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You searched for subject:( SNP). Showing records 1 – 30 of 771 total matches.

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1. Coulet, Adrien. Construction et utilisation d'une base de connaissances pharmacogénomique pour l'intégration de données et la découverte de connaissances : Construction and use of a pharmacogenomic knowledge base for data integration and knowledge discovery.

Degree: Docteur es, Informatique, 2008, Université Henri Poincaré – Nancy I

Cette thèse porte sur l’utilisation d’ontologies et de bases de connaissances pour guider différentes étapes du processus d’extraction de connaissances à partir de bases de… (more)

Subjects/Keywords: SNP

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

APA (6th Edition):

Coulet, A. (2008). Construction et utilisation d'une base de connaissances pharmacogénomique pour l'intégration de données et la découverte de connaissances : Construction and use of a pharmacogenomic knowledge base for data integration and knowledge discovery. (Doctoral Dissertation). Université Henri Poincaré – Nancy I. Retrieved from http://www.theses.fr/2008NAN10047

Chicago Manual of Style (16th Edition):

Coulet, Adrien. “Construction et utilisation d'une base de connaissances pharmacogénomique pour l'intégration de données et la découverte de connaissances : Construction and use of a pharmacogenomic knowledge base for data integration and knowledge discovery.” 2008. Doctoral Dissertation, Université Henri Poincaré – Nancy I. Accessed November 29, 2020. http://www.theses.fr/2008NAN10047.

MLA Handbook (7th Edition):

Coulet, Adrien. “Construction et utilisation d'une base de connaissances pharmacogénomique pour l'intégration de données et la découverte de connaissances : Construction and use of a pharmacogenomic knowledge base for data integration and knowledge discovery.” 2008. Web. 29 Nov 2020.

Vancouver:

Coulet A. Construction et utilisation d'une base de connaissances pharmacogénomique pour l'intégration de données et la découverte de connaissances : Construction and use of a pharmacogenomic knowledge base for data integration and knowledge discovery. [Internet] [Doctoral dissertation]. Université Henri Poincaré – Nancy I; 2008. [cited 2020 Nov 29]. Available from: http://www.theses.fr/2008NAN10047.

Council of Science Editors:

Coulet A. Construction et utilisation d'une base de connaissances pharmacogénomique pour l'intégration de données et la découverte de connaissances : Construction and use of a pharmacogenomic knowledge base for data integration and knowledge discovery. [Doctoral Dissertation]. Université Henri Poincaré – Nancy I; 2008. Available from: http://www.theses.fr/2008NAN10047


University of Debrecen

2. Juhász, Emőke. A myogenin gén 3’ UTR-ben lévő MspI polimorfizmusának vizsgálata hibrid sertésállományban .

Degree: DE – Általános Orvostudományi Kar, 2014, University of Debrecen

Dolgozatomban a myogenin 3'UTR régiójában vizsgáltunk egy SNP-nek a hatását. Genotipizálást végeztünk majd a termelési paraméterek adatait összevetettük a kapott genotípusokkal. Ezt pedig statisztikailag elemeztük. Advisors/Committee Members: Babinszky, László (advisor), Takarmány- és Élelmiszer Biotechnológiai Tanszék (advisor).

Subjects/Keywords: myogenin; SNP

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APA (6th Edition):

Juhász, E. (2014). A myogenin gén 3’ UTR-ben lévő MspI polimorfizmusának vizsgálata hibrid sertésállományban . (Thesis). University of Debrecen. Retrieved from http://hdl.handle.net/2437/194824

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):

Juhász, Emőke. “A myogenin gén 3’ UTR-ben lévő MspI polimorfizmusának vizsgálata hibrid sertésállományban .” 2014. Thesis, University of Debrecen. Accessed November 29, 2020. http://hdl.handle.net/2437/194824.

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

MLA Handbook (7th Edition):

Juhász, Emőke. “A myogenin gén 3’ UTR-ben lévő MspI polimorfizmusának vizsgálata hibrid sertésállományban .” 2014. Web. 29 Nov 2020.

Vancouver:

Juhász E. A myogenin gén 3’ UTR-ben lévő MspI polimorfizmusának vizsgálata hibrid sertésállományban . [Internet] [Thesis]. University of Debrecen; 2014. [cited 2020 Nov 29]. Available from: http://hdl.handle.net/2437/194824.

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

Council of Science Editors:

Juhász E. A myogenin gén 3’ UTR-ben lévő MspI polimorfizmusának vizsgálata hibrid sertésállományban . [Thesis]. University of Debrecen; 2014. Available from: http://hdl.handle.net/2437/194824

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


California State University – Sacramento

3. Wu, Dean. Association analysis of galectin gene promoter polymorphisms with multiple cancers.

Degree: MS, Biological Science (Molecular and Cellular Biology, 2011, California State University – Sacramento

 Galectins are a family of carbohydrate-binding proteins with diverse functions in a wide range of cellular processes. A number of galectins play roles in tumorigenesis… (more)

Subjects/Keywords: SNP; Cancer

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APA (6th Edition):

Wu, D. (2011). Association analysis of galectin gene promoter polymorphisms with multiple cancers. (Masters Thesis). California State University – Sacramento. Retrieved from http://hdl.handle.net/10211.9/1234

Chicago Manual of Style (16th Edition):

Wu, Dean. “Association analysis of galectin gene promoter polymorphisms with multiple cancers.” 2011. Masters Thesis, California State University – Sacramento. Accessed November 29, 2020. http://hdl.handle.net/10211.9/1234.

MLA Handbook (7th Edition):

Wu, Dean. “Association analysis of galectin gene promoter polymorphisms with multiple cancers.” 2011. Web. 29 Nov 2020.

Vancouver:

Wu D. Association analysis of galectin gene promoter polymorphisms with multiple cancers. [Internet] [Masters thesis]. California State University – Sacramento; 2011. [cited 2020 Nov 29]. Available from: http://hdl.handle.net/10211.9/1234.

Council of Science Editors:

Wu D. Association analysis of galectin gene promoter polymorphisms with multiple cancers. [Masters Thesis]. California State University – Sacramento; 2011. Available from: http://hdl.handle.net/10211.9/1234

4. Ana Maria Bezerra Oliveira LÃbo. Estudo genÃtico de caracterÃsticas de importÃncia econÃmica em uma populaÃÃo multirracial de ovinos de corte: uma abordagem quantitativa e molecular .

Degree: Master, 2008, Universidade Federal do Ceará

 Atualmente, existe uma grande possibilidade de associaÃÃo entre as Ãreas de genÃtica quantitativa e de genÃtica molecular. Isto pode causar importante impacto na seleÃÃo de… (more)

Subjects/Keywords: ZOOTECNIA; Aromatase; Polimorfismo; SNP; Polymorphism; SNP

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APA (6th Edition):

LÃbo, A. M. B. O. (2008). Estudo genÃtico de caracterÃsticas de importÃncia econÃmica em uma populaÃÃo multirracial de ovinos de corte: uma abordagem quantitativa e molecular . (Masters Thesis). Universidade Federal do Ceará. Retrieved from http://www.teses.ufc.br/tde_busca/arquivo.php?codArquivo=4317 ;

Chicago Manual of Style (16th Edition):

LÃbo, Ana Maria Bezerra Oliveira. “Estudo genÃtico de caracterÃsticas de importÃncia econÃmica em uma populaÃÃo multirracial de ovinos de corte: uma abordagem quantitativa e molecular .” 2008. Masters Thesis, Universidade Federal do Ceará. Accessed November 29, 2020. http://www.teses.ufc.br/tde_busca/arquivo.php?codArquivo=4317 ;.

MLA Handbook (7th Edition):

LÃbo, Ana Maria Bezerra Oliveira. “Estudo genÃtico de caracterÃsticas de importÃncia econÃmica em uma populaÃÃo multirracial de ovinos de corte: uma abordagem quantitativa e molecular .” 2008. Web. 29 Nov 2020.

Vancouver:

LÃbo AMBO. Estudo genÃtico de caracterÃsticas de importÃncia econÃmica em uma populaÃÃo multirracial de ovinos de corte: uma abordagem quantitativa e molecular . [Internet] [Masters thesis]. Universidade Federal do Ceará 2008. [cited 2020 Nov 29]. Available from: http://www.teses.ufc.br/tde_busca/arquivo.php?codArquivo=4317 ;.

Council of Science Editors:

LÃbo AMBO. Estudo genÃtico de caracterÃsticas de importÃncia econÃmica em uma populaÃÃo multirracial de ovinos de corte: uma abordagem quantitativa e molecular . [Masters Thesis]. Universidade Federal do Ceará 2008. Available from: http://www.teses.ufc.br/tde_busca/arquivo.php?codArquivo=4317 ;

5. Donatoni, Flavia Aline Bressani. Prospecção de SNPs por eletroforese capilar e sua identificação em genes candidatos relacionados à resistência de caprinos a nematóides gastrintestinais.

Degree: PhD, Química Analítica e Inorgânica, 2012, University of São Paulo

Citocinas são pequenas moléculas de sinalização celular que desempenham um papel muito importante no sistema imunológico e atuam na comunicação intracelular. Escolheu-se cinco genes pertencentes… (more)

Subjects/Keywords: caprinos; goats; marcadores; markers; SNP; SNP

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APA (6th Edition):

Donatoni, F. A. B. (2012). Prospecção de SNPs por eletroforese capilar e sua identificação em genes candidatos relacionados à resistência de caprinos a nematóides gastrintestinais. (Doctoral Dissertation). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/75/75135/tde-24072012-163708/ ;

Chicago Manual of Style (16th Edition):

Donatoni, Flavia Aline Bressani. “Prospecção de SNPs por eletroforese capilar e sua identificação em genes candidatos relacionados à resistência de caprinos a nematóides gastrintestinais.” 2012. Doctoral Dissertation, University of São Paulo. Accessed November 29, 2020. http://www.teses.usp.br/teses/disponiveis/75/75135/tde-24072012-163708/ ;.

MLA Handbook (7th Edition):

Donatoni, Flavia Aline Bressani. “Prospecção de SNPs por eletroforese capilar e sua identificação em genes candidatos relacionados à resistência de caprinos a nematóides gastrintestinais.” 2012. Web. 29 Nov 2020.

Vancouver:

Donatoni FAB. Prospecção de SNPs por eletroforese capilar e sua identificação em genes candidatos relacionados à resistência de caprinos a nematóides gastrintestinais. [Internet] [Doctoral dissertation]. University of São Paulo; 2012. [cited 2020 Nov 29]. Available from: http://www.teses.usp.br/teses/disponiveis/75/75135/tde-24072012-163708/ ;.

Council of Science Editors:

Donatoni FAB. Prospecção de SNPs por eletroforese capilar e sua identificação em genes candidatos relacionados à resistência de caprinos a nematóides gastrintestinais. [Doctoral Dissertation]. University of São Paulo; 2012. Available from: http://www.teses.usp.br/teses/disponiveis/75/75135/tde-24072012-163708/ ;


University of Alberta

6. Clark, Laura Ashley. The Effect of Mutations in Stearoyl CoA Desaturase Gene and Fatty Acid Synthase on Milk Composition and Fatty Acid Profile in Milk Fat of Dairy Cows.

Degree: MS, Department of Agricultural, Food, and Nutritional Science, 2009, University of Alberta

 The effects of diet on milk fatty acid profile, including conjugated linoleic acid (CLA) have been well documented, however, there is limited information on the… (more)

Subjects/Keywords: CLA; SCD; SNP

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APA (6th Edition):

Clark, L. A. (2009). The Effect of Mutations in Stearoyl CoA Desaturase Gene and Fatty Acid Synthase on Milk Composition and Fatty Acid Profile in Milk Fat of Dairy Cows. (Masters Thesis). University of Alberta. Retrieved from https://era.library.ualberta.ca/files/2227mq21k

Chicago Manual of Style (16th Edition):

Clark, Laura Ashley. “The Effect of Mutations in Stearoyl CoA Desaturase Gene and Fatty Acid Synthase on Milk Composition and Fatty Acid Profile in Milk Fat of Dairy Cows.” 2009. Masters Thesis, University of Alberta. Accessed November 29, 2020. https://era.library.ualberta.ca/files/2227mq21k.

MLA Handbook (7th Edition):

Clark, Laura Ashley. “The Effect of Mutations in Stearoyl CoA Desaturase Gene and Fatty Acid Synthase on Milk Composition and Fatty Acid Profile in Milk Fat of Dairy Cows.” 2009. Web. 29 Nov 2020.

Vancouver:

Clark LA. The Effect of Mutations in Stearoyl CoA Desaturase Gene and Fatty Acid Synthase on Milk Composition and Fatty Acid Profile in Milk Fat of Dairy Cows. [Internet] [Masters thesis]. University of Alberta; 2009. [cited 2020 Nov 29]. Available from: https://era.library.ualberta.ca/files/2227mq21k.

Council of Science Editors:

Clark LA. The Effect of Mutations in Stearoyl CoA Desaturase Gene and Fatty Acid Synthase on Milk Composition and Fatty Acid Profile in Milk Fat of Dairy Cows. [Masters Thesis]. University of Alberta; 2009. Available from: https://era.library.ualberta.ca/files/2227mq21k

7. BARBOSA, Alexandre Domingues. Polimorfismos do gene codificante do receptor da vitamina d (vdr): associação com a susceptibilidade à osteoporose pós‐menopausa e gravidade da doença .

Degree: 2013, Universidade Federal de Pernambuco

 A osteoporose é uma doença esquelética caracterizada pelo comprometimento da resistência óssea, predispondo ao risco aumentado de fraturas. A resistência óssea reflete a integração de… (more)

Subjects/Keywords: Osteoporose; VDR; SNP

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APA (6th Edition):

BARBOSA, A. D. (2013). Polimorfismos do gene codificante do receptor da vitamina d (vdr): associação com a susceptibilidade à osteoporose pós‐menopausa e gravidade da doença . (Thesis). Universidade Federal de Pernambuco. Retrieved from http://repositorio.ufpe.br/handle/123456789/12005

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):

BARBOSA, Alexandre Domingues. “Polimorfismos do gene codificante do receptor da vitamina d (vdr): associação com a susceptibilidade à osteoporose pós‐menopausa e gravidade da doença .” 2013. Thesis, Universidade Federal de Pernambuco. Accessed November 29, 2020. http://repositorio.ufpe.br/handle/123456789/12005.

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

MLA Handbook (7th Edition):

BARBOSA, Alexandre Domingues. “Polimorfismos do gene codificante do receptor da vitamina d (vdr): associação com a susceptibilidade à osteoporose pós‐menopausa e gravidade da doença .” 2013. Web. 29 Nov 2020.

Vancouver:

BARBOSA AD. Polimorfismos do gene codificante do receptor da vitamina d (vdr): associação com a susceptibilidade à osteoporose pós‐menopausa e gravidade da doença . [Internet] [Thesis]. Universidade Federal de Pernambuco; 2013. [cited 2020 Nov 29]. Available from: http://repositorio.ufpe.br/handle/123456789/12005.

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

Council of Science Editors:

BARBOSA AD. Polimorfismos do gene codificante do receptor da vitamina d (vdr): associação com a susceptibilidade à osteoporose pós‐menopausa e gravidade da doença . [Thesis]. Universidade Federal de Pernambuco; 2013. Available from: http://repositorio.ufpe.br/handle/123456789/12005

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


Cornell University

8. Wernimont, Susan. Genetic And Nutritional Variation In The Folate-Mediated One-Carbon Metabolic Network And Cardiovascular Disease (Cvd) Risk.

Degree: PhD, Nutrition, 2011, Cornell University

 The aim of this research was to investigate the role of genetic and nutritional variation within the folate-mediated one-carbon network in relation to cardiovascular disease… (more)

Subjects/Keywords: Folate; snp; Cardiovascular

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APA (6th Edition):

Wernimont, S. (2011). Genetic And Nutritional Variation In The Folate-Mediated One-Carbon Metabolic Network And Cardiovascular Disease (Cvd) Risk. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/33624

Chicago Manual of Style (16th Edition):

Wernimont, Susan. “Genetic And Nutritional Variation In The Folate-Mediated One-Carbon Metabolic Network And Cardiovascular Disease (Cvd) Risk.” 2011. Doctoral Dissertation, Cornell University. Accessed November 29, 2020. http://hdl.handle.net/1813/33624.

MLA Handbook (7th Edition):

Wernimont, Susan. “Genetic And Nutritional Variation In The Folate-Mediated One-Carbon Metabolic Network And Cardiovascular Disease (Cvd) Risk.” 2011. Web. 29 Nov 2020.

Vancouver:

Wernimont S. Genetic And Nutritional Variation In The Folate-Mediated One-Carbon Metabolic Network And Cardiovascular Disease (Cvd) Risk. [Internet] [Doctoral dissertation]. Cornell University; 2011. [cited 2020 Nov 29]. Available from: http://hdl.handle.net/1813/33624.

Council of Science Editors:

Wernimont S. Genetic And Nutritional Variation In The Folate-Mediated One-Carbon Metabolic Network And Cardiovascular Disease (Cvd) Risk. [Doctoral Dissertation]. Cornell University; 2011. Available from: http://hdl.handle.net/1813/33624


Vanderbilt University

9. Baerenwald, Devin August. Extending Genome-Wide Association Study Data Through Analysis of SNPs in the G6PC2 Gene.

Degree: MS, Molecular Physiology and Biophysics, 2012, Vanderbilt University

 This project and the experiments discussed in this document sought to contribute a functional basis for SNPs within G6PC2 significantly associated with variations in fasting… (more)

Subjects/Keywords: FPG; SNP; G6PC2

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APA (6th Edition):

Baerenwald, D. A. (2012). Extending Genome-Wide Association Study Data Through Analysis of SNPs in the G6PC2 Gene. (Thesis). Vanderbilt University. Retrieved from http://hdl.handle.net/1803/10481

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):

Baerenwald, Devin August. “Extending Genome-Wide Association Study Data Through Analysis of SNPs in the G6PC2 Gene.” 2012. Thesis, Vanderbilt University. Accessed November 29, 2020. http://hdl.handle.net/1803/10481.

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

MLA Handbook (7th Edition):

Baerenwald, Devin August. “Extending Genome-Wide Association Study Data Through Analysis of SNPs in the G6PC2 Gene.” 2012. Web. 29 Nov 2020.

Vancouver:

Baerenwald DA. Extending Genome-Wide Association Study Data Through Analysis of SNPs in the G6PC2 Gene. [Internet] [Thesis]. Vanderbilt University; 2012. [cited 2020 Nov 29]. Available from: http://hdl.handle.net/1803/10481.

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

Council of Science Editors:

Baerenwald DA. Extending Genome-Wide Association Study Data Through Analysis of SNPs in the G6PC2 Gene. [Thesis]. Vanderbilt University; 2012. Available from: http://hdl.handle.net/1803/10481

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


University of Saskatchewan

10. Thomas, Tina. Understanding the Genetic Basis of Carotenoid Concentration in Lentil (Lens culinaris Medik.) Seeds.

Degree: 2015, University of Saskatchewan

 Lentils are an inexpensive source of protein, vitamins and minerals. Lentil seeds contain carotenoids that have antioxidant properties and play an important nutritional role as… (more)

Subjects/Keywords: HPLC; GLM; SNP

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APA (6th Edition):

Thomas, T. (2015). Understanding the Genetic Basis of Carotenoid Concentration in Lentil (Lens culinaris Medik.) Seeds. (Thesis). University of Saskatchewan. Retrieved from http://hdl.handle.net/10388/ETD-2015-12-2381

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):

Thomas, Tina. “Understanding the Genetic Basis of Carotenoid Concentration in Lentil (Lens culinaris Medik.) Seeds.” 2015. Thesis, University of Saskatchewan. Accessed November 29, 2020. http://hdl.handle.net/10388/ETD-2015-12-2381.

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

MLA Handbook (7th Edition):

Thomas, Tina. “Understanding the Genetic Basis of Carotenoid Concentration in Lentil (Lens culinaris Medik.) Seeds.” 2015. Web. 29 Nov 2020.

Vancouver:

Thomas T. Understanding the Genetic Basis of Carotenoid Concentration in Lentil (Lens culinaris Medik.) Seeds. [Internet] [Thesis]. University of Saskatchewan; 2015. [cited 2020 Nov 29]. Available from: http://hdl.handle.net/10388/ETD-2015-12-2381.

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

Council of Science Editors:

Thomas T. Understanding the Genetic Basis of Carotenoid Concentration in Lentil (Lens culinaris Medik.) Seeds. [Thesis]. University of Saskatchewan; 2015. Available from: http://hdl.handle.net/10388/ETD-2015-12-2381

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


Ruhr Universität Bochum

11. Fritz, Antigone. Der T393C Genpolymorphismus im Gen GNAS 1 als unabhängiger Prognosefaktor für den Erkrankungsverlauf beim malignen Melanom.

Degree: 2009, Ruhr Universität Bochum

 Wir postulieren, dass der T393C Genpolymorphismus im Gen GNAS 1 für den klinischen Erkrankungsverlauf beim malignen Melanom einen prognostischen Marker darstellt. Es wurde eine retrospektive,… (more)

Subjects/Keywords: Polymorphismus; Hautkrebs; SNP; Prognose; Krankheitsverlauf

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APA (6th Edition):

Fritz, A. (2009). Der T393C Genpolymorphismus im Gen GNAS 1 als unabhängiger Prognosefaktor für den Erkrankungsverlauf beim malignen Melanom. (Thesis). Ruhr Universität Bochum. Retrieved from http://nbn-resolving.de/urn/resolver.pl?urn=urn:nbn:de:hbz:294-27385

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):

Fritz, Antigone. “Der T393C Genpolymorphismus im Gen GNAS 1 als unabhängiger Prognosefaktor für den Erkrankungsverlauf beim malignen Melanom.” 2009. Thesis, Ruhr Universität Bochum. Accessed November 29, 2020. http://nbn-resolving.de/urn/resolver.pl?urn=urn:nbn:de:hbz:294-27385.

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

MLA Handbook (7th Edition):

Fritz, Antigone. “Der T393C Genpolymorphismus im Gen GNAS 1 als unabhängiger Prognosefaktor für den Erkrankungsverlauf beim malignen Melanom.” 2009. Web. 29 Nov 2020.

Vancouver:

Fritz A. Der T393C Genpolymorphismus im Gen GNAS 1 als unabhängiger Prognosefaktor für den Erkrankungsverlauf beim malignen Melanom. [Internet] [Thesis]. Ruhr Universität Bochum; 2009. [cited 2020 Nov 29]. Available from: http://nbn-resolving.de/urn/resolver.pl?urn=urn:nbn:de:hbz:294-27385.

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

Council of Science Editors:

Fritz A. Der T393C Genpolymorphismus im Gen GNAS 1 als unabhängiger Prognosefaktor für den Erkrankungsverlauf beim malignen Melanom. [Thesis]. Ruhr Universität Bochum; 2009. Available from: http://nbn-resolving.de/urn/resolver.pl?urn=urn:nbn:de:hbz:294-27385

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


Ruhr Universität Bochum

12. Heckmann, Michael. Charakterisierung der Wegenersche Granulomatose assoziierten Region auf Chromosom 6p21.3 mittels tagSNP-basierter Feintypisierung.

Degree: 2010, Ruhr Universität Bochum

 Die Prädisposition zur Wegenerschen Granulomatose (WG) ist in hohem Maße mit einer genomischen Region auf Chromosom 6p21.3 (enthält u.a. das HLA-DPB1 Gen) assoziiert worden. Aufgrund… (more)

Subjects/Keywords: Vasculitis; Prädisposition; SNP; Allel; Genotypisierung

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APA (6th Edition):

Heckmann, M. (2010). Charakterisierung der Wegenersche Granulomatose assoziierten Region auf Chromosom 6p21.3 mittels tagSNP-basierter Feintypisierung. (Thesis). Ruhr Universität Bochum. Retrieved from http://nbn-resolving.de/urn/resolver.pl?urn=urn:nbn:de:hbz:294-27667

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):

Heckmann, Michael. “Charakterisierung der Wegenersche Granulomatose assoziierten Region auf Chromosom 6p21.3 mittels tagSNP-basierter Feintypisierung.” 2010. Thesis, Ruhr Universität Bochum. Accessed November 29, 2020. http://nbn-resolving.de/urn/resolver.pl?urn=urn:nbn:de:hbz:294-27667.

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

MLA Handbook (7th Edition):

Heckmann, Michael. “Charakterisierung der Wegenersche Granulomatose assoziierten Region auf Chromosom 6p21.3 mittels tagSNP-basierter Feintypisierung.” 2010. Web. 29 Nov 2020.

Vancouver:

Heckmann M. Charakterisierung der Wegenersche Granulomatose assoziierten Region auf Chromosom 6p21.3 mittels tagSNP-basierter Feintypisierung. [Internet] [Thesis]. Ruhr Universität Bochum; 2010. [cited 2020 Nov 29]. Available from: http://nbn-resolving.de/urn/resolver.pl?urn=urn:nbn:de:hbz:294-27667.

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

Council of Science Editors:

Heckmann M. Charakterisierung der Wegenersche Granulomatose assoziierten Region auf Chromosom 6p21.3 mittels tagSNP-basierter Feintypisierung. [Thesis]. Ruhr Universität Bochum; 2010. Available from: http://nbn-resolving.de/urn/resolver.pl?urn=urn:nbn:de:hbz:294-27667

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


Universiteit Utrecht

13. Castelijns, B. The Role of Genome-Wide Association Studies in Understanding Sporadic Parkinson’s Disease Susceptibility.

Degree: 2014, Universiteit Utrecht

 Parkinson’s disease is one of the most common neurodegenerative diseases, occurring mainly in individuals older than 60 years. The disease causes severe motor disabilities of… (more)

Subjects/Keywords: Parkinson's Disease; GWAS; SNP

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

APA (6th Edition):

Castelijns, B. (2014). The Role of Genome-Wide Association Studies in Understanding Sporadic Parkinson’s Disease Susceptibility. (Masters Thesis). Universiteit Utrecht. Retrieved from http://dspace.library.uu.nl:8080/handle/1874/298193

Chicago Manual of Style (16th Edition):

Castelijns, B. “The Role of Genome-Wide Association Studies in Understanding Sporadic Parkinson’s Disease Susceptibility.” 2014. Masters Thesis, Universiteit Utrecht. Accessed November 29, 2020. http://dspace.library.uu.nl:8080/handle/1874/298193.

MLA Handbook (7th Edition):

Castelijns, B. “The Role of Genome-Wide Association Studies in Understanding Sporadic Parkinson’s Disease Susceptibility.” 2014. Web. 29 Nov 2020.

Vancouver:

Castelijns B. The Role of Genome-Wide Association Studies in Understanding Sporadic Parkinson’s Disease Susceptibility. [Internet] [Masters thesis]. Universiteit Utrecht; 2014. [cited 2020 Nov 29]. Available from: http://dspace.library.uu.nl:8080/handle/1874/298193.

Council of Science Editors:

Castelijns B. The Role of Genome-Wide Association Studies in Understanding Sporadic Parkinson’s Disease Susceptibility. [Masters Thesis]. Universiteit Utrecht; 2014. Available from: http://dspace.library.uu.nl:8080/handle/1874/298193

14. Cavalcanti, Catarina Addobbati Jordão. Polimorfismos do gene fyb (proteína ligante de fyn): associação com o lúpus eritematoso sistêmico .

Degree: 2013, Universidade Federal de Pernambuco

 Lúpus Eritematoso Sistêmico (LES) é uma doença autoimune que afeta diversos órgãos e sistemas. Embora os fatores que contribuem para a patogenia da doença não… (more)

Subjects/Keywords: Lúpus Eritematoso Sistêmico; FYB; SNP

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APA (6th Edition):

Cavalcanti, C. A. J. (2013). Polimorfismos do gene fyb (proteína ligante de fyn): associação com o lúpus eritematoso sistêmico . (Thesis). Universidade Federal de Pernambuco. Retrieved from http://repositorio.ufpe.br/handle/123456789/12039

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):

Cavalcanti, Catarina Addobbati Jordão. “Polimorfismos do gene fyb (proteína ligante de fyn): associação com o lúpus eritematoso sistêmico .” 2013. Thesis, Universidade Federal de Pernambuco. Accessed November 29, 2020. http://repositorio.ufpe.br/handle/123456789/12039.

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

MLA Handbook (7th Edition):

Cavalcanti, Catarina Addobbati Jordão. “Polimorfismos do gene fyb (proteína ligante de fyn): associação com o lúpus eritematoso sistêmico .” 2013. Web. 29 Nov 2020.

Vancouver:

Cavalcanti CAJ. Polimorfismos do gene fyb (proteína ligante de fyn): associação com o lúpus eritematoso sistêmico . [Internet] [Thesis]. Universidade Federal de Pernambuco; 2013. [cited 2020 Nov 29]. Available from: http://repositorio.ufpe.br/handle/123456789/12039.

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

Council of Science Editors:

Cavalcanti CAJ. Polimorfismos do gene fyb (proteína ligante de fyn): associação com o lúpus eritematoso sistêmico . [Thesis]. Universidade Federal de Pernambuco; 2013. Available from: http://repositorio.ufpe.br/handle/123456789/12039

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


Cornell University

15. Wang, Wei. Characterization Of Genetic Variation In North African And Spanish Populations.

Degree: M.S., Biometry, Biometry, 2011, Cornell University

 High-density Single Nucleotide Polymorphism (SNP) scans of the human genome have been applied in many populations worldwide to investigate their genetic characteristics. However, populations in… (more)

Subjects/Keywords: genetic variation; population genetics; snp

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APA (6th Edition):

Wang, W. (2011). Characterization Of Genetic Variation In North African And Spanish Populations. (Masters Thesis). Cornell University. Retrieved from http://hdl.handle.net/1813/29511

Chicago Manual of Style (16th Edition):

Wang, Wei. “Characterization Of Genetic Variation In North African And Spanish Populations.” 2011. Masters Thesis, Cornell University. Accessed November 29, 2020. http://hdl.handle.net/1813/29511.

MLA Handbook (7th Edition):

Wang, Wei. “Characterization Of Genetic Variation In North African And Spanish Populations.” 2011. Web. 29 Nov 2020.

Vancouver:

Wang W. Characterization Of Genetic Variation In North African And Spanish Populations. [Internet] [Masters thesis]. Cornell University; 2011. [cited 2020 Nov 29]. Available from: http://hdl.handle.net/1813/29511.

Council of Science Editors:

Wang W. Characterization Of Genetic Variation In North African And Spanish Populations. [Masters Thesis]. Cornell University; 2011. Available from: http://hdl.handle.net/1813/29511


Vanderbilt University

16. Oetjens, Matthew Thomas. Pharmacogenetic Discovery in an EMR-Biorepository.

Degree: PhD, Human Genetics, 2014, Vanderbilt University

 Adverse drug reactions (ADRs) can be highly influenced by genetic variation. For example, immunosuppressants prescribed to patients who have undergone organ transplantation have severe nephrotoxic… (more)

Subjects/Keywords: Pharmacogenetics; SNP; genetics; genomics; BioVU

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APA (6th Edition):

Oetjens, M. T. (2014). Pharmacogenetic Discovery in an EMR-Biorepository. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://hdl.handle.net/1803/11314

Chicago Manual of Style (16th Edition):

Oetjens, Matthew Thomas. “Pharmacogenetic Discovery in an EMR-Biorepository.” 2014. Doctoral Dissertation, Vanderbilt University. Accessed November 29, 2020. http://hdl.handle.net/1803/11314.

MLA Handbook (7th Edition):

Oetjens, Matthew Thomas. “Pharmacogenetic Discovery in an EMR-Biorepository.” 2014. Web. 29 Nov 2020.

Vancouver:

Oetjens MT. Pharmacogenetic Discovery in an EMR-Biorepository. [Internet] [Doctoral dissertation]. Vanderbilt University; 2014. [cited 2020 Nov 29]. Available from: http://hdl.handle.net/1803/11314.

Council of Science Editors:

Oetjens MT. Pharmacogenetic Discovery in an EMR-Biorepository. [Doctoral Dissertation]. Vanderbilt University; 2014. Available from: http://hdl.handle.net/1803/11314


Colorado State University

17. Hernandez Cordero, Ana Isabel. Predictive potential of genotypes within the prolactin, growth hormone and insulin -like growth factor-I pathways in genetic evaluation of 305 days milk yield in Holstein cows in Sonora, Mexico.

Degree: MS(M.S.), Animal Sciences, 2015, Colorado State University

 The objective of this study was to calculate a molecular breeding value (MBV) using single nucleotide polymorphims (SNP) within genes of the prolactin (PRL) and… (more)

Subjects/Keywords: IGF1; prolactin; GH; SNP; MBV

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

APA (6th Edition):

Hernandez Cordero, A. I. (2015). Predictive potential of genotypes within the prolactin, growth hormone and insulin -like growth factor-I pathways in genetic evaluation of 305 days milk yield in Holstein cows in Sonora, Mexico. (Masters Thesis). Colorado State University. Retrieved from http://hdl.handle.net/10217/167095

Chicago Manual of Style (16th Edition):

Hernandez Cordero, Ana Isabel. “Predictive potential of genotypes within the prolactin, growth hormone and insulin -like growth factor-I pathways in genetic evaluation of 305 days milk yield in Holstein cows in Sonora, Mexico.” 2015. Masters Thesis, Colorado State University. Accessed November 29, 2020. http://hdl.handle.net/10217/167095.

MLA Handbook (7th Edition):

Hernandez Cordero, Ana Isabel. “Predictive potential of genotypes within the prolactin, growth hormone and insulin -like growth factor-I pathways in genetic evaluation of 305 days milk yield in Holstein cows in Sonora, Mexico.” 2015. Web. 29 Nov 2020.

Vancouver:

Hernandez Cordero AI. Predictive potential of genotypes within the prolactin, growth hormone and insulin -like growth factor-I pathways in genetic evaluation of 305 days milk yield in Holstein cows in Sonora, Mexico. [Internet] [Masters thesis]. Colorado State University; 2015. [cited 2020 Nov 29]. Available from: http://hdl.handle.net/10217/167095.

Council of Science Editors:

Hernandez Cordero AI. Predictive potential of genotypes within the prolactin, growth hormone and insulin -like growth factor-I pathways in genetic evaluation of 305 days milk yield in Holstein cows in Sonora, Mexico. [Masters Thesis]. Colorado State University; 2015. Available from: http://hdl.handle.net/10217/167095


Universidade do Rio Grande do Norte

18. Ferreira, Leonardo Capistrano. Genes candidatos de suscetibilidade a pré-eclampsia: estudo de associação .

Degree: 2010, Universidade do Rio Grande do Norte

 Preeclampsia is a multifactorial disease of unknown etiology that features with wide clinical symptoms, ranging from mild preeclampsia to severe forms, as eclampsia and HELLP… (more)

Subjects/Keywords: Pré-eclâmpsia; Associação genética; SNP

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APA (6th Edition):

Ferreira, L. C. (2010). Genes candidatos de suscetibilidade a pré-eclampsia: estudo de associação . (Thesis). Universidade do Rio Grande do Norte. Retrieved from http://repositorio.ufrn.br/handle/123456789/12565

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):

Ferreira, Leonardo Capistrano. “Genes candidatos de suscetibilidade a pré-eclampsia: estudo de associação .” 2010. Thesis, Universidade do Rio Grande do Norte. Accessed November 29, 2020. http://repositorio.ufrn.br/handle/123456789/12565.

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

MLA Handbook (7th Edition):

Ferreira, Leonardo Capistrano. “Genes candidatos de suscetibilidade a pré-eclampsia: estudo de associação .” 2010. Web. 29 Nov 2020.

Vancouver:

Ferreira LC. Genes candidatos de suscetibilidade a pré-eclampsia: estudo de associação . [Internet] [Thesis]. Universidade do Rio Grande do Norte; 2010. [cited 2020 Nov 29]. Available from: http://repositorio.ufrn.br/handle/123456789/12565.

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

Council of Science Editors:

Ferreira LC. Genes candidatos de suscetibilidade a pré-eclampsia: estudo de associação . [Thesis]. Universidade do Rio Grande do Norte; 2010. Available from: http://repositorio.ufrn.br/handle/123456789/12565

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


Harvard University

19. Chiu, Darren Jianjhih. Non-Coding Functional SNPs Within the Arthritis-Associated TRAF1-C5 Locus.

Degree: Master of Medical Sciences, 2018, Harvard University

The TRAF1-C5 locus is associated by genome-wide association studies (GWAS) with susceptibility to rheumatoid arthritis and juvenile idiopathic arthritis. Monocytes from healthy individuals with the… (more)

Subjects/Keywords: TRAF1-C5; SNP; arthritis; monocyte

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APA (6th Edition):

Chiu, D. J. (2018). Non-Coding Functional SNPs Within the Arthritis-Associated TRAF1-C5 Locus. (Masters Thesis). Harvard University. Retrieved from http://nrs.harvard.edu/urn-3:HUL.InstRepos:42076544

Chicago Manual of Style (16th Edition):

Chiu, Darren Jianjhih. “Non-Coding Functional SNPs Within the Arthritis-Associated TRAF1-C5 Locus.” 2018. Masters Thesis, Harvard University. Accessed November 29, 2020. http://nrs.harvard.edu/urn-3:HUL.InstRepos:42076544.

MLA Handbook (7th Edition):

Chiu, Darren Jianjhih. “Non-Coding Functional SNPs Within the Arthritis-Associated TRAF1-C5 Locus.” 2018. Web. 29 Nov 2020.

Vancouver:

Chiu DJ. Non-Coding Functional SNPs Within the Arthritis-Associated TRAF1-C5 Locus. [Internet] [Masters thesis]. Harvard University; 2018. [cited 2020 Nov 29]. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:42076544.

Council of Science Editors:

Chiu DJ. Non-Coding Functional SNPs Within the Arthritis-Associated TRAF1-C5 Locus. [Masters Thesis]. Harvard University; 2018. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:42076544

20. Enami, Nobuko; Itaya-Hironaka, Asako; Yamauchi, Akiyo; Sakuramoto-Tsuchida, Sumiyo; Takasawa, Shin. The CD38 genotype (rs1800561 (4693C>T): R140W) is associated with an increased risk of admission to the neonatal intensive care unit. : CD38 genotype (rs1800561 (4693C > T): R140W)は新生児集中治療室への入院のリスク増加に関連する.

Degree: 博士(医学), 2015, Nara Medical University / 奈良県立医科大学

BACKGROUNDS:Preterm birth (PTB)/admission to the neonatal intensive care unit (NICU) is a complex disorder associated with significant neonatal mortality and morbidity and long-term adverse health… (more)

Subjects/Keywords: CD38; Preterm birth; OXTR; SNP

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APA (6th Edition):

Enami, Nobuko; Itaya-Hironaka, Asako; Yamauchi, Akiyo; Sakuramoto-Tsuchida, Sumiyo; Takasawa, S. (2015). The CD38 genotype (rs1800561 (4693C>T): R140W) is associated with an increased risk of admission to the neonatal intensive care unit. : CD38 genotype (rs1800561 (4693C > T): R140W)は新生児集中治療室への入院のリスク増加に関連する. (Thesis). Nara Medical University / 奈良県立医科大学. Retrieved from http://hdl.handle.net/10564/3100

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):

Enami, Nobuko; Itaya-Hironaka, Asako; Yamauchi, Akiyo; Sakuramoto-Tsuchida, Sumiyo; Takasawa, Shin. “The CD38 genotype (rs1800561 (4693C>T): R140W) is associated with an increased risk of admission to the neonatal intensive care unit. : CD38 genotype (rs1800561 (4693C > T): R140W)は新生児集中治療室への入院のリスク増加に関連する.” 2015. Thesis, Nara Medical University / 奈良県立医科大学. Accessed November 29, 2020. http://hdl.handle.net/10564/3100.

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

MLA Handbook (7th Edition):

Enami, Nobuko; Itaya-Hironaka, Asako; Yamauchi, Akiyo; Sakuramoto-Tsuchida, Sumiyo; Takasawa, Shin. “The CD38 genotype (rs1800561 (4693C>T): R140W) is associated with an increased risk of admission to the neonatal intensive care unit. : CD38 genotype (rs1800561 (4693C > T): R140W)は新生児集中治療室への入院のリスク増加に関連する.” 2015. Web. 29 Nov 2020.

Vancouver:

Enami, Nobuko; Itaya-Hironaka, Asako; Yamauchi, Akiyo; Sakuramoto-Tsuchida, Sumiyo; Takasawa S. The CD38 genotype (rs1800561 (4693C>T): R140W) is associated with an increased risk of admission to the neonatal intensive care unit. : CD38 genotype (rs1800561 (4693C > T): R140W)は新生児集中治療室への入院のリスク増加に関連する. [Internet] [Thesis]. Nara Medical University / 奈良県立医科大学; 2015. [cited 2020 Nov 29]. Available from: http://hdl.handle.net/10564/3100.

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

Council of Science Editors:

Enami, Nobuko; Itaya-Hironaka, Asako; Yamauchi, Akiyo; Sakuramoto-Tsuchida, Sumiyo; Takasawa S. The CD38 genotype (rs1800561 (4693C>T): R140W) is associated with an increased risk of admission to the neonatal intensive care unit. : CD38 genotype (rs1800561 (4693C > T): R140W)は新生児集中治療室への入院のリスク増加に関連する. [Thesis]. Nara Medical University / 奈良県立医科大学; 2015. Available from: http://hdl.handle.net/10564/3100

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

21. Pereira, João Pedro. Farmacogenética na terapêutica das leucemias.

Degree: 2014, RCAAP

Dissertação para obtenção do grau de Mestre no Instituto Superior de Ciências da Saúde Egas Moniz

A leucemia é uma doença neoplásica que afecta a… (more)

Subjects/Keywords: Leucemia; Farmacogenética; SNP; Imatinib

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APA (6th Edition):

Pereira, J. P. (2014). Farmacogenética na terapêutica das leucemias. (Thesis). RCAAP. Retrieved from https://www.rcaap.pt/detail.jsp?id=oai:comum.rcaap.pt:10400.26/13058

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):

Pereira, João Pedro. “Farmacogenética na terapêutica das leucemias.” 2014. Thesis, RCAAP. Accessed November 29, 2020. https://www.rcaap.pt/detail.jsp?id=oai:comum.rcaap.pt:10400.26/13058.

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

MLA Handbook (7th Edition):

Pereira, João Pedro. “Farmacogenética na terapêutica das leucemias.” 2014. Web. 29 Nov 2020.

Vancouver:

Pereira JP. Farmacogenética na terapêutica das leucemias. [Internet] [Thesis]. RCAAP; 2014. [cited 2020 Nov 29]. Available from: https://www.rcaap.pt/detail.jsp?id=oai:comum.rcaap.pt:10400.26/13058.

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

Council of Science Editors:

Pereira JP. Farmacogenética na terapêutica das leucemias. [Thesis]. RCAAP; 2014. Available from: https://www.rcaap.pt/detail.jsp?id=oai:comum.rcaap.pt:10400.26/13058

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


University of Adelaide

22. O’Callaghan, Michael E. The Australian cerebral palsy research study - epidemiological and genetic associations with cerebral palsy.

Degree: 2011, University of Adelaide

 Introduction Twenty two mostly small studies have reported associations between cerebral palsy (CP) and specific single nucleotide polymorphisms (SNPs). These data require prospective confirmation in… (more)

Subjects/Keywords: cerebral palsy; SNP; epidemiology

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APA (6th Edition):

O’Callaghan, M. E. (2011). The Australian cerebral palsy research study - epidemiological and genetic associations with cerebral palsy. (Thesis). University of Adelaide. Retrieved from http://hdl.handle.net/2440/71717

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):

O’Callaghan, Michael E. “The Australian cerebral palsy research study - epidemiological and genetic associations with cerebral palsy.” 2011. Thesis, University of Adelaide. Accessed November 29, 2020. http://hdl.handle.net/2440/71717.

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

MLA Handbook (7th Edition):

O’Callaghan, Michael E. “The Australian cerebral palsy research study - epidemiological and genetic associations with cerebral palsy.” 2011. Web. 29 Nov 2020.

Vancouver:

O’Callaghan ME. The Australian cerebral palsy research study - epidemiological and genetic associations with cerebral palsy. [Internet] [Thesis]. University of Adelaide; 2011. [cited 2020 Nov 29]. Available from: http://hdl.handle.net/2440/71717.

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

Council of Science Editors:

O’Callaghan ME. The Australian cerebral palsy research study - epidemiological and genetic associations with cerebral palsy. [Thesis]. University of Adelaide; 2011. Available from: http://hdl.handle.net/2440/71717

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


University of Adelaide

23. Wooley, Oliver. Methodological challenges to study the nuclear evolutionary history of an ancient bison species.

Degree: 2015, University of Adelaide

 A Masters thesis investigating the evolutionary context of Bison priscus at a genomic scale using advanced sequencing and bioinformatics tools. The thesis describes a workflow… (more)

Subjects/Keywords: Bison; bioinformatics; phylogenetics; SNP

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APA (6th Edition):

Wooley, O. (2015). Methodological challenges to study the nuclear evolutionary history of an ancient bison species. (Thesis). University of Adelaide. Retrieved from http://hdl.handle.net/2440/96824

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):

Wooley, Oliver. “Methodological challenges to study the nuclear evolutionary history of an ancient bison species.” 2015. Thesis, University of Adelaide. Accessed November 29, 2020. http://hdl.handle.net/2440/96824.

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

MLA Handbook (7th Edition):

Wooley, Oliver. “Methodological challenges to study the nuclear evolutionary history of an ancient bison species.” 2015. Web. 29 Nov 2020.

Vancouver:

Wooley O. Methodological challenges to study the nuclear evolutionary history of an ancient bison species. [Internet] [Thesis]. University of Adelaide; 2015. [cited 2020 Nov 29]. Available from: http://hdl.handle.net/2440/96824.

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

Council of Science Editors:

Wooley O. Methodological challenges to study the nuclear evolutionary history of an ancient bison species. [Thesis]. University of Adelaide; 2015. Available from: http://hdl.handle.net/2440/96824

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

24. Naychov, Zheko Dimitrov. TIMP-1 c.T372C Genetic Polymorphism as a Possible Predictor for Acute Aortic Dissection : TIMP-1 c.T372C遺伝子多型による急性大動脈解離の予測可能性.

Degree: 博士(医学), 2014, Hiroshima University / 広島大学

 While single nucleotide polymorphisms (SNP) have been extensively researched in atherosclerotic aortic aneurysms, there are too few data about acute aortic dissection (AAD). The matrix… (more)

Subjects/Keywords: Aortic dissection; SNP; TIMP-1

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APA (6th Edition):

Naychov, Z. D. (2014). TIMP-1 c.T372C Genetic Polymorphism as a Possible Predictor for Acute Aortic Dissection : TIMP-1 c.T372C遺伝子多型による急性大動脈解離の予測可能性. (Thesis). Hiroshima University / 広島大学. Retrieved from http://ir.lib.hiroshima-u.ac.jp/00036322

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):

Naychov, Zheko Dimitrov. “TIMP-1 c.T372C Genetic Polymorphism as a Possible Predictor for Acute Aortic Dissection : TIMP-1 c.T372C遺伝子多型による急性大動脈解離の予測可能性.” 2014. Thesis, Hiroshima University / 広島大学. Accessed November 29, 2020. http://ir.lib.hiroshima-u.ac.jp/00036322.

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

MLA Handbook (7th Edition):

Naychov, Zheko Dimitrov. “TIMP-1 c.T372C Genetic Polymorphism as a Possible Predictor for Acute Aortic Dissection : TIMP-1 c.T372C遺伝子多型による急性大動脈解離の予測可能性.” 2014. Web. 29 Nov 2020.

Vancouver:

Naychov ZD. TIMP-1 c.T372C Genetic Polymorphism as a Possible Predictor for Acute Aortic Dissection : TIMP-1 c.T372C遺伝子多型による急性大動脈解離の予測可能性. [Internet] [Thesis]. Hiroshima University / 広島大学; 2014. [cited 2020 Nov 29]. Available from: http://ir.lib.hiroshima-u.ac.jp/00036322.

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

Council of Science Editors:

Naychov ZD. TIMP-1 c.T372C Genetic Polymorphism as a Possible Predictor for Acute Aortic Dissection : TIMP-1 c.T372C遺伝子多型による急性大動脈解離の予測可能性. [Thesis]. Hiroshima University / 広島大学; 2014. Available from: http://ir.lib.hiroshima-u.ac.jp/00036322

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


Universidade do Rio Grande do Norte

25. Ferreira, Leonardo Capistrano. Genes candidatos de suscetibilidade a pré-eclampsia: estudo de associação .

Degree: 2010, Universidade do Rio Grande do Norte

 Preeclampsia is a multifactorial disease of unknown etiology that features with wide clinical symptoms, ranging from mild preeclampsia to severe forms, as eclampsia and HELLP… (more)

Subjects/Keywords: Pré-eclâmpsia; Associação genética; SNP

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APA (6th Edition):

Ferreira, L. C. (2010). Genes candidatos de suscetibilidade a pré-eclampsia: estudo de associação . (Masters Thesis). Universidade do Rio Grande do Norte. Retrieved from http://repositorio.ufrn.br/handle/123456789/12565

Chicago Manual of Style (16th Edition):

Ferreira, Leonardo Capistrano. “Genes candidatos de suscetibilidade a pré-eclampsia: estudo de associação .” 2010. Masters Thesis, Universidade do Rio Grande do Norte. Accessed November 29, 2020. http://repositorio.ufrn.br/handle/123456789/12565.

MLA Handbook (7th Edition):

Ferreira, Leonardo Capistrano. “Genes candidatos de suscetibilidade a pré-eclampsia: estudo de associação .” 2010. Web. 29 Nov 2020.

Vancouver:

Ferreira LC. Genes candidatos de suscetibilidade a pré-eclampsia: estudo de associação . [Internet] [Masters thesis]. Universidade do Rio Grande do Norte; 2010. [cited 2020 Nov 29]. Available from: http://repositorio.ufrn.br/handle/123456789/12565.

Council of Science Editors:

Ferreira LC. Genes candidatos de suscetibilidade a pré-eclampsia: estudo de associação . [Masters Thesis]. Universidade do Rio Grande do Norte; 2010. Available from: http://repositorio.ufrn.br/handle/123456789/12565


University of Colorado

26. Simonson, Matthew A. Polygenic Analysis of Genome‐Wide SNP Data.

Degree: PhD, Psychology & Neuroscience, 2013, University of Colorado

  One of the central motivators behind genetic research is to understand how genetic variation relates to human health and disease. Recently, there has been… (more)

Subjects/Keywords: GWAS; Polygenic; SNP; Bioinformatics; Genetics

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APA (6th Edition):

Simonson, M. A. (2013). Polygenic Analysis of Genome‐Wide SNP Data. (Doctoral Dissertation). University of Colorado. Retrieved from https://scholar.colorado.edu/psyc_gradetds/43

Chicago Manual of Style (16th Edition):

Simonson, Matthew A. “Polygenic Analysis of Genome‐Wide SNP Data.” 2013. Doctoral Dissertation, University of Colorado. Accessed November 29, 2020. https://scholar.colorado.edu/psyc_gradetds/43.

MLA Handbook (7th Edition):

Simonson, Matthew A. “Polygenic Analysis of Genome‐Wide SNP Data.” 2013. Web. 29 Nov 2020.

Vancouver:

Simonson MA. Polygenic Analysis of Genome‐Wide SNP Data. [Internet] [Doctoral dissertation]. University of Colorado; 2013. [cited 2020 Nov 29]. Available from: https://scholar.colorado.edu/psyc_gradetds/43.

Council of Science Editors:

Simonson MA. Polygenic Analysis of Genome‐Wide SNP Data. [Doctoral Dissertation]. University of Colorado; 2013. Available from: https://scholar.colorado.edu/psyc_gradetds/43


University of Southern California

27. Lehmann, Kjong-Van. Understanding the characteristic of single nucleotide variants.

Degree: PhD, Computational Biology and Bioinformatics, 2013, University of Southern California

 This thesis explores a variety of characteristics towards their use in ranking single nucleotide polymorphisms. The thousand genomes project and many similar ongoing large-scale sequencing… (more)

Subjects/Keywords: functional variants; genomic annotation; snp

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

APA (6th Edition):

Lehmann, K. (2013). Understanding the characteristic of single nucleotide variants. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/114943/rec/7681

Chicago Manual of Style (16th Edition):

Lehmann, Kjong-Van. “Understanding the characteristic of single nucleotide variants.” 2013. Doctoral Dissertation, University of Southern California. Accessed November 29, 2020. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/114943/rec/7681.

MLA Handbook (7th Edition):

Lehmann, Kjong-Van. “Understanding the characteristic of single nucleotide variants.” 2013. Web. 29 Nov 2020.

Vancouver:

Lehmann K. Understanding the characteristic of single nucleotide variants. [Internet] [Doctoral dissertation]. University of Southern California; 2013. [cited 2020 Nov 29]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/114943/rec/7681.

Council of Science Editors:

Lehmann K. Understanding the characteristic of single nucleotide variants. [Doctoral Dissertation]. University of Southern California; 2013. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/114943/rec/7681


University of Florida

28. Ortega Obando, Martha Sophia. Candidate Genes Associated with Fertility and Embryonic Development in Dairy Cattle.

Degree: PhD, Animal Molecular and Cellular Biology, 2017, University of Florida

 The overall goal was to identify genes containing single nucleotide polymorphisms (SNP) explaining some of the genetic variation in fertility in Holstein cows. Identification of… (more)

Subjects/Keywords: cow  – fertility  – genetics  – snp

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APA (6th Edition):

Ortega Obando, M. S. (2017). Candidate Genes Associated with Fertility and Embryonic Development in Dairy Cattle. (Doctoral Dissertation). University of Florida. Retrieved from https://ufdc.ufl.edu/UFE0050689

Chicago Manual of Style (16th Edition):

Ortega Obando, Martha Sophia. “Candidate Genes Associated with Fertility and Embryonic Development in Dairy Cattle.” 2017. Doctoral Dissertation, University of Florida. Accessed November 29, 2020. https://ufdc.ufl.edu/UFE0050689.

MLA Handbook (7th Edition):

Ortega Obando, Martha Sophia. “Candidate Genes Associated with Fertility and Embryonic Development in Dairy Cattle.” 2017. Web. 29 Nov 2020.

Vancouver:

Ortega Obando MS. Candidate Genes Associated with Fertility and Embryonic Development in Dairy Cattle. [Internet] [Doctoral dissertation]. University of Florida; 2017. [cited 2020 Nov 29]. Available from: https://ufdc.ufl.edu/UFE0050689.

Council of Science Editors:

Ortega Obando MS. Candidate Genes Associated with Fertility and Embryonic Development in Dairy Cattle. [Doctoral Dissertation]. University of Florida; 2017. Available from: https://ufdc.ufl.edu/UFE0050689


University of Florida

29. Harris, Theodore Hunter. The Role of P2RX7 in the Hyper-Inflammatory Response of Localized Aggressive Periodontitis Patients.

Degree: PhD, Medical Sciences - Genetics (IDP), 2018, University of Florida

 The purpose of this study is to investigate the involvement of the P2X7 receptor in the inflammatory response in localized aggressive periodontitis (LAP). Blood was… (more)

Subjects/Keywords: inflammation  – p2rx7  – periodontitis  – snp

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

APA (6th Edition):

Harris, T. H. (2018). The Role of P2RX7 in the Hyper-Inflammatory Response of Localized Aggressive Periodontitis Patients. (Doctoral Dissertation). University of Florida. Retrieved from https://ufdc.ufl.edu/UFE0054003

Chicago Manual of Style (16th Edition):

Harris, Theodore Hunter. “The Role of P2RX7 in the Hyper-Inflammatory Response of Localized Aggressive Periodontitis Patients.” 2018. Doctoral Dissertation, University of Florida. Accessed November 29, 2020. https://ufdc.ufl.edu/UFE0054003.

MLA Handbook (7th Edition):

Harris, Theodore Hunter. “The Role of P2RX7 in the Hyper-Inflammatory Response of Localized Aggressive Periodontitis Patients.” 2018. Web. 29 Nov 2020.

Vancouver:

Harris TH. The Role of P2RX7 in the Hyper-Inflammatory Response of Localized Aggressive Periodontitis Patients. [Internet] [Doctoral dissertation]. University of Florida; 2018. [cited 2020 Nov 29]. Available from: https://ufdc.ufl.edu/UFE0054003.

Council of Science Editors:

Harris TH. The Role of P2RX7 in the Hyper-Inflammatory Response of Localized Aggressive Periodontitis Patients. [Doctoral Dissertation]. University of Florida; 2018. Available from: https://ufdc.ufl.edu/UFE0054003


Universitat de Valencia

30. Amat Martínez, Paula. Influencia de los polimorfismos genéticos en la Leucemia Mieloide Crónica .

Degree: 2016, Universitat de Valencia

 La leucemia mieloide crónica (LMC) es una neoplasia mieloproliferativa crónica de carácter clonal con origen en una célula madre pluripotencial común a las tres series… (more)

Subjects/Keywords: leucemia mieloide crónica; SNP; imatinib

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

APA (6th Edition):

Amat Martínez, P. (2016). Influencia de los polimorfismos genéticos en la Leucemia Mieloide Crónica . (Doctoral Dissertation). Universitat de Valencia. Retrieved from http://hdl.handle.net/10550/50156

Chicago Manual of Style (16th Edition):

Amat Martínez, Paula. “Influencia de los polimorfismos genéticos en la Leucemia Mieloide Crónica .” 2016. Doctoral Dissertation, Universitat de Valencia. Accessed November 29, 2020. http://hdl.handle.net/10550/50156.

MLA Handbook (7th Edition):

Amat Martínez, Paula. “Influencia de los polimorfismos genéticos en la Leucemia Mieloide Crónica .” 2016. Web. 29 Nov 2020.

Vancouver:

Amat Martínez P. Influencia de los polimorfismos genéticos en la Leucemia Mieloide Crónica . [Internet] [Doctoral dissertation]. Universitat de Valencia; 2016. [cited 2020 Nov 29]. Available from: http://hdl.handle.net/10550/50156.

Council of Science Editors:

Amat Martínez P. Influencia de los polimorfismos genéticos en la Leucemia Mieloide Crónica . [Doctoral Dissertation]. Universitat de Valencia; 2016. Available from: http://hdl.handle.net/10550/50156

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