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You searched for subject:(Single Nucleotide Polymorphisms SNP ). Showing records 1 – 30 of 10247 total matches.

[1] [2] [3] [4] [5] … [342]

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University of Waikato

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

Degree: 2011, University of Waikato

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

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

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APA (6th Edition):

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

Chicago Manual of Style (16th Edition):

McCormick, Helen Margaret. “Molecular Studies of House Mice in Southern New Zealand .” 2011. Masters Thesis, University of Waikato. Accessed October 30, 2020. http://hdl.handle.net/10289/5908.

MLA Handbook (7th Edition):

McCormick, Helen Margaret. “Molecular Studies of House Mice in Southern New Zealand .” 2011. Web. 30 Oct 2020.

Vancouver:

McCormick HM. Molecular Studies of House Mice in Southern New Zealand . [Internet] [Masters thesis]. University of Waikato; 2011. [cited 2020 Oct 30]. Available from: http://hdl.handle.net/10289/5908.

Council of Science Editors:

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


University of Technology, Sydney

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

Degree: 2014, University of Technology, Sydney

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

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

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APA (6th Edition):

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

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

Chicago Manual of Style (16th Edition):

Castel, CV. “Inference of biogeographical ancestry and pigmentation phenotype using single nucleotide polymorphisms.” 2014. Thesis, University of Technology, Sydney. Accessed October 30, 2020. http://hdl.handle.net/10453/29232.

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

MLA Handbook (7th Edition):

Castel, CV. “Inference of biogeographical ancestry and pigmentation phenotype using single nucleotide polymorphisms.” 2014. Web. 30 Oct 2020.

Vancouver:

Castel C. Inference of biogeographical ancestry and pigmentation phenotype using single nucleotide polymorphisms. [Internet] [Thesis]. University of Technology, Sydney; 2014. [cited 2020 Oct 30]. Available from: http://hdl.handle.net/10453/29232.

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

Council of Science Editors:

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

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


University of Oxford

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

Degree: PhD, 2011, University of Oxford

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

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

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APA (6th Edition):

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

Chicago Manual of Style (16th Edition):

Grochola, Lukasz Filip. “Identification and functional analysis of single nucleotide polymorphisms that affect human cancer.” 2011. Doctoral Dissertation, University of Oxford. Accessed October 30, 2020. http://ora.ox.ac.uk/objects/uuid:aacc7084-81a8-4e97-b1ac-024d9bed106e ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.558392.

MLA Handbook (7th Edition):

Grochola, Lukasz Filip. “Identification and functional analysis of single nucleotide polymorphisms that affect human cancer.” 2011. Web. 30 Oct 2020.

Vancouver:

Grochola LF. Identification and functional analysis of single nucleotide polymorphisms that affect human cancer. [Internet] [Doctoral dissertation]. University of Oxford; 2011. [cited 2020 Oct 30]. Available from: http://ora.ox.ac.uk/objects/uuid:aacc7084-81a8-4e97-b1ac-024d9bed106e ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.558392.

Council of Science Editors:

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


University of Edinburgh

4. Zahoor, Imran. Genetics of muscle and meat quality in chicken.

Degree: PhD, 2013, University of Edinburgh

 Skeletal muscles in broilers are generally characterised by pathological muscle damage, indicated by greater plasma creatine kinase (CK) activity, higher incidence of haemorrhages, lighter and… (more)

Subjects/Keywords: heat stress; chicken; genes; SNP; single nucleotide polymorphisms; muscle quality; meat quality

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APA (6th Edition):

Zahoor, I. (2013). Genetics of muscle and meat quality in chicken. (Doctoral Dissertation). University of Edinburgh. Retrieved from http://hdl.handle.net/1842/8085

Chicago Manual of Style (16th Edition):

Zahoor, Imran. “Genetics of muscle and meat quality in chicken.” 2013. Doctoral Dissertation, University of Edinburgh. Accessed October 30, 2020. http://hdl.handle.net/1842/8085.

MLA Handbook (7th Edition):

Zahoor, Imran. “Genetics of muscle and meat quality in chicken.” 2013. Web. 30 Oct 2020.

Vancouver:

Zahoor I. Genetics of muscle and meat quality in chicken. [Internet] [Doctoral dissertation]. University of Edinburgh; 2013. [cited 2020 Oct 30]. Available from: http://hdl.handle.net/1842/8085.

Council of Science Editors:

Zahoor I. Genetics of muscle and meat quality in chicken. [Doctoral Dissertation]. University of Edinburgh; 2013. Available from: http://hdl.handle.net/1842/8085

5. VILLAR, Kamila de Melo. Associação de polimorfismos no gene IL22RA1 como os níveis séricos de IL-22 e com parâmetros clínicos de pacientes portadores de artrite reumatoide .

Degree: 2015, Universidade Federal de Pernambuco

 O processo inflamatório associado à liberação de citocinas está diretamente envolvido na patogênese da artrite reumatóide (AR). Um estudo anterior do nosso grupo relatou que… (more)

Subjects/Keywords: Artrite Reumatóide, IL-22, IL22RA1, SNP (Polimorfismo de Nucleotídeo Único).; Rheumatoid Arthritis,IL22, IL22RA1. Polymorphisms, SNP (Single Nucleotide Polymorphism

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APA (6th Edition):

VILLAR, K. d. M. (2015). Associação de polimorfismos no gene IL22RA1 como os níveis séricos de IL-22 e com parâmetros clínicos de pacientes portadores de artrite reumatoide . (Thesis). Universidade Federal de Pernambuco. Retrieved from http://repositorio.ufpe.br/handle/123456789/17169

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):

VILLAR, Kamila de Melo. “Associação de polimorfismos no gene IL22RA1 como os níveis séricos de IL-22 e com parâmetros clínicos de pacientes portadores de artrite reumatoide .” 2015. Thesis, Universidade Federal de Pernambuco. Accessed October 30, 2020. http://repositorio.ufpe.br/handle/123456789/17169.

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

MLA Handbook (7th Edition):

VILLAR, Kamila de Melo. “Associação de polimorfismos no gene IL22RA1 como os níveis séricos de IL-22 e com parâmetros clínicos de pacientes portadores de artrite reumatoide .” 2015. Web. 30 Oct 2020.

Vancouver:

VILLAR KdM. Associação de polimorfismos no gene IL22RA1 como os níveis séricos de IL-22 e com parâmetros clínicos de pacientes portadores de artrite reumatoide . [Internet] [Thesis]. Universidade Federal de Pernambuco; 2015. [cited 2020 Oct 30]. Available from: http://repositorio.ufpe.br/handle/123456789/17169.

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

Council of Science Editors:

VILLAR KdM. Associação de polimorfismos no gene IL22RA1 como os níveis séricos de IL-22 e com parâmetros clínicos de pacientes portadores de artrite reumatoide . [Thesis]. Universidade Federal de Pernambuco; 2015. Available from: http://repositorio.ufpe.br/handle/123456789/17169

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


IUPUI

6. Bhushan, Sushant. DACS‐DB: AN ANNOTATION AND DISSEMINATION MODEL FOR DISEASE ASSOCIATED CYTOKINE SNPs.

Degree: 2011, IUPUI

Indiana University-Purdue University Indianapolis (IUPUI)

Cytokines mediate crucial functions in innate and adaptive immunity. They play valuable roles in immune cell growth and lineage specification,… (more)

Subjects/Keywords: Cytokine, SNP, Disease, Curated and annotated database; Genetic polymorphisms  – Databases; Cytokines  – Diseases  – Databases; Medicine  – Databases; Polymorphisms, Single Nucleotide

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APA (6th Edition):

Bhushan, S. (2011). DACS‐DB: AN ANNOTATION AND DISSEMINATION MODEL FOR DISEASE ASSOCIATED CYTOKINE SNPs. (Thesis). IUPUI. Retrieved from http://hdl.handle.net/1805/2683

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):

Bhushan, Sushant. “DACS‐DB: AN ANNOTATION AND DISSEMINATION MODEL FOR DISEASE ASSOCIATED CYTOKINE SNPs.” 2011. Thesis, IUPUI. Accessed October 30, 2020. http://hdl.handle.net/1805/2683.

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

MLA Handbook (7th Edition):

Bhushan, Sushant. “DACS‐DB: AN ANNOTATION AND DISSEMINATION MODEL FOR DISEASE ASSOCIATED CYTOKINE SNPs.” 2011. Web. 30 Oct 2020.

Vancouver:

Bhushan S. DACS‐DB: AN ANNOTATION AND DISSEMINATION MODEL FOR DISEASE ASSOCIATED CYTOKINE SNPs. [Internet] [Thesis]. IUPUI; 2011. [cited 2020 Oct 30]. Available from: http://hdl.handle.net/1805/2683.

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

Council of Science Editors:

Bhushan S. DACS‐DB: AN ANNOTATION AND DISSEMINATION MODEL FOR DISEASE ASSOCIATED CYTOKINE SNPs. [Thesis]. IUPUI; 2011. Available from: http://hdl.handle.net/1805/2683

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

7. 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 October 30, 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. 30 Oct 2020.

Vancouver:

Bhasin Y. Single nucleotide polymorphisms (SNPs) in complex disorders: a genome-widw computational analysis. [Internet] [Thesis]. University of Pune; 2009. [cited 2020 Oct 30]. 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

8. Dubois, Julie. Syndromes myélodysplasiques de novo et secondaires à un traitement anti-cancéreux : recherche de marqueurs génétiques de susceptibilité individuelle : Therapy-related myelodysplastic syndromes : identification of genetic markers of individual susceptibility.

Degree: Docteur es, Sciences, technologie, santé. Biologie cellulaire et physiopathologie, 2012, Université de Bordeaux Segalen

Les syndromes myélodysplasiques (SMD) sont des hémopathies myéloïdes clonales évoluant vers une leucémie aiguë (LA). Les SMD et LA secondaires, survenant après traitement par chimiothérapie… (more)

Subjects/Keywords: SMD/LA secondaires; Polymorphismes génétiques SNP; Puce « à façon » de génotypage; Therapy-related MDS/AML; Single Nucleotide Polymorphisms (SNP); Custom-made SNP array

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APA (6th Edition):

Dubois, J. (2012). Syndromes myélodysplasiques de novo et secondaires à un traitement anti-cancéreux : recherche de marqueurs génétiques de susceptibilité individuelle : Therapy-related myelodysplastic syndromes : identification of genetic markers of individual susceptibility. (Doctoral Dissertation). Université de Bordeaux Segalen. Retrieved from http://www.theses.fr/2012BOR21990

Chicago Manual of Style (16th Edition):

Dubois, Julie. “Syndromes myélodysplasiques de novo et secondaires à un traitement anti-cancéreux : recherche de marqueurs génétiques de susceptibilité individuelle : Therapy-related myelodysplastic syndromes : identification of genetic markers of individual susceptibility.” 2012. Doctoral Dissertation, Université de Bordeaux Segalen. Accessed October 30, 2020. http://www.theses.fr/2012BOR21990.

MLA Handbook (7th Edition):

Dubois, Julie. “Syndromes myélodysplasiques de novo et secondaires à un traitement anti-cancéreux : recherche de marqueurs génétiques de susceptibilité individuelle : Therapy-related myelodysplastic syndromes : identification of genetic markers of individual susceptibility.” 2012. Web. 30 Oct 2020.

Vancouver:

Dubois J. Syndromes myélodysplasiques de novo et secondaires à un traitement anti-cancéreux : recherche de marqueurs génétiques de susceptibilité individuelle : Therapy-related myelodysplastic syndromes : identification of genetic markers of individual susceptibility. [Internet] [Doctoral dissertation]. Université de Bordeaux Segalen; 2012. [cited 2020 Oct 30]. Available from: http://www.theses.fr/2012BOR21990.

Council of Science Editors:

Dubois J. Syndromes myélodysplasiques de novo et secondaires à un traitement anti-cancéreux : recherche de marqueurs génétiques de susceptibilité individuelle : Therapy-related myelodysplastic syndromes : identification of genetic markers of individual susceptibility. [Doctoral Dissertation]. Université de Bordeaux Segalen; 2012. Available from: http://www.theses.fr/2012BOR21990


Virginia Commonwealth University

9. Shukry, Sally Gamal. FUNCTIONAL AND BIOCHEMICAL CONSEQUENCES OF SINGLE NUCLEOTIDE POLYMORPHISMS IN THE HUMAN VESICULAR MONOAMINE TRANSPORTER 1 GENE (SLC18A1) By Sally Gamal Shukry, B.S.

Degree: MS, Biology, 2012, Virginia Commonwealth University

 Abstract FUNCTIONAL AND BIOCHEMICAL CONSEQUENCES OF SINGLE NUCLEOTIDE POLYMORPHISMS IN THE HUMAN VESICULAR MONOAMINE TRANSPORTER 1 GENE (SLC18A1) By Sally Gamal Shukry, B.S. A thesis… (more)

Subjects/Keywords: SNP; VMAT1; SLC18A1; Vesicular Monoamine Transporter 1; Single Nucleotide Polymorphisms; Schizophrenia; Bipolar Disorder; Biology; Life Sciences

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APA (6th Edition):

Shukry, S. G. (2012). FUNCTIONAL AND BIOCHEMICAL CONSEQUENCES OF SINGLE NUCLEOTIDE POLYMORPHISMS IN THE HUMAN VESICULAR MONOAMINE TRANSPORTER 1 GENE (SLC18A1) By Sally Gamal Shukry, B.S. (Thesis). Virginia Commonwealth University. Retrieved from https://doi.org/10.25772/B65Q-7P33 ; https://scholarscompass.vcu.edu/etd/360

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):

Shukry, Sally Gamal. “FUNCTIONAL AND BIOCHEMICAL CONSEQUENCES OF SINGLE NUCLEOTIDE POLYMORPHISMS IN THE HUMAN VESICULAR MONOAMINE TRANSPORTER 1 GENE (SLC18A1) By Sally Gamal Shukry, B.S.” 2012. Thesis, Virginia Commonwealth University. Accessed October 30, 2020. https://doi.org/10.25772/B65Q-7P33 ; https://scholarscompass.vcu.edu/etd/360.

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

MLA Handbook (7th Edition):

Shukry, Sally Gamal. “FUNCTIONAL AND BIOCHEMICAL CONSEQUENCES OF SINGLE NUCLEOTIDE POLYMORPHISMS IN THE HUMAN VESICULAR MONOAMINE TRANSPORTER 1 GENE (SLC18A1) By Sally Gamal Shukry, B.S.” 2012. Web. 30 Oct 2020.

Vancouver:

Shukry SG. FUNCTIONAL AND BIOCHEMICAL CONSEQUENCES OF SINGLE NUCLEOTIDE POLYMORPHISMS IN THE HUMAN VESICULAR MONOAMINE TRANSPORTER 1 GENE (SLC18A1) By Sally Gamal Shukry, B.S. [Internet] [Thesis]. Virginia Commonwealth University; 2012. [cited 2020 Oct 30]. Available from: https://doi.org/10.25772/B65Q-7P33 ; https://scholarscompass.vcu.edu/etd/360.

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

Council of Science Editors:

Shukry SG. FUNCTIONAL AND BIOCHEMICAL CONSEQUENCES OF SINGLE NUCLEOTIDE POLYMORPHISMS IN THE HUMAN VESICULAR MONOAMINE TRANSPORTER 1 GENE (SLC18A1) By Sally Gamal Shukry, B.S. [Thesis]. Virginia Commonwealth University; 2012. Available from: https://doi.org/10.25772/B65Q-7P33 ; https://scholarscompass.vcu.edu/etd/360

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


University of Illinois – Chicago

10. Jhun, Ellie H. Pain Pharmacogenetics in Sickle Cell Disease.

Degree: 2016, University of Illinois – Chicago

 Pain is the most conspicuous aspect of sickle cell disease (SCD) to those that are affected that even African tribes have been calling it onomatopoetic… (more)

Subjects/Keywords: Pain; Sickle cell disease; single nucleotide polymorphisms; genetic; monoamine neurotransmitter system; polygenic; candidate gene; SNP; acute pain crisis; chronic pain

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APA (6th Edition):

Jhun, E. H. (2016). Pain Pharmacogenetics in Sickle Cell Disease. (Thesis). University of Illinois – Chicago. Retrieved from http://hdl.handle.net/10027/21347

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):

Jhun, Ellie H. “Pain Pharmacogenetics in Sickle Cell Disease.” 2016. Thesis, University of Illinois – Chicago. Accessed October 30, 2020. http://hdl.handle.net/10027/21347.

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

MLA Handbook (7th Edition):

Jhun, Ellie H. “Pain Pharmacogenetics in Sickle Cell Disease.” 2016. Web. 30 Oct 2020.

Vancouver:

Jhun EH. Pain Pharmacogenetics in Sickle Cell Disease. [Internet] [Thesis]. University of Illinois – Chicago; 2016. [cited 2020 Oct 30]. Available from: http://hdl.handle.net/10027/21347.

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

Council of Science Editors:

Jhun EH. Pain Pharmacogenetics in Sickle Cell Disease. [Thesis]. University of Illinois – Chicago; 2016. Available from: http://hdl.handle.net/10027/21347

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

11. Assis, Alexandro Mangueira Lima de. Análise hierárquica de marcadores bialélicos do cromossomo Y e demografia histórica de populações quilombolas de Alagoas, Brasil.

Degree: 2011, Universidade Federal de Alagoas

The slave trade across the Atlantic brought an estimated four million Africans to Brazil since the beginning of the XVI century until mid-XIX century, thus… (more)

Subjects/Keywords: Genética humana; Quilombolas (AL); Cromossomo Y; Marcadores genéticos; Poliformismo de Nucleotídeo Único (SNP); Human genetics; Quilombolas (AL); Y-Chromosome; Genetic markers; Single Nucleotide Polymorphisms (SNP); CNPQ::CIENCIAS DA SAUDE

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APA (6th Edition):

Assis, A. M. L. d. (2011). Análise hierárquica de marcadores bialélicos do cromossomo Y e demografia histórica de populações quilombolas de Alagoas, Brasil. (Masters Thesis). Universidade Federal de Alagoas. Retrieved from http://www.repositorio.ufal.br/handle/riufal/943

Chicago Manual of Style (16th Edition):

Assis, Alexandro Mangueira Lima de. “Análise hierárquica de marcadores bialélicos do cromossomo Y e demografia histórica de populações quilombolas de Alagoas, Brasil.” 2011. Masters Thesis, Universidade Federal de Alagoas. Accessed October 30, 2020. http://www.repositorio.ufal.br/handle/riufal/943.

MLA Handbook (7th Edition):

Assis, Alexandro Mangueira Lima de. “Análise hierárquica de marcadores bialélicos do cromossomo Y e demografia histórica de populações quilombolas de Alagoas, Brasil.” 2011. Web. 30 Oct 2020.

Vancouver:

Assis AMLd. Análise hierárquica de marcadores bialélicos do cromossomo Y e demografia histórica de populações quilombolas de Alagoas, Brasil. [Internet] [Masters thesis]. Universidade Federal de Alagoas; 2011. [cited 2020 Oct 30]. Available from: http://www.repositorio.ufal.br/handle/riufal/943.

Council of Science Editors:

Assis AMLd. Análise hierárquica de marcadores bialélicos do cromossomo Y e demografia histórica de populações quilombolas de Alagoas, Brasil. [Masters Thesis]. Universidade Federal de Alagoas; 2011. Available from: http://www.repositorio.ufal.br/handle/riufal/943

12. Curti, Maira Ladeia Rodrigues. Associação de poliformismos de genes relacionados à obesidade e comorbidades com resposta à intervenção no estilo de vida de indivíduos de risco cardiometabólico.

Degree: Mestrado, Nutrição em Saúde Pública, 2012, University of São Paulo

Introdução: Fatores genéticos estão entre os determinantes de obesidade, podendo influenciar a resposta a intervenções em estilo de vida. O impacto de polimorfismos de nucleotídeo… (more)

Subjects/Keywords: Cardiometabolic Risk; Estilo de Vida; Intervenção; Intervention on Lifestyle; Nutrigenética; Nutrigenetics; Polimorfismos de nucleotídeo único (SNP); Risco Cardiometabólico; Single Nucleotide polymorphisms (SNP)

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APA (6th Edition):

Curti, M. L. R. (2012). Associação de poliformismos de genes relacionados à obesidade e comorbidades com resposta à intervenção no estilo de vida de indivíduos de risco cardiometabólico. (Masters Thesis). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/6/6138/tde-23082012-143922/ ;

Chicago Manual of Style (16th Edition):

Curti, Maira Ladeia Rodrigues. “Associação de poliformismos de genes relacionados à obesidade e comorbidades com resposta à intervenção no estilo de vida de indivíduos de risco cardiometabólico.” 2012. Masters Thesis, University of São Paulo. Accessed October 30, 2020. http://www.teses.usp.br/teses/disponiveis/6/6138/tde-23082012-143922/ ;.

MLA Handbook (7th Edition):

Curti, Maira Ladeia Rodrigues. “Associação de poliformismos de genes relacionados à obesidade e comorbidades com resposta à intervenção no estilo de vida de indivíduos de risco cardiometabólico.” 2012. Web. 30 Oct 2020.

Vancouver:

Curti MLR. Associação de poliformismos de genes relacionados à obesidade e comorbidades com resposta à intervenção no estilo de vida de indivíduos de risco cardiometabólico. [Internet] [Masters thesis]. University of São Paulo; 2012. [cited 2020 Oct 30]. Available from: http://www.teses.usp.br/teses/disponiveis/6/6138/tde-23082012-143922/ ;.

Council of Science Editors:

Curti MLR. Associação de poliformismos de genes relacionados à obesidade e comorbidades com resposta à intervenção no estilo de vida de indivíduos de risco cardiometabólico. [Masters Thesis]. University of São Paulo; 2012. Available from: http://www.teses.usp.br/teses/disponiveis/6/6138/tde-23082012-143922/ ;


University of Waikato

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

Degree: 2012, University of Waikato

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

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

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APA (6th Edition):

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

Chicago Manual of Style (16th Edition):

Mulholland, Claire Vignette. “Single nucleotide polymorphisms associated with the human electroencephalogram during desflurane anaesthesia .” 2012. Masters Thesis, University of Waikato. Accessed October 30, 2020. http://hdl.handle.net/10289/6678.

MLA Handbook (7th Edition):

Mulholland, Claire Vignette. “Single nucleotide polymorphisms associated with the human electroencephalogram during desflurane anaesthesia .” 2012. Web. 30 Oct 2020.

Vancouver:

Mulholland CV. Single nucleotide polymorphisms associated with the human electroencephalogram during desflurane anaesthesia . [Internet] [Masters thesis]. University of Waikato; 2012. [cited 2020 Oct 30]. Available from: http://hdl.handle.net/10289/6678.

Council of Science Editors:

Mulholland CV. Single nucleotide polymorphisms associated with the human electroencephalogram during desflurane anaesthesia . [Masters Thesis]. University of Waikato; 2012. Available from: http://hdl.handle.net/10289/6678


University of Limerick

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

Degree: 2014, University of Limerick

peer-reviewed

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

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

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APA (6th Edition):

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

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

Chicago Manual of Style (16th Edition):

Sheikhi, Ali. “Statistical methods for the detection of single nucleotide polymorphisms (SNPs) using new generation genome sequencers.” 2014. Thesis, University of Limerick. Accessed October 30, 2020. http://hdl.handle.net/10344/5996.

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

MLA Handbook (7th Edition):

Sheikhi, Ali. “Statistical methods for the detection of single nucleotide polymorphisms (SNPs) using new generation genome sequencers.” 2014. Web. 30 Oct 2020.

Vancouver:

Sheikhi A. Statistical methods for the detection of single nucleotide polymorphisms (SNPs) using new generation genome sequencers. [Internet] [Thesis]. University of Limerick; 2014. [cited 2020 Oct 30]. Available from: http://hdl.handle.net/10344/5996.

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

Council of Science Editors:

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

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


Columbia University

15. 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 October 30, 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. 30 Oct 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 Oct 30]. 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


Hong Kong University of Science and Technology

16. 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 (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 October 30, 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. 30 Oct 2020.

Vancouver:

Yang G. Permutation tests for genome-wide association studies. [Internet] [Thesis]. Hong Kong University of Science and Technology; 2014. [cited 2020 Oct 30]. 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


University of the Western Cape

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

Degree: 2013, University of the Western Cape

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

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

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APA (6th Edition):

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

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

Chicago Manual of Style (16th Edition):

October, Firzana. “Proteomic and SNP analysis of the Cadherin 10 type-II (CDH10) gene, in the South African autistic population .” 2013. Thesis, University of the Western Cape. Accessed October 30, 2020. http://hdl.handle.net/11394/4826.

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

MLA Handbook (7th Edition):

October, Firzana. “Proteomic and SNP analysis of the Cadherin 10 type-II (CDH10) gene, in the South African autistic population .” 2013. Web. 30 Oct 2020.

Vancouver:

October F. Proteomic and SNP analysis of the Cadherin 10 type-II (CDH10) gene, in the South African autistic population . [Internet] [Thesis]. University of the Western Cape; 2013. [cited 2020 Oct 30]. Available from: http://hdl.handle.net/11394/4826.

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

Council of Science Editors:

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

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


University of New Mexico

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

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

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

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

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APA (6th Edition):

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

Chicago Manual of Style (16th Edition):

Glenn, Elizabeth M. “Prevalence of Artemisinin Resistance Associated Single Nucleotide Polymorphisms in Kenyan Isolates.” 2018. Masters Thesis, University of New Mexico. Accessed October 30, 2020. https://digitalrepository.unm.edu/biol_etds/262.

MLA Handbook (7th Edition):

Glenn, Elizabeth M. “Prevalence of Artemisinin Resistance Associated Single Nucleotide Polymorphisms in Kenyan Isolates.” 2018. Web. 30 Oct 2020.

Vancouver:

Glenn EM. Prevalence of Artemisinin Resistance Associated Single Nucleotide Polymorphisms in Kenyan Isolates. [Internet] [Masters thesis]. University of New Mexico; 2018. [cited 2020 Oct 30]. Available from: https://digitalrepository.unm.edu/biol_etds/262.

Council of Science Editors:

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


University of Missouri – Columbia

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

Degree: 2015, University of Missouri – Columbia

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

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

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APA (6th Edition):

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

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

Chicago Manual of Style (16th Edition):

Ramey, Holly Rene. “Mapping natural and artificial selection events in animal genomes.” 2015. Thesis, University of Missouri – Columbia. Accessed October 30, 2020. http://hdl.handle.net/10355/46894.

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

MLA Handbook (7th Edition):

Ramey, Holly Rene. “Mapping natural and artificial selection events in animal genomes.” 2015. Web. 30 Oct 2020.

Vancouver:

Ramey HR. Mapping natural and artificial selection events in animal genomes. [Internet] [Thesis]. University of Missouri – Columbia; 2015. [cited 2020 Oct 30]. Available from: http://hdl.handle.net/10355/46894.

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

Council of Science Editors:

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

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

20. Jenkins, T. Connectivity between MPAs : selecting appropriate taxa and assessing genetic connectivity in two benthic marine invertebrates.

Degree: PhD, 2019, University of Exeter

 Connectivity is fundamental for the persistence of many populations of marine species and is formally identified as one of five key principles for designing an… (more)

Subjects/Keywords: 570; Marine connectivity; Population genetics; RAD sequencing; Phylogeography; Lobster; Pink sea fan; Single nucleotide polymorphisms; SNP; Population structure; Genetic connectivity; Conservation; Fisheries

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

APA (6th Edition):

Jenkins, T. (2019). Connectivity between MPAs : selecting appropriate taxa and assessing genetic connectivity in two benthic marine invertebrates. (Doctoral Dissertation). University of Exeter. Retrieved from http://hdl.handle.net/10871/35541

Chicago Manual of Style (16th Edition):

Jenkins, T. “Connectivity between MPAs : selecting appropriate taxa and assessing genetic connectivity in two benthic marine invertebrates.” 2019. Doctoral Dissertation, University of Exeter. Accessed October 30, 2020. http://hdl.handle.net/10871/35541.

MLA Handbook (7th Edition):

Jenkins, T. “Connectivity between MPAs : selecting appropriate taxa and assessing genetic connectivity in two benthic marine invertebrates.” 2019. Web. 30 Oct 2020.

Vancouver:

Jenkins T. Connectivity between MPAs : selecting appropriate taxa and assessing genetic connectivity in two benthic marine invertebrates. [Internet] [Doctoral dissertation]. University of Exeter; 2019. [cited 2020 Oct 30]. Available from: http://hdl.handle.net/10871/35541.

Council of Science Editors:

Jenkins T. Connectivity between MPAs : selecting appropriate taxa and assessing genetic connectivity in two benthic marine invertebrates. [Doctoral Dissertation]. University of Exeter; 2019. Available from: http://hdl.handle.net/10871/35541


University of Illinois – Urbana-Champaign

21. Serao, Nicola. Study of genetic by environmental interactions at transcriptomic and genomic levels.

Degree: PhD, 0002, 2013, University of Illinois – Urbana-Champaign

 Many phenotypes in humans and animals are resulted by the interaction between genes and environment. For example, animals from distinct breeds may have different nutritional… (more)

Subjects/Keywords: Genome-wide association study (GWAS); feed efficiency; gene expression; glioblastoma; genetic by environment interaction; beef cattle; survival analysis; brain cancer; association study; single nucleotide polymorphisms (SNP); residual feed intake (RFI)

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APA (6th Edition):

Serao, N. (2013). Study of genetic by environmental interactions at transcriptomic and genomic levels. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/42457

Chicago Manual of Style (16th Edition):

Serao, Nicola. “Study of genetic by environmental interactions at transcriptomic and genomic levels.” 2013. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed October 30, 2020. http://hdl.handle.net/2142/42457.

MLA Handbook (7th Edition):

Serao, Nicola. “Study of genetic by environmental interactions at transcriptomic and genomic levels.” 2013. Web. 30 Oct 2020.

Vancouver:

Serao N. Study of genetic by environmental interactions at transcriptomic and genomic levels. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2013. [cited 2020 Oct 30]. Available from: http://hdl.handle.net/2142/42457.

Council of Science Editors:

Serao N. Study of genetic by environmental interactions at transcriptomic and genomic levels. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2013. Available from: http://hdl.handle.net/2142/42457


University of Illinois – Chicago

22. 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 October 30, 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. 30 Oct 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 Oct 30]. 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

23. 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 October 30, 2020. https://dspace.sunyconnect.suny.edu/handle/1951/71105.

MLA Handbook (7th Edition):

Hasper, John. “Next Generation Sequencing Guided SNP Mapping .” 2018. Web. 30 Oct 2020.

Vancouver:

Hasper J. Next Generation Sequencing Guided SNP Mapping . [Internet] [Masters thesis]. SUNY College at Fredonia; 2018. [cited 2020 Oct 30]. 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


Rice University

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

Degree: MS, Engineering, 2015, Rice University

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

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

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

APA (6th Edition):

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

Chicago Manual of Style (16th Edition):

Zafar, Hamim. “A SNP Calling And Genotyping Method For Single-cell Sequencing Data.” 2015. Masters Thesis, Rice University. Accessed October 30, 2020. http://hdl.handle.net/1911/88187.

MLA Handbook (7th Edition):

Zafar, Hamim. “A SNP Calling And Genotyping Method For Single-cell Sequencing Data.” 2015. Web. 30 Oct 2020.

Vancouver:

Zafar H. A SNP Calling And Genotyping Method For Single-cell Sequencing Data. [Internet] [Masters thesis]. Rice University; 2015. [cited 2020 Oct 30]. Available from: http://hdl.handle.net/1911/88187.

Council of Science Editors:

Zafar H. A SNP Calling And Genotyping Method For Single-cell Sequencing Data. [Masters Thesis]. Rice University; 2015. Available from: http://hdl.handle.net/1911/88187


Brno University of Technology

25. Beňková, Daniela. Srovnávací studie působení léčiv vybraného onemocnění na základě genových polymorfismů člověka: Comparative study of the drug effect on selected disease based on the human genetic polymorphisms.

Degree: 2018, Brno University of Technology

 This bachelor thesis is dealing with topic of effects of medicine from the viewpoint of the genetic polymorphism occurrence in human being. The main targets… (more)

Subjects/Keywords: Alzheimerova choroba; ADMET; farmakogenomika; jednonukleotidový polymorfismus; SNP; Alzheimer’s disease; ADMET; pharmacogenomics; single nucleotide polymorphism; SNP

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APA (6th Edition):

Beňková, D. (2018). Srovnávací studie působení léčiv vybraného onemocnění na základě genových polymorfismů člověka: Comparative study of the drug effect on selected disease based on the human genetic polymorphisms. (Thesis). Brno University of Technology. Retrieved from http://hdl.handle.net/11012/61718

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):

Beňková, Daniela. “Srovnávací studie působení léčiv vybraného onemocnění na základě genových polymorfismů člověka: Comparative study of the drug effect on selected disease based on the human genetic polymorphisms.” 2018. Thesis, Brno University of Technology. Accessed October 30, 2020. http://hdl.handle.net/11012/61718.

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

MLA Handbook (7th Edition):

Beňková, Daniela. “Srovnávací studie působení léčiv vybraného onemocnění na základě genových polymorfismů člověka: Comparative study of the drug effect on selected disease based on the human genetic polymorphisms.” 2018. Web. 30 Oct 2020.

Vancouver:

Beňková D. Srovnávací studie působení léčiv vybraného onemocnění na základě genových polymorfismů člověka: Comparative study of the drug effect on selected disease based on the human genetic polymorphisms. [Internet] [Thesis]. Brno University of Technology; 2018. [cited 2020 Oct 30]. Available from: http://hdl.handle.net/11012/61718.

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

Council of Science Editors:

Beňková D. Srovnávací studie působení léčiv vybraného onemocnění na základě genových polymorfismů člověka: Comparative study of the drug effect on selected disease based on the human genetic polymorphisms. [Thesis]. Brno University of Technology; 2018. Available from: http://hdl.handle.net/11012/61718

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


University of the Western Cape

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

Degree: 2016, University of the Western Cape

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

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

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APA (6th Edition):

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

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

Chicago Manual of Style (16th Edition):

Veldsman, Werner Pieter. “SNP based literature and data retrieval .” 2016. Thesis, University of the Western Cape. Accessed October 30, 2020. http://hdl.handle.net/11394/5345.

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

MLA Handbook (7th Edition):

Veldsman, Werner Pieter. “SNP based literature and data retrieval .” 2016. Web. 30 Oct 2020.

Vancouver:

Veldsman WP. SNP based literature and data retrieval . [Internet] [Thesis]. University of the Western Cape; 2016. [cited 2020 Oct 30]. Available from: http://hdl.handle.net/11394/5345.

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

Council of Science Editors:

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

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


Queensland University of Technology

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

Degree: 2010, Queensland University of Technology

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

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

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

APA (6th Edition):

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

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

Chicago Manual of Style (16th Edition):

Costello, Mary-Ellen Clare. “Single nucleotide polymorphism (SNP) - genotyping of Community Acquired Methicillin-Resistant Staphylococcus aureus, including the subtyping of PVL toxin producers using Real-Time PCR.” 2010. Thesis, Queensland University of Technology. Accessed October 30, 2020. https://eprints.qut.edu.au/37662/.

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

MLA Handbook (7th Edition):

Costello, Mary-Ellen Clare. “Single nucleotide polymorphism (SNP) - genotyping of Community Acquired Methicillin-Resistant Staphylococcus aureus, including the subtyping of PVL toxin producers using Real-Time PCR.” 2010. Web. 30 Oct 2020.

Vancouver:

Costello MC. Single nucleotide polymorphism (SNP) - genotyping of Community Acquired Methicillin-Resistant Staphylococcus aureus, including the subtyping of PVL toxin producers using Real-Time PCR. [Internet] [Thesis]. Queensland University of Technology; 2010. [cited 2020 Oct 30]. Available from: https://eprints.qut.edu.au/37662/.

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

Council of Science Editors:

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

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


University of Alberta

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

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

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

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

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

APA (6th Edition):

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

Chicago Manual of Style (16th Edition):

Christiaens, Inge. “Chronic Maternal Stress and Genetic Variants in the Etiology of Spontaneous Preterm Birth.” 2012. Doctoral Dissertation, University of Alberta. Accessed October 30, 2020. https://era.library.ualberta.ca/files/8336h231m.

MLA Handbook (7th Edition):

Christiaens, Inge. “Chronic Maternal Stress and Genetic Variants in the Etiology of Spontaneous Preterm Birth.” 2012. Web. 30 Oct 2020.

Vancouver:

Christiaens I. Chronic Maternal Stress and Genetic Variants in the Etiology of Spontaneous Preterm Birth. [Internet] [Doctoral dissertation]. University of Alberta; 2012. [cited 2020 Oct 30]. Available from: https://era.library.ualberta.ca/files/8336h231m.

Council of Science Editors:

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


Stellenbosch University

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

Degree: MMedSc, Pathology, 2013, Stellenbosch University

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

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

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

APA (6th Edition):

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

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

Chicago Manual of Style (16th Edition):

Davis, William Henry. “Development of a high-throughput genotyping assay for detection of functional polymorphisms involved in homocysteine metabolism and the methylation process implicated in multiple sclerosis.” 2013. Thesis, Stellenbosch University. Accessed October 30, 2020. http://hdl.handle.net/10019.1/95457.

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

MLA Handbook (7th Edition):

Davis, William Henry. “Development of a high-throughput genotyping assay for detection of functional polymorphisms involved in homocysteine metabolism and the methylation process implicated in multiple sclerosis.” 2013. Web. 30 Oct 2020.

Vancouver:

Davis WH. Development of a high-throughput genotyping assay for detection of functional polymorphisms involved in homocysteine metabolism and the methylation process implicated in multiple sclerosis. [Internet] [Thesis]. Stellenbosch University; 2013. [cited 2020 Oct 30]. Available from: http://hdl.handle.net/10019.1/95457.

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

Council of Science Editors:

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

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


University of Alaska – Fairbanks

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

Degree: 2008, University of Alaska – Fairbanks

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

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

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

APA (6th Edition):

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

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

Chicago Manual of Style (16th Edition):

Pasker, Renee Leigh. “Gene by environment interactions between three candidate genes for obesity and omega-3 polyunsaturated fatty acids .” 2008. Thesis, University of Alaska – Fairbanks. Accessed October 30, 2020. http://hdl.handle.net/11122/87.

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

MLA Handbook (7th Edition):

Pasker, Renee Leigh. “Gene by environment interactions between three candidate genes for obesity and omega-3 polyunsaturated fatty acids .” 2008. Web. 30 Oct 2020.

Vancouver:

Pasker RL. Gene by environment interactions between three candidate genes for obesity and omega-3 polyunsaturated fatty acids . [Internet] [Thesis]. University of Alaska – Fairbanks; 2008. [cited 2020 Oct 30]. Available from: http://hdl.handle.net/11122/87.

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

Council of Science Editors:

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

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

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