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You searched for subject:(single nucleotide polymorphism). Showing records 1 – 30 of 362 total matches.

[1] [2] [3] [4] [5] … [13]

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University of Georgia

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

Degree: MS, Statistics, 2013, 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)

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APA (6th Edition):

Sprolden, T. L. (2013). Double eQTL mapping method to improve identification of trans eQTLs and construct intermediate gene networks. (Masters Thesis). University of Georgia. Retrieved from http://purl.galileo.usg.edu/uga_etd/sprolden_tracy_l_201305_ms

Chicago Manual of Style (16th Edition):

Sprolden, Tracy Lashonda. “Double eQTL mapping method to improve identification of trans eQTLs and construct intermediate gene networks.” 2013. Masters Thesis, University of Georgia. Accessed January 17, 2020. http://purl.galileo.usg.edu/uga_etd/sprolden_tracy_l_201305_ms.

MLA Handbook (7th Edition):

Sprolden, Tracy Lashonda. “Double eQTL mapping method to improve identification of trans eQTLs and construct intermediate gene networks.” 2013. Web. 17 Jan 2020.

Vancouver:

Sprolden TL. Double eQTL mapping method to improve identification of trans eQTLs and construct intermediate gene networks. [Internet] [Masters thesis]. University of Georgia; 2013. [cited 2020 Jan 17]. Available from: http://purl.galileo.usg.edu/uga_etd/sprolden_tracy_l_201305_ms.

Council of Science Editors:

Sprolden TL. Double eQTL mapping method to improve identification of trans eQTLs and construct intermediate gene networks. [Masters Thesis]. University of Georgia; 2013. Available from: http://purl.galileo.usg.edu/uga_etd/sprolden_tracy_l_201305_ms


University of Waikato

2. 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 January 17, 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. 17 Jan 2020.

Vancouver:

Mulholland CV. Single nucleotide polymorphisms associated with the human electroencephalogram during desflurane anaesthesia . [Internet] [Masters thesis]. University of Waikato; 2012. [cited 2020 Jan 17]. 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 Cincinnati

3. Hrabik, Sarah A. The Clinical Utility of a SNP Microarray in Patients with Epilepsy at a Tertiary Medical Center.

Degree: MS, Medicine: Genetic Counseling, 2013, University of Cincinnati

 Background: Microarray testing has revolutionized clinical cytogenetics, as it provides a significantly higher resolution and greater clinical yield than karyotype analysis. Previously, microarray studies have… (more)

Subjects/Keywords: Genetics; epilepsy; genetics; Single Nucleotide Polymorphism microarray

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APA (6th Edition):

Hrabik, S. A. (2013). The Clinical Utility of a SNP Microarray in Patients with Epilepsy at a Tertiary Medical Center. (Masters Thesis). University of Cincinnati. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=ucin1368024881

Chicago Manual of Style (16th Edition):

Hrabik, Sarah A. “The Clinical Utility of a SNP Microarray in Patients with Epilepsy at a Tertiary Medical Center.” 2013. Masters Thesis, University of Cincinnati. Accessed January 17, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1368024881.

MLA Handbook (7th Edition):

Hrabik, Sarah A. “The Clinical Utility of a SNP Microarray in Patients with Epilepsy at a Tertiary Medical Center.” 2013. Web. 17 Jan 2020.

Vancouver:

Hrabik SA. The Clinical Utility of a SNP Microarray in Patients with Epilepsy at a Tertiary Medical Center. [Internet] [Masters thesis]. University of Cincinnati; 2013. [cited 2020 Jan 17]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ucin1368024881.

Council of Science Editors:

Hrabik SA. The Clinical Utility of a SNP Microarray in Patients with Epilepsy at a Tertiary Medical Center. [Masters Thesis]. University of Cincinnati; 2013. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ucin1368024881


McMaster University

4. Hua, Wenjing. Genotypic and phenotypic analyses of two model strains of Cryptococcus neoformans.

Degree: MSc, 2017, McMaster University

The human pathogenic Cryptococcus neoformans species complex are agents of a common AIDS-defining disease, which causes about 181,000 deaths each year. There are several specific… (more)

Subjects/Keywords: Cryptococcus neoformans; phenotype; Single nucleotide polymorphism

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APA (6th Edition):

Hua, W. (2017). Genotypic and phenotypic analyses of two model strains of Cryptococcus neoformans. (Masters Thesis). McMaster University. Retrieved from http://hdl.handle.net/11375/22202

Chicago Manual of Style (16th Edition):

Hua, Wenjing. “Genotypic and phenotypic analyses of two model strains of Cryptococcus neoformans.” 2017. Masters Thesis, McMaster University. Accessed January 17, 2020. http://hdl.handle.net/11375/22202.

MLA Handbook (7th Edition):

Hua, Wenjing. “Genotypic and phenotypic analyses of two model strains of Cryptococcus neoformans.” 2017. Web. 17 Jan 2020.

Vancouver:

Hua W. Genotypic and phenotypic analyses of two model strains of Cryptococcus neoformans. [Internet] [Masters thesis]. McMaster University; 2017. [cited 2020 Jan 17]. Available from: http://hdl.handle.net/11375/22202.

Council of Science Editors:

Hua W. Genotypic and phenotypic analyses of two model strains of Cryptococcus neoformans. [Masters Thesis]. McMaster University; 2017. Available from: http://hdl.handle.net/11375/22202


University of New South Wales

5. Hettiaratchi, Anusha. Single nucleotide polymorphisms in matrix metalloproteinase genes and their association with carcinoma.

Degree: Medical Sciences, 2010, University of New South Wales

 Matrix metalloproteinases (MMPs) are proteolytic enzymes with a selective and specific ability to denature structural proteins and thus have been implicated in tumour invasion and… (more)

Subjects/Keywords: Carcinoma; Matrix Metalloproteinase; Single nucleotide polymorphism

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APA (6th Edition):

Hettiaratchi, A. (2010). Single nucleotide polymorphisms in matrix metalloproteinase genes and their association with carcinoma. (Doctoral Dissertation). University of New South Wales. Retrieved from http://handle.unsw.edu.au/1959.4/51259 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:9940/SOURCE02?view=true

Chicago Manual of Style (16th Edition):

Hettiaratchi, Anusha. “Single nucleotide polymorphisms in matrix metalloproteinase genes and their association with carcinoma.” 2010. Doctoral Dissertation, University of New South Wales. Accessed January 17, 2020. http://handle.unsw.edu.au/1959.4/51259 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:9940/SOURCE02?view=true.

MLA Handbook (7th Edition):

Hettiaratchi, Anusha. “Single nucleotide polymorphisms in matrix metalloproteinase genes and their association with carcinoma.” 2010. Web. 17 Jan 2020.

Vancouver:

Hettiaratchi A. Single nucleotide polymorphisms in matrix metalloproteinase genes and their association with carcinoma. [Internet] [Doctoral dissertation]. University of New South Wales; 2010. [cited 2020 Jan 17]. Available from: http://handle.unsw.edu.au/1959.4/51259 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:9940/SOURCE02?view=true.

Council of Science Editors:

Hettiaratchi A. Single nucleotide polymorphisms in matrix metalloproteinase genes and their association with carcinoma. [Doctoral Dissertation]. University of New South Wales; 2010. Available from: http://handle.unsw.edu.au/1959.4/51259 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:9940/SOURCE02?view=true

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

Degree: 2014, Univerisyt of Limerick

 A single nucleotide polymorphism, or SNP, is a site of the genome where variation occurs within a population. Almost all SNPs have only two alleles… (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). Univerisyt 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, Univerisyt of Limerick. Accessed January 17, 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. 17 Jan 2020.

Vancouver:

Sheikhi A. Statistical methods for the detection of single nucleotide polymorphisms (SNPs) using new generation genome sequencers. [Internet] [Thesis]. Univerisyt of Limerick; 2014. [cited 2020 Jan 17]. 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]. Univerisyt 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

7. 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 January 17, 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. 17 Jan 2020.

Vancouver:

Zafar H. A SNP Calling And Genotyping Method For Single-cell Sequencing Data. [Internet] [Masters thesis]. Rice University; 2015. [cited 2020 Jan 17]. 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


Texas A&M University

8. Hulse-Kemp, Amanda M. Development of Genomic Markers and Mapping Tools for Assembling the Allotetraploid Gossypium hirsutum L. Draft Genome Sequence.

Degree: 2015, Texas A&M University

 Cotton (Gossypium spp.) is the largest producer of natural textile fibers. Most worldwide and domestic cotton fiber production is based on cultivars of G. hirsutum… (more)

Subjects/Keywords: Cotton; Genome Sequence; Single Nucleotide Polymorphism; Resequencing; Physical Mapping; Intraspecific; Interspecific

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APA (6th Edition):

Hulse-Kemp, A. M. (2015). Development of Genomic Markers and Mapping Tools for Assembling the Allotetraploid Gossypium hirsutum L. Draft Genome Sequence. (Thesis). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/155055

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):

Hulse-Kemp, Amanda M. “Development of Genomic Markers and Mapping Tools for Assembling the Allotetraploid Gossypium hirsutum L. Draft Genome Sequence.” 2015. Thesis, Texas A&M University. Accessed January 17, 2020. http://hdl.handle.net/1969.1/155055.

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

MLA Handbook (7th Edition):

Hulse-Kemp, Amanda M. “Development of Genomic Markers and Mapping Tools for Assembling the Allotetraploid Gossypium hirsutum L. Draft Genome Sequence.” 2015. Web. 17 Jan 2020.

Vancouver:

Hulse-Kemp AM. Development of Genomic Markers and Mapping Tools for Assembling the Allotetraploid Gossypium hirsutum L. Draft Genome Sequence. [Internet] [Thesis]. Texas A&M University; 2015. [cited 2020 Jan 17]. Available from: http://hdl.handle.net/1969.1/155055.

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

Council of Science Editors:

Hulse-Kemp AM. Development of Genomic Markers and Mapping Tools for Assembling the Allotetraploid Gossypium hirsutum L. Draft Genome Sequence. [Thesis]. Texas A&M University; 2015. Available from: http://hdl.handle.net/1969.1/155055

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


University of Edinburgh

9. Huffman, Jennifer Elizabeth. Genetic analysis of protein N-glycosylation.

Degree: PhD, 2014, University of Edinburgh

 The majority of human proteins are post-translationally modified by covalent addition of one or more complex oligosaccharides (glycans). Alterations in glycosylation processing are associated with… (more)

Subjects/Keywords: 572; genomewide association studies; glycan; single nucleotide polymorphism

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APA (6th Edition):

Huffman, J. E. (2014). Genetic analysis of protein N-glycosylation. (Doctoral Dissertation). University of Edinburgh. Retrieved from http://hdl.handle.net/1842/10038

Chicago Manual of Style (16th Edition):

Huffman, Jennifer Elizabeth. “Genetic analysis of protein N-glycosylation.” 2014. Doctoral Dissertation, University of Edinburgh. Accessed January 17, 2020. http://hdl.handle.net/1842/10038.

MLA Handbook (7th Edition):

Huffman, Jennifer Elizabeth. “Genetic analysis of protein N-glycosylation.” 2014. Web. 17 Jan 2020.

Vancouver:

Huffman JE. Genetic analysis of protein N-glycosylation. [Internet] [Doctoral dissertation]. University of Edinburgh; 2014. [cited 2020 Jan 17]. Available from: http://hdl.handle.net/1842/10038.

Council of Science Editors:

Huffman JE. Genetic analysis of protein N-glycosylation. [Doctoral Dissertation]. University of Edinburgh; 2014. Available from: http://hdl.handle.net/1842/10038


Lincoln University

10. Lange, Claudia. The genome and beyond: phenotypic determinants of two Trichoderma cf. atroviride sister strains.

Degree: 2015, Lincoln University

 Trichoderma cf. atroviride isolate LU132 is used commercially in New Zealand as a biological control agent (BCA) on various economically important plants to protect against… (more)

Subjects/Keywords: biocontrol; genomics; epigenetics; cytosine methylation; Trichoderma atroviride; mycoviruses; single nucleotide polymorphism

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APA (6th Edition):

Lange, C. (2015). The genome and beyond: phenotypic determinants of two Trichoderma cf. atroviride sister strains. (Thesis). Lincoln University. Retrieved from http://hdl.handle.net/10182/6675

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):

Lange, Claudia. “The genome and beyond: phenotypic determinants of two Trichoderma cf. atroviride sister strains.” 2015. Thesis, Lincoln University. Accessed January 17, 2020. http://hdl.handle.net/10182/6675.

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

MLA Handbook (7th Edition):

Lange, Claudia. “The genome and beyond: phenotypic determinants of two Trichoderma cf. atroviride sister strains.” 2015. Web. 17 Jan 2020.

Vancouver:

Lange C. The genome and beyond: phenotypic determinants of two Trichoderma cf. atroviride sister strains. [Internet] [Thesis]. Lincoln University; 2015. [cited 2020 Jan 17]. Available from: http://hdl.handle.net/10182/6675.

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

Council of Science Editors:

Lange C. The genome and beyond: phenotypic determinants of two Trichoderma cf. atroviride sister strains. [Thesis]. Lincoln University; 2015. Available from: http://hdl.handle.net/10182/6675

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


University of Southern California

11. Rhie, Suhn Kyong. Breast epithelial cell type specific enhancers and functional annotation of breast cancer risk loci.

Degree: PhD, Genetic, Molecular and Cellular Biology, 2013, University of Southern California

 Breast Cancer (BCa) genome-wide association studies (GWAS) revealed allelic frequency differences between cases and controls at index single nucleotide polymorphisms (SNPs). To date 71 loci… (more)

Subjects/Keywords: breast cancer; GWAS; enhancer; single nucleotide polymorphism; epigenetics; predisposition

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APA (6th Edition):

Rhie, S. K. (2013). Breast epithelial cell type specific enhancers and functional annotation of breast cancer risk loci. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/241673/rec/1161

Chicago Manual of Style (16th Edition):

Rhie, Suhn Kyong. “Breast epithelial cell type specific enhancers and functional annotation of breast cancer risk loci.” 2013. Doctoral Dissertation, University of Southern California. Accessed January 17, 2020. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/241673/rec/1161.

MLA Handbook (7th Edition):

Rhie, Suhn Kyong. “Breast epithelial cell type specific enhancers and functional annotation of breast cancer risk loci.” 2013. Web. 17 Jan 2020.

Vancouver:

Rhie SK. Breast epithelial cell type specific enhancers and functional annotation of breast cancer risk loci. [Internet] [Doctoral dissertation]. University of Southern California; 2013. [cited 2020 Jan 17]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/241673/rec/1161.

Council of Science Editors:

Rhie SK. Breast epithelial cell type specific enhancers and functional annotation of breast cancer risk loci. [Doctoral Dissertation]. University of Southern California; 2013. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/241673/rec/1161


University of Kansas

12. Flynn, Colleen A. FEXOFENADINE AND ORGANIC ANION TRANSPORTING POLYPEPTIDES (OATPs): TRANSPORT AND DRUG-DRUG INTERACTIONS.

Degree: PhD, Pharmacology, Toxicology & Therapeutics, 2011, University of Kansas

 Transporters play a major role in the absorption and disposition of fexofenadine, suggesting this drug could be used as a probe of transporter activity. When… (more)

Subjects/Keywords: Toxicology; Drug-drug interactions; Fexofenadine; Oatp; Probe cocktail; Single nucleotide polymorphism

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APA (6th Edition):

Flynn, C. A. (2011). FEXOFENADINE AND ORGANIC ANION TRANSPORTING POLYPEPTIDES (OATPs): TRANSPORT AND DRUG-DRUG INTERACTIONS. (Doctoral Dissertation). University of Kansas. Retrieved from http://hdl.handle.net/1808/9723

Chicago Manual of Style (16th Edition):

Flynn, Colleen A. “FEXOFENADINE AND ORGANIC ANION TRANSPORTING POLYPEPTIDES (OATPs): TRANSPORT AND DRUG-DRUG INTERACTIONS.” 2011. Doctoral Dissertation, University of Kansas. Accessed January 17, 2020. http://hdl.handle.net/1808/9723.

MLA Handbook (7th Edition):

Flynn, Colleen A. “FEXOFENADINE AND ORGANIC ANION TRANSPORTING POLYPEPTIDES (OATPs): TRANSPORT AND DRUG-DRUG INTERACTIONS.” 2011. Web. 17 Jan 2020.

Vancouver:

Flynn CA. FEXOFENADINE AND ORGANIC ANION TRANSPORTING POLYPEPTIDES (OATPs): TRANSPORT AND DRUG-DRUG INTERACTIONS. [Internet] [Doctoral dissertation]. University of Kansas; 2011. [cited 2020 Jan 17]. Available from: http://hdl.handle.net/1808/9723.

Council of Science Editors:

Flynn CA. FEXOFENADINE AND ORGANIC ANION TRANSPORTING POLYPEPTIDES (OATPs): TRANSPORT AND DRUG-DRUG INTERACTIONS. [Doctoral Dissertation]. University of Kansas; 2011. Available from: http://hdl.handle.net/1808/9723


University of Toledo Health Science Campus

13. Yatskiv, Yuriy Romanovich. A Haplotype Analysis of an Archaic Denisovan Genome.

Degree: MS, Biomedical Sciences (Bioinformatics and Proteomics/Genomics), 2016, University of Toledo Health Science Campus

 We computationally processed 1720 chromosomal segments from 22 autosomes that contained Yin, Yang, and Mosaic haplotypes (minor allele frequency of greater than 25%) of modern… (more)

Subjects/Keywords: Bioinformatics; Genetics; Denisovan; Haplotype; Genome; Single Nucleotide Polymorphism

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APA (6th Edition):

Yatskiv, Y. R. (2016). A Haplotype Analysis of an Archaic Denisovan Genome. (Masters Thesis). University of Toledo Health Science Campus. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=mco1481145733356233

Chicago Manual of Style (16th Edition):

Yatskiv, Yuriy Romanovich. “A Haplotype Analysis of an Archaic Denisovan Genome.” 2016. Masters Thesis, University of Toledo Health Science Campus. Accessed January 17, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=mco1481145733356233.

MLA Handbook (7th Edition):

Yatskiv, Yuriy Romanovich. “A Haplotype Analysis of an Archaic Denisovan Genome.” 2016. Web. 17 Jan 2020.

Vancouver:

Yatskiv YR. A Haplotype Analysis of an Archaic Denisovan Genome. [Internet] [Masters thesis]. University of Toledo Health Science Campus; 2016. [cited 2020 Jan 17]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=mco1481145733356233.

Council of Science Editors:

Yatskiv YR. A Haplotype Analysis of an Archaic Denisovan Genome. [Masters Thesis]. University of Toledo Health Science Campus; 2016. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=mco1481145733356233


University of Edinburgh

14. Cong, Duanduan. Identification of functional single nucleotide polymorphisms (SNPs) in High Risk-Human Papillomavirus (HR-HPV) related diseases.

Degree: PhD, 2018, University of Edinburgh

 Persistent infection of the cervix with high risk (HR) types of Human Papilloma Virus (HPV) (HR-HPV) can result in precancerous lesions and cancers. However, most… (more)

Subjects/Keywords: Human papillomavirus; HPV; HR-HPV; single nucleotide polymorphism; CXCR1; biomarkers

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APA (6th Edition):

Cong, D. (2018). Identification of functional single nucleotide polymorphisms (SNPs) in High Risk-Human Papillomavirus (HR-HPV) related diseases. (Doctoral Dissertation). University of Edinburgh. Retrieved from http://hdl.handle.net/1842/31174

Chicago Manual of Style (16th Edition):

Cong, Duanduan. “Identification of functional single nucleotide polymorphisms (SNPs) in High Risk-Human Papillomavirus (HR-HPV) related diseases.” 2018. Doctoral Dissertation, University of Edinburgh. Accessed January 17, 2020. http://hdl.handle.net/1842/31174.

MLA Handbook (7th Edition):

Cong, Duanduan. “Identification of functional single nucleotide polymorphisms (SNPs) in High Risk-Human Papillomavirus (HR-HPV) related diseases.” 2018. Web. 17 Jan 2020.

Vancouver:

Cong D. Identification of functional single nucleotide polymorphisms (SNPs) in High Risk-Human Papillomavirus (HR-HPV) related diseases. [Internet] [Doctoral dissertation]. University of Edinburgh; 2018. [cited 2020 Jan 17]. Available from: http://hdl.handle.net/1842/31174.

Council of Science Editors:

Cong D. Identification of functional single nucleotide polymorphisms (SNPs) in High Risk-Human Papillomavirus (HR-HPV) related diseases. [Doctoral Dissertation]. University of Edinburgh; 2018. Available from: http://hdl.handle.net/1842/31174


Queensland University of Technology

15. 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 January 17, 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. 17 Jan 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 Jan 17]. 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


Robert Gordon University

16. Bhatta, Prabhakar. An investigation of genetic polymorphism in association with Type 2 diabetes and metabolic syndrome.

Degree: PhD, 2018, Robert Gordon University

 Type 2 diabetes and metabolic syndrome are the metabolic disorders which constitute a major public health problem in both developed and developing countries. Various studies… (more)

Subjects/Keywords: 610; Type 2 diabetes; Metabolic syndrome; Single nucleotide polymorphism

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APA (6th Edition):

Bhatta, P. (2018). An investigation of genetic polymorphism in association with Type 2 diabetes and metabolic syndrome. (Doctoral Dissertation). Robert Gordon University. Retrieved from http://hdl.handle.net/10059/3105

Chicago Manual of Style (16th Edition):

Bhatta, Prabhakar. “An investigation of genetic polymorphism in association with Type 2 diabetes and metabolic syndrome.” 2018. Doctoral Dissertation, Robert Gordon University. Accessed January 17, 2020. http://hdl.handle.net/10059/3105.

MLA Handbook (7th Edition):

Bhatta, Prabhakar. “An investigation of genetic polymorphism in association with Type 2 diabetes and metabolic syndrome.” 2018. Web. 17 Jan 2020.

Vancouver:

Bhatta P. An investigation of genetic polymorphism in association with Type 2 diabetes and metabolic syndrome. [Internet] [Doctoral dissertation]. Robert Gordon University; 2018. [cited 2020 Jan 17]. Available from: http://hdl.handle.net/10059/3105.

Council of Science Editors:

Bhatta P. An investigation of genetic polymorphism in association with Type 2 diabetes and metabolic syndrome. [Doctoral Dissertation]. Robert Gordon University; 2018. Available from: http://hdl.handle.net/10059/3105

17. 水無瀬, 学. Single-nucleotide polymorphisms in the human RAD21L gene may be a genetic risk factor for Japanese patients with azoospermia caused by meiotic arrest and Sertoli cell-only syndrome : 減数分裂停止及びSertoli cell-only syndromeに起因する日本人無精子症患者におけるヒトRAD21L遺伝子の解析に関する研究.

Degree: 博士(医学), 2018, Asahikawa Medical University / 旭川医科大学

 Genetic mechanisms are implicated in some cases of male infertility. Recently, it was demonstrated that male mice lacking the gene for RAD21L exhibited azoospermia caused… (more)

Subjects/Keywords: Azoospermia; RAD21L; SCOS; meiotic arrest; single-nucleotide polymorphism

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APA (6th Edition):

水無瀬, . (2018). Single-nucleotide polymorphisms in the human RAD21L gene may be a genetic risk factor for Japanese patients with azoospermia caused by meiotic arrest and Sertoli cell-only syndrome : 減数分裂停止及びSertoli cell-only syndromeに起因する日本人無精子症患者におけるヒトRAD21L遺伝子の解析に関する研究. (Thesis). Asahikawa Medical University / 旭川医科大学. Retrieved from http://amcor.asahikawa-med.ac.jp/modules/xoonips/detail.php?id=20180323_K523

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):

水無瀬, 学. “Single-nucleotide polymorphisms in the human RAD21L gene may be a genetic risk factor for Japanese patients with azoospermia caused by meiotic arrest and Sertoli cell-only syndrome : 減数分裂停止及びSertoli cell-only syndromeに起因する日本人無精子症患者におけるヒトRAD21L遺伝子の解析に関する研究.” 2018. Thesis, Asahikawa Medical University / 旭川医科大学. Accessed January 17, 2020. http://amcor.asahikawa-med.ac.jp/modules/xoonips/detail.php?id=20180323_K523.

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

MLA Handbook (7th Edition):

水無瀬, 学. “Single-nucleotide polymorphisms in the human RAD21L gene may be a genetic risk factor for Japanese patients with azoospermia caused by meiotic arrest and Sertoli cell-only syndrome : 減数分裂停止及びSertoli cell-only syndromeに起因する日本人無精子症患者におけるヒトRAD21L遺伝子の解析に関する研究.” 2018. Web. 17 Jan 2020.

Vancouver:

水無瀬 . Single-nucleotide polymorphisms in the human RAD21L gene may be a genetic risk factor for Japanese patients with azoospermia caused by meiotic arrest and Sertoli cell-only syndrome : 減数分裂停止及びSertoli cell-only syndromeに起因する日本人無精子症患者におけるヒトRAD21L遺伝子の解析に関する研究. [Internet] [Thesis]. Asahikawa Medical University / 旭川医科大学; 2018. [cited 2020 Jan 17]. Available from: http://amcor.asahikawa-med.ac.jp/modules/xoonips/detail.php?id=20180323_K523.

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

Council of Science Editors:

水無瀬 . Single-nucleotide polymorphisms in the human RAD21L gene may be a genetic risk factor for Japanese patients with azoospermia caused by meiotic arrest and Sertoli cell-only syndrome : 減数分裂停止及びSertoli cell-only syndromeに起因する日本人無精子症患者におけるヒトRAD21L遺伝子の解析に関する研究. [Thesis]. Asahikawa Medical University / 旭川医科大学; 2018. Available from: http://amcor.asahikawa-med.ac.jp/modules/xoonips/detail.php?id=20180323_K523

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


University of Ghana

18. Yabani, J.E. Phenotypic and Genotypic Analysis of Onchocerca Volvulus Response To Ivermectin Treatment .

Degree: 2017, University of Ghana

 Ivermectin remains the only potent drug for the control and mass treatment of onchocerciasis. Nonetheless, recent studies indicate sub-optimal responses and genetic changes in some… (more)

Subjects/Keywords: Ivermectin; Onchocerca volvulus; mutations; DNA fragment; microfilaria; single nucleotide polymorphism

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APA (6th Edition):

Yabani, J. E. (2017). Phenotypic and Genotypic Analysis of Onchocerca Volvulus Response To Ivermectin Treatment . (Masters Thesis). University of Ghana. Retrieved from http://ugspace.ug.edu.gh/handle/123456789/24730

Chicago Manual of Style (16th Edition):

Yabani, J E. “Phenotypic and Genotypic Analysis of Onchocerca Volvulus Response To Ivermectin Treatment .” 2017. Masters Thesis, University of Ghana. Accessed January 17, 2020. http://ugspace.ug.edu.gh/handle/123456789/24730.

MLA Handbook (7th Edition):

Yabani, J E. “Phenotypic and Genotypic Analysis of Onchocerca Volvulus Response To Ivermectin Treatment .” 2017. Web. 17 Jan 2020.

Vancouver:

Yabani JE. Phenotypic and Genotypic Analysis of Onchocerca Volvulus Response To Ivermectin Treatment . [Internet] [Masters thesis]. University of Ghana; 2017. [cited 2020 Jan 17]. Available from: http://ugspace.ug.edu.gh/handle/123456789/24730.

Council of Science Editors:

Yabani JE. Phenotypic and Genotypic Analysis of Onchocerca Volvulus Response To Ivermectin Treatment . [Masters Thesis]. University of Ghana; 2017. Available from: http://ugspace.ug.edu.gh/handle/123456789/24730


University of the Western Cape

19. Willemse, Gratia-Lize. The role of arylamine N-acetyltransferase 1 (NAT1) in the clinical therapy of tuberculosis .

Degree: 2017, University of the Western Cape

 Despite attempts to develop new drugs to reduce the worldwide mortality rate attributable to tuberculosis (TB), the illness remains a threat. Isoniazid (INH) has been… (more)

Subjects/Keywords: Acetylation; Mycobacterium tuberculosis; NAT1; PAS; PABA; Protein expression; Single nucleotide polymorphism

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APA (6th Edition):

Willemse, G. (2017). The role of arylamine N-acetyltransferase 1 (NAT1) in the clinical therapy of tuberculosis . (Thesis). University of the Western Cape. Retrieved from http://hdl.handle.net/11394/6351

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):

Willemse, Gratia-Lize. “The role of arylamine N-acetyltransferase 1 (NAT1) in the clinical therapy of tuberculosis .” 2017. Thesis, University of the Western Cape. Accessed January 17, 2020. http://hdl.handle.net/11394/6351.

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

MLA Handbook (7th Edition):

Willemse, Gratia-Lize. “The role of arylamine N-acetyltransferase 1 (NAT1) in the clinical therapy of tuberculosis .” 2017. Web. 17 Jan 2020.

Vancouver:

Willemse G. The role of arylamine N-acetyltransferase 1 (NAT1) in the clinical therapy of tuberculosis . [Internet] [Thesis]. University of the Western Cape; 2017. [cited 2020 Jan 17]. Available from: http://hdl.handle.net/11394/6351.

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

Council of Science Editors:

Willemse G. The role of arylamine N-acetyltransferase 1 (NAT1) in the clinical therapy of tuberculosis . [Thesis]. University of the Western Cape; 2017. Available from: http://hdl.handle.net/11394/6351

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


University of the Western Cape

20. 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 January 17, 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. 17 Jan 2020.

Vancouver:

Veldsman WP. SNP based literature and data retrieval . [Internet] [Thesis]. University of the Western Cape; 2016. [cited 2020 Jan 17]. 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


University of New South Wales

21. Schmidt, Heather-Marie Ann. The role of Helicobacter pylori virulence and host genetic factors in gastroduodenal disease.

Degree: Biotechnology & Biomolecular Sciences, 2010, University of New South Wales

 Helicobacter pylori, a gastric bacterial pathogen, colonises >50% of the world’s population. Colonisation invariably leads to chronic gastritis, with a small but significant proportion progressing… (more)

Subjects/Keywords: Single nucleotide polymorphism; Helicobacter pylori; Gastric cancer; CagA; Ethnic diversity

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APA (6th Edition):

Schmidt, H. A. (2010). The role of Helicobacter pylori virulence and host genetic factors in gastroduodenal disease. (Doctoral Dissertation). University of New South Wales. Retrieved from http://handle.unsw.edu.au/1959.4/50234 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:9112/SOURCE02?view=true

Chicago Manual of Style (16th Edition):

Schmidt, Heather-Marie Ann. “The role of Helicobacter pylori virulence and host genetic factors in gastroduodenal disease.” 2010. Doctoral Dissertation, University of New South Wales. Accessed January 17, 2020. http://handle.unsw.edu.au/1959.4/50234 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:9112/SOURCE02?view=true.

MLA Handbook (7th Edition):

Schmidt, Heather-Marie Ann. “The role of Helicobacter pylori virulence and host genetic factors in gastroduodenal disease.” 2010. Web. 17 Jan 2020.

Vancouver:

Schmidt HA. The role of Helicobacter pylori virulence and host genetic factors in gastroduodenal disease. [Internet] [Doctoral dissertation]. University of New South Wales; 2010. [cited 2020 Jan 17]. Available from: http://handle.unsw.edu.au/1959.4/50234 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:9112/SOURCE02?view=true.

Council of Science Editors:

Schmidt HA. The role of Helicobacter pylori virulence and host genetic factors in gastroduodenal disease. [Doctoral Dissertation]. University of New South Wales; 2010. Available from: http://handle.unsw.edu.au/1959.4/50234 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:9112/SOURCE02?view=true


University of Guelph

22. Kroezen, Victoria. Genetic Markers for Resistance to Ketosis in Dairy Cattle .

Degree: 2017, University of Guelph

 High-yielding dairy cattle are susceptible to ketosis, a metabolic disease which negatively affects the health, fertility and production of the cow. The goal of this… (more)

Subjects/Keywords: ketosis; dairy cattle; single-nucleotide polymorphism; candidate gene; energy metabolism

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APA (6th Edition):

Kroezen, V. (2017). Genetic Markers for Resistance to Ketosis in Dairy Cattle . (Thesis). University of Guelph. Retrieved from https://atrium.lib.uoguelph.ca/xmlui/handle/10214/10253

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):

Kroezen, Victoria. “Genetic Markers for Resistance to Ketosis in Dairy Cattle .” 2017. Thesis, University of Guelph. Accessed January 17, 2020. https://atrium.lib.uoguelph.ca/xmlui/handle/10214/10253.

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

MLA Handbook (7th Edition):

Kroezen, Victoria. “Genetic Markers for Resistance to Ketosis in Dairy Cattle .” 2017. Web. 17 Jan 2020.

Vancouver:

Kroezen V. Genetic Markers for Resistance to Ketosis in Dairy Cattle . [Internet] [Thesis]. University of Guelph; 2017. [cited 2020 Jan 17]. Available from: https://atrium.lib.uoguelph.ca/xmlui/handle/10214/10253.

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

Council of Science Editors:

Kroezen V. Genetic Markers for Resistance to Ketosis in Dairy Cattle . [Thesis]. University of Guelph; 2017. Available from: https://atrium.lib.uoguelph.ca/xmlui/handle/10214/10253

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


Queens University

23. Chan, Yuen Man. Functional analysis of single nucleotide polymorphisms in the proximal promoter regions of the multidrug transporter genes MRP1/ABCC1 and MRP4/ABCC4 .

Degree: Pathology and Molecular Medicine, 2007, Queens University

 The ATP-binding cassette (ABC) transporter superfamily consists of 49 members, to which both Multidrug Resistance Protein 1 (MRP1/gene symbol: ABCC1) and MRP4 (ABCC4) belong. Single(more)

Subjects/Keywords: Multidrug resistance; Single nucleotide polymorphism

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APA (6th Edition):

Chan, Y. M. (2007). Functional analysis of single nucleotide polymorphisms in the proximal promoter regions of the multidrug transporter genes MRP1/ABCC1 and MRP4/ABCC4 . (Thesis). Queens University. Retrieved from http://hdl.handle.net/1974/730

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):

Chan, Yuen Man. “Functional analysis of single nucleotide polymorphisms in the proximal promoter regions of the multidrug transporter genes MRP1/ABCC1 and MRP4/ABCC4 .” 2007. Thesis, Queens University. Accessed January 17, 2020. http://hdl.handle.net/1974/730.

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

MLA Handbook (7th Edition):

Chan, Yuen Man. “Functional analysis of single nucleotide polymorphisms in the proximal promoter regions of the multidrug transporter genes MRP1/ABCC1 and MRP4/ABCC4 .” 2007. Web. 17 Jan 2020.

Vancouver:

Chan YM. Functional analysis of single nucleotide polymorphisms in the proximal promoter regions of the multidrug transporter genes MRP1/ABCC1 and MRP4/ABCC4 . [Internet] [Thesis]. Queens University; 2007. [cited 2020 Jan 17]. Available from: http://hdl.handle.net/1974/730.

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

Council of Science Editors:

Chan YM. Functional analysis of single nucleotide polymorphisms in the proximal promoter regions of the multidrug transporter genes MRP1/ABCC1 and MRP4/ABCC4 . [Thesis]. Queens University; 2007. Available from: http://hdl.handle.net/1974/730

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

24. Stenberg, Jenny. Optimization and validation of the method lactose intolerance genotyping with real-time PCR.

Degree: Medical Biochemistry and Microbiology, 2011, Uppsala UniversityUppsala UniversityUppsala UniversityUppsala University

  Abstract Primary lactose intolerance has been associated with a single nucleotide polymorphism located upstream of the lactase gene. The most common diagnostic tests for… (more)

Subjects/Keywords: lactose intolerance; single nucleotide polymorphism; real-time PCR; genotype; optimization.

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APA (6th Edition):

Stenberg, J. (2011). Optimization and validation of the method lactose intolerance genotyping with real-time PCR. (Thesis). Uppsala UniversityUppsala UniversityUppsala UniversityUppsala University. Retrieved from http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-150810

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):

Stenberg, Jenny. “Optimization and validation of the method lactose intolerance genotyping with real-time PCR.” 2011. Thesis, Uppsala UniversityUppsala UniversityUppsala UniversityUppsala University. Accessed January 17, 2020. http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-150810.

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

MLA Handbook (7th Edition):

Stenberg, Jenny. “Optimization and validation of the method lactose intolerance genotyping with real-time PCR.” 2011. Web. 17 Jan 2020.

Vancouver:

Stenberg J. Optimization and validation of the method lactose intolerance genotyping with real-time PCR. [Internet] [Thesis]. Uppsala UniversityUppsala UniversityUppsala UniversityUppsala University; 2011. [cited 2020 Jan 17]. Available from: http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-150810.

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

Council of Science Editors:

Stenberg J. Optimization and validation of the method lactose intolerance genotyping with real-time PCR. [Thesis]. Uppsala UniversityUppsala UniversityUppsala UniversityUppsala University; 2011. Available from: http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-150810

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

25. Mahmoudi, Abd-elrachid. Etude génotypique et phénotypique des polymorphismes du récepteur du complément de type 1 (CR1,CD35) dans la maladie d’Alzheimer : Genotype and phenotype study of complement receptor type 1 polymorphisms (CR1, CD35) in Alzheimer’s disease.

Degree: Docteur es, Médecine - STS, 2015, Reims

Les études d'association pangénomiques ont permis d'identifier de nouveaux loci, dont le gène CR1 comme associé au risque de maladie d'Alzheimer (MA). Le récepteur du… (more)

Subjects/Keywords: Maladie D'Alzheimer; Cr1; Polymorphisme de longueur; Complément; Risque génétique; Single nucleotide polymorphism; Alzheimer’s disease; Cr1; Length Polymorphism; Complement; Genetic risk; Single nucleotide polymorphism; 610

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APA (6th Edition):

Mahmoudi, A. (2015). Etude génotypique et phénotypique des polymorphismes du récepteur du complément de type 1 (CR1,CD35) dans la maladie d’Alzheimer : Genotype and phenotype study of complement receptor type 1 polymorphisms (CR1, CD35) in Alzheimer’s disease. (Doctoral Dissertation). Reims. Retrieved from http://www.theses.fr/2015REIMM201

Chicago Manual of Style (16th Edition):

Mahmoudi, Abd-elrachid. “Etude génotypique et phénotypique des polymorphismes du récepteur du complément de type 1 (CR1,CD35) dans la maladie d’Alzheimer : Genotype and phenotype study of complement receptor type 1 polymorphisms (CR1, CD35) in Alzheimer’s disease.” 2015. Doctoral Dissertation, Reims. Accessed January 17, 2020. http://www.theses.fr/2015REIMM201.

MLA Handbook (7th Edition):

Mahmoudi, Abd-elrachid. “Etude génotypique et phénotypique des polymorphismes du récepteur du complément de type 1 (CR1,CD35) dans la maladie d’Alzheimer : Genotype and phenotype study of complement receptor type 1 polymorphisms (CR1, CD35) in Alzheimer’s disease.” 2015. Web. 17 Jan 2020.

Vancouver:

Mahmoudi A. Etude génotypique et phénotypique des polymorphismes du récepteur du complément de type 1 (CR1,CD35) dans la maladie d’Alzheimer : Genotype and phenotype study of complement receptor type 1 polymorphisms (CR1, CD35) in Alzheimer’s disease. [Internet] [Doctoral dissertation]. Reims; 2015. [cited 2020 Jan 17]. Available from: http://www.theses.fr/2015REIMM201.

Council of Science Editors:

Mahmoudi A. Etude génotypique et phénotypique des polymorphismes du récepteur du complément de type 1 (CR1,CD35) dans la maladie d’Alzheimer : Genotype and phenotype study of complement receptor type 1 polymorphisms (CR1, CD35) in Alzheimer’s disease. [Doctoral Dissertation]. Reims; 2015. Available from: http://www.theses.fr/2015REIMM201


North-West University

26. Mbongwa, Hlengiwe Prosperity. Characterisation of the SULT1A1 polymorphism in a South African Tswana population group / y Hlengiwe P. Mbongwa.

Degree: 2010, North-West University

 This dissertation brings to the fore the “Characterization of the SULT1A1 polymorphism in a South Africa Tswana population group.” The primary experimental group studied came… (more)

Subjects/Keywords: PURE study; South African Tswana population; Copy number polymorphism; Single nucleotide polymorphism; SULT1A1 polymorphism; Sulfotransferases; Targeted metabolomics

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APA (6th Edition):

Mbongwa, H. P. (2010). Characterisation of the SULT1A1 polymorphism in a South African Tswana population group / y Hlengiwe P. Mbongwa. (Thesis). North-West University. Retrieved from http://hdl.handle.net/10394/4225

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):

Mbongwa, Hlengiwe Prosperity. “Characterisation of the SULT1A1 polymorphism in a South African Tswana population group / y Hlengiwe P. Mbongwa. ” 2010. Thesis, North-West University. Accessed January 17, 2020. http://hdl.handle.net/10394/4225.

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

MLA Handbook (7th Edition):

Mbongwa, Hlengiwe Prosperity. “Characterisation of the SULT1A1 polymorphism in a South African Tswana population group / y Hlengiwe P. Mbongwa. ” 2010. Web. 17 Jan 2020.

Vancouver:

Mbongwa HP. Characterisation of the SULT1A1 polymorphism in a South African Tswana population group / y Hlengiwe P. Mbongwa. [Internet] [Thesis]. North-West University; 2010. [cited 2020 Jan 17]. Available from: http://hdl.handle.net/10394/4225.

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

Council of Science Editors:

Mbongwa HP. Characterisation of the SULT1A1 polymorphism in a South African Tswana population group / y Hlengiwe P. Mbongwa. [Thesis]. North-West University; 2010. Available from: http://hdl.handle.net/10394/4225

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

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

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 January 17, 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. 17 Jan 2020.

Vancouver:

Schwender H. Statistical analysis of genotype and gene expression data. [Internet] [Thesis]. Technische Universität Dortmund; 2007. [cited 2020 Jan 17]. 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

28. Rossi, Giulio Antonino. FOXP3, ICOS and ICOSL polymorphisms in an Italian population affected by systemic sclerosis.

Degree: 2017, Università degli Studi di Catania

 Associated with substantial morbidity and mortality rates, systemic sclerosis (SSc) is an autoimmune disorder characterized by vasculopathy, inflammation, progressive perivascular and interstitial fibrosis. SSc pathogenesis… (more)

Subjects/Keywords: Area 05 - Scienze biologiche; Systemic sclerosis; single nucleotide polymorphism; GWAS; autoimmune disease

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

APA (6th Edition):

Rossi, G. A. (2017). FOXP3, ICOS and ICOSL polymorphisms in an Italian population affected by systemic sclerosis. (Thesis). Università degli Studi di Catania. Retrieved from http://hdl.handle.net/10761/4031

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):

Rossi, Giulio Antonino. “FOXP3, ICOS and ICOSL polymorphisms in an Italian population affected by systemic sclerosis.” 2017. Thesis, Università degli Studi di Catania. Accessed January 17, 2020. http://hdl.handle.net/10761/4031.

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

MLA Handbook (7th Edition):

Rossi, Giulio Antonino. “FOXP3, ICOS and ICOSL polymorphisms in an Italian population affected by systemic sclerosis.” 2017. Web. 17 Jan 2020.

Vancouver:

Rossi GA. FOXP3, ICOS and ICOSL polymorphisms in an Italian population affected by systemic sclerosis. [Internet] [Thesis]. Università degli Studi di Catania; 2017. [cited 2020 Jan 17]. Available from: http://hdl.handle.net/10761/4031.

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

Council of Science Editors:

Rossi GA. FOXP3, ICOS and ICOSL polymorphisms in an Italian population affected by systemic sclerosis. [Thesis]. Università degli Studi di Catania; 2017. Available from: http://hdl.handle.net/10761/4031

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

29. Oki, Erica. Associação entre polimorfismos de nucleotídeo único relacionados aos genes da proteína C reativa, TNF- e IL-10 e ácidos graxos plasmáticos e seus efeitos sobre um padrão inflamatório sistêmico em estudo de base populacional - ISA.

Degree: Mestrado, Nutrição em Saúde Pública, 2015, University of São Paulo

 Introdução: Variações genéticas podem influenciar a relação entre ácidos graxos (AG) do plasma e concentração plasmática de biomarcadores inflamatórios. Objetivo: Verificar a associação entre polimorfismos… (more)

Subjects/Keywords: Biomarcadores Inflamatórios; Inflammatory Biomarkers; Lipídios; Lipids; Nutrigenética; Nutrigenetics; Polimorfismos de Nucleotídeo Único; Single Nucleotide Polymorphism

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

APA (6th Edition):

Oki, E. (2015). Associação entre polimorfismos de nucleotídeo único relacionados aos genes da proteína C reativa, TNF- e IL-10 e ácidos graxos plasmáticos e seus efeitos sobre um padrão inflamatório sistêmico em estudo de base populacional - ISA. (Masters Thesis). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/6/6138/tde-18092015-113817/ ;

Chicago Manual of Style (16th Edition):

Oki, Erica. “Associação entre polimorfismos de nucleotídeo único relacionados aos genes da proteína C reativa, TNF- e IL-10 e ácidos graxos plasmáticos e seus efeitos sobre um padrão inflamatório sistêmico em estudo de base populacional - ISA.” 2015. Masters Thesis, University of São Paulo. Accessed January 17, 2020. http://www.teses.usp.br/teses/disponiveis/6/6138/tde-18092015-113817/ ;.

MLA Handbook (7th Edition):

Oki, Erica. “Associação entre polimorfismos de nucleotídeo único relacionados aos genes da proteína C reativa, TNF- e IL-10 e ácidos graxos plasmáticos e seus efeitos sobre um padrão inflamatório sistêmico em estudo de base populacional - ISA.” 2015. Web. 17 Jan 2020.

Vancouver:

Oki E. Associação entre polimorfismos de nucleotídeo único relacionados aos genes da proteína C reativa, TNF- e IL-10 e ácidos graxos plasmáticos e seus efeitos sobre um padrão inflamatório sistêmico em estudo de base populacional - ISA. [Internet] [Masters thesis]. University of São Paulo; 2015. [cited 2020 Jan 17]. Available from: http://www.teses.usp.br/teses/disponiveis/6/6138/tde-18092015-113817/ ;.

Council of Science Editors:

Oki E. Associação entre polimorfismos de nucleotídeo único relacionados aos genes da proteína C reativa, TNF- e IL-10 e ácidos graxos plasmáticos e seus efeitos sobre um padrão inflamatório sistêmico em estudo de base populacional - ISA. [Masters Thesis]. University of São Paulo; 2015. Available from: http://www.teses.usp.br/teses/disponiveis/6/6138/tde-18092015-113817/ ;


University of Alberta

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

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 January 17, 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. 17 Jan 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 Jan 17]. 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

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