Advanced search options

Advanced Search Options 🞨

Browse by author name (“Author name starts with…”).

Find ETDs with:

in
/  
in
/  
in
/  
in

Written in Published in Earliest date Latest date

Sorted by

Results per page:

Sorted by: relevance · author · university · dateNew search

You searched for subject:(Single nucleotide polymorphisms). Showing records 1 – 30 of 176 total matches.

[1] [2] [3] [4] [5] [6]

Search Limiters

Last 2 Years | English Only

Levels

Languages

Country

▼ Search Limiters

1. Bhasin, Yasha. Single nucleotide polymorphisms (SNPs) in complex disorders: a genome-widw computational analysis.

Degree: 2009, University of Pune

Common complex disorders, also known as multifactorial disorders, are characterized by the interactions of multiple genetic and/or environmental factors that influence the expression of a… (more)

Subjects/Keywords: Biotechnology; Single Nucleotide Polymorphisms

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Bhasin, Y. (2009). Single nucleotide polymorphisms (SNPs) in complex disorders: a genome-widw computational analysis. (Thesis). University of Pune. Retrieved from http://shodhganga.inflibnet.ac.in/handle/10603/3417

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):

Bhasin, Yasha. “Single nucleotide polymorphisms (SNPs) in complex disorders: a genome-widw computational analysis.” 2009. Thesis, University of Pune. Accessed October 18, 2019. http://shodhganga.inflibnet.ac.in/handle/10603/3417.

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

MLA Handbook (7th Edition):

Bhasin, Yasha. “Single nucleotide polymorphisms (SNPs) in complex disorders: a genome-widw computational analysis.” 2009. Web. 18 Oct 2019.

Vancouver:

Bhasin Y. Single nucleotide polymorphisms (SNPs) in complex disorders: a genome-widw computational analysis. [Internet] [Thesis]. University of Pune; 2009. [cited 2019 Oct 18]. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/3417.

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

Council of Science Editors:

Bhasin Y. Single nucleotide polymorphisms (SNPs) in complex disorders: a genome-widw computational analysis. [Thesis]. University of Pune; 2009. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/3417

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


Central Connecticut State University

2. Bigiarelli, Krista J. Using SNP analysis to refine a genetic map for the "curly whiskers" mutation in mice.

Degree: Department of Biomolecular Sciences, 2019, Central Connecticut State University

The "curly whiskers" mutation in mice (abbreviated cw) causes recessive hair curling and may also generate a single-gene barrier to tissue-graft acceptance, a combination of… (more)

Subjects/Keywords: Single nucleotide polymorphisms.; Mice.

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Bigiarelli, K. J. (2019). Using SNP analysis to refine a genetic map for the "curly whiskers" mutation in mice. (Thesis). Central Connecticut State University. Retrieved from http://content.library.ccsu.edu/u?/ccsutheses,2929

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):

Bigiarelli, Krista J. “Using SNP analysis to refine a genetic map for the "curly whiskers" mutation in mice.” 2019. Thesis, Central Connecticut State University. Accessed October 18, 2019. http://content.library.ccsu.edu/u?/ccsutheses,2929.

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

MLA Handbook (7th Edition):

Bigiarelli, Krista J. “Using SNP analysis to refine a genetic map for the "curly whiskers" mutation in mice.” 2019. Web. 18 Oct 2019.

Vancouver:

Bigiarelli KJ. Using SNP analysis to refine a genetic map for the "curly whiskers" mutation in mice. [Internet] [Thesis]. Central Connecticut State University; 2019. [cited 2019 Oct 18]. Available from: http://content.library.ccsu.edu/u?/ccsutheses,2929.

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

Council of Science Editors:

Bigiarelli KJ. Using SNP analysis to refine a genetic map for the "curly whiskers" mutation in mice. [Thesis]. Central Connecticut State University; 2019. Available from: http://content.library.ccsu.edu/u?/ccsutheses,2929

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


Hong Kong University of Science and Technology

3. Yang, Guangyuan. Permutation tests for genome-wide association studies.

Degree: 2014, Hong Kong University of Science and Technology

 In genome wide association studies (GWAS), there are single-nucleotide polymorphism (SNP) pairs which have significant associations with diseases via the combination of their main effects… (more)

Subjects/Keywords: Single nucleotide polymorphisms; Testing; Data processing

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Yang, G. (2014). Permutation tests for genome-wide association studies. (Thesis). Hong Kong University of Science and Technology. Retrieved from https://doi.org/10.14711/thesis-b1432208 ; http://repository.ust.hk/ir/bitstream/1783.1-88026/1/th_redirect.html

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

Chicago Manual of Style (16th Edition):

Yang, Guangyuan. “Permutation tests for genome-wide association studies.” 2014. Thesis, Hong Kong University of Science and Technology. Accessed October 18, 2019. https://doi.org/10.14711/thesis-b1432208 ; http://repository.ust.hk/ir/bitstream/1783.1-88026/1/th_redirect.html.

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

MLA Handbook (7th Edition):

Yang, Guangyuan. “Permutation tests for genome-wide association studies.” 2014. Web. 18 Oct 2019.

Vancouver:

Yang G. Permutation tests for genome-wide association studies. [Internet] [Thesis]. Hong Kong University of Science and Technology; 2014. [cited 2019 Oct 18]. Available from: https://doi.org/10.14711/thesis-b1432208 ; http://repository.ust.hk/ir/bitstream/1783.1-88026/1/th_redirect.html.

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

Council of Science Editors:

Yang G. Permutation tests for genome-wide association studies. [Thesis]. Hong Kong University of Science and Technology; 2014. Available from: https://doi.org/10.14711/thesis-b1432208 ; http://repository.ust.hk/ir/bitstream/1783.1-88026/1/th_redirect.html

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


University of Louisville

4. Leggett, Carmine Simone. Functional effects of CYP1A2, NAT1, and NAT2 genetic variants in nucleotide excision repair-deficient human fibroblasts : implications for toxicological risk from environmental arylamines.

Degree: MS, 2010, University of Louisville

 Arylamine N-acetyltransferase 1 (NAT1) and 2 (NAT2) catalyze the detoxification and/or activation of aromatic and heterocyclic amine carcinogens by two pathways. This metabolism reaction can… (more)

Subjects/Keywords: N-acetyltransferase; Arylamines; Single nucleotide polymorphisms (SNPs)

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Leggett, C. S. (2010). Functional effects of CYP1A2, NAT1, and NAT2 genetic variants in nucleotide excision repair-deficient human fibroblasts : implications for toxicological risk from environmental arylamines. (Masters Thesis). University of Louisville. Retrieved from 10.18297/etd/811 ; https://ir.library.louisville.edu/etd/811

Chicago Manual of Style (16th Edition):

Leggett, Carmine Simone. “Functional effects of CYP1A2, NAT1, and NAT2 genetic variants in nucleotide excision repair-deficient human fibroblasts : implications for toxicological risk from environmental arylamines.” 2010. Masters Thesis, University of Louisville. Accessed October 18, 2019. 10.18297/etd/811 ; https://ir.library.louisville.edu/etd/811.

MLA Handbook (7th Edition):

Leggett, Carmine Simone. “Functional effects of CYP1A2, NAT1, and NAT2 genetic variants in nucleotide excision repair-deficient human fibroblasts : implications for toxicological risk from environmental arylamines.” 2010. Web. 18 Oct 2019.

Vancouver:

Leggett CS. Functional effects of CYP1A2, NAT1, and NAT2 genetic variants in nucleotide excision repair-deficient human fibroblasts : implications for toxicological risk from environmental arylamines. [Internet] [Masters thesis]. University of Louisville; 2010. [cited 2019 Oct 18]. Available from: 10.18297/etd/811 ; https://ir.library.louisville.edu/etd/811.

Council of Science Editors:

Leggett CS. Functional effects of CYP1A2, NAT1, and NAT2 genetic variants in nucleotide excision repair-deficient human fibroblasts : implications for toxicological risk from environmental arylamines. [Masters Thesis]. University of Louisville; 2010. Available from: 10.18297/etd/811 ; https://ir.library.louisville.edu/etd/811


University of the Western Cape

5. October, Firzana. Proteomic and SNP analysis of the Cadherin 10 type-II (CDH10) gene, in the South African autistic population .

Degree: 2013, University of the Western Cape

 Autism or autism spectrum disorder (ASD) is a very diverse neurological disorder that manifests specifically in children and infants between the ages of two to… (more)

Subjects/Keywords: Autism; Biomarkers; Mass spectrometry; Single nucleotide polymorphisms

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

October, F. (2013). Proteomic and SNP analysis of the Cadherin 10 type-II (CDH10) gene, in the South African autistic population . (Thesis). University of the Western Cape. Retrieved from http://hdl.handle.net/11394/4826

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):

October, Firzana. “Proteomic and SNP analysis of the Cadherin 10 type-II (CDH10) gene, in the South African autistic population .” 2013. Thesis, University of the Western Cape. Accessed October 18, 2019. http://hdl.handle.net/11394/4826.

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

MLA Handbook (7th Edition):

October, Firzana. “Proteomic and SNP analysis of the Cadherin 10 type-II (CDH10) gene, in the South African autistic population .” 2013. Web. 18 Oct 2019.

Vancouver:

October F. Proteomic and SNP analysis of the Cadherin 10 type-II (CDH10) gene, in the South African autistic population . [Internet] [Thesis]. University of the Western Cape; 2013. [cited 2019 Oct 18]. Available from: http://hdl.handle.net/11394/4826.

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

Council of Science Editors:

October F. Proteomic and SNP analysis of the Cadherin 10 type-II (CDH10) gene, in the South African autistic population . [Thesis]. University of the Western Cape; 2013. Available from: http://hdl.handle.net/11394/4826

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


Columbia University

6. Cho, Youngjin. Development of Single Molecule Electronic SNP Assays using Polymer Tagged Nucleotides and Nanopore Detection.

Degree: 2018, Columbia University

 As knowledge of the human genome has accelerated, various diseases and individuals’ responses to drugs have been pinpointed to specific DNA variations in one’s genome.… (more)

Subjects/Keywords: Biochemistry; Biomedical engineering; Nanopores; Single nucleotide polymorphisms

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Cho, Y. (2018). Development of Single Molecule Electronic SNP Assays using Polymer Tagged Nucleotides and Nanopore Detection. (Doctoral Dissertation). Columbia University. Retrieved from https://doi.org/10.7916/D8QC1FDG

Chicago Manual of Style (16th Edition):

Cho, Youngjin. “Development of Single Molecule Electronic SNP Assays using Polymer Tagged Nucleotides and Nanopore Detection.” 2018. Doctoral Dissertation, Columbia University. Accessed October 18, 2019. https://doi.org/10.7916/D8QC1FDG.

MLA Handbook (7th Edition):

Cho, Youngjin. “Development of Single Molecule Electronic SNP Assays using Polymer Tagged Nucleotides and Nanopore Detection.” 2018. Web. 18 Oct 2019.

Vancouver:

Cho Y. Development of Single Molecule Electronic SNP Assays using Polymer Tagged Nucleotides and Nanopore Detection. [Internet] [Doctoral dissertation]. Columbia University; 2018. [cited 2019 Oct 18]. Available from: https://doi.org/10.7916/D8QC1FDG.

Council of Science Editors:

Cho Y. Development of Single Molecule Electronic SNP Assays using Polymer Tagged Nucleotides and Nanopore Detection. [Doctoral Dissertation]. Columbia University; 2018. Available from: https://doi.org/10.7916/D8QC1FDG


University of New Mexico

7. Glenn, Elizabeth M. Prevalence of Artemisinin Resistance Associated Single Nucleotide Polymorphisms in Kenyan Isolates.

Degree: UNM Biology Department, 2018, University of New Mexico

  Malaria has had an unspeakable toll on human economy and wellbeing. Every year, there are approximately 212 million malaria infections caused by Plasmodium falciparum… (more)

Subjects/Keywords: Malaria; single nucleotide polymorphisms; artemisinin; resistance; Biology

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Glenn, E. M. (2018). Prevalence of Artemisinin Resistance Associated Single Nucleotide Polymorphisms in Kenyan Isolates. (Masters Thesis). University of New Mexico. Retrieved from https://digitalrepository.unm.edu/biol_etds/262

Chicago Manual of Style (16th Edition):

Glenn, Elizabeth M. “Prevalence of Artemisinin Resistance Associated Single Nucleotide Polymorphisms in Kenyan Isolates.” 2018. Masters Thesis, University of New Mexico. Accessed October 18, 2019. https://digitalrepository.unm.edu/biol_etds/262.

MLA Handbook (7th Edition):

Glenn, Elizabeth M. “Prevalence of Artemisinin Resistance Associated Single Nucleotide Polymorphisms in Kenyan Isolates.” 2018. Web. 18 Oct 2019.

Vancouver:

Glenn EM. Prevalence of Artemisinin Resistance Associated Single Nucleotide Polymorphisms in Kenyan Isolates. [Internet] [Masters thesis]. University of New Mexico; 2018. [cited 2019 Oct 18]. Available from: https://digitalrepository.unm.edu/biol_etds/262.

Council of Science Editors:

Glenn EM. Prevalence of Artemisinin Resistance Associated Single Nucleotide Polymorphisms in Kenyan Isolates. [Masters Thesis]. University of New Mexico; 2018. Available from: https://digitalrepository.unm.edu/biol_etds/262


University of Guelph

8. Notay, Karambir. Genetic polymorphisms in skeletal muscle metaboreceptors are associated with blood pressure responses to exercise .

Degree: 2018, University of Guelph

 This thesis examined whether single-nucleotide polymorphisms (SNPs) in genes encoding for metaboreceptors present in skeletal muscle afferents can influence responses to exercise. Two hundred healthy… (more)

Subjects/Keywords: Single Nucleotide Polymorphisms; Blood Pressure; Muscle metaboreflex

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Notay, K. (2018). Genetic polymorphisms in skeletal muscle metaboreceptors are associated with blood pressure responses to exercise . (Thesis). University of Guelph. Retrieved from https://atrium.lib.uoguelph.ca/xmlui/handle/10214/13894

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):

Notay, Karambir. “Genetic polymorphisms in skeletal muscle metaboreceptors are associated with blood pressure responses to exercise .” 2018. Thesis, University of Guelph. Accessed October 18, 2019. https://atrium.lib.uoguelph.ca/xmlui/handle/10214/13894.

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

MLA Handbook (7th Edition):

Notay, Karambir. “Genetic polymorphisms in skeletal muscle metaboreceptors are associated with blood pressure responses to exercise .” 2018. Web. 18 Oct 2019.

Vancouver:

Notay K. Genetic polymorphisms in skeletal muscle metaboreceptors are associated with blood pressure responses to exercise . [Internet] [Thesis]. University of Guelph; 2018. [cited 2019 Oct 18]. Available from: https://atrium.lib.uoguelph.ca/xmlui/handle/10214/13894.

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

Council of Science Editors:

Notay K. Genetic polymorphisms in skeletal muscle metaboreceptors are associated with blood pressure responses to exercise . [Thesis]. University of Guelph; 2018. Available from: https://atrium.lib.uoguelph.ca/xmlui/handle/10214/13894

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


University of Missouri – Columbia

9. Ramey, Holly Rene. Mapping natural and artificial selection events in animal genomes.

Degree: 2015, University of Missouri – Columbia

 Selection events, of both artificial (human-imposed) and natural origin, have left their mark on animal genomes. These signatures are detectable through a variety of analyses… (more)

Subjects/Keywords: Genomics; Heterozygosity; Single nucleotide polymorphisms; Domestic animals

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Ramey, H. R. (2015). Mapping natural and artificial selection events in animal genomes. (Thesis). University of Missouri – Columbia. Retrieved from http://hdl.handle.net/10355/46894

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):

Ramey, Holly Rene. “Mapping natural and artificial selection events in animal genomes.” 2015. Thesis, University of Missouri – Columbia. Accessed October 18, 2019. http://hdl.handle.net/10355/46894.

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

MLA Handbook (7th Edition):

Ramey, Holly Rene. “Mapping natural and artificial selection events in animal genomes.” 2015. Web. 18 Oct 2019.

Vancouver:

Ramey HR. Mapping natural and artificial selection events in animal genomes. [Internet] [Thesis]. University of Missouri – Columbia; 2015. [cited 2019 Oct 18]. Available from: http://hdl.handle.net/10355/46894.

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

Council of Science Editors:

Ramey HR. Mapping natural and artificial selection events in animal genomes. [Thesis]. University of Missouri – Columbia; 2015. Available from: http://hdl.handle.net/10355/46894

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


University of Illinois – Chicago

10. Obando, Julio E. Assessment of the Clinical Validity and Utility of SNPs When Used as Predictors for Periodontitis.

Degree: 2017, University of Illinois – Chicago

 BACKGROUND Chronic periodontitis is an inflammatory disease, influenced by a multifactorial etiology; susceptible host, environmental factors, microbial colonization and genetic variations. As genes determine qualitative… (more)

Subjects/Keywords: periodontitis; polymorphisms; genetics; single nucleotide polymorphisms; genetic testing

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Obando, J. E. (2017). Assessment of the Clinical Validity and Utility of SNPs When Used as Predictors for Periodontitis. (Thesis). University of Illinois – Chicago. Retrieved from http://hdl.handle.net/10027/21820

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):

Obando, Julio E. “Assessment of the Clinical Validity and Utility of SNPs When Used as Predictors for Periodontitis.” 2017. Thesis, University of Illinois – Chicago. Accessed October 18, 2019. http://hdl.handle.net/10027/21820.

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

MLA Handbook (7th Edition):

Obando, Julio E. “Assessment of the Clinical Validity and Utility of SNPs When Used as Predictors for Periodontitis.” 2017. Web. 18 Oct 2019.

Vancouver:

Obando JE. Assessment of the Clinical Validity and Utility of SNPs When Used as Predictors for Periodontitis. [Internet] [Thesis]. University of Illinois – Chicago; 2017. [cited 2019 Oct 18]. Available from: http://hdl.handle.net/10027/21820.

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

Council of Science Editors:

Obando JE. Assessment of the Clinical Validity and Utility of SNPs When Used as Predictors for Periodontitis. [Thesis]. University of Illinois – Chicago; 2017. Available from: http://hdl.handle.net/10027/21820

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

11. Kohrn, Brendan F. An Efficient Pipeline for Assaying Whole-Genome Plastid Variation for Population Genetics and Phylogeography.

Degree: MS(M.S.) in Biology, Biology, 2017, Portland State University

  Tracking seed dispersal using traditional, direct measurement approaches is difficult and generally underestimates dispersal distances. Variation in chloroplast haplotypes (cpDNA) offers a way to… (more)

Subjects/Keywords: Phylogeography; Chloroplast DNA; Seeds  – Dispersal; Single nucleotide polymorphisms; Biology; Plant Sciences

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Kohrn, B. F. (2017). An Efficient Pipeline for Assaying Whole-Genome Plastid Variation for Population Genetics and Phylogeography. (Masters Thesis). Portland State University. Retrieved from https://pdxscholar.library.pdx.edu/open_access_etds/4007

Chicago Manual of Style (16th Edition):

Kohrn, Brendan F. “An Efficient Pipeline for Assaying Whole-Genome Plastid Variation for Population Genetics and Phylogeography.” 2017. Masters Thesis, Portland State University. Accessed October 18, 2019. https://pdxscholar.library.pdx.edu/open_access_etds/4007.

MLA Handbook (7th Edition):

Kohrn, Brendan F. “An Efficient Pipeline for Assaying Whole-Genome Plastid Variation for Population Genetics and Phylogeography.” 2017. Web. 18 Oct 2019.

Vancouver:

Kohrn BF. An Efficient Pipeline for Assaying Whole-Genome Plastid Variation for Population Genetics and Phylogeography. [Internet] [Masters thesis]. Portland State University; 2017. [cited 2019 Oct 18]. Available from: https://pdxscholar.library.pdx.edu/open_access_etds/4007.

Council of Science Editors:

Kohrn BF. An Efficient Pipeline for Assaying Whole-Genome Plastid Variation for Population Genetics and Phylogeography. [Masters Thesis]. Portland State University; 2017. Available from: https://pdxscholar.library.pdx.edu/open_access_etds/4007


University of Alberta

12. Christiaens, Inge. Chronic Maternal Stress and Genetic Variants in the Etiology of Spontaneous Preterm Birth.

Degree: PhD, Department of Physiology, 2012, University of Alberta

 Preterm birth is the leading cause of mortality and morbidity in newborn infants. With an estimated 15 million preterm births annually worldwide, the global burden… (more)

Subjects/Keywords: preterm birth; single nucleotide polymorphisms; chronic maternal stress

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Christiaens, I. (2012). Chronic Maternal Stress and Genetic Variants in the Etiology of Spontaneous Preterm Birth. (Doctoral Dissertation). University of Alberta. Retrieved from https://era.library.ualberta.ca/files/8336h231m

Chicago Manual of Style (16th Edition):

Christiaens, Inge. “Chronic Maternal Stress and Genetic Variants in the Etiology of Spontaneous Preterm Birth.” 2012. Doctoral Dissertation, University of Alberta. Accessed October 18, 2019. https://era.library.ualberta.ca/files/8336h231m.

MLA Handbook (7th Edition):

Christiaens, Inge. “Chronic Maternal Stress and Genetic Variants in the Etiology of Spontaneous Preterm Birth.” 2012. Web. 18 Oct 2019.

Vancouver:

Christiaens I. Chronic Maternal Stress and Genetic Variants in the Etiology of Spontaneous Preterm Birth. [Internet] [Doctoral dissertation]. University of Alberta; 2012. [cited 2019 Oct 18]. Available from: https://era.library.ualberta.ca/files/8336h231m.

Council of Science Editors:

Christiaens I. Chronic Maternal Stress and Genetic Variants in the Etiology of Spontaneous Preterm Birth. [Doctoral Dissertation]. University of Alberta; 2012. Available from: https://era.library.ualberta.ca/files/8336h231m


University of Technology, Sydney

13. Castel, CV. Inference of biogeographical ancestry and pigmentation phenotype using single nucleotide polymorphisms.

Degree: 2014, University of Technology, Sydney

 Conventional DNA profiling of Short Tandem Repeats (STR) provides little evidentiary value in the absence of reference profiles or in the case of a non-match.… (more)

Subjects/Keywords: SNP.; Single nucleotide polymorphisms.; Biogeographical ancestry.; DNA.; Externally visible characteristics.

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Castel, C. (2014). Inference of biogeographical ancestry and pigmentation phenotype using single nucleotide polymorphisms. (Thesis). University of Technology, Sydney. Retrieved from http://hdl.handle.net/10453/29232

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):

Castel, CV. “Inference of biogeographical ancestry and pigmentation phenotype using single nucleotide polymorphisms.” 2014. Thesis, University of Technology, Sydney. Accessed October 18, 2019. http://hdl.handle.net/10453/29232.

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

MLA Handbook (7th Edition):

Castel, CV. “Inference of biogeographical ancestry and pigmentation phenotype using single nucleotide polymorphisms.” 2014. Web. 18 Oct 2019.

Vancouver:

Castel C. Inference of biogeographical ancestry and pigmentation phenotype using single nucleotide polymorphisms. [Internet] [Thesis]. University of Technology, Sydney; 2014. [cited 2019 Oct 18]. Available from: http://hdl.handle.net/10453/29232.

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

Council of Science Editors:

Castel C. Inference of biogeographical ancestry and pigmentation phenotype using single nucleotide polymorphisms. [Thesis]. University of Technology, Sydney; 2014. Available from: http://hdl.handle.net/10453/29232

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


East Tennessee State University

14. Mullersman, Jerald Eric. Effect of Gender on the Association of Single-Nucleotide Polymorphisms with Bipolar Disorder.

Degree: MPH (Master of Public Health), Public Health, 2011, East Tennessee State University

  Bipolar disorder is a relatively common form of mental illness that depends strongly on genetic inheritance for expression. The author of this study has… (more)

Subjects/Keywords: genome-wide association; bipolar disorder; single nucleotide polymorphisms; gender; Public Health

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Mullersman, J. E. (2011). Effect of Gender on the Association of Single-Nucleotide Polymorphisms with Bipolar Disorder. (Masters Thesis). East Tennessee State University. Retrieved from https://dc.etsu.edu/etd/1230

Chicago Manual of Style (16th Edition):

Mullersman, Jerald Eric. “Effect of Gender on the Association of Single-Nucleotide Polymorphisms with Bipolar Disorder.” 2011. Masters Thesis, East Tennessee State University. Accessed October 18, 2019. https://dc.etsu.edu/etd/1230.

MLA Handbook (7th Edition):

Mullersman, Jerald Eric. “Effect of Gender on the Association of Single-Nucleotide Polymorphisms with Bipolar Disorder.” 2011. Web. 18 Oct 2019.

Vancouver:

Mullersman JE. Effect of Gender on the Association of Single-Nucleotide Polymorphisms with Bipolar Disorder. [Internet] [Masters thesis]. East Tennessee State University; 2011. [cited 2019 Oct 18]. Available from: https://dc.etsu.edu/etd/1230.

Council of Science Editors:

Mullersman JE. Effect of Gender on the Association of Single-Nucleotide Polymorphisms with Bipolar Disorder. [Masters Thesis]. East Tennessee State University; 2011. Available from: https://dc.etsu.edu/etd/1230


University of Alaska – Fairbanks

15. Pasker, Renee Leigh. Gene by environment interactions between three candidate genes for obesity and omega-3 polyunsaturated fatty acids .

Degree: 2008, University of Alaska – Fairbanks

 Multi-factorial diseases, like obesity, are caused by genetic and environmental factors. Few studies examine potential interactions between genetic and environmental factors. Understanding these interactions can… (more)

Subjects/Keywords: Yup'ik Eskimos; omega-3 fatty acids; single nucleotide polymorphisms

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Pasker, R. L. (2008). Gene by environment interactions between three candidate genes for obesity and omega-3 polyunsaturated fatty acids . (Thesis). University of Alaska – Fairbanks. Retrieved from http://hdl.handle.net/11122/87

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):

Pasker, Renee Leigh. “Gene by environment interactions between three candidate genes for obesity and omega-3 polyunsaturated fatty acids .” 2008. Thesis, University of Alaska – Fairbanks. Accessed October 18, 2019. http://hdl.handle.net/11122/87.

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

MLA Handbook (7th Edition):

Pasker, Renee Leigh. “Gene by environment interactions between three candidate genes for obesity and omega-3 polyunsaturated fatty acids .” 2008. Web. 18 Oct 2019.

Vancouver:

Pasker RL. Gene by environment interactions between three candidate genes for obesity and omega-3 polyunsaturated fatty acids . [Internet] [Thesis]. University of Alaska – Fairbanks; 2008. [cited 2019 Oct 18]. Available from: http://hdl.handle.net/11122/87.

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

Council of Science Editors:

Pasker RL. Gene by environment interactions between three candidate genes for obesity and omega-3 polyunsaturated fatty acids . [Thesis]. University of Alaska – Fairbanks; 2008. Available from: http://hdl.handle.net/11122/87

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


Queen Mary, University of London

16. Ren, Meixia. A functional study of blood-pressure-associated SNPs at natriuretic peptide receptor C gene locus.

Degree: PhD, 2016, Queen Mary, University of London

 Background: Essential hypertension is regarded as a complex disease, the phenotype of which results from interactions between numerous genes and environmental factors. Genome-wide association studies… (more)

Subjects/Keywords: Medicine; Essential hypertension; single nucleotide polymorphisms; blood pressure

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Ren, M. (2016). A functional study of blood-pressure-associated SNPs at natriuretic peptide receptor C gene locus. (Doctoral Dissertation). Queen Mary, University of London. Retrieved from http://qmro.qmul.ac.uk/xmlui/handle/123456789/12912 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.765779

Chicago Manual of Style (16th Edition):

Ren, Meixia. “A functional study of blood-pressure-associated SNPs at natriuretic peptide receptor C gene locus.” 2016. Doctoral Dissertation, Queen Mary, University of London. Accessed October 18, 2019. http://qmro.qmul.ac.uk/xmlui/handle/123456789/12912 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.765779.

MLA Handbook (7th Edition):

Ren, Meixia. “A functional study of blood-pressure-associated SNPs at natriuretic peptide receptor C gene locus.” 2016. Web. 18 Oct 2019.

Vancouver:

Ren M. A functional study of blood-pressure-associated SNPs at natriuretic peptide receptor C gene locus. [Internet] [Doctoral dissertation]. Queen Mary, University of London; 2016. [cited 2019 Oct 18]. Available from: http://qmro.qmul.ac.uk/xmlui/handle/123456789/12912 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.765779.

Council of Science Editors:

Ren M. A functional study of blood-pressure-associated SNPs at natriuretic peptide receptor C gene locus. [Doctoral Dissertation]. Queen Mary, University of London; 2016. Available from: http://qmro.qmul.ac.uk/xmlui/handle/123456789/12912 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.765779


University of Waikato

17. McCormick, Helen Margaret. Molecular Studies of House Mice in Southern New Zealand .

Degree: 2011, University of Waikato

 The house mouse, Mus Musculus, was first introduced into New Zealand in significant numbers in the mid nineteenth century. Earlier research suggests that multiple introductions… (more)

Subjects/Keywords: mus musculus; mouse SNP; hybrid mice; single nucleotide polymorphisms

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

McCormick, H. M. (2011). Molecular Studies of House Mice in Southern New Zealand . (Masters Thesis). University of Waikato. Retrieved from http://hdl.handle.net/10289/5908

Chicago Manual of Style (16th Edition):

McCormick, Helen Margaret. “Molecular Studies of House Mice in Southern New Zealand .” 2011. Masters Thesis, University of Waikato. Accessed October 18, 2019. http://hdl.handle.net/10289/5908.

MLA Handbook (7th Edition):

McCormick, Helen Margaret. “Molecular Studies of House Mice in Southern New Zealand .” 2011. Web. 18 Oct 2019.

Vancouver:

McCormick HM. Molecular Studies of House Mice in Southern New Zealand . [Internet] [Masters thesis]. University of Waikato; 2011. [cited 2019 Oct 18]. Available from: http://hdl.handle.net/10289/5908.

Council of Science Editors:

McCormick HM. Molecular Studies of House Mice in Southern New Zealand . [Masters Thesis]. University of Waikato; 2011. Available from: http://hdl.handle.net/10289/5908


Stellenbosch University

18. Davis, William Henry. Development of a high-throughput genotyping assay for detection of functional polymorphisms involved in homocysteine metabolism and the methylation process implicated in multiple sclerosis.

Degree: MMedSc, Pathology, 2013, Stellenbosch University

 ENGLISH ABSTRACT: The aetiology of multiple sclerosis (MS) remains largely unknown due to the multifactorial nature of disease susceptibility determined by both environmental and genetic… (more)

Subjects/Keywords: Multiple sclerosis (MS); Homocysteine  – Metabolism; Single nucleotide polymorphisms; UCTD

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Davis, W. H. (2013). Development of a high-throughput genotyping assay for detection of functional polymorphisms involved in homocysteine metabolism and the methylation process implicated in multiple sclerosis. (Thesis). Stellenbosch University. Retrieved from http://hdl.handle.net/10019.1/95457

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):

Davis, William Henry. “Development of a high-throughput genotyping assay for detection of functional polymorphisms involved in homocysteine metabolism and the methylation process implicated in multiple sclerosis.” 2013. Thesis, Stellenbosch University. Accessed October 18, 2019. http://hdl.handle.net/10019.1/95457.

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

MLA Handbook (7th Edition):

Davis, William Henry. “Development of a high-throughput genotyping assay for detection of functional polymorphisms involved in homocysteine metabolism and the methylation process implicated in multiple sclerosis.” 2013. Web. 18 Oct 2019.

Vancouver:

Davis WH. Development of a high-throughput genotyping assay for detection of functional polymorphisms involved in homocysteine metabolism and the methylation process implicated in multiple sclerosis. [Internet] [Thesis]. Stellenbosch University; 2013. [cited 2019 Oct 18]. Available from: http://hdl.handle.net/10019.1/95457.

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

Council of Science Editors:

Davis WH. Development of a high-throughput genotyping assay for detection of functional polymorphisms involved in homocysteine metabolism and the methylation process implicated in multiple sclerosis. [Thesis]. Stellenbosch University; 2013. Available from: http://hdl.handle.net/10019.1/95457

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

19. Khalil, Mahmoud Salah. Transforming growth factor beta 1 : role in the progression of chronic renal failure.

Degree: PhD, 2002, Sheffield Hallam University

 TGF-beta1 plays an important role in the pathogenesis of experimental and clinical glomerulosclerosis and tubufointerstitial fibrosis. Associations have been described between polymorphisms of cytokine and… (more)

Subjects/Keywords: 616; Single nucleotide polymorphisms

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Khalil, M. S. (2002). Transforming growth factor beta 1 : role in the progression of chronic renal failure. (Doctoral Dissertation). Sheffield Hallam University. Retrieved from http://shura.shu.ac.uk/19437/ ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.247628

Chicago Manual of Style (16th Edition):

Khalil, Mahmoud Salah. “Transforming growth factor beta 1 : role in the progression of chronic renal failure.” 2002. Doctoral Dissertation, Sheffield Hallam University. Accessed October 18, 2019. http://shura.shu.ac.uk/19437/ ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.247628.

MLA Handbook (7th Edition):

Khalil, Mahmoud Salah. “Transforming growth factor beta 1 : role in the progression of chronic renal failure.” 2002. Web. 18 Oct 2019.

Vancouver:

Khalil MS. Transforming growth factor beta 1 : role in the progression of chronic renal failure. [Internet] [Doctoral dissertation]. Sheffield Hallam University; 2002. [cited 2019 Oct 18]. Available from: http://shura.shu.ac.uk/19437/ ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.247628.

Council of Science Editors:

Khalil MS. Transforming growth factor beta 1 : role in the progression of chronic renal failure. [Doctoral Dissertation]. Sheffield Hallam University; 2002. Available from: http://shura.shu.ac.uk/19437/ ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.247628


Columbia University

20. Argos, Maria. Genetic Susceptibility to Arsenic Exposure and Arsenical Skin Lesion Prevalence in Bangladesh.

Degree: 2011, Columbia University

 Elevated concentrations of arsenic in groundwater pose a public health threat to millions of people worldwide. While arsenic is an established human carcinogen, a mode… (more)

Subjects/Keywords: Epidemiology; Environmental health; Arsenic – Physiological effect; Arsenic – Carcinogenicity; Single nucleotide polymorphisms

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Argos, M. (2011). Genetic Susceptibility to Arsenic Exposure and Arsenical Skin Lesion Prevalence in Bangladesh. (Doctoral Dissertation). Columbia University. Retrieved from https://doi.org/10.7916/D8CC16NM

Chicago Manual of Style (16th Edition):

Argos, Maria. “Genetic Susceptibility to Arsenic Exposure and Arsenical Skin Lesion Prevalence in Bangladesh.” 2011. Doctoral Dissertation, Columbia University. Accessed October 18, 2019. https://doi.org/10.7916/D8CC16NM.

MLA Handbook (7th Edition):

Argos, Maria. “Genetic Susceptibility to Arsenic Exposure and Arsenical Skin Lesion Prevalence in Bangladesh.” 2011. Web. 18 Oct 2019.

Vancouver:

Argos M. Genetic Susceptibility to Arsenic Exposure and Arsenical Skin Lesion Prevalence in Bangladesh. [Internet] [Doctoral dissertation]. Columbia University; 2011. [cited 2019 Oct 18]. Available from: https://doi.org/10.7916/D8CC16NM.

Council of Science Editors:

Argos M. Genetic Susceptibility to Arsenic Exposure and Arsenical Skin Lesion Prevalence in Bangladesh. [Doctoral Dissertation]. Columbia University; 2011. Available from: https://doi.org/10.7916/D8CC16NM

21. Kearns, James Kalman. Field Portable Methods for the Determination of Arsenic in Environmental Samples.

Degree: PhD, Chemistry, 2010, U of Massachusetts : PhD

 Arsenic contamination of the environment is a worldwide health hazard. This research project focused on four areas: development and testing of low cost, field portable… (more)

Subjects/Keywords: Arsenic; Field Portable Determination; Single Nucleotide Polymorphisms; Chemistry

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Kearns, J. K. (2010). Field Portable Methods for the Determination of Arsenic in Environmental Samples. (Doctoral Dissertation). U of Massachusetts : PhD. Retrieved from https://scholarworks.umass.edu/open_access_dissertations/285

Chicago Manual of Style (16th Edition):

Kearns, James Kalman. “Field Portable Methods for the Determination of Arsenic in Environmental Samples.” 2010. Doctoral Dissertation, U of Massachusetts : PhD. Accessed October 18, 2019. https://scholarworks.umass.edu/open_access_dissertations/285.

MLA Handbook (7th Edition):

Kearns, James Kalman. “Field Portable Methods for the Determination of Arsenic in Environmental Samples.” 2010. Web. 18 Oct 2019.

Vancouver:

Kearns JK. Field Portable Methods for the Determination of Arsenic in Environmental Samples. [Internet] [Doctoral dissertation]. U of Massachusetts : PhD; 2010. [cited 2019 Oct 18]. Available from: https://scholarworks.umass.edu/open_access_dissertations/285.

Council of Science Editors:

Kearns JK. Field Portable Methods for the Determination of Arsenic in Environmental Samples. [Doctoral Dissertation]. U of Massachusetts : PhD; 2010. Available from: https://scholarworks.umass.edu/open_access_dissertations/285


New Jersey Institute of Technology

22. Shahidain, Seif. Ranking single nucleotide polymorphisms with support vector regression in continuous phenotypes.

Degree: MSin Computational Biology - (M.S.), Mathematical Sciences, 2011, New Jersey Institute of Technology

  Support vector machines (SVM) have been used to improve the ranking of single nucleotide polymorphisms (SNPs) over traditional chi-square tests in disease case studies… (more)

Subjects/Keywords: Support vector machines; Single nucleotide polymorphisms; Continuous phenotypes; Biostatistics; Computer Sciences

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Shahidain, S. (2011). Ranking single nucleotide polymorphisms with support vector regression in continuous phenotypes. (Thesis). New Jersey Institute of Technology. Retrieved from https://digitalcommons.njit.edu/theses/95

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):

Shahidain, Seif. “Ranking single nucleotide polymorphisms with support vector regression in continuous phenotypes.” 2011. Thesis, New Jersey Institute of Technology. Accessed October 18, 2019. https://digitalcommons.njit.edu/theses/95.

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

MLA Handbook (7th Edition):

Shahidain, Seif. “Ranking single nucleotide polymorphisms with support vector regression in continuous phenotypes.” 2011. Web. 18 Oct 2019.

Vancouver:

Shahidain S. Ranking single nucleotide polymorphisms with support vector regression in continuous phenotypes. [Internet] [Thesis]. New Jersey Institute of Technology; 2011. [cited 2019 Oct 18]. Available from: https://digitalcommons.njit.edu/theses/95.

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

Council of Science Editors:

Shahidain S. Ranking single nucleotide polymorphisms with support vector regression in continuous phenotypes. [Thesis]. New Jersey Institute of Technology; 2011. Available from: https://digitalcommons.njit.edu/theses/95

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


Rutgers University

23. Giarratana, Anna Obee, 1987-. The effects of genetic polymorphisms on recovery after repeated mild traumatic brain injury in a mouse model and personalized treatment approaches.

Degree: PhD, Traumatic brain injury, 2019, Rutgers University

Traumatic Brain Injury (TBI) is a serious and potentially life-threatening clinical problem. In 2013, there were 2.5 million TBIs in the United States, 50,000 of… (more)

Subjects/Keywords: Neuroscience; Brain  – Wounds and injuries; Single nucleotide polymorphisms

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Giarratana, Anna Obee, 1. (2019). The effects of genetic polymorphisms on recovery after repeated mild traumatic brain injury in a mouse model and personalized treatment approaches. (Doctoral Dissertation). Rutgers University. Retrieved from https://rucore.libraries.rutgers.edu/rutgers-lib/60759/

Chicago Manual of Style (16th Edition):

Giarratana, Anna Obee, 1987-. “The effects of genetic polymorphisms on recovery after repeated mild traumatic brain injury in a mouse model and personalized treatment approaches.” 2019. Doctoral Dissertation, Rutgers University. Accessed October 18, 2019. https://rucore.libraries.rutgers.edu/rutgers-lib/60759/.

MLA Handbook (7th Edition):

Giarratana, Anna Obee, 1987-. “The effects of genetic polymorphisms on recovery after repeated mild traumatic brain injury in a mouse model and personalized treatment approaches.” 2019. Web. 18 Oct 2019.

Vancouver:

Giarratana, Anna Obee 1. The effects of genetic polymorphisms on recovery after repeated mild traumatic brain injury in a mouse model and personalized treatment approaches. [Internet] [Doctoral dissertation]. Rutgers University; 2019. [cited 2019 Oct 18]. Available from: https://rucore.libraries.rutgers.edu/rutgers-lib/60759/.

Council of Science Editors:

Giarratana, Anna Obee 1. The effects of genetic polymorphisms on recovery after repeated mild traumatic brain injury in a mouse model and personalized treatment approaches. [Doctoral Dissertation]. Rutgers University; 2019. Available from: https://rucore.libraries.rutgers.edu/rutgers-lib/60759/


Hong Kong University of Science and Technology

24. Pu, Yu ECE. Statistical fine-mapping and summary statistics imputation in genome-wide association studies.

Degree: 2019, Hong Kong University of Science and Technology

 In genome-wide association studies (GWASs), a large number of trait-associated single-nucleotide polymorphisms (SNPs) have been detected. Among these associations, not all SNPs are the causal… (more)

Subjects/Keywords: Genomics ; Data processing ; Mathematical models ; Statistical methods ; Single nucleotide polymorphisms

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Pu, Y. E. (2019). Statistical fine-mapping and summary statistics imputation in genome-wide association studies. (Thesis). Hong Kong University of Science and Technology. Retrieved from http://repository.ust.hk/ir/Record/1783.1-99558 ; https://doi.org/10.14711/thesis-991012710761503412 ; http://repository.ust.hk/ir/bitstream/1783.1-99558/1/th_redirect.html

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

Chicago Manual of Style (16th Edition):

Pu, Yu ECE. “Statistical fine-mapping and summary statistics imputation in genome-wide association studies.” 2019. Thesis, Hong Kong University of Science and Technology. Accessed October 18, 2019. http://repository.ust.hk/ir/Record/1783.1-99558 ; https://doi.org/10.14711/thesis-991012710761503412 ; http://repository.ust.hk/ir/bitstream/1783.1-99558/1/th_redirect.html.

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

MLA Handbook (7th Edition):

Pu, Yu ECE. “Statistical fine-mapping and summary statistics imputation in genome-wide association studies.” 2019. Web. 18 Oct 2019.

Vancouver:

Pu YE. Statistical fine-mapping and summary statistics imputation in genome-wide association studies. [Internet] [Thesis]. Hong Kong University of Science and Technology; 2019. [cited 2019 Oct 18]. Available from: http://repository.ust.hk/ir/Record/1783.1-99558 ; https://doi.org/10.14711/thesis-991012710761503412 ; http://repository.ust.hk/ir/bitstream/1783.1-99558/1/th_redirect.html.

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

Council of Science Editors:

Pu YE. Statistical fine-mapping and summary statistics imputation in genome-wide association studies. [Thesis]. Hong Kong University of Science and Technology; 2019. Available from: http://repository.ust.hk/ir/Record/1783.1-99558 ; https://doi.org/10.14711/thesis-991012710761503412 ; http://repository.ust.hk/ir/bitstream/1783.1-99558/1/th_redirect.html

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


Johannes Gutenberg Universität Mainz

25. Bogus, Magdalena. Multiplex-Genotypisierung forensisch relevanter SNPs unter Verwendung von Microarrays auf chemisch aktivierten Glasflächen.

Degree: 2010, Johannes Gutenberg Universität Mainz

 Die Analyse tandem-repetitiver DNA-Sequenzen hat einen festen Platz als genetisches Typisierungsverfahren in den Breichen der stammesgeschichtlichen Untersuchung, der Verwandtschaftsanalyse und vor allem in der forensischen… (more)

Subjects/Keywords: Microarray, SNPs, forensisch, Single Nucletide Polymorphisms, Multiplex; microarray, SNPs, forensic, single nucleotide polymorphisms, multiplex; Life sciences

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Bogus, M. (2010). Multiplex-Genotypisierung forensisch relevanter SNPs unter Verwendung von Microarrays auf chemisch aktivierten Glasflächen. (Doctoral Dissertation). Johannes Gutenberg Universität Mainz. Retrieved from http://ubm.opus.hbz-nrw.de/volltexte/2011/2741/

Chicago Manual of Style (16th Edition):

Bogus, Magdalena. “Multiplex-Genotypisierung forensisch relevanter SNPs unter Verwendung von Microarrays auf chemisch aktivierten Glasflächen.” 2010. Doctoral Dissertation, Johannes Gutenberg Universität Mainz. Accessed October 18, 2019. http://ubm.opus.hbz-nrw.de/volltexte/2011/2741/.

MLA Handbook (7th Edition):

Bogus, Magdalena. “Multiplex-Genotypisierung forensisch relevanter SNPs unter Verwendung von Microarrays auf chemisch aktivierten Glasflächen.” 2010. Web. 18 Oct 2019.

Vancouver:

Bogus M. Multiplex-Genotypisierung forensisch relevanter SNPs unter Verwendung von Microarrays auf chemisch aktivierten Glasflächen. [Internet] [Doctoral dissertation]. Johannes Gutenberg Universität Mainz; 2010. [cited 2019 Oct 18]. Available from: http://ubm.opus.hbz-nrw.de/volltexte/2011/2741/.

Council of Science Editors:

Bogus M. Multiplex-Genotypisierung forensisch relevanter SNPs unter Verwendung von Microarrays auf chemisch aktivierten Glasflächen. [Doctoral Dissertation]. Johannes Gutenberg Universität Mainz; 2010. Available from: http://ubm.opus.hbz-nrw.de/volltexte/2011/2741/

26. Souza, Roberto Antonio de. Genotipagem de linhagens de Yersinia spp. por high-resolution melting analysis.

Degree: PhD, Biociências Aplicadas à Farmácia, 2013, University of São Paulo

 O gênero Yersinia pertence à família Enterobacteriaceae e compreende 17 espécies. Y. pestis, Y. pseudotuberculosis e Y. enterocolitica são reconhecidamente patógenos de humanos e animais.… (more)

Subjects/Keywords: Epidemiologia molecular; Gênero Yersinia; Genotipagem; Genotyping; Genus Yersinia; High-resolution melting analysis; High-resolution melting analysis; Molecular epidemiology; Single-nucleotide polymorphisms; Single-nucleotide polymorphisms

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Souza, R. A. d. (2013). Genotipagem de linhagens de Yersinia spp. por high-resolution melting analysis. (Doctoral Dissertation). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/60/60135/tde-27062013-151724/ ;

Chicago Manual of Style (16th Edition):

Souza, Roberto Antonio de. “Genotipagem de linhagens de Yersinia spp. por high-resolution melting analysis.” 2013. Doctoral Dissertation, University of São Paulo. Accessed October 18, 2019. http://www.teses.usp.br/teses/disponiveis/60/60135/tde-27062013-151724/ ;.

MLA Handbook (7th Edition):

Souza, Roberto Antonio de. “Genotipagem de linhagens de Yersinia spp. por high-resolution melting analysis.” 2013. Web. 18 Oct 2019.

Vancouver:

Souza RAd. Genotipagem de linhagens de Yersinia spp. por high-resolution melting analysis. [Internet] [Doctoral dissertation]. University of São Paulo; 2013. [cited 2019 Oct 18]. Available from: http://www.teses.usp.br/teses/disponiveis/60/60135/tde-27062013-151724/ ;.

Council of Science Editors:

Souza RAd. Genotipagem de linhagens de Yersinia spp. por high-resolution melting analysis. [Doctoral Dissertation]. University of São Paulo; 2013. Available from: http://www.teses.usp.br/teses/disponiveis/60/60135/tde-27062013-151724/ ;


University of Oxford

27. Grochola, Lukasz Filip. Identification and functional analysis of single nucleotide polymorphisms that affect human cancer.

Degree: PhD, 2011, University of Oxford

 Aims: The p53 regulatory network is crucial in directing the suppression of cancer formation and mediating the response to commonly used cancer therapies. Functional genetic… (more)

Subjects/Keywords: 616.994071; Biology; Life Sciences; Genetics (life sciences); Medical sciences; single nucleotide polymorphisms; snp; p53 pathway

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Grochola, L. F. (2011). Identification and functional analysis of single nucleotide polymorphisms that affect human cancer. (Doctoral Dissertation). University of Oxford. Retrieved from http://ora.ox.ac.uk/objects/uuid:aacc7084-81a8-4e97-b1ac-024d9bed106e ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.558392

Chicago Manual of Style (16th Edition):

Grochola, Lukasz Filip. “Identification and functional analysis of single nucleotide polymorphisms that affect human cancer.” 2011. Doctoral Dissertation, University of Oxford. Accessed October 18, 2019. http://ora.ox.ac.uk/objects/uuid:aacc7084-81a8-4e97-b1ac-024d9bed106e ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.558392.

MLA Handbook (7th Edition):

Grochola, Lukasz Filip. “Identification and functional analysis of single nucleotide polymorphisms that affect human cancer.” 2011. Web. 18 Oct 2019.

Vancouver:

Grochola LF. Identification and functional analysis of single nucleotide polymorphisms that affect human cancer. [Internet] [Doctoral dissertation]. University of Oxford; 2011. [cited 2019 Oct 18]. Available from: http://ora.ox.ac.uk/objects/uuid:aacc7084-81a8-4e97-b1ac-024d9bed106e ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.558392.

Council of Science Editors:

Grochola LF. Identification and functional analysis of single nucleotide polymorphisms that affect human cancer. [Doctoral Dissertation]. University of Oxford; 2011. Available from: http://ora.ox.ac.uk/objects/uuid:aacc7084-81a8-4e97-b1ac-024d9bed106e ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.558392


Bond University

28. Barash, Mark. Identification of single nucleotide polymorphisms (SNPs) involved in the determination of craniofacial morphology.

Degree: 2014, Bond University

 Current methods of forensic DNA analysis are mainly used for identification purposes and require a reference sample for comparison to an evidence DNA profile. The… (more)

Subjects/Keywords: DNA physiology; Forensic genetics; Single nucleotide polymorphisms.; Health Sciences, General (0566); Genetic Structures; Medical Genetics

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Barash, M. (2014). Identification of single nucleotide polymorphisms (SNPs) involved in the determination of craniofacial morphology. (Thesis). Bond University. Retrieved from https://epublications.bond.edu.au/theses/144

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):

Barash, Mark. “Identification of single nucleotide polymorphisms (SNPs) involved in the determination of craniofacial morphology.” 2014. Thesis, Bond University. Accessed October 18, 2019. https://epublications.bond.edu.au/theses/144.

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

MLA Handbook (7th Edition):

Barash, Mark. “Identification of single nucleotide polymorphisms (SNPs) involved in the determination of craniofacial morphology.” 2014. Web. 18 Oct 2019.

Vancouver:

Barash M. Identification of single nucleotide polymorphisms (SNPs) involved in the determination of craniofacial morphology. [Internet] [Thesis]. Bond University; 2014. [cited 2019 Oct 18]. Available from: https://epublications.bond.edu.au/theses/144.

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

Council of Science Editors:

Barash M. Identification of single nucleotide polymorphisms (SNPs) involved in the determination of craniofacial morphology. [Thesis]. Bond University; 2014. Available from: https://epublications.bond.edu.au/theses/144

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

29. Simou, Maria. Διερεύνηση της σχέσης της ετεroγενειας των γονιδίων των γλυκοπρωτεϊνικών υποδοχέων και δια κυτταρικών συνδέσμων των αιμοπεταλίων μητρικής και εμβρυικής προέλευσης με την εκδήλωση ενδομήτριας περιορισμένης ανάπτυξης του εμβρύου.

Degree: 2017, National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ)

Vascular thrombotic tendency may lead to fetal growth restriction (FGR). Altered platelet function and genetic heterogeneity may play a role in this procedure. We investigated… (more)

Subjects/Keywords: Αιμοπετάλια; Ενδομήτριος περιορισμός της αύξησης; Πολυμορφισμοί; Single Nucleotide Polymorphisms, SNPs; Platelets; FGR; Pyrosequencing

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Simou, M. (2017). Διερεύνηση της σχέσης της ετεroγενειας των γονιδίων των γλυκοπρωτεϊνικών υποδοχέων και δια κυτταρικών συνδέσμων των αιμοπεταλίων μητρικής και εμβρυικής προέλευσης με την εκδήλωση ενδομήτριας περιορισμένης ανάπτυξης του εμβρύου. (Thesis). National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ). Retrieved from http://hdl.handle.net/10442/hedi/41711

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):

Simou, Maria. “Διερεύνηση της σχέσης της ετεroγενειας των γονιδίων των γλυκοπρωτεϊνικών υποδοχέων και δια κυτταρικών συνδέσμων των αιμοπεταλίων μητρικής και εμβρυικής προέλευσης με την εκδήλωση ενδομήτριας περιορισμένης ανάπτυξης του εμβρύου.” 2017. Thesis, National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ). Accessed October 18, 2019. http://hdl.handle.net/10442/hedi/41711.

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

MLA Handbook (7th Edition):

Simou, Maria. “Διερεύνηση της σχέσης της ετεroγενειας των γονιδίων των γλυκοπρωτεϊνικών υποδοχέων και δια κυτταρικών συνδέσμων των αιμοπεταλίων μητρικής και εμβρυικής προέλευσης με την εκδήλωση ενδομήτριας περιορισμένης ανάπτυξης του εμβρύου.” 2017. Web. 18 Oct 2019.

Vancouver:

Simou M. Διερεύνηση της σχέσης της ετεroγενειας των γονιδίων των γλυκοπρωτεϊνικών υποδοχέων και δια κυτταρικών συνδέσμων των αιμοπεταλίων μητρικής και εμβρυικής προέλευσης με την εκδήλωση ενδομήτριας περιορισμένης ανάπτυξης του εμβρύου. [Internet] [Thesis]. National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ); 2017. [cited 2019 Oct 18]. Available from: http://hdl.handle.net/10442/hedi/41711.

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

Council of Science Editors:

Simou M. Διερεύνηση της σχέσης της ετεroγενειας των γονιδίων των γλυκοπρωτεϊνικών υποδοχέων και δια κυτταρικών συνδέσμων των αιμοπεταλίων μητρικής και εμβρυικής προέλευσης με την εκδήλωση ενδομήτριας περιορισμένης ανάπτυξης του εμβρύου. [Thesis]. National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ); 2017. Available from: http://hdl.handle.net/10442/hedi/41711

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


Aristotle University Of Thessaloniki (AUTH); Αριστοτέλειο Πανεπιστήμιο Θεσσαλονίκης (ΑΠΘ)

30. Kanata, Eirini. Ανίχνευση μορίων και πολυμορφισμών που πιθανόν επηρεάζουν την παθογένεση των νευροεκφυλιστικών νοσημάτων συμπεριλαμβανομένων των ασθενειών Prion.

Degree: 2014, Aristotle University Of Thessaloniki (AUTH); Αριστοτέλειο Πανεπιστήμιο Θεσσαλονίκης (ΑΠΘ)

Scrapie is a fatal neurodegenerative disease of sheep and goats, characterized by the conformational conversion of the normal PrPC protein (encoded by the prnp gene).… (more)

Subjects/Keywords: Τρομώδης νόσος; Αίγες; Μονονουκλεοτιδικοί πολυμορφισμοί; Ανθεκτικότητα; Scrapie; Goats; Single nucleotide polymorphisms; Resistance

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Kanata, E. (2014). Ανίχνευση μορίων και πολυμορφισμών που πιθανόν επηρεάζουν την παθογένεση των νευροεκφυλιστικών νοσημάτων συμπεριλαμβανομένων των ασθενειών Prion. (Thesis). Aristotle University Of Thessaloniki (AUTH); Αριστοτέλειο Πανεπιστήμιο Θεσσαλονίκης (ΑΠΘ). Retrieved from http://hdl.handle.net/10442/hedi/40872

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):

Kanata, Eirini. “Ανίχνευση μορίων και πολυμορφισμών που πιθανόν επηρεάζουν την παθογένεση των νευροεκφυλιστικών νοσημάτων συμπεριλαμβανομένων των ασθενειών Prion.” 2014. Thesis, Aristotle University Of Thessaloniki (AUTH); Αριστοτέλειο Πανεπιστήμιο Θεσσαλονίκης (ΑΠΘ). Accessed October 18, 2019. http://hdl.handle.net/10442/hedi/40872.

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

MLA Handbook (7th Edition):

Kanata, Eirini. “Ανίχνευση μορίων και πολυμορφισμών που πιθανόν επηρεάζουν την παθογένεση των νευροεκφυλιστικών νοσημάτων συμπεριλαμβανομένων των ασθενειών Prion.” 2014. Web. 18 Oct 2019.

Vancouver:

Kanata E. Ανίχνευση μορίων και πολυμορφισμών που πιθανόν επηρεάζουν την παθογένεση των νευροεκφυλιστικών νοσημάτων συμπεριλαμβανομένων των ασθενειών Prion. [Internet] [Thesis]. Aristotle University Of Thessaloniki (AUTH); Αριστοτέλειο Πανεπιστήμιο Θεσσαλονίκης (ΑΠΘ); 2014. [cited 2019 Oct 18]. Available from: http://hdl.handle.net/10442/hedi/40872.

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

Council of Science Editors:

Kanata E. Ανίχνευση μορίων και πολυμορφισμών που πιθανόν επηρεάζουν την παθογένεση των νευροεκφυλιστικών νοσημάτων συμπεριλαμβανομένων των ασθενειών Prion. [Thesis]. Aristotle University Of Thessaloniki (AUTH); Αριστοτέλειο Πανεπιστήμιο Θεσσαλονίκης (ΑΠΘ); 2014. Available from: http://hdl.handle.net/10442/hedi/40872

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

[1] [2] [3] [4] [5] [6]

.