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You searched for subject:(Transcriptional regulation). Showing records 1 – 30 of 526 total matches.

[1] [2] [3] [4] [5] … [18]

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University of Gothenburg / Göteborgs Universitet

1. Nilsson, Daniel. Post-transcriptional regulation after stress in Schizosaccharomyces pombe.

Degree: 2011, University of Gothenburg / Göteborgs Universitet

 Post transcriptional regulation is part of the gene expression control and is important for many cellular processes. It influences how mRNAs are selected for translation,… (more)

Subjects/Keywords: Post transcriptional regulation

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APA (6th Edition):

Nilsson, D. (2011). Post-transcriptional regulation after stress in Schizosaccharomyces pombe. (Thesis). University of Gothenburg / Göteborgs Universitet. Retrieved from http://hdl.handle.net/2077/24467

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):

Nilsson, Daniel. “Post-transcriptional regulation after stress in Schizosaccharomyces pombe.” 2011. Thesis, University of Gothenburg / Göteborgs Universitet. Accessed October 16, 2019. http://hdl.handle.net/2077/24467.

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

MLA Handbook (7th Edition):

Nilsson, Daniel. “Post-transcriptional regulation after stress in Schizosaccharomyces pombe.” 2011. Web. 16 Oct 2019.

Vancouver:

Nilsson D. Post-transcriptional regulation after stress in Schizosaccharomyces pombe. [Internet] [Thesis]. University of Gothenburg / Göteborgs Universitet; 2011. [cited 2019 Oct 16]. Available from: http://hdl.handle.net/2077/24467.

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

Council of Science Editors:

Nilsson D. Post-transcriptional regulation after stress in Schizosaccharomyces pombe. [Thesis]. University of Gothenburg / Göteborgs Universitet; 2011. Available from: http://hdl.handle.net/2077/24467

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


University of Toronto

2. Baczyk, Dorota. DREAM-mediated Regulation of GCM1 in the Human Placental Trophoblast.

Degree: 2010, University of Toronto

The trophoblast transcription factor glial cell missing-1 (GCM1) regulates asymmetric division of placental cytotrophoblast to form the differentiated syncytiotrophoblast. Reduced GCM1 expression is a key… (more)

Subjects/Keywords: placenta; transcriptional regulation

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APA (6th Edition):

Baczyk, D. (2010). DREAM-mediated Regulation of GCM1 in the Human Placental Trophoblast. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/24234

Chicago Manual of Style (16th Edition):

Baczyk, Dorota. “DREAM-mediated Regulation of GCM1 in the Human Placental Trophoblast.” 2010. Masters Thesis, University of Toronto. Accessed October 16, 2019. http://hdl.handle.net/1807/24234.

MLA Handbook (7th Edition):

Baczyk, Dorota. “DREAM-mediated Regulation of GCM1 in the Human Placental Trophoblast.” 2010. Web. 16 Oct 2019.

Vancouver:

Baczyk D. DREAM-mediated Regulation of GCM1 in the Human Placental Trophoblast. [Internet] [Masters thesis]. University of Toronto; 2010. [cited 2019 Oct 16]. Available from: http://hdl.handle.net/1807/24234.

Council of Science Editors:

Baczyk D. DREAM-mediated Regulation of GCM1 in the Human Placental Trophoblast. [Masters Thesis]. University of Toronto; 2010. Available from: http://hdl.handle.net/1807/24234


Cornell University

3. Welsh, Ian. Giving Shape To Genomic Regulatory Networks Controlling Craniofacial And Asymmetric Organ Morphogenesis .

Degree: 2016, Cornell University

 Morphogenesis is the most critical and dynamic utilization of genomic information in the life history of an organism and a powerful system for advancing our… (more)

Subjects/Keywords: genomics; morphogenesis; transcriptional regulation

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APA (6th Edition):

Welsh, I. (2016). Giving Shape To Genomic Regulatory Networks Controlling Craniofacial And Asymmetric Organ Morphogenesis . (Thesis). Cornell University. Retrieved from http://hdl.handle.net/1813/43625

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):

Welsh, Ian. “Giving Shape To Genomic Regulatory Networks Controlling Craniofacial And Asymmetric Organ Morphogenesis .” 2016. Thesis, Cornell University. Accessed October 16, 2019. http://hdl.handle.net/1813/43625.

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

MLA Handbook (7th Edition):

Welsh, Ian. “Giving Shape To Genomic Regulatory Networks Controlling Craniofacial And Asymmetric Organ Morphogenesis .” 2016. Web. 16 Oct 2019.

Vancouver:

Welsh I. Giving Shape To Genomic Regulatory Networks Controlling Craniofacial And Asymmetric Organ Morphogenesis . [Internet] [Thesis]. Cornell University; 2016. [cited 2019 Oct 16]. Available from: http://hdl.handle.net/1813/43625.

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

Council of Science Editors:

Welsh I. Giving Shape To Genomic Regulatory Networks Controlling Craniofacial And Asymmetric Organ Morphogenesis . [Thesis]. Cornell University; 2016. Available from: http://hdl.handle.net/1813/43625

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


University of Miami

4. Han, Xiaoqing. Identification and Characterization of a Notch Transcriptional Repressor Complex.

Degree: PhD, Cancer Biology (Medicine), 2017, University of Miami

 It is well established that Notch functions as a transcriptional activator through the formation of a ternary complex that comprises Notch, Maml and CSL. This… (more)

Subjects/Keywords: Notch; PRC2; LSD1; Transcriptional Regulation

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APA (6th Edition):

Han, X. (2017). Identification and Characterization of a Notch Transcriptional Repressor Complex. (Doctoral Dissertation). University of Miami. Retrieved from https://scholarlyrepository.miami.edu/oa_dissertations/1906

Chicago Manual of Style (16th Edition):

Han, Xiaoqing. “Identification and Characterization of a Notch Transcriptional Repressor Complex.” 2017. Doctoral Dissertation, University of Miami. Accessed October 16, 2019. https://scholarlyrepository.miami.edu/oa_dissertations/1906.

MLA Handbook (7th Edition):

Han, Xiaoqing. “Identification and Characterization of a Notch Transcriptional Repressor Complex.” 2017. Web. 16 Oct 2019.

Vancouver:

Han X. Identification and Characterization of a Notch Transcriptional Repressor Complex. [Internet] [Doctoral dissertation]. University of Miami; 2017. [cited 2019 Oct 16]. Available from: https://scholarlyrepository.miami.edu/oa_dissertations/1906.

Council of Science Editors:

Han X. Identification and Characterization of a Notch Transcriptional Repressor Complex. [Doctoral Dissertation]. University of Miami; 2017. Available from: https://scholarlyrepository.miami.edu/oa_dissertations/1906


University of Toronto

5. Orlowicz, Agata. Mechanisms of Vts1-Mediated Repression in S. cerevisiae.

Degree: 2011, University of Toronto

Vts1p is the Saccharomyces cerevisiae member of the Smaug family of post-transcriptional regulators, which is a group of sequence-specific RNA-binding proteins that regulate target mRNA… (more)

Subjects/Keywords: Vts1; post-transcriptional regulation; 0487

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APA (6th Edition):

Orlowicz, A. (2011). Mechanisms of Vts1-Mediated Repression in S. cerevisiae. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/29596

Chicago Manual of Style (16th Edition):

Orlowicz, Agata. “Mechanisms of Vts1-Mediated Repression in S. cerevisiae.” 2011. Masters Thesis, University of Toronto. Accessed October 16, 2019. http://hdl.handle.net/1807/29596.

MLA Handbook (7th Edition):

Orlowicz, Agata. “Mechanisms of Vts1-Mediated Repression in S. cerevisiae.” 2011. Web. 16 Oct 2019.

Vancouver:

Orlowicz A. Mechanisms of Vts1-Mediated Repression in S. cerevisiae. [Internet] [Masters thesis]. University of Toronto; 2011. [cited 2019 Oct 16]. Available from: http://hdl.handle.net/1807/29596.

Council of Science Editors:

Orlowicz A. Mechanisms of Vts1-Mediated Repression in S. cerevisiae. [Masters Thesis]. University of Toronto; 2011. Available from: http://hdl.handle.net/1807/29596


University of New South Wales

6. Md Azahri, Nor Saadah. Role of TRAIL and its transcriptional regulation in stimulated vascular smooth muscle cells.

Degree: Medical Sciences, 2012, University of New South Wales

 Abnormal migration of vascular smooth muscle cells (VSMCs) from the media to the intima of the vessel and subsequent proliferation are key underlying events contributing… (more)

Subjects/Keywords: VSMC; TRAIL; Transcriptional regulation

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APA (6th Edition):

Md Azahri, N. S. (2012). Role of TRAIL and its transcriptional regulation in stimulated vascular smooth muscle cells. (Doctoral Dissertation). University of New South Wales. Retrieved from http://handle.unsw.edu.au/1959.4/54045 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:12761/SOURCE02?view=true

Chicago Manual of Style (16th Edition):

Md Azahri, Nor Saadah. “Role of TRAIL and its transcriptional regulation in stimulated vascular smooth muscle cells.” 2012. Doctoral Dissertation, University of New South Wales. Accessed October 16, 2019. http://handle.unsw.edu.au/1959.4/54045 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:12761/SOURCE02?view=true.

MLA Handbook (7th Edition):

Md Azahri, Nor Saadah. “Role of TRAIL and its transcriptional regulation in stimulated vascular smooth muscle cells.” 2012. Web. 16 Oct 2019.

Vancouver:

Md Azahri NS. Role of TRAIL and its transcriptional regulation in stimulated vascular smooth muscle cells. [Internet] [Doctoral dissertation]. University of New South Wales; 2012. [cited 2019 Oct 16]. Available from: http://handle.unsw.edu.au/1959.4/54045 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:12761/SOURCE02?view=true.

Council of Science Editors:

Md Azahri NS. Role of TRAIL and its transcriptional regulation in stimulated vascular smooth muscle cells. [Doctoral Dissertation]. University of New South Wales; 2012. Available from: http://handle.unsw.edu.au/1959.4/54045 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:12761/SOURCE02?view=true


University of New South Wales

7. Liu, Shengyi. Transcriptional regulation of human thrombopoietin (TPO)-characterization of a novel gene repressor and PF4-mediated suppression.

Degree: Clinical School - St George Hospital, 2013, University of New South Wales

 Human thrombopoietin (TPO) is the primary regulator of megakaryopoiesis. It is known that TPO levels in blood are regulated by a mechanism involving its uptake… (more)

Subjects/Keywords: PF4; Transcriptional regulation; Thrombopoietin

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APA (6th Edition):

Liu, S. (2013). Transcriptional regulation of human thrombopoietin (TPO)-characterization of a novel gene repressor and PF4-mediated suppression. (Doctoral Dissertation). University of New South Wales. Retrieved from http://handle.unsw.edu.au/1959.4/52962 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:11640/SOURCE01?view=true

Chicago Manual of Style (16th Edition):

Liu, Shengyi. “Transcriptional regulation of human thrombopoietin (TPO)-characterization of a novel gene repressor and PF4-mediated suppression.” 2013. Doctoral Dissertation, University of New South Wales. Accessed October 16, 2019. http://handle.unsw.edu.au/1959.4/52962 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:11640/SOURCE01?view=true.

MLA Handbook (7th Edition):

Liu, Shengyi. “Transcriptional regulation of human thrombopoietin (TPO)-characterization of a novel gene repressor and PF4-mediated suppression.” 2013. Web. 16 Oct 2019.

Vancouver:

Liu S. Transcriptional regulation of human thrombopoietin (TPO)-characterization of a novel gene repressor and PF4-mediated suppression. [Internet] [Doctoral dissertation]. University of New South Wales; 2013. [cited 2019 Oct 16]. Available from: http://handle.unsw.edu.au/1959.4/52962 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:11640/SOURCE01?view=true.

Council of Science Editors:

Liu S. Transcriptional regulation of human thrombopoietin (TPO)-characterization of a novel gene repressor and PF4-mediated suppression. [Doctoral Dissertation]. University of New South Wales; 2013. Available from: http://handle.unsw.edu.au/1959.4/52962 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:11640/SOURCE01?view=true


University of Cambridge

8. Janga, Sarath Chandra. Exploiting network-based approaches for understanding gene regulation and function .

Degree: 2010, University of Cambridge

 It is increasingly becoming clear in the post-genomic era that proteins in a cell do not work in isolation but rather work in the context… (more)

Subjects/Keywords: Transcriptional regulation; Networks; Function prediction; Systems biology; Post-transcriptional regulation; Genomics

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APA (6th Edition):

Janga, S. C. (2010). Exploiting network-based approaches for understanding gene regulation and function . (Thesis). University of Cambridge. Retrieved from http://www.dspace.cam.ac.uk/handle/1810/236171

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):

Janga, Sarath Chandra. “Exploiting network-based approaches for understanding gene regulation and function .” 2010. Thesis, University of Cambridge. Accessed October 16, 2019. http://www.dspace.cam.ac.uk/handle/1810/236171.

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

MLA Handbook (7th Edition):

Janga, Sarath Chandra. “Exploiting network-based approaches for understanding gene regulation and function .” 2010. Web. 16 Oct 2019.

Vancouver:

Janga SC. Exploiting network-based approaches for understanding gene regulation and function . [Internet] [Thesis]. University of Cambridge; 2010. [cited 2019 Oct 16]. Available from: http://www.dspace.cam.ac.uk/handle/1810/236171.

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

Council of Science Editors:

Janga SC. Exploiting network-based approaches for understanding gene regulation and function . [Thesis]. University of Cambridge; 2010. Available from: http://www.dspace.cam.ac.uk/handle/1810/236171

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


University of Washington

9. Raubitschek, Antony C. Pre-programmed regulatory networks and poised chromatin potentiate lineage-specific differentiation of CD4+ T cells.

Degree: PhD, 2014, University of Washington

 How the interactions of transcription factors (TFs) with specific regions of chromatin control the basis for cellular function and identity remains an open question. Here,… (more)

Subjects/Keywords: Chromatin Landscape; Epigenetics; Transcriptional Networks; Transcriptional Regulation; Immunology; immunology

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APA (6th Edition):

Raubitschek, A. C. (2014). Pre-programmed regulatory networks and poised chromatin potentiate lineage-specific differentiation of CD4+ T cells. (Doctoral Dissertation). University of Washington. Retrieved from http://hdl.handle.net/1773/24990

Chicago Manual of Style (16th Edition):

Raubitschek, Antony C. “Pre-programmed regulatory networks and poised chromatin potentiate lineage-specific differentiation of CD4+ T cells.” 2014. Doctoral Dissertation, University of Washington. Accessed October 16, 2019. http://hdl.handle.net/1773/24990.

MLA Handbook (7th Edition):

Raubitschek, Antony C. “Pre-programmed regulatory networks and poised chromatin potentiate lineage-specific differentiation of CD4+ T cells.” 2014. Web. 16 Oct 2019.

Vancouver:

Raubitschek AC. Pre-programmed regulatory networks and poised chromatin potentiate lineage-specific differentiation of CD4+ T cells. [Internet] [Doctoral dissertation]. University of Washington; 2014. [cited 2019 Oct 16]. Available from: http://hdl.handle.net/1773/24990.

Council of Science Editors:

Raubitschek AC. Pre-programmed regulatory networks and poised chromatin potentiate lineage-specific differentiation of CD4+ T cells. [Doctoral Dissertation]. University of Washington; 2014. Available from: http://hdl.handle.net/1773/24990


Queensland University of Technology

10. Chua, Xin-Yi. Prediction of transcriptional regulatory interactions in bacteria : a comparative genomics approach.

Degree: 2012, Queensland University of Technology

 Exponential growth of genomic data in the last two decades has made manual analyses impractical for all but trial studies. As genomic analyses have become… (more)

Subjects/Keywords: transcriptional regulatory interactions; bacteria; genomics approach; gene regulation; transcriptional regulatory network

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APA (6th Edition):

Chua, X. (2012). Prediction of transcriptional regulatory interactions in bacteria : a comparative genomics approach. (Thesis). Queensland University of Technology. Retrieved from https://eprints.qut.edu.au/55249/

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):

Chua, Xin-Yi. “Prediction of transcriptional regulatory interactions in bacteria : a comparative genomics approach.” 2012. Thesis, Queensland University of Technology. Accessed October 16, 2019. https://eprints.qut.edu.au/55249/.

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

MLA Handbook (7th Edition):

Chua, Xin-Yi. “Prediction of transcriptional regulatory interactions in bacteria : a comparative genomics approach.” 2012. Web. 16 Oct 2019.

Vancouver:

Chua X. Prediction of transcriptional regulatory interactions in bacteria : a comparative genomics approach. [Internet] [Thesis]. Queensland University of Technology; 2012. [cited 2019 Oct 16]. Available from: https://eprints.qut.edu.au/55249/.

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

Council of Science Editors:

Chua X. Prediction of transcriptional regulatory interactions in bacteria : a comparative genomics approach. [Thesis]. Queensland University of Technology; 2012. Available from: https://eprints.qut.edu.au/55249/

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


University of Illinois – Chicago

11. Pan, Xian. Transcriptional Regulation of Cytochrome P450 2D6 by Small Heterodimer Partner.

Degree: 2015, University of Illinois – Chicago

 Cytochrome P450 2D6 (CYP2D6) is a major drug-metabolizing enzyme, responsible for eliminating ~20% of marketed drugs. Of note, CYP2D6 activity exhibits large interindividual variability, but… (more)

Subjects/Keywords: CYP2D6; SHP; transcriptional regulation; pregnancy; interindividual variability

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APA (6th Edition):

Pan, X. (2015). Transcriptional Regulation of Cytochrome P450 2D6 by Small Heterodimer Partner. (Thesis). University of Illinois – Chicago. Retrieved from http://hdl.handle.net/10027/19796

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):

Pan, Xian. “Transcriptional Regulation of Cytochrome P450 2D6 by Small Heterodimer Partner.” 2015. Thesis, University of Illinois – Chicago. Accessed October 16, 2019. http://hdl.handle.net/10027/19796.

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

MLA Handbook (7th Edition):

Pan, Xian. “Transcriptional Regulation of Cytochrome P450 2D6 by Small Heterodimer Partner.” 2015. Web. 16 Oct 2019.

Vancouver:

Pan X. Transcriptional Regulation of Cytochrome P450 2D6 by Small Heterodimer Partner. [Internet] [Thesis]. University of Illinois – Chicago; 2015. [cited 2019 Oct 16]. Available from: http://hdl.handle.net/10027/19796.

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

Council of Science Editors:

Pan X. Transcriptional Regulation of Cytochrome P450 2D6 by Small Heterodimer Partner. [Thesis]. University of Illinois – Chicago; 2015. Available from: http://hdl.handle.net/10027/19796

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


The Ohio State University

12. Hu, Rong. Regulation of osteoclast differentiation by transcription factors MITF, PU.1 and EOS.

Degree: PhD, Molecular, Cellular, and Developmental Biology, 2007, The Ohio State University

 The microphthalmia-associated transcription factor (MITF), a basic helix-loop-helix leucine zipper (bHLH-Zip) transcription factor, regulates distinct target genes in several cell types including osteoclasts. Osteoclasts are… (more)

Subjects/Keywords: Biology, Molecular; Cell differentiation; osteoclasts; transcriptional regulation

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APA (6th Edition):

Hu, R. (2007). Regulation of osteoclast differentiation by transcription factors MITF, PU.1 and EOS. (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1166644761

Chicago Manual of Style (16th Edition):

Hu, Rong. “Regulation of osteoclast differentiation by transcription factors MITF, PU.1 and EOS.” 2007. Doctoral Dissertation, The Ohio State University. Accessed October 16, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=osu1166644761.

MLA Handbook (7th Edition):

Hu, Rong. “Regulation of osteoclast differentiation by transcription factors MITF, PU.1 and EOS.” 2007. Web. 16 Oct 2019.

Vancouver:

Hu R. Regulation of osteoclast differentiation by transcription factors MITF, PU.1 and EOS. [Internet] [Doctoral dissertation]. The Ohio State University; 2007. [cited 2019 Oct 16]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1166644761.

Council of Science Editors:

Hu R. Regulation of osteoclast differentiation by transcription factors MITF, PU.1 and EOS. [Doctoral Dissertation]. The Ohio State University; 2007. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1166644761


Georgia Tech

13. Jung, Jeenah. Development of optical imaging method for detecting RNA-protein interactions.

Degree: PhD, Biomedical Engineering (Joint GT/Emory Department), 2014, Georgia Tech

 The localization and translation of messenger ribonucleic acids (mRNAs) play crucial roles in cellular function and diseases, and are regulated by numerous RNA-binding proteins (RBPs)… (more)

Subjects/Keywords: RNA-protein interactions; Post-transcriptional regulation

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APA (6th Edition):

Jung, J. (2014). Development of optical imaging method for detecting RNA-protein interactions. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/54278

Chicago Manual of Style (16th Edition):

Jung, Jeenah. “Development of optical imaging method for detecting RNA-protein interactions.” 2014. Doctoral Dissertation, Georgia Tech. Accessed October 16, 2019. http://hdl.handle.net/1853/54278.

MLA Handbook (7th Edition):

Jung, Jeenah. “Development of optical imaging method for detecting RNA-protein interactions.” 2014. Web. 16 Oct 2019.

Vancouver:

Jung J. Development of optical imaging method for detecting RNA-protein interactions. [Internet] [Doctoral dissertation]. Georgia Tech; 2014. [cited 2019 Oct 16]. Available from: http://hdl.handle.net/1853/54278.

Council of Science Editors:

Jung J. Development of optical imaging method for detecting RNA-protein interactions. [Doctoral Dissertation]. Georgia Tech; 2014. Available from: http://hdl.handle.net/1853/54278


Penn State University

14. Roff, Alanna Nichole. Post-Transcriptional Regulation of Human Meprin Alpha.

Degree: MS, Cell and Molecular Biology, 2011, Penn State University

 Meprins are multimeric proteases that are expressed in a tissue-specific manner and process a wide variety of substrates. Meprins are also regulated via numerous forms… (more)

Subjects/Keywords: post-transcriptional regulation; inflammation; meprin alpha

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APA (6th Edition):

Roff, A. N. (2011). Post-Transcriptional Regulation of Human Meprin Alpha. (Masters Thesis). Penn State University. Retrieved from https://etda.libraries.psu.edu/catalog/12064

Chicago Manual of Style (16th Edition):

Roff, Alanna Nichole. “Post-Transcriptional Regulation of Human Meprin Alpha.” 2011. Masters Thesis, Penn State University. Accessed October 16, 2019. https://etda.libraries.psu.edu/catalog/12064.

MLA Handbook (7th Edition):

Roff, Alanna Nichole. “Post-Transcriptional Regulation of Human Meprin Alpha.” 2011. Web. 16 Oct 2019.

Vancouver:

Roff AN. Post-Transcriptional Regulation of Human Meprin Alpha. [Internet] [Masters thesis]. Penn State University; 2011. [cited 2019 Oct 16]. Available from: https://etda.libraries.psu.edu/catalog/12064.

Council of Science Editors:

Roff AN. Post-Transcriptional Regulation of Human Meprin Alpha. [Masters Thesis]. Penn State University; 2011. Available from: https://etda.libraries.psu.edu/catalog/12064


University of California – Berkeley

15. Steakley, David Lee. Mechanisms of Heterochromatin Silencing in Saccharomyces cerevisiae.

Degree: Molecular & Cell Biology, 2013, University of California – Berkeley

 Sir proteins are responsible for maintaining stable transcriptional repression and silencing of telomeres, rDNA, and silent mating-type loci in S. cerevisiae. Decades of research identify… (more)

Subjects/Keywords: Genetics; Gene Regulation; Heterochromatin; Saccharomyces; Transcriptional Silencing

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APA (6th Edition):

Steakley, D. L. (2013). Mechanisms of Heterochromatin Silencing in Saccharomyces cerevisiae. (Thesis). University of California – Berkeley. Retrieved from http://www.escholarship.org/uc/item/87q1494q

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):

Steakley, David Lee. “Mechanisms of Heterochromatin Silencing in Saccharomyces cerevisiae.” 2013. Thesis, University of California – Berkeley. Accessed October 16, 2019. http://www.escholarship.org/uc/item/87q1494q.

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

MLA Handbook (7th Edition):

Steakley, David Lee. “Mechanisms of Heterochromatin Silencing in Saccharomyces cerevisiae.” 2013. Web. 16 Oct 2019.

Vancouver:

Steakley DL. Mechanisms of Heterochromatin Silencing in Saccharomyces cerevisiae. [Internet] [Thesis]. University of California – Berkeley; 2013. [cited 2019 Oct 16]. Available from: http://www.escholarship.org/uc/item/87q1494q.

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

Council of Science Editors:

Steakley DL. Mechanisms of Heterochromatin Silencing in Saccharomyces cerevisiae. [Thesis]. University of California – Berkeley; 2013. Available from: http://www.escholarship.org/uc/item/87q1494q

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


University of Melbourne

16. Carradice, Duncan Peter. Genetic basis of congenital myeloid failure syndromes in mutant zebrafish.

Degree: 2010, University of Melbourne

 Zinc finger and BTB domain containing proteins (BTB-ZF) are transcriptional repressors from a family including members with critical roles in haematopoiesis and oncogenesis. From an… (more)

Subjects/Keywords: myelopoiesis; zebrafish; transcriptional regulation; genetic screen

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APA (6th Edition):

Carradice, D. P. (2010). Genetic basis of congenital myeloid failure syndromes in mutant zebrafish. (Doctoral Dissertation). University of Melbourne. Retrieved from http://hdl.handle.net/11343/35545

Chicago Manual of Style (16th Edition):

Carradice, Duncan Peter. “Genetic basis of congenital myeloid failure syndromes in mutant zebrafish.” 2010. Doctoral Dissertation, University of Melbourne. Accessed October 16, 2019. http://hdl.handle.net/11343/35545.

MLA Handbook (7th Edition):

Carradice, Duncan Peter. “Genetic basis of congenital myeloid failure syndromes in mutant zebrafish.” 2010. Web. 16 Oct 2019.

Vancouver:

Carradice DP. Genetic basis of congenital myeloid failure syndromes in mutant zebrafish. [Internet] [Doctoral dissertation]. University of Melbourne; 2010. [cited 2019 Oct 16]. Available from: http://hdl.handle.net/11343/35545.

Council of Science Editors:

Carradice DP. Genetic basis of congenital myeloid failure syndromes in mutant zebrafish. [Doctoral Dissertation]. University of Melbourne; 2010. Available from: http://hdl.handle.net/11343/35545


Vanderbilt University

17. Dimitrova, Yoana Nantcheva. Biochemical and structural analyses of TBL1: insights into the function of a transcriptional regulator.

Degree: PhD, Biochemistry, 2010, Vanderbilt University

 The mechanism controlling the switch between gene activation and repression is critically important for understanding the process of transcriptional regulation. Gene expression is highly controlled… (more)

Subjects/Keywords: transcriptional regulation; ubiquitination; beta-catenin; TBL1

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APA (6th Edition):

Dimitrova, Y. N. (2010). Biochemical and structural analyses of TBL1: insights into the function of a transcriptional regulator. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://etd.library.vanderbilt.edu/available/etd-10282010-173834/ ;

Chicago Manual of Style (16th Edition):

Dimitrova, Yoana Nantcheva. “Biochemical and structural analyses of TBL1: insights into the function of a transcriptional regulator.” 2010. Doctoral Dissertation, Vanderbilt University. Accessed October 16, 2019. http://etd.library.vanderbilt.edu/available/etd-10282010-173834/ ;.

MLA Handbook (7th Edition):

Dimitrova, Yoana Nantcheva. “Biochemical and structural analyses of TBL1: insights into the function of a transcriptional regulator.” 2010. Web. 16 Oct 2019.

Vancouver:

Dimitrova YN. Biochemical and structural analyses of TBL1: insights into the function of a transcriptional regulator. [Internet] [Doctoral dissertation]. Vanderbilt University; 2010. [cited 2019 Oct 16]. Available from: http://etd.library.vanderbilt.edu/available/etd-10282010-173834/ ;.

Council of Science Editors:

Dimitrova YN. Biochemical and structural analyses of TBL1: insights into the function of a transcriptional regulator. [Doctoral Dissertation]. Vanderbilt University; 2010. Available from: http://etd.library.vanderbilt.edu/available/etd-10282010-173834/ ;


University of New Mexico

18. Sun, Xiaobo. Transcriptional networks of lung airway epithelial ciliogenesis.

Degree: Biomedical Sciences Graduate Program, 2009, University of New Mexico

 Motile cilia of the mammalian airway play an essential role in innate defense. The coordinated transcriptional regulation of cilial axoneme genes remains to be elucidated.… (more)

Subjects/Keywords: Transcriptional Regulation; Lung Airway Epithelium; Cilia; Ciliogenesis

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APA (6th Edition):

Sun, X. (2009). Transcriptional networks of lung airway epithelial ciliogenesis. (Masters Thesis). University of New Mexico. Retrieved from https://digitalrepository.unm.edu/biom_etds/107

Chicago Manual of Style (16th Edition):

Sun, Xiaobo. “Transcriptional networks of lung airway epithelial ciliogenesis.” 2009. Masters Thesis, University of New Mexico. Accessed October 16, 2019. https://digitalrepository.unm.edu/biom_etds/107.

MLA Handbook (7th Edition):

Sun, Xiaobo. “Transcriptional networks of lung airway epithelial ciliogenesis.” 2009. Web. 16 Oct 2019.

Vancouver:

Sun X. Transcriptional networks of lung airway epithelial ciliogenesis. [Internet] [Masters thesis]. University of New Mexico; 2009. [cited 2019 Oct 16]. Available from: https://digitalrepository.unm.edu/biom_etds/107.

Council of Science Editors:

Sun X. Transcriptional networks of lung airway epithelial ciliogenesis. [Masters Thesis]. University of New Mexico; 2009. Available from: https://digitalrepository.unm.edu/biom_etds/107


University of Illinois – Urbana-Champaign

19. Blatti, Charles. Understanding co-expressed gene sets by identifying regulators and modeling genomic elements.

Degree: PhD, Computer Science, 2015, University of Illinois – Urbana-Champaign

 Genomic researchers commonly study complex phenotypes by identifying experimentally derived sets of functionally related genes with similar transcriptional profiles. These gene sets are then frequently… (more)

Subjects/Keywords: heterogeneous networks; gene set analysis; transcriptional regulation

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APA (6th Edition):

Blatti, C. (2015). Understanding co-expressed gene sets by identifying regulators and modeling genomic elements. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/78301

Chicago Manual of Style (16th Edition):

Blatti, Charles. “Understanding co-expressed gene sets by identifying regulators and modeling genomic elements.” 2015. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed October 16, 2019. http://hdl.handle.net/2142/78301.

MLA Handbook (7th Edition):

Blatti, Charles. “Understanding co-expressed gene sets by identifying regulators and modeling genomic elements.” 2015. Web. 16 Oct 2019.

Vancouver:

Blatti C. Understanding co-expressed gene sets by identifying regulators and modeling genomic elements. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2015. [cited 2019 Oct 16]. Available from: http://hdl.handle.net/2142/78301.

Council of Science Editors:

Blatti C. Understanding co-expressed gene sets by identifying regulators and modeling genomic elements. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2015. Available from: http://hdl.handle.net/2142/78301


University of Illinois – Urbana-Champaign

20. Henke, Sarah K. Regulatory function and interdomain communication of group II biotin protein ligases.

Degree: PhD, Microbiology, 2017, University of Illinois – Urbana-Champaign

 Biotin is a cofactor required for function of essential biotin dependent enzymes that are involved in metabolic processes including fatty acid biosynthesis, gluconeogenesis, and amino… (more)

Subjects/Keywords: Biotin; Biotin protein ligase; BirA; Transcriptional regulation

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APA (6th Edition):

Henke, S. K. (2017). Regulatory function and interdomain communication of group II biotin protein ligases. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/99277

Chicago Manual of Style (16th Edition):

Henke, Sarah K. “Regulatory function and interdomain communication of group II biotin protein ligases.” 2017. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed October 16, 2019. http://hdl.handle.net/2142/99277.

MLA Handbook (7th Edition):

Henke, Sarah K. “Regulatory function and interdomain communication of group II biotin protein ligases.” 2017. Web. 16 Oct 2019.

Vancouver:

Henke SK. Regulatory function and interdomain communication of group II biotin protein ligases. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2017. [cited 2019 Oct 16]. Available from: http://hdl.handle.net/2142/99277.

Council of Science Editors:

Henke SK. Regulatory function and interdomain communication of group II biotin protein ligases. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2017. Available from: http://hdl.handle.net/2142/99277


University of Southern California

21. Ianculescu, Irina. One play, many actors: the many roles coregulators play in nuclear receptor mediated transcription.

Degree: PhD, Genetic, Molecular and Cellular Biology, 2011, University of Southern California

 It is becoming increasingly evident that transcriptional coregulators are a diverse group of proteins of central importance to gene expression. Although some appear to be… (more)

Subjects/Keywords: transcriptional regulation; nuclear receptor coactivators; p300/CBP

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APA (6th Edition):

Ianculescu, I. (2011). One play, many actors: the many roles coregulators play in nuclear receptor mediated transcription. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/175732/rec/4561

Chicago Manual of Style (16th Edition):

Ianculescu, Irina. “One play, many actors: the many roles coregulators play in nuclear receptor mediated transcription.” 2011. Doctoral Dissertation, University of Southern California. Accessed October 16, 2019. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/175732/rec/4561.

MLA Handbook (7th Edition):

Ianculescu, Irina. “One play, many actors: the many roles coregulators play in nuclear receptor mediated transcription.” 2011. Web. 16 Oct 2019.

Vancouver:

Ianculescu I. One play, many actors: the many roles coregulators play in nuclear receptor mediated transcription. [Internet] [Doctoral dissertation]. University of Southern California; 2011. [cited 2019 Oct 16]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/175732/rec/4561.

Council of Science Editors:

Ianculescu I. One play, many actors: the many roles coregulators play in nuclear receptor mediated transcription. [Doctoral Dissertation]. University of Southern California; 2011. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/175732/rec/4561


University of New South Wales

22. Piggin, Catherine. Mechanisms of action of ELF5 in breast cancer.

Degree: Garvan Institute of Medical Research, 2018, University of New South Wales

 The ETS transcription factor ELF5 is a critical regulator of cell fate. In the mammary epithelium, ELF5 drives the development of the ER-negative milk-producing alveolar… (more)

Subjects/Keywords: Transcription; ELF5; Breast cancer; Transcriptional regulation; FOXA1

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APA (6th Edition):

Piggin, C. (2018). Mechanisms of action of ELF5 in breast cancer. (Doctoral Dissertation). University of New South Wales. Retrieved from http://handle.unsw.edu.au/1959.4/59565

Chicago Manual of Style (16th Edition):

Piggin, Catherine. “Mechanisms of action of ELF5 in breast cancer.” 2018. Doctoral Dissertation, University of New South Wales. Accessed October 16, 2019. http://handle.unsw.edu.au/1959.4/59565.

MLA Handbook (7th Edition):

Piggin, Catherine. “Mechanisms of action of ELF5 in breast cancer.” 2018. Web. 16 Oct 2019.

Vancouver:

Piggin C. Mechanisms of action of ELF5 in breast cancer. [Internet] [Doctoral dissertation]. University of New South Wales; 2018. [cited 2019 Oct 16]. Available from: http://handle.unsw.edu.au/1959.4/59565.

Council of Science Editors:

Piggin C. Mechanisms of action of ELF5 in breast cancer. [Doctoral Dissertation]. University of New South Wales; 2018. Available from: http://handle.unsw.edu.au/1959.4/59565


University of Toronto

23. Cheng, Matthew. Characterization of the N-terminal Region of the RNA-Binding Protein Smaug in Post-transcriptional Regulation During Drosophila Embryogenesis.

Degree: 2013, University of Toronto

The Drosophila sequence-specific RNA-binding protein Smaug (Smg) regulates the expression of mRNAs in the early fly embryo. It is the founding member of a conserved… (more)

Subjects/Keywords: Smaug; post-transcriptional regulation; Drosophila; RNA; 0487

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APA (6th Edition):

Cheng, M. (2013). Characterization of the N-terminal Region of the RNA-Binding Protein Smaug in Post-transcriptional Regulation During Drosophila Embryogenesis. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/70038

Chicago Manual of Style (16th Edition):

Cheng, Matthew. “Characterization of the N-terminal Region of the RNA-Binding Protein Smaug in Post-transcriptional Regulation During Drosophila Embryogenesis.” 2013. Masters Thesis, University of Toronto. Accessed October 16, 2019. http://hdl.handle.net/1807/70038.

MLA Handbook (7th Edition):

Cheng, Matthew. “Characterization of the N-terminal Region of the RNA-Binding Protein Smaug in Post-transcriptional Regulation During Drosophila Embryogenesis.” 2013. Web. 16 Oct 2019.

Vancouver:

Cheng M. Characterization of the N-terminal Region of the RNA-Binding Protein Smaug in Post-transcriptional Regulation During Drosophila Embryogenesis. [Internet] [Masters thesis]. University of Toronto; 2013. [cited 2019 Oct 16]. Available from: http://hdl.handle.net/1807/70038.

Council of Science Editors:

Cheng M. Characterization of the N-terminal Region of the RNA-Binding Protein Smaug in Post-transcriptional Regulation During Drosophila Embryogenesis. [Masters Thesis]. University of Toronto; 2013. Available from: http://hdl.handle.net/1807/70038


Queens University

24. Genge, Christine E. Scaling of Metabolic Enzymes: Transcriptional Basis of Interspecies Variation in Mitochondrial Content .

Degree: Biology, 2010, Queens University

 Mitochondrial content, an important determinant of muscle metabolic capacity, changes in individuals during development, and in response to physiological and environmental challenges. This phenotypic plasticity… (more)

Subjects/Keywords: Mitochondria; Allometric Scaling; Transcriptional Regulation; PGC-1alpha

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APA (6th Edition):

Genge, C. E. (2010). Scaling of Metabolic Enzymes: Transcriptional Basis of Interspecies Variation in Mitochondrial Content . (Thesis). Queens University. Retrieved from http://hdl.handle.net/1974/5710

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):

Genge, Christine E. “Scaling of Metabolic Enzymes: Transcriptional Basis of Interspecies Variation in Mitochondrial Content .” 2010. Thesis, Queens University. Accessed October 16, 2019. http://hdl.handle.net/1974/5710.

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

MLA Handbook (7th Edition):

Genge, Christine E. “Scaling of Metabolic Enzymes: Transcriptional Basis of Interspecies Variation in Mitochondrial Content .” 2010. Web. 16 Oct 2019.

Vancouver:

Genge CE. Scaling of Metabolic Enzymes: Transcriptional Basis of Interspecies Variation in Mitochondrial Content . [Internet] [Thesis]. Queens University; 2010. [cited 2019 Oct 16]. Available from: http://hdl.handle.net/1974/5710.

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

Council of Science Editors:

Genge CE. Scaling of Metabolic Enzymes: Transcriptional Basis of Interspecies Variation in Mitochondrial Content . [Thesis]. Queens University; 2010. Available from: http://hdl.handle.net/1974/5710

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


University of Arizona

25. Peterson, Maureen. Transposon Regulation: Control of Expression in Drosophila Melanogaster and Consequences of Disregulation in Human Cells .

Degree: 2011, University of Arizona

 Transposons were first discovered as "jumping genes" by Barbara McClintock, who continued to study them in maize through the 1940's and 1950's. Since then, transposons… (more)

Subjects/Keywords: transposons; Genetics; post-transcriptional gene regulation; SINEs

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APA (6th Edition):

Peterson, M. (2011). Transposon Regulation: Control of Expression in Drosophila Melanogaster and Consequences of Disregulation in Human Cells . (Doctoral Dissertation). University of Arizona. Retrieved from http://hdl.handle.net/10150/203469

Chicago Manual of Style (16th Edition):

Peterson, Maureen. “Transposon Regulation: Control of Expression in Drosophila Melanogaster and Consequences of Disregulation in Human Cells .” 2011. Doctoral Dissertation, University of Arizona. Accessed October 16, 2019. http://hdl.handle.net/10150/203469.

MLA Handbook (7th Edition):

Peterson, Maureen. “Transposon Regulation: Control of Expression in Drosophila Melanogaster and Consequences of Disregulation in Human Cells .” 2011. Web. 16 Oct 2019.

Vancouver:

Peterson M. Transposon Regulation: Control of Expression in Drosophila Melanogaster and Consequences of Disregulation in Human Cells . [Internet] [Doctoral dissertation]. University of Arizona; 2011. [cited 2019 Oct 16]. Available from: http://hdl.handle.net/10150/203469.

Council of Science Editors:

Peterson M. Transposon Regulation: Control of Expression in Drosophila Melanogaster and Consequences of Disregulation in Human Cells . [Doctoral Dissertation]. University of Arizona; 2011. Available from: http://hdl.handle.net/10150/203469


Temple University

26. Zumbrun, Steven David. Distinct Mechanisms Regulate Induction of Stress Effector, gadd45b.

Degree: PhD, 2008, Temple University

Molecular Biology and Genetics

The GADD45 family of proteins consists of three small nuclear proteins, GADD45A, GADD45B, and GADD45G, which are implicated in modulating the… (more)

Subjects/Keywords: Biology, Molecular; gadd45b; MMS; post-transcriptional regulation; Sorbitol; stress response; transcriptional regulation

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APA (6th Edition):

Zumbrun, S. D. (2008). Distinct Mechanisms Regulate Induction of Stress Effector, gadd45b. (Doctoral Dissertation). Temple University. Retrieved from http://digital.library.temple.edu/u?/p245801coll10,23355

Chicago Manual of Style (16th Edition):

Zumbrun, Steven David. “Distinct Mechanisms Regulate Induction of Stress Effector, gadd45b.” 2008. Doctoral Dissertation, Temple University. Accessed October 16, 2019. http://digital.library.temple.edu/u?/p245801coll10,23355.

MLA Handbook (7th Edition):

Zumbrun, Steven David. “Distinct Mechanisms Regulate Induction of Stress Effector, gadd45b.” 2008. Web. 16 Oct 2019.

Vancouver:

Zumbrun SD. Distinct Mechanisms Regulate Induction of Stress Effector, gadd45b. [Internet] [Doctoral dissertation]. Temple University; 2008. [cited 2019 Oct 16]. Available from: http://digital.library.temple.edu/u?/p245801coll10,23355.

Council of Science Editors:

Zumbrun SD. Distinct Mechanisms Regulate Induction of Stress Effector, gadd45b. [Doctoral Dissertation]. Temple University; 2008. Available from: http://digital.library.temple.edu/u?/p245801coll10,23355


University of Cambridge

27. Janga, Sarath Chandra. Exploiting network-based approaches for understanding gene regulation and function.

Degree: PhD, 2010, University of Cambridge

 It is increasingly becoming clear in the post-genomic era that proteins in a cell do not work in isolation but rather work in the context… (more)

Subjects/Keywords: 572.8; Transcriptional regulation; Networks; Function prediction; Systems biology; Post-transcriptional regulation; Genomics

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APA (6th Edition):

Janga, S. C. (2010). Exploiting network-based approaches for understanding gene regulation and function. (Doctoral Dissertation). University of Cambridge. Retrieved from https://www.repository.cam.ac.uk/handle/1810/236171 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.541759

Chicago Manual of Style (16th Edition):

Janga, Sarath Chandra. “Exploiting network-based approaches for understanding gene regulation and function.” 2010. Doctoral Dissertation, University of Cambridge. Accessed October 16, 2019. https://www.repository.cam.ac.uk/handle/1810/236171 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.541759.

MLA Handbook (7th Edition):

Janga, Sarath Chandra. “Exploiting network-based approaches for understanding gene regulation and function.” 2010. Web. 16 Oct 2019.

Vancouver:

Janga SC. Exploiting network-based approaches for understanding gene regulation and function. [Internet] [Doctoral dissertation]. University of Cambridge; 2010. [cited 2019 Oct 16]. Available from: https://www.repository.cam.ac.uk/handle/1810/236171 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.541759.

Council of Science Editors:

Janga SC. Exploiting network-based approaches for understanding gene regulation and function. [Doctoral Dissertation]. University of Cambridge; 2010. Available from: https://www.repository.cam.ac.uk/handle/1810/236171 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.541759


University of Vienna

28. Machacek, Christian. The search for novel mRNAs targeted by the RNA-destabilizing protein tristetraprolin for degradation.

Degree: 2010, University of Vienna

Genexpression ist auf den Ebenen der Transkription, mRNA Stabilität und Translation reguliert. Die Stabilität der mRNA wird in den meisten Fällen von regulatorischen Elementen, welche… (more)

Subjects/Keywords: 42.13 Molekularbiologie; 42.15 Zellbiologie; Tristetraprolin / Posttranskriptionelle Regulation; Tristetraprolin / post-transcriptional regulation

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APA (6th Edition):

Machacek, C. (2010). The search for novel mRNAs targeted by the RNA-destabilizing protein tristetraprolin for degradation. (Thesis). University of Vienna. Retrieved from http://othes.univie.ac.at/10357/

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):

Machacek, Christian. “The search for novel mRNAs targeted by the RNA-destabilizing protein tristetraprolin for degradation.” 2010. Thesis, University of Vienna. Accessed October 16, 2019. http://othes.univie.ac.at/10357/.

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

MLA Handbook (7th Edition):

Machacek, Christian. “The search for novel mRNAs targeted by the RNA-destabilizing protein tristetraprolin for degradation.” 2010. Web. 16 Oct 2019.

Vancouver:

Machacek C. The search for novel mRNAs targeted by the RNA-destabilizing protein tristetraprolin for degradation. [Internet] [Thesis]. University of Vienna; 2010. [cited 2019 Oct 16]. Available from: http://othes.univie.ac.at/10357/.

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

Council of Science Editors:

Machacek C. The search for novel mRNAs targeted by the RNA-destabilizing protein tristetraprolin for degradation. [Thesis]. University of Vienna; 2010. Available from: http://othes.univie.ac.at/10357/

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


University of Southern California

29. Fromm, Jody Arlene. Mechanisms for regulating the expression of the TATA-binding protein.

Degree: PhD, Biochemistry & Molecular Biology, 2009, University of Southern California

 The Epidermal Growth Factor Receptor (EGFR) family regulates essential biological processes upon receptor activation and deregulation of these receptors is detrimental to cellular homeostasis. HER2… (more)

Subjects/Keywords: oncogenes; transcriptional regulation; gene regulation; Elk-1; AP-1; TBP; EGFR

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APA (6th Edition):

Fromm, J. A. (2009). Mechanisms for regulating the expression of the TATA-binding protein. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/506625/rec/4007

Chicago Manual of Style (16th Edition):

Fromm, Jody Arlene. “Mechanisms for regulating the expression of the TATA-binding protein.” 2009. Doctoral Dissertation, University of Southern California. Accessed October 16, 2019. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/506625/rec/4007.

MLA Handbook (7th Edition):

Fromm, Jody Arlene. “Mechanisms for regulating the expression of the TATA-binding protein.” 2009. Web. 16 Oct 2019.

Vancouver:

Fromm JA. Mechanisms for regulating the expression of the TATA-binding protein. [Internet] [Doctoral dissertation]. University of Southern California; 2009. [cited 2019 Oct 16]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/506625/rec/4007.

Council of Science Editors:

Fromm JA. Mechanisms for regulating the expression of the TATA-binding protein. [Doctoral Dissertation]. University of Southern California; 2009. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/506625/rec/4007


University of New South Wales

30. Howe, Vicky. SQUALENE MONOOXYGENASE: Insights into the regulation of a key cholesterol synthesis enzyme.

Degree: Biotechnology & Biomolecular Sciences, 2018, University of New South Wales

 Cholesterol is an essential biological molecule, important in maintaining cell membrane integrity and fluidity, cell signalling, and being a precursor for bile acids and steroid… (more)

Subjects/Keywords: Transcriptional regulation; Cholesterol; Squalene monooxygenase; Post-translational regulation

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APA (6th Edition):

Howe, V. (2018). SQUALENE MONOOXYGENASE: Insights into the regulation of a key cholesterol synthesis enzyme. (Doctoral Dissertation). University of New South Wales. Retrieved from http://handle.unsw.edu.au/1959.4/60151 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:51226/SOURCE02?view=true

Chicago Manual of Style (16th Edition):

Howe, Vicky. “SQUALENE MONOOXYGENASE: Insights into the regulation of a key cholesterol synthesis enzyme.” 2018. Doctoral Dissertation, University of New South Wales. Accessed October 16, 2019. http://handle.unsw.edu.au/1959.4/60151 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:51226/SOURCE02?view=true.

MLA Handbook (7th Edition):

Howe, Vicky. “SQUALENE MONOOXYGENASE: Insights into the regulation of a key cholesterol synthesis enzyme.” 2018. Web. 16 Oct 2019.

Vancouver:

Howe V. SQUALENE MONOOXYGENASE: Insights into the regulation of a key cholesterol synthesis enzyme. [Internet] [Doctoral dissertation]. University of New South Wales; 2018. [cited 2019 Oct 16]. Available from: http://handle.unsw.edu.au/1959.4/60151 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:51226/SOURCE02?view=true.

Council of Science Editors:

Howe V. SQUALENE MONOOXYGENASE: Insights into the regulation of a key cholesterol synthesis enzyme. [Doctoral Dissertation]. University of New South Wales; 2018. Available from: http://handle.unsw.edu.au/1959.4/60151 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:51226/SOURCE02?view=true

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