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You searched for subject:(Polymorphisms). Showing records 1 – 30 of 862 total matches.

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University of Pretoria

1. [No author]. New tools for comparative genomics based on oligonucleotide compositional constraints and single nucleotide polymorphisms .

Degree: 2010, University of Pretoria

 Tuberculosis is one of the leading causes of mortality globally. Although this disease has been around for many generations, treatment and management of the disease… (more)

Subjects/Keywords: Nucleotide polymorphisms; Comparative genomics; UCTD

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APA (6th Edition):

author], [. (2010). New tools for comparative genomics based on oligonucleotide compositional constraints and single nucleotide polymorphisms . (Doctoral Dissertation). University of Pretoria. Retrieved from http://upetd.up.ac.za/thesis/available/etd-06042010-004142/

Chicago Manual of Style (16th Edition):

author], [No. “New tools for comparative genomics based on oligonucleotide compositional constraints and single nucleotide polymorphisms .” 2010. Doctoral Dissertation, University of Pretoria. Accessed November 28, 2020. http://upetd.up.ac.za/thesis/available/etd-06042010-004142/.

MLA Handbook (7th Edition):

author], [No. “New tools for comparative genomics based on oligonucleotide compositional constraints and single nucleotide polymorphisms .” 2010. Web. 28 Nov 2020.

Vancouver:

author] [. New tools for comparative genomics based on oligonucleotide compositional constraints and single nucleotide polymorphisms . [Internet] [Doctoral dissertation]. University of Pretoria; 2010. [cited 2020 Nov 28]. Available from: http://upetd.up.ac.za/thesis/available/etd-06042010-004142/.

Council of Science Editors:

author] [. New tools for comparative genomics based on oligonucleotide compositional constraints and single nucleotide polymorphisms . [Doctoral Dissertation]. University of Pretoria; 2010. Available from: http://upetd.up.ac.za/thesis/available/etd-06042010-004142/

2. Sapkota, Shraddha. Synergistic Associations of Genetic, Demographic, Health, and Lifestyle Risk Factors on Neurocognitive Performance and Change in Aging.

Degree: PhD, Centre for Neuroscience, 2016, University of Alberta

 Objective: Neurocognitive phenotypes observed in aging have been linked to select combinations of candidate genetic polymorphisms and modifiable risk factors. In this dissertation, I test… (more)

Subjects/Keywords: Aging; Neurocognitive Performance; Genetic Polymorphisms

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APA (6th Edition):

Sapkota, S. (2016). Synergistic Associations of Genetic, Demographic, Health, and Lifestyle Risk Factors on Neurocognitive Performance and Change in Aging. (Doctoral Dissertation). University of Alberta. Retrieved from https://era.library.ualberta.ca/files/csn009x77d

Chicago Manual of Style (16th Edition):

Sapkota, Shraddha. “Synergistic Associations of Genetic, Demographic, Health, and Lifestyle Risk Factors on Neurocognitive Performance and Change in Aging.” 2016. Doctoral Dissertation, University of Alberta. Accessed November 28, 2020. https://era.library.ualberta.ca/files/csn009x77d.

MLA Handbook (7th Edition):

Sapkota, Shraddha. “Synergistic Associations of Genetic, Demographic, Health, and Lifestyle Risk Factors on Neurocognitive Performance and Change in Aging.” 2016. Web. 28 Nov 2020.

Vancouver:

Sapkota S. Synergistic Associations of Genetic, Demographic, Health, and Lifestyle Risk Factors on Neurocognitive Performance and Change in Aging. [Internet] [Doctoral dissertation]. University of Alberta; 2016. [cited 2020 Nov 28]. Available from: https://era.library.ualberta.ca/files/csn009x77d.

Council of Science Editors:

Sapkota S. Synergistic Associations of Genetic, Demographic, Health, and Lifestyle Risk Factors on Neurocognitive Performance and Change in Aging. [Doctoral Dissertation]. University of Alberta; 2016. Available from: https://era.library.ualberta.ca/files/csn009x77d


University of Pretoria

3. Ganesan, Hamilton. New tools for comparative genomics based on oligonucleotide compositional constraints and single nucleotide polymorphisms.

Degree: Biochemistry, 2010, University of Pretoria

 Tuberculosis is one of the leading causes of mortality globally. Although this disease has been around for many generations, treatment and management of the disease… (more)

Subjects/Keywords: Nucleotide polymorphisms; Comparative genomics; UCTD

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APA (6th Edition):

Ganesan, H. (2010). New tools for comparative genomics based on oligonucleotide compositional constraints and single nucleotide polymorphisms. (Doctoral Dissertation). University of Pretoria. Retrieved from http://hdl.handle.net/2263/25245

Chicago Manual of Style (16th Edition):

Ganesan, Hamilton. “New tools for comparative genomics based on oligonucleotide compositional constraints and single nucleotide polymorphisms.” 2010. Doctoral Dissertation, University of Pretoria. Accessed November 28, 2020. http://hdl.handle.net/2263/25245.

MLA Handbook (7th Edition):

Ganesan, Hamilton. “New tools for comparative genomics based on oligonucleotide compositional constraints and single nucleotide polymorphisms.” 2010. Web. 28 Nov 2020.

Vancouver:

Ganesan H. New tools for comparative genomics based on oligonucleotide compositional constraints and single nucleotide polymorphisms. [Internet] [Doctoral dissertation]. University of Pretoria; 2010. [cited 2020 Nov 28]. Available from: http://hdl.handle.net/2263/25245.

Council of Science Editors:

Ganesan H. New tools for comparative genomics based on oligonucleotide compositional constraints and single nucleotide polymorphisms. [Doctoral Dissertation]. University of Pretoria; 2010. Available from: http://hdl.handle.net/2263/25245


Oregon State University

4. McDonald, John H. Ecological genetics of two polymorphic enzymes in three species of Megalorchestia (Amphipoda:Talitridae).

Degree: MS, Oceanography, 1983, Oregon State University

Subjects/Keywords: Genetic polymorphisms

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APA (6th Edition):

McDonald, J. H. (1983). Ecological genetics of two polymorphic enzymes in three species of Megalorchestia (Amphipoda:Talitridae). (Masters Thesis). Oregon State University. Retrieved from http://hdl.handle.net/1957/28199

Chicago Manual of Style (16th Edition):

McDonald, John H. “Ecological genetics of two polymorphic enzymes in three species of Megalorchestia (Amphipoda:Talitridae).” 1983. Masters Thesis, Oregon State University. Accessed November 28, 2020. http://hdl.handle.net/1957/28199.

MLA Handbook (7th Edition):

McDonald, John H. “Ecological genetics of two polymorphic enzymes in three species of Megalorchestia (Amphipoda:Talitridae).” 1983. Web. 28 Nov 2020.

Vancouver:

McDonald JH. Ecological genetics of two polymorphic enzymes in three species of Megalorchestia (Amphipoda:Talitridae). [Internet] [Masters thesis]. Oregon State University; 1983. [cited 2020 Nov 28]. Available from: http://hdl.handle.net/1957/28199.

Council of Science Editors:

McDonald JH. Ecological genetics of two polymorphic enzymes in three species of Megalorchestia (Amphipoda:Talitridae). [Masters Thesis]. Oregon State University; 1983. Available from: http://hdl.handle.net/1957/28199

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

Degree: 2009, University of Pune

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

Subjects/Keywords: Biotechnology; Single Nucleotide Polymorphisms

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APA (6th Edition):

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

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

Chicago Manual of Style (16th Edition):

Bhasin, Yasha. “Single nucleotide polymorphisms (SNPs) in complex disorders: a genome-widw computational analysis.” 2009. Thesis, University of Pune. Accessed November 28, 2020. http://shodhganga.inflibnet.ac.in/handle/10603/3417.

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

MLA Handbook (7th Edition):

Bhasin, Yasha. “Single nucleotide polymorphisms (SNPs) in complex disorders: a genome-widw computational analysis.” 2009. Web. 28 Nov 2020.

Vancouver:

Bhasin Y. Single nucleotide polymorphisms (SNPs) in complex disorders: a genome-widw computational analysis. [Internet] [Thesis]. University of Pune; 2009. [cited 2020 Nov 28]. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/3417.

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

Council of Science Editors:

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

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

6. Bali, Prerna. Toll like receptor polymorphisms in relation to malaria in the Indian population; -.

Degree: Zoology, 2013, University of Delhi

Available

Bibliography p.98-115, Appendix p.122-128

Advisors/Committee Members: Singh, A K and Adak, T.

Subjects/Keywords: Polymorphisms; Malaria

Page 1

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APA (6th Edition):

Bali, P. (2013). Toll like receptor polymorphisms in relation to malaria in the Indian population; -. (Thesis). University of Delhi. Retrieved from http://shodhganga.inflibnet.ac.in/handle/10603/26844

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):

Bali, Prerna. “Toll like receptor polymorphisms in relation to malaria in the Indian population; -.” 2013. Thesis, University of Delhi. Accessed November 28, 2020. http://shodhganga.inflibnet.ac.in/handle/10603/26844.

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

MLA Handbook (7th Edition):

Bali, Prerna. “Toll like receptor polymorphisms in relation to malaria in the Indian population; -.” 2013. Web. 28 Nov 2020.

Vancouver:

Bali P. Toll like receptor polymorphisms in relation to malaria in the Indian population; -. [Internet] [Thesis]. University of Delhi; 2013. [cited 2020 Nov 28]. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/26844.

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

Council of Science Editors:

Bali P. Toll like receptor polymorphisms in relation to malaria in the Indian population; -. [Thesis]. University of Delhi; 2013. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/26844

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


Oregon State University

7. Templeton, Joe Wayne, 1941-. Genetic polymorphism of sheep hemoglobin.

Degree: PhD, Genetics, 1968, Oregon State University

 Five breeds of sheep (Columbia, Targhee, Rambouillet, Lincoln, and Suffolk) were found to possess two hemoglobin types (Hb. A and Hb. B) when their hemoglobins… (more)

Subjects/Keywords: Genetic polymorphisms

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APA (6th Edition):

Templeton, Joe Wayne, 1. (1968). Genetic polymorphism of sheep hemoglobin. (Doctoral Dissertation). Oregon State University. Retrieved from http://hdl.handle.net/1957/46356

Chicago Manual of Style (16th Edition):

Templeton, Joe Wayne, 1941-. “Genetic polymorphism of sheep hemoglobin.” 1968. Doctoral Dissertation, Oregon State University. Accessed November 28, 2020. http://hdl.handle.net/1957/46356.

MLA Handbook (7th Edition):

Templeton, Joe Wayne, 1941-. “Genetic polymorphism of sheep hemoglobin.” 1968. Web. 28 Nov 2020.

Vancouver:

Templeton, Joe Wayne 1. Genetic polymorphism of sheep hemoglobin. [Internet] [Doctoral dissertation]. Oregon State University; 1968. [cited 2020 Nov 28]. Available from: http://hdl.handle.net/1957/46356.

Council of Science Editors:

Templeton, Joe Wayne 1. Genetic polymorphism of sheep hemoglobin. [Doctoral Dissertation]. Oregon State University; 1968. Available from: http://hdl.handle.net/1957/46356


Laurentian University

8. Baath, Simran. Genetic background and environmental effects on single nucleotide polymorphisms in the NADPH pathway .

Degree: 2018, Laurentian University

 A major focus in modern genomics is determining the connection between genotypes and quantifying phenotypes. In this connection, many factors come into play including different… (more)

Subjects/Keywords: Nucleotide polymorphisms; NADPH; phenotypes; genotypes

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APA (6th Edition):

Baath, S. (2018). Genetic background and environmental effects on single nucleotide polymorphisms in the NADPH pathway . (Thesis). Laurentian University. Retrieved from https://zone.biblio.laurentian.ca/handle/10219/3236

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):

Baath, Simran. “Genetic background and environmental effects on single nucleotide polymorphisms in the NADPH pathway .” 2018. Thesis, Laurentian University. Accessed November 28, 2020. https://zone.biblio.laurentian.ca/handle/10219/3236.

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

MLA Handbook (7th Edition):

Baath, Simran. “Genetic background and environmental effects on single nucleotide polymorphisms in the NADPH pathway .” 2018. Web. 28 Nov 2020.

Vancouver:

Baath S. Genetic background and environmental effects on single nucleotide polymorphisms in the NADPH pathway . [Internet] [Thesis]. Laurentian University; 2018. [cited 2020 Nov 28]. Available from: https://zone.biblio.laurentian.ca/handle/10219/3236.

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

Council of Science Editors:

Baath S. Genetic background and environmental effects on single nucleotide polymorphisms in the NADPH pathway . [Thesis]. Laurentian University; 2018. Available from: https://zone.biblio.laurentian.ca/handle/10219/3236

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


University of Louisville

9. Connor, Avonne Elish. The beta-2 adrenergic receptor polymorphisms and risk of breast cancer among hispanic and non-hispanic white women from the 4-corners breast cancer study : a population-based case-control examination.

Degree: PhD, 2011, University of Louisville

Polymorphisms in the adrenergic receptor beta-2 (ADRB2) gene have been studied in relation to risk of Type 2 diabetes and obesity, but few studies have… (more)

Subjects/Keywords: Breast cancer; Ethnicity; Epidemiology; Polymorphisms

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APA (6th Edition):

Connor, A. E. (2011). The beta-2 adrenergic receptor polymorphisms and risk of breast cancer among hispanic and non-hispanic white women from the 4-corners breast cancer study : a population-based case-control examination. (Doctoral Dissertation). University of Louisville. Retrieved from 10.18297/etd/271 ; https://ir.library.louisville.edu/etd/271

Chicago Manual of Style (16th Edition):

Connor, Avonne Elish. “The beta-2 adrenergic receptor polymorphisms and risk of breast cancer among hispanic and non-hispanic white women from the 4-corners breast cancer study : a population-based case-control examination.” 2011. Doctoral Dissertation, University of Louisville. Accessed November 28, 2020. 10.18297/etd/271 ; https://ir.library.louisville.edu/etd/271.

MLA Handbook (7th Edition):

Connor, Avonne Elish. “The beta-2 adrenergic receptor polymorphisms and risk of breast cancer among hispanic and non-hispanic white women from the 4-corners breast cancer study : a population-based case-control examination.” 2011. Web. 28 Nov 2020.

Vancouver:

Connor AE. The beta-2 adrenergic receptor polymorphisms and risk of breast cancer among hispanic and non-hispanic white women from the 4-corners breast cancer study : a population-based case-control examination. [Internet] [Doctoral dissertation]. University of Louisville; 2011. [cited 2020 Nov 28]. Available from: 10.18297/etd/271 ; https://ir.library.louisville.edu/etd/271.

Council of Science Editors:

Connor AE. The beta-2 adrenergic receptor polymorphisms and risk of breast cancer among hispanic and non-hispanic white women from the 4-corners breast cancer study : a population-based case-control examination. [Doctoral Dissertation]. University of Louisville; 2011. Available from: 10.18297/etd/271 ; https://ir.library.louisville.edu/etd/271


Rutgers University

10. Misra, Ashish, 1981. Analysis of single nucleotide polymorphisms using molecular affinity separation and mass spectrometry.

Degree: PhD, Chemical and Biochemical Engineering, 2009, Rutgers University

Single nucleotide polymorphisms (SNP) constitute the most abundant human genetic variations and are important markers for studying interindividual variability with many different techniques having being… (more)

Subjects/Keywords: Genetic polymorphisms

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APA (6th Edition):

Misra, Ashish, 1. (2009). Analysis of single nucleotide polymorphisms using molecular affinity separation and mass spectrometry. (Doctoral Dissertation). Rutgers University. Retrieved from http://hdl.rutgers.edu/1782.2/rucore10001600001.ETD.000051381

Chicago Manual of Style (16th Edition):

Misra, Ashish, 1981. “Analysis of single nucleotide polymorphisms using molecular affinity separation and mass spectrometry.” 2009. Doctoral Dissertation, Rutgers University. Accessed November 28, 2020. http://hdl.rutgers.edu/1782.2/rucore10001600001.ETD.000051381.

MLA Handbook (7th Edition):

Misra, Ashish, 1981. “Analysis of single nucleotide polymorphisms using molecular affinity separation and mass spectrometry.” 2009. Web. 28 Nov 2020.

Vancouver:

Misra, Ashish 1. Analysis of single nucleotide polymorphisms using molecular affinity separation and mass spectrometry. [Internet] [Doctoral dissertation]. Rutgers University; 2009. [cited 2020 Nov 28]. Available from: http://hdl.rutgers.edu/1782.2/rucore10001600001.ETD.000051381.

Council of Science Editors:

Misra, Ashish 1. Analysis of single nucleotide polymorphisms using molecular affinity separation and mass spectrometry. [Doctoral Dissertation]. Rutgers University; 2009. Available from: http://hdl.rutgers.edu/1782.2/rucore10001600001.ETD.000051381


University of New South Wales

11. Tang, Joyce Chi Man. Studies on the Vitamin C transporter gene SLC23A2 and cardiac conduction.

Degree: Rural Clinical School, 2017, University of New South Wales

 This thesis considers the role of Vitamin C genes on cardiac conduction. Firstly we performed a systematic literature review to ascertain the protective effects of… (more)

Subjects/Keywords: Polymorphisms; Vitamin C; Cardiac Conduction

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APA (6th Edition):

Tang, J. C. M. (2017). Studies on the Vitamin C transporter gene SLC23A2 and cardiac conduction. (Masters Thesis). University of New South Wales. Retrieved from http://handle.unsw.edu.au/1959.4/58655 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:46543/SOURCE02?view=true

Chicago Manual of Style (16th Edition):

Tang, Joyce Chi Man. “Studies on the Vitamin C transporter gene SLC23A2 and cardiac conduction.” 2017. Masters Thesis, University of New South Wales. Accessed November 28, 2020. http://handle.unsw.edu.au/1959.4/58655 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:46543/SOURCE02?view=true.

MLA Handbook (7th Edition):

Tang, Joyce Chi Man. “Studies on the Vitamin C transporter gene SLC23A2 and cardiac conduction.” 2017. Web. 28 Nov 2020.

Vancouver:

Tang JCM. Studies on the Vitamin C transporter gene SLC23A2 and cardiac conduction. [Internet] [Masters thesis]. University of New South Wales; 2017. [cited 2020 Nov 28]. Available from: http://handle.unsw.edu.au/1959.4/58655 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:46543/SOURCE02?view=true.

Council of Science Editors:

Tang JCM. Studies on the Vitamin C transporter gene SLC23A2 and cardiac conduction. [Masters Thesis]. University of New South Wales; 2017. Available from: http://handle.unsw.edu.au/1959.4/58655 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:46543/SOURCE02?view=true


University of Illinois – Chicago

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

Degree: 2017, University of Illinois – Chicago

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

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

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APA (6th Edition):

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

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

Chicago Manual of Style (16th Edition):

Obando, Julio E. “Assessment of the Clinical Validity and Utility of SNPs When Used as Predictors for Periodontitis.” 2017. Thesis, University of Illinois – Chicago. Accessed November 28, 2020. http://hdl.handle.net/10027/21820.

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

MLA Handbook (7th Edition):

Obando, Julio E. “Assessment of the Clinical Validity and Utility of SNPs When Used as Predictors for Periodontitis.” 2017. Web. 28 Nov 2020.

Vancouver:

Obando JE. Assessment of the Clinical Validity and Utility of SNPs When Used as Predictors for Periodontitis. [Internet] [Thesis]. University of Illinois – Chicago; 2017. [cited 2020 Nov 28]. Available from: http://hdl.handle.net/10027/21820.

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

Council of Science Editors:

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

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

13. Hasper, John. Next Generation Sequencing Guided SNP Mapping .

Degree: 2018, SUNY College at Fredonia

 Oogenesis is dependent on precise translational control and localization of numerous morphogens within the oocyte to achieve faithful patterning. Gurken, (Grk) is one such protein… (more)

Subjects/Keywords: Single nucleotide polymorphisms; Genetic polymorphisms; Genetic recombination; Oogenesis.

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APA (6th Edition):

Hasper, J. (2018). Next Generation Sequencing Guided SNP Mapping . (Masters Thesis). SUNY College at Fredonia. Retrieved from https://dspace.sunyconnect.suny.edu/handle/1951/71105

Chicago Manual of Style (16th Edition):

Hasper, John. “Next Generation Sequencing Guided SNP Mapping .” 2018. Masters Thesis, SUNY College at Fredonia. Accessed November 28, 2020. https://dspace.sunyconnect.suny.edu/handle/1951/71105.

MLA Handbook (7th Edition):

Hasper, John. “Next Generation Sequencing Guided SNP Mapping .” 2018. Web. 28 Nov 2020.

Vancouver:

Hasper J. Next Generation Sequencing Guided SNP Mapping . [Internet] [Masters thesis]. SUNY College at Fredonia; 2018. [cited 2020 Nov 28]. Available from: https://dspace.sunyconnect.suny.edu/handle/1951/71105.

Council of Science Editors:

Hasper J. Next Generation Sequencing Guided SNP Mapping . [Masters Thesis]. SUNY College at Fredonia; 2018. Available from: https://dspace.sunyconnect.suny.edu/handle/1951/71105


Durban University of Technology

14. Makamure, Michelle. A genetic epidemiological study of prevalence and association of genetic polymorphisms in asthma related phenotypes among children in Durban, Kwazulu-Natal.

Degree: 2012, Durban University of Technology

Submitted in fulfillment of the requirements for the degree of Master of Technology: Health Sciences, Durban University of Technology, Durban, South Africa, 2013.

Several genes… (more)

Subjects/Keywords: Genetic polymorphisms; Asthma in children; Respiratory allergy

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APA (6th Edition):

Makamure, M. (2012). A genetic epidemiological study of prevalence and association of genetic polymorphisms in asthma related phenotypes among children in Durban, Kwazulu-Natal. (Thesis). Durban University of Technology. Retrieved from http://hdl.handle.net/10321/2980

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):

Makamure, Michelle. “A genetic epidemiological study of prevalence and association of genetic polymorphisms in asthma related phenotypes among children in Durban, Kwazulu-Natal.” 2012. Thesis, Durban University of Technology. Accessed November 28, 2020. http://hdl.handle.net/10321/2980.

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

MLA Handbook (7th Edition):

Makamure, Michelle. “A genetic epidemiological study of prevalence and association of genetic polymorphisms in asthma related phenotypes among children in Durban, Kwazulu-Natal.” 2012. Web. 28 Nov 2020.

Vancouver:

Makamure M. A genetic epidemiological study of prevalence and association of genetic polymorphisms in asthma related phenotypes among children in Durban, Kwazulu-Natal. [Internet] [Thesis]. Durban University of Technology; 2012. [cited 2020 Nov 28]. Available from: http://hdl.handle.net/10321/2980.

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

Council of Science Editors:

Makamure M. A genetic epidemiological study of prevalence and association of genetic polymorphisms in asthma related phenotypes among children in Durban, Kwazulu-Natal. [Thesis]. Durban University of Technology; 2012. Available from: http://hdl.handle.net/10321/2980

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


University of Missouri – Kansas City

15. Jain, Piyush K., 1985-. Light-activated biomacromolecules.

Degree: 2013, University of Missouri – Kansas City

 Biomacromolecules, mainly nucleic acids and proteins, are involved in every cellular process and therefore their aberrant level or function is linked with most of the… (more)

Subjects/Keywords: Insulin; Labeling; Light; Genetic polymorphisms; Macromolecules; Biomolecules

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APA (6th Edition):

Jain, Piyush K., 1. (2013). Light-activated biomacromolecules. (Thesis). University of Missouri – Kansas City. Retrieved from http://hdl.handle.net/10355/45499

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):

Jain, Piyush K., 1985-. “Light-activated biomacromolecules.” 2013. Thesis, University of Missouri – Kansas City. Accessed November 28, 2020. http://hdl.handle.net/10355/45499.

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

MLA Handbook (7th Edition):

Jain, Piyush K., 1985-. “Light-activated biomacromolecules.” 2013. Web. 28 Nov 2020.

Vancouver:

Jain, Piyush K. 1. Light-activated biomacromolecules. [Internet] [Thesis]. University of Missouri – Kansas City; 2013. [cited 2020 Nov 28]. Available from: http://hdl.handle.net/10355/45499.

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

Council of Science Editors:

Jain, Piyush K. 1. Light-activated biomacromolecules. [Thesis]. University of Missouri – Kansas City; 2013. Available from: http://hdl.handle.net/10355/45499

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


University of Utah

16. Carr, Brian Allen. Function and regulation of pulmonary expressed cytochrome P450 enzymes;.

Degree: PhD, Pharmacology & Toxicology;, 2003, University of Utah

 Humans are exposed to a variety of inhaled and systemic xenobiotic compounds that cause respiratory toxicity. Cytochrome P450 enzymes, expressed specifically in lung tissues, are… (more)

Subjects/Keywords: Xenobiotic; Metabolism; Polymorphisms

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

APA (6th Edition):

Carr, B. A. (2003). Function and regulation of pulmonary expressed cytochrome P450 enzymes;. (Doctoral Dissertation). University of Utah. Retrieved from http://content.lib.utah.edu/cdm/singleitem/collection/etd1/id/715/rec/546

Chicago Manual of Style (16th Edition):

Carr, Brian Allen. “Function and regulation of pulmonary expressed cytochrome P450 enzymes;.” 2003. Doctoral Dissertation, University of Utah. Accessed November 28, 2020. http://content.lib.utah.edu/cdm/singleitem/collection/etd1/id/715/rec/546.

MLA Handbook (7th Edition):

Carr, Brian Allen. “Function and regulation of pulmonary expressed cytochrome P450 enzymes;.” 2003. Web. 28 Nov 2020.

Vancouver:

Carr BA. Function and regulation of pulmonary expressed cytochrome P450 enzymes;. [Internet] [Doctoral dissertation]. University of Utah; 2003. [cited 2020 Nov 28]. Available from: http://content.lib.utah.edu/cdm/singleitem/collection/etd1/id/715/rec/546.

Council of Science Editors:

Carr BA. Function and regulation of pulmonary expressed cytochrome P450 enzymes;. [Doctoral Dissertation]. University of Utah; 2003. Available from: http://content.lib.utah.edu/cdm/singleitem/collection/etd1/id/715/rec/546

17. Custódio, Aline Cadurin. Análise de polimorfismos em tumores gliais humanos.

Degree: PhD, Genética, 2011, University of São Paulo

Os tumores do sistema nervoso central representam aproximadamente 2% de todos os tipos de cânceres. Embora a incidência dos tumores do SNC seja pequena, comparada… (more)

Subjects/Keywords: Astrocitomas; Astrocytomas; Glioblastoma; Glioblastomas; Polimorfismo; Polymorphisms

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APA (6th Edition):

Custódio, A. C. (2011). Análise de polimorfismos em tumores gliais humanos. (Doctoral Dissertation). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/17/17135/tde-25052011-153254/ ;

Chicago Manual of Style (16th Edition):

Custódio, Aline Cadurin. “Análise de polimorfismos em tumores gliais humanos.” 2011. Doctoral Dissertation, University of São Paulo. Accessed November 28, 2020. http://www.teses.usp.br/teses/disponiveis/17/17135/tde-25052011-153254/ ;.

MLA Handbook (7th Edition):

Custódio, Aline Cadurin. “Análise de polimorfismos em tumores gliais humanos.” 2011. Web. 28 Nov 2020.

Vancouver:

Custódio AC. Análise de polimorfismos em tumores gliais humanos. [Internet] [Doctoral dissertation]. University of São Paulo; 2011. [cited 2020 Nov 28]. Available from: http://www.teses.usp.br/teses/disponiveis/17/17135/tde-25052011-153254/ ;.

Council of Science Editors:

Custódio AC. Análise de polimorfismos em tumores gliais humanos. [Doctoral Dissertation]. University of São Paulo; 2011. Available from: http://www.teses.usp.br/teses/disponiveis/17/17135/tde-25052011-153254/ ;

18. Fragkioudaki, Sofia. Διερεύνηση συμβολής κλινικοεργαστηριακών και γενετικών παραγόντων στη λεμφωματογένεση στο σύνδρομο Sjogren.

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

The heightened risk of non-Hodgkin lymphoma (NHL) development in primary Sjogren syndrome (SS) is well established. Several adverse clinical and laboratory predictors have been described.… (more)

Subjects/Keywords: Λέμφωμα; Μεθυλίωση; Πολυμορφισμοί; Lymphoma; Methylation; Polymorphisms

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APA (6th Edition):

Fragkioudaki, S. (2017). Διερεύνηση συμβολής κλινικοεργαστηριακών και γενετικών παραγόντων στη λεμφωματογένεση στο σύνδρομο Sjogren. (Thesis). National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ). Retrieved from http://hdl.handle.net/10442/hedi/42170

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):

Fragkioudaki, Sofia. “Διερεύνηση συμβολής κλινικοεργαστηριακών και γενετικών παραγόντων στη λεμφωματογένεση στο σύνδρομο Sjogren.” 2017. Thesis, National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ). Accessed November 28, 2020. http://hdl.handle.net/10442/hedi/42170.

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

MLA Handbook (7th Edition):

Fragkioudaki, Sofia. “Διερεύνηση συμβολής κλινικοεργαστηριακών και γενετικών παραγόντων στη λεμφωματογένεση στο σύνδρομο Sjogren.” 2017. Web. 28 Nov 2020.

Vancouver:

Fragkioudaki S. Διερεύνηση συμβολής κλινικοεργαστηριακών και γενετικών παραγόντων στη λεμφωματογένεση στο σύνδρομο Sjogren. [Internet] [Thesis]. National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ); 2017. [cited 2020 Nov 28]. Available from: http://hdl.handle.net/10442/hedi/42170.

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

Council of Science Editors:

Fragkioudaki S. Διερεύνηση συμβολής κλινικοεργαστηριακών και γενετικών παραγόντων στη λεμφωματογένεση στο σύνδρομο Sjogren. [Thesis]. National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ); 2017. Available from: http://hdl.handle.net/10442/hedi/42170

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


Universidade Estadual de Campinas

19. Isabel Cristina Jacinto de Faria. Polymorphisms in the TGFB1, CD14, IL4, IL4-Ra, e ADAM33 genes and asthma severity.

Degree: Faculdade de Ciências Médicas, 2007, Universidade Estadual de Campinas

A Asma é uma doença inflamatória crônica de vias aéreas, na qual várias células têm papel fundamental, tais como os eosinófilos, mastócitos e linfócitos T.… (more)

Subjects/Keywords: Genes; Gene; Polymorphisms; Asma; Polimorfismos (Genetica); Asthma

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

APA (6th Edition):

Faria, I. C. J. d. (2007). Polymorphisms in the TGFB1, CD14, IL4, IL4-Ra, e ADAM33 genes and asthma severity. (Thesis). Universidade Estadual de Campinas. Retrieved from http://libdigi.unicamp.br/document/?code=vtls000416073

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):

Faria, Isabel Cristina Jacinto de. “Polymorphisms in the TGFB1, CD14, IL4, IL4-Ra, e ADAM33 genes and asthma severity.” 2007. Thesis, Universidade Estadual de Campinas. Accessed November 28, 2020. http://libdigi.unicamp.br/document/?code=vtls000416073.

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

MLA Handbook (7th Edition):

Faria, Isabel Cristina Jacinto de. “Polymorphisms in the TGFB1, CD14, IL4, IL4-Ra, e ADAM33 genes and asthma severity.” 2007. Web. 28 Nov 2020.

Vancouver:

Faria ICJd. Polymorphisms in the TGFB1, CD14, IL4, IL4-Ra, e ADAM33 genes and asthma severity. [Internet] [Thesis]. Universidade Estadual de Campinas; 2007. [cited 2020 Nov 28]. Available from: http://libdigi.unicamp.br/document/?code=vtls000416073.

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

Council of Science Editors:

Faria ICJd. Polymorphisms in the TGFB1, CD14, IL4, IL4-Ra, e ADAM33 genes and asthma severity. [Thesis]. Universidade Estadual de Campinas; 2007. Available from: http://libdigi.unicamp.br/document/?code=vtls000416073

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


Universidade Estadual de Campinas

20. Ana Carolina Zimiani de Paiva. Associação dos polimorfismos Gln27, Glu27, Arg16 e Gly16 do gene ADRB2R com asma.

Degree: Faculdade de Ciências Médicas, 2007, Universidade Estadual de Campinas

The atopic asthma is an illness with 20% of average prevalence in the Brazilian population. It?s estimated that 60% of the asthma cases are intermittent… (more)

Subjects/Keywords: Asma; Asthma; Polimorfismos (Genetica); Polymorphisms (Genetic)

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

APA (6th Edition):

Paiva, A. C. Z. d. (2007). Associação dos polimorfismos Gln27, Glu27, Arg16 e Gly16 do gene ADRB2R com asma. (Thesis). Universidade Estadual de Campinas. Retrieved from http://libdigi.unicamp.br/document/?code=vtls000417683

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):

Paiva, Ana Carolina Zimiani de. “Associação dos polimorfismos Gln27, Glu27, Arg16 e Gly16 do gene ADRB2R com asma.” 2007. Thesis, Universidade Estadual de Campinas. Accessed November 28, 2020. http://libdigi.unicamp.br/document/?code=vtls000417683.

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

MLA Handbook (7th Edition):

Paiva, Ana Carolina Zimiani de. “Associação dos polimorfismos Gln27, Glu27, Arg16 e Gly16 do gene ADRB2R com asma.” 2007. Web. 28 Nov 2020.

Vancouver:

Paiva ACZd. Associação dos polimorfismos Gln27, Glu27, Arg16 e Gly16 do gene ADRB2R com asma. [Internet] [Thesis]. Universidade Estadual de Campinas; 2007. [cited 2020 Nov 28]. Available from: http://libdigi.unicamp.br/document/?code=vtls000417683.

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

Council of Science Editors:

Paiva ACZd. Associação dos polimorfismos Gln27, Glu27, Arg16 e Gly16 do gene ADRB2R com asma. [Thesis]. Universidade Estadual de Campinas; 2007. Available from: http://libdigi.unicamp.br/document/?code=vtls000417683

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


University of Adelaide

21. Andraweera, Prabha Hemamali. Angiogenesis regulating gene polymorphisms in adverse pregnancy outcomes.

Degree: 2012, University of Adelaide

 Introduction: Both placental vascular defects and a genetic contribution are documented in pregnancies complicated by preeclampsia, small-for-gestational-age infants (SGA) and spontaneous preterm birth (sPTB). Our… (more)

Subjects/Keywords: polymorphisms; angiogenesis; preeclampsia; SGA infants; preterm birth

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APA (6th Edition):

Andraweera, P. H. (2012). Angiogenesis regulating gene polymorphisms in adverse pregnancy outcomes. (Thesis). University of Adelaide. Retrieved from http://hdl.handle.net/2440/95878

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):

Andraweera, Prabha Hemamali. “Angiogenesis regulating gene polymorphisms in adverse pregnancy outcomes.” 2012. Thesis, University of Adelaide. Accessed November 28, 2020. http://hdl.handle.net/2440/95878.

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

MLA Handbook (7th Edition):

Andraweera, Prabha Hemamali. “Angiogenesis regulating gene polymorphisms in adverse pregnancy outcomes.” 2012. Web. 28 Nov 2020.

Vancouver:

Andraweera PH. Angiogenesis regulating gene polymorphisms in adverse pregnancy outcomes. [Internet] [Thesis]. University of Adelaide; 2012. [cited 2020 Nov 28]. Available from: http://hdl.handle.net/2440/95878.

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

Council of Science Editors:

Andraweera PH. Angiogenesis regulating gene polymorphisms in adverse pregnancy outcomes. [Thesis]. University of Adelaide; 2012. Available from: http://hdl.handle.net/2440/95878

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


Univerzitet u Beogradu

22. Ilić, Vesna M., 1965-. Uloga polimorfizama gena za angiotenzinogen, angiotenzin-konvertujući enzim i AT1 receptor u razvoju nefropatije u dijabetesu tipa I.

Degree: Biološki fakultet, 2015, Univerzitet u Beogradu

Biologija - Genetika / Biology - Genetics

Dijabetesna nefropatija (DN) je jedna od najozbiljnijih mikrovaskularnih komplikacija, kako u tipu I, tako i u tipu II dijabetesa...

Advisors/Committee Members: Cvetković, Dragana, 1961-.

Subjects/Keywords: diabetic nephropathy; renin-angiotensin system; gene polymorphisms

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APA (6th Edition):

Ilić, Vesna M., 1. (2015). Uloga polimorfizama gena za angiotenzinogen, angiotenzin-konvertujući enzim i AT1 receptor u razvoju nefropatije u dijabetesu tipa I. (Thesis). Univerzitet u Beogradu. Retrieved from https://fedorabg.bg.ac.rs/fedora/get/o:9144/bdef:Content/get

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

Chicago Manual of Style (16th Edition):

Ilić, Vesna M., 1965-. “Uloga polimorfizama gena za angiotenzinogen, angiotenzin-konvertujući enzim i AT1 receptor u razvoju nefropatije u dijabetesu tipa I.” 2015. Thesis, Univerzitet u Beogradu. Accessed November 28, 2020. https://fedorabg.bg.ac.rs/fedora/get/o:9144/bdef:Content/get.

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

MLA Handbook (7th Edition):

Ilić, Vesna M., 1965-. “Uloga polimorfizama gena za angiotenzinogen, angiotenzin-konvertujući enzim i AT1 receptor u razvoju nefropatije u dijabetesu tipa I.” 2015. Web. 28 Nov 2020.

Vancouver:

Ilić, Vesna M. 1. Uloga polimorfizama gena za angiotenzinogen, angiotenzin-konvertujući enzim i AT1 receptor u razvoju nefropatije u dijabetesu tipa I. [Internet] [Thesis]. Univerzitet u Beogradu; 2015. [cited 2020 Nov 28]. Available from: https://fedorabg.bg.ac.rs/fedora/get/o:9144/bdef:Content/get.

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

Council of Science Editors:

Ilić, Vesna M. 1. Uloga polimorfizama gena za angiotenzinogen, angiotenzin-konvertujući enzim i AT1 receptor u razvoju nefropatije u dijabetesu tipa I. [Thesis]. Univerzitet u Beogradu; 2015. Available from: https://fedorabg.bg.ac.rs/fedora/get/o:9144/bdef:Content/get

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


Univerzitet u Beogradu

23. Popović-Kuzmanović, Dragana V. Analiza polimorfizama gena značajnih za diferencijaciju T(H)17 i T regulatornih ćelija kod bolesnika sa antifosfolipidnim sindromom.

Degree: Medicinski fakultet, 2015, Univerzitet u Beogradu

 Uvod: Antifosfolipidni sindrom (AFS) je autoimunska bolest koju karakteri#e pojava arterijskih i venskih tromboza, gubitak ploda i prisustvo antifosfolipidnih antitela u serumu. AFS, kao i… (more)

Subjects/Keywords: Th17; Treg; Antiphospholipid syndrome; gene polymorphisms

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APA (6th Edition):

Popović-Kuzmanović, D. V. (2015). Analiza polimorfizama gena značajnih za diferencijaciju T(H)17 i T regulatornih ćelija kod bolesnika sa antifosfolipidnim sindromom. (Thesis). Univerzitet u Beogradu. Retrieved from https://fedorabg.bg.ac.rs/fedora/get/o:9848/bdef:Content/get

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

Chicago Manual of Style (16th Edition):

Popović-Kuzmanović, Dragana V. “Analiza polimorfizama gena značajnih za diferencijaciju T(H)17 i T regulatornih ćelija kod bolesnika sa antifosfolipidnim sindromom.” 2015. Thesis, Univerzitet u Beogradu. Accessed November 28, 2020. https://fedorabg.bg.ac.rs/fedora/get/o:9848/bdef:Content/get.

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

MLA Handbook (7th Edition):

Popović-Kuzmanović, Dragana V. “Analiza polimorfizama gena značajnih za diferencijaciju T(H)17 i T regulatornih ćelija kod bolesnika sa antifosfolipidnim sindromom.” 2015. Web. 28 Nov 2020.

Vancouver:

Popović-Kuzmanović DV. Analiza polimorfizama gena značajnih za diferencijaciju T(H)17 i T regulatornih ćelija kod bolesnika sa antifosfolipidnim sindromom. [Internet] [Thesis]. Univerzitet u Beogradu; 2015. [cited 2020 Nov 28]. Available from: https://fedorabg.bg.ac.rs/fedora/get/o:9848/bdef:Content/get.

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

Council of Science Editors:

Popović-Kuzmanović DV. Analiza polimorfizama gena značajnih za diferencijaciju T(H)17 i T regulatornih ćelija kod bolesnika sa antifosfolipidnim sindromom. [Thesis]. Univerzitet u Beogradu; 2015. Available from: https://fedorabg.bg.ac.rs/fedora/get/o:9848/bdef:Content/get

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


Columbia University

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

Degree: 2018, Columbia University

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

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

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APA (6th Edition):

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

Chicago Manual of Style (16th Edition):

Cho, Youngjin. “Development of Single Molecule Electronic SNP Assays using Polymer Tagged Nucleotides and Nanopore Detection.” 2018. Doctoral Dissertation, Columbia University. Accessed November 28, 2020. https://doi.org/10.7916/D8QC1FDG.

MLA Handbook (7th Edition):

Cho, Youngjin. “Development of Single Molecule Electronic SNP Assays using Polymer Tagged Nucleotides and Nanopore Detection.” 2018. Web. 28 Nov 2020.

Vancouver:

Cho Y. Development of Single Molecule Electronic SNP Assays using Polymer Tagged Nucleotides and Nanopore Detection. [Internet] [Doctoral dissertation]. Columbia University; 2018. [cited 2020 Nov 28]. Available from: https://doi.org/10.7916/D8QC1FDG.

Council of Science Editors:

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


Univerzitet u Beogradu

25. Popović, Bojana M., 1976-. Uticaj utreniranosti i polimorfizama u genima za glukokortikoidni, mineralokortikoidni i adrenokortikotropni receptor na fiziološku adaptaciju hipotalamo-hipofizno-nadbubrežne osovine na hronično ponavljani fizički stres.

Degree: Medicinski fakultet, 2019, Univerzitet u Beogradu

Medicina -Interna medicina - endokrinologija / Medicine - internal medicine - endocrinology

Svaka forma stresa ima višestruke efekte na ceo organizam, ali reakcije i adaptacije… (more)

Subjects/Keywords: stress; HPA axis; athletes; receptor gene polymorphisms

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APA (6th Edition):

Popović, Bojana M., 1. (2019). Uticaj utreniranosti i polimorfizama u genima za glukokortikoidni, mineralokortikoidni i adrenokortikotropni receptor na fiziološku adaptaciju hipotalamo-hipofizno-nadbubrežne osovine na hronično ponavljani fizički stres. (Thesis). Univerzitet u Beogradu. Retrieved from https://fedorabg.bg.ac.rs/fedora/get/o:19407/bdef:Content/get

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

Chicago Manual of Style (16th Edition):

Popović, Bojana M., 1976-. “Uticaj utreniranosti i polimorfizama u genima za glukokortikoidni, mineralokortikoidni i adrenokortikotropni receptor na fiziološku adaptaciju hipotalamo-hipofizno-nadbubrežne osovine na hronično ponavljani fizički stres.” 2019. Thesis, Univerzitet u Beogradu. Accessed November 28, 2020. https://fedorabg.bg.ac.rs/fedora/get/o:19407/bdef:Content/get.

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

MLA Handbook (7th Edition):

Popović, Bojana M., 1976-. “Uticaj utreniranosti i polimorfizama u genima za glukokortikoidni, mineralokortikoidni i adrenokortikotropni receptor na fiziološku adaptaciju hipotalamo-hipofizno-nadbubrežne osovine na hronično ponavljani fizički stres.” 2019. Web. 28 Nov 2020.

Vancouver:

Popović, Bojana M. 1. Uticaj utreniranosti i polimorfizama u genima za glukokortikoidni, mineralokortikoidni i adrenokortikotropni receptor na fiziološku adaptaciju hipotalamo-hipofizno-nadbubrežne osovine na hronično ponavljani fizički stres. [Internet] [Thesis]. Univerzitet u Beogradu; 2019. [cited 2020 Nov 28]. Available from: https://fedorabg.bg.ac.rs/fedora/get/o:19407/bdef:Content/get.

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

Council of Science Editors:

Popović, Bojana M. 1. Uticaj utreniranosti i polimorfizama u genima za glukokortikoidni, mineralokortikoidni i adrenokortikotropni receptor na fiziološku adaptaciju hipotalamo-hipofizno-nadbubrežne osovine na hronično ponavljani fizički stres. [Thesis]. Univerzitet u Beogradu; 2019. Available from: https://fedorabg.bg.ac.rs/fedora/get/o:19407/bdef:Content/get

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


University of Manchester

26. Dhaygude, Ajay. Epidemiology, genetic differences and clinical outcomes of antineutrophil cytoplasmic autoantibody associated systemic vasculitis.

Degree: Thesis (M.D.), 2012, University of Manchester

 Introduction: The two subtypes of Antineutrophil Cytoplasmic autoantibody associated systemic vasculitis (AASV) cANCA and pANCA associated vasculitis are the commonest causes of rapidly progressive glomerulonephritis.… (more)

Subjects/Keywords: 616.07; ANCA, vasculitis, epidemiology, cytokine, polymorphisms, metabolomics

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

APA (6th Edition):

Dhaygude, A. (2012). Epidemiology, genetic differences and clinical outcomes of antineutrophil cytoplasmic autoantibody associated systemic vasculitis. (Doctoral Dissertation). University of Manchester. Retrieved from https://www.research.manchester.ac.uk/portal/en/theses/epidemiology-genetic-differencesand-clinical-outcomes-ofantineutrophil-cytoplasmicautoantibody-associated-systemicvasculitis(1d4bf70b-3046-4997-9bdb-82206b6a8264).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.549027

Chicago Manual of Style (16th Edition):

Dhaygude, Ajay. “Epidemiology, genetic differences and clinical outcomes of antineutrophil cytoplasmic autoantibody associated systemic vasculitis.” 2012. Doctoral Dissertation, University of Manchester. Accessed November 28, 2020. https://www.research.manchester.ac.uk/portal/en/theses/epidemiology-genetic-differencesand-clinical-outcomes-ofantineutrophil-cytoplasmicautoantibody-associated-systemicvasculitis(1d4bf70b-3046-4997-9bdb-82206b6a8264).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.549027.

MLA Handbook (7th Edition):

Dhaygude, Ajay. “Epidemiology, genetic differences and clinical outcomes of antineutrophil cytoplasmic autoantibody associated systemic vasculitis.” 2012. Web. 28 Nov 2020.

Vancouver:

Dhaygude A. Epidemiology, genetic differences and clinical outcomes of antineutrophil cytoplasmic autoantibody associated systemic vasculitis. [Internet] [Doctoral dissertation]. University of Manchester; 2012. [cited 2020 Nov 28]. Available from: https://www.research.manchester.ac.uk/portal/en/theses/epidemiology-genetic-differencesand-clinical-outcomes-ofantineutrophil-cytoplasmicautoantibody-associated-systemicvasculitis(1d4bf70b-3046-4997-9bdb-82206b6a8264).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.549027.

Council of Science Editors:

Dhaygude A. Epidemiology, genetic differences and clinical outcomes of antineutrophil cytoplasmic autoantibody associated systemic vasculitis. [Doctoral Dissertation]. University of Manchester; 2012. Available from: https://www.research.manchester.ac.uk/portal/en/theses/epidemiology-genetic-differencesand-clinical-outcomes-ofantineutrophil-cytoplasmicautoantibody-associated-systemicvasculitis(1d4bf70b-3046-4997-9bdb-82206b6a8264).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.549027


Brunel University

27. Liozidou, Maria. Genetic epidemiology of breast cancer in Cyprus : a case-control study of DNA repair genes.

Degree: PhD, 2009, Brunel University

 The occurrence of early-onset breast cancer (EOBC) has been associated with germline mutations in the BRCA1 and BRCA2 genes. The first aim of this thesis… (more)

Subjects/Keywords: 610.7343; Polymorphisms; Risk

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APA (6th Edition):

Liozidou, M. (2009). Genetic epidemiology of breast cancer in Cyprus : a case-control study of DNA repair genes. (Doctoral Dissertation). Brunel University. Retrieved from http://bura.brunel.ac.uk/handle/2438/4111 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.508838

Chicago Manual of Style (16th Edition):

Liozidou, Maria. “Genetic epidemiology of breast cancer in Cyprus : a case-control study of DNA repair genes.” 2009. Doctoral Dissertation, Brunel University. Accessed November 28, 2020. http://bura.brunel.ac.uk/handle/2438/4111 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.508838.

MLA Handbook (7th Edition):

Liozidou, Maria. “Genetic epidemiology of breast cancer in Cyprus : a case-control study of DNA repair genes.” 2009. Web. 28 Nov 2020.

Vancouver:

Liozidou M. Genetic epidemiology of breast cancer in Cyprus : a case-control study of DNA repair genes. [Internet] [Doctoral dissertation]. Brunel University; 2009. [cited 2020 Nov 28]. Available from: http://bura.brunel.ac.uk/handle/2438/4111 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.508838.

Council of Science Editors:

Liozidou M. Genetic epidemiology of breast cancer in Cyprus : a case-control study of DNA repair genes. [Doctoral Dissertation]. Brunel University; 2009. Available from: http://bura.brunel.ac.uk/handle/2438/4111 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.508838


Hong Kong University of Science and Technology

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

Degree: 2014, Hong Kong University of Science and Technology

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

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

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

APA (6th Edition):

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

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

Chicago Manual of Style (16th Edition):

Yang, Guangyuan. “Permutation tests for genome-wide association studies.” 2014. Thesis, Hong Kong University of Science and Technology. Accessed November 28, 2020. http://repository.ust.hk/ir/Record/1783.1-88026 ; https://doi.org/10.14711/thesis-b1432208 ; http://repository.ust.hk/ir/bitstream/1783.1-88026/1/th_redirect.html.

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

MLA Handbook (7th Edition):

Yang, Guangyuan. “Permutation tests for genome-wide association studies.” 2014. Web. 28 Nov 2020.

Vancouver:

Yang G. Permutation tests for genome-wide association studies. [Internet] [Thesis]. Hong Kong University of Science and Technology; 2014. [cited 2020 Nov 28]. Available from: http://repository.ust.hk/ir/Record/1783.1-88026 ; https://doi.org/10.14711/thesis-b1432208 ; http://repository.ust.hk/ir/bitstream/1783.1-88026/1/th_redirect.html.

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

Council of Science Editors:

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

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


Florida International University

29. Li, Jiaojiao. Arsenic Biotransformations in Microbes and Humans, and Catalytic Properties of Human AS3MT Variants.

Degree: PhD, Biomedical Sciences, 2017, Florida International University

  Arsenic is the most pervasive environmental toxic substance. As a consequence of its ubiquity, nearly every organism has genes for resistance to inorganic arsenic.… (more)

Subjects/Keywords: Arsenic; Human AS3MT; Polymorphisms; Methyltransferase; Microbes

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

APA (6th Edition):

Li, J. (2017). Arsenic Biotransformations in Microbes and Humans, and Catalytic Properties of Human AS3MT Variants. (Doctoral Dissertation). Florida International University. Retrieved from https://digitalcommons.fiu.edu/etd/3460 ; 10.25148/etd.FIDC001934 ; FIDC001934

Chicago Manual of Style (16th Edition):

Li, Jiaojiao. “Arsenic Biotransformations in Microbes and Humans, and Catalytic Properties of Human AS3MT Variants.” 2017. Doctoral Dissertation, Florida International University. Accessed November 28, 2020. https://digitalcommons.fiu.edu/etd/3460 ; 10.25148/etd.FIDC001934 ; FIDC001934.

MLA Handbook (7th Edition):

Li, Jiaojiao. “Arsenic Biotransformations in Microbes and Humans, and Catalytic Properties of Human AS3MT Variants.” 2017. Web. 28 Nov 2020.

Vancouver:

Li J. Arsenic Biotransformations in Microbes and Humans, and Catalytic Properties of Human AS3MT Variants. [Internet] [Doctoral dissertation]. Florida International University; 2017. [cited 2020 Nov 28]. Available from: https://digitalcommons.fiu.edu/etd/3460 ; 10.25148/etd.FIDC001934 ; FIDC001934.

Council of Science Editors:

Li J. Arsenic Biotransformations in Microbes and Humans, and Catalytic Properties of Human AS3MT Variants. [Doctoral Dissertation]. Florida International University; 2017. Available from: https://digitalcommons.fiu.edu/etd/3460 ; 10.25148/etd.FIDC001934 ; FIDC001934


University of Iowa

30. Badtke, Laura Elise. The influence of gene polymorphisms, modifiable lifestyle factors, and toxicants on the protective effects of the paraoxonase genes.

Degree: PhD, Human Toxicology, 2014, University of Iowa

  The paraoxonase gene family consists of three members (PON1, PON2, and PON3) with both distinct and overlapping roles in human health. These enzymes influence… (more)

Subjects/Keywords: aging; Drosophila; Paraoxonases; polymorphisms; twins; Toxicology

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

APA (6th Edition):

Badtke, L. E. (2014). The influence of gene polymorphisms, modifiable lifestyle factors, and toxicants on the protective effects of the paraoxonase genes. (Doctoral Dissertation). University of Iowa. Retrieved from https://ir.uiowa.edu/etd/4567

Chicago Manual of Style (16th Edition):

Badtke, Laura Elise. “The influence of gene polymorphisms, modifiable lifestyle factors, and toxicants on the protective effects of the paraoxonase genes.” 2014. Doctoral Dissertation, University of Iowa. Accessed November 28, 2020. https://ir.uiowa.edu/etd/4567.

MLA Handbook (7th Edition):

Badtke, Laura Elise. “The influence of gene polymorphisms, modifiable lifestyle factors, and toxicants on the protective effects of the paraoxonase genes.” 2014. Web. 28 Nov 2020.

Vancouver:

Badtke LE. The influence of gene polymorphisms, modifiable lifestyle factors, and toxicants on the protective effects of the paraoxonase genes. [Internet] [Doctoral dissertation]. University of Iowa; 2014. [cited 2020 Nov 28]. Available from: https://ir.uiowa.edu/etd/4567.

Council of Science Editors:

Badtke LE. The influence of gene polymorphisms, modifiable lifestyle factors, and toxicants on the protective effects of the paraoxonase genes. [Doctoral Dissertation]. University of Iowa; 2014. Available from: https://ir.uiowa.edu/etd/4567

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