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You searched for subject:(candidate gene study). Showing records 1 – 25 of 25 total matches.

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University of Edinburgh

1. Frenken, Hannah. Neuroticism, stress and psychological wellbeing: the role of CRHR1 and HSD11B1 in neuroticism, anxiety and depression.

Degree: 2012, University of Edinburgh

 Personality factors are increasingly being recognised as valuable predictors of psychopathology. Neuroticism has been a focus of epidemiologically-oriented personality research, and has been associated with… (more)

Subjects/Keywords: Neuroticism; HSD11B1; CRHR1; Candidate gene study

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APA (6th Edition):

Frenken, H. (2012). Neuroticism, stress and psychological wellbeing: the role of CRHR1 and HSD11B1 in neuroticism, anxiety and depression. (Thesis). University of Edinburgh. Retrieved from http://hdl.handle.net/1842/8456

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):

Frenken, Hannah. “Neuroticism, stress and psychological wellbeing: the role of CRHR1 and HSD11B1 in neuroticism, anxiety and depression.” 2012. Thesis, University of Edinburgh. Accessed April 16, 2021. http://hdl.handle.net/1842/8456.

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

MLA Handbook (7th Edition):

Frenken, Hannah. “Neuroticism, stress and psychological wellbeing: the role of CRHR1 and HSD11B1 in neuroticism, anxiety and depression.” 2012. Web. 16 Apr 2021.

Vancouver:

Frenken H. Neuroticism, stress and psychological wellbeing: the role of CRHR1 and HSD11B1 in neuroticism, anxiety and depression. [Internet] [Thesis]. University of Edinburgh; 2012. [cited 2021 Apr 16]. Available from: http://hdl.handle.net/1842/8456.

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

Council of Science Editors:

Frenken H. Neuroticism, stress and psychological wellbeing: the role of CRHR1 and HSD11B1 in neuroticism, anxiety and depression. [Thesis]. University of Edinburgh; 2012. Available from: http://hdl.handle.net/1842/8456

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


Vanderbilt University

2. Dumitrescu, Logan Caneel. Identificatiion and Characterization of Genetic Variants Associated with Lipid and Lipoprotein Levels.

Degree: PhD, Human Genetics, 2011, Vanderbilt University

 Low-density lipoprotein cholesterol (LDL-C), high-density lipoprotein cholesterol (HDL-C), and triglyceride (TG) levels are well known independent risk factors for cardiovascular disease. Other lipoproteins, such as… (more)

Subjects/Keywords: genetics; epidemiology; gwas; candidate gene study; lipids; lipoproteins; cardiovascular disease

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APA (6th Edition):

Dumitrescu, L. C. (2011). Identificatiion and Characterization of Genetic Variants Associated with Lipid and Lipoprotein Levels. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://hdl.handle.net/1803/11282

Chicago Manual of Style (16th Edition):

Dumitrescu, Logan Caneel. “Identificatiion and Characterization of Genetic Variants Associated with Lipid and Lipoprotein Levels.” 2011. Doctoral Dissertation, Vanderbilt University. Accessed April 16, 2021. http://hdl.handle.net/1803/11282.

MLA Handbook (7th Edition):

Dumitrescu, Logan Caneel. “Identificatiion and Characterization of Genetic Variants Associated with Lipid and Lipoprotein Levels.” 2011. Web. 16 Apr 2021.

Vancouver:

Dumitrescu LC. Identificatiion and Characterization of Genetic Variants Associated with Lipid and Lipoprotein Levels. [Internet] [Doctoral dissertation]. Vanderbilt University; 2011. [cited 2021 Apr 16]. Available from: http://hdl.handle.net/1803/11282.

Council of Science Editors:

Dumitrescu LC. Identificatiion and Characterization of Genetic Variants Associated with Lipid and Lipoprotein Levels. [Doctoral Dissertation]. Vanderbilt University; 2011. Available from: http://hdl.handle.net/1803/11282

3. He, Yuan. A Candidate Gene Study of the Association of TLR4 Polymorphisms rs4986790 and rs4986791 with HIV Disease Progression and Response to HAART Treatment in Men.

Degree: 2015, Johns Hopkins University

 Background. Host genetic factors have been shown to be associated with the diversity in the HIV/AIDS disease progression. In addition, lipopolysaccharides (LPSs) are recognized by… (more)

Subjects/Keywords: HIV; HAART; candidate gene study

…active transcription regions, which may lead to active gene expression8. HIV infection in the… …defect of 32-nucleotide deletion in beta-chemokine receptor 5 (CCR5) gene. CCR5 on… …study in HIV infected children showed that younger children have more rapid growth… …response to HAART. A 8 cross-sectional study showed that obesity and overweight was more common… …and rs4986790 in TLR4 RS4986791 (C1196T) is a non-synonymous SNP in TLR4 gene with… 

Page 1 Page 2 Page 3 Page 4 Page 5 Page 6 Page 7 Sample image

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APA (6th Edition):

He, Y. (2015). A Candidate Gene Study of the Association of TLR4 Polymorphisms rs4986790 and rs4986791 with HIV Disease Progression and Response to HAART Treatment in Men. (Thesis). Johns Hopkins University. Retrieved from http://jhir.library.jhu.edu/handle/1774.2/38048

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):

He, Yuan. “A Candidate Gene Study of the Association of TLR4 Polymorphisms rs4986790 and rs4986791 with HIV Disease Progression and Response to HAART Treatment in Men.” 2015. Thesis, Johns Hopkins University. Accessed April 16, 2021. http://jhir.library.jhu.edu/handle/1774.2/38048.

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

MLA Handbook (7th Edition):

He, Yuan. “A Candidate Gene Study of the Association of TLR4 Polymorphisms rs4986790 and rs4986791 with HIV Disease Progression and Response to HAART Treatment in Men.” 2015. Web. 16 Apr 2021.

Vancouver:

He Y. A Candidate Gene Study of the Association of TLR4 Polymorphisms rs4986790 and rs4986791 with HIV Disease Progression and Response to HAART Treatment in Men. [Internet] [Thesis]. Johns Hopkins University; 2015. [cited 2021 Apr 16]. Available from: http://jhir.library.jhu.edu/handle/1774.2/38048.

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

Council of Science Editors:

He Y. A Candidate Gene Study of the Association of TLR4 Polymorphisms rs4986790 and rs4986791 with HIV Disease Progression and Response to HAART Treatment in Men. [Thesis]. Johns Hopkins University; 2015. Available from: http://jhir.library.jhu.edu/handle/1774.2/38048

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


University of Illinois – Urbana-Champaign

4. Potts, Sarah. Identification of QTL and candidate genes for plant density tolerance in maize.

Degree: PhD, 0030, 2014, University of Illinois – Urbana-Champaign

 The global population is growing and up to three billion people will be added to the population within the next 35 years. Meanwhile, the amount… (more)

Subjects/Keywords: Candidate gene; Genome-wide association study (GWAS); Maize; Plant density tolerance; quantitative trait loci (QTL)

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APA (6th Edition):

Potts, S. (2014). Identification of QTL and candidate genes for plant density tolerance in maize. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/49814

Chicago Manual of Style (16th Edition):

Potts, Sarah. “Identification of QTL and candidate genes for plant density tolerance in maize.” 2014. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed April 16, 2021. http://hdl.handle.net/2142/49814.

MLA Handbook (7th Edition):

Potts, Sarah. “Identification of QTL and candidate genes for plant density tolerance in maize.” 2014. Web. 16 Apr 2021.

Vancouver:

Potts S. Identification of QTL and candidate genes for plant density tolerance in maize. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2014. [cited 2021 Apr 16]. Available from: http://hdl.handle.net/2142/49814.

Council of Science Editors:

Potts S. Identification of QTL and candidate genes for plant density tolerance in maize. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2014. Available from: http://hdl.handle.net/2142/49814


Texas A&M University

5. Kim, Seung Kyum. Genetic Regulation of Intrinsic Endothelial Function and Endothelial Responses to Exercise Training.

Degree: PhD, Kinesiology, 2015, Texas A&M University

 Endothelial dysfunction is a fundamental component of cardiovascular disease. Exercise training is known to prevent/improve endothelial dysfunction. However, the genetic basis for endothelial function is… (more)

Subjects/Keywords: Endothelial function; Genome-wide association study; Quantitative trait loci; Candidate genes; Exercise training; Training Intensity; Gene expression profiling; Pathway analysis

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APA (6th Edition):

Kim, S. K. (2015). Genetic Regulation of Intrinsic Endothelial Function and Endothelial Responses to Exercise Training. (Doctoral Dissertation). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/156421

Chicago Manual of Style (16th Edition):

Kim, Seung Kyum. “Genetic Regulation of Intrinsic Endothelial Function and Endothelial Responses to Exercise Training.” 2015. Doctoral Dissertation, Texas A&M University. Accessed April 16, 2021. http://hdl.handle.net/1969.1/156421.

MLA Handbook (7th Edition):

Kim, Seung Kyum. “Genetic Regulation of Intrinsic Endothelial Function and Endothelial Responses to Exercise Training.” 2015. Web. 16 Apr 2021.

Vancouver:

Kim SK. Genetic Regulation of Intrinsic Endothelial Function and Endothelial Responses to Exercise Training. [Internet] [Doctoral dissertation]. Texas A&M University; 2015. [cited 2021 Apr 16]. Available from: http://hdl.handle.net/1969.1/156421.

Council of Science Editors:

Kim SK. Genetic Regulation of Intrinsic Endothelial Function and Endothelial Responses to Exercise Training. [Doctoral Dissertation]. Texas A&M University; 2015. Available from: http://hdl.handle.net/1969.1/156421


University of Helsinki

6. Klemetti, Miira M. An RGS2 3'UTR Polymorphism is Associated with Preeclampsia in Overweight Women.

Degree: Medicinska fakulteten, 2016, University of Helsinki

 Background Preeclampsia is a common and heterogeneous vascular syndrome of pregnancy. Its genetic risk profile is yet unknown and may vary between individuals and populations.… (more)

Subjects/Keywords: preeclampsia; pregnancy; regulator of G-protein signaling 2; candidate gene study; Medical Genetics; Lääketieteellinen genetiikka ja perinnöllisyyslääketiede; Medicinsk genetik

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

APA (6th Edition):

Klemetti, M. M. (2016). An RGS2 3'UTR Polymorphism is Associated with Preeclampsia in Overweight Women. (Masters Thesis). University of Helsinki. Retrieved from http://hdl.handle.net/10138/169756

Chicago Manual of Style (16th Edition):

Klemetti, Miira M. “An RGS2 3'UTR Polymorphism is Associated with Preeclampsia in Overweight Women.” 2016. Masters Thesis, University of Helsinki. Accessed April 16, 2021. http://hdl.handle.net/10138/169756.

MLA Handbook (7th Edition):

Klemetti, Miira M. “An RGS2 3'UTR Polymorphism is Associated with Preeclampsia in Overweight Women.” 2016. Web. 16 Apr 2021.

Vancouver:

Klemetti MM. An RGS2 3'UTR Polymorphism is Associated with Preeclampsia in Overweight Women. [Internet] [Masters thesis]. University of Helsinki; 2016. [cited 2021 Apr 16]. Available from: http://hdl.handle.net/10138/169756.

Council of Science Editors:

Klemetti MM. An RGS2 3'UTR Polymorphism is Associated with Preeclampsia in Overweight Women. [Masters Thesis]. University of Helsinki; 2016. Available from: http://hdl.handle.net/10138/169756

7. S. DE MATTEIS. INTERACTION BETWEEN GENETIC AND OCCUPATIONAL FACTORS IN LUNG CANCER ETIOLOGY.A POPULATION-BASED CASE-CONTROL STUDY.

Degree: 2013, Università degli Studi di Milano

 Background: Exposure to occupational carcinogens is an important preventable cause of lung cancer. Single nucleotide polymorphisms (SNPs) have been reported in association with lung cancer… (more)

Subjects/Keywords: lung neoplasms; case-control study; carcinogens; occupational health; genetic polymorphisms; gene-environment interaction; candidate gene approach; Settore MED/44 - Medicina del Lavoro

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APA (6th Edition):

MATTEIS, S. D. (2013). INTERACTION BETWEEN GENETIC AND OCCUPATIONAL FACTORS IN LUNG CANCER ETIOLOGY.A POPULATION-BASED CASE-CONTROL STUDY. (Thesis). Università degli Studi di Milano. Retrieved from http://hdl.handle.net/2434/216405

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):

MATTEIS, S. DE. “INTERACTION BETWEEN GENETIC AND OCCUPATIONAL FACTORS IN LUNG CANCER ETIOLOGY.A POPULATION-BASED CASE-CONTROL STUDY.” 2013. Thesis, Università degli Studi di Milano. Accessed April 16, 2021. http://hdl.handle.net/2434/216405.

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

MLA Handbook (7th Edition):

MATTEIS, S. DE. “INTERACTION BETWEEN GENETIC AND OCCUPATIONAL FACTORS IN LUNG CANCER ETIOLOGY.A POPULATION-BASED CASE-CONTROL STUDY.” 2013. Web. 16 Apr 2021.

Vancouver:

MATTEIS SD. INTERACTION BETWEEN GENETIC AND OCCUPATIONAL FACTORS IN LUNG CANCER ETIOLOGY.A POPULATION-BASED CASE-CONTROL STUDY. [Internet] [Thesis]. Università degli Studi di Milano; 2013. [cited 2021 Apr 16]. Available from: http://hdl.handle.net/2434/216405.

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

Council of Science Editors:

MATTEIS SD. INTERACTION BETWEEN GENETIC AND OCCUPATIONAL FACTORS IN LUNG CANCER ETIOLOGY.A POPULATION-BASED CASE-CONTROL STUDY. [Thesis]. Università degli Studi di Milano; 2013. Available from: http://hdl.handle.net/2434/216405

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

8. LIANG XIAOHUI. Evaluation of the impact of polymorphisms on candidate genes of allergic rhinitis and asthma on disease outcomes in the Singapore population.

Degree: 2006, National University of Singapore

Subjects/Keywords: Atopic diseases; candidate gene; polymorphisms; association study; functional study; Singapore population

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APA (6th Edition):

XIAOHUI, L. (2006). Evaluation of the impact of polymorphisms on candidate genes of allergic rhinitis and asthma on disease outcomes in the Singapore population. (Thesis). National University of Singapore. Retrieved from http://scholarbank.nus.edu.sg/handle/10635/15676

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):

XIAOHUI, LIANG. “Evaluation of the impact of polymorphisms on candidate genes of allergic rhinitis and asthma on disease outcomes in the Singapore population.” 2006. Thesis, National University of Singapore. Accessed April 16, 2021. http://scholarbank.nus.edu.sg/handle/10635/15676.

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

MLA Handbook (7th Edition):

XIAOHUI, LIANG. “Evaluation of the impact of polymorphisms on candidate genes of allergic rhinitis and asthma on disease outcomes in the Singapore population.” 2006. Web. 16 Apr 2021.

Vancouver:

XIAOHUI L. Evaluation of the impact of polymorphisms on candidate genes of allergic rhinitis and asthma on disease outcomes in the Singapore population. [Internet] [Thesis]. National University of Singapore; 2006. [cited 2021 Apr 16]. Available from: http://scholarbank.nus.edu.sg/handle/10635/15676.

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

Council of Science Editors:

XIAOHUI L. Evaluation of the impact of polymorphisms on candidate genes of allergic rhinitis and asthma on disease outcomes in the Singapore population. [Thesis]. National University of Singapore; 2006. Available from: http://scholarbank.nus.edu.sg/handle/10635/15676

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


Tartu University

9. Lokk, Kaie. Comparative genome-wide DNA methylation studies of healthy human tissues and non-small cell lung cancer tissue .

Degree: 2016, Tartu University

 Metüleeritud tsütosiinil on suur roll imetajate organismi arengus. CpG dinukleotiidis asuvad tsütosiinid võivad olla kas metüleeritud või metüleerimata olekus. Kuna DNA metülatsioon on eluliselt vajalik… (more)

Subjects/Keywords: DNA metüülimine; geeniekspressioon; koed; vähk (med.); kopsuvähk; biomarkerid; kantserogenees; kasvaja markerid; võrdlevuuringud; geneetilised assotsiatsiooniuuringud; DNA methylation; gene expression; tissues; cancer (medicine); lung cancer; biochemical markers; cancerogenesis; tumor markers; comparative research; candidate gene association study

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APA (6th Edition):

Lokk, K. (2016). Comparative genome-wide DNA methylation studies of healthy human tissues and non-small cell lung cancer tissue . (Thesis). Tartu University. Retrieved from http://hdl.handle.net/10062/55064

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):

Lokk, Kaie. “Comparative genome-wide DNA methylation studies of healthy human tissues and non-small cell lung cancer tissue .” 2016. Thesis, Tartu University. Accessed April 16, 2021. http://hdl.handle.net/10062/55064.

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

MLA Handbook (7th Edition):

Lokk, Kaie. “Comparative genome-wide DNA methylation studies of healthy human tissues and non-small cell lung cancer tissue .” 2016. Web. 16 Apr 2021.

Vancouver:

Lokk K. Comparative genome-wide DNA methylation studies of healthy human tissues and non-small cell lung cancer tissue . [Internet] [Thesis]. Tartu University; 2016. [cited 2021 Apr 16]. Available from: http://hdl.handle.net/10062/55064.

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

Council of Science Editors:

Lokk K. Comparative genome-wide DNA methylation studies of healthy human tissues and non-small cell lung cancer tissue . [Thesis]. Tartu University; 2016. Available from: http://hdl.handle.net/10062/55064

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


Tampere University

10. Seppälä, Eija. Heterogeneity in Genetic Susceptibility to Prostate Cancer .

Degree: Lääketieteellisen teknologian instituutti - Institute of Medical Technology, 2006, Tampere University

 Eturauhassyöpä on geneettisesti hyvin heterogeeninen sairaus Eturauhassyöpä on nykyisin miesten yleisin syöpä. Se on myös toiseksi yleisin syöpäkuolemien syy keuhkosyövän jälkeen. Taudin syyt ja riskitekijät… (more)

Subjects/Keywords: eturauhassyöpä ; perinnöllisyys ; ehdokasgeeni ; genetiikka ; assosiaatiotutkimus ; prostate cancer ; candidate gene ; genetic susceptibility ; susceptibility gene ; association study

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APA (6th Edition):

Seppälä, E. (2006). Heterogeneity in Genetic Susceptibility to Prostate Cancer . (Doctoral Dissertation). Tampere University. Retrieved from https://trepo.tuni.fi/handle/10024/67661

Chicago Manual of Style (16th Edition):

Seppälä, Eija. “Heterogeneity in Genetic Susceptibility to Prostate Cancer .” 2006. Doctoral Dissertation, Tampere University. Accessed April 16, 2021. https://trepo.tuni.fi/handle/10024/67661.

MLA Handbook (7th Edition):

Seppälä, Eija. “Heterogeneity in Genetic Susceptibility to Prostate Cancer .” 2006. Web. 16 Apr 2021.

Vancouver:

Seppälä E. Heterogeneity in Genetic Susceptibility to Prostate Cancer . [Internet] [Doctoral dissertation]. Tampere University; 2006. [cited 2021 Apr 16]. Available from: https://trepo.tuni.fi/handle/10024/67661.

Council of Science Editors:

Seppälä E. Heterogeneity in Genetic Susceptibility to Prostate Cancer . [Doctoral Dissertation]. Tampere University; 2006. Available from: https://trepo.tuni.fi/handle/10024/67661


University of Oxford

11. Link, Emma. Genome-wide association of statin-induced myopathy.

Degree: PhD, 2009, University of Oxford

 Lowering LDL-cholesterol with statin therapy produces substantial reductions in cardiovascular events, and larger cholesterol reductions may produce larger benefits. Rarely, myopathy occurs with statins, especially… (more)

Subjects/Keywords: 616.042; Medical Sciences; Cardiovascular disease; Epidemiology; Genetics (medical sciences); statin; myopathy; rhabdomyolysis; genome-wide association study; candidate gene study

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APA (6th Edition):

Link, E. (2009). Genome-wide association of statin-induced myopathy. (Doctoral Dissertation). University of Oxford. Retrieved from http://ora.ox.ac.uk/objects/uuid:ca675486-d678-4200-8bb4-988a923e9c4c ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.504424

Chicago Manual of Style (16th Edition):

Link, Emma. “Genome-wide association of statin-induced myopathy.” 2009. Doctoral Dissertation, University of Oxford. Accessed April 16, 2021. http://ora.ox.ac.uk/objects/uuid:ca675486-d678-4200-8bb4-988a923e9c4c ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.504424.

MLA Handbook (7th Edition):

Link, Emma. “Genome-wide association of statin-induced myopathy.” 2009. Web. 16 Apr 2021.

Vancouver:

Link E. Genome-wide association of statin-induced myopathy. [Internet] [Doctoral dissertation]. University of Oxford; 2009. [cited 2021 Apr 16]. Available from: http://ora.ox.ac.uk/objects/uuid:ca675486-d678-4200-8bb4-988a923e9c4c ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.504424.

Council of Science Editors:

Link E. Genome-wide association of statin-induced myopathy. [Doctoral Dissertation]. University of Oxford; 2009. Available from: http://ora.ox.ac.uk/objects/uuid:ca675486-d678-4200-8bb4-988a923e9c4c ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.504424


Universiteit Utrecht

12. Bakker, Steven Cornelis. Unravelling the genetics of schizophrenia and ADHD.

Degree: 2005, Universiteit Utrecht

 The susceptibility to common psychiatric disorders is largely determined by genetic factors. Knowledge of these factors may give insight into the causes of these disorders,… (more)

Subjects/Keywords: Geneeskunde; schizophrenia; Attention-Deficit Hyperactivity Disorder; DNA pooling; SNP analysis; microsatellite; genetic association study; sib pair analysis; candidate gene

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APA (6th Edition):

Bakker, S. C. (2005). Unravelling the genetics of schizophrenia and ADHD. (Doctoral Dissertation). Universiteit Utrecht. Retrieved from http://dspace.library.uu.nl:8080/handle/1874/3189

Chicago Manual of Style (16th Edition):

Bakker, Steven Cornelis. “Unravelling the genetics of schizophrenia and ADHD.” 2005. Doctoral Dissertation, Universiteit Utrecht. Accessed April 16, 2021. http://dspace.library.uu.nl:8080/handle/1874/3189.

MLA Handbook (7th Edition):

Bakker, Steven Cornelis. “Unravelling the genetics of schizophrenia and ADHD.” 2005. Web. 16 Apr 2021.

Vancouver:

Bakker SC. Unravelling the genetics of schizophrenia and ADHD. [Internet] [Doctoral dissertation]. Universiteit Utrecht; 2005. [cited 2021 Apr 16]. Available from: http://dspace.library.uu.nl:8080/handle/1874/3189.

Council of Science Editors:

Bakker SC. Unravelling the genetics of schizophrenia and ADHD. [Doctoral Dissertation]. Universiteit Utrecht; 2005. Available from: http://dspace.library.uu.nl:8080/handle/1874/3189


University of Otago

13. Moir-Meyer, Gemma Louise. Endometrial Cancer and Copy Number Variation .

Degree: 2013, University of Otago

 Endometrial cancer is the most common gynaecological cancer in New Zealand and the incidence is increasing as the population ages. Genetic predictors of endometrial cancer… (more)

Subjects/Keywords: copy number variation; CNV; loading; CNV load; mismatch repair pathway; candidate gene; MSH2; MSH6; MUTYH; RPA3; TGFBR3; genome wide association study; GWAS; PennCNV; CNV frequency; rare CNVs; common CNVs; deletion; duplication; copy number gain; copy number loss; endometrial cancer

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APA (6th Edition):

Moir-Meyer, G. L. (2013). Endometrial Cancer and Copy Number Variation . (Masters Thesis). University of Otago. Retrieved from http://hdl.handle.net/10523/4170

Chicago Manual of Style (16th Edition):

Moir-Meyer, Gemma Louise. “Endometrial Cancer and Copy Number Variation .” 2013. Masters Thesis, University of Otago. Accessed April 16, 2021. http://hdl.handle.net/10523/4170.

MLA Handbook (7th Edition):

Moir-Meyer, Gemma Louise. “Endometrial Cancer and Copy Number Variation .” 2013. Web. 16 Apr 2021.

Vancouver:

Moir-Meyer GL. Endometrial Cancer and Copy Number Variation . [Internet] [Masters thesis]. University of Otago; 2013. [cited 2021 Apr 16]. Available from: http://hdl.handle.net/10523/4170.

Council of Science Editors:

Moir-Meyer GL. Endometrial Cancer and Copy Number Variation . [Masters Thesis]. University of Otago; 2013. Available from: http://hdl.handle.net/10523/4170


Rhodes University

14. Kimuda, Magambo Phillip. Computer aided approaches against Human African Trypanosomiasis.

Degree: Faculty of Science, Biochemistry and Microbiology, 2020, Rhodes University

 The thesis presented here is divided into two parts under a common theme that is the use of computer based tools, genomics, and in vitro… (more)

Subjects/Keywords: African trypanosomiasis; African trypanosomiasis  – Chemotherapy; Genomics; Macrophage migration inhibitory factor; Trypanosoma brucei; Pteridines; Tetrahydrofolate dehydrogenase; Adenylic acid; Molecular dynamics; Principal components analysis; Bioinformatics; Single nucleotide polymorphisms; Single Nucleotide Variants; Candidate Gene Association Study (CGAS)

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

APA (6th Edition):

Kimuda, M. P. (2020). Computer aided approaches against Human African Trypanosomiasis. (Thesis). Rhodes University. Retrieved from http://hdl.handle.net/10962/142542

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):

Kimuda, Magambo Phillip. “Computer aided approaches against Human African Trypanosomiasis.” 2020. Thesis, Rhodes University. Accessed April 16, 2021. http://hdl.handle.net/10962/142542.

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

MLA Handbook (7th Edition):

Kimuda, Magambo Phillip. “Computer aided approaches against Human African Trypanosomiasis.” 2020. Web. 16 Apr 2021.

Vancouver:

Kimuda MP. Computer aided approaches against Human African Trypanosomiasis. [Internet] [Thesis]. Rhodes University; 2020. [cited 2021 Apr 16]. Available from: http://hdl.handle.net/10962/142542.

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

Council of Science Editors:

Kimuda MP. Computer aided approaches against Human African Trypanosomiasis. [Thesis]. Rhodes University; 2020. Available from: http://hdl.handle.net/10962/142542

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

15. Bakker, Steven Cornelis. Unravelling the genetics of schizophrenia and ADHD.

Degree: 2005, University Utrecht

 The susceptibility to common psychiatric disorders is largely determined by genetic factors. Knowledge of these factors may give insight into the causes of these disorders,… (more)

Subjects/Keywords: schizophrenia; Attention-Deficit Hyperactivity Disorder; DNA pooling; SNP analysis; microsatellite; genetic association study; sib pair analysis; candidate gene

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APA (6th Edition):

Bakker, S. C. (2005). Unravelling the genetics of schizophrenia and ADHD. (Doctoral Dissertation). University Utrecht. Retrieved from https://dspace.library.uu.nl/handle/1874/3189 ; URN:NBN:NL:UI:10-1874-3189 ; urn:isbn:90-393-3952-X ; URN:NBN:NL:UI:10-1874-3189 ; https://dspace.library.uu.nl/handle/1874/3189

Chicago Manual of Style (16th Edition):

Bakker, Steven Cornelis. “Unravelling the genetics of schizophrenia and ADHD.” 2005. Doctoral Dissertation, University Utrecht. Accessed April 16, 2021. https://dspace.library.uu.nl/handle/1874/3189 ; URN:NBN:NL:UI:10-1874-3189 ; urn:isbn:90-393-3952-X ; URN:NBN:NL:UI:10-1874-3189 ; https://dspace.library.uu.nl/handle/1874/3189.

MLA Handbook (7th Edition):

Bakker, Steven Cornelis. “Unravelling the genetics of schizophrenia and ADHD.” 2005. Web. 16 Apr 2021.

Vancouver:

Bakker SC. Unravelling the genetics of schizophrenia and ADHD. [Internet] [Doctoral dissertation]. University Utrecht; 2005. [cited 2021 Apr 16]. Available from: https://dspace.library.uu.nl/handle/1874/3189 ; URN:NBN:NL:UI:10-1874-3189 ; urn:isbn:90-393-3952-X ; URN:NBN:NL:UI:10-1874-3189 ; https://dspace.library.uu.nl/handle/1874/3189.

Council of Science Editors:

Bakker SC. Unravelling the genetics of schizophrenia and ADHD. [Doctoral Dissertation]. University Utrecht; 2005. Available from: https://dspace.library.uu.nl/handle/1874/3189 ; URN:NBN:NL:UI:10-1874-3189 ; urn:isbn:90-393-3952-X ; URN:NBN:NL:UI:10-1874-3189 ; https://dspace.library.uu.nl/handle/1874/3189


University of Cincinnati

16. SMELSER, DIANE T. A COMPARISON OF OBESITY CANDIDATE GENES IN THE ANABOLIC NEUROPEPTIDE PATHWAY IN THE SAMOAN AND AMERICAN SAMOAN POPULATIONS.

Degree: PhD, Medicine : Epidemiology (Environmental Health), 2006, University of Cincinnati

 Obesity is a significant public health problem with substantial morbidity and mortality costs, increasing at an alarming rate. The literature suggests that obesity is a… (more)

Subjects/Keywords: Health Sciences, Public Health; Obesity; Samoan Population; Anabolic Neuropeptide Pathway; Candidate Gene Association Study; Neuropeptide Y

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APA (6th Edition):

SMELSER, D. T. (2006). A COMPARISON OF OBESITY CANDIDATE GENES IN THE ANABOLIC NEUROPEPTIDE PATHWAY IN THE SAMOAN AND AMERICAN SAMOAN POPULATIONS. (Doctoral Dissertation). University of Cincinnati. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=ucin1163647875

Chicago Manual of Style (16th Edition):

SMELSER, DIANE T. “A COMPARISON OF OBESITY CANDIDATE GENES IN THE ANABOLIC NEUROPEPTIDE PATHWAY IN THE SAMOAN AND AMERICAN SAMOAN POPULATIONS.” 2006. Doctoral Dissertation, University of Cincinnati. Accessed April 16, 2021. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1163647875.

MLA Handbook (7th Edition):

SMELSER, DIANE T. “A COMPARISON OF OBESITY CANDIDATE GENES IN THE ANABOLIC NEUROPEPTIDE PATHWAY IN THE SAMOAN AND AMERICAN SAMOAN POPULATIONS.” 2006. Web. 16 Apr 2021.

Vancouver:

SMELSER DT. A COMPARISON OF OBESITY CANDIDATE GENES IN THE ANABOLIC NEUROPEPTIDE PATHWAY IN THE SAMOAN AND AMERICAN SAMOAN POPULATIONS. [Internet] [Doctoral dissertation]. University of Cincinnati; 2006. [cited 2021 Apr 16]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ucin1163647875.

Council of Science Editors:

SMELSER DT. A COMPARISON OF OBESITY CANDIDATE GENES IN THE ANABOLIC NEUROPEPTIDE PATHWAY IN THE SAMOAN AND AMERICAN SAMOAN POPULATIONS. [Doctoral Dissertation]. University of Cincinnati; 2006. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ucin1163647875

17. Zeng, Rong. Molecular genetic studies in canine inherited diseases including neonatal cerebellar ataxia, degenerative myelopathy and multiple system degeneration.

Degree: 2013, University of Missouri – Columbia

 [ACCESS RESTRICTED TO THE UNIVERSITY OF MISSOURI AT AUTHOR'S REQUEST.] The inherited diseases of the domestic dog mimic a wide spectrum of common human disorders.… (more)

Subjects/Keywords: whole genome sequencing; genome association study; candidate gene analysis; inherited diseases; canine diseases

Page 1

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

APA (6th Edition):

Zeng, R. (2013). Molecular genetic studies in canine inherited diseases including neonatal cerebellar ataxia, degenerative myelopathy and multiple system degeneration. (Thesis). University of Missouri – Columbia. Retrieved from http://hdl.handle.net/10355/37874

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):

Zeng, Rong. “Molecular genetic studies in canine inherited diseases including neonatal cerebellar ataxia, degenerative myelopathy and multiple system degeneration.” 2013. Thesis, University of Missouri – Columbia. Accessed April 16, 2021. http://hdl.handle.net/10355/37874.

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

MLA Handbook (7th Edition):

Zeng, Rong. “Molecular genetic studies in canine inherited diseases including neonatal cerebellar ataxia, degenerative myelopathy and multiple system degeneration.” 2013. Web. 16 Apr 2021.

Vancouver:

Zeng R. Molecular genetic studies in canine inherited diseases including neonatal cerebellar ataxia, degenerative myelopathy and multiple system degeneration. [Internet] [Thesis]. University of Missouri – Columbia; 2013. [cited 2021 Apr 16]. Available from: http://hdl.handle.net/10355/37874.

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

Council of Science Editors:

Zeng R. Molecular genetic studies in canine inherited diseases including neonatal cerebellar ataxia, degenerative myelopathy and multiple system degeneration. [Thesis]. University of Missouri – Columbia; 2013. Available from: http://hdl.handle.net/10355/37874

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

18. Bakker, Steven Cornelis. Unravelling the genetics of schizophrenia and ADHD.

Degree: 2005, University Utrecht

 The susceptibility to common psychiatric disorders is largely determined by genetic factors. Knowledge of these factors may give insight into the causes of these disorders,… (more)

Subjects/Keywords: schizophrenia; Attention-Deficit Hyperactivity Disorder; DNA pooling; SNP analysis; microsatellite; genetic association study; sib pair analysis; candidate gene

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

APA (6th Edition):

Bakker, S. C. (2005). Unravelling the genetics of schizophrenia and ADHD. (Doctoral Dissertation). University Utrecht. Retrieved from https://dspace.library.uu.nl/handle/1874/3189 ; URN:NBN:NL:UI:10-1874-3189 ; 1874/3189 ; urn:isbn:903933952X ; URN:NBN:NL:UI:10-1874-3189 ; https://dspace.library.uu.nl/handle/1874/3189

Chicago Manual of Style (16th Edition):

Bakker, Steven Cornelis. “Unravelling the genetics of schizophrenia and ADHD.” 2005. Doctoral Dissertation, University Utrecht. Accessed April 16, 2021. https://dspace.library.uu.nl/handle/1874/3189 ; URN:NBN:NL:UI:10-1874-3189 ; 1874/3189 ; urn:isbn:903933952X ; URN:NBN:NL:UI:10-1874-3189 ; https://dspace.library.uu.nl/handle/1874/3189.

MLA Handbook (7th Edition):

Bakker, Steven Cornelis. “Unravelling the genetics of schizophrenia and ADHD.” 2005. Web. 16 Apr 2021.

Vancouver:

Bakker SC. Unravelling the genetics of schizophrenia and ADHD. [Internet] [Doctoral dissertation]. University Utrecht; 2005. [cited 2021 Apr 16]. Available from: https://dspace.library.uu.nl/handle/1874/3189 ; URN:NBN:NL:UI:10-1874-3189 ; 1874/3189 ; urn:isbn:903933952X ; URN:NBN:NL:UI:10-1874-3189 ; https://dspace.library.uu.nl/handle/1874/3189.

Council of Science Editors:

Bakker SC. Unravelling the genetics of schizophrenia and ADHD. [Doctoral Dissertation]. University Utrecht; 2005. Available from: https://dspace.library.uu.nl/handle/1874/3189 ; URN:NBN:NL:UI:10-1874-3189 ; 1874/3189 ; urn:isbn:903933952X ; URN:NBN:NL:UI:10-1874-3189 ; https://dspace.library.uu.nl/handle/1874/3189


University of Oulu

19. Mahlman, M. (Mari). Genetic background and antenatal risk factors of bronchopulmonary dysplasia.

Degree: 2018, University of Oulu

Abstract Advances over the past few decades in ante- and neonatal care have led to the survival of a growing number of premature infants of… (more)

Subjects/Keywords: C-reactive protein; Kit ligand; bronchopulmonary dysplasia; candidate gene study; genetic association study; genetic polymorphism; genome-wide association study; premature birth; premature infant; pulmonary inflammation; twins; vascular endothelial growth factor; vascular endothelial growth factor receptor 2; C-reaktiivinen proteiini; Kit ligandi; bronkopulmonaalinen dysplasia; ehdokasgeenitutkimus; ennenaikainen syntymä; geenipolymorfismi; geneettinen assosiaatiotutkimus; kaksoset; keskosen krooninen keuhkosairaus; keskosuus; keuhkojen tulehdusreaktio; koko genomin assosiaatiotutkimus; verisuonten endoteelikasvutekijä

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APA (6th Edition):

Mahlman, M. (. (2018). Genetic background and antenatal risk factors of bronchopulmonary dysplasia. (Doctoral Dissertation). University of Oulu. Retrieved from http://urn.fi/urn:isbn:9789526219530

Chicago Manual of Style (16th Edition):

Mahlman, M (Mari). “Genetic background and antenatal risk factors of bronchopulmonary dysplasia.” 2018. Doctoral Dissertation, University of Oulu. Accessed April 16, 2021. http://urn.fi/urn:isbn:9789526219530.

MLA Handbook (7th Edition):

Mahlman, M (Mari). “Genetic background and antenatal risk factors of bronchopulmonary dysplasia.” 2018. Web. 16 Apr 2021.

Vancouver:

Mahlman M(. Genetic background and antenatal risk factors of bronchopulmonary dysplasia. [Internet] [Doctoral dissertation]. University of Oulu; 2018. [cited 2021 Apr 16]. Available from: http://urn.fi/urn:isbn:9789526219530.

Council of Science Editors:

Mahlman M(. Genetic background and antenatal risk factors of bronchopulmonary dysplasia. [Doctoral Dissertation]. University of Oulu; 2018. Available from: http://urn.fi/urn:isbn:9789526219530

20. 荒木, 千鶴. The evidence of genetic polymorphisms of genes involved in the P2RX7 signaling pathway as predictive biomarkers for response and loss of response to infliximab against Crohn's disease : P2RX7のシグナル伝達経路にある遺伝子の遺伝子多型はクローン病の治療薬インフリキシマブの応答性と不応答性を予測するバイオマーカーである.

Degree: 博士(薬学), 2017, Nagasaki University / 長崎大学

 Infliximab (IFX) is a chimeric anti-tumor necrosis factor-α monoclonal antibody exerting the therapeutic effect for Crohn’s disease (CD). To identify certain genes related to the… (more)

Subjects/Keywords: P2RX7 signaling pathway; single nucleotide polymorphism; infliximab; drug-responsibility gene; Crohn's disease; candidate gene-based association study; DNA-based biomarker

Gene C/C 54 (55.7) 13 (68.4) C/A 38 (39.2) 5 (26.3… …x29; Inheritance model* P value OR 95% CI Allele 0.096 2.904 0.836-10.08 Gene Tag… …gene-gene interaction in response to IFX after 1 year of treatment Likewise, in order to… …sensitivity, specificity, and positive predictive value (Table 9). Discussion This study… …Gene-gene interaction among P2RX7, CARD8, and CASP1 genotypes for response to IFX after 1… 

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APA (6th Edition):

荒木, . (2017). The evidence of genetic polymorphisms of genes involved in the P2RX7 signaling pathway as predictive biomarkers for response and loss of response to infliximab against Crohn's disease : P2RX7のシグナル伝達経路にある遺伝子の遺伝子多型はクローン病の治療薬インフリキシマブの応答性と不応答性を予測するバイオマーカーである. (Thesis). Nagasaki University / 長崎大学. Retrieved from http://hdl.handle.net/10069/37158

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):

荒木, 千鶴. “The evidence of genetic polymorphisms of genes involved in the P2RX7 signaling pathway as predictive biomarkers for response and loss of response to infliximab against Crohn's disease : P2RX7のシグナル伝達経路にある遺伝子の遺伝子多型はクローン病の治療薬インフリキシマブの応答性と不応答性を予測するバイオマーカーである.” 2017. Thesis, Nagasaki University / 長崎大学. Accessed April 16, 2021. http://hdl.handle.net/10069/37158.

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

MLA Handbook (7th Edition):

荒木, 千鶴. “The evidence of genetic polymorphisms of genes involved in the P2RX7 signaling pathway as predictive biomarkers for response and loss of response to infliximab against Crohn's disease : P2RX7のシグナル伝達経路にある遺伝子の遺伝子多型はクローン病の治療薬インフリキシマブの応答性と不応答性を予測するバイオマーカーである.” 2017. Web. 16 Apr 2021.

Vancouver:

荒木 . The evidence of genetic polymorphisms of genes involved in the P2RX7 signaling pathway as predictive biomarkers for response and loss of response to infliximab against Crohn's disease : P2RX7のシグナル伝達経路にある遺伝子の遺伝子多型はクローン病の治療薬インフリキシマブの応答性と不応答性を予測するバイオマーカーである. [Internet] [Thesis]. Nagasaki University / 長崎大学; 2017. [cited 2021 Apr 16]. Available from: http://hdl.handle.net/10069/37158.

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

Council of Science Editors:

荒木 . The evidence of genetic polymorphisms of genes involved in the P2RX7 signaling pathway as predictive biomarkers for response and loss of response to infliximab against Crohn's disease : P2RX7のシグナル伝達経路にある遺伝子の遺伝子多型はクローン病の治療薬インフリキシマブの応答性と不応答性を予測するバイオマーカーである. [Thesis]. Nagasaki University / 長崎大学; 2017. Available from: http://hdl.handle.net/10069/37158

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

21. 고, 은희. Identification of novel genes involved in precocious puberty by integrated genomic analyses.

Degree: 2019, Ajou University

Precocious puberty is a multifactorial disease that occurs in one out of 5,000-10,000 children with the appearance of secondary sexual characteristics before 8 years in… (more)

Subjects/Keywords: precocious puberty; genetic biomarker; early diagnosis; whole-genome RNA sequencing; gene expression; next-generation sequencing (NGS); candidate gene-based association study; single nucleotide polymorphism (SNP); hypothalamus; gonadotrophin-releasing hormone (GnRH); 성조숙증; 유전자 바이오마커; 조기진단; 전장유전체 RNA 시퀀싱; 차세대염기서열분석(NGS); 유전자발현; 후보유전자 연관성분석; 단일염기다형성(SNP); 시상하부; 생식샘자극호르몬 방출호르몬 (GnRH)

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APA (6th Edition):

고, . (2019). Identification of novel genes involved in precocious puberty by integrated genomic analyses. (Thesis). Ajou University. Retrieved from http://repository.ajou.ac.kr/handle/201003/17897 ; http://dcoll.ajou.ac.kr:9080/dcollection/jsp/common/DcLoOrgPer.jsp?sItemId=000000028361

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):

고, 은희. “Identification of novel genes involved in precocious puberty by integrated genomic analyses.” 2019. Thesis, Ajou University. Accessed April 16, 2021. http://repository.ajou.ac.kr/handle/201003/17897 ; http://dcoll.ajou.ac.kr:9080/dcollection/jsp/common/DcLoOrgPer.jsp?sItemId=000000028361.

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

MLA Handbook (7th Edition):

고, 은희. “Identification of novel genes involved in precocious puberty by integrated genomic analyses.” 2019. Web. 16 Apr 2021.

Vancouver:

고 . Identification of novel genes involved in precocious puberty by integrated genomic analyses. [Internet] [Thesis]. Ajou University; 2019. [cited 2021 Apr 16]. Available from: http://repository.ajou.ac.kr/handle/201003/17897 ; http://dcoll.ajou.ac.kr:9080/dcollection/jsp/common/DcLoOrgPer.jsp?sItemId=000000028361.

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

Council of Science Editors:

고 . Identification of novel genes involved in precocious puberty by integrated genomic analyses. [Thesis]. Ajou University; 2019. Available from: http://repository.ajou.ac.kr/handle/201003/17897 ; http://dcoll.ajou.ac.kr:9080/dcollection/jsp/common/DcLoOrgPer.jsp?sItemId=000000028361

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

22. Loos, Matthijs. Molecular Genetics and Hormones: New Frontiers in Entrepreneurship Research.

Degree: 2013, Erasmus Research Institute of Management

 textabstractRecent studies suggest that entrepreneurship is partly heritable, but are unable to pinpoint the specific genes involved. This thesis presents results from novel research aiming… (more)

Subjects/Keywords: candidate gene study; entrepreneurship; gcta; genetics; genome-wide association study; heritability; microeconomics; molecular genetic architecture; prediction; self-employment; testosterone; twin study

candidate gene study suggests that a genetic variant in the DRD3 gene is associated with… …entrepreneur, in a group of 1,335 British subjects. In this candidate gene study, polymorphisms in a… …candidate gene study and our replication study, not all 18 reported SNPs were readily available in… …the Rotterdam Study cohorts. Therefore, we im- 15 16 CANDIDATE GENE STUDIES puted these… …candidate gene study. Although we cannot reject the hypothesis that the DRD3 gene is associated… 

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APA (6th Edition):

Loos, M. (2013). Molecular Genetics and Hormones: New Frontiers in Entrepreneurship Research. (Doctoral Dissertation). Erasmus Research Institute of Management. Retrieved from http://hdl.handle.net/1765/40081

Chicago Manual of Style (16th Edition):

Loos, Matthijs. “Molecular Genetics and Hormones: New Frontiers in Entrepreneurship Research.” 2013. Doctoral Dissertation, Erasmus Research Institute of Management. Accessed April 16, 2021. http://hdl.handle.net/1765/40081.

MLA Handbook (7th Edition):

Loos, Matthijs. “Molecular Genetics and Hormones: New Frontiers in Entrepreneurship Research.” 2013. Web. 16 Apr 2021.

Vancouver:

Loos M. Molecular Genetics and Hormones: New Frontiers in Entrepreneurship Research. [Internet] [Doctoral dissertation]. Erasmus Research Institute of Management; 2013. [cited 2021 Apr 16]. Available from: http://hdl.handle.net/1765/40081.

Council of Science Editors:

Loos M. Molecular Genetics and Hormones: New Frontiers in Entrepreneurship Research. [Doctoral Dissertation]. Erasmus Research Institute of Management; 2013. Available from: http://hdl.handle.net/1765/40081


University of Oxford

23. Karaderi, Tugce. Genetics of ankylosing spondylitis.

Degree: PhD, 2012, University of Oxford

 Ankylosing spondylitis (AS) is a common inflammatory arthritis of the spine and other affected joints, which is highly heritable, being strongly influenced by the HLA-B27… (more)

Subjects/Keywords: 616.73; Bioinformatics (life sciences); Biology; Genetics (life sciences); Biology and other natural sciences (mathematics); Medical Sciences; Clinical genetics; Biology (medical sciences); Epidemiology; Genetics (medical sciences); Immunology; Orthopaedics; Rheumotology; Multiple Sclerosis; Molecular genetics; Computationally-intensive statistics; Mathematical genetics and bioinformatics (statistics); ankylosing spondylitis; genetics; imputation; candidate gene study; Genomewide Association study; interleukin 23 receptor; tumour necrosis factor receptor 1; immunology; TH-17 pathway; endoplasmic reticulumn associated protease 1; endoplasmic reticulumn associated protease 2; imputation accuracy; 1000 Genomes Project; low frequency variants; rare variants; variant discovery; sequencing; polyphred; polymerase chain reaction; logistic regression; case control study; stratified analysis; meta-analysis; inflammatory bowel disease; Crohn's disease; ulcerative colitis; HapMap Project; Mach2Dat; rheumatology; inflammation; spine; uveitis; iritis; psoriasis; anti-TNF; CCRaVAT; C-Alpha; statistical power; Genetic Association Study

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APA (6th Edition):

Karaderi, T. (2012). Genetics of ankylosing spondylitis. (Doctoral Dissertation). University of Oxford. Retrieved from http://ora.ox.ac.uk/objects/uuid:8c0e848a-e712-4603-b923-a96a2f1644ac ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.422700

Chicago Manual of Style (16th Edition):

Karaderi, Tugce. “Genetics of ankylosing spondylitis.” 2012. Doctoral Dissertation, University of Oxford. Accessed April 16, 2021. http://ora.ox.ac.uk/objects/uuid:8c0e848a-e712-4603-b923-a96a2f1644ac ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.422700.

MLA Handbook (7th Edition):

Karaderi, Tugce. “Genetics of ankylosing spondylitis.” 2012. Web. 16 Apr 2021.

Vancouver:

Karaderi T. Genetics of ankylosing spondylitis. [Internet] [Doctoral dissertation]. University of Oxford; 2012. [cited 2021 Apr 16]. Available from: http://ora.ox.ac.uk/objects/uuid:8c0e848a-e712-4603-b923-a96a2f1644ac ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.422700.

Council of Science Editors:

Karaderi T. Genetics of ankylosing spondylitis. [Doctoral Dissertation]. University of Oxford; 2012. Available from: http://ora.ox.ac.uk/objects/uuid:8c0e848a-e712-4603-b923-a96a2f1644ac ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.422700


Université de Montréal

24. Krupoves, Alfreda. Investigating the role of potential genetic markers that can predict risk for steroid refractory inflammatory bowel disease.

Degree: 2011, Université de Montréal

Subjects/Keywords: Épidémiologie génétique; Genetic epidemiology; Étude d’association génétique; Genetic association study; Gène candidat; Gene candidate; Maladie inflammatoire de l’intestin; Inflammatory bowel disease; Maladie de Crohn; Crohn’s disease; Réponse aux médicaments; Drug response; Variations interindividuelles; Inter-individual variations; ABCB1; ABCB1; NR3C1; NR3C1; Polymorphismes d’un nucléotide simple (SNPs); Single nucleotide polymorphisms (SNPs); Health Sciences - Epidemiology / Sciences de la santé - Épidémiologie (UMI : 0766)

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

APA (6th Edition):

Krupoves, A. (2011). Investigating the role of potential genetic markers that can predict risk for steroid refractory inflammatory bowel disease. (Thesis). Université de Montréal. Retrieved from http://hdl.handle.net/1866/5427

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):

Krupoves, Alfreda. “Investigating the role of potential genetic markers that can predict risk for steroid refractory inflammatory bowel disease.” 2011. Thesis, Université de Montréal. Accessed April 16, 2021. http://hdl.handle.net/1866/5427.

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

MLA Handbook (7th Edition):

Krupoves, Alfreda. “Investigating the role of potential genetic markers that can predict risk for steroid refractory inflammatory bowel disease.” 2011. Web. 16 Apr 2021.

Vancouver:

Krupoves A. Investigating the role of potential genetic markers that can predict risk for steroid refractory inflammatory bowel disease. [Internet] [Thesis]. Université de Montréal; 2011. [cited 2021 Apr 16]. Available from: http://hdl.handle.net/1866/5427.

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

Council of Science Editors:

Krupoves A. Investigating the role of potential genetic markers that can predict risk for steroid refractory inflammatory bowel disease. [Thesis]. Université de Montréal; 2011. Available from: http://hdl.handle.net/1866/5427

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


University of Aberdeen

25. Mierzwińska, Monika Ewa.; University of Aberdeen.Dept. of Plant and Soil Science. Natural variation in root morphology and adaptation to soil conditions in Arabidopsis thaliana.

Degree: Dept. of Plant and Soil Science., 2016, University of Aberdeen

Subjects/Keywords: Intraspecific variation within the genetic model plant Arabidopsis thaliana has been used to research numerous potentially adaptive and economically important traits. In this thesis I used this tool to investigate root morphology and adaptation of plants to edaphic conditions. Firstly I tested local adaptation of chosen A. thaliana wild genotypes collected from north eastern Scotland, to two soil types with contrasting textures. When local adaptation is defined as fitness advantage (reproductive output) in local soil, I did not find clear signs of local adaptation. Additionally, I observed significant phenotypic variation between collected accessions for both mineral nutrient uptake and growth in the two soil types. Together these results may suggest the mixing of adapted genotypes due to extensive human disturbance in north eastern Scotland. Secondly I focused on two linked aspects of root biology: endodermal development and root system architecture. The characteristic features of the endodermis include Casparian strips (CS) that form a barrier to apoplastic transport. Some mutants with an altered CS are sensitive to growth on media with elevated magnesium (Mg) and reduced calcium (Ca). In order to potentially identify novel alleles of genes involved in CS biosynthesis I took advantage of this growth phenotype and performed genome wide association (GWA) analysis on response of plants to low Ca/Mg ratio of the growth medium. As a result I compiled a list of genes for the future research by choosing candidate genes identified in the GWA study for both plant weight and elemental composition. This list was further refined using knowledge on gene expression in the endodermis. Accessions with the most extreme response to this low Ca/Mg treatment were analysed further. I identify a link between both lateral root number and total root length with performance on growth medium containing a low Ca/Mg ratio.; Arabidopsis thaliana.; Roots (Botany); Arabidopsis thaliana

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

APA (6th Edition):

Mierzwińska, M. E. ;. U. o. A. D. o. P. a. S. S. (2016). Natural variation in root morphology and adaptation to soil conditions in Arabidopsis thaliana. (Doctoral Dissertation). University of Aberdeen. Retrieved from http://digitool.abdn.ac.uk:80/webclient/DeliveryManager?application=DIGITOOL-3&owner=resourcediscovery&custom_att_2=simple_viewer&pid=230164 ; http://digitool.abdn.ac.uk:1801/webclient/DeliveryManager?pid=230164&custom_att_2=simple_viewer

Chicago Manual of Style (16th Edition):

Mierzwińska, Monika Ewa ; University of Aberdeen Dept of Plant and Soil Science. “Natural variation in root morphology and adaptation to soil conditions in Arabidopsis thaliana.” 2016. Doctoral Dissertation, University of Aberdeen. Accessed April 16, 2021. http://digitool.abdn.ac.uk:80/webclient/DeliveryManager?application=DIGITOOL-3&owner=resourcediscovery&custom_att_2=simple_viewer&pid=230164 ; http://digitool.abdn.ac.uk:1801/webclient/DeliveryManager?pid=230164&custom_att_2=simple_viewer.

MLA Handbook (7th Edition):

Mierzwińska, Monika Ewa ; University of Aberdeen Dept of Plant and Soil Science. “Natural variation in root morphology and adaptation to soil conditions in Arabidopsis thaliana.” 2016. Web. 16 Apr 2021.

Vancouver:

Mierzwińska ME;UoADoPaSS. Natural variation in root morphology and adaptation to soil conditions in Arabidopsis thaliana. [Internet] [Doctoral dissertation]. University of Aberdeen; 2016. [cited 2021 Apr 16]. Available from: http://digitool.abdn.ac.uk:80/webclient/DeliveryManager?application=DIGITOOL-3&owner=resourcediscovery&custom_att_2=simple_viewer&pid=230164 ; http://digitool.abdn.ac.uk:1801/webclient/DeliveryManager?pid=230164&custom_att_2=simple_viewer.

Council of Science Editors:

Mierzwińska ME;UoADoPaSS. Natural variation in root morphology and adaptation to soil conditions in Arabidopsis thaliana. [Doctoral Dissertation]. University of Aberdeen; 2016. Available from: http://digitool.abdn.ac.uk:80/webclient/DeliveryManager?application=DIGITOOL-3&owner=resourcediscovery&custom_att_2=simple_viewer&pid=230164 ; http://digitool.abdn.ac.uk:1801/webclient/DeliveryManager?pid=230164&custom_att_2=simple_viewer

.