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You searched for subject:(Protein translocation). Showing records 1 – 30 of 71 total matches.

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Université de Neuchâtel

1. Martin, Meryll Michael. Proprotein import in chloroplast biogenesis: identification and characterisation of a strong dimerisation mutant of atToc159.

Degree: 2011, Université de Neuchâtel

 The chloroplast is the hallmark organelle of plant having evolved from the endosymbiotic event. Most chloroplast proteins are synthesized as preproteins in the cytosol. The… (more)

Subjects/Keywords: protein translocation

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APA (6th Edition):

Martin, M. M. (2011). Proprotein import in chloroplast biogenesis: identification and characterisation of a strong dimerisation mutant of atToc159. (Thesis). Université de Neuchâtel. Retrieved from http://doc.rero.ch/record/28475

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):

Martin, Meryll Michael. “Proprotein import in chloroplast biogenesis: identification and characterisation of a strong dimerisation mutant of atToc159.” 2011. Thesis, Université de Neuchâtel. Accessed June 24, 2019. http://doc.rero.ch/record/28475.

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

MLA Handbook (7th Edition):

Martin, Meryll Michael. “Proprotein import in chloroplast biogenesis: identification and characterisation of a strong dimerisation mutant of atToc159.” 2011. Web. 24 Jun 2019.

Vancouver:

Martin MM. Proprotein import in chloroplast biogenesis: identification and characterisation of a strong dimerisation mutant of atToc159. [Internet] [Thesis]. Université de Neuchâtel; 2011. [cited 2019 Jun 24]. Available from: http://doc.rero.ch/record/28475.

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

Council of Science Editors:

Martin MM. Proprotein import in chloroplast biogenesis: identification and characterisation of a strong dimerisation mutant of atToc159. [Thesis]. Université de Neuchâtel; 2011. Available from: http://doc.rero.ch/record/28475

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


The Ohio State University

2. Shoji, Shinichiro. Molecular Analysis of tRNA-mRNA movement in the Ribosome.

Degree: PhD, Microbiology, 2009, The Ohio State University

  Ribosomes are megadalton ribonucleoprotein particles dedicated to protein synthesis. The process of protein synthesis, also called translation, is one of the major targets of… (more)

Subjects/Keywords: Biochemistry; Microbiology; translation; protein synthesis; translocation; antibiotics; reverse translocation; LepA

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APA (6th Edition):

Shoji, S. (2009). Molecular Analysis of tRNA-mRNA movement in the Ribosome. (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1243195638

Chicago Manual of Style (16th Edition):

Shoji, Shinichiro. “Molecular Analysis of tRNA-mRNA movement in the Ribosome.” 2009. Doctoral Dissertation, The Ohio State University. Accessed June 24, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=osu1243195638.

MLA Handbook (7th Edition):

Shoji, Shinichiro. “Molecular Analysis of tRNA-mRNA movement in the Ribosome.” 2009. Web. 24 Jun 2019.

Vancouver:

Shoji S. Molecular Analysis of tRNA-mRNA movement in the Ribosome. [Internet] [Doctoral dissertation]. The Ohio State University; 2009. [cited 2019 Jun 24]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1243195638.

Council of Science Editors:

Shoji S. Molecular Analysis of tRNA-mRNA movement in the Ribosome. [Doctoral Dissertation]. The Ohio State University; 2009. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1243195638


University of Missouri – Columbia

3. Peters, Kristen N. Yersinia pestis YopK contributes to immune evasion and cell death to promote plague.

Degree: 2012, University of Missouri – Columbia

 [ACCESS RESTRICTED TO THE UNIVERSITY OF MISSOURI AT AUTHOR'S REQUEST.] YopK is a 21-kilodalton protein that is secreted and translocated by the type three secretion… (more)

Subjects/Keywords: effector protein; translocation; CCR2+ cells; GTPase mimic

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APA (6th Edition):

Peters, K. N. (2012). Yersinia pestis YopK contributes to immune evasion and cell death to promote plague. (Thesis). University of Missouri – Columbia. Retrieved from http://hdl.handle.net/10355/35204

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):

Peters, Kristen N. “Yersinia pestis YopK contributes to immune evasion and cell death to promote plague.” 2012. Thesis, University of Missouri – Columbia. Accessed June 24, 2019. http://hdl.handle.net/10355/35204.

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

MLA Handbook (7th Edition):

Peters, Kristen N. “Yersinia pestis YopK contributes to immune evasion and cell death to promote plague.” 2012. Web. 24 Jun 2019.

Vancouver:

Peters KN. Yersinia pestis YopK contributes to immune evasion and cell death to promote plague. [Internet] [Thesis]. University of Missouri – Columbia; 2012. [cited 2019 Jun 24]. Available from: http://hdl.handle.net/10355/35204.

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

Council of Science Editors:

Peters KN. Yersinia pestis YopK contributes to immune evasion and cell death to promote plague. [Thesis]. University of Missouri – Columbia; 2012. Available from: http://hdl.handle.net/10355/35204

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


Indian Institute of Science

4. Sinha, Devanjan. Unraveling the Intricate Architecture of Human Mitochondrial Presequence Translocase - Insights on its Evolution and Role in Tumourigenesis.

Degree: 2013, Indian Institute of Science

 The present thesis focuses on the elucidation of human mitochondrial inner membrane presequence-translocation machinery with implications on cancer cell proliferation. Mitochondria are the endosymbiotic organelles… (more)

Subjects/Keywords: Mitochondrial Protein Translocation; Mitochondria; Human Mitochondria Biogenesis; Mitochondrial J-Proteins; Humam Mitochondrial Presequence Translocation; Organellar Protein Translocation; Mitochondrial Protein Translocation; Cancer - Mitochondria; Apoptosis - Mitochondria; Tumourigenesis; Mitocondria - Tumourigenicity; Biochemistry

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APA (6th Edition):

Sinha, D. (2013). Unraveling the Intricate Architecture of Human Mitochondrial Presequence Translocase - Insights on its Evolution and Role in Tumourigenesis. (Thesis). Indian Institute of Science. Retrieved from http://etd.iisc.ernet.in/2005/3445 ; http://etd.iisc.ernet.in/abstracts/4312/G25967-Abs.pdf

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):

Sinha, Devanjan. “Unraveling the Intricate Architecture of Human Mitochondrial Presequence Translocase - Insights on its Evolution and Role in Tumourigenesis.” 2013. Thesis, Indian Institute of Science. Accessed June 24, 2019. http://etd.iisc.ernet.in/2005/3445 ; http://etd.iisc.ernet.in/abstracts/4312/G25967-Abs.pdf.

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

MLA Handbook (7th Edition):

Sinha, Devanjan. “Unraveling the Intricate Architecture of Human Mitochondrial Presequence Translocase - Insights on its Evolution and Role in Tumourigenesis.” 2013. Web. 24 Jun 2019.

Vancouver:

Sinha D. Unraveling the Intricate Architecture of Human Mitochondrial Presequence Translocase - Insights on its Evolution and Role in Tumourigenesis. [Internet] [Thesis]. Indian Institute of Science; 2013. [cited 2019 Jun 24]. Available from: http://etd.iisc.ernet.in/2005/3445 ; http://etd.iisc.ernet.in/abstracts/4312/G25967-Abs.pdf.

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

Council of Science Editors:

Sinha D. Unraveling the Intricate Architecture of Human Mitochondrial Presequence Translocase - Insights on its Evolution and Role in Tumourigenesis. [Thesis]. Indian Institute of Science; 2013. Available from: http://etd.iisc.ernet.in/2005/3445 ; http://etd.iisc.ernet.in/abstracts/4312/G25967-Abs.pdf

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


University of Cincinnati

5. Kravats, Andrea N. Coarse grained molecular dynamics simulations of the coupling between the allosteric mechanism of the ClpY nanomachine and threading of a substrate protein.

Degree: PhD, Arts and Sciences: Chemistry, 2013, University of Cincinnati

Protein quality control is critical in maintaining cell viability. Recognitionand degradation of aberrant proteins in the cellular environment is essential,as many neurodegenerative diseases are linked… (more)

Subjects/Keywords: Physical Chemistry; ATPase; protein unfolding; protein translocation; coarse grained simulations

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APA (6th Edition):

Kravats, A. N. (2013). Coarse grained molecular dynamics simulations of the coupling between the allosteric mechanism of the ClpY nanomachine and threading of a substrate protein. (Doctoral Dissertation). University of Cincinnati. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=ucin1384849649

Chicago Manual of Style (16th Edition):

Kravats, Andrea N. “Coarse grained molecular dynamics simulations of the coupling between the allosteric mechanism of the ClpY nanomachine and threading of a substrate protein.” 2013. Doctoral Dissertation, University of Cincinnati. Accessed June 24, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1384849649.

MLA Handbook (7th Edition):

Kravats, Andrea N. “Coarse grained molecular dynamics simulations of the coupling between the allosteric mechanism of the ClpY nanomachine and threading of a substrate protein.” 2013. Web. 24 Jun 2019.

Vancouver:

Kravats AN. Coarse grained molecular dynamics simulations of the coupling between the allosteric mechanism of the ClpY nanomachine and threading of a substrate protein. [Internet] [Doctoral dissertation]. University of Cincinnati; 2013. [cited 2019 Jun 24]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ucin1384849649.

Council of Science Editors:

Kravats AN. Coarse grained molecular dynamics simulations of the coupling between the allosteric mechanism of the ClpY nanomachine and threading of a substrate protein. [Doctoral Dissertation]. University of Cincinnati; 2013. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ucin1384849649


University of Cincinnati

6. Tonddast-Navaei, Sam, M.S. Mechanism of Substrate Protein Remodeling by Allosteric Motions of AAA+ Nanomachines.

Degree: PhD, Arts and Sciences: Chemistry, 2014, University of Cincinnati

 Proteins are large complex molecules that play important roles in cellular activities such as DNA replication, molecular transport, cell immunity, and regulatory activities. Based on… (more)

Subjects/Keywords: Physical Chemistry; Protein unfolding; Protein translocation; Protein degradation; ATPase; p97; Molecular Dynamics

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APA (6th Edition):

Tonddast-Navaei, Sam, M. S. (2014). Mechanism of Substrate Protein Remodeling by Allosteric Motions of AAA+ Nanomachines. (Doctoral Dissertation). University of Cincinnati. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=ucin1384869946

Chicago Manual of Style (16th Edition):

Tonddast-Navaei, Sam, M S. “Mechanism of Substrate Protein Remodeling by Allosteric Motions of AAA+ Nanomachines.” 2014. Doctoral Dissertation, University of Cincinnati. Accessed June 24, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1384869946.

MLA Handbook (7th Edition):

Tonddast-Navaei, Sam, M S. “Mechanism of Substrate Protein Remodeling by Allosteric Motions of AAA+ Nanomachines.” 2014. Web. 24 Jun 2019.

Vancouver:

Tonddast-Navaei, Sam MS. Mechanism of Substrate Protein Remodeling by Allosteric Motions of AAA+ Nanomachines. [Internet] [Doctoral dissertation]. University of Cincinnati; 2014. [cited 2019 Jun 24]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ucin1384869946.

Council of Science Editors:

Tonddast-Navaei, Sam MS. Mechanism of Substrate Protein Remodeling by Allosteric Motions of AAA+ Nanomachines. [Doctoral Dissertation]. University of Cincinnati; 2014. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ucin1384869946


University of Manchester

7. Casson, Joe. Investigating the role of TRC40 in post-translational protein delivery and quality control.

Degree: 2017, University of Manchester

 Membrane compartmentalisation allows eukaryotic cells to perform complex processes by combining dedicated sets of proteins in the same organelle. To achieve this, the cell must… (more)

Subjects/Keywords: BAG6; Endoplasmic reticulum; Protein translocation; Membrane protein; SND; SRP; BAG6; Protein quality control

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

APA (6th Edition):

Casson, J. (2017). Investigating the role of TRC40 in post-translational protein delivery and quality control. (Doctoral Dissertation). University of Manchester. Retrieved from http://www.manchester.ac.uk/escholar/uk-ac-man-scw:312279

Chicago Manual of Style (16th Edition):

Casson, Joe. “Investigating the role of TRC40 in post-translational protein delivery and quality control.” 2017. Doctoral Dissertation, University of Manchester. Accessed June 24, 2019. http://www.manchester.ac.uk/escholar/uk-ac-man-scw:312279.

MLA Handbook (7th Edition):

Casson, Joe. “Investigating the role of TRC40 in post-translational protein delivery and quality control.” 2017. Web. 24 Jun 2019.

Vancouver:

Casson J. Investigating the role of TRC40 in post-translational protein delivery and quality control. [Internet] [Doctoral dissertation]. University of Manchester; 2017. [cited 2019 Jun 24]. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:312279.

Council of Science Editors:

Casson J. Investigating the role of TRC40 in post-translational protein delivery and quality control. [Doctoral Dissertation]. University of Manchester; 2017. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:312279


University of Manchester

8. Casson, Joe. Investigating the role of TRC40 in post-translational protein delivery and quality control.

Degree: PhD, 2017, University of Manchester

 Membrane compartmentalisation allows eukaryotic cells to perform complex processes by combining dedicated sets of proteins in the same organelle. To achieve this, the cell must… (more)

Subjects/Keywords: BAG6; SRP; SND; Protein quality control; Protein translocation; Endoplasmic reticulum; Membrane protein

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APA (6th Edition):

Casson, J. (2017). Investigating the role of TRC40 in post-translational protein delivery and quality control. (Doctoral Dissertation). University of Manchester. Retrieved from https://www.research.manchester.ac.uk/portal/en/theses/investigating-the-role-of-trc40-in-posttranslational-protein-delivery-and-quality-control(02dac94c-857b-4c66-9ea7-8813241dcbce).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.764518

Chicago Manual of Style (16th Edition):

Casson, Joe. “Investigating the role of TRC40 in post-translational protein delivery and quality control.” 2017. Doctoral Dissertation, University of Manchester. Accessed June 24, 2019. https://www.research.manchester.ac.uk/portal/en/theses/investigating-the-role-of-trc40-in-posttranslational-protein-delivery-and-quality-control(02dac94c-857b-4c66-9ea7-8813241dcbce).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.764518.

MLA Handbook (7th Edition):

Casson, Joe. “Investigating the role of TRC40 in post-translational protein delivery and quality control.” 2017. Web. 24 Jun 2019.

Vancouver:

Casson J. Investigating the role of TRC40 in post-translational protein delivery and quality control. [Internet] [Doctoral dissertation]. University of Manchester; 2017. [cited 2019 Jun 24]. Available from: https://www.research.manchester.ac.uk/portal/en/theses/investigating-the-role-of-trc40-in-posttranslational-protein-delivery-and-quality-control(02dac94c-857b-4c66-9ea7-8813241dcbce).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.764518.

Council of Science Editors:

Casson J. Investigating the role of TRC40 in post-translational protein delivery and quality control. [Doctoral Dissertation]. University of Manchester; 2017. Available from: https://www.research.manchester.ac.uk/portal/en/theses/investigating-the-role-of-trc40-in-posttranslational-protein-delivery-and-quality-control(02dac94c-857b-4c66-9ea7-8813241dcbce).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.764518


University of California – San Diego

9. Nelson, Katelyn. Functional Characterization of Oncogenic Driver FGFR3-TACC3.

Degree: Chemistry, 2018, University of California – San Diego

 Fibroblast Growth Factor Receptors (FGFRs) are critical for cell proliferation and differentiation. Mutation and/or translocation of FGFRs lead to aberrant signaling that often results in… (more)

Subjects/Keywords: Biochemistry; Cellular biology; cancer; FGFR; fusion protein; TACC; translocation

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APA (6th Edition):

Nelson, K. (2018). Functional Characterization of Oncogenic Driver FGFR3-TACC3. (Thesis). University of California – San Diego. Retrieved from http://www.escholarship.org/uc/item/9tj8f2k3

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):

Nelson, Katelyn. “Functional Characterization of Oncogenic Driver FGFR3-TACC3.” 2018. Thesis, University of California – San Diego. Accessed June 24, 2019. http://www.escholarship.org/uc/item/9tj8f2k3.

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

MLA Handbook (7th Edition):

Nelson, Katelyn. “Functional Characterization of Oncogenic Driver FGFR3-TACC3.” 2018. Web. 24 Jun 2019.

Vancouver:

Nelson K. Functional Characterization of Oncogenic Driver FGFR3-TACC3. [Internet] [Thesis]. University of California – San Diego; 2018. [cited 2019 Jun 24]. Available from: http://www.escholarship.org/uc/item/9tj8f2k3.

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

Council of Science Editors:

Nelson K. Functional Characterization of Oncogenic Driver FGFR3-TACC3. [Thesis]. University of California – San Diego; 2018. Available from: http://www.escholarship.org/uc/item/9tj8f2k3

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


UCLA

10. Maland, Matthew Dean. Dissecting Mitochondrial Redox-Regulated Protein Translocation Using Small Molecule Probes.

Degree: Biochemistry & Molecular Biology, 2016, UCLA

 Mitochondria are responsible for a multitude of cellular functions that almost always require nuclear encoded proteins to be translocated. Defects in mitochondrial import pathways result… (more)

Subjects/Keywords: Biochemistry; Erv1; Mia40; Mitochondria; protein translocation; Small molecule tools

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APA (6th Edition):

Maland, M. D. (2016). Dissecting Mitochondrial Redox-Regulated Protein Translocation Using Small Molecule Probes. (Thesis). UCLA. Retrieved from http://www.escholarship.org/uc/item/1n4516dd

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):

Maland, Matthew Dean. “Dissecting Mitochondrial Redox-Regulated Protein Translocation Using Small Molecule Probes.” 2016. Thesis, UCLA. Accessed June 24, 2019. http://www.escholarship.org/uc/item/1n4516dd.

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

MLA Handbook (7th Edition):

Maland, Matthew Dean. “Dissecting Mitochondrial Redox-Regulated Protein Translocation Using Small Molecule Probes.” 2016. Web. 24 Jun 2019.

Vancouver:

Maland MD. Dissecting Mitochondrial Redox-Regulated Protein Translocation Using Small Molecule Probes. [Internet] [Thesis]. UCLA; 2016. [cited 2019 Jun 24]. Available from: http://www.escholarship.org/uc/item/1n4516dd.

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

Council of Science Editors:

Maland MD. Dissecting Mitochondrial Redox-Regulated Protein Translocation Using Small Molecule Probes. [Thesis]. UCLA; 2016. Available from: http://www.escholarship.org/uc/item/1n4516dd

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


UCLA

11. Cheung, Tsz Mei Jesmine. A small molecule dissociates the PAM motor from the TIM23 channel.

Degree: Biochemistry & Molecular Biology, 2017, UCLA

 Mitochondrial dysfunction is a contributing factor in various neural and muscular degenerative diseases. Modulation of mitochondrial protein pathways can have regulatory effects on mitochondrial function.… (more)

Subjects/Keywords: Biochemistry; Molecular biology; Mitochondria; Protein translocation; Small Molecule; TIM23 channel

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APA (6th Edition):

Cheung, T. M. J. (2017). A small molecule dissociates the PAM motor from the TIM23 channel. (Thesis). UCLA. Retrieved from http://www.escholarship.org/uc/item/9kh6586x

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):

Cheung, Tsz Mei Jesmine. “A small molecule dissociates the PAM motor from the TIM23 channel.” 2017. Thesis, UCLA. Accessed June 24, 2019. http://www.escholarship.org/uc/item/9kh6586x.

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

MLA Handbook (7th Edition):

Cheung, Tsz Mei Jesmine. “A small molecule dissociates the PAM motor from the TIM23 channel.” 2017. Web. 24 Jun 2019.

Vancouver:

Cheung TMJ. A small molecule dissociates the PAM motor from the TIM23 channel. [Internet] [Thesis]. UCLA; 2017. [cited 2019 Jun 24]. Available from: http://www.escholarship.org/uc/item/9kh6586x.

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

Council of Science Editors:

Cheung TMJ. A small molecule dissociates the PAM motor from the TIM23 channel. [Thesis]. UCLA; 2017. Available from: http://www.escholarship.org/uc/item/9kh6586x

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


Wayne State University

12. Kern, Stephanie Marie. Development of a cargo delivery system and inhibition studies focused on clostridium difficile toxin a.

Degree: PhD, Chemistry, 2012, Wayne State University

  Virulence factors of pathogenic bacteria are to be blamed for life-threatening infections such as diphtheria, anthrax, botulism, and tentanus. In the case of enzymatic… (more)

Subjects/Keywords: Cargo delivery, Clostridium difficile, Protein delivery, Toxin A, Translocation; Biochemistry; Chemistry

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APA (6th Edition):

Kern, S. M. (2012). Development of a cargo delivery system and inhibition studies focused on clostridium difficile toxin a. (Doctoral Dissertation). Wayne State University. Retrieved from https://digitalcommons.wayne.edu/oa_dissertations/449

Chicago Manual of Style (16th Edition):

Kern, Stephanie Marie. “Development of a cargo delivery system and inhibition studies focused on clostridium difficile toxin a.” 2012. Doctoral Dissertation, Wayne State University. Accessed June 24, 2019. https://digitalcommons.wayne.edu/oa_dissertations/449.

MLA Handbook (7th Edition):

Kern, Stephanie Marie. “Development of a cargo delivery system and inhibition studies focused on clostridium difficile toxin a.” 2012. Web. 24 Jun 2019.

Vancouver:

Kern SM. Development of a cargo delivery system and inhibition studies focused on clostridium difficile toxin a. [Internet] [Doctoral dissertation]. Wayne State University; 2012. [cited 2019 Jun 24]. Available from: https://digitalcommons.wayne.edu/oa_dissertations/449.

Council of Science Editors:

Kern SM. Development of a cargo delivery system and inhibition studies focused on clostridium difficile toxin a. [Doctoral Dissertation]. Wayne State University; 2012. Available from: https://digitalcommons.wayne.edu/oa_dissertations/449


Wesleyan University

13. Blum, Amy Elana. Assessment of the Functionality of the Back-to-back Conformation of the SecYEG.

Degree: Molecular Biology and Biochemistry, 2015, Wesleyan University

  Approximately 30% of proteins produced in E. coli are translocated through the universally conserved SecYEG channel, either for co-translational insertion into the cytoplasmic membrane,… (more)

Subjects/Keywords: SecYEG; Protein Translocation; SecA; Oligomerization; Dimer; E. coli

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APA (6th Edition):

Blum, A. E. (2015). Assessment of the Functionality of the Back-to-back Conformation of the SecYEG. (Masters Thesis). Wesleyan University. Retrieved from https://wesscholar.wesleyan.edu/etd_mas_theses/105

Chicago Manual of Style (16th Edition):

Blum, Amy Elana. “Assessment of the Functionality of the Back-to-back Conformation of the SecYEG.” 2015. Masters Thesis, Wesleyan University. Accessed June 24, 2019. https://wesscholar.wesleyan.edu/etd_mas_theses/105.

MLA Handbook (7th Edition):

Blum, Amy Elana. “Assessment of the Functionality of the Back-to-back Conformation of the SecYEG.” 2015. Web. 24 Jun 2019.

Vancouver:

Blum AE. Assessment of the Functionality of the Back-to-back Conformation of the SecYEG. [Internet] [Masters thesis]. Wesleyan University; 2015. [cited 2019 Jun 24]. Available from: https://wesscholar.wesleyan.edu/etd_mas_theses/105.

Council of Science Editors:

Blum AE. Assessment of the Functionality of the Back-to-back Conformation of the SecYEG. [Masters Thesis]. Wesleyan University; 2015. Available from: https://wesscholar.wesleyan.edu/etd_mas_theses/105


University of California – Berkeley

14. Rodriguez Aliaga, Piere. A Finely Tuned Molecular Motor: Mechanochemistry and Power Efficiency in the AAA+ Protease Machine ClpXP.

Degree: Biophysics, 2016, University of California – Berkeley

 Molecular motors transduce chemical energy –usually from ATP hydrolysis– into directed motion and mechanical work, which is used to perform key functions in almost every… (more)

Subjects/Keywords: Biophysics; Molecular biology; Biochemistry; Mechanochemistry; Molecular Motors; Optical Tweezers; Protein translocation; Protein unfolding; Single Molecule

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APA (6th Edition):

Rodriguez Aliaga, P. (2016). A Finely Tuned Molecular Motor: Mechanochemistry and Power Efficiency in the AAA+ Protease Machine ClpXP. (Thesis). University of California – Berkeley. Retrieved from http://www.escholarship.org/uc/item/89s8r174

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):

Rodriguez Aliaga, Piere. “A Finely Tuned Molecular Motor: Mechanochemistry and Power Efficiency in the AAA+ Protease Machine ClpXP.” 2016. Thesis, University of California – Berkeley. Accessed June 24, 2019. http://www.escholarship.org/uc/item/89s8r174.

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

MLA Handbook (7th Edition):

Rodriguez Aliaga, Piere. “A Finely Tuned Molecular Motor: Mechanochemistry and Power Efficiency in the AAA+ Protease Machine ClpXP.” 2016. Web. 24 Jun 2019.

Vancouver:

Rodriguez Aliaga P. A Finely Tuned Molecular Motor: Mechanochemistry and Power Efficiency in the AAA+ Protease Machine ClpXP. [Internet] [Thesis]. University of California – Berkeley; 2016. [cited 2019 Jun 24]. Available from: http://www.escholarship.org/uc/item/89s8r174.

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

Council of Science Editors:

Rodriguez Aliaga P. A Finely Tuned Molecular Motor: Mechanochemistry and Power Efficiency in the AAA+ Protease Machine ClpXP. [Thesis]. University of California – Berkeley; 2016. Available from: http://www.escholarship.org/uc/item/89s8r174

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


University of Notre Dame

15. Esther Braselmann. Investigating the secretion and folding mechanism of a beta-sheet rich virulence protein</h1>.

Degree: PhD, Chemistry and Biochemistry, 2014, University of Notre Dame

  Autotransporter (AT) proteins are the largest family of virulence proteins secreted from Gram-negative bacterial pathogens. They are synthesized with an N-terminal signal sequence, a… (more)

Subjects/Keywords: protein folding; beta-helix; outer membrane translocation; autotransporter secretion; virulence protein; vectorial folding

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APA (6th Edition):

Braselmann, E. (2014). Investigating the secretion and folding mechanism of a beta-sheet rich virulence protein</h1>. (Doctoral Dissertation). University of Notre Dame. Retrieved from https://curate.nd.edu/show/3b59183387t

Chicago Manual of Style (16th Edition):

Braselmann, Esther. “Investigating the secretion and folding mechanism of a beta-sheet rich virulence protein</h1>.” 2014. Doctoral Dissertation, University of Notre Dame. Accessed June 24, 2019. https://curate.nd.edu/show/3b59183387t.

MLA Handbook (7th Edition):

Braselmann, Esther. “Investigating the secretion and folding mechanism of a beta-sheet rich virulence protein</h1>.” 2014. Web. 24 Jun 2019.

Vancouver:

Braselmann E. Investigating the secretion and folding mechanism of a beta-sheet rich virulence protein</h1>. [Internet] [Doctoral dissertation]. University of Notre Dame; 2014. [cited 2019 Jun 24]. Available from: https://curate.nd.edu/show/3b59183387t.

Council of Science Editors:

Braselmann E. Investigating the secretion and folding mechanism of a beta-sheet rich virulence protein</h1>. [Doctoral Dissertation]. University of Notre Dame; 2014. Available from: https://curate.nd.edu/show/3b59183387t


Texas A&M University

16. Whitaker, Neal William 1982-. Deciphering the Mechanism of E. coli tat Protein Transport: Kinetic Substeps and Cargo Properties.

Degree: 2012, Texas A&M University

 The Escherichia coli twin-arginine translocation (Tat) system transports fully folded and assembled proteins across the inner membrane into the periplasmic space. The E. coli Tat… (more)

Subjects/Keywords: Protein Translocation; Protein Targeting; Protein Secretion; Protein Export; Membrane Proteins; Intracellular Trafficking; Fluorescence Resonance Energy Transfer (FRET); Escherichia coli

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APA (6th Edition):

Whitaker, N. W. 1. (2012). Deciphering the Mechanism of E. coli tat Protein Transport: Kinetic Substeps and Cargo Properties. (Thesis). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/148188

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):

Whitaker, Neal William 1982-. “Deciphering the Mechanism of E. coli tat Protein Transport: Kinetic Substeps and Cargo Properties.” 2012. Thesis, Texas A&M University. Accessed June 24, 2019. http://hdl.handle.net/1969.1/148188.

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

MLA Handbook (7th Edition):

Whitaker, Neal William 1982-. “Deciphering the Mechanism of E. coli tat Protein Transport: Kinetic Substeps and Cargo Properties.” 2012. Web. 24 Jun 2019.

Vancouver:

Whitaker NW1. Deciphering the Mechanism of E. coli tat Protein Transport: Kinetic Substeps and Cargo Properties. [Internet] [Thesis]. Texas A&M University; 2012. [cited 2019 Jun 24]. Available from: http://hdl.handle.net/1969.1/148188.

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

Council of Science Editors:

Whitaker NW1. Deciphering the Mechanism of E. coli tat Protein Transport: Kinetic Substeps and Cargo Properties. [Thesis]. Texas A&M University; 2012. Available from: http://hdl.handle.net/1969.1/148188

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

17. Jiang, Qiyang. Cryo-microscopie électronique des complexes de l'adressage et de la translocation co-traductionnelle chez E. coli : Electron cryo-microscopy of complexes in E. coli co-translational targeting and translocation.

Degree: Docteur es, Chimie, 2015, Grenoble Alpes

 La membrane cellulaire est la barrière qui sépare l'intérieur des cellules de l'environnement extérieur. Elle se compose de lipides et de protéines. Les gènes codant… (more)

Subjects/Keywords: Cryo-microscopie électronique; Protéine membranaire; Ribosome; Adressage des protéines; Translocation des protéines; Electron cryo-microscopy; Membrane protein; Ribosome; Protein targeting; Protein translocation; 500; 570

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APA (6th Edition):

Jiang, Q. (2015). Cryo-microscopie électronique des complexes de l'adressage et de la translocation co-traductionnelle chez E. coli : Electron cryo-microscopy of complexes in E. coli co-translational targeting and translocation. (Doctoral Dissertation). Grenoble Alpes. Retrieved from http://www.theses.fr/2015GREAV058

Chicago Manual of Style (16th Edition):

Jiang, Qiyang. “Cryo-microscopie électronique des complexes de l'adressage et de la translocation co-traductionnelle chez E. coli : Electron cryo-microscopy of complexes in E. coli co-translational targeting and translocation.” 2015. Doctoral Dissertation, Grenoble Alpes. Accessed June 24, 2019. http://www.theses.fr/2015GREAV058.

MLA Handbook (7th Edition):

Jiang, Qiyang. “Cryo-microscopie électronique des complexes de l'adressage et de la translocation co-traductionnelle chez E. coli : Electron cryo-microscopy of complexes in E. coli co-translational targeting and translocation.” 2015. Web. 24 Jun 2019.

Vancouver:

Jiang Q. Cryo-microscopie électronique des complexes de l'adressage et de la translocation co-traductionnelle chez E. coli : Electron cryo-microscopy of complexes in E. coli co-translational targeting and translocation. [Internet] [Doctoral dissertation]. Grenoble Alpes; 2015. [cited 2019 Jun 24]. Available from: http://www.theses.fr/2015GREAV058.

Council of Science Editors:

Jiang Q. Cryo-microscopie électronique des complexes de l'adressage et de la translocation co-traductionnelle chez E. coli : Electron cryo-microscopy of complexes in E. coli co-translational targeting and translocation. [Doctoral Dissertation]. Grenoble Alpes; 2015. Available from: http://www.theses.fr/2015GREAV058


University of Cambridge

18. Liu, Dandan. A study of protein-DNA interactions using atomic force microscopy and DNA origami .

Degree: 2019, University of Cambridge

 The development and application of genome editing tools has accelerated in recent years. However, their widespread application, especially in the medical field, is delayed for… (more)

Subjects/Keywords: restriction enzyme; DNA origami; atomic force microscopy; EcoRV; BcgI; quantitative studies; protein translocation; protein-DNA interaction; recognition site; recognition sites; translocation mechanism; protein-complex; Type II restriction enzymes; DNA-cutting

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APA (6th Edition):

Liu, D. (2019). A study of protein-DNA interactions using atomic force microscopy and DNA origami . (Thesis). University of Cambridge. Retrieved from https://www.repository.cam.ac.uk/handle/1810/291911

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):

Liu, Dandan. “A study of protein-DNA interactions using atomic force microscopy and DNA origami .” 2019. Thesis, University of Cambridge. Accessed June 24, 2019. https://www.repository.cam.ac.uk/handle/1810/291911.

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

MLA Handbook (7th Edition):

Liu, Dandan. “A study of protein-DNA interactions using atomic force microscopy and DNA origami .” 2019. Web. 24 Jun 2019.

Vancouver:

Liu D. A study of protein-DNA interactions using atomic force microscopy and DNA origami . [Internet] [Thesis]. University of Cambridge; 2019. [cited 2019 Jun 24]. Available from: https://www.repository.cam.ac.uk/handle/1810/291911.

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

Council of Science Editors:

Liu D. A study of protein-DNA interactions using atomic force microscopy and DNA origami . [Thesis]. University of Cambridge; 2019. Available from: https://www.repository.cam.ac.uk/handle/1810/291911

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

19. Agiasotelli, Danai. Αξιολόγηση των επιπέδων της πρωτεΐνης-δέσμευσης-λιποπολυσακχαρίτη στον ορό και το ασκιτικό υγρό σε ασθενείς με κίρρωση ήπατος με και χωρίς επιπλοκές.

Degree: 2017, National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ)

Lipopolysaccharide-binding protein (LBP) is an acute-phase protein produced by the liver. Changes in LBP levels are associated with dynamics of bacterial translocation and intestinal permeability… (more)

Subjects/Keywords: Πρωτεΐνη – δέσμευσης – λιποπολυσακχαρίτη; Μη αντιρροπούμενη κίρρωση; Βακτηριακή μετατόπιση; Lipopolysaccharide - binding protein; Decompensated cirrhosis; Bacterial translocation

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APA (6th Edition):

Agiasotelli, D. (2017). Αξιολόγηση των επιπέδων της πρωτεΐνης-δέσμευσης-λιποπολυσακχαρίτη στον ορό και το ασκιτικό υγρό σε ασθενείς με κίρρωση ήπατος με και χωρίς επιπλοκές. (Thesis). National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ). Retrieved from http://hdl.handle.net/10442/hedi/40681

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):

Agiasotelli, Danai. “Αξιολόγηση των επιπέδων της πρωτεΐνης-δέσμευσης-λιποπολυσακχαρίτη στον ορό και το ασκιτικό υγρό σε ασθενείς με κίρρωση ήπατος με και χωρίς επιπλοκές.” 2017. Thesis, National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ). Accessed June 24, 2019. http://hdl.handle.net/10442/hedi/40681.

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

MLA Handbook (7th Edition):

Agiasotelli, Danai. “Αξιολόγηση των επιπέδων της πρωτεΐνης-δέσμευσης-λιποπολυσακχαρίτη στον ορό και το ασκιτικό υγρό σε ασθενείς με κίρρωση ήπατος με και χωρίς επιπλοκές.” 2017. Web. 24 Jun 2019.

Vancouver:

Agiasotelli D. Αξιολόγηση των επιπέδων της πρωτεΐνης-δέσμευσης-λιποπολυσακχαρίτη στον ορό και το ασκιτικό υγρό σε ασθενείς με κίρρωση ήπατος με και χωρίς επιπλοκές. [Internet] [Thesis]. National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ); 2017. [cited 2019 Jun 24]. Available from: http://hdl.handle.net/10442/hedi/40681.

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

Council of Science Editors:

Agiasotelli D. Αξιολόγηση των επιπέδων της πρωτεΐνης-δέσμευσης-λιποπολυσακχαρίτη στον ορό και το ασκιτικό υγρό σε ασθενείς με κίρρωση ήπατος με και χωρίς επιπλοκές. [Thesis]. National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ); 2017. Available from: http://hdl.handle.net/10442/hedi/40681

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


University of Kentucky

20. Wang, Shaoying. Development of New Biological Nanopores and Their Application for Biosensing and Disease Detection.

Degree: 2016, University of Kentucky

 Nanopore technology has recently emerged as a new real-time single molecule sensing method. The current dominant technologies, such as mass spectrometry and immunoassay, for protein(more)

Subjects/Keywords: Biological nanopore; peptide translocation; bacteriophage; RNA Nanotechnology; protein sequencing; Biology; Biotechnology; Nanotechnology

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APA (6th Edition):

Wang, S. (2016). Development of New Biological Nanopores and Their Application for Biosensing and Disease Detection. (Doctoral Dissertation). University of Kentucky. Retrieved from http://uknowledge.uky.edu/pharmacy_etds/64

Chicago Manual of Style (16th Edition):

Wang, Shaoying. “Development of New Biological Nanopores and Their Application for Biosensing and Disease Detection.” 2016. Doctoral Dissertation, University of Kentucky. Accessed June 24, 2019. http://uknowledge.uky.edu/pharmacy_etds/64.

MLA Handbook (7th Edition):

Wang, Shaoying. “Development of New Biological Nanopores and Their Application for Biosensing and Disease Detection.” 2016. Web. 24 Jun 2019.

Vancouver:

Wang S. Development of New Biological Nanopores and Their Application for Biosensing and Disease Detection. [Internet] [Doctoral dissertation]. University of Kentucky; 2016. [cited 2019 Jun 24]. Available from: http://uknowledge.uky.edu/pharmacy_etds/64.

Council of Science Editors:

Wang S. Development of New Biological Nanopores and Their Application for Biosensing and Disease Detection. [Doctoral Dissertation]. University of Kentucky; 2016. Available from: http://uknowledge.uky.edu/pharmacy_etds/64

21. Iatmanen, Soria. Production et caractérisation structurale et fonctionnelle de la protéine membranaire recombinante TSPO : Production and structural and functional characterization of recombinant membrane protein TSPO.

Degree: Docteur es, Biologie Moléculaire et Biochimie, 2014, Université Pierre et Marie Curie – Paris VI

La TSPO préalablement connue sous le nom de récepteur périphérique aux benzodiazépines (PBR), est une protéine membranaire principalement impliquée dans le transport du cholestérol du… (more)

Subjects/Keywords: TSPO; PBR; Protéine membranaire; Structure; Fonction; Translocation Protein; Peripherical Benzodiazepine Receptor; 572.8

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APA (6th Edition):

Iatmanen, S. (2014). Production et caractérisation structurale et fonctionnelle de la protéine membranaire recombinante TSPO : Production and structural and functional characterization of recombinant membrane protein TSPO. (Doctoral Dissertation). Université Pierre et Marie Curie – Paris VI. Retrieved from http://www.theses.fr/2014PA066561

Chicago Manual of Style (16th Edition):

Iatmanen, Soria. “Production et caractérisation structurale et fonctionnelle de la protéine membranaire recombinante TSPO : Production and structural and functional characterization of recombinant membrane protein TSPO.” 2014. Doctoral Dissertation, Université Pierre et Marie Curie – Paris VI. Accessed June 24, 2019. http://www.theses.fr/2014PA066561.

MLA Handbook (7th Edition):

Iatmanen, Soria. “Production et caractérisation structurale et fonctionnelle de la protéine membranaire recombinante TSPO : Production and structural and functional characterization of recombinant membrane protein TSPO.” 2014. Web. 24 Jun 2019.

Vancouver:

Iatmanen S. Production et caractérisation structurale et fonctionnelle de la protéine membranaire recombinante TSPO : Production and structural and functional characterization of recombinant membrane protein TSPO. [Internet] [Doctoral dissertation]. Université Pierre et Marie Curie – Paris VI; 2014. [cited 2019 Jun 24]. Available from: http://www.theses.fr/2014PA066561.

Council of Science Editors:

Iatmanen S. Production et caractérisation structurale et fonctionnelle de la protéine membranaire recombinante TSPO : Production and structural and functional characterization of recombinant membrane protein TSPO. [Doctoral Dissertation]. Université Pierre et Marie Curie – Paris VI; 2014. Available from: http://www.theses.fr/2014PA066561


Virginia Tech

22. Cao, Zhenning. Microfluidic Engineering for Ultrasensitive Molecular Analysis of cells.

Degree: PhD, Biomedical Engineering, 2015, Virginia Tech

 The main focus of this research was the development of microfluidic technology for ultrasensitive and fast molecular analysis of cells. Chromatin immunoprecipitation (ChIP) assay followed… (more)

Subjects/Keywords: chromatin immunoprecipitation(ChIP); next generation sequencing; microfluidics; droplet sorting; protein translocation; sonication

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APA (6th Edition):

Cao, Z. (2015). Microfluidic Engineering for Ultrasensitive Molecular Analysis of cells. (Doctoral Dissertation). Virginia Tech. Retrieved from http://hdl.handle.net/10919/76721

Chicago Manual of Style (16th Edition):

Cao, Zhenning. “Microfluidic Engineering for Ultrasensitive Molecular Analysis of cells.” 2015. Doctoral Dissertation, Virginia Tech. Accessed June 24, 2019. http://hdl.handle.net/10919/76721.

MLA Handbook (7th Edition):

Cao, Zhenning. “Microfluidic Engineering for Ultrasensitive Molecular Analysis of cells.” 2015. Web. 24 Jun 2019.

Vancouver:

Cao Z. Microfluidic Engineering for Ultrasensitive Molecular Analysis of cells. [Internet] [Doctoral dissertation]. Virginia Tech; 2015. [cited 2019 Jun 24]. Available from: http://hdl.handle.net/10919/76721.

Council of Science Editors:

Cao Z. Microfluidic Engineering for Ultrasensitive Molecular Analysis of cells. [Doctoral Dissertation]. Virginia Tech; 2015. Available from: http://hdl.handle.net/10919/76721

23. Bulushev, Roman. Nanocapillaries combined with optical tweezers as a single molecule technique for studying DNA-protein complexes.

Degree: 2017, EPFL

 Interactions of proteins with DNA are essential for carrying out DNA's biological functions and performing a cellular cycle. Such processes as DNA replication, expression and… (more)

Subjects/Keywords: optical tweezers; glass nanocapillary; solid-state nanopore; DNA translocation; single molecule measurements; force measurements; DNA-protein complex; protein binding site

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APA (6th Edition):

Bulushev, R. (2017). Nanocapillaries combined with optical tweezers as a single molecule technique for studying DNA-protein complexes. (Thesis). EPFL. Retrieved from http://infoscience.epfl.ch/record/227088

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):

Bulushev, Roman. “Nanocapillaries combined with optical tweezers as a single molecule technique for studying DNA-protein complexes.” 2017. Thesis, EPFL. Accessed June 24, 2019. http://infoscience.epfl.ch/record/227088.

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

MLA Handbook (7th Edition):

Bulushev, Roman. “Nanocapillaries combined with optical tweezers as a single molecule technique for studying DNA-protein complexes.” 2017. Web. 24 Jun 2019.

Vancouver:

Bulushev R. Nanocapillaries combined with optical tweezers as a single molecule technique for studying DNA-protein complexes. [Internet] [Thesis]. EPFL; 2017. [cited 2019 Jun 24]. Available from: http://infoscience.epfl.ch/record/227088.

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

Council of Science Editors:

Bulushev R. Nanocapillaries combined with optical tweezers as a single molecule technique for studying DNA-protein complexes. [Thesis]. EPFL; 2017. Available from: http://infoscience.epfl.ch/record/227088

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


Cornell University

24. Chang, Matthew. Development Of A Tat Enabled Antibody Selection Platform Within The Cytoplasm Of Escherichia Coli .

Degree: 2016, Cornell University

Subjects/Keywords: Antibody selection; Protein protein interactions; Twin-arginine translocation

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APA (6th Edition):

Chang, M. (2016). Development Of A Tat Enabled Antibody Selection Platform Within The Cytoplasm Of Escherichia Coli . (Thesis). Cornell University. Retrieved from http://hdl.handle.net/1813/45286

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. “Development Of A Tat Enabled Antibody Selection Platform Within The Cytoplasm Of Escherichia Coli .” 2016. Thesis, Cornell University. Accessed June 24, 2019. http://hdl.handle.net/1813/45286.

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. “Development Of A Tat Enabled Antibody Selection Platform Within The Cytoplasm Of Escherichia Coli .” 2016. Web. 24 Jun 2019.

Vancouver:

Chang M. Development Of A Tat Enabled Antibody Selection Platform Within The Cytoplasm Of Escherichia Coli . [Internet] [Thesis]. Cornell University; 2016. [cited 2019 Jun 24]. Available from: http://hdl.handle.net/1813/45286.

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

Council of Science Editors:

Chang M. Development Of A Tat Enabled Antibody Selection Platform Within The Cytoplasm Of Escherichia Coli . [Thesis]. Cornell University; 2016. Available from: http://hdl.handle.net/1813/45286

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


University of Florida

25. Williams, Matthew L. YlxM a Novel Component of the Streptococcus Mutans Signal Recognition Particle Pathway.

Degree: PhD, Medical Sciences - Immunology and Microbiology (IDP), 2015, University of Florida

 Dental caries is the most common infectious disease in humans and causes significant health and economic burdens. Streptococcus mutans is a pathogen that is strongly… (more)

Subjects/Keywords: Bacteria; Membrane proteins; Operon; Protein transport; Proteins; Ribosomes; RNA; Signals; Small cytoplasmic RNA; Streptococcus mutans; caries  – protein  – smutans  – srp  – translocation  – ylxm

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APA (6th Edition):

Williams, M. L. (2015). YlxM a Novel Component of the Streptococcus Mutans Signal Recognition Particle Pathway. (Doctoral Dissertation). University of Florida. Retrieved from http://ufdc.ufl.edu/UFE0049247

Chicago Manual of Style (16th Edition):

Williams, Matthew L. “YlxM a Novel Component of the Streptococcus Mutans Signal Recognition Particle Pathway.” 2015. Doctoral Dissertation, University of Florida. Accessed June 24, 2019. http://ufdc.ufl.edu/UFE0049247.

MLA Handbook (7th Edition):

Williams, Matthew L. “YlxM a Novel Component of the Streptococcus Mutans Signal Recognition Particle Pathway.” 2015. Web. 24 Jun 2019.

Vancouver:

Williams ML. YlxM a Novel Component of the Streptococcus Mutans Signal Recognition Particle Pathway. [Internet] [Doctoral dissertation]. University of Florida; 2015. [cited 2019 Jun 24]. Available from: http://ufdc.ufl.edu/UFE0049247.

Council of Science Editors:

Williams ML. YlxM a Novel Component of the Streptococcus Mutans Signal Recognition Particle Pathway. [Doctoral Dissertation]. University of Florida; 2015. Available from: http://ufdc.ufl.edu/UFE0049247


Indian Institute of Science

26. Pareek, Gautam. Understanding the Dynamic Organization of the Presequence-Translocase in Translocation of Preproteins Across Mitochondrial Inner Membrane.

Degree: 2014, Indian Institute of Science

 Mitochondrion is an endosymbiotic organelle synthesizing ~1% of its proteome, while remaining ~99% of the proteins are encoded by the nuclear genome and translated on… (more)

Subjects/Keywords: Mitochondria; Nucleotide Binding; Mitochondrial Biogenesis; Mitochondrial Inner Membrane Protein Translocation; Mitochondrial Presquence Translocase; Preprotein Translocation; Saccharomyces Cerevisiae; Presequence Translocase Tim23; Mitochondrial Inner Membrane; Mitochondrial Hsp70s; Biochemistry

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

APA (6th Edition):

Pareek, G. (2014). Understanding the Dynamic Organization of the Presequence-Translocase in Translocation of Preproteins Across Mitochondrial Inner Membrane. (Thesis). Indian Institute of Science. Retrieved from http://etd.iisc.ernet.in/2005/3486 ; http://etd.iisc.ernet.in/abstracts/4353/G26385-Abs.PDF

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):

Pareek, Gautam. “Understanding the Dynamic Organization of the Presequence-Translocase in Translocation of Preproteins Across Mitochondrial Inner Membrane.” 2014. Thesis, Indian Institute of Science. Accessed June 24, 2019. http://etd.iisc.ernet.in/2005/3486 ; http://etd.iisc.ernet.in/abstracts/4353/G26385-Abs.PDF.

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

MLA Handbook (7th Edition):

Pareek, Gautam. “Understanding the Dynamic Organization of the Presequence-Translocase in Translocation of Preproteins Across Mitochondrial Inner Membrane.” 2014. Web. 24 Jun 2019.

Vancouver:

Pareek G. Understanding the Dynamic Organization of the Presequence-Translocase in Translocation of Preproteins Across Mitochondrial Inner Membrane. [Internet] [Thesis]. Indian Institute of Science; 2014. [cited 2019 Jun 24]. Available from: http://etd.iisc.ernet.in/2005/3486 ; http://etd.iisc.ernet.in/abstracts/4353/G26385-Abs.PDF.

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

Council of Science Editors:

Pareek G. Understanding the Dynamic Organization of the Presequence-Translocase in Translocation of Preproteins Across Mitochondrial Inner Membrane. [Thesis]. Indian Institute of Science; 2014. Available from: http://etd.iisc.ernet.in/2005/3486 ; http://etd.iisc.ernet.in/abstracts/4353/G26385-Abs.PDF

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


Université de Montréal

27. Kasakov, Velichko M. Intracellular trafficking of protease : Activated Receptor 2 (PAR2) by members of sorting nexins family .

Degree: 2010, Université de Montréal

 Le dogme voulant que les récepteurs couplés aux protéines G (GPCRs) activent des voies de signalisation seulement lorsqu’ils sont localisés à la membrane plasmatique, a… (more)

Subjects/Keywords: Récepteurs couplés à la protéine G; Sorting nexins; Récepteurs activés par la protéase; Translocation nucléaire; Membrane nucléaire; Signal nucléaire; G – Protein coupled receptors; Protease-activated receptors; Nuclear translocation; Nuclear membrane

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

APA (6th Edition):

Kasakov, V. M. (2010). Intracellular trafficking of protease : Activated Receptor 2 (PAR2) by members of sorting nexins family . (Thesis). Université de Montréal. Retrieved from http://hdl.handle.net/1866/4320

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):

Kasakov, Velichko M. “Intracellular trafficking of protease : Activated Receptor 2 (PAR2) by members of sorting nexins family .” 2010. Thesis, Université de Montréal. Accessed June 24, 2019. http://hdl.handle.net/1866/4320.

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

MLA Handbook (7th Edition):

Kasakov, Velichko M. “Intracellular trafficking of protease : Activated Receptor 2 (PAR2) by members of sorting nexins family .” 2010. Web. 24 Jun 2019.

Vancouver:

Kasakov VM. Intracellular trafficking of protease : Activated Receptor 2 (PAR2) by members of sorting nexins family . [Internet] [Thesis]. Université de Montréal; 2010. [cited 2019 Jun 24]. Available from: http://hdl.handle.net/1866/4320.

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

Council of Science Editors:

Kasakov VM. Intracellular trafficking of protease : Activated Receptor 2 (PAR2) by members of sorting nexins family . [Thesis]. Université de Montréal; 2010. Available from: http://hdl.handle.net/1866/4320

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

28. Chauzeix, Jasmine. Impact des anomalies moléculaires dans l'histoire naturelle de la leucémie lymphoïde chronique : Impact of molecular abnormalities in chronic lymphocytic leukemia natural history.

Degree: Docteur es, Biologie, médecine et santé, 2018, Limoges

La leucémie lymphoïde chronique (LLC) est le lymphome avec phase circulante le plus fréquent chez l’adulte dans les pays occidentaux. Elle est caractérisée par une… (more)

Subjects/Keywords: Leucémie lymphoide chronique; Translocation; Immunoglobuline; IncRNA; Séquençage haut débit; Électrophorèse des protéines sériques; Chronic lymphocytic leukemia; Translocation; Immunoglobulin; IncRNA; High throughput sequencing; Serum protein electrophoresis; 616.994

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

APA (6th Edition):

Chauzeix, J. (2018). Impact des anomalies moléculaires dans l'histoire naturelle de la leucémie lymphoïde chronique : Impact of molecular abnormalities in chronic lymphocytic leukemia natural history. (Doctoral Dissertation). Limoges. Retrieved from http://www.theses.fr/2018LIMO0051

Chicago Manual of Style (16th Edition):

Chauzeix, Jasmine. “Impact des anomalies moléculaires dans l'histoire naturelle de la leucémie lymphoïde chronique : Impact of molecular abnormalities in chronic lymphocytic leukemia natural history.” 2018. Doctoral Dissertation, Limoges. Accessed June 24, 2019. http://www.theses.fr/2018LIMO0051.

MLA Handbook (7th Edition):

Chauzeix, Jasmine. “Impact des anomalies moléculaires dans l'histoire naturelle de la leucémie lymphoïde chronique : Impact of molecular abnormalities in chronic lymphocytic leukemia natural history.” 2018. Web. 24 Jun 2019.

Vancouver:

Chauzeix J. Impact des anomalies moléculaires dans l'histoire naturelle de la leucémie lymphoïde chronique : Impact of molecular abnormalities in chronic lymphocytic leukemia natural history. [Internet] [Doctoral dissertation]. Limoges; 2018. [cited 2019 Jun 24]. Available from: http://www.theses.fr/2018LIMO0051.

Council of Science Editors:

Chauzeix J. Impact des anomalies moléculaires dans l'histoire naturelle de la leucémie lymphoïde chronique : Impact of molecular abnormalities in chronic lymphocytic leukemia natural history. [Doctoral Dissertation]. Limoges; 2018. Available from: http://www.theses.fr/2018LIMO0051


Georgia State University

29. Chaudhary, Arpana S. Inhibitors of SecA as Potential Antimicrobial Agents.

Degree: PhD, Chemistry, 2013, Georgia State University

Protein translocation is essential for bacterial survival and the most important translocation mechanism in bacteria is the secretion (Sec) pathway. Thus targeting Sec pathway… (more)

Subjects/Keywords: SecA inhibitors; Sec pathway inhibition; Thiouracil; 1; 2; 4-Triazole; Novel antibacterial therapeutics; Protein translocation inhibition

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

APA (6th Edition):

Chaudhary, A. S. (2013). Inhibitors of SecA as Potential Antimicrobial Agents. (Doctoral Dissertation). Georgia State University. Retrieved from https://scholarworks.gsu.edu/chemistry_diss/77

Chicago Manual of Style (16th Edition):

Chaudhary, Arpana S. “Inhibitors of SecA as Potential Antimicrobial Agents.” 2013. Doctoral Dissertation, Georgia State University. Accessed June 24, 2019. https://scholarworks.gsu.edu/chemistry_diss/77.

MLA Handbook (7th Edition):

Chaudhary, Arpana S. “Inhibitors of SecA as Potential Antimicrobial Agents.” 2013. Web. 24 Jun 2019.

Vancouver:

Chaudhary AS. Inhibitors of SecA as Potential Antimicrobial Agents. [Internet] [Doctoral dissertation]. Georgia State University; 2013. [cited 2019 Jun 24]. Available from: https://scholarworks.gsu.edu/chemistry_diss/77.

Council of Science Editors:

Chaudhary AS. Inhibitors of SecA as Potential Antimicrobial Agents. [Doctoral Dissertation]. Georgia State University; 2013. Available from: https://scholarworks.gsu.edu/chemistry_diss/77


University of California – Berkeley

30. Brown, Michael Joseph. Anthrax lethal toxin unfolding and translocation via a charge-state ratchet.

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

 A fundamental problem in biochemistry is how molecular machines convert chemical potential energy into mechanical work. Here, this problem is addressed in terms of how… (more)

Subjects/Keywords: Molecular biology; Biochemistry; Biophysics; anthrax toxin; bacterial toxins; Brownian ratchet; molecular motors; pH gradient; protein translocation

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

APA (6th Edition):

Brown, M. J. (2013). Anthrax lethal toxin unfolding and translocation via a charge-state ratchet. (Thesis). University of California – Berkeley. Retrieved from http://www.escholarship.org/uc/item/2fv818v7

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):

Brown, Michael Joseph. “Anthrax lethal toxin unfolding and translocation via a charge-state ratchet.” 2013. Thesis, University of California – Berkeley. Accessed June 24, 2019. http://www.escholarship.org/uc/item/2fv818v7.

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

MLA Handbook (7th Edition):

Brown, Michael Joseph. “Anthrax lethal toxin unfolding and translocation via a charge-state ratchet.” 2013. Web. 24 Jun 2019.

Vancouver:

Brown MJ. Anthrax lethal toxin unfolding and translocation via a charge-state ratchet. [Internet] [Thesis]. University of California – Berkeley; 2013. [cited 2019 Jun 24]. Available from: http://www.escholarship.org/uc/item/2fv818v7.

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

Council of Science Editors:

Brown MJ. Anthrax lethal toxin unfolding and translocation via a charge-state ratchet. [Thesis]. University of California – Berkeley; 2013. Available from: http://www.escholarship.org/uc/item/2fv818v7

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

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