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You searched for subject:(genetic predisposition to disease). Showing records 1 – 30 of 74199 total matches.

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University of Utah

1. Spancake, Kimberly Michelle. Contributions of retinoblastoma and p53 to breast carcinogenesis;.

Degree: PhD, Human Genetics;, 1999, University of Utah

 The lifetime risk for a woman to develop breast cancer is 1 in 9 and yet relatively little is known about the early events and… (more)

Subjects/Keywords: Genetic Predisposition to Disease

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APA (6th Edition):

Spancake, K. M. (1999). Contributions of retinoblastoma and p53 to breast carcinogenesis;. (Doctoral Dissertation). University of Utah. Retrieved from http://content.lib.utah.edu/cdm/singleitem/collection/etd1/id/1311/rec/244

Chicago Manual of Style (16th Edition):

Spancake, Kimberly Michelle. “Contributions of retinoblastoma and p53 to breast carcinogenesis;.” 1999. Doctoral Dissertation, University of Utah. Accessed April 18, 2021. http://content.lib.utah.edu/cdm/singleitem/collection/etd1/id/1311/rec/244.

MLA Handbook (7th Edition):

Spancake, Kimberly Michelle. “Contributions of retinoblastoma and p53 to breast carcinogenesis;.” 1999. Web. 18 Apr 2021.

Vancouver:

Spancake KM. Contributions of retinoblastoma and p53 to breast carcinogenesis;. [Internet] [Doctoral dissertation]. University of Utah; 1999. [cited 2021 Apr 18]. Available from: http://content.lib.utah.edu/cdm/singleitem/collection/etd1/id/1311/rec/244.

Council of Science Editors:

Spancake KM. Contributions of retinoblastoma and p53 to breast carcinogenesis;. [Doctoral Dissertation]. University of Utah; 1999. Available from: http://content.lib.utah.edu/cdm/singleitem/collection/etd1/id/1311/rec/244


University of Oulu

2. Erkko, H. (Hannele). TOPBP1, CLSPN and PALB2 genes in familial breast cancer susceptibility.

Degree: 2008, University of Oulu

 Abstract The currently known susceptibility genes account for approximately 25% of familial breast cancer predisposition. Additional factors contributing to the pathogenesis of breast cancer are,… (more)

Subjects/Keywords: CLSPN; Genetic predisposition to disease; PALB2; TOPBP1; breast neoplasms; mutation; penetrance

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APA (6th Edition):

Erkko, H. (. (2008). TOPBP1, CLSPN and PALB2 genes in familial breast cancer susceptibility. (Doctoral Dissertation). University of Oulu. Retrieved from http://urn.fi/urn:isbn:9789514289682

Chicago Manual of Style (16th Edition):

Erkko, H (Hannele). “TOPBP1, CLSPN and PALB2 genes in familial breast cancer susceptibility.” 2008. Doctoral Dissertation, University of Oulu. Accessed April 18, 2021. http://urn.fi/urn:isbn:9789514289682.

MLA Handbook (7th Edition):

Erkko, H (Hannele). “TOPBP1, CLSPN and PALB2 genes in familial breast cancer susceptibility.” 2008. Web. 18 Apr 2021.

Vancouver:

Erkko H(. TOPBP1, CLSPN and PALB2 genes in familial breast cancer susceptibility. [Internet] [Doctoral dissertation]. University of Oulu; 2008. [cited 2021 Apr 18]. Available from: http://urn.fi/urn:isbn:9789514289682.

Council of Science Editors:

Erkko H(. TOPBP1, CLSPN and PALB2 genes in familial breast cancer susceptibility. [Doctoral Dissertation]. University of Oulu; 2008. Available from: http://urn.fi/urn:isbn:9789514289682


Florida International University

3. Kennedy, Amy. Genetic Markers, Birth Characteristics, and Childhood Leukemia Risk.

Degree: PhD, Public Health, 2013, Florida International University

  The cause for childhood acute lymphoblastic leukemia (ALL) remains unknown, but male gender is a risk factor, and among ethnicities, Hispanics have the highest… (more)

Subjects/Keywords: Genetic associations; genetic predisposition to disease; childhood leukemia; iron homeostasis; birth weight; Epidemiology; Public Health

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APA (6th Edition):

Kennedy, A. (2013). Genetic Markers, Birth Characteristics, and Childhood Leukemia Risk. (Doctoral Dissertation). Florida International University. Retrieved from https://digitalcommons.fiu.edu/etd/992 ; 10.25148/etd.FI13120601 ; FI13120601

Chicago Manual of Style (16th Edition):

Kennedy, Amy. “Genetic Markers, Birth Characteristics, and Childhood Leukemia Risk.” 2013. Doctoral Dissertation, Florida International University. Accessed April 18, 2021. https://digitalcommons.fiu.edu/etd/992 ; 10.25148/etd.FI13120601 ; FI13120601.

MLA Handbook (7th Edition):

Kennedy, Amy. “Genetic Markers, Birth Characteristics, and Childhood Leukemia Risk.” 2013. Web. 18 Apr 2021.

Vancouver:

Kennedy A. Genetic Markers, Birth Characteristics, and Childhood Leukemia Risk. [Internet] [Doctoral dissertation]. Florida International University; 2013. [cited 2021 Apr 18]. Available from: https://digitalcommons.fiu.edu/etd/992 ; 10.25148/etd.FI13120601 ; FI13120601.

Council of Science Editors:

Kennedy A. Genetic Markers, Birth Characteristics, and Childhood Leukemia Risk. [Doctoral Dissertation]. Florida International University; 2013. Available from: https://digitalcommons.fiu.edu/etd/992 ; 10.25148/etd.FI13120601 ; FI13120601

4. Jovanović Nataša. Polimorfizmi gena lipidnog metabolizma kod pacijenata sa metaboličkim sindromom.

Degree: 2014, University of Novi Sad

  Metabolic syndrome is a complex polygene multifactor metabolic disorder. By knowing genetic predisposition, environment factors which are subject to change can be corrected, which… (more)

Subjects/Keywords: Metabolic Syndrome; Genetic Predisposition to Disease; Apolipoprotein E; Lipoprotein Receptors; Genetic Polymorphism

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APA (6th Edition):

Nataša, J. (2014). Polimorfizmi gena lipidnog metabolizma kod pacijenata sa metaboličkim sindromom. (Thesis). University of Novi Sad. Retrieved from https://www.cris.uns.ac.rs/DownloadFileServlet/DisertacijaNatasa Jovanovic disertacija.pdf?controlNumber=(BISIS)84442&fileName=Natasa Jovanovic disertacija.pdf&id=1005&source=OATD&language=en ; https://www.cris.uns.ac.rs/record.jsf?recordId=84442&source=OATD&language=en ; http://dx.doi.org/10.2298/NS20140110JOVANOVIC ; http://vbs.rs/scripts/cobiss?command=SEARCH&base=99999&select=ID=viagra sample coupon 1world2go.com coupon for prescription

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):

Nataša, Jovanović. “Polimorfizmi gena lipidnog metabolizma kod pacijenata sa metaboličkim sindromom.” 2014. Thesis, University of Novi Sad. Accessed April 18, 2021. https://www.cris.uns.ac.rs/DownloadFileServlet/DisertacijaNatasa Jovanovic disertacija.pdf?controlNumber=(BISIS)84442&fileName=Natasa Jovanovic disertacija.pdf&id=1005&source=OATD&language=en ; https://www.cris.uns.ac.rs/record.jsf?recordId=84442&source=OATD&language=en ; http://dx.doi.org/10.2298/NS20140110JOVANOVIC ; http://vbs.rs/scripts/cobiss?command=SEARCH&base=99999&select=ID=viagra sample coupon 1world2go.com coupon for prescription.

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

MLA Handbook (7th Edition):

Nataša, Jovanović. “Polimorfizmi gena lipidnog metabolizma kod pacijenata sa metaboličkim sindromom.” 2014. Web. 18 Apr 2021.

Vancouver:

Nataša J. Polimorfizmi gena lipidnog metabolizma kod pacijenata sa metaboličkim sindromom. [Internet] [Thesis]. University of Novi Sad; 2014. [cited 2021 Apr 18]. Available from: https://www.cris.uns.ac.rs/DownloadFileServlet/DisertacijaNatasa Jovanovic disertacija.pdf?controlNumber=(BISIS)84442&fileName=Natasa Jovanovic disertacija.pdf&id=1005&source=OATD&language=en ; https://www.cris.uns.ac.rs/record.jsf?recordId=84442&source=OATD&language=en ; http://dx.doi.org/10.2298/NS20140110JOVANOVIC ; http://vbs.rs/scripts/cobiss?command=SEARCH&base=99999&select=ID=viagra sample coupon 1world2go.com coupon for prescription.

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

Council of Science Editors:

Nataša J. Polimorfizmi gena lipidnog metabolizma kod pacijenata sa metaboličkim sindromom. [Thesis]. University of Novi Sad; 2014. Available from: https://www.cris.uns.ac.rs/DownloadFileServlet/DisertacijaNatasa Jovanovic disertacija.pdf?controlNumber=(BISIS)84442&fileName=Natasa Jovanovic disertacija.pdf&id=1005&source=OATD&language=en ; https://www.cris.uns.ac.rs/record.jsf?recordId=84442&source=OATD&language=en ; http://dx.doi.org/10.2298/NS20140110JOVANOVIC ; http://vbs.rs/scripts/cobiss?command=SEARCH&base=99999&select=ID=viagra sample coupon 1world2go.com coupon for prescription

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


University of Oulu

5. Karppinen, S.-M. (Sanna-Maria). The role of BACH1, BARD1 and TOPBP1 genes in familial breast cancer.

Degree: 2009, University of Oulu

 Abstract Approximately 5–10% of all breast cancer cases are estimated to result from a hereditary predisposition to the disease. Currently no more than 25–30% of… (more)

Subjects/Keywords: BACH1; BARD1; BRCA1; DNA mutational analysis; TOPBP1; breast neoplasms; genetic predisposition to disease; germ-line mutation; hereditary cancer syndromes

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

APA (6th Edition):

Karppinen, S. -. (. (2009). The role of BACH1, BARD1 and TOPBP1 genes in familial breast cancer. (Doctoral Dissertation). University of Oulu. Retrieved from http://urn.fi/urn:isbn:9789514291593

Chicago Manual of Style (16th Edition):

Karppinen, S -M (Sanna-Maria). “The role of BACH1, BARD1 and TOPBP1 genes in familial breast cancer.” 2009. Doctoral Dissertation, University of Oulu. Accessed April 18, 2021. http://urn.fi/urn:isbn:9789514291593.

MLA Handbook (7th Edition):

Karppinen, S -M (Sanna-Maria). “The role of BACH1, BARD1 and TOPBP1 genes in familial breast cancer.” 2009. Web. 18 Apr 2021.

Vancouver:

Karppinen S-(. The role of BACH1, BARD1 and TOPBP1 genes in familial breast cancer. [Internet] [Doctoral dissertation]. University of Oulu; 2009. [cited 2021 Apr 18]. Available from: http://urn.fi/urn:isbn:9789514291593.

Council of Science Editors:

Karppinen S-(. The role of BACH1, BARD1 and TOPBP1 genes in familial breast cancer. [Doctoral Dissertation]. University of Oulu; 2009. Available from: http://urn.fi/urn:isbn:9789514291593


University of Texas Southwestern Medical Center

6. Kulkarni, Vinayak Vaman. Analysis of Coding Region SNPs and Its Propensity to Cause Disease.

Degree: 2007, University of Texas Southwestern Medical Center

 Single Nucleotide Polymorphisms or (SNPs) are the most abundant form of variation present in the human genome. These variations in individuals are considered to be… (more)

Subjects/Keywords: Polymorphism, Single Nucleotide; Genetic Predisposition to Disease; Likelihood Functions

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APA (6th Edition):

Kulkarni, V. V. (2007). Analysis of Coding Region SNPs and Its Propensity to Cause Disease. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/693

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):

Kulkarni, Vinayak Vaman. “Analysis of Coding Region SNPs and Its Propensity to Cause Disease.” 2007. Thesis, University of Texas Southwestern Medical Center. Accessed April 18, 2021. http://hdl.handle.net/2152.5/693.

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

MLA Handbook (7th Edition):

Kulkarni, Vinayak Vaman. “Analysis of Coding Region SNPs and Its Propensity to Cause Disease.” 2007. Web. 18 Apr 2021.

Vancouver:

Kulkarni VV. Analysis of Coding Region SNPs and Its Propensity to Cause Disease. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2007. [cited 2021 Apr 18]. Available from: http://hdl.handle.net/2152.5/693.

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

Council of Science Editors:

Kulkarni VV. Analysis of Coding Region SNPs and Its Propensity to Cause Disease. [Thesis]. University of Texas Southwestern Medical Center; 2007. Available from: http://hdl.handle.net/2152.5/693

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


University of Helsinki

7. Tanskanen, Tomas. Exome sequencing in diagnostic evaluation of colorectal cancer predisposition in young patients.

Degree: Medicinska fakulteten, 2013, University of Helsinki

 Objective. Early-onset colorectal cancer (CRC), defined here as age of onset less than 40 years, develops frequently in genetically predisposed individuals. Next-generation sequencing is an… (more)

Subjects/Keywords: age of onset; colorectal neoplasms; exome; genetic predisposition to disease; mutation; Medical Genetics; Lääketieteellinen genetiikka ja perinnöllisyyslääketiede; Medicinsk genetik

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APA (6th Edition):

Tanskanen, T. (2013). Exome sequencing in diagnostic evaluation of colorectal cancer predisposition in young patients. (Masters Thesis). University of Helsinki. Retrieved from http://hdl.handle.net/10138/159908

Chicago Manual of Style (16th Edition):

Tanskanen, Tomas. “Exome sequencing in diagnostic evaluation of colorectal cancer predisposition in young patients.” 2013. Masters Thesis, University of Helsinki. Accessed April 18, 2021. http://hdl.handle.net/10138/159908.

MLA Handbook (7th Edition):

Tanskanen, Tomas. “Exome sequencing in diagnostic evaluation of colorectal cancer predisposition in young patients.” 2013. Web. 18 Apr 2021.

Vancouver:

Tanskanen T. Exome sequencing in diagnostic evaluation of colorectal cancer predisposition in young patients. [Internet] [Masters thesis]. University of Helsinki; 2013. [cited 2021 Apr 18]. Available from: http://hdl.handle.net/10138/159908.

Council of Science Editors:

Tanskanen T. Exome sequencing in diagnostic evaluation of colorectal cancer predisposition in young patients. [Masters Thesis]. University of Helsinki; 2013. Available from: http://hdl.handle.net/10138/159908


University of Texas Southwestern Medical Center

8. Neumann, Joanie. A Mutation in Alk6b Causes Impaired Germ Cell Differentation and Testicular Germ Cell Tumors in Zebrafish.

Degree: 2010, University of Texas Southwestern Medical Center

 Germ cell tumors (GCTs) affect infants, children and young adults and are increasing in incidence worldwide. GCTs arise from pluripotent germ cells and can exhibit… (more)

Subjects/Keywords: Zebrafish; Disease Models, Animal; Genetic Predisposition to Disease; Neoplasms, Germ Cell and Embryonal

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APA (6th Edition):

Neumann, J. (2010). A Mutation in Alk6b Causes Impaired Germ Cell Differentation and Testicular Germ Cell Tumors in Zebrafish. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/816

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):

Neumann, Joanie. “A Mutation in Alk6b Causes Impaired Germ Cell Differentation and Testicular Germ Cell Tumors in Zebrafish.” 2010. Thesis, University of Texas Southwestern Medical Center. Accessed April 18, 2021. http://hdl.handle.net/2152.5/816.

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

MLA Handbook (7th Edition):

Neumann, Joanie. “A Mutation in Alk6b Causes Impaired Germ Cell Differentation and Testicular Germ Cell Tumors in Zebrafish.” 2010. Web. 18 Apr 2021.

Vancouver:

Neumann J. A Mutation in Alk6b Causes Impaired Germ Cell Differentation and Testicular Germ Cell Tumors in Zebrafish. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2010. [cited 2021 Apr 18]. Available from: http://hdl.handle.net/2152.5/816.

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

Council of Science Editors:

Neumann J. A Mutation in Alk6b Causes Impaired Germ Cell Differentation and Testicular Germ Cell Tumors in Zebrafish. [Thesis]. University of Texas Southwestern Medical Center; 2010. Available from: http://hdl.handle.net/2152.5/816

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

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

Degree: PhD, 2008, University of Alabama – Birmingham

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

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

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APA (6th Edition):

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

Chicago Manual of Style (16th Edition):

Azuero, Andres. “Comparisons of sequential testing approaches for detection of association between disease and haplotype blocks.” 2008. Doctoral Dissertation, University of Alabama – Birmingham. Accessed April 18, 2021. http://contentdm.mhsl.uab.edu/u?/etd,430.

MLA Handbook (7th Edition):

Azuero, Andres. “Comparisons of sequential testing approaches for detection of association between disease and haplotype blocks.” 2008. Web. 18 Apr 2021.

Vancouver:

Azuero A. Comparisons of sequential testing approaches for detection of association between disease and haplotype blocks. [Internet] [Doctoral dissertation]. University of Alabama – Birmingham; 2008. [cited 2021 Apr 18]. Available from: http://contentdm.mhsl.uab.edu/u?/etd,430.

Council of Science Editors:

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

10. Carla Renata Graça. Estudos dos polimorfismos dos genes GSTT1, GSTM1 e NINJURIN1 em indivíduos com Hanseníase.

Degree: 2011, Faculdade de Medicina de São José do Rio Preto

 A hanseníase é uma doença infecciosa crônica causada pelo bacilo álcool-ácido resistente Mycobacterium leprae (M. leprae), patógeno intracelular obrigatório, que afeta a pele e o… (more)

Subjects/Keywords: Hanseníase; Polimorfismo de nucleotídeo único; NINJURIN1; Glutatião S-Transferase; Reação em cadeia da polimerase; Mycobacterium leprae; DERMATOLOGIA; Leprosy; Ninjurin; Single nucleotide polymorphism; Glutathione STransferase; Genetic Predisposition to Disease

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APA (6th Edition):

Graça, C. R. (2011). Estudos dos polimorfismos dos genes GSTT1, GSTM1 e NINJURIN1 em indivíduos com Hanseníase. (Thesis). Faculdade de Medicina de São José do Rio Preto. Retrieved from http://bdtd.famerp.br//tde_busca/arquivo.php?codArquivo=314

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):

Graça, Carla Renata. “Estudos dos polimorfismos dos genes GSTT1, GSTM1 e NINJURIN1 em indivíduos com Hanseníase.” 2011. Thesis, Faculdade de Medicina de São José do Rio Preto. Accessed April 18, 2021. http://bdtd.famerp.br//tde_busca/arquivo.php?codArquivo=314.

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

MLA Handbook (7th Edition):

Graça, Carla Renata. “Estudos dos polimorfismos dos genes GSTT1, GSTM1 e NINJURIN1 em indivíduos com Hanseníase.” 2011. Web. 18 Apr 2021.

Vancouver:

Graça CR. Estudos dos polimorfismos dos genes GSTT1, GSTM1 e NINJURIN1 em indivíduos com Hanseníase. [Internet] [Thesis]. Faculdade de Medicina de São José do Rio Preto; 2011. [cited 2021 Apr 18]. Available from: http://bdtd.famerp.br//tde_busca/arquivo.php?codArquivo=314.

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

Council of Science Editors:

Graça CR. Estudos dos polimorfismos dos genes GSTT1, GSTM1 e NINJURIN1 em indivíduos com Hanseníase. [Thesis]. Faculdade de Medicina de São José do Rio Preto; 2011. Available from: http://bdtd.famerp.br//tde_busca/arquivo.php?codArquivo=314

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


University of Oulu

11. Solyom, S. (Szilvia). BRCA/Fanconi anemia pathway genes in hereditary predisposition to breast cancer.

Degree: 2011, University of Oulu

Abstract Two major genes are involved in hereditary predisposition to breast and ovarian cancer – BRCA1 and BRCA2. However, germline mutations in these tumor suppressors… (more)

Subjects/Keywords: Fanconi anemia; breast cancer; genetic predisposition to disease; germline mutation; Fanconin anemia; ituradan muutos; perinnöllinen alttius; rintasyöpä; ABRAXAS; BRIP1; CHK1; FANCA; FANCJ; MERIT40

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

APA (6th Edition):

Solyom, S. (. (2011). BRCA/Fanconi anemia pathway genes in hereditary predisposition to breast cancer. (Doctoral Dissertation). University of Oulu. Retrieved from http://urn.fi/urn:isbn:9789514294099

Chicago Manual of Style (16th Edition):

Solyom, S (Szilvia). “BRCA/Fanconi anemia pathway genes in hereditary predisposition to breast cancer.” 2011. Doctoral Dissertation, University of Oulu. Accessed April 18, 2021. http://urn.fi/urn:isbn:9789514294099.

MLA Handbook (7th Edition):

Solyom, S (Szilvia). “BRCA/Fanconi anemia pathway genes in hereditary predisposition to breast cancer.” 2011. Web. 18 Apr 2021.

Vancouver:

Solyom S(. BRCA/Fanconi anemia pathway genes in hereditary predisposition to breast cancer. [Internet] [Doctoral dissertation]. University of Oulu; 2011. [cited 2021 Apr 18]. Available from: http://urn.fi/urn:isbn:9789514294099.

Council of Science Editors:

Solyom S(. BRCA/Fanconi anemia pathway genes in hereditary predisposition to breast cancer. [Doctoral Dissertation]. University of Oulu; 2011. Available from: http://urn.fi/urn:isbn:9789514294099


University of Oulu

12. Haanpää, M. (Maria). Hereditary predisposition to breast cancer – with a focus on AATF, MRG15, PALB2, and three Fanconi anaemia genes.

Degree: 2014, University of Oulu

Abstract Around 5−10% of all breast cancer cases are estimated to result from a strong hereditary predisposition to the disease. However, mutations in the currently… (more)

Subjects/Keywords: DNA damage response; DNA repair; Fanconi anaemia; breast cancer; genetic predisposition to disease; germline mutation; DNA-korjaus; DNA-vauriovaste; Fanconin anemia; ituradan mutaatio; perinnöllinen rintasyöpäalttius; rintasyöpä; AATF; MRG15; PALB2

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

APA (6th Edition):

Haanpää, M. (. (2014). Hereditary predisposition to breast cancer – with a focus on AATF, MRG15, PALB2, and three Fanconi anaemia genes. (Doctoral Dissertation). University of Oulu. Retrieved from http://urn.fi/urn:isbn:9789526204581

Chicago Manual of Style (16th Edition):

Haanpää, M (Maria). “Hereditary predisposition to breast cancer – with a focus on AATF, MRG15, PALB2, and three Fanconi anaemia genes.” 2014. Doctoral Dissertation, University of Oulu. Accessed April 18, 2021. http://urn.fi/urn:isbn:9789526204581.

MLA Handbook (7th Edition):

Haanpää, M (Maria). “Hereditary predisposition to breast cancer – with a focus on AATF, MRG15, PALB2, and three Fanconi anaemia genes.” 2014. Web. 18 Apr 2021.

Vancouver:

Haanpää M(. Hereditary predisposition to breast cancer – with a focus on AATF, MRG15, PALB2, and three Fanconi anaemia genes. [Internet] [Doctoral dissertation]. University of Oulu; 2014. [cited 2021 Apr 18]. Available from: http://urn.fi/urn:isbn:9789526204581.

Council of Science Editors:

Haanpää M(. Hereditary predisposition to breast cancer – with a focus on AATF, MRG15, PALB2, and three Fanconi anaemia genes. [Doctoral Dissertation]. University of Oulu; 2014. Available from: http://urn.fi/urn:isbn:9789526204581

13. Lopes, Antonio Luiz Ribeiro Boechat. Influencia de polimorfismos dos genes TNF e PTPN22 sobre a artrite reumatoide e a tuberculose no Amazonas, Brasil.

Degree: 2010, Universidade Federal do Amazonas

A Artrite Reumatoide (AR) é uma doença autoimune que afeta 1% da população geral, promovendo poliartrite e destruição articular com variados graus de incapacidade. Cerca… (more)

Subjects/Keywords: Predisposição genética à doença; Drogas Anti-TNF; Artrite reumatoide; Tuberculose; TNF -308 G/A; PTPN22 1858 C/T; Genetic predisposition to disease; Anti-TNF drugs; Rheumatoid arthritis; Tuberculosis; CIÊNCIAS BIOLÓGICAS

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APA (6th Edition):

Lopes, A. L. R. B. (2010). Influencia de polimorfismos dos genes TNF e PTPN22 sobre a artrite reumatoide e a tuberculose no Amazonas, Brasil. (Doctoral Dissertation). Universidade Federal do Amazonas. Retrieved from http://tede.ufam.edu.br/handle/tede/4302

Chicago Manual of Style (16th Edition):

Lopes, Antonio Luiz Ribeiro Boechat. “Influencia de polimorfismos dos genes TNF e PTPN22 sobre a artrite reumatoide e a tuberculose no Amazonas, Brasil.” 2010. Doctoral Dissertation, Universidade Federal do Amazonas. Accessed April 18, 2021. http://tede.ufam.edu.br/handle/tede/4302.

MLA Handbook (7th Edition):

Lopes, Antonio Luiz Ribeiro Boechat. “Influencia de polimorfismos dos genes TNF e PTPN22 sobre a artrite reumatoide e a tuberculose no Amazonas, Brasil.” 2010. Web. 18 Apr 2021.

Vancouver:

Lopes ALRB. Influencia de polimorfismos dos genes TNF e PTPN22 sobre a artrite reumatoide e a tuberculose no Amazonas, Brasil. [Internet] [Doctoral dissertation]. Universidade Federal do Amazonas; 2010. [cited 2021 Apr 18]. Available from: http://tede.ufam.edu.br/handle/tede/4302.

Council of Science Editors:

Lopes ALRB. Influencia de polimorfismos dos genes TNF e PTPN22 sobre a artrite reumatoide e a tuberculose no Amazonas, Brasil. [Doctoral Dissertation]. Universidade Federal do Amazonas; 2010. Available from: http://tede.ufam.edu.br/handle/tede/4302

14. Karla Fabiana Brasil Gomes. A influência da estratificação populacional na susceptibilidade genética ao diabetes mellitus tipo 1 em uma população brasileira.

Degree: 2016, University of São Paulo

 Introdução: A investigação de genes associados a doenças complexas em estudos caso-controle, baseada na frequência de variantes polimórficas, pode não ser adequada na presença de… (more)

Subjects/Keywords: Diabetes mellitus tipo 1; Genética; Genética populacional; Grupos populacionais; Miscigenação; Predisposição genética para doença; Genetic predisposition to disease, Population groups; Genetics; Genetics population; Miscigenation; Type 1 diabetes mellitus

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APA (6th Edition):

Gomes, K. F. B. (2016). A influência da estratificação populacional na susceptibilidade genética ao diabetes mellitus tipo 1 em uma população brasileira. (Doctoral Dissertation). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/5/5135/tde-22082016-161854/

Chicago Manual of Style (16th Edition):

Gomes, Karla Fabiana Brasil. “A influência da estratificação populacional na susceptibilidade genética ao diabetes mellitus tipo 1 em uma população brasileira.” 2016. Doctoral Dissertation, University of São Paulo. Accessed April 18, 2021. http://www.teses.usp.br/teses/disponiveis/5/5135/tde-22082016-161854/.

MLA Handbook (7th Edition):

Gomes, Karla Fabiana Brasil. “A influência da estratificação populacional na susceptibilidade genética ao diabetes mellitus tipo 1 em uma população brasileira.” 2016. Web. 18 Apr 2021.

Vancouver:

Gomes KFB. A influência da estratificação populacional na susceptibilidade genética ao diabetes mellitus tipo 1 em uma população brasileira. [Internet] [Doctoral dissertation]. University of São Paulo; 2016. [cited 2021 Apr 18]. Available from: http://www.teses.usp.br/teses/disponiveis/5/5135/tde-22082016-161854/.

Council of Science Editors:

Gomes KFB. A influência da estratificação populacional na susceptibilidade genética ao diabetes mellitus tipo 1 em uma população brasileira. [Doctoral Dissertation]. University of São Paulo; 2016. Available from: http://www.teses.usp.br/teses/disponiveis/5/5135/tde-22082016-161854/


Universidade Estadual de Campinas

15. Araujo, Priscila Pereira Costa, 1976-. Estudo da expressão da proteína grelina em carcinoma papilífero da tireoide : um novo marcador de predisposição?.

Degree: Faculdade de Ciências Médicas; Programa de Pós-Graduação em Clínica Médica, 2013, Universidade Estadual de Campinas

Orientador: Laura Sterian Ward

Tese (doutorado) - Universidade Estadual de Campinas, Faculdade de Ciências Médicas

Made available in DSpace on 2018-08-23T21:47:49Z (GMT). No. of bitstreams:… (more)

Subjects/Keywords: Neoplasias da glândula tireoide; Obesidade; Grelina; Predisposição genetica para doenças; Carcinoma da glândula tireoide não medular; Thyroid neoplasms; Obesity; Ghrelin; Genetic predisposition to disease; Thyroid Carcinoma, Nonmedullary 1

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APA (6th Edition):

Araujo, Priscila Pereira Costa, 1. (2013). Estudo da expressão da proteína grelina em carcinoma papilífero da tireoide : um novo marcador de predisposição?. (Doctoral Dissertation). Universidade Estadual de Campinas. Retrieved from ARAUJO, Priscila Pereira Costa. Estudo da expressão da proteína grelina em carcinoma papilífero da tireoide: um novo marcador de predisposição?. 2013. 100p. Tese (doutorado) - Universidade Estadual de Campinas, Faculdade de Ciências Médicas, Campinas, SP. Disponível em: <http://www.repositorio.unicamp.br/handle/REPOSIP/308625>. Acesso em: 23 ago. 2018. ; http://repositorio.unicamp.br/jspui/handle/REPOSIP/308625

Chicago Manual of Style (16th Edition):

Araujo, Priscila Pereira Costa, 1976-. “Estudo da expressão da proteína grelina em carcinoma papilífero da tireoide : um novo marcador de predisposição?.” 2013. Doctoral Dissertation, Universidade Estadual de Campinas. Accessed April 18, 2021. ARAUJO, Priscila Pereira Costa. Estudo da expressão da proteína grelina em carcinoma papilífero da tireoide: um novo marcador de predisposição?. 2013. 100p. Tese (doutorado) - Universidade Estadual de Campinas, Faculdade de Ciências Médicas, Campinas, SP. Disponível em: <http://www.repositorio.unicamp.br/handle/REPOSIP/308625>. Acesso em: 23 ago. 2018. ; http://repositorio.unicamp.br/jspui/handle/REPOSIP/308625.

MLA Handbook (7th Edition):

Araujo, Priscila Pereira Costa, 1976-. “Estudo da expressão da proteína grelina em carcinoma papilífero da tireoide : um novo marcador de predisposição?.” 2013. Web. 18 Apr 2021.

Vancouver:

Araujo, Priscila Pereira Costa 1. Estudo da expressão da proteína grelina em carcinoma papilífero da tireoide : um novo marcador de predisposição?. [Internet] [Doctoral dissertation]. Universidade Estadual de Campinas; 2013. [cited 2021 Apr 18]. Available from: ARAUJO, Priscila Pereira Costa. Estudo da expressão da proteína grelina em carcinoma papilífero da tireoide: um novo marcador de predisposição?. 2013. 100p. Tese (doutorado) - Universidade Estadual de Campinas, Faculdade de Ciências Médicas, Campinas, SP. Disponível em: <http://www.repositorio.unicamp.br/handle/REPOSIP/308625>. Acesso em: 23 ago. 2018. ; http://repositorio.unicamp.br/jspui/handle/REPOSIP/308625.

Council of Science Editors:

Araujo, Priscila Pereira Costa 1. Estudo da expressão da proteína grelina em carcinoma papilífero da tireoide : um novo marcador de predisposição?. [Doctoral Dissertation]. Universidade Estadual de Campinas; 2013. Available from: ARAUJO, Priscila Pereira Costa. Estudo da expressão da proteína grelina em carcinoma papilífero da tireoide: um novo marcador de predisposição?. 2013. 100p. Tese (doutorado) - Universidade Estadual de Campinas, Faculdade de Ciências Médicas, Campinas, SP. Disponível em: <http://www.repositorio.unicamp.br/handle/REPOSIP/308625>. Acesso em: 23 ago. 2018. ; http://repositorio.unicamp.br/jspui/handle/REPOSIP/308625

16. Tatiane Katsue Furuya. Associação entre polimorfismos em genes relacionados à resposta inflamatória e a suscetibilidade, progressão e prognóstico do câncer gástrico.

Degree: 2017, University of São Paulo

 INTRODUÇÃO: A persistência de um microambiente cronicamente inflamado no estômago tem sido descrita como um componente crítico tanto para a iniciação, quanto para a progressão… (more)

Subjects/Keywords: Análise de Sobrevida; Estudos de associação genética; Inflamação; Neoplasias gástricas; Polimorfismo genético; Predisposição genética para doença; Prognóstico; Progressão da doença; Disease progression; Genetic association studies; Genetic predisposition to disease; Inflammation; Polymorphism genetic; Prognosis; Stomach neoplasms; Survival analysis

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APA (6th Edition):

Furuya, T. K. (2017). Associação entre polimorfismos em genes relacionados à resposta inflamatória e a suscetibilidade, progressão e prognóstico do câncer gástrico. (Doctoral Dissertation). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/5/5155/tde-11052017-083936/

Chicago Manual of Style (16th Edition):

Furuya, Tatiane Katsue. “Associação entre polimorfismos em genes relacionados à resposta inflamatória e a suscetibilidade, progressão e prognóstico do câncer gástrico.” 2017. Doctoral Dissertation, University of São Paulo. Accessed April 18, 2021. http://www.teses.usp.br/teses/disponiveis/5/5155/tde-11052017-083936/.

MLA Handbook (7th Edition):

Furuya, Tatiane Katsue. “Associação entre polimorfismos em genes relacionados à resposta inflamatória e a suscetibilidade, progressão e prognóstico do câncer gástrico.” 2017. Web. 18 Apr 2021.

Vancouver:

Furuya TK. Associação entre polimorfismos em genes relacionados à resposta inflamatória e a suscetibilidade, progressão e prognóstico do câncer gástrico. [Internet] [Doctoral dissertation]. University of São Paulo; 2017. [cited 2021 Apr 18]. Available from: http://www.teses.usp.br/teses/disponiveis/5/5155/tde-11052017-083936/.

Council of Science Editors:

Furuya TK. Associação entre polimorfismos em genes relacionados à resposta inflamatória e a suscetibilidade, progressão e prognóstico do câncer gástrico. [Doctoral Dissertation]. University of São Paulo; 2017. Available from: http://www.teses.usp.br/teses/disponiveis/5/5155/tde-11052017-083936/

17. Konstantinidou, Maria-Kalliopi. Μοριακή ανάλυση των μορίων CD14, Toll-like Receptors και συναφών παραγόντων σε αθηρωματικές αλλοιώσεις στεφανιαίων αγγείων.

Degree: 2016, National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ)

BACKGROUND - AIM: Inflammatory mechanisms are the key to the pathogenesis of atherosclerosis. The functional polymorphisms of TLR-4, Asp299Gly and Thr399Ile, CD14 promoter area C260T… (more)

Subjects/Keywords: Στεφανιαία νόσος; Γενετική προδιάθεση; Αθηρωματική νόσος; Coronary artery disease; Genetic predisposition; Atheroma

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APA (6th Edition):

Konstantinidou, M. (2016). Μοριακή ανάλυση των μορίων CD14, Toll-like Receptors και συναφών παραγόντων σε αθηρωματικές αλλοιώσεις στεφανιαίων αγγείων. (Thesis). National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ). Retrieved from http://hdl.handle.net/10442/hedi/39257

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):

Konstantinidou, Maria-Kalliopi. “Μοριακή ανάλυση των μορίων CD14, Toll-like Receptors και συναφών παραγόντων σε αθηρωματικές αλλοιώσεις στεφανιαίων αγγείων.” 2016. Thesis, National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ). Accessed April 18, 2021. http://hdl.handle.net/10442/hedi/39257.

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

MLA Handbook (7th Edition):

Konstantinidou, Maria-Kalliopi. “Μοριακή ανάλυση των μορίων CD14, Toll-like Receptors και συναφών παραγόντων σε αθηρωματικές αλλοιώσεις στεφανιαίων αγγείων.” 2016. Web. 18 Apr 2021.

Vancouver:

Konstantinidou M. Μοριακή ανάλυση των μορίων CD14, Toll-like Receptors και συναφών παραγόντων σε αθηρωματικές αλλοιώσεις στεφανιαίων αγγείων. [Internet] [Thesis]. National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ); 2016. [cited 2021 Apr 18]. Available from: http://hdl.handle.net/10442/hedi/39257.

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

Council of Science Editors:

Konstantinidou M. Μοριακή ανάλυση των μορίων CD14, Toll-like Receptors και συναφών παραγόντων σε αθηρωματικές αλλοιώσεις στεφανιαίων αγγείων. [Thesis]. National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ); 2016. Available from: http://hdl.handle.net/10442/hedi/39257

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

18. Cintia Semzezem. Variantes nos genes dos receptores das interleucinas IL-17A e IL-21 em pacientes com diabete melito autoimune.

Degree: 2017, University of São Paulo

 Diabete Melito tipo 1A (DM1A) é uma doença autoimune resultante da interação de fatores ambientais, alterações imunológicas e predisposição genética. Decorre da perda da tolerância… (more)

Subjects/Keywords: Autoimunidade; Diabetes mellitus tipo 1; Polimorfismo genético; Predisposição genética para doença; Receptores de interleucina-17; Receptores de interleucina-21; Autoimmunity; Diabetes mellitus type 1; Genetic predisposition to disease; Polymorphism genetic; Receptors interleukin-17; Receptors interleukin-21

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APA (6th Edition):

Semzezem, C. (2017). Variantes nos genes dos receptores das interleucinas IL-17A e IL-21 em pacientes com diabete melito autoimune. (Masters Thesis). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/5/5135/tde-05102017-114232/

Chicago Manual of Style (16th Edition):

Semzezem, Cintia. “Variantes nos genes dos receptores das interleucinas IL-17A e IL-21 em pacientes com diabete melito autoimune.” 2017. Masters Thesis, University of São Paulo. Accessed April 18, 2021. http://www.teses.usp.br/teses/disponiveis/5/5135/tde-05102017-114232/.

MLA Handbook (7th Edition):

Semzezem, Cintia. “Variantes nos genes dos receptores das interleucinas IL-17A e IL-21 em pacientes com diabete melito autoimune.” 2017. Web. 18 Apr 2021.

Vancouver:

Semzezem C. Variantes nos genes dos receptores das interleucinas IL-17A e IL-21 em pacientes com diabete melito autoimune. [Internet] [Masters thesis]. University of São Paulo; 2017. [cited 2021 Apr 18]. Available from: http://www.teses.usp.br/teses/disponiveis/5/5135/tde-05102017-114232/.

Council of Science Editors:

Semzezem C. Variantes nos genes dos receptores das interleucinas IL-17A e IL-21 em pacientes com diabete melito autoimune. [Masters Thesis]. University of São Paulo; 2017. Available from: http://www.teses.usp.br/teses/disponiveis/5/5135/tde-05102017-114232/

19. Stojšić Vladimir. Učestalost i prognostički značaj genskih alteracija u tumorskim ćelijama i njihova povezanost sa kliničko-patološkim karakteristikama bolesnika sa ranim stadijumom adenokarcinoma bronha.

Degree: 2018, University of Novi Sad

  Napredak na polju molekularne biologije omogućio je identifikaciju molekularnih markera za karcinom bronha sa vrednim prognostičkim i prediktivnim značajem i njihova uloga kod uznapredovalog,… (more)

Subjects/Keywords: neoplazme bronha; adenokarcinom; genetska predispozicija prema bolesti; tumorski biomarkeri; prognoza; stadijum neoplazmi; preživljavanje; preživljavanje bez povratka bolesti; mutacija; rana dijagnoza karcinoma; Bronchial Neoplasms; Adenocarcinoma; Genetic Predisposition to Disease; Biomarkers, Tumor; Prognosis; Neoplasm Staging; Survival; Disease-Free Survival; Mutation; Early Diagnosis of Cancer

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APA (6th Edition):

Vladimir, S. (2018). Učestalost i prognostički značaj genskih alteracija u tumorskim ćelijama i njihova povezanost sa kliničko-patološkim karakteristikama bolesnika sa ranim stadijumom adenokarcinoma bronha. (Thesis). University of Novi Sad. Retrieved from https://www.cris.uns.ac.rs/DownloadFileServlet/Disertacija150839780477797.pdf?controlNumber=(BISIS)105379&fileName=150839780477797.pdf&id=10574&source=OATD&language=en ; https://www.cris.uns.ac.rs/record.jsf?recordId=105379&source=OATD&language=en

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):

Vladimir, Stojšić. “Učestalost i prognostički značaj genskih alteracija u tumorskim ćelijama i njihova povezanost sa kliničko-patološkim karakteristikama bolesnika sa ranim stadijumom adenokarcinoma bronha.” 2018. Thesis, University of Novi Sad. Accessed April 18, 2021. https://www.cris.uns.ac.rs/DownloadFileServlet/Disertacija150839780477797.pdf?controlNumber=(BISIS)105379&fileName=150839780477797.pdf&id=10574&source=OATD&language=en ; https://www.cris.uns.ac.rs/record.jsf?recordId=105379&source=OATD&language=en.

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

MLA Handbook (7th Edition):

Vladimir, Stojšić. “Učestalost i prognostički značaj genskih alteracija u tumorskim ćelijama i njihova povezanost sa kliničko-patološkim karakteristikama bolesnika sa ranim stadijumom adenokarcinoma bronha.” 2018. Web. 18 Apr 2021.

Vancouver:

Vladimir S. Učestalost i prognostički značaj genskih alteracija u tumorskim ćelijama i njihova povezanost sa kliničko-patološkim karakteristikama bolesnika sa ranim stadijumom adenokarcinoma bronha. [Internet] [Thesis]. University of Novi Sad; 2018. [cited 2021 Apr 18]. Available from: https://www.cris.uns.ac.rs/DownloadFileServlet/Disertacija150839780477797.pdf?controlNumber=(BISIS)105379&fileName=150839780477797.pdf&id=10574&source=OATD&language=en ; https://www.cris.uns.ac.rs/record.jsf?recordId=105379&source=OATD&language=en.

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

Council of Science Editors:

Vladimir S. Učestalost i prognostički značaj genskih alteracija u tumorskim ćelijama i njihova povezanost sa kliničko-patološkim karakteristikama bolesnika sa ranim stadijumom adenokarcinoma bronha. [Thesis]. University of Novi Sad; 2018. Available from: https://www.cris.uns.ac.rs/DownloadFileServlet/Disertacija150839780477797.pdf?controlNumber=(BISIS)105379&fileName=150839780477797.pdf&id=10574&source=OATD&language=en ; https://www.cris.uns.ac.rs/record.jsf?recordId=105379&source=OATD&language=en

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

20. Nyaku, Mawuli K. Association between CC Chemokine ligand 3-Like-1 (CCL3L1) gene copy number and rheumatoid arthritis in African Americans.

Degree: D.P.H., 2012, University of Alabama – Birmingham

Purpose: Gene copy number of the CC Chemokine ligand 3-Like-1 (CCL3L1) located on chromosome 17 position q12 varies between ethnicities. Previously, gene copy number of… (more)

Subjects/Keywords: African Americans<; br>; Arthritis, Rheumatoid  – genetics<; br>; Chemokines, CC  – genetics<; br>; Gene Dosage<; br>; Genetic Predisposition to Disease<; br>; Risk Factors

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APA (6th Edition):

Nyaku, M. K. (2012). Association between CC Chemokine ligand 3-Like-1 (CCL3L1) gene copy number and rheumatoid arthritis in African Americans. (Doctoral Dissertation). University of Alabama – Birmingham. Retrieved from http://contentdm.mhsl.uab.edu/u?/etd,1144

Chicago Manual of Style (16th Edition):

Nyaku, Mawuli K. “Association between CC Chemokine ligand 3-Like-1 (CCL3L1) gene copy number and rheumatoid arthritis in African Americans.” 2012. Doctoral Dissertation, University of Alabama – Birmingham. Accessed April 18, 2021. http://contentdm.mhsl.uab.edu/u?/etd,1144.

MLA Handbook (7th Edition):

Nyaku, Mawuli K. “Association between CC Chemokine ligand 3-Like-1 (CCL3L1) gene copy number and rheumatoid arthritis in African Americans.” 2012. Web. 18 Apr 2021.

Vancouver:

Nyaku MK. Association between CC Chemokine ligand 3-Like-1 (CCL3L1) gene copy number and rheumatoid arthritis in African Americans. [Internet] [Doctoral dissertation]. University of Alabama – Birmingham; 2012. [cited 2021 Apr 18]. Available from: http://contentdm.mhsl.uab.edu/u?/etd,1144.

Council of Science Editors:

Nyaku MK. Association between CC Chemokine ligand 3-Like-1 (CCL3L1) gene copy number and rheumatoid arthritis in African Americans. [Doctoral Dissertation]. University of Alabama – Birmingham; 2012. Available from: http://contentdm.mhsl.uab.edu/u?/etd,1144

21. Dickson, Marguerite Mulryan. Genetic and psychiatric treatment related risk factors for type 2 diabetes in schizophrenia and schizoaffective disorder patients.

Degree: PhD, 2008, University of Alabama – Birmingham

Type 2 diabetes (T2D) is a complex disease with genetic and environmental components. An increased prevalence of T2D in patients with schizophrenia (SCZ) has been… (more)

Subjects/Keywords: Antipsychotic Agents  – adverse effects<; br>; Diabetes Mellitus, Type 2  – chemically induced<; br>; Genetic Predisposition to Disease<; br>; Psychotic Disorders  – drug therapy<; br>; Risk Factors<; br>; Schizophrenia  – drug therapy<; br>; Weight Gain  – drug effects

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

APA (6th Edition):

Dickson, M. M. (2008). Genetic and psychiatric treatment related risk factors for type 2 diabetes in schizophrenia and schizoaffective disorder patients. (Doctoral Dissertation). University of Alabama – Birmingham. Retrieved from http://contentdm.mhsl.uab.edu/u?/etd,388

Chicago Manual of Style (16th Edition):

Dickson, Marguerite Mulryan. “Genetic and psychiatric treatment related risk factors for type 2 diabetes in schizophrenia and schizoaffective disorder patients.” 2008. Doctoral Dissertation, University of Alabama – Birmingham. Accessed April 18, 2021. http://contentdm.mhsl.uab.edu/u?/etd,388.

MLA Handbook (7th Edition):

Dickson, Marguerite Mulryan. “Genetic and psychiatric treatment related risk factors for type 2 diabetes in schizophrenia and schizoaffective disorder patients.” 2008. Web. 18 Apr 2021.

Vancouver:

Dickson MM. Genetic and psychiatric treatment related risk factors for type 2 diabetes in schizophrenia and schizoaffective disorder patients. [Internet] [Doctoral dissertation]. University of Alabama – Birmingham; 2008. [cited 2021 Apr 18]. Available from: http://contentdm.mhsl.uab.edu/u?/etd,388.

Council of Science Editors:

Dickson MM. Genetic and psychiatric treatment related risk factors for type 2 diabetes in schizophrenia and schizoaffective disorder patients. [Doctoral Dissertation]. University of Alabama – Birmingham; 2008. Available from: http://contentdm.mhsl.uab.edu/u?/etd,388

22. Wineinger, Nathan E. Statistical methods in the analysis of copy number variation data.

Degree: PhD, 2011, University of Alabama – Birmingham

Copy number variation is a significant form of genetic variation that has been shown to influence many traits. However, current methods used to estimate copy… (more)

Subjects/Keywords: African Americans  – genetics<; br>; DNA Copy Number Variations  – genetics<; br>; Genetic Predisposition to Disease<; br>; Hypertension  – pathology<; br>; Polymorphism, Single Nucleotide<; br>; Sequence Analysis, DNA

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

APA (6th Edition):

Wineinger, N. E. (2011). Statistical methods in the analysis of copy number variation data. (Doctoral Dissertation). University of Alabama – Birmingham. Retrieved from http://contentdm.mhsl.uab.edu/u?/etd,967

Chicago Manual of Style (16th Edition):

Wineinger, Nathan E. “Statistical methods in the analysis of copy number variation data.” 2011. Doctoral Dissertation, University of Alabama – Birmingham. Accessed April 18, 2021. http://contentdm.mhsl.uab.edu/u?/etd,967.

MLA Handbook (7th Edition):

Wineinger, Nathan E. “Statistical methods in the analysis of copy number variation data.” 2011. Web. 18 Apr 2021.

Vancouver:

Wineinger NE. Statistical methods in the analysis of copy number variation data. [Internet] [Doctoral dissertation]. University of Alabama – Birmingham; 2011. [cited 2021 Apr 18]. Available from: http://contentdm.mhsl.uab.edu/u?/etd,967.

Council of Science Editors:

Wineinger NE. Statistical methods in the analysis of copy number variation data. [Doctoral Dissertation]. University of Alabama – Birmingham; 2011. Available from: http://contentdm.mhsl.uab.edu/u?/etd,967

23. Farmer, Tyesha Latrece. Genome copy number of African-American and European-American early-onset breast cancer.

Degree: PhD, 2009, University of Alabama – Birmingham

Breast cancer is the second leading cause of cancer related death among women in the United States, surpassed only by lung cancer. It is estimated… (more)

Subjects/Keywords: African Americans  – genetics<; br>; Breast Neoplasms  – genetics<; br>; DNA Copy Number Variations  – genetics<; br>; European Continental Ancestry Group  – genetics<; br>; Genetic Predisposition to Disease<; br>; Genomics

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APA (6th Edition):

Farmer, T. L. (2009). Genome copy number of African-American and European-American early-onset breast cancer. (Doctoral Dissertation). University of Alabama – Birmingham. Retrieved from http://contentdm.mhsl.uab.edu/u?/etd,1001

Chicago Manual of Style (16th Edition):

Farmer, Tyesha Latrece. “Genome copy number of African-American and European-American early-onset breast cancer.” 2009. Doctoral Dissertation, University of Alabama – Birmingham. Accessed April 18, 2021. http://contentdm.mhsl.uab.edu/u?/etd,1001.

MLA Handbook (7th Edition):

Farmer, Tyesha Latrece. “Genome copy number of African-American and European-American early-onset breast cancer.” 2009. Web. 18 Apr 2021.

Vancouver:

Farmer TL. Genome copy number of African-American and European-American early-onset breast cancer. [Internet] [Doctoral dissertation]. University of Alabama – Birmingham; 2009. [cited 2021 Apr 18]. Available from: http://contentdm.mhsl.uab.edu/u?/etd,1001.

Council of Science Editors:

Farmer TL. Genome copy number of African-American and European-American early-onset breast cancer. [Doctoral Dissertation]. University of Alabama – Birmingham; 2009. Available from: http://contentdm.mhsl.uab.edu/u?/etd,1001


University of Oulu

24. Pylkäs, K. (Katri). ATM, ATR and Mre11 complex genes in hereditary susceptibility to breast cancer.

Degree: 2007, University of Oulu

 Abstract Mutations in BRCA1 and BRCA2 explain only about 20% of familial aggregation of breast cancer, suggesting involvement of additional susceptibility genes. In this study… (more)

Subjects/Keywords: ATM; ATR; DNA double-strand break response; MRE11; NBS1; RAD50; breast neoplasms; genetic predisposition to disease

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APA (6th Edition):

Pylkäs, K. (. (2007). ATM, ATR and Mre11 complex genes in hereditary susceptibility to breast cancer. (Doctoral Dissertation). University of Oulu. Retrieved from http://urn.fi/urn:isbn:9789514283833

Chicago Manual of Style (16th Edition):

Pylkäs, K (Katri). “ATM, ATR and Mre11 complex genes in hereditary susceptibility to breast cancer.” 2007. Doctoral Dissertation, University of Oulu. Accessed April 18, 2021. http://urn.fi/urn:isbn:9789514283833.

MLA Handbook (7th Edition):

Pylkäs, K (Katri). “ATM, ATR and Mre11 complex genes in hereditary susceptibility to breast cancer.” 2007. Web. 18 Apr 2021.

Vancouver:

Pylkäs K(. ATM, ATR and Mre11 complex genes in hereditary susceptibility to breast cancer. [Internet] [Doctoral dissertation]. University of Oulu; 2007. [cited 2021 Apr 18]. Available from: http://urn.fi/urn:isbn:9789514283833.

Council of Science Editors:

Pylkäs K(. ATM, ATR and Mre11 complex genes in hereditary susceptibility to breast cancer. [Doctoral Dissertation]. University of Oulu; 2007. Available from: http://urn.fi/urn:isbn:9789514283833

25. Busarčević Ivan. Značaj testa inhibicije hemaglutinacije pljuvačke i Lewis fenotipa u ispitivanju udruženosti sekretornog statusa i seronegativnih spondiloartropatija.

Degree: 2017, University of Novi Sad

  Uvod: Pojam "sekretor” ili „nesekretor" se odnosi na sposobnost pojedinca da luči antigene krvnih grupa ABO sistema u telesnim tečnostima. Određivanje ABO krvne grupe… (more)

Subjects/Keywords: spondiloartropatije; testovi inhibicije hemaglutinacije; Lewis sistem krvnih grupa; ABO sistem krvnih grupa; HLA-B27 antigen; pljuvačka; genetska predispozicija prema bolesti; biomarkeri; Spondylarthropathies; Hemagglutination Inhibition Tests; Lewis Blood Group System; ABO Blood Group-System; HLA-B27 Antigen; Saliva; Genetic Predisposition to Disease; Biomarkers

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APA (6th Edition):

Ivan, B. (2017). Značaj testa inhibicije hemaglutinacije pljuvačke i Lewis fenotipa u ispitivanju udruženosti sekretornog statusa i seronegativnih spondiloartropatija. (Thesis). University of Novi Sad. Retrieved from https://www.cris.uns.ac.rs/DownloadFileServlet/Disertacija147789930495195.pdf?controlNumber=(BISIS)102337&fileName=147789930495195.pdf&id=7007&source=OATD&language=en ; https://www.cris.uns.ac.rs/record.jsf?recordId=102337&source=OATD&language=en

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):

Ivan, Busarčević. “Značaj testa inhibicije hemaglutinacije pljuvačke i Lewis fenotipa u ispitivanju udruženosti sekretornog statusa i seronegativnih spondiloartropatija.” 2017. Thesis, University of Novi Sad. Accessed April 18, 2021. https://www.cris.uns.ac.rs/DownloadFileServlet/Disertacija147789930495195.pdf?controlNumber=(BISIS)102337&fileName=147789930495195.pdf&id=7007&source=OATD&language=en ; https://www.cris.uns.ac.rs/record.jsf?recordId=102337&source=OATD&language=en.

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

MLA Handbook (7th Edition):

Ivan, Busarčević. “Značaj testa inhibicije hemaglutinacije pljuvačke i Lewis fenotipa u ispitivanju udruženosti sekretornog statusa i seronegativnih spondiloartropatija.” 2017. Web. 18 Apr 2021.

Vancouver:

Ivan B. Značaj testa inhibicije hemaglutinacije pljuvačke i Lewis fenotipa u ispitivanju udruženosti sekretornog statusa i seronegativnih spondiloartropatija. [Internet] [Thesis]. University of Novi Sad; 2017. [cited 2021 Apr 18]. Available from: https://www.cris.uns.ac.rs/DownloadFileServlet/Disertacija147789930495195.pdf?controlNumber=(BISIS)102337&fileName=147789930495195.pdf&id=7007&source=OATD&language=en ; https://www.cris.uns.ac.rs/record.jsf?recordId=102337&source=OATD&language=en.

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

Council of Science Editors:

Ivan B. Značaj testa inhibicije hemaglutinacije pljuvačke i Lewis fenotipa u ispitivanju udruženosti sekretornog statusa i seronegativnih spondiloartropatija. [Thesis]. University of Novi Sad; 2017. Available from: https://www.cris.uns.ac.rs/DownloadFileServlet/Disertacija147789930495195.pdf?controlNumber=(BISIS)102337&fileName=147789930495195.pdf&id=7007&source=OATD&language=en ; https://www.cris.uns.ac.rs/record.jsf?recordId=102337&source=OATD&language=en

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

26. Mihaescu, Raluca. Genetic risk prediction for common diseases : methodology and applications.

Degree: 2013, Erasmus University Medical Center

 textabstractThis thesis describes methodological and empirical studies of genetic risk prediction of common diseases. The methodological studies involved the evaluation of traditional and new methods… (more)

Subjects/Keywords: genetic predisposition to disease; models (statistical); polymorphism; risk assessment; single nucleotide

…potential to predict risk of disease (51-55). The cumulative effect of multiple genetic… …genetic polymorphisms and conventional risk factors to predict coronary heart disease in… …methods and technologies are explored to detect stronger genetic risk variants. In the future… …applications include the identification of genetic profiles associated with increased risk to develop… …Prediction of disease 14 | Chapter 1 This thesis focuses on a broad application of genetic tests… 

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

APA (6th Edition):

Mihaescu, R. (2013). Genetic risk prediction for common diseases : methodology and applications. (Doctoral Dissertation). Erasmus University Medical Center. Retrieved from http://hdl.handle.net/1765/41430

Chicago Manual of Style (16th Edition):

Mihaescu, Raluca. “Genetic risk prediction for common diseases : methodology and applications.” 2013. Doctoral Dissertation, Erasmus University Medical Center. Accessed April 18, 2021. http://hdl.handle.net/1765/41430.

MLA Handbook (7th Edition):

Mihaescu, Raluca. “Genetic risk prediction for common diseases : methodology and applications.” 2013. Web. 18 Apr 2021.

Vancouver:

Mihaescu R. Genetic risk prediction for common diseases : methodology and applications. [Internet] [Doctoral dissertation]. Erasmus University Medical Center; 2013. [cited 2021 Apr 18]. Available from: http://hdl.handle.net/1765/41430.

Council of Science Editors:

Mihaescu R. Genetic risk prediction for common diseases : methodology and applications. [Doctoral Dissertation]. Erasmus University Medical Center; 2013. Available from: http://hdl.handle.net/1765/41430

27. Tiago Barreto de Castro e Silva. Percepção de risco para câncer e comportamentos preventivos em uma amostra de usuários de um ambulatório de aconselhamento genético oncológico.

Degree: 2010, University of São Paulo

O presente estudo investigou a percepção de risco para o desenvolvimento de neoplasias e os comportamentos preventivos em indivíduos com suspeita de síndromes neoplásicas hereditárias.… (more)

Subjects/Keywords: Enfermagem; Neoplasias; Predisposição genética para doença; Risco; Genetic Predisposition to Disease; Neoplasms; Nursing; Risk

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APA (6th Edition):

Silva, T. B. d. C. e. (2010). Percepção de risco para câncer e comportamentos preventivos em uma amostra de usuários de um ambulatório de aconselhamento genético oncológico. (Masters Thesis). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/22/22133/tde-04082010-152456/

Chicago Manual of Style (16th Edition):

Silva, Tiago Barreto de Castro e. “Percepção de risco para câncer e comportamentos preventivos em uma amostra de usuários de um ambulatório de aconselhamento genético oncológico.” 2010. Masters Thesis, University of São Paulo. Accessed April 18, 2021. http://www.teses.usp.br/teses/disponiveis/22/22133/tde-04082010-152456/.

MLA Handbook (7th Edition):

Silva, Tiago Barreto de Castro e. “Percepção de risco para câncer e comportamentos preventivos em uma amostra de usuários de um ambulatório de aconselhamento genético oncológico.” 2010. Web. 18 Apr 2021.

Vancouver:

Silva TBdCe. Percepção de risco para câncer e comportamentos preventivos em uma amostra de usuários de um ambulatório de aconselhamento genético oncológico. [Internet] [Masters thesis]. University of São Paulo; 2010. [cited 2021 Apr 18]. Available from: http://www.teses.usp.br/teses/disponiveis/22/22133/tde-04082010-152456/.

Council of Science Editors:

Silva TBdCe. Percepção de risco para câncer e comportamentos preventivos em uma amostra de usuários de um ambulatório de aconselhamento genético oncológico. [Masters Thesis]. University of São Paulo; 2010. Available from: http://www.teses.usp.br/teses/disponiveis/22/22133/tde-04082010-152456/

28. Ricardo Vessoni Perez. Os polimorfismos de um único nucleotídeo rs713041 no GPX4 e rs17883901 no GCLC modulam a susceptibilidade à retinopatia diabética em pacientes com diabetes mellitus tipo 1.

Degree: 2017, University of São Paulo

 INTRODUÇÃO: A retinopatia diabética (RD) é uma das complicações mais frequentes dos diabetes mellitus tipo 1 (DM1). Durante a hiperglicemia, as células endoteliais da retina… (more)

Subjects/Keywords: Antioxidantes; Complicações do diabetes; Diabetes mellitus tipo 1; Glutationa; Glutationa peroxidase/genética; Polimorfismo de nucleotídeo único; Retinopatia diabética; Suscetibilidade genética; Antioxidants; Diabetes complications; Diabetes mellitus type 1; Diabetic retinopathy; Genetic predisposition to disease; Glutathione; Glutathione peroxidase; Polymorphism single nucleotide

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APA (6th Edition):

Perez, R. V. (2017). Os polimorfismos de um único nucleotídeo rs713041 no GPX4 e rs17883901 no GCLC modulam a susceptibilidade à retinopatia diabética em pacientes com diabetes mellitus tipo 1. (Doctoral Dissertation). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/5/5135/tde-18122017-101252/

Chicago Manual of Style (16th Edition):

Perez, Ricardo Vessoni. “Os polimorfismos de um único nucleotídeo rs713041 no GPX4 e rs17883901 no GCLC modulam a susceptibilidade à retinopatia diabética em pacientes com diabetes mellitus tipo 1.” 2017. Doctoral Dissertation, University of São Paulo. Accessed April 18, 2021. http://www.teses.usp.br/teses/disponiveis/5/5135/tde-18122017-101252/.

MLA Handbook (7th Edition):

Perez, Ricardo Vessoni. “Os polimorfismos de um único nucleotídeo rs713041 no GPX4 e rs17883901 no GCLC modulam a susceptibilidade à retinopatia diabética em pacientes com diabetes mellitus tipo 1.” 2017. Web. 18 Apr 2021.

Vancouver:

Perez RV. Os polimorfismos de um único nucleotídeo rs713041 no GPX4 e rs17883901 no GCLC modulam a susceptibilidade à retinopatia diabética em pacientes com diabetes mellitus tipo 1. [Internet] [Doctoral dissertation]. University of São Paulo; 2017. [cited 2021 Apr 18]. Available from: http://www.teses.usp.br/teses/disponiveis/5/5135/tde-18122017-101252/.

Council of Science Editors:

Perez RV. Os polimorfismos de um único nucleotídeo rs713041 no GPX4 e rs17883901 no GCLC modulam a susceptibilidade à retinopatia diabética em pacientes com diabetes mellitus tipo 1. [Doctoral Dissertation]. University of São Paulo; 2017. Available from: http://www.teses.usp.br/teses/disponiveis/5/5135/tde-18122017-101252/

29. Camila Maciel de Oliveira. Herdabilidade dos fatores envolvidos na síndrome metabólica.

Degree: 2007, University of São Paulo

Muitos estudos têm sido conduzidos em diferentes populações visando a identificação da proporção da variância fenotípica total atribuída a efeitos genéticos. A herdabilidade de fatores… (more)

Subjects/Keywords: Hereditariedade; Predisposição genética para doença; Pressão arterial; Síndrome X metabólica; Blood pressure; Genetic predisposition to disease; Genetics; Metabolic syndrome X

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APA (6th Edition):

Oliveira, C. M. d. (2007). Herdabilidade dos fatores envolvidos na síndrome metabólica. (Doctoral Dissertation). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/5/5131/tde-16022009-162349/

Chicago Manual of Style (16th Edition):

Oliveira, Camila Maciel de. “Herdabilidade dos fatores envolvidos na síndrome metabólica.” 2007. Doctoral Dissertation, University of São Paulo. Accessed April 18, 2021. http://www.teses.usp.br/teses/disponiveis/5/5131/tde-16022009-162349/.

MLA Handbook (7th Edition):

Oliveira, Camila Maciel de. “Herdabilidade dos fatores envolvidos na síndrome metabólica.” 2007. Web. 18 Apr 2021.

Vancouver:

Oliveira CMd. Herdabilidade dos fatores envolvidos na síndrome metabólica. [Internet] [Doctoral dissertation]. University of São Paulo; 2007. [cited 2021 Apr 18]. Available from: http://www.teses.usp.br/teses/disponiveis/5/5131/tde-16022009-162349/.

Council of Science Editors:

Oliveira CMd. Herdabilidade dos fatores envolvidos na síndrome metabólica. [Doctoral Dissertation]. University of São Paulo; 2007. Available from: http://www.teses.usp.br/teses/disponiveis/5/5131/tde-16022009-162349/

30. Samantha Kuwada Teixeira. Identificação e análise estrutural e funcional de genes candidatos do cromossomo 4 de ratos SHR que possam influenciar a hipertensão essencial.

Degree: 2013, University of São Paulo

O emprego de \"Total Genome Scanëm modelos genéticos de doenças complexas tem sido fundamental para seleção de regiões cromossômicas envolvidas com traços complexos. Em nosso… (more)

Subjects/Keywords: Animais congênicos; Expressão gênica; Hipertensão/genética; Identificação de genes candidatos; Predisposição genética para doenças; Ratos endogâmicos SHR; Candidate genes identification; Congenic strains; Gene expression; Genetic predisposition to disease; Hypertension/genetics; Rats inbred SHR

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APA (6th Edition):

Teixeira, S. K. (2013). Identificação e análise estrutural e funcional de genes candidatos do cromossomo 4 de ratos SHR que possam influenciar a hipertensão essencial. (Masters Thesis). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/5/5166/tde-10052016-122534/

Chicago Manual of Style (16th Edition):

Teixeira, Samantha Kuwada. “Identificação e análise estrutural e funcional de genes candidatos do cromossomo 4 de ratos SHR que possam influenciar a hipertensão essencial.” 2013. Masters Thesis, University of São Paulo. Accessed April 18, 2021. http://www.teses.usp.br/teses/disponiveis/5/5166/tde-10052016-122534/.

MLA Handbook (7th Edition):

Teixeira, Samantha Kuwada. “Identificação e análise estrutural e funcional de genes candidatos do cromossomo 4 de ratos SHR que possam influenciar a hipertensão essencial.” 2013. Web. 18 Apr 2021.

Vancouver:

Teixeira SK. Identificação e análise estrutural e funcional de genes candidatos do cromossomo 4 de ratos SHR que possam influenciar a hipertensão essencial. [Internet] [Masters thesis]. University of São Paulo; 2013. [cited 2021 Apr 18]. Available from: http://www.teses.usp.br/teses/disponiveis/5/5166/tde-10052016-122534/.

Council of Science Editors:

Teixeira SK. Identificação e análise estrutural e funcional de genes candidatos do cromossomo 4 de ratos SHR que possam influenciar a hipertensão essencial. [Masters Thesis]. University of São Paulo; 2013. Available from: http://www.teses.usp.br/teses/disponiveis/5/5166/tde-10052016-122534/

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