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You searched for subject:(translational biology). Showing records 1 – 30 of 167 total matches.

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1. Seefeldt, Alexandra. Inhibition of the bacterial ribosome by nascent and antimicrobial peptides : Inhibition du ribosome bactérien par les peptides naissants et antimicrobiens.

Degree: Docteur es, Biochimie, 2017, Bordeaux

Le ribosome bactérien (70S) catalyse la formation de la liaison peptidique et représente une cible majeure pour les antibiotiques. Le peptide synthétisé passe à travers… (more)

Subjects/Keywords: Antibiotiques; Ribosome; Biologie structurale; Peptides d’arrêt; Antibiotics; Ribosomes; Nascent-chain mediated translational arrest; Structure biology

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

APA (6th Edition):

Seefeldt, A. (2017). Inhibition of the bacterial ribosome by nascent and antimicrobial peptides : Inhibition du ribosome bactérien par les peptides naissants et antimicrobiens. (Doctoral Dissertation). Bordeaux. Retrieved from http://www.theses.fr/2017BORD0856

Chicago Manual of Style (16th Edition):

Seefeldt, Alexandra. “Inhibition of the bacterial ribosome by nascent and antimicrobial peptides : Inhibition du ribosome bactérien par les peptides naissants et antimicrobiens.” 2017. Doctoral Dissertation, Bordeaux. Accessed January 26, 2021. http://www.theses.fr/2017BORD0856.

MLA Handbook (7th Edition):

Seefeldt, Alexandra. “Inhibition of the bacterial ribosome by nascent and antimicrobial peptides : Inhibition du ribosome bactérien par les peptides naissants et antimicrobiens.” 2017. Web. 26 Jan 2021.

Vancouver:

Seefeldt A. Inhibition of the bacterial ribosome by nascent and antimicrobial peptides : Inhibition du ribosome bactérien par les peptides naissants et antimicrobiens. [Internet] [Doctoral dissertation]. Bordeaux; 2017. [cited 2021 Jan 26]. Available from: http://www.theses.fr/2017BORD0856.

Council of Science Editors:

Seefeldt A. Inhibition of the bacterial ribosome by nascent and antimicrobial peptides : Inhibition du ribosome bactérien par les peptides naissants et antimicrobiens. [Doctoral Dissertation]. Bordeaux; 2017. Available from: http://www.theses.fr/2017BORD0856


University of Helsinki

2. Chen, Shuo. Simultaneous Targeting of Multiple Angiogenic Pathways in Cancer.

Degree: Medicinska fakulteten, 2016, University of Helsinki

 Tumor cells exhibit uncontrolled proliferation, which is supported and accelerated by a constant supply of nutrients carried by blood vessels. Tumor angiogenesis, the formation of… (more)

Subjects/Keywords: angiogenesis; cancer; Translational Cancer Biology; Translationaalinen syöpäbiologia

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APA (6th Edition):

Chen, S. (2016). Simultaneous Targeting of Multiple Angiogenic Pathways in Cancer. (Masters Thesis). University of Helsinki. Retrieved from http://hdl.handle.net/10138/161642

Chicago Manual of Style (16th Edition):

Chen, Shuo. “Simultaneous Targeting of Multiple Angiogenic Pathways in Cancer.” 2016. Masters Thesis, University of Helsinki. Accessed January 26, 2021. http://hdl.handle.net/10138/161642.

MLA Handbook (7th Edition):

Chen, Shuo. “Simultaneous Targeting of Multiple Angiogenic Pathways in Cancer.” 2016. Web. 26 Jan 2021.

Vancouver:

Chen S. Simultaneous Targeting of Multiple Angiogenic Pathways in Cancer. [Internet] [Masters thesis]. University of Helsinki; 2016. [cited 2021 Jan 26]. Available from: http://hdl.handle.net/10138/161642.

Council of Science Editors:

Chen S. Simultaneous Targeting of Multiple Angiogenic Pathways in Cancer. [Masters Thesis]. University of Helsinki; 2016. Available from: http://hdl.handle.net/10138/161642


University of Illinois – Urbana-Champaign

3. Sung, Jaeyun. Systems approaches to identify molecular signatures from high-throughput expression data: towards next generation patient diagnostics.

Degree: PhD, 0300, 2012, University of Illinois – Urbana-Champaign

 The advent of high-throughput (so called “omics”) technologies for the comprehensive and rapid measurement of virtually all molecular components within human cells, tissues, organs, and… (more)

Subjects/Keywords: Translational Bioinformatics; Systems Biology; Transcriptomics; Classification

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APA (6th Edition):

Sung, J. (2012). Systems approaches to identify molecular signatures from high-throughput expression data: towards next generation patient diagnostics. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/34469

Chicago Manual of Style (16th Edition):

Sung, Jaeyun. “Systems approaches to identify molecular signatures from high-throughput expression data: towards next generation patient diagnostics.” 2012. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed January 26, 2021. http://hdl.handle.net/2142/34469.

MLA Handbook (7th Edition):

Sung, Jaeyun. “Systems approaches to identify molecular signatures from high-throughput expression data: towards next generation patient diagnostics.” 2012. Web. 26 Jan 2021.

Vancouver:

Sung J. Systems approaches to identify molecular signatures from high-throughput expression data: towards next generation patient diagnostics. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2012. [cited 2021 Jan 26]. Available from: http://hdl.handle.net/2142/34469.

Council of Science Editors:

Sung J. Systems approaches to identify molecular signatures from high-throughput expression data: towards next generation patient diagnostics. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2012. Available from: http://hdl.handle.net/2142/34469


University of Kentucky

4. Keesling, David C. INVESTIGATING THE PED PROTEIN AND ITS EFFECT ON TRANSLATIONAL CONTROL IN DROSOPHILA MELANOGASTER SPERMATOGENESIS.

Degree: 2012, University of Kentucky

 Inactive mutants of the ped gene cause two phenotypes in Drosophila melanogaster: male sterility and the early translation of DHODH within spermatogenesis. Investigation of the… (more)

Subjects/Keywords: translational control; deubiquitination; spermatogenesis; otubain; proteolysis; Biology

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APA (6th Edition):

Keesling, D. C. (2012). INVESTIGATING THE PED PROTEIN AND ITS EFFECT ON TRANSLATIONAL CONTROL IN DROSOPHILA MELANOGASTER SPERMATOGENESIS. (Masters Thesis). University of Kentucky. Retrieved from https://uknowledge.uky.edu/biology_etds/2

Chicago Manual of Style (16th Edition):

Keesling, David C. “INVESTIGATING THE PED PROTEIN AND ITS EFFECT ON TRANSLATIONAL CONTROL IN DROSOPHILA MELANOGASTER SPERMATOGENESIS.” 2012. Masters Thesis, University of Kentucky. Accessed January 26, 2021. https://uknowledge.uky.edu/biology_etds/2.

MLA Handbook (7th Edition):

Keesling, David C. “INVESTIGATING THE PED PROTEIN AND ITS EFFECT ON TRANSLATIONAL CONTROL IN DROSOPHILA MELANOGASTER SPERMATOGENESIS.” 2012. Web. 26 Jan 2021.

Vancouver:

Keesling DC. INVESTIGATING THE PED PROTEIN AND ITS EFFECT ON TRANSLATIONAL CONTROL IN DROSOPHILA MELANOGASTER SPERMATOGENESIS. [Internet] [Masters thesis]. University of Kentucky; 2012. [cited 2021 Jan 26]. Available from: https://uknowledge.uky.edu/biology_etds/2.

Council of Science Editors:

Keesling DC. INVESTIGATING THE PED PROTEIN AND ITS EFFECT ON TRANSLATIONAL CONTROL IN DROSOPHILA MELANOGASTER SPERMATOGENESIS. [Masters Thesis]. University of Kentucky; 2012. Available from: https://uknowledge.uky.edu/biology_etds/2


University of Oxford

5. Feng, Tianshu. Characterisation of 2-oxoglutarate- and fe(II)-dependent oxygenases targeting the protein synthesis apparatus.

Degree: PhD, 2014, University of Oxford

 Members of the 2-oxoglutarate (2OG)- and Fe(II)-dependent oxygenase (2OG oxygenase) superfamily catalyse a wide range of oxidative reactions in biology. 2OG oxygenases require Fe(II) and… (more)

Subjects/Keywords: 572; Biochemistry; Cell Biology; oxygen sensing; protein synthesis; translational termination; ribosome; post-translational modification

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APA (6th Edition):

Feng, T. (2014). Characterisation of 2-oxoglutarate- and fe(II)-dependent oxygenases targeting the protein synthesis apparatus. (Doctoral Dissertation). University of Oxford. Retrieved from http://ora.ox.ac.uk/objects/uuid:406a311b-dae6-48c6-9785-1e2f0b889e45 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.655026

Chicago Manual of Style (16th Edition):

Feng, Tianshu. “Characterisation of 2-oxoglutarate- and fe(II)-dependent oxygenases targeting the protein synthesis apparatus.” 2014. Doctoral Dissertation, University of Oxford. Accessed January 26, 2021. http://ora.ox.ac.uk/objects/uuid:406a311b-dae6-48c6-9785-1e2f0b889e45 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.655026.

MLA Handbook (7th Edition):

Feng, Tianshu. “Characterisation of 2-oxoglutarate- and fe(II)-dependent oxygenases targeting the protein synthesis apparatus.” 2014. Web. 26 Jan 2021.

Vancouver:

Feng T. Characterisation of 2-oxoglutarate- and fe(II)-dependent oxygenases targeting the protein synthesis apparatus. [Internet] [Doctoral dissertation]. University of Oxford; 2014. [cited 2021 Jan 26]. Available from: http://ora.ox.ac.uk/objects/uuid:406a311b-dae6-48c6-9785-1e2f0b889e45 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.655026.

Council of Science Editors:

Feng T. Characterisation of 2-oxoglutarate- and fe(II)-dependent oxygenases targeting the protein synthesis apparatus. [Doctoral Dissertation]. University of Oxford; 2014. Available from: http://ora.ox.ac.uk/objects/uuid:406a311b-dae6-48c6-9785-1e2f0b889e45 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.655026


Freie Universität Berlin

6. Hou, Jingyi. Globale Studie der cis-regulatorischen Effekte auf die Translation in Säugetierzellen.

Degree: 2016, Freie Universität Berlin

 Diese Dissertation setzt sich aus zwei Teilen zusammen: Der erste Teil beschreibt eine globale Studie von cis-regulatorischen Divergenzen in der mRNA Translationseffizienz von Säugetierzellen. Hierzu… (more)

Subjects/Keywords: translational regulation; cis-regulatory elements; allele-specific gene expression; transcript leaders; 500 Naturwissenschaften und Mathematik::570 Biowissenschaften; Biologie::570 Biowissenschaften; Biologie

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

APA (6th Edition):

Hou, J. (2016). Globale Studie der cis-regulatorischen Effekte auf die Translation in Säugetierzellen. (Thesis). Freie Universität Berlin. Retrieved from http://dx.doi.org/10.17169/refubium-6902

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):

Hou, Jingyi. “Globale Studie der cis-regulatorischen Effekte auf die Translation in Säugetierzellen.” 2016. Thesis, Freie Universität Berlin. Accessed January 26, 2021. http://dx.doi.org/10.17169/refubium-6902.

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

MLA Handbook (7th Edition):

Hou, Jingyi. “Globale Studie der cis-regulatorischen Effekte auf die Translation in Säugetierzellen.” 2016. Web. 26 Jan 2021.

Vancouver:

Hou J. Globale Studie der cis-regulatorischen Effekte auf die Translation in Säugetierzellen. [Internet] [Thesis]. Freie Universität Berlin; 2016. [cited 2021 Jan 26]. Available from: http://dx.doi.org/10.17169/refubium-6902.

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

Council of Science Editors:

Hou J. Globale Studie der cis-regulatorischen Effekte auf die Translation in Säugetierzellen. [Thesis]. Freie Universität Berlin; 2016. Available from: http://dx.doi.org/10.17169/refubium-6902

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


University of California – San Francisco

7. Chang, Matthew Tsn-Wei. Systematic identification of driver mutations in cancer.

Degree: Pharmaceutical Sciences and Pharmacogenomics, 2016, University of California – San Francisco

 The advent of next-generation sequencing has accelerated the search for somatic mutations that drive the initiation and progression of human cancers. Much emphasis has been… (more)

Subjects/Keywords: Bioinformatics; Oncology; Biology; Bioinformatics; Biology; Cancer genomics; Oncology; Translational research

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APA (6th Edition):

Chang, M. T. (2016). Systematic identification of driver mutations in cancer. (Thesis). University of California – San Francisco. Retrieved from http://www.escholarship.org/uc/item/0s53q62g

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):

Chang, Matthew Tsn-Wei. “Systematic identification of driver mutations in cancer.” 2016. Thesis, University of California – San Francisco. Accessed January 26, 2021. http://www.escholarship.org/uc/item/0s53q62g.

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

MLA Handbook (7th Edition):

Chang, Matthew Tsn-Wei. “Systematic identification of driver mutations in cancer.” 2016. Web. 26 Jan 2021.

Vancouver:

Chang MT. Systematic identification of driver mutations in cancer. [Internet] [Thesis]. University of California – San Francisco; 2016. [cited 2021 Jan 26]. Available from: http://www.escholarship.org/uc/item/0s53q62g.

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

Council of Science Editors:

Chang MT. Systematic identification of driver mutations in cancer. [Thesis]. University of California – San Francisco; 2016. Available from: http://www.escholarship.org/uc/item/0s53q62g

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


Princeton University

8. Dann, Geoffrey Paul. Diverse Regulation of ISWI Family ATP-dependent Chromatin Remodeling Enzymes by Nucleosome Modifications .

Degree: PhD, 2017, Princeton University

 ATP-dependent chromatin remodelers regulate access to genetic information by controlling nucleosome positions in vivo. However, the mechanism by which remodelers discriminate between different nucleosome substrates… (more)

Subjects/Keywords: Chemical Biology; Chromatin Biology; Chromatin Remodeling; Epigenetics; Histones; Post-translational modifications

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APA (6th Edition):

Dann, G. P. (2017). Diverse Regulation of ISWI Family ATP-dependent Chromatin Remodeling Enzymes by Nucleosome Modifications . (Doctoral Dissertation). Princeton University. Retrieved from http://arks.princeton.edu/ark:/88435/dsp01j9602327k

Chicago Manual of Style (16th Edition):

Dann, Geoffrey Paul. “Diverse Regulation of ISWI Family ATP-dependent Chromatin Remodeling Enzymes by Nucleosome Modifications .” 2017. Doctoral Dissertation, Princeton University. Accessed January 26, 2021. http://arks.princeton.edu/ark:/88435/dsp01j9602327k.

MLA Handbook (7th Edition):

Dann, Geoffrey Paul. “Diverse Regulation of ISWI Family ATP-dependent Chromatin Remodeling Enzymes by Nucleosome Modifications .” 2017. Web. 26 Jan 2021.

Vancouver:

Dann GP. Diverse Regulation of ISWI Family ATP-dependent Chromatin Remodeling Enzymes by Nucleosome Modifications . [Internet] [Doctoral dissertation]. Princeton University; 2017. [cited 2021 Jan 26]. Available from: http://arks.princeton.edu/ark:/88435/dsp01j9602327k.

Council of Science Editors:

Dann GP. Diverse Regulation of ISWI Family ATP-dependent Chromatin Remodeling Enzymes by Nucleosome Modifications . [Doctoral Dissertation]. Princeton University; 2017. Available from: http://arks.princeton.edu/ark:/88435/dsp01j9602327k


University of California – Irvine

9. Hachey, Stephanie. Effect of BRAF V600E Heterogeneity on Melanoma Pathogenesis.

Degree: Biomedical and Translational Science, 2014, University of California – Irvine

 To determine if BRAF V600E is conserved during melanoma disease progression and the effect of heterogeneity on patient outcomes, clinical data was collected from 17… (more)

Subjects/Keywords: Molecular biology; Medicine; Cancer; Clinical; Genetic; Melanoma; Metastasis; Translational

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APA (6th Edition):

Hachey, S. (2014). Effect of BRAF V600E Heterogeneity on Melanoma Pathogenesis. (Thesis). University of California – Irvine. Retrieved from http://www.escholarship.org/uc/item/8px4d4tf

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):

Hachey, Stephanie. “Effect of BRAF V600E Heterogeneity on Melanoma Pathogenesis.” 2014. Thesis, University of California – Irvine. Accessed January 26, 2021. http://www.escholarship.org/uc/item/8px4d4tf.

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

MLA Handbook (7th Edition):

Hachey, Stephanie. “Effect of BRAF V600E Heterogeneity on Melanoma Pathogenesis.” 2014. Web. 26 Jan 2021.

Vancouver:

Hachey S. Effect of BRAF V600E Heterogeneity on Melanoma Pathogenesis. [Internet] [Thesis]. University of California – Irvine; 2014. [cited 2021 Jan 26]. Available from: http://www.escholarship.org/uc/item/8px4d4tf.

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

Council of Science Editors:

Hachey S. Effect of BRAF V600E Heterogeneity on Melanoma Pathogenesis. [Thesis]. University of California – Irvine; 2014. Available from: http://www.escholarship.org/uc/item/8px4d4tf

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


Texas A&M University

10. Wang, Zhipeng. The Chemical Synthetic Investigation of Proteins with Sitespecific Lysine Post-Translational Modifications.

Degree: PhD, Chemistry, 2018, Texas A&M University

 In the recent decade, an increasing amount of protein post-translational modifications (PTMs) have been discovered, which are important epigenetic markers widespread on nucleic and cytoplasmic… (more)

Subjects/Keywords: Protein chemical biology; Post-translational modification; Lysine; noncanonical amino acids

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APA (6th Edition):

Wang, Z. (2018). The Chemical Synthetic Investigation of Proteins with Sitespecific Lysine Post-Translational Modifications. (Doctoral Dissertation). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/173444

Chicago Manual of Style (16th Edition):

Wang, Zhipeng. “The Chemical Synthetic Investigation of Proteins with Sitespecific Lysine Post-Translational Modifications.” 2018. Doctoral Dissertation, Texas A&M University. Accessed January 26, 2021. http://hdl.handle.net/1969.1/173444.

MLA Handbook (7th Edition):

Wang, Zhipeng. “The Chemical Synthetic Investigation of Proteins with Sitespecific Lysine Post-Translational Modifications.” 2018. Web. 26 Jan 2021.

Vancouver:

Wang Z. The Chemical Synthetic Investigation of Proteins with Sitespecific Lysine Post-Translational Modifications. [Internet] [Doctoral dissertation]. Texas A&M University; 2018. [cited 2021 Jan 26]. Available from: http://hdl.handle.net/1969.1/173444.

Council of Science Editors:

Wang Z. The Chemical Synthetic Investigation of Proteins with Sitespecific Lysine Post-Translational Modifications. [Doctoral Dissertation]. Texas A&M University; 2018. Available from: http://hdl.handle.net/1969.1/173444


Penn State University

11. Tian, Tian. development of a biophysical model of translational coupling to coordinate protein expression.

Degree: 2012, Penn State University

Translational coupling is a common phenomenon in polycistronic bacterial operons, where translation of the downstream gene expression is dependent and coupled to translation of an… (more)

Subjects/Keywords: Translational coupling; Biophysical model; Protein expression; Synthetic biology; Escherichia coli

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APA (6th Edition):

Tian, T. (2012). development of a biophysical model of translational coupling to coordinate protein expression. (Thesis). Penn State University. Retrieved from https://submit-etda.libraries.psu.edu/catalog/15480

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):

Tian, Tian. “development of a biophysical model of translational coupling to coordinate protein expression.” 2012. Thesis, Penn State University. Accessed January 26, 2021. https://submit-etda.libraries.psu.edu/catalog/15480.

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

MLA Handbook (7th Edition):

Tian, Tian. “development of a biophysical model of translational coupling to coordinate protein expression.” 2012. Web. 26 Jan 2021.

Vancouver:

Tian T. development of a biophysical model of translational coupling to coordinate protein expression. [Internet] [Thesis]. Penn State University; 2012. [cited 2021 Jan 26]. Available from: https://submit-etda.libraries.psu.edu/catalog/15480.

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

Council of Science Editors:

Tian T. development of a biophysical model of translational coupling to coordinate protein expression. [Thesis]. Penn State University; 2012. Available from: https://submit-etda.libraries.psu.edu/catalog/15480

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


Virginia Commonwealth University

12. Quinn, Bridget A. Novel Therapeutic Strategies for Pancreatic Cancer.

Degree: PhD, Human Genetics, 2014, Virginia Commonwealth University

  Pancreatic cancer is a devastating disease that leaves patients with a very poor prognosis and few therapeutic options. Many of the treatment options available… (more)

Subjects/Keywords: Medical Cell Biology; Medical Genetics; Neoplasms; Oncology; Translational Medical Research

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APA (6th Edition):

Quinn, B. A. (2014). Novel Therapeutic Strategies for Pancreatic Cancer. (Doctoral Dissertation). Virginia Commonwealth University. Retrieved from https://doi.org/10.25772/T39H-KJ31 ; https://scholarscompass.vcu.edu/etd/4671

Chicago Manual of Style (16th Edition):

Quinn, Bridget A. “Novel Therapeutic Strategies for Pancreatic Cancer.” 2014. Doctoral Dissertation, Virginia Commonwealth University. Accessed January 26, 2021. https://doi.org/10.25772/T39H-KJ31 ; https://scholarscompass.vcu.edu/etd/4671.

MLA Handbook (7th Edition):

Quinn, Bridget A. “Novel Therapeutic Strategies for Pancreatic Cancer.” 2014. Web. 26 Jan 2021.

Vancouver:

Quinn BA. Novel Therapeutic Strategies for Pancreatic Cancer. [Internet] [Doctoral dissertation]. Virginia Commonwealth University; 2014. [cited 2021 Jan 26]. Available from: https://doi.org/10.25772/T39H-KJ31 ; https://scholarscompass.vcu.edu/etd/4671.

Council of Science Editors:

Quinn BA. Novel Therapeutic Strategies for Pancreatic Cancer. [Doctoral Dissertation]. Virginia Commonwealth University; 2014. Available from: https://doi.org/10.25772/T39H-KJ31 ; https://scholarscompass.vcu.edu/etd/4671


University of Vermont

13. Romano, Joseph D. Exploring Complex Disease Gene Relationships Using Simultaneous Analysis.

Degree: Microbiology and Molecular Genetics, 2014, University of Vermont

  The characterization of complex diseases remains a great challenge for biomedical researchers due to the myriad interactions of genetic and environmental factors. Adaptation of… (more)

Subjects/Keywords: Translational Bioinformatics; Comparative Genomics; Computational Biology; Bioinformatics; Alzheimer Disease; Phylogenomics

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APA (6th Edition):

Romano, J. D. (2014). Exploring Complex Disease Gene Relationships Using Simultaneous Analysis. (Thesis). University of Vermont. Retrieved from https://scholarworks.uvm.edu/hcoltheses/35

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):

Romano, Joseph D. “Exploring Complex Disease Gene Relationships Using Simultaneous Analysis.” 2014. Thesis, University of Vermont. Accessed January 26, 2021. https://scholarworks.uvm.edu/hcoltheses/35.

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

MLA Handbook (7th Edition):

Romano, Joseph D. “Exploring Complex Disease Gene Relationships Using Simultaneous Analysis.” 2014. Web. 26 Jan 2021.

Vancouver:

Romano JD. Exploring Complex Disease Gene Relationships Using Simultaneous Analysis. [Internet] [Thesis]. University of Vermont; 2014. [cited 2021 Jan 26]. Available from: https://scholarworks.uvm.edu/hcoltheses/35.

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

Council of Science Editors:

Romano JD. Exploring Complex Disease Gene Relationships Using Simultaneous Analysis. [Thesis]. University of Vermont; 2014. Available from: https://scholarworks.uvm.edu/hcoltheses/35

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

14. Hasin, Naushaba. Functional significance of Hsp70 post-translational modification in prion propagation and cellular function.

Degree: 2012, RIAN

 The term prion (proteinaceous infectious particles) was first coined by Stanley Prusiner while naming the causative agent responsible for a group of invariably fatal neurodegenerative… (more)

Subjects/Keywords: Biology; Hsp70 post-translational modification; prion propagation; cellular function

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APA (6th Edition):

Hasin, N. (2012). Functional significance of Hsp70 post-translational modification in prion propagation and cellular function. (Thesis). RIAN. Retrieved from http://eprints.maynoothuniversity.ie/4077/

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):

Hasin, Naushaba. “Functional significance of Hsp70 post-translational modification in prion propagation and cellular function.” 2012. Thesis, RIAN. Accessed January 26, 2021. http://eprints.maynoothuniversity.ie/4077/.

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

MLA Handbook (7th Edition):

Hasin, Naushaba. “Functional significance of Hsp70 post-translational modification in prion propagation and cellular function.” 2012. Web. 26 Jan 2021.

Vancouver:

Hasin N. Functional significance of Hsp70 post-translational modification in prion propagation and cellular function. [Internet] [Thesis]. RIAN; 2012. [cited 2021 Jan 26]. Available from: http://eprints.maynoothuniversity.ie/4077/.

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

Council of Science Editors:

Hasin N. Functional significance of Hsp70 post-translational modification in prion propagation and cellular function. [Thesis]. RIAN; 2012. Available from: http://eprints.maynoothuniversity.ie/4077/

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


University of Western Ontario

15. Singh, Randeep K. Regulation of E2F1 in Keratinocytes During UV-Damage and Differentiation.

Degree: 2016, University of Western Ontario

 The E2F1 transcription factor regulates the expression of key genes involved in cell proliferation and differentiation to maintain skin homeostasis. The expression of E2F1 is… (more)

Subjects/Keywords: Keratinocytes; E2F; post-translational modification; hHR23; DNA photodamage; Cdh1.; Cancer Biology

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APA (6th Edition):

Singh, R. K. (2016). Regulation of E2F1 in Keratinocytes During UV-Damage and Differentiation. (Thesis). University of Western Ontario. Retrieved from https://ir.lib.uwo.ca/etd/4202

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):

Singh, Randeep K. “Regulation of E2F1 in Keratinocytes During UV-Damage and Differentiation.” 2016. Thesis, University of Western Ontario. Accessed January 26, 2021. https://ir.lib.uwo.ca/etd/4202.

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

MLA Handbook (7th Edition):

Singh, Randeep K. “Regulation of E2F1 in Keratinocytes During UV-Damage and Differentiation.” 2016. Web. 26 Jan 2021.

Vancouver:

Singh RK. Regulation of E2F1 in Keratinocytes During UV-Damage and Differentiation. [Internet] [Thesis]. University of Western Ontario; 2016. [cited 2021 Jan 26]. Available from: https://ir.lib.uwo.ca/etd/4202.

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

Council of Science Editors:

Singh RK. Regulation of E2F1 in Keratinocytes During UV-Damage and Differentiation. [Thesis]. University of Western Ontario; 2016. Available from: https://ir.lib.uwo.ca/etd/4202

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


University of Minnesota

16. Liu, Katherine. Reconceptualizing Cancer: The development of new models and frameworks.

Degree: PhD, Ecology, Evolution and Behavior, 2018, University of Minnesota

 Cancer research secures an enormous amount of money each year, and researchers are generally quite productive with that money. The trend over the recent years… (more)

Subjects/Keywords: cancer; evolution; models; modularity; philosophy of biology; translational research

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APA (6th Edition):

Liu, K. (2018). Reconceptualizing Cancer: The development of new models and frameworks. (Doctoral Dissertation). University of Minnesota. Retrieved from http://hdl.handle.net/11299/202170

Chicago Manual of Style (16th Edition):

Liu, Katherine. “Reconceptualizing Cancer: The development of new models and frameworks.” 2018. Doctoral Dissertation, University of Minnesota. Accessed January 26, 2021. http://hdl.handle.net/11299/202170.

MLA Handbook (7th Edition):

Liu, Katherine. “Reconceptualizing Cancer: The development of new models and frameworks.” 2018. Web. 26 Jan 2021.

Vancouver:

Liu K. Reconceptualizing Cancer: The development of new models and frameworks. [Internet] [Doctoral dissertation]. University of Minnesota; 2018. [cited 2021 Jan 26]. Available from: http://hdl.handle.net/11299/202170.

Council of Science Editors:

Liu K. Reconceptualizing Cancer: The development of new models and frameworks. [Doctoral Dissertation]. University of Minnesota; 2018. Available from: http://hdl.handle.net/11299/202170

17. Hasin, Naushaba. Functional significance of Hsp70 post-translational modification in prion propagation and cellular function.

Degree: 2012, RIAN

 The term prion (proteinaceous infectious particles) was first coined by Stanley Prusiner while naming the causative agent responsible for a group of invariably fatal neurodegenerative… (more)

Subjects/Keywords: Biology; Hsp70 post-translational modification; prion propagation; cellular function

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APA (6th Edition):

Hasin, N. (2012). Functional significance of Hsp70 post-translational modification in prion propagation and cellular function. (Thesis). RIAN. Retrieved from http://mural.maynoothuniversity.ie/4077/

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):

Hasin, Naushaba. “Functional significance of Hsp70 post-translational modification in prion propagation and cellular function.” 2012. Thesis, RIAN. Accessed January 26, 2021. http://mural.maynoothuniversity.ie/4077/.

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

MLA Handbook (7th Edition):

Hasin, Naushaba. “Functional significance of Hsp70 post-translational modification in prion propagation and cellular function.” 2012. Web. 26 Jan 2021.

Vancouver:

Hasin N. Functional significance of Hsp70 post-translational modification in prion propagation and cellular function. [Internet] [Thesis]. RIAN; 2012. [cited 2021 Jan 26]. Available from: http://mural.maynoothuniversity.ie/4077/.

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

Council of Science Editors:

Hasin N. Functional significance of Hsp70 post-translational modification in prion propagation and cellular function. [Thesis]. RIAN; 2012. Available from: http://mural.maynoothuniversity.ie/4077/

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


University of Maryland

18. Bowen, Alicia Marie. The Core of Eukaryotic Ribosomal Protein uS19 Functions as a Pivot Point Enhancing Eukaryotic Ribosome Flexibility.

Degree: Biochemistry, 2015, University of Maryland

 While most ribosomal elements are highly conserved in the three domains of life, over the course of evolution, significant differences have emerged as ribosomes have… (more)

Subjects/Keywords: Biochemistry; Molecular biology; protein translation; ribosomal protein; ribosomes; translational fidelity

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APA (6th Edition):

Bowen, A. M. (2015). The Core of Eukaryotic Ribosomal Protein uS19 Functions as a Pivot Point Enhancing Eukaryotic Ribosome Flexibility. (Thesis). University of Maryland. Retrieved from http://hdl.handle.net/1903/16608

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):

Bowen, Alicia Marie. “The Core of Eukaryotic Ribosomal Protein uS19 Functions as a Pivot Point Enhancing Eukaryotic Ribosome Flexibility.” 2015. Thesis, University of Maryland. Accessed January 26, 2021. http://hdl.handle.net/1903/16608.

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

MLA Handbook (7th Edition):

Bowen, Alicia Marie. “The Core of Eukaryotic Ribosomal Protein uS19 Functions as a Pivot Point Enhancing Eukaryotic Ribosome Flexibility.” 2015. Web. 26 Jan 2021.

Vancouver:

Bowen AM. The Core of Eukaryotic Ribosomal Protein uS19 Functions as a Pivot Point Enhancing Eukaryotic Ribosome Flexibility. [Internet] [Thesis]. University of Maryland; 2015. [cited 2021 Jan 26]. Available from: http://hdl.handle.net/1903/16608.

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

Council of Science Editors:

Bowen AM. The Core of Eukaryotic Ribosomal Protein uS19 Functions as a Pivot Point Enhancing Eukaryotic Ribosome Flexibility. [Thesis]. University of Maryland; 2015. Available from: http://hdl.handle.net/1903/16608

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


University of Helsinki

19. Li, Huini. Neuropilin-1 (NRP1) regulates glioblastoma cell autophagy in association with p62/Sequestosome 1 (SQSTM1).

Degree: Medicinska fakulteten, 2016, University of Helsinki

 Glioblastoma Multiforme (GBM) is the most common and aggressive types of glioma in adults. Autophagy allows degradation and recycling of cellular components such as damaged… (more)

Subjects/Keywords: p62/SQSTM1; Neuropilin-1; Autophagy; Glioblastoma; Translational Cancer Biology; Translationaalinen syöpäbiologia

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APA (6th Edition):

Li, H. (2016). Neuropilin-1 (NRP1) regulates glioblastoma cell autophagy in association with p62/Sequestosome 1 (SQSTM1). (Masters Thesis). University of Helsinki. Retrieved from http://hdl.handle.net/10138/164160

Chicago Manual of Style (16th Edition):

Li, Huini. “Neuropilin-1 (NRP1) regulates glioblastoma cell autophagy in association with p62/Sequestosome 1 (SQSTM1).” 2016. Masters Thesis, University of Helsinki. Accessed January 26, 2021. http://hdl.handle.net/10138/164160.

MLA Handbook (7th Edition):

Li, Huini. “Neuropilin-1 (NRP1) regulates glioblastoma cell autophagy in association with p62/Sequestosome 1 (SQSTM1).” 2016. Web. 26 Jan 2021.

Vancouver:

Li H. Neuropilin-1 (NRP1) regulates glioblastoma cell autophagy in association with p62/Sequestosome 1 (SQSTM1). [Internet] [Masters thesis]. University of Helsinki; 2016. [cited 2021 Jan 26]. Available from: http://hdl.handle.net/10138/164160.

Council of Science Editors:

Li H. Neuropilin-1 (NRP1) regulates glioblastoma cell autophagy in association with p62/Sequestosome 1 (SQSTM1). [Masters Thesis]. University of Helsinki; 2016. Available from: http://hdl.handle.net/10138/164160


University of Cincinnati

20. Tang, Xiaofang. Regulation of Wingless secretion, distribution and signaling.

Degree: PhD, Medicine: Molecular and Developmental Biology, 2012, University of Cincinnati

  The evolutionarily conserved Wnt (Wingless and INT-1) family proteins are secreted cysteine-rich glycoproteins essential for embryonic patterning and adult homeostasis. Wnt signaling is highly… (more)

Subjects/Keywords: Developmental Biology; Wingless; Wntless; post-translational modification; secretion; signal transduction

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APA (6th Edition):

Tang, X. (2012). Regulation of Wingless secretion, distribution and signaling. (Doctoral Dissertation). University of Cincinnati. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=ucin1353100929

Chicago Manual of Style (16th Edition):

Tang, Xiaofang. “Regulation of Wingless secretion, distribution and signaling.” 2012. Doctoral Dissertation, University of Cincinnati. Accessed January 26, 2021. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1353100929.

MLA Handbook (7th Edition):

Tang, Xiaofang. “Regulation of Wingless secretion, distribution and signaling.” 2012. Web. 26 Jan 2021.

Vancouver:

Tang X. Regulation of Wingless secretion, distribution and signaling. [Internet] [Doctoral dissertation]. University of Cincinnati; 2012. [cited 2021 Jan 26]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ucin1353100929.

Council of Science Editors:

Tang X. Regulation of Wingless secretion, distribution and signaling. [Doctoral Dissertation]. University of Cincinnati; 2012. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ucin1353100929


University of Texas – Austin

21. Mayfield, Joshua Edward. Post-translational modification of the C-terminal domain of RNA polymerase II : identification and cross talk.

Degree: PhD, Biochemistry, 2020, University of Texas – Austin

 RNA polymerase II is a highly regulated protein complex that transcribes all protein coding mRNA and many non-coding RNAs. A key mechanism that facilitates its… (more)

Subjects/Keywords: Transcription; Post-translational modification; Phosphorylation; Proline isomerization; Mass spectrometry; Chemical biology

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APA (6th Edition):

Mayfield, J. E. (2020). Post-translational modification of the C-terminal domain of RNA polymerase II : identification and cross talk. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://dx.doi.org/10.26153/tsw/7505

Chicago Manual of Style (16th Edition):

Mayfield, Joshua Edward. “Post-translational modification of the C-terminal domain of RNA polymerase II : identification and cross talk.” 2020. Doctoral Dissertation, University of Texas – Austin. Accessed January 26, 2021. http://dx.doi.org/10.26153/tsw/7505.

MLA Handbook (7th Edition):

Mayfield, Joshua Edward. “Post-translational modification of the C-terminal domain of RNA polymerase II : identification and cross talk.” 2020. Web. 26 Jan 2021.

Vancouver:

Mayfield JE. Post-translational modification of the C-terminal domain of RNA polymerase II : identification and cross talk. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2020. [cited 2021 Jan 26]. Available from: http://dx.doi.org/10.26153/tsw/7505.

Council of Science Editors:

Mayfield JE. Post-translational modification of the C-terminal domain of RNA polymerase II : identification and cross talk. [Doctoral Dissertation]. University of Texas – Austin; 2020. Available from: http://dx.doi.org/10.26153/tsw/7505


Temple University

22. Romasko, Edward Joseph. Translational Control of Maternal mRNA in Mouse Oocytes.

Degree: PhD, 2014, Temple University

Molecular Biology and Genetics

In contrast to other species, localized maternal mRNAs are not believed to be prominent features of mammalian oocytes. Due to the… (more)

Subjects/Keywords: Molecular biology; Genetics; Developmental biology;

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APA (6th Edition):

Romasko, E. J. (2014). Translational Control of Maternal mRNA in Mouse Oocytes. (Doctoral Dissertation). Temple University. Retrieved from http://digital.library.temple.edu/u?/p245801coll10,273206

Chicago Manual of Style (16th Edition):

Romasko, Edward Joseph. “Translational Control of Maternal mRNA in Mouse Oocytes.” 2014. Doctoral Dissertation, Temple University. Accessed January 26, 2021. http://digital.library.temple.edu/u?/p245801coll10,273206.

MLA Handbook (7th Edition):

Romasko, Edward Joseph. “Translational Control of Maternal mRNA in Mouse Oocytes.” 2014. Web. 26 Jan 2021.

Vancouver:

Romasko EJ. Translational Control of Maternal mRNA in Mouse Oocytes. [Internet] [Doctoral dissertation]. Temple University; 2014. [cited 2021 Jan 26]. Available from: http://digital.library.temple.edu/u?/p245801coll10,273206.

Council of Science Editors:

Romasko EJ. Translational Control of Maternal mRNA in Mouse Oocytes. [Doctoral Dissertation]. Temple University; 2014. Available from: http://digital.library.temple.edu/u?/p245801coll10,273206


Cornell University

23. Negron Abril, Yashira Liz. TUMOR PROMOTING FUNCTIONS FOR THE METABOLIC REGULATOR SIRT5.

Degree: PhD, Chemistry and Chemical Biology, 2018, Cornell University

 Cancer is among the leading causes of death worldwide, highlighting the urgent need for identification of new targets and the development of new strategies to… (more)

Subjects/Keywords: Mice; Post-translational modifications; SIRT5; Sirtuins; Small molecules; Biology; Molecular biology; Chemistry; cancer

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APA (6th Edition):

Negron Abril, Y. L. (2018). TUMOR PROMOTING FUNCTIONS FOR THE METABOLIC REGULATOR SIRT5. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/59440

Chicago Manual of Style (16th Edition):

Negron Abril, Yashira Liz. “TUMOR PROMOTING FUNCTIONS FOR THE METABOLIC REGULATOR SIRT5.” 2018. Doctoral Dissertation, Cornell University. Accessed January 26, 2021. http://hdl.handle.net/1813/59440.

MLA Handbook (7th Edition):

Negron Abril, Yashira Liz. “TUMOR PROMOTING FUNCTIONS FOR THE METABOLIC REGULATOR SIRT5.” 2018. Web. 26 Jan 2021.

Vancouver:

Negron Abril YL. TUMOR PROMOTING FUNCTIONS FOR THE METABOLIC REGULATOR SIRT5. [Internet] [Doctoral dissertation]. Cornell University; 2018. [cited 2021 Jan 26]. Available from: http://hdl.handle.net/1813/59440.

Council of Science Editors:

Negron Abril YL. TUMOR PROMOTING FUNCTIONS FOR THE METABOLIC REGULATOR SIRT5. [Doctoral Dissertation]. Cornell University; 2018. Available from: http://hdl.handle.net/1813/59440


Wayne State University

24. Jessmon, Philip. Human trophoblast survival and invasion in the developing placenta: autocrine regulation by hbegf.

Degree: PhD, Anatomy and Cell Biology, 2011, Wayne State University

  HBEGF is a multifunctional protein in early pregnancy that induces cytotrophoblast (CTB) cell differentiation to an invasive phenotype, protects against apoptosis, and is involved… (more)

Subjects/Keywords: HBEGF, integrin switching, miRNA, placenta, translational regulation, trophoblast; Cell Biology; Molecular Biology; Obstetrics and Gynecology

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APA (6th Edition):

Jessmon, P. (2011). Human trophoblast survival and invasion in the developing placenta: autocrine regulation by hbegf. (Doctoral Dissertation). Wayne State University. Retrieved from https://digitalcommons.wayne.edu/oa_dissertations/353

Chicago Manual of Style (16th Edition):

Jessmon, Philip. “Human trophoblast survival and invasion in the developing placenta: autocrine regulation by hbegf.” 2011. Doctoral Dissertation, Wayne State University. Accessed January 26, 2021. https://digitalcommons.wayne.edu/oa_dissertations/353.

MLA Handbook (7th Edition):

Jessmon, Philip. “Human trophoblast survival and invasion in the developing placenta: autocrine regulation by hbegf.” 2011. Web. 26 Jan 2021.

Vancouver:

Jessmon P. Human trophoblast survival and invasion in the developing placenta: autocrine regulation by hbegf. [Internet] [Doctoral dissertation]. Wayne State University; 2011. [cited 2021 Jan 26]. Available from: https://digitalcommons.wayne.edu/oa_dissertations/353.

Council of Science Editors:

Jessmon P. Human trophoblast survival and invasion in the developing placenta: autocrine regulation by hbegf. [Doctoral Dissertation]. Wayne State University; 2011. Available from: https://digitalcommons.wayne.edu/oa_dissertations/353

25. Chicoine, Kay-ellen. Characterization of the Role of Testis-Specific Serine Kinase1 (tssk1) in Human Sperm Capacitation.

Degree: MS(M.S.), Animal Science, 2013, U of Massachusetts : Masters

  The ability of a sperm to fertilize an egg involves a complex series of events, referred to as capacitation. Capacitation involves sperm acquiring a… (more)

Subjects/Keywords: kinase; TSSK1; human; sperm; post-translational modification; CASA; Cell Biology; Molecular Biology

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APA (6th Edition):

Chicoine, K. (2013). Characterization of the Role of Testis-Specific Serine Kinase1 (tssk1) in Human Sperm Capacitation. (Masters Thesis). U of Massachusetts : Masters. Retrieved from http://scholarworks.umass.edu/theses/1112

Chicago Manual of Style (16th Edition):

Chicoine, Kay-ellen. “Characterization of the Role of Testis-Specific Serine Kinase1 (tssk1) in Human Sperm Capacitation.” 2013. Masters Thesis, U of Massachusetts : Masters. Accessed January 26, 2021. http://scholarworks.umass.edu/theses/1112.

MLA Handbook (7th Edition):

Chicoine, Kay-ellen. “Characterization of the Role of Testis-Specific Serine Kinase1 (tssk1) in Human Sperm Capacitation.” 2013. Web. 26 Jan 2021.

Vancouver:

Chicoine K. Characterization of the Role of Testis-Specific Serine Kinase1 (tssk1) in Human Sperm Capacitation. [Internet] [Masters thesis]. U of Massachusetts : Masters; 2013. [cited 2021 Jan 26]. Available from: http://scholarworks.umass.edu/theses/1112.

Council of Science Editors:

Chicoine K. Characterization of the Role of Testis-Specific Serine Kinase1 (tssk1) in Human Sperm Capacitation. [Masters Thesis]. U of Massachusetts : Masters; 2013. Available from: http://scholarworks.umass.edu/theses/1112


Universiteit Utrecht

26. Kloosterman, W.P. The expression and function of microRNAs in vertebrate embryonic development.

Degree: 2007, Universiteit Utrecht

 MicroRNAs regulate gene expression at the posttranscriptional level by binding to the 3'UTR of mRNAs. These small RNA molecules (~22 bases in length) are processed… (more)

Subjects/Keywords: Biologie; microRNA; small RNA; zebrafish; gene silencing; Locked Nucleic Acid; in situ; embryo; RNAi; translational inhibition; morpholino

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APA (6th Edition):

Kloosterman, W. P. (2007). The expression and function of microRNAs in vertebrate embryonic development. (Doctoral Dissertation). Universiteit Utrecht. Retrieved from http://dspace.library.uu.nl:8080/handle/1874/22653

Chicago Manual of Style (16th Edition):

Kloosterman, W P. “The expression and function of microRNAs in vertebrate embryonic development.” 2007. Doctoral Dissertation, Universiteit Utrecht. Accessed January 26, 2021. http://dspace.library.uu.nl:8080/handle/1874/22653.

MLA Handbook (7th Edition):

Kloosterman, W P. “The expression and function of microRNAs in vertebrate embryonic development.” 2007. Web. 26 Jan 2021.

Vancouver:

Kloosterman WP. The expression and function of microRNAs in vertebrate embryonic development. [Internet] [Doctoral dissertation]. Universiteit Utrecht; 2007. [cited 2021 Jan 26]. Available from: http://dspace.library.uu.nl:8080/handle/1874/22653.

Council of Science Editors:

Kloosterman WP. The expression and function of microRNAs in vertebrate embryonic development. [Doctoral Dissertation]. Universiteit Utrecht; 2007. Available from: http://dspace.library.uu.nl:8080/handle/1874/22653


University of California – Berkeley

27. Carroll, Johanna Shumway. Post-transcriptional regulation of gene expression by the DExD/H-box protein Dhh1.

Degree: Molecular & Cell Biology, 2011, University of California – Berkeley

 By repressing translation and promoting mRNA decay, cells are able to modulate gene expression and respond swiftly to changing environmental signals and developmental cues. Although… (more)

Subjects/Keywords: Molecular biology; DExD/H box ATPases; mRNA turnover; P bodies; translational control

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APA (6th Edition):

Carroll, J. S. (2011). Post-transcriptional regulation of gene expression by the DExD/H-box protein Dhh1. (Thesis). University of California – Berkeley. Retrieved from http://www.escholarship.org/uc/item/88t4n3v7

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):

Carroll, Johanna Shumway. “Post-transcriptional regulation of gene expression by the DExD/H-box protein Dhh1.” 2011. Thesis, University of California – Berkeley. Accessed January 26, 2021. http://www.escholarship.org/uc/item/88t4n3v7.

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

MLA Handbook (7th Edition):

Carroll, Johanna Shumway. “Post-transcriptional regulation of gene expression by the DExD/H-box protein Dhh1.” 2011. Web. 26 Jan 2021.

Vancouver:

Carroll JS. Post-transcriptional regulation of gene expression by the DExD/H-box protein Dhh1. [Internet] [Thesis]. University of California – Berkeley; 2011. [cited 2021 Jan 26]. Available from: http://www.escholarship.org/uc/item/88t4n3v7.

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

Council of Science Editors:

Carroll JS. Post-transcriptional regulation of gene expression by the DExD/H-box protein Dhh1. [Thesis]. University of California – Berkeley; 2011. Available from: http://www.escholarship.org/uc/item/88t4n3v7

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


UCLA

28. David, John M. The Hidden Costs of Housing Practices: the importance of murine cold-stress to science.

Degree: Molec & Med Pharmacology, 2014, UCLA

 Laboratory mice housed in modern vivariums are chronically cold-stressed. Cold-stressed mice exhibit compensatory non-shivering thermogenesis that drives a significant increase in total energy expenditure. In… (more)

Subjects/Keywords: Veterinary medicine; Medical imaging and radiology; Biology; Caging; Cold-stress; Experimental reproducibility; Mouse; Translational research

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APA (6th Edition):

David, J. M. (2014). The Hidden Costs of Housing Practices: the importance of murine cold-stress to science. (Thesis). UCLA. Retrieved from http://www.escholarship.org/uc/item/9g3430xs

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):

David, John M. “The Hidden Costs of Housing Practices: the importance of murine cold-stress to science.” 2014. Thesis, UCLA. Accessed January 26, 2021. http://www.escholarship.org/uc/item/9g3430xs.

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

MLA Handbook (7th Edition):

David, John M. “The Hidden Costs of Housing Practices: the importance of murine cold-stress to science.” 2014. Web. 26 Jan 2021.

Vancouver:

David JM. The Hidden Costs of Housing Practices: the importance of murine cold-stress to science. [Internet] [Thesis]. UCLA; 2014. [cited 2021 Jan 26]. Available from: http://www.escholarship.org/uc/item/9g3430xs.

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

Council of Science Editors:

David JM. The Hidden Costs of Housing Practices: the importance of murine cold-stress to science. [Thesis]. UCLA; 2014. Available from: http://www.escholarship.org/uc/item/9g3430xs

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


UCLA

29. Dzialo, Maria Charlene. Found in Translation: The Search for Functional Roles of Translation Elongation Factor Methylation and the Discovery of a Novel Type of Protein Methylation.

Degree: Biochemistry & Molecular Biology, 2015, UCLA

 Methylation has emerged as an essential modification of small molecules, lipids, nucleic acids, and proteins. Given the variety of potential substrates, the effects the addition… (more)

Subjects/Keywords: Biochemistry; Molecular biology; Lysine methylation; Methylation; Methyltransferases; Post-translational modifications; Protein; Saccharomyces cerevisiae

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APA (6th Edition):

Dzialo, M. C. (2015). Found in Translation: The Search for Functional Roles of Translation Elongation Factor Methylation and the Discovery of a Novel Type of Protein Methylation. (Thesis). UCLA. Retrieved from http://www.escholarship.org/uc/item/0w7998h0

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):

Dzialo, Maria Charlene. “Found in Translation: The Search for Functional Roles of Translation Elongation Factor Methylation and the Discovery of a Novel Type of Protein Methylation.” 2015. Thesis, UCLA. Accessed January 26, 2021. http://www.escholarship.org/uc/item/0w7998h0.

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

MLA Handbook (7th Edition):

Dzialo, Maria Charlene. “Found in Translation: The Search for Functional Roles of Translation Elongation Factor Methylation and the Discovery of a Novel Type of Protein Methylation.” 2015. Web. 26 Jan 2021.

Vancouver:

Dzialo MC. Found in Translation: The Search for Functional Roles of Translation Elongation Factor Methylation and the Discovery of a Novel Type of Protein Methylation. [Internet] [Thesis]. UCLA; 2015. [cited 2021 Jan 26]. Available from: http://www.escholarship.org/uc/item/0w7998h0.

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

Council of Science Editors:

Dzialo MC. Found in Translation: The Search for Functional Roles of Translation Elongation Factor Methylation and the Discovery of a Novel Type of Protein Methylation. [Thesis]. UCLA; 2015. Available from: http://www.escholarship.org/uc/item/0w7998h0

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


Vanderbilt University

30. Gallant, Jean-Nicolas. EGFR Rearrangements as Oncogenic Drivers and Therapeutic Targets in Lung Cancer.

Degree: PhD, Cancer Biology, 2017, Vanderbilt University

 Lung cancer is the leading cause of cancer deaths worldwide. More than 40% of lung cancers are classified as lung adenocarcinoma (LUAD), which is defined… (more)

Subjects/Keywords: targeted therapy; EGFR; gene rearrangement; gene fusion; lung cancer; translational medicine; structural biology; personalized medicine

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

APA (6th Edition):

Gallant, J. (2017). EGFR Rearrangements as Oncogenic Drivers and Therapeutic Targets in Lung Cancer. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://hdl.handle.net/1803/10873

Chicago Manual of Style (16th Edition):

Gallant, Jean-Nicolas. “EGFR Rearrangements as Oncogenic Drivers and Therapeutic Targets in Lung Cancer.” 2017. Doctoral Dissertation, Vanderbilt University. Accessed January 26, 2021. http://hdl.handle.net/1803/10873.

MLA Handbook (7th Edition):

Gallant, Jean-Nicolas. “EGFR Rearrangements as Oncogenic Drivers and Therapeutic Targets in Lung Cancer.” 2017. Web. 26 Jan 2021.

Vancouver:

Gallant J. EGFR Rearrangements as Oncogenic Drivers and Therapeutic Targets in Lung Cancer. [Internet] [Doctoral dissertation]. Vanderbilt University; 2017. [cited 2021 Jan 26]. Available from: http://hdl.handle.net/1803/10873.

Council of Science Editors:

Gallant J. EGFR Rearrangements as Oncogenic Drivers and Therapeutic Targets in Lung Cancer. [Doctoral Dissertation]. Vanderbilt University; 2017. Available from: http://hdl.handle.net/1803/10873

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