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You searched for subject:(Single Nucleotide Polymorphism SNP ). Showing records 1 – 30 of 10794 total matches.

[1] [2] [3] [4] [5] … [360]

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University of Waikato

1. Mulholland, Claire Vignette. Single nucleotide polymorphisms associated with the human electroencephalogram during desflurane anaesthesia .

Degree: 2012, University of Waikato

 General anaesthesia is an induced state that enables a person to endure surgical procedures without pain or recollection. There is substantial individual variability in the… (more)

Subjects/Keywords: single nucleotide polymorphism; polymorphism; SNP; anaesthesia; electroencephalogram

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APA (6th Edition):

Mulholland, C. V. (2012). Single nucleotide polymorphisms associated with the human electroencephalogram during desflurane anaesthesia . (Masters Thesis). University of Waikato. Retrieved from http://hdl.handle.net/10289/6678

Chicago Manual of Style (16th Edition):

Mulholland, Claire Vignette. “Single nucleotide polymorphisms associated with the human electroencephalogram during desflurane anaesthesia .” 2012. Masters Thesis, University of Waikato. Accessed October 20, 2020. http://hdl.handle.net/10289/6678.

MLA Handbook (7th Edition):

Mulholland, Claire Vignette. “Single nucleotide polymorphisms associated with the human electroencephalogram during desflurane anaesthesia .” 2012. Web. 20 Oct 2020.

Vancouver:

Mulholland CV. Single nucleotide polymorphisms associated with the human electroencephalogram during desflurane anaesthesia . [Internet] [Masters thesis]. University of Waikato; 2012. [cited 2020 Oct 20]. Available from: http://hdl.handle.net/10289/6678.

Council of Science Editors:

Mulholland CV. Single nucleotide polymorphisms associated with the human electroencephalogram during desflurane anaesthesia . [Masters Thesis]. University of Waikato; 2012. Available from: http://hdl.handle.net/10289/6678


University of Limerick

2. Sheikhi, Ali. Statistical methods for the detection of single nucleotide polymorphisms (SNPs) using new generation genome sequencers.

Degree: 2014, University of Limerick

peer-reviewed

A single nucleotide polymorphism, or SNP, is a site of the genome where variation occurs within a population. Almost all SNPs have only two… (more)

Subjects/Keywords: single nucleotide polymorphism; SNP; DNA sequences

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APA (6th Edition):

Sheikhi, A. (2014). Statistical methods for the detection of single nucleotide polymorphisms (SNPs) using new generation genome sequencers. (Thesis). University of Limerick. Retrieved from http://hdl.handle.net/10344/5996

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):

Sheikhi, Ali. “Statistical methods for the detection of single nucleotide polymorphisms (SNPs) using new generation genome sequencers.” 2014. Thesis, University of Limerick. Accessed October 20, 2020. http://hdl.handle.net/10344/5996.

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

MLA Handbook (7th Edition):

Sheikhi, Ali. “Statistical methods for the detection of single nucleotide polymorphisms (SNPs) using new generation genome sequencers.” 2014. Web. 20 Oct 2020.

Vancouver:

Sheikhi A. Statistical methods for the detection of single nucleotide polymorphisms (SNPs) using new generation genome sequencers. [Internet] [Thesis]. University of Limerick; 2014. [cited 2020 Oct 20]. Available from: http://hdl.handle.net/10344/5996.

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

Council of Science Editors:

Sheikhi A. Statistical methods for the detection of single nucleotide polymorphisms (SNPs) using new generation genome sequencers. [Thesis]. University of Limerick; 2014. Available from: http://hdl.handle.net/10344/5996

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


Rice University

3. Zafar, Hamim. A SNP Calling And Genotyping Method For Single-cell Sequencing Data.

Degree: MS, Engineering, 2015, Rice University

 In this thesis, we propose a single nucleotide polymorphism (SNP) calling and genotyping algorithm for single-cell sequencing data generated by the recently developed single-cell sequencing… (more)

Subjects/Keywords: Single Nucleotide Polymorphism; SNP calling; Genotyping; Single Cell sequencing; Algorithm

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APA (6th Edition):

Zafar, H. (2015). A SNP Calling And Genotyping Method For Single-cell Sequencing Data. (Masters Thesis). Rice University. Retrieved from http://hdl.handle.net/1911/88187

Chicago Manual of Style (16th Edition):

Zafar, Hamim. “A SNP Calling And Genotyping Method For Single-cell Sequencing Data.” 2015. Masters Thesis, Rice University. Accessed October 20, 2020. http://hdl.handle.net/1911/88187.

MLA Handbook (7th Edition):

Zafar, Hamim. “A SNP Calling And Genotyping Method For Single-cell Sequencing Data.” 2015. Web. 20 Oct 2020.

Vancouver:

Zafar H. A SNP Calling And Genotyping Method For Single-cell Sequencing Data. [Internet] [Masters thesis]. Rice University; 2015. [cited 2020 Oct 20]. Available from: http://hdl.handle.net/1911/88187.

Council of Science Editors:

Zafar H. A SNP Calling And Genotyping Method For Single-cell Sequencing Data. [Masters Thesis]. Rice University; 2015. Available from: http://hdl.handle.net/1911/88187


University of the Western Cape

4. Veldsman, Werner Pieter. SNP based literature and data retrieval .

Degree: 2016, University of the Western Cape

 Reference single nucleotide polymorphism (refSNP) identifiers are used to earmark SNPs in the human genome. These identifiers are often found in variant call format (VCF)… (more)

Subjects/Keywords: API (Application Programming Interface); Bioinformatics; Data mining; SNP (Single Nucleotide Polymorphism)

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APA (6th Edition):

Veldsman, W. P. (2016). SNP based literature and data retrieval . (Thesis). University of the Western Cape. Retrieved from http://hdl.handle.net/11394/5345

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):

Veldsman, Werner Pieter. “SNP based literature and data retrieval .” 2016. Thesis, University of the Western Cape. Accessed October 20, 2020. http://hdl.handle.net/11394/5345.

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

MLA Handbook (7th Edition):

Veldsman, Werner Pieter. “SNP based literature and data retrieval .” 2016. Web. 20 Oct 2020.

Vancouver:

Veldsman WP. SNP based literature and data retrieval . [Internet] [Thesis]. University of the Western Cape; 2016. [cited 2020 Oct 20]. Available from: http://hdl.handle.net/11394/5345.

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

Council of Science Editors:

Veldsman WP. SNP based literature and data retrieval . [Thesis]. University of the Western Cape; 2016. Available from: http://hdl.handle.net/11394/5345

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


Queensland University of Technology

5. Costello, Mary-Ellen Clare. Single nucleotide polymorphism (SNP) - genotyping of Community Acquired Methicillin-Resistant Staphylococcus aureus, including the subtyping of PVL toxin producers using Real-Time PCR.

Degree: 2010, Queensland University of Technology

 Staphylococcus aureus is a common pathogen that causes a variety of infections including soft tissue infections, impetigo, septicemia toxic shock and scalded skin syndrome. Traditionally,… (more)

Subjects/Keywords: Single nucleotide polymorphism (SNP); genotyping; Community Acquired Methicillin-Resistant Staphylococcus aureus

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APA (6th Edition):

Costello, M. C. (2010). Single nucleotide polymorphism (SNP) - genotyping of Community Acquired Methicillin-Resistant Staphylococcus aureus, including the subtyping of PVL toxin producers using Real-Time PCR. (Thesis). Queensland University of Technology. Retrieved from https://eprints.qut.edu.au/37662/

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):

Costello, Mary-Ellen Clare. “Single nucleotide polymorphism (SNP) - genotyping of Community Acquired Methicillin-Resistant Staphylococcus aureus, including the subtyping of PVL toxin producers using Real-Time PCR.” 2010. Thesis, Queensland University of Technology. Accessed October 20, 2020. https://eprints.qut.edu.au/37662/.

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

MLA Handbook (7th Edition):

Costello, Mary-Ellen Clare. “Single nucleotide polymorphism (SNP) - genotyping of Community Acquired Methicillin-Resistant Staphylococcus aureus, including the subtyping of PVL toxin producers using Real-Time PCR.” 2010. Web. 20 Oct 2020.

Vancouver:

Costello MC. Single nucleotide polymorphism (SNP) - genotyping of Community Acquired Methicillin-Resistant Staphylococcus aureus, including the subtyping of PVL toxin producers using Real-Time PCR. [Internet] [Thesis]. Queensland University of Technology; 2010. [cited 2020 Oct 20]. Available from: https://eprints.qut.edu.au/37662/.

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

Council of Science Editors:

Costello MC. Single nucleotide polymorphism (SNP) - genotyping of Community Acquired Methicillin-Resistant Staphylococcus aureus, including the subtyping of PVL toxin producers using Real-Time PCR. [Thesis]. Queensland University of Technology; 2010. Available from: https://eprints.qut.edu.au/37662/

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


Brno University of Technology

6. Beňková, Daniela. Srovnávací studie působení léčiv vybraného onemocnění na základě genových polymorfismů člověka: Comparative study of the drug effect on selected disease based on the human genetic polymorphisms.

Degree: 2018, Brno University of Technology

 This bachelor thesis is dealing with topic of effects of medicine from the viewpoint of the genetic polymorphism occurrence in human being. The main targets… (more)

Subjects/Keywords: Alzheimerova choroba; ADMET; farmakogenomika; jednonukleotidový polymorfismus; SNP; Alzheimer’s disease; ADMET; pharmacogenomics; single nucleotide polymorphism; SNP

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APA (6th Edition):

Beňková, D. (2018). Srovnávací studie působení léčiv vybraného onemocnění na základě genových polymorfismů člověka: Comparative study of the drug effect on selected disease based on the human genetic polymorphisms. (Thesis). Brno University of Technology. Retrieved from http://hdl.handle.net/11012/61718

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):

Beňková, Daniela. “Srovnávací studie působení léčiv vybraného onemocnění na základě genových polymorfismů člověka: Comparative study of the drug effect on selected disease based on the human genetic polymorphisms.” 2018. Thesis, Brno University of Technology. Accessed October 20, 2020. http://hdl.handle.net/11012/61718.

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

MLA Handbook (7th Edition):

Beňková, Daniela. “Srovnávací studie působení léčiv vybraného onemocnění na základě genových polymorfismů člověka: Comparative study of the drug effect on selected disease based on the human genetic polymorphisms.” 2018. Web. 20 Oct 2020.

Vancouver:

Beňková D. Srovnávací studie působení léčiv vybraného onemocnění na základě genových polymorfismů člověka: Comparative study of the drug effect on selected disease based on the human genetic polymorphisms. [Internet] [Thesis]. Brno University of Technology; 2018. [cited 2020 Oct 20]. Available from: http://hdl.handle.net/11012/61718.

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

Council of Science Editors:

Beňková D. Srovnávací studie působení léčiv vybraného onemocnění na základě genových polymorfismů člověka: Comparative study of the drug effect on selected disease based on the human genetic polymorphisms. [Thesis]. Brno University of Technology; 2018. Available from: http://hdl.handle.net/11012/61718

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


Université Paris-Sud – Paris XI

7. Wang, Xiao Wei. IDH1/2 (isocitrate dehydrogenase 1/2) Mutations in Gliomas : genotype-Phenotype Correlation, Prognostic impact, and Response to Irradiation : Les mutations IDH1/2 (isocitrate déshydrogénase 1/2) dans les gliomes : Corrélation au profile génomique, facteur pronostique, et implication dans la réponse à l’irradiation.

Degree: Docteur es, Cancérologie - Biochimie, Biologie cellulaire et moléculaire, 2012, Université Paris-Sud – Paris XI

Depuis que Parsons et col. ont découvert en 2008 que le gène de l’isocitrate déhydrogénase 1 (IDH1) est fréquemment muté dans les glioblastomes (12%), de… (more)

Subjects/Keywords: Gliomes; Isocitrate déshydrogénase 1 (IDH1); Polymorphism nucléotide (SNP); Radiothérapie; Radiosensibilité; Gliomas; Isocitrate dehydrogenase 1 (IDH1); Single nucleotide polymorphism (SNP); Irradiation

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APA (6th Edition):

Wang, X. W. (2012). IDH1/2 (isocitrate dehydrogenase 1/2) Mutations in Gliomas : genotype-Phenotype Correlation, Prognostic impact, and Response to Irradiation : Les mutations IDH1/2 (isocitrate déshydrogénase 1/2) dans les gliomes : Corrélation au profile génomique, facteur pronostique, et implication dans la réponse à l’irradiation. (Doctoral Dissertation). Université Paris-Sud – Paris XI. Retrieved from http://www.theses.fr/2012PA11T033

Chicago Manual of Style (16th Edition):

Wang, Xiao Wei. “IDH1/2 (isocitrate dehydrogenase 1/2) Mutations in Gliomas : genotype-Phenotype Correlation, Prognostic impact, and Response to Irradiation : Les mutations IDH1/2 (isocitrate déshydrogénase 1/2) dans les gliomes : Corrélation au profile génomique, facteur pronostique, et implication dans la réponse à l’irradiation.” 2012. Doctoral Dissertation, Université Paris-Sud – Paris XI. Accessed October 20, 2020. http://www.theses.fr/2012PA11T033.

MLA Handbook (7th Edition):

Wang, Xiao Wei. “IDH1/2 (isocitrate dehydrogenase 1/2) Mutations in Gliomas : genotype-Phenotype Correlation, Prognostic impact, and Response to Irradiation : Les mutations IDH1/2 (isocitrate déshydrogénase 1/2) dans les gliomes : Corrélation au profile génomique, facteur pronostique, et implication dans la réponse à l’irradiation.” 2012. Web. 20 Oct 2020.

Vancouver:

Wang XW. IDH1/2 (isocitrate dehydrogenase 1/2) Mutations in Gliomas : genotype-Phenotype Correlation, Prognostic impact, and Response to Irradiation : Les mutations IDH1/2 (isocitrate déshydrogénase 1/2) dans les gliomes : Corrélation au profile génomique, facteur pronostique, et implication dans la réponse à l’irradiation. [Internet] [Doctoral dissertation]. Université Paris-Sud – Paris XI; 2012. [cited 2020 Oct 20]. Available from: http://www.theses.fr/2012PA11T033.

Council of Science Editors:

Wang XW. IDH1/2 (isocitrate dehydrogenase 1/2) Mutations in Gliomas : genotype-Phenotype Correlation, Prognostic impact, and Response to Irradiation : Les mutations IDH1/2 (isocitrate déshydrogénase 1/2) dans les gliomes : Corrélation au profile génomique, facteur pronostique, et implication dans la réponse à l’irradiation. [Doctoral Dissertation]. Université Paris-Sud – Paris XI; 2012. Available from: http://www.theses.fr/2012PA11T033


University of Guelph

8. Wong, Jeremy. Investigating single-nucleotide variants in swine associated with common infectious pathogens and diseases, with a focus on Streptococcus suis infection, using a genome-wide association study approach.

Degree: MS, Department of Pathobiology, 2020, University of Guelph

 Infectious diseases are major burdens for the swine industry. Host genetics is an important factor in the outcome of host-pathogen interactions. Single-nucleotide variants in pigs… (more)

Subjects/Keywords: gwas; pigs; disease; infectious; pathogen; streptococcus; suis; genome; genome-wide; association; nursery; gene; snp; snv; single-nucleotide variant; single-nucleotide polymorphism

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APA (6th Edition):

Wong, J. (2020). Investigating single-nucleotide variants in swine associated with common infectious pathogens and diseases, with a focus on Streptococcus suis infection, using a genome-wide association study approach. (Masters Thesis). University of Guelph. Retrieved from https://atrium.lib.uoguelph.ca/xmlui/handle/10214/18037

Chicago Manual of Style (16th Edition):

Wong, Jeremy. “Investigating single-nucleotide variants in swine associated with common infectious pathogens and diseases, with a focus on Streptococcus suis infection, using a genome-wide association study approach.” 2020. Masters Thesis, University of Guelph. Accessed October 20, 2020. https://atrium.lib.uoguelph.ca/xmlui/handle/10214/18037.

MLA Handbook (7th Edition):

Wong, Jeremy. “Investigating single-nucleotide variants in swine associated with common infectious pathogens and diseases, with a focus on Streptococcus suis infection, using a genome-wide association study approach.” 2020. Web. 20 Oct 2020.

Vancouver:

Wong J. Investigating single-nucleotide variants in swine associated with common infectious pathogens and diseases, with a focus on Streptococcus suis infection, using a genome-wide association study approach. [Internet] [Masters thesis]. University of Guelph; 2020. [cited 2020 Oct 20]. Available from: https://atrium.lib.uoguelph.ca/xmlui/handle/10214/18037.

Council of Science Editors:

Wong J. Investigating single-nucleotide variants in swine associated with common infectious pathogens and diseases, with a focus on Streptococcus suis infection, using a genome-wide association study approach. [Masters Thesis]. University of Guelph; 2020. Available from: https://atrium.lib.uoguelph.ca/xmlui/handle/10214/18037

9. Schwender, Holger. Statistical analysis of genotype and gene expression data.

Degree: 2007, Technische Universität Dortmund

 A common and important goal in cancer research is the identification of genetic markers such as genes or genetic variations that enable to determine if… (more)

Subjects/Keywords: Cancer risk; Classification; Microarray; Preprocessing; Single nucleotide polymorphism; SNP; Variable selection; 310

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APA (6th Edition):

Schwender, H. (2007). Statistical analysis of genotype and gene expression data. (Thesis). Technische Universität Dortmund. Retrieved from http://hdl.handle.net/2003/23306

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):

Schwender, Holger. “Statistical analysis of genotype and gene expression data.” 2007. Thesis, Technische Universität Dortmund. Accessed October 20, 2020. http://hdl.handle.net/2003/23306.

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

MLA Handbook (7th Edition):

Schwender, Holger. “Statistical analysis of genotype and gene expression data.” 2007. Web. 20 Oct 2020.

Vancouver:

Schwender H. Statistical analysis of genotype and gene expression data. [Internet] [Thesis]. Technische Universität Dortmund; 2007. [cited 2020 Oct 20]. Available from: http://hdl.handle.net/2003/23306.

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

Council of Science Editors:

Schwender H. Statistical analysis of genotype and gene expression data. [Thesis]. Technische Universität Dortmund; 2007. Available from: http://hdl.handle.net/2003/23306

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


University of Alberta

10. Islam, Khandker Khaldun. Association analyses of SNPs in candidate genes with body fat deposition and carcass merit traits in beef cattle.

Degree: MS, Department of Agricultural, Food and Nutritional Science, 2009, University of Alberta

 A candidate gene approach was used to identify single nucleotide polymorphisms (SNPs) and their associations with body fat deposition and carcass merit traits in beef… (more)

Subjects/Keywords: Beef cattle; Association analyses; Body fat deposition; Carcass trait; Single nucleotide polymorphism; Candidate gene; SNP

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APA (6th Edition):

Islam, K. K. (2009). Association analyses of SNPs in candidate genes with body fat deposition and carcass merit traits in beef cattle. (Masters Thesis). University of Alberta. Retrieved from https://era.library.ualberta.ca/files/pv63g042c

Chicago Manual of Style (16th Edition):

Islam, Khandker Khaldun. “Association analyses of SNPs in candidate genes with body fat deposition and carcass merit traits in beef cattle.” 2009. Masters Thesis, University of Alberta. Accessed October 20, 2020. https://era.library.ualberta.ca/files/pv63g042c.

MLA Handbook (7th Edition):

Islam, Khandker Khaldun. “Association analyses of SNPs in candidate genes with body fat deposition and carcass merit traits in beef cattle.” 2009. Web. 20 Oct 2020.

Vancouver:

Islam KK. Association analyses of SNPs in candidate genes with body fat deposition and carcass merit traits in beef cattle. [Internet] [Masters thesis]. University of Alberta; 2009. [cited 2020 Oct 20]. Available from: https://era.library.ualberta.ca/files/pv63g042c.

Council of Science Editors:

Islam KK. Association analyses of SNPs in candidate genes with body fat deposition and carcass merit traits in beef cattle. [Masters Thesis]. University of Alberta; 2009. Available from: https://era.library.ualberta.ca/files/pv63g042c


University of Tasmania

11. Hadjigol, S. Evidence for natural selection acting on genes affecting lignin and cellulose biosynthesis in Eucalyptus globulus.

Degree: 2012, University of Tasmania

 Eucalyptus globulus (Myrtaceae) is a forest tree species that is native to South-eastern Australia, including the island of Tasmania. It is the main eucalypt species… (more)

Subjects/Keywords: natural selection; wood properties; molecular approach; candidate gene; Eglobulus; single nucleotide Polymorphism (SNP)

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APA (6th Edition):

Hadjigol, S. (2012). Evidence for natural selection acting on genes affecting lignin and cellulose biosynthesis in Eucalyptus globulus. (Thesis). University of Tasmania. Retrieved from https://eprints.utas.edu.au/12930/2/Whole_thesis_030112.pdf

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):

Hadjigol, S. “Evidence for natural selection acting on genes affecting lignin and cellulose biosynthesis in Eucalyptus globulus.” 2012. Thesis, University of Tasmania. Accessed October 20, 2020. https://eprints.utas.edu.au/12930/2/Whole_thesis_030112.pdf.

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

MLA Handbook (7th Edition):

Hadjigol, S. “Evidence for natural selection acting on genes affecting lignin and cellulose biosynthesis in Eucalyptus globulus.” 2012. Web. 20 Oct 2020.

Vancouver:

Hadjigol S. Evidence for natural selection acting on genes affecting lignin and cellulose biosynthesis in Eucalyptus globulus. [Internet] [Thesis]. University of Tasmania; 2012. [cited 2020 Oct 20]. Available from: https://eprints.utas.edu.au/12930/2/Whole_thesis_030112.pdf.

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

Council of Science Editors:

Hadjigol S. Evidence for natural selection acting on genes affecting lignin and cellulose biosynthesis in Eucalyptus globulus. [Thesis]. University of Tasmania; 2012. Available from: https://eprints.utas.edu.au/12930/2/Whole_thesis_030112.pdf

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


University of Georgia

12. Sprolden, Tracy Lashonda. Double eQTL mapping method to improve identification of trans eQTLs and construct intermediate gene networks.

Degree: 2014, University of Georgia

 A double eQTL mapping method for identifying trans eQTLs that reduces multiple testing and increases the statistical power of eQTL mapping is described. The first… (more)

Subjects/Keywords: Single nucleotide polymorphism (SNP); Expression quantitative trait loci (eQTL); Microarray; Cis eQTL; Trans eQTL

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APA (6th Edition):

Sprolden, T. L. (2014). Double eQTL mapping method to improve identification of trans eQTLs and construct intermediate gene networks. (Thesis). University of Georgia. Retrieved from http://hdl.handle.net/10724/28916

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):

Sprolden, Tracy Lashonda. “Double eQTL mapping method to improve identification of trans eQTLs and construct intermediate gene networks.” 2014. Thesis, University of Georgia. Accessed October 20, 2020. http://hdl.handle.net/10724/28916.

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

MLA Handbook (7th Edition):

Sprolden, Tracy Lashonda. “Double eQTL mapping method to improve identification of trans eQTLs and construct intermediate gene networks.” 2014. Web. 20 Oct 2020.

Vancouver:

Sprolden TL. Double eQTL mapping method to improve identification of trans eQTLs and construct intermediate gene networks. [Internet] [Thesis]. University of Georgia; 2014. [cited 2020 Oct 20]. Available from: http://hdl.handle.net/10724/28916.

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

Council of Science Editors:

Sprolden TL. Double eQTL mapping method to improve identification of trans eQTLs and construct intermediate gene networks. [Thesis]. University of Georgia; 2014. Available from: http://hdl.handle.net/10724/28916

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


Stellenbosch University

13. Sandenbergh, Lise. Identification of SNPs associated with robustness and greater reproductive success in the South African merino sheep using SNP chip technology.

Degree: PhD, Genetics, 2015, Stellenbosch University

 ENGLISH ABSTRACT: Reproduction and robustness traits are integral in ensuring sustainable, efficient and profitable sheep farming. Increases in genetic gain of reproduction and robustness traits… (more)

Subjects/Keywords: Merino sheep  – South Africa; Merino sheep  – South Africa  – Breeding; SNP (Single nucleotide polymorphism); UCTD

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APA (6th Edition):

Sandenbergh, L. (2015). Identification of SNPs associated with robustness and greater reproductive success in the South African merino sheep using SNP chip technology. (Doctoral Dissertation). Stellenbosch University. Retrieved from http://hdl.handle.net/10019.1/97093

Chicago Manual of Style (16th Edition):

Sandenbergh, Lise. “Identification of SNPs associated with robustness and greater reproductive success in the South African merino sheep using SNP chip technology.” 2015. Doctoral Dissertation, Stellenbosch University. Accessed October 20, 2020. http://hdl.handle.net/10019.1/97093.

MLA Handbook (7th Edition):

Sandenbergh, Lise. “Identification of SNPs associated with robustness and greater reproductive success in the South African merino sheep using SNP chip technology.” 2015. Web. 20 Oct 2020.

Vancouver:

Sandenbergh L. Identification of SNPs associated with robustness and greater reproductive success in the South African merino sheep using SNP chip technology. [Internet] [Doctoral dissertation]. Stellenbosch University; 2015. [cited 2020 Oct 20]. Available from: http://hdl.handle.net/10019.1/97093.

Council of Science Editors:

Sandenbergh L. Identification of SNPs associated with robustness and greater reproductive success in the South African merino sheep using SNP chip technology. [Doctoral Dissertation]. Stellenbosch University; 2015. Available from: http://hdl.handle.net/10019.1/97093

14. 김, 보영. The Role of Annexin A6 in Osteoporosis.

Degree: 2011, Ajou University

 Osteoporosis is a common calcium and metabolic skeletal disease which is characterized by decreased bone mass, microarchitectural deterioration of bone tissue and impaired bone strength,… (more)

Subjects/Keywords: osteoporosis; Annexin A6 (ANXA6); osteoblast; bone mineral density (BMD); single nucleotide polymorphism (SNP)

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

APA (6th Edition):

김, . (2011). The Role of Annexin A6 in Osteoporosis. (Thesis). Ajou University. Retrieved from http://repository.ajou.ac.kr/handle/201003/4392 ; http://dcoll.ajou.ac.kr:9080/dcollection/jsp/common/DcLoOrgPer.jsp?sItemId=000000011786

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):

김, 보영. “The Role of Annexin A6 in Osteoporosis.” 2011. Thesis, Ajou University. Accessed October 20, 2020. http://repository.ajou.ac.kr/handle/201003/4392 ; http://dcoll.ajou.ac.kr:9080/dcollection/jsp/common/DcLoOrgPer.jsp?sItemId=000000011786.

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

MLA Handbook (7th Edition):

김, 보영. “The Role of Annexin A6 in Osteoporosis.” 2011. Web. 20 Oct 2020.

Vancouver:

김 . The Role of Annexin A6 in Osteoporosis. [Internet] [Thesis]. Ajou University; 2011. [cited 2020 Oct 20]. Available from: http://repository.ajou.ac.kr/handle/201003/4392 ; http://dcoll.ajou.ac.kr:9080/dcollection/jsp/common/DcLoOrgPer.jsp?sItemId=000000011786.

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

Council of Science Editors:

김 . The Role of Annexin A6 in Osteoporosis. [Thesis]. Ajou University; 2011. Available from: http://repository.ajou.ac.kr/handle/201003/4392 ; http://dcoll.ajou.ac.kr:9080/dcollection/jsp/common/DcLoOrgPer.jsp?sItemId=000000011786

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


Univerzitet u Beogradu

15. Đorđević, Jelena Z., 1974-. Značaj genskih polimorfizama IL28B u predikciji stabilnog virusološkog odgovora pacijanta sa hroničnim C hepatitisom.

Degree: Medicinski fakultet, 2015, Univerzitet u Beogradu

gastroenterologija i hepatologija / gastroenterology and hepatology

UVOD: IL28B polimorfizmi se smatraju važnim prognostičkim faktorom za ishod terapije pacijenata sa hroničnim C hepatitisom koji se… (more)

Subjects/Keywords: IL28B; Hepatitis C virus (HCV); single nucleotide polymorphism (SNP); sustained virological response (SVR)

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

APA (6th Edition):

Đorđević, Jelena Z., 1. (2015). Značaj genskih polimorfizama IL28B u predikciji stabilnog virusološkog odgovora pacijanta sa hroničnim C hepatitisom. (Thesis). Univerzitet u Beogradu. Retrieved from https://fedorabg.bg.ac.rs/fedora/get/o:9829/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):

Đorđević, Jelena Z., 1974-. “Značaj genskih polimorfizama IL28B u predikciji stabilnog virusološkog odgovora pacijanta sa hroničnim C hepatitisom.” 2015. Thesis, Univerzitet u Beogradu. Accessed October 20, 2020. https://fedorabg.bg.ac.rs/fedora/get/o:9829/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):

Đorđević, Jelena Z., 1974-. “Značaj genskih polimorfizama IL28B u predikciji stabilnog virusološkog odgovora pacijanta sa hroničnim C hepatitisom.” 2015. Web. 20 Oct 2020.

Vancouver:

Đorđević, Jelena Z. 1. Značaj genskih polimorfizama IL28B u predikciji stabilnog virusološkog odgovora pacijanta sa hroničnim C hepatitisom. [Internet] [Thesis]. Univerzitet u Beogradu; 2015. [cited 2020 Oct 20]. Available from: https://fedorabg.bg.ac.rs/fedora/get/o:9829/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:

Đorđević, Jelena Z. 1. Značaj genskih polimorfizama IL28B u predikciji stabilnog virusološkog odgovora pacijanta sa hroničnim C hepatitisom. [Thesis]. Univerzitet u Beogradu; 2015. Available from: https://fedorabg.bg.ac.rs/fedora/get/o:9829/bdef:Content/get

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


George Mason University

16. Harrif, Khatera Noor. The Use of “Omics” in Next Generation SNP Analysis: Future of Forensic Phenotyping .

Degree: 2012, George Mason University

 When a crime occurs, investigators collect samples from the crime scene and interview witnesses to learn the External Visible Characteristics (EVCs) of the suspect. This… (more)

Subjects/Keywords: Forensic Phenotyping; Next Generation Sequencing; External Visible Characteristics; Single Nucleotide Polymorphism; EVCS; SNP Analysis

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

APA (6th Edition):

Harrif, K. N. (2012). The Use of “Omics” in Next Generation SNP Analysis: Future of Forensic Phenotyping . (Thesis). George Mason University. Retrieved from http://hdl.handle.net/1920/7862

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):

Harrif, Khatera Noor. “The Use of “Omics” in Next Generation SNP Analysis: Future of Forensic Phenotyping .” 2012. Thesis, George Mason University. Accessed October 20, 2020. http://hdl.handle.net/1920/7862.

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

MLA Handbook (7th Edition):

Harrif, Khatera Noor. “The Use of “Omics” in Next Generation SNP Analysis: Future of Forensic Phenotyping .” 2012. Web. 20 Oct 2020.

Vancouver:

Harrif KN. The Use of “Omics” in Next Generation SNP Analysis: Future of Forensic Phenotyping . [Internet] [Thesis]. George Mason University; 2012. [cited 2020 Oct 20]. Available from: http://hdl.handle.net/1920/7862.

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

Council of Science Editors:

Harrif KN. The Use of “Omics” in Next Generation SNP Analysis: Future of Forensic Phenotyping . [Thesis]. George Mason University; 2012. Available from: http://hdl.handle.net/1920/7862

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


University of Western Ontario

17. Findlay, Scott D. Comprehensive Molecular Characterization of Human NODAL.

Degree: 2016, University of Western Ontario

 Nodal and related ligands are highly conserved members of the TGF-beta superfamily with well-established and essential roles in the early embryonic development of vertebrates, and… (more)

Subjects/Keywords: NODAL; human embryonic stem cells; pluripotency; cancer; single nucleotide polymorphism (SNP); alternative splicing; Molecular Biology

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APA (6th Edition):

Findlay, S. D. (2016). Comprehensive Molecular Characterization of Human NODAL. (Thesis). University of Western Ontario. Retrieved from https://ir.lib.uwo.ca/etd/4277

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):

Findlay, Scott D. “Comprehensive Molecular Characterization of Human NODAL.” 2016. Thesis, University of Western Ontario. Accessed October 20, 2020. https://ir.lib.uwo.ca/etd/4277.

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

MLA Handbook (7th Edition):

Findlay, Scott D. “Comprehensive Molecular Characterization of Human NODAL.” 2016. Web. 20 Oct 2020.

Vancouver:

Findlay SD. Comprehensive Molecular Characterization of Human NODAL. [Internet] [Thesis]. University of Western Ontario; 2016. [cited 2020 Oct 20]. Available from: https://ir.lib.uwo.ca/etd/4277.

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

Council of Science Editors:

Findlay SD. Comprehensive Molecular Characterization of Human NODAL. [Thesis]. University of Western Ontario; 2016. Available from: https://ir.lib.uwo.ca/etd/4277

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


University of Southern California

18. Rand, Kristin Alyse. Genetic risk factors in multiple myeloma.

Degree: PhD, Epidemiology, 2012, University of Southern California

 Multiple myeloma (MM) is a malignancy of the plasma cells, accounting for 1% of all cancer deaths and 20% of all hematological cancer deaths. In… (more)

Subjects/Keywords: multiple myeloma; epidemiology; single nucleotide polymorphism; SNP; genetic risk factors; hematologic malignancy

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

APA (6th Edition):

Rand, K. A. (2012). Genetic risk factors in multiple myeloma. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/119332/rec/3008

Chicago Manual of Style (16th Edition):

Rand, Kristin Alyse. “Genetic risk factors in multiple myeloma.” 2012. Doctoral Dissertation, University of Southern California. Accessed October 20, 2020. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/119332/rec/3008.

MLA Handbook (7th Edition):

Rand, Kristin Alyse. “Genetic risk factors in multiple myeloma.” 2012. Web. 20 Oct 2020.

Vancouver:

Rand KA. Genetic risk factors in multiple myeloma. [Internet] [Doctoral dissertation]. University of Southern California; 2012. [cited 2020 Oct 20]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/119332/rec/3008.

Council of Science Editors:

Rand KA. Genetic risk factors in multiple myeloma. [Doctoral Dissertation]. University of Southern California; 2012. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/119332/rec/3008


NSYSU

19. Wu, Nein-chi. Single Nucleotide Polymorphism Analysis of the Metastasis Supressor RECK Gene Promoter and Itâs Clinical Significance.

Degree: Master, Institute of Biomedical Sciences, 2011, NSYSU

 Reversion-inducing cysteine-rich with Kazal motif (RECK) is a cell surface anchoring protein, which known for the ability to inhibit matrix metalloproteinases (MMPs) and participate in… (more)

Subjects/Keywords: RECK promoter; Reversion-inducing cysteine-rich with Kazal motif; RECK; RECK SNP; SNP; single nucleotide polymorphism

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

APA (6th Edition):

Wu, N. (2011). Single Nucleotide Polymorphism Analysis of the Metastasis Supressor RECK Gene Promoter and Itâs Clinical Significance. (Thesis). NSYSU. Retrieved from http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0809111-202826

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, Nein-chi. “Single Nucleotide Polymorphism Analysis of the Metastasis Supressor RECK Gene Promoter and Itâs Clinical Significance.” 2011. Thesis, NSYSU. Accessed October 20, 2020. http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0809111-202826.

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

MLA Handbook (7th Edition):

Wu, Nein-chi. “Single Nucleotide Polymorphism Analysis of the Metastasis Supressor RECK Gene Promoter and Itâs Clinical Significance.” 2011. Web. 20 Oct 2020.

Vancouver:

Wu N. Single Nucleotide Polymorphism Analysis of the Metastasis Supressor RECK Gene Promoter and Itâs Clinical Significance. [Internet] [Thesis]. NSYSU; 2011. [cited 2020 Oct 20]. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0809111-202826.

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

Council of Science Editors:

Wu N. Single Nucleotide Polymorphism Analysis of the Metastasis Supressor RECK Gene Promoter and Itâs Clinical Significance. [Thesis]. NSYSU; 2011. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0809111-202826

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

20. VILLAR, Kamila de Melo. Associação de polimorfismos no gene IL22RA1 como os níveis séricos de IL-22 e com parâmetros clínicos de pacientes portadores de artrite reumatoide .

Degree: 2015, Universidade Federal de Pernambuco

 O processo inflamatório associado à liberação de citocinas está diretamente envolvido na patogênese da artrite reumatóide (AR). Um estudo anterior do nosso grupo relatou que… (more)

Subjects/Keywords: Artrite Reumatóide, IL-22, IL22RA1, SNP (Polimorfismo de Nucleotídeo Único).; Rheumatoid Arthritis,IL22, IL22RA1. Polymorphisms, SNP (Single Nucleotide Polymorphism

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APA (6th Edition):

VILLAR, K. d. M. (2015). Associação de polimorfismos no gene IL22RA1 como os níveis séricos de IL-22 e com parâmetros clínicos de pacientes portadores de artrite reumatoide . (Thesis). Universidade Federal de Pernambuco. Retrieved from http://repositorio.ufpe.br/handle/123456789/17169

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):

VILLAR, Kamila de Melo. “Associação de polimorfismos no gene IL22RA1 como os níveis séricos de IL-22 e com parâmetros clínicos de pacientes portadores de artrite reumatoide .” 2015. Thesis, Universidade Federal de Pernambuco. Accessed October 20, 2020. http://repositorio.ufpe.br/handle/123456789/17169.

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

MLA Handbook (7th Edition):

VILLAR, Kamila de Melo. “Associação de polimorfismos no gene IL22RA1 como os níveis séricos de IL-22 e com parâmetros clínicos de pacientes portadores de artrite reumatoide .” 2015. Web. 20 Oct 2020.

Vancouver:

VILLAR KdM. Associação de polimorfismos no gene IL22RA1 como os níveis séricos de IL-22 e com parâmetros clínicos de pacientes portadores de artrite reumatoide . [Internet] [Thesis]. Universidade Federal de Pernambuco; 2015. [cited 2020 Oct 20]. Available from: http://repositorio.ufpe.br/handle/123456789/17169.

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

Council of Science Editors:

VILLAR KdM. Associação de polimorfismos no gene IL22RA1 como os níveis séricos de IL-22 e com parâmetros clínicos de pacientes portadores de artrite reumatoide . [Thesis]. Universidade Federal de Pernambuco; 2015. Available from: http://repositorio.ufpe.br/handle/123456789/17169

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

21. Paulos Pinheiro, Sofia. Epidemiologia genética do Acidente Vascular Cerebral: identificação de genes envolvidos na susceptibilidade e na recuperação do doente.

Degree: 2012, RCAAP

Dissertação de Mestrado em Biologia Humana e Ambiente apresentada à Faculdade de Ciências de Universidade de Lisboa, 2012.

Dissertação defendida e aprovada em 12 de… (more)

Subjects/Keywords: AVC; Susceptibilidade; Recuperação; Single Nucleotide Polymorphism (SNP); Genome Wide Association Study (GWAS); Genes Candidatos; Doenças Cardio e Cérebro-vasculares

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APA (6th Edition):

Paulos Pinheiro, S. (2012). Epidemiologia genética do Acidente Vascular Cerebral: identificação de genes envolvidos na susceptibilidade e na recuperação do doente. (Thesis). RCAAP. Retrieved from http://www.rcaap.pt/detail.jsp?id=oai:repositorio.insa.pt:10400.18/1234

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):

Paulos Pinheiro, Sofia. “Epidemiologia genética do Acidente Vascular Cerebral: identificação de genes envolvidos na susceptibilidade e na recuperação do doente.” 2012. Thesis, RCAAP. Accessed October 20, 2020. http://www.rcaap.pt/detail.jsp?id=oai:repositorio.insa.pt:10400.18/1234.

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

MLA Handbook (7th Edition):

Paulos Pinheiro, Sofia. “Epidemiologia genética do Acidente Vascular Cerebral: identificação de genes envolvidos na susceptibilidade e na recuperação do doente.” 2012. Web. 20 Oct 2020.

Vancouver:

Paulos Pinheiro S. Epidemiologia genética do Acidente Vascular Cerebral: identificação de genes envolvidos na susceptibilidade e na recuperação do doente. [Internet] [Thesis]. RCAAP; 2012. [cited 2020 Oct 20]. Available from: http://www.rcaap.pt/detail.jsp?id=oai:repositorio.insa.pt:10400.18/1234.

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

Council of Science Editors:

Paulos Pinheiro S. Epidemiologia genética do Acidente Vascular Cerebral: identificação de genes envolvidos na susceptibilidade e na recuperação do doente. [Thesis]. RCAAP; 2012. Available from: http://www.rcaap.pt/detail.jsp?id=oai:repositorio.insa.pt:10400.18/1234

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

22. Müller, Tina. Local analysis of high dimensional genetic data considering interaction effects.

Degree: 2010, Technische Universität Dortmund

Subjects/Keywords: Cluster; Klassifikation; Single Nucleotide Polymorphism; SNP; 310

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

APA (6th Edition):

Müller, T. (2010). Local analysis of high dimensional genetic data considering interaction effects. (Thesis). Technische Universität Dortmund. Retrieved from http://hdl.handle.net/2003/26997

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):

Müller, Tina. “Local analysis of high dimensional genetic data considering interaction effects.” 2010. Thesis, Technische Universität Dortmund. Accessed October 20, 2020. http://hdl.handle.net/2003/26997.

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

MLA Handbook (7th Edition):

Müller, Tina. “Local analysis of high dimensional genetic data considering interaction effects.” 2010. Web. 20 Oct 2020.

Vancouver:

Müller T. Local analysis of high dimensional genetic data considering interaction effects. [Internet] [Thesis]. Technische Universität Dortmund; 2010. [cited 2020 Oct 20]. Available from: http://hdl.handle.net/2003/26997.

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

Council of Science Editors:

Müller T. Local analysis of high dimensional genetic data considering interaction effects. [Thesis]. Technische Universität Dortmund; 2010. Available from: http://hdl.handle.net/2003/26997

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


Texas A&M University

23. Jones, Brittany. Genetic and Phylogenetic Studies of Toll-Like Receptor 5 (TLR5) in River Buffalo (Bubalus Bubalis).

Degree: PhD, Veterinary Microbiology, 2012, Texas A&M University

 River buffalo are economically important to many countries and only recently has their genome been explored for the purpose of mapping genetic variation in traits… (more)

Subjects/Keywords: radiation hybrid (RH) mapping; phylogenetics; single-nucleotide polymorphism (SNP); toll-like receptor 5 (TLR5); innate immunity; river buffalo

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APA (6th Edition):

Jones, B. (2012). Genetic and Phylogenetic Studies of Toll-Like Receptor 5 (TLR5) in River Buffalo (Bubalus Bubalis). (Doctoral Dissertation). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/148100

Chicago Manual of Style (16th Edition):

Jones, Brittany. “Genetic and Phylogenetic Studies of Toll-Like Receptor 5 (TLR5) in River Buffalo (Bubalus Bubalis).” 2012. Doctoral Dissertation, Texas A&M University. Accessed October 20, 2020. http://hdl.handle.net/1969.1/148100.

MLA Handbook (7th Edition):

Jones, Brittany. “Genetic and Phylogenetic Studies of Toll-Like Receptor 5 (TLR5) in River Buffalo (Bubalus Bubalis).” 2012. Web. 20 Oct 2020.

Vancouver:

Jones B. Genetic and Phylogenetic Studies of Toll-Like Receptor 5 (TLR5) in River Buffalo (Bubalus Bubalis). [Internet] [Doctoral dissertation]. Texas A&M University; 2012. [cited 2020 Oct 20]. Available from: http://hdl.handle.net/1969.1/148100.

Council of Science Editors:

Jones B. Genetic and Phylogenetic Studies of Toll-Like Receptor 5 (TLR5) in River Buffalo (Bubalus Bubalis). [Doctoral Dissertation]. Texas A&M University; 2012. Available from: http://hdl.handle.net/1969.1/148100


Brigham Young University

24. Eldon, Desiree Rochelle. Population Genetic Structure of Bromus tectorum in the American Desert Southwest.

Degree: MS, 2013, Brigham Young University

  Following its introduction to North America in the late nineteenth century, Bromus tectorum L., an inbreeding invasive winter annual grass, has become dominant on… (more)

Subjects/Keywords: Bromus tectorum; cheatgrass; single nucleotide polymorphism; SNP genotyping; Mojave Desert; Intermountain West; invasive species; ecological genetics; Animal Sciences

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APA (6th Edition):

Eldon, D. R. (2013). Population Genetic Structure of Bromus tectorum in the American Desert Southwest. (Masters Thesis). Brigham Young University. Retrieved from https://scholarsarchive.byu.edu/cgi/viewcontent.cgi?article=5272&context=etd

Chicago Manual of Style (16th Edition):

Eldon, Desiree Rochelle. “Population Genetic Structure of Bromus tectorum in the American Desert Southwest.” 2013. Masters Thesis, Brigham Young University. Accessed October 20, 2020. https://scholarsarchive.byu.edu/cgi/viewcontent.cgi?article=5272&context=etd.

MLA Handbook (7th Edition):

Eldon, Desiree Rochelle. “Population Genetic Structure of Bromus tectorum in the American Desert Southwest.” 2013. Web. 20 Oct 2020.

Vancouver:

Eldon DR. Population Genetic Structure of Bromus tectorum in the American Desert Southwest. [Internet] [Masters thesis]. Brigham Young University; 2013. [cited 2020 Oct 20]. Available from: https://scholarsarchive.byu.edu/cgi/viewcontent.cgi?article=5272&context=etd.

Council of Science Editors:

Eldon DR. Population Genetic Structure of Bromus tectorum in the American Desert Southwest. [Masters Thesis]. Brigham Young University; 2013. Available from: https://scholarsarchive.byu.edu/cgi/viewcontent.cgi?article=5272&context=etd

25. Müller, Tina. Local analysis of high dimensional genetic data considering interaction effects.

Degree: 2010, Technische Universität Dortmund

Subjects/Keywords: SNP; Klassifikation; Cluster; Single Nucleotide Polymorphism; 310

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Müller, T. (2010). Local analysis of high dimensional genetic data considering interaction effects. (Doctoral Dissertation). Technische Universität Dortmund. Retrieved from http://dx.doi.org/10.17877/DE290R-34

Chicago Manual of Style (16th Edition):

Müller, Tina. “Local analysis of high dimensional genetic data considering interaction effects.” 2010. Doctoral Dissertation, Technische Universität Dortmund. Accessed October 20, 2020. http://dx.doi.org/10.17877/DE290R-34.

MLA Handbook (7th Edition):

Müller, Tina. “Local analysis of high dimensional genetic data considering interaction effects.” 2010. Web. 20 Oct 2020.

Vancouver:

Müller T. Local analysis of high dimensional genetic data considering interaction effects. [Internet] [Doctoral dissertation]. Technische Universität Dortmund; 2010. [cited 2020 Oct 20]. Available from: http://dx.doi.org/10.17877/DE290R-34.

Council of Science Editors:

Müller T. Local analysis of high dimensional genetic data considering interaction effects. [Doctoral Dissertation]. Technische Universität Dortmund; 2010. Available from: http://dx.doi.org/10.17877/DE290R-34


Queensland University of Technology

26. Carter, Shea L. The genetic basis of human height : the role of estrogen.

Degree: 2008, Queensland University of Technology

 Height is a complex physical trait that displays strong heritability. Adult height is related to length of the long bones, which is determined by growth… (more)

Subjects/Keywords: estrogen; growth hormone; matrix metalloproteinase 13 (MMP13); chondrocytes; height; longitudinal bone growth; epiphyseal growth plate; single nucleotide polymorphism (SNP); chondrosarcoma; osteoarthritis

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

APA (6th Edition):

Carter, S. L. (2008). The genetic basis of human height : the role of estrogen. (Thesis). Queensland University of Technology. Retrieved from https://eprints.qut.edu.au/28390/

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):

Carter, Shea L. “The genetic basis of human height : the role of estrogen.” 2008. Thesis, Queensland University of Technology. Accessed October 20, 2020. https://eprints.qut.edu.au/28390/.

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

MLA Handbook (7th Edition):

Carter, Shea L. “The genetic basis of human height : the role of estrogen.” 2008. Web. 20 Oct 2020.

Vancouver:

Carter SL. The genetic basis of human height : the role of estrogen. [Internet] [Thesis]. Queensland University of Technology; 2008. [cited 2020 Oct 20]. Available from: https://eprints.qut.edu.au/28390/.

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

Council of Science Editors:

Carter SL. The genetic basis of human height : the role of estrogen. [Thesis]. Queensland University of Technology; 2008. Available from: https://eprints.qut.edu.au/28390/

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


University of Guelph

27. Diaz Castro, Esteban. Quantitative Trait Loci (QTL) for Common Bacterial Blight Resistance and Agronomic and Developmental Traits in Common Bean (Phaseolus vulgaris L.).

Degree: MS, Department of Plant Agriculture, 2015, University of Guelph

 Common Bacterial Blight (CBB; caused by Xanthomonas axonopodis pv. phaseoli) is a major constraint in dry bean (Phaseolus vulgaris L.) production worldwide. Mapping of quantitative… (more)

Subjects/Keywords: Common bean; Phaseolus vulgaris L.; QTL mapping; Single Nucleotide Polymorphism; SNP; Common bacterial blight; Development traits

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

APA (6th Edition):

Diaz Castro, E. (2015). Quantitative Trait Loci (QTL) for Common Bacterial Blight Resistance and Agronomic and Developmental Traits in Common Bean (Phaseolus vulgaris L.). (Masters Thesis). University of Guelph. Retrieved from https://atrium.lib.uoguelph.ca/xmlui/handle/10214/9294

Chicago Manual of Style (16th Edition):

Diaz Castro, Esteban. “Quantitative Trait Loci (QTL) for Common Bacterial Blight Resistance and Agronomic and Developmental Traits in Common Bean (Phaseolus vulgaris L.).” 2015. Masters Thesis, University of Guelph. Accessed October 20, 2020. https://atrium.lib.uoguelph.ca/xmlui/handle/10214/9294.

MLA Handbook (7th Edition):

Diaz Castro, Esteban. “Quantitative Trait Loci (QTL) for Common Bacterial Blight Resistance and Agronomic and Developmental Traits in Common Bean (Phaseolus vulgaris L.).” 2015. Web. 20 Oct 2020.

Vancouver:

Diaz Castro E. Quantitative Trait Loci (QTL) for Common Bacterial Blight Resistance and Agronomic and Developmental Traits in Common Bean (Phaseolus vulgaris L.). [Internet] [Masters thesis]. University of Guelph; 2015. [cited 2020 Oct 20]. Available from: https://atrium.lib.uoguelph.ca/xmlui/handle/10214/9294.

Council of Science Editors:

Diaz Castro E. Quantitative Trait Loci (QTL) for Common Bacterial Blight Resistance and Agronomic and Developmental Traits in Common Bean (Phaseolus vulgaris L.). [Masters Thesis]. University of Guelph; 2015. Available from: https://atrium.lib.uoguelph.ca/xmlui/handle/10214/9294


Brigham Young University

28. Byers, Robert L. Marker Discovery in Allotetraploid Cotton Using 454 Pyrosequencing.

Degree: MS, 2011, Brigham Young University

  A narrow germplasm base and a complex allotetraploid genome have historically made the discovery of single nucleotide polymorphism (SNP) markers difficult in cotton (Gossypium… (more)

Subjects/Keywords: allotetraploid; cotton; EST; expressed sequence tag; genetic map; Gossypium; genome reduction; pyrosequencing; polyploidy; single nucleotide polymorphism; SNP; Animal Sciences

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

APA (6th Edition):

Byers, R. L. (2011). Marker Discovery in Allotetraploid Cotton Using 454 Pyrosequencing. (Masters Thesis). Brigham Young University. Retrieved from https://scholarsarchive.byu.edu/cgi/viewcontent.cgi?article=3662&context=etd

Chicago Manual of Style (16th Edition):

Byers, Robert L. “Marker Discovery in Allotetraploid Cotton Using 454 Pyrosequencing.” 2011. Masters Thesis, Brigham Young University. Accessed October 20, 2020. https://scholarsarchive.byu.edu/cgi/viewcontent.cgi?article=3662&context=etd.

MLA Handbook (7th Edition):

Byers, Robert L. “Marker Discovery in Allotetraploid Cotton Using 454 Pyrosequencing.” 2011. Web. 20 Oct 2020.

Vancouver:

Byers RL. Marker Discovery in Allotetraploid Cotton Using 454 Pyrosequencing. [Internet] [Masters thesis]. Brigham Young University; 2011. [cited 2020 Oct 20]. Available from: https://scholarsarchive.byu.edu/cgi/viewcontent.cgi?article=3662&context=etd.

Council of Science Editors:

Byers RL. Marker Discovery in Allotetraploid Cotton Using 454 Pyrosequencing. [Masters Thesis]. Brigham Young University; 2011. Available from: https://scholarsarchive.byu.edu/cgi/viewcontent.cgi?article=3662&context=etd


Freie Universität Berlin

29. Rau, Carolin. Implication of the erythropoietin promotor polymorphism rs1617640 in premature infants with severe retinopathy of prematurity.

Degree: 2016, Freie Universität Berlin

 Introduction: Very premature infants can develop a proliferative retinopathy (ROP) caused by excessive retinal neovascularizations which can lead to retinal detachment and blindness. These neovascularizations… (more)

Subjects/Keywords: retinopathy; prematurity; erythropoietin; rhEpo; single nucleotide polymorphism; SNP; promotor; rs1617640; neuroprotection; 600 Technik, Medizin, angewandte Wissenschaften::610 Medizin und Gesundheit

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

APA (6th Edition):

Rau, C. (2016). Implication of the erythropoietin promotor polymorphism rs1617640 in premature infants with severe retinopathy of prematurity. (Thesis). Freie Universität Berlin. Retrieved from http://dx.doi.org/10.17169/refubium-10047

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):

Rau, Carolin. “Implication of the erythropoietin promotor polymorphism rs1617640 in premature infants with severe retinopathy of prematurity.” 2016. Thesis, Freie Universität Berlin. Accessed October 20, 2020. http://dx.doi.org/10.17169/refubium-10047.

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

MLA Handbook (7th Edition):

Rau, Carolin. “Implication of the erythropoietin promotor polymorphism rs1617640 in premature infants with severe retinopathy of prematurity.” 2016. Web. 20 Oct 2020.

Vancouver:

Rau C. Implication of the erythropoietin promotor polymorphism rs1617640 in premature infants with severe retinopathy of prematurity. [Internet] [Thesis]. Freie Universität Berlin; 2016. [cited 2020 Oct 20]. Available from: http://dx.doi.org/10.17169/refubium-10047.

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

Council of Science Editors:

Rau C. Implication of the erythropoietin promotor polymorphism rs1617640 in premature infants with severe retinopathy of prematurity. [Thesis]. Freie Universität Berlin; 2016. Available from: http://dx.doi.org/10.17169/refubium-10047

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

30. Kroscher, Kellie Ann. Creation and characterization of mice with a mutation disrupting binding of a transcriptional repressor of insulin-like growth factor 2.

Degree: MS, Animal Sciences, 2017, University of Illinois – Urbana-Champaign

 Insulin-like growth factor-2 (IGF2) is a key regulator of myogenesis as it promotes differentiation of myoblasts during embryonic and fetal development. A single nucleotide polymorphism(more)

Subjects/Keywords: Insulin-like growth factor-2 (IGF2); Mice; Transcription activator-like effector nucleases (TALEN); Single nucleotide polymorphism (SNP)

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

APA (6th Edition):

Kroscher, K. A. (2017). Creation and characterization of mice with a mutation disrupting binding of a transcriptional repressor of insulin-like growth factor 2. (Thesis). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/98425

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):

Kroscher, Kellie Ann. “Creation and characterization of mice with a mutation disrupting binding of a transcriptional repressor of insulin-like growth factor 2.” 2017. Thesis, University of Illinois – Urbana-Champaign. Accessed October 20, 2020. http://hdl.handle.net/2142/98425.

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

MLA Handbook (7th Edition):

Kroscher, Kellie Ann. “Creation and characterization of mice with a mutation disrupting binding of a transcriptional repressor of insulin-like growth factor 2.” 2017. Web. 20 Oct 2020.

Vancouver:

Kroscher KA. Creation and characterization of mice with a mutation disrupting binding of a transcriptional repressor of insulin-like growth factor 2. [Internet] [Thesis]. University of Illinois – Urbana-Champaign; 2017. [cited 2020 Oct 20]. Available from: http://hdl.handle.net/2142/98425.

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

Council of Science Editors:

Kroscher KA. Creation and characterization of mice with a mutation disrupting binding of a transcriptional repressor of insulin-like growth factor 2. [Thesis]. University of Illinois – Urbana-Champaign; 2017. Available from: http://hdl.handle.net/2142/98425

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

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