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You searched for subject:( Luciferase assay). Showing records 1 – 30 of 39 total matches.

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1. 五條堀,孝廣. Signaling pathways of electroliticaly-generated acid functional water in epithelial cells : 上皮細胞における電解酸性機能水のシグナル伝達経路.

Degree: 博士(歯学), 2015, Nihon University / 日本大学

Subjects/Keywords: 電解酸性機能水; electrolyticaly-generated acid functional water; 2 本鎖 RNA; double-stranded RNA; ルシフェラーゼアッセイ; luciferase assay; hBD2; human β-defensin 2; IL-8; interleukin 8

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APA (6th Edition):

五條堀,孝廣. (2015). Signaling pathways of electroliticaly-generated acid functional water in epithelial cells : 上皮細胞における電解酸性機能水のシグナル伝達経路. (Thesis). Nihon University / 日本大学. Retrieved from http://repository.nihon-u.ac.jp/xmlui/handle/11263/554 ; http://dx.doi.org/10.15006/32665A4948

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

Chicago Manual of Style (16th Edition):

五條堀,孝廣. “Signaling pathways of electroliticaly-generated acid functional water in epithelial cells : 上皮細胞における電解酸性機能水のシグナル伝達経路.” 2015. Thesis, Nihon University / 日本大学. Accessed December 13, 2019. http://repository.nihon-u.ac.jp/xmlui/handle/11263/554 ; http://dx.doi.org/10.15006/32665A4948.

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

MLA Handbook (7th Edition):

五條堀,孝廣. “Signaling pathways of electroliticaly-generated acid functional water in epithelial cells : 上皮細胞における電解酸性機能水のシグナル伝達経路.” 2015. Web. 13 Dec 2019.

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete

Vancouver:

五條堀,孝廣. Signaling pathways of electroliticaly-generated acid functional water in epithelial cells : 上皮細胞における電解酸性機能水のシグナル伝達経路. [Internet] [Thesis]. Nihon University / 日本大学; 2015. [cited 2019 Dec 13]. Available from: http://repository.nihon-u.ac.jp/xmlui/handle/11263/554 ; http://dx.doi.org/10.15006/32665A4948.

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

Council of Science Editors:

五條堀,孝廣. Signaling pathways of electroliticaly-generated acid functional water in epithelial cells : 上皮細胞における電解酸性機能水のシグナル伝達経路. [Thesis]. Nihon University / 日本大学; 2015. Available from: http://repository.nihon-u.ac.jp/xmlui/handle/11263/554 ; http://dx.doi.org/10.15006/32665A4948

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


NSYSU

2. Aqib Raza Khan, Mo. Studies on the Chemical Components of Marine-Derived Fungus, Aspergillus terreus and Their Biological Activities.

Degree: Master, Marine Biotechnology and Resources, 2016, NSYSU

 Abstract Marine microbes are regarded as one of the worthiest treasures for bioactive chemical Scaffolds. To search for anti-microbial secondary metabolites from marine environment, we… (more)

Subjects/Keywords: luciferase assay activity; Acinetobacter baumannii; Anti-microbial activity; Aspegillus terreus; MTS cell viability effect; Iron chelating effects

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APA (6th Edition):

Aqib Raza Khan, M. (2016). Studies on the Chemical Components of Marine-Derived Fungus, Aspergillus terreus and Their Biological Activities. (Thesis). NSYSU. Retrieved from http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0801116-154952

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):

Aqib Raza Khan, Mo. “Studies on the Chemical Components of Marine-Derived Fungus, Aspergillus terreus and Their Biological Activities.” 2016. Thesis, NSYSU. Accessed December 13, 2019. http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0801116-154952.

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

MLA Handbook (7th Edition):

Aqib Raza Khan, Mo. “Studies on the Chemical Components of Marine-Derived Fungus, Aspergillus terreus and Their Biological Activities.” 2016. Web. 13 Dec 2019.

Vancouver:

Aqib Raza Khan M. Studies on the Chemical Components of Marine-Derived Fungus, Aspergillus terreus and Their Biological Activities. [Internet] [Thesis]. NSYSU; 2016. [cited 2019 Dec 13]. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0801116-154952.

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

Council of Science Editors:

Aqib Raza Khan M. Studies on the Chemical Components of Marine-Derived Fungus, Aspergillus terreus and Their Biological Activities. [Thesis]. NSYSU; 2016. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0801116-154952

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


Rhode Island College

3. Bock, Timothy. Homology Modeling of the Squalus Acanthias AHR1 To Locate Structural Determinants of Function.

Degree: MA, 2019, Rhode Island College

  The aryl hydrocarbon receptor (AHR) is a ligand-activated transcription factor that mediates a toxic response to many environmental contaminants. Cartilaginous fishes, due to gene… (more)

Subjects/Keywords:

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APA (6th Edition):

Bock, T. (2019). Homology Modeling of the Squalus Acanthias AHR1 To Locate Structural Determinants of Function. (Masters Thesis). Rhode Island College. Retrieved from https://digitalcommons.ric.edu/etd/307

Chicago Manual of Style (16th Edition):

Bock, Timothy. “Homology Modeling of the Squalus Acanthias AHR1 To Locate Structural Determinants of Function.” 2019. Masters Thesis, Rhode Island College. Accessed December 13, 2019. https://digitalcommons.ric.edu/etd/307.

MLA Handbook (7th Edition):

Bock, Timothy. “Homology Modeling of the Squalus Acanthias AHR1 To Locate Structural Determinants of Function.” 2019. Web. 13 Dec 2019.

Vancouver:

Bock T. Homology Modeling of the Squalus Acanthias AHR1 To Locate Structural Determinants of Function. [Internet] [Masters thesis]. Rhode Island College; 2019. [cited 2019 Dec 13]. Available from: https://digitalcommons.ric.edu/etd/307.

Council of Science Editors:

Bock T. Homology Modeling of the Squalus Acanthias AHR1 To Locate Structural Determinants of Function. [Masters Thesis]. Rhode Island College; 2019. Available from: https://digitalcommons.ric.edu/etd/307


University of Newcastle

4. Carroll, Adam. Genomic characterisation of small RNA-mediated post-transcriptional gene regulation.

Degree: PhD, 2013, University of Newcastle

Research Doctorate - Doctor of Philosophy (PhD)

microRNA (miRNA) are small non-coding RNA molecules that function to guide the miRNA-induced silencing complex (miRISC) to regions… (more)

Subjects/Keywords: miRNA; schizophrenia; thesis by publication; target identification; luciferase assay; miR-181b; miR-107; miR-17; miR-20a; miR-16; expression

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APA (6th Edition):

Carroll, A. (2013). Genomic characterisation of small RNA-mediated post-transcriptional gene regulation. (Doctoral Dissertation). University of Newcastle. Retrieved from http://hdl.handle.net/1959.13/1037796

Chicago Manual of Style (16th Edition):

Carroll, Adam. “Genomic characterisation of small RNA-mediated post-transcriptional gene regulation.” 2013. Doctoral Dissertation, University of Newcastle. Accessed December 13, 2019. http://hdl.handle.net/1959.13/1037796.

MLA Handbook (7th Edition):

Carroll, Adam. “Genomic characterisation of small RNA-mediated post-transcriptional gene regulation.” 2013. Web. 13 Dec 2019.

Vancouver:

Carroll A. Genomic characterisation of small RNA-mediated post-transcriptional gene regulation. [Internet] [Doctoral dissertation]. University of Newcastle; 2013. [cited 2019 Dec 13]. Available from: http://hdl.handle.net/1959.13/1037796.

Council of Science Editors:

Carroll A. Genomic characterisation of small RNA-mediated post-transcriptional gene regulation. [Doctoral Dissertation]. University of Newcastle; 2013. Available from: http://hdl.handle.net/1959.13/1037796


Texas Medical Center

5. Chiang, Yun-Chen. Development of HIF-1α/HIF-1β heterodimerization inhibitors using a novel bioluminescence reporter assay system for in vitro high throughput screening and in vivo imaging.

Degree: PhD, 2013, Texas Medical Center

  Tumor growth often outpaces its vascularization, leading to development of a hypoxic tumor microenvironment. In response, an intracellular hypoxia survival pathway is initiated by… (more)

Subjects/Keywords: HIF-1α/β heterodimerization; HIF-1α inhibitor; cancer therapy; molecular imaging; high-content screnning; split luciferase complementation assay; Medical Biotechnology; Medical Molecular Biology; Medicine and Health Sciences; Pharmaceutics and Drug Design; Therapeutics

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APA (6th Edition):

Chiang, Y. (2013). Development of HIF-1α/HIF-1β heterodimerization inhibitors using a novel bioluminescence reporter assay system for in vitro high throughput screening and in vivo imaging. (Doctoral Dissertation). Texas Medical Center. Retrieved from http://digitalcommons.library.tmc.edu/utgsbs_dissertations/383

Chicago Manual of Style (16th Edition):

Chiang, Yun-Chen. “Development of HIF-1α/HIF-1β heterodimerization inhibitors using a novel bioluminescence reporter assay system for in vitro high throughput screening and in vivo imaging.” 2013. Doctoral Dissertation, Texas Medical Center. Accessed December 13, 2019. http://digitalcommons.library.tmc.edu/utgsbs_dissertations/383.

MLA Handbook (7th Edition):

Chiang, Yun-Chen. “Development of HIF-1α/HIF-1β heterodimerization inhibitors using a novel bioluminescence reporter assay system for in vitro high throughput screening and in vivo imaging.” 2013. Web. 13 Dec 2019.

Vancouver:

Chiang Y. Development of HIF-1α/HIF-1β heterodimerization inhibitors using a novel bioluminescence reporter assay system for in vitro high throughput screening and in vivo imaging. [Internet] [Doctoral dissertation]. Texas Medical Center; 2013. [cited 2019 Dec 13]. Available from: http://digitalcommons.library.tmc.edu/utgsbs_dissertations/383.

Council of Science Editors:

Chiang Y. Development of HIF-1α/HIF-1β heterodimerization inhibitors using a novel bioluminescence reporter assay system for in vitro high throughput screening and in vivo imaging. [Doctoral Dissertation]. Texas Medical Center; 2013. Available from: http://digitalcommons.library.tmc.edu/utgsbs_dissertations/383


Louisiana State University

6. Dale, Renee. Mathematical Model of the Split Firefly Luciferase Assay.

Degree: MS, 2015, Louisiana State University

 The firefly luciferase complementation assay is widely used as a bioluminescent reporter technology to detect protein-protein interactions in vitro and in vivo. Firefly luciferase oxidates… (more)

Subjects/Keywords: firefly luciferase; complementation assay; bioluminesence; reporter assay; mathematical model

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APA (6th Edition):

Dale, R. (2015). Mathematical Model of the Split Firefly Luciferase Assay. (Masters Thesis). Louisiana State University. Retrieved from etd-07022015-161605 ; https://digitalcommons.lsu.edu/gradschool_theses/855

Chicago Manual of Style (16th Edition):

Dale, Renee. “Mathematical Model of the Split Firefly Luciferase Assay.” 2015. Masters Thesis, Louisiana State University. Accessed December 13, 2019. etd-07022015-161605 ; https://digitalcommons.lsu.edu/gradschool_theses/855.

MLA Handbook (7th Edition):

Dale, Renee. “Mathematical Model of the Split Firefly Luciferase Assay.” 2015. Web. 13 Dec 2019.

Vancouver:

Dale R. Mathematical Model of the Split Firefly Luciferase Assay. [Internet] [Masters thesis]. Louisiana State University; 2015. [cited 2019 Dec 13]. Available from: etd-07022015-161605 ; https://digitalcommons.lsu.edu/gradschool_theses/855.

Council of Science Editors:

Dale R. Mathematical Model of the Split Firefly Luciferase Assay. [Masters Thesis]. Louisiana State University; 2015. Available from: etd-07022015-161605 ; https://digitalcommons.lsu.edu/gradschool_theses/855


Duquesne University

7. Das, Ranajit. Molecular Evolution of Hominoid Primates: Phylogeny and Regulation.

Degree: PhD, Biological Sciences, 2014, Duquesne University

 The complete mtDNA of one eastern gorilla was sequenced to provide the most accurate date for the mitochondrial divergence of gorillas. The most recent common… (more)

Subjects/Keywords: Eastern Lowland Gorilla; In vitro Luciferase Assay; Promoter-Silencer Interaction; Seminal plasma proteins; TMRCA; Unique hominoid miRNAs

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APA (6th Edition):

Das, R. (2014). Molecular Evolution of Hominoid Primates: Phylogeny and Regulation. (Doctoral Dissertation). Duquesne University. Retrieved from https://dsc.duq.edu/etd/461

Chicago Manual of Style (16th Edition):

Das, Ranajit. “Molecular Evolution of Hominoid Primates: Phylogeny and Regulation.” 2014. Doctoral Dissertation, Duquesne University. Accessed December 13, 2019. https://dsc.duq.edu/etd/461.

MLA Handbook (7th Edition):

Das, Ranajit. “Molecular Evolution of Hominoid Primates: Phylogeny and Regulation.” 2014. Web. 13 Dec 2019.

Vancouver:

Das R. Molecular Evolution of Hominoid Primates: Phylogeny and Regulation. [Internet] [Doctoral dissertation]. Duquesne University; 2014. [cited 2019 Dec 13]. Available from: https://dsc.duq.edu/etd/461.

Council of Science Editors:

Das R. Molecular Evolution of Hominoid Primates: Phylogeny and Regulation. [Doctoral Dissertation]. Duquesne University; 2014. Available from: https://dsc.duq.edu/etd/461

8. Fath, Puria Motamed. Construction of a Copper Bioreporter Screening, characterization and genetic improvement of copper-sensitive bacteria.

Degree: Engineering, 2010, University of Borås

  In the nature, lots of organism apply different kinds of lights such as flourscence or luminoscence for some purposes such as defence or hunting.… (more)

Subjects/Keywords: copper bioreporter; luciferase assay; cop operon; pgl3; e. coli bl-21; Engineering and Technology; Teknik och teknologier

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APA (6th Edition):

Fath, P. M. (2010). Construction of a Copper Bioreporter Screening, characterization and genetic improvement of copper-sensitive bacteria. (Thesis). University of Borås. Retrieved from http://urn.kb.se/resolve?urn=urn:nbn:se:hb:diva-19682

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):

Fath, Puria Motamed. “Construction of a Copper Bioreporter Screening, characterization and genetic improvement of copper-sensitive bacteria.” 2010. Thesis, University of Borås. Accessed December 13, 2019. http://urn.kb.se/resolve?urn=urn:nbn:se:hb:diva-19682.

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

MLA Handbook (7th Edition):

Fath, Puria Motamed. “Construction of a Copper Bioreporter Screening, characterization and genetic improvement of copper-sensitive bacteria.” 2010. Web. 13 Dec 2019.

Vancouver:

Fath PM. Construction of a Copper Bioreporter Screening, characterization and genetic improvement of copper-sensitive bacteria. [Internet] [Thesis]. University of Borås; 2010. [cited 2019 Dec 13]. Available from: http://urn.kb.se/resolve?urn=urn:nbn:se:hb:diva-19682.

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

Council of Science Editors:

Fath PM. Construction of a Copper Bioreporter Screening, characterization and genetic improvement of copper-sensitive bacteria. [Thesis]. University of Borås; 2010. Available from: http://urn.kb.se/resolve?urn=urn:nbn:se:hb:diva-19682

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


Université de Montréal

9. Forget, Amélie. La voie de régulation de la traduction de l’ARNm ASH1 : une concertation entre Khd1, Puf6 et Loc1 .

Degree: 2014, Université de Montréal

 La localisation des ARNm par transport dirigé joue un rôle dans le développement, la motilité cellulaire, la plasticité synaptique et la division cellulaire asymétrique. Chez… (more)

Subjects/Keywords: localisation d’ARNm dirigé; ARNm ASH1; Saccharomyces cerevisiæ; division cellulaire asymétrique; mécanismes de régulation de la traduction; répresseurs traductionnels; Khd1; Puf6; Loc1; She2; Spt4-Spt5/DSIF; co-IP; ChIP; luciferase assay; mRNA localization; ASH1 mRNA; yeast; asymmetric cellular division; translation regulation pathway

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APA (6th Edition):

Forget, A. (2014). La voie de régulation de la traduction de l’ARNm ASH1 : une concertation entre Khd1, Puf6 et Loc1 . (Thesis). Université de Montréal. Retrieved from http://hdl.handle.net/1866/11329

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):

Forget, Amélie. “La voie de régulation de la traduction de l’ARNm ASH1 : une concertation entre Khd1, Puf6 et Loc1 .” 2014. Thesis, Université de Montréal. Accessed December 13, 2019. http://hdl.handle.net/1866/11329.

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

MLA Handbook (7th Edition):

Forget, Amélie. “La voie de régulation de la traduction de l’ARNm ASH1 : une concertation entre Khd1, Puf6 et Loc1 .” 2014. Web. 13 Dec 2019.

Vancouver:

Forget A. La voie de régulation de la traduction de l’ARNm ASH1 : une concertation entre Khd1, Puf6 et Loc1 . [Internet] [Thesis]. Université de Montréal; 2014. [cited 2019 Dec 13]. Available from: http://hdl.handle.net/1866/11329.

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

Council of Science Editors:

Forget A. La voie de régulation de la traduction de l’ARNm ASH1 : une concertation entre Khd1, Puf6 et Loc1 . [Thesis]. Université de Montréal; 2014. Available from: http://hdl.handle.net/1866/11329

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


University of Helsinki

10. Gao, Song. Detection of protein- protein interactions in planta by BiFC and split luciferase assays.

Degree: Department of Agricultural Sciences; Helsingfors universitet, Agrikultur- och forstvetenskapliga fakulteten, Institutionen för lantsbruksvetenskaper, 2010, University of Helsinki

 Molecular biology has created a new pathway for plant breeding in cut flower industry. It focuses on studying flower gene functions and provides a more… (more)

Subjects/Keywords: protein- protein interactions; BiFC; split luciferase assay; electroporation; agroinfiltration; Växtproduktions biologi (trädgårdsvetenskap); Plant Production Biology (Horticulture); Kasvintuotannon biologia (puutarhatiede); protein- protein interactions; BiFC; split luciferase assay; electroporation; agroinfiltration

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APA (6th Edition):

Gao, S. (2010). Detection of protein- protein interactions in planta by BiFC and split luciferase assays. (Masters Thesis). University of Helsinki. Retrieved from http://hdl.handle.net/10138/18107

Chicago Manual of Style (16th Edition):

Gao, Song. “Detection of protein- protein interactions in planta by BiFC and split luciferase assays.” 2010. Masters Thesis, University of Helsinki. Accessed December 13, 2019. http://hdl.handle.net/10138/18107.

MLA Handbook (7th Edition):

Gao, Song. “Detection of protein- protein interactions in planta by BiFC and split luciferase assays.” 2010. Web. 13 Dec 2019.

Vancouver:

Gao S. Detection of protein- protein interactions in planta by BiFC and split luciferase assays. [Internet] [Masters thesis]. University of Helsinki; 2010. [cited 2019 Dec 13]. Available from: http://hdl.handle.net/10138/18107.

Council of Science Editors:

Gao S. Detection of protein- protein interactions in planta by BiFC and split luciferase assays. [Masters Thesis]. University of Helsinki; 2010. Available from: http://hdl.handle.net/10138/18107


Universitat Pompeu Fabra

11. Guidi, Mònica. Micro RNA-Mediated regulation of the full-length and truncated isoforms of human neurotrophic tyrosine kinase receptor type 3 (NTRK 3).

Degree: Departament de Ciències Experimentals i de la Salut, 2009, Universitat Pompeu Fabra

 Las neurotrofinas y sus receptores constituyen una familia de factores cruciales para el desarrollo del sistema nervioso. La neurotrofina 3 ejerce su función principalmente a… (more)

Subjects/Keywords: RISC complex; retinoic acid; renilla luciferase; real-time quantitative PCR; PTBP1; pri-miRNA; pre-miRNA; post-transcriptional regulation; piRNA; PicTar; pGL4.13; PCR; P-body; p75NTR; overexpression; NTRK3; NTRK2; NTRK1; non-coding RNAs; NGF; neurotrophin; neurotrophic signaling; neuronal differentiation; neurodevelopment; neuroblastoma; nervous system; mRNA; miRNA target prediction; miRNA profiling; miRNA mimic; miRNA microarray; miRNA inhibitor; miRanda; microRNA; microarray; luciferase assay; Ingenuity Pathway Analysis (IPA); heLa cells; gene silencing; gene regulation; full-length isoform (FL-NTRK3); firefly luciferase; ERK; disease; dicer; cancer development; BDNF; argonaute; alternative splicing; 3'UTR; RNAhybrid; RT-PCR; SH-SY5Y cells; siRNA; standard error; synaptic plasticity; target validation; TargetScan; transfection; translational repression; TrkA; TrkB; TrkC; truncated isoform (TR-NTRK3); tyrosine kinase (TK); western blot; 575; 61

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APA (6th Edition):

Guidi, M. (2009). Micro RNA-Mediated regulation of the full-length and truncated isoforms of human neurotrophic tyrosine kinase receptor type 3 (NTRK 3). (Thesis). Universitat Pompeu Fabra. Retrieved from http://hdl.handle.net/10803/7114

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):

Guidi, Mònica. “Micro RNA-Mediated regulation of the full-length and truncated isoforms of human neurotrophic tyrosine kinase receptor type 3 (NTRK 3).” 2009. Thesis, Universitat Pompeu Fabra. Accessed December 13, 2019. http://hdl.handle.net/10803/7114.

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

MLA Handbook (7th Edition):

Guidi, Mònica. “Micro RNA-Mediated regulation of the full-length and truncated isoforms of human neurotrophic tyrosine kinase receptor type 3 (NTRK 3).” 2009. Web. 13 Dec 2019.

Vancouver:

Guidi M. Micro RNA-Mediated regulation of the full-length and truncated isoforms of human neurotrophic tyrosine kinase receptor type 3 (NTRK 3). [Internet] [Thesis]. Universitat Pompeu Fabra; 2009. [cited 2019 Dec 13]. Available from: http://hdl.handle.net/10803/7114.

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

Council of Science Editors:

Guidi M. Micro RNA-Mediated regulation of the full-length and truncated isoforms of human neurotrophic tyrosine kinase receptor type 3 (NTRK 3). [Thesis]. Universitat Pompeu Fabra; 2009. Available from: http://hdl.handle.net/10803/7114

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


Uppsala University

12. Handin, Niklas. Identification of new regulatory mechanisms that determine coagulation FXI plasma concentration.

Degree: Biology Education Centre, 2015, Uppsala University

  FXI is a protein in the coagulation cascade in humans proven to be involved in the propagation and stabilization of developing thrombi in previous… (more)

Subjects/Keywords: FXI; F11; blood plasma; coagulation; GWAS; Meta-analysis; pathway analysis; eQTL; miRNA; luciferase reporter assay

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APA (6th Edition):

Handin, N. (2015). Identification of new regulatory mechanisms that determine coagulation FXI plasma concentration. (Thesis). Uppsala University. Retrieved from http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-261267

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):

Handin, Niklas. “Identification of new regulatory mechanisms that determine coagulation FXI plasma concentration.” 2015. Thesis, Uppsala University. Accessed December 13, 2019. http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-261267.

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

MLA Handbook (7th Edition):

Handin, Niklas. “Identification of new regulatory mechanisms that determine coagulation FXI plasma concentration.” 2015. Web. 13 Dec 2019.

Vancouver:

Handin N. Identification of new regulatory mechanisms that determine coagulation FXI plasma concentration. [Internet] [Thesis]. Uppsala University; 2015. [cited 2019 Dec 13]. Available from: http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-261267.

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

Council of Science Editors:

Handin N. Identification of new regulatory mechanisms that determine coagulation FXI plasma concentration. [Thesis]. Uppsala University; 2015. Available from: http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-261267

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


Université de Montréal

13. Hannou, Lydia. La régulation transcriptionnelle de Neuroligine-1 par les facteurs de transcription de l’horloge .

Degree: 2018, Université de Montréal

Subjects/Keywords: Neuroligine-1; Transcription; Protéines de l’horloge; Essai luciférase; Expression génique; Souris; Neuroligin-1; Transcription; Clock proteins; Luciferase assay; Gene expression; Mice

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APA (6th Edition):

Hannou, L. (2018). La régulation transcriptionnelle de Neuroligine-1 par les facteurs de transcription de l’horloge . (Thesis). Université de Montréal. Retrieved from http://hdl.handle.net/1866/20787

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):

Hannou, Lydia. “La régulation transcriptionnelle de Neuroligine-1 par les facteurs de transcription de l’horloge .” 2018. Thesis, Université de Montréal. Accessed December 13, 2019. http://hdl.handle.net/1866/20787.

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

MLA Handbook (7th Edition):

Hannou, Lydia. “La régulation transcriptionnelle de Neuroligine-1 par les facteurs de transcription de l’horloge .” 2018. Web. 13 Dec 2019.

Vancouver:

Hannou L. La régulation transcriptionnelle de Neuroligine-1 par les facteurs de transcription de l’horloge . [Internet] [Thesis]. Université de Montréal; 2018. [cited 2019 Dec 13]. Available from: http://hdl.handle.net/1866/20787.

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

Council of Science Editors:

Hannou L. La régulation transcriptionnelle de Neuroligine-1 par les facteurs de transcription de l’horloge . [Thesis]. Université de Montréal; 2018. Available from: http://hdl.handle.net/1866/20787

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

14. Hogel, Matthew. INVESTIGATING THE MECHANISM OF PROMOTER-SPECIFIC N-TERMINAL MUTANT HUNTINGTIN-MEDIATED TRANSCRIPTIONAL DYSREGULATION.

Degree: PhD, Department of Pharmacology with Neuroscience, 2012, Dalhousie University

 Huntington’s disease (HD) is a neurodegenerative disorder caused by the inheritance of one mutant copy of the huntingtin gene. Mutant huntingtin protein (mHtt) contains an… (more)

Subjects/Keywords: Huntington's; Transcription; Repression; Huntingtin; Polyglutamine; Transcriptional Dysregulation; in vitro transcription; N548; ST14A; Dual-luciferase assay; Chromatin Immunoprecipitation; Promoter Deletion; Linker Scanning Mutagenesis; Quantitative PCR; Promoter binding assay; TBP; RAP30

…3.4 Diagram of the luciferase reporter assay… …of the luciferase assay… …3.9 CMV-driven luciferase activity was decreased in the presence of N-mHtt ... 111 3.10… …The relationship between luciferase activity and luc+ mRNA copy number was similar in N548wt… …and N548hd cells but not in ST14A cells .................. 112 3.11 Luciferase activity… 

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APA (6th Edition):

Hogel, M. (2012). INVESTIGATING THE MECHANISM OF PROMOTER-SPECIFIC N-TERMINAL MUTANT HUNTINGTIN-MEDIATED TRANSCRIPTIONAL DYSREGULATION. (Doctoral Dissertation). Dalhousie University. Retrieved from http://hdl.handle.net/10222/15723

Chicago Manual of Style (16th Edition):

Hogel, Matthew. “INVESTIGATING THE MECHANISM OF PROMOTER-SPECIFIC N-TERMINAL MUTANT HUNTINGTIN-MEDIATED TRANSCRIPTIONAL DYSREGULATION.” 2012. Doctoral Dissertation, Dalhousie University. Accessed December 13, 2019. http://hdl.handle.net/10222/15723.

MLA Handbook (7th Edition):

Hogel, Matthew. “INVESTIGATING THE MECHANISM OF PROMOTER-SPECIFIC N-TERMINAL MUTANT HUNTINGTIN-MEDIATED TRANSCRIPTIONAL DYSREGULATION.” 2012. Web. 13 Dec 2019.

Vancouver:

Hogel M. INVESTIGATING THE MECHANISM OF PROMOTER-SPECIFIC N-TERMINAL MUTANT HUNTINGTIN-MEDIATED TRANSCRIPTIONAL DYSREGULATION. [Internet] [Doctoral dissertation]. Dalhousie University; 2012. [cited 2019 Dec 13]. Available from: http://hdl.handle.net/10222/15723.

Council of Science Editors:

Hogel M. INVESTIGATING THE MECHANISM OF PROMOTER-SPECIFIC N-TERMINAL MUTANT HUNTINGTIN-MEDIATED TRANSCRIPTIONAL DYSREGULATION. [Doctoral Dissertation]. Dalhousie University; 2012. Available from: http://hdl.handle.net/10222/15723

15. Hsia, Hung-Ching. Identification of Targets and Pathways Controlled by the Chicken MicroRNAs miR-10a and miR-143.

Degree: MS, Animal Science, 2009, North Carolina State University

 MicroRNAs are small non-coding RNAs that regulate gene expression at the posttranscriptional level. The importance of microRNAs in development, tumorogenesis, immune system function, and infectious… (more)

Subjects/Keywords: spleen; chicken; microRNA; luciferase assay; microarray

…39 Luciferase Assay… …49 Luciferase Assay… …62 Luciferase Assay… …55 Figure 3.5 Luciferase Assay for miR-10a Target Validation… …56 Figure 3.6 Luciferase Assay for miR-143 Target Validation… 

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APA (6th Edition):

Hsia, H. (2009). Identification of Targets and Pathways Controlled by the Chicken MicroRNAs miR-10a and miR-143. (Thesis). North Carolina State University. Retrieved from http://www.lib.ncsu.edu/resolver/1840.16/942

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):

Hsia, Hung-Ching. “Identification of Targets and Pathways Controlled by the Chicken MicroRNAs miR-10a and miR-143.” 2009. Thesis, North Carolina State University. Accessed December 13, 2019. http://www.lib.ncsu.edu/resolver/1840.16/942.

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

MLA Handbook (7th Edition):

Hsia, Hung-Ching. “Identification of Targets and Pathways Controlled by the Chicken MicroRNAs miR-10a and miR-143.” 2009. Web. 13 Dec 2019.

Vancouver:

Hsia H. Identification of Targets and Pathways Controlled by the Chicken MicroRNAs miR-10a and miR-143. [Internet] [Thesis]. North Carolina State University; 2009. [cited 2019 Dec 13]. Available from: http://www.lib.ncsu.edu/resolver/1840.16/942.

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

Council of Science Editors:

Hsia H. Identification of Targets and Pathways Controlled by the Chicken MicroRNAs miR-10a and miR-143. [Thesis]. North Carolina State University; 2009. Available from: http://www.lib.ncsu.edu/resolver/1840.16/942

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


Kyoto University / 京都大学

16. Isobe, Masanori. Polymorphism within a neuronal activity-dependent enhancer of NgR1 is associated with corpus callosum morphology in humans : NgR1遺伝子の神経活動依存性エンハンサー領域の遺伝子多型はヒトの脳梁の形態に関連する.

Degree: 博士(医学), 2015, Kyoto University / 京都大学

新制・課程博士

甲第19270号

医博第4034号

Subjects/Keywords: Nogo-66 receptor 1 (NgR1); Corpus callosum; Diffusion tensor imaging (DTI); Epigenomics; Luciferase assay; Neuronal activity dependent enhancer

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APA (6th Edition):

Isobe, M. (2015). Polymorphism within a neuronal activity-dependent enhancer of NgR1 is associated with corpus callosum morphology in humans : NgR1遺伝子の神経活動依存性エンハンサー領域の遺伝子多型はヒトの脳梁の形態に関連する. (Thesis). Kyoto University / 京都大学. Retrieved from http://hdl.handle.net/2433/202673 ; http://dx.doi.org/10.14989/doctor.k19270

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):

Isobe, Masanori. “Polymorphism within a neuronal activity-dependent enhancer of NgR1 is associated with corpus callosum morphology in humans : NgR1遺伝子の神経活動依存性エンハンサー領域の遺伝子多型はヒトの脳梁の形態に関連する.” 2015. Thesis, Kyoto University / 京都大学. Accessed December 13, 2019. http://hdl.handle.net/2433/202673 ; http://dx.doi.org/10.14989/doctor.k19270.

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

MLA Handbook (7th Edition):

Isobe, Masanori. “Polymorphism within a neuronal activity-dependent enhancer of NgR1 is associated with corpus callosum morphology in humans : NgR1遺伝子の神経活動依存性エンハンサー領域の遺伝子多型はヒトの脳梁の形態に関連する.” 2015. Web. 13 Dec 2019.

Vancouver:

Isobe M. Polymorphism within a neuronal activity-dependent enhancer of NgR1 is associated with corpus callosum morphology in humans : NgR1遺伝子の神経活動依存性エンハンサー領域の遺伝子多型はヒトの脳梁の形態に関連する. [Internet] [Thesis]. Kyoto University / 京都大学; 2015. [cited 2019 Dec 13]. Available from: http://hdl.handle.net/2433/202673 ; http://dx.doi.org/10.14989/doctor.k19270.

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

Council of Science Editors:

Isobe M. Polymorphism within a neuronal activity-dependent enhancer of NgR1 is associated with corpus callosum morphology in humans : NgR1遺伝子の神経活動依存性エンハンサー領域の遺伝子多型はヒトの脳梁の形態に関連する. [Thesis]. Kyoto University / 京都大学; 2015. Available from: http://hdl.handle.net/2433/202673 ; http://dx.doi.org/10.14989/doctor.k19270

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

17. Isobe, Masanori. Polymorphism within a neuronal activity-dependent enhancer of NgR1 is associated with corpus callosum morphology in humans .

Degree: 2015, Kyoto University

Subjects/Keywords: Nogo-66 receptor 1 (NgR1); Corpus callosum; Diffusion tensor imaging (DTI); Epigenomics; Luciferase assay; Neuronal activity dependent enhancer

Page 1 Page 2

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APA (6th Edition):

Isobe, M. (2015). Polymorphism within a neuronal activity-dependent enhancer of NgR1 is associated with corpus callosum morphology in humans . (Thesis). Kyoto University. Retrieved from http://hdl.handle.net/2433/202673

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):

Isobe, Masanori. “Polymorphism within a neuronal activity-dependent enhancer of NgR1 is associated with corpus callosum morphology in humans .” 2015. Thesis, Kyoto University. Accessed December 13, 2019. http://hdl.handle.net/2433/202673.

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

MLA Handbook (7th Edition):

Isobe, Masanori. “Polymorphism within a neuronal activity-dependent enhancer of NgR1 is associated with corpus callosum morphology in humans .” 2015. Web. 13 Dec 2019.

Vancouver:

Isobe M. Polymorphism within a neuronal activity-dependent enhancer of NgR1 is associated with corpus callosum morphology in humans . [Internet] [Thesis]. Kyoto University; 2015. [cited 2019 Dec 13]. Available from: http://hdl.handle.net/2433/202673.

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

Council of Science Editors:

Isobe M. Polymorphism within a neuronal activity-dependent enhancer of NgR1 is associated with corpus callosum morphology in humans . [Thesis]. Kyoto University; 2015. Available from: http://hdl.handle.net/2433/202673

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

18. Jahanshahi-Anbuhi, Sana. Development of Ready-to-Use Biosensors for Diagnostics and Biosensing.

Degree: DEng, 2014, McMaster University

 Ideally, every person in the world should have access to a safe and clean water supply; if not all sources of water are clean and… (more)

Subjects/Keywords: Biosensor; Microfluidic; Bio-active Paper; Paper Based Microfluidic Devices; Pullulan; Pill Based Assay; Reagent Release; Enzyme Stabilization; Organophosphate Pesticide; E. coli; Luciferase; Luminescent; Lab on Pills; Pullulan Tablet; Pullulan Capsule

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APA (6th Edition):

Jahanshahi-Anbuhi, S. (2014). Development of Ready-to-Use Biosensors for Diagnostics and Biosensing. (Doctoral Dissertation). McMaster University. Retrieved from http://hdl.handle.net/11375/16501

Chicago Manual of Style (16th Edition):

Jahanshahi-Anbuhi, Sana. “Development of Ready-to-Use Biosensors for Diagnostics and Biosensing.” 2014. Doctoral Dissertation, McMaster University. Accessed December 13, 2019. http://hdl.handle.net/11375/16501.

MLA Handbook (7th Edition):

Jahanshahi-Anbuhi, Sana. “Development of Ready-to-Use Biosensors for Diagnostics and Biosensing.” 2014. Web. 13 Dec 2019.

Vancouver:

Jahanshahi-Anbuhi S. Development of Ready-to-Use Biosensors for Diagnostics and Biosensing. [Internet] [Doctoral dissertation]. McMaster University; 2014. [cited 2019 Dec 13]. Available from: http://hdl.handle.net/11375/16501.

Council of Science Editors:

Jahanshahi-Anbuhi S. Development of Ready-to-Use Biosensors for Diagnostics and Biosensing. [Doctoral Dissertation]. McMaster University; 2014. Available from: http://hdl.handle.net/11375/16501


University of Helsinki

19. Jokinen, Nora. Assay optimization and screening for hepatitis C virus replication inhibitors from marine-derived substances.

Degree: Farmaceutiska fakulteten, 2013, University of Helsinki

 Maailmassa on arviolta 180 miljoonaa hepatiitti C -viruksen kantajaa. C-hepatiitti aiheuttaa usein oireettomia maksasairauksia. Krooniset infektiot voivat aiheuttaa maksakirroosia, johtaa elinsiirtoon tai maksasyöpään. Lääkkeiden kehitys… (more)

Subjects/Keywords: Hepatitis C virus; replication inhibitor; antiviral screening; cell-based assay; luciferase reporter; Farmakognosi; Pharmacognosy; Farmakognosia

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APA (6th Edition):

Jokinen, N. (2013). Assay optimization and screening for hepatitis C virus replication inhibitors from marine-derived substances. (Masters Thesis). University of Helsinki. Retrieved from http://hdl.handle.net/10138/40773

Chicago Manual of Style (16th Edition):

Jokinen, Nora. “Assay optimization and screening for hepatitis C virus replication inhibitors from marine-derived substances.” 2013. Masters Thesis, University of Helsinki. Accessed December 13, 2019. http://hdl.handle.net/10138/40773.

MLA Handbook (7th Edition):

Jokinen, Nora. “Assay optimization and screening for hepatitis C virus replication inhibitors from marine-derived substances.” 2013. Web. 13 Dec 2019.

Vancouver:

Jokinen N. Assay optimization and screening for hepatitis C virus replication inhibitors from marine-derived substances. [Internet] [Masters thesis]. University of Helsinki; 2013. [cited 2019 Dec 13]. Available from: http://hdl.handle.net/10138/40773.

Council of Science Editors:

Jokinen N. Assay optimization and screening for hepatitis C virus replication inhibitors from marine-derived substances. [Masters Thesis]. University of Helsinki; 2013. Available from: http://hdl.handle.net/10138/40773


University of Lund

20. Kotarsky, Knut. Development of sensitive cellular assay systems and their application to the identification of "orphan" seven-transmembrane receptors.

Degree: 2003, University of Lund

 Seven-transmembrane, G-protein coupled receptors play a central role in physiology since they facilitate cell communication in multicellular organisms by recognition of a broad range of… (more)

Subjects/Keywords: Neurovetenskaper; Biokemi; Metabolism; Biochemistry; metabolism; leukotrieneB4; thiazolidinedione; 9-HODE; fatty acid; luciferase; GFP; reporter gene; preclinical assay; receptor; GPCR

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APA (6th Edition):

Kotarsky, K. (2003). Development of sensitive cellular assay systems and their application to the identification of "orphan" seven-transmembrane receptors. (Doctoral Dissertation). University of Lund. Retrieved from http://lup.lub.lu.se/record/465640 ; http://portal.research.lu.se/ws/files/5657663/1692971.pdf

Chicago Manual of Style (16th Edition):

Kotarsky, Knut. “Development of sensitive cellular assay systems and their application to the identification of "orphan" seven-transmembrane receptors.” 2003. Doctoral Dissertation, University of Lund. Accessed December 13, 2019. http://lup.lub.lu.se/record/465640 ; http://portal.research.lu.se/ws/files/5657663/1692971.pdf.

MLA Handbook (7th Edition):

Kotarsky, Knut. “Development of sensitive cellular assay systems and their application to the identification of "orphan" seven-transmembrane receptors.” 2003. Web. 13 Dec 2019.

Vancouver:

Kotarsky K. Development of sensitive cellular assay systems and their application to the identification of "orphan" seven-transmembrane receptors. [Internet] [Doctoral dissertation]. University of Lund; 2003. [cited 2019 Dec 13]. Available from: http://lup.lub.lu.se/record/465640 ; http://portal.research.lu.se/ws/files/5657663/1692971.pdf.

Council of Science Editors:

Kotarsky K. Development of sensitive cellular assay systems and their application to the identification of "orphan" seven-transmembrane receptors. [Doctoral Dissertation]. University of Lund; 2003. Available from: http://lup.lub.lu.se/record/465640 ; http://portal.research.lu.se/ws/files/5657663/1692971.pdf


Tampere University

21. Lahtinen, Suvi. Optimizing a method to reliably detect the furin activity at cellular level and identify the regulators of its activity .

Degree: 2015, Tampere University

Subjects/Keywords: furin; S2 cells; direct cell assay; RNA-interference; genome-wide screening; luciferase reporter gene

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APA (6th Edition):

Lahtinen, S. (2015). Optimizing a method to reliably detect the furin activity at cellular level and identify the regulators of its activity . (Masters Thesis). Tampere University. Retrieved from https://trepo.tuni.fi/handle/10024/97773

Chicago Manual of Style (16th Edition):

Lahtinen, Suvi. “Optimizing a method to reliably detect the furin activity at cellular level and identify the regulators of its activity .” 2015. Masters Thesis, Tampere University. Accessed December 13, 2019. https://trepo.tuni.fi/handle/10024/97773.

MLA Handbook (7th Edition):

Lahtinen, Suvi. “Optimizing a method to reliably detect the furin activity at cellular level and identify the regulators of its activity .” 2015. Web. 13 Dec 2019.

Vancouver:

Lahtinen S. Optimizing a method to reliably detect the furin activity at cellular level and identify the regulators of its activity . [Internet] [Masters thesis]. Tampere University; 2015. [cited 2019 Dec 13]. Available from: https://trepo.tuni.fi/handle/10024/97773.

Council of Science Editors:

Lahtinen S. Optimizing a method to reliably detect the furin activity at cellular level and identify the regulators of its activity . [Masters Thesis]. Tampere University; 2015. Available from: https://trepo.tuni.fi/handle/10024/97773


Queensland University of Technology

22. Lai, John. Functional analyses of polymorphisms in the promoters of the KLK3 and KLK4 genes in prostate cancer.

Degree: 2006, Queensland University of Technology

 This PhD aimed to elucidate the mechanisms by which polymorphisms may alter androgen-induced transactivation of androgen receptor (AR) target genes which may be important in… (more)

Subjects/Keywords: prostate cancer; single nucleotide polymorphism (SNP); kallikreins (KLKs); kallikrein 4 (KLK4); prostate specific antigen (PSA); androgens; hormones; androgen receptor (AR); androgen receptor DNA binding domain (AR-DBD); androgen response element (ARE); electromobility shift assay (EMSA); luciferase reporter assay

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APA (6th Edition):

Lai, J. (2006). Functional analyses of polymorphisms in the promoters of the KLK3 and KLK4 genes in prostate cancer. (Thesis). Queensland University of Technology. Retrieved from https://eprints.qut.edu.au/16454/

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):

Lai, John. “Functional analyses of polymorphisms in the promoters of the KLK3 and KLK4 genes in prostate cancer.” 2006. Thesis, Queensland University of Technology. Accessed December 13, 2019. https://eprints.qut.edu.au/16454/.

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

MLA Handbook (7th Edition):

Lai, John. “Functional analyses of polymorphisms in the promoters of the KLK3 and KLK4 genes in prostate cancer.” 2006. Web. 13 Dec 2019.

Vancouver:

Lai J. Functional analyses of polymorphisms in the promoters of the KLK3 and KLK4 genes in prostate cancer. [Internet] [Thesis]. Queensland University of Technology; 2006. [cited 2019 Dec 13]. Available from: https://eprints.qut.edu.au/16454/.

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

Council of Science Editors:

Lai J. Functional analyses of polymorphisms in the promoters of the KLK3 and KLK4 genes in prostate cancer. [Thesis]. Queensland University of Technology; 2006. Available from: https://eprints.qut.edu.au/16454/

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


Northeastern University

23. Lau, Joyce Yuk-Ting. Evolution and function of the globin gene complexes of Antarctic Dragonfishes (Notothenioidei: Bathydraconidae).

Degree: MS, Department of Biology, 2009, Northeastern University

 As the Southern Ocean cooled to -1.8°C over the past 40 million years, the teleostean clade Notothenioidei became less reliant on hemoglobin and red blood… (more)

Subjects/Keywords: alpha/beta globin intergenic regulatory region; Bathydraconidae; luciferase reporter assay; murine erythroleukemia cell (MEL); Nototheniidae; notothenioid fish suborder; Pterois volitans – Evolution; Biology

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APA (6th Edition):

Lau, J. Y. (2009). Evolution and function of the globin gene complexes of Antarctic Dragonfishes (Notothenioidei: Bathydraconidae). (Masters Thesis). Northeastern University. Retrieved from http://hdl.handle.net/2047/d20000336

Chicago Manual of Style (16th Edition):

Lau, Joyce Yuk-Ting. “Evolution and function of the globin gene complexes of Antarctic Dragonfishes (Notothenioidei: Bathydraconidae).” 2009. Masters Thesis, Northeastern University. Accessed December 13, 2019. http://hdl.handle.net/2047/d20000336.

MLA Handbook (7th Edition):

Lau, Joyce Yuk-Ting. “Evolution and function of the globin gene complexes of Antarctic Dragonfishes (Notothenioidei: Bathydraconidae).” 2009. Web. 13 Dec 2019.

Vancouver:

Lau JY. Evolution and function of the globin gene complexes of Antarctic Dragonfishes (Notothenioidei: Bathydraconidae). [Internet] [Masters thesis]. Northeastern University; 2009. [cited 2019 Dec 13]. Available from: http://hdl.handle.net/2047/d20000336.

Council of Science Editors:

Lau JY. Evolution and function of the globin gene complexes of Antarctic Dragonfishes (Notothenioidei: Bathydraconidae). [Masters Thesis]. Northeastern University; 2009. Available from: http://hdl.handle.net/2047/d20000336

24. Lind, Liza. Non-coding RNA in T cell activation and function.

Degree: Faculty of Health Sciences, 2013, Linköping UniversityLinköping University

  For a long time research has focused on the protein-coding mRNA, but there is a complex world of non-coding RNAs regulating the human body… (more)

Subjects/Keywords: ncRNA 886; non-coding RNA 886; microRNA 150; miRNA 150; PKR; T cell activation; luciferase assay

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APA (6th Edition):

Lind, L. (2013). Non-coding RNA in T cell activation and function. (Thesis). Linköping UniversityLinköping University. Retrieved from http://urn.kb.se/resolve?urn=urn:nbn:se:liu:diva-96966

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):

Lind, Liza. “Non-coding RNA in T cell activation and function.” 2013. Thesis, Linköping UniversityLinköping University. Accessed December 13, 2019. http://urn.kb.se/resolve?urn=urn:nbn:se:liu:diva-96966.

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

MLA Handbook (7th Edition):

Lind, Liza. “Non-coding RNA in T cell activation and function.” 2013. Web. 13 Dec 2019.

Vancouver:

Lind L. Non-coding RNA in T cell activation and function. [Internet] [Thesis]. Linköping UniversityLinköping University; 2013. [cited 2019 Dec 13]. Available from: http://urn.kb.se/resolve?urn=urn:nbn:se:liu:diva-96966.

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

Council of Science Editors:

Lind L. Non-coding RNA in T cell activation and function. [Thesis]. Linköping UniversityLinköping University; 2013. Available from: http://urn.kb.se/resolve?urn=urn:nbn:se:liu:diva-96966

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


Universitat Pompeu Fabra

25. Muiños Gimeno, Margarita. Analysis of genetic variation in microrna-mediated regulation and the susceptibility to anxiety disorders.

Degree: Departament de Ciències Experimentals i de la Salut, 2009, Universitat Pompeu Fabra

 Hem investigat la variació genètica a la regulació mediada per microRNAs com a factors de susceptibilitat pels trastorns d'ansietat seguint dues aproximacions diferents. Primer vam… (more)

Subjects/Keywords: isoforma; anàlisi de transcriptoma; PCR; assaig de luciferasa; variant comuna; variant rara; reseqüenciar; estudis d'associació; poly-miRTS; trastorn obsessiu-compulsiu; trastorn de pànic; trastorn d'ansietat; variació genètica intraespecífica; SNP; NTRK3; gen candidat; element regulador; microRNA; variació genòmica; desordres poligènics; trets complexes; isoform; transcriptome analysis; PCR; luciferase assay; common variant; rare variant; re-sequencing; association studies; poly-miRTS; obsessive-compulsive disorder; panic disorder; anxiety disorder; genetic variation within species; SNP; NTRK3; candidate gene; regulatory element; microRNA; genome variation; polygenic disorders; complex traits; 57

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

APA (6th Edition):

Muiños Gimeno, M. (2009). Analysis of genetic variation in microrna-mediated regulation and the susceptibility to anxiety disorders. (Thesis). Universitat Pompeu Fabra. Retrieved from http://hdl.handle.net/10803/7192

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):

Muiños Gimeno, Margarita. “Analysis of genetic variation in microrna-mediated regulation and the susceptibility to anxiety disorders.” 2009. Thesis, Universitat Pompeu Fabra. Accessed December 13, 2019. http://hdl.handle.net/10803/7192.

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

MLA Handbook (7th Edition):

Muiños Gimeno, Margarita. “Analysis of genetic variation in microrna-mediated regulation and the susceptibility to anxiety disorders.” 2009. Web. 13 Dec 2019.

Vancouver:

Muiños Gimeno M. Analysis of genetic variation in microrna-mediated regulation and the susceptibility to anxiety disorders. [Internet] [Thesis]. Universitat Pompeu Fabra; 2009. [cited 2019 Dec 13]. Available from: http://hdl.handle.net/10803/7192.

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

Council of Science Editors:

Muiños Gimeno M. Analysis of genetic variation in microrna-mediated regulation and the susceptibility to anxiety disorders. [Thesis]. Universitat Pompeu Fabra; 2009. Available from: http://hdl.handle.net/10803/7192

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

26. Muthusamy, Sasikumar. Evaluation of interaction and combined toxicity of polyaromatic hydrocarbons (PAHs) and metals using human cell-based bioassays.

Degree: School of Medicine, 2016, University of Queensland

Subjects/Keywords: Mixture toxicity; In vitro assays; Cytotoxicity; Oxidative stress; Genotoxicity; Flow cytometry; Luciferase assay; Reporter gene system; Regulatory toxicology; Health risk assessment; 050204 Environmental Impact Assessment; 0601 Biochemistry and Cell Biology; 111506 Toxicology (incl.Clinical Toxicology)

…genotoxicity, flow cytometry, luciferase assay, reporter gene system, regulatory toxicology, health… …luciferase assay CAFLUX- chemically activated fluorescent assay CAS- chemical abstract registry Cd… …23 2.8.1. Luciferase Assays… …31 3.4. Cytotoxicity assay… …37 4.2.3. Cytotoxicity assay… 

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

APA (6th Edition):

Muthusamy, S. (2016). Evaluation of interaction and combined toxicity of polyaromatic hydrocarbons (PAHs) and metals using human cell-based bioassays. (Thesis). University of Queensland. Retrieved from http://espace.library.uq.edu.au/view/UQ:409659

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):

Muthusamy, Sasikumar. “Evaluation of interaction and combined toxicity of polyaromatic hydrocarbons (PAHs) and metals using human cell-based bioassays.” 2016. Thesis, University of Queensland. Accessed December 13, 2019. http://espace.library.uq.edu.au/view/UQ:409659.

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

MLA Handbook (7th Edition):

Muthusamy, Sasikumar. “Evaluation of interaction and combined toxicity of polyaromatic hydrocarbons (PAHs) and metals using human cell-based bioassays.” 2016. Web. 13 Dec 2019.

Vancouver:

Muthusamy S. Evaluation of interaction and combined toxicity of polyaromatic hydrocarbons (PAHs) and metals using human cell-based bioassays. [Internet] [Thesis]. University of Queensland; 2016. [cited 2019 Dec 13]. Available from: http://espace.library.uq.edu.au/view/UQ:409659.

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

Council of Science Editors:

Muthusamy S. Evaluation of interaction and combined toxicity of polyaromatic hydrocarbons (PAHs) and metals using human cell-based bioassays. [Thesis]. University of Queensland; 2016. Available from: http://espace.library.uq.edu.au/view/UQ:409659

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


University of Texas Medical Branch – Galveston

27. [No author]. Targeting protein: protein interaction sites for drug development against voltage-gated sodium channels .

Degree: University of Texas Medical Branch – Galveston

 Voltage-gated sodium (Nav) channels are responsible for initiation and propagation of action potentials, which contribute to control of neuronal excitability. Malfunction of specific Nav channel… (more)

Subjects/Keywords: FGF14; Fibroblast growth factor 14 Nav channel; Voltage-gated sodium channel; PPI; Protein: protein interactions; LCA; Luciferase complementation assay; Small Peptide

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

APA (6th Edition):

author], [. (n.d.). Targeting protein: protein interaction sites for drug development against voltage-gated sodium channels . (Thesis). University of Texas Medical Branch – Galveston. Retrieved from http://hdl.handle.net/2152.3/11197

Note: this citation may be lacking information needed for this citation format:
No year of publication.
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

author], [No. “Targeting protein: protein interaction sites for drug development against voltage-gated sodium channels .” Thesis, University of Texas Medical Branch – Galveston. Accessed December 13, 2019. http://hdl.handle.net/2152.3/11197.

Note: this citation may be lacking information needed for this citation format:
No year of publication.
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

author], [No. “Targeting protein: protein interaction sites for drug development against voltage-gated sodium channels .” Web. 13 Dec 2019.

Note: this citation may be lacking information needed for this citation format:
No year of publication.

Vancouver:

author] [. Targeting protein: protein interaction sites for drug development against voltage-gated sodium channels . [Internet] [Thesis]. University of Texas Medical Branch – Galveston; [cited 2019 Dec 13]. Available from: http://hdl.handle.net/2152.3/11197.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation
No year of publication.

Council of Science Editors:

author] [. Targeting protein: protein interaction sites for drug development against voltage-gated sodium channels . [Thesis]. University of Texas Medical Branch – Galveston; Available from: http://hdl.handle.net/2152.3/11197

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation
No year of publication.


University of Texas Medical Branch – Galveston

28. [No author]. Degradational and Transcriptional Investigations of the RAF Kinase Inhibitory Protein .

Degree: University of Texas Medical Branch – Galveston

 RKIP (Raf-1 kinase inhibitory protein) is a novel potent metastasis suppressor by its function of inhibiting ERK pathway, NF-κB pathway, and GRK-2. RKIP expression level… (more)

Subjects/Keywords: RKIP; degradation; transcription; phosphorylation; ubiquitination; luciferase assay

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

APA (6th Edition):

author], [. (n.d.). Degradational and Transcriptional Investigations of the RAF Kinase Inhibitory Protein . (Thesis). University of Texas Medical Branch – Galveston. Retrieved from http://hdl.handle.net/2152.3/801

Note: this citation may be lacking information needed for this citation format:
No year of publication.
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

author], [No. “Degradational and Transcriptional Investigations of the RAF Kinase Inhibitory Protein .” Thesis, University of Texas Medical Branch – Galveston. Accessed December 13, 2019. http://hdl.handle.net/2152.3/801.

Note: this citation may be lacking information needed for this citation format:
No year of publication.
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

author], [No. “Degradational and Transcriptional Investigations of the RAF Kinase Inhibitory Protein .” Web. 13 Dec 2019.

Note: this citation may be lacking information needed for this citation format:
No year of publication.

Vancouver:

author] [. Degradational and Transcriptional Investigations of the RAF Kinase Inhibitory Protein . [Internet] [Thesis]. University of Texas Medical Branch – Galveston; [cited 2019 Dec 13]. Available from: http://hdl.handle.net/2152.3/801.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation
No year of publication.

Council of Science Editors:

author] [. Degradational and Transcriptional Investigations of the RAF Kinase Inhibitory Protein . [Thesis]. University of Texas Medical Branch – Galveston; Available from: http://hdl.handle.net/2152.3/801

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation
No year of publication.


University of Oxford

29. Prapansilp, Panote. Molecular pathological investigation of the pathophysiology of fatal malaria.

Degree: PhD, 2012, University of Oxford

 Malaria remains one of the world's major health problems, especially in developing countries. A better understanding of the pathology and pathophysiology of severe malaria is… (more)

Subjects/Keywords: 616.9; Malaria; Pathology; Tropical medicine; Cerebral malaria; Infectious diseases; molecular pathology; autopsy; tissue quality; african; asian; angiopoietin; tie-2; hypoxia; cell culture; acute kidney injury; malaria associated acute renal failure; microRNA; microarray; cloning; luciferase assay

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

APA (6th Edition):

Prapansilp, P. (2012). Molecular pathological investigation of the pathophysiology of fatal malaria. (Doctoral Dissertation). University of Oxford. Retrieved from http://ora.ox.ac.uk/objects/uuid:e966a2f2-a37d-4586-b09e-2bb616e5dce2 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.658384

Chicago Manual of Style (16th Edition):

Prapansilp, Panote. “Molecular pathological investigation of the pathophysiology of fatal malaria.” 2012. Doctoral Dissertation, University of Oxford. Accessed December 13, 2019. http://ora.ox.ac.uk/objects/uuid:e966a2f2-a37d-4586-b09e-2bb616e5dce2 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.658384.

MLA Handbook (7th Edition):

Prapansilp, Panote. “Molecular pathological investigation of the pathophysiology of fatal malaria.” 2012. Web. 13 Dec 2019.

Vancouver:

Prapansilp P. Molecular pathological investigation of the pathophysiology of fatal malaria. [Internet] [Doctoral dissertation]. University of Oxford; 2012. [cited 2019 Dec 13]. Available from: http://ora.ox.ac.uk/objects/uuid:e966a2f2-a37d-4586-b09e-2bb616e5dce2 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.658384.

Council of Science Editors:

Prapansilp P. Molecular pathological investigation of the pathophysiology of fatal malaria. [Doctoral Dissertation]. University of Oxford; 2012. Available from: http://ora.ox.ac.uk/objects/uuid:e966a2f2-a37d-4586-b09e-2bb616e5dce2 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.658384


University of Queensland

30. Pretorius, Lara-Simone. Investigation of virus-induced defence modulations during plant-virus interactions.

Degree: School of Agriculture & Food Sciences, 2018, University of Queensland

Subjects/Keywords: Biogenesis pathway; Defence pathways; Dual-luciferase assay; Gene expression; Jasmonic acid; med18; Small RNAs; Turnip mosaic virus; Viral evolution; 0604 Genetics; 0605 Microbiology; 0607 Plant Biology

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

APA (6th Edition):

Pretorius, L. (2018). Investigation of virus-induced defence modulations during plant-virus interactions. (Thesis). University of Queensland. Retrieved from http://espace.library.uq.edu.au/view/UQ:8

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):

Pretorius, Lara-Simone. “Investigation of virus-induced defence modulations during plant-virus interactions.” 2018. Thesis, University of Queensland. Accessed December 13, 2019. http://espace.library.uq.edu.au/view/UQ:8.

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

MLA Handbook (7th Edition):

Pretorius, Lara-Simone. “Investigation of virus-induced defence modulations during plant-virus interactions.” 2018. Web. 13 Dec 2019.

Vancouver:

Pretorius L. Investigation of virus-induced defence modulations during plant-virus interactions. [Internet] [Thesis]. University of Queensland; 2018. [cited 2019 Dec 13]. Available from: http://espace.library.uq.edu.au/view/UQ:8.

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

Council of Science Editors:

Pretorius L. Investigation of virus-induced defence modulations during plant-virus interactions. [Thesis]. University of Queensland; 2018. Available from: http://espace.library.uq.edu.au/view/UQ:8

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

[1] [2]

.