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You searched for subject:(Single nucleotide polymorphism). Showing records 1 – 30 of 390 total matches.

[1] [2] [3] [4] [5] … [13]

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University of Waikato

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

Degree: 2012, University of Waikato

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

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

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APA (6th Edition):

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

Chicago Manual of Style (16th Edition):

Mulholland, Claire Vignette. “Single nucleotide polymorphisms associated with the human electroencephalogram during desflurane anaesthesia .” 2012. Masters Thesis, University of Waikato. Accessed October 22, 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. 22 Oct 2020.

Vancouver:

Mulholland CV. Single nucleotide polymorphisms associated with the human electroencephalogram during desflurane anaesthesia . [Internet] [Masters thesis]. University of Waikato; 2012. [cited 2020 Oct 22]. 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


McMaster University

2. 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 October 22, 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. 22 Oct 2020.

Vancouver:

Hua W. Genotypic and phenotypic analyses of two model strains of Cryptococcus neoformans. [Internet] [Masters thesis]. McMaster University; 2017. [cited 2020 Oct 22]. 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


Penn State University

3. Garvin, Nathan Michael. ASSOCIATION OF VARIABILITY IN CARDIOVASCULAR RESPONSIVENESS TO REFLEX ACTIVATION OF THE AUTONOMIC NERVOUS SYSTEM WITH GENETICS OF PERIPHERAL SENSORY RECEPTORS.

Degree: 2017, Penn State University

 Cardiovascular disease accounts for approximately 1 in 3 deaths in the United States and high blood pressure (BP) is one of the risk factors implicated.… (more)

Subjects/Keywords: blood pressure; autonomic; single nucleotide polymorphism

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APA (6th Edition):

Garvin, N. M. (2017). ASSOCIATION OF VARIABILITY IN CARDIOVASCULAR RESPONSIVENESS TO REFLEX ACTIVATION OF THE AUTONOMIC NERVOUS SYSTEM WITH GENETICS OF PERIPHERAL SENSORY RECEPTORS. (Thesis). Penn State University. Retrieved from https://submit-etda.libraries.psu.edu/catalog/14295nmg5181

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):

Garvin, Nathan Michael. “ASSOCIATION OF VARIABILITY IN CARDIOVASCULAR RESPONSIVENESS TO REFLEX ACTIVATION OF THE AUTONOMIC NERVOUS SYSTEM WITH GENETICS OF PERIPHERAL SENSORY RECEPTORS.” 2017. Thesis, Penn State University. Accessed October 22, 2020. https://submit-etda.libraries.psu.edu/catalog/14295nmg5181.

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

MLA Handbook (7th Edition):

Garvin, Nathan Michael. “ASSOCIATION OF VARIABILITY IN CARDIOVASCULAR RESPONSIVENESS TO REFLEX ACTIVATION OF THE AUTONOMIC NERVOUS SYSTEM WITH GENETICS OF PERIPHERAL SENSORY RECEPTORS.” 2017. Web. 22 Oct 2020.

Vancouver:

Garvin NM. ASSOCIATION OF VARIABILITY IN CARDIOVASCULAR RESPONSIVENESS TO REFLEX ACTIVATION OF THE AUTONOMIC NERVOUS SYSTEM WITH GENETICS OF PERIPHERAL SENSORY RECEPTORS. [Internet] [Thesis]. Penn State University; 2017. [cited 2020 Oct 22]. Available from: https://submit-etda.libraries.psu.edu/catalog/14295nmg5181.

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

Council of Science Editors:

Garvin NM. ASSOCIATION OF VARIABILITY IN CARDIOVASCULAR RESPONSIVENESS TO REFLEX ACTIVATION OF THE AUTONOMIC NERVOUS SYSTEM WITH GENETICS OF PERIPHERAL SENSORY RECEPTORS. [Thesis]. Penn State University; 2017. Available from: https://submit-etda.libraries.psu.edu/catalog/14295nmg5181

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


University of Limerick

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

Degree: 2014, University of Limerick

peer-reviewed

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

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

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APA (6th Edition):

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

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

Chicago Manual of Style (16th Edition):

Sheikhi, Ali. “Statistical methods for the detection of single nucleotide polymorphisms (SNPs) using new generation genome sequencers.” 2014. Thesis, University of Limerick. Accessed October 22, 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. 22 Oct 2020.

Vancouver:

Sheikhi A. Statistical methods for the detection of single nucleotide polymorphisms (SNPs) using new generation genome sequencers. [Internet] [Thesis]. University of Limerick; 2014. [cited 2020 Oct 22]. Available from: http://hdl.handle.net/10344/5996.

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

Council of Science Editors:

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

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


University of Cincinnati

5. 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 October 22, 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. 22 Oct 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 Oct 22]. 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


Rice University

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

Degree: MS, Engineering, 2015, Rice University

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

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

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APA (6th Edition):

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

Chicago Manual of Style (16th Edition):

Zafar, Hamim. “A SNP Calling And Genotyping Method For Single-cell Sequencing Data.” 2015. Masters Thesis, Rice University. Accessed October 22, 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. 22 Oct 2020.

Vancouver:

Zafar H. A SNP Calling And Genotyping Method For Single-cell Sequencing Data. [Internet] [Masters thesis]. Rice University; 2015. [cited 2020 Oct 22]. 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


Universidade Estadual de Campinas

7. Zago, Vanessa Helena de Souza, 1984-. Estudo molecular dos genes ABCA1, ABCG1, ABCG5, ABCG8 e SCARB1 em amostra populacional brasileira assintomática: Molecular study of ABCA1, ABCG1, ABCG5, ABCG8 and SCARB1 genes in an asymptomatic brazilian population sample.

Degree: 2015, Universidade Estadual de Campinas

 Abstract: Given the important role played by ATP binding cassete transporters A1 (ABCA1), G1 (ABCG1), G5 (ABCG5), G8 (ABCG8) and by scavenger receptor class B… (more)

Subjects/Keywords: Lipoproteinas; Polimorfismo de nucleotídeo único; MicroRNAs; Lipoproteins; Polymorphism, Single nucleotide; MicroRNAs

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APA (6th Edition):

Zago, Vanessa Helena de Souza, 1. (2015). Estudo molecular dos genes ABCA1, ABCG1, ABCG5, ABCG8 e SCARB1 em amostra populacional brasileira assintomática: Molecular study of ABCA1, ABCG1, ABCG5, ABCG8 and SCARB1 genes in an asymptomatic brazilian population sample. (Thesis). Universidade Estadual de Campinas. Retrieved from http://repositorio.unicamp.br/jspui/handle/REPOSIP/312594

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):

Zago, Vanessa Helena de Souza, 1984-. “Estudo molecular dos genes ABCA1, ABCG1, ABCG5, ABCG8 e SCARB1 em amostra populacional brasileira assintomática: Molecular study of ABCA1, ABCG1, ABCG5, ABCG8 and SCARB1 genes in an asymptomatic brazilian population sample.” 2015. Thesis, Universidade Estadual de Campinas. Accessed October 22, 2020. http://repositorio.unicamp.br/jspui/handle/REPOSIP/312594.

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

MLA Handbook (7th Edition):

Zago, Vanessa Helena de Souza, 1984-. “Estudo molecular dos genes ABCA1, ABCG1, ABCG5, ABCG8 e SCARB1 em amostra populacional brasileira assintomática: Molecular study of ABCA1, ABCG1, ABCG5, ABCG8 and SCARB1 genes in an asymptomatic brazilian population sample.” 2015. Web. 22 Oct 2020.

Vancouver:

Zago, Vanessa Helena de Souza 1. Estudo molecular dos genes ABCA1, ABCG1, ABCG5, ABCG8 e SCARB1 em amostra populacional brasileira assintomática: Molecular study of ABCA1, ABCG1, ABCG5, ABCG8 and SCARB1 genes in an asymptomatic brazilian population sample. [Internet] [Thesis]. Universidade Estadual de Campinas; 2015. [cited 2020 Oct 22]. Available from: http://repositorio.unicamp.br/jspui/handle/REPOSIP/312594.

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

Council of Science Editors:

Zago, Vanessa Helena de Souza 1. Estudo molecular dos genes ABCA1, ABCG1, ABCG5, ABCG8 e SCARB1 em amostra populacional brasileira assintomática: Molecular study of ABCA1, ABCG1, ABCG5, ABCG8 and SCARB1 genes in an asymptomatic brazilian population sample. [Thesis]. Universidade Estadual de Campinas; 2015. Available from: http://repositorio.unicamp.br/jspui/handle/REPOSIP/312594

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


Universidade Estadual de Campinas

8. Messetti, Ana Camila Pereira, 1980-. Estudo multicêntrico brasileiro sobre a associação entre polimorfismos nos genes CRISPLD2 e JARID2 e fissuras orais não-sindrômicas = Brazilian multicenter study of association between polymorphisms in CRISPLD2 and JARID2 nonsyndromic oral cleft: Brazilian multicenter study of association between polymorphisms in CRISPLD2 and JARID2 nonsyndromic oral cleft.

Degree: 2016, Universidade Estadual de Campinas

 Abstract: Variants in the cysteine-rich secretory protein LCCL domain containing 2 gene (CRISPLD2) and in the jumonji, AT-rich interaction domain 2 gene (JARID2) were previously… (more)

Subjects/Keywords: Fenda labial; Polimorfismo de nucleotídeo único; Cleft lip; Polymorphism single nucleotide

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APA (6th Edition):

Messetti, Ana Camila Pereira, 1. (2016). Estudo multicêntrico brasileiro sobre a associação entre polimorfismos nos genes CRISPLD2 e JARID2 e fissuras orais não-sindrômicas = Brazilian multicenter study of association between polymorphisms in CRISPLD2 and JARID2 nonsyndromic oral cleft: Brazilian multicenter study of association between polymorphisms in CRISPLD2 and JARID2 nonsyndromic oral cleft. (Thesis). Universidade Estadual de Campinas. Retrieved from http://repositorio.unicamp.br/jspui/handle/REPOSIP/321295

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):

Messetti, Ana Camila Pereira, 1980-. “Estudo multicêntrico brasileiro sobre a associação entre polimorfismos nos genes CRISPLD2 e JARID2 e fissuras orais não-sindrômicas = Brazilian multicenter study of association between polymorphisms in CRISPLD2 and JARID2 nonsyndromic oral cleft: Brazilian multicenter study of association between polymorphisms in CRISPLD2 and JARID2 nonsyndromic oral cleft.” 2016. Thesis, Universidade Estadual de Campinas. Accessed October 22, 2020. http://repositorio.unicamp.br/jspui/handle/REPOSIP/321295.

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

MLA Handbook (7th Edition):

Messetti, Ana Camila Pereira, 1980-. “Estudo multicêntrico brasileiro sobre a associação entre polimorfismos nos genes CRISPLD2 e JARID2 e fissuras orais não-sindrômicas = Brazilian multicenter study of association between polymorphisms in CRISPLD2 and JARID2 nonsyndromic oral cleft: Brazilian multicenter study of association between polymorphisms in CRISPLD2 and JARID2 nonsyndromic oral cleft.” 2016. Web. 22 Oct 2020.

Vancouver:

Messetti, Ana Camila Pereira 1. Estudo multicêntrico brasileiro sobre a associação entre polimorfismos nos genes CRISPLD2 e JARID2 e fissuras orais não-sindrômicas = Brazilian multicenter study of association between polymorphisms in CRISPLD2 and JARID2 nonsyndromic oral cleft: Brazilian multicenter study of association between polymorphisms in CRISPLD2 and JARID2 nonsyndromic oral cleft. [Internet] [Thesis]. Universidade Estadual de Campinas; 2016. [cited 2020 Oct 22]. Available from: http://repositorio.unicamp.br/jspui/handle/REPOSIP/321295.

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

Council of Science Editors:

Messetti, Ana Camila Pereira 1. Estudo multicêntrico brasileiro sobre a associação entre polimorfismos nos genes CRISPLD2 e JARID2 e fissuras orais não-sindrômicas = Brazilian multicenter study of association between polymorphisms in CRISPLD2 and JARID2 nonsyndromic oral cleft: Brazilian multicenter study of association between polymorphisms in CRISPLD2 and JARID2 nonsyndromic oral cleft. [Thesis]. Universidade Estadual de Campinas; 2016. Available from: http://repositorio.unicamp.br/jspui/handle/REPOSIP/321295

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


Texas A&M University

9. Gunaratna, Ramesh Tharindu. Dynamic Role of the Codon 72 P53 Single Nucleotide Polymorphism in Mammary Tumorigenesis in a Humanized Mouse Model.

Degree: PhD, Genetics, 2018, Texas A&M University

 Female breast cancer (BrCa) is the most common noncutaneous cancer among women in the United States. Human epidemiological studies reveal that p53 codon 72 single(more)

Subjects/Keywords: p53; single nucleotide polymorphism; mammary tumorigenesis; SASP; inflammation; macrophages

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APA (6th Edition):

Gunaratna, R. T. (2018). Dynamic Role of the Codon 72 P53 Single Nucleotide Polymorphism in Mammary Tumorigenesis in a Humanized Mouse Model. (Doctoral Dissertation). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/173408

Chicago Manual of Style (16th Edition):

Gunaratna, Ramesh Tharindu. “Dynamic Role of the Codon 72 P53 Single Nucleotide Polymorphism in Mammary Tumorigenesis in a Humanized Mouse Model.” 2018. Doctoral Dissertation, Texas A&M University. Accessed October 22, 2020. http://hdl.handle.net/1969.1/173408.

MLA Handbook (7th Edition):

Gunaratna, Ramesh Tharindu. “Dynamic Role of the Codon 72 P53 Single Nucleotide Polymorphism in Mammary Tumorigenesis in a Humanized Mouse Model.” 2018. Web. 22 Oct 2020.

Vancouver:

Gunaratna RT. Dynamic Role of the Codon 72 P53 Single Nucleotide Polymorphism in Mammary Tumorigenesis in a Humanized Mouse Model. [Internet] [Doctoral dissertation]. Texas A&M University; 2018. [cited 2020 Oct 22]. Available from: http://hdl.handle.net/1969.1/173408.

Council of Science Editors:

Gunaratna RT. Dynamic Role of the Codon 72 P53 Single Nucleotide Polymorphism in Mammary Tumorigenesis in a Humanized Mouse Model. [Doctoral Dissertation]. Texas A&M University; 2018. Available from: http://hdl.handle.net/1969.1/173408


Texas A&M University

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

Degree: PhD, Genetics, 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. (Doctoral Dissertation). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/155055

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. Doctoral Dissertation, Texas A&M University. Accessed October 22, 2020. http://hdl.handle.net/1969.1/155055.

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. 22 Oct 2020.

Vancouver:

Hulse-Kemp AM. Development of Genomic Markers and Mapping Tools for Assembling the Allotetraploid Gossypium hirsutum L. Draft Genome Sequence. [Internet] [Doctoral dissertation]. Texas A&M University; 2015. [cited 2020 Oct 22]. Available from: http://hdl.handle.net/1969.1/155055.

Council of Science Editors:

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


Penn State University

11. Vasquez, Kate. Post-embryonic mutations are inherited in the next generation of corals.

Degree: 2019, Penn State University

 Increasingly frequent wide-spread coral bleaching caused by rising seawater temperatures is a strong selective force that is changing the genetic composition of surviving coral populations.… (more)

Subjects/Keywords: Post-embryonic mutation; parthenogenesis; Acropora palmata; Microsatellite; Single Nucleotide Polymorphism

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APA (6th Edition):

Vasquez, K. (2019). Post-embryonic mutations are inherited in the next generation of corals. (Thesis). Penn State University. Retrieved from https://submit-etda.libraries.psu.edu/catalog/17223klv9

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):

Vasquez, Kate. “Post-embryonic mutations are inherited in the next generation of corals.” 2019. Thesis, Penn State University. Accessed October 22, 2020. https://submit-etda.libraries.psu.edu/catalog/17223klv9.

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

MLA Handbook (7th Edition):

Vasquez, Kate. “Post-embryonic mutations are inherited in the next generation of corals.” 2019. Web. 22 Oct 2020.

Vancouver:

Vasquez K. Post-embryonic mutations are inherited in the next generation of corals. [Internet] [Thesis]. Penn State University; 2019. [cited 2020 Oct 22]. Available from: https://submit-etda.libraries.psu.edu/catalog/17223klv9.

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

Council of Science Editors:

Vasquez K. Post-embryonic mutations are inherited in the next generation of corals. [Thesis]. Penn State University; 2019. Available from: https://submit-etda.libraries.psu.edu/catalog/17223klv9

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


University of Ghana

12. 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 October 22, 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. 22 Oct 2020.

Vancouver:

Yabani JE. Phenotypic and Genotypic Analysis of Onchocerca Volvulus Response To Ivermectin Treatment . [Internet] [Masters thesis]. University of Ghana; 2017. [cited 2020 Oct 22]. 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 Edinburgh

13. 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: 616.9; 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 October 22, 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. 22 Oct 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 Oct 22]. 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


University of the Western Cape

14. 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 October 22, 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. 22 Oct 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 Oct 22]. 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

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

Degree: 2016, University of the Western Cape

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

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

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APA (6th Edition):

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

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

Chicago Manual of Style (16th Edition):

Veldsman, Werner Pieter. “SNP based literature and data retrieval .” 2016. Thesis, University of the Western Cape. Accessed October 22, 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. 22 Oct 2020.

Vancouver:

Veldsman WP. SNP based literature and data retrieval . [Internet] [Thesis]. University of the Western Cape; 2016. [cited 2020 Oct 22]. Available from: http://hdl.handle.net/11394/5345.

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

Council of Science Editors:

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

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


Queensland University of Technology

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

Degree: 2010, Queensland University of Technology

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

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

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APA (6th Edition):

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

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

Chicago Manual of Style (16th Edition):

Costello, Mary-Ellen Clare. “Single nucleotide polymorphism (SNP) - genotyping of Community Acquired Methicillin-Resistant Staphylococcus aureus, including the subtyping of PVL toxin producers using Real-Time PCR.” 2010. Thesis, Queensland University of Technology. Accessed October 22, 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. 22 Oct 2020.

Vancouver:

Costello MC. Single nucleotide polymorphism (SNP) - genotyping of Community Acquired Methicillin-Resistant Staphylococcus aureus, including the subtyping of PVL toxin producers using Real-Time PCR. [Internet] [Thesis]. Queensland University of Technology; 2010. [cited 2020 Oct 22]. 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

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 October 22, 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. 22 Oct 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 Oct 22]. 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


Robert Gordon University

18. 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 https://rgu-repository.worktribe.com/output/248956 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.758176

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 October 22, 2020. https://rgu-repository.worktribe.com/output/248956 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.758176.

MLA Handbook (7th Edition):

Bhatta, Prabhakar. “An investigation of genetic polymorphism in association with Type 2 diabetes and metabolic syndrome.” 2018. Web. 22 Oct 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 Oct 22]. Available from: https://rgu-repository.worktribe.com/output/248956 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.758176.

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: https://rgu-repository.worktribe.com/output/248956 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.758176


University of Edinburgh

19. 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 October 22, 2020. http://hdl.handle.net/1842/10038.

MLA Handbook (7th Edition):

Huffman, Jennifer Elizabeth. “Genetic analysis of protein N-glycosylation.” 2014. Web. 22 Oct 2020.

Vancouver:

Huffman JE. Genetic analysis of protein N-glycosylation. [Internet] [Doctoral dissertation]. University of Edinburgh; 2014. [cited 2020 Oct 22]. 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

20. 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 October 22, 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. 22 Oct 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 Oct 22]. 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


University of Toronto

21. Bani-Fatemi, Ali. Genetics and Epigenetics of Suicidal Behavior.

Degree: PhD, 2018, University of Toronto

 According to the latest World Health Organization report (2012), suicide was the second leading cause of death among people. Approximately 90% of suicide victims or… (more)

Subjects/Keywords: CpG; DNA methylation; Epigenetics; Schizophrenia; single-nucleotide polymorphism; Suicidal behavior; 0369

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APA (6th Edition):

Bani-Fatemi, A. (2018). Genetics and Epigenetics of Suicidal Behavior. (Doctoral Dissertation). University of Toronto. Retrieved from http://hdl.handle.net/1807/91878

Chicago Manual of Style (16th Edition):

Bani-Fatemi, Ali. “Genetics and Epigenetics of Suicidal Behavior.” 2018. Doctoral Dissertation, University of Toronto. Accessed October 22, 2020. http://hdl.handle.net/1807/91878.

MLA Handbook (7th Edition):

Bani-Fatemi, Ali. “Genetics and Epigenetics of Suicidal Behavior.” 2018. Web. 22 Oct 2020.

Vancouver:

Bani-Fatemi A. Genetics and Epigenetics of Suicidal Behavior. [Internet] [Doctoral dissertation]. University of Toronto; 2018. [cited 2020 Oct 22]. Available from: http://hdl.handle.net/1807/91878.

Council of Science Editors:

Bani-Fatemi A. Genetics and Epigenetics of Suicidal Behavior. [Doctoral Dissertation]. University of Toronto; 2018. Available from: http://hdl.handle.net/1807/91878


University of Southern California

22. 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/1163

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 October 22, 2020. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/241673/rec/1163.

MLA Handbook (7th Edition):

Rhie, Suhn Kyong. “Breast epithelial cell type specific enhancers and functional annotation of breast cancer risk loci.” 2013. Web. 22 Oct 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 Oct 22]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/241673/rec/1163.

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/1163


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 October 22, 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. 22 Oct 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 Oct 22]. 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


University of Ottawa

24. Fatima, Fizza. Genome-Wide Association Study for Disease Traits In Wheat and Its Wild Relatives.

Degree: MSc, Sciences / Science, 2020, University of Ottawa

 Wheat is the most widely grown crop in the world and as such, is an essential source of energy and nutrition. The challenges that breeders… (more)

Subjects/Keywords: Wheat; Leaf rust; GWAS; Genotyping; Single nucleotide polymorphism; Triticum aestivum

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APA (6th Edition):

Fatima, F. (2020). Genome-Wide Association Study for Disease Traits In Wheat and Its Wild Relatives. (Masters Thesis). University of Ottawa. Retrieved from http://dx.doi.org/10.20381/ruor-25126

Chicago Manual of Style (16th Edition):

Fatima, Fizza. “Genome-Wide Association Study for Disease Traits In Wheat and Its Wild Relatives.” 2020. Masters Thesis, University of Ottawa. Accessed October 22, 2020. http://dx.doi.org/10.20381/ruor-25126.

MLA Handbook (7th Edition):

Fatima, Fizza. “Genome-Wide Association Study for Disease Traits In Wheat and Its Wild Relatives.” 2020. Web. 22 Oct 2020.

Vancouver:

Fatima F. Genome-Wide Association Study for Disease Traits In Wheat and Its Wild Relatives. [Internet] [Masters thesis]. University of Ottawa; 2020. [cited 2020 Oct 22]. Available from: http://dx.doi.org/10.20381/ruor-25126.

Council of Science Editors:

Fatima F. Genome-Wide Association Study for Disease Traits In Wheat and Its Wild Relatives. [Masters Thesis]. University of Ottawa; 2020. Available from: http://dx.doi.org/10.20381/ruor-25126


University of Kansas

25. 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 October 22, 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. 22 Oct 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 Oct 22]. 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

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

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 October 22, 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. 22 Oct 2020.

Vancouver:

Yatskiv YR. A Haplotype Analysis of an Archaic Denisovan Genome. [Internet] [Masters thesis]. University of Toledo Health Science Campus; 2016. [cited 2020 Oct 22]. 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

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

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 October 22, 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. 22 Oct 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 Oct 22]. 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

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

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 October 22, 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. 22 Oct 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 Oct 22]. 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


University of Guelph

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

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

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

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

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

APA (6th Edition):

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

Chicago Manual of Style (16th Edition):

Wong, Jeremy. “Investigating single-nucleotide variants in swine associated with common infectious pathogens and diseases, with a focus on Streptococcus suis infection, using a genome-wide association study approach.” 2020. Masters Thesis, University of Guelph. Accessed October 22, 2020. https://atrium.lib.uoguelph.ca/xmlui/handle/10214/18037.

MLA Handbook (7th Edition):

Wong, Jeremy. “Investigating single-nucleotide variants in swine associated with common infectious pathogens and diseases, with a focus on Streptococcus suis infection, using a genome-wide association study approach.” 2020. Web. 22 Oct 2020.

Vancouver:

Wong J. Investigating single-nucleotide variants in swine associated with common infectious pathogens and diseases, with a focus on Streptococcus suis infection, using a genome-wide association study approach. [Internet] [Masters thesis]. University of Guelph; 2020. [cited 2020 Oct 22]. Available from: https://atrium.lib.uoguelph.ca/xmlui/handle/10214/18037.

Council of Science Editors:

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


NSYSU

30. Chen, I-ya. Costimulatory molecules as genetic markers for relapse of Gravesâ disease.

Degree: Master, Biological Sciences, 2009, NSYSU

 Gravesâ disease (GD), an organ specific autoimmune disease, requires two signals to activate the T cells. In addition to the specific binding of T cell… (more)

Subjects/Keywords: CD40; PDCD-1; ICOS; CTLA-4; CD28; costimulatory factor; Graves' disease; haplotype; single nucleotide polymorphism

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

APA (6th Edition):

Chen, I. (2009). Costimulatory molecules as genetic markers for relapse of Gravesâ disease. (Thesis). NSYSU. Retrieved from http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0323109-115415

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):

Chen, I-ya. “Costimulatory molecules as genetic markers for relapse of Gravesâ disease.” 2009. Thesis, NSYSU. Accessed October 22, 2020. http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0323109-115415.

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

MLA Handbook (7th Edition):

Chen, I-ya. “Costimulatory molecules as genetic markers for relapse of Gravesâ disease.” 2009. Web. 22 Oct 2020.

Vancouver:

Chen I. Costimulatory molecules as genetic markers for relapse of Gravesâ disease. [Internet] [Thesis]. NSYSU; 2009. [cited 2020 Oct 22]. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0323109-115415.

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

Council of Science Editors:

Chen I. Costimulatory molecules as genetic markers for relapse of Gravesâ disease. [Thesis]. NSYSU; 2009. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0323109-115415

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

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