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You searched for subject:(Acetyltransferases). Showing records 1 – 29 of 29 total matches.

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University of Texas Southwestern Medical Center

1. Chu, Chih-Wen. The Substrate and Regulator of Acetyltransferase San.

Degree: 2010, University of Texas Southwestern Medical Center

 Lysine acetylation is one of the most common protein modifications in eukaryotes and plays critical roles in numerous cellular events. San is an acetyltransferase required… (more)

Subjects/Keywords: Acetyltransferases; Tubulin; Microtubules

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APA (6th Edition):

Chu, C. (2010). The Substrate and Regulator of Acetyltransferase San. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/721

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):

Chu, Chih-Wen. “The Substrate and Regulator of Acetyltransferase San.” 2010. Thesis, University of Texas Southwestern Medical Center. Accessed October 17, 2019. http://hdl.handle.net/2152.5/721.

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

MLA Handbook (7th Edition):

Chu, Chih-Wen. “The Substrate and Regulator of Acetyltransferase San.” 2010. Web. 17 Oct 2019.

Vancouver:

Chu C. The Substrate and Regulator of Acetyltransferase San. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2010. [cited 2019 Oct 17]. Available from: http://hdl.handle.net/2152.5/721.

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

Council of Science Editors:

Chu C. The Substrate and Regulator of Acetyltransferase San. [Thesis]. University of Texas Southwestern Medical Center; 2010. Available from: http://hdl.handle.net/2152.5/721

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


Virginia Tech

2. Mehere, Prajwalini V. Towards the Characterization of Enzymes Involved in the Metabolism of Tyrosine and Tyrosine Derivatives.

Degree: PhD, Biochemistry, 2010, Virginia Tech

 Tyrosine is involved in many biological processes including protein synthesis. This dissertation is focused on two different aspects: tyrosine catabolism and tyrosine derivative metabolism. Tyrosine… (more)

Subjects/Keywords: arylalkylamine; Tyrosine; aminotransferase; acetyltransferases

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APA (6th Edition):

Mehere, P. V. (2010). Towards the Characterization of Enzymes Involved in the Metabolism of Tyrosine and Tyrosine Derivatives. (Doctoral Dissertation). Virginia Tech. Retrieved from http://hdl.handle.net/10919/77289

Chicago Manual of Style (16th Edition):

Mehere, Prajwalini V. “Towards the Characterization of Enzymes Involved in the Metabolism of Tyrosine and Tyrosine Derivatives.” 2010. Doctoral Dissertation, Virginia Tech. Accessed October 17, 2019. http://hdl.handle.net/10919/77289.

MLA Handbook (7th Edition):

Mehere, Prajwalini V. “Towards the Characterization of Enzymes Involved in the Metabolism of Tyrosine and Tyrosine Derivatives.” 2010. Web. 17 Oct 2019.

Vancouver:

Mehere PV. Towards the Characterization of Enzymes Involved in the Metabolism of Tyrosine and Tyrosine Derivatives. [Internet] [Doctoral dissertation]. Virginia Tech; 2010. [cited 2019 Oct 17]. Available from: http://hdl.handle.net/10919/77289.

Council of Science Editors:

Mehere PV. Towards the Characterization of Enzymes Involved in the Metabolism of Tyrosine and Tyrosine Derivatives. [Doctoral Dissertation]. Virginia Tech; 2010. Available from: http://hdl.handle.net/10919/77289


University of Oxford

3. Brooke, Edward W. Protein-ligand interactions of arylamine N-acetyltransferase from Mycobacterium smegmatis.

Degree: 2003, University of Oxford

 Tuberculosis is the world's largest cause of death from an infectious agent. Treatment is by an extended period of combination chemotherapy. Drug resistance is an… (more)

Subjects/Keywords: 616.995061; Tuberculosis : Acetyltransferases : Mycobacterium tuberculosis

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APA (6th Edition):

Brooke, E. W. (2003). Protein-ligand interactions of arylamine N-acetyltransferase from Mycobacterium smegmatis. (Doctoral Dissertation). University of Oxford. Retrieved from http://ora.ox.ac.uk/objects/uuid:f13c3191-b098-4a85-84c3-90590b365d30 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.400066

Chicago Manual of Style (16th Edition):

Brooke, Edward W. “Protein-ligand interactions of arylamine N-acetyltransferase from Mycobacterium smegmatis.” 2003. Doctoral Dissertation, University of Oxford. Accessed October 17, 2019. http://ora.ox.ac.uk/objects/uuid:f13c3191-b098-4a85-84c3-90590b365d30 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.400066.

MLA Handbook (7th Edition):

Brooke, Edward W. “Protein-ligand interactions of arylamine N-acetyltransferase from Mycobacterium smegmatis.” 2003. Web. 17 Oct 2019.

Vancouver:

Brooke EW. Protein-ligand interactions of arylamine N-acetyltransferase from Mycobacterium smegmatis. [Internet] [Doctoral dissertation]. University of Oxford; 2003. [cited 2019 Oct 17]. Available from: http://ora.ox.ac.uk/objects/uuid:f13c3191-b098-4a85-84c3-90590b365d30 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.400066.

Council of Science Editors:

Brooke EW. Protein-ligand interactions of arylamine N-acetyltransferase from Mycobacterium smegmatis. [Doctoral Dissertation]. University of Oxford; 2003. Available from: http://ora.ox.ac.uk/objects/uuid:f13c3191-b098-4a85-84c3-90590b365d30 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.400066


Rhodes University

4. Olivieri, Gianfranco. The regulation of Serotonin N-acetyltransferase in the rat pineal gland.

Degree: PhD, Faculty of Science, Biochemistry, Microbiology and Biotechnology, 1993, Rhodes University

 The synthesis of the pineal hormone, melatonin, is finely regulated by the pineal enzyme serotonin N-acetyltransferase (NAT). In the absence of light, the activity of… (more)

Subjects/Keywords: Serotonin  – Research; Pineal gland; Acetyltransferases

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APA (6th Edition):

Olivieri, G. (1993). The regulation of Serotonin N-acetyltransferase in the rat pineal gland. (Doctoral Dissertation). Rhodes University. Retrieved from http://hdl.handle.net/10962/d1004112

Chicago Manual of Style (16th Edition):

Olivieri, Gianfranco. “The regulation of Serotonin N-acetyltransferase in the rat pineal gland.” 1993. Doctoral Dissertation, Rhodes University. Accessed October 17, 2019. http://hdl.handle.net/10962/d1004112.

MLA Handbook (7th Edition):

Olivieri, Gianfranco. “The regulation of Serotonin N-acetyltransferase in the rat pineal gland.” 1993. Web. 17 Oct 2019.

Vancouver:

Olivieri G. The regulation of Serotonin N-acetyltransferase in the rat pineal gland. [Internet] [Doctoral dissertation]. Rhodes University; 1993. [cited 2019 Oct 17]. Available from: http://hdl.handle.net/10962/d1004112.

Council of Science Editors:

Olivieri G. The regulation of Serotonin N-acetyltransferase in the rat pineal gland. [Doctoral Dissertation]. Rhodes University; 1993. Available from: http://hdl.handle.net/10962/d1004112


Universiteit Utrecht

5. Sachini, N.N. The role of lysine acetylation,histone acetyltransferases and bromocontaining proteins in cancer development.

Degree: 2013, Universiteit Utrecht

 Histone lysine acetylation is a key regulator of gene expression. Cancer manifests because of both genetic and epigenetic alterations. In several solid tumours and haematological… (more)

Subjects/Keywords: epigenetics; lysine acetylation; transcription; histone acetyltransferases; bromocontaining proteins; cancer development; epidrugs

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APA (6th Edition):

Sachini, N. N. (2013). The role of lysine acetylation,histone acetyltransferases and bromocontaining proteins in cancer development. (Masters Thesis). Universiteit Utrecht. Retrieved from http://dspace.library.uu.nl:8080/handle/1874/273357

Chicago Manual of Style (16th Edition):

Sachini, N N. “The role of lysine acetylation,histone acetyltransferases and bromocontaining proteins in cancer development.” 2013. Masters Thesis, Universiteit Utrecht. Accessed October 17, 2019. http://dspace.library.uu.nl:8080/handle/1874/273357.

MLA Handbook (7th Edition):

Sachini, N N. “The role of lysine acetylation,histone acetyltransferases and bromocontaining proteins in cancer development.” 2013. Web. 17 Oct 2019.

Vancouver:

Sachini NN. The role of lysine acetylation,histone acetyltransferases and bromocontaining proteins in cancer development. [Internet] [Masters thesis]. Universiteit Utrecht; 2013. [cited 2019 Oct 17]. Available from: http://dspace.library.uu.nl:8080/handle/1874/273357.

Council of Science Editors:

Sachini NN. The role of lysine acetylation,histone acetyltransferases and bromocontaining proteins in cancer development. [Masters Thesis]. Universiteit Utrecht; 2013. Available from: http://dspace.library.uu.nl:8080/handle/1874/273357


Hong Kong University of Science and Technology

6. Chan, Jonathan Ka Lok. Functional characterization of the regulation of transcription factor MEF2C by histone acetyltransferase p300 and histone deacetylase 4.

Degree: 2004, Hong Kong University of Science and Technology

 Two families of transcription factors are important for executing the differentiation program in proliferating myoblasts to become contractile myotubes. These are the myocyte enhancer factors… (more)

Subjects/Keywords: Acetyltransferases; Histone deacetylase; Transcription factors

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APA (6th Edition):

Chan, J. K. L. (2004). Functional characterization of the regulation of transcription factor MEF2C by histone acetyltransferase p300 and histone deacetylase 4. (Thesis). Hong Kong University of Science and Technology. Retrieved from https://doi.org/10.14711/thesis-b839591 ; http://repository.ust.hk/ir/bitstream/1783.1-2093/1/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):

Chan, Jonathan Ka Lok. “Functional characterization of the regulation of transcription factor MEF2C by histone acetyltransferase p300 and histone deacetylase 4.” 2004. Thesis, Hong Kong University of Science and Technology. Accessed October 17, 2019. https://doi.org/10.14711/thesis-b839591 ; http://repository.ust.hk/ir/bitstream/1783.1-2093/1/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):

Chan, Jonathan Ka Lok. “Functional characterization of the regulation of transcription factor MEF2C by histone acetyltransferase p300 and histone deacetylase 4.” 2004. Web. 17 Oct 2019.

Vancouver:

Chan JKL. Functional characterization of the regulation of transcription factor MEF2C by histone acetyltransferase p300 and histone deacetylase 4. [Internet] [Thesis]. Hong Kong University of Science and Technology; 2004. [cited 2019 Oct 17]. Available from: https://doi.org/10.14711/thesis-b839591 ; http://repository.ust.hk/ir/bitstream/1783.1-2093/1/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:

Chan JKL. Functional characterization of the regulation of transcription factor MEF2C by histone acetyltransferase p300 and histone deacetylase 4. [Thesis]. Hong Kong University of Science and Technology; 2004. Available from: https://doi.org/10.14711/thesis-b839591 ; http://repository.ust.hk/ir/bitstream/1783.1-2093/1/th_redirect.html

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


University of North Carolina – Greensboro

7. Baghaee, Ravari Soodeh. Ionic modulation of QPX stability as a nano - switch regulating gene expression in neurons.

Degree: 2016, University of North Carolina – Greensboro

 G-quadruplexes (G-QPX) have been the subject of intense research due to their unique structural configuration and potential applications, particularly their functionality in biological process as… (more)

Subjects/Keywords: Quadruplex nucleic acids; Acetyltransferases; Neurons; Genetic regulation; Gene expression; Biochemistry; Nanoscience

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APA (6th Edition):

Baghaee, R. S. (2016). Ionic modulation of QPX stability as a nano - switch regulating gene expression in neurons. (Doctoral Dissertation). University of North Carolina – Greensboro. Retrieved from http://libres.uncg.edu/ir/listing.aspx?styp=ti&id=20927

Chicago Manual of Style (16th Edition):

Baghaee, Ravari Soodeh. “Ionic modulation of QPX stability as a nano - switch regulating gene expression in neurons.” 2016. Doctoral Dissertation, University of North Carolina – Greensboro. Accessed October 17, 2019. http://libres.uncg.edu/ir/listing.aspx?styp=ti&id=20927.

MLA Handbook (7th Edition):

Baghaee, Ravari Soodeh. “Ionic modulation of QPX stability as a nano - switch regulating gene expression in neurons.” 2016. Web. 17 Oct 2019.

Vancouver:

Baghaee RS. Ionic modulation of QPX stability as a nano - switch regulating gene expression in neurons. [Internet] [Doctoral dissertation]. University of North Carolina – Greensboro; 2016. [cited 2019 Oct 17]. Available from: http://libres.uncg.edu/ir/listing.aspx?styp=ti&id=20927.

Council of Science Editors:

Baghaee RS. Ionic modulation of QPX stability as a nano - switch regulating gene expression in neurons. [Doctoral Dissertation]. University of North Carolina – Greensboro; 2016. Available from: http://libres.uncg.edu/ir/listing.aspx?styp=ti&id=20927


University of Lethbridge

8. University of Lethbridge. Faculty of Arts and Science. Isolation, partial purification and characterization of an N-acetyltransferase from Streptomyces akiyoshiensis L-138 .

Degree: 2003, University of Lethbridge

 A novel N-acetyltranferase (NAT) with high specificity for L-dopa was partially purified and characterized during this study. Streptomyces akiyoshiensis NAT was isolated from liquid cultures… (more)

Subjects/Keywords: Dissertations, Academic; Streptomyces; Acetyltransferases  – Purification

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APA (6th Edition):

Science, U. o. L. F. o. A. a. (2003). Isolation, partial purification and characterization of an N-acetyltransferase from Streptomyces akiyoshiensis L-138 . (Thesis). University of Lethbridge. Retrieved from http://hdl.handle.net/10133/234

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):

Science, University of Lethbridge. Faculty of Arts and. “Isolation, partial purification and characterization of an N-acetyltransferase from Streptomyces akiyoshiensis L-138 .” 2003. Thesis, University of Lethbridge. Accessed October 17, 2019. http://hdl.handle.net/10133/234.

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

MLA Handbook (7th Edition):

Science, University of Lethbridge. Faculty of Arts and. “Isolation, partial purification and characterization of an N-acetyltransferase from Streptomyces akiyoshiensis L-138 .” 2003. Web. 17 Oct 2019.

Vancouver:

Science UoLFoAa. Isolation, partial purification and characterization of an N-acetyltransferase from Streptomyces akiyoshiensis L-138 . [Internet] [Thesis]. University of Lethbridge; 2003. [cited 2019 Oct 17]. Available from: http://hdl.handle.net/10133/234.

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

Council of Science Editors:

Science UoLFoAa. Isolation, partial purification and characterization of an N-acetyltransferase from Streptomyces akiyoshiensis L-138 . [Thesis]. University of Lethbridge; 2003. Available from: http://hdl.handle.net/10133/234

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


IUPUI

9. Dixon, Stacey E. GCN5-B is a Novel Nuclear Histone Acetyltransferase that is Crucial for Viability in the Protozoan Parasite Toxoplasma gondii.

Degree: 2011, IUPUI

Indiana University-Purdue University Indianapolis (IUPUI)

Infection with the single-celled parasite Toxoplasma gondii (phylum Apicomplexa) is usually benign in normal healthy individuals, but can cause congenital… (more)

Subjects/Keywords: GCN5; histone acetyltransferase; nuclear localization signal; epigenetic; Toxoplasma; Toxoplasma gondii; Acetyltransferases

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APA (6th Edition):

Dixon, S. E. (2011). GCN5-B is a Novel Nuclear Histone Acetyltransferase that is Crucial for Viability in the Protozoan Parasite Toxoplasma gondii. (Thesis). IUPUI. Retrieved from http://hdl.handle.net/1805/2524

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):

Dixon, Stacey E. “GCN5-B is a Novel Nuclear Histone Acetyltransferase that is Crucial for Viability in the Protozoan Parasite Toxoplasma gondii.” 2011. Thesis, IUPUI. Accessed October 17, 2019. http://hdl.handle.net/1805/2524.

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

MLA Handbook (7th Edition):

Dixon, Stacey E. “GCN5-B is a Novel Nuclear Histone Acetyltransferase that is Crucial for Viability in the Protozoan Parasite Toxoplasma gondii.” 2011. Web. 17 Oct 2019.

Vancouver:

Dixon SE. GCN5-B is a Novel Nuclear Histone Acetyltransferase that is Crucial for Viability in the Protozoan Parasite Toxoplasma gondii. [Internet] [Thesis]. IUPUI; 2011. [cited 2019 Oct 17]. Available from: http://hdl.handle.net/1805/2524.

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

Council of Science Editors:

Dixon SE. GCN5-B is a Novel Nuclear Histone Acetyltransferase that is Crucial for Viability in the Protozoan Parasite Toxoplasma gondii. [Thesis]. IUPUI; 2011. Available from: http://hdl.handle.net/1805/2524

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


University of Texas Southwestern Medical Center

10. Vetter, Ali Jean. Protein Acetylation and Regulation of CFTR Expression.

Degree: 2015, University of Texas Southwestern Medical Center

 Cystic Fibrosis (CF) is an autosomal recessive disease caused by a loss of function of a chloride channel encoded by the cystic fibrosis conductance regulator… (more)

Subjects/Keywords: Cystic Fibrosis Transmembrane Conductance Regulator; Gene Expression Regulation; N-Terminal Acetyltransferases

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APA (6th Edition):

Vetter, A. J. (2015). Protein Acetylation and Regulation of CFTR Expression. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/5289

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):

Vetter, Ali Jean. “Protein Acetylation and Regulation of CFTR Expression.” 2015. Thesis, University of Texas Southwestern Medical Center. Accessed October 17, 2019. http://hdl.handle.net/2152.5/5289.

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

MLA Handbook (7th Edition):

Vetter, Ali Jean. “Protein Acetylation and Regulation of CFTR Expression.” 2015. Web. 17 Oct 2019.

Vancouver:

Vetter AJ. Protein Acetylation and Regulation of CFTR Expression. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2015. [cited 2019 Oct 17]. Available from: http://hdl.handle.net/2152.5/5289.

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

Council of Science Editors:

Vetter AJ. Protein Acetylation and Regulation of CFTR Expression. [Thesis]. University of Texas Southwestern Medical Center; 2015. Available from: http://hdl.handle.net/2152.5/5289

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


University of Arizona

11. Gunawardhana, Lhanoo, 1959-. Human liver slices: An in vitro system for determination of N-acetylation and acetylator status .

Degree: 1989, University of Arizona

 An in vitro system has been developed to study N-acetyltransferase (NAT) activity using human liver slices in dynamic organ culture. Acetylation of para-aminobenzoic acid (PABA)… (more)

Subjects/Keywords: Acetyltransferases.; Liver function tests.

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APA (6th Edition):

Gunawardhana, Lhanoo, 1. (1989). Human liver slices: An in vitro system for determination of N-acetylation and acetylator status . (Masters Thesis). University of Arizona. Retrieved from http://hdl.handle.net/10150/291394

Chicago Manual of Style (16th Edition):

Gunawardhana, Lhanoo, 1959-. “Human liver slices: An in vitro system for determination of N-acetylation and acetylator status .” 1989. Masters Thesis, University of Arizona. Accessed October 17, 2019. http://hdl.handle.net/10150/291394.

MLA Handbook (7th Edition):

Gunawardhana, Lhanoo, 1959-. “Human liver slices: An in vitro system for determination of N-acetylation and acetylator status .” 1989. Web. 17 Oct 2019.

Vancouver:

Gunawardhana, Lhanoo 1. Human liver slices: An in vitro system for determination of N-acetylation and acetylator status . [Internet] [Masters thesis]. University of Arizona; 1989. [cited 2019 Oct 17]. Available from: http://hdl.handle.net/10150/291394.

Council of Science Editors:

Gunawardhana, Lhanoo 1. Human liver slices: An in vitro system for determination of N-acetylation and acetylator status . [Masters Thesis]. University of Arizona; 1989. Available from: http://hdl.handle.net/10150/291394


Georgia State University

12. Wu, Jiang. Development of Inhibitors and Assay Methods for Histone Acetyltransferases.

Degree: PhD, Chemistry, 2011, Georgia State University

  Histone acetyltransferases (HATs) are important enzymes in transcriptional control and potential targets for chemotherapeutic intervention in malignant diseases. Among different HAT members, the yeast… (more)

Subjects/Keywords: Histone acetyltransferases; Tip60; Substrate-based analogs; Virtual screening; Computer modeling; Fluorescent reporters; Chemistry

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APA (6th Edition):

Wu, J. (2011). Development of Inhibitors and Assay Methods for Histone Acetyltransferases. (Doctoral Dissertation). Georgia State University. Retrieved from https://scholarworks.gsu.edu/chemistry_diss/52

Chicago Manual of Style (16th Edition):

Wu, Jiang. “Development of Inhibitors and Assay Methods for Histone Acetyltransferases.” 2011. Doctoral Dissertation, Georgia State University. Accessed October 17, 2019. https://scholarworks.gsu.edu/chemistry_diss/52.

MLA Handbook (7th Edition):

Wu, Jiang. “Development of Inhibitors and Assay Methods for Histone Acetyltransferases.” 2011. Web. 17 Oct 2019.

Vancouver:

Wu J. Development of Inhibitors and Assay Methods for Histone Acetyltransferases. [Internet] [Doctoral dissertation]. Georgia State University; 2011. [cited 2019 Oct 17]. Available from: https://scholarworks.gsu.edu/chemistry_diss/52.

Council of Science Editors:

Wu J. Development of Inhibitors and Assay Methods for Histone Acetyltransferases. [Doctoral Dissertation]. Georgia State University; 2011. Available from: https://scholarworks.gsu.edu/chemistry_diss/52


University of the Western Cape

13. Akurugu, Wisdom Alemya. Effects of nucleotide variation on the structure and function of human arylamine n-acetyltransferase 1 .

Degree: 2012, University of the Western Cape

 The human arylamine N-acetyltransferase 1 (NAT1) is critical in determining the duration of action and pharmacokinetics of amine-containing drugs such as para-aminosalicylic acid and para-aminobenzoyl… (more)

Subjects/Keywords: Homology modelling; NAT1; NAT2; N-acetyltransferases; Sequence conservation; Single nucleotide polymorphisms; Tuberculosis; Xenobiotic-metabolizing enzymes

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APA (6th Edition):

Akurugu, W. A. (2012). Effects of nucleotide variation on the structure and function of human arylamine n-acetyltransferase 1 . (Thesis). University of the Western Cape. Retrieved from http://hdl.handle.net/11394/3816

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):

Akurugu, Wisdom Alemya. “Effects of nucleotide variation on the structure and function of human arylamine n-acetyltransferase 1 .” 2012. Thesis, University of the Western Cape. Accessed October 17, 2019. http://hdl.handle.net/11394/3816.

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

MLA Handbook (7th Edition):

Akurugu, Wisdom Alemya. “Effects of nucleotide variation on the structure and function of human arylamine n-acetyltransferase 1 .” 2012. Web. 17 Oct 2019.

Vancouver:

Akurugu WA. Effects of nucleotide variation on the structure and function of human arylamine n-acetyltransferase 1 . [Internet] [Thesis]. University of the Western Cape; 2012. [cited 2019 Oct 17]. Available from: http://hdl.handle.net/11394/3816.

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

Council of Science Editors:

Akurugu WA. Effects of nucleotide variation on the structure and function of human arylamine n-acetyltransferase 1 . [Thesis]. University of the Western Cape; 2012. Available from: http://hdl.handle.net/11394/3816

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


University of Missouri – Columbia

14. Ladipo, Paul B. The effects of histone acetylation on the maize allele PL1-blotched.

Degree: 2007, University of Missouri – Columbia

 Covalent modifications of DNA and nucleosomal histone proteins associated with eukaryotic chromatin have the potential to alter expression of a gene without change in its… (more)

Subjects/Keywords: Histones; Acetylation; DNA; Genetic regulation; Acetyltransferases

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APA (6th Edition):

Ladipo, P. B. (2007). The effects of histone acetylation on the maize allele PL1-blotched. (Thesis). University of Missouri – Columbia. Retrieved from https://doi.org/10.32469/10355/5038

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):

Ladipo, Paul B. “The effects of histone acetylation on the maize allele PL1-blotched.” 2007. Thesis, University of Missouri – Columbia. Accessed October 17, 2019. https://doi.org/10.32469/10355/5038.

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

MLA Handbook (7th Edition):

Ladipo, Paul B. “The effects of histone acetylation on the maize allele PL1-blotched.” 2007. Web. 17 Oct 2019.

Vancouver:

Ladipo PB. The effects of histone acetylation on the maize allele PL1-blotched. [Internet] [Thesis]. University of Missouri – Columbia; 2007. [cited 2019 Oct 17]. Available from: https://doi.org/10.32469/10355/5038.

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

Council of Science Editors:

Ladipo PB. The effects of histone acetylation on the maize allele PL1-blotched. [Thesis]. University of Missouri – Columbia; 2007. Available from: https://doi.org/10.32469/10355/5038

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

15. Ravens, Sarina. A genome-wide characterization of Mof or Tip60 containing complexes in mouse embryonic stem cells : L'analyse génomique des complexes contenant les acétyltransférases Mof ou Tip60 révèle des fonctions à la fois redondantes mais aussi spécifiques dans les cellules souches embryonnaire de souris.

Degree: Docteur es, Aspects moléculaires et cellulaires de la biologie, 2014, Université de Strasbourg

L’acétylation des histones est associée à une activation transcriptionnelle. Cette acétylation est mise en place par des histone acétyltransférases (HATs) qui sont le plus souvent… (more)

Subjects/Keywords: Histone acétyltransférases; Epigénetique; Mof; Tip60; Cellules souches embryonnaires de souris; Histone acetyltransferases; Epigenetic control; Mof; Tip60; Mouse embryonic stem cells; 572.8

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APA (6th Edition):

Ravens, S. (2014). A genome-wide characterization of Mof or Tip60 containing complexes in mouse embryonic stem cells : L'analyse génomique des complexes contenant les acétyltransférases Mof ou Tip60 révèle des fonctions à la fois redondantes mais aussi spécifiques dans les cellules souches embryonnaire de souris. (Doctoral Dissertation). Université de Strasbourg. Retrieved from http://www.theses.fr/2014STRAJ097

Chicago Manual of Style (16th Edition):

Ravens, Sarina. “A genome-wide characterization of Mof or Tip60 containing complexes in mouse embryonic stem cells : L'analyse génomique des complexes contenant les acétyltransférases Mof ou Tip60 révèle des fonctions à la fois redondantes mais aussi spécifiques dans les cellules souches embryonnaire de souris.” 2014. Doctoral Dissertation, Université de Strasbourg. Accessed October 17, 2019. http://www.theses.fr/2014STRAJ097.

MLA Handbook (7th Edition):

Ravens, Sarina. “A genome-wide characterization of Mof or Tip60 containing complexes in mouse embryonic stem cells : L'analyse génomique des complexes contenant les acétyltransférases Mof ou Tip60 révèle des fonctions à la fois redondantes mais aussi spécifiques dans les cellules souches embryonnaire de souris.” 2014. Web. 17 Oct 2019.

Vancouver:

Ravens S. A genome-wide characterization of Mof or Tip60 containing complexes in mouse embryonic stem cells : L'analyse génomique des complexes contenant les acétyltransférases Mof ou Tip60 révèle des fonctions à la fois redondantes mais aussi spécifiques dans les cellules souches embryonnaire de souris. [Internet] [Doctoral dissertation]. Université de Strasbourg; 2014. [cited 2019 Oct 17]. Available from: http://www.theses.fr/2014STRAJ097.

Council of Science Editors:

Ravens S. A genome-wide characterization of Mof or Tip60 containing complexes in mouse embryonic stem cells : L'analyse génomique des complexes contenant les acétyltransférases Mof ou Tip60 révèle des fonctions à la fois redondantes mais aussi spécifiques dans les cellules souches embryonnaire de souris. [Doctoral Dissertation]. Université de Strasbourg; 2014. Available from: http://www.theses.fr/2014STRAJ097


McGill University

16. Oguine, Adaora. The effect of food access schedule and diet composition on the rhythmicity of serum melatonin and pineal N-acetyltransferase activity in rats.

Degree: MS, School of Dietetics and Human Nutrition., 2002, McGill University

 Melatonin is a hormone secreted by the pineal gland, which is known to modulate biological rhythms in mammals. This study investigated the effect of food… (more)

Subjects/Keywords: Melatonin  – Synthesis.; Acetyltransferases.; Rats  – Food.; Tryptophan  – Physiological effect.

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APA (6th Edition):

Oguine, A. (2002). The effect of food access schedule and diet composition on the rhythmicity of serum melatonin and pineal N-acetyltransferase activity in rats. (Masters Thesis). McGill University. Retrieved from http://digitool.library.mcgill.ca/thesisfile33816.pdf

Chicago Manual of Style (16th Edition):

Oguine, Adaora. “The effect of food access schedule and diet composition on the rhythmicity of serum melatonin and pineal N-acetyltransferase activity in rats.” 2002. Masters Thesis, McGill University. Accessed October 17, 2019. http://digitool.library.mcgill.ca/thesisfile33816.pdf.

MLA Handbook (7th Edition):

Oguine, Adaora. “The effect of food access schedule and diet composition on the rhythmicity of serum melatonin and pineal N-acetyltransferase activity in rats.” 2002. Web. 17 Oct 2019.

Vancouver:

Oguine A. The effect of food access schedule and diet composition on the rhythmicity of serum melatonin and pineal N-acetyltransferase activity in rats. [Internet] [Masters thesis]. McGill University; 2002. [cited 2019 Oct 17]. Available from: http://digitool.library.mcgill.ca/thesisfile33816.pdf.

Council of Science Editors:

Oguine A. The effect of food access schedule and diet composition on the rhythmicity of serum melatonin and pineal N-acetyltransferase activity in rats. [Masters Thesis]. McGill University; 2002. Available from: http://digitool.library.mcgill.ca/thesisfile33816.pdf


IUPUI

17. Bhatti, Micah M. Functions of the Unique N-terminus of a GCN5 Histone Acetylase in Toxoplasma gondii.

Degree: 2007, IUPUI

Indiana University-Purdue University Indianapolis (IUPUI)

GCN5 is a histone acetyltransferase (HAT) that remodels chromatin by acetylating lysine residues of histones. The GCN5 HAT identified in… (more)

Subjects/Keywords: Parasitology; HAT; nuclear localization; Apicomplexan; Acetyltransferases; Histones; Apicomplexa; Parasitology

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APA (6th Edition):

Bhatti, M. M. (2007). Functions of the Unique N-terminus of a GCN5 Histone Acetylase in Toxoplasma gondii. (Thesis). IUPUI. Retrieved from http://hdl.handle.net/1805/897

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):

Bhatti, Micah M. “Functions of the Unique N-terminus of a GCN5 Histone Acetylase in Toxoplasma gondii.” 2007. Thesis, IUPUI. Accessed October 17, 2019. http://hdl.handle.net/1805/897.

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

MLA Handbook (7th Edition):

Bhatti, Micah M. “Functions of the Unique N-terminus of a GCN5 Histone Acetylase in Toxoplasma gondii.” 2007. Web. 17 Oct 2019.

Vancouver:

Bhatti MM. Functions of the Unique N-terminus of a GCN5 Histone Acetylase in Toxoplasma gondii. [Internet] [Thesis]. IUPUI; 2007. [cited 2019 Oct 17]. Available from: http://hdl.handle.net/1805/897.

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

Council of Science Editors:

Bhatti MM. Functions of the Unique N-terminus of a GCN5 Histone Acetylase in Toxoplasma gondii. [Thesis]. IUPUI; 2007. Available from: http://hdl.handle.net/1805/897

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

18. Chen, Poshen B. Function and Regulation of the Tip60-p400 Complex in Embryonic Stem Cells: A Dissertation.

Degree: Interdisciplinary Graduate Program, Molecular, Cell and Cancer Biology Department, 2015, U of Massachusetts : Med

  The following work examines the mechanisms by which Tip60-p400 chromatin remodeling complex regulates gene expression in embryonic stem cells (ESCs). Tip60-p400 complex has distinct… (more)

Subjects/Keywords: Chromatin; Embryonic Stem Cells; Developmental Gene Expression Regulation; Histone Acetyltransferases; Cell Biology; Developmental Biology; Genetics and Genomics

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APA (6th Edition):

Chen, P. B. (2015). Function and Regulation of the Tip60-p400 Complex in Embryonic Stem Cells: A Dissertation. (Doctoral Dissertation). U of Massachusetts : Med. Retrieved from https://escholarship.umassmed.edu/gsbs_diss/785

Chicago Manual of Style (16th Edition):

Chen, Poshen B. “Function and Regulation of the Tip60-p400 Complex in Embryonic Stem Cells: A Dissertation.” 2015. Doctoral Dissertation, U of Massachusetts : Med. Accessed October 17, 2019. https://escholarship.umassmed.edu/gsbs_diss/785.

MLA Handbook (7th Edition):

Chen, Poshen B. “Function and Regulation of the Tip60-p400 Complex in Embryonic Stem Cells: A Dissertation.” 2015. Web. 17 Oct 2019.

Vancouver:

Chen PB. Function and Regulation of the Tip60-p400 Complex in Embryonic Stem Cells: A Dissertation. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 2015. [cited 2019 Oct 17]. Available from: https://escholarship.umassmed.edu/gsbs_diss/785.

Council of Science Editors:

Chen PB. Function and Regulation of the Tip60-p400 Complex in Embryonic Stem Cells: A Dissertation. [Doctoral Dissertation]. U of Massachusetts : Med; 2015. Available from: https://escholarship.umassmed.edu/gsbs_diss/785

19. He, Ti. Molecular regulation of Pax5-mediated biological functions.

Degree: PhD, 2008, University of Alabama – Birmingham

B lineage cells are major players in the adaptive immune system. Pax5 is essential for B lineage cell development and function. Pax5 controls B lineage… (more)

Subjects/Keywords: B-Cell-Specific Activator Protein <; br>; Gene Expression Regulation <; br>; Histone Acetyltransferases  – metabolism <; br>; Transcription Factors <; br>; Transcription, Genetic

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APA (6th Edition):

He, T. (2008). Molecular regulation of Pax5-mediated biological functions. (Doctoral Dissertation). University of Alabama – Birmingham. Retrieved from http://contentdm.mhsl.uab.edu/u?/etd,329

Chicago Manual of Style (16th Edition):

He, Ti. “Molecular regulation of Pax5-mediated biological functions.” 2008. Doctoral Dissertation, University of Alabama – Birmingham. Accessed October 17, 2019. http://contentdm.mhsl.uab.edu/u?/etd,329.

MLA Handbook (7th Edition):

He, Ti. “Molecular regulation of Pax5-mediated biological functions.” 2008. Web. 17 Oct 2019.

Vancouver:

He T. Molecular regulation of Pax5-mediated biological functions. [Internet] [Doctoral dissertation]. University of Alabama – Birmingham; 2008. [cited 2019 Oct 17]. Available from: http://contentdm.mhsl.uab.edu/u?/etd,329.

Council of Science Editors:

He T. Molecular regulation of Pax5-mediated biological functions. [Doctoral Dissertation]. University of Alabama – Birmingham; 2008. Available from: http://contentdm.mhsl.uab.edu/u?/etd,329

20. Huang, Ping, Ph.D. O-GlcNAc modification in muscle development.

Degree: PhD, 2007, University of Alabama – Birmingham

O-glycosylation, a type of posttranslational modification, is abundant and dy-namic in the cell, yet its function in cell signaling and destiny regulation is far from… (more)

Subjects/Keywords: Acetyltransferases  – metabolism<; br>; Glycosylation<; br>; Muscle Proteins  – chemistry<; br>; Muscle, Skeletal  – metabolism<; br>; Proteasome Endopeptidase Complex

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APA (6th Edition):

Huang, Ping, P. D. (2007). O-GlcNAc modification in muscle development. (Doctoral Dissertation). University of Alabama – Birmingham. Retrieved from http://contentdm.mhsl.uab.edu/u?/etd,521

Chicago Manual of Style (16th Edition):

Huang, Ping, Ph D. “O-GlcNAc modification in muscle development.” 2007. Doctoral Dissertation, University of Alabama – Birmingham. Accessed October 17, 2019. http://contentdm.mhsl.uab.edu/u?/etd,521.

MLA Handbook (7th Edition):

Huang, Ping, Ph D. “O-GlcNAc modification in muscle development.” 2007. Web. 17 Oct 2019.

Vancouver:

Huang, Ping PD. O-GlcNAc modification in muscle development. [Internet] [Doctoral dissertation]. University of Alabama – Birmingham; 2007. [cited 2019 Oct 17]. Available from: http://contentdm.mhsl.uab.edu/u?/etd,521.

Council of Science Editors:

Huang, Ping PD. O-GlcNAc modification in muscle development. [Doctoral Dissertation]. University of Alabama – Birmingham; 2007. Available from: http://contentdm.mhsl.uab.edu/u?/etd,521

21. Abshiru, Nebiyu. Quantitative proteomics methods for the analysis of histone post-translational modifications .

Degree: 2016, Université de Montréal

 Les histones sont des protéines nucléaires hautement conservées chez les cellules des eucaryotes. Elles permettent d’organiser et de compacter l’ADN sous la forme de nucléosomes,… (more)

Subjects/Keywords: Spectrométrie de masse; Histones; Modifications post-traductionnelles; Peptides isomérique; Histones acétyltranférases; Histones déacétylases; Mass spectrometry; Histones; Post-translational modifications; Isomeric peptides; Histones acetyltransferases; Histone deacetylases

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APA (6th Edition):

Abshiru, N. (2016). Quantitative proteomics methods for the analysis of histone post-translational modifications . (Thesis). Université de Montréal. Retrieved from http://hdl.handle.net/1866/13563

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):

Abshiru, Nebiyu. “Quantitative proteomics methods for the analysis of histone post-translational modifications .” 2016. Thesis, Université de Montréal. Accessed October 17, 2019. http://hdl.handle.net/1866/13563.

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

MLA Handbook (7th Edition):

Abshiru, Nebiyu. “Quantitative proteomics methods for the analysis of histone post-translational modifications .” 2016. Web. 17 Oct 2019.

Vancouver:

Abshiru N. Quantitative proteomics methods for the analysis of histone post-translational modifications . [Internet] [Thesis]. Université de Montréal; 2016. [cited 2019 Oct 17]. Available from: http://hdl.handle.net/1866/13563.

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

Council of Science Editors:

Abshiru N. Quantitative proteomics methods for the analysis of histone post-translational modifications . [Thesis]. Université de Montréal; 2016. Available from: http://hdl.handle.net/1866/13563

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

22. Yang, Chao. Enzymatic Mechanisms and Chemical Probes of the Myst Family of Histone Acetyltransferases.

Degree: PhD, Chemistry, 2013, Georgia State University

  As an important posttranslational modification, protein acetylation plays critical roles in many biological processes such as gene transcription, DNA damage repair, apoptosis and metabolism.… (more)

Subjects/Keywords: Histone acetyltransferases; MYST HATs; Autoacetylation; Deacetylation; Chemical probe; Click chemistry

…15 2.2 Enzymatic Mechanisms of the MYST Family of Histone Acetyltransferases… …21 2.3 Chemical Probes of the MYST Family of Histone Acetyltransferases… …55 3.3 Chemical probes of the MYST family of histone acetyltransferases… …157 x LIST OF TABLES Table 1.1 Histone acetyltransferases and substrate specificity.63… …Histone acetyltransferases (HATs) Protein lysine acetyltransferases (KATs)… 

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APA (6th Edition):

Yang, C. (2013). Enzymatic Mechanisms and Chemical Probes of the Myst Family of Histone Acetyltransferases. (Doctoral Dissertation). Georgia State University. Retrieved from https://scholarworks.gsu.edu/chemistry_diss/80

Chicago Manual of Style (16th Edition):

Yang, Chao. “Enzymatic Mechanisms and Chemical Probes of the Myst Family of Histone Acetyltransferases.” 2013. Doctoral Dissertation, Georgia State University. Accessed October 17, 2019. https://scholarworks.gsu.edu/chemistry_diss/80.

MLA Handbook (7th Edition):

Yang, Chao. “Enzymatic Mechanisms and Chemical Probes of the Myst Family of Histone Acetyltransferases.” 2013. Web. 17 Oct 2019.

Vancouver:

Yang C. Enzymatic Mechanisms and Chemical Probes of the Myst Family of Histone Acetyltransferases. [Internet] [Doctoral dissertation]. Georgia State University; 2013. [cited 2019 Oct 17]. Available from: https://scholarworks.gsu.edu/chemistry_diss/80.

Council of Science Editors:

Yang C. Enzymatic Mechanisms and Chemical Probes of the Myst Family of Histone Acetyltransferases. [Doctoral Dissertation]. Georgia State University; 2013. Available from: https://scholarworks.gsu.edu/chemistry_diss/80


University of Missouri – Columbia

23. Choudhury, Mahua, 1977-. Alcohol induced histone acetylation mediated by histone acetyl transferase GCN5 in liver.

Degree: 2008, University of Missouri – Columbia

 Although several mechanisms have identified for alcoholic liver disease, at present there are no precise mechanisms for liver injury. We have observed that surrogate alcohols… (more)

Subjects/Keywords: Alcoholic liver diseases; Histones  – Metabolism; Histones  – Effect of drugs on; Acetyltransferases; Alcohols  – Receptors  – Effect of drugs on; Histone deacetylase  – Metabolism; Liver Diseases, Alcoholic  – etiology; Histones  – metabolism; Histones  – drug effects; Histone Acetyltransferases; Alcohols  – pharmacology; Histone Deacetylases  – metabolism

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APA (6th Edition):

Choudhury, Mahua, 1. (2008). Alcohol induced histone acetylation mediated by histone acetyl transferase GCN5 in liver. (Thesis). University of Missouri – Columbia. Retrieved from https://doi.org/10.32469/10355/6866

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):

Choudhury, Mahua, 1977-. “Alcohol induced histone acetylation mediated by histone acetyl transferase GCN5 in liver.” 2008. Thesis, University of Missouri – Columbia. Accessed October 17, 2019. https://doi.org/10.32469/10355/6866.

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

MLA Handbook (7th Edition):

Choudhury, Mahua, 1977-. “Alcohol induced histone acetylation mediated by histone acetyl transferase GCN5 in liver.” 2008. Web. 17 Oct 2019.

Vancouver:

Choudhury, Mahua 1. Alcohol induced histone acetylation mediated by histone acetyl transferase GCN5 in liver. [Internet] [Thesis]. University of Missouri – Columbia; 2008. [cited 2019 Oct 17]. Available from: https://doi.org/10.32469/10355/6866.

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

Council of Science Editors:

Choudhury, Mahua 1. Alcohol induced histone acetylation mediated by histone acetyl transferase GCN5 in liver. [Thesis]. University of Missouri – Columbia; 2008. Available from: https://doi.org/10.32469/10355/6866

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

24. Lopes da Rosa-Spiegler, Jessica. Targeting the Histone Acetyl-Transferase, RTT109, for Novel Anti-Fungal Drug Development: A Dissertation.

Degree: Interdisciplinary Graduate Program, Molecular, Cell and Cancer Biology, 2012, U of Massachusetts : Med

  Discovery of new antifungal chemo-therapeutics for humans is limited by the large degree of conservation among eukaryotic organisms. In recent years, the histone acetyl-transferase… (more)

Subjects/Keywords: Histone Acetyltransferases; Candida albicans; Antifungal Agents; Molecular Targeted Therapy; Biochemistry, Biophysics, and Structural Biology; Cells; Chemical Actions and Uses; Enzymes and Coenzymes; Fungi; Hemic and Immune Systems; Immunology and Infectious Disease; Microbiology; Pathology; Pharmaceutical Preparations; Therapeutics

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APA (6th Edition):

Lopes da Rosa-Spiegler, J. (2012). Targeting the Histone Acetyl-Transferase, RTT109, for Novel Anti-Fungal Drug Development: A Dissertation. (Doctoral Dissertation). U of Massachusetts : Med. Retrieved from https://escholarship.umassmed.edu/gsbs_diss/624

Chicago Manual of Style (16th Edition):

Lopes da Rosa-Spiegler, Jessica. “Targeting the Histone Acetyl-Transferase, RTT109, for Novel Anti-Fungal Drug Development: A Dissertation.” 2012. Doctoral Dissertation, U of Massachusetts : Med. Accessed October 17, 2019. https://escholarship.umassmed.edu/gsbs_diss/624.

MLA Handbook (7th Edition):

Lopes da Rosa-Spiegler, Jessica. “Targeting the Histone Acetyl-Transferase, RTT109, for Novel Anti-Fungal Drug Development: A Dissertation.” 2012. Web. 17 Oct 2019.

Vancouver:

Lopes da Rosa-Spiegler J. Targeting the Histone Acetyl-Transferase, RTT109, for Novel Anti-Fungal Drug Development: A Dissertation. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 2012. [cited 2019 Oct 17]. Available from: https://escholarship.umassmed.edu/gsbs_diss/624.

Council of Science Editors:

Lopes da Rosa-Spiegler J. Targeting the Histone Acetyl-Transferase, RTT109, for Novel Anti-Fungal Drug Development: A Dissertation. [Doctoral Dissertation]. U of Massachusetts : Med; 2012. Available from: https://escholarship.umassmed.edu/gsbs_diss/624


IUPUI

25. Stilger, Krista L. Identification of TgElp3 as an essential, tail-anchored mitochondrial lysine acetyltransferase in the protozoan pathogen toxoplasma gondii.

Degree: 2014, IUPUI

Indiana University-Purdue University Indianapolis (IUPUI)

Toxoplasma gondii, a single-celled eukaryotic pathogen, has infected one-third of the world’s population and is the causative agent of toxoplasmosis.… (more)

Subjects/Keywords: lysine acetyltransferase; Toxoplasma gondii; mitochondria; Toxoplasma gondii  – Research  – Analysis; Toxoplasmosis; Immunosuppression; Parasites  – Physiology; Parasitic diseases  – Immunological aspects; Lysine; Cellular signal transduction; Acetylation; Acetyltransferases; Eukaryotic cells; Prokaryotes; Virulence (Microbiology)  – Genetic aspects; Mitochondria; Membranes (Biology); Immune response  – Regulation; Post-translational modification

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APA (6th Edition):

Stilger, K. L. (2014). Identification of TgElp3 as an essential, tail-anchored mitochondrial lysine acetyltransferase in the protozoan pathogen toxoplasma gondii. (Thesis). IUPUI. Retrieved from http://hdl.handle.net/1805/4660

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):

Stilger, Krista L. “Identification of TgElp3 as an essential, tail-anchored mitochondrial lysine acetyltransferase in the protozoan pathogen toxoplasma gondii.” 2014. Thesis, IUPUI. Accessed October 17, 2019. http://hdl.handle.net/1805/4660.

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

MLA Handbook (7th Edition):

Stilger, Krista L. “Identification of TgElp3 as an essential, tail-anchored mitochondrial lysine acetyltransferase in the protozoan pathogen toxoplasma gondii.” 2014. Web. 17 Oct 2019.

Vancouver:

Stilger KL. Identification of TgElp3 as an essential, tail-anchored mitochondrial lysine acetyltransferase in the protozoan pathogen toxoplasma gondii. [Internet] [Thesis]. IUPUI; 2014. [cited 2019 Oct 17]. Available from: http://hdl.handle.net/1805/4660.

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

Council of Science Editors:

Stilger KL. Identification of TgElp3 as an essential, tail-anchored mitochondrial lysine acetyltransferase in the protozoan pathogen toxoplasma gondii. [Thesis]. IUPUI; 2014. Available from: http://hdl.handle.net/1805/4660

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


Queens University

26. Edgett, Brittany. Regulation of SIRT1, SIRT3, PGC-1α, and LRP130 in Response to Energetic Stress in Human Skeletal Muscle .

Degree: Kinesiology and Health Studies, Queens University

 The purpose of this dissertation was to investigate how the regulation of transcriptional coactivators (PGC-1α, LRP130) and protein deacetylases (SIRT1, SIRT3), which are shown to… (more)

Subjects/Keywords: Acetyltransferases; Deacetylases; Exercise; Fasting; GCN5; KAT2A; LRP130; LRPPRC; Mitochondria; PGC-1α; PPARGC1A; SIRT1; SIRT3; Skeletal Muscle; Transcriptional Coactivators

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APA (6th Edition):

Edgett, B. (n.d.). Regulation of SIRT1, SIRT3, PGC-1α, and LRP130 in Response to Energetic Stress in Human Skeletal Muscle . (Thesis). Queens University. Retrieved from http://hdl.handle.net/1974/15409

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):

Edgett, Brittany. “Regulation of SIRT1, SIRT3, PGC-1α, and LRP130 in Response to Energetic Stress in Human Skeletal Muscle .” Thesis, Queens University. Accessed October 17, 2019. http://hdl.handle.net/1974/15409.

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):

Edgett, Brittany. “Regulation of SIRT1, SIRT3, PGC-1α, and LRP130 in Response to Energetic Stress in Human Skeletal Muscle .” Web. 17 Oct 2019.

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

Vancouver:

Edgett B. Regulation of SIRT1, SIRT3, PGC-1α, and LRP130 in Response to Energetic Stress in Human Skeletal Muscle . [Internet] [Thesis]. Queens University; [cited 2019 Oct 17]. Available from: http://hdl.handle.net/1974/15409.

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:

Edgett B. Regulation of SIRT1, SIRT3, PGC-1α, and LRP130 in Response to Energetic Stress in Human Skeletal Muscle . [Thesis]. Queens University; Available from: http://hdl.handle.net/1974/15409

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


Universidad de Extremadura

27. Diop, Sokhna Maryama Seydina Yakhine. Acetilación, autofagia y Enfermedad de Parkinson.

Degree: 2018, Universidad de Extremadura

Subjects/Keywords: Acetilación; Acetil-coenzima A; Enfermedad de Parkinson; Histonas acetiltransferasas; Histonas desacetilasas; LRRK2; Mitocondria; Acetylation; Acetyl-coenzyme A; Parkinson’s disease; Histone acetyltransferases; Histone deacetylases; LRRK2; Mitochondrion; 2302 Bioquímica; 3207.04 Patología Cardiovascular; 3205.06 Nefrología; 3207.11 Neuropatología; 2410.07 Genética Humana

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

APA (6th Edition):

Diop, S. M. S. Y. (2018). Acetilación, autofagia y Enfermedad de Parkinson. (Thesis). Universidad de Extremadura. Retrieved from http://hdl.handle.net/10662/4027

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):

Diop, Sokhna Maryama Seydina Yakhine. “Acetilación, autofagia y Enfermedad de Parkinson.” 2018. Thesis, Universidad de Extremadura. Accessed October 17, 2019. http://hdl.handle.net/10662/4027.

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

MLA Handbook (7th Edition):

Diop, Sokhna Maryama Seydina Yakhine. “Acetilación, autofagia y Enfermedad de Parkinson.” 2018. Web. 17 Oct 2019.

Vancouver:

Diop SMSY. Acetilación, autofagia y Enfermedad de Parkinson. [Internet] [Thesis]. Universidad de Extremadura; 2018. [cited 2019 Oct 17]. Available from: http://hdl.handle.net/10662/4027.

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

Council of Science Editors:

Diop SMSY. Acetilación, autofagia y Enfermedad de Parkinson. [Thesis]. Universidad de Extremadura; 2018. Available from: http://hdl.handle.net/10662/4027

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

28. Wang, Jiachen. Lysine acetyltransferase Gcn5-B regulates the expression of crucial genes in Toxoplasma and its function is regulated through lysine acetylation.

Degree: 2014, IUPUI

Indiana University-Purdue University Indianapolis (IUPUI)

Histone acetylation has been linked to developmental changes in gene expression and is a validated drug target of apicomplexan parasites,… (more)

Subjects/Keywords: epigenetics, chromatin, Apicomplexa, parasite, gene regulation; Toxoplasma gondii  – Research; Apicomplexa  – Research  – Methodology  – Evaluation; Molecular parasitology  – Research; Acetyltransferases; Lysine; Chromatin; Epigenesis  – Research  – Methodology; Parasite antigens; Histones; Acetylation; Gene expression; Genetic regulation; DNA microarrays; Polymerase chain reaction  – Diagnostic use

…is catalyzed by lysine acetyltransferases (KATs) and reversed by lysine… …assembly. When GCN5 histone acetyltransferases were found to have non-histone substrates as well… …they became referred to as lysine (K) acetyltransferases (KATs) [40… …activation. Nuclear KATs can be divided into five families, GCN5-related N-acetyltransferases (… 

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

APA (6th Edition):

Wang, J. (2014). Lysine acetyltransferase Gcn5-B regulates the expression of crucial genes in Toxoplasma and its function is regulated through lysine acetylation. (Thesis). IUPUI. Retrieved from http://hdl.handle.net/1805/4211

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, Jiachen. “Lysine acetyltransferase Gcn5-B regulates the expression of crucial genes in Toxoplasma and its function is regulated through lysine acetylation.” 2014. Thesis, IUPUI. Accessed October 17, 2019. http://hdl.handle.net/1805/4211.

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

MLA Handbook (7th Edition):

Wang, Jiachen. “Lysine acetyltransferase Gcn5-B regulates the expression of crucial genes in Toxoplasma and its function is regulated through lysine acetylation.” 2014. Web. 17 Oct 2019.

Vancouver:

Wang J. Lysine acetyltransferase Gcn5-B regulates the expression of crucial genes in Toxoplasma and its function is regulated through lysine acetylation. [Internet] [Thesis]. IUPUI; 2014. [cited 2019 Oct 17]. Available from: http://hdl.handle.net/1805/4211.

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

Council of Science Editors:

Wang J. Lysine acetyltransferase Gcn5-B regulates the expression of crucial genes in Toxoplasma and its function is regulated through lysine acetylation. [Thesis]. IUPUI; 2014. Available from: http://hdl.handle.net/1805/4211

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

29. Calix, Juan Jose. Discovery And Characterization Of Streptococcus Pneumoniae Serotype 11e Reveals A Novel Model Of Serotype Evolution.

Degree: 2012, University of Alabama – Birmingham

The facultative pathogen Streptococcus pneumoniae is capable of producing a polysaccharide (PS) capsule that prevents bacterial recognition and clearance by the host immune system. Over… (more)

Subjects/Keywords: Acetyltransferases<; br>; Bacterial Capsules – chemistry.<; br>; Bacterial Proteins – chemistry<; br>; Carrier State – microbiology.<; br>; Gene Expression Regulation, Bacterial – physiology.<; br>; Genes, Bacterial<; br>; Genetic Variation<; br>; Oligosaccharides – metabolism.<; br>; Pneumococcal Infections – microbiology<; br>; Polysaccharides, Bacterial<; br>; Streptococcus pneumoniae

…acetate substitutions may be mediated by integral membrane O-acetyltransferases. CDP, cytosine… …acetyltransferases (OAcT) are important accessory genes, as reflected by the presence of 14… 

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

APA (6th Edition):

Calix, J. J. (2012). Discovery And Characterization Of Streptococcus Pneumoniae Serotype 11e Reveals A Novel Model Of Serotype Evolution. (Thesis). University of Alabama – Birmingham. Retrieved from http://contentdm.mhsl.uab.edu/u?/etd,1506

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):

Calix, Juan Jose. “Discovery And Characterization Of Streptococcus Pneumoniae Serotype 11e Reveals A Novel Model Of Serotype Evolution.” 2012. Thesis, University of Alabama – Birmingham. Accessed October 17, 2019. http://contentdm.mhsl.uab.edu/u?/etd,1506.

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

MLA Handbook (7th Edition):

Calix, Juan Jose. “Discovery And Characterization Of Streptococcus Pneumoniae Serotype 11e Reveals A Novel Model Of Serotype Evolution.” 2012. Web. 17 Oct 2019.

Vancouver:

Calix JJ. Discovery And Characterization Of Streptococcus Pneumoniae Serotype 11e Reveals A Novel Model Of Serotype Evolution. [Internet] [Thesis]. University of Alabama – Birmingham; 2012. [cited 2019 Oct 17]. Available from: http://contentdm.mhsl.uab.edu/u?/etd,1506.

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

Council of Science Editors:

Calix JJ. Discovery And Characterization Of Streptococcus Pneumoniae Serotype 11e Reveals A Novel Model Of Serotype Evolution. [Thesis]. University of Alabama – Birmingham; 2012. Available from: http://contentdm.mhsl.uab.edu/u?/etd,1506

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

.