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You searched for subject:( regulation of gene expression). Showing records 1 – 30 of 247294 total matches.

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University of Texas Southwestern Medical Center

1. Young, Melissa Rasar. Paxillin is a Novel Regulator of Xenopus Oocyte Maturation.

Degree: 2010, University of Texas Southwestern Medical Center

 Oocyte maturation is triggered by steroids in a transcription-independent fashion that involves an unusual positive feedback loop whereby MOS (a germ cell specific Raf) activates… (more)

Subjects/Keywords: Oocytes; Paxillin; Gene Expression Regulation

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

APA (6th Edition):

Young, M. R. (2010). Paxillin is a Novel Regulator of Xenopus Oocyte Maturation. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/786

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):

Young, Melissa Rasar. “Paxillin is a Novel Regulator of Xenopus Oocyte Maturation.” 2010. Thesis, University of Texas Southwestern Medical Center. Accessed January 21, 2020. http://hdl.handle.net/2152.5/786.

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

MLA Handbook (7th Edition):

Young, Melissa Rasar. “Paxillin is a Novel Regulator of Xenopus Oocyte Maturation.” 2010. Web. 21 Jan 2020.

Vancouver:

Young MR. Paxillin is a Novel Regulator of Xenopus Oocyte Maturation. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2010. [cited 2020 Jan 21]. Available from: http://hdl.handle.net/2152.5/786.

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

Council of Science Editors:

Young MR. Paxillin is a Novel Regulator of Xenopus Oocyte Maturation. [Thesis]. University of Texas Southwestern Medical Center; 2010. Available from: http://hdl.handle.net/2152.5/786

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


Rutgers University

2. Caratozzolo, Rose Marie, 1978-. Studies of polyadenylation regulation of U1A mRNA by an RNP complex containing U1A and U1 snRNP.

Degree: PhD, Biochemistry, 2011, Rutgers University

The 3’-end processing of nearly all eukaryotic pre-mRNAs comprises multiple steps which culminate in the addition of a poly(A) tail, which is essential for mRNA… (more)

Subjects/Keywords: Gene expression; Genetic regulation; RNA

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APA (6th Edition):

Caratozzolo, Rose Marie, 1. (2011). Studies of polyadenylation regulation of U1A mRNA by an RNP complex containing U1A and U1 snRNP. (Doctoral Dissertation). Rutgers University. Retrieved from http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000057530

Chicago Manual of Style (16th Edition):

Caratozzolo, Rose Marie, 1978-. “Studies of polyadenylation regulation of U1A mRNA by an RNP complex containing U1A and U1 snRNP.” 2011. Doctoral Dissertation, Rutgers University. Accessed January 21, 2020. http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000057530.

MLA Handbook (7th Edition):

Caratozzolo, Rose Marie, 1978-. “Studies of polyadenylation regulation of U1A mRNA by an RNP complex containing U1A and U1 snRNP.” 2011. Web. 21 Jan 2020.

Vancouver:

Caratozzolo, Rose Marie 1. Studies of polyadenylation regulation of U1A mRNA by an RNP complex containing U1A and U1 snRNP. [Internet] [Doctoral dissertation]. Rutgers University; 2011. [cited 2020 Jan 21]. Available from: http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000057530.

Council of Science Editors:

Caratozzolo, Rose Marie 1. Studies of polyadenylation regulation of U1A mRNA by an RNP complex containing U1A and U1 snRNP. [Doctoral Dissertation]. Rutgers University; 2011. Available from: http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000057530

3. LIMA, Gustavo Barbosa de. Avaliação da importância para a viabilidade celular de três homólogos do fator de iniciação da tradução EIF4E de Leishmania sp .

Degree: 2016, Universidade Federal de Pernambuco

 A família de protozoários tripanosomatídeos apresenta características moleculares diferenciadas dos demais eucariotos, onde a regulação da expressão gênica é feita principalmente em nível pós-transcricional. Como… (more)

Subjects/Keywords: eIF4F; EIF4E; Expressão gênica; tripanosomatídeos; eIF4F; Regulation of gene expression; Trypanosomatids

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APA (6th Edition):

LIMA, G. B. d. (2016). Avaliação da importância para a viabilidade celular de três homólogos do fator de iniciação da tradução EIF4E de Leishmania sp . (Masters Thesis). Universidade Federal de Pernambuco. Retrieved from https://repositorio.ufpe.br/handle/123456789/19537

Chicago Manual of Style (16th Edition):

LIMA, Gustavo Barbosa de. “Avaliação da importância para a viabilidade celular de três homólogos do fator de iniciação da tradução EIF4E de Leishmania sp .” 2016. Masters Thesis, Universidade Federal de Pernambuco. Accessed January 21, 2020. https://repositorio.ufpe.br/handle/123456789/19537.

MLA Handbook (7th Edition):

LIMA, Gustavo Barbosa de. “Avaliação da importância para a viabilidade celular de três homólogos do fator de iniciação da tradução EIF4E de Leishmania sp .” 2016. Web. 21 Jan 2020.

Vancouver:

LIMA GBd. Avaliação da importância para a viabilidade celular de três homólogos do fator de iniciação da tradução EIF4E de Leishmania sp . [Internet] [Masters thesis]. Universidade Federal de Pernambuco; 2016. [cited 2020 Jan 21]. Available from: https://repositorio.ufpe.br/handle/123456789/19537.

Council of Science Editors:

LIMA GBd. Avaliação da importância para a viabilidade celular de três homólogos do fator de iniciação da tradução EIF4E de Leishmania sp . [Masters Thesis]. Universidade Federal de Pernambuco; 2016. Available from: https://repositorio.ufpe.br/handle/123456789/19537


Tampere University

4. Pillai, Mukundan. The identification and study of transcription factors and co-factors other than androgen receptor that could have important role in the regulation of gene expression in prostate tumor .

Degree: 2018, Tampere University

 The overall aim of this study is to computationally identify and analyze the nature of transcription factors other than androgen receptor (AR) that play an… (more)

Subjects/Keywords: prostate cancer; androgen receptors; regulation of gene expression; transcription factors; clustering

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APA (6th Edition):

Pillai, M. (2018). The identification and study of transcription factors and co-factors other than androgen receptor that could have important role in the regulation of gene expression in prostate tumor . (Masters Thesis). Tampere University. Retrieved from https://trepo.tuni.fi/handle/10024/104829

Chicago Manual of Style (16th Edition):

Pillai, Mukundan. “The identification and study of transcription factors and co-factors other than androgen receptor that could have important role in the regulation of gene expression in prostate tumor .” 2018. Masters Thesis, Tampere University. Accessed January 21, 2020. https://trepo.tuni.fi/handle/10024/104829.

MLA Handbook (7th Edition):

Pillai, Mukundan. “The identification and study of transcription factors and co-factors other than androgen receptor that could have important role in the regulation of gene expression in prostate tumor .” 2018. Web. 21 Jan 2020.

Vancouver:

Pillai M. The identification and study of transcription factors and co-factors other than androgen receptor that could have important role in the regulation of gene expression in prostate tumor . [Internet] [Masters thesis]. Tampere University; 2018. [cited 2020 Jan 21]. Available from: https://trepo.tuni.fi/handle/10024/104829.

Council of Science Editors:

Pillai M. The identification and study of transcription factors and co-factors other than androgen receptor that could have important role in the regulation of gene expression in prostate tumor . [Masters Thesis]. Tampere University; 2018. Available from: https://trepo.tuni.fi/handle/10024/104829


Univerzitet u Beogradu

5. Pruner, Iva B., 1984-. Funkcionalna analiza genske varijante C20068T u 3' kraju gena za protrombin čoveka i njena uloga u patogenezi trombofilije.

Degree: Biološki fakultet, 2016, Univerzitet u Beogradu

Biologija - Molekularna biologija / Biology - Molecular biology

Protrombin (Faktor II) je prekursor trombina, jednog od ključnih molekula u održavanju hemostazne ravnoteže. Povišeni nivo… (more)

Subjects/Keywords: prothrombin; 3end of the prothrombin gene; C20068T gene variant; synonymous gene variant; gene expression regulation; thrombophilia

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APA (6th Edition):

Pruner, Iva B., 1. (2016). Funkcionalna analiza genske varijante C20068T u 3' kraju gena za protrombin čoveka i njena uloga u patogenezi trombofilije. (Thesis). Univerzitet u Beogradu. Retrieved from https://fedorabg.bg.ac.rs/fedora/get/o:11393/bdef:Content/get

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):

Pruner, Iva B., 1984-. “Funkcionalna analiza genske varijante C20068T u 3' kraju gena za protrombin čoveka i njena uloga u patogenezi trombofilije.” 2016. Thesis, Univerzitet u Beogradu. Accessed January 21, 2020. https://fedorabg.bg.ac.rs/fedora/get/o:11393/bdef:Content/get.

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

MLA Handbook (7th Edition):

Pruner, Iva B., 1984-. “Funkcionalna analiza genske varijante C20068T u 3' kraju gena za protrombin čoveka i njena uloga u patogenezi trombofilije.” 2016. Web. 21 Jan 2020.

Vancouver:

Pruner, Iva B. 1. Funkcionalna analiza genske varijante C20068T u 3' kraju gena za protrombin čoveka i njena uloga u patogenezi trombofilije. [Internet] [Thesis]. Univerzitet u Beogradu; 2016. [cited 2020 Jan 21]. Available from: https://fedorabg.bg.ac.rs/fedora/get/o:11393/bdef:Content/get.

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

Council of Science Editors:

Pruner, Iva B. 1. Funkcionalna analiza genske varijante C20068T u 3' kraju gena za protrombin čoveka i njena uloga u patogenezi trombofilije. [Thesis]. Univerzitet u Beogradu; 2016. Available from: https://fedorabg.bg.ac.rs/fedora/get/o:11393/bdef:Content/get

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


University of Saskatchewan

6. Narayanan, Karthikeyan. SCREENING AND CHARACTERIZATION OF ARABIDOPSIS THALIANA MUTANTS WITH ALTERED CAROTENOID PROFILE.

Degree: 2014, University of Saskatchewan

 Carotenoids are organic pigments that are mainly found in the chloroplasts and chromoplasts of plants and other photosynthetic organisms. Carotenoid molecules containing oxygen, such as… (more)

Subjects/Keywords: Carotneoids; RBP47; KCS19; Gene expression; Gene regulation

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APA (6th Edition):

Narayanan, K. (2014). SCREENING AND CHARACTERIZATION OF ARABIDOPSIS THALIANA MUTANTS WITH ALTERED CAROTENOID PROFILE. (Thesis). University of Saskatchewan. Retrieved from http://hdl.handle.net/10388/ETD-2014-06-1601

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):

Narayanan, Karthikeyan. “SCREENING AND CHARACTERIZATION OF ARABIDOPSIS THALIANA MUTANTS WITH ALTERED CAROTENOID PROFILE.” 2014. Thesis, University of Saskatchewan. Accessed January 21, 2020. http://hdl.handle.net/10388/ETD-2014-06-1601.

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

MLA Handbook (7th Edition):

Narayanan, Karthikeyan. “SCREENING AND CHARACTERIZATION OF ARABIDOPSIS THALIANA MUTANTS WITH ALTERED CAROTENOID PROFILE.” 2014. Web. 21 Jan 2020.

Vancouver:

Narayanan K. SCREENING AND CHARACTERIZATION OF ARABIDOPSIS THALIANA MUTANTS WITH ALTERED CAROTENOID PROFILE. [Internet] [Thesis]. University of Saskatchewan; 2014. [cited 2020 Jan 21]. Available from: http://hdl.handle.net/10388/ETD-2014-06-1601.

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

Council of Science Editors:

Narayanan K. SCREENING AND CHARACTERIZATION OF ARABIDOPSIS THALIANA MUTANTS WITH ALTERED CAROTENOID PROFILE. [Thesis]. University of Saskatchewan; 2014. Available from: http://hdl.handle.net/10388/ETD-2014-06-1601

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

7. Alasoo, Kaur. Regulation of gene expression in macrophage immune response.

Degree: PhD, 2017, University of Cambridge

Gene expression quantitative trait loci (eQTL) mapping studies can provide mechanistic insights into the functions of disease-associated variants. However, many eQTLs are cell type and… (more)

Subjects/Keywords: Gene expression; Gene regulation; Chromatin; Genetics

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APA (6th Edition):

Alasoo, K. (2017). Regulation of gene expression in macrophage immune response. (Doctoral Dissertation). University of Cambridge. Retrieved from https://www.repository.cam.ac.uk/handle/1810/263855

Chicago Manual of Style (16th Edition):

Alasoo, Kaur. “Regulation of gene expression in macrophage immune response.” 2017. Doctoral Dissertation, University of Cambridge. Accessed January 21, 2020. https://www.repository.cam.ac.uk/handle/1810/263855.

MLA Handbook (7th Edition):

Alasoo, Kaur. “Regulation of gene expression in macrophage immune response.” 2017. Web. 21 Jan 2020.

Vancouver:

Alasoo K. Regulation of gene expression in macrophage immune response. [Internet] [Doctoral dissertation]. University of Cambridge; 2017. [cited 2020 Jan 21]. Available from: https://www.repository.cam.ac.uk/handle/1810/263855.

Council of Science Editors:

Alasoo K. Regulation of gene expression in macrophage immune response. [Doctoral Dissertation]. University of Cambridge; 2017. Available from: https://www.repository.cam.ac.uk/handle/1810/263855


University of Cambridge

8. Alasoo, Kaur. Regulation of gene expression in macrophage immune response.

Degree: PhD, 2017, University of Cambridge

Gene expression quantitative trait loci (eQTL) mapping studies can provide mechanistic insights into the functions of disease-associated variants. However, many eQTLs are cell type and… (more)

Subjects/Keywords: 616.07; Gene expression; Gene regulation; Chromatin; Genetics

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APA (6th Edition):

Alasoo, K. (2017). Regulation of gene expression in macrophage immune response. (Doctoral Dissertation). University of Cambridge. Retrieved from https://www.repository.cam.ac.uk/handle/1810/263855 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.715945

Chicago Manual of Style (16th Edition):

Alasoo, Kaur. “Regulation of gene expression in macrophage immune response.” 2017. Doctoral Dissertation, University of Cambridge. Accessed January 21, 2020. https://www.repository.cam.ac.uk/handle/1810/263855 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.715945.

MLA Handbook (7th Edition):

Alasoo, Kaur. “Regulation of gene expression in macrophage immune response.” 2017. Web. 21 Jan 2020.

Vancouver:

Alasoo K. Regulation of gene expression in macrophage immune response. [Internet] [Doctoral dissertation]. University of Cambridge; 2017. [cited 2020 Jan 21]. Available from: https://www.repository.cam.ac.uk/handle/1810/263855 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.715945.

Council of Science Editors:

Alasoo K. Regulation of gene expression in macrophage immune response. [Doctoral Dissertation]. University of Cambridge; 2017. Available from: https://www.repository.cam.ac.uk/handle/1810/263855 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.715945

9. Velloso, Fernando Janczur. Expressão de isoformas da proteína do retardo mental do X frágil (FMRP) e sua regulação.

Degree: Mestrado, Biologia (Genética), 2008, University of São Paulo

Entre as modificações sofridas pelo transcrito primário de RNA de eucariontes, o splicing é responsável pela colocação lado a lado das sequências expressas alinhando a… (more)

Subjects/Keywords: splicing; splicing; FMR1; FMR1; Regulação da expressão gênica; Regulation of gene expression

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APA (6th Edition):

Velloso, F. J. (2008). Expressão de isoformas da proteína do retardo mental do X frágil (FMRP) e sua regulação. (Masters Thesis). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/41/41131/tde-19032009-144613/ ;

Chicago Manual of Style (16th Edition):

Velloso, Fernando Janczur. “Expressão de isoformas da proteína do retardo mental do X frágil (FMRP) e sua regulação.” 2008. Masters Thesis, University of São Paulo. Accessed January 21, 2020. http://www.teses.usp.br/teses/disponiveis/41/41131/tde-19032009-144613/ ;.

MLA Handbook (7th Edition):

Velloso, Fernando Janczur. “Expressão de isoformas da proteína do retardo mental do X frágil (FMRP) e sua regulação.” 2008. Web. 21 Jan 2020.

Vancouver:

Velloso FJ. Expressão de isoformas da proteína do retardo mental do X frágil (FMRP) e sua regulação. [Internet] [Masters thesis]. University of São Paulo; 2008. [cited 2020 Jan 21]. Available from: http://www.teses.usp.br/teses/disponiveis/41/41131/tde-19032009-144613/ ;.

Council of Science Editors:

Velloso FJ. Expressão de isoformas da proteína do retardo mental do X frágil (FMRP) e sua regulação. [Masters Thesis]. University of São Paulo; 2008. Available from: http://www.teses.usp.br/teses/disponiveis/41/41131/tde-19032009-144613/ ;


University of Pennsylvania

10. Brady, Lauren Kathleen. Transcriptome-Wide Analysis Of Hypoxic Cancer Cells Identify Alternative Splicing As A Mechanism To Inhibit Translation.

Degree: 2017, University of Pennsylvania

 Cellular adaptation to hypoxia involves downregulation of energy-consuming processes such as macromolecular synthesis, and leads to tumor aggressiveness and resistance to therapies for many solid… (more)

Subjects/Keywords: Alternative splicing; Hypoxia; Regulation of gene expression; Translational control; Tumor microenvironment; Bioinformatics; Genetics; Molecular Biology

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APA (6th Edition):

Brady, L. K. (2017). Transcriptome-Wide Analysis Of Hypoxic Cancer Cells Identify Alternative Splicing As A Mechanism To Inhibit Translation. (Thesis). University of Pennsylvania. Retrieved from https://repository.upenn.edu/edissertations/2196

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):

Brady, Lauren Kathleen. “Transcriptome-Wide Analysis Of Hypoxic Cancer Cells Identify Alternative Splicing As A Mechanism To Inhibit Translation.” 2017. Thesis, University of Pennsylvania. Accessed January 21, 2020. https://repository.upenn.edu/edissertations/2196.

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

MLA Handbook (7th Edition):

Brady, Lauren Kathleen. “Transcriptome-Wide Analysis Of Hypoxic Cancer Cells Identify Alternative Splicing As A Mechanism To Inhibit Translation.” 2017. Web. 21 Jan 2020.

Vancouver:

Brady LK. Transcriptome-Wide Analysis Of Hypoxic Cancer Cells Identify Alternative Splicing As A Mechanism To Inhibit Translation. [Internet] [Thesis]. University of Pennsylvania; 2017. [cited 2020 Jan 21]. Available from: https://repository.upenn.edu/edissertations/2196.

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

Council of Science Editors:

Brady LK. Transcriptome-Wide Analysis Of Hypoxic Cancer Cells Identify Alternative Splicing As A Mechanism To Inhibit Translation. [Thesis]. University of Pennsylvania; 2017. Available from: https://repository.upenn.edu/edissertations/2196

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


University of Alberta

11. Gesner, Emily. Structural and Functional Characterization of T.thermophilus CasE.

Degree: PhD, Department of Biochemistry, 2011, University of Alberta

 Powerful mechanisms of genetic interference in both unicellular and multicellular organisms are based on the sequence-directed targeting of DNA or RNA by small effector RNAs.… (more)

Subjects/Keywords: CRISPR, RNA, Prokaryotes, gene expression regulation, endonuclease

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APA (6th Edition):

Gesner, E. (2011). Structural and Functional Characterization of T.thermophilus CasE. (Doctoral Dissertation). University of Alberta. Retrieved from https://era.library.ualberta.ca/files/3b591b15d

Chicago Manual of Style (16th Edition):

Gesner, Emily. “Structural and Functional Characterization of T.thermophilus CasE.” 2011. Doctoral Dissertation, University of Alberta. Accessed January 21, 2020. https://era.library.ualberta.ca/files/3b591b15d.

MLA Handbook (7th Edition):

Gesner, Emily. “Structural and Functional Characterization of T.thermophilus CasE.” 2011. Web. 21 Jan 2020.

Vancouver:

Gesner E. Structural and Functional Characterization of T.thermophilus CasE. [Internet] [Doctoral dissertation]. University of Alberta; 2011. [cited 2020 Jan 21]. Available from: https://era.library.ualberta.ca/files/3b591b15d.

Council of Science Editors:

Gesner E. Structural and Functional Characterization of T.thermophilus CasE. [Doctoral Dissertation]. University of Alberta; 2011. Available from: https://era.library.ualberta.ca/files/3b591b15d


University of Southern California

12. Zhang, Jing. Isoform quantification and splicing regulation analysis in RNA-seq studies.

Degree: PhD, Electrical Engineering, 2015, University of Southern California

 The rapid advances in high-throughput sequencing technologies provide us an opportunity to dissect transcriptomes with unprecedented resolution. Based on RNA-seq studies, alternative splicing has become… (more)

Subjects/Keywords: RNA-seq; alternative splicing; gene expression regulation

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APA (6th Edition):

Zhang, J. (2015). Isoform quantification and splicing regulation analysis in RNA-seq studies. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/343497/rec/3662

Chicago Manual of Style (16th Edition):

Zhang, Jing. “Isoform quantification and splicing regulation analysis in RNA-seq studies.” 2015. Doctoral Dissertation, University of Southern California. Accessed January 21, 2020. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/343497/rec/3662.

MLA Handbook (7th Edition):

Zhang, Jing. “Isoform quantification and splicing regulation analysis in RNA-seq studies.” 2015. Web. 21 Jan 2020.

Vancouver:

Zhang J. Isoform quantification and splicing regulation analysis in RNA-seq studies. [Internet] [Doctoral dissertation]. University of Southern California; 2015. [cited 2020 Jan 21]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/343497/rec/3662.

Council of Science Editors:

Zhang J. Isoform quantification and splicing regulation analysis in RNA-seq studies. [Doctoral Dissertation]. University of Southern California; 2015. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/343497/rec/3662


University of Victoria

13. Busby, Ellen Rain. Expression, regulation and evolution of proglucagon genes in vertebrates.

Degree: Department of Biochemistry and Microbiology, 2018, University of Victoria

 Three biologically active peptide hormones, glucagon, glucagon-like peptide (GLP)-1, and GLP-2, are co-encoded by the precursor proglucagon. As all three peptides have distinct functions, regulation(more)

Subjects/Keywords: Gene expression; Genetic regulation; Vertebrates; Genetics

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APA (6th Edition):

Busby, E. R. (2018). Expression, regulation and evolution of proglucagon genes in vertebrates. (Thesis). University of Victoria. Retrieved from https://dspace.library.uvic.ca//handle/1828/10358

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):

Busby, Ellen Rain. “Expression, regulation and evolution of proglucagon genes in vertebrates.” 2018. Thesis, University of Victoria. Accessed January 21, 2020. https://dspace.library.uvic.ca//handle/1828/10358.

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

MLA Handbook (7th Edition):

Busby, Ellen Rain. “Expression, regulation and evolution of proglucagon genes in vertebrates.” 2018. Web. 21 Jan 2020.

Vancouver:

Busby ER. Expression, regulation and evolution of proglucagon genes in vertebrates. [Internet] [Thesis]. University of Victoria; 2018. [cited 2020 Jan 21]. Available from: https://dspace.library.uvic.ca//handle/1828/10358.

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

Council of Science Editors:

Busby ER. Expression, regulation and evolution of proglucagon genes in vertebrates. [Thesis]. University of Victoria; 2018. Available from: https://dspace.library.uvic.ca//handle/1828/10358

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

14. Attanasio, Catia. Evaluation of the regulatory potential of HSA21q conserved non-coding sequences (CNCs).

Degree: 2007, Université de Genève

 The comparative analysis of the human and mouse genomes has resulted in the identification of a large number of evolutionarily conserved sequences. The occurence of… (more)

Subjects/Keywords: gene expression regulation

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

APA (6th Edition):

Attanasio, C. (2007). Evaluation of the regulatory potential of HSA21q conserved non-coding sequences (CNCs). (Thesis). Université de Genève. Retrieved from http://doc.rero.ch/record/8776

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):

Attanasio, Catia. “Evaluation of the regulatory potential of HSA21q conserved non-coding sequences (CNCs).” 2007. Thesis, Université de Genève. Accessed January 21, 2020. http://doc.rero.ch/record/8776.

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

MLA Handbook (7th Edition):

Attanasio, Catia. “Evaluation of the regulatory potential of HSA21q conserved non-coding sequences (CNCs).” 2007. Web. 21 Jan 2020.

Vancouver:

Attanasio C. Evaluation of the regulatory potential of HSA21q conserved non-coding sequences (CNCs). [Internet] [Thesis]. Université de Genève; 2007. [cited 2020 Jan 21]. Available from: http://doc.rero.ch/record/8776.

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

Council of Science Editors:

Attanasio C. Evaluation of the regulatory potential of HSA21q conserved non-coding sequences (CNCs). [Thesis]. Université de Genève; 2007. Available from: http://doc.rero.ch/record/8776

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


Rutgers University

15. Li, You. Regulation of mammalian mRNA decapping.

Degree: PhD, Cell and Developmental Biology, 2011, Rutgers University

The modulation of mRNA degradation plays a critical role for regulation of gene expression. A major mRNA decay pathway in mammals proceeding from the 5'… (more)

Subjects/Keywords: Messenger RNA; Gene expression; Genetic regulation

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

APA (6th Edition):

Li, Y. (2011). Regulation of mammalian mRNA decapping. (Doctoral Dissertation). Rutgers University. Retrieved from http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000061329

Chicago Manual of Style (16th Edition):

Li, You. “Regulation of mammalian mRNA decapping.” 2011. Doctoral Dissertation, Rutgers University. Accessed January 21, 2020. http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000061329.

MLA Handbook (7th Edition):

Li, You. “Regulation of mammalian mRNA decapping.” 2011. Web. 21 Jan 2020.

Vancouver:

Li Y. Regulation of mammalian mRNA decapping. [Internet] [Doctoral dissertation]. Rutgers University; 2011. [cited 2020 Jan 21]. Available from: http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000061329.

Council of Science Editors:

Li Y. Regulation of mammalian mRNA decapping. [Doctoral Dissertation]. Rutgers University; 2011. Available from: http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000061329


Rutgers University

16. Hammond, Gifty Naa Ayeley, 1981-. Defining the nanoRNA regulon and the mechanism by which gene expression is controlled and manifested.

Degree: MS, Microbiology and Molecular Genetics, 2014, Rutgers University

Gene transcription is mediated by the enzyme RNA polymerase (RNAP). RNAP is a multi subunit nucleotidyl transferase that polymerizes ribonucleotides at the 3’ end of… (more)

Subjects/Keywords: Gene expression; Genetic regulation; Reverse transcriptase

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APA (6th Edition):

Hammond, Gifty Naa Ayeley, 1. (2014). Defining the nanoRNA regulon and the mechanism by which gene expression is controlled and manifested. (Masters Thesis). Rutgers University. Retrieved from https://rucore.libraries.rutgers.edu/rutgers-lib/42394/

Chicago Manual of Style (16th Edition):

Hammond, Gifty Naa Ayeley, 1981-. “Defining the nanoRNA regulon and the mechanism by which gene expression is controlled and manifested.” 2014. Masters Thesis, Rutgers University. Accessed January 21, 2020. https://rucore.libraries.rutgers.edu/rutgers-lib/42394/.

MLA Handbook (7th Edition):

Hammond, Gifty Naa Ayeley, 1981-. “Defining the nanoRNA regulon and the mechanism by which gene expression is controlled and manifested.” 2014. Web. 21 Jan 2020.

Vancouver:

Hammond, Gifty Naa Ayeley 1. Defining the nanoRNA regulon and the mechanism by which gene expression is controlled and manifested. [Internet] [Masters thesis]. Rutgers University; 2014. [cited 2020 Jan 21]. Available from: https://rucore.libraries.rutgers.edu/rutgers-lib/42394/.

Council of Science Editors:

Hammond, Gifty Naa Ayeley 1. Defining the nanoRNA regulon and the mechanism by which gene expression is controlled and manifested. [Masters Thesis]. Rutgers University; 2014. Available from: https://rucore.libraries.rutgers.edu/rutgers-lib/42394/


Jawaharlal Nehru University

17. Saha, Gautam Kumar. Mechanism of regulation of c-jun gene expression; -.

Degree: Biotechnology, 2005, Jawaharlal Nehru University

None

Bibliography p.86-103 Appendices p.104-106

Advisors/Committee Members: Dixit, Aparna.

Subjects/Keywords: Biotechnology; regulation of c-jun gene; gene expression; Mechanism

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APA (6th Edition):

Saha, G. K. (2005). Mechanism of regulation of c-jun gene expression; -. (Thesis). Jawaharlal Nehru University. Retrieved from http://shodhganga.inflibnet.ac.in/handle/10603/18881

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):

Saha, Gautam Kumar. “Mechanism of regulation of c-jun gene expression; -.” 2005. Thesis, Jawaharlal Nehru University. Accessed January 21, 2020. http://shodhganga.inflibnet.ac.in/handle/10603/18881.

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

MLA Handbook (7th Edition):

Saha, Gautam Kumar. “Mechanism of regulation of c-jun gene expression; -.” 2005. Web. 21 Jan 2020.

Vancouver:

Saha GK. Mechanism of regulation of c-jun gene expression; -. [Internet] [Thesis]. Jawaharlal Nehru University; 2005. [cited 2020 Jan 21]. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/18881.

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

Council of Science Editors:

Saha GK. Mechanism of regulation of c-jun gene expression; -. [Thesis]. Jawaharlal Nehru University; 2005. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/18881

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


Univerzitet u Beogradu

18. Gvozdenov, Maja Ž., 1988-. Funkcionalna analiza genskih varijanti FIIc.1787G>A (protrombin, Beograd) i FIIc.*64_*66del i njihova povezanost sa trombofolijom.

Degree: Biološki fakultet, 2017, Univerzitet u Beogradu

Biologija - Molekularna biologija / Biology - Molecular biology

Protrombin predstavlja zimogen trombina (koagulacinog faktora II), koji ima centralnu ulogu u održanju hemostazne ravnoteže. Zahvaljujući… (more)

Subjects/Keywords: FIIc.1787G>; A, prothrombin Belgrade, FIIc.*64_*66del, prothrombin, 3end of gene, antithrombin resistance, gene expression regulation, thrombophilia

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APA (6th Edition):

Gvozdenov, Maja Ž., 1. (2017). Funkcionalna analiza genskih varijanti FIIc.1787G>A (protrombin, Beograd) i FIIc.*64_*66del i njihova povezanost sa trombofolijom. (Thesis). Univerzitet u Beogradu. Retrieved from https://fedorabg.bg.ac.rs/fedora/get/o:15910/bdef:Content/get

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):

Gvozdenov, Maja Ž., 1988-. “Funkcionalna analiza genskih varijanti FIIc.1787G>A (protrombin, Beograd) i FIIc.*64_*66del i njihova povezanost sa trombofolijom.” 2017. Thesis, Univerzitet u Beogradu. Accessed January 21, 2020. https://fedorabg.bg.ac.rs/fedora/get/o:15910/bdef:Content/get.

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

MLA Handbook (7th Edition):

Gvozdenov, Maja Ž., 1988-. “Funkcionalna analiza genskih varijanti FIIc.1787G>A (protrombin, Beograd) i FIIc.*64_*66del i njihova povezanost sa trombofolijom.” 2017. Web. 21 Jan 2020.

Vancouver:

Gvozdenov, Maja Ž. 1. Funkcionalna analiza genskih varijanti FIIc.1787G>A (protrombin, Beograd) i FIIc.*64_*66del i njihova povezanost sa trombofolijom. [Internet] [Thesis]. Univerzitet u Beogradu; 2017. [cited 2020 Jan 21]. Available from: https://fedorabg.bg.ac.rs/fedora/get/o:15910/bdef:Content/get.

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

Council of Science Editors:

Gvozdenov, Maja Ž. 1. Funkcionalna analiza genskih varijanti FIIc.1787G>A (protrombin, Beograd) i FIIc.*64_*66del i njihova povezanost sa trombofolijom. [Thesis]. Univerzitet u Beogradu; 2017. Available from: https://fedorabg.bg.ac.rs/fedora/get/o:15910/bdef:Content/get

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


Massey University

19. Yang, Tian. Development of a tetracycline-inducible lentiviral vector with an instant regulatory system.

Degree: MSc, Biochemistry, 2013, Massey University

 Lentiviral vectors, originally derived from human immunodeficiency virus, provide highly efficient viral gene delivery vehicles. Lentiviral vectors often use a constitutive promoter to drive the… (more)

Subjects/Keywords: Lentiviral vectors; Gene therapy; Gene expression; Gene regulation; Tetracycline; Genetic vectors

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APA (6th Edition):

Yang, T. (2013). Development of a tetracycline-inducible lentiviral vector with an instant regulatory system. (Masters Thesis). Massey University. Retrieved from http://hdl.handle.net/10179/4319

Chicago Manual of Style (16th Edition):

Yang, Tian. “Development of a tetracycline-inducible lentiviral vector with an instant regulatory system.” 2013. Masters Thesis, Massey University. Accessed January 21, 2020. http://hdl.handle.net/10179/4319.

MLA Handbook (7th Edition):

Yang, Tian. “Development of a tetracycline-inducible lentiviral vector with an instant regulatory system.” 2013. Web. 21 Jan 2020.

Vancouver:

Yang T. Development of a tetracycline-inducible lentiviral vector with an instant regulatory system. [Internet] [Masters thesis]. Massey University; 2013. [cited 2020 Jan 21]. Available from: http://hdl.handle.net/10179/4319.

Council of Science Editors:

Yang T. Development of a tetracycline-inducible lentiviral vector with an instant regulatory system. [Masters Thesis]. Massey University; 2013. Available from: http://hdl.handle.net/10179/4319

20. Meireles, Diogo de Abreu. Estudo da função do gene kerV de Pseudomonas aeruginosa.

Degree: PhD, Bioquímica, 2011, University of São Paulo

 P. aeruginosa PA14 é uma linhagem isolada de queimadura que apresenta vários fatores de patogenicidade comuns no quadro de infecção de hospedeiros filogeneticamente distintos (plantas,… (more)

Subjects/Keywords: Gene regulation; Metiltransferase dependentes de S-adenosil-metionina; Pathogenicity; Patogenicidade; Pseudomonas aeruginosa; Pseudomonas aeruginosa; Regulação da expressão gênica; Regulação gênica; Regulation of gene expression; SAM dependent methyltransferase

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APA (6th Edition):

Meireles, D. d. A. (2011). Estudo da função do gene kerV de Pseudomonas aeruginosa. (Doctoral Dissertation). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/46/46131/tde-05122011-150318/ ;

Chicago Manual of Style (16th Edition):

Meireles, Diogo de Abreu. “Estudo da função do gene kerV de Pseudomonas aeruginosa.” 2011. Doctoral Dissertation, University of São Paulo. Accessed January 21, 2020. http://www.teses.usp.br/teses/disponiveis/46/46131/tde-05122011-150318/ ;.

MLA Handbook (7th Edition):

Meireles, Diogo de Abreu. “Estudo da função do gene kerV de Pseudomonas aeruginosa.” 2011. Web. 21 Jan 2020.

Vancouver:

Meireles DdA. Estudo da função do gene kerV de Pseudomonas aeruginosa. [Internet] [Doctoral dissertation]. University of São Paulo; 2011. [cited 2020 Jan 21]. Available from: http://www.teses.usp.br/teses/disponiveis/46/46131/tde-05122011-150318/ ;.

Council of Science Editors:

Meireles DdA. Estudo da função do gene kerV de Pseudomonas aeruginosa. [Doctoral Dissertation]. University of São Paulo; 2011. Available from: http://www.teses.usp.br/teses/disponiveis/46/46131/tde-05122011-150318/ ;


Columbia University

21. Lachmann, Alexander. Confounding effects in gene expression and their impact on downstream analysis.

Degree: 2016, Columbia University

 The reconstruction of gene regulatory networks is one of the milestones of computational system biology. We introduce a new implementation of ARACNe (Algorithm for the… (more)

Subjects/Keywords: Genetic regulation; Genetic regulation – Data processing; Gene expression; Gene expression – Data processing; Bioinformatics; Gene regulatory networks; Genetics

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APA (6th Edition):

Lachmann, A. (2016). Confounding effects in gene expression and their impact on downstream analysis. (Doctoral Dissertation). Columbia University. Retrieved from https://doi.org/10.7916/D82J6BRF

Chicago Manual of Style (16th Edition):

Lachmann, Alexander. “Confounding effects in gene expression and their impact on downstream analysis.” 2016. Doctoral Dissertation, Columbia University. Accessed January 21, 2020. https://doi.org/10.7916/D82J6BRF.

MLA Handbook (7th Edition):

Lachmann, Alexander. “Confounding effects in gene expression and their impact on downstream analysis.” 2016. Web. 21 Jan 2020.

Vancouver:

Lachmann A. Confounding effects in gene expression and their impact on downstream analysis. [Internet] [Doctoral dissertation]. Columbia University; 2016. [cited 2020 Jan 21]. Available from: https://doi.org/10.7916/D82J6BRF.

Council of Science Editors:

Lachmann A. Confounding effects in gene expression and their impact on downstream analysis. [Doctoral Dissertation]. Columbia University; 2016. Available from: https://doi.org/10.7916/D82J6BRF

22. Vineetha, S. “Reconstruction of Gene Regulatory Network from Expression Profile of Plasma RNA Data of Colorectal Cancer Patients using Soft Computing Techniques”.

Degree: 2012, Cochin University of Science and Technology

Microarray data analysis is one of data mining tool which is used to extract meaningful information hidden in biological data. One of the major focuses… (more)

Subjects/Keywords: Gene Expression Dataset; Colorectal Cancer; Colon Carcinogenesis; Gene Regulation

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APA (6th Edition):

Vineetha, S. (2012). “Reconstruction of Gene Regulatory Network from Expression Profile of Plasma RNA Data of Colorectal Cancer Patients using Soft Computing Techniques”. (Thesis). Cochin University of Science and Technology. Retrieved from http://dyuthi.cusat.ac.in/purl/3760

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):

Vineetha, S. ““Reconstruction of Gene Regulatory Network from Expression Profile of Plasma RNA Data of Colorectal Cancer Patients using Soft Computing Techniques”.” 2012. Thesis, Cochin University of Science and Technology. Accessed January 21, 2020. http://dyuthi.cusat.ac.in/purl/3760.

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

MLA Handbook (7th Edition):

Vineetha, S. ““Reconstruction of Gene Regulatory Network from Expression Profile of Plasma RNA Data of Colorectal Cancer Patients using Soft Computing Techniques”.” 2012. Web. 21 Jan 2020.

Vancouver:

Vineetha S. “Reconstruction of Gene Regulatory Network from Expression Profile of Plasma RNA Data of Colorectal Cancer Patients using Soft Computing Techniques”. [Internet] [Thesis]. Cochin University of Science and Technology; 2012. [cited 2020 Jan 21]. Available from: http://dyuthi.cusat.ac.in/purl/3760.

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

Council of Science Editors:

Vineetha S. “Reconstruction of Gene Regulatory Network from Expression Profile of Plasma RNA Data of Colorectal Cancer Patients using Soft Computing Techniques”. [Thesis]. Cochin University of Science and Technology; 2012. Available from: http://dyuthi.cusat.ac.in/purl/3760

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


University of Saskatchewan

23. Degenhardt, Rory Frank. The Ribosomal Protein L23a Family of Arabidopsis thaliana.

Degree: 2008, University of Saskatchewan

 The 80 S cytoplasmic ribosome is the largest of three populations of ribosomes responsible for protein synthesis in plants. It is comprised of two RNA/protein… (more)

Subjects/Keywords: gene regulation; gene expression

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APA (6th Edition):

Degenhardt, R. F. (2008). The Ribosomal Protein L23a Family of Arabidopsis thaliana. (Thesis). University of Saskatchewan. Retrieved from http://hdl.handle.net/10388/etd-07142008-061230

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):

Degenhardt, Rory Frank. “The Ribosomal Protein L23a Family of Arabidopsis thaliana.” 2008. Thesis, University of Saskatchewan. Accessed January 21, 2020. http://hdl.handle.net/10388/etd-07142008-061230.

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

MLA Handbook (7th Edition):

Degenhardt, Rory Frank. “The Ribosomal Protein L23a Family of Arabidopsis thaliana.” 2008. Web. 21 Jan 2020.

Vancouver:

Degenhardt RF. The Ribosomal Protein L23a Family of Arabidopsis thaliana. [Internet] [Thesis]. University of Saskatchewan; 2008. [cited 2020 Jan 21]. Available from: http://hdl.handle.net/10388/etd-07142008-061230.

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

Council of Science Editors:

Degenhardt RF. The Ribosomal Protein L23a Family of Arabidopsis thaliana. [Thesis]. University of Saskatchewan; 2008. Available from: http://hdl.handle.net/10388/etd-07142008-061230

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


Cornell University

24. Kremling, Karl. Regulators of expression in Zea mays .

Degree: 2018, Cornell University

 To assess the impact of regulatory variation on a genomic scale, a large scale gene expression resource was created from seven tissues profiled using 3’… (more)

Subjects/Keywords: GWAS; eQTL; transcriptome; Genetics; Gene regulation; Gene expression; Agriculture; Plant sciences

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APA (6th Edition):

Kremling, K. (2018). Regulators of expression in Zea mays . (Thesis). Cornell University. Retrieved from http://hdl.handle.net/1813/59415

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):

Kremling, Karl. “Regulators of expression in Zea mays .” 2018. Thesis, Cornell University. Accessed January 21, 2020. http://hdl.handle.net/1813/59415.

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

MLA Handbook (7th Edition):

Kremling, Karl. “Regulators of expression in Zea mays .” 2018. Web. 21 Jan 2020.

Vancouver:

Kremling K. Regulators of expression in Zea mays . [Internet] [Thesis]. Cornell University; 2018. [cited 2020 Jan 21]. Available from: http://hdl.handle.net/1813/59415.

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

Council of Science Editors:

Kremling K. Regulators of expression in Zea mays . [Thesis]. Cornell University; 2018. Available from: http://hdl.handle.net/1813/59415

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


University of Manitoba

25. Lei, Lei. Differential roles of RNA binding proteins hnRNP L and LL in hormone production in rat pituitary cells.

Degree: Physiology and Pathophysiology, 2015, University of Manitoba

 OBJECTIVES: The role of heterogeneous nuclear ribonucleoproteins in controlling hormone production is not well-understood. This study aims to determine the regulatory roles of hnRNP L… (more)

Subjects/Keywords: Endocrine; Hormones; RNA; Splicing; Processing; Gene regulation; Gene expression; Molecular biology

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APA (6th Edition):

Lei, L. (2015). Differential roles of RNA binding proteins hnRNP L and LL in hormone production in rat pituitary cells. (Masters Thesis). University of Manitoba. Retrieved from http://hdl.handle.net/1993/30848

Chicago Manual of Style (16th Edition):

Lei, Lei. “Differential roles of RNA binding proteins hnRNP L and LL in hormone production in rat pituitary cells.” 2015. Masters Thesis, University of Manitoba. Accessed January 21, 2020. http://hdl.handle.net/1993/30848.

MLA Handbook (7th Edition):

Lei, Lei. “Differential roles of RNA binding proteins hnRNP L and LL in hormone production in rat pituitary cells.” 2015. Web. 21 Jan 2020.

Vancouver:

Lei L. Differential roles of RNA binding proteins hnRNP L and LL in hormone production in rat pituitary cells. [Internet] [Masters thesis]. University of Manitoba; 2015. [cited 2020 Jan 21]. Available from: http://hdl.handle.net/1993/30848.

Council of Science Editors:

Lei L. Differential roles of RNA binding proteins hnRNP L and LL in hormone production in rat pituitary cells. [Masters Thesis]. University of Manitoba; 2015. Available from: http://hdl.handle.net/1993/30848


IUPUI

26. Robison, Jennifer Dawn. Molecular and Physiological Responses of Soybean (Glycine max) to Cold and the Stress Hormone Ethylene.

Degree: 2019, IUPUI

Indiana University-Purdue University Indianapolis (IUPUI)

Abiotic stresses, such as cold, are serious agricultural problems resulting in substantial crop and revenue losses. Soybean (Glycine max) is… (more)

Subjects/Keywords: CBF/DREB; Ethylene; Cold stress; Gene expression; Gene regulation; Soybean; Photosynthesis

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APA (6th Edition):

Robison, J. D. (2019). Molecular and Physiological Responses of Soybean (Glycine max) to Cold and the Stress Hormone Ethylene. (Thesis). IUPUI. Retrieved from http://hdl.handle.net/1805/18927

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):

Robison, Jennifer Dawn. “Molecular and Physiological Responses of Soybean (Glycine max) to Cold and the Stress Hormone Ethylene.” 2019. Thesis, IUPUI. Accessed January 21, 2020. http://hdl.handle.net/1805/18927.

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

MLA Handbook (7th Edition):

Robison, Jennifer Dawn. “Molecular and Physiological Responses of Soybean (Glycine max) to Cold and the Stress Hormone Ethylene.” 2019. Web. 21 Jan 2020.

Vancouver:

Robison JD. Molecular and Physiological Responses of Soybean (Glycine max) to Cold and the Stress Hormone Ethylene. [Internet] [Thesis]. IUPUI; 2019. [cited 2020 Jan 21]. Available from: http://hdl.handle.net/1805/18927.

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

Council of Science Editors:

Robison JD. Molecular and Physiological Responses of Soybean (Glycine max) to Cold and the Stress Hormone Ethylene. [Thesis]. IUPUI; 2019. Available from: http://hdl.handle.net/1805/18927

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


Massey University

27. Hayashi, Amanda Aparecida. Regulation of protein synthesis in the mammary gland.

Degree: PhD, Animal Science, 2007, Massey University

 This thesis examines the signaling pathways involved in the regulation of milk protein synthesis in the lactating mammary gland and their control. The protein synthetic… (more)

Subjects/Keywords: Regulation of protein synthesis; Milk proteins; Gene expression

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

APA (6th Edition):

Hayashi, A. A. (2007). Regulation of protein synthesis in the mammary gland. (Doctoral Dissertation). Massey University. Retrieved from http://hdl.handle.net/10179/795

Chicago Manual of Style (16th Edition):

Hayashi, Amanda Aparecida. “Regulation of protein synthesis in the mammary gland.” 2007. Doctoral Dissertation, Massey University. Accessed January 21, 2020. http://hdl.handle.net/10179/795.

MLA Handbook (7th Edition):

Hayashi, Amanda Aparecida. “Regulation of protein synthesis in the mammary gland.” 2007. Web. 21 Jan 2020.

Vancouver:

Hayashi AA. Regulation of protein synthesis in the mammary gland. [Internet] [Doctoral dissertation]. Massey University; 2007. [cited 2020 Jan 21]. Available from: http://hdl.handle.net/10179/795.

Council of Science Editors:

Hayashi AA. Regulation of protein synthesis in the mammary gland. [Doctoral Dissertation]. Massey University; 2007. Available from: http://hdl.handle.net/10179/795


Univerzitet u Beogradu

28. Spasovski, Vesna M., 1971-. Molekularni mehanizmi patogeneze mijeloproliferativnih neoplazija : poremećaj ekspresije gena uključenih u proliferaciju i apoptozu.

Degree: Biološki fakultet, 2013, Univerzitet u Beogradu

BIOLOGIJA - MOLEKULARNA BIOLOGIJA / BIOLOGY - MOLECULAR BIOLOGY

Mijeloproliferativne neoplazije (MPN) su hronični hematološki maligniteti koji se odlikuju autonomnom proliferacijom opredeljenih progenitora hematopoeze i… (more)

Subjects/Keywords: Myeloproliferative neoplasms; JAK2-V617F-mutation; 46/1 haplotype; transcriptional regulation; expression of the JAK2 gene; apoptosis

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

APA (6th Edition):

Spasovski, Vesna M., 1. (2013). Molekularni mehanizmi patogeneze mijeloproliferativnih neoplazija : poremećaj ekspresije gena uključenih u proliferaciju i apoptozu. (Thesis). Univerzitet u Beogradu. Retrieved from https://fedorabg.bg.ac.rs/fedora/get/o:5396/bdef:Content/get

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):

Spasovski, Vesna M., 1971-. “Molekularni mehanizmi patogeneze mijeloproliferativnih neoplazija : poremećaj ekspresije gena uključenih u proliferaciju i apoptozu.” 2013. Thesis, Univerzitet u Beogradu. Accessed January 21, 2020. https://fedorabg.bg.ac.rs/fedora/get/o:5396/bdef:Content/get.

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

MLA Handbook (7th Edition):

Spasovski, Vesna M., 1971-. “Molekularni mehanizmi patogeneze mijeloproliferativnih neoplazija : poremećaj ekspresije gena uključenih u proliferaciju i apoptozu.” 2013. Web. 21 Jan 2020.

Vancouver:

Spasovski, Vesna M. 1. Molekularni mehanizmi patogeneze mijeloproliferativnih neoplazija : poremećaj ekspresije gena uključenih u proliferaciju i apoptozu. [Internet] [Thesis]. Univerzitet u Beogradu; 2013. [cited 2020 Jan 21]. Available from: https://fedorabg.bg.ac.rs/fedora/get/o:5396/bdef:Content/get.

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

Council of Science Editors:

Spasovski, Vesna M. 1. Molekularni mehanizmi patogeneze mijeloproliferativnih neoplazija : poremećaj ekspresije gena uključenih u proliferaciju i apoptozu. [Thesis]. Univerzitet u Beogradu; 2013. Available from: https://fedorabg.bg.ac.rs/fedora/get/o:5396/bdef:Content/get

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


University of Michigan

29. Swanson, Christina Ione. Structure, Function, and Evolution of a Signal-Regulated Enhancer.

Degree: PhD, Cell and Developmental Biology, 2010, University of Michigan

 Enhancers are cis-regulatory elements that control the level, timing, and cell-type specificity of gene expression. Despite the central role that enhancers play in transcriptional regulation,… (more)

Subjects/Keywords: Enhancers; Cis-regulatory Elements; Regulation of Gene Expression; Enhancer Evolution; Molecular, Cellular and Developmental Biology; Health Sciences

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

APA (6th Edition):

Swanson, C. I. (2010). Structure, Function, and Evolution of a Signal-Regulated Enhancer. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/76017

Chicago Manual of Style (16th Edition):

Swanson, Christina Ione. “Structure, Function, and Evolution of a Signal-Regulated Enhancer.” 2010. Doctoral Dissertation, University of Michigan. Accessed January 21, 2020. http://hdl.handle.net/2027.42/76017.

MLA Handbook (7th Edition):

Swanson, Christina Ione. “Structure, Function, and Evolution of a Signal-Regulated Enhancer.” 2010. Web. 21 Jan 2020.

Vancouver:

Swanson CI. Structure, Function, and Evolution of a Signal-Regulated Enhancer. [Internet] [Doctoral dissertation]. University of Michigan; 2010. [cited 2020 Jan 21]. Available from: http://hdl.handle.net/2027.42/76017.

Council of Science Editors:

Swanson CI. Structure, Function, and Evolution of a Signal-Regulated Enhancer. [Doctoral Dissertation]. University of Michigan; 2010. Available from: http://hdl.handle.net/2027.42/76017


Uniwersytet im. Adama Mickiewicza w Poznaniu

30. Rosikiewicz, Wojciech. Identyfikacja i analiza ekspresji nakładających się genów u człowieka i myszy .

Degree: 2017, Uniwersytet im. Adama Mickiewicza w Poznaniu

 Zjawisko nakładania się genów może pełnić wiele funkcji regulatorowych, a większość prowadzonych obecnie w tym temacie badań skupia się na parach genów kodujących białka, nakładających… (more)

Subjects/Keywords: geny nakładające; overlapping genes; regulacja ekspresji genów; regulation of gene expression; geny kodujące białka; protein-coding genes; interferencja transkrypcji; transcription interference

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

APA (6th Edition):

Rosikiewicz, W. (2017). Identyfikacja i analiza ekspresji nakładających się genów u człowieka i myszy . (Doctoral Dissertation). Uniwersytet im. Adama Mickiewicza w Poznaniu. Retrieved from http://hdl.handle.net/10593/19347

Chicago Manual of Style (16th Edition):

Rosikiewicz, Wojciech. “Identyfikacja i analiza ekspresji nakładających się genów u człowieka i myszy .” 2017. Doctoral Dissertation, Uniwersytet im. Adama Mickiewicza w Poznaniu. Accessed January 21, 2020. http://hdl.handle.net/10593/19347.

MLA Handbook (7th Edition):

Rosikiewicz, Wojciech. “Identyfikacja i analiza ekspresji nakładających się genów u człowieka i myszy .” 2017. Web. 21 Jan 2020.

Vancouver:

Rosikiewicz W. Identyfikacja i analiza ekspresji nakładających się genów u człowieka i myszy . [Internet] [Doctoral dissertation]. Uniwersytet im. Adama Mickiewicza w Poznaniu; 2017. [cited 2020 Jan 21]. Available from: http://hdl.handle.net/10593/19347.

Council of Science Editors:

Rosikiewicz W. Identyfikacja i analiza ekspresji nakładających się genów u człowieka i myszy . [Doctoral Dissertation]. Uniwersytet im. Adama Mickiewicza w Poznaniu; 2017. Available from: http://hdl.handle.net/10593/19347

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