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You searched for subject:(zinc fingers). Showing records 1 – 27 of 27 total matches.

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University of Texas Southwestern Medical Center

1. Barker, Jenny. Site-Specific Genome Engineering in Mouse Primary Fibroblasts.

Degree: 2014, University of Texas Southwestern Medical Center

 Site-specific genome engineering is a powerful tool for medical therapeutics and basic scientific research. As the name implies, site-specific genome engineering describes the ability to… (more)

Subjects/Keywords: Endonucleases; Genetic Therapy; Zinc Fingers

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

APA (6th Edition):

Barker, J. (2014). Site-Specific Genome Engineering in Mouse Primary Fibroblasts. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/3302

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):

Barker, Jenny. “Site-Specific Genome Engineering in Mouse Primary Fibroblasts.” 2014. Thesis, University of Texas Southwestern Medical Center. Accessed January 21, 2018. http://hdl.handle.net/2152.5/3302.

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

MLA Handbook (7th Edition):

Barker, Jenny. “Site-Specific Genome Engineering in Mouse Primary Fibroblasts.” 2014. Web. 21 Jan 2018.

Vancouver:

Barker J. Site-Specific Genome Engineering in Mouse Primary Fibroblasts. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2014. [cited 2018 Jan 21]. Available from: http://hdl.handle.net/2152.5/3302.

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

Council of Science Editors:

Barker J. Site-Specific Genome Engineering in Mouse Primary Fibroblasts. [Thesis]. University of Texas Southwestern Medical Center; 2014. Available from: http://hdl.handle.net/2152.5/3302

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

2. Chaikind, Brian Robb. Targeting bifurcated methyltransferases towards user-defined DNA sequences.

Degree: 2014, Johns Hopkins University

 There would be great value in targeting methylation toward user-defined DNA sequences. Directing methylation toward single CpG sites within a genome would provide a means… (more)

Subjects/Keywords: methyltransferases; protein engineering; directed evolution; zinc fingers

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APA (6th Edition):

Chaikind, B. R. (2014). Targeting bifurcated methyltransferases towards user-defined DNA sequences. (Thesis). Johns Hopkins University. Retrieved from http://jhir.library.jhu.edu/handle/1774.2/38017

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):

Chaikind, Brian Robb. “Targeting bifurcated methyltransferases towards user-defined DNA sequences.” 2014. Thesis, Johns Hopkins University. Accessed January 21, 2018. http://jhir.library.jhu.edu/handle/1774.2/38017.

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

MLA Handbook (7th Edition):

Chaikind, Brian Robb. “Targeting bifurcated methyltransferases towards user-defined DNA sequences.” 2014. Web. 21 Jan 2018.

Vancouver:

Chaikind BR. Targeting bifurcated methyltransferases towards user-defined DNA sequences. [Internet] [Thesis]. Johns Hopkins University; 2014. [cited 2018 Jan 21]. Available from: http://jhir.library.jhu.edu/handle/1774.2/38017.

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

Council of Science Editors:

Chaikind BR. Targeting bifurcated methyltransferases towards user-defined DNA sequences. [Thesis]. Johns Hopkins University; 2014. Available from: http://jhir.library.jhu.edu/handle/1774.2/38017

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

3. Pruett-Miller, Shondra M. Optimizing Zinc Finger Nucleases for Use in Mammalian Cells.

Degree: 2009, University of Texas Southwestern Medical Center

 Homologous recombination is a well-established technique that has been used to manipulate the genomes of multiple model organisms with great precision and is therefore being… (more)

Subjects/Keywords: Genetic Diseases; Zinc Fingers; Targeted Gene Repair

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APA (6th Edition):

Pruett-Miller, S. M. (2009). Optimizing Zinc Finger Nucleases for Use in Mammalian Cells. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/420

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):

Pruett-Miller, Shondra M. “Optimizing Zinc Finger Nucleases for Use in Mammalian Cells.” 2009. Thesis, University of Texas Southwestern Medical Center. Accessed January 21, 2018. http://hdl.handle.net/2152.5/420.

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

MLA Handbook (7th Edition):

Pruett-Miller, Shondra M. “Optimizing Zinc Finger Nucleases for Use in Mammalian Cells.” 2009. Web. 21 Jan 2018.

Vancouver:

Pruett-Miller SM. Optimizing Zinc Finger Nucleases for Use in Mammalian Cells. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2009. [cited 2018 Jan 21]. Available from: http://hdl.handle.net/2152.5/420.

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

Council of Science Editors:

Pruett-Miller SM. Optimizing Zinc Finger Nucleases for Use in Mammalian Cells. [Thesis]. University of Texas Southwestern Medical Center; 2009. Available from: http://hdl.handle.net/2152.5/420

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


University of Toronto

4. Lam, Kathy. A Phage Display System to Profile the DNA-binding Specificities of C2H2 Zinc Fingers.

Degree: 2010, University of Toronto

Knowing the sequence specificities of transcription factors allows us to surmise their functions and establish their regulatory roles in genomes. The most common DNA-binding domain… (more)

Subjects/Keywords: C2H2; zinc fingers; phage display; modular; DNA-binding specificity; 0307

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APA (6th Edition):

Lam, K. (2010). A Phage Display System to Profile the DNA-binding Specificities of C2H2 Zinc Fingers. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/25742

Chicago Manual of Style (16th Edition):

Lam, Kathy. “A Phage Display System to Profile the DNA-binding Specificities of C2H2 Zinc Fingers.” 2010. Masters Thesis, University of Toronto. Accessed January 21, 2018. http://hdl.handle.net/1807/25742.

MLA Handbook (7th Edition):

Lam, Kathy. “A Phage Display System to Profile the DNA-binding Specificities of C2H2 Zinc Fingers.” 2010. Web. 21 Jan 2018.

Vancouver:

Lam K. A Phage Display System to Profile the DNA-binding Specificities of C2H2 Zinc Fingers. [Internet] [Masters thesis]. University of Toronto; 2010. [cited 2018 Jan 21]. Available from: http://hdl.handle.net/1807/25742.

Council of Science Editors:

Lam K. A Phage Display System to Profile the DNA-binding Specificities of C2H2 Zinc Fingers. [Masters Thesis]. University of Toronto; 2010. Available from: http://hdl.handle.net/1807/25742


University of Texas Southwestern Medical Center

5. Wilson, Kimberly Anne. The Design and Development of Artificial Zinc Finger Transcription Factors and Zinc Finger Nucleases to the hTERT Locus.

Degree: 2011, University of Texas Southwestern Medical Center

 The ability to direct hTERT expression through genetic control or tunable regulatory factors would advance our understanding of the transcriptional regulation of hTERT, and also… (more)

Subjects/Keywords: Zinc Fingers; Gene Expression Regulation; Telomerase; Transcription Factors

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APA (6th Edition):

Wilson, K. A. (2011). The Design and Development of Artificial Zinc Finger Transcription Factors and Zinc Finger Nucleases to the hTERT Locus. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/861

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):

Wilson, Kimberly Anne. “The Design and Development of Artificial Zinc Finger Transcription Factors and Zinc Finger Nucleases to the hTERT Locus.” 2011. Thesis, University of Texas Southwestern Medical Center. Accessed January 21, 2018. http://hdl.handle.net/2152.5/861.

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

MLA Handbook (7th Edition):

Wilson, Kimberly Anne. “The Design and Development of Artificial Zinc Finger Transcription Factors and Zinc Finger Nucleases to the hTERT Locus.” 2011. Web. 21 Jan 2018.

Vancouver:

Wilson KA. The Design and Development of Artificial Zinc Finger Transcription Factors and Zinc Finger Nucleases to the hTERT Locus. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2011. [cited 2018 Jan 21]. Available from: http://hdl.handle.net/2152.5/861.

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

Council of Science Editors:

Wilson KA. The Design and Development of Artificial Zinc Finger Transcription Factors and Zinc Finger Nucleases to the hTERT Locus. [Thesis]. University of Texas Southwestern Medical Center; 2011. Available from: http://hdl.handle.net/2152.5/861

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


Lincoln University

6. Emami-Khoyi, Arsalan. Population and diet of the New Zealand fur seal (Arctocephalus forsteri): molecular approaches.

Degree: 2015, Lincoln University

 The recent increase in the New Zealand fur seal (Arctocephalus forsteri) population has given rise to socio-economic concerns regarding the potential conflicts with human interests.… (more)

Subjects/Keywords: New Zealand fur seal; Banks Peninsula; mitochondrial DNA; zinc fingers; population genetics; diet composition; diet

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APA (6th Edition):

Emami-Khoyi, A. (2015). Population and diet of the New Zealand fur seal (Arctocephalus forsteri): molecular approaches. (Thesis). Lincoln University. Retrieved from http://hdl.handle.net/10182/6758

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):

Emami-Khoyi, Arsalan. “Population and diet of the New Zealand fur seal (Arctocephalus forsteri): molecular approaches.” 2015. Thesis, Lincoln University. Accessed January 21, 2018. http://hdl.handle.net/10182/6758.

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

MLA Handbook (7th Edition):

Emami-Khoyi, Arsalan. “Population and diet of the New Zealand fur seal (Arctocephalus forsteri): molecular approaches.” 2015. Web. 21 Jan 2018.

Vancouver:

Emami-Khoyi A. Population and diet of the New Zealand fur seal (Arctocephalus forsteri): molecular approaches. [Internet] [Thesis]. Lincoln University; 2015. [cited 2018 Jan 21]. Available from: http://hdl.handle.net/10182/6758.

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

Council of Science Editors:

Emami-Khoyi A. Population and diet of the New Zealand fur seal (Arctocephalus forsteri): molecular approaches. [Thesis]. Lincoln University; 2015. Available from: http://hdl.handle.net/10182/6758

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


University of Oregon

7. Purcell, Jamie. Investigating the RNA Binding Domains of MBNL1 and the Alternative Splicing Motifs They Recognize.

Degree: 2012, University of Oregon

 Muscleblind-like 1 (MBNL1) is a ubiquitously expressed RNA binding protein that regulates the alternative splicing of a variety of transcripts. In Myotonic Dystrophy (DM) aberrant… (more)

Subjects/Keywords: Alternative splicing; Muscleblind (MBNL1); Myotonic Dystrophy (DM); RNA-binding proteins; Splicing factors; Zinc fingers

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APA (6th Edition):

Purcell, J. (2012). Investigating the RNA Binding Domains of MBNL1 and the Alternative Splicing Motifs They Recognize. (Thesis). University of Oregon. Retrieved from http://hdl.handle.net/1794/12331

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):

Purcell, Jamie. “Investigating the RNA Binding Domains of MBNL1 and the Alternative Splicing Motifs They Recognize.” 2012. Thesis, University of Oregon. Accessed January 21, 2018. http://hdl.handle.net/1794/12331.

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

MLA Handbook (7th Edition):

Purcell, Jamie. “Investigating the RNA Binding Domains of MBNL1 and the Alternative Splicing Motifs They Recognize.” 2012. Web. 21 Jan 2018.

Vancouver:

Purcell J. Investigating the RNA Binding Domains of MBNL1 and the Alternative Splicing Motifs They Recognize. [Internet] [Thesis]. University of Oregon; 2012. [cited 2018 Jan 21]. Available from: http://hdl.handle.net/1794/12331.

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

Council of Science Editors:

Purcell J. Investigating the RNA Binding Domains of MBNL1 and the Alternative Splicing Motifs They Recognize. [Thesis]. University of Oregon; 2012. Available from: http://hdl.handle.net/1794/12331

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


Université de Grenoble

8. Lebrun, Vincent. Doigts de zinc et stress oxydant : réactivité vis-à-vis de l'oxygène singulet et l'acide hypochloreux : Zinc Fingers and oxidative stress : reactivity towards hypochlorous acid and singlet oxygen.

Degree: Docteur es, Chimie, 2014, Université de Grenoble

Très répandues dans le monde vivant, les protéines à doigt de zinc constituent une super-famille dont les membres possèdent un site à zinc de formule… (more)

Subjects/Keywords: Oxygène singulet; Acide hypochloreux; Doigts de zinc; Peptide; Stress oxydant; Singlet oxygen; Hypochlorous acid; Zinc fingers; Peptide; Oxidative stress; 540

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APA (6th Edition):

Lebrun, V. (2014). Doigts de zinc et stress oxydant : réactivité vis-à-vis de l'oxygène singulet et l'acide hypochloreux : Zinc Fingers and oxidative stress : reactivity towards hypochlorous acid and singlet oxygen. (Doctoral Dissertation). Université de Grenoble. Retrieved from http://www.theses.fr/2014GRENV068

Chicago Manual of Style (16th Edition):

Lebrun, Vincent. “Doigts de zinc et stress oxydant : réactivité vis-à-vis de l'oxygène singulet et l'acide hypochloreux : Zinc Fingers and oxidative stress : reactivity towards hypochlorous acid and singlet oxygen.” 2014. Doctoral Dissertation, Université de Grenoble. Accessed January 21, 2018. http://www.theses.fr/2014GRENV068.

MLA Handbook (7th Edition):

Lebrun, Vincent. “Doigts de zinc et stress oxydant : réactivité vis-à-vis de l'oxygène singulet et l'acide hypochloreux : Zinc Fingers and oxidative stress : reactivity towards hypochlorous acid and singlet oxygen.” 2014. Web. 21 Jan 2018.

Vancouver:

Lebrun V. Doigts de zinc et stress oxydant : réactivité vis-à-vis de l'oxygène singulet et l'acide hypochloreux : Zinc Fingers and oxidative stress : reactivity towards hypochlorous acid and singlet oxygen. [Internet] [Doctoral dissertation]. Université de Grenoble; 2014. [cited 2018 Jan 21]. Available from: http://www.theses.fr/2014GRENV068.

Council of Science Editors:

Lebrun V. Doigts de zinc et stress oxydant : réactivité vis-à-vis de l'oxygène singulet et l'acide hypochloreux : Zinc Fingers and oxidative stress : reactivity towards hypochlorous acid and singlet oxygen. [Doctoral Dissertation]. Université de Grenoble; 2014. Available from: http://www.theses.fr/2014GRENV068


University of Utah

9. Hurban, Patrick. Isolation and characterization of ecdysone-inducible genes from Drosophila;.

Degree: PhD, Human Genetics;, 1994, University of Utah

 Metamorphosis in Drosophila melanogaster is initiated by a pulse of the steroid hormone ecdysone. The genetic response to ecdysone can be visualized in the reproducible… (more)

Subjects/Keywords: Zinc Fingers; Cytochrome P-450; Molecular Biology

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APA (6th Edition):

Hurban, P. (1994). Isolation and characterization of ecdysone-inducible genes from Drosophila;. (Doctoral Dissertation). University of Utah. Retrieved from http://content.lib.utah.edu/cdm/singleitem/collection/etd1/id/1228/rec/732

Chicago Manual of Style (16th Edition):

Hurban, Patrick. “Isolation and characterization of ecdysone-inducible genes from Drosophila;.” 1994. Doctoral Dissertation, University of Utah. Accessed January 21, 2018. http://content.lib.utah.edu/cdm/singleitem/collection/etd1/id/1228/rec/732.

MLA Handbook (7th Edition):

Hurban, Patrick. “Isolation and characterization of ecdysone-inducible genes from Drosophila;.” 1994. Web. 21 Jan 2018.

Vancouver:

Hurban P. Isolation and characterization of ecdysone-inducible genes from Drosophila;. [Internet] [Doctoral dissertation]. University of Utah; 1994. [cited 2018 Jan 21]. Available from: http://content.lib.utah.edu/cdm/singleitem/collection/etd1/id/1228/rec/732.

Council of Science Editors:

Hurban P. Isolation and characterization of ecdysone-inducible genes from Drosophila;. [Doctoral Dissertation]. University of Utah; 1994. Available from: http://content.lib.utah.edu/cdm/singleitem/collection/etd1/id/1228/rec/732


Indian Institute of Science

10. Tripathi, Pankaj. Selective Binding Of Meiosis-Specific Yeast Hop1 Protein, or Its ZnF Motif, To The Holliday Junction Distorts The DNA Structure : Implications For Junction Migration And Resolution.

Degree: 2008, Indian Institute of Science

 Saccharomyces cerevisiae HOP1, which encodes a component of the synaptonemal complex, plays an important role in both gene conversion and crossing over between homologs, as… (more)

Subjects/Keywords: DNA - Molecular Structure; Yeast Hop1 Protein; Holliday Junction; Hop1 Zinc Fingers; Meiotic Recombination; Meiosis; Saccharomyces cerevisiae; Holliday Junction Migration; Biochemical Genetics

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APA (6th Edition):

Tripathi, P. (2008). Selective Binding Of Meiosis-Specific Yeast Hop1 Protein, or Its ZnF Motif, To The Holliday Junction Distorts The DNA Structure : Implications For Junction Migration And Resolution. (Thesis). Indian Institute of Science. Retrieved from http://hdl.handle.net/2005/894

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):

Tripathi, Pankaj. “Selective Binding Of Meiosis-Specific Yeast Hop1 Protein, or Its ZnF Motif, To The Holliday Junction Distorts The DNA Structure : Implications For Junction Migration And Resolution.” 2008. Thesis, Indian Institute of Science. Accessed January 21, 2018. http://hdl.handle.net/2005/894.

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

MLA Handbook (7th Edition):

Tripathi, Pankaj. “Selective Binding Of Meiosis-Specific Yeast Hop1 Protein, or Its ZnF Motif, To The Holliday Junction Distorts The DNA Structure : Implications For Junction Migration And Resolution.” 2008. Web. 21 Jan 2018.

Vancouver:

Tripathi P. Selective Binding Of Meiosis-Specific Yeast Hop1 Protein, or Its ZnF Motif, To The Holliday Junction Distorts The DNA Structure : Implications For Junction Migration And Resolution. [Internet] [Thesis]. Indian Institute of Science; 2008. [cited 2018 Jan 21]. Available from: http://hdl.handle.net/2005/894.

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

Council of Science Editors:

Tripathi P. Selective Binding Of Meiosis-Specific Yeast Hop1 Protein, or Its ZnF Motif, To The Holliday Junction Distorts The DNA Structure : Implications For Junction Migration And Resolution. [Thesis]. Indian Institute of Science; 2008. Available from: http://hdl.handle.net/2005/894

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


University of Sydney

11. Kwan, Ann Hau Yu. Protein Design Based on a PHD Scaffold .

Degree: 2004, University of Sydney

 The plant homeodomain (PHD) is a protein domain of ~45�100 residues characterised by a Cys4-His-Cys3 zinc-binding motif. When we commenced our study of the PHD… (more)

Subjects/Keywords: protein design; PHD; nmr spectroscopy; zinc fingers; LMO

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APA (6th Edition):

Kwan, A. H. Y. (2004). Protein Design Based on a PHD Scaffold . (Thesis). University of Sydney. Retrieved from http://hdl.handle.net/2123/564

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):

Kwan, Ann Hau Yu. “Protein Design Based on a PHD Scaffold .” 2004. Thesis, University of Sydney. Accessed January 21, 2018. http://hdl.handle.net/2123/564.

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

MLA Handbook (7th Edition):

Kwan, Ann Hau Yu. “Protein Design Based on a PHD Scaffold .” 2004. Web. 21 Jan 2018.

Vancouver:

Kwan AHY. Protein Design Based on a PHD Scaffold . [Internet] [Thesis]. University of Sydney; 2004. [cited 2018 Jan 21]. Available from: http://hdl.handle.net/2123/564.

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

Council of Science Editors:

Kwan AHY. Protein Design Based on a PHD Scaffold . [Thesis]. University of Sydney; 2004. Available from: http://hdl.handle.net/2123/564

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


University of Sydney

12. Simpson, Raina Jui Yu. The multiple roles of zinc finger domains .

Degree: 2004, University of Sydney

Zinc finger (ZnF) domains are prevalent in eukaryotes and play crucial roles in mediating protein-DNA and protein-protein interactions. This Thesis focuses on the molecular details… (more)

Subjects/Keywords: zinc fingers; protein-protein; protein-DNA; interactions

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APA (6th Edition):

Simpson, R. J. Y. (2004). The multiple roles of zinc finger domains . (Thesis). University of Sydney. Retrieved from http://hdl.handle.net/2123/655

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):

Simpson, Raina Jui Yu. “The multiple roles of zinc finger domains .” 2004. Thesis, University of Sydney. Accessed January 21, 2018. http://hdl.handle.net/2123/655.

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

MLA Handbook (7th Edition):

Simpson, Raina Jui Yu. “The multiple roles of zinc finger domains .” 2004. Web. 21 Jan 2018.

Vancouver:

Simpson RJY. The multiple roles of zinc finger domains . [Internet] [Thesis]. University of Sydney; 2004. [cited 2018 Jan 21]. Available from: http://hdl.handle.net/2123/655.

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

Council of Science Editors:

Simpson RJY. The multiple roles of zinc finger domains . [Thesis]. University of Sydney; 2004. Available from: http://hdl.handle.net/2123/655

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


University of Kentucky

13. Creasy, Kate Townsend. ZHX2 REGULATION OF LIPID METABOLISM AND THE BALANCE BETWEEN CARDIOVASCULAR AND HEPATIC HEALTH.

Degree: 2015, University of Kentucky

 The growing obesity epidemic in America carries with it numerous health risks, including diabetes, increased serum lipid levels, and excess fat accumulation in the liver.… (more)

Subjects/Keywords: Zinc fingers and homeoboxes 2; gene regulation; lipid metabolism; cancer; cardiovascular disease; Molecular, Genetic, and Biochemical Nutrition

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APA (6th Edition):

Creasy, K. T. (2015). ZHX2 REGULATION OF LIPID METABOLISM AND THE BALANCE BETWEEN CARDIOVASCULAR AND HEPATIC HEALTH. (Doctoral Dissertation). University of Kentucky. Retrieved from http://uknowledge.uky.edu/pharmacol_etds/10

Chicago Manual of Style (16th Edition):

Creasy, Kate Townsend. “ZHX2 REGULATION OF LIPID METABOLISM AND THE BALANCE BETWEEN CARDIOVASCULAR AND HEPATIC HEALTH.” 2015. Doctoral Dissertation, University of Kentucky. Accessed January 21, 2018. http://uknowledge.uky.edu/pharmacol_etds/10.

MLA Handbook (7th Edition):

Creasy, Kate Townsend. “ZHX2 REGULATION OF LIPID METABOLISM AND THE BALANCE BETWEEN CARDIOVASCULAR AND HEPATIC HEALTH.” 2015. Web. 21 Jan 2018.

Vancouver:

Creasy KT. ZHX2 REGULATION OF LIPID METABOLISM AND THE BALANCE BETWEEN CARDIOVASCULAR AND HEPATIC HEALTH. [Internet] [Doctoral dissertation]. University of Kentucky; 2015. [cited 2018 Jan 21]. Available from: http://uknowledge.uky.edu/pharmacol_etds/10.

Council of Science Editors:

Creasy KT. ZHX2 REGULATION OF LIPID METABOLISM AND THE BALANCE BETWEEN CARDIOVASCULAR AND HEPATIC HEALTH. [Doctoral Dissertation]. University of Kentucky; 2015. Available from: http://uknowledge.uky.edu/pharmacol_etds/10


University of Texas Southwestern Medical Center

14. Kathiriya, Irfan S. GATA Co-Factors : Collaborators in Cardiac Development, Conspirators in Cardiac Disease.

Degree: 2005, University of Texas Southwestern Medical Center

 Disruption of fetal gene expression during cardiac development can result in congenital heart defects (CHDs), the most common developmental anomaly in humans and the leading… (more)

Subjects/Keywords: Heart, Embryology; GATA4 Transcription Factor; Zinc Fingers

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APA (6th Edition):

Kathiriya, I. S. (2005). GATA Co-Factors : Collaborators in Cardiac Development, Conspirators in Cardiac Disease. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/292

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):

Kathiriya, Irfan S. “GATA Co-Factors : Collaborators in Cardiac Development, Conspirators in Cardiac Disease.” 2005. Thesis, University of Texas Southwestern Medical Center. Accessed January 21, 2018. http://hdl.handle.net/2152.5/292.

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

MLA Handbook (7th Edition):

Kathiriya, Irfan S. “GATA Co-Factors : Collaborators in Cardiac Development, Conspirators in Cardiac Disease.” 2005. Web. 21 Jan 2018.

Vancouver:

Kathiriya IS. GATA Co-Factors : Collaborators in Cardiac Development, Conspirators in Cardiac Disease. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2005. [cited 2018 Jan 21]. Available from: http://hdl.handle.net/2152.5/292.

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

Council of Science Editors:

Kathiriya IS. GATA Co-Factors : Collaborators in Cardiac Development, Conspirators in Cardiac Disease. [Thesis]. University of Texas Southwestern Medical Center; 2005. Available from: http://hdl.handle.net/2152.5/292

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

15. Connelly, Jon Patrick. Gene Targeting in a Novel Mouse Model and the Chicken DT40 Cell Line.

Degree: 2010, University of Texas Southwestern Medical Center

 Gene targeting has the power to create precise changes at specific sites within the genome. In the context of gene therapy, this technology may be… (more)

Subjects/Keywords: Genetic Diseases; Targeted Gene Repair; Zinc Fingers

…double-strand break at the target site. These breaks can be created by proteins called zinc… …11 Development of Zinc Finger Nucleases… …57 CHAPTER IV: GENE CORRECTION BY HOMOLOGOUS RECOMBINATION WITH ZINC FINGER NUCLEASES IN… …correction by homologous recombination with zinc finger nucleases in primary cells from a mouse… …Connelly JP, Maeder ML, Joung JK, Porteus MH. (2008) Comparison of zinc finger… 

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APA (6th Edition):

Connelly, J. P. (2010). Gene Targeting in a Novel Mouse Model and the Chicken DT40 Cell Line. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/719

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):

Connelly, Jon Patrick. “Gene Targeting in a Novel Mouse Model and the Chicken DT40 Cell Line.” 2010. Thesis, University of Texas Southwestern Medical Center. Accessed January 21, 2018. http://hdl.handle.net/2152.5/719.

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

MLA Handbook (7th Edition):

Connelly, Jon Patrick. “Gene Targeting in a Novel Mouse Model and the Chicken DT40 Cell Line.” 2010. Web. 21 Jan 2018.

Vancouver:

Connelly JP. Gene Targeting in a Novel Mouse Model and the Chicken DT40 Cell Line. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2010. [cited 2018 Jan 21]. Available from: http://hdl.handle.net/2152.5/719.

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

Council of Science Editors:

Connelly JP. Gene Targeting in a Novel Mouse Model and the Chicken DT40 Cell Line. [Thesis]. University of Texas Southwestern Medical Center; 2010. Available from: http://hdl.handle.net/2152.5/719

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


Université de Grenoble

16. Jacques, Aurélie. Interaction de l'or avec des peptides modèles de doigts de zinc : caractérisation de la complexation des sels d'or et application à la toxicologie des nanoparticules d'or : Interaction between gold and zinc finger models : characterization of gold(I) complexes and relevance for toxicology of gold nanoparticles.

Degree: Docteur es, Chimie bio-inorganique, 2013, Université de Grenoble

Les complexes d'or(I) tels que l'auranofine et l'aurothiomalate ont été utilisés dans le traitement de la polyarthrite rhumatoïde depuis plusieurs décennies. Plus récemment, de nombreux… (more)

Subjects/Keywords: Doigts de zinc; Sels d'or; Nanoparticules d'or; Peptides; Échange de métaux; Cinétique; Zinc fingers; Gold solts; Gold nanoparticles; Peptides; Metal exchange; Kinetic; 540

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APA (6th Edition):

Jacques, A. (2013). Interaction de l'or avec des peptides modèles de doigts de zinc : caractérisation de la complexation des sels d'or et application à la toxicologie des nanoparticules d'or : Interaction between gold and zinc finger models : characterization of gold(I) complexes and relevance for toxicology of gold nanoparticles. (Doctoral Dissertation). Université de Grenoble. Retrieved from http://www.theses.fr/2013GRENV075

Chicago Manual of Style (16th Edition):

Jacques, Aurélie. “Interaction de l'or avec des peptides modèles de doigts de zinc : caractérisation de la complexation des sels d'or et application à la toxicologie des nanoparticules d'or : Interaction between gold and zinc finger models : characterization of gold(I) complexes and relevance for toxicology of gold nanoparticles.” 2013. Doctoral Dissertation, Université de Grenoble. Accessed January 21, 2018. http://www.theses.fr/2013GRENV075.

MLA Handbook (7th Edition):

Jacques, Aurélie. “Interaction de l'or avec des peptides modèles de doigts de zinc : caractérisation de la complexation des sels d'or et application à la toxicologie des nanoparticules d'or : Interaction between gold and zinc finger models : characterization of gold(I) complexes and relevance for toxicology of gold nanoparticles.” 2013. Web. 21 Jan 2018.

Vancouver:

Jacques A. Interaction de l'or avec des peptides modèles de doigts de zinc : caractérisation de la complexation des sels d'or et application à la toxicologie des nanoparticules d'or : Interaction between gold and zinc finger models : characterization of gold(I) complexes and relevance for toxicology of gold nanoparticles. [Internet] [Doctoral dissertation]. Université de Grenoble; 2013. [cited 2018 Jan 21]. Available from: http://www.theses.fr/2013GRENV075.

Council of Science Editors:

Jacques A. Interaction de l'or avec des peptides modèles de doigts de zinc : caractérisation de la complexation des sels d'or et application à la toxicologie des nanoparticules d'or : Interaction between gold and zinc finger models : characterization of gold(I) complexes and relevance for toxicology of gold nanoparticles. [Doctoral Dissertation]. Université de Grenoble; 2013. Available from: http://www.theses.fr/2013GRENV075


McGill University

17. Drolet, Jessica Ann. Evidence for the involvement of the zinc cluster protein Asg1p in the transcriptional regulation of some stress response genes in Saccharomyces cerevisiae.

Degree: MS, Department of Microbiology and Immunology., 2007, McGill University

 Saccharomyces cerevisiae has developed mechanisms in order to survive harsh environmental conditions. This species responds to stresses such as ethanol, heat, and weak acid exposure… (more)

Subjects/Keywords: Saccharomyces cerevisiae Proteins  – metabolism.; Gene Expression Regulation, Fungal  – genetics.; Zinc  – metabolism.; Zinc Fingers.

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APA (6th Edition):

Drolet, J. A. (2007). Evidence for the involvement of the zinc cluster protein Asg1p in the transcriptional regulation of some stress response genes in Saccharomyces cerevisiae. (Masters Thesis). McGill University. Retrieved from http://digitool.library.mcgill.ca/thesisfile112617.pdf

Chicago Manual of Style (16th Edition):

Drolet, Jessica Ann. “Evidence for the involvement of the zinc cluster protein Asg1p in the transcriptional regulation of some stress response genes in Saccharomyces cerevisiae.” 2007. Masters Thesis, McGill University. Accessed January 21, 2018. http://digitool.library.mcgill.ca/thesisfile112617.pdf.

MLA Handbook (7th Edition):

Drolet, Jessica Ann. “Evidence for the involvement of the zinc cluster protein Asg1p in the transcriptional regulation of some stress response genes in Saccharomyces cerevisiae.” 2007. Web. 21 Jan 2018.

Vancouver:

Drolet JA. Evidence for the involvement of the zinc cluster protein Asg1p in the transcriptional regulation of some stress response genes in Saccharomyces cerevisiae. [Internet] [Masters thesis]. McGill University; 2007. [cited 2018 Jan 21]. Available from: http://digitool.library.mcgill.ca/thesisfile112617.pdf.

Council of Science Editors:

Drolet JA. Evidence for the involvement of the zinc cluster protein Asg1p in the transcriptional regulation of some stress response genes in Saccharomyces cerevisiae. [Masters Thesis]. McGill University; 2007. Available from: http://digitool.library.mcgill.ca/thesisfile112617.pdf

18. Valeije, Ana Claudia Mancusi. Utilização de informações termodinâmicas e estruturais na predição de sítios de ligação de receptores nucleares ao DNA: uma abordagem computacional.

Degree: Mestrado, Bioinformática, 2015, University of São Paulo

 Os projetos genoma têm fornecido uma grande quantidade de informação sobre a arquitetura gênica e sobre a configuração física de suas respectivas regiões flanqueadoras (RF).… (more)

Subjects/Keywords: Dedos de zinco; DNA binding sites; Fatores de transcrição; Interação proteína-DNA; Nuclear receptors; Protein-DNA interactions; Receptores nucleares; Sítios de ligação ao DNA; TFBS; TFBS; Transcription factors; Zinc fingers

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APA (6th Edition):

Valeije, A. C. M. (2015). Utilização de informações termodinâmicas e estruturais na predição de sítios de ligação de receptores nucleares ao DNA: uma abordagem computacional. (Masters Thesis). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/95/95131/tde-23042015-133407/ ;

Chicago Manual of Style (16th Edition):

Valeije, Ana Claudia Mancusi. “Utilização de informações termodinâmicas e estruturais na predição de sítios de ligação de receptores nucleares ao DNA: uma abordagem computacional.” 2015. Masters Thesis, University of São Paulo. Accessed January 21, 2018. http://www.teses.usp.br/teses/disponiveis/95/95131/tde-23042015-133407/ ;.

MLA Handbook (7th Edition):

Valeije, Ana Claudia Mancusi. “Utilização de informações termodinâmicas e estruturais na predição de sítios de ligação de receptores nucleares ao DNA: uma abordagem computacional.” 2015. Web. 21 Jan 2018.

Vancouver:

Valeije ACM. Utilização de informações termodinâmicas e estruturais na predição de sítios de ligação de receptores nucleares ao DNA: uma abordagem computacional. [Internet] [Masters thesis]. University of São Paulo; 2015. [cited 2018 Jan 21]. Available from: http://www.teses.usp.br/teses/disponiveis/95/95131/tde-23042015-133407/ ;.

Council of Science Editors:

Valeije ACM. Utilização de informações termodinâmicas e estruturais na predição de sítios de ligação de receptores nucleares ao DNA: uma abordagem computacional. [Masters Thesis]. University of São Paulo; 2015. Available from: http://www.teses.usp.br/teses/disponiveis/95/95131/tde-23042015-133407/ ;


Brigham Young University

19. Parker, Tory L. The Effects of Selenium on Estrogen-regulated Gene Expression in LNCaP Prostate Cancer Cells.

Degree: MS, 2004, Brigham Young University

  Prostate cancer is the most frequently diagnosed cancer in American men and the second leading cause of cancer deaths. Supplementation with Se has reduced… (more)

Subjects/Keywords: selenium; estrogen; estrogen receptor; LNCaP; prostate cancer; zinc fingers; Food Science; Nutrition

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APA (6th Edition):

Parker, T. L. (2004). The Effects of Selenium on Estrogen-regulated Gene Expression in LNCaP Prostate Cancer Cells. (Thesis). Brigham Young University. Retrieved from https://scholarsarchive.byu.edu/etd/637

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):

Parker, Tory L. “The Effects of Selenium on Estrogen-regulated Gene Expression in LNCaP Prostate Cancer Cells.” 2004. Thesis, Brigham Young University. Accessed January 21, 2018. https://scholarsarchive.byu.edu/etd/637.

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

MLA Handbook (7th Edition):

Parker, Tory L. “The Effects of Selenium on Estrogen-regulated Gene Expression in LNCaP Prostate Cancer Cells.” 2004. Web. 21 Jan 2018.

Vancouver:

Parker TL. The Effects of Selenium on Estrogen-regulated Gene Expression in LNCaP Prostate Cancer Cells. [Internet] [Thesis]. Brigham Young University; 2004. [cited 2018 Jan 21]. Available from: https://scholarsarchive.byu.edu/etd/637.

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

Council of Science Editors:

Parker TL. The Effects of Selenium on Estrogen-regulated Gene Expression in LNCaP Prostate Cancer Cells. [Thesis]. Brigham Young University; 2004. Available from: https://scholarsarchive.byu.edu/etd/637

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

20. MANJEET MUKHERJEE. STRUCTURAL AND FUNCTIONAL STUDIES OF A NOVEL PHOSPHOTYROSINE-BINDING DOMAIN IN HAKAI, THE HYB DOMAIN, THAT TARGETS E-CADHERIN AND OTHER SRC SUBSTRATES.

Degree: 2013, National University of Singapore

Subjects/Keywords: Hakai; phosphotyrosine-binding domain; zinc fingers; HYB; Src substrates; structural biology

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APA (6th Edition):

MUKHERJEE, M. (2013). STRUCTURAL AND FUNCTIONAL STUDIES OF A NOVEL PHOSPHOTYROSINE-BINDING DOMAIN IN HAKAI, THE HYB DOMAIN, THAT TARGETS E-CADHERIN AND OTHER SRC SUBSTRATES. (Thesis). National University of Singapore. Retrieved from http://scholarbank.nus.edu.sg/handle/10635/49247 ; http://scholarbank.nus.edu.sg/bitstream/10635%2F49247/2/bitstream ; http://scholarbank.nus.edu.sg/bitstream/10635%2F49247/1/bitstream

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):

MUKHERJEE, MANJEET. “STRUCTURAL AND FUNCTIONAL STUDIES OF A NOVEL PHOSPHOTYROSINE-BINDING DOMAIN IN HAKAI, THE HYB DOMAIN, THAT TARGETS E-CADHERIN AND OTHER SRC SUBSTRATES.” 2013. Thesis, National University of Singapore. Accessed January 21, 2018. http://scholarbank.nus.edu.sg/handle/10635/49247 ; http://scholarbank.nus.edu.sg/bitstream/10635%2F49247/2/bitstream ; http://scholarbank.nus.edu.sg/bitstream/10635%2F49247/1/bitstream.

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

MLA Handbook (7th Edition):

MUKHERJEE, MANJEET. “STRUCTURAL AND FUNCTIONAL STUDIES OF A NOVEL PHOSPHOTYROSINE-BINDING DOMAIN IN HAKAI, THE HYB DOMAIN, THAT TARGETS E-CADHERIN AND OTHER SRC SUBSTRATES.” 2013. Web. 21 Jan 2018.

Vancouver:

MUKHERJEE M. STRUCTURAL AND FUNCTIONAL STUDIES OF A NOVEL PHOSPHOTYROSINE-BINDING DOMAIN IN HAKAI, THE HYB DOMAIN, THAT TARGETS E-CADHERIN AND OTHER SRC SUBSTRATES. [Internet] [Thesis]. National University of Singapore; 2013. [cited 2018 Jan 21]. Available from: http://scholarbank.nus.edu.sg/handle/10635/49247 ; http://scholarbank.nus.edu.sg/bitstream/10635%2F49247/2/bitstream ; http://scholarbank.nus.edu.sg/bitstream/10635%2F49247/1/bitstream.

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

Council of Science Editors:

MUKHERJEE M. STRUCTURAL AND FUNCTIONAL STUDIES OF A NOVEL PHOSPHOTYROSINE-BINDING DOMAIN IN HAKAI, THE HYB DOMAIN, THAT TARGETS E-CADHERIN AND OTHER SRC SUBSTRATES. [Thesis]. National University of Singapore; 2013. Available from: http://scholarbank.nus.edu.sg/handle/10635/49247 ; http://scholarbank.nus.edu.sg/bitstream/10635%2F49247/2/bitstream ; http://scholarbank.nus.edu.sg/bitstream/10635%2F49247/1/bitstream

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


University of Otago

21. Ahokovi Tukia, Richard Katavake Taka-I-Utukakai. Investigation of the Wilms' tumour suppressor protein (WT1) .

Degree: 2011, University of Otago

 Wilms’ tumour is a paediatric nephroblastoma which affects 1: 10,000 live births, and is the most common form of solid tumour in children under 5… (more)

Subjects/Keywords: Wilms' tumour; Wilms' tumour suppressor protein; WT1; wt1 gene; Kidney; Nephroblastoma; Pediatric nephroblastoma; Invitrogen GateWay cloning; Electrophoretic mobility shift assay; Self association; zinc fingers; cancer; tumour suppressor

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APA (6th Edition):

Ahokovi Tukia, R. K. T. (2011). Investigation of the Wilms' tumour suppressor protein (WT1) . (Masters Thesis). University of Otago. Retrieved from http://hdl.handle.net/10523/2029

Chicago Manual of Style (16th Edition):

Ahokovi Tukia, Richard Katavake Taka-I-Utukakai. “Investigation of the Wilms' tumour suppressor protein (WT1) .” 2011. Masters Thesis, University of Otago. Accessed January 21, 2018. http://hdl.handle.net/10523/2029.

MLA Handbook (7th Edition):

Ahokovi Tukia, Richard Katavake Taka-I-Utukakai. “Investigation of the Wilms' tumour suppressor protein (WT1) .” 2011. Web. 21 Jan 2018.

Vancouver:

Ahokovi Tukia RKT. Investigation of the Wilms' tumour suppressor protein (WT1) . [Internet] [Masters thesis]. University of Otago; 2011. [cited 2018 Jan 21]. Available from: http://hdl.handle.net/10523/2029.

Council of Science Editors:

Ahokovi Tukia RKT. Investigation of the Wilms' tumour suppressor protein (WT1) . [Masters Thesis]. University of Otago; 2011. Available from: http://hdl.handle.net/10523/2029

22. Deveau, Laura M. Characterizing the Disorder in Tristetraprolin and its Contribution to Post-Transcriptional Gene Regulation: A Dissertation.

Degree: Biochemistry and Molecular Pharmacology, Biochemistry and Molecular Pharmacology, 2016, U of Massachusetts : Med

  RNA-binding proteins (RBPs) are important for a wide variety of biological processes involved in gene regulation. However, the structural and dynamic contributions to their… (more)

Subjects/Keywords: RNA-Binding Proteins; Tristetraprolin; Zinc Fingers; Messenger RNA; Post-Transcriptional Gene Regulation; Amino Acids, Peptides, and Proteins; Biochemistry; Biophysics; Molecular Biology; Structural Biology

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APA (6th Edition):

Deveau, L. M. (2016). Characterizing the Disorder in Tristetraprolin and its Contribution to Post-Transcriptional Gene Regulation: A Dissertation. (Doctoral Dissertation). U of Massachusetts : Med. Retrieved from http://escholarship.umassmed.edu/gsbs_diss/855

Chicago Manual of Style (16th Edition):

Deveau, Laura M. “Characterizing the Disorder in Tristetraprolin and its Contribution to Post-Transcriptional Gene Regulation: A Dissertation.” 2016. Doctoral Dissertation, U of Massachusetts : Med. Accessed January 21, 2018. http://escholarship.umassmed.edu/gsbs_diss/855.

MLA Handbook (7th Edition):

Deveau, Laura M. “Characterizing the Disorder in Tristetraprolin and its Contribution to Post-Transcriptional Gene Regulation: A Dissertation.” 2016. Web. 21 Jan 2018.

Vancouver:

Deveau LM. Characterizing the Disorder in Tristetraprolin and its Contribution to Post-Transcriptional Gene Regulation: A Dissertation. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 2016. [cited 2018 Jan 21]. Available from: http://escholarship.umassmed.edu/gsbs_diss/855.

Council of Science Editors:

Deveau LM. Characterizing the Disorder in Tristetraprolin and its Contribution to Post-Transcriptional Gene Regulation: A Dissertation. [Doctoral Dissertation]. U of Massachusetts : Med; 2016. Available from: http://escholarship.umassmed.edu/gsbs_diss/855

23. Mikles, David C. Physicochemical Insights Into the EGR1-DNA Interaction.

Degree: PhD, Biochemistry and Molecular Biology (Medicine), 2014, University of Miami

 Early growth response 1 (EGR1) transcription factor orchestrates a plethora of signaling cascades in response to a wide variety of stimuli such as growth factors… (more)

Subjects/Keywords: intracellular pH; protein–DNA thermodynamics; zinc fingers; salt tolerance; polyelectrolyte effect; single nucleotide polymorphisms

…is characterized by three tandem copies of C2H2-type zinc fingers. Intuitively, the DB… …extensively studied. It should be noted that creating synthetic zinc fingers that can recognize… …within the 9-bp GCGTGGGCG consensus motif (Figure 1-3b). The three zinc fingers… …three zinc fingers, the protein-DNA contacts are largely afforded by the α-helix, which fits… …domain is comprised of three tandem C2H2-type zinc fingers, designated herein ZF-I (green… 

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APA (6th Edition):

Mikles, D. C. (2014). Physicochemical Insights Into the EGR1-DNA Interaction. (Doctoral Dissertation). University of Miami. Retrieved from http://scholarlyrepository.miami.edu/oa_dissertations/1161

Chicago Manual of Style (16th Edition):

Mikles, David C. “Physicochemical Insights Into the EGR1-DNA Interaction.” 2014. Doctoral Dissertation, University of Miami. Accessed January 21, 2018. http://scholarlyrepository.miami.edu/oa_dissertations/1161.

MLA Handbook (7th Edition):

Mikles, David C. “Physicochemical Insights Into the EGR1-DNA Interaction.” 2014. Web. 21 Jan 2018.

Vancouver:

Mikles DC. Physicochemical Insights Into the EGR1-DNA Interaction. [Internet] [Doctoral dissertation]. University of Miami; 2014. [cited 2018 Jan 21]. Available from: http://scholarlyrepository.miami.edu/oa_dissertations/1161.

Council of Science Editors:

Mikles DC. Physicochemical Insights Into the EGR1-DNA Interaction. [Doctoral Dissertation]. University of Miami; 2014. Available from: http://scholarlyrepository.miami.edu/oa_dissertations/1161


University of Southern California

24. Franzman, Matthew A. Solution-phase synthesis of metal chalcogenide nanocrystals at low temperatures using dialkyl dichalcogenide precursors.

Degree: PhD, Chemistry, 2010, University of Southern California

 Solution-phase synthetic reactions have proven to be viable routes toward semiconductor metal chalcogenide nanocrystals; however, these reactions are often reliant upon high temperatures, designer single-source… (more)

Subjects/Keywords: semiconductor; nanocrystal; nanorods; synthesis; nanocrystal synthesis; nanocrystal growth; growth kinetics; dichalcogenide; peroxide; disulfide; diselenide; green chemistry; inorganic chemistry; indium oxide; In2O3; indium sulfide; In2S3; copper indium sulfide; CuInS2; CIS; tin sulfide; SnS; tin selenide; SnSe; zinc fingers; aurothiomalate; myochrysine; auranofin; gold drugs

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APA (6th Edition):

Franzman, M. A. (2010). Solution-phase synthesis of metal chalcogenide nanocrystals at low temperatures using dialkyl dichalcogenide precursors. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/291102/rec/5928

Chicago Manual of Style (16th Edition):

Franzman, Matthew A. “Solution-phase synthesis of metal chalcogenide nanocrystals at low temperatures using dialkyl dichalcogenide precursors.” 2010. Doctoral Dissertation, University of Southern California. Accessed January 21, 2018. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/291102/rec/5928.

MLA Handbook (7th Edition):

Franzman, Matthew A. “Solution-phase synthesis of metal chalcogenide nanocrystals at low temperatures using dialkyl dichalcogenide precursors.” 2010. Web. 21 Jan 2018.

Vancouver:

Franzman MA. Solution-phase synthesis of metal chalcogenide nanocrystals at low temperatures using dialkyl dichalcogenide precursors. [Internet] [Doctoral dissertation]. University of Southern California; 2010. [cited 2018 Jan 21]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/291102/rec/5928.

Council of Science Editors:

Franzman MA. Solution-phase synthesis of metal chalcogenide nanocrystals at low temperatures using dialkyl dichalcogenide precursors. [Doctoral Dissertation]. University of Southern California; 2010. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/291102/rec/5928


McGill University

25. Soontorngun, Nitnipa. Functional characterization of zinc cluster transcriptional regulators in Saccharomyces cerevisiae and Candida albicans.

Degree: PhD, Department of Biochemistry., 2008, McGill University

Zinc cluster proteins form a major class of fungal-specific transcriptional regulators in Saccharmyces cerevisiae. They are characterized by a well-conserved zinc cluster motif essential for… (more)

Subjects/Keywords: Drug Resistance, Fungal.; Azoles  – pharmacology.; Saccharomyces cerevisiae  – drug effects.; Saccharomyces cerevisiae Proteins  – metabolism.; Candida albicans  – drug effects.; Transcription Factors  – metabolism.; Zinc  – metabolism.; Zinc Fingers.

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APA (6th Edition):

Soontorngun, N. (2008). Functional characterization of zinc cluster transcriptional regulators in Saccharomyces cerevisiae and Candida albicans. (Doctoral Dissertation). McGill University. Retrieved from http://digitool.library.mcgill.ca/thesisfile114030.pdf

Chicago Manual of Style (16th Edition):

Soontorngun, Nitnipa. “Functional characterization of zinc cluster transcriptional regulators in Saccharomyces cerevisiae and Candida albicans.” 2008. Doctoral Dissertation, McGill University. Accessed January 21, 2018. http://digitool.library.mcgill.ca/thesisfile114030.pdf.

MLA Handbook (7th Edition):

Soontorngun, Nitnipa. “Functional characterization of zinc cluster transcriptional regulators in Saccharomyces cerevisiae and Candida albicans.” 2008. Web. 21 Jan 2018.

Vancouver:

Soontorngun N. Functional characterization of zinc cluster transcriptional regulators in Saccharomyces cerevisiae and Candida albicans. [Internet] [Doctoral dissertation]. McGill University; 2008. [cited 2018 Jan 21]. Available from: http://digitool.library.mcgill.ca/thesisfile114030.pdf.

Council of Science Editors:

Soontorngun N. Functional characterization of zinc cluster transcriptional regulators in Saccharomyces cerevisiae and Candida albicans. [Doctoral Dissertation]. McGill University; 2008. Available from: http://digitool.library.mcgill.ca/thesisfile114030.pdf

26. França, Marcela Moura. Análise dos genes GHRH e GL12 em pacientes com deficiência de hormônio do crescimento congênita.

Degree: PhD, Endocrinologia, 2012, University of São Paulo

 Introdução: Alterações em genes relacionados com a secreção de GH ou a organogênese hipofisária foram identificadas em pacientes com deficiência de hormônio do crescimento (DGH)… (more)

Subjects/Keywords: Dedos de zinco; Fatores de transcrição; GLI2 protein; GLI2 proteína; Growth hormone-releasing hormone/genetics; Growth hormone/deficiency; Growth hormone/genetics; Hipófise/embriologia; Hipopituitarismo/etiologia; Hormônio do crescimento/deficiência; Hormônio do crescimento/genética; Hormônio liberador de hormônio do crescimento/genética; Hypopituitarism/etiology; Neuroipófise/anormalidades; Pituitary gland posterior/abnormalities; Pituitary/embryology; Transcription factors; Zinc fingers

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

APA (6th Edition):

França, M. M. (2012). Análise dos genes GHRH e GL12 em pacientes com deficiência de hormônio do crescimento congênita. (Doctoral Dissertation). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/5/5135/tde-25042012-142522/ ;

Chicago Manual of Style (16th Edition):

França, Marcela Moura. “Análise dos genes GHRH e GL12 em pacientes com deficiência de hormônio do crescimento congênita.” 2012. Doctoral Dissertation, University of São Paulo. Accessed January 21, 2018. http://www.teses.usp.br/teses/disponiveis/5/5135/tde-25042012-142522/ ;.

MLA Handbook (7th Edition):

França, Marcela Moura. “Análise dos genes GHRH e GL12 em pacientes com deficiência de hormônio do crescimento congênita.” 2012. Web. 21 Jan 2018.

Vancouver:

França MM. Análise dos genes GHRH e GL12 em pacientes com deficiência de hormônio do crescimento congênita. [Internet] [Doctoral dissertation]. University of São Paulo; 2012. [cited 2018 Jan 21]. Available from: http://www.teses.usp.br/teses/disponiveis/5/5135/tde-25042012-142522/ ;.

Council of Science Editors:

França MM. Análise dos genes GHRH e GL12 em pacientes com deficiência de hormônio do crescimento congênita. [Doctoral Dissertation]. University of São Paulo; 2012. Available from: http://www.teses.usp.br/teses/disponiveis/5/5135/tde-25042012-142522/ ;

27. Zhou, Ying, 1977-. Studies of the metal binding properties and DNA recognition mode of the unusual zinc fingers in poly(ADP-ribose) Polymerase-1 and the investigation of its interaction with apoptosis inducing factor (AIF).

Degree: Cellular and Molecular Biology, 2009, University of Texas – Austin

 Poly(ADP-ribosyl)ation, a covalent modification of proteins catalyzed by poly(ADP-ribose) polymerases (PARPs), plays a crucial role in regulating DNA repair, DNA replication, and cell death. Poly(ADP-ribose)… (more)

Subjects/Keywords: DNA repair; Poly(ADP-ribosyl)ation; Poly(ADP-ribose) polymerases; Poly(ADP-ribose) Polymerase-1; Zinc fingers; PARP; DNA-binding protein; DNA-binding properties; Apoptosis

…45 Chapter 2 Spectroscopic Determination of Metal Binding to PARP-1 Zinc Fingers and… …108 Chapter 3 PARP Zinc Fingers are Differentially Required for Damage Recognition… …127 3.1 Design and construction of PARP-1 zinc fingers and their mutants… …127 3.2 Single zinc fingers play different roles in DNA binding .............128 3.3… …154 4.1 PARP-1 zinc fingers play different roles in DNA binding and damage sensing… 

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

APA (6th Edition):

Zhou, Ying, 1. (2009). Studies of the metal binding properties and DNA recognition mode of the unusual zinc fingers in poly(ADP-ribose) Polymerase-1 and the investigation of its interaction with apoptosis inducing factor (AIF). (Thesis). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/21906

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):

Zhou, Ying, 1977-. “Studies of the metal binding properties and DNA recognition mode of the unusual zinc fingers in poly(ADP-ribose) Polymerase-1 and the investigation of its interaction with apoptosis inducing factor (AIF).” 2009. Thesis, University of Texas – Austin. Accessed January 21, 2018. http://hdl.handle.net/2152/21906.

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

MLA Handbook (7th Edition):

Zhou, Ying, 1977-. “Studies of the metal binding properties and DNA recognition mode of the unusual zinc fingers in poly(ADP-ribose) Polymerase-1 and the investigation of its interaction with apoptosis inducing factor (AIF).” 2009. Web. 21 Jan 2018.

Vancouver:

Zhou, Ying 1. Studies of the metal binding properties and DNA recognition mode of the unusual zinc fingers in poly(ADP-ribose) Polymerase-1 and the investigation of its interaction with apoptosis inducing factor (AIF). [Internet] [Thesis]. University of Texas – Austin; 2009. [cited 2018 Jan 21]. Available from: http://hdl.handle.net/2152/21906.

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

Council of Science Editors:

Zhou, Ying 1. Studies of the metal binding properties and DNA recognition mode of the unusual zinc fingers in poly(ADP-ribose) Polymerase-1 and the investigation of its interaction with apoptosis inducing factor (AIF). [Thesis]. University of Texas – Austin; 2009. Available from: http://hdl.handle.net/2152/21906

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

.