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You searched for subject:(Ubiquitin). Showing records 1 – 30 of 41 total matches.

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Universiteit Utrecht

1. Flierman, D. Cytomegalovirus-induced destruction of MHC class I molecules provides insight into ER-associated protein degradation.

Degree: 2007, Universiteit Utrecht

 In living cells, proteins are produced continuously. To carry out its specific functions, proteins need to be correctly folded. Proteins that are secreted or function… (more)

Subjects/Keywords: Diergeneeskunde; ubiquitin; endoplasmic reticulum; degradation; cytomegalovirus; US11; E2-25K; proteasome; ERAD

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APA (6th Edition):

Flierman, D. (2007). Cytomegalovirus-induced destruction of MHC class I molecules provides insight into ER-associated protein degradation. (Doctoral Dissertation). Universiteit Utrecht. Retrieved from http://dspace.library.uu.nl:8080/handle/1874/20846

Chicago Manual of Style (16th Edition):

Flierman, D. “Cytomegalovirus-induced destruction of MHC class I molecules provides insight into ER-associated protein degradation.” 2007. Doctoral Dissertation, Universiteit Utrecht. Accessed July 19, 2019. http://dspace.library.uu.nl:8080/handle/1874/20846.

MLA Handbook (7th Edition):

Flierman, D. “Cytomegalovirus-induced destruction of MHC class I molecules provides insight into ER-associated protein degradation.” 2007. Web. 19 Jul 2019.

Vancouver:

Flierman D. Cytomegalovirus-induced destruction of MHC class I molecules provides insight into ER-associated protein degradation. [Internet] [Doctoral dissertation]. Universiteit Utrecht; 2007. [cited 2019 Jul 19]. Available from: http://dspace.library.uu.nl:8080/handle/1874/20846.

Council of Science Editors:

Flierman D. Cytomegalovirus-induced destruction of MHC class I molecules provides insight into ER-associated protein degradation. [Doctoral Dissertation]. Universiteit Utrecht; 2007. Available from: http://dspace.library.uu.nl:8080/handle/1874/20846


Universiteit Utrecht

2. D'Annibale, S. Mechanisms of crosstalk between phosphorylation and ubiquitylation in the regulation of cell proliferation.

Degree: 2014, Universiteit Utrecht

 Cell cycle progression is tightly controlled by the ubiquitin-proteasome system. Cullin-RING ubiquitin ligases are the major players responsible for the periodic proteolysis of many regulators… (more)

Subjects/Keywords: Geneeskunde; cell growth and proliferation; ubiquitin-proteasome system; phosphorylation; SCFβTrCP; cancer

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APA (6th Edition):

D'Annibale, S. (2014). Mechanisms of crosstalk between phosphorylation and ubiquitylation in the regulation of cell proliferation. (Doctoral Dissertation). Universiteit Utrecht. Retrieved from http://dspace.library.uu.nl:8080/handle/1874/300358

Chicago Manual of Style (16th Edition):

D'Annibale, S. “Mechanisms of crosstalk between phosphorylation and ubiquitylation in the regulation of cell proliferation.” 2014. Doctoral Dissertation, Universiteit Utrecht. Accessed July 19, 2019. http://dspace.library.uu.nl:8080/handle/1874/300358.

MLA Handbook (7th Edition):

D'Annibale, S. “Mechanisms of crosstalk between phosphorylation and ubiquitylation in the regulation of cell proliferation.” 2014. Web. 19 Jul 2019.

Vancouver:

D'Annibale S. Mechanisms of crosstalk between phosphorylation and ubiquitylation in the regulation of cell proliferation. [Internet] [Doctoral dissertation]. Universiteit Utrecht; 2014. [cited 2019 Jul 19]. Available from: http://dspace.library.uu.nl:8080/handle/1874/300358.

Council of Science Editors:

D'Annibale S. Mechanisms of crosstalk between phosphorylation and ubiquitylation in the regulation of cell proliferation. [Doctoral Dissertation]. Universiteit Utrecht; 2014. Available from: http://dspace.library.uu.nl:8080/handle/1874/300358

3. van de Pasch, L.A.L. Ubiquitin and ubiquitine-like systems in Saccharomyces cerevisiae.

Degree: 2012, University Utrecht

Ubiquitin and ubiquitin-like modifiers are small proteins that exist in all eukaryotes, from yeast to humans. Ubiquitin(-like) modifiers can be coupled to other proteins, which… (more)

Subjects/Keywords: ubiquitination; ubiquitin-like modification; ubiquitin-proteasome system; mitosis; gene expression; microarray; yeast

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APA (6th Edition):

van de Pasch, L. A. L. (2012). Ubiquitin and ubiquitine-like systems in Saccharomyces cerevisiae. (Doctoral Dissertation). University Utrecht. Retrieved from http://dspace.library.uu.nl/handle/1874/256081 ; URN:NBN:NL:UI:10-1874-256081 ; urn:isbn:978-90-393-5855-9 ; URN:NBN:NL:UI:10-1874-256081 ; http://dspace.library.uu.nl/handle/1874/256081

Chicago Manual of Style (16th Edition):

van de Pasch, L A L. “Ubiquitin and ubiquitine-like systems in Saccharomyces cerevisiae.” 2012. Doctoral Dissertation, University Utrecht. Accessed July 19, 2019. http://dspace.library.uu.nl/handle/1874/256081 ; URN:NBN:NL:UI:10-1874-256081 ; urn:isbn:978-90-393-5855-9 ; URN:NBN:NL:UI:10-1874-256081 ; http://dspace.library.uu.nl/handle/1874/256081.

MLA Handbook (7th Edition):

van de Pasch, L A L. “Ubiquitin and ubiquitine-like systems in Saccharomyces cerevisiae.” 2012. Web. 19 Jul 2019.

Vancouver:

van de Pasch LAL. Ubiquitin and ubiquitine-like systems in Saccharomyces cerevisiae. [Internet] [Doctoral dissertation]. University Utrecht; 2012. [cited 2019 Jul 19]. Available from: http://dspace.library.uu.nl/handle/1874/256081 ; URN:NBN:NL:UI:10-1874-256081 ; urn:isbn:978-90-393-5855-9 ; URN:NBN:NL:UI:10-1874-256081 ; http://dspace.library.uu.nl/handle/1874/256081.

Council of Science Editors:

van de Pasch LAL. Ubiquitin and ubiquitine-like systems in Saccharomyces cerevisiae. [Doctoral Dissertation]. University Utrecht; 2012. Available from: http://dspace.library.uu.nl/handle/1874/256081 ; URN:NBN:NL:UI:10-1874-256081 ; urn:isbn:978-90-393-5855-9 ; URN:NBN:NL:UI:10-1874-256081 ; http://dspace.library.uu.nl/handle/1874/256081

4. van de Pasch, L.A.L. Ubiquitin and ubiquitine-like systems in Saccharomyces cerevisiae.

Degree: 2012, University Utrecht

Ubiquitin and ubiquitin-like modifiers are small proteins that exist in all eukaryotes, from yeast to humans. Ubiquitin(-like) modifiers can be coupled to other proteins, which… (more)

Subjects/Keywords: ubiquitination; ubiquitin-like modification; ubiquitin-proteasome system; mitosis; gene expression; microarray; yeast

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APA (6th Edition):

van de Pasch, L. A. L. (2012). Ubiquitin and ubiquitine-like systems in Saccharomyces cerevisiae. (Doctoral Dissertation). University Utrecht. Retrieved from http://dspace.library.uu.nl/handle/1874/256081 ; URN:NBN:NL:UI:10-1874-256081 ; urn:isbn:978-90-393-5855-9 ; URN:NBN:NL:UI:10-1874-256081 ; http://dspace.library.uu.nl/handle/1874/256081

Chicago Manual of Style (16th Edition):

van de Pasch, L A L. “Ubiquitin and ubiquitine-like systems in Saccharomyces cerevisiae.” 2012. Doctoral Dissertation, University Utrecht. Accessed July 19, 2019. http://dspace.library.uu.nl/handle/1874/256081 ; URN:NBN:NL:UI:10-1874-256081 ; urn:isbn:978-90-393-5855-9 ; URN:NBN:NL:UI:10-1874-256081 ; http://dspace.library.uu.nl/handle/1874/256081.

MLA Handbook (7th Edition):

van de Pasch, L A L. “Ubiquitin and ubiquitine-like systems in Saccharomyces cerevisiae.” 2012. Web. 19 Jul 2019.

Vancouver:

van de Pasch LAL. Ubiquitin and ubiquitine-like systems in Saccharomyces cerevisiae. [Internet] [Doctoral dissertation]. University Utrecht; 2012. [cited 2019 Jul 19]. Available from: http://dspace.library.uu.nl/handle/1874/256081 ; URN:NBN:NL:UI:10-1874-256081 ; urn:isbn:978-90-393-5855-9 ; URN:NBN:NL:UI:10-1874-256081 ; http://dspace.library.uu.nl/handle/1874/256081.

Council of Science Editors:

van de Pasch LAL. Ubiquitin and ubiquitine-like systems in Saccharomyces cerevisiae. [Doctoral Dissertation]. University Utrecht; 2012. Available from: http://dspace.library.uu.nl/handle/1874/256081 ; URN:NBN:NL:UI:10-1874-256081 ; urn:isbn:978-90-393-5855-9 ; URN:NBN:NL:UI:10-1874-256081 ; http://dspace.library.uu.nl/handle/1874/256081


Universiteit Utrecht

5. Kim, Jihoon. F-box proteins, cell cycle and cancer.

Degree: 2015, Universiteit Utrecht

 E3 ubiquitin ligases are enzymes that confer specificity to the ubiquitin-proteasome system by directly binding the proteins that are targeted for degradation. E3s are encoded… (more)

Subjects/Keywords: Geneeskunde; Ubiquitin; Proteasome; Proteolysis; F-box protein; Cell cycle; cancer; checkpoint recovery; DNA damage

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APA (6th Edition):

Kim, J. (2015). F-box proteins, cell cycle and cancer. (Doctoral Dissertation). Universiteit Utrecht. Retrieved from http://dspace.library.uu.nl:8080/handle/1874/302855

Chicago Manual of Style (16th Edition):

Kim, Jihoon. “F-box proteins, cell cycle and cancer.” 2015. Doctoral Dissertation, Universiteit Utrecht. Accessed July 19, 2019. http://dspace.library.uu.nl:8080/handle/1874/302855.

MLA Handbook (7th Edition):

Kim, Jihoon. “F-box proteins, cell cycle and cancer.” 2015. Web. 19 Jul 2019.

Vancouver:

Kim J. F-box proteins, cell cycle and cancer. [Internet] [Doctoral dissertation]. Universiteit Utrecht; 2015. [cited 2019 Jul 19]. Available from: http://dspace.library.uu.nl:8080/handle/1874/302855.

Council of Science Editors:

Kim J. F-box proteins, cell cycle and cancer. [Doctoral Dissertation]. Universiteit Utrecht; 2015. Available from: http://dspace.library.uu.nl:8080/handle/1874/302855


Vrije Universiteit Amsterdam

6. Schreiber, J. Synaptic functions of the ubiquitin ligase TRIM3 .

Degree: 2016, Vrije Universiteit Amsterdam

Subjects/Keywords: TRIM3; Ubiquitin; PTMs; Synapse; Learning; LTP; Brain; Hippocampus

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APA (6th Edition):

Schreiber, J. (2016). Synaptic functions of the ubiquitin ligase TRIM3 . (Doctoral Dissertation). Vrije Universiteit Amsterdam. Retrieved from http://hdl.handle.net/1871/54134

Chicago Manual of Style (16th Edition):

Schreiber, J. “Synaptic functions of the ubiquitin ligase TRIM3 .” 2016. Doctoral Dissertation, Vrije Universiteit Amsterdam. Accessed July 19, 2019. http://hdl.handle.net/1871/54134.

MLA Handbook (7th Edition):

Schreiber, J. “Synaptic functions of the ubiquitin ligase TRIM3 .” 2016. Web. 19 Jul 2019.

Vancouver:

Schreiber J. Synaptic functions of the ubiquitin ligase TRIM3 . [Internet] [Doctoral dissertation]. Vrije Universiteit Amsterdam; 2016. [cited 2019 Jul 19]. Available from: http://hdl.handle.net/1871/54134.

Council of Science Editors:

Schreiber J. Synaptic functions of the ubiquitin ligase TRIM3 . [Doctoral Dissertation]. Vrije Universiteit Amsterdam; 2016. Available from: http://hdl.handle.net/1871/54134

7. Alves dos Santos, M.C.M. (Maria Cristina Miranda). Ubiquitin System-Dependent Regulation of Growth Hormone Receptor Signal Transduction and Effects of Oxidative Stress.

Degree: 2001, University Utrecht

 The ubiquitin-proteasome system is known to be involved in GHR endocytosis, where an active ubiquitin system is necessary for receptor ubiquitination and its consequent internalization.… (more)

Subjects/Keywords: Growth Hormone Receptor; Growth Hormone; Ubiquitin; Proteasome; Signal Transduction

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APA (6th Edition):

Alves dos Santos, M. C. M. (. C. M. (2001). Ubiquitin System-Dependent Regulation of Growth Hormone Receptor Signal Transduction and Effects of Oxidative Stress. (Doctoral Dissertation). University Utrecht. Retrieved from http://dspace.library.uu.nl/handle/1874/456 ; URN:NBN:NL:UI:10-1874-456 ; URN:NBN:NL:UI:10-1874-456 ; http://dspace.library.uu.nl/handle/1874/456

Chicago Manual of Style (16th Edition):

Alves dos Santos, M C M (Maria Cristina Miranda). “Ubiquitin System-Dependent Regulation of Growth Hormone Receptor Signal Transduction and Effects of Oxidative Stress.” 2001. Doctoral Dissertation, University Utrecht. Accessed July 19, 2019. http://dspace.library.uu.nl/handle/1874/456 ; URN:NBN:NL:UI:10-1874-456 ; URN:NBN:NL:UI:10-1874-456 ; http://dspace.library.uu.nl/handle/1874/456.

MLA Handbook (7th Edition):

Alves dos Santos, M C M (Maria Cristina Miranda). “Ubiquitin System-Dependent Regulation of Growth Hormone Receptor Signal Transduction and Effects of Oxidative Stress.” 2001. Web. 19 Jul 2019.

Vancouver:

Alves dos Santos MCM(CM. Ubiquitin System-Dependent Regulation of Growth Hormone Receptor Signal Transduction and Effects of Oxidative Stress. [Internet] [Doctoral dissertation]. University Utrecht; 2001. [cited 2019 Jul 19]. Available from: http://dspace.library.uu.nl/handle/1874/456 ; URN:NBN:NL:UI:10-1874-456 ; URN:NBN:NL:UI:10-1874-456 ; http://dspace.library.uu.nl/handle/1874/456.

Council of Science Editors:

Alves dos Santos MCM(CM. Ubiquitin System-Dependent Regulation of Growth Hormone Receptor Signal Transduction and Effects of Oxidative Stress. [Doctoral Dissertation]. University Utrecht; 2001. Available from: http://dspace.library.uu.nl/handle/1874/456 ; URN:NBN:NL:UI:10-1874-456 ; URN:NBN:NL:UI:10-1874-456 ; http://dspace.library.uu.nl/handle/1874/456

8. Alves dos Santos, M.C.M. (Maria Cristina Miranda). Ubiquitin System-Dependent Regulation of Growth Hormone Receptor Signal Transduction and Effects of Oxidative Stress.

Degree: 2001, University Utrecht

 The ubiquitin-proteasome system is known to be involved in GHR endocytosis, where an active ubiquitin system is necessary for receptor ubiquitination and its consequent internalization.… (more)

Subjects/Keywords: Growth Hormone Receptor; Growth Hormone; Ubiquitin; Proteasome; Signal Transduction

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APA (6th Edition):

Alves dos Santos, M. C. M. (. C. M. (2001). Ubiquitin System-Dependent Regulation of Growth Hormone Receptor Signal Transduction and Effects of Oxidative Stress. (Doctoral Dissertation). University Utrecht. Retrieved from http://dspace.library.uu.nl/handle/1874/456 ; URN:NBN:NL:UI:10-1874-456 ; URN:NBN:NL:UI:10-1874-456 ; http://dspace.library.uu.nl/handle/1874/456

Chicago Manual of Style (16th Edition):

Alves dos Santos, M C M (Maria Cristina Miranda). “Ubiquitin System-Dependent Regulation of Growth Hormone Receptor Signal Transduction and Effects of Oxidative Stress.” 2001. Doctoral Dissertation, University Utrecht. Accessed July 19, 2019. http://dspace.library.uu.nl/handle/1874/456 ; URN:NBN:NL:UI:10-1874-456 ; URN:NBN:NL:UI:10-1874-456 ; http://dspace.library.uu.nl/handle/1874/456.

MLA Handbook (7th Edition):

Alves dos Santos, M C M (Maria Cristina Miranda). “Ubiquitin System-Dependent Regulation of Growth Hormone Receptor Signal Transduction and Effects of Oxidative Stress.” 2001. Web. 19 Jul 2019.

Vancouver:

Alves dos Santos MCM(CM. Ubiquitin System-Dependent Regulation of Growth Hormone Receptor Signal Transduction and Effects of Oxidative Stress. [Internet] [Doctoral dissertation]. University Utrecht; 2001. [cited 2019 Jul 19]. Available from: http://dspace.library.uu.nl/handle/1874/456 ; URN:NBN:NL:UI:10-1874-456 ; URN:NBN:NL:UI:10-1874-456 ; http://dspace.library.uu.nl/handle/1874/456.

Council of Science Editors:

Alves dos Santos MCM(CM. Ubiquitin System-Dependent Regulation of Growth Hormone Receptor Signal Transduction and Effects of Oxidative Stress. [Doctoral Dissertation]. University Utrecht; 2001. Available from: http://dspace.library.uu.nl/handle/1874/456 ; URN:NBN:NL:UI:10-1874-456 ; URN:NBN:NL:UI:10-1874-456 ; http://dspace.library.uu.nl/handle/1874/456

9. J.J. Smit (Judith). Ubiquitin chain formation by RBR E3-ligases.

Degree: 2013, Erasmus University Rotterdam

 Ubiquitination is an important posttranslational modification that plays a role in virtually all cellular pathways. Ubiquitin signals are made out of one or multiple ubiquitin(more)

Subjects/Keywords: E3-ligase; HOIP; LUBAC; RING; triad1; ubiquitin

…protein is used to signal on its own, as well as in a variety of different types of ubiquitin… …chains that function in many different cellular processes. Ubiquitination Ubiquitin is a 76… …ubiquitin was first linked to the proteasomal degradation of proteins5. However, now it is… …recognized that ubiquitin has many different signalling functions in cells6, 7. It forms an… …ubiquitin signalling is associated with the initiation and progression of various human diseases… 

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APA (6th Edition):

(Judith), J. S. (2013). Ubiquitin chain formation by RBR E3-ligases. (Thesis). Erasmus University Rotterdam. Retrieved from http://hdl.handle.net/1765/40175

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):

(Judith), J.J. Smit. “Ubiquitin chain formation by RBR E3-ligases.” 2013. Thesis, Erasmus University Rotterdam. Accessed July 19, 2019. http://hdl.handle.net/1765/40175.

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

MLA Handbook (7th Edition):

(Judith), J.J. Smit. “Ubiquitin chain formation by RBR E3-ligases.” 2013. Web. 19 Jul 2019.

Vancouver:

(Judith) JS. Ubiquitin chain formation by RBR E3-ligases. [Internet] [Thesis]. Erasmus University Rotterdam; 2013. [cited 2019 Jul 19]. Available from: http://hdl.handle.net/1765/40175.

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

Council of Science Editors:

(Judith) JS. Ubiquitin chain formation by RBR E3-ligases. [Thesis]. Erasmus University Rotterdam; 2013. Available from: http://hdl.handle.net/1765/40175

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

10. Kasteren, Puck Bertyne van. Arterivirus PLP2: an OTU deubiquitinase that counteracts Innate Immunity.

Degree: 2014, Department of Medical Microbiology, Faculty of Medicine / Leiden University Medical Center (LUMC), Leiden University

 The work described in this thesis provides novel insights into the structural and (multi)functional characteristics of arterivirus PLP2. This enzyme plays an essential role in… (more)

Subjects/Keywords: Interferon; Arterivirus; Deubiquitinase; Nidovirus; Protease; Innate immunity; Crystal structure; Ubiquitin; Interferon; Arterivirus; Deubiquitinase; Nidovirus; Protease; Innate immunity; Crystal structure; Ubiquitin

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APA (6th Edition):

Kasteren, P. B. v. (2014). Arterivirus PLP2: an OTU deubiquitinase that counteracts Innate Immunity. (Doctoral Dissertation). Department of Medical Microbiology, Faculty of Medicine / Leiden University Medical Center (LUMC), Leiden University. Retrieved from http://hdl.handle.net/1887/29907

Chicago Manual of Style (16th Edition):

Kasteren, Puck Bertyne van. “Arterivirus PLP2: an OTU deubiquitinase that counteracts Innate Immunity.” 2014. Doctoral Dissertation, Department of Medical Microbiology, Faculty of Medicine / Leiden University Medical Center (LUMC), Leiden University. Accessed July 19, 2019. http://hdl.handle.net/1887/29907.

MLA Handbook (7th Edition):

Kasteren, Puck Bertyne van. “Arterivirus PLP2: an OTU deubiquitinase that counteracts Innate Immunity.” 2014. Web. 19 Jul 2019.

Vancouver:

Kasteren PBv. Arterivirus PLP2: an OTU deubiquitinase that counteracts Innate Immunity. [Internet] [Doctoral dissertation]. Department of Medical Microbiology, Faculty of Medicine / Leiden University Medical Center (LUMC), Leiden University; 2014. [cited 2019 Jul 19]. Available from: http://hdl.handle.net/1887/29907.

Council of Science Editors:

Kasteren PBv. Arterivirus PLP2: an OTU deubiquitinase that counteracts Innate Immunity. [Doctoral Dissertation]. Department of Medical Microbiology, Faculty of Medicine / Leiden University Medical Center (LUMC), Leiden University; 2014. Available from: http://hdl.handle.net/1887/29907

11. Meulmeester, Erik. Regulation of Mdmx and its role in the p53 pathway.

Degree: 2006, Dept. of Molecular Cell Biology, Faculty of Medicine, LUMC, Leiden University

 The p53 protein is an important tumor suppressor that acts as a key regulator of the integrity of the genome. Two essential regulators of the… (more)

Subjects/Keywords: P53; Ubiquitin; Mdmx; Mdm2; Hdmx; Hdm2; HAUSP; SUMO; P53; Ubiquitin; Mdmx; Mdm2; Hdmx; Hdm2; HAUSP; SUMO

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APA (6th Edition):

Meulmeester, E. (2006). Regulation of Mdmx and its role in the p53 pathway. (Doctoral Dissertation). Dept. of Molecular Cell Biology, Faculty of Medicine, LUMC, Leiden University. Retrieved from http://hdl.handle.net/1887/4280

Chicago Manual of Style (16th Edition):

Meulmeester, Erik. “Regulation of Mdmx and its role in the p53 pathway.” 2006. Doctoral Dissertation, Dept. of Molecular Cell Biology, Faculty of Medicine, LUMC, Leiden University. Accessed July 19, 2019. http://hdl.handle.net/1887/4280.

MLA Handbook (7th Edition):

Meulmeester, Erik. “Regulation of Mdmx and its role in the p53 pathway.” 2006. Web. 19 Jul 2019.

Vancouver:

Meulmeester E. Regulation of Mdmx and its role in the p53 pathway. [Internet] [Doctoral dissertation]. Dept. of Molecular Cell Biology, Faculty of Medicine, LUMC, Leiden University; 2006. [cited 2019 Jul 19]. Available from: http://hdl.handle.net/1887/4280.

Council of Science Editors:

Meulmeester E. Regulation of Mdmx and its role in the p53 pathway. [Doctoral Dissertation]. Dept. of Molecular Cell Biology, Faculty of Medicine, LUMC, Leiden University; 2006. Available from: http://hdl.handle.net/1887/4280

12. Hassink, Gerrit Cornelis. The role of the ubiquitin system in human cytomegalovirus-mediated degradation of MHC class I heavy chains.

Degree: 2006, Medical Microbiology, Faculty of Medicine, Leiden University

 One of the mechanisms used by HCMV to downregulate cell surface expression of the MHC class I complex involves the dislocation of newly synthesized class… (more)

Subjects/Keywords: ubiquitin; ER associated degradation; MHC class I; HCMV; ubiquitin; ER associated degradation; MHC class I; HCMV

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APA (6th Edition):

Hassink, G. C. (2006). The role of the ubiquitin system in human cytomegalovirus-mediated degradation of MHC class I heavy chains. (Doctoral Dissertation). Medical Microbiology, Faculty of Medicine, Leiden University. Retrieved from http://hdl.handle.net/1887/4414

Chicago Manual of Style (16th Edition):

Hassink, Gerrit Cornelis. “The role of the ubiquitin system in human cytomegalovirus-mediated degradation of MHC class I heavy chains.” 2006. Doctoral Dissertation, Medical Microbiology, Faculty of Medicine, Leiden University. Accessed July 19, 2019. http://hdl.handle.net/1887/4414.

MLA Handbook (7th Edition):

Hassink, Gerrit Cornelis. “The role of the ubiquitin system in human cytomegalovirus-mediated degradation of MHC class I heavy chains.” 2006. Web. 19 Jul 2019.

Vancouver:

Hassink GC. The role of the ubiquitin system in human cytomegalovirus-mediated degradation of MHC class I heavy chains. [Internet] [Doctoral dissertation]. Medical Microbiology, Faculty of Medicine, Leiden University; 2006. [cited 2019 Jul 19]. Available from: http://hdl.handle.net/1887/4414.

Council of Science Editors:

Hassink GC. The role of the ubiquitin system in human cytomegalovirus-mediated degradation of MHC class I heavy chains. [Doctoral Dissertation]. Medical Microbiology, Faculty of Medicine, Leiden University; 2006. Available from: http://hdl.handle.net/1887/4414

13. Groothuis, Tom Alphonsus Maria. Manipulations of the ubiquitin proteasome system and their effects on antigen presentation.

Degree: 2006, Netherlands Cancer Institute, Department of Tumorbiology.Faculty of Medicine / Leiden University Medical Center (LUMC), Leiden University

 Surgery is the most effective cancer therapy, followed by radiotherapy. These techniques usually target tumour specific tissue only, unlike most forms of chemotherapy as is… (more)

Subjects/Keywords: Antigen prestentation; Cancer; Cross-presentation; MHC class I; Proteasome; Ubiquitin; Antigen prestentation; Cancer; Cross-presentation; MHC class I; Proteasome; Ubiquitin

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APA (6th Edition):

Groothuis, T. A. M. (2006). Manipulations of the ubiquitin proteasome system and their effects on antigen presentation. (Doctoral Dissertation). Netherlands Cancer Institute, Department of Tumorbiology.Faculty of Medicine / Leiden University Medical Center (LUMC), Leiden University. Retrieved from http://hdl.handle.net/1887/4956

Chicago Manual of Style (16th Edition):

Groothuis, Tom Alphonsus Maria. “Manipulations of the ubiquitin proteasome system and their effects on antigen presentation.” 2006. Doctoral Dissertation, Netherlands Cancer Institute, Department of Tumorbiology.Faculty of Medicine / Leiden University Medical Center (LUMC), Leiden University. Accessed July 19, 2019. http://hdl.handle.net/1887/4956.

MLA Handbook (7th Edition):

Groothuis, Tom Alphonsus Maria. “Manipulations of the ubiquitin proteasome system and their effects on antigen presentation.” 2006. Web. 19 Jul 2019.

Vancouver:

Groothuis TAM. Manipulations of the ubiquitin proteasome system and their effects on antigen presentation. [Internet] [Doctoral dissertation]. Netherlands Cancer Institute, Department of Tumorbiology.Faculty of Medicine / Leiden University Medical Center (LUMC), Leiden University; 2006. [cited 2019 Jul 19]. Available from: http://hdl.handle.net/1887/4956.

Council of Science Editors:

Groothuis TAM. Manipulations of the ubiquitin proteasome system and their effects on antigen presentation. [Doctoral Dissertation]. Netherlands Cancer Institute, Department of Tumorbiology.Faculty of Medicine / Leiden University Medical Center (LUMC), Leiden University; 2006. Available from: http://hdl.handle.net/1887/4956


Universiteit Utrecht

14. Alves dos Santos, M.C.M. (Maria Cristina Miranda). Ubiquitin System-Dependent Regulation of Growth Hormone Receptor Signal Transduction and Effects of Oxidative Stress.

Degree: 2001, Universiteit Utrecht

 The ubiquitin-proteasome system is known to be involved in GHR endocytosis, where an active ubiquitin system is necessary for receptor ubiquitination and its consequent internalization.… (more)

Subjects/Keywords: Geneeskunde; Growth Hormone Receptor; Growth Hormone; Ubiquitin; Proteasome; Signal Transduction

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APA (6th Edition):

Alves dos Santos, M. C. M. (. C. M. (2001). Ubiquitin System-Dependent Regulation of Growth Hormone Receptor Signal Transduction and Effects of Oxidative Stress. (Doctoral Dissertation). Universiteit Utrecht. Retrieved from http://dspace.library.uu.nl:8080/handle/1874/456

Chicago Manual of Style (16th Edition):

Alves dos Santos, M C M (Maria Cristina Miranda). “Ubiquitin System-Dependent Regulation of Growth Hormone Receptor Signal Transduction and Effects of Oxidative Stress.” 2001. Doctoral Dissertation, Universiteit Utrecht. Accessed July 19, 2019. http://dspace.library.uu.nl:8080/handle/1874/456.

MLA Handbook (7th Edition):

Alves dos Santos, M C M (Maria Cristina Miranda). “Ubiquitin System-Dependent Regulation of Growth Hormone Receptor Signal Transduction and Effects of Oxidative Stress.” 2001. Web. 19 Jul 2019.

Vancouver:

Alves dos Santos MCM(CM. Ubiquitin System-Dependent Regulation of Growth Hormone Receptor Signal Transduction and Effects of Oxidative Stress. [Internet] [Doctoral dissertation]. Universiteit Utrecht; 2001. [cited 2019 Jul 19]. Available from: http://dspace.library.uu.nl:8080/handle/1874/456.

Council of Science Editors:

Alves dos Santos MCM(CM. Ubiquitin System-Dependent Regulation of Growth Hormone Receptor Signal Transduction and Effects of Oxidative Stress. [Doctoral Dissertation]. Universiteit Utrecht; 2001. Available from: http://dspace.library.uu.nl:8080/handle/1874/456

15. Schmidt, R. Ubiquitin & Wnt: The diverse roles of ubiquitin in canonical Wnt signalling.

Degree: 2013, Universiteit Utrecht

 The Wnt signalling pathway plays a major role in both the embryonic development and adult homeostasis of metazoans. Canonical Wnt signalling, which converges on the… (more)

Subjects/Keywords: Canonical Wnt signalling; Wnt; cancer; β-catenin; Ubiquitin

…Choi et al., 2004). Recently, HectD1 was identified as an E3 ubiquitin ligase that is… …signalosome (CSN) regulates Cullin-RING E3 ubiquitin ligases (CRLs), and… …2009b). In a wild type situation, APC is stabilised by the DUB ubiquitin-specific… …2009b). In addition, the HECT E3 ubiquitin ligase and tumour suppressor E3 isolated by… …chains, making up as much as 30% of the total cellular ubiquitin content (Xu et al., 2009… 

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APA (6th Edition):

Schmidt, R. (2013). Ubiquitin & Wnt: The diverse roles of ubiquitin in canonical Wnt signalling. (Masters Thesis). Universiteit Utrecht. Retrieved from http://dspace.library.uu.nl:8080/handle/1874/287111

Chicago Manual of Style (16th Edition):

Schmidt, R. “Ubiquitin & Wnt: The diverse roles of ubiquitin in canonical Wnt signalling.” 2013. Masters Thesis, Universiteit Utrecht. Accessed July 19, 2019. http://dspace.library.uu.nl:8080/handle/1874/287111.

MLA Handbook (7th Edition):

Schmidt, R. “Ubiquitin & Wnt: The diverse roles of ubiquitin in canonical Wnt signalling.” 2013. Web. 19 Jul 2019.

Vancouver:

Schmidt R. Ubiquitin & Wnt: The diverse roles of ubiquitin in canonical Wnt signalling. [Internet] [Masters thesis]. Universiteit Utrecht; 2013. [cited 2019 Jul 19]. Available from: http://dspace.library.uu.nl:8080/handle/1874/287111.

Council of Science Editors:

Schmidt R. Ubiquitin & Wnt: The diverse roles of ubiquitin in canonical Wnt signalling. [Masters Thesis]. Universiteit Utrecht; 2013. Available from: http://dspace.library.uu.nl:8080/handle/1874/287111

16. Kim, Jihoon. F-box proteins, cell cycle and cancer.

Degree: 2015, University Utrecht

 E3 ubiquitin ligases are enzymes that confer specificity to the ubiquitin-proteasome system by directly binding the proteins that are targeted for degradation. E3s are encoded… (more)

Subjects/Keywords: Ubiquitin; Proteasome; Proteolysis; F-box protein; Cell cycle; cancer; checkpoint recovery; DNA damage

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APA (6th Edition):

Kim, J. (2015). F-box proteins, cell cycle and cancer. (Doctoral Dissertation). University Utrecht. Retrieved from http://dspace.library.uu.nl/handle/1874/302855 ; URN:NBN:NL:UI:10-1874-302855 ; urn:isbn:978-94-6203-741-0 ; URN:NBN:NL:UI:10-1874-302855 ; http://dspace.library.uu.nl/handle/1874/302855

Chicago Manual of Style (16th Edition):

Kim, Jihoon. “F-box proteins, cell cycle and cancer.” 2015. Doctoral Dissertation, University Utrecht. Accessed July 19, 2019. http://dspace.library.uu.nl/handle/1874/302855 ; URN:NBN:NL:UI:10-1874-302855 ; urn:isbn:978-94-6203-741-0 ; URN:NBN:NL:UI:10-1874-302855 ; http://dspace.library.uu.nl/handle/1874/302855.

MLA Handbook (7th Edition):

Kim, Jihoon. “F-box proteins, cell cycle and cancer.” 2015. Web. 19 Jul 2019.

Vancouver:

Kim J. F-box proteins, cell cycle and cancer. [Internet] [Doctoral dissertation]. University Utrecht; 2015. [cited 2019 Jul 19]. Available from: http://dspace.library.uu.nl/handle/1874/302855 ; URN:NBN:NL:UI:10-1874-302855 ; urn:isbn:978-94-6203-741-0 ; URN:NBN:NL:UI:10-1874-302855 ; http://dspace.library.uu.nl/handle/1874/302855.

Council of Science Editors:

Kim J. F-box proteins, cell cycle and cancer. [Doctoral Dissertation]. University Utrecht; 2015. Available from: http://dspace.library.uu.nl/handle/1874/302855 ; URN:NBN:NL:UI:10-1874-302855 ; urn:isbn:978-94-6203-741-0 ; URN:NBN:NL:UI:10-1874-302855 ; http://dspace.library.uu.nl/handle/1874/302855

17. Bergink, Steven. Interplay of the Ubiquitin Proteasome System with Nucleotide Excision Repair.

Degree: Department of Molecular Genetics, 2006, Erasmus University Medical Center

 textabstractDit proefschrift kwam tot stand binnen de vakgroep Celbiologie en Genetica van de faculteit der Geneeskunde en Gezondheidswetenschappen van de Erasmus Universiteit Rotterdam. De vakgroep… (more)

Subjects/Keywords: ATR; DNA damage response; DNA repair; H2AX; chromatin; histone; ubiquitin–proteasome system

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APA (6th Edition):

Bergink, S. (2006). Interplay of the Ubiquitin Proteasome System with Nucleotide Excision Repair. (Doctoral Dissertation). Erasmus University Medical Center. Retrieved from http://hdl.handle.net/1765/7843

Chicago Manual of Style (16th Edition):

Bergink, Steven. “Interplay of the Ubiquitin Proteasome System with Nucleotide Excision Repair.” 2006. Doctoral Dissertation, Erasmus University Medical Center. Accessed July 19, 2019. http://hdl.handle.net/1765/7843.

MLA Handbook (7th Edition):

Bergink, Steven. “Interplay of the Ubiquitin Proteasome System with Nucleotide Excision Repair.” 2006. Web. 19 Jul 2019.

Vancouver:

Bergink S. Interplay of the Ubiquitin Proteasome System with Nucleotide Excision Repair. [Internet] [Doctoral dissertation]. Erasmus University Medical Center; 2006. [cited 2019 Jul 19]. Available from: http://hdl.handle.net/1765/7843.

Council of Science Editors:

Bergink S. Interplay of the Ubiquitin Proteasome System with Nucleotide Excision Repair. [Doctoral Dissertation]. Erasmus University Medical Center; 2006. Available from: http://hdl.handle.net/1765/7843


Erasmus University Rotterdam

18. Kim, Robbert. Structural and Mechanistic Studies on Deubiquitinating Enzymes USP7 and USP40.

Degree: 2019, Erasmus University Rotterdam

 textabstractIn this thesis we investigated the molecular mechanism of a subset of USPs (Ubiquitin-Specific Proteases), a class of deubiquitinating enzymes. Our findings describe how USP7,… (more)

Subjects/Keywords: USP7; Ubiquitin; protease; enzymatic activity; structural biology; biochemistry; biophysical analysis; activity mechanism; protein

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APA (6th Edition):

Kim, R. (2019). Structural and Mechanistic Studies on Deubiquitinating Enzymes USP7 and USP40. (Doctoral Dissertation). Erasmus University Rotterdam. Retrieved from http://hdl.handle.net/1765/115598

Chicago Manual of Style (16th Edition):

Kim, Robbert. “Structural and Mechanistic Studies on Deubiquitinating Enzymes USP7 and USP40.” 2019. Doctoral Dissertation, Erasmus University Rotterdam. Accessed July 19, 2019. http://hdl.handle.net/1765/115598.

MLA Handbook (7th Edition):

Kim, Robbert. “Structural and Mechanistic Studies on Deubiquitinating Enzymes USP7 and USP40.” 2019. Web. 19 Jul 2019.

Vancouver:

Kim R. Structural and Mechanistic Studies on Deubiquitinating Enzymes USP7 and USP40. [Internet] [Doctoral dissertation]. Erasmus University Rotterdam; 2019. [cited 2019 Jul 19]. Available from: http://hdl.handle.net/1765/115598.

Council of Science Editors:

Kim R. Structural and Mechanistic Studies on Deubiquitinating Enzymes USP7 and USP40. [Doctoral Dissertation]. Erasmus University Rotterdam; 2019. Available from: http://hdl.handle.net/1765/115598

19. D'Annibale, S. Mechanisms of crosstalk between phosphorylation and ubiquitylation in the regulation of cell proliferation.

Degree: 2014, University Utrecht

 Cell cycle progression is tightly controlled by the ubiquitin-proteasome system. Cullin-RING ubiquitin ligases are the major players responsible for the periodic proteolysis of many regulators… (more)

Subjects/Keywords: cell growth and proliferation; ubiquitin-proteasome system; phosphorylation; SCFβTrCP; cancer

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APA (6th Edition):

D'Annibale, S. (2014). Mechanisms of crosstalk between phosphorylation and ubiquitylation in the regulation of cell proliferation. (Doctoral Dissertation). University Utrecht. Retrieved from http://dspace.library.uu.nl/handle/1874/300358 ; URN:NBN:NL:UI:10-1874-300358 ; urn:isbn:978-90-393-6223-5 ; URN:NBN:NL:UI:10-1874-300358 ; http://dspace.library.uu.nl/handle/1874/300358

Chicago Manual of Style (16th Edition):

D'Annibale, S. “Mechanisms of crosstalk between phosphorylation and ubiquitylation in the regulation of cell proliferation.” 2014. Doctoral Dissertation, University Utrecht. Accessed July 19, 2019. http://dspace.library.uu.nl/handle/1874/300358 ; URN:NBN:NL:UI:10-1874-300358 ; urn:isbn:978-90-393-6223-5 ; URN:NBN:NL:UI:10-1874-300358 ; http://dspace.library.uu.nl/handle/1874/300358.

MLA Handbook (7th Edition):

D'Annibale, S. “Mechanisms of crosstalk between phosphorylation and ubiquitylation in the regulation of cell proliferation.” 2014. Web. 19 Jul 2019.

Vancouver:

D'Annibale S. Mechanisms of crosstalk between phosphorylation and ubiquitylation in the regulation of cell proliferation. [Internet] [Doctoral dissertation]. University Utrecht; 2014. [cited 2019 Jul 19]. Available from: http://dspace.library.uu.nl/handle/1874/300358 ; URN:NBN:NL:UI:10-1874-300358 ; urn:isbn:978-90-393-6223-5 ; URN:NBN:NL:UI:10-1874-300358 ; http://dspace.library.uu.nl/handle/1874/300358.

Council of Science Editors:

D'Annibale S. Mechanisms of crosstalk between phosphorylation and ubiquitylation in the regulation of cell proliferation. [Doctoral Dissertation]. University Utrecht; 2014. Available from: http://dspace.library.uu.nl/handle/1874/300358 ; URN:NBN:NL:UI:10-1874-300358 ; urn:isbn:978-90-393-6223-5 ; URN:NBN:NL:UI:10-1874-300358 ; http://dspace.library.uu.nl/handle/1874/300358

20. da Silva Almeida, A.C. Understanding the Growth Hormone Receptor-βTrCP interactions: Molecular Tools for controlling Growth Hormone Sensitivity.

Degree: 2011, University Utrecht

 Growth hormone (GH) signaling plays major roles in the organism and, therefore, the sensitivity of the cells to GH and the signaling duration are under… (more)

Subjects/Keywords: Growth Hormone; Growth Hormone Receptor; Endocytosis; Ubiquitin dependent endocytosis; betaTrCP; Cachexia

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APA (6th Edition):

da Silva Almeida, A. C. (2011). Understanding the Growth Hormone Receptor-βTrCP interactions: Molecular Tools for controlling Growth Hormone Sensitivity. (Doctoral Dissertation). University Utrecht. Retrieved from http://dspace.library.uu.nl/handle/1874/350510 ; URN:NBN:NL:UI:10-1874-350510 ; URN:NBN:NL:UI:10-1874-350510 ; http://dspace.library.uu.nl/handle/1874/350510

Chicago Manual of Style (16th Edition):

da Silva Almeida, A C. “Understanding the Growth Hormone Receptor-βTrCP interactions: Molecular Tools for controlling Growth Hormone Sensitivity.” 2011. Doctoral Dissertation, University Utrecht. Accessed July 19, 2019. http://dspace.library.uu.nl/handle/1874/350510 ; URN:NBN:NL:UI:10-1874-350510 ; URN:NBN:NL:UI:10-1874-350510 ; http://dspace.library.uu.nl/handle/1874/350510.

MLA Handbook (7th Edition):

da Silva Almeida, A C. “Understanding the Growth Hormone Receptor-βTrCP interactions: Molecular Tools for controlling Growth Hormone Sensitivity.” 2011. Web. 19 Jul 2019.

Vancouver:

da Silva Almeida AC. Understanding the Growth Hormone Receptor-βTrCP interactions: Molecular Tools for controlling Growth Hormone Sensitivity. [Internet] [Doctoral dissertation]. University Utrecht; 2011. [cited 2019 Jul 19]. Available from: http://dspace.library.uu.nl/handle/1874/350510 ; URN:NBN:NL:UI:10-1874-350510 ; URN:NBN:NL:UI:10-1874-350510 ; http://dspace.library.uu.nl/handle/1874/350510.

Council of Science Editors:

da Silva Almeida AC. Understanding the Growth Hormone Receptor-βTrCP interactions: Molecular Tools for controlling Growth Hormone Sensitivity. [Doctoral Dissertation]. University Utrecht; 2011. Available from: http://dspace.library.uu.nl/handle/1874/350510 ; URN:NBN:NL:UI:10-1874-350510 ; URN:NBN:NL:UI:10-1874-350510 ; http://dspace.library.uu.nl/handle/1874/350510

21. da Silva Almeida, A.C. Understanding the Growth Hormone Receptor-βTrCP interactions: Molecular Tools for controlling Growth Hormone Sensitivity.

Degree: 2011, University Utrecht

 Growth hormone (GH) signaling plays major roles in the organism and, therefore, the sensitivity of the cells to GH and the signaling duration are under… (more)

Subjects/Keywords: Growth Hormone; Growth Hormone Receptor; Endocytosis; Ubiquitin dependent endocytosis; betaTrCP; Cachexia

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

APA (6th Edition):

da Silva Almeida, A. C. (2011). Understanding the Growth Hormone Receptor-βTrCP interactions: Molecular Tools for controlling Growth Hormone Sensitivity. (Doctoral Dissertation). University Utrecht. Retrieved from http://dspace.library.uu.nl/handle/1874/350510 ; URN:NBN:NL:UI:10-1874-350510 ; URN:NBN:NL:UI:10-1874-350510 ; http://dspace.library.uu.nl/handle/1874/350510

Chicago Manual of Style (16th Edition):

da Silva Almeida, A C. “Understanding the Growth Hormone Receptor-βTrCP interactions: Molecular Tools for controlling Growth Hormone Sensitivity.” 2011. Doctoral Dissertation, University Utrecht. Accessed July 19, 2019. http://dspace.library.uu.nl/handle/1874/350510 ; URN:NBN:NL:UI:10-1874-350510 ; URN:NBN:NL:UI:10-1874-350510 ; http://dspace.library.uu.nl/handle/1874/350510.

MLA Handbook (7th Edition):

da Silva Almeida, A C. “Understanding the Growth Hormone Receptor-βTrCP interactions: Molecular Tools for controlling Growth Hormone Sensitivity.” 2011. Web. 19 Jul 2019.

Vancouver:

da Silva Almeida AC. Understanding the Growth Hormone Receptor-βTrCP interactions: Molecular Tools for controlling Growth Hormone Sensitivity. [Internet] [Doctoral dissertation]. University Utrecht; 2011. [cited 2019 Jul 19]. Available from: http://dspace.library.uu.nl/handle/1874/350510 ; URN:NBN:NL:UI:10-1874-350510 ; URN:NBN:NL:UI:10-1874-350510 ; http://dspace.library.uu.nl/handle/1874/350510.

Council of Science Editors:

da Silva Almeida AC. Understanding the Growth Hormone Receptor-βTrCP interactions: Molecular Tools for controlling Growth Hormone Sensitivity. [Doctoral Dissertation]. University Utrecht; 2011. Available from: http://dspace.library.uu.nl/handle/1874/350510 ; URN:NBN:NL:UI:10-1874-350510 ; URN:NBN:NL:UI:10-1874-350510 ; http://dspace.library.uu.nl/handle/1874/350510

22. D'Annibale, S. Mechanisms of crosstalk between phosphorylation and ubiquitylation in the regulation of cell proliferation.

Degree: 2014, University Utrecht

 Cell cycle progression is tightly controlled by the ubiquitin-proteasome system. Cullin-RING ubiquitin ligases are the major players responsible for the periodic proteolysis of many regulators… (more)

Subjects/Keywords: cell growth and proliferation; ubiquitin-proteasome system; phosphorylation; SCFβTrCP; cancer

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

APA (6th Edition):

D'Annibale, S. (2014). Mechanisms of crosstalk between phosphorylation and ubiquitylation in the regulation of cell proliferation. (Doctoral Dissertation). University Utrecht. Retrieved from http://dspace.library.uu.nl/handle/1874/300358 ; URN:NBN:NL:UI:10-1874-300358 ; urn:isbn:978-90-393-6223-5 ; URN:NBN:NL:UI:10-1874-300358 ; http://dspace.library.uu.nl/handle/1874/300358

Chicago Manual of Style (16th Edition):

D'Annibale, S. “Mechanisms of crosstalk between phosphorylation and ubiquitylation in the regulation of cell proliferation.” 2014. Doctoral Dissertation, University Utrecht. Accessed July 19, 2019. http://dspace.library.uu.nl/handle/1874/300358 ; URN:NBN:NL:UI:10-1874-300358 ; urn:isbn:978-90-393-6223-5 ; URN:NBN:NL:UI:10-1874-300358 ; http://dspace.library.uu.nl/handle/1874/300358.

MLA Handbook (7th Edition):

D'Annibale, S. “Mechanisms of crosstalk between phosphorylation and ubiquitylation in the regulation of cell proliferation.” 2014. Web. 19 Jul 2019.

Vancouver:

D'Annibale S. Mechanisms of crosstalk between phosphorylation and ubiquitylation in the regulation of cell proliferation. [Internet] [Doctoral dissertation]. University Utrecht; 2014. [cited 2019 Jul 19]. Available from: http://dspace.library.uu.nl/handle/1874/300358 ; URN:NBN:NL:UI:10-1874-300358 ; urn:isbn:978-90-393-6223-5 ; URN:NBN:NL:UI:10-1874-300358 ; http://dspace.library.uu.nl/handle/1874/300358.

Council of Science Editors:

D'Annibale S. Mechanisms of crosstalk between phosphorylation and ubiquitylation in the regulation of cell proliferation. [Doctoral Dissertation]. University Utrecht; 2014. Available from: http://dspace.library.uu.nl/handle/1874/300358 ; URN:NBN:NL:UI:10-1874-300358 ; urn:isbn:978-90-393-6223-5 ; URN:NBN:NL:UI:10-1874-300358 ; http://dspace.library.uu.nl/handle/1874/300358

23. Kim, Jihoon. F-box proteins, cell cycle and cancer.

Degree: 2015, University Utrecht

 E3 ubiquitin ligases are enzymes that confer specificity to the ubiquitin-proteasome system by directly binding the proteins that are targeted for degradation. E3s are encoded… (more)

Subjects/Keywords: Ubiquitin; Proteasome; Proteolysis; F-box protein; Cell cycle; cancer; checkpoint recovery; DNA damage

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

APA (6th Edition):

Kim, J. (2015). F-box proteins, cell cycle and cancer. (Doctoral Dissertation). University Utrecht. Retrieved from http://dspace.library.uu.nl/handle/1874/302855 ; URN:NBN:NL:UI:10-1874-302855 ; urn:isbn:978-94-6203-741-0 ; URN:NBN:NL:UI:10-1874-302855 ; http://dspace.library.uu.nl/handle/1874/302855

Chicago Manual of Style (16th Edition):

Kim, Jihoon. “F-box proteins, cell cycle and cancer.” 2015. Doctoral Dissertation, University Utrecht. Accessed July 19, 2019. http://dspace.library.uu.nl/handle/1874/302855 ; URN:NBN:NL:UI:10-1874-302855 ; urn:isbn:978-94-6203-741-0 ; URN:NBN:NL:UI:10-1874-302855 ; http://dspace.library.uu.nl/handle/1874/302855.

MLA Handbook (7th Edition):

Kim, Jihoon. “F-box proteins, cell cycle and cancer.” 2015. Web. 19 Jul 2019.

Vancouver:

Kim J. F-box proteins, cell cycle and cancer. [Internet] [Doctoral dissertation]. University Utrecht; 2015. [cited 2019 Jul 19]. Available from: http://dspace.library.uu.nl/handle/1874/302855 ; URN:NBN:NL:UI:10-1874-302855 ; urn:isbn:978-94-6203-741-0 ; URN:NBN:NL:UI:10-1874-302855 ; http://dspace.library.uu.nl/handle/1874/302855.

Council of Science Editors:

Kim J. F-box proteins, cell cycle and cancer. [Doctoral Dissertation]. University Utrecht; 2015. Available from: http://dspace.library.uu.nl/handle/1874/302855 ; URN:NBN:NL:UI:10-1874-302855 ; urn:isbn:978-94-6203-741-0 ; URN:NBN:NL:UI:10-1874-302855 ; http://dspace.library.uu.nl/handle/1874/302855

24. Flierman, D. Cytomegalovirus-induced destruction of MHC class I molecules provides insight into ER-associated protein degradation.

Degree: 2007, University Utrecht

 In living cells, proteins are produced continuously. To carry out its specific functions, proteins need to be correctly folded. Proteins that are secreted or function… (more)

Subjects/Keywords: ubiquitin; endoplasmic reticulum; degradation; cytomegalovirus; US11; E2-25K; proteasome; ERAD

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APA (6th Edition):

Flierman, D. (2007). Cytomegalovirus-induced destruction of MHC class I molecules provides insight into ER-associated protein degradation. (Doctoral Dissertation). University Utrecht. Retrieved from http://dspace.library.uu.nl/handle/1874/20846 ; URN:NBN:NL:UI:10-1874-20846 ; urn:isbn:978-90-3934476-7 ; URN:NBN:NL:UI:10-1874-20846 ; http://dspace.library.uu.nl/handle/1874/20846

Chicago Manual of Style (16th Edition):

Flierman, D. “Cytomegalovirus-induced destruction of MHC class I molecules provides insight into ER-associated protein degradation.” 2007. Doctoral Dissertation, University Utrecht. Accessed July 19, 2019. http://dspace.library.uu.nl/handle/1874/20846 ; URN:NBN:NL:UI:10-1874-20846 ; urn:isbn:978-90-3934476-7 ; URN:NBN:NL:UI:10-1874-20846 ; http://dspace.library.uu.nl/handle/1874/20846.

MLA Handbook (7th Edition):

Flierman, D. “Cytomegalovirus-induced destruction of MHC class I molecules provides insight into ER-associated protein degradation.” 2007. Web. 19 Jul 2019.

Vancouver:

Flierman D. Cytomegalovirus-induced destruction of MHC class I molecules provides insight into ER-associated protein degradation. [Internet] [Doctoral dissertation]. University Utrecht; 2007. [cited 2019 Jul 19]. Available from: http://dspace.library.uu.nl/handle/1874/20846 ; URN:NBN:NL:UI:10-1874-20846 ; urn:isbn:978-90-3934476-7 ; URN:NBN:NL:UI:10-1874-20846 ; http://dspace.library.uu.nl/handle/1874/20846.

Council of Science Editors:

Flierman D. Cytomegalovirus-induced destruction of MHC class I molecules provides insight into ER-associated protein degradation. [Doctoral Dissertation]. University Utrecht; 2007. Available from: http://dspace.library.uu.nl/handle/1874/20846 ; URN:NBN:NL:UI:10-1874-20846 ; urn:isbn:978-90-3934476-7 ; URN:NBN:NL:UI:10-1874-20846 ; http://dspace.library.uu.nl/handle/1874/20846

25. Kerkhof, P.J.M. van. The Ubiquitin-Proteasome Pathway and the Regulation of Growth Hormone Receptor Availability.

Degree: 2001, University Utrecht

 Growth hormone (GH) promotes postnatal longitudinal growth in children and is active throughout an individual’s live in protein, fat and carbohydrate metabolism. GH is an… (more)

Subjects/Keywords: ubiquitin; endocytosis; growth hormone; down-regulation; sorting; lysosome; receptor; antagonist; multivescular body; proteasome

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APA (6th Edition):

Kerkhof, P. J. M. v. (2001). The Ubiquitin-Proteasome Pathway and the Regulation of Growth Hormone Receptor Availability. (Doctoral Dissertation). University Utrecht. Retrieved from http://dspace.library.uu.nl/handle/1874/426 ; URN:NBN:NL:UI:10-1874-426 ; URN:NBN:NL:UI:10-1874-426 ; http://dspace.library.uu.nl/handle/1874/426

Chicago Manual of Style (16th Edition):

Kerkhof, P J M van. “The Ubiquitin-Proteasome Pathway and the Regulation of Growth Hormone Receptor Availability.” 2001. Doctoral Dissertation, University Utrecht. Accessed July 19, 2019. http://dspace.library.uu.nl/handle/1874/426 ; URN:NBN:NL:UI:10-1874-426 ; URN:NBN:NL:UI:10-1874-426 ; http://dspace.library.uu.nl/handle/1874/426.

MLA Handbook (7th Edition):

Kerkhof, P J M van. “The Ubiquitin-Proteasome Pathway and the Regulation of Growth Hormone Receptor Availability.” 2001. Web. 19 Jul 2019.

Vancouver:

Kerkhof PJMv. The Ubiquitin-Proteasome Pathway and the Regulation of Growth Hormone Receptor Availability. [Internet] [Doctoral dissertation]. University Utrecht; 2001. [cited 2019 Jul 19]. Available from: http://dspace.library.uu.nl/handle/1874/426 ; URN:NBN:NL:UI:10-1874-426 ; URN:NBN:NL:UI:10-1874-426 ; http://dspace.library.uu.nl/handle/1874/426.

Council of Science Editors:

Kerkhof PJMv. The Ubiquitin-Proteasome Pathway and the Regulation of Growth Hormone Receptor Availability. [Doctoral Dissertation]. University Utrecht; 2001. Available from: http://dspace.library.uu.nl/handle/1874/426 ; URN:NBN:NL:UI:10-1874-426 ; URN:NBN:NL:UI:10-1874-426 ; http://dspace.library.uu.nl/handle/1874/426

26. Kerkhof, P.J.M. van. The Ubiquitin-Proteasome Pathway and the Regulation of Growth Hormone Receptor Availability.

Degree: 2001, University Utrecht

 Growth hormone (GH) promotes postnatal longitudinal growth in children and is active throughout an individual’s live in protein, fat and carbohydrate metabolism. GH is an… (more)

Subjects/Keywords: ubiquitin; endocytosis; growth hormone; down-regulation; sorting; lysosome; receptor; antagonist; multivescular body; proteasome

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

APA (6th Edition):

Kerkhof, P. J. M. v. (2001). The Ubiquitin-Proteasome Pathway and the Regulation of Growth Hormone Receptor Availability. (Doctoral Dissertation). University Utrecht. Retrieved from http://dspace.library.uu.nl/handle/1874/426 ; URN:NBN:NL:UI:10-1874-426 ; URN:NBN:NL:UI:10-1874-426 ; http://dspace.library.uu.nl/handle/1874/426

Chicago Manual of Style (16th Edition):

Kerkhof, P J M van. “The Ubiquitin-Proteasome Pathway and the Regulation of Growth Hormone Receptor Availability.” 2001. Doctoral Dissertation, University Utrecht. Accessed July 19, 2019. http://dspace.library.uu.nl/handle/1874/426 ; URN:NBN:NL:UI:10-1874-426 ; URN:NBN:NL:UI:10-1874-426 ; http://dspace.library.uu.nl/handle/1874/426.

MLA Handbook (7th Edition):

Kerkhof, P J M van. “The Ubiquitin-Proteasome Pathway and the Regulation of Growth Hormone Receptor Availability.” 2001. Web. 19 Jul 2019.

Vancouver:

Kerkhof PJMv. The Ubiquitin-Proteasome Pathway and the Regulation of Growth Hormone Receptor Availability. [Internet] [Doctoral dissertation]. University Utrecht; 2001. [cited 2019 Jul 19]. Available from: http://dspace.library.uu.nl/handle/1874/426 ; URN:NBN:NL:UI:10-1874-426 ; URN:NBN:NL:UI:10-1874-426 ; http://dspace.library.uu.nl/handle/1874/426.

Council of Science Editors:

Kerkhof PJMv. The Ubiquitin-Proteasome Pathway and the Regulation of Growth Hormone Receptor Availability. [Doctoral Dissertation]. University Utrecht; 2001. Available from: http://dspace.library.uu.nl/handle/1874/426 ; URN:NBN:NL:UI:10-1874-426 ; URN:NBN:NL:UI:10-1874-426 ; http://dspace.library.uu.nl/handle/1874/426

27. King, C.R. Dissecting the role of Fbxo41 in neuronal development and signaling.

Degree: 2018, NARCIS

Subjects/Keywords: Neurons; F-box proteins; synapse; dendrite; neuronal morphology; neuroscience; ubiquitin; ups; synaptic plasticity

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APA (6th Edition):

King, C. R. (2018). Dissecting the role of Fbxo41 in neuronal development and signaling. (Doctoral Dissertation). NARCIS. Retrieved from https://research.vu.nl/en/publications/d25b22bd-a20a-48ee-a61a-2bc6d3f16e78 ; urn:nbn:nl:ui:31-d25b22bd-a20a-48ee-a61a-2bc6d3f16e78 ; d25b22bd-a20a-48ee-a61a-2bc6d3f16e78 ; 1871.1/d25b22bd-a20a-48ee-a61a-2bc6d3f16e78 ; urn:isbn:9789462999176 ; urn:nbn:nl:ui:31-d25b22bd-a20a-48ee-a61a-2bc6d3f16e78 ; https://research.vu.nl/en/publications/d25b22bd-a20a-48ee-a61a-2bc6d3f16e78

Chicago Manual of Style (16th Edition):

King, C R. “Dissecting the role of Fbxo41 in neuronal development and signaling.” 2018. Doctoral Dissertation, NARCIS. Accessed July 19, 2019. https://research.vu.nl/en/publications/d25b22bd-a20a-48ee-a61a-2bc6d3f16e78 ; urn:nbn:nl:ui:31-d25b22bd-a20a-48ee-a61a-2bc6d3f16e78 ; d25b22bd-a20a-48ee-a61a-2bc6d3f16e78 ; 1871.1/d25b22bd-a20a-48ee-a61a-2bc6d3f16e78 ; urn:isbn:9789462999176 ; urn:nbn:nl:ui:31-d25b22bd-a20a-48ee-a61a-2bc6d3f16e78 ; https://research.vu.nl/en/publications/d25b22bd-a20a-48ee-a61a-2bc6d3f16e78.

MLA Handbook (7th Edition):

King, C R. “Dissecting the role of Fbxo41 in neuronal development and signaling.” 2018. Web. 19 Jul 2019.

Vancouver:

King CR. Dissecting the role of Fbxo41 in neuronal development and signaling. [Internet] [Doctoral dissertation]. NARCIS; 2018. [cited 2019 Jul 19]. Available from: https://research.vu.nl/en/publications/d25b22bd-a20a-48ee-a61a-2bc6d3f16e78 ; urn:nbn:nl:ui:31-d25b22bd-a20a-48ee-a61a-2bc6d3f16e78 ; d25b22bd-a20a-48ee-a61a-2bc6d3f16e78 ; 1871.1/d25b22bd-a20a-48ee-a61a-2bc6d3f16e78 ; urn:isbn:9789462999176 ; urn:nbn:nl:ui:31-d25b22bd-a20a-48ee-a61a-2bc6d3f16e78 ; https://research.vu.nl/en/publications/d25b22bd-a20a-48ee-a61a-2bc6d3f16e78.

Council of Science Editors:

King CR. Dissecting the role of Fbxo41 in neuronal development and signaling. [Doctoral Dissertation]. NARCIS; 2018. Available from: https://research.vu.nl/en/publications/d25b22bd-a20a-48ee-a61a-2bc6d3f16e78 ; urn:nbn:nl:ui:31-d25b22bd-a20a-48ee-a61a-2bc6d3f16e78 ; d25b22bd-a20a-48ee-a61a-2bc6d3f16e78 ; 1871.1/d25b22bd-a20a-48ee-a61a-2bc6d3f16e78 ; urn:isbn:9789462999176 ; urn:nbn:nl:ui:31-d25b22bd-a20a-48ee-a61a-2bc6d3f16e78 ; https://research.vu.nl/en/publications/d25b22bd-a20a-48ee-a61a-2bc6d3f16e78

28. Santos Maraschin, Felipe dos. Protein ubiquitination in auxin signaling and transport.

Degree: 2009, Sections Plant Cell Physiology/Molecular and Developmental Genetics, Institute of Biology, Leiden University

 What makes plant shoots grow towards the light, and plant roots grow down into the soil? This was a question that Charles Darwin asked himself,… (more)

Subjects/Keywords: Aux/IAA; F-box protein; PINOID; Proteasome; Protein degradation; Protoplast; Signalosome; Ubiquitin; Aux/IAA; F-box protein; PINOID; Proteasome; Protein degradation; Protoplast; Signalosome; Ubiquitin

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APA (6th Edition):

Santos Maraschin, F. d. (2009). Protein ubiquitination in auxin signaling and transport. (Doctoral Dissertation). Sections Plant Cell Physiology/Molecular and Developmental Genetics, Institute of Biology, Leiden University. Retrieved from http://hdl.handle.net/1887/13868

Chicago Manual of Style (16th Edition):

Santos Maraschin, Felipe dos. “Protein ubiquitination in auxin signaling and transport.” 2009. Doctoral Dissertation, Sections Plant Cell Physiology/Molecular and Developmental Genetics, Institute of Biology, Leiden University. Accessed July 19, 2019. http://hdl.handle.net/1887/13868.

MLA Handbook (7th Edition):

Santos Maraschin, Felipe dos. “Protein ubiquitination in auxin signaling and transport.” 2009. Web. 19 Jul 2019.

Vancouver:

Santos Maraschin Fd. Protein ubiquitination in auxin signaling and transport. [Internet] [Doctoral dissertation]. Sections Plant Cell Physiology/Molecular and Developmental Genetics, Institute of Biology, Leiden University; 2009. [cited 2019 Jul 19]. Available from: http://hdl.handle.net/1887/13868.

Council of Science Editors:

Santos Maraschin Fd. Protein ubiquitination in auxin signaling and transport. [Doctoral Dissertation]. Sections Plant Cell Physiology/Molecular and Developmental Genetics, Institute of Biology, Leiden University; 2009. Available from: http://hdl.handle.net/1887/13868

29. Pril, Remko de. The ubiquitin proteasome system in Huntington disease: impairment of the proteolytic machinery aggravates huntingtin aggregation and toxicity.

Degree: 2011, Department of Neurology, Faculty of Medicine, Leiden University Medical Center (LUMC), Leiden University

 Huntington disease (HD) is the best know of the polyglutamine disorders which are caused by the excessive expansion of a CAG repeat in a transcribed… (more)

Subjects/Keywords: Huntington; Ubiquitin Proteasome System; Neurodegeneration; Transgenic mic; Inclusions; E2-25K/Hip2; Protein aggregation; Huntington; Ubiquitin Proteasome System; Neurodegeneration; Transgenic mic; Inclusions; E2-25K/Hip2; Protein aggregation

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

APA (6th Edition):

Pril, R. d. (2011). The ubiquitin proteasome system in Huntington disease: impairment of the proteolytic machinery aggravates huntingtin aggregation and toxicity. (Doctoral Dissertation). Department of Neurology, Faculty of Medicine, Leiden University Medical Center (LUMC), Leiden University. Retrieved from http://hdl.handle.net/1887/16530

Chicago Manual of Style (16th Edition):

Pril, Remko de. “The ubiquitin proteasome system in Huntington disease: impairment of the proteolytic machinery aggravates huntingtin aggregation and toxicity.” 2011. Doctoral Dissertation, Department of Neurology, Faculty of Medicine, Leiden University Medical Center (LUMC), Leiden University. Accessed July 19, 2019. http://hdl.handle.net/1887/16530.

MLA Handbook (7th Edition):

Pril, Remko de. “The ubiquitin proteasome system in Huntington disease: impairment of the proteolytic machinery aggravates huntingtin aggregation and toxicity.” 2011. Web. 19 Jul 2019.

Vancouver:

Pril Rd. The ubiquitin proteasome system in Huntington disease: impairment of the proteolytic machinery aggravates huntingtin aggregation and toxicity. [Internet] [Doctoral dissertation]. Department of Neurology, Faculty of Medicine, Leiden University Medical Center (LUMC), Leiden University; 2011. [cited 2019 Jul 19]. Available from: http://hdl.handle.net/1887/16530.

Council of Science Editors:

Pril Rd. The ubiquitin proteasome system in Huntington disease: impairment of the proteolytic machinery aggravates huntingtin aggregation and toxicity. [Doctoral Dissertation]. Department of Neurology, Faculty of Medicine, Leiden University Medical Center (LUMC), Leiden University; 2011. Available from: http://hdl.handle.net/1887/16530

30. Niu, Xiaolei. Functional analysis of agrobacterium virulence genes.

Degree: 2013, Molecular and Development Genetics Department, Institute of Biology, Faculty of Science, Leiden University

 Agrobacterium tumefaciens is a gram-negative soil bacterium that induces plant tumors by transferring a segment of DNA, called T-DNA, into plant cells. Under laboratory conditions,… (more)

Subjects/Keywords: Agrobacterium tumefaciens; F-box protein; RNA-seq; Saccharomyces cerevisiae; Ubiquitin; VirE3; VirF; Agrobacterium tumefaciens; F-box protein; RNA-seq; Saccharomyces cerevisiae; Ubiquitin; VirE3; VirF

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

APA (6th Edition):

Niu, X. (2013). Functional analysis of agrobacterium virulence genes. (Doctoral Dissertation). Molecular and Development Genetics Department, Institute of Biology, Faculty of Science, Leiden University. Retrieved from http://hdl.handle.net/1887/21014

Chicago Manual of Style (16th Edition):

Niu, Xiaolei. “Functional analysis of agrobacterium virulence genes.” 2013. Doctoral Dissertation, Molecular and Development Genetics Department, Institute of Biology, Faculty of Science, Leiden University. Accessed July 19, 2019. http://hdl.handle.net/1887/21014.

MLA Handbook (7th Edition):

Niu, Xiaolei. “Functional analysis of agrobacterium virulence genes.” 2013. Web. 19 Jul 2019.

Vancouver:

Niu X. Functional analysis of agrobacterium virulence genes. [Internet] [Doctoral dissertation]. Molecular and Development Genetics Department, Institute of Biology, Faculty of Science, Leiden University; 2013. [cited 2019 Jul 19]. Available from: http://hdl.handle.net/1887/21014.

Council of Science Editors:

Niu X. Functional analysis of agrobacterium virulence genes. [Doctoral Dissertation]. Molecular and Development Genetics Department, Institute of Biology, Faculty of Science, Leiden University; 2013. Available from: http://hdl.handle.net/1887/21014

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