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You searched for subject:(mutagenesis). Showing records 1 – 30 of 841 total matches.

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University of Rochester

1. Coles, Garry L. KIF7 and Microtubule Dynamics Function to Regulate Cellular Proliferation and Cell Cycle Progression.

Degree: PhD, 2015, University of Rochester

 Respiratory diseases such as lung cancer, COPD, and asthma are the second leading cause of death in the United States. These diseases are heterogeneous and… (more)

Subjects/Keywords: ENU mutagenesis

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APA (6th Edition):

Coles, G. L. (2015). KIF7 and Microtubule Dynamics Function to Regulate Cellular Proliferation and Cell Cycle Progression. (Doctoral Dissertation). University of Rochester. Retrieved from http://hdl.handle.net/1802/30258

Chicago Manual of Style (16th Edition):

Coles, Garry L. “KIF7 and Microtubule Dynamics Function to Regulate Cellular Proliferation and Cell Cycle Progression.” 2015. Doctoral Dissertation, University of Rochester. Accessed September 22, 2020. http://hdl.handle.net/1802/30258.

MLA Handbook (7th Edition):

Coles, Garry L. “KIF7 and Microtubule Dynamics Function to Regulate Cellular Proliferation and Cell Cycle Progression.” 2015. Web. 22 Sep 2020.

Vancouver:

Coles GL. KIF7 and Microtubule Dynamics Function to Regulate Cellular Proliferation and Cell Cycle Progression. [Internet] [Doctoral dissertation]. University of Rochester; 2015. [cited 2020 Sep 22]. Available from: http://hdl.handle.net/1802/30258.

Council of Science Editors:

Coles GL. KIF7 and Microtubule Dynamics Function to Regulate Cellular Proliferation and Cell Cycle Progression. [Doctoral Dissertation]. University of Rochester; 2015. Available from: http://hdl.handle.net/1802/30258

2. Chrabaszcz, Elodie. Comment la proximité des lésions module les voies de tolérance des dommages de l'ADN in vivo : How the proximity of lesions modulates the DNA damage tolerance pathways in vivo.

Degree: Docteur es, Biologie. Génétique, 2017, Aix Marseille Université

Le génome de tous les organismes vivants est constamment menacé par de nombreux agents qui causent des dommages à l'ADN. Lorsque la fourche de réplication… (more)

Subjects/Keywords: Mutagenèse; Mutagenesis

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APA (6th Edition):

Chrabaszcz, E. (2017). Comment la proximité des lésions module les voies de tolérance des dommages de l'ADN in vivo : How the proximity of lesions modulates the DNA damage tolerance pathways in vivo. (Doctoral Dissertation). Aix Marseille Université. Retrieved from http://www.theses.fr/2017AIXM0661

Chicago Manual of Style (16th Edition):

Chrabaszcz, Elodie. “Comment la proximité des lésions module les voies de tolérance des dommages de l'ADN in vivo : How the proximity of lesions modulates the DNA damage tolerance pathways in vivo.” 2017. Doctoral Dissertation, Aix Marseille Université. Accessed September 22, 2020. http://www.theses.fr/2017AIXM0661.

MLA Handbook (7th Edition):

Chrabaszcz, Elodie. “Comment la proximité des lésions module les voies de tolérance des dommages de l'ADN in vivo : How the proximity of lesions modulates the DNA damage tolerance pathways in vivo.” 2017. Web. 22 Sep 2020.

Vancouver:

Chrabaszcz E. Comment la proximité des lésions module les voies de tolérance des dommages de l'ADN in vivo : How the proximity of lesions modulates the DNA damage tolerance pathways in vivo. [Internet] [Doctoral dissertation]. Aix Marseille Université 2017. [cited 2020 Sep 22]. Available from: http://www.theses.fr/2017AIXM0661.

Council of Science Editors:

Chrabaszcz E. Comment la proximité des lésions module les voies de tolérance des dommages de l'ADN in vivo : How the proximity of lesions modulates the DNA damage tolerance pathways in vivo. [Doctoral Dissertation]. Aix Marseille Université 2017. Available from: http://www.theses.fr/2017AIXM0661


Oregon State University

3. Lundquist, Amy J. Mechanism of action of Escherichia coli uracil-DNA glycosylase and interaction with the bacteriophage PBS-2 uracil-DNA glycosylase inhibitor protein.

Degree: PhD, Biochemistry and Biophysics, 1999, Oregon State University

Subjects/Keywords: Mutagenesis

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APA (6th Edition):

Lundquist, A. J. (1999). Mechanism of action of Escherichia coli uracil-DNA glycosylase and interaction with the bacteriophage PBS-2 uracil-DNA glycosylase inhibitor protein. (Doctoral Dissertation). Oregon State University. Retrieved from http://hdl.handle.net/1957/33247

Chicago Manual of Style (16th Edition):

Lundquist, Amy J. “Mechanism of action of Escherichia coli uracil-DNA glycosylase and interaction with the bacteriophage PBS-2 uracil-DNA glycosylase inhibitor protein.” 1999. Doctoral Dissertation, Oregon State University. Accessed September 22, 2020. http://hdl.handle.net/1957/33247.

MLA Handbook (7th Edition):

Lundquist, Amy J. “Mechanism of action of Escherichia coli uracil-DNA glycosylase and interaction with the bacteriophage PBS-2 uracil-DNA glycosylase inhibitor protein.” 1999. Web. 22 Sep 2020.

Vancouver:

Lundquist AJ. Mechanism of action of Escherichia coli uracil-DNA glycosylase and interaction with the bacteriophage PBS-2 uracil-DNA glycosylase inhibitor protein. [Internet] [Doctoral dissertation]. Oregon State University; 1999. [cited 2020 Sep 22]. Available from: http://hdl.handle.net/1957/33247.

Council of Science Editors:

Lundquist AJ. Mechanism of action of Escherichia coli uracil-DNA glycosylase and interaction with the bacteriophage PBS-2 uracil-DNA glycosylase inhibitor protein. [Doctoral Dissertation]. Oregon State University; 1999. Available from: http://hdl.handle.net/1957/33247


Oregon State University

4. Zhang, Xiaolin. Mutagenic mechanisms associated with DNA cytosine methylation, DNA base sequence context and DNA precursor pool asymmetry.

Degree: PhD, Genetics, 1995, Oregon State University

Subjects/Keywords: Mutagenesis

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APA (6th Edition):

Zhang, X. (1995). Mutagenic mechanisms associated with DNA cytosine methylation, DNA base sequence context and DNA precursor pool asymmetry. (Doctoral Dissertation). Oregon State University. Retrieved from http://hdl.handle.net/1957/35148

Chicago Manual of Style (16th Edition):

Zhang, Xiaolin. “Mutagenic mechanisms associated with DNA cytosine methylation, DNA base sequence context and DNA precursor pool asymmetry.” 1995. Doctoral Dissertation, Oregon State University. Accessed September 22, 2020. http://hdl.handle.net/1957/35148.

MLA Handbook (7th Edition):

Zhang, Xiaolin. “Mutagenic mechanisms associated with DNA cytosine methylation, DNA base sequence context and DNA precursor pool asymmetry.” 1995. Web. 22 Sep 2020.

Vancouver:

Zhang X. Mutagenic mechanisms associated with DNA cytosine methylation, DNA base sequence context and DNA precursor pool asymmetry. [Internet] [Doctoral dissertation]. Oregon State University; 1995. [cited 2020 Sep 22]. Available from: http://hdl.handle.net/1957/35148.

Council of Science Editors:

Zhang X. Mutagenic mechanisms associated with DNA cytosine methylation, DNA base sequence context and DNA precursor pool asymmetry. [Doctoral Dissertation]. Oregon State University; 1995. Available from: http://hdl.handle.net/1957/35148


University of Ottawa

5. Styles, George. Redesigning Nature: Developing a More Potent BMP2 Molecule for Expression in a Transgenic Puroindoline-Rice Expression System .

Degree: 2016, University of Ottawa

 Bone Morphogenetic Protein 2 (BMP2) is a cytokine growth factor that elicits de novo bone formation in adult mammals. The use of BMP2 in surgical… (more)

Subjects/Keywords: Mutagenesis; Growth Factor

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APA (6th Edition):

Styles, G. (2016). Redesigning Nature: Developing a More Potent BMP2 Molecule for Expression in a Transgenic Puroindoline-Rice Expression System . (Thesis). University of Ottawa. Retrieved from http://hdl.handle.net/10393/34177

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):

Styles, George. “Redesigning Nature: Developing a More Potent BMP2 Molecule for Expression in a Transgenic Puroindoline-Rice Expression System .” 2016. Thesis, University of Ottawa. Accessed September 22, 2020. http://hdl.handle.net/10393/34177.

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

MLA Handbook (7th Edition):

Styles, George. “Redesigning Nature: Developing a More Potent BMP2 Molecule for Expression in a Transgenic Puroindoline-Rice Expression System .” 2016. Web. 22 Sep 2020.

Vancouver:

Styles G. Redesigning Nature: Developing a More Potent BMP2 Molecule for Expression in a Transgenic Puroindoline-Rice Expression System . [Internet] [Thesis]. University of Ottawa; 2016. [cited 2020 Sep 22]. Available from: http://hdl.handle.net/10393/34177.

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

Council of Science Editors:

Styles G. Redesigning Nature: Developing a More Potent BMP2 Molecule for Expression in a Transgenic Puroindoline-Rice Expression System . [Thesis]. University of Ottawa; 2016. Available from: http://hdl.handle.net/10393/34177

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


Tulane University

6. Hodel, Karl. Investigation of human DNA polymerase epsilon mutants in cancer: Mutagenic capacity, mutation spectrum & influence of mismatch repair correction.

Degree: 2018, Tulane University

[email protected]

The bulk of nuclear DNA synthesis during replication of the eukaryotic genome is carried out by three DNA Polymerases (Pols): Pols α, δ and… (more)

Subjects/Keywords: Polymerase; mutagenesis; Cancer

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APA (6th Edition):

Hodel, K. (2018). Investigation of human DNA polymerase epsilon mutants in cancer: Mutagenic capacity, mutation spectrum & influence of mismatch repair correction. (Thesis). Tulane University. Retrieved from https://digitallibrary.tulane.edu/islandora/object/tulane:110739

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):

Hodel, Karl. “Investigation of human DNA polymerase epsilon mutants in cancer: Mutagenic capacity, mutation spectrum & influence of mismatch repair correction.” 2018. Thesis, Tulane University. Accessed September 22, 2020. https://digitallibrary.tulane.edu/islandora/object/tulane:110739.

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

MLA Handbook (7th Edition):

Hodel, Karl. “Investigation of human DNA polymerase epsilon mutants in cancer: Mutagenic capacity, mutation spectrum & influence of mismatch repair correction.” 2018. Web. 22 Sep 2020.

Vancouver:

Hodel K. Investigation of human DNA polymerase epsilon mutants in cancer: Mutagenic capacity, mutation spectrum & influence of mismatch repair correction. [Internet] [Thesis]. Tulane University; 2018. [cited 2020 Sep 22]. Available from: https://digitallibrary.tulane.edu/islandora/object/tulane:110739.

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

Council of Science Editors:

Hodel K. Investigation of human DNA polymerase epsilon mutants in cancer: Mutagenic capacity, mutation spectrum & influence of mismatch repair correction. [Thesis]. Tulane University; 2018. Available from: https://digitallibrary.tulane.edu/islandora/object/tulane:110739

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


University of Melbourne

7. Brown, Fiona Claire. Analysis of erythropoiesis through ENU mutagenesis.

Degree: 2013, University of Melbourne

 Abnormalities in erythrocytes, the cells essential for normal respiratory exchange throughout the body, are amongst the most common disorders worldwide. The regulation of erythropoiesis is… (more)

Subjects/Keywords: ENU mutagenesis; erythropoiesis

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APA (6th Edition):

Brown, F. C. (2013). Analysis of erythropoiesis through ENU mutagenesis. (Doctoral Dissertation). University of Melbourne. Retrieved from http://hdl.handle.net/11343/38178

Chicago Manual of Style (16th Edition):

Brown, Fiona Claire. “Analysis of erythropoiesis through ENU mutagenesis.” 2013. Doctoral Dissertation, University of Melbourne. Accessed September 22, 2020. http://hdl.handle.net/11343/38178.

MLA Handbook (7th Edition):

Brown, Fiona Claire. “Analysis of erythropoiesis through ENU mutagenesis.” 2013. Web. 22 Sep 2020.

Vancouver:

Brown FC. Analysis of erythropoiesis through ENU mutagenesis. [Internet] [Doctoral dissertation]. University of Melbourne; 2013. [cited 2020 Sep 22]. Available from: http://hdl.handle.net/11343/38178.

Council of Science Editors:

Brown FC. Analysis of erythropoiesis through ENU mutagenesis. [Doctoral Dissertation]. University of Melbourne; 2013. Available from: http://hdl.handle.net/11343/38178


Cornell University

8. Wang, Gaoyan. Purification, Characterization, Site-Directed Mutagenesis And Mode Of Action Studies Of The Bacillus Bacteriocin Thurincin H.

Degree: PhD, Food Science and Technology, 2014, Cornell University

 Bacteriocins are ribosomally synthesized antimicrobial peptides or proteins produced by bacteria, which usually inhibit the growth of closely related species. Bacteriocins produced by Bacillus species… (more)

Subjects/Keywords: Bacteriocin; Mutagenesis; mode of action

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APA (6th Edition):

Wang, G. (2014). Purification, Characterization, Site-Directed Mutagenesis And Mode Of Action Studies Of The Bacillus Bacteriocin Thurincin H. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/36078

Chicago Manual of Style (16th Edition):

Wang, Gaoyan. “Purification, Characterization, Site-Directed Mutagenesis And Mode Of Action Studies Of The Bacillus Bacteriocin Thurincin H.” 2014. Doctoral Dissertation, Cornell University. Accessed September 22, 2020. http://hdl.handle.net/1813/36078.

MLA Handbook (7th Edition):

Wang, Gaoyan. “Purification, Characterization, Site-Directed Mutagenesis And Mode Of Action Studies Of The Bacillus Bacteriocin Thurincin H.” 2014. Web. 22 Sep 2020.

Vancouver:

Wang G. Purification, Characterization, Site-Directed Mutagenesis And Mode Of Action Studies Of The Bacillus Bacteriocin Thurincin H. [Internet] [Doctoral dissertation]. Cornell University; 2014. [cited 2020 Sep 22]. Available from: http://hdl.handle.net/1813/36078.

Council of Science Editors:

Wang G. Purification, Characterization, Site-Directed Mutagenesis And Mode Of Action Studies Of The Bacillus Bacteriocin Thurincin H. [Doctoral Dissertation]. Cornell University; 2014. Available from: http://hdl.handle.net/1813/36078

9. Muricken, Deepa G. Cloning, expression and site-directed mutagenesis of the bowman-birk inhibitor of horsegram (dolichos biflorus); -.

Degree: Biochemistry, 2011, University of Mysore

Bowman Birk inhibitors (BBI) are small protease inhibitors found in the seeds of legumes in particular. Their molecular masses are in the range of 6-… (more)

Subjects/Keywords: biochemistry; horsegram; dolichos biflorus; mutagenesis

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APA (6th Edition):

Muricken, D. G. (2011). Cloning, expression and site-directed mutagenesis of the bowman-birk inhibitor of horsegram (dolichos biflorus); -. (Thesis). University of Mysore. Retrieved from http://shodhganga.inflibnet.ac.in/handle/10603/11032

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):

Muricken, Deepa G. “Cloning, expression and site-directed mutagenesis of the bowman-birk inhibitor of horsegram (dolichos biflorus); -.” 2011. Thesis, University of Mysore. Accessed September 22, 2020. http://shodhganga.inflibnet.ac.in/handle/10603/11032.

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

MLA Handbook (7th Edition):

Muricken, Deepa G. “Cloning, expression and site-directed mutagenesis of the bowman-birk inhibitor of horsegram (dolichos biflorus); -.” 2011. Web. 22 Sep 2020.

Vancouver:

Muricken DG. Cloning, expression and site-directed mutagenesis of the bowman-birk inhibitor of horsegram (dolichos biflorus); -. [Internet] [Thesis]. University of Mysore; 2011. [cited 2020 Sep 22]. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/11032.

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

Council of Science Editors:

Muricken DG. Cloning, expression and site-directed mutagenesis of the bowman-birk inhibitor of horsegram (dolichos biflorus); -. [Thesis]. University of Mysore; 2011. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/11032

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


Texas Tech University

10. Mishra, Deepika. Improvement of cotton fiber quality with chemical mutagenesis.

Degree: PhD, Plant and Soil Science, 2016, Texas Tech University

 Cotton (Gossypium hirsutum L.) is world’s most important natural fiber crop. For the U.S. cotton industry to compete in international markets, we need to develop… (more)

Subjects/Keywords: Fiber quality chemical mutagenesis

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APA (6th Edition):

Mishra, D. (2016). Improvement of cotton fiber quality with chemical mutagenesis. (Doctoral Dissertation). Texas Tech University. Retrieved from http://hdl.handle.net/2346/72296

Chicago Manual of Style (16th Edition):

Mishra, Deepika. “Improvement of cotton fiber quality with chemical mutagenesis.” 2016. Doctoral Dissertation, Texas Tech University. Accessed September 22, 2020. http://hdl.handle.net/2346/72296.

MLA Handbook (7th Edition):

Mishra, Deepika. “Improvement of cotton fiber quality with chemical mutagenesis.” 2016. Web. 22 Sep 2020.

Vancouver:

Mishra D. Improvement of cotton fiber quality with chemical mutagenesis. [Internet] [Doctoral dissertation]. Texas Tech University; 2016. [cited 2020 Sep 22]. Available from: http://hdl.handle.net/2346/72296.

Council of Science Editors:

Mishra D. Improvement of cotton fiber quality with chemical mutagenesis. [Doctoral Dissertation]. Texas Tech University; 2016. Available from: http://hdl.handle.net/2346/72296


Texas Tech University

11. -4621-5627. Characterization, mutagenesis and mechanistic analysis of the sterol C24-methyltransferase: Implications for understanding active site requirements for sterol biosynthesis.

Degree: PhD, Chemistry, 2016, Texas Tech University

 Previous studies that have defined regions of the sterol C24-methyltransferase (SMT) primary structure involved with catalysis failed to show the full identity of essential amino… (more)

Subjects/Keywords: sterol; methyltransferase; mutagenesis; inhibitor

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APA (6th Edition):

-4621-5627. (2016). Characterization, mutagenesis and mechanistic analysis of the sterol C24-methyltransferase: Implications for understanding active site requirements for sterol biosynthesis. (Doctoral Dissertation). Texas Tech University. Retrieved from http://hdl.handle.net/2346/72372

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

Chicago Manual of Style (16th Edition):

-4621-5627. “Characterization, mutagenesis and mechanistic analysis of the sterol C24-methyltransferase: Implications for understanding active site requirements for sterol biosynthesis.” 2016. Doctoral Dissertation, Texas Tech University. Accessed September 22, 2020. http://hdl.handle.net/2346/72372.

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

MLA Handbook (7th Edition):

-4621-5627. “Characterization, mutagenesis and mechanistic analysis of the sterol C24-methyltransferase: Implications for understanding active site requirements for sterol biosynthesis.” 2016. Web. 22 Sep 2020.

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

Vancouver:

-4621-5627. Characterization, mutagenesis and mechanistic analysis of the sterol C24-methyltransferase: Implications for understanding active site requirements for sterol biosynthesis. [Internet] [Doctoral dissertation]. Texas Tech University; 2016. [cited 2020 Sep 22]. Available from: http://hdl.handle.net/2346/72372.

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

Council of Science Editors:

-4621-5627. Characterization, mutagenesis and mechanistic analysis of the sterol C24-methyltransferase: Implications for understanding active site requirements for sterol biosynthesis. [Doctoral Dissertation]. Texas Tech University; 2016. Available from: http://hdl.handle.net/2346/72372

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


University of Glasgow

12. Laverty, Hugh Gerard. Isolation and characterisation of a locus disrupted in a transgenic mouse mutant exhibiting sex-linked cleft palate.

Degree: PhD, 1995, University of Glasgow

 A unique transgenic mouse line displayed the phenotype of sex-linked cleft palate. As no other mouse line expressing this transgene demonstrated a similar phenotype, it… (more)

Subjects/Keywords: 572.8; Mutagenesis

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APA (6th Edition):

Laverty, H. G. (1995). Isolation and characterisation of a locus disrupted in a transgenic mouse mutant exhibiting sex-linked cleft palate. (Doctoral Dissertation). University of Glasgow. Retrieved from http://theses.gla.ac.uk/71681/ ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.296959

Chicago Manual of Style (16th Edition):

Laverty, Hugh Gerard. “Isolation and characterisation of a locus disrupted in a transgenic mouse mutant exhibiting sex-linked cleft palate.” 1995. Doctoral Dissertation, University of Glasgow. Accessed September 22, 2020. http://theses.gla.ac.uk/71681/ ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.296959.

MLA Handbook (7th Edition):

Laverty, Hugh Gerard. “Isolation and characterisation of a locus disrupted in a transgenic mouse mutant exhibiting sex-linked cleft palate.” 1995. Web. 22 Sep 2020.

Vancouver:

Laverty HG. Isolation and characterisation of a locus disrupted in a transgenic mouse mutant exhibiting sex-linked cleft palate. [Internet] [Doctoral dissertation]. University of Glasgow; 1995. [cited 2020 Sep 22]. Available from: http://theses.gla.ac.uk/71681/ ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.296959.

Council of Science Editors:

Laverty HG. Isolation and characterisation of a locus disrupted in a transgenic mouse mutant exhibiting sex-linked cleft palate. [Doctoral Dissertation]. University of Glasgow; 1995. Available from: http://theses.gla.ac.uk/71681/ ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.296959


University of Glasgow

13. Arnold, Patricia Hazel. Mutants of Tn3 resolvase.

Degree: PhD, 1997, University of Glasgow

 Prior to this work, no mutants of Tn3 resolvase had been isolated. To construct a variety of mutants, a suitable plasmid for mutagenesis purposes was… (more)

Subjects/Keywords: 572.8; Mutagenesis

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APA (6th Edition):

Arnold, P. H. (1997). Mutants of Tn3 resolvase. (Doctoral Dissertation). University of Glasgow. Retrieved from http://theses.gla.ac.uk/74844/ ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.363154

Chicago Manual of Style (16th Edition):

Arnold, Patricia Hazel. “Mutants of Tn3 resolvase.” 1997. Doctoral Dissertation, University of Glasgow. Accessed September 22, 2020. http://theses.gla.ac.uk/74844/ ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.363154.

MLA Handbook (7th Edition):

Arnold, Patricia Hazel. “Mutants of Tn3 resolvase.” 1997. Web. 22 Sep 2020.

Vancouver:

Arnold PH. Mutants of Tn3 resolvase. [Internet] [Doctoral dissertation]. University of Glasgow; 1997. [cited 2020 Sep 22]. Available from: http://theses.gla.ac.uk/74844/ ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.363154.

Council of Science Editors:

Arnold PH. Mutants of Tn3 resolvase. [Doctoral Dissertation]. University of Glasgow; 1997. Available from: http://theses.gla.ac.uk/74844/ ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.363154


University of Miami

14. Nichols, Andrew S. Subunit Contributions to the Structure and Function of Insect Olfactory Receptors.

Degree: PhD, Molecular and Cellular Pharmacology (Medicine), 2010, University of Miami

  Insects detect specific chemicals in the environment with olfactory receptors (ORs), which represent a novel class of ligand-gated ion channel. Insect ORs are comprised… (more)

Subjects/Keywords: Electrophysiology; Xenopus; Receptor; Mutagenesis; Orco

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APA (6th Edition):

Nichols, A. S. (2010). Subunit Contributions to the Structure and Function of Insect Olfactory Receptors. (Doctoral Dissertation). University of Miami. Retrieved from https://scholarlyrepository.miami.edu/oa_dissertations/361

Chicago Manual of Style (16th Edition):

Nichols, Andrew S. “Subunit Contributions to the Structure and Function of Insect Olfactory Receptors.” 2010. Doctoral Dissertation, University of Miami. Accessed September 22, 2020. https://scholarlyrepository.miami.edu/oa_dissertations/361.

MLA Handbook (7th Edition):

Nichols, Andrew S. “Subunit Contributions to the Structure and Function of Insect Olfactory Receptors.” 2010. Web. 22 Sep 2020.

Vancouver:

Nichols AS. Subunit Contributions to the Structure and Function of Insect Olfactory Receptors. [Internet] [Doctoral dissertation]. University of Miami; 2010. [cited 2020 Sep 22]. Available from: https://scholarlyrepository.miami.edu/oa_dissertations/361.

Council of Science Editors:

Nichols AS. Subunit Contributions to the Structure and Function of Insect Olfactory Receptors. [Doctoral Dissertation]. University of Miami; 2010. Available from: https://scholarlyrepository.miami.edu/oa_dissertations/361


East Carolina University

15. Kuyateh, Abu-Bakarr. THE DEVELOPMENT OF BETA-ACTIN MUTANTS WITH ALTERED BINDING AFFINITES FOR ATP AND ADP.

Degree: MS, MS-Chemistry, 2018, East Carolina University

 A number of neurodegenerative diseases are accompanied by the formation of cofilin-actin rods in neural cells. These rods can cause synaptic dysfunction and block transport… (more)

Subjects/Keywords: Optogenetics; Mutagenesis; Microfilament proteins

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APA (6th Edition):

Kuyateh, A. (2018). THE DEVELOPMENT OF BETA-ACTIN MUTANTS WITH ALTERED BINDING AFFINITES FOR ATP AND ADP. (Masters Thesis). East Carolina University. Retrieved from http://hdl.handle.net/10342/7027

Chicago Manual of Style (16th Edition):

Kuyateh, Abu-Bakarr. “THE DEVELOPMENT OF BETA-ACTIN MUTANTS WITH ALTERED BINDING AFFINITES FOR ATP AND ADP.” 2018. Masters Thesis, East Carolina University. Accessed September 22, 2020. http://hdl.handle.net/10342/7027.

MLA Handbook (7th Edition):

Kuyateh, Abu-Bakarr. “THE DEVELOPMENT OF BETA-ACTIN MUTANTS WITH ALTERED BINDING AFFINITES FOR ATP AND ADP.” 2018. Web. 22 Sep 2020.

Vancouver:

Kuyateh A. THE DEVELOPMENT OF BETA-ACTIN MUTANTS WITH ALTERED BINDING AFFINITES FOR ATP AND ADP. [Internet] [Masters thesis]. East Carolina University; 2018. [cited 2020 Sep 22]. Available from: http://hdl.handle.net/10342/7027.

Council of Science Editors:

Kuyateh A. THE DEVELOPMENT OF BETA-ACTIN MUTANTS WITH ALTERED BINDING AFFINITES FOR ATP AND ADP. [Masters Thesis]. East Carolina University; 2018. Available from: http://hdl.handle.net/10342/7027


University of Victoria

16. Yang, Haiyan. Mutagenesis and antimutagenesis in Big Blue ® lacI transgenic rats.

Degree: Department of Biology, 2018, University of Victoria

 The initiation of the cancer process is associated with mutations. Analysis of environmental exposure to chemical or physical agents causing these genetic alterations is of… (more)

Subjects/Keywords: Mutagenesis; Cancer; Genetic aspects

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APA (6th Edition):

Yang, H. (2018). Mutagenesis and antimutagenesis in Big Blue ® lacI transgenic rats. (Thesis). University of Victoria. Retrieved from https://dspace.library.uvic.ca//handle/1828/10175

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):

Yang, Haiyan. “Mutagenesis and antimutagenesis in Big Blue ® lacI transgenic rats.” 2018. Thesis, University of Victoria. Accessed September 22, 2020. https://dspace.library.uvic.ca//handle/1828/10175.

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

MLA Handbook (7th Edition):

Yang, Haiyan. “Mutagenesis and antimutagenesis in Big Blue ® lacI transgenic rats.” 2018. Web. 22 Sep 2020.

Vancouver:

Yang H. Mutagenesis and antimutagenesis in Big Blue ® lacI transgenic rats. [Internet] [Thesis]. University of Victoria; 2018. [cited 2020 Sep 22]. Available from: https://dspace.library.uvic.ca//handle/1828/10175.

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

Council of Science Editors:

Yang H. Mutagenesis and antimutagenesis in Big Blue ® lacI transgenic rats. [Thesis]. University of Victoria; 2018. Available from: https://dspace.library.uvic.ca//handle/1828/10175

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


University of New South Wales

17. Murray, Jayne. Suppression of neuroblastoma tumorigenesis using ENU mutagenesis in the Th-MYCN mouse model of neuroblastoma.

Degree: Women's & Children's Health, 2017, University of New South Wales

 Neuroblastoma, a disease of the neural crest and the most common solid tumour of infancy, accounts for 7-10% of all childhood cancer. The disease arises… (more)

Subjects/Keywords: Runx1t1; Neuroblastoma; ENU mutagenesis

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APA (6th Edition):

Murray, J. (2017). Suppression of neuroblastoma tumorigenesis using ENU mutagenesis in the Th-MYCN mouse model of neuroblastoma. (Doctoral Dissertation). University of New South Wales. Retrieved from http://handle.unsw.edu.au/1959.4/60088 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:51377/SOURCE02?view=true

Chicago Manual of Style (16th Edition):

Murray, Jayne. “Suppression of neuroblastoma tumorigenesis using ENU mutagenesis in the Th-MYCN mouse model of neuroblastoma.” 2017. Doctoral Dissertation, University of New South Wales. Accessed September 22, 2020. http://handle.unsw.edu.au/1959.4/60088 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:51377/SOURCE02?view=true.

MLA Handbook (7th Edition):

Murray, Jayne. “Suppression of neuroblastoma tumorigenesis using ENU mutagenesis in the Th-MYCN mouse model of neuroblastoma.” 2017. Web. 22 Sep 2020.

Vancouver:

Murray J. Suppression of neuroblastoma tumorigenesis using ENU mutagenesis in the Th-MYCN mouse model of neuroblastoma. [Internet] [Doctoral dissertation]. University of New South Wales; 2017. [cited 2020 Sep 22]. Available from: http://handle.unsw.edu.au/1959.4/60088 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:51377/SOURCE02?view=true.

Council of Science Editors:

Murray J. Suppression of neuroblastoma tumorigenesis using ENU mutagenesis in the Th-MYCN mouse model of neuroblastoma. [Doctoral Dissertation]. University of New South Wales; 2017. Available from: http://handle.unsw.edu.au/1959.4/60088 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:51377/SOURCE02?view=true


University of Minnesota

18. Starrett, Gabriel. Overlapping functions of APOBEC enzymes in antiviral immunity and cancer.

Degree: PhD, Microbiology, Immunology and Cancer Biology, 2017, University of Minnesota

 APOBEC enzymes are a family of innate antiviral enzymes that form an important barrier against DNA-based pathogens. Encoding and expressing these DNA mutating enzymes, however,… (more)

Subjects/Keywords: APOBEC; Cancer; mutagenesis; viruses

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APA (6th Edition):

Starrett, G. (2017). Overlapping functions of APOBEC enzymes in antiviral immunity and cancer. (Doctoral Dissertation). University of Minnesota. Retrieved from http://hdl.handle.net/11299/191441

Chicago Manual of Style (16th Edition):

Starrett, Gabriel. “Overlapping functions of APOBEC enzymes in antiviral immunity and cancer.” 2017. Doctoral Dissertation, University of Minnesota. Accessed September 22, 2020. http://hdl.handle.net/11299/191441.

MLA Handbook (7th Edition):

Starrett, Gabriel. “Overlapping functions of APOBEC enzymes in antiviral immunity and cancer.” 2017. Web. 22 Sep 2020.

Vancouver:

Starrett G. Overlapping functions of APOBEC enzymes in antiviral immunity and cancer. [Internet] [Doctoral dissertation]. University of Minnesota; 2017. [cited 2020 Sep 22]. Available from: http://hdl.handle.net/11299/191441.

Council of Science Editors:

Starrett G. Overlapping functions of APOBEC enzymes in antiviral immunity and cancer. [Doctoral Dissertation]. University of Minnesota; 2017. Available from: http://hdl.handle.net/11299/191441


University of Louisville

19. Stallons, Lindsey Jay, 1983-. DNA polymerase iota promotes G2/M checkpoint activation and genetic stability after UV-induced DNA damage.

Degree: PhD, 2011, University of Louisville

 Unrepaired DNA damage poses a serious threat to the genetic stability of a replicating cell. One mechanism of tolerating this damage is translesion DNA synthesis… (more)

Subjects/Keywords: Mutagenesis; Cell cycle; Polymerase iota

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APA (6th Edition):

Stallons, Lindsey Jay, 1. (2011). DNA polymerase iota promotes G2/M checkpoint activation and genetic stability after UV-induced DNA damage. (Doctoral Dissertation). University of Louisville. Retrieved from 10.18297/etd/1369 ; https://ir.library.louisville.edu/etd/1369

Chicago Manual of Style (16th Edition):

Stallons, Lindsey Jay, 1983-. “DNA polymerase iota promotes G2/M checkpoint activation and genetic stability after UV-induced DNA damage.” 2011. Doctoral Dissertation, University of Louisville. Accessed September 22, 2020. 10.18297/etd/1369 ; https://ir.library.louisville.edu/etd/1369.

MLA Handbook (7th Edition):

Stallons, Lindsey Jay, 1983-. “DNA polymerase iota promotes G2/M checkpoint activation and genetic stability after UV-induced DNA damage.” 2011. Web. 22 Sep 2020.

Vancouver:

Stallons, Lindsey Jay 1. DNA polymerase iota promotes G2/M checkpoint activation and genetic stability after UV-induced DNA damage. [Internet] [Doctoral dissertation]. University of Louisville; 2011. [cited 2020 Sep 22]. Available from: 10.18297/etd/1369 ; https://ir.library.louisville.edu/etd/1369.

Council of Science Editors:

Stallons, Lindsey Jay 1. DNA polymerase iota promotes G2/M checkpoint activation and genetic stability after UV-induced DNA damage. [Doctoral Dissertation]. University of Louisville; 2011. Available from: 10.18297/etd/1369 ; https://ir.library.louisville.edu/etd/1369


Kansas State University

20. Kotek, Joseph John. Mutagenesis of human lymphoblast cells.

Degree: 1976, Kansas State University

Subjects/Keywords: Mutagenesis; Cytogenetics

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APA (6th Edition):

Kotek, J. J. (1976). Mutagenesis of human lymphoblast cells. (Thesis). Kansas State University. Retrieved from http://hdl.handle.net/2097/11381

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):

Kotek, Joseph John. “Mutagenesis of human lymphoblast cells.” 1976. Thesis, Kansas State University. Accessed September 22, 2020. http://hdl.handle.net/2097/11381.

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

MLA Handbook (7th Edition):

Kotek, Joseph John. “Mutagenesis of human lymphoblast cells.” 1976. Web. 22 Sep 2020.

Vancouver:

Kotek JJ. Mutagenesis of human lymphoblast cells. [Internet] [Thesis]. Kansas State University; 1976. [cited 2020 Sep 22]. Available from: http://hdl.handle.net/2097/11381.

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

Council of Science Editors:

Kotek JJ. Mutagenesis of human lymphoblast cells. [Thesis]. Kansas State University; 1976. Available from: http://hdl.handle.net/2097/11381

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


Michigan State University

21. Liu, Philip Kuocherng. Isolation and characterization of an aphidicolin-resistant mutator mutant of Chinese hamster cells.

Degree: PhD, Genetics Interdepartmental Program, 1981, Michigan State University

Subjects/Keywords: Mutagenesis; Chemical mutagenesis; Mutagenicity testing

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APA (6th Edition):

Liu, P. K. (1981). Isolation and characterization of an aphidicolin-resistant mutator mutant of Chinese hamster cells. (Doctoral Dissertation). Michigan State University. Retrieved from http://etd.lib.msu.edu/islandora/object/etd:35713

Chicago Manual of Style (16th Edition):

Liu, Philip Kuocherng. “Isolation and characterization of an aphidicolin-resistant mutator mutant of Chinese hamster cells.” 1981. Doctoral Dissertation, Michigan State University. Accessed September 22, 2020. http://etd.lib.msu.edu/islandora/object/etd:35713.

MLA Handbook (7th Edition):

Liu, Philip Kuocherng. “Isolation and characterization of an aphidicolin-resistant mutator mutant of Chinese hamster cells.” 1981. Web. 22 Sep 2020.

Vancouver:

Liu PK. Isolation and characterization of an aphidicolin-resistant mutator mutant of Chinese hamster cells. [Internet] [Doctoral dissertation]. Michigan State University; 1981. [cited 2020 Sep 22]. Available from: http://etd.lib.msu.edu/islandora/object/etd:35713.

Council of Science Editors:

Liu PK. Isolation and characterization of an aphidicolin-resistant mutator mutant of Chinese hamster cells. [Doctoral Dissertation]. Michigan State University; 1981. Available from: http://etd.lib.msu.edu/islandora/object/etd:35713


Indian Institute of Science

22. Bajaj, Kanika. Determinants Of Globular Protein Stability And Temperature Sensitivity Inferred From Saturation Mutagenesis Of CcdB.

Degree: PhD, Faculty of Science, 2011, Indian Institute of Science

 The unique native structure is a basic requirement for normal functioning of most proteins. Many diseases stem from mutations in proteins that destabilize the protein… (more)

Subjects/Keywords: Mutagenesis; Protein Stability; Protein Metabolism; CcdB; Protein Structure; Protein Folding; Temperature Sensitive Mutants; Proline Scanning Mutagenesis; Scanning Mutagenesis; Molecular Biology

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APA (6th Edition):

Bajaj, K. (2011). Determinants Of Globular Protein Stability And Temperature Sensitivity Inferred From Saturation Mutagenesis Of CcdB. (Doctoral Dissertation). Indian Institute of Science. Retrieved from http://etd.iisc.ac.in/handle/2005/1082

Chicago Manual of Style (16th Edition):

Bajaj, Kanika. “Determinants Of Globular Protein Stability And Temperature Sensitivity Inferred From Saturation Mutagenesis Of CcdB.” 2011. Doctoral Dissertation, Indian Institute of Science. Accessed September 22, 2020. http://etd.iisc.ac.in/handle/2005/1082.

MLA Handbook (7th Edition):

Bajaj, Kanika. “Determinants Of Globular Protein Stability And Temperature Sensitivity Inferred From Saturation Mutagenesis Of CcdB.” 2011. Web. 22 Sep 2020.

Vancouver:

Bajaj K. Determinants Of Globular Protein Stability And Temperature Sensitivity Inferred From Saturation Mutagenesis Of CcdB. [Internet] [Doctoral dissertation]. Indian Institute of Science; 2011. [cited 2020 Sep 22]. Available from: http://etd.iisc.ac.in/handle/2005/1082.

Council of Science Editors:

Bajaj K. Determinants Of Globular Protein Stability And Temperature Sensitivity Inferred From Saturation Mutagenesis Of CcdB. [Doctoral Dissertation]. Indian Institute of Science; 2011. Available from: http://etd.iisc.ac.in/handle/2005/1082


The Ohio State University

23. Ahmed, Farid El-Mamoun Mohamed. Environmental genetics : a model to investigate pollutants producing genetic damage.

Degree: PhD, Graduate School, 1975, The Ohio State University

Subjects/Keywords: Biophysics; Radiogenetics; Mutagenesis

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APA (6th Edition):

Ahmed, F. E. M. (1975). Environmental genetics : a model to investigate pollutants producing genetic damage. (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1486993975342046

Chicago Manual of Style (16th Edition):

Ahmed, Farid El-Mamoun Mohamed. “Environmental genetics : a model to investigate pollutants producing genetic damage.” 1975. Doctoral Dissertation, The Ohio State University. Accessed September 22, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=osu1486993975342046.

MLA Handbook (7th Edition):

Ahmed, Farid El-Mamoun Mohamed. “Environmental genetics : a model to investigate pollutants producing genetic damage.” 1975. Web. 22 Sep 2020.

Vancouver:

Ahmed FEM. Environmental genetics : a model to investigate pollutants producing genetic damage. [Internet] [Doctoral dissertation]. The Ohio State University; 1975. [cited 2020 Sep 22]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1486993975342046.

Council of Science Editors:

Ahmed FEM. Environmental genetics : a model to investigate pollutants producing genetic damage. [Doctoral Dissertation]. The Ohio State University; 1975. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1486993975342046


University of Utah

24. Kalyanasundaram, Sandhlya. Characterization of a behevior in Caenorhabditis elegans ADAR mutants;.

Degree: MS;, Biochemistry;, 2006, University of Utah

 Adenosine deaminases that act on RNA (ADARs) are RNA editing enzymes that convert adenosine (A) to inosine (I) and are highly expressed in the nervous… (more)

Subjects/Keywords: Adenosine Deaminase; Mutagenesis

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APA (6th Edition):

Kalyanasundaram, S. (2006). Characterization of a behevior in Caenorhabditis elegans ADAR mutants;. (Masters Thesis). University of Utah. Retrieved from http://content.lib.utah.edu/cdm/singleitem/collection/etd1/id/741/rec/135

Chicago Manual of Style (16th Edition):

Kalyanasundaram, Sandhlya. “Characterization of a behevior in Caenorhabditis elegans ADAR mutants;.” 2006. Masters Thesis, University of Utah. Accessed September 22, 2020. http://content.lib.utah.edu/cdm/singleitem/collection/etd1/id/741/rec/135.

MLA Handbook (7th Edition):

Kalyanasundaram, Sandhlya. “Characterization of a behevior in Caenorhabditis elegans ADAR mutants;.” 2006. Web. 22 Sep 2020.

Vancouver:

Kalyanasundaram S. Characterization of a behevior in Caenorhabditis elegans ADAR mutants;. [Internet] [Masters thesis]. University of Utah; 2006. [cited 2020 Sep 22]. Available from: http://content.lib.utah.edu/cdm/singleitem/collection/etd1/id/741/rec/135.

Council of Science Editors:

Kalyanasundaram S. Characterization of a behevior in Caenorhabditis elegans ADAR mutants;. [Masters Thesis]. University of Utah; 2006. Available from: http://content.lib.utah.edu/cdm/singleitem/collection/etd1/id/741/rec/135

25. Khan, Mohd. Nisar. Induced Mutagenesis In BlackGrame;.

Degree: Agriculture Botany, 2014, Chaudhary Charan Singh University

Induced Mutagenesis In BlackGrame newline

Advisors/Committee Members: Balyan, H. S..

Subjects/Keywords: Induced Mutagenesis; BlackGrame

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APA (6th Edition):

Khan, M. N. (2014). Induced Mutagenesis In BlackGrame;. (Thesis). Chaudhary Charan Singh University. Retrieved from http://shodhganga.inflibnet.ac.in/handle/10603/19525

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):

Khan, Mohd Nisar. “Induced Mutagenesis In BlackGrame;.” 2014. Thesis, Chaudhary Charan Singh University. Accessed September 22, 2020. http://shodhganga.inflibnet.ac.in/handle/10603/19525.

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

MLA Handbook (7th Edition):

Khan, Mohd Nisar. “Induced Mutagenesis In BlackGrame;.” 2014. Web. 22 Sep 2020.

Vancouver:

Khan MN. Induced Mutagenesis In BlackGrame;. [Internet] [Thesis]. Chaudhary Charan Singh University; 2014. [cited 2020 Sep 22]. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/19525.

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

Council of Science Editors:

Khan MN. Induced Mutagenesis In BlackGrame;. [Thesis]. Chaudhary Charan Singh University; 2014. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/19525

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


Stellenbosch University

26. De Villiers, Jacques Izak. Mutagenesis studies of a glycoside hydrolase family 2 enzyme.

Degree: MSc, Genetics, 2015, Stellenbosch University

ENGLISH ABSTRACT: Galactooligosaccharides are produced by the transglycosylation activity of β-galactosidases (β-gal, EC 3.2.1.23) when utilising lactose as a substrate. They have emerged as important… (more)

Subjects/Keywords: Beta-galactosidase; Site directed-mutagenesis; Exopolymer; UCTD

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APA (6th Edition):

De Villiers, J. I. (2015). Mutagenesis studies of a glycoside hydrolase family 2 enzyme. (Masters Thesis). Stellenbosch University. Retrieved from http://hdl.handle.net/10019.1/98110

Chicago Manual of Style (16th Edition):

De Villiers, Jacques Izak. “Mutagenesis studies of a glycoside hydrolase family 2 enzyme.” 2015. Masters Thesis, Stellenbosch University. Accessed September 22, 2020. http://hdl.handle.net/10019.1/98110.

MLA Handbook (7th Edition):

De Villiers, Jacques Izak. “Mutagenesis studies of a glycoside hydrolase family 2 enzyme.” 2015. Web. 22 Sep 2020.

Vancouver:

De Villiers JI. Mutagenesis studies of a glycoside hydrolase family 2 enzyme. [Internet] [Masters thesis]. Stellenbosch University; 2015. [cited 2020 Sep 22]. Available from: http://hdl.handle.net/10019.1/98110.

Council of Science Editors:

De Villiers JI. Mutagenesis studies of a glycoside hydrolase family 2 enzyme. [Masters Thesis]. Stellenbosch University; 2015. Available from: http://hdl.handle.net/10019.1/98110


Texas A&M University

27. Rowin, Kristina D. Identifying Coxiella burnetii Genes Essential for Subversion of the Host Immune System.

Degree: MS, Medical Sciences, 2014, Texas A&M University

 Coxiella burnetii, the causative agent of Q fever in humans, is a Gram-negative intracellular bacterium. Although the organism was first isolated in the 1930s, little… (more)

Subjects/Keywords: Coxiella burnetii; transposon mutagenesis; Himar1; TraDIS

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APA (6th Edition):

Rowin, K. D. (2014). Identifying Coxiella burnetii Genes Essential for Subversion of the Host Immune System. (Masters Thesis). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/154065

Chicago Manual of Style (16th Edition):

Rowin, Kristina D. “Identifying Coxiella burnetii Genes Essential for Subversion of the Host Immune System.” 2014. Masters Thesis, Texas A&M University. Accessed September 22, 2020. http://hdl.handle.net/1969.1/154065.

MLA Handbook (7th Edition):

Rowin, Kristina D. “Identifying Coxiella burnetii Genes Essential for Subversion of the Host Immune System.” 2014. Web. 22 Sep 2020.

Vancouver:

Rowin KD. Identifying Coxiella burnetii Genes Essential for Subversion of the Host Immune System. [Internet] [Masters thesis]. Texas A&M University; 2014. [cited 2020 Sep 22]. Available from: http://hdl.handle.net/1969.1/154065.

Council of Science Editors:

Rowin KD. Identifying Coxiella burnetii Genes Essential for Subversion of the Host Immune System. [Masters Thesis]. Texas A&M University; 2014. Available from: http://hdl.handle.net/1969.1/154065


Univerzitet u Beogradu

28. Kostić, Tatjana, 1959-. Molekularna osnova genetičkih rearanžmana izazvanih IS5 elementima u polA1 mutatorskom soju Escherichia coli K12.

Degree: Biološki fakultet, 2020, Univerzitet u Beogradu

Mолекуларна биологија / Molecular biology

U našem prethodnom radu na polA1 mutantima pokazali smo da polA1 kreira mutacije isključivo tipa minus fs i delecija. U… (more)

Subjects/Keywords: mutagenesis - polA1- recombination – deletions - IS5 – PCR

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APA (6th Edition):

Kostić, Tatjana, 1. (2020). Molekularna osnova genetičkih rearanžmana izazvanih IS5 elementima u polA1 mutatorskom soju Escherichia coli K12. (Thesis). Univerzitet u Beogradu. Retrieved from https://fedorabg.bg.ac.rs/fedora/get/o:20765/bdef:Content/get

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):

Kostić, Tatjana, 1959-. “Molekularna osnova genetičkih rearanžmana izazvanih IS5 elementima u polA1 mutatorskom soju Escherichia coli K12.” 2020. Thesis, Univerzitet u Beogradu. Accessed September 22, 2020. https://fedorabg.bg.ac.rs/fedora/get/o:20765/bdef:Content/get.

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

MLA Handbook (7th Edition):

Kostić, Tatjana, 1959-. “Molekularna osnova genetičkih rearanžmana izazvanih IS5 elementima u polA1 mutatorskom soju Escherichia coli K12.” 2020. Web. 22 Sep 2020.

Vancouver:

Kostić, Tatjana 1. Molekularna osnova genetičkih rearanžmana izazvanih IS5 elementima u polA1 mutatorskom soju Escherichia coli K12. [Internet] [Thesis]. Univerzitet u Beogradu; 2020. [cited 2020 Sep 22]. Available from: https://fedorabg.bg.ac.rs/fedora/get/o:20765/bdef:Content/get.

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

Council of Science Editors:

Kostić, Tatjana 1. Molekularna osnova genetičkih rearanžmana izazvanih IS5 elementima u polA1 mutatorskom soju Escherichia coli K12. [Thesis]. Univerzitet u Beogradu; 2020. Available from: https://fedorabg.bg.ac.rs/fedora/get/o:20765/bdef:Content/get

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


NSYSU

29. Wu, Chun-Yi. Interaction between KLIP1 and SUMO-1.

Degree: Master, Biological Sciences, 2011, NSYSU

 Nuclear protein KLIP1 cooperates with myeloid leukemia factor 1 (MLF1) to inhibit the programmed cell death resulting in tumor formation. It also inhibits the activity… (more)

Subjects/Keywords: KLIP1; SUMO-1; site-directed mutagenesis

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APA (6th Edition):

Wu, C. (2011). Interaction between KLIP1 and SUMO-1. (Thesis). NSYSU. Retrieved from http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0905111-105014

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

Chicago Manual of Style (16th Edition):

Wu, Chun-Yi. “Interaction between KLIP1 and SUMO-1.” 2011. Thesis, NSYSU. Accessed September 22, 2020. http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0905111-105014.

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

MLA Handbook (7th Edition):

Wu, Chun-Yi. “Interaction between KLIP1 and SUMO-1.” 2011. Web. 22 Sep 2020.

Vancouver:

Wu C. Interaction between KLIP1 and SUMO-1. [Internet] [Thesis]. NSYSU; 2011. [cited 2020 Sep 22]. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0905111-105014.

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

Council of Science Editors:

Wu C. Interaction between KLIP1 and SUMO-1. [Thesis]. NSYSU; 2011. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0905111-105014

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


University of Alberta

30. Liu, Qin. Functional and Topological Analysis of Acyl-CoA:Diacylglycerol Acyltransferase 2 From Saccharomyces cerevisiae.

Degree: PhD, Department of Agricultural, Food, and Nutritional Science, 2011, University of Alberta

 Acyl-CoA:diacylglycerol acyltransferase (EC 2.3.1.20, DGAT or DAGAT) is a membrane protein found mainly in the endoplasmic reticulum (ER). It catalyzes the final step in the… (more)

Subjects/Keywords: Mutagenesis; TAG; Yeast; DGAT2; Structure/Function; Topology

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

APA (6th Edition):

Liu, Q. (2011). Functional and Topological Analysis of Acyl-CoA:Diacylglycerol Acyltransferase 2 From Saccharomyces cerevisiae. (Doctoral Dissertation). University of Alberta. Retrieved from https://era.library.ualberta.ca/files/b8515n990

Chicago Manual of Style (16th Edition):

Liu, Qin. “Functional and Topological Analysis of Acyl-CoA:Diacylglycerol Acyltransferase 2 From Saccharomyces cerevisiae.” 2011. Doctoral Dissertation, University of Alberta. Accessed September 22, 2020. https://era.library.ualberta.ca/files/b8515n990.

MLA Handbook (7th Edition):

Liu, Qin. “Functional and Topological Analysis of Acyl-CoA:Diacylglycerol Acyltransferase 2 From Saccharomyces cerevisiae.” 2011. Web. 22 Sep 2020.

Vancouver:

Liu Q. Functional and Topological Analysis of Acyl-CoA:Diacylglycerol Acyltransferase 2 From Saccharomyces cerevisiae. [Internet] [Doctoral dissertation]. University of Alberta; 2011. [cited 2020 Sep 22]. Available from: https://era.library.ualberta.ca/files/b8515n990.

Council of Science Editors:

Liu Q. Functional and Topological Analysis of Acyl-CoA:Diacylglycerol Acyltransferase 2 From Saccharomyces cerevisiae. [Doctoral Dissertation]. University of Alberta; 2011. Available from: https://era.library.ualberta.ca/files/b8515n990

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