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You searched for subject:(Mutation Genetics ). Showing records 1 – 30 of 267 total matches.

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University of Pennsylvania

1. Singh, Tanya. Hypermutability in Asexuals: Investigating the Effects of Deleterious Mutations.

Degree: 2016, University of Pennsylvania

Mutation is the ultimate source of the genetic variation—including genetic variation for mutation rate itself—that fuels evolution. Selection to increase the genomic mutation rate, driven… (more)

Subjects/Keywords: Deleterious Mutation; Evolutionary Genetics; Mutation; Mutation Accumulation; Mutation Rate Evolution; Neutral Mutation; Biology; Microbiology

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

APA (6th Edition):

Singh, T. (2016). Hypermutability in Asexuals: Investigating the Effects of Deleterious Mutations. (Thesis). University of Pennsylvania. Retrieved from https://repository.upenn.edu/edissertations/2020

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):

Singh, Tanya. “Hypermutability in Asexuals: Investigating the Effects of Deleterious Mutations.” 2016. Thesis, University of Pennsylvania. Accessed January 17, 2020. https://repository.upenn.edu/edissertations/2020.

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

MLA Handbook (7th Edition):

Singh, Tanya. “Hypermutability in Asexuals: Investigating the Effects of Deleterious Mutations.” 2016. Web. 17 Jan 2020.

Vancouver:

Singh T. Hypermutability in Asexuals: Investigating the Effects of Deleterious Mutations. [Internet] [Thesis]. University of Pennsylvania; 2016. [cited 2020 Jan 17]. Available from: https://repository.upenn.edu/edissertations/2020.

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

Council of Science Editors:

Singh T. Hypermutability in Asexuals: Investigating the Effects of Deleterious Mutations. [Thesis]. University of Pennsylvania; 2016. Available from: https://repository.upenn.edu/edissertations/2020

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


Dalhousie University

2. Kozela, Christopher Paul. ENVIRONMENT-DEPENDENT CAUSES AND CONSEQUENCES OF MUTATION IN SACCHAROMYCES CEREVISIAE.

Degree: PhD, Department of Biology, 2012, Dalhousie University

 Environmental effects on mutation have been documented for many years but have concentrated on agents that directly interact with DNA. Mutation research in its early… (more)

Subjects/Keywords: Evolutionary Genetics; Mutation; Environmental Stress

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APA (6th Edition):

Kozela, C. P. (2012). ENVIRONMENT-DEPENDENT CAUSES AND CONSEQUENCES OF MUTATION IN SACCHAROMYCES CEREVISIAE. (Doctoral Dissertation). Dalhousie University. Retrieved from http://hdl.handle.net/10222/14821

Chicago Manual of Style (16th Edition):

Kozela, Christopher Paul. “ENVIRONMENT-DEPENDENT CAUSES AND CONSEQUENCES OF MUTATION IN SACCHAROMYCES CEREVISIAE.” 2012. Doctoral Dissertation, Dalhousie University. Accessed January 17, 2020. http://hdl.handle.net/10222/14821.

MLA Handbook (7th Edition):

Kozela, Christopher Paul. “ENVIRONMENT-DEPENDENT CAUSES AND CONSEQUENCES OF MUTATION IN SACCHAROMYCES CEREVISIAE.” 2012. Web. 17 Jan 2020.

Vancouver:

Kozela CP. ENVIRONMENT-DEPENDENT CAUSES AND CONSEQUENCES OF MUTATION IN SACCHAROMYCES CEREVISIAE. [Internet] [Doctoral dissertation]. Dalhousie University; 2012. [cited 2020 Jan 17]. Available from: http://hdl.handle.net/10222/14821.

Council of Science Editors:

Kozela CP. ENVIRONMENT-DEPENDENT CAUSES AND CONSEQUENCES OF MUTATION IN SACCHAROMYCES CEREVISIAE. [Doctoral Dissertation]. Dalhousie University; 2012. Available from: http://hdl.handle.net/10222/14821

3. Curry, John Duncan. Mutation monitoring in human populations.

Degree: Department of Biology, 2017, University of Victoria

 Currently, the most widely used in vivo mutation monitoring system in humans is the hypoxanthine-guanine phosphoribosyltransferase (hprt) T-cell clonal assay. This dissertation examines the current… (more)

Subjects/Keywords: Mutation (Biology); Human population genetics

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APA (6th Edition):

Curry, J. D. (2017). Mutation monitoring in human populations. (Thesis). University of Victoria. Retrieved from https://dspace.library.uvic.ca//handle/1828/8811

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):

Curry, John Duncan. “Mutation monitoring in human populations.” 2017. Thesis, University of Victoria. Accessed January 17, 2020. https://dspace.library.uvic.ca//handle/1828/8811.

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

MLA Handbook (7th Edition):

Curry, John Duncan. “Mutation monitoring in human populations.” 2017. Web. 17 Jan 2020.

Vancouver:

Curry JD. Mutation monitoring in human populations. [Internet] [Thesis]. University of Victoria; 2017. [cited 2020 Jan 17]. Available from: https://dspace.library.uvic.ca//handle/1828/8811.

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

Council of Science Editors:

Curry JD. Mutation monitoring in human populations. [Thesis]. University of Victoria; 2017. Available from: https://dspace.library.uvic.ca//handle/1828/8811

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


Oregon State University

4. Bollmann, Stephanie R. Reversion reporters in Arabidopsis thaliana to detect all six base substitution pathways.

Degree: PhD, Genetics, 2008, Oregon State University

 Maintaining genome integrity is essential for an organism, as mutation accumulation can lead to cancer, reduced fitness, and heritable diseases in offspring. Therefore the study… (more)

Subjects/Keywords: mutation reporter; Arabidopsis thaliana  – Genetics

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APA (6th Edition):

Bollmann, S. R. (2008). Reversion reporters in Arabidopsis thaliana to detect all six base substitution pathways. (Doctoral Dissertation). Oregon State University. Retrieved from http://hdl.handle.net/1957/8924

Chicago Manual of Style (16th Edition):

Bollmann, Stephanie R. “Reversion reporters in Arabidopsis thaliana to detect all six base substitution pathways.” 2008. Doctoral Dissertation, Oregon State University. Accessed January 17, 2020. http://hdl.handle.net/1957/8924.

MLA Handbook (7th Edition):

Bollmann, Stephanie R. “Reversion reporters in Arabidopsis thaliana to detect all six base substitution pathways.” 2008. Web. 17 Jan 2020.

Vancouver:

Bollmann SR. Reversion reporters in Arabidopsis thaliana to detect all six base substitution pathways. [Internet] [Doctoral dissertation]. Oregon State University; 2008. [cited 2020 Jan 17]. Available from: http://hdl.handle.net/1957/8924.

Council of Science Editors:

Bollmann SR. Reversion reporters in Arabidopsis thaliana to detect all six base substitution pathways. [Doctoral Dissertation]. Oregon State University; 2008. Available from: http://hdl.handle.net/1957/8924


University of Otago

5. Sharma, Utsav. Genetic basis of the activation of the cryptic dct genes in Mesorhizobium loti .

Degree: 2010, University of Otago

 Previous studies showed that, although non-symbiotic mesorhizobia carry a copy of the dctABD genes responsible for C4-dicarboxylate transport, most strains isolated from soil were unable… (more)

Subjects/Keywords: Cryptic genes; Mutation; Bacteria; Genetics

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APA (6th Edition):

Sharma, U. (2010). Genetic basis of the activation of the cryptic dct genes in Mesorhizobium loti . (Masters Thesis). University of Otago. Retrieved from http://hdl.handle.net/10523/387

Chicago Manual of Style (16th Edition):

Sharma, Utsav. “Genetic basis of the activation of the cryptic dct genes in Mesorhizobium loti .” 2010. Masters Thesis, University of Otago. Accessed January 17, 2020. http://hdl.handle.net/10523/387.

MLA Handbook (7th Edition):

Sharma, Utsav. “Genetic basis of the activation of the cryptic dct genes in Mesorhizobium loti .” 2010. Web. 17 Jan 2020.

Vancouver:

Sharma U. Genetic basis of the activation of the cryptic dct genes in Mesorhizobium loti . [Internet] [Masters thesis]. University of Otago; 2010. [cited 2020 Jan 17]. Available from: http://hdl.handle.net/10523/387.

Council of Science Editors:

Sharma U. Genetic basis of the activation of the cryptic dct genes in Mesorhizobium loti . [Masters Thesis]. University of Otago; 2010. Available from: http://hdl.handle.net/10523/387


Columbia University

6. Simons, Yuval Benjamin. Population Genetics of Mutation Load and Quantitative Traits in Humans.

Degree: 2019, Columbia University

 The past fifteen years have seen a revolution in human population genetics. We have gone from anecdotal genetic data from a few individuals at a… (more)

Subjects/Keywords: Genetics; Biology; Human population genetics; Mutation (Biology)

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APA (6th Edition):

Simons, Y. B. (2019). Population Genetics of Mutation Load and Quantitative Traits in Humans. (Doctoral Dissertation). Columbia University. Retrieved from https://doi.org/10.7916/D8H71ZQG

Chicago Manual of Style (16th Edition):

Simons, Yuval Benjamin. “Population Genetics of Mutation Load and Quantitative Traits in Humans.” 2019. Doctoral Dissertation, Columbia University. Accessed January 17, 2020. https://doi.org/10.7916/D8H71ZQG.

MLA Handbook (7th Edition):

Simons, Yuval Benjamin. “Population Genetics of Mutation Load and Quantitative Traits in Humans.” 2019. Web. 17 Jan 2020.

Vancouver:

Simons YB. Population Genetics of Mutation Load and Quantitative Traits in Humans. [Internet] [Doctoral dissertation]. Columbia University; 2019. [cited 2020 Jan 17]. Available from: https://doi.org/10.7916/D8H71ZQG.

Council of Science Editors:

Simons YB. Population Genetics of Mutation Load and Quantitative Traits in Humans. [Doctoral Dissertation]. Columbia University; 2019. Available from: https://doi.org/10.7916/D8H71ZQG


Portland State University

7. Goodman, David Andrew. Comparative Genetic and Genomic Analysis of the Novel Fusellovirus Sulfolobus Spindle-shaped Virus 10.

Degree: MS(M.S.) in Biology, Biology, 2018, Portland State University

  Viruses that infect thermophilic Archaea are unique in both their structure and genetic makeup. The lemon-shaped fuselloviruses - which infect members of the order… (more)

Subjects/Keywords: Viruses; Mutation (Biology); Archaebacteria; Biology; Genetics; Virology

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APA (6th Edition):

Goodman, D. A. (2018). Comparative Genetic and Genomic Analysis of the Novel Fusellovirus Sulfolobus Spindle-shaped Virus 10. (Masters Thesis). Portland State University. Retrieved from https://pdxscholar.library.pdx.edu/open_access_etds/4496

Chicago Manual of Style (16th Edition):

Goodman, David Andrew. “Comparative Genetic and Genomic Analysis of the Novel Fusellovirus Sulfolobus Spindle-shaped Virus 10.” 2018. Masters Thesis, Portland State University. Accessed January 17, 2020. https://pdxscholar.library.pdx.edu/open_access_etds/4496.

MLA Handbook (7th Edition):

Goodman, David Andrew. “Comparative Genetic and Genomic Analysis of the Novel Fusellovirus Sulfolobus Spindle-shaped Virus 10.” 2018. Web. 17 Jan 2020.

Vancouver:

Goodman DA. Comparative Genetic and Genomic Analysis of the Novel Fusellovirus Sulfolobus Spindle-shaped Virus 10. [Internet] [Masters thesis]. Portland State University; 2018. [cited 2020 Jan 17]. Available from: https://pdxscholar.library.pdx.edu/open_access_etds/4496.

Council of Science Editors:

Goodman DA. Comparative Genetic and Genomic Analysis of the Novel Fusellovirus Sulfolobus Spindle-shaped Virus 10. [Masters Thesis]. Portland State University; 2018. Available from: https://pdxscholar.library.pdx.edu/open_access_etds/4496


McMaster University

8. Sathiasothy, Sharmila. Environmental Selection of Phenotypic Switching of the RpoS-dependent Response in Escherichia coli.

Degree: MSc, 2011, McMaster University

<h1>Abstract</h1> Understanding the adaptive mechanisms of large regulatory networks can provide insight into long-term survival of bacterial populations in nature. The RpoS master stress… (more)

Subjects/Keywords: mutation; selection; sigma factor; bacterial stress resistance; Molecular genetics; Molecular genetics

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APA (6th Edition):

Sathiasothy, S. (2011). Environmental Selection of Phenotypic Switching of the RpoS-dependent Response in Escherichia coli. (Masters Thesis). McMaster University. Retrieved from http://hdl.handle.net/11375/11480

Chicago Manual of Style (16th Edition):

Sathiasothy, Sharmila. “Environmental Selection of Phenotypic Switching of the RpoS-dependent Response in Escherichia coli.” 2011. Masters Thesis, McMaster University. Accessed January 17, 2020. http://hdl.handle.net/11375/11480.

MLA Handbook (7th Edition):

Sathiasothy, Sharmila. “Environmental Selection of Phenotypic Switching of the RpoS-dependent Response in Escherichia coli.” 2011. Web. 17 Jan 2020.

Vancouver:

Sathiasothy S. Environmental Selection of Phenotypic Switching of the RpoS-dependent Response in Escherichia coli. [Internet] [Masters thesis]. McMaster University; 2011. [cited 2020 Jan 17]. Available from: http://hdl.handle.net/11375/11480.

Council of Science Editors:

Sathiasothy S. Environmental Selection of Phenotypic Switching of the RpoS-dependent Response in Escherichia coli. [Masters Thesis]. McMaster University; 2011. Available from: http://hdl.handle.net/11375/11480


Michigan State University

9. Chari, Sudarshan R. Understanding the role of standing genetic variation in functional genetics and compensatory evolution.

Degree: 2014, Michigan State University

Thesis Ph. D. Michigan State University. Zoology 2014.

Conventionally the phenotypic outcome of a mutation is considered to be due to a specific DNA lesion.… (more)

Subjects/Keywords: Mutation (Biology); Epistasis (Genetics); Evolution (Biology); Genetics; Evolution & development; Animal behavior

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APA (6th Edition):

Chari, S. R. (2014). Understanding the role of standing genetic variation in functional genetics and compensatory evolution. (Thesis). Michigan State University. Retrieved from http://etd.lib.msu.edu/islandora/object/etd:2897

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):

Chari, Sudarshan R. “Understanding the role of standing genetic variation in functional genetics and compensatory evolution.” 2014. Thesis, Michigan State University. Accessed January 17, 2020. http://etd.lib.msu.edu/islandora/object/etd:2897.

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

MLA Handbook (7th Edition):

Chari, Sudarshan R. “Understanding the role of standing genetic variation in functional genetics and compensatory evolution.” 2014. Web. 17 Jan 2020.

Vancouver:

Chari SR. Understanding the role of standing genetic variation in functional genetics and compensatory evolution. [Internet] [Thesis]. Michigan State University; 2014. [cited 2020 Jan 17]. Available from: http://etd.lib.msu.edu/islandora/object/etd:2897.

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

Council of Science Editors:

Chari SR. Understanding the role of standing genetic variation in functional genetics and compensatory evolution. [Thesis]. Michigan State University; 2014. Available from: http://etd.lib.msu.edu/islandora/object/etd:2897

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


University of Washington

10. Geisheker, Madeleine. De novo missense mutations in neurodevelopmental disorders.

Degree: PhD, 2019, University of Washington

 Autism spectrum disorder (ASD) is a pervasive neurodevelopmental disorder (NDD) with a high prevalence in the US (1 in 59 children). It is commonly comorbid… (more)

Subjects/Keywords: Autism; Clustering; De novo; Mutation; Neurodevelopmental disorders; Genetics; Neurosciences; Genetics

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APA (6th Edition):

Geisheker, M. (2019). De novo missense mutations in neurodevelopmental disorders. (Doctoral Dissertation). University of Washington. Retrieved from http://hdl.handle.net/1773/44273

Chicago Manual of Style (16th Edition):

Geisheker, Madeleine. “De novo missense mutations in neurodevelopmental disorders.” 2019. Doctoral Dissertation, University of Washington. Accessed January 17, 2020. http://hdl.handle.net/1773/44273.

MLA Handbook (7th Edition):

Geisheker, Madeleine. “De novo missense mutations in neurodevelopmental disorders.” 2019. Web. 17 Jan 2020.

Vancouver:

Geisheker M. De novo missense mutations in neurodevelopmental disorders. [Internet] [Doctoral dissertation]. University of Washington; 2019. [cited 2020 Jan 17]. Available from: http://hdl.handle.net/1773/44273.

Council of Science Editors:

Geisheker M. De novo missense mutations in neurodevelopmental disorders. [Doctoral Dissertation]. University of Washington; 2019. Available from: http://hdl.handle.net/1773/44273

11. Dillon, Marcus M. The rate, spectrum and effects of spontaneous mutation in bacteria with multiple chromosomes.

Degree: PhD, 2016, University of New Hampshire

  Despite their essentiality for evolutionary change and role in many diseases, spontaneous mutations remain understudied because of both biological and technical barriers. Prokaryotic mutation(more)

Subjects/Keywords: distribution of fitness effects; experimental evolution; mutation rate; mutation spectra; Microbiology; Evolution & development; Genetics

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APA (6th Edition):

Dillon, M. M. (2016). The rate, spectrum and effects of spontaneous mutation in bacteria with multiple chromosomes. (Doctoral Dissertation). University of New Hampshire. Retrieved from https://scholars.unh.edu/dissertation/2247

Chicago Manual of Style (16th Edition):

Dillon, Marcus M. “The rate, spectrum and effects of spontaneous mutation in bacteria with multiple chromosomes.” 2016. Doctoral Dissertation, University of New Hampshire. Accessed January 17, 2020. https://scholars.unh.edu/dissertation/2247.

MLA Handbook (7th Edition):

Dillon, Marcus M. “The rate, spectrum and effects of spontaneous mutation in bacteria with multiple chromosomes.” 2016. Web. 17 Jan 2020.

Vancouver:

Dillon MM. The rate, spectrum and effects of spontaneous mutation in bacteria with multiple chromosomes. [Internet] [Doctoral dissertation]. University of New Hampshire; 2016. [cited 2020 Jan 17]. Available from: https://scholars.unh.edu/dissertation/2247.

Council of Science Editors:

Dillon MM. The rate, spectrum and effects of spontaneous mutation in bacteria with multiple chromosomes. [Doctoral Dissertation]. University of New Hampshire; 2016. Available from: https://scholars.unh.edu/dissertation/2247


University of Oxford

12. Jiang, Hongyu. Population genetics genealogies under selection.

Degree: PhD, 2013, University of Oxford

 In the presence of selection and mutation, the genealogy of a given sample configuration can be described by two classes of ancestral processes, namely the… (more)

Subjects/Keywords: 576.5; Mathematical Population Genetics; strong selection; strong mutation; selection-mutation balance; additive selection

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APA (6th Edition):

Jiang, H. (2013). Population genetics genealogies under selection. (Doctoral Dissertation). University of Oxford. Retrieved from http://ora.ox.ac.uk/objects/uuid:141f4e19-d13a-409e-a7c7-aeaabd6b9b88 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.639972

Chicago Manual of Style (16th Edition):

Jiang, Hongyu. “Population genetics genealogies under selection.” 2013. Doctoral Dissertation, University of Oxford. Accessed January 17, 2020. http://ora.ox.ac.uk/objects/uuid:141f4e19-d13a-409e-a7c7-aeaabd6b9b88 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.639972.

MLA Handbook (7th Edition):

Jiang, Hongyu. “Population genetics genealogies under selection.” 2013. Web. 17 Jan 2020.

Vancouver:

Jiang H. Population genetics genealogies under selection. [Internet] [Doctoral dissertation]. University of Oxford; 2013. [cited 2020 Jan 17]. Available from: http://ora.ox.ac.uk/objects/uuid:141f4e19-d13a-409e-a7c7-aeaabd6b9b88 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.639972.

Council of Science Editors:

Jiang H. Population genetics genealogies under selection. [Doctoral Dissertation]. University of Oxford; 2013. Available from: http://ora.ox.ac.uk/objects/uuid:141f4e19-d13a-409e-a7c7-aeaabd6b9b88 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.639972


University of Pennsylvania

13. Aggarwala, Varun. Human Mutation/substitution Rate: Variability, Modeling And Applications.

Degree: 2016, University of Pennsylvania

Mutation generates genetic variation, and in turn selection purges deleterious variants from the population. Understanding both is critical for discovering causal genes and variants behind… (more)

Subjects/Keywords: Computational Biology; Evolutionary Biology; Human Genetics; Mutation Rate; Statistical Genetics; Bioinformatics; Genetics

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APA (6th Edition):

Aggarwala, V. (2016). Human Mutation/substitution Rate: Variability, Modeling And Applications. (Thesis). University of Pennsylvania. Retrieved from https://repository.upenn.edu/edissertations/2158

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):

Aggarwala, Varun. “Human Mutation/substitution Rate: Variability, Modeling And Applications.” 2016. Thesis, University of Pennsylvania. Accessed January 17, 2020. https://repository.upenn.edu/edissertations/2158.

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

MLA Handbook (7th Edition):

Aggarwala, Varun. “Human Mutation/substitution Rate: Variability, Modeling And Applications.” 2016. Web. 17 Jan 2020.

Vancouver:

Aggarwala V. Human Mutation/substitution Rate: Variability, Modeling And Applications. [Internet] [Thesis]. University of Pennsylvania; 2016. [cited 2020 Jan 17]. Available from: https://repository.upenn.edu/edissertations/2158.

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

Council of Science Editors:

Aggarwala V. Human Mutation/substitution Rate: Variability, Modeling And Applications. [Thesis]. University of Pennsylvania; 2016. Available from: https://repository.upenn.edu/edissertations/2158

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

14. Klaver, Stefanie Gomes. Defeitos genético-moleculares e aspectos clínicos de pacientes com síndrome de hiper IgM autossômica.

Degree: Mestrado, Imunologia, 2011, University of São Paulo

A síndrome de HIGM é uma imunodeficiência, caracterizada por níveis séricos normais ou elevados de IgM associados com baixos níveis de IgG, IgA e IgE.… (more)

Subjects/Keywords: Genetic mutation; Genética molecular; Immunogenetics; Imunogenética; Molecular genetics; Mutação genética

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APA (6th Edition):

Klaver, S. G. (2011). Defeitos genético-moleculares e aspectos clínicos de pacientes com síndrome de hiper IgM autossômica. (Masters Thesis). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/42/42133/tde-09022012-124352/ ;

Chicago Manual of Style (16th Edition):

Klaver, Stefanie Gomes. “Defeitos genético-moleculares e aspectos clínicos de pacientes com síndrome de hiper IgM autossômica.” 2011. Masters Thesis, University of São Paulo. Accessed January 17, 2020. http://www.teses.usp.br/teses/disponiveis/42/42133/tde-09022012-124352/ ;.

MLA Handbook (7th Edition):

Klaver, Stefanie Gomes. “Defeitos genético-moleculares e aspectos clínicos de pacientes com síndrome de hiper IgM autossômica.” 2011. Web. 17 Jan 2020.

Vancouver:

Klaver SG. Defeitos genético-moleculares e aspectos clínicos de pacientes com síndrome de hiper IgM autossômica. [Internet] [Masters thesis]. University of São Paulo; 2011. [cited 2020 Jan 17]. Available from: http://www.teses.usp.br/teses/disponiveis/42/42133/tde-09022012-124352/ ;.

Council of Science Editors:

Klaver SG. Defeitos genético-moleculares e aspectos clínicos de pacientes com síndrome de hiper IgM autossômica. [Masters Thesis]. University of São Paulo; 2011. Available from: http://www.teses.usp.br/teses/disponiveis/42/42133/tde-09022012-124352/ ;


University of Hong Kong

15. Zeng, Shuai. Predicting functional impact of nonsynonymous mutations by quantifying conservation information and detect indels using split-read approach.

Degree: PhD, 2014, University of Hong Kong

 The rapidly developing sequencing technology has brought up an opportunity to scientists to look into the detailed genotype information in human genome. Computational programs have… (more)

Subjects/Keywords: Medical genetics; Nucleotide sequence - Data processing; Mutation (Biology)

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APA (6th Edition):

Zeng, S. (2014). Predicting functional impact of nonsynonymous mutations by quantifying conservation information and detect indels using split-read approach. (Doctoral Dissertation). University of Hong Kong. Retrieved from Zeng, S. [曾帥]. (2014). Predicting functional impact of nonsynonymous mutations by quantifying conservation information and detect indels using split-read approach. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5204922 ; http://dx.doi.org/10.5353/th_b5204922 ; http://hdl.handle.net/10722/198818

Chicago Manual of Style (16th Edition):

Zeng, Shuai. “Predicting functional impact of nonsynonymous mutations by quantifying conservation information and detect indels using split-read approach.” 2014. Doctoral Dissertation, University of Hong Kong. Accessed January 17, 2020. Zeng, S. [曾帥]. (2014). Predicting functional impact of nonsynonymous mutations by quantifying conservation information and detect indels using split-read approach. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5204922 ; http://dx.doi.org/10.5353/th_b5204922 ; http://hdl.handle.net/10722/198818.

MLA Handbook (7th Edition):

Zeng, Shuai. “Predicting functional impact of nonsynonymous mutations by quantifying conservation information and detect indels using split-read approach.” 2014. Web. 17 Jan 2020.

Vancouver:

Zeng S. Predicting functional impact of nonsynonymous mutations by quantifying conservation information and detect indels using split-read approach. [Internet] [Doctoral dissertation]. University of Hong Kong; 2014. [cited 2020 Jan 17]. Available from: Zeng, S. [曾帥]. (2014). Predicting functional impact of nonsynonymous mutations by quantifying conservation information and detect indels using split-read approach. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5204922 ; http://dx.doi.org/10.5353/th_b5204922 ; http://hdl.handle.net/10722/198818.

Council of Science Editors:

Zeng S. Predicting functional impact of nonsynonymous mutations by quantifying conservation information and detect indels using split-read approach. [Doctoral Dissertation]. University of Hong Kong; 2014. Available from: Zeng, S. [曾帥]. (2014). Predicting functional impact of nonsynonymous mutations by quantifying conservation information and detect indels using split-read approach. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5204922 ; http://dx.doi.org/10.5353/th_b5204922 ; http://hdl.handle.net/10722/198818


The Ohio State University

16. Paisie, Carolyn Anne. Definition of mechanisms of mutation generation in tissues and embryonic stem cellsof the constitutive Fhit knockout mouse.

Degree: PhD, Integrated Biomedical Science Graduate Program, 2015, The Ohio State University

 Genome instability, which can be defined as an increase in changes at both the nucleotide and chromosomal level (e.g. point mutations, chromosomal translocations), results from… (more)

Subjects/Keywords: Genetics; Genome instability; mutation signatures; constitutive knockout mouse strains; exome sequence

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APA (6th Edition):

Paisie, C. A. (2015). Definition of mechanisms of mutation generation in tissues and embryonic stem cellsof the constitutive Fhit knockout mouse. (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1436542716

Chicago Manual of Style (16th Edition):

Paisie, Carolyn Anne. “Definition of mechanisms of mutation generation in tissues and embryonic stem cellsof the constitutive Fhit knockout mouse.” 2015. Doctoral Dissertation, The Ohio State University. Accessed January 17, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=osu1436542716.

MLA Handbook (7th Edition):

Paisie, Carolyn Anne. “Definition of mechanisms of mutation generation in tissues and embryonic stem cellsof the constitutive Fhit knockout mouse.” 2015. Web. 17 Jan 2020.

Vancouver:

Paisie CA. Definition of mechanisms of mutation generation in tissues and embryonic stem cellsof the constitutive Fhit knockout mouse. [Internet] [Doctoral dissertation]. The Ohio State University; 2015. [cited 2020 Jan 17]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1436542716.

Council of Science Editors:

Paisie CA. Definition of mechanisms of mutation generation in tissues and embryonic stem cellsof the constitutive Fhit knockout mouse. [Doctoral Dissertation]. The Ohio State University; 2015. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1436542716


University of California – Berkeley

17. Brega, Moorea. An Analysis of the Distribution of Genotypes for a Recent Model in Population Genetics.

Degree: Statistics, 2011, University of California – Berkeley

 Recent genetic studies suggest that many age-related diseases may be attributed not to a single or small number of mutations, but rather to a large… (more)

Subjects/Keywords: Statistics; Biostatistics; Demography; biodemography; mutation accumulation; population genetics; recombination

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APA (6th Edition):

Brega, M. (2011). An Analysis of the Distribution of Genotypes for a Recent Model in Population Genetics. (Thesis). University of California – Berkeley. Retrieved from http://www.escholarship.org/uc/item/23w4s1jc

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):

Brega, Moorea. “An Analysis of the Distribution of Genotypes for a Recent Model in Population Genetics.” 2011. Thesis, University of California – Berkeley. Accessed January 17, 2020. http://www.escholarship.org/uc/item/23w4s1jc.

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

MLA Handbook (7th Edition):

Brega, Moorea. “An Analysis of the Distribution of Genotypes for a Recent Model in Population Genetics.” 2011. Web. 17 Jan 2020.

Vancouver:

Brega M. An Analysis of the Distribution of Genotypes for a Recent Model in Population Genetics. [Internet] [Thesis]. University of California – Berkeley; 2011. [cited 2020 Jan 17]. Available from: http://www.escholarship.org/uc/item/23w4s1jc.

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

Council of Science Editors:

Brega M. An Analysis of the Distribution of Genotypes for a Recent Model in Population Genetics. [Thesis]. University of California – Berkeley; 2011. Available from: http://www.escholarship.org/uc/item/23w4s1jc

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


Portland State University

18. Wendel, Brian Michael. Completion of DNA Replication in <i>Escherichia coli</i>.

Degree: PhD, Biology, 2018, Portland State University

  To maintain genomic integrity, all cells must accurately duplicate their genetic material in order to provide intact and complete copies to each daughter cell… (more)

Subjects/Keywords: DNA replication  – Research; Chromosome replication; Mutation (Biology); Biology; Genetics

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APA (6th Edition):

Wendel, B. M. (2018). Completion of DNA Replication in <i>Escherichia coli</i>. (Doctoral Dissertation). Portland State University. Retrieved from https://pdxscholar.library.pdx.edu/open_access_etds/4406

Chicago Manual of Style (16th Edition):

Wendel, Brian Michael. “Completion of DNA Replication in <i>Escherichia coli</i>.” 2018. Doctoral Dissertation, Portland State University. Accessed January 17, 2020. https://pdxscholar.library.pdx.edu/open_access_etds/4406.

MLA Handbook (7th Edition):

Wendel, Brian Michael. “Completion of DNA Replication in <i>Escherichia coli</i>.” 2018. Web. 17 Jan 2020.

Vancouver:

Wendel BM. Completion of DNA Replication in <i>Escherichia coli</i>. [Internet] [Doctoral dissertation]. Portland State University; 2018. [cited 2020 Jan 17]. Available from: https://pdxscholar.library.pdx.edu/open_access_etds/4406.

Council of Science Editors:

Wendel BM. Completion of DNA Replication in <i>Escherichia coli</i>. [Doctoral Dissertation]. Portland State University; 2018. Available from: https://pdxscholar.library.pdx.edu/open_access_etds/4406


McGill University

19. Boutis, Paula. Viable maternal-effect mutations in the nematode Caenorhabditis elegans.

Degree: MS, Department of Biology, 1995, McGill University

Note:

In an effort to find new genes affecting developmental processes in the nematode Caenorhabditis elegans, a screen for viable maternal-effect mutations was performed. Wild… (more)

Subjects/Keywords: Caenorhabditis elegans  – Genetics.; Animal mutation.

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APA (6th Edition):

Boutis, P. (1995). Viable maternal-effect mutations in the nematode Caenorhabditis elegans. (Masters Thesis). McGill University. Retrieved from http://digitool.library.mcgill.ca/thesisfile156825.pdf

Chicago Manual of Style (16th Edition):

Boutis, Paula. “Viable maternal-effect mutations in the nematode Caenorhabditis elegans.” 1995. Masters Thesis, McGill University. Accessed January 17, 2020. http://digitool.library.mcgill.ca/thesisfile156825.pdf.

MLA Handbook (7th Edition):

Boutis, Paula. “Viable maternal-effect mutations in the nematode Caenorhabditis elegans.” 1995. Web. 17 Jan 2020.

Vancouver:

Boutis P. Viable maternal-effect mutations in the nematode Caenorhabditis elegans. [Internet] [Masters thesis]. McGill University; 1995. [cited 2020 Jan 17]. Available from: http://digitool.library.mcgill.ca/thesisfile156825.pdf.

Council of Science Editors:

Boutis P. Viable maternal-effect mutations in the nematode Caenorhabditis elegans. [Masters Thesis]. McGill University; 1995. Available from: http://digitool.library.mcgill.ca/thesisfile156825.pdf


Oregon State University

20. Pomraning, Kyle R. Characterization of Neurospora crassa and Fusarium graminearum mutants defective in repeat-induced point mutation.

Degree: PhD, Molecular and Cellular Biology, 2012, Oregon State University

Mutation of repetitive DNA by repeat-induced point mutation (RIP) is a process that occurs in many filamentous fungi of the Ascomycota during the sexual cycle.… (more)

Subjects/Keywords: repeat-induced point mutation; Neurospora crassa  – Molecular genetics

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APA (6th Edition):

Pomraning, K. R. (2012). Characterization of Neurospora crassa and Fusarium graminearum mutants defective in repeat-induced point mutation. (Doctoral Dissertation). Oregon State University. Retrieved from http://hdl.handle.net/1957/35582

Chicago Manual of Style (16th Edition):

Pomraning, Kyle R. “Characterization of Neurospora crassa and Fusarium graminearum mutants defective in repeat-induced point mutation.” 2012. Doctoral Dissertation, Oregon State University. Accessed January 17, 2020. http://hdl.handle.net/1957/35582.

MLA Handbook (7th Edition):

Pomraning, Kyle R. “Characterization of Neurospora crassa and Fusarium graminearum mutants defective in repeat-induced point mutation.” 2012. Web. 17 Jan 2020.

Vancouver:

Pomraning KR. Characterization of Neurospora crassa and Fusarium graminearum mutants defective in repeat-induced point mutation. [Internet] [Doctoral dissertation]. Oregon State University; 2012. [cited 2020 Jan 17]. Available from: http://hdl.handle.net/1957/35582.

Council of Science Editors:

Pomraning KR. Characterization of Neurospora crassa and Fusarium graminearum mutants defective in repeat-induced point mutation. [Doctoral Dissertation]. Oregon State University; 2012. Available from: http://hdl.handle.net/1957/35582


University of Adelaide

21. Fullston, Tod. The role of Aristaless related homeobox (ARX) gene mutations in intellectual disability.

Degree: 2012, University of Adelaide

 Intellectual disability (ID) affects ~1-3% of the population, profoundly impacting the lives of affected individuals and their families. An approximate 30% excess of males with… (more)

Subjects/Keywords: genetics; mutation screening; ARX gene; cell based studies; protein localistion

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APA (6th Edition):

Fullston, T. (2012). The role of Aristaless related homeobox (ARX) gene mutations in intellectual disability. (Thesis). University of Adelaide. Retrieved from http://hdl.handle.net/2440/73327

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):

Fullston, Tod. “The role of Aristaless related homeobox (ARX) gene mutations in intellectual disability.” 2012. Thesis, University of Adelaide. Accessed January 17, 2020. http://hdl.handle.net/2440/73327.

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

MLA Handbook (7th Edition):

Fullston, Tod. “The role of Aristaless related homeobox (ARX) gene mutations in intellectual disability.” 2012. Web. 17 Jan 2020.

Vancouver:

Fullston T. The role of Aristaless related homeobox (ARX) gene mutations in intellectual disability. [Internet] [Thesis]. University of Adelaide; 2012. [cited 2020 Jan 17]. Available from: http://hdl.handle.net/2440/73327.

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

Council of Science Editors:

Fullston T. The role of Aristaless related homeobox (ARX) gene mutations in intellectual disability. [Thesis]. University of Adelaide; 2012. Available from: http://hdl.handle.net/2440/73327

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


University of Arizona

22. Clark, Dale Rogers. Methods of screening for induced apomictic mutants in barley (Hordeum vulgare L.).

Degree: 1988, University of Arizona

 Plants that are heterozygous for genetic markers but do not produce segregating progeny may be suspected of carrying a mutation conditioning apomixis. Seed stocks in… (more)

Subjects/Keywords: Barley  – Genetics.; Apomixis.; Plant mutation.

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

APA (6th Edition):

Clark, D. R. (1988). Methods of screening for induced apomictic mutants in barley (Hordeum vulgare L.). (Doctoral Dissertation). University of Arizona. Retrieved from http://hdl.handle.net/10150/184354

Chicago Manual of Style (16th Edition):

Clark, Dale Rogers. “Methods of screening for induced apomictic mutants in barley (Hordeum vulgare L.). ” 1988. Doctoral Dissertation, University of Arizona. Accessed January 17, 2020. http://hdl.handle.net/10150/184354.

MLA Handbook (7th Edition):

Clark, Dale Rogers. “Methods of screening for induced apomictic mutants in barley (Hordeum vulgare L.). ” 1988. Web. 17 Jan 2020.

Vancouver:

Clark DR. Methods of screening for induced apomictic mutants in barley (Hordeum vulgare L.). [Internet] [Doctoral dissertation]. University of Arizona; 1988. [cited 2020 Jan 17]. Available from: http://hdl.handle.net/10150/184354.

Council of Science Editors:

Clark DR. Methods of screening for induced apomictic mutants in barley (Hordeum vulgare L.). [Doctoral Dissertation]. University of Arizona; 1988. Available from: http://hdl.handle.net/10150/184354


University of Arizona

23. Hernandez-Soriano, Juan Maria, 1945-. INDUCTION OF HAPLO-VIABLE MUTANTS IN BARLEY (HORDEUM VULGARE L.) .

Degree: 1975, University of Arizona

Subjects/Keywords: Barley  – Genetics.; Plant mutation.

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APA (6th Edition):

Hernandez-Soriano, Juan Maria, 1. (1975). INDUCTION OF HAPLO-VIABLE MUTANTS IN BARLEY (HORDEUM VULGARE L.) . (Doctoral Dissertation). University of Arizona. Retrieved from http://hdl.handle.net/10150/288388

Chicago Manual of Style (16th Edition):

Hernandez-Soriano, Juan Maria, 1945-. “INDUCTION OF HAPLO-VIABLE MUTANTS IN BARLEY (HORDEUM VULGARE L.) .” 1975. Doctoral Dissertation, University of Arizona. Accessed January 17, 2020. http://hdl.handle.net/10150/288388.

MLA Handbook (7th Edition):

Hernandez-Soriano, Juan Maria, 1945-. “INDUCTION OF HAPLO-VIABLE MUTANTS IN BARLEY (HORDEUM VULGARE L.) .” 1975. Web. 17 Jan 2020.

Vancouver:

Hernandez-Soriano, Juan Maria 1. INDUCTION OF HAPLO-VIABLE MUTANTS IN BARLEY (HORDEUM VULGARE L.) . [Internet] [Doctoral dissertation]. University of Arizona; 1975. [cited 2020 Jan 17]. Available from: http://hdl.handle.net/10150/288388.

Council of Science Editors:

Hernandez-Soriano, Juan Maria 1. INDUCTION OF HAPLO-VIABLE MUTANTS IN BARLEY (HORDEUM VULGARE L.) . [Doctoral Dissertation]. University of Arizona; 1975. Available from: http://hdl.handle.net/10150/288388


Columbia University

24. Bost, Alyssa. An Investigation into the Function and Specification of Enteroendocrine cells in Drosophila melanogaster and Mus musculus.

Degree: 2013, Columbia University

 Enteroendocrine cells (EEs) are critical components in our bodies' ability to maintain homeostasis after eating a meal. Hormones released by EEs mediate processes ranging from… (more)

Subjects/Keywords: Endocrine glands; Mutation (Biology); Drosophila melanogaster; Genetics; Endocrinology

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APA (6th Edition):

Bost, A. (2013). An Investigation into the Function and Specification of Enteroendocrine cells in Drosophila melanogaster and Mus musculus. (Doctoral Dissertation). Columbia University. Retrieved from https://doi.org/10.7916/D8Z31WS6

Chicago Manual of Style (16th Edition):

Bost, Alyssa. “An Investigation into the Function and Specification of Enteroendocrine cells in Drosophila melanogaster and Mus musculus.” 2013. Doctoral Dissertation, Columbia University. Accessed January 17, 2020. https://doi.org/10.7916/D8Z31WS6.

MLA Handbook (7th Edition):

Bost, Alyssa. “An Investigation into the Function and Specification of Enteroendocrine cells in Drosophila melanogaster and Mus musculus.” 2013. Web. 17 Jan 2020.

Vancouver:

Bost A. An Investigation into the Function and Specification of Enteroendocrine cells in Drosophila melanogaster and Mus musculus. [Internet] [Doctoral dissertation]. Columbia University; 2013. [cited 2020 Jan 17]. Available from: https://doi.org/10.7916/D8Z31WS6.

Council of Science Editors:

Bost A. An Investigation into the Function and Specification of Enteroendocrine cells in Drosophila melanogaster and Mus musculus. [Doctoral Dissertation]. Columbia University; 2013. Available from: https://doi.org/10.7916/D8Z31WS6


Cornell University

25. Onaga, Lisa. Silkworm, Science, And Nation: A Sericultural History Of Genetics In Modern Japan .

Degree: 2012, Cornell University

 This dissertation describes how and why the source of raw silk, the domesticated silkworm (Bombyx mori), emerged as an organism that scientists in Japan researched… (more)

Subjects/Keywords: sericulture; genetics; breeding; Japan; hybridization; mutation; silk; Toyama Kametaro; Tanaka Yoshimaro

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APA (6th Edition):

Onaga, L. (2012). Silkworm, Science, And Nation: A Sericultural History Of Genetics In Modern Japan . (Thesis). Cornell University. Retrieved from http://hdl.handle.net/1813/29385

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):

Onaga, Lisa. “Silkworm, Science, And Nation: A Sericultural History Of Genetics In Modern Japan .” 2012. Thesis, Cornell University. Accessed January 17, 2020. http://hdl.handle.net/1813/29385.

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

MLA Handbook (7th Edition):

Onaga, Lisa. “Silkworm, Science, And Nation: A Sericultural History Of Genetics In Modern Japan .” 2012. Web. 17 Jan 2020.

Vancouver:

Onaga L. Silkworm, Science, And Nation: A Sericultural History Of Genetics In Modern Japan . [Internet] [Thesis]. Cornell University; 2012. [cited 2020 Jan 17]. Available from: http://hdl.handle.net/1813/29385.

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

Council of Science Editors:

Onaga L. Silkworm, Science, And Nation: A Sericultural History Of Genetics In Modern Japan . [Thesis]. Cornell University; 2012. Available from: http://hdl.handle.net/1813/29385

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


Columbia University

26. Chen, Chen. The generation and phenotypic effect of human genetic mutations.

Degree: 2018, Columbia University

 Mutations cause genetic variations among cells within an individual as well as variations between individuals within a species. It is the fuel for evolution and… (more)

Subjects/Keywords: Bioinformatics; Computer science; Mutation (Biology); Human genetics – Variation; Machine learning

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APA (6th Edition):

Chen, C. (2018). The generation and phenotypic effect of human genetic mutations. (Doctoral Dissertation). Columbia University. Retrieved from https://doi.org/10.7916/D8Z625XQ

Chicago Manual of Style (16th Edition):

Chen, Chen. “The generation and phenotypic effect of human genetic mutations.” 2018. Doctoral Dissertation, Columbia University. Accessed January 17, 2020. https://doi.org/10.7916/D8Z625XQ.

MLA Handbook (7th Edition):

Chen, Chen. “The generation and phenotypic effect of human genetic mutations.” 2018. Web. 17 Jan 2020.

Vancouver:

Chen C. The generation and phenotypic effect of human genetic mutations. [Internet] [Doctoral dissertation]. Columbia University; 2018. [cited 2020 Jan 17]. Available from: https://doi.org/10.7916/D8Z625XQ.

Council of Science Editors:

Chen C. The generation and phenotypic effect of human genetic mutations. [Doctoral Dissertation]. Columbia University; 2018. Available from: https://doi.org/10.7916/D8Z625XQ


Massey University

27. Shewaramani, Sonal. Effects of aerobic and anaerobic environments on bacterial mutation rates and mutation spectra assessed by whole genome analyses.

Degree: PhD, Genetics, 2015, Massey University

 For organisms that are exposed to different environments, the rates and types of spontaneous mutations that arise in each environment can vary, and potentially impact… (more)

Subjects/Keywords: Mutation; Bacterial genetics; Molecular evolution; Gross chromosomal rearrangements (GCR)

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APA (6th Edition):

Shewaramani, S. (2015). Effects of aerobic and anaerobic environments on bacterial mutation rates and mutation spectra assessed by whole genome analyses. (Doctoral Dissertation). Massey University. Retrieved from http://hdl.handle.net/10179/7166

Chicago Manual of Style (16th Edition):

Shewaramani, Sonal. “Effects of aerobic and anaerobic environments on bacterial mutation rates and mutation spectra assessed by whole genome analyses.” 2015. Doctoral Dissertation, Massey University. Accessed January 17, 2020. http://hdl.handle.net/10179/7166.

MLA Handbook (7th Edition):

Shewaramani, Sonal. “Effects of aerobic and anaerobic environments on bacterial mutation rates and mutation spectra assessed by whole genome analyses.” 2015. Web. 17 Jan 2020.

Vancouver:

Shewaramani S. Effects of aerobic and anaerobic environments on bacterial mutation rates and mutation spectra assessed by whole genome analyses. [Internet] [Doctoral dissertation]. Massey University; 2015. [cited 2020 Jan 17]. Available from: http://hdl.handle.net/10179/7166.

Council of Science Editors:

Shewaramani S. Effects of aerobic and anaerobic environments on bacterial mutation rates and mutation spectra assessed by whole genome analyses. [Doctoral Dissertation]. Massey University; 2015. Available from: http://hdl.handle.net/10179/7166


University of North Texas

28. Prombutara, Pinidphon. Identification of Genes Involved in Flocculation by Whole Genome Sequencing of Thauera aminoaromatica Strain MZ1T Floc-defective Mutants.

Degree: 2015, University of North Texas

 Thauera aminoaromatica MZ1T, a floc-forming bacterium isolated from an industrial activated sludge wastewater treatment plant, overproduces exopolysaccharide (EPS) leading to viscous bulking. This phenomenon results… (more)

Subjects/Keywords: whole genome sequencing; flocculation; thauera MZIT; Bacterial genetics.; Flocculation.; Mutation (Biology)

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APA (6th Edition):

Prombutara, P. (2015). Identification of Genes Involved in Flocculation by Whole Genome Sequencing of Thauera aminoaromatica Strain MZ1T Floc-defective Mutants. (Thesis). University of North Texas. Retrieved from https://digital.library.unt.edu/ark:/67531/metadc822777/

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):

Prombutara, Pinidphon. “Identification of Genes Involved in Flocculation by Whole Genome Sequencing of Thauera aminoaromatica Strain MZ1T Floc-defective Mutants.” 2015. Thesis, University of North Texas. Accessed January 17, 2020. https://digital.library.unt.edu/ark:/67531/metadc822777/.

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

MLA Handbook (7th Edition):

Prombutara, Pinidphon. “Identification of Genes Involved in Flocculation by Whole Genome Sequencing of Thauera aminoaromatica Strain MZ1T Floc-defective Mutants.” 2015. Web. 17 Jan 2020.

Vancouver:

Prombutara P. Identification of Genes Involved in Flocculation by Whole Genome Sequencing of Thauera aminoaromatica Strain MZ1T Floc-defective Mutants. [Internet] [Thesis]. University of North Texas; 2015. [cited 2020 Jan 17]. Available from: https://digital.library.unt.edu/ark:/67531/metadc822777/.

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

Council of Science Editors:

Prombutara P. Identification of Genes Involved in Flocculation by Whole Genome Sequencing of Thauera aminoaromatica Strain MZ1T Floc-defective Mutants. [Thesis]. University of North Texas; 2015. Available from: https://digital.library.unt.edu/ark:/67531/metadc822777/

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


University of Michigan

29. Melfi, Andrew. Theoretical and Numerical Analyses of Deviations Between Kingman's Coalescent and the Wright-Fisher Model.

Degree: PhD, Applied and Interdisciplinary Mathematics, 2019, University of Michigan

 The Kingman Coalescent is a commonly used model in genetics, which is often justified with reference to the Wright-Fisher (WF) model. In this thesis we… (more)

Subjects/Keywords: Coalescent; Wright-Fisher; Variable mutation rate; Genetics; Mathematics; Science

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APA (6th Edition):

Melfi, A. (2019). Theoretical and Numerical Analyses of Deviations Between Kingman's Coalescent and the Wright-Fisher Model. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/149920

Chicago Manual of Style (16th Edition):

Melfi, Andrew. “Theoretical and Numerical Analyses of Deviations Between Kingman's Coalescent and the Wright-Fisher Model.” 2019. Doctoral Dissertation, University of Michigan. Accessed January 17, 2020. http://hdl.handle.net/2027.42/149920.

MLA Handbook (7th Edition):

Melfi, Andrew. “Theoretical and Numerical Analyses of Deviations Between Kingman's Coalescent and the Wright-Fisher Model.” 2019. Web. 17 Jan 2020.

Vancouver:

Melfi A. Theoretical and Numerical Analyses of Deviations Between Kingman's Coalescent and the Wright-Fisher Model. [Internet] [Doctoral dissertation]. University of Michigan; 2019. [cited 2020 Jan 17]. Available from: http://hdl.handle.net/2027.42/149920.

Council of Science Editors:

Melfi A. Theoretical and Numerical Analyses of Deviations Between Kingman's Coalescent and the Wright-Fisher Model. [Doctoral Dissertation]. University of Michigan; 2019. Available from: http://hdl.handle.net/2027.42/149920


University of Arizona

30. Hernandez-Soriano, Juan Maria, 1945-. Desynaptic mutants in Betzes barley .

Degree: 1973, University of Arizona

Subjects/Keywords: Plant mutation.; Barley  – Genetics.

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APA (6th Edition):

Hernandez-Soriano, Juan Maria, 1. (1973). Desynaptic mutants in Betzes barley . (Masters Thesis). University of Arizona. Retrieved from http://hdl.handle.net/10150/554463

Chicago Manual of Style (16th Edition):

Hernandez-Soriano, Juan Maria, 1945-. “Desynaptic mutants in Betzes barley .” 1973. Masters Thesis, University of Arizona. Accessed January 17, 2020. http://hdl.handle.net/10150/554463.

MLA Handbook (7th Edition):

Hernandez-Soriano, Juan Maria, 1945-. “Desynaptic mutants in Betzes barley .” 1973. Web. 17 Jan 2020.

Vancouver:

Hernandez-Soriano, Juan Maria 1. Desynaptic mutants in Betzes barley . [Internet] [Masters thesis]. University of Arizona; 1973. [cited 2020 Jan 17]. Available from: http://hdl.handle.net/10150/554463.

Council of Science Editors:

Hernandez-Soriano, Juan Maria 1. Desynaptic mutants in Betzes barley . [Masters Thesis]. University of Arizona; 1973. Available from: http://hdl.handle.net/10150/554463

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