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You searched for subject:(methylation). Showing records 1 – 30 of 1343 total matches.

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University of Georgia

1. Shi, Jinghua. Partitioning of the maize epigenome by the number of methyl groups on histone H3 lysines 9 and 27 & mapping maize centromeres and centormere evolution.

Degree: PhD, Plant Biology, 2009, University of Georgia

 Taking advantage of 3D light microscopy and the fine cytological resolution of maize pachytene chromosomes, we compared the distribution of individual methylation events to each… (more)

Subjects/Keywords: Histone methylation

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APA (6th Edition):

Shi, J. (2009). Partitioning of the maize epigenome by the number of methyl groups on histone H3 lysines 9 and 27 & mapping maize centromeres and centormere evolution. (Doctoral Dissertation). University of Georgia. Retrieved from http://purl.galileo.usg.edu/uga_etd/shi_jinghua_200905_phd

Chicago Manual of Style (16th Edition):

Shi, Jinghua. “Partitioning of the maize epigenome by the number of methyl groups on histone H3 lysines 9 and 27 & mapping maize centromeres and centormere evolution.” 2009. Doctoral Dissertation, University of Georgia. Accessed December 13, 2018. http://purl.galileo.usg.edu/uga_etd/shi_jinghua_200905_phd.

MLA Handbook (7th Edition):

Shi, Jinghua. “Partitioning of the maize epigenome by the number of methyl groups on histone H3 lysines 9 and 27 & mapping maize centromeres and centormere evolution.” 2009. Web. 13 Dec 2018.

Vancouver:

Shi J. Partitioning of the maize epigenome by the number of methyl groups on histone H3 lysines 9 and 27 & mapping maize centromeres and centormere evolution. [Internet] [Doctoral dissertation]. University of Georgia; 2009. [cited 2018 Dec 13]. Available from: http://purl.galileo.usg.edu/uga_etd/shi_jinghua_200905_phd.

Council of Science Editors:

Shi J. Partitioning of the maize epigenome by the number of methyl groups on histone H3 lysines 9 and 27 & mapping maize centromeres and centormere evolution. [Doctoral Dissertation]. University of Georgia; 2009. Available from: http://purl.galileo.usg.edu/uga_etd/shi_jinghua_200905_phd


University of Georgia

2. Taniguchi, Yu. The relationship between DNA methylation and nucleosome occupancy involving in a transcriptional activity of SOX2.

Degree: BS, Biochemistry and Molecular Biology, 2010, University of Georgia

 Histone modifications, DNA methylation, and nucleosome occupancy are known to play an important role in regulation of transcription. The purpose of the study was to… (more)

Subjects/Keywords: DNA methylation

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APA (6th Edition):

Taniguchi, Y. (2010). The relationship between DNA methylation and nucleosome occupancy involving in a transcriptional activity of SOX2. (Thesis). University of Georgia. Retrieved from http://purl.galileo.usg.edu/uga_etd/taniguchi_yu_201005_bs

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):

Taniguchi, Yu. “The relationship between DNA methylation and nucleosome occupancy involving in a transcriptional activity of SOX2.” 2010. Thesis, University of Georgia. Accessed December 13, 2018. http://purl.galileo.usg.edu/uga_etd/taniguchi_yu_201005_bs.

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

MLA Handbook (7th Edition):

Taniguchi, Yu. “The relationship between DNA methylation and nucleosome occupancy involving in a transcriptional activity of SOX2.” 2010. Web. 13 Dec 2018.

Vancouver:

Taniguchi Y. The relationship between DNA methylation and nucleosome occupancy involving in a transcriptional activity of SOX2. [Internet] [Thesis]. University of Georgia; 2010. [cited 2018 Dec 13]. Available from: http://purl.galileo.usg.edu/uga_etd/taniguchi_yu_201005_bs.

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

Council of Science Editors:

Taniguchi Y. The relationship between DNA methylation and nucleosome occupancy involving in a transcriptional activity of SOX2. [Thesis]. University of Georgia; 2010. Available from: http://purl.galileo.usg.edu/uga_etd/taniguchi_yu_201005_bs

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


University of Hong Kong

3. Kwan, Chun-kit, Peter. Development and application of a single mouse embryo DNA methylation-detection assay.

Degree: M. Phil., 2014, University of Hong Kong

 During preimplantation embryonic development, imprinting genes are susceptible to methylation changes by artificial manipulation, which may lead to developmental abnormalities. In addition, environmental endocrine disruptors… (more)

Subjects/Keywords: DNA - Methylation

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APA (6th Edition):

Kwan, Chun-kit, P. (2014). Development and application of a single mouse embryo DNA methylation-detection assay. (Masters Thesis). University of Hong Kong. Retrieved from Kwan, C. P. [關駿傑]. (2014). Development and application of a single mouse embryo DNA methylation-detection assay. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5194756 ; http://dx.doi.org/10.5353/th_b5194756 ; http://hdl.handle.net/10722/197532

Chicago Manual of Style (16th Edition):

Kwan, Chun-kit, Peter. “Development and application of a single mouse embryo DNA methylation-detection assay.” 2014. Masters Thesis, University of Hong Kong. Accessed December 13, 2018. Kwan, C. P. [關駿傑]. (2014). Development and application of a single mouse embryo DNA methylation-detection assay. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5194756 ; http://dx.doi.org/10.5353/th_b5194756 ; http://hdl.handle.net/10722/197532.

MLA Handbook (7th Edition):

Kwan, Chun-kit, Peter. “Development and application of a single mouse embryo DNA methylation-detection assay.” 2014. Web. 13 Dec 2018.

Vancouver:

Kwan, Chun-kit P. Development and application of a single mouse embryo DNA methylation-detection assay. [Internet] [Masters thesis]. University of Hong Kong; 2014. [cited 2018 Dec 13]. Available from: Kwan, C. P. [關駿傑]. (2014). Development and application of a single mouse embryo DNA methylation-detection assay. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5194756 ; http://dx.doi.org/10.5353/th_b5194756 ; http://hdl.handle.net/10722/197532.

Council of Science Editors:

Kwan, Chun-kit P. Development and application of a single mouse embryo DNA methylation-detection assay. [Masters Thesis]. University of Hong Kong; 2014. Available from: Kwan, C. P. [關駿傑]. (2014). Development and application of a single mouse embryo DNA methylation-detection assay. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5194756 ; http://dx.doi.org/10.5353/th_b5194756 ; http://hdl.handle.net/10722/197532


UCLA

4. Al-Hadid, Qais K. Identification and Biological Characterization of Ribosomal Protein Methyltransferases in Yeast and Humans.

Degree: Biochemistry & Molecular Biology, 2015, UCLA

 Post-translational modifications (PTMs) of proteins is key to the functionality of complex cellular processes. Methylation is one of the most common PTMs in nature. I… (more)

Subjects/Keywords: Biochemistry; Histidine Methylation; Lysine Methylation; Methylation; Methyltransferases; N-terminal Methylation; Ribosomes

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APA (6th Edition):

Al-Hadid, Q. K. (2015). Identification and Biological Characterization of Ribosomal Protein Methyltransferases in Yeast and Humans. (Thesis). UCLA. Retrieved from http://www.escholarship.org/uc/item/86d09939

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):

Al-Hadid, Qais K. “Identification and Biological Characterization of Ribosomal Protein Methyltransferases in Yeast and Humans.” 2015. Thesis, UCLA. Accessed December 13, 2018. http://www.escholarship.org/uc/item/86d09939.

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

MLA Handbook (7th Edition):

Al-Hadid, Qais K. “Identification and Biological Characterization of Ribosomal Protein Methyltransferases in Yeast and Humans.” 2015. Web. 13 Dec 2018.

Vancouver:

Al-Hadid QK. Identification and Biological Characterization of Ribosomal Protein Methyltransferases in Yeast and Humans. [Internet] [Thesis]. UCLA; 2015. [cited 2018 Dec 13]. Available from: http://www.escholarship.org/uc/item/86d09939.

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

Council of Science Editors:

Al-Hadid QK. Identification and Biological Characterization of Ribosomal Protein Methyltransferases in Yeast and Humans. [Thesis]. UCLA; 2015. Available from: http://www.escholarship.org/uc/item/86d09939

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


Oregon State University

5. Botsford, James Lawrence. Terminal methylation reactions in Saccharomyces cerevisiae.

Degree: PhD, Microbiology, 1968, Oregon State University

 A cell-free system for assessing the role of S-adenosyl-methionine in the methylation of homocysteine deriving the methyl group from serine has been developed. No role… (more)

Subjects/Keywords: Methylation

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APA (6th Edition):

Botsford, J. L. (1968). Terminal methylation reactions in Saccharomyces cerevisiae. (Doctoral Dissertation). Oregon State University. Retrieved from http://hdl.handle.net/1957/46584

Chicago Manual of Style (16th Edition):

Botsford, James Lawrence. “Terminal methylation reactions in Saccharomyces cerevisiae.” 1968. Doctoral Dissertation, Oregon State University. Accessed December 13, 2018. http://hdl.handle.net/1957/46584.

MLA Handbook (7th Edition):

Botsford, James Lawrence. “Terminal methylation reactions in Saccharomyces cerevisiae.” 1968. Web. 13 Dec 2018.

Vancouver:

Botsford JL. Terminal methylation reactions in Saccharomyces cerevisiae. [Internet] [Doctoral dissertation]. Oregon State University; 1968. [cited 2018 Dec 13]. Available from: http://hdl.handle.net/1957/46584.

Council of Science Editors:

Botsford JL. Terminal methylation reactions in Saccharomyces cerevisiae. [Doctoral Dissertation]. Oregon State University; 1968. Available from: http://hdl.handle.net/1957/46584


University of Southern California

6. Triche, Timothy J., Jr. Preprocessing and analysis of DNA methylation microarrays.

Degree: PhD, Statistical Genetics and Genetic Epidemiology, 2013, University of Southern California

 In the first chapter of this dissertation, I review the importance of cytosine methylation in vertebrate genomes. In the second chapter, I present methods which… (more)

Subjects/Keywords: DNA methylation

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APA (6th Edition):

Triche, Timothy J., J. (2013). Preprocessing and analysis of DNA methylation microarrays. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/298429/rec/5200

Chicago Manual of Style (16th Edition):

Triche, Timothy J., Jr. “Preprocessing and analysis of DNA methylation microarrays.” 2013. Doctoral Dissertation, University of Southern California. Accessed December 13, 2018. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/298429/rec/5200.

MLA Handbook (7th Edition):

Triche, Timothy J., Jr. “Preprocessing and analysis of DNA methylation microarrays.” 2013. Web. 13 Dec 2018.

Vancouver:

Triche, Timothy J. J. Preprocessing and analysis of DNA methylation microarrays. [Internet] [Doctoral dissertation]. University of Southern California; 2013. [cited 2018 Dec 13]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/298429/rec/5200.

Council of Science Editors:

Triche, Timothy J. J. Preprocessing and analysis of DNA methylation microarrays. [Doctoral Dissertation]. University of Southern California; 2013. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/298429/rec/5200


Wake Forest University

7. Cammarata, Michael Wesley. DNA Methylation and Gene Expression of P2RY12 in a Multi-Ethnic Cohort.

Degree: 2015, Wake Forest University

Background: P2Y12 receptor is the target for thienopyridine mediated platelet inhibition. Epigenetic factors, including DNA methylation could influence gene expression and subsequent in vitro and clinical response to thienopyridine therapy. Our aim was to determine the relationships between DNA methylation at cis acting CpG sites and P2RY12 gene expression.

Subjects/Keywords: DNA Methylation

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APA (6th Edition):

Cammarata, M. W. (2015). DNA Methylation and Gene Expression of P2RY12 in a Multi-Ethnic Cohort. (Thesis). Wake Forest University. Retrieved from http://hdl.handle.net/10339/57275

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):

Cammarata, Michael Wesley. “DNA Methylation and Gene Expression of P2RY12 in a Multi-Ethnic Cohort.” 2015. Thesis, Wake Forest University. Accessed December 13, 2018. http://hdl.handle.net/10339/57275.

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

MLA Handbook (7th Edition):

Cammarata, Michael Wesley. “DNA Methylation and Gene Expression of P2RY12 in a Multi-Ethnic Cohort.” 2015. Web. 13 Dec 2018.

Vancouver:

Cammarata MW. DNA Methylation and Gene Expression of P2RY12 in a Multi-Ethnic Cohort. [Internet] [Thesis]. Wake Forest University; 2015. [cited 2018 Dec 13]. Available from: http://hdl.handle.net/10339/57275.

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

Council of Science Editors:

Cammarata MW. DNA Methylation and Gene Expression of P2RY12 in a Multi-Ethnic Cohort. [Thesis]. Wake Forest University; 2015. Available from: http://hdl.handle.net/10339/57275

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

8. Accomando, William Paul. Epigenetic Biomarkers for the Detection and Quantification of Human Leukocytes in Blood and Tissue.

Degree: PhD, Pathobiology, 2013, Brown University

 Different types of human cells, defined by function and morphology, are typically detected and enumerated in complex mixtures using a variety of physical, optical and… (more)

Subjects/Keywords: DNA methylation

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APA (6th Edition):

Accomando, W. P. (2013). Epigenetic Biomarkers for the Detection and Quantification of Human Leukocytes in Blood and Tissue. (Doctoral Dissertation). Brown University. Retrieved from https://repository.library.brown.edu/studio/item/bdr:320602/

Chicago Manual of Style (16th Edition):

Accomando, William Paul. “Epigenetic Biomarkers for the Detection and Quantification of Human Leukocytes in Blood and Tissue.” 2013. Doctoral Dissertation, Brown University. Accessed December 13, 2018. https://repository.library.brown.edu/studio/item/bdr:320602/.

MLA Handbook (7th Edition):

Accomando, William Paul. “Epigenetic Biomarkers for the Detection and Quantification of Human Leukocytes in Blood and Tissue.” 2013. Web. 13 Dec 2018.

Vancouver:

Accomando WP. Epigenetic Biomarkers for the Detection and Quantification of Human Leukocytes in Blood and Tissue. [Internet] [Doctoral dissertation]. Brown University; 2013. [cited 2018 Dec 13]. Available from: https://repository.library.brown.edu/studio/item/bdr:320602/.

Council of Science Editors:

Accomando WP. Epigenetic Biomarkers for the Detection and Quantification of Human Leukocytes in Blood and Tissue. [Doctoral Dissertation]. Brown University; 2013. Available from: https://repository.library.brown.edu/studio/item/bdr:320602/

9. Smith, Ashley A. Integration of Genetic and Epigenetic Alterations in the Discovery of Molecular Drivers of Malignancy in Glioma.

Degree: PhD, Pathobiology, 2014, Brown University

 Gliomas are a family of extremely aggressive brain cancers, which, despite current treatment options, have poor prognoses. There are distinct subtypes of gliomas, and accurately… (more)

Subjects/Keywords: DNA methylation

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APA (6th Edition):

Smith, A. A. (2014). Integration of Genetic and Epigenetic Alterations in the Discovery of Molecular Drivers of Malignancy in Glioma. (Doctoral Dissertation). Brown University. Retrieved from https://repository.library.brown.edu/studio/item/bdr:386178/

Chicago Manual of Style (16th Edition):

Smith, Ashley A. “Integration of Genetic and Epigenetic Alterations in the Discovery of Molecular Drivers of Malignancy in Glioma.” 2014. Doctoral Dissertation, Brown University. Accessed December 13, 2018. https://repository.library.brown.edu/studio/item/bdr:386178/.

MLA Handbook (7th Edition):

Smith, Ashley A. “Integration of Genetic and Epigenetic Alterations in the Discovery of Molecular Drivers of Malignancy in Glioma.” 2014. Web. 13 Dec 2018.

Vancouver:

Smith AA. Integration of Genetic and Epigenetic Alterations in the Discovery of Molecular Drivers of Malignancy in Glioma. [Internet] [Doctoral dissertation]. Brown University; 2014. [cited 2018 Dec 13]. Available from: https://repository.library.brown.edu/studio/item/bdr:386178/.

Council of Science Editors:

Smith AA. Integration of Genetic and Epigenetic Alterations in the Discovery of Molecular Drivers of Malignancy in Glioma. [Doctoral Dissertation]. Brown University; 2014. Available from: https://repository.library.brown.edu/studio/item/bdr:386178/

10. Cash, Haley L. DNA Methylation of Repeat Regions in Human Cancer and Metabolic Disease.

Degree: PhD, Pathobiology, 2011, Brown University

 Non-communicable diseases have recently surpassed communicable diseases as the number one cause of death globally. These conditions not only lead to increased rates of mortality,… (more)

Subjects/Keywords: DNA methylation

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APA (6th Edition):

Cash, H. L. (2011). DNA Methylation of Repeat Regions in Human Cancer and Metabolic Disease. (Doctoral Dissertation). Brown University. Retrieved from https://repository.library.brown.edu/studio/item/bdr:11329/

Chicago Manual of Style (16th Edition):

Cash, Haley L. “DNA Methylation of Repeat Regions in Human Cancer and Metabolic Disease.” 2011. Doctoral Dissertation, Brown University. Accessed December 13, 2018. https://repository.library.brown.edu/studio/item/bdr:11329/.

MLA Handbook (7th Edition):

Cash, Haley L. “DNA Methylation of Repeat Regions in Human Cancer and Metabolic Disease.” 2011. Web. 13 Dec 2018.

Vancouver:

Cash HL. DNA Methylation of Repeat Regions in Human Cancer and Metabolic Disease. [Internet] [Doctoral dissertation]. Brown University; 2011. [cited 2018 Dec 13]. Available from: https://repository.library.brown.edu/studio/item/bdr:11329/.

Council of Science Editors:

Cash HL. DNA Methylation of Repeat Regions in Human Cancer and Metabolic Disease. [Doctoral Dissertation]. Brown University; 2011. Available from: https://repository.library.brown.edu/studio/item/bdr:11329/


Kaunas University of Medicine

11. Kaselytė, Agnė. Assay of epigenetics changes in SFRP2 gene in grade II and grade III gliomas able to infleunce drug effects.

Degree: Master, Pharmacy, 2010, Kaunas University of Medicine

Two different mechanisms participate in the loss of SFRPs expression in cancer cells: allelic loss and epigenetic silencing [1]. Methylation status in grade II and… (more)

Subjects/Keywords: Glioma; Methylation; SFRP2 gene; Glioma; SFRP2; Methylation

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APA (6th Edition):

Kaselytė, Agnė. (2010). Assay of epigenetics changes in SFRP2 gene in grade II and grade III gliomas able to infleunce drug effects. (Masters Thesis). Kaunas University of Medicine. Retrieved from http://vddb.laba.lt/obj/LT-eLABa-0001:E.02~2010~D_20100621_092807-14356 ;

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete

Chicago Manual of Style (16th Edition):

Kaselytė, Agnė. “Assay of epigenetics changes in SFRP2 gene in grade II and grade III gliomas able to infleunce drug effects.” 2010. Masters Thesis, Kaunas University of Medicine. Accessed December 13, 2018. http://vddb.laba.lt/obj/LT-eLABa-0001:E.02~2010~D_20100621_092807-14356 ;.

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete

MLA Handbook (7th Edition):

Kaselytė, Agnė. “Assay of epigenetics changes in SFRP2 gene in grade II and grade III gliomas able to infleunce drug effects.” 2010. Web. 13 Dec 2018.

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete

Vancouver:

Kaselytė, Agnė. Assay of epigenetics changes in SFRP2 gene in grade II and grade III gliomas able to infleunce drug effects. [Internet] [Masters thesis]. Kaunas University of Medicine; 2010. [cited 2018 Dec 13]. Available from: http://vddb.laba.lt/obj/LT-eLABa-0001:E.02~2010~D_20100621_092807-14356 ;.

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete

Council of Science Editors:

Kaselytė, Agnė. Assay of epigenetics changes in SFRP2 gene in grade II and grade III gliomas able to infleunce drug effects. [Masters Thesis]. Kaunas University of Medicine; 2010. Available from: http://vddb.laba.lt/obj/LT-eLABa-0001:E.02~2010~D_20100621_092807-14356 ;

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete


University of Edinburgh

12. Termanis, Ausma. Regulators of DNA methylation in mammalian cells.

Degree: PhD, 2013, University of Edinburgh

 Although the many cells within a mammal share the same DNA sequence, their gene expression programmes are highly heterogeneous, and their functions correspondingly diverse. This… (more)

Subjects/Keywords: 572.8; epigenetics; DNA methylation; X chromosome methylation

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APA (6th Edition):

Termanis, A. (2013). Regulators of DNA methylation in mammalian cells. (Doctoral Dissertation). University of Edinburgh. Retrieved from http://hdl.handle.net/1842/11749

Chicago Manual of Style (16th Edition):

Termanis, Ausma. “Regulators of DNA methylation in mammalian cells.” 2013. Doctoral Dissertation, University of Edinburgh. Accessed December 13, 2018. http://hdl.handle.net/1842/11749.

MLA Handbook (7th Edition):

Termanis, Ausma. “Regulators of DNA methylation in mammalian cells.” 2013. Web. 13 Dec 2018.

Vancouver:

Termanis A. Regulators of DNA methylation in mammalian cells. [Internet] [Doctoral dissertation]. University of Edinburgh; 2013. [cited 2018 Dec 13]. Available from: http://hdl.handle.net/1842/11749.

Council of Science Editors:

Termanis A. Regulators of DNA methylation in mammalian cells. [Doctoral Dissertation]. University of Edinburgh; 2013. Available from: http://hdl.handle.net/1842/11749


University of Oxford

13. 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 December 13, 2018. 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. 13 Dec 2018.

Vancouver:

Lu Y. Arginine methylation on E2F1. [Internet] [Doctoral dissertation]. University of Oxford; 2014. [cited 2018 Dec 13]. 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 Hawaii – Manoa

14. Song, Min-Ae. Identification of aberrant epigenetic events in MSS/CIMP-negative colon cancer.

Degree: 2015, University of Hawaii – Manoa

Ph.D. University of Hawaii at Manoa 2014.

My research project focused on the identification of aberrant epigenetic changes via non-coding RNAs and DNA methylation in… (more)

Subjects/Keywords: RNAs; DNA methylation

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APA (6th Edition):

Song, M. (2015). Identification of aberrant epigenetic events in MSS/CIMP-negative colon cancer. (Thesis). University of Hawaii – Manoa. Retrieved from http://hdl.handle.net/10125/100485

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):

Song, Min-Ae. “Identification of aberrant epigenetic events in MSS/CIMP-negative colon cancer.” 2015. Thesis, University of Hawaii – Manoa. Accessed December 13, 2018. http://hdl.handle.net/10125/100485.

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

MLA Handbook (7th Edition):

Song, Min-Ae. “Identification of aberrant epigenetic events in MSS/CIMP-negative colon cancer.” 2015. Web. 13 Dec 2018.

Vancouver:

Song M. Identification of aberrant epigenetic events in MSS/CIMP-negative colon cancer. [Internet] [Thesis]. University of Hawaii – Manoa; 2015. [cited 2018 Dec 13]. Available from: http://hdl.handle.net/10125/100485.

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

Council of Science Editors:

Song M. Identification of aberrant epigenetic events in MSS/CIMP-negative colon cancer. [Thesis]. University of Hawaii – Manoa; 2015. Available from: http://hdl.handle.net/10125/100485

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


University of Hong Kong

15. Li, Tao. Structural and mechanistic insights into UHRF1-coordinated maintenance DNA methylation by DNMT1.

Degree: M. Phil., 2016, University of Hong Kong

DNA methylation is a crucial epigenetic modification and functions as a key factor in controlling gene expression and mammalian development. The DNA methyltransferase DNMT1 is… (more)

Subjects/Keywords: Ubiquitin; DNA - Methylation

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APA (6th Edition):

Li, T. (2016). Structural and mechanistic insights into UHRF1-coordinated maintenance DNA methylation by DNMT1. (Masters Thesis). University of Hong Kong. Retrieved from http://hdl.handle.net/10722/240653

Chicago Manual of Style (16th Edition):

Li, Tao. “Structural and mechanistic insights into UHRF1-coordinated maintenance DNA methylation by DNMT1.” 2016. Masters Thesis, University of Hong Kong. Accessed December 13, 2018. http://hdl.handle.net/10722/240653.

MLA Handbook (7th Edition):

Li, Tao. “Structural and mechanistic insights into UHRF1-coordinated maintenance DNA methylation by DNMT1.” 2016. Web. 13 Dec 2018.

Vancouver:

Li T. Structural and mechanistic insights into UHRF1-coordinated maintenance DNA methylation by DNMT1. [Internet] [Masters thesis]. University of Hong Kong; 2016. [cited 2018 Dec 13]. Available from: http://hdl.handle.net/10722/240653.

Council of Science Editors:

Li T. Structural and mechanistic insights into UHRF1-coordinated maintenance DNA methylation by DNMT1. [Masters Thesis]. University of Hong Kong; 2016. Available from: http://hdl.handle.net/10722/240653


University of Southern California

16. Houston, Sabrina Ishimaru. Studies of the biological relevance of Histone H4 Lysine 20 monomethylation: discovery of its role in the cell cycle and localization within the human genome.

Degree: PhD, Biochemistry & Molecular Biology, 2009, University of Southern California

 The post-translational modification of histones is thought to play a critical role in directing nuclear events involving chromatin. One such modification, Histone H4 Lysine 20… (more)

Subjects/Keywords: epigenetics; histone methylation

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APA (6th Edition):

Houston, S. I. (2009). Studies of the biological relevance of Histone H4 Lysine 20 monomethylation: discovery of its role in the cell cycle and localization within the human genome. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/558150/rec/6159

Chicago Manual of Style (16th Edition):

Houston, Sabrina Ishimaru. “Studies of the biological relevance of Histone H4 Lysine 20 monomethylation: discovery of its role in the cell cycle and localization within the human genome.” 2009. Doctoral Dissertation, University of Southern California. Accessed December 13, 2018. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/558150/rec/6159.

MLA Handbook (7th Edition):

Houston, Sabrina Ishimaru. “Studies of the biological relevance of Histone H4 Lysine 20 monomethylation: discovery of its role in the cell cycle and localization within the human genome.” 2009. Web. 13 Dec 2018.

Vancouver:

Houston SI. Studies of the biological relevance of Histone H4 Lysine 20 monomethylation: discovery of its role in the cell cycle and localization within the human genome. [Internet] [Doctoral dissertation]. University of Southern California; 2009. [cited 2018 Dec 13]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/558150/rec/6159.

Council of Science Editors:

Houston SI. Studies of the biological relevance of Histone H4 Lysine 20 monomethylation: discovery of its role in the cell cycle and localization within the human genome. [Doctoral Dissertation]. University of Southern California; 2009. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/558150/rec/6159


University of Montana

17. Barney, Patrick Anthony. THE DESIGN AND SYNTHESIS OF SMALL MOLECULE DRUGS TO INHIBIT EPIGENETIC ALTERATIONS CAUSED BY DNA METHYLTRANSFERASE 1.

Degree: PhD, 2016, University of Montana

 The acquisition of genomic alterations is a defining feature of human cancers. Many cancer chemotherapies rely upon an apoptotic pathway to eradicate cells containing those… (more)

Subjects/Keywords: DNMT1; inhibitor; methylation

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APA (6th Edition):

Barney, P. A. (2016). THE DESIGN AND SYNTHESIS OF SMALL MOLECULE DRUGS TO INHIBIT EPIGENETIC ALTERATIONS CAUSED BY DNA METHYLTRANSFERASE 1. (Doctoral Dissertation). University of Montana. Retrieved from https://scholarworks.umt.edu/etd/10737

Chicago Manual of Style (16th Edition):

Barney, Patrick Anthony. “THE DESIGN AND SYNTHESIS OF SMALL MOLECULE DRUGS TO INHIBIT EPIGENETIC ALTERATIONS CAUSED BY DNA METHYLTRANSFERASE 1.” 2016. Doctoral Dissertation, University of Montana. Accessed December 13, 2018. https://scholarworks.umt.edu/etd/10737.

MLA Handbook (7th Edition):

Barney, Patrick Anthony. “THE DESIGN AND SYNTHESIS OF SMALL MOLECULE DRUGS TO INHIBIT EPIGENETIC ALTERATIONS CAUSED BY DNA METHYLTRANSFERASE 1.” 2016. Web. 13 Dec 2018.

Vancouver:

Barney PA. THE DESIGN AND SYNTHESIS OF SMALL MOLECULE DRUGS TO INHIBIT EPIGENETIC ALTERATIONS CAUSED BY DNA METHYLTRANSFERASE 1. [Internet] [Doctoral dissertation]. University of Montana; 2016. [cited 2018 Dec 13]. Available from: https://scholarworks.umt.edu/etd/10737.

Council of Science Editors:

Barney PA. THE DESIGN AND SYNTHESIS OF SMALL MOLECULE DRUGS TO INHIBIT EPIGENETIC ALTERATIONS CAUSED BY DNA METHYLTRANSFERASE 1. [Doctoral Dissertation]. University of Montana; 2016. Available from: https://scholarworks.umt.edu/etd/10737


University of Edinburgh

18. Playfoot, Christopher James. Genome defence in hypomethylated developmental contexts.

Degree: PhD, 2017, University of Edinburgh

 Retrotransposons constitute around 40% of the mammalian genome and their aberrant activation can have wide ranging detrimental consequences, both throughout development and into somatic lineages.… (more)

Subjects/Keywords: DNA methylation; Tex19.1; retrotransposons

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APA (6th Edition):

Playfoot, C. J. (2017). Genome defence in hypomethylated developmental contexts. (Doctoral Dissertation). University of Edinburgh. Retrieved from http://hdl.handle.net/1842/28783

Chicago Manual of Style (16th Edition):

Playfoot, Christopher James. “Genome defence in hypomethylated developmental contexts.” 2017. Doctoral Dissertation, University of Edinburgh. Accessed December 13, 2018. http://hdl.handle.net/1842/28783.

MLA Handbook (7th Edition):

Playfoot, Christopher James. “Genome defence in hypomethylated developmental contexts.” 2017. Web. 13 Dec 2018.

Vancouver:

Playfoot CJ. Genome defence in hypomethylated developmental contexts. [Internet] [Doctoral dissertation]. University of Edinburgh; 2017. [cited 2018 Dec 13]. Available from: http://hdl.handle.net/1842/28783.

Council of Science Editors:

Playfoot CJ. Genome defence in hypomethylated developmental contexts. [Doctoral Dissertation]. University of Edinburgh; 2017. Available from: http://hdl.handle.net/1842/28783


University of Edinburgh

19. Perricone, Sara Maria. The role of DNA methylation in transcriptional regulation.

Degree: PhD, 2015, University of Edinburgh

 In mammals, the correct spatio-temporal patterns of gene expression are coordinated by transcription factor networks in combination with epigenetic signalling pathways. CpG methylation is an… (more)

Subjects/Keywords: 572.8; DNA methylation; transcription; hypomethylation

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APA (6th Edition):

Perricone, S. M. (2015). The role of DNA methylation in transcriptional regulation. (Doctoral Dissertation). University of Edinburgh. Retrieved from http://hdl.handle.net/1842/17866

Chicago Manual of Style (16th Edition):

Perricone, Sara Maria. “The role of DNA methylation in transcriptional regulation.” 2015. Doctoral Dissertation, University of Edinburgh. Accessed December 13, 2018. http://hdl.handle.net/1842/17866.

MLA Handbook (7th Edition):

Perricone, Sara Maria. “The role of DNA methylation in transcriptional regulation.” 2015. Web. 13 Dec 2018.

Vancouver:

Perricone SM. The role of DNA methylation in transcriptional regulation. [Internet] [Doctoral dissertation]. University of Edinburgh; 2015. [cited 2018 Dec 13]. Available from: http://hdl.handle.net/1842/17866.

Council of Science Editors:

Perricone SM. The role of DNA methylation in transcriptional regulation. [Doctoral Dissertation]. University of Edinburgh; 2015. Available from: http://hdl.handle.net/1842/17866


University of Alberta

20. Heit, Ryan. Epigenetic Regulation of Centromere Formation and Kinetochore Function.

Degree: MS, Department of Oncology, 2009, University of Alberta

 One form of protein regulation is accomplished by post-translational modification (PTM). In order to test the importance one type of PTM, methylation, in chromosome segregation,… (more)

Subjects/Keywords: centromere; methylation; mitosis; histones

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APA (6th Edition):

Heit, R. (2009). Epigenetic Regulation of Centromere Formation and Kinetochore Function. (Masters Thesis). University of Alberta. Retrieved from https://era.library.ualberta.ca/files/fx719n183

Chicago Manual of Style (16th Edition):

Heit, Ryan. “Epigenetic Regulation of Centromere Formation and Kinetochore Function.” 2009. Masters Thesis, University of Alberta. Accessed December 13, 2018. https://era.library.ualberta.ca/files/fx719n183.

MLA Handbook (7th Edition):

Heit, Ryan. “Epigenetic Regulation of Centromere Formation and Kinetochore Function.” 2009. Web. 13 Dec 2018.

Vancouver:

Heit R. Epigenetic Regulation of Centromere Formation and Kinetochore Function. [Internet] [Masters thesis]. University of Alberta; 2009. [cited 2018 Dec 13]. Available from: https://era.library.ualberta.ca/files/fx719n183.

Council of Science Editors:

Heit R. Epigenetic Regulation of Centromere Formation and Kinetochore Function. [Masters Thesis]. University of Alberta; 2009. Available from: https://era.library.ualberta.ca/files/fx719n183


University of Edinburgh

21. Ho, Kok Lian. Structural studies of MeCP2 in complex with methylated DNA.

Degree: 2009, University of Edinburgh

 DNA methylation is a common epigenetic mark that affects gene regulation, genomic stability and chromatin structure. In mammals, methylation is mainly found in the CpG… (more)

Subjects/Keywords: 571.4; DNA methylation; Rett mutations

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APA (6th Edition):

Ho, K. L. (2009). Structural studies of MeCP2 in complex with methylated DNA. (Doctoral Dissertation). University of Edinburgh. Retrieved from http://hdl.handle.net/1842/3801

Chicago Manual of Style (16th Edition):

Ho, Kok Lian. “Structural studies of MeCP2 in complex with methylated DNA.” 2009. Doctoral Dissertation, University of Edinburgh. Accessed December 13, 2018. http://hdl.handle.net/1842/3801.

MLA Handbook (7th Edition):

Ho, Kok Lian. “Structural studies of MeCP2 in complex with methylated DNA.” 2009. Web. 13 Dec 2018.

Vancouver:

Ho KL. Structural studies of MeCP2 in complex with methylated DNA. [Internet] [Doctoral dissertation]. University of Edinburgh; 2009. [cited 2018 Dec 13]. Available from: http://hdl.handle.net/1842/3801.

Council of Science Editors:

Ho KL. Structural studies of MeCP2 in complex with methylated DNA. [Doctoral Dissertation]. University of Edinburgh; 2009. Available from: http://hdl.handle.net/1842/3801

22. Choi, Chang-Sui. Change of DNA methylation status in response to environmental stress : 環境に応答したDNAメチル化の変化; カンキョウ ニ オウトウシタ DNA メチルカ ノ ヘンカ.

Degree: Nara Institute of Science and Technology / 奈良先端科学技術大学院大学

Subjects/Keywords: DNA methylation

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APA (6th Edition):

Choi, C. (n.d.). Change of DNA methylation status in response to environmental stress : 環境に応答したDNAメチル化の変化; カンキョウ ニ オウトウシタ DNA メチルカ ノ ヘンカ. (Thesis). Nara Institute of Science and Technology / 奈良先端科学技術大学院大学. Retrieved from http://hdl.handle.net/10061/4135

Note: this citation may be lacking information needed for this citation format:
No year of publication.
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Choi, Chang-Sui. “Change of DNA methylation status in response to environmental stress : 環境に応答したDNAメチル化の変化; カンキョウ ニ オウトウシタ DNA メチルカ ノ ヘンカ.” Thesis, Nara Institute of Science and Technology / 奈良先端科学技術大学院大学. Accessed December 13, 2018. http://hdl.handle.net/10061/4135.

Note: this citation may be lacking information needed for this citation format:
No year of publication.
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Choi, Chang-Sui. “Change of DNA methylation status in response to environmental stress : 環境に応答したDNAメチル化の変化; カンキョウ ニ オウトウシタ DNA メチルカ ノ ヘンカ.” Web. 13 Dec 2018.

Note: this citation may be lacking information needed for this citation format:
No year of publication.

Vancouver:

Choi C. Change of DNA methylation status in response to environmental stress : 環境に応答したDNAメチル化の変化; カンキョウ ニ オウトウシタ DNA メチルカ ノ ヘンカ. [Internet] [Thesis]. Nara Institute of Science and Technology / 奈良先端科学技術大学院大学; [cited 2018 Dec 13]. Available from: http://hdl.handle.net/10061/4135.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation
No year of publication.

Council of Science Editors:

Choi C. Change of DNA methylation status in response to environmental stress : 環境に応答したDNAメチル化の変化; カンキョウ ニ オウトウシタ DNA メチルカ ノ ヘンカ. [Thesis]. Nara Institute of Science and Technology / 奈良先端科学技術大学院大学; Available from: http://hdl.handle.net/10061/4135

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation
No year of publication.

23. Wada, Yuko. Biochemical properties and physiological function of DNA methyltransferases from tobacco plants : タバコDNAメチル化酵素の生化学的特徴と生理機能; タバコ DNA メチルカ コウソ ノ セイカガクテキ トクチョウ ト セイリ キノウ.

Degree: Nara Institute of Science and Technology / 奈良先端科学技術大学院大学

Subjects/Keywords: DNA methylation

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APA (6th Edition):

Wada, Y. (n.d.). Biochemical properties and physiological function of DNA methyltransferases from tobacco plants : タバコDNAメチル化酵素の生化学的特徴と生理機能; タバコ DNA メチルカ コウソ ノ セイカガクテキ トクチョウ ト セイリ キノウ. (Thesis). Nara Institute of Science and Technology / 奈良先端科学技術大学院大学. Retrieved from http://hdl.handle.net/10061/2817

Note: this citation may be lacking information needed for this citation format:
No year of publication.
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Wada, Yuko. “Biochemical properties and physiological function of DNA methyltransferases from tobacco plants : タバコDNAメチル化酵素の生化学的特徴と生理機能; タバコ DNA メチルカ コウソ ノ セイカガクテキ トクチョウ ト セイリ キノウ.” Thesis, Nara Institute of Science and Technology / 奈良先端科学技術大学院大学. Accessed December 13, 2018. http://hdl.handle.net/10061/2817.

Note: this citation may be lacking information needed for this citation format:
No year of publication.
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Wada, Yuko. “Biochemical properties and physiological function of DNA methyltransferases from tobacco plants : タバコDNAメチル化酵素の生化学的特徴と生理機能; タバコ DNA メチルカ コウソ ノ セイカガクテキ トクチョウ ト セイリ キノウ.” Web. 13 Dec 2018.

Note: this citation may be lacking information needed for this citation format:
No year of publication.

Vancouver:

Wada Y. Biochemical properties and physiological function of DNA methyltransferases from tobacco plants : タバコDNAメチル化酵素の生化学的特徴と生理機能; タバコ DNA メチルカ コウソ ノ セイカガクテキ トクチョウ ト セイリ キノウ. [Internet] [Thesis]. Nara Institute of Science and Technology / 奈良先端科学技術大学院大学; [cited 2018 Dec 13]. Available from: http://hdl.handle.net/10061/2817.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation
No year of publication.

Council of Science Editors:

Wada Y. Biochemical properties and physiological function of DNA methyltransferases from tobacco plants : タバコDNAメチル化酵素の生化学的特徴と生理機能; タバコ DNA メチルカ コウソ ノ セイカガクテキ トクチョウ ト セイリ キノウ. [Thesis]. Nara Institute of Science and Technology / 奈良先端科学技術大学院大学; Available from: http://hdl.handle.net/10061/2817

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation
No year of publication.


University of Edinburgh

24. Roberts, Kirsty Anne. Analysis of 14-3-3σ methylation and associated changes in gene expression and function in colorectal carcinoma.

Degree: PhD, 2010, University of Edinburgh

 The aims of the work presented in this thesis were: to investigate the role of methylation of 14-3-3σ (a key regulator of p53-mediated G2/M arrest… (more)

Subjects/Keywords: 616.994; cancer; epigenetics; methylation

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APA (6th Edition):

Roberts, K. A. (2010). Analysis of 14-3-3σ methylation and associated changes in gene expression and function in colorectal carcinoma. (Doctoral Dissertation). University of Edinburgh. Retrieved from http://hdl.handle.net/1842/4821

Chicago Manual of Style (16th Edition):

Roberts, Kirsty Anne. “Analysis of 14-3-3σ methylation and associated changes in gene expression and function in colorectal carcinoma.” 2010. Doctoral Dissertation, University of Edinburgh. Accessed December 13, 2018. http://hdl.handle.net/1842/4821.

MLA Handbook (7th Edition):

Roberts, Kirsty Anne. “Analysis of 14-3-3σ methylation and associated changes in gene expression and function in colorectal carcinoma.” 2010. Web. 13 Dec 2018.

Vancouver:

Roberts KA. Analysis of 14-3-3σ methylation and associated changes in gene expression and function in colorectal carcinoma. [Internet] [Doctoral dissertation]. University of Edinburgh; 2010. [cited 2018 Dec 13]. Available from: http://hdl.handle.net/1842/4821.

Council of Science Editors:

Roberts KA. Analysis of 14-3-3σ methylation and associated changes in gene expression and function in colorectal carcinoma. [Doctoral Dissertation]. University of Edinburgh; 2010. Available from: http://hdl.handle.net/1842/4821


Hong Kong University of Science and Technology

25. Kan, Junsuo. General replicators and replication origins in human cells and the role of yeast ORC in mediating histone methylation.

Degree: 2009, Hong Kong University of Science and Technology

 Initiation of DNA replication is controlled by the cis-acting replicators and the trans-acting initiator and initiation proteins that interact with replicators to initiate replication at… (more)

Subjects/Keywords: DNA replication; Histones; Methylation

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APA (6th Edition):

Kan, J. (2009). General replicators and replication origins in human cells and the role of yeast ORC in mediating histone methylation. (Thesis). Hong Kong University of Science and Technology. Retrieved from https://doi.org/10.14711/thesis-b1041255 ; http://repository.ust.hk/ir/bitstream/1783.1-6981/1/th_redirect.html

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

Chicago Manual of Style (16th Edition):

Kan, Junsuo. “General replicators and replication origins in human cells and the role of yeast ORC in mediating histone methylation.” 2009. Thesis, Hong Kong University of Science and Technology. Accessed December 13, 2018. https://doi.org/10.14711/thesis-b1041255 ; http://repository.ust.hk/ir/bitstream/1783.1-6981/1/th_redirect.html.

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

MLA Handbook (7th Edition):

Kan, Junsuo. “General replicators and replication origins in human cells and the role of yeast ORC in mediating histone methylation.” 2009. Web. 13 Dec 2018.

Vancouver:

Kan J. General replicators and replication origins in human cells and the role of yeast ORC in mediating histone methylation. [Internet] [Thesis]. Hong Kong University of Science and Technology; 2009. [cited 2018 Dec 13]. Available from: https://doi.org/10.14711/thesis-b1041255 ; http://repository.ust.hk/ir/bitstream/1783.1-6981/1/th_redirect.html.

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

Council of Science Editors:

Kan J. General replicators and replication origins in human cells and the role of yeast ORC in mediating histone methylation. [Thesis]. Hong Kong University of Science and Technology; 2009. Available from: https://doi.org/10.14711/thesis-b1041255 ; http://repository.ust.hk/ir/bitstream/1783.1-6981/1/th_redirect.html

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


University of Hong Kong

26. Wong, Kin-yiu. Correlation of TSPY expression level and its promoter methylation status in liver cancer.

Degree: Master of Medical Sciences, 2016, University of Hong Kong

Background: Hepatocellular carcinoma (HCC) is the 6th most common cancer and the 2nd leading cause of cancer deaths globally. TSPY (Testis-specific protein Y-encoded) is normally… (more)

Subjects/Keywords: Nucleoproteins; Liver - Cancer; DNA - Methylation

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APA (6th Edition):

Wong, K. (2016). Correlation of TSPY expression level and its promoter methylation status in liver cancer. (Masters Thesis). University of Hong Kong. Retrieved from http://hdl.handle.net/10722/237202

Chicago Manual of Style (16th Edition):

Wong, Kin-yiu. “Correlation of TSPY expression level and its promoter methylation status in liver cancer.” 2016. Masters Thesis, University of Hong Kong. Accessed December 13, 2018. http://hdl.handle.net/10722/237202.

MLA Handbook (7th Edition):

Wong, Kin-yiu. “Correlation of TSPY expression level and its promoter methylation status in liver cancer.” 2016. Web. 13 Dec 2018.

Vancouver:

Wong K. Correlation of TSPY expression level and its promoter methylation status in liver cancer. [Internet] [Masters thesis]. University of Hong Kong; 2016. [cited 2018 Dec 13]. Available from: http://hdl.handle.net/10722/237202.

Council of Science Editors:

Wong K. Correlation of TSPY expression level and its promoter methylation status in liver cancer. [Masters Thesis]. University of Hong Kong; 2016. Available from: http://hdl.handle.net/10722/237202


University of Edinburgh

27. Moffat, Michael. Aberrant DNA modification profiles in embryonic stem cells lacking polycomb repressive complexes.

Degree: PhD, 2016, University of Edinburgh

 Transcriptional repression is maintained by many molecular processes, including DNA methylation and polycomb repression. These two systems are both associated with chromatin modification at the… (more)

Subjects/Keywords: DNA methylation; chromatin; epigenetics; polycomb

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APA (6th Edition):

Moffat, M. (2016). Aberrant DNA modification profiles in embryonic stem cells lacking polycomb repressive complexes. (Doctoral Dissertation). University of Edinburgh. Retrieved from http://hdl.handle.net/1842/25711

Chicago Manual of Style (16th Edition):

Moffat, Michael. “Aberrant DNA modification profiles in embryonic stem cells lacking polycomb repressive complexes.” 2016. Doctoral Dissertation, University of Edinburgh. Accessed December 13, 2018. http://hdl.handle.net/1842/25711.

MLA Handbook (7th Edition):

Moffat, Michael. “Aberrant DNA modification profiles in embryonic stem cells lacking polycomb repressive complexes.” 2016. Web. 13 Dec 2018.

Vancouver:

Moffat M. Aberrant DNA modification profiles in embryonic stem cells lacking polycomb repressive complexes. [Internet] [Doctoral dissertation]. University of Edinburgh; 2016. [cited 2018 Dec 13]. Available from: http://hdl.handle.net/1842/25711.

Council of Science Editors:

Moffat M. Aberrant DNA modification profiles in embryonic stem cells lacking polycomb repressive complexes. [Doctoral Dissertation]. University of Edinburgh; 2016. Available from: http://hdl.handle.net/1842/25711


University of Hong Kong

28. Yeung, Kit-san. The use of genome-wide DNA methylation microarray to study both the common and rare diseases.

Degree: M. Phil., 2014, University of Hong Kong

 DNA methylation plays many important roles in human physiology such as imprinting and X chromosome inactivation (XCI), and therefore disruption in DNA methylation can lead… (more)

Subjects/Keywords: DNA - Methylation; Medical genetics

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APA (6th Edition):

Yeung, K. (2014). The use of genome-wide DNA methylation microarray to study both the common and rare diseases. (Masters Thesis). University of Hong Kong. Retrieved from Yeung, K. [楊傑燊]. (2014). The use of genome-wide DNA methylation microarray to study both the common and rare diseases. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5334844 ; http://dx.doi.org/10.5353/th_b5334844 ; http://hdl.handle.net/10722/220770

Chicago Manual of Style (16th Edition):

Yeung, Kit-san. “The use of genome-wide DNA methylation microarray to study both the common and rare diseases.” 2014. Masters Thesis, University of Hong Kong. Accessed December 13, 2018. Yeung, K. [楊傑燊]. (2014). The use of genome-wide DNA methylation microarray to study both the common and rare diseases. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5334844 ; http://dx.doi.org/10.5353/th_b5334844 ; http://hdl.handle.net/10722/220770.

MLA Handbook (7th Edition):

Yeung, Kit-san. “The use of genome-wide DNA methylation microarray to study both the common and rare diseases.” 2014. Web. 13 Dec 2018.

Vancouver:

Yeung K. The use of genome-wide DNA methylation microarray to study both the common and rare diseases. [Internet] [Masters thesis]. University of Hong Kong; 2014. [cited 2018 Dec 13]. Available from: Yeung, K. [楊傑燊]. (2014). The use of genome-wide DNA methylation microarray to study both the common and rare diseases. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5334844 ; http://dx.doi.org/10.5353/th_b5334844 ; http://hdl.handle.net/10722/220770.

Council of Science Editors:

Yeung K. The use of genome-wide DNA methylation microarray to study both the common and rare diseases. [Masters Thesis]. University of Hong Kong; 2014. Available from: Yeung, K. [楊傑燊]. (2014). The use of genome-wide DNA methylation microarray to study both the common and rare diseases. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5334844 ; http://dx.doi.org/10.5353/th_b5334844 ; http://hdl.handle.net/10722/220770


University of North Carolina – Greensboro

29. Rumph, Candie. Aberrant DNA methylation and patterns of histone modifications at the WNT5A Promoter B in osteosarcoma cells.

Degree: 2014, University of North Carolina – Greensboro

 WNT5A is a secreted ligand involved in differentiation, proliferation, cell movement and apoptosis. WNT5A is often misregulated in cancer and is known to be involved… (more)

Subjects/Keywords: Wnt proteins; DNA – Methylation; Osteosarcoma

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

APA (6th Edition):

Rumph, C. (2014). Aberrant DNA methylation and patterns of histone modifications at the WNT5A Promoter B in osteosarcoma cells. (Masters Thesis). University of North Carolina – Greensboro. Retrieved from http://libres.uncg.edu/ir/listing.aspx?styp=ti&id=16604

Chicago Manual of Style (16th Edition):

Rumph, Candie. “Aberrant DNA methylation and patterns of histone modifications at the WNT5A Promoter B in osteosarcoma cells.” 2014. Masters Thesis, University of North Carolina – Greensboro. Accessed December 13, 2018. http://libres.uncg.edu/ir/listing.aspx?styp=ti&id=16604.

MLA Handbook (7th Edition):

Rumph, Candie. “Aberrant DNA methylation and patterns of histone modifications at the WNT5A Promoter B in osteosarcoma cells.” 2014. Web. 13 Dec 2018.

Vancouver:

Rumph C. Aberrant DNA methylation and patterns of histone modifications at the WNT5A Promoter B in osteosarcoma cells. [Internet] [Masters thesis]. University of North Carolina – Greensboro; 2014. [cited 2018 Dec 13]. Available from: http://libres.uncg.edu/ir/listing.aspx?styp=ti&id=16604.

Council of Science Editors:

Rumph C. Aberrant DNA methylation and patterns of histone modifications at the WNT5A Promoter B in osteosarcoma cells. [Masters Thesis]. University of North Carolina – Greensboro; 2014. Available from: http://libres.uncg.edu/ir/listing.aspx?styp=ti&id=16604


Penn State University

30. Abu Bakar, Nur Suhada. Transgenerational inheritance of epigenetic regulation by Unstable factor for orange1 in maize.

Degree: MS, Agronomy, 2013, Penn State University

 Epigenetics is the study of heritable changes in gene expression or cellular phenotype that are attributable to mechanisms other than changes in DNA sequence. In… (more)

Subjects/Keywords: epigenetics; DNA methylation; inheritance

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

APA (6th Edition):

Abu Bakar, N. S. (2013). Transgenerational inheritance of epigenetic regulation by Unstable factor for orange1 in maize. (Masters Thesis). Penn State University. Retrieved from https://etda.libraries.psu.edu/catalog/18226

Chicago Manual of Style (16th Edition):

Abu Bakar, Nur Suhada. “Transgenerational inheritance of epigenetic regulation by Unstable factor for orange1 in maize.” 2013. Masters Thesis, Penn State University. Accessed December 13, 2018. https://etda.libraries.psu.edu/catalog/18226.

MLA Handbook (7th Edition):

Abu Bakar, Nur Suhada. “Transgenerational inheritance of epigenetic regulation by Unstable factor for orange1 in maize.” 2013. Web. 13 Dec 2018.

Vancouver:

Abu Bakar NS. Transgenerational inheritance of epigenetic regulation by Unstable factor for orange1 in maize. [Internet] [Masters thesis]. Penn State University; 2013. [cited 2018 Dec 13]. Available from: https://etda.libraries.psu.edu/catalog/18226.

Council of Science Editors:

Abu Bakar NS. Transgenerational inheritance of epigenetic regulation by Unstable factor for orange1 in maize. [Masters Thesis]. Penn State University; 2013. Available from: https://etda.libraries.psu.edu/catalog/18226

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