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You searched for subject:(stress granule). Showing records 1 – 28 of 28 total matches.

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University of Colorado

1. Matheny, Tyler. Composition and Dynamics of Stress Granules.

Degree: PhD, 2018, University of Colorado

Stress granules are non-membranous assemblies of RNA and protein that form during conditions in which translation initiation is limited. Stress granules are of interest… (more)

Subjects/Keywords: microscopy; rna; rnp granule; stress granule; transcriptomics; Biochemistry; Molecular Biology

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APA (6th Edition):

Matheny, T. (2018). Composition and Dynamics of Stress Granules. (Doctoral Dissertation). University of Colorado. Retrieved from https://scholar.colorado.edu/chem_gradetds/286

Chicago Manual of Style (16th Edition):

Matheny, Tyler. “Composition and Dynamics of Stress Granules.” 2018. Doctoral Dissertation, University of Colorado. Accessed April 13, 2021. https://scholar.colorado.edu/chem_gradetds/286.

MLA Handbook (7th Edition):

Matheny, Tyler. “Composition and Dynamics of Stress Granules.” 2018. Web. 13 Apr 2021.

Vancouver:

Matheny T. Composition and Dynamics of Stress Granules. [Internet] [Doctoral dissertation]. University of Colorado; 2018. [cited 2021 Apr 13]. Available from: https://scholar.colorado.edu/chem_gradetds/286.

Council of Science Editors:

Matheny T. Composition and Dynamics of Stress Granules. [Doctoral Dissertation]. University of Colorado; 2018. Available from: https://scholar.colorado.edu/chem_gradetds/286


University of Colorado

2. Protter, David Stephen Warren. Contributions of Intrinsically Disordered Regions of Proteins to the Assembly of Ribonucleoprotein Granules.

Degree: PhD, Chemistry & Biochemistry, 2017, University of Colorado

  Cells assemble large, non-membrane bound granules of protein and RNA, termed Ri- bonucleoprotein granules (RNP granules), often in response to a wide variety of… (more)

Subjects/Keywords: intrinsically disordered region; phase separation; RNP granule; stress granule; Biochemistry

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APA (6th Edition):

Protter, D. S. W. (2017). Contributions of Intrinsically Disordered Regions of Proteins to the Assembly of Ribonucleoprotein Granules. (Doctoral Dissertation). University of Colorado. Retrieved from https://scholar.colorado.edu/chem_gradetds/242

Chicago Manual of Style (16th Edition):

Protter, David Stephen Warren. “Contributions of Intrinsically Disordered Regions of Proteins to the Assembly of Ribonucleoprotein Granules.” 2017. Doctoral Dissertation, University of Colorado. Accessed April 13, 2021. https://scholar.colorado.edu/chem_gradetds/242.

MLA Handbook (7th Edition):

Protter, David Stephen Warren. “Contributions of Intrinsically Disordered Regions of Proteins to the Assembly of Ribonucleoprotein Granules.” 2017. Web. 13 Apr 2021.

Vancouver:

Protter DSW. Contributions of Intrinsically Disordered Regions of Proteins to the Assembly of Ribonucleoprotein Granules. [Internet] [Doctoral dissertation]. University of Colorado; 2017. [cited 2021 Apr 13]. Available from: https://scholar.colorado.edu/chem_gradetds/242.

Council of Science Editors:

Protter DSW. Contributions of Intrinsically Disordered Regions of Proteins to the Assembly of Ribonucleoprotein Granules. [Doctoral Dissertation]. University of Colorado; 2017. Available from: https://scholar.colorado.edu/chem_gradetds/242


Université Montpellier II

3. Martin, Sophie. Le composant des granules de stress G3BP : caractérisation phénotypique de souris KO, et identification de son interactome ribonucléoprotéique dans le cerveau de souris : The stress granules component G3BP : functional characterization from KO mouse and identification of its ribonucleoprotein interactome in mouse brain.

Degree: Docteur es, Biologie Santé, 2012, Université Montpellier II

Les protéines capables de lier des ARNs sont essentielles pour les différentes étapes de maturation de l'ARN messager (ARNm), en dirigeant leur localisation et leur… (more)

Subjects/Keywords: Stabilité ARN; Plasticité synaptique; Granule de stress; RNA stability; Synaptic plasticity; Stress granule

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APA (6th Edition):

Martin, S. (2012). Le composant des granules de stress G3BP : caractérisation phénotypique de souris KO, et identification de son interactome ribonucléoprotéique dans le cerveau de souris : The stress granules component G3BP : functional characterization from KO mouse and identification of its ribonucleoprotein interactome in mouse brain. (Doctoral Dissertation). Université Montpellier II. Retrieved from http://www.theses.fr/2012MON20247

Chicago Manual of Style (16th Edition):

Martin, Sophie. “Le composant des granules de stress G3BP : caractérisation phénotypique de souris KO, et identification de son interactome ribonucléoprotéique dans le cerveau de souris : The stress granules component G3BP : functional characterization from KO mouse and identification of its ribonucleoprotein interactome in mouse brain.” 2012. Doctoral Dissertation, Université Montpellier II. Accessed April 13, 2021. http://www.theses.fr/2012MON20247.

MLA Handbook (7th Edition):

Martin, Sophie. “Le composant des granules de stress G3BP : caractérisation phénotypique de souris KO, et identification de son interactome ribonucléoprotéique dans le cerveau de souris : The stress granules component G3BP : functional characterization from KO mouse and identification of its ribonucleoprotein interactome in mouse brain.” 2012. Web. 13 Apr 2021.

Vancouver:

Martin S. Le composant des granules de stress G3BP : caractérisation phénotypique de souris KO, et identification de son interactome ribonucléoprotéique dans le cerveau de souris : The stress granules component G3BP : functional characterization from KO mouse and identification of its ribonucleoprotein interactome in mouse brain. [Internet] [Doctoral dissertation]. Université Montpellier II; 2012. [cited 2021 Apr 13]. Available from: http://www.theses.fr/2012MON20247.

Council of Science Editors:

Martin S. Le composant des granules de stress G3BP : caractérisation phénotypique de souris KO, et identification de son interactome ribonucléoprotéique dans le cerveau de souris : The stress granules component G3BP : functional characterization from KO mouse and identification of its ribonucleoprotein interactome in mouse brain. [Doctoral Dissertation]. Université Montpellier II; 2012. Available from: http://www.theses.fr/2012MON20247


University of Colorado

4. Wheeler, Joshua Riley. Investigations into Higher Order Assemblies of RNA and Protein in Health and Disease.

Degree: PhD, 2018, University of Colorado

  RNA and proteins (RNPs) can form highly ordered aggregates in living organisms with functional or toxic properties. Clumps of toxic, cytoplasmic RNP aggregates are… (more)

Subjects/Keywords: amyotrophic lateral sclerosis; neurodegeneration; rnp granule; skeletal muscle; stress granule; tdp-43; Biochemistry; Tissues

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APA (6th Edition):

Wheeler, J. R. (2018). Investigations into Higher Order Assemblies of RNA and Protein in Health and Disease. (Doctoral Dissertation). University of Colorado. Retrieved from https://scholar.colorado.edu/chem_gradetds/262

Chicago Manual of Style (16th Edition):

Wheeler, Joshua Riley. “Investigations into Higher Order Assemblies of RNA and Protein in Health and Disease.” 2018. Doctoral Dissertation, University of Colorado. Accessed April 13, 2021. https://scholar.colorado.edu/chem_gradetds/262.

MLA Handbook (7th Edition):

Wheeler, Joshua Riley. “Investigations into Higher Order Assemblies of RNA and Protein in Health and Disease.” 2018. Web. 13 Apr 2021.

Vancouver:

Wheeler JR. Investigations into Higher Order Assemblies of RNA and Protein in Health and Disease. [Internet] [Doctoral dissertation]. University of Colorado; 2018. [cited 2021 Apr 13]. Available from: https://scholar.colorado.edu/chem_gradetds/262.

Council of Science Editors:

Wheeler JR. Investigations into Higher Order Assemblies of RNA and Protein in Health and Disease. [Doctoral Dissertation]. University of Colorado; 2018. Available from: https://scholar.colorado.edu/chem_gradetds/262


Boston University

5. Apicco, Daniel. Emerging roles for RNA binding proteins in the pathogenesis of Alzheimer's disease and frontotemporal dementia.

Degree: PhD, Pharmacology, 2017, Boston University

 Abnormal aggregation of microtubule associated protein tau is the defining pathological hallmark of tauopathies, which include Alzheimer’s disease (AD) and related frontotemporal dementias (FTLD-tau). However,… (more)

Subjects/Keywords: Neurosciences; RNA binding protein; Tau; TIA1; Dementia; Neurodegeneration; Stress granule

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APA (6th Edition):

Apicco, D. (2017). Emerging roles for RNA binding proteins in the pathogenesis of Alzheimer's disease and frontotemporal dementia. (Doctoral Dissertation). Boston University. Retrieved from http://hdl.handle.net/2144/23406

Chicago Manual of Style (16th Edition):

Apicco, Daniel. “Emerging roles for RNA binding proteins in the pathogenesis of Alzheimer's disease and frontotemporal dementia.” 2017. Doctoral Dissertation, Boston University. Accessed April 13, 2021. http://hdl.handle.net/2144/23406.

MLA Handbook (7th Edition):

Apicco, Daniel. “Emerging roles for RNA binding proteins in the pathogenesis of Alzheimer's disease and frontotemporal dementia.” 2017. Web. 13 Apr 2021.

Vancouver:

Apicco D. Emerging roles for RNA binding proteins in the pathogenesis of Alzheimer's disease and frontotemporal dementia. [Internet] [Doctoral dissertation]. Boston University; 2017. [cited 2021 Apr 13]. Available from: http://hdl.handle.net/2144/23406.

Council of Science Editors:

Apicco D. Emerging roles for RNA binding proteins in the pathogenesis of Alzheimer's disease and frontotemporal dementia. [Doctoral Dissertation]. Boston University; 2017. Available from: http://hdl.handle.net/2144/23406


University of Melbourne

6. Sui, Xiaojing. The impact of proteostasis imbalance on proteome solubility.

Degree: 2019, University of Melbourne

 A hallmark of neurodegenerative diseases is that certain proteins abnormally aggregate into insoluble deposits. A leading hypothesis is that a breakdown in protein folding quality… (more)

Subjects/Keywords: proteostasis; protein aggregation; protein misfolding; Huntington Disease; chaperone; protein misfolding; nuclear pore; stress granule formation

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APA (6th Edition):

Sui, X. (2019). The impact of proteostasis imbalance on proteome solubility. (Doctoral Dissertation). University of Melbourne. Retrieved from http://hdl.handle.net/11343/222169

Chicago Manual of Style (16th Edition):

Sui, Xiaojing. “The impact of proteostasis imbalance on proteome solubility.” 2019. Doctoral Dissertation, University of Melbourne. Accessed April 13, 2021. http://hdl.handle.net/11343/222169.

MLA Handbook (7th Edition):

Sui, Xiaojing. “The impact of proteostasis imbalance on proteome solubility.” 2019. Web. 13 Apr 2021.

Vancouver:

Sui X. The impact of proteostasis imbalance on proteome solubility. [Internet] [Doctoral dissertation]. University of Melbourne; 2019. [cited 2021 Apr 13]. Available from: http://hdl.handle.net/11343/222169.

Council of Science Editors:

Sui X. The impact of proteostasis imbalance on proteome solubility. [Doctoral Dissertation]. University of Melbourne; 2019. Available from: http://hdl.handle.net/11343/222169


Wright State University

7. Hayden, Elliott. Rescue of ALS Protein FUS Toxicity by TAF.

Degree: PhD, Biomedical Sciences PhD, 2019, Wright State University

 Amyotrophic Lateral Scleroses (ALS) is a neurodegenerative disease characterized by the degeneration of upper and lower motor neurons in the brain and spinal cord leading… (more)

Subjects/Keywords: Molecular Biology; yeast; neurodegeneration; ALS; protein aggregation; amyotrophic lateral sclerosis; stress granule; p-bodies

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APA (6th Edition):

Hayden, E. (2019). Rescue of ALS Protein FUS Toxicity by TAF. (Doctoral Dissertation). Wright State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=wright1559680404963737

Chicago Manual of Style (16th Edition):

Hayden, Elliott. “Rescue of ALS Protein FUS Toxicity by TAF.” 2019. Doctoral Dissertation, Wright State University. Accessed April 13, 2021. http://rave.ohiolink.edu/etdc/view?acc_num=wright1559680404963737.

MLA Handbook (7th Edition):

Hayden, Elliott. “Rescue of ALS Protein FUS Toxicity by TAF.” 2019. Web. 13 Apr 2021.

Vancouver:

Hayden E. Rescue of ALS Protein FUS Toxicity by TAF. [Internet] [Doctoral dissertation]. Wright State University; 2019. [cited 2021 Apr 13]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=wright1559680404963737.

Council of Science Editors:

Hayden E. Rescue of ALS Protein FUS Toxicity by TAF. [Doctoral Dissertation]. Wright State University; 2019. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=wright1559680404963737

8. Salinger, Ari. Study of stress granule disassembly in Saccharomyces cerevisae.

Degree: 2012, Brandeis University

 In order for cells to remain viable, they need to have the capacity to survive during times of stress. Eukaryotic cells, in order to endure… (more)

Subjects/Keywords: Saccharomyces cerevisae; Stress Granule; Fluorescent Microscopy; Stress

…Motif SC Synthetic Media SG Stress Granule STE Stabilizer Elements TAP Tandem Affinity… …proteins bind and aggregate to form SGs (10). 3 1.2 Stress granule function Stress… …association with cytotoxic granules in killer T cells (10). Regarding stress granule… …proteins to stress granule structure: TIA1 and Pub1 TIA-1 is a multifunctional protein. It is… …confirmed that a truncated TIA-1 protein can still form stress granule-like aggregates so long as… 

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APA (6th Edition):

Salinger, A. (2012). Study of stress granule disassembly in Saccharomyces cerevisae. (Thesis). Brandeis University. Retrieved from http://hdl.handle.net/10192/76

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):

Salinger, Ari. “Study of stress granule disassembly in Saccharomyces cerevisae.” 2012. Thesis, Brandeis University. Accessed April 13, 2021. http://hdl.handle.net/10192/76.

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

MLA Handbook (7th Edition):

Salinger, Ari. “Study of stress granule disassembly in Saccharomyces cerevisae.” 2012. Web. 13 Apr 2021.

Vancouver:

Salinger A. Study of stress granule disassembly in Saccharomyces cerevisae. [Internet] [Thesis]. Brandeis University; 2012. [cited 2021 Apr 13]. Available from: http://hdl.handle.net/10192/76.

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

Council of Science Editors:

Salinger A. Study of stress granule disassembly in Saccharomyces cerevisae. [Thesis]. Brandeis University; 2012. Available from: http://hdl.handle.net/10192/76

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


Kyoto University / 京都大学

9. Yoo, Ji Seung. INVESTIGATIONS INTO THE ROLES OF PKR-INDUCED ANTIVIRAL STRESS GRANULE AND DHX36 IN RIG-I SIGNALING : PKRによって誘導される抗ウイルスストレス顆粒とRIG-IによるシグナルにおけるDHX36の機能の研究.

Degree: 博士(生命科学), 2014, Kyoto University / 京都大学

新制・課程博士

甲第18485号

生博第314号

Subjects/Keywords: DHX36; RIG-I; PKR; Stress Granule; Innate Immunity

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APA (6th Edition):

Yoo, J. S. (2014). INVESTIGATIONS INTO THE ROLES OF PKR-INDUCED ANTIVIRAL STRESS GRANULE AND DHX36 IN RIG-I SIGNALING : PKRによって誘導される抗ウイルスストレス顆粒とRIG-IによるシグナルにおけるDHX36の機能の研究. (Thesis). Kyoto University / 京都大学. Retrieved from http://hdl.handle.net/2433/189378 ; http://dx.doi.org/10.14989/doctor.k18485

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):

Yoo, Ji Seung. “INVESTIGATIONS INTO THE ROLES OF PKR-INDUCED ANTIVIRAL STRESS GRANULE AND DHX36 IN RIG-I SIGNALING : PKRによって誘導される抗ウイルスストレス顆粒とRIG-IによるシグナルにおけるDHX36の機能の研究.” 2014. Thesis, Kyoto University / 京都大学. Accessed April 13, 2021. http://hdl.handle.net/2433/189378 ; http://dx.doi.org/10.14989/doctor.k18485.

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

MLA Handbook (7th Edition):

Yoo, Ji Seung. “INVESTIGATIONS INTO THE ROLES OF PKR-INDUCED ANTIVIRAL STRESS GRANULE AND DHX36 IN RIG-I SIGNALING : PKRによって誘導される抗ウイルスストレス顆粒とRIG-IによるシグナルにおけるDHX36の機能の研究.” 2014. Web. 13 Apr 2021.

Vancouver:

Yoo JS. INVESTIGATIONS INTO THE ROLES OF PKR-INDUCED ANTIVIRAL STRESS GRANULE AND DHX36 IN RIG-I SIGNALING : PKRによって誘導される抗ウイルスストレス顆粒とRIG-IによるシグナルにおけるDHX36の機能の研究. [Internet] [Thesis]. Kyoto University / 京都大学; 2014. [cited 2021 Apr 13]. Available from: http://hdl.handle.net/2433/189378 ; http://dx.doi.org/10.14989/doctor.k18485.

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

Council of Science Editors:

Yoo JS. INVESTIGATIONS INTO THE ROLES OF PKR-INDUCED ANTIVIRAL STRESS GRANULE AND DHX36 IN RIG-I SIGNALING : PKRによって誘導される抗ウイルスストレス顆粒とRIG-IによるシグナルにおけるDHX36の機能の研究. [Thesis]. Kyoto University / 京都大学; 2014. Available from: http://hdl.handle.net/2433/189378 ; http://dx.doi.org/10.14989/doctor.k18485

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


University of California – San Diego

10. Fang, Mark Yang. Modulation of RNA-dependent Interactions in Stress Granules Prevents Persistent TPD-43 accumulation in ALS/FTD.

Degree: Biomedical Sciences, 2019, University of California – San Diego

Stress granules (SG) form during cellular stress and have been linked to neurodegenerative diseases such as amyotrophic lateral sclerosis and frontotemporal dementia (ALS/FTD). Strategies to… (more)

Subjects/Keywords: Neurosciences; Cellular biology; ALS; intrinsically disordered region; RNA binding protein; screening; stem cell disease model; stress granule

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APA (6th Edition):

Fang, M. Y. (2019). Modulation of RNA-dependent Interactions in Stress Granules Prevents Persistent TPD-43 accumulation in ALS/FTD. (Thesis). University of California – San Diego. Retrieved from http://www.escholarship.org/uc/item/1c0562nh

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):

Fang, Mark Yang. “Modulation of RNA-dependent Interactions in Stress Granules Prevents Persistent TPD-43 accumulation in ALS/FTD.” 2019. Thesis, University of California – San Diego. Accessed April 13, 2021. http://www.escholarship.org/uc/item/1c0562nh.

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

MLA Handbook (7th Edition):

Fang, Mark Yang. “Modulation of RNA-dependent Interactions in Stress Granules Prevents Persistent TPD-43 accumulation in ALS/FTD.” 2019. Web. 13 Apr 2021.

Vancouver:

Fang MY. Modulation of RNA-dependent Interactions in Stress Granules Prevents Persistent TPD-43 accumulation in ALS/FTD. [Internet] [Thesis]. University of California – San Diego; 2019. [cited 2021 Apr 13]. Available from: http://www.escholarship.org/uc/item/1c0562nh.

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

Council of Science Editors:

Fang MY. Modulation of RNA-dependent Interactions in Stress Granules Prevents Persistent TPD-43 accumulation in ALS/FTD. [Thesis]. University of California – San Diego; 2019. Available from: http://www.escholarship.org/uc/item/1c0562nh

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


Brigham Young University

11. Holladay, Seth R. Optimized Simulation of Granular Materials.

Degree: PhD, 2013, Brigham Young University

 Visual effects for film and animation often require simulated granular materials, such as sand, wheat, or dirt, to meet a director's needs. Simulating granular materials… (more)

Subjects/Keywords: Granular simulation; simulation; optimization; fluid dynamics; rigid body dynamics; culling; frictional stress; artistic control; granule deposition; contact resolution; Computer Sciences

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APA (6th Edition):

Holladay, S. R. (2013). Optimized Simulation of Granular Materials. (Doctoral Dissertation). Brigham Young University. Retrieved from https://scholarsarchive.byu.edu/cgi/viewcontent.cgi?article=4855&context=etd

Chicago Manual of Style (16th Edition):

Holladay, Seth R. “Optimized Simulation of Granular Materials.” 2013. Doctoral Dissertation, Brigham Young University. Accessed April 13, 2021. https://scholarsarchive.byu.edu/cgi/viewcontent.cgi?article=4855&context=etd.

MLA Handbook (7th Edition):

Holladay, Seth R. “Optimized Simulation of Granular Materials.” 2013. Web. 13 Apr 2021.

Vancouver:

Holladay SR. Optimized Simulation of Granular Materials. [Internet] [Doctoral dissertation]. Brigham Young University; 2013. [cited 2021 Apr 13]. Available from: https://scholarsarchive.byu.edu/cgi/viewcontent.cgi?article=4855&context=etd.

Council of Science Editors:

Holladay SR. Optimized Simulation of Granular Materials. [Doctoral Dissertation]. Brigham Young University; 2013. Available from: https://scholarsarchive.byu.edu/cgi/viewcontent.cgi?article=4855&context=etd


Kyoto University

12. Yoo, Ji Seung. INVESTIGATIONS INTO THE ROLES OF PKR-INDUCED ANTIVIRAL STRESS GRANULE AND DHX36 IN RIG-I SIGNALING .

Degree: 2014, Kyoto University

Subjects/Keywords: DHX36; RIG-I; PKR; Stress Granule; Innate Immunity

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

APA (6th Edition):

Yoo, J. S. (2014). INVESTIGATIONS INTO THE ROLES OF PKR-INDUCED ANTIVIRAL STRESS GRANULE AND DHX36 IN RIG-I SIGNALING . (Thesis). Kyoto University. Retrieved from http://hdl.handle.net/2433/189378

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):

Yoo, Ji Seung. “INVESTIGATIONS INTO THE ROLES OF PKR-INDUCED ANTIVIRAL STRESS GRANULE AND DHX36 IN RIG-I SIGNALING .” 2014. Thesis, Kyoto University. Accessed April 13, 2021. http://hdl.handle.net/2433/189378.

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

MLA Handbook (7th Edition):

Yoo, Ji Seung. “INVESTIGATIONS INTO THE ROLES OF PKR-INDUCED ANTIVIRAL STRESS GRANULE AND DHX36 IN RIG-I SIGNALING .” 2014. Web. 13 Apr 2021.

Vancouver:

Yoo JS. INVESTIGATIONS INTO THE ROLES OF PKR-INDUCED ANTIVIRAL STRESS GRANULE AND DHX36 IN RIG-I SIGNALING . [Internet] [Thesis]. Kyoto University; 2014. [cited 2021 Apr 13]. Available from: http://hdl.handle.net/2433/189378.

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

Council of Science Editors:

Yoo JS. INVESTIGATIONS INTO THE ROLES OF PKR-INDUCED ANTIVIRAL STRESS GRANULE AND DHX36 IN RIG-I SIGNALING . [Thesis]. Kyoto University; 2014. Available from: http://hdl.handle.net/2433/189378

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


University of Melbourne

13. James, Janine Louise. Development and application of advanced bioimaging techniques to investigate stress pathways and drug action in neurodegeneration.

Degree: 2019, University of Melbourne

 Neurodegenerative diseases such as Frontotemporal Dementia (FTD), and Amyotrophic Lateral Sclerosis (ALS), also known as Motor Neuron Disease (MND), have limited therapeutics available, placing a… (more)

Subjects/Keywords: neurodegeneration; amyotrophic lateral sclerosis; dementia; stress granule; RNA binding protein; bioimaging; FUS; TDP-43; RNA granule; microscopy; frontotemporal dementia; motor neuron disease; pathological mutations; hnRNP; cell culture; cell stress; in vitro; bioimaging; sub-cellular; protein distribution; biometal

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APA (6th Edition):

James, J. L. (2019). Development and application of advanced bioimaging techniques to investigate stress pathways and drug action in neurodegeneration. (Doctoral Dissertation). University of Melbourne. Retrieved from http://hdl.handle.net/11343/228831

Chicago Manual of Style (16th Edition):

James, Janine Louise. “Development and application of advanced bioimaging techniques to investigate stress pathways and drug action in neurodegeneration.” 2019. Doctoral Dissertation, University of Melbourne. Accessed April 13, 2021. http://hdl.handle.net/11343/228831.

MLA Handbook (7th Edition):

James, Janine Louise. “Development and application of advanced bioimaging techniques to investigate stress pathways and drug action in neurodegeneration.” 2019. Web. 13 Apr 2021.

Vancouver:

James JL. Development and application of advanced bioimaging techniques to investigate stress pathways and drug action in neurodegeneration. [Internet] [Doctoral dissertation]. University of Melbourne; 2019. [cited 2021 Apr 13]. Available from: http://hdl.handle.net/11343/228831.

Council of Science Editors:

James JL. Development and application of advanced bioimaging techniques to investigate stress pathways and drug action in neurodegeneration. [Doctoral Dissertation]. University of Melbourne; 2019. Available from: http://hdl.handle.net/11343/228831


Kyoto University / 京都大学

14. Ng Chen Seng. INHIBITION OF HOST INNATE IMMUNE RESPONSES THROUGH THE MODULATION OF CYTOPLASMIC STRESS GRANULES BY ENCEPHALOMYOCARDITIS VIRUS PROTEASE : 脳心筋炎ウイルス(EMCV)プロテアーゼによる細胞性ストレス顆粒形成の制御と抗ウイルス自然免疫応答の阻害機構.

Degree: 博士(生命科学), 2014, Kyoto University / 京都大学

新制・課程博士

甲第18627号

生博第318号

Subjects/Keywords: EMCV; Stress granule; MDA5; interferon; PKR; antiviral; innate immune response

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

APA (6th Edition):

Seng, N. C. (2014). INHIBITION OF HOST INNATE IMMUNE RESPONSES THROUGH THE MODULATION OF CYTOPLASMIC STRESS GRANULES BY ENCEPHALOMYOCARDITIS VIRUS PROTEASE : 脳心筋炎ウイルス(EMCV)プロテアーゼによる細胞性ストレス顆粒形成の制御と抗ウイルス自然免疫応答の阻害機構. (Thesis). Kyoto University / 京都大学. Retrieved from http://hdl.handle.net/2433/192227 ; http://dx.doi.org/10.14989/doctor.k18627

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):

Seng, Ng Chen. “INHIBITION OF HOST INNATE IMMUNE RESPONSES THROUGH THE MODULATION OF CYTOPLASMIC STRESS GRANULES BY ENCEPHALOMYOCARDITIS VIRUS PROTEASE : 脳心筋炎ウイルス(EMCV)プロテアーゼによる細胞性ストレス顆粒形成の制御と抗ウイルス自然免疫応答の阻害機構.” 2014. Thesis, Kyoto University / 京都大学. Accessed April 13, 2021. http://hdl.handle.net/2433/192227 ; http://dx.doi.org/10.14989/doctor.k18627.

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

MLA Handbook (7th Edition):

Seng, Ng Chen. “INHIBITION OF HOST INNATE IMMUNE RESPONSES THROUGH THE MODULATION OF CYTOPLASMIC STRESS GRANULES BY ENCEPHALOMYOCARDITIS VIRUS PROTEASE : 脳心筋炎ウイルス(EMCV)プロテアーゼによる細胞性ストレス顆粒形成の制御と抗ウイルス自然免疫応答の阻害機構.” 2014. Web. 13 Apr 2021.

Vancouver:

Seng NC. INHIBITION OF HOST INNATE IMMUNE RESPONSES THROUGH THE MODULATION OF CYTOPLASMIC STRESS GRANULES BY ENCEPHALOMYOCARDITIS VIRUS PROTEASE : 脳心筋炎ウイルス(EMCV)プロテアーゼによる細胞性ストレス顆粒形成の制御と抗ウイルス自然免疫応答の阻害機構. [Internet] [Thesis]. Kyoto University / 京都大学; 2014. [cited 2021 Apr 13]. Available from: http://hdl.handle.net/2433/192227 ; http://dx.doi.org/10.14989/doctor.k18627.

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

Council of Science Editors:

Seng NC. INHIBITION OF HOST INNATE IMMUNE RESPONSES THROUGH THE MODULATION OF CYTOPLASMIC STRESS GRANULES BY ENCEPHALOMYOCARDITIS VIRUS PROTEASE : 脳心筋炎ウイルス(EMCV)プロテアーゼによる細胞性ストレス顆粒形成の制御と抗ウイルス自然免疫応答の阻害機構. [Thesis]. Kyoto University / 京都大学; 2014. Available from: http://hdl.handle.net/2433/192227 ; http://dx.doi.org/10.14989/doctor.k18627

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

15. Oh, Seong-Wook. Functional Analysis of RIG-I and RNP Complexes in the Antiviral Interferon System : 抗ウイルスIFNシステムにおけるRIG-IとRNP複合体の機能解析.

Degree: 博士(生命科学), 2016, Kyoto University / 京都大学

新制・課程博士

甲第19907号

生博第354号

Subjects/Keywords: interferon; RIG-I; innate immunity; RNA virus; stress granule; read-through transccript

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APA (6th Edition):

Oh, S. (2016). Functional Analysis of RIG-I and RNP Complexes in the Antiviral Interferon System : 抗ウイルスIFNシステムにおけるRIG-IとRNP複合体の機能解析. (Thesis). Kyoto University / 京都大学. Retrieved from http://hdl.handle.net/2433/215973 ; http://dx.doi.org/10.14989/doctor.k19907

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):

Oh, Seong-Wook. “Functional Analysis of RIG-I and RNP Complexes in the Antiviral Interferon System : 抗ウイルスIFNシステムにおけるRIG-IとRNP複合体の機能解析.” 2016. Thesis, Kyoto University / 京都大学. Accessed April 13, 2021. http://hdl.handle.net/2433/215973 ; http://dx.doi.org/10.14989/doctor.k19907.

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

MLA Handbook (7th Edition):

Oh, Seong-Wook. “Functional Analysis of RIG-I and RNP Complexes in the Antiviral Interferon System : 抗ウイルスIFNシステムにおけるRIG-IとRNP複合体の機能解析.” 2016. Web. 13 Apr 2021.

Vancouver:

Oh S. Functional Analysis of RIG-I and RNP Complexes in the Antiviral Interferon System : 抗ウイルスIFNシステムにおけるRIG-IとRNP複合体の機能解析. [Internet] [Thesis]. Kyoto University / 京都大学; 2016. [cited 2021 Apr 13]. Available from: http://hdl.handle.net/2433/215973 ; http://dx.doi.org/10.14989/doctor.k19907.

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

Council of Science Editors:

Oh S. Functional Analysis of RIG-I and RNP Complexes in the Antiviral Interferon System : 抗ウイルスIFNシステムにおけるRIG-IとRNP複合体の機能解析. [Thesis]. Kyoto University / 京都大学; 2016. Available from: http://hdl.handle.net/2433/215973 ; http://dx.doi.org/10.14989/doctor.k19907

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

16. Oh, Seong-Wook. Functional Analysis of RIG-I and RNP Complexes in the Antiviral Interferon System .

Degree: 2016, Kyoto University

Subjects/Keywords: interferon; RIG-I; innate immunity; RNA virus; stress granule; read-through transccript

Page 1 Page 2 Page 3

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

APA (6th Edition):

Oh, S. (2016). Functional Analysis of RIG-I and RNP Complexes in the Antiviral Interferon System . (Thesis). Kyoto University. Retrieved from http://hdl.handle.net/2433/215973

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):

Oh, Seong-Wook. “Functional Analysis of RIG-I and RNP Complexes in the Antiviral Interferon System .” 2016. Thesis, Kyoto University. Accessed April 13, 2021. http://hdl.handle.net/2433/215973.

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

MLA Handbook (7th Edition):

Oh, Seong-Wook. “Functional Analysis of RIG-I and RNP Complexes in the Antiviral Interferon System .” 2016. Web. 13 Apr 2021.

Vancouver:

Oh S. Functional Analysis of RIG-I and RNP Complexes in the Antiviral Interferon System . [Internet] [Thesis]. Kyoto University; 2016. [cited 2021 Apr 13]. Available from: http://hdl.handle.net/2433/215973.

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

Council of Science Editors:

Oh S. Functional Analysis of RIG-I and RNP Complexes in the Antiviral Interferon System . [Thesis]. Kyoto University; 2016. Available from: http://hdl.handle.net/2433/215973

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


Kyoto University

17. Yatsuzuka, Kenji. Live-cell imaging of multiple endogenous mRNAs permits the direct observation of RNA granule dynamics .

Degree: 2019, Kyoto University

Subjects/Keywords: RNA imaging; Stress granule; Live-cell imaging; Fluorescent probe; Chemical biology

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APA (6th Edition):

Yatsuzuka, K. (2019). Live-cell imaging of multiple endogenous mRNAs permits the direct observation of RNA granule dynamics . (Thesis). Kyoto University. Retrieved from http://hdl.handle.net/2433/242400

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):

Yatsuzuka, Kenji. “Live-cell imaging of multiple endogenous mRNAs permits the direct observation of RNA granule dynamics .” 2019. Thesis, Kyoto University. Accessed April 13, 2021. http://hdl.handle.net/2433/242400.

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

MLA Handbook (7th Edition):

Yatsuzuka, Kenji. “Live-cell imaging of multiple endogenous mRNAs permits the direct observation of RNA granule dynamics .” 2019. Web. 13 Apr 2021.

Vancouver:

Yatsuzuka K. Live-cell imaging of multiple endogenous mRNAs permits the direct observation of RNA granule dynamics . [Internet] [Thesis]. Kyoto University; 2019. [cited 2021 Apr 13]. Available from: http://hdl.handle.net/2433/242400.

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

Council of Science Editors:

Yatsuzuka K. Live-cell imaging of multiple endogenous mRNAs permits the direct observation of RNA granule dynamics . [Thesis]. Kyoto University; 2019. Available from: http://hdl.handle.net/2433/242400

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

18. Ng Chen Seng. INHIBITION OF HOST INNATE IMMUNE RESPONSES THROUGH THE MODULATION OF CYTOPLASMIC STRESS GRANULES BY ENCEPHALOMYOCARDITIS VIRUS PROTEASE .

Degree: 2014, Kyoto University

Subjects/Keywords: EMCV; Stress granule; MDA5; interferon; PKR; antiviral; innate immune response

…associated factor 3/6 dsRNA double-stranded ribonucleic-acids SG stress granule mRNA… …Sindbis virus vSG virus-induced stress granule VSV Vesicular stomatitis virus VV Vaccina… …pathway from the perspective of host defense. 1.4 Stress response pathway and stress granule… …assortment of cellular host mRNA inside the stress granule could further protect these naked mRNA… …Under stress response, Pbody foci are recruited and juxtaposition with stress granule (… 

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

APA (6th Edition):

Seng, N. C. (2014). INHIBITION OF HOST INNATE IMMUNE RESPONSES THROUGH THE MODULATION OF CYTOPLASMIC STRESS GRANULES BY ENCEPHALOMYOCARDITIS VIRUS PROTEASE . (Thesis). Kyoto University. Retrieved from http://hdl.handle.net/2433/192227

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):

Seng, Ng Chen. “INHIBITION OF HOST INNATE IMMUNE RESPONSES THROUGH THE MODULATION OF CYTOPLASMIC STRESS GRANULES BY ENCEPHALOMYOCARDITIS VIRUS PROTEASE .” 2014. Thesis, Kyoto University. Accessed April 13, 2021. http://hdl.handle.net/2433/192227.

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

MLA Handbook (7th Edition):

Seng, Ng Chen. “INHIBITION OF HOST INNATE IMMUNE RESPONSES THROUGH THE MODULATION OF CYTOPLASMIC STRESS GRANULES BY ENCEPHALOMYOCARDITIS VIRUS PROTEASE .” 2014. Web. 13 Apr 2021.

Vancouver:

Seng NC. INHIBITION OF HOST INNATE IMMUNE RESPONSES THROUGH THE MODULATION OF CYTOPLASMIC STRESS GRANULES BY ENCEPHALOMYOCARDITIS VIRUS PROTEASE . [Internet] [Thesis]. Kyoto University; 2014. [cited 2021 Apr 13]. Available from: http://hdl.handle.net/2433/192227.

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

Council of Science Editors:

Seng NC. INHIBITION OF HOST INNATE IMMUNE RESPONSES THROUGH THE MODULATION OF CYTOPLASMIC STRESS GRANULES BY ENCEPHALOMYOCARDITIS VIRUS PROTEASE . [Thesis]. Kyoto University; 2014. Available from: http://hdl.handle.net/2433/192227

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


Université de Montréal

19. McDonald, Karli K. TAR DNA-Binding protein 43 (TDP-43) regulates stress granule dynamics via differential regulation of G3BP and TIA-1.

Degree: 2011, Université de Montréal

Subjects/Keywords: TDP-43; Stress granule; Granule de stress; hnRNP A2; G3BP; TIA-1; Sclérose latérale amyotrophique; Amyotrophic lateral sclerosis; Biology - Cell / Biologie - Cellule (UMI : 0379)

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APA (6th Edition):

McDonald, K. K. (2011). TAR DNA-Binding protein 43 (TDP-43) regulates stress granule dynamics via differential regulation of G3BP and TIA-1. (Thesis). Université de Montréal. Retrieved from http://hdl.handle.net/1866/5134

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):

McDonald, Karli K. “TAR DNA-Binding protein 43 (TDP-43) regulates stress granule dynamics via differential regulation of G3BP and TIA-1.” 2011. Thesis, Université de Montréal. Accessed April 13, 2021. http://hdl.handle.net/1866/5134.

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

MLA Handbook (7th Edition):

McDonald, Karli K. “TAR DNA-Binding protein 43 (TDP-43) regulates stress granule dynamics via differential regulation of G3BP and TIA-1.” 2011. Web. 13 Apr 2021.

Vancouver:

McDonald KK. TAR DNA-Binding protein 43 (TDP-43) regulates stress granule dynamics via differential regulation of G3BP and TIA-1. [Internet] [Thesis]. Université de Montréal; 2011. [cited 2021 Apr 13]. Available from: http://hdl.handle.net/1866/5134.

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

Council of Science Editors:

McDonald KK. TAR DNA-Binding protein 43 (TDP-43) regulates stress granule dynamics via differential regulation of G3BP and TIA-1. [Thesis]. Université de Montréal; 2011. Available from: http://hdl.handle.net/1866/5134

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


Université de Montréal

20. Aulas, Anaïs. TDP-43 régule la dynamique et la fonction des Granules de Stress via G3BP1.

Degree: 2015, Université de Montréal

Subjects/Keywords: TDP-43; G3BP1; FUS; Granule de Stress; P-Body; Sclérose Latérale Amyotrophique; ARNm; Réponse au stress; Stress Granule; mRNA; Amyotrophic Lateral Sclerosis; Stress response; Biology - Cell / Biologie - Cellule (UMI : 0379)

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APA (6th Edition):

Aulas, A. (2015). TDP-43 régule la dynamique et la fonction des Granules de Stress via G3BP1. (Thesis). Université de Montréal. Retrieved from http://hdl.handle.net/1866/12069

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):

Aulas, Anaïs. “TDP-43 régule la dynamique et la fonction des Granules de Stress via G3BP1.” 2015. Thesis, Université de Montréal. Accessed April 13, 2021. http://hdl.handle.net/1866/12069.

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

MLA Handbook (7th Edition):

Aulas, Anaïs. “TDP-43 régule la dynamique et la fonction des Granules de Stress via G3BP1.” 2015. Web. 13 Apr 2021.

Vancouver:

Aulas A. TDP-43 régule la dynamique et la fonction des Granules de Stress via G3BP1. [Internet] [Thesis]. Université de Montréal; 2015. [cited 2021 Apr 13]. Available from: http://hdl.handle.net/1866/12069.

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

Council of Science Editors:

Aulas A. TDP-43 régule la dynamique et la fonction des Granules de Stress via G3BP1. [Thesis]. Université de Montréal; 2015. Available from: http://hdl.handle.net/1866/12069

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

21. 田中,融. イオンチャネルを介する神経刺激に応じたYB-1タンパク質による迅速な翻訳調節機構の解析とストレス応答におけるYB-1タンパク質の役割 : Mechanism of YB-1-mediated translational induction in response to neural activity through ionotropic receptors and roles of YB-1 under oxidative stress.

Degree: 博士(薬学), 2014, Nihon University / 日本大学

Subjects/Keywords: YB-1; 翻訳調節; translational regulation; GluR2 mRNA; ストレス顆粒; stress granule; HSP70

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APA (6th Edition):

田中,融. (2014). イオンチャネルを介する神経刺激に応じたYB-1タンパク質による迅速な翻訳調節機構の解析とストレス応答におけるYB-1タンパク質の役割 : Mechanism of YB-1-mediated translational induction in response to neural activity through ionotropic receptors and roles of YB-1 under oxidative stress. (Thesis). Nihon University / 日本大学. Retrieved from http://repository.nihon-u.ac.jp/xmlui/handle/11263/222 ; http://dx.doi.org/10.15006/32665A4849

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

Chicago Manual of Style (16th Edition):

田中,融. “イオンチャネルを介する神経刺激に応じたYB-1タンパク質による迅速な翻訳調節機構の解析とストレス応答におけるYB-1タンパク質の役割 : Mechanism of YB-1-mediated translational induction in response to neural activity through ionotropic receptors and roles of YB-1 under oxidative stress.” 2014. Thesis, Nihon University / 日本大学. Accessed April 13, 2021. http://repository.nihon-u.ac.jp/xmlui/handle/11263/222 ; http://dx.doi.org/10.15006/32665A4849.

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

MLA Handbook (7th Edition):

田中,融. “イオンチャネルを介する神経刺激に応じたYB-1タンパク質による迅速な翻訳調節機構の解析とストレス応答におけるYB-1タンパク質の役割 : Mechanism of YB-1-mediated translational induction in response to neural activity through ionotropic receptors and roles of YB-1 under oxidative stress.” 2014. Web. 13 Apr 2021.

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

Vancouver:

田中,融. イオンチャネルを介する神経刺激に応じたYB-1タンパク質による迅速な翻訳調節機構の解析とストレス応答におけるYB-1タンパク質の役割 : Mechanism of YB-1-mediated translational induction in response to neural activity through ionotropic receptors and roles of YB-1 under oxidative stress. [Internet] [Thesis]. Nihon University / 日本大学; 2014. [cited 2021 Apr 13]. Available from: http://repository.nihon-u.ac.jp/xmlui/handle/11263/222 ; http://dx.doi.org/10.15006/32665A4849.

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

Council of Science Editors:

田中,融. イオンチャネルを介する神経刺激に応じたYB-1タンパク質による迅速な翻訳調節機構の解析とストレス応答におけるYB-1タンパク質の役割 : Mechanism of YB-1-mediated translational induction in response to neural activity through ionotropic receptors and roles of YB-1 under oxidative stress. [Thesis]. Nihon University / 日本大学; 2014. Available from: http://repository.nihon-u.ac.jp/xmlui/handle/11263/222 ; http://dx.doi.org/10.15006/32665A4849

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

22. Sorenson, Reed Stephen. Role of the RNA-Binding Protein UBP1C in Translational Repression During Hypoxia in Arabidopsis thaliana.

Degree: Plant Biology, 2012, University of California – Riverside

 Oxygen deficient plants suffer an energy limitation that can suppress growth and development and lead to premature cell death. Underlying adaptation, plants have evolved integrated… (more)

Subjects/Keywords: Plant biology; Cellular biology; Molecular biology; Arabidopsis; hypoxia; polysome; stress granule; translation; UBP1

…References 21 Chapter 2. Processing body and stress granule protein genes: Cellular localization… …among other putative stress granule and processing body component gene mutants 44 2.4.4… …Putative stress granule and processing body proteins localize to granules in conditions of low… …nucleocytoplasmic transport, and mRNA stability 91 3.2.4 Stress granule aggregation and repression of… …fluorescent protein-tagged overexpression lines of putative stress granule or processing body… 

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APA (6th Edition):

Sorenson, R. S. (2012). Role of the RNA-Binding Protein UBP1C in Translational Repression During Hypoxia in Arabidopsis thaliana. (Thesis). University of California – Riverside. Retrieved from http://www.escholarship.org/uc/item/6db908pg

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):

Sorenson, Reed Stephen. “Role of the RNA-Binding Protein UBP1C in Translational Repression During Hypoxia in Arabidopsis thaliana.” 2012. Thesis, University of California – Riverside. Accessed April 13, 2021. http://www.escholarship.org/uc/item/6db908pg.

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

MLA Handbook (7th Edition):

Sorenson, Reed Stephen. “Role of the RNA-Binding Protein UBP1C in Translational Repression During Hypoxia in Arabidopsis thaliana.” 2012. Web. 13 Apr 2021.

Vancouver:

Sorenson RS. Role of the RNA-Binding Protein UBP1C in Translational Repression During Hypoxia in Arabidopsis thaliana. [Internet] [Thesis]. University of California – Riverside; 2012. [cited 2021 Apr 13]. Available from: http://www.escholarship.org/uc/item/6db908pg.

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

Council of Science Editors:

Sorenson RS. Role of the RNA-Binding Protein UBP1C in Translational Repression During Hypoxia in Arabidopsis thaliana. [Thesis]. University of California – Riverside; 2012. Available from: http://www.escholarship.org/uc/item/6db908pg

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


University of Oulu

23. Mattila, R. (Riikka). The roles of virulence factors Us3 and γ134.5 during different phases of HSV-1 life cycle.

Degree: 2015, University of Oulu

Abstract Herpes simplex virus type 1 (HSV-1) is a common pathogen with an age-standardized seroprevalence of 52% in Finland. The most common manifestation of HSV-1… (more)

Subjects/Keywords: Us3 protein kinase; ganglion culture; herpes simplex virus type 1; immune evasion; innate immunity; latency; neurovirulence; stress granule; viral culture; γ₁34.5 protein; Us3-proteiinikinaasi; ganglioviljely; herpes simplex virus tyyppi 1; immuunivasteiden välttely; latenssi; luontainen immuniteetti; neurovirulenssi; virusviljely; γ₁34.5 proteiini

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APA (6th Edition):

Mattila, R. (. (2015). The roles of virulence factors Us3 and γ134.5 during different phases of HSV-1 life cycle. (Doctoral Dissertation). University of Oulu. Retrieved from http://urn.fi/urn:isbn:9789526210469

Chicago Manual of Style (16th Edition):

Mattila, R (Riikka). “The roles of virulence factors Us3 and γ134.5 during different phases of HSV-1 life cycle.” 2015. Doctoral Dissertation, University of Oulu. Accessed April 13, 2021. http://urn.fi/urn:isbn:9789526210469.

MLA Handbook (7th Edition):

Mattila, R (Riikka). “The roles of virulence factors Us3 and γ134.5 during different phases of HSV-1 life cycle.” 2015. Web. 13 Apr 2021.

Vancouver:

Mattila R(. The roles of virulence factors Us3 and γ134.5 during different phases of HSV-1 life cycle. [Internet] [Doctoral dissertation]. University of Oulu; 2015. [cited 2021 Apr 13]. Available from: http://urn.fi/urn:isbn:9789526210469.

Council of Science Editors:

Mattila R(. The roles of virulence factors Us3 and γ134.5 during different phases of HSV-1 life cycle. [Doctoral Dissertation]. University of Oulu; 2015. Available from: http://urn.fi/urn:isbn:9789526210469

24. Vanderweyde, Tara Elizabeth. Regulated protein aggregation: how it takes TIA1 to tangle.

Degree: PhD, Pharmacology, 2015, Boston University

 The eukaryotic stress response involves translational suppression of non-housekeeping proteins, and the sequestration of unnecessary mRNA transcripts into stress granules (SGs). This process is dependent… (more)

Subjects/Keywords: Neurosciences; Alzheimer's disease; RNA-binding protein; Tau; TIA1; Neurodegeneration; Stress granule

…animal tissues to complete the stress granule panel in transgenic mouse models of tauopathy and… …without you. I am proud to be able to pass the tau and stress granule torch to a friend and know… …63 CHAPTER THREE: CONTRASTING PATHOLOGY OF STRESS GRANULE PROTEINS IN ALZHEIMER’S DISEASE… …120 CHAPTER FOUR: TAU EXPRESSION INCREASES TIA-1 STRESS GRANULE FORMATION AND ALTERS GRANULE… …21 Figure 4: A model of stress granule assembly… 

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APA (6th Edition):

Vanderweyde, T. E. (2015). Regulated protein aggregation: how it takes TIA1 to tangle. (Doctoral Dissertation). Boston University. Retrieved from http://hdl.handle.net/2144/16021

Chicago Manual of Style (16th Edition):

Vanderweyde, Tara Elizabeth. “Regulated protein aggregation: how it takes TIA1 to tangle.” 2015. Doctoral Dissertation, Boston University. Accessed April 13, 2021. http://hdl.handle.net/2144/16021.

MLA Handbook (7th Edition):

Vanderweyde, Tara Elizabeth. “Regulated protein aggregation: how it takes TIA1 to tangle.” 2015. Web. 13 Apr 2021.

Vancouver:

Vanderweyde TE. Regulated protein aggregation: how it takes TIA1 to tangle. [Internet] [Doctoral dissertation]. Boston University; 2015. [cited 2021 Apr 13]. Available from: http://hdl.handle.net/2144/16021.

Council of Science Editors:

Vanderweyde TE. Regulated protein aggregation: how it takes TIA1 to tangle. [Doctoral Dissertation]. Boston University; 2015. Available from: http://hdl.handle.net/2144/16021

25. Ebata, Atsushi. Development of TDP-43 granule inhibitors as potential amyotrophic lateral sclerosis and frontotemporal lobar degeneration therapies.

Degree: PhD, Pathology & Laboratory Medicine, 2016, Boston University

 The 43 kDa TAR DNA binding protein (TDP-43) has been identified as one of the major proteins that accumulates in the cytoplasm of brain and… (more)

Subjects/Keywords: Pharmacology; TARDBP; TDP-43; Therapy; Amyotrophic lateral sclerosis; Frontotemporal lobar degeneration; Stress granule

…27 Subsection One: Stress Granule… …24 Figure 5. Stress granule formation… …formation by regaining normal function of TDP-43 as a dynamic stress-granule protein… …stress granule SHH… …26 Section Three: TDP-43 and Stress Granules… 

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APA (6th Edition):

Ebata, A. (2016). Development of TDP-43 granule inhibitors as potential amyotrophic lateral sclerosis and frontotemporal lobar degeneration therapies. (Doctoral Dissertation). Boston University. Retrieved from http://hdl.handle.net/2144/14606

Chicago Manual of Style (16th Edition):

Ebata, Atsushi. “Development of TDP-43 granule inhibitors as potential amyotrophic lateral sclerosis and frontotemporal lobar degeneration therapies.” 2016. Doctoral Dissertation, Boston University. Accessed April 13, 2021. http://hdl.handle.net/2144/14606.

MLA Handbook (7th Edition):

Ebata, Atsushi. “Development of TDP-43 granule inhibitors as potential amyotrophic lateral sclerosis and frontotemporal lobar degeneration therapies.” 2016. Web. 13 Apr 2021.

Vancouver:

Ebata A. Development of TDP-43 granule inhibitors as potential amyotrophic lateral sclerosis and frontotemporal lobar degeneration therapies. [Internet] [Doctoral dissertation]. Boston University; 2016. [cited 2021 Apr 13]. Available from: http://hdl.handle.net/2144/14606.

Council of Science Editors:

Ebata A. Development of TDP-43 granule inhibitors as potential amyotrophic lateral sclerosis and frontotemporal lobar degeneration therapies. [Doctoral Dissertation]. Boston University; 2016. Available from: http://hdl.handle.net/2144/14606


The Ohio State University

26. Pomeranz, Marcelo Christian. The Role of the AtTZF1 Tandem CCCH Zinc Finger Gene in Plant Growth, Development, and Stress Response.

Degree: PhD, Horticulture and Crop Science, 2011, The Ohio State University

  TZF proteins are characterized by two CCCH Zinc Finger motifs arranged in tandem. In animals, TZFs can localize to specialized cytoplasmic RNA processing centers… (more)

Subjects/Keywords: Plant Biology; AtTZF1; AtTZF; TZF; Processing Body; Stress Granule PB; SG; ABA; GA; Germination

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APA (6th Edition):

Pomeranz, M. C. (2011). The Role of the AtTZF1 Tandem CCCH Zinc Finger Gene in Plant Growth, Development, and Stress Response. (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1299525118

Chicago Manual of Style (16th Edition):

Pomeranz, Marcelo Christian. “The Role of the AtTZF1 Tandem CCCH Zinc Finger Gene in Plant Growth, Development, and Stress Response.” 2011. Doctoral Dissertation, The Ohio State University. Accessed April 13, 2021. http://rave.ohiolink.edu/etdc/view?acc_num=osu1299525118.

MLA Handbook (7th Edition):

Pomeranz, Marcelo Christian. “The Role of the AtTZF1 Tandem CCCH Zinc Finger Gene in Plant Growth, Development, and Stress Response.” 2011. Web. 13 Apr 2021.

Vancouver:

Pomeranz MC. The Role of the AtTZF1 Tandem CCCH Zinc Finger Gene in Plant Growth, Development, and Stress Response. [Internet] [Doctoral dissertation]. The Ohio State University; 2011. [cited 2021 Apr 13]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1299525118.

Council of Science Editors:

Pomeranz MC. The Role of the AtTZF1 Tandem CCCH Zinc Finger Gene in Plant Growth, Development, and Stress Response. [Doctoral Dissertation]. The Ohio State University; 2011. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1299525118


University of Illinois – Urbana-Champaign

27. Park, Seongjin. Cellular responses to external threats probed by super-resolution microscopy.

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

 Fluorescence microscopy has been an essential tool in biology. However, its imaging resolution has been limited around >200 nm in lateral dimensions, and >500 nm… (more)

Subjects/Keywords: super-resolution; microscopy; biophysics; fluorescence; Stochastic Optical Reconstruction Microscopy (STORM); Photoactivated localization microscopy (PALM); retinoic acid-inducible gene-I (RIG-I); antiviral; SOS; RecA; Plantazolicin; Plantazolicin (PZN); influenza; nonstructural one (ns1); T-cell restricted intracellular antigen-related protein (TIAR); stress granule; antiviral granules (AVG); stress granules (SG); structural illumination microscopy (SIM); structural illumination; deoxyribonucleic acid (DNA); virus; antibiotics; resolution limit; optical microscopy

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APA (6th Edition):

Park, S. (2015). Cellular responses to external threats probed by super-resolution microscopy. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/89208

Chicago Manual of Style (16th Edition):

Park, Seongjin. “Cellular responses to external threats probed by super-resolution microscopy.” 2015. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed April 13, 2021. http://hdl.handle.net/2142/89208.

MLA Handbook (7th Edition):

Park, Seongjin. “Cellular responses to external threats probed by super-resolution microscopy.” 2015. Web. 13 Apr 2021.

Vancouver:

Park S. Cellular responses to external threats probed by super-resolution microscopy. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2015. [cited 2021 Apr 13]. Available from: http://hdl.handle.net/2142/89208.

Council of Science Editors:

Park S. Cellular responses to external threats probed by super-resolution microscopy. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2015. Available from: http://hdl.handle.net/2142/89208


Universitat Pompeu Fabra

28. Agostini, Federico, 1985-. Predictions of RNA-binding ability and aggregation propensity of proteins.

Degree: Departament de Ciències Experimentals i de la Salut, 2014, Universitat Pompeu Fabra

 Las proteínas de unión de ARN son responsables de controlar el destino de una multitud de transcriptos codificantes y no codificantes. De hecho, la formación… (more)

Subjects/Keywords: Intrinsically disordered region (IDR); Long non-coding RNA (lncRNA); Low-complexity sequence (LCS); Protein aggregate; Ribonucleoprotein complex (RNP complex); RNA granule; RNA recognition element (RRE); RNA-binding protein (RBP); Stress granules; Región intrínsecamente desordenada; ARN largo no codificante; Secuencia de baja complejidad; Agregado proteico; Complejo de ribonucleoproteína; Gránulo de ARN; Elemento de reconocimiento de ARN; Proteína de unión al ARN; Gránulos de estrés; 577

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APA (6th Edition):

Agostini, Federico, 1. (2014). Predictions of RNA-binding ability and aggregation propensity of proteins. (Thesis). Universitat Pompeu Fabra. Retrieved from http://hdl.handle.net/10803/318159

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):

Agostini, Federico, 1985-. “Predictions of RNA-binding ability and aggregation propensity of proteins.” 2014. Thesis, Universitat Pompeu Fabra. Accessed April 13, 2021. http://hdl.handle.net/10803/318159.

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

MLA Handbook (7th Edition):

Agostini, Federico, 1985-. “Predictions of RNA-binding ability and aggregation propensity of proteins.” 2014. Web. 13 Apr 2021.

Vancouver:

Agostini, Federico 1. Predictions of RNA-binding ability and aggregation propensity of proteins. [Internet] [Thesis]. Universitat Pompeu Fabra; 2014. [cited 2021 Apr 13]. Available from: http://hdl.handle.net/10803/318159.

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

Council of Science Editors:

Agostini, Federico 1. Predictions of RNA-binding ability and aggregation propensity of proteins. [Thesis]. Universitat Pompeu Fabra; 2014. Available from: http://hdl.handle.net/10803/318159

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

.