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You searched for subject:(Histone Modifications). Showing records 1 – 30 of 146 total matches.

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Texas A&M University

1. Veazey, Kylee Jordan. An Epigenetic Basis to the Etiology of Fetal Alcohol Spectrum Disorders.

Degree: PhD, Genetics, 2015, Texas A&M University

 Observations from a number of independent laboratories indicate that ethanol has the capacity to act as a powerful epigenetic disruptor and potentially derail the process… (more)

Subjects/Keywords: Epigenetics; FASD; Histone Modifications

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APA (6th Edition):

Veazey, K. J. (2015). An Epigenetic Basis to the Etiology of Fetal Alcohol Spectrum Disorders. (Doctoral Dissertation). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/156462

Chicago Manual of Style (16th Edition):

Veazey, Kylee Jordan. “An Epigenetic Basis to the Etiology of Fetal Alcohol Spectrum Disorders.” 2015. Doctoral Dissertation, Texas A&M University. Accessed January 24, 2021. http://hdl.handle.net/1969.1/156462.

MLA Handbook (7th Edition):

Veazey, Kylee Jordan. “An Epigenetic Basis to the Etiology of Fetal Alcohol Spectrum Disorders.” 2015. Web. 24 Jan 2021.

Vancouver:

Veazey KJ. An Epigenetic Basis to the Etiology of Fetal Alcohol Spectrum Disorders. [Internet] [Doctoral dissertation]. Texas A&M University; 2015. [cited 2021 Jan 24]. Available from: http://hdl.handle.net/1969.1/156462.

Council of Science Editors:

Veazey KJ. An Epigenetic Basis to the Etiology of Fetal Alcohol Spectrum Disorders. [Doctoral Dissertation]. Texas A&M University; 2015. Available from: http://hdl.handle.net/1969.1/156462


Linköping University

2. Wettermark, Anna. Histone modifications and their role in splicing.

Degree: Biology, 2020, Linköping University

  Splicing is the process when introns gets removed and exons are spliced together. This is an important step to form a clean mRNA with… (more)

Subjects/Keywords: Splicing; Spliceosome; Histone modifications; epigenetics; histone methylation; histone acetylation; histone phosphorylation; histone ubiquitination; Genetics; Genetik

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APA (6th Edition):

Wettermark, A. (2020). Histone modifications and their role in splicing. (Thesis). Linköping University. Retrieved from http://urn.kb.se/resolve?urn=urn:nbn:se:liu:diva-166639

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):

Wettermark, Anna. “Histone modifications and their role in splicing.” 2020. Thesis, Linköping University. Accessed January 24, 2021. http://urn.kb.se/resolve?urn=urn:nbn:se:liu:diva-166639.

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

MLA Handbook (7th Edition):

Wettermark, Anna. “Histone modifications and their role in splicing.” 2020. Web. 24 Jan 2021.

Vancouver:

Wettermark A. Histone modifications and their role in splicing. [Internet] [Thesis]. Linköping University; 2020. [cited 2021 Jan 24]. Available from: http://urn.kb.se/resolve?urn=urn:nbn:se:liu:diva-166639.

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

Council of Science Editors:

Wettermark A. Histone modifications and their role in splicing. [Thesis]. Linköping University; 2020. Available from: http://urn.kb.se/resolve?urn=urn:nbn:se:liu:diva-166639

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


Princeton University

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

Degree: PhD, 2014, Princeton University

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

Subjects/Keywords: histone post translational modifications; mass spectrometry

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APA (6th Edition):

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

Chicago Manual of Style (16th Edition):

Britton, Laura-Mae. “Serine, Threonine and Tyrosine O-Acetylation in the Chromatin Landscape .” 2014. Doctoral Dissertation, Princeton University. Accessed January 24, 2021. http://arks.princeton.edu/ark:/88435/dsp016969z300m.

MLA Handbook (7th Edition):

Britton, Laura-Mae. “Serine, Threonine and Tyrosine O-Acetylation in the Chromatin Landscape .” 2014. Web. 24 Jan 2021.

Vancouver:

Britton L. Serine, Threonine and Tyrosine O-Acetylation in the Chromatin Landscape . [Internet] [Doctoral dissertation]. Princeton University; 2014. [cited 2021 Jan 24]. Available from: http://arks.princeton.edu/ark:/88435/dsp016969z300m.

Council of Science Editors:

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


University of Illinois – Urbana-Champaign

4. Li, Mingxi. Quantitative proteomic analysis of cellular senescence: from systems biology to targeted signaling pathways.

Degree: PhD, 0318, 2012, University of Illinois – Urbana-Champaign

 Cellular senescence, an irreversible cell cycle arrest induced by a diversity of stimuli, has been considered as an innate tumor suppressing mechanism with implications and… (more)

Subjects/Keywords: quantitative proteomics; cellular senescence; histone modifications

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APA (6th Edition):

Li, M. (2012). Quantitative proteomic analysis of cellular senescence: from systems biology to targeted signaling pathways. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/29510

Chicago Manual of Style (16th Edition):

Li, Mingxi. “Quantitative proteomic analysis of cellular senescence: from systems biology to targeted signaling pathways.” 2012. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed January 24, 2021. http://hdl.handle.net/2142/29510.

MLA Handbook (7th Edition):

Li, Mingxi. “Quantitative proteomic analysis of cellular senescence: from systems biology to targeted signaling pathways.” 2012. Web. 24 Jan 2021.

Vancouver:

Li M. Quantitative proteomic analysis of cellular senescence: from systems biology to targeted signaling pathways. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2012. [cited 2021 Jan 24]. Available from: http://hdl.handle.net/2142/29510.

Council of Science Editors:

Li M. Quantitative proteomic analysis of cellular senescence: from systems biology to targeted signaling pathways. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2012. Available from: http://hdl.handle.net/2142/29510

5. Abd Hadi, Nur Annies Binti. DNA methylation dynamics and epigenetic diversity in development.

Degree: PhD, 2017, University of Edinburgh

 Epigenetics refers to heritable changes in phenotype without alterations to the genotype. Epigenetic changes involve two main mechanisms: DNA methylation and histone modification. Methylation of… (more)

Subjects/Keywords: DNA methylation; epigenetics; histone modifications; 5hmC

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APA (6th Edition):

Abd Hadi, N. A. B. (2017). DNA methylation dynamics and epigenetic diversity in development. (Doctoral Dissertation). University of Edinburgh. Retrieved from http://hdl.handle.net/1842/28778

Chicago Manual of Style (16th Edition):

Abd Hadi, Nur Annies Binti. “DNA methylation dynamics and epigenetic diversity in development.” 2017. Doctoral Dissertation, University of Edinburgh. Accessed January 24, 2021. http://hdl.handle.net/1842/28778.

MLA Handbook (7th Edition):

Abd Hadi, Nur Annies Binti. “DNA methylation dynamics and epigenetic diversity in development.” 2017. Web. 24 Jan 2021.

Vancouver:

Abd Hadi NAB. DNA methylation dynamics and epigenetic diversity in development. [Internet] [Doctoral dissertation]. University of Edinburgh; 2017. [cited 2021 Jan 24]. Available from: http://hdl.handle.net/1842/28778.

Council of Science Editors:

Abd Hadi NAB. DNA methylation dynamics and epigenetic diversity in development. [Doctoral Dissertation]. University of Edinburgh; 2017. Available from: http://hdl.handle.net/1842/28778


University of Georgia

6. Wang, Li. Interplay between transcription and chromatin dynamics.

Degree: 2016, University of Georgia

 Transcription of nuclear genes in eukaryotic organisms occurs in a chromatin environment, where the template DNA is wrapped around histone octamers to form nucleosomes. The… (more)

Subjects/Keywords: Transcription; Chromatin Dynamics; Heat Stress; Nucleosome Positioning; Histone Variants; Histone Modifications; Histone Methyltransferase; H3K27me3S28ph

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APA (6th Edition):

Wang, L. (2016). Interplay between transcription and chromatin dynamics. (Thesis). University of Georgia. Retrieved from http://hdl.handle.net/10724/34758

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):

Wang, Li. “Interplay between transcription and chromatin dynamics.” 2016. Thesis, University of Georgia. Accessed January 24, 2021. http://hdl.handle.net/10724/34758.

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

MLA Handbook (7th Edition):

Wang, Li. “Interplay between transcription and chromatin dynamics.” 2016. Web. 24 Jan 2021.

Vancouver:

Wang L. Interplay between transcription and chromatin dynamics. [Internet] [Thesis]. University of Georgia; 2016. [cited 2021 Jan 24]. Available from: http://hdl.handle.net/10724/34758.

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

Council of Science Editors:

Wang L. Interplay between transcription and chromatin dynamics. [Thesis]. University of Georgia; 2016. Available from: http://hdl.handle.net/10724/34758

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

7. M. Rubino. EPIGENETIC MODIFICATIONS ABOLISH THE EXPRESSION OF THE LONG PENTRAXIN PTX3 IN HUMAN TUMORS.

Degree: 2015, Università degli Studi di Milano

 PTX3 is a fluid-phase pattern recognition receptor that participates in innate immunity and inflammation by modulating complement activation, leukocyte recruitment, extracellular matrix deposition and angiogenesis.… (more)

Subjects/Keywords: PTX3; cancer; epigenetics modifications; enhancers; miRNAs; DNA methylation; histone modifications; Settore MED/04 - Patologia Generale

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APA (6th Edition):

Rubino, M. (2015). EPIGENETIC MODIFICATIONS ABOLISH THE EXPRESSION OF THE LONG PENTRAXIN PTX3 IN HUMAN TUMORS. (Thesis). Università degli Studi di Milano. Retrieved from http://hdl.handle.net/2434/254345

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):

Rubino, M.. “EPIGENETIC MODIFICATIONS ABOLISH THE EXPRESSION OF THE LONG PENTRAXIN PTX3 IN HUMAN TUMORS.” 2015. Thesis, Università degli Studi di Milano. Accessed January 24, 2021. http://hdl.handle.net/2434/254345.

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

MLA Handbook (7th Edition):

Rubino, M.. “EPIGENETIC MODIFICATIONS ABOLISH THE EXPRESSION OF THE LONG PENTRAXIN PTX3 IN HUMAN TUMORS.” 2015. Web. 24 Jan 2021.

Vancouver:

Rubino M. EPIGENETIC MODIFICATIONS ABOLISH THE EXPRESSION OF THE LONG PENTRAXIN PTX3 IN HUMAN TUMORS. [Internet] [Thesis]. Università degli Studi di Milano; 2015. [cited 2021 Jan 24]. Available from: http://hdl.handle.net/2434/254345.

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

Council of Science Editors:

Rubino M. EPIGENETIC MODIFICATIONS ABOLISH THE EXPRESSION OF THE LONG PENTRAXIN PTX3 IN HUMAN TUMORS. [Thesis]. Università degli Studi di Milano; 2015. Available from: http://hdl.handle.net/2434/254345

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


Wayne State University

8. Gajan, Ambikai. Analyzing The Interactions Of Kdm5/lid And Sin3 In Drosophila Melanogaster.

Degree: PhD, Biological Sciences, 2015, Wayne State University

  SIN3, the scaffold protein of a histone modifying complex is conserved from yeast to mammals. Drosophila SIN3 associates with both a histone deactylase RPD3… (more)

Subjects/Keywords: Cell proliferation; Development; Drosophila; Gene expression; Histone demethylase; Histone modifications; Biochemistry; Biology; Molecular Biology

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APA (6th Edition):

Gajan, A. (2015). Analyzing The Interactions Of Kdm5/lid And Sin3 In Drosophila Melanogaster. (Doctoral Dissertation). Wayne State University. Retrieved from https://digitalcommons.wayne.edu/oa_dissertations/1129

Chicago Manual of Style (16th Edition):

Gajan, Ambikai. “Analyzing The Interactions Of Kdm5/lid And Sin3 In Drosophila Melanogaster.” 2015. Doctoral Dissertation, Wayne State University. Accessed January 24, 2021. https://digitalcommons.wayne.edu/oa_dissertations/1129.

MLA Handbook (7th Edition):

Gajan, Ambikai. “Analyzing The Interactions Of Kdm5/lid And Sin3 In Drosophila Melanogaster.” 2015. Web. 24 Jan 2021.

Vancouver:

Gajan A. Analyzing The Interactions Of Kdm5/lid And Sin3 In Drosophila Melanogaster. [Internet] [Doctoral dissertation]. Wayne State University; 2015. [cited 2021 Jan 24]. Available from: https://digitalcommons.wayne.edu/oa_dissertations/1129.

Council of Science Editors:

Gajan A. Analyzing The Interactions Of Kdm5/lid And Sin3 In Drosophila Melanogaster. [Doctoral Dissertation]. Wayne State University; 2015. Available from: https://digitalcommons.wayne.edu/oa_dissertations/1129


University of Edinburgh

9. Aguilar Sanchez, Cristina. Epigenetic transitions in cardiovascular development and cell reprogramming.

Degree: PhD, 2017, University of Edinburgh

 Epigenetic modifications are alterations in the cell nucleus that affect gene expression and can occur in chromatin at the level of DNA methylation or histone(more)

Subjects/Keywords: epigenetics; post­-translational modifications; histone acetylation; histone methylation; cardiomyocytes; cardiomyocyte formation; cardiac heterochromatin; H3K9me3

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APA (6th Edition):

Aguilar Sanchez, C. (2017). Epigenetic transitions in cardiovascular development and cell reprogramming. (Doctoral Dissertation). University of Edinburgh. Retrieved from http://hdl.handle.net/1842/28787

Chicago Manual of Style (16th Edition):

Aguilar Sanchez, Cristina. “Epigenetic transitions in cardiovascular development and cell reprogramming.” 2017. Doctoral Dissertation, University of Edinburgh. Accessed January 24, 2021. http://hdl.handle.net/1842/28787.

MLA Handbook (7th Edition):

Aguilar Sanchez, Cristina. “Epigenetic transitions in cardiovascular development and cell reprogramming.” 2017. Web. 24 Jan 2021.

Vancouver:

Aguilar Sanchez C. Epigenetic transitions in cardiovascular development and cell reprogramming. [Internet] [Doctoral dissertation]. University of Edinburgh; 2017. [cited 2021 Jan 24]. Available from: http://hdl.handle.net/1842/28787.

Council of Science Editors:

Aguilar Sanchez C. Epigenetic transitions in cardiovascular development and cell reprogramming. [Doctoral Dissertation]. University of Edinburgh; 2017. Available from: http://hdl.handle.net/1842/28787

10. M. Soldi. ESTABLISHMENT AND OPTIMIZATION OF THE CHROP APPROACH, COMBINING CHIP AND MS-BASED PROTEOMICS, FOR THE CHARACTERIZATION OF THE CHROMATOME AT DISTINCT FUNCTIONAL DOMAINS.

Degree: 2013, Università degli Studi di Milano

 Chromatin is a highly dynamic, well-structured nucleoprotein complex of DNA and proteins that controls virtually all DNA-transactions. Chromatin dynamicity is regulated at specific loci by… (more)

Subjects/Keywords: chromatin; histone post-translational modifications; epigenetics; mass spectrometry; proteomics; SILAC; histone code readers; histone variants; Settore BIO/10 - Biochimica

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APA (6th Edition):

Soldi, M. (2013). ESTABLISHMENT AND OPTIMIZATION OF THE CHROP APPROACH, COMBINING CHIP AND MS-BASED PROTEOMICS, FOR THE CHARACTERIZATION OF THE CHROMATOME AT DISTINCT FUNCTIONAL DOMAINS. (Thesis). Università degli Studi di Milano. Retrieved from http://hdl.handle.net/2434/219069

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):

Soldi, M.. “ESTABLISHMENT AND OPTIMIZATION OF THE CHROP APPROACH, COMBINING CHIP AND MS-BASED PROTEOMICS, FOR THE CHARACTERIZATION OF THE CHROMATOME AT DISTINCT FUNCTIONAL DOMAINS.” 2013. Thesis, Università degli Studi di Milano. Accessed January 24, 2021. http://hdl.handle.net/2434/219069.

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

MLA Handbook (7th Edition):

Soldi, M.. “ESTABLISHMENT AND OPTIMIZATION OF THE CHROP APPROACH, COMBINING CHIP AND MS-BASED PROTEOMICS, FOR THE CHARACTERIZATION OF THE CHROMATOME AT DISTINCT FUNCTIONAL DOMAINS.” 2013. Web. 24 Jan 2021.

Vancouver:

Soldi M. ESTABLISHMENT AND OPTIMIZATION OF THE CHROP APPROACH, COMBINING CHIP AND MS-BASED PROTEOMICS, FOR THE CHARACTERIZATION OF THE CHROMATOME AT DISTINCT FUNCTIONAL DOMAINS. [Internet] [Thesis]. Università degli Studi di Milano; 2013. [cited 2021 Jan 24]. Available from: http://hdl.handle.net/2434/219069.

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

Council of Science Editors:

Soldi M. ESTABLISHMENT AND OPTIMIZATION OF THE CHROP APPROACH, COMBINING CHIP AND MS-BASED PROTEOMICS, FOR THE CHARACTERIZATION OF THE CHROMATOME AT DISTINCT FUNCTIONAL DOMAINS. [Thesis]. Università degli Studi di Milano; 2013. Available from: http://hdl.handle.net/2434/219069

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

11. Peterson, J.C. The histone code: what proteomics has taught us.

Degree: 2014, Universiteit Utrecht

 Within eukaryotic cells chromatin plays an important role in the regulation of gene expression. Nucleosomes form the fundamental repeating unit within chromatin. Nucleosomes consist each… (more)

Subjects/Keywords: Proteomics; Histone modifications; histone code; histone PTMs.

…properties when compared to other histones.[16] The histone code Histone modifications… …The great variety of histone modifications quickly led to the idea of a ‘histone code’. This… …histone code hypothesis explains how specific histone modifications located on one or more N… …core, blue indicates DNA, pink represents the protruding histone tails. Histone modifications… …modifications either on histone tails or the DNA itself. These modifications are known as epigenetic… 

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APA (6th Edition):

Peterson, J. C. (2014). The histone code: what proteomics has taught us. (Masters Thesis). Universiteit Utrecht. Retrieved from http://dspace.library.uu.nl:8080/handle/1874/294773

Chicago Manual of Style (16th Edition):

Peterson, J C. “The histone code: what proteomics has taught us.” 2014. Masters Thesis, Universiteit Utrecht. Accessed January 24, 2021. http://dspace.library.uu.nl:8080/handle/1874/294773.

MLA Handbook (7th Edition):

Peterson, J C. “The histone code: what proteomics has taught us.” 2014. Web. 24 Jan 2021.

Vancouver:

Peterson JC. The histone code: what proteomics has taught us. [Internet] [Masters thesis]. Universiteit Utrecht; 2014. [cited 2021 Jan 24]. Available from: http://dspace.library.uu.nl:8080/handle/1874/294773.

Council of Science Editors:

Peterson JC. The histone code: what proteomics has taught us. [Masters Thesis]. Universiteit Utrecht; 2014. Available from: http://dspace.library.uu.nl:8080/handle/1874/294773

12. Vossaert, Liesbeth. Histone H3 clipping in human embryonic stem cells: in pursuit of an epigenetic outcast.

Degree: 2014, Ghent University

 Epigenetic mechanisms such as posttranslational histone modifications (PTM) regulate gene expression (variations) without altering the DNA sequence itself. Human embryonic stem cells (hESC) are a… (more)

Subjects/Keywords: Biology and Life Sciences; Histone modifications; Epigenetics; Human embryonic stem cells; Histone proteolysis; Histone clipping; Proteomics; Quantitative PCR; Reference genes

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APA (6th Edition):

Vossaert, L. (2014). Histone H3 clipping in human embryonic stem cells: in pursuit of an epigenetic outcast. (Thesis). Ghent University. Retrieved from http://hdl.handle.net/1854/LU-5782946

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):

Vossaert, Liesbeth. “Histone H3 clipping in human embryonic stem cells: in pursuit of an epigenetic outcast.” 2014. Thesis, Ghent University. Accessed January 24, 2021. http://hdl.handle.net/1854/LU-5782946.

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

MLA Handbook (7th Edition):

Vossaert, Liesbeth. “Histone H3 clipping in human embryonic stem cells: in pursuit of an epigenetic outcast.” 2014. Web. 24 Jan 2021.

Vancouver:

Vossaert L. Histone H3 clipping in human embryonic stem cells: in pursuit of an epigenetic outcast. [Internet] [Thesis]. Ghent University; 2014. [cited 2021 Jan 24]. Available from: http://hdl.handle.net/1854/LU-5782946.

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

Council of Science Editors:

Vossaert L. Histone H3 clipping in human embryonic stem cells: in pursuit of an epigenetic outcast. [Thesis]. Ghent University; 2014. Available from: http://hdl.handle.net/1854/LU-5782946

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

13. Hsieh, Tsung-Han S. Three-dimensional Folding of Eukaryotic Genomes.

Degree: Interdisciplinary Graduate Program, Biochemistry and Molecular Pharmacology, 2017, U of Massachusetts : Med

  Chromatin packages eukaryotic genomes via a hierarchical series of folding steps, encrypting multiple layers of epigenetic information, which are capable of regulating nuclear transactions… (more)

Subjects/Keywords: Chromatin; Nucleosome; 3D genome; Histone modifications; Biotechnology; Genetics; Genomics; Molecular Biology

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APA (6th Edition):

Hsieh, T. S. (2017). Three-dimensional Folding of Eukaryotic Genomes. (Doctoral Dissertation). U of Massachusetts : Med. Retrieved from http://escholarship.umassmed.edu/gsbs_diss/903

Chicago Manual of Style (16th Edition):

Hsieh, Tsung-Han S. “Three-dimensional Folding of Eukaryotic Genomes.” 2017. Doctoral Dissertation, U of Massachusetts : Med. Accessed January 24, 2021. http://escholarship.umassmed.edu/gsbs_diss/903.

MLA Handbook (7th Edition):

Hsieh, Tsung-Han S. “Three-dimensional Folding of Eukaryotic Genomes.” 2017. Web. 24 Jan 2021.

Vancouver:

Hsieh TS. Three-dimensional Folding of Eukaryotic Genomes. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 2017. [cited 2021 Jan 24]. Available from: http://escholarship.umassmed.edu/gsbs_diss/903.

Council of Science Editors:

Hsieh TS. Three-dimensional Folding of Eukaryotic Genomes. [Doctoral Dissertation]. U of Massachusetts : Med; 2017. Available from: http://escholarship.umassmed.edu/gsbs_diss/903


Penn State University

14. Dogan, Nergiz. Elucidating Biological Function of Genomic DNA with Robust Signals of Biochemical Activity: Integrative Genome-wide Studies of Enhancers.

Degree: 2014, Penn State University

 Genome-wide measurements of epigenetic features such as histone modifications, occupancy by transcription factors and coactivators provide the opportunity to understand more globally how genes are… (more)

Subjects/Keywords: Functional genomics; Gene regulation; TAL1; GATA1; Histone modifications; Enhancer assay

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APA (6th Edition):

Dogan, N. (2014). Elucidating Biological Function of Genomic DNA with Robust Signals of Biochemical Activity: Integrative Genome-wide Studies of Enhancers. (Thesis). Penn State University. Retrieved from https://submit-etda.libraries.psu.edu/catalog/22714

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):

Dogan, Nergiz. “Elucidating Biological Function of Genomic DNA with Robust Signals of Biochemical Activity: Integrative Genome-wide Studies of Enhancers.” 2014. Thesis, Penn State University. Accessed January 24, 2021. https://submit-etda.libraries.psu.edu/catalog/22714.

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

MLA Handbook (7th Edition):

Dogan, Nergiz. “Elucidating Biological Function of Genomic DNA with Robust Signals of Biochemical Activity: Integrative Genome-wide Studies of Enhancers.” 2014. Web. 24 Jan 2021.

Vancouver:

Dogan N. Elucidating Biological Function of Genomic DNA with Robust Signals of Biochemical Activity: Integrative Genome-wide Studies of Enhancers. [Internet] [Thesis]. Penn State University; 2014. [cited 2021 Jan 24]. Available from: https://submit-etda.libraries.psu.edu/catalog/22714.

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

Council of Science Editors:

Dogan N. Elucidating Biological Function of Genomic DNA with Robust Signals of Biochemical Activity: Integrative Genome-wide Studies of Enhancers. [Thesis]. Penn State University; 2014. Available from: https://submit-etda.libraries.psu.edu/catalog/22714

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


Penn State University

15. Bulynko, Yaroslava. Role of Cysteine Protease Cathepsin L in Maintenance of Epigenetic Histone Modifications and Constitutive Heterochromatin .

Degree: 2008, Penn State University

 Cathepsin L (catL) is a lysosomal cysteine protease ubiquitously expressed in mammalian cells. It was recently shown to modulate several important chromatin-binding factors, however its… (more)

Subjects/Keywords: histone modifications; protease; chromatin

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APA (6th Edition):

Bulynko, Y. (2008). Role of Cysteine Protease Cathepsin L in Maintenance of Epigenetic Histone Modifications and Constitutive Heterochromatin . (Thesis). Penn State University. Retrieved from https://submit-etda.libraries.psu.edu/catalog/7247

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):

Bulynko, Yaroslava. “Role of Cysteine Protease Cathepsin L in Maintenance of Epigenetic Histone Modifications and Constitutive Heterochromatin .” 2008. Thesis, Penn State University. Accessed January 24, 2021. https://submit-etda.libraries.psu.edu/catalog/7247.

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

MLA Handbook (7th Edition):

Bulynko, Yaroslava. “Role of Cysteine Protease Cathepsin L in Maintenance of Epigenetic Histone Modifications and Constitutive Heterochromatin .” 2008. Web. 24 Jan 2021.

Vancouver:

Bulynko Y. Role of Cysteine Protease Cathepsin L in Maintenance of Epigenetic Histone Modifications and Constitutive Heterochromatin . [Internet] [Thesis]. Penn State University; 2008. [cited 2021 Jan 24]. Available from: https://submit-etda.libraries.psu.edu/catalog/7247.

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

Council of Science Editors:

Bulynko Y. Role of Cysteine Protease Cathepsin L in Maintenance of Epigenetic Histone Modifications and Constitutive Heterochromatin . [Thesis]. Penn State University; 2008. Available from: https://submit-etda.libraries.psu.edu/catalog/7247

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


Penn State University

16. Wu, Weisheng. ROLES OF HISTONE MODIFICATIONS AND TRANSCRIPTION FACTORS IN TRANSCRIPTION REGULATION IN ERYTHROPOIESIS.

Degree: 2011, Penn State University

 Cellular differentiation is a process in which pluripotent cells become morphologically and functionally more specialized cells, which happens in the development from monocellular zygote into… (more)

Subjects/Keywords: Histone modifications; transcription factors; erythropoiesis; epigenetics; chromatin states

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APA (6th Edition):

Wu, W. (2011). ROLES OF HISTONE MODIFICATIONS AND TRANSCRIPTION FACTORS IN TRANSCRIPTION REGULATION IN ERYTHROPOIESIS. (Thesis). Penn State University. Retrieved from https://submit-etda.libraries.psu.edu/catalog/12534

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, Weisheng. “ROLES OF HISTONE MODIFICATIONS AND TRANSCRIPTION FACTORS IN TRANSCRIPTION REGULATION IN ERYTHROPOIESIS.” 2011. Thesis, Penn State University. Accessed January 24, 2021. https://submit-etda.libraries.psu.edu/catalog/12534.

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

MLA Handbook (7th Edition):

Wu, Weisheng. “ROLES OF HISTONE MODIFICATIONS AND TRANSCRIPTION FACTORS IN TRANSCRIPTION REGULATION IN ERYTHROPOIESIS.” 2011. Web. 24 Jan 2021.

Vancouver:

Wu W. ROLES OF HISTONE MODIFICATIONS AND TRANSCRIPTION FACTORS IN TRANSCRIPTION REGULATION IN ERYTHROPOIESIS. [Internet] [Thesis]. Penn State University; 2011. [cited 2021 Jan 24]. Available from: https://submit-etda.libraries.psu.edu/catalog/12534.

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

Council of Science Editors:

Wu W. ROLES OF HISTONE MODIFICATIONS AND TRANSCRIPTION FACTORS IN TRANSCRIPTION REGULATION IN ERYTHROPOIESIS. [Thesis]. Penn State University; 2011. Available from: https://submit-etda.libraries.psu.edu/catalog/12534

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


University of Saskatchewan

17. Turner, Emma. The Anaphase-Promoting Complex Interacts with Histone Modification Proteins and Chromatin Assembly Factors.

Degree: 2011, University of Saskatchewan

 The Anaphase-Promoting Complex (APC) plays an important role in cell cycle progression. This evolutionarily conserved multi-subunit ubiquitin ligase is responsible for targeting proteins that hinder… (more)

Subjects/Keywords: Anaphase-promoting complex; histone modifications; genetics; protein degradation

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APA (6th Edition):

Turner, E. (2011). The Anaphase-Promoting Complex Interacts with Histone Modification Proteins and Chromatin Assembly Factors. (Thesis). University of Saskatchewan. Retrieved from http://hdl.handle.net/10388/ETD-2011-08-78

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):

Turner, Emma. “The Anaphase-Promoting Complex Interacts with Histone Modification Proteins and Chromatin Assembly Factors.” 2011. Thesis, University of Saskatchewan. Accessed January 24, 2021. http://hdl.handle.net/10388/ETD-2011-08-78.

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

MLA Handbook (7th Edition):

Turner, Emma. “The Anaphase-Promoting Complex Interacts with Histone Modification Proteins and Chromatin Assembly Factors.” 2011. Web. 24 Jan 2021.

Vancouver:

Turner E. The Anaphase-Promoting Complex Interacts with Histone Modification Proteins and Chromatin Assembly Factors. [Internet] [Thesis]. University of Saskatchewan; 2011. [cited 2021 Jan 24]. Available from: http://hdl.handle.net/10388/ETD-2011-08-78.

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

Council of Science Editors:

Turner E. The Anaphase-Promoting Complex Interacts with Histone Modification Proteins and Chromatin Assembly Factors. [Thesis]. University of Saskatchewan; 2011. Available from: http://hdl.handle.net/10388/ETD-2011-08-78

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


University of Toronto

18. Chen, Chih-yu. Identifying Tissue Specific Distal Regulatory Sequences in the Mouse Genome.

Degree: 2011, University of Toronto

Epigenetic modifications, transcription factor (TF) availability and chromatin conformation influence how a genome is interpreted by the transcriptional machinery responsible for gene expression. Enhancers buried… (more)

Subjects/Keywords: Enhancers; Epigenetics; Bioinformatics; Machine learning; Histone modifications; 0715; 0307

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APA (6th Edition):

Chen, C. (2011). Identifying Tissue Specific Distal Regulatory Sequences in the Mouse Genome. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/30544

Chicago Manual of Style (16th Edition):

Chen, Chih-yu. “Identifying Tissue Specific Distal Regulatory Sequences in the Mouse Genome.” 2011. Masters Thesis, University of Toronto. Accessed January 24, 2021. http://hdl.handle.net/1807/30544.

MLA Handbook (7th Edition):

Chen, Chih-yu. “Identifying Tissue Specific Distal Regulatory Sequences in the Mouse Genome.” 2011. Web. 24 Jan 2021.

Vancouver:

Chen C. Identifying Tissue Specific Distal Regulatory Sequences in the Mouse Genome. [Internet] [Masters thesis]. University of Toronto; 2011. [cited 2021 Jan 24]. Available from: http://hdl.handle.net/1807/30544.

Council of Science Editors:

Chen C. Identifying Tissue Specific Distal Regulatory Sequences in the Mouse Genome. [Masters Thesis]. University of Toronto; 2011. Available from: http://hdl.handle.net/1807/30544


Washington University in St. Louis

19. He, Yu. Developing Tools for Identifying Tissue-Specific Epigenetic Marks and Predicting DNA hydroxy/methylation.

Degree: PhD, Biology & Biomedical Sciences (Computational & Systems Biology), 2020, Washington University in St. Louis

 A single genome can derive phenotypically unique cell types through various epigenetic modifications that instruct specific gene expression patterns. Histone modifications, DNA methylation, and DNA… (more)

Subjects/Keywords: DNA hydroxymethylation, DNA methylation, epigenetics, histone modifications, tissue-specific enhancers; Genetics

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APA (6th Edition):

He, Y. (2020). Developing Tools for Identifying Tissue-Specific Epigenetic Marks and Predicting DNA hydroxy/methylation. (Doctoral Dissertation). Washington University in St. Louis. Retrieved from https://openscholarship.wustl.edu/art_sci_etds/2197

Chicago Manual of Style (16th Edition):

He, Yu. “Developing Tools for Identifying Tissue-Specific Epigenetic Marks and Predicting DNA hydroxy/methylation.” 2020. Doctoral Dissertation, Washington University in St. Louis. Accessed January 24, 2021. https://openscholarship.wustl.edu/art_sci_etds/2197.

MLA Handbook (7th Edition):

He, Yu. “Developing Tools for Identifying Tissue-Specific Epigenetic Marks and Predicting DNA hydroxy/methylation.” 2020. Web. 24 Jan 2021.

Vancouver:

He Y. Developing Tools for Identifying Tissue-Specific Epigenetic Marks and Predicting DNA hydroxy/methylation. [Internet] [Doctoral dissertation]. Washington University in St. Louis; 2020. [cited 2021 Jan 24]. Available from: https://openscholarship.wustl.edu/art_sci_etds/2197.

Council of Science Editors:

He Y. Developing Tools for Identifying Tissue-Specific Epigenetic Marks and Predicting DNA hydroxy/methylation. [Doctoral Dissertation]. Washington University in St. Louis; 2020. Available from: https://openscholarship.wustl.edu/art_sci_etds/2197


Harvard University

20. Larson, Jessica. Hidden Markov Models Predict Epigenetic Chromatin Domains.

Degree: PhD, Biostatistics, 2012, Harvard University

 Epigenetics is an important layer of transcriptional control necessary for cell-type specific gene regulation. We developed computational methods to analyze the combinatorial effect and large-scale… (more)

Subjects/Keywords: biostatistics; bioinformatics; chromatin; chromatin domains; epigenetics; hidden Markov models; histone modifications

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APA (6th Edition):

Larson, J. (2012). Hidden Markov Models Predict Epigenetic Chromatin Domains. (Doctoral Dissertation). Harvard University. Retrieved from http://nrs.harvard.edu/urn-3:HUL.InstRepos:10087396

Chicago Manual of Style (16th Edition):

Larson, Jessica. “Hidden Markov Models Predict Epigenetic Chromatin Domains.” 2012. Doctoral Dissertation, Harvard University. Accessed January 24, 2021. http://nrs.harvard.edu/urn-3:HUL.InstRepos:10087396.

MLA Handbook (7th Edition):

Larson, Jessica. “Hidden Markov Models Predict Epigenetic Chromatin Domains.” 2012. Web. 24 Jan 2021.

Vancouver:

Larson J. Hidden Markov Models Predict Epigenetic Chromatin Domains. [Internet] [Doctoral dissertation]. Harvard University; 2012. [cited 2021 Jan 24]. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:10087396.

Council of Science Editors:

Larson J. Hidden Markov Models Predict Epigenetic Chromatin Domains. [Doctoral Dissertation]. Harvard University; 2012. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:10087396

21. A. Russo. DIET-SPECIFIC EPIGENETIC SIGNATURE REVEALED BY H3K4ME3 AND H3K27ME3 DATA ANALYSIS IN C57BL6 MICE.

Degree: 2016, Università degli Studi di Milano

 Increasing evidences demonstrate that adapting to different environmental conditions is mediated by epigenetic changes, which can participate in cellular processes. In particular, the adaptation to… (more)

Subjects/Keywords: Epigenetics; Diet; NGS; Histone Modifications; Bioinformatics; Settore BIO/11 - Biologia Molecolare

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APA (6th Edition):

Russo, A. (2016). DIET-SPECIFIC EPIGENETIC SIGNATURE REVEALED BY H3K4ME3 AND H3K27ME3 DATA ANALYSIS IN C57BL6 MICE. (Thesis). Università degli Studi di Milano. Retrieved from http://hdl.handle.net/2434/365343

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):

Russo, A.. “DIET-SPECIFIC EPIGENETIC SIGNATURE REVEALED BY H3K4ME3 AND H3K27ME3 DATA ANALYSIS IN C57BL6 MICE.” 2016. Thesis, Università degli Studi di Milano. Accessed January 24, 2021. http://hdl.handle.net/2434/365343.

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

MLA Handbook (7th Edition):

Russo, A.. “DIET-SPECIFIC EPIGENETIC SIGNATURE REVEALED BY H3K4ME3 AND H3K27ME3 DATA ANALYSIS IN C57BL6 MICE.” 2016. Web. 24 Jan 2021.

Vancouver:

Russo A. DIET-SPECIFIC EPIGENETIC SIGNATURE REVEALED BY H3K4ME3 AND H3K27ME3 DATA ANALYSIS IN C57BL6 MICE. [Internet] [Thesis]. Università degli Studi di Milano; 2016. [cited 2021 Jan 24]. Available from: http://hdl.handle.net/2434/365343.

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

Council of Science Editors:

Russo A. DIET-SPECIFIC EPIGENETIC SIGNATURE REVEALED BY H3K4ME3 AND H3K27ME3 DATA ANALYSIS IN C57BL6 MICE. [Thesis]. Università degli Studi di Milano; 2016. Available from: http://hdl.handle.net/2434/365343

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


Swedish University of Agricultural Sciences

22. Kralemann, Lejon. Genetic and epigenetic mechanisms underlying the regulation of flowering time.

Degree: 2019, Swedish University of Agricultural Sciences

 Developmental transitions and responses to the environment have a tight epigenetic control. Especially the switch to flowering is important for plants because it allows (sexual)… (more)

Subjects/Keywords: Arabidopsis; Ambrosia; FT; TFL1; epigenetics; histone modifications; PRC1; PRC2; UBP12; UBP13

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APA (6th Edition):

Kralemann, L. (2019). Genetic and epigenetic mechanisms underlying the regulation of flowering time. (Doctoral Dissertation). Swedish University of Agricultural Sciences. Retrieved from https://pub.epsilon.slu.se/16266/

Chicago Manual of Style (16th Edition):

Kralemann, Lejon. “Genetic and epigenetic mechanisms underlying the regulation of flowering time.” 2019. Doctoral Dissertation, Swedish University of Agricultural Sciences. Accessed January 24, 2021. https://pub.epsilon.slu.se/16266/.

MLA Handbook (7th Edition):

Kralemann, Lejon. “Genetic and epigenetic mechanisms underlying the regulation of flowering time.” 2019. Web. 24 Jan 2021.

Vancouver:

Kralemann L. Genetic and epigenetic mechanisms underlying the regulation of flowering time. [Internet] [Doctoral dissertation]. Swedish University of Agricultural Sciences; 2019. [cited 2021 Jan 24]. Available from: https://pub.epsilon.slu.se/16266/.

Council of Science Editors:

Kralemann L. Genetic and epigenetic mechanisms underlying the regulation of flowering time. [Doctoral Dissertation]. Swedish University of Agricultural Sciences; 2019. Available from: https://pub.epsilon.slu.se/16266/


Brunel University

23. Gokhan, Ezgi. The Repo-Man/PP1 complex role in chromatin remodelling, nuclear structure and cancer progression.

Degree: PhD, 2016, Brunel University

 Repo-Man is a chromatin-associated PP1 targeting subunit that coordinates chromosome re-organisation and nuclear envelope reassembly during mitotic exit. At the onset of mitosis, Repo-Man association… (more)

Subjects/Keywords: 616.99; Phosphatases; Mitotic exit; Cell cycle; Breast cancer; Histone modifications

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APA (6th Edition):

Gokhan, E. (2016). The Repo-Man/PP1 complex role in chromatin remodelling, nuclear structure and cancer progression. (Doctoral Dissertation). Brunel University. Retrieved from http://bura.brunel.ac.uk/handle/2438/14731 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.715884

Chicago Manual of Style (16th Edition):

Gokhan, Ezgi. “The Repo-Man/PP1 complex role in chromatin remodelling, nuclear structure and cancer progression.” 2016. Doctoral Dissertation, Brunel University. Accessed January 24, 2021. http://bura.brunel.ac.uk/handle/2438/14731 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.715884.

MLA Handbook (7th Edition):

Gokhan, Ezgi. “The Repo-Man/PP1 complex role in chromatin remodelling, nuclear structure and cancer progression.” 2016. Web. 24 Jan 2021.

Vancouver:

Gokhan E. The Repo-Man/PP1 complex role in chromatin remodelling, nuclear structure and cancer progression. [Internet] [Doctoral dissertation]. Brunel University; 2016. [cited 2021 Jan 24]. Available from: http://bura.brunel.ac.uk/handle/2438/14731 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.715884.

Council of Science Editors:

Gokhan E. The Repo-Man/PP1 complex role in chromatin remodelling, nuclear structure and cancer progression. [Doctoral Dissertation]. Brunel University; 2016. Available from: http://bura.brunel.ac.uk/handle/2438/14731 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.715884


University of Dundee

24. Baker, Katie. The chromatin landscape of barley : gene expression, evolution and epigenetics.

Degree: PhD, 2015, University of Dundee

 Barley (Hordeum vulgare) is an economically important crop species with a large diploid genome. Around a half of the barley genome and a fifth of… (more)

Subjects/Keywords: 580; Chromatin; Barley; Epigenomics; Pericentromere; Recombination; Histone modifications; Gene evolution

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APA (6th Edition):

Baker, K. (2015). The chromatin landscape of barley : gene expression, evolution and epigenetics. (Doctoral Dissertation). University of Dundee. Retrieved from https://discovery.dundee.ac.uk/en/studentTheses/13a096cd-f45b-4e34-babd-ccb3ff3607ca ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.656026

Chicago Manual of Style (16th Edition):

Baker, Katie. “The chromatin landscape of barley : gene expression, evolution and epigenetics.” 2015. Doctoral Dissertation, University of Dundee. Accessed January 24, 2021. https://discovery.dundee.ac.uk/en/studentTheses/13a096cd-f45b-4e34-babd-ccb3ff3607ca ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.656026.

MLA Handbook (7th Edition):

Baker, Katie. “The chromatin landscape of barley : gene expression, evolution and epigenetics.” 2015. Web. 24 Jan 2021.

Vancouver:

Baker K. The chromatin landscape of barley : gene expression, evolution and epigenetics. [Internet] [Doctoral dissertation]. University of Dundee; 2015. [cited 2021 Jan 24]. Available from: https://discovery.dundee.ac.uk/en/studentTheses/13a096cd-f45b-4e34-babd-ccb3ff3607ca ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.656026.

Council of Science Editors:

Baker K. The chromatin landscape of barley : gene expression, evolution and epigenetics. [Doctoral Dissertation]. University of Dundee; 2015. Available from: https://discovery.dundee.ac.uk/en/studentTheses/13a096cd-f45b-4e34-babd-ccb3ff3607ca ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.656026


Princeton University

25. Cope, Michelle Martine Gonzales. The Role of Histone Modifications in Pluripotency .

Degree: PhD, 2015, Princeton University

 Pluripotent cells have the potential to differentiate into different cell types while having the same genetic material. Fibroblasts can be reprogrammed into induced pluripotent stem… (more)

Subjects/Keywords: histone modifications; induced pluripotent stem cells; mass spectrometry; pluripotency

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APA (6th Edition):

Cope, M. M. G. (2015). The Role of Histone Modifications in Pluripotency . (Doctoral Dissertation). Princeton University. Retrieved from http://arks.princeton.edu/ark:/88435/dsp01b2773x92r

Chicago Manual of Style (16th Edition):

Cope, Michelle Martine Gonzales. “The Role of Histone Modifications in Pluripotency .” 2015. Doctoral Dissertation, Princeton University. Accessed January 24, 2021. http://arks.princeton.edu/ark:/88435/dsp01b2773x92r.

MLA Handbook (7th Edition):

Cope, Michelle Martine Gonzales. “The Role of Histone Modifications in Pluripotency .” 2015. Web. 24 Jan 2021.

Vancouver:

Cope MMG. The Role of Histone Modifications in Pluripotency . [Internet] [Doctoral dissertation]. Princeton University; 2015. [cited 2021 Jan 24]. Available from: http://arks.princeton.edu/ark:/88435/dsp01b2773x92r.

Council of Science Editors:

Cope MMG. The Role of Histone Modifications in Pluripotency . [Doctoral Dissertation]. Princeton University; 2015. Available from: http://arks.princeton.edu/ark:/88435/dsp01b2773x92r


University of Illinois – Urbana-Champaign

26. Li, Qian. Genistein suppresses colon cancer metastasis through epigenetic regulations.

Degree: PhD, 0037, 2014, University of Illinois – Urbana-Champaign

 Colorectal cancer (CRC) is the third most common cancer in the United States. Approximately 90% of colon cancer deaths arise from cancer metastasis, the process… (more)

Subjects/Keywords: Colon cancer; Metastasis; Nutrition; Epigenetics; Histone modifications; DNA methylation; Soy genistein

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APA (6th Edition):

Li, Q. (2014). Genistein suppresses colon cancer metastasis through epigenetic regulations. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/50436

Chicago Manual of Style (16th Edition):

Li, Qian. “Genistein suppresses colon cancer metastasis through epigenetic regulations.” 2014. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed January 24, 2021. http://hdl.handle.net/2142/50436.

MLA Handbook (7th Edition):

Li, Qian. “Genistein suppresses colon cancer metastasis through epigenetic regulations.” 2014. Web. 24 Jan 2021.

Vancouver:

Li Q. Genistein suppresses colon cancer metastasis through epigenetic regulations. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2014. [cited 2021 Jan 24]. Available from: http://hdl.handle.net/2142/50436.

Council of Science Editors:

Li Q. Genistein suppresses colon cancer metastasis through epigenetic regulations. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2014. Available from: http://hdl.handle.net/2142/50436


University of Edinburgh

27. Zhang, Tuo. Maintenance of genomic imprinting by G9a/GLP complex of histone methyltransferases in embryonic stem (ES) cells.

Degree: PhD, 2014, University of Edinburgh

 DNA methylation refers to an addition of a methyl group to the 5 position of the cytosine pyrimidine ring. As the best characterized epigenetic mark,… (more)

Subjects/Keywords: 572.8; genomic imprinting; epigenetics; histone modifications; DNA methylation; embryonic stem cells

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APA (6th Edition):

Zhang, T. (2014). Maintenance of genomic imprinting by G9a/GLP complex of histone methyltransferases in embryonic stem (ES) cells. (Doctoral Dissertation). University of Edinburgh. Retrieved from http://hdl.handle.net/1842/9967

Chicago Manual of Style (16th Edition):

Zhang, Tuo. “Maintenance of genomic imprinting by G9a/GLP complex of histone methyltransferases in embryonic stem (ES) cells.” 2014. Doctoral Dissertation, University of Edinburgh. Accessed January 24, 2021. http://hdl.handle.net/1842/9967.

MLA Handbook (7th Edition):

Zhang, Tuo. “Maintenance of genomic imprinting by G9a/GLP complex of histone methyltransferases in embryonic stem (ES) cells.” 2014. Web. 24 Jan 2021.

Vancouver:

Zhang T. Maintenance of genomic imprinting by G9a/GLP complex of histone methyltransferases in embryonic stem (ES) cells. [Internet] [Doctoral dissertation]. University of Edinburgh; 2014. [cited 2021 Jan 24]. Available from: http://hdl.handle.net/1842/9967.

Council of Science Editors:

Zhang T. Maintenance of genomic imprinting by G9a/GLP complex of histone methyltransferases in embryonic stem (ES) cells. [Doctoral Dissertation]. University of Edinburgh; 2014. Available from: http://hdl.handle.net/1842/9967


University of Maryland

28. Mitra, Apratim. Genome-Wide Analysis of Histone Modification Enrichments Induced by Marek's Disease Virus in Inbred Chicken Lines.

Degree: Animal Sciences, 2013, University of Maryland

 Covalent histone modifications constitute a complex network of transcriptional regulation involved in diverse biological processes ranging from stem cell differentiation to immune response. The advent… (more)

Subjects/Keywords: Bioinformatics; Mathematics; Statistics; differential chromatin; histone modifications; Marek's disease; wavelets

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APA (6th Edition):

Mitra, A. (2013). Genome-Wide Analysis of Histone Modification Enrichments Induced by Marek's Disease Virus in Inbred Chicken Lines. (Thesis). University of Maryland. Retrieved from http://hdl.handle.net/1903/14177

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):

Mitra, Apratim. “Genome-Wide Analysis of Histone Modification Enrichments Induced by Marek's Disease Virus in Inbred Chicken Lines.” 2013. Thesis, University of Maryland. Accessed January 24, 2021. http://hdl.handle.net/1903/14177.

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

MLA Handbook (7th Edition):

Mitra, Apratim. “Genome-Wide Analysis of Histone Modification Enrichments Induced by Marek's Disease Virus in Inbred Chicken Lines.” 2013. Web. 24 Jan 2021.

Vancouver:

Mitra A. Genome-Wide Analysis of Histone Modification Enrichments Induced by Marek's Disease Virus in Inbred Chicken Lines. [Internet] [Thesis]. University of Maryland; 2013. [cited 2021 Jan 24]. Available from: http://hdl.handle.net/1903/14177.

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

Council of Science Editors:

Mitra A. Genome-Wide Analysis of Histone Modification Enrichments Induced by Marek's Disease Virus in Inbred Chicken Lines. [Thesis]. University of Maryland; 2013. Available from: http://hdl.handle.net/1903/14177

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


University of Tasmania

29. Phipps, AJ. DNA methylation and histone modification dynamics in neurons in aging and Alzheimer’s disease.

Degree: 2019, University of Tasmania

 The epigenome dynamically regulates chromatin structure to control cellular function and homeostasis in a highly specific fashion and mediates the complex interaction between the DNA… (more)

Subjects/Keywords: epigenetics; Alzheimers disease; DNA Methylation; histone modifications; aging

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APA (6th Edition):

Phipps, A. (2019). DNA methylation and histone modification dynamics in neurons in aging and Alzheimer’s disease. (Thesis). University of Tasmania. Retrieved from https://eprints.utas.edu.au/34331/1/Phipps_whole_thesis.pdf ; Phipps, AJ ORCID: 0000-0003-4689-1198 <https://orcid.org/0000-0003-4689-1198> 2019 , 'DNA methylation and histone modification dynamics in neurons in aging and Alzheimer’s disease', PhD thesis, University of Tasmania.

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):

Phipps, AJ. “DNA methylation and histone modification dynamics in neurons in aging and Alzheimer’s disease.” 2019. Thesis, University of Tasmania. Accessed January 24, 2021. https://eprints.utas.edu.au/34331/1/Phipps_whole_thesis.pdf ; Phipps, AJ ORCID: 0000-0003-4689-1198 <https://orcid.org/0000-0003-4689-1198> 2019 , 'DNA methylation and histone modification dynamics in neurons in aging and Alzheimer’s disease', PhD thesis, University of Tasmania..

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

MLA Handbook (7th Edition):

Phipps, AJ. “DNA methylation and histone modification dynamics in neurons in aging and Alzheimer’s disease.” 2019. Web. 24 Jan 2021.

Vancouver:

Phipps A. DNA methylation and histone modification dynamics in neurons in aging and Alzheimer’s disease. [Internet] [Thesis]. University of Tasmania; 2019. [cited 2021 Jan 24]. Available from: https://eprints.utas.edu.au/34331/1/Phipps_whole_thesis.pdf ; Phipps, AJ ORCID: 0000-0003-4689-1198 <https://orcid.org/0000-0003-4689-1198> 2019 , 'DNA methylation and histone modification dynamics in neurons in aging and Alzheimer’s disease', PhD thesis, University of Tasmania..

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

Council of Science Editors:

Phipps A. DNA methylation and histone modification dynamics in neurons in aging and Alzheimer’s disease. [Thesis]. University of Tasmania; 2019. Available from: https://eprints.utas.edu.au/34331/1/Phipps_whole_thesis.pdf ; Phipps, AJ ORCID: 0000-0003-4689-1198 <https://orcid.org/0000-0003-4689-1198> 2019 , 'DNA methylation and histone modification dynamics in neurons in aging and Alzheimer’s disease', PhD thesis, University of Tasmania.

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


University of Oxford

30. Howe, Françoise Sara. Crosstalk between histone modifications in Saccharomyces cerevisiae.

Degree: PhD, 2012, University of Oxford

 The N-terminal tails of histone proteins protrude from the nucleosome core and are extensively post-translationally modified. These modifications are proposed to affect many DNA-based processes… (more)

Subjects/Keywords: 579.5; Biochemistry; Genetics (life sciences); Molecular genetics; chromatin; histone H3; histone modifications; histone methylation; histone acetylation; proline isomerisation; crosstalk; gene expression; transcription; yeast; Saccharomyces cerevisiae

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

APA (6th Edition):

Howe, F. S. (2012). Crosstalk between histone modifications in Saccharomyces cerevisiae. (Doctoral Dissertation). University of Oxford. Retrieved from http://ora.ox.ac.uk/objects/uuid:1e2e128e-1ec3-4d41-8ab5-b27e5930a654 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.580995

Chicago Manual of Style (16th Edition):

Howe, Françoise Sara. “Crosstalk between histone modifications in Saccharomyces cerevisiae.” 2012. Doctoral Dissertation, University of Oxford. Accessed January 24, 2021. http://ora.ox.ac.uk/objects/uuid:1e2e128e-1ec3-4d41-8ab5-b27e5930a654 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.580995.

MLA Handbook (7th Edition):

Howe, Françoise Sara. “Crosstalk between histone modifications in Saccharomyces cerevisiae.” 2012. Web. 24 Jan 2021.

Vancouver:

Howe FS. Crosstalk between histone modifications in Saccharomyces cerevisiae. [Internet] [Doctoral dissertation]. University of Oxford; 2012. [cited 2021 Jan 24]. Available from: http://ora.ox.ac.uk/objects/uuid:1e2e128e-1ec3-4d41-8ab5-b27e5930a654 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.580995.

Council of Science Editors:

Howe FS. Crosstalk between histone modifications in Saccharomyces cerevisiae. [Doctoral Dissertation]. University of Oxford; 2012. Available from: http://ora.ox.ac.uk/objects/uuid:1e2e128e-1ec3-4d41-8ab5-b27e5930a654 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.580995

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