)

La protéine arginine méthyltransférase 5 est la majeure arginine méthyltransférase de type II chez les mammifères, responsable de la génération de la majorité des arginines… (more)

Subjects/Keywords: PRMT5; LKB1; Methylation des arginines; Phosphorylation des threonines; Cancer du sein; Interaction proteique; PRMT5; LKB1; Arginine methylation; Threonine Phosphorylation; Breast Cancer; Protein Interaction; 616.99

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APA (6th Edition):

Lattouf, H. (2017). Crosstalk entre la kinase LKB1 et l'arginine methyltransferase PRMT5 dans le cancer du sein : Crosstalk between the kinase LKB1 and the arginine methyltransferase PRMT5 in breast cancer. (Doctoral Dissertation). Lyon; École Doctorale des Sciences et de Technologie (Beyrouth). Retrieved from http://www.theses.fr/2017LYSE1252

Chicago Manual of Style (16th Edition):

Lattouf, Hanine. “Crosstalk entre la kinase LKB1 et l'arginine methyltransferase PRMT5 dans le cancer du sein : Crosstalk between the kinase LKB1 and the arginine methyltransferase PRMT5 in breast cancer.” 2017. Doctoral Dissertation, Lyon; École Doctorale des Sciences et de Technologie (Beyrouth). Accessed July 21, 2019. http://www.theses.fr/2017LYSE1252.

MLA Handbook (7th Edition):

Lattouf, Hanine. “Crosstalk entre la kinase LKB1 et l'arginine methyltransferase PRMT5 dans le cancer du sein : Crosstalk between the kinase LKB1 and the arginine methyltransferase PRMT5 in breast cancer.” 2017. Web. 21 Jul 2019.

Vancouver:

Lattouf H. Crosstalk entre la kinase LKB1 et l'arginine methyltransferase PRMT5 dans le cancer du sein : Crosstalk between the kinase LKB1 and the arginine methyltransferase PRMT5 in breast cancer. [Internet] [Doctoral dissertation]. Lyon; École Doctorale des Sciences et de Technologie (Beyrouth); 2017. [cited 2019 Jul 21]. Available from: http://www.theses.fr/2017LYSE1252.

Council of Science Editors:

Lattouf H. Crosstalk entre la kinase LKB1 et l'arginine methyltransferase PRMT5 dans le cancer du sein : Crosstalk between the kinase LKB1 and the arginine methyltransferase PRMT5 in breast cancer. [Doctoral Dissertation]. Lyon; École Doctorale des Sciences et de Technologie (Beyrouth); 2017. Available from: http://www.theses.fr/2017LYSE1252

27. Stavride, Phoebe. Διαφορική ρύθμιση των γονιδίων του μείζονος συμπλόκου ιστοσυμβατότητας τάξης ΙΙ από τη μεθυλοτρανσφεράση PRMT6, μέσω μιας AT-hook, μιας νέας πρωτεϊνικής επικράτειας του RFX5.

Degree: 2011, University of Crete (UOC); Πανεπιστήμιο Κρήτης

The MHCII family of genes is of central importance to the development and function of the adaptive immune system. Transcription of all members of the… (more)

Subjects/Keywords: Μείζον σύμπλοκο ιστοσυμβατότητας τάξης ΙΙ; Μεθυλίωση αργινίνης; Μεθυλίωση αργινινών; MHCII; Major histocompatibility complex class II; HLA-DR; HLA-DQ; RFX5; PRMT6; AT-hook; Arginine methylation

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

APA (6th Edition):

Stavride, P. (2011). Διαφορική ρύθμιση των γονιδίων του μείζονος συμπλόκου ιστοσυμβατότητας τάξης ΙΙ από τη μεθυλοτρανσφεράση PRMT6, μέσω μιας AT-hook, μιας νέας πρωτεϊνικής επικράτειας του RFX5. (Thesis). University of Crete (UOC); Πανεπιστήμιο Κρήτης. Retrieved from http://hdl.handle.net/10442/hedi/34993

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):

Stavride, Phoebe. “Διαφορική ρύθμιση των γονιδίων του μείζονος συμπλόκου ιστοσυμβατότητας τάξης ΙΙ από τη μεθυλοτρανσφεράση PRMT6, μέσω μιας AT-hook, μιας νέας πρωτεϊνικής επικράτειας του RFX5.” 2011. Thesis, University of Crete (UOC); Πανεπιστήμιο Κρήτης. Accessed July 21, 2019. http://hdl.handle.net/10442/hedi/34993.

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

MLA Handbook (7th Edition):

Stavride, Phoebe. “Διαφορική ρύθμιση των γονιδίων του μείζονος συμπλόκου ιστοσυμβατότητας τάξης ΙΙ από τη μεθυλοτρανσφεράση PRMT6, μέσω μιας AT-hook, μιας νέας πρωτεϊνικής επικράτειας του RFX5.” 2011. Web. 21 Jul 2019.

Vancouver:

Stavride P. Διαφορική ρύθμιση των γονιδίων του μείζονος συμπλόκου ιστοσυμβατότητας τάξης ΙΙ από τη μεθυλοτρανσφεράση PRMT6, μέσω μιας AT-hook, μιας νέας πρωτεϊνικής επικράτειας του RFX5. [Internet] [Thesis]. University of Crete (UOC); Πανεπιστήμιο Κρήτης; 2011. [cited 2019 Jul 21]. Available from: http://hdl.handle.net/10442/hedi/34993.

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

Council of Science Editors:

Stavride P. Διαφορική ρύθμιση των γονιδίων του μείζονος συμπλόκου ιστοσυμβατότητας τάξης ΙΙ από τη μεθυλοτρανσφεράση PRMT6, μέσω μιας AT-hook, μιας νέας πρωτεϊνικής επικράτειας του RFX5. [Thesis]. University of Crete (UOC); Πανεπιστήμιο Κρήτης; 2011. Available from: http://hdl.handle.net/10442/hedi/34993

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

28. 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

…2 Figure 1.2- Protein arginine methylation mediated by PRMTs… …modifications include lysine acetylating, methylation, and ubiquitination, arginine methylation… …x5B;17] 4 Figure 1.2- Protein arginine methylation mediated by PRMTs PRMT1 and… …1 1.3 Protein arginine methyltransferase… …14 2.1.5 PRMT1 and PRMT6 methylation and interaction… 

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

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 July 21, 2019. 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. 21 Jul 2019.

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 2019 Jul 21]. 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

29. Bouchekioua-Bouzaghou, Katia. Étude de la régulation de la méthylation du récepteur aux œstrogènes de type alpha dans la carcinogenèse mammaire : rôle de la protéine kinase LKB1 : Regulation of estrogen receptor alpha methylation in breast carcinogenesis : involvment of the protein kinase LKB1.

Degree: Docteur es, Biologie moléculaire, cellulaire et oncologie, 2012, Université Claude Bernard – Lyon I

Parallèlement à leur action nucléaire, les œstrogènes exercent également des effets via une signalisation cytoplasmique par des mécanismes pas complètement élucidés. Nous avons mis en… (more)

Subjects/Keywords: Récepteur des oestrogènes; Voies non génomiques; Méthylation des arginines; PRMT1; LKB1; Cancer du sein; Estrogen receptor; Non genomic pathways; Arginine methylation; PRMT1; LKB1; Breast cancer; 616.994

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

APA (6th Edition):

Bouchekioua-Bouzaghou, K. (2012). Étude de la régulation de la méthylation du récepteur aux œstrogènes de type alpha dans la carcinogenèse mammaire : rôle de la protéine kinase LKB1 : Regulation of estrogen receptor alpha methylation in breast carcinogenesis : involvment of the protein kinase LKB1. (Doctoral Dissertation). Université Claude Bernard – Lyon I. Retrieved from http://www.theses.fr/2012LYO10088

Chicago Manual of Style (16th Edition):

Bouchekioua-Bouzaghou, Katia. “Étude de la régulation de la méthylation du récepteur aux œstrogènes de type alpha dans la carcinogenèse mammaire : rôle de la protéine kinase LKB1 : Regulation of estrogen receptor alpha methylation in breast carcinogenesis : involvment of the protein kinase LKB1.” 2012. Doctoral Dissertation, Université Claude Bernard – Lyon I. Accessed July 21, 2019. http://www.theses.fr/2012LYO10088.

MLA Handbook (7th Edition):

Bouchekioua-Bouzaghou, Katia. “Étude de la régulation de la méthylation du récepteur aux œstrogènes de type alpha dans la carcinogenèse mammaire : rôle de la protéine kinase LKB1 : Regulation of estrogen receptor alpha methylation in breast carcinogenesis : involvment of the protein kinase LKB1.” 2012. Web. 21 Jul 2019.

Vancouver:

Bouchekioua-Bouzaghou K. Étude de la régulation de la méthylation du récepteur aux œstrogènes de type alpha dans la carcinogenèse mammaire : rôle de la protéine kinase LKB1 : Regulation of estrogen receptor alpha methylation in breast carcinogenesis : involvment of the protein kinase LKB1. [Internet] [Doctoral dissertation]. Université Claude Bernard – Lyon I; 2012. [cited 2019 Jul 21]. Available from: http://www.theses.fr/2012LYO10088.

Council of Science Editors:

Bouchekioua-Bouzaghou K. Étude de la régulation de la méthylation du récepteur aux œstrogènes de type alpha dans la carcinogenèse mammaire : rôle de la protéine kinase LKB1 : Regulation of estrogen receptor alpha methylation in breast carcinogenesis : involvment of the protein kinase LKB1. [Doctoral Dissertation]. Université Claude Bernard – Lyon I; 2012. Available from: http://www.theses.fr/2012LYO10088

30. Poulard, Coralie. Étude de la régulation de la méthylation du récepteur aux œstrogènes de type alpha dans le cancer du sein : Regulation of estrogen receptor alpha methylation in breast cancer.

Degree: Docteur es, Aspects moléculaires et cellulaires de la biologie, 2013, Université Claude Bernard – Lyon I

Le cancer du sein représente une cause de mortalité élevée chez la femme. Le cancer du sein est un cancer hormono-dépendant. De ce fait, il… (more)

Subjects/Keywords: Récepteur aux oestrogènes; Voies non génomiques; Méthylation des arginines; PRMT1; Déméthylation; LKB1; JMJD6; Cancer du sein; Estrogen receptor; Non genomic signaling; Arginine methylation; PRMT1; Demethylation; LKB1; JMJD6; Breast cancer; 616.99

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

APA (6th Edition):

Poulard, C. (2013). Étude de la régulation de la méthylation du récepteur aux œstrogènes de type alpha dans le cancer du sein : Regulation of estrogen receptor alpha methylation in breast cancer. (Doctoral Dissertation). Université Claude Bernard – Lyon I. Retrieved from http://www.theses.fr/2013LYO10142

Chicago Manual of Style (16th Edition):

Poulard, Coralie. “Étude de la régulation de la méthylation du récepteur aux œstrogènes de type alpha dans le cancer du sein : Regulation of estrogen receptor alpha methylation in breast cancer.” 2013. Doctoral Dissertation, Université Claude Bernard – Lyon I. Accessed July 21, 2019. http://www.theses.fr/2013LYO10142.

MLA Handbook (7th Edition):

Poulard, Coralie. “Étude de la régulation de la méthylation du récepteur aux œstrogènes de type alpha dans le cancer du sein : Regulation of estrogen receptor alpha methylation in breast cancer.” 2013. Web. 21 Jul 2019.

Vancouver:

Poulard C. Étude de la régulation de la méthylation du récepteur aux œstrogènes de type alpha dans le cancer du sein : Regulation of estrogen receptor alpha methylation in breast cancer. [Internet] [Doctoral dissertation]. Université Claude Bernard – Lyon I; 2013. [cited 2019 Jul 21]. Available from: http://www.theses.fr/2013LYO10142.

Council of Science Editors:

Poulard C. Étude de la régulation de la méthylation du récepteur aux œstrogènes de type alpha dans le cancer du sein : Regulation of estrogen receptor alpha methylation in breast cancer. [Doctoral Dissertation]. Université Claude Bernard – Lyon I; 2013. Available from: http://www.theses.fr/2013LYO10142

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