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You searched for subject:(Human polymorphism). Showing records 1 – 30 of 41 total matches.

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University of Edinburgh

1. 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 January 24, 2021. 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. 24 Jan 2021.

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 2021 Jan 24]. 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


Univerzitet u Beogradu

2. Andrić, Zorana P., 1965-. Određivanje polimorfizma lokusa humanih leukocitnih antigena u populaciji potencijalnih davalaca matičnih ćelija hematopoeze u Srbiji.

Degree: Medicinski fakultet, 2015, Univerzitet u Beogradu

Medicina - Transfuziologija / Medicine - Transfusion Medicine

Uvod: Kompleks gena koji kodira sistema humanih leukocitnih antigen (HLA) je najpolimorfniji deo humanog genoma. Složenost polimorfizma… (more)

Subjects/Keywords: Human leukocyte antigens; polymorphism; Serbian population; bone marrow donor registry

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APA (6th Edition):

Andrić, Zorana P., 1. (2015). Određivanje polimorfizma lokusa humanih leukocitnih antigena u populaciji potencijalnih davalaca matičnih ćelija hematopoeze u Srbiji. (Thesis). Univerzitet u Beogradu. Retrieved from https://fedorabg.bg.ac.rs/fedora/get/o:9824/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):

Andrić, Zorana P., 1965-. “Određivanje polimorfizma lokusa humanih leukocitnih antigena u populaciji potencijalnih davalaca matičnih ćelija hematopoeze u Srbiji.” 2015. Thesis, Univerzitet u Beogradu. Accessed January 24, 2021. https://fedorabg.bg.ac.rs/fedora/get/o:9824/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):

Andrić, Zorana P., 1965-. “Određivanje polimorfizma lokusa humanih leukocitnih antigena u populaciji potencijalnih davalaca matičnih ćelija hematopoeze u Srbiji.” 2015. Web. 24 Jan 2021.

Vancouver:

Andrić, Zorana P. 1. Određivanje polimorfizma lokusa humanih leukocitnih antigena u populaciji potencijalnih davalaca matičnih ćelija hematopoeze u Srbiji. [Internet] [Thesis]. Univerzitet u Beogradu; 2015. [cited 2021 Jan 24]. Available from: https://fedorabg.bg.ac.rs/fedora/get/o:9824/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:

Andrić, Zorana P. 1. Određivanje polimorfizma lokusa humanih leukocitnih antigena u populaciji potencijalnih davalaca matičnih ćelija hematopoeze u Srbiji. [Thesis]. Univerzitet u Beogradu; 2015. Available from: https://fedorabg.bg.ac.rs/fedora/get/o:9824/bdef:Content/get

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


University of Western Ontario

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

Degree: 2016, University of Western Ontario

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

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

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APA (6th Edition):

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

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

Chicago Manual of Style (16th Edition):

Findlay, Scott D. “Comprehensive Molecular Characterization of Human NODAL.” 2016. Thesis, University of Western Ontario. Accessed January 24, 2021. https://ir.lib.uwo.ca/etd/4277.

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

MLA Handbook (7th Edition):

Findlay, Scott D. “Comprehensive Molecular Characterization of Human NODAL.” 2016. Web. 24 Jan 2021.

Vancouver:

Findlay SD. Comprehensive Molecular Characterization of Human NODAL. [Internet] [Thesis]. University of Western Ontario; 2016. [cited 2021 Jan 24]. Available from: https://ir.lib.uwo.ca/etd/4277.

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

Council of Science Editors:

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

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


University of Lund

4. Jongruamklang, Philaiphon. Studies of Thai blood group and platelet polymorphism. Implications for malaria susceptibility.

Degree: 2020, University of Lund

 The objectives of the thesis were to seek a better understanding of polymorphic RBC surface molecules in the Thai, and to investigate the role of… (more)

Subjects/Keywords: Hematology; Thai; Blood group polymorphism; Human platelet antigens; Malaria susceptibility; Plasmodium falciparum

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APA (6th Edition):

Jongruamklang, P. (2020). Studies of Thai blood group and platelet polymorphism. Implications for malaria susceptibility. (Doctoral Dissertation). University of Lund. Retrieved from https://lup.lub.lu.se/record/144d8aca-f1ba-4d3c-8f10-2377284eda25 ; https://portal.research.lu.se/ws/files/78945059/dokumentdatablad_Philaiphon_J.pdf

Chicago Manual of Style (16th Edition):

Jongruamklang, Philaiphon. “Studies of Thai blood group and platelet polymorphism. Implications for malaria susceptibility.” 2020. Doctoral Dissertation, University of Lund. Accessed January 24, 2021. https://lup.lub.lu.se/record/144d8aca-f1ba-4d3c-8f10-2377284eda25 ; https://portal.research.lu.se/ws/files/78945059/dokumentdatablad_Philaiphon_J.pdf.

MLA Handbook (7th Edition):

Jongruamklang, Philaiphon. “Studies of Thai blood group and platelet polymorphism. Implications for malaria susceptibility.” 2020. Web. 24 Jan 2021.

Vancouver:

Jongruamklang P. Studies of Thai blood group and platelet polymorphism. Implications for malaria susceptibility. [Internet] [Doctoral dissertation]. University of Lund; 2020. [cited 2021 Jan 24]. Available from: https://lup.lub.lu.se/record/144d8aca-f1ba-4d3c-8f10-2377284eda25 ; https://portal.research.lu.se/ws/files/78945059/dokumentdatablad_Philaiphon_J.pdf.

Council of Science Editors:

Jongruamklang P. Studies of Thai blood group and platelet polymorphism. Implications for malaria susceptibility. [Doctoral Dissertation]. University of Lund; 2020. Available from: https://lup.lub.lu.se/record/144d8aca-f1ba-4d3c-8f10-2377284eda25 ; https://portal.research.lu.se/ws/files/78945059/dokumentdatablad_Philaiphon_J.pdf


University of Pennsylvania

5. Joseph, Paule Valery. Sucrose Thresholds and Genetic Polymorphisms of Sweet and Bitter Taste Receptor Genes in Children.

Degree: 2015, University of Pennsylvania

 SUCROSE THRESHOLDS AND GENETIC POLYMORPHISMS OF SWEET AND BITTER TASTE RECEPTOR GENES IN CHILDREN Paule Valery Joseph Charlene Compher, PhD, RD Background: Many illnesses of… (more)

Subjects/Keywords: Diet; Genetics; Obesity; Polymorphism; Sucrose; Thresholds; Genetics; Human and Clinical Nutrition; Nursing; Nutrition

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APA (6th Edition):

Joseph, P. V. (2015). Sucrose Thresholds and Genetic Polymorphisms of Sweet and Bitter Taste Receptor Genes in Children. (Thesis). University of Pennsylvania. Retrieved from https://repository.upenn.edu/edissertations/1793

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):

Joseph, Paule Valery. “Sucrose Thresholds and Genetic Polymorphisms of Sweet and Bitter Taste Receptor Genes in Children.” 2015. Thesis, University of Pennsylvania. Accessed January 24, 2021. https://repository.upenn.edu/edissertations/1793.

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

MLA Handbook (7th Edition):

Joseph, Paule Valery. “Sucrose Thresholds and Genetic Polymorphisms of Sweet and Bitter Taste Receptor Genes in Children.” 2015. Web. 24 Jan 2021.

Vancouver:

Joseph PV. Sucrose Thresholds and Genetic Polymorphisms of Sweet and Bitter Taste Receptor Genes in Children. [Internet] [Thesis]. University of Pennsylvania; 2015. [cited 2021 Jan 24]. Available from: https://repository.upenn.edu/edissertations/1793.

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

Council of Science Editors:

Joseph PV. Sucrose Thresholds and Genetic Polymorphisms of Sweet and Bitter Taste Receptor Genes in Children. [Thesis]. University of Pennsylvania; 2015. Available from: https://repository.upenn.edu/edissertations/1793

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

6. Dubay, Christopher J. Genomics of chromosome 11 : exclusion mapping of episodic ataxia on human chromosomes 6p and 17 : characterization of DNA probes which detect restriction fragment length polymorphisms on human chromosome 11q : a database management system for the entry, organization and transer of family genotypes for linkage analysis.

Degree: PhD, 1990, Oregon Health Sciences University

Subjects/Keywords: Genome, Human; Information Services; Genetics; Polymorphism, Genetic

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APA (6th Edition):

Dubay, C. J. (1990). Genomics of chromosome 11 : exclusion mapping of episodic ataxia on human chromosomes 6p and 17 : characterization of DNA probes which detect restriction fragment length polymorphisms on human chromosome 11q : a database management system for the entry, organization and transer of family genotypes for linkage analysis. (Doctoral Dissertation). Oregon Health Sciences University. Retrieved from doi:10.6083/M4T43R6K ; http://digitalcommons.ohsu.edu/etd/1828

Chicago Manual of Style (16th Edition):

Dubay, Christopher J. “Genomics of chromosome 11 : exclusion mapping of episodic ataxia on human chromosomes 6p and 17 : characterization of DNA probes which detect restriction fragment length polymorphisms on human chromosome 11q : a database management system for the entry, organization and transer of family genotypes for linkage analysis.” 1990. Doctoral Dissertation, Oregon Health Sciences University. Accessed January 24, 2021. doi:10.6083/M4T43R6K ; http://digitalcommons.ohsu.edu/etd/1828.

MLA Handbook (7th Edition):

Dubay, Christopher J. “Genomics of chromosome 11 : exclusion mapping of episodic ataxia on human chromosomes 6p and 17 : characterization of DNA probes which detect restriction fragment length polymorphisms on human chromosome 11q : a database management system for the entry, organization and transer of family genotypes for linkage analysis.” 1990. Web. 24 Jan 2021.

Vancouver:

Dubay CJ. Genomics of chromosome 11 : exclusion mapping of episodic ataxia on human chromosomes 6p and 17 : characterization of DNA probes which detect restriction fragment length polymorphisms on human chromosome 11q : a database management system for the entry, organization and transer of family genotypes for linkage analysis. [Internet] [Doctoral dissertation]. Oregon Health Sciences University; 1990. [cited 2021 Jan 24]. Available from: doi:10.6083/M4T43R6K ; http://digitalcommons.ohsu.edu/etd/1828.

Council of Science Editors:

Dubay CJ. Genomics of chromosome 11 : exclusion mapping of episodic ataxia on human chromosomes 6p and 17 : characterization of DNA probes which detect restriction fragment length polymorphisms on human chromosome 11q : a database management system for the entry, organization and transer of family genotypes for linkage analysis. [Doctoral Dissertation]. Oregon Health Sciences University; 1990. Available from: doi:10.6083/M4T43R6K ; http://digitalcommons.ohsu.edu/etd/1828

7. QUIXABEIRA, Dafne Carolina Alves. Estudo dos polimorfismos genéticos da metalproteinase de matriz 2 envolvidos na carcinogênese cervical .

Degree: 2016, Universidade Federal de Pernambuco

 O câncer de colo do útero apresenta distribuição a nível mundial, correspondendo ao quarto mais incidente entre as mulheres. Está associado à infecção prévia pelo… (more)

Subjects/Keywords: Lesão Cervical; Metaloproteinase de matriz 2; Polimorfismo; Papillomavírus Humano; Cervical Lesion; Matrix metalloproteinase 2; Polymorphism; Human Papillomavirus

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APA (6th Edition):

QUIXABEIRA, D. C. A. (2016). Estudo dos polimorfismos genéticos da metalproteinase de matriz 2 envolvidos na carcinogênese cervical . (Masters Thesis). Universidade Federal de Pernambuco. Retrieved from https://repositorio.ufpe.br/handle/123456789/18894

Chicago Manual of Style (16th Edition):

QUIXABEIRA, Dafne Carolina Alves. “Estudo dos polimorfismos genéticos da metalproteinase de matriz 2 envolvidos na carcinogênese cervical .” 2016. Masters Thesis, Universidade Federal de Pernambuco. Accessed January 24, 2021. https://repositorio.ufpe.br/handle/123456789/18894.

MLA Handbook (7th Edition):

QUIXABEIRA, Dafne Carolina Alves. “Estudo dos polimorfismos genéticos da metalproteinase de matriz 2 envolvidos na carcinogênese cervical .” 2016. Web. 24 Jan 2021.

Vancouver:

QUIXABEIRA DCA. Estudo dos polimorfismos genéticos da metalproteinase de matriz 2 envolvidos na carcinogênese cervical . [Internet] [Masters thesis]. Universidade Federal de Pernambuco; 2016. [cited 2021 Jan 24]. Available from: https://repositorio.ufpe.br/handle/123456789/18894.

Council of Science Editors:

QUIXABEIRA DCA. Estudo dos polimorfismos genéticos da metalproteinase de matriz 2 envolvidos na carcinogênese cervical . [Masters Thesis]. Universidade Federal de Pernambuco; 2016. Available from: https://repositorio.ufpe.br/handle/123456789/18894

8. Lynch, Joshua. Identifying Host-Microbiome Interactions in Genomic Data.

Degree: MS, Biomedical Informatics and Computational Biology, 2015, University of Minnesota

 The human microbiome has been identified as a significant biological aspect of the human body with correlations to many characteristics of the host including age,… (more)

Subjects/Keywords: human microbiome; LASSO regression; single nucleotide polymorphism

…1. Introduction The microorganisms living on and inside the human body are called… …the ‘human microbiome’. This large and varied collection of organisms has been studied… …community. The human microbiome has been compared to an organ (Baquero and Nombela, 2012… …of the human microbiome to understanding human biology and treating human disease. The… …microbiota of the human body consist of thousands of taxonomically distinct organisms including… 

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APA (6th Edition):

Lynch, J. (2015). Identifying Host-Microbiome Interactions in Genomic Data. (Masters Thesis). University of Minnesota. Retrieved from http://hdl.handle.net/11299/174809

Chicago Manual of Style (16th Edition):

Lynch, Joshua. “Identifying Host-Microbiome Interactions in Genomic Data.” 2015. Masters Thesis, University of Minnesota. Accessed January 24, 2021. http://hdl.handle.net/11299/174809.

MLA Handbook (7th Edition):

Lynch, Joshua. “Identifying Host-Microbiome Interactions in Genomic Data.” 2015. Web. 24 Jan 2021.

Vancouver:

Lynch J. Identifying Host-Microbiome Interactions in Genomic Data. [Internet] [Masters thesis]. University of Minnesota; 2015. [cited 2021 Jan 24]. Available from: http://hdl.handle.net/11299/174809.

Council of Science Editors:

Lynch J. Identifying Host-Microbiome Interactions in Genomic Data. [Masters Thesis]. University of Minnesota; 2015. Available from: http://hdl.handle.net/11299/174809


Indian Institute of Science

9. Mukherjee, Sumanta. Multi-scale Modelling of HLA Diversity and Its Effect on Cytotoxic Immune Responses in Influenza H1N1 Infection.

Degree: PhD, Faculty of Science, 2018, Indian Institute of Science

 Cytotoxic T-lymphocytes (CTLs) are important components of the adaptive immune system and function by scanning the intracellular environment so as to detect and de-stroy infected… (more)

Subjects/Keywords: Influenza H1N1 Infection; Cytotoxic T-lymphocytes (CTLs); Human Leucocyte Antigen (HLA); Cytotoxic Immune Responses Modeling; Human Immune System; Peptide Binding; Genetic Heterogeneity; Human Leucocyte Antigen (HLA) Genotype Modeling; Human Leucotyte Antigen (HLA) Gene Polymorphism; Structural Bioinformatics; HLAClassify; HLAffy; Flutope; Disease Spreader Network (DSN); Disease Dynamics; Mathematics

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APA (6th Edition):

Mukherjee, S. (2018). Multi-scale Modelling of HLA Diversity and Its Effect on Cytotoxic Immune Responses in Influenza H1N1 Infection. (Doctoral Dissertation). Indian Institute of Science. Retrieved from http://etd.iisc.ac.in/handle/2005/3665

Chicago Manual of Style (16th Edition):

Mukherjee, Sumanta. “Multi-scale Modelling of HLA Diversity and Its Effect on Cytotoxic Immune Responses in Influenza H1N1 Infection.” 2018. Doctoral Dissertation, Indian Institute of Science. Accessed January 24, 2021. http://etd.iisc.ac.in/handle/2005/3665.

MLA Handbook (7th Edition):

Mukherjee, Sumanta. “Multi-scale Modelling of HLA Diversity and Its Effect on Cytotoxic Immune Responses in Influenza H1N1 Infection.” 2018. Web. 24 Jan 2021.

Vancouver:

Mukherjee S. Multi-scale Modelling of HLA Diversity and Its Effect on Cytotoxic Immune Responses in Influenza H1N1 Infection. [Internet] [Doctoral dissertation]. Indian Institute of Science; 2018. [cited 2021 Jan 24]. Available from: http://etd.iisc.ac.in/handle/2005/3665.

Council of Science Editors:

Mukherjee S. Multi-scale Modelling of HLA Diversity and Its Effect on Cytotoxic Immune Responses in Influenza H1N1 Infection. [Doctoral Dissertation]. Indian Institute of Science; 2018. Available from: http://etd.iisc.ac.in/handle/2005/3665


Universidade do Rio Grande do Sul

10. Bueno, Larissa Souza Mario. Vitamina D, polimorfismos do gene VDR e neurofibromatose 1.

Degree: 2012, Universidade do Rio Grande do Sul

Introdução: A Neurofibromatose tipo 1 (NF1) é uma doença genética autossômica dominante causada por mutação no gene NF1 (17q11.2; proteína neurofibromina). A incidência é de… (more)

Subjects/Keywords: Vitamina D; Neurofibromatosis type 1; Polimorfismo genético; Vitamin D; Neurofibromatose 1; Neurofibromas; Hypovitaminosis D; Deficiência de vitamina D; BsmI e FokI Polymorphism; VDR gene; Human; Brazil

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APA (6th Edition):

Bueno, L. S. M. (2012). Vitamina D, polimorfismos do gene VDR e neurofibromatose 1. (Thesis). Universidade do Rio Grande do Sul. Retrieved from http://hdl.handle.net/10183/52955

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):

Bueno, Larissa Souza Mario. “Vitamina D, polimorfismos do gene VDR e neurofibromatose 1.” 2012. Thesis, Universidade do Rio Grande do Sul. Accessed January 24, 2021. http://hdl.handle.net/10183/52955.

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

MLA Handbook (7th Edition):

Bueno, Larissa Souza Mario. “Vitamina D, polimorfismos do gene VDR e neurofibromatose 1.” 2012. Web. 24 Jan 2021.

Vancouver:

Bueno LSM. Vitamina D, polimorfismos do gene VDR e neurofibromatose 1. [Internet] [Thesis]. Universidade do Rio Grande do Sul; 2012. [cited 2021 Jan 24]. Available from: http://hdl.handle.net/10183/52955.

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

Council of Science Editors:

Bueno LSM. Vitamina D, polimorfismos do gene VDR e neurofibromatose 1. [Thesis]. Universidade do Rio Grande do Sul; 2012. Available from: http://hdl.handle.net/10183/52955

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

11. Sharma, Vikram. The Cloning and characterization of microsatellite polymorphisms from chromosome 21.

Degree: PhD, 1992, Oregon Health Sciences University

Subjects/Keywords: Genetic Markers; Chromosomes, Human, Pair 21; Polymorphism, Genetic; Polymerase Chain Reaction

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APA (6th Edition):

Sharma, V. (1992). The Cloning and characterization of microsatellite polymorphisms from chromosome 21. (Doctoral Dissertation). Oregon Health Sciences University. Retrieved from doi:10.6083/M4M32SXT ; http://digitalcommons.ohsu.edu/etd/1729

Chicago Manual of Style (16th Edition):

Sharma, Vikram. “The Cloning and characterization of microsatellite polymorphisms from chromosome 21.” 1992. Doctoral Dissertation, Oregon Health Sciences University. Accessed January 24, 2021. doi:10.6083/M4M32SXT ; http://digitalcommons.ohsu.edu/etd/1729.

MLA Handbook (7th Edition):

Sharma, Vikram. “The Cloning and characterization of microsatellite polymorphisms from chromosome 21.” 1992. Web. 24 Jan 2021.

Vancouver:

Sharma V. The Cloning and characterization of microsatellite polymorphisms from chromosome 21. [Internet] [Doctoral dissertation]. Oregon Health Sciences University; 1992. [cited 2021 Jan 24]. Available from: doi:10.6083/M4M32SXT ; http://digitalcommons.ohsu.edu/etd/1729.

Council of Science Editors:

Sharma V. The Cloning and characterization of microsatellite polymorphisms from chromosome 21. [Doctoral Dissertation]. Oregon Health Sciences University; 1992. Available from: doi:10.6083/M4M32SXT ; http://digitalcommons.ohsu.edu/etd/1729

12. Azuero, Andres. Comparisons of sequential testing approaches for detection of association between disease and haplotype blocks.

Degree: PhD, 2008, University of Alabama – Birmingham

Since Wald's development of the Sequential Probability Ratio Test (SPRT) in 1945, sequential analysis has evolved into a rich and well-developed field. Sequential methods are… (more)

Subjects/Keywords: Algorithms<; br>; Genetic Predisposition to Disease<; br>; Genome, Human<; br>; Haplotypes<; br>; Linkage Disequilibrium<; br>; Polymorphism, Single Nucleotide.

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APA (6th Edition):

Azuero, A. (2008). Comparisons of sequential testing approaches for detection of association between disease and haplotype blocks. (Doctoral Dissertation). University of Alabama – Birmingham. Retrieved from http://contentdm.mhsl.uab.edu/u?/etd,430

Chicago Manual of Style (16th Edition):

Azuero, Andres. “Comparisons of sequential testing approaches for detection of association between disease and haplotype blocks.” 2008. Doctoral Dissertation, University of Alabama – Birmingham. Accessed January 24, 2021. http://contentdm.mhsl.uab.edu/u?/etd,430.

MLA Handbook (7th Edition):

Azuero, Andres. “Comparisons of sequential testing approaches for detection of association between disease and haplotype blocks.” 2008. Web. 24 Jan 2021.

Vancouver:

Azuero A. Comparisons of sequential testing approaches for detection of association between disease and haplotype blocks. [Internet] [Doctoral dissertation]. University of Alabama – Birmingham; 2008. [cited 2021 Jan 24]. Available from: http://contentdm.mhsl.uab.edu/u?/etd,430.

Council of Science Editors:

Azuero A. Comparisons of sequential testing approaches for detection of association between disease and haplotype blocks. [Doctoral Dissertation]. University of Alabama – Birmingham; 2008. Available from: http://contentdm.mhsl.uab.edu/u?/etd,430


Universidade Estadual de Campinas

13. Gomez, Selma Michèle Linda, 1984-. Identificação de SNPs e haplótipos do gene BCL11A em pacientes com anemia falciforme e suas associações com níveis de hemoglobina fetal: Identification of SNPs and haplotype of BCL11A gene in sickle cell anemia patients and their associations with fetal hemoglobin levels.

Degree: 2018, Universidade Estadual de Campinas

 Abstract: Sickle cell anemia is one of the most common inherited hematologic diseases in the world, with about 300,000 new cases each year. Studies that… (more)

Subjects/Keywords: Anemia falciforme; Polimorfismo (Genética); Haplótipos; Proteína BCL11a humana; Hemoglobina fetal; Expressão gênica; Sickle cell anemia; Polymorphism, Genetic; Haplotypes; BCL11A protein, human; Fetal hemoglobin; Gene expression

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APA (6th Edition):

Gomez, Selma Michèle Linda, 1. (2018). Identificação de SNPs e haplótipos do gene BCL11A em pacientes com anemia falciforme e suas associações com níveis de hemoglobina fetal: Identification of SNPs and haplotype of BCL11A gene in sickle cell anemia patients and their associations with fetal hemoglobin levels. (Thesis). Universidade Estadual de Campinas. Retrieved from http://repositorio.unicamp.br/jspui/handle/REPOSIP/332586

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):

Gomez, Selma Michèle Linda, 1984-. “Identificação de SNPs e haplótipos do gene BCL11A em pacientes com anemia falciforme e suas associações com níveis de hemoglobina fetal: Identification of SNPs and haplotype of BCL11A gene in sickle cell anemia patients and their associations with fetal hemoglobin levels.” 2018. Thesis, Universidade Estadual de Campinas. Accessed January 24, 2021. http://repositorio.unicamp.br/jspui/handle/REPOSIP/332586.

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

MLA Handbook (7th Edition):

Gomez, Selma Michèle Linda, 1984-. “Identificação de SNPs e haplótipos do gene BCL11A em pacientes com anemia falciforme e suas associações com níveis de hemoglobina fetal: Identification of SNPs and haplotype of BCL11A gene in sickle cell anemia patients and their associations with fetal hemoglobin levels.” 2018. Web. 24 Jan 2021.

Vancouver:

Gomez, Selma Michèle Linda 1. Identificação de SNPs e haplótipos do gene BCL11A em pacientes com anemia falciforme e suas associações com níveis de hemoglobina fetal: Identification of SNPs and haplotype of BCL11A gene in sickle cell anemia patients and their associations with fetal hemoglobin levels. [Internet] [Thesis]. Universidade Estadual de Campinas; 2018. [cited 2021 Jan 24]. Available from: http://repositorio.unicamp.br/jspui/handle/REPOSIP/332586.

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

Council of Science Editors:

Gomez, Selma Michèle Linda 1. Identificação de SNPs e haplótipos do gene BCL11A em pacientes com anemia falciforme e suas associações com níveis de hemoglobina fetal: Identification of SNPs and haplotype of BCL11A gene in sickle cell anemia patients and their associations with fetal hemoglobin levels. [Thesis]. Universidade Estadual de Campinas; 2018. Available from: http://repositorio.unicamp.br/jspui/handle/REPOSIP/332586

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

14. Shyamala, K. V. Single nucleotide polymorphism analysis of candidate genes of developmental dyslexia in India;.

Degree: 2013, University of Mysore

newline

Advisors/Committee Members: Ramachandra, N. B..

Subjects/Keywords:

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APA (6th Edition):

Shyamala, K. V. (2013). Single nucleotide polymorphism analysis of candidate genes of developmental dyslexia in India;. (Thesis). University of Mysore. Retrieved from http://shodhganga.inflibnet.ac.in/handle/10603/36538

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):

Shyamala, K V. “Single nucleotide polymorphism analysis of candidate genes of developmental dyslexia in India;.” 2013. Thesis, University of Mysore. Accessed January 24, 2021. http://shodhganga.inflibnet.ac.in/handle/10603/36538.

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

MLA Handbook (7th Edition):

Shyamala, K V. “Single nucleotide polymorphism analysis of candidate genes of developmental dyslexia in India;.” 2013. Web. 24 Jan 2021.

Vancouver:

Shyamala KV. Single nucleotide polymorphism analysis of candidate genes of developmental dyslexia in India;. [Internet] [Thesis]. University of Mysore; 2013. [cited 2021 Jan 24]. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/36538.

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

Council of Science Editors:

Shyamala KV. Single nucleotide polymorphism analysis of candidate genes of developmental dyslexia in India;. [Thesis]. University of Mysore; 2013. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/36538

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

15. Song, Zehua. Agents antimicrobiens ciblant le complexe III de la chaine respiratoire mitochondriale : Etudes des déterminants structuraux de la sensibilité différentielle et du développement de la résistance, en utilisant la levure comme organisme modèle : Anti-microbial agents targeting complex III of the mitochondrial respiratory chain : Studying the structural determinants of differential sensitivity and the development of resistance, using yeast as a model organism.

Degree: Docteur es, Sciences de la vie et de la santé, 2016, Université Paris-Saclay (ComUE)

Le complexe bc₁ de la chaîne respiratoire mitochondriale est une bonne cible thérapeutique pour traiter le paludisme car cette enzyme est essentielle au parasite. Ses… (more)

Subjects/Keywords: Mitochondrie; Complexe III respiratoire; Mutation de résistance; Modèle levure; Drogues antipaludique; Polymorphisme humain; Mitochondrion; Respiratory complex III; Resistance mutation; Yeast model; Antimalarial drugs; Human polymorphism

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APA (6th Edition):

Song, Z. (2016). Agents antimicrobiens ciblant le complexe III de la chaine respiratoire mitochondriale : Etudes des déterminants structuraux de la sensibilité différentielle et du développement de la résistance, en utilisant la levure comme organisme modèle : Anti-microbial agents targeting complex III of the mitochondrial respiratory chain : Studying the structural determinants of differential sensitivity and the development of resistance, using yeast as a model organism. (Doctoral Dissertation). Université Paris-Saclay (ComUE). Retrieved from http://www.theses.fr/2016SACLS281

Chicago Manual of Style (16th Edition):

Song, Zehua. “Agents antimicrobiens ciblant le complexe III de la chaine respiratoire mitochondriale : Etudes des déterminants structuraux de la sensibilité différentielle et du développement de la résistance, en utilisant la levure comme organisme modèle : Anti-microbial agents targeting complex III of the mitochondrial respiratory chain : Studying the structural determinants of differential sensitivity and the development of resistance, using yeast as a model organism.” 2016. Doctoral Dissertation, Université Paris-Saclay (ComUE). Accessed January 24, 2021. http://www.theses.fr/2016SACLS281.

MLA Handbook (7th Edition):

Song, Zehua. “Agents antimicrobiens ciblant le complexe III de la chaine respiratoire mitochondriale : Etudes des déterminants structuraux de la sensibilité différentielle et du développement de la résistance, en utilisant la levure comme organisme modèle : Anti-microbial agents targeting complex III of the mitochondrial respiratory chain : Studying the structural determinants of differential sensitivity and the development of resistance, using yeast as a model organism.” 2016. Web. 24 Jan 2021.

Vancouver:

Song Z. Agents antimicrobiens ciblant le complexe III de la chaine respiratoire mitochondriale : Etudes des déterminants structuraux de la sensibilité différentielle et du développement de la résistance, en utilisant la levure comme organisme modèle : Anti-microbial agents targeting complex III of the mitochondrial respiratory chain : Studying the structural determinants of differential sensitivity and the development of resistance, using yeast as a model organism. [Internet] [Doctoral dissertation]. Université Paris-Saclay (ComUE); 2016. [cited 2021 Jan 24]. Available from: http://www.theses.fr/2016SACLS281.

Council of Science Editors:

Song Z. Agents antimicrobiens ciblant le complexe III de la chaine respiratoire mitochondriale : Etudes des déterminants structuraux de la sensibilité différentielle et du développement de la résistance, en utilisant la levure comme organisme modèle : Anti-microbial agents targeting complex III of the mitochondrial respiratory chain : Studying the structural determinants of differential sensitivity and the development of resistance, using yeast as a model organism. [Doctoral Dissertation]. Université Paris-Saclay (ComUE); 2016. Available from: http://www.theses.fr/2016SACLS281


University of Adelaide

16. Soubrier, Julien Benoit Adrien. What (molecular) time is it? : using ancient DNA to date evolutionary events.

Degree: 2012, University of Adelaide

 This work aims to explore the use of genetic sequences sampled serially through time (heterochronous data), to infer the timescale of past evolutionary events. Such… (more)

Subjects/Keywords: molecular clock; substitution rate; mutation rate; phylogenetics; calibration; ancient DNA; time-dependent rates; among-site rate variation; divergence times; human; bison; hyena; single nucleotide polymorphism; mitochondrial genome

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APA (6th Edition):

Soubrier, J. B. A. (2012). What (molecular) time is it? : using ancient DNA to date evolutionary events. (Thesis). University of Adelaide. Retrieved from http://hdl.handle.net/2440/96464

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):

Soubrier, Julien Benoit Adrien. “What (molecular) time is it? : using ancient DNA to date evolutionary events.” 2012. Thesis, University of Adelaide. Accessed January 24, 2021. http://hdl.handle.net/2440/96464.

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

MLA Handbook (7th Edition):

Soubrier, Julien Benoit Adrien. “What (molecular) time is it? : using ancient DNA to date evolutionary events.” 2012. Web. 24 Jan 2021.

Vancouver:

Soubrier JBA. What (molecular) time is it? : using ancient DNA to date evolutionary events. [Internet] [Thesis]. University of Adelaide; 2012. [cited 2021 Jan 24]. Available from: http://hdl.handle.net/2440/96464.

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

Council of Science Editors:

Soubrier JBA. What (molecular) time is it? : using ancient DNA to date evolutionary events. [Thesis]. University of Adelaide; 2012. Available from: http://hdl.handle.net/2440/96464

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


Freie Universität Berlin

17. Caglayan, Safak. SORLA/SORL1 als genetischer Risikofaktor bei der Alzheimer-Krankheit.

Degree: 2013, Freie Universität Berlin

 SORLA („sorting protein-related receptor with A-type repeats“) ist ein Typ-I- Transmembranrezeptor, welcher zur Familie der Rezeptoren mit VPS10P („vacuolar protein-sorting 10 protein“)-Domäne gehört. Im Gehirn… (more)

Subjects/Keywords: SORLA; SORL1; Alzheimer disease; human genetics; single nucleotide polymorphism; amyloid beta; catabolism; transgenic mice; 500 Naturwissenschaften und Mathematik; 600 Technik, Medizin, angewandte Wissenschaften

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APA (6th Edition):

Caglayan, S. (2013). SORLA/SORL1 als genetischer Risikofaktor bei der Alzheimer-Krankheit. (Thesis). Freie Universität Berlin. Retrieved from https://refubium.fu-berlin.de/handle/fub188/10410

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):

Caglayan, Safak. “SORLA/SORL1 als genetischer Risikofaktor bei der Alzheimer-Krankheit.” 2013. Thesis, Freie Universität Berlin. Accessed January 24, 2021. https://refubium.fu-berlin.de/handle/fub188/10410.

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

MLA Handbook (7th Edition):

Caglayan, Safak. “SORLA/SORL1 als genetischer Risikofaktor bei der Alzheimer-Krankheit.” 2013. Web. 24 Jan 2021.

Vancouver:

Caglayan S. SORLA/SORL1 als genetischer Risikofaktor bei der Alzheimer-Krankheit. [Internet] [Thesis]. Freie Universität Berlin; 2013. [cited 2021 Jan 24]. Available from: https://refubium.fu-berlin.de/handle/fub188/10410.

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

Council of Science Editors:

Caglayan S. SORLA/SORL1 als genetischer Risikofaktor bei der Alzheimer-Krankheit. [Thesis]. Freie Universität Berlin; 2013. Available from: https://refubium.fu-berlin.de/handle/fub188/10410

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


Hong Kong University of Science and Technology

18. Liu, Shuk Ming. Single nucleotide polymorphism in human microsomal glutathione s-transferase gene and colorectal cancer.

Degree: 2003, Hong Kong University of Science and Technology

 GST is a big family of isoezymes, and based on their locations they can be divided into cytosolic and microsomal GST. The major role of… (more)

Subjects/Keywords: Glutathione transferase ; Colon (Anatomy)  – Cancer ; Rectum  – Cancer ; Genetic polymorphisms ; Human genetics ; Chromosome polymorphism

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APA (6th Edition):

Liu, S. M. (2003). Single nucleotide polymorphism in human microsomal glutathione s-transferase gene and colorectal cancer. (Thesis). Hong Kong University of Science and Technology. Retrieved from http://repository.ust.hk/ir/Record/1783.1-3899 ; https://doi.org/10.14711/thesis-b802027 ; http://repository.ust.hk/ir/bitstream/1783.1-3899/1/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):

Liu, Shuk Ming. “Single nucleotide polymorphism in human microsomal glutathione s-transferase gene and colorectal cancer.” 2003. Thesis, Hong Kong University of Science and Technology. Accessed January 24, 2021. http://repository.ust.hk/ir/Record/1783.1-3899 ; https://doi.org/10.14711/thesis-b802027 ; http://repository.ust.hk/ir/bitstream/1783.1-3899/1/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):

Liu, Shuk Ming. “Single nucleotide polymorphism in human microsomal glutathione s-transferase gene and colorectal cancer.” 2003. Web. 24 Jan 2021.

Vancouver:

Liu SM. Single nucleotide polymorphism in human microsomal glutathione s-transferase gene and colorectal cancer. [Internet] [Thesis]. Hong Kong University of Science and Technology; 2003. [cited 2021 Jan 24]. Available from: http://repository.ust.hk/ir/Record/1783.1-3899 ; https://doi.org/10.14711/thesis-b802027 ; http://repository.ust.hk/ir/bitstream/1783.1-3899/1/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:

Liu SM. Single nucleotide polymorphism in human microsomal glutathione s-transferase gene and colorectal cancer. [Thesis]. Hong Kong University of Science and Technology; 2003. Available from: http://repository.ust.hk/ir/Record/1783.1-3899 ; https://doi.org/10.14711/thesis-b802027 ; http://repository.ust.hk/ir/bitstream/1783.1-3899/1/th_redirect.html

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


University of Western Ontario

19. Hattlmann, Clayton. Restriction of HIV-1 replication by unique TRIM22 isoforms.

Degree: 2012, University of Western Ontario

 Understanding how the immune system reacts to HIV infection and why normal antiviral defenses are insufficient to fight infection is a key step towards creating… (more)

Subjects/Keywords: Human immunodeficiency virus type 1; TRIM22; antiviral; interferon; restriction factor; single nucleotide polymorphism; Immune System Diseases; Immunity; Immunology of Infectious Disease; Virology; Virus Diseases

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APA (6th Edition):

Hattlmann, C. (2012). Restriction of HIV-1 replication by unique TRIM22 isoforms. (Thesis). University of Western Ontario. Retrieved from https://ir.lib.uwo.ca/etd/392

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):

Hattlmann, Clayton. “Restriction of HIV-1 replication by unique TRIM22 isoforms.” 2012. Thesis, University of Western Ontario. Accessed January 24, 2021. https://ir.lib.uwo.ca/etd/392.

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

MLA Handbook (7th Edition):

Hattlmann, Clayton. “Restriction of HIV-1 replication by unique TRIM22 isoforms.” 2012. Web. 24 Jan 2021.

Vancouver:

Hattlmann C. Restriction of HIV-1 replication by unique TRIM22 isoforms. [Internet] [Thesis]. University of Western Ontario; 2012. [cited 2021 Jan 24]. Available from: https://ir.lib.uwo.ca/etd/392.

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

Council of Science Editors:

Hattlmann C. Restriction of HIV-1 replication by unique TRIM22 isoforms. [Thesis]. University of Western Ontario; 2012. Available from: https://ir.lib.uwo.ca/etd/392

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

20. Golem, Scott Matthew Bradley. Human Endogenous Retrovirus (HERV) Insertional Polymorphisms .

Degree: Centre for Biotechnology, 2013, Brock University

Human endogenous retroviruses (HERVs) are the result of ancient germ cell infections of human germ cells by exogenous retroviruses. HERVs belong to the long terminal… (more)

Subjects/Keywords: HERV; Classification Nomenclature; Human Endogenous Retrovirus; Insertion; Polymorphism

…certain level of transposition activity in the human genome and their level of polymorphism may… …activity and polymorphism level of HERV insertions in the human genome, as well as their… …Human endogenous retrovirus (HERV) Human MMTV-like (HML) Long terminal… …x28;RNA) Single nucleotide polymorphism (SNP) Solo-long terminal repeat (… …Transposable insertion polymorphisms in the human reference genome but absent in the test genome… 

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APA (6th Edition):

Golem, S. M. B. (2013). Human Endogenous Retrovirus (HERV) Insertional Polymorphisms . (Thesis). Brock University. Retrieved from http://hdl.handle.net/10464/4743

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):

Golem, Scott Matthew Bradley. “Human Endogenous Retrovirus (HERV) Insertional Polymorphisms .” 2013. Thesis, Brock University. Accessed January 24, 2021. http://hdl.handle.net/10464/4743.

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

MLA Handbook (7th Edition):

Golem, Scott Matthew Bradley. “Human Endogenous Retrovirus (HERV) Insertional Polymorphisms .” 2013. Web. 24 Jan 2021.

Vancouver:

Golem SMB. Human Endogenous Retrovirus (HERV) Insertional Polymorphisms . [Internet] [Thesis]. Brock University; 2013. [cited 2021 Jan 24]. Available from: http://hdl.handle.net/10464/4743.

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

Council of Science Editors:

Golem SMB. Human Endogenous Retrovirus (HERV) Insertional Polymorphisms . [Thesis]. Brock University; 2013. Available from: http://hdl.handle.net/10464/4743

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


University of Cincinnati

21. Aswathanarayanan, Subramanian. A STUDY OF THE EFFECT OF SINGLE NUCLEOTIDE POLYMORPHISMS IN HUMAN GENOME ON THE SECONDARY STRUCTURE OF PROTEINS.

Degree: MS, Engineering : Computer Science, 2002, University of Cincinnati

 Geneticists throughout the world are involved in deciphering the genetic code of various organisms including that of human beings. With the discovery of more single… (more)

Subjects/Keywords: SNP; Single Nucleotide Polymorphism; Secondary Structure of Protiens; Human Genome

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APA (6th Edition):

Aswathanarayanan, S. (2002). A STUDY OF THE EFFECT OF SINGLE NUCLEOTIDE POLYMORPHISMS IN HUMAN GENOME ON THE SECONDARY STRUCTURE OF PROTEINS. (Masters Thesis). University of Cincinnati. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=ucin1024675762

Chicago Manual of Style (16th Edition):

Aswathanarayanan, Subramanian. “A STUDY OF THE EFFECT OF SINGLE NUCLEOTIDE POLYMORPHISMS IN HUMAN GENOME ON THE SECONDARY STRUCTURE OF PROTEINS.” 2002. Masters Thesis, University of Cincinnati. Accessed January 24, 2021. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1024675762.

MLA Handbook (7th Edition):

Aswathanarayanan, Subramanian. “A STUDY OF THE EFFECT OF SINGLE NUCLEOTIDE POLYMORPHISMS IN HUMAN GENOME ON THE SECONDARY STRUCTURE OF PROTEINS.” 2002. Web. 24 Jan 2021.

Vancouver:

Aswathanarayanan S. A STUDY OF THE EFFECT OF SINGLE NUCLEOTIDE POLYMORPHISMS IN HUMAN GENOME ON THE SECONDARY STRUCTURE OF PROTEINS. [Internet] [Masters thesis]. University of Cincinnati; 2002. [cited 2021 Jan 24]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ucin1024675762.

Council of Science Editors:

Aswathanarayanan S. A STUDY OF THE EFFECT OF SINGLE NUCLEOTIDE POLYMORPHISMS IN HUMAN GENOME ON THE SECONDARY STRUCTURE OF PROTEINS. [Masters Thesis]. University of Cincinnati; 2002. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ucin1024675762

22. Feve, Marie. Utilisation d'une approche de chimie biologie intégrative dans la recherche de nouvelles molécules actives sur la prolifération et la différenciation des cellules souches cancéreuses : A chemical biology approach for the discovery of molecules acting on tumour initiating cells isolated from glioblastomas.

Degree: Docteur es, Aspects moléculaires et cellulaires de la biologie, 2012, Université de Strasbourg

Depuis l’émergence du concept de cellules souches cancéreuses (CSC), de telles cellules ont été isolées à partir de diverses tumeurs solides, dont les glioblastomes. Les… (more)

Subjects/Keywords: Glioblastomes humains; Cellules Souches Cancéreuses; Quiescence; Single Nucleotide Polymorphism; Récepteurs couplés aux protéines G; Transcriptomique; Chimie-Biologie Intégrative; Criblage; Chimiothèque; Relation Structure-Activité; Human Glioblastoma; Cancer Stem Cells; Quiescence; Single Nucleotide Polymorphism; G protein-coupled receptors; Transcriptomics; Integrative Biological Chemistry; Screening; Chemical Library; Structure-Activity Relationship; 571.8; 572.8; 616.99

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APA (6th Edition):

Feve, M. (2012). Utilisation d'une approche de chimie biologie intégrative dans la recherche de nouvelles molécules actives sur la prolifération et la différenciation des cellules souches cancéreuses : A chemical biology approach for the discovery of molecules acting on tumour initiating cells isolated from glioblastomas. (Doctoral Dissertation). Université de Strasbourg. Retrieved from http://www.theses.fr/2012STRAJ075

Chicago Manual of Style (16th Edition):

Feve, Marie. “Utilisation d'une approche de chimie biologie intégrative dans la recherche de nouvelles molécules actives sur la prolifération et la différenciation des cellules souches cancéreuses : A chemical biology approach for the discovery of molecules acting on tumour initiating cells isolated from glioblastomas.” 2012. Doctoral Dissertation, Université de Strasbourg. Accessed January 24, 2021. http://www.theses.fr/2012STRAJ075.

MLA Handbook (7th Edition):

Feve, Marie. “Utilisation d'une approche de chimie biologie intégrative dans la recherche de nouvelles molécules actives sur la prolifération et la différenciation des cellules souches cancéreuses : A chemical biology approach for the discovery of molecules acting on tumour initiating cells isolated from glioblastomas.” 2012. Web. 24 Jan 2021.

Vancouver:

Feve M. Utilisation d'une approche de chimie biologie intégrative dans la recherche de nouvelles molécules actives sur la prolifération et la différenciation des cellules souches cancéreuses : A chemical biology approach for the discovery of molecules acting on tumour initiating cells isolated from glioblastomas. [Internet] [Doctoral dissertation]. Université de Strasbourg; 2012. [cited 2021 Jan 24]. Available from: http://www.theses.fr/2012STRAJ075.

Council of Science Editors:

Feve M. Utilisation d'une approche de chimie biologie intégrative dans la recherche de nouvelles molécules actives sur la prolifération et la différenciation des cellules souches cancéreuses : A chemical biology approach for the discovery of molecules acting on tumour initiating cells isolated from glioblastomas. [Doctoral Dissertation]. Université de Strasbourg; 2012. Available from: http://www.theses.fr/2012STRAJ075

23. Hauge, Xue Ya. A Genetic linkage index map of the human chromosome 11q composed mainly of microsatellite markers.

Degree: PhD, 1992, Oregon Health Sciences University

Subjects/Keywords: Chromosomes, Human, Pair 11; Genetic Linkage; Polymorphism, Genetic; Repetitive Sequences, Nucleic Acid; Genetic Markers; Genome, Human

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APA (6th Edition):

Hauge, X. Y. (1992). A Genetic linkage index map of the human chromosome 11q composed mainly of microsatellite markers. (Doctoral Dissertation). Oregon Health Sciences University. Retrieved from doi:10.6083/M4QV3JN7 ; http://digitalcommons.ohsu.edu/etd/1728

Chicago Manual of Style (16th Edition):

Hauge, Xue Ya. “A Genetic linkage index map of the human chromosome 11q composed mainly of microsatellite markers.” 1992. Doctoral Dissertation, Oregon Health Sciences University. Accessed January 24, 2021. doi:10.6083/M4QV3JN7 ; http://digitalcommons.ohsu.edu/etd/1728.

MLA Handbook (7th Edition):

Hauge, Xue Ya. “A Genetic linkage index map of the human chromosome 11q composed mainly of microsatellite markers.” 1992. Web. 24 Jan 2021.

Vancouver:

Hauge XY. A Genetic linkage index map of the human chromosome 11q composed mainly of microsatellite markers. [Internet] [Doctoral dissertation]. Oregon Health Sciences University; 1992. [cited 2021 Jan 24]. Available from: doi:10.6083/M4QV3JN7 ; http://digitalcommons.ohsu.edu/etd/1728.

Council of Science Editors:

Hauge XY. A Genetic linkage index map of the human chromosome 11q composed mainly of microsatellite markers. [Doctoral Dissertation]. Oregon Health Sciences University; 1992. Available from: doi:10.6083/M4QV3JN7 ; http://digitalcommons.ohsu.edu/etd/1728

24. Maslen, Cheryl L. The Cloning and characterizaion of DNA probes which detect restriction fragement length polymorphisms on human chromosomes 11q and 16q.

Degree: PhD, 1987, Oregon Health Sciences University

Subjects/Keywords: DNA, Recombinant; Chromosomes, Human, Pair 11; Chromosomes, Human, Pair 16; Genetic Markers; Polymorphism, Genetic

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APA (6th Edition):

Maslen, C. L. (1987). The Cloning and characterizaion of DNA probes which detect restriction fragement length polymorphisms on human chromosomes 11q and 16q. (Doctoral Dissertation). Oregon Health Sciences University. Retrieved from doi:10.6083/M4PG1PW5 ; http://digitalcommons.ohsu.edu/etd/2007

Chicago Manual of Style (16th Edition):

Maslen, Cheryl L. “The Cloning and characterizaion of DNA probes which detect restriction fragement length polymorphisms on human chromosomes 11q and 16q.” 1987. Doctoral Dissertation, Oregon Health Sciences University. Accessed January 24, 2021. doi:10.6083/M4PG1PW5 ; http://digitalcommons.ohsu.edu/etd/2007.

MLA Handbook (7th Edition):

Maslen, Cheryl L. “The Cloning and characterizaion of DNA probes which detect restriction fragement length polymorphisms on human chromosomes 11q and 16q.” 1987. Web. 24 Jan 2021.

Vancouver:

Maslen CL. The Cloning and characterizaion of DNA probes which detect restriction fragement length polymorphisms on human chromosomes 11q and 16q. [Internet] [Doctoral dissertation]. Oregon Health Sciences University; 1987. [cited 2021 Jan 24]. Available from: doi:10.6083/M4PG1PW5 ; http://digitalcommons.ohsu.edu/etd/2007.

Council of Science Editors:

Maslen CL. The Cloning and characterizaion of DNA probes which detect restriction fragement length polymorphisms on human chromosomes 11q and 16q. [Doctoral Dissertation]. Oregon Health Sciences University; 1987. Available from: doi:10.6083/M4PG1PW5 ; http://digitalcommons.ohsu.edu/etd/2007


Swedish University of Agricultural Sciences

25. Dicksved, Johan. Exploring the human intestinal microbiome in health and disease.

Degree: 2008, Swedish University of Agricultural Sciences

 In this thesis, molecular tools were used to study bacteria inhabiting the gastrointestinal tract of humans. One aim was to determine whether certain lifestyle factors,… (more)

Subjects/Keywords: microbial flora; intestines; bacteria; human diseases; intestinal diseases; neoplasms; siblings; rflp; Microbiota; terminal-restriction fragment length polymorphism (T-RFLP); gastrointestinal tract; identical twins; inflammatory bowel disease (IBD); Crohn's disease; gastric cancer; Faecalibacterium prausnitzii; lifestyle; diversity.

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

APA (6th Edition):

Dicksved, J. (2008). Exploring the human intestinal microbiome in health and disease. (Doctoral Dissertation). Swedish University of Agricultural Sciences. Retrieved from http://pub.epsilon.slu.se/1760/

Chicago Manual of Style (16th Edition):

Dicksved, Johan. “Exploring the human intestinal microbiome in health and disease.” 2008. Doctoral Dissertation, Swedish University of Agricultural Sciences. Accessed January 24, 2021. http://pub.epsilon.slu.se/1760/.

MLA Handbook (7th Edition):

Dicksved, Johan. “Exploring the human intestinal microbiome in health and disease.” 2008. Web. 24 Jan 2021.

Vancouver:

Dicksved J. Exploring the human intestinal microbiome in health and disease. [Internet] [Doctoral dissertation]. Swedish University of Agricultural Sciences; 2008. [cited 2021 Jan 24]. Available from: http://pub.epsilon.slu.se/1760/.

Council of Science Editors:

Dicksved J. Exploring the human intestinal microbiome in health and disease. [Doctoral Dissertation]. Swedish University of Agricultural Sciences; 2008. Available from: http://pub.epsilon.slu.se/1760/

26. Cunha, Joel da. Estudo da atividade e polimorfismos da Paraoxonase-1 em indivíduos infectados pelo vírus da imunodeficiência humana tipo-1 (HIV-1) tratados com inibidores de protease.

Degree: PhD, Alergia e Imunopatologia, 2012, University of São Paulo

A enzima Paraoxonase-1 (PON1) possui atividades paraoxonase, arilestearase e lactonase, entre outras. É a mais estuda da família das PONs que é composta pela PON1,… (more)

Subjects/Keywords: Anti-retrovirais; Antiretrovirals; Genetic polymorphism; HIV-1; HIV-1; human; Inibidores de proteases; LDL proteins; Lipoproteína de baixa densidade oxidada; Oxidized low-density lipoprotein; Paraoxon/blood; Paraoxon/sangue; Polimorfismo genético; PON1 protein; PON1 proteína humana; Protease inhibitors; Proteínas LDL

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APA (6th Edition):

Cunha, J. d. (2012). Estudo da atividade e polimorfismos da Paraoxonase-1 em indivíduos infectados pelo vírus da imunodeficiência humana tipo-1 (HIV-1) tratados com inibidores de protease. (Doctoral Dissertation). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/5/5146/tde-10052013-095130/ ;

Chicago Manual of Style (16th Edition):

Cunha, Joel da. “Estudo da atividade e polimorfismos da Paraoxonase-1 em indivíduos infectados pelo vírus da imunodeficiência humana tipo-1 (HIV-1) tratados com inibidores de protease.” 2012. Doctoral Dissertation, University of São Paulo. Accessed January 24, 2021. http://www.teses.usp.br/teses/disponiveis/5/5146/tde-10052013-095130/ ;.

MLA Handbook (7th Edition):

Cunha, Joel da. “Estudo da atividade e polimorfismos da Paraoxonase-1 em indivíduos infectados pelo vírus da imunodeficiência humana tipo-1 (HIV-1) tratados com inibidores de protease.” 2012. Web. 24 Jan 2021.

Vancouver:

Cunha Jd. Estudo da atividade e polimorfismos da Paraoxonase-1 em indivíduos infectados pelo vírus da imunodeficiência humana tipo-1 (HIV-1) tratados com inibidores de protease. [Internet] [Doctoral dissertation]. University of São Paulo; 2012. [cited 2021 Jan 24]. Available from: http://www.teses.usp.br/teses/disponiveis/5/5146/tde-10052013-095130/ ;.

Council of Science Editors:

Cunha Jd. Estudo da atividade e polimorfismos da Paraoxonase-1 em indivíduos infectados pelo vírus da imunodeficiência humana tipo-1 (HIV-1) tratados com inibidores de protease. [Doctoral Dissertation]. University of São Paulo; 2012. Available from: http://www.teses.usp.br/teses/disponiveis/5/5146/tde-10052013-095130/ ;


Universidade do Estado do Rio de Janeiro

27. Fernanda Saloum de Neves Manta. Marcadores Inserção/Deleção (Indel): estudo de ancestralidade e identificação humana na população brasileira.

Degree: PhD, 2013, Universidade do Estado do Rio de Janeiro

 Os polimorfismos denominados Indels são variações de comprimento geradas por inserção ou deleção de um ou mais nucleotídeos em uma sequência de DNA. Estes marcadores… (more)

Subjects/Keywords: Polimorfismo genético; Indels; População brasileira; Ancestralidade; Identificação humana; Genetic Polymorphism; Indels; Brazilian population; Ancestry; Human Identification; GENETICA; Polimorfismo (Genética) - Teses; Genética forense - Teses; Antropologia forense Teses; Brasil População Teses; Hereditariedade - Teses; Genética da população humana - Teses; Mutação INDEL

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APA (6th Edition):

Manta, F. S. d. N. (2013). Marcadores Inserção/Deleção (Indel): estudo de ancestralidade e identificação humana na população brasileira. (Doctoral Dissertation). Universidade do Estado do Rio de Janeiro. Retrieved from http://www.bdtd.uerj.br/tde_busca/arquivo.php?codArquivo=7194 ;

Chicago Manual of Style (16th Edition):

Manta, Fernanda Saloum de Neves. “Marcadores Inserção/Deleção (Indel): estudo de ancestralidade e identificação humana na população brasileira.” 2013. Doctoral Dissertation, Universidade do Estado do Rio de Janeiro. Accessed January 24, 2021. http://www.bdtd.uerj.br/tde_busca/arquivo.php?codArquivo=7194 ;.

MLA Handbook (7th Edition):

Manta, Fernanda Saloum de Neves. “Marcadores Inserção/Deleção (Indel): estudo de ancestralidade e identificação humana na população brasileira.” 2013. Web. 24 Jan 2021.

Vancouver:

Manta FSdN. Marcadores Inserção/Deleção (Indel): estudo de ancestralidade e identificação humana na população brasileira. [Internet] [Doctoral dissertation]. Universidade do Estado do Rio de Janeiro; 2013. [cited 2021 Jan 24]. Available from: http://www.bdtd.uerj.br/tde_busca/arquivo.php?codArquivo=7194 ;.

Council of Science Editors:

Manta FSdN. Marcadores Inserção/Deleção (Indel): estudo de ancestralidade e identificação humana na população brasileira. [Doctoral Dissertation]. Universidade do Estado do Rio de Janeiro; 2013. Available from: http://www.bdtd.uerj.br/tde_busca/arquivo.php?codArquivo=7194 ;

28. Jeanmougin, Marc. Imputation HLA et analyse génomique de la coinfection VIH/VHC : HLA imputation and genomic analysis of HIV/HCV coinfection.

Degree: Docteur es, Biochimie et biologie moléculaire. Bioinformatique, 2017, Paris, CNAM

La génomique d'association cherche à déterminer des liens entre le génome et des traits ou phénotypes, notamment dans le contexte de maladies. Aujourd'hui, les études… (more)

Subjects/Keywords: GWAS; Cirrhose; Coinfection VIH/VHC; HLA; Imputation; Génétique d'association; SNP; Polymorphisme nucléotidique; Antigènes des leucocytes humains; CMH; Complexe majeur d'histocompatibilité; GWAS; Cirrhosis; HIV/HCV Coinfection; HLA; Imputation; Association genetics; SNP; Single Nucleotide Polymorphism; Human leukocyte antigen; MHC; Major histocompatibility complex; 616.042; 616.362; 616.979 2

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

APA (6th Edition):

Jeanmougin, M. (2017). Imputation HLA et analyse génomique de la coinfection VIH/VHC : HLA imputation and genomic analysis of HIV/HCV coinfection. (Doctoral Dissertation). Paris, CNAM. Retrieved from http://www.theses.fr/2017CNAM1164

Chicago Manual of Style (16th Edition):

Jeanmougin, Marc. “Imputation HLA et analyse génomique de la coinfection VIH/VHC : HLA imputation and genomic analysis of HIV/HCV coinfection.” 2017. Doctoral Dissertation, Paris, CNAM. Accessed January 24, 2021. http://www.theses.fr/2017CNAM1164.

MLA Handbook (7th Edition):

Jeanmougin, Marc. “Imputation HLA et analyse génomique de la coinfection VIH/VHC : HLA imputation and genomic analysis of HIV/HCV coinfection.” 2017. Web. 24 Jan 2021.

Vancouver:

Jeanmougin M. Imputation HLA et analyse génomique de la coinfection VIH/VHC : HLA imputation and genomic analysis of HIV/HCV coinfection. [Internet] [Doctoral dissertation]. Paris, CNAM; 2017. [cited 2021 Jan 24]. Available from: http://www.theses.fr/2017CNAM1164.

Council of Science Editors:

Jeanmougin M. Imputation HLA et analyse génomique de la coinfection VIH/VHC : HLA imputation and genomic analysis of HIV/HCV coinfection. [Doctoral Dissertation]. Paris, CNAM; 2017. Available from: http://www.theses.fr/2017CNAM1164


Queensland University of Technology

29. Graf, Justin T. Membrane associated transporter protein gene (SLC45A2) and the genetic basis of normal human pigmentation variation.

Degree: 2008, Queensland University of Technology

 This work is concerned with the genetic basis of normal human pigmentation variation. Specifically, the role of polymorphisms within the solute carrier family 45 member… (more)

Subjects/Keywords: membrane associated transporter protein (MATP), solute carrier family 45 member 2 (SLC45A2), antigen in melanoma (AIM1), underwhite, single nucleotide polymorphism (SNP), normal human pigmentation variation, promoter, hair, skin and eye colour, genotyping; association study

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APA (6th Edition):

Graf, J. T. (2008). Membrane associated transporter protein gene (SLC45A2) and the genetic basis of normal human pigmentation variation. (Thesis). Queensland University of Technology. Retrieved from https://eprints.qut.edu.au/25913/

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):

Graf, Justin T. “Membrane associated transporter protein gene (SLC45A2) and the genetic basis of normal human pigmentation variation.” 2008. Thesis, Queensland University of Technology. Accessed January 24, 2021. https://eprints.qut.edu.au/25913/.

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

MLA Handbook (7th Edition):

Graf, Justin T. “Membrane associated transporter protein gene (SLC45A2) and the genetic basis of normal human pigmentation variation.” 2008. Web. 24 Jan 2021.

Vancouver:

Graf JT. Membrane associated transporter protein gene (SLC45A2) and the genetic basis of normal human pigmentation variation. [Internet] [Thesis]. Queensland University of Technology; 2008. [cited 2021 Jan 24]. Available from: https://eprints.qut.edu.au/25913/.

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

Council of Science Editors:

Graf JT. Membrane associated transporter protein gene (SLC45A2) and the genetic basis of normal human pigmentation variation. [Thesis]. Queensland University of Technology; 2008. Available from: https://eprints.qut.edu.au/25913/

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

30. YU HONGXIANG. HLA associations with nasopharyngeal carcinoma: Implications in pathogenesis and immunotherarpy.

Degree: 2006, National University of Singapore

Subjects/Keywords: Human Leukocyte Antigen; Nasopharyngeal Carcinoma; Single Nucleotide Polymorphism; Epstein-Barr Virus; epitope; Chromosome 6p

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APA (6th Edition):

HONGXIANG, Y. (2006). HLA associations with nasopharyngeal carcinoma: Implications in pathogenesis and immunotherarpy. (Thesis). National University of Singapore. Retrieved from http://scholarbank.nus.edu.sg/handle/10635/15174

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):

HONGXIANG, YU. “HLA associations with nasopharyngeal carcinoma: Implications in pathogenesis and immunotherarpy.” 2006. Thesis, National University of Singapore. Accessed January 24, 2021. http://scholarbank.nus.edu.sg/handle/10635/15174.

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

MLA Handbook (7th Edition):

HONGXIANG, YU. “HLA associations with nasopharyngeal carcinoma: Implications in pathogenesis and immunotherarpy.” 2006. Web. 24 Jan 2021.

Vancouver:

HONGXIANG Y. HLA associations with nasopharyngeal carcinoma: Implications in pathogenesis and immunotherarpy. [Internet] [Thesis]. National University of Singapore; 2006. [cited 2021 Jan 24]. Available from: http://scholarbank.nus.edu.sg/handle/10635/15174.

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

Council of Science Editors:

HONGXIANG Y. HLA associations with nasopharyngeal carcinoma: Implications in pathogenesis and immunotherarpy. [Thesis]. National University of Singapore; 2006. Available from: http://scholarbank.nus.edu.sg/handle/10635/15174

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

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