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You searched for subject:(Furin). Showing records 1 – 24 of 24 total matches.

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University of New Mexico

1. Flores, Sonya Persia. The role of furin in human papillomavirus infection.

Degree: Biomedical Sciences Graduate Program, 2012, University of New Mexico

 Human papillomaviruses (HPVs) are the causative agent of cervical cancer and infect skin and mucosal membranes. Through wounding the virus establishes infection in the basal… (more)

Subjects/Keywords: HPV; Furin

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APA (6th Edition):

Flores, S. P. (2012). The role of furin in human papillomavirus infection. (Masters Thesis). University of New Mexico. Retrieved from https://digitalrepository.unm.edu/biom_etds/60

Chicago Manual of Style (16th Edition):

Flores, Sonya Persia. “The role of furin in human papillomavirus infection.” 2012. Masters Thesis, University of New Mexico. Accessed July 20, 2019. https://digitalrepository.unm.edu/biom_etds/60.

MLA Handbook (7th Edition):

Flores, Sonya Persia. “The role of furin in human papillomavirus infection.” 2012. Web. 20 Jul 2019.

Vancouver:

Flores SP. The role of furin in human papillomavirus infection. [Internet] [Masters thesis]. University of New Mexico; 2012. [cited 2019 Jul 20]. Available from: https://digitalrepository.unm.edu/biom_etds/60.

Council of Science Editors:

Flores SP. The role of furin in human papillomavirus infection. [Masters Thesis]. University of New Mexico; 2012. Available from: https://digitalrepository.unm.edu/biom_etds/60


University of Arizona

2. Bronnimann, Matthew Phillip. Penetration of Host Membrane Barriers by Human Papillomavirus During Infection .

Degree: 2016, University of Arizona

 Human Papillomaviruses (HPVs) are circular double-stranded DNA (dsDNA) viruses that infect human cutaneous and mucosal tissue. Most HPV infections are benign or cause only minor… (more)

Subjects/Keywords: L2; Membrane; Papillomavirus; furin

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APA (6th Edition):

Bronnimann, M. P. (2016). Penetration of Host Membrane Barriers by Human Papillomavirus During Infection . (Doctoral Dissertation). University of Arizona. Retrieved from http://hdl.handle.net/10150/623159

Chicago Manual of Style (16th Edition):

Bronnimann, Matthew Phillip. “Penetration of Host Membrane Barriers by Human Papillomavirus During Infection .” 2016. Doctoral Dissertation, University of Arizona. Accessed July 20, 2019. http://hdl.handle.net/10150/623159.

MLA Handbook (7th Edition):

Bronnimann, Matthew Phillip. “Penetration of Host Membrane Barriers by Human Papillomavirus During Infection .” 2016. Web. 20 Jul 2019.

Vancouver:

Bronnimann MP. Penetration of Host Membrane Barriers by Human Papillomavirus During Infection . [Internet] [Doctoral dissertation]. University of Arizona; 2016. [cited 2019 Jul 20]. Available from: http://hdl.handle.net/10150/623159.

Council of Science Editors:

Bronnimann MP. Penetration of Host Membrane Barriers by Human Papillomavirus During Infection . [Doctoral Dissertation]. University of Arizona; 2016. Available from: http://hdl.handle.net/10150/623159


Boston University

3. Li, Erik. The proteolytic cleavage of SEMA3F may be mediated by non-furin proprotein convertases.

Degree: MS, Medical Sciences, 2014, Boston University

 Class III Semaphorins (SEMA3) comprise a family of chemokines that have been implicated as negative regulators of axonal guidance, angiogenesis and tumor progression. It has… (more)

Subjects/Keywords: Biology; Furin; SEMA3F; Semaphorin; Angiogenesis; Cancer; Cleavage

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APA (6th Edition):

Li, E. (2014). The proteolytic cleavage of SEMA3F may be mediated by non-furin proprotein convertases. (Masters Thesis). Boston University. Retrieved from http://hdl.handle.net/2144/15074

Chicago Manual of Style (16th Edition):

Li, Erik. “The proteolytic cleavage of SEMA3F may be mediated by non-furin proprotein convertases.” 2014. Masters Thesis, Boston University. Accessed July 20, 2019. http://hdl.handle.net/2144/15074.

MLA Handbook (7th Edition):

Li, Erik. “The proteolytic cleavage of SEMA3F may be mediated by non-furin proprotein convertases.” 2014. Web. 20 Jul 2019.

Vancouver:

Li E. The proteolytic cleavage of SEMA3F may be mediated by non-furin proprotein convertases. [Internet] [Masters thesis]. Boston University; 2014. [cited 2019 Jul 20]. Available from: http://hdl.handle.net/2144/15074.

Council of Science Editors:

Li E. The proteolytic cleavage of SEMA3F may be mediated by non-furin proprotein convertases. [Masters Thesis]. Boston University; 2014. Available from: http://hdl.handle.net/2144/15074


North Carolina State University

4. Nelson, Steevenson. Characterization of Furin Protease Sensitive Site Processing and Its Effects on Sindbis Virus Assembly and Budding.

Degree: PhD, Biochemistry, 2006, North Carolina State University

 Sindbis virus particles are composed of three structural proteins (C/E2/E1). The E1 glycoprotein is organized into a highly constrained, energy-rich conformation. Its hypothesized that this… (more)

Subjects/Keywords: Furin; proteins; truncated

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APA (6th Edition):

Nelson, S. (2006). Characterization of Furin Protease Sensitive Site Processing and Its Effects on Sindbis Virus Assembly and Budding. (Doctoral Dissertation). North Carolina State University. Retrieved from http://www.lib.ncsu.edu/resolver/1840.16/5050

Chicago Manual of Style (16th Edition):

Nelson, Steevenson. “Characterization of Furin Protease Sensitive Site Processing and Its Effects on Sindbis Virus Assembly and Budding.” 2006. Doctoral Dissertation, North Carolina State University. Accessed July 20, 2019. http://www.lib.ncsu.edu/resolver/1840.16/5050.

MLA Handbook (7th Edition):

Nelson, Steevenson. “Characterization of Furin Protease Sensitive Site Processing and Its Effects on Sindbis Virus Assembly and Budding.” 2006. Web. 20 Jul 2019.

Vancouver:

Nelson S. Characterization of Furin Protease Sensitive Site Processing and Its Effects on Sindbis Virus Assembly and Budding. [Internet] [Doctoral dissertation]. North Carolina State University; 2006. [cited 2019 Jul 20]. Available from: http://www.lib.ncsu.edu/resolver/1840.16/5050.

Council of Science Editors:

Nelson S. Characterization of Furin Protease Sensitive Site Processing and Its Effects on Sindbis Virus Assembly and Budding. [Doctoral Dissertation]. North Carolina State University; 2006. Available from: http://www.lib.ncsu.edu/resolver/1840.16/5050


University of Central Florida

5. Limaye, Arati. Receptor Mediated Oral Delivery Of Bioencapsulated Green Fluorescent Protein Expressed In Transgenic Chloroplasts.

Degree: 2005, University of Central Florida

 The skyrocketing costs of prescription medicine in developed countries and their lack of availability in developing countries are the most challenging problems of human health.… (more)

Subjects/Keywords: Furin; Ganglioside; CTB

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APA (6th Edition):

Limaye, A. (2005). Receptor Mediated Oral Delivery Of Bioencapsulated Green Fluorescent Protein Expressed In Transgenic Chloroplasts. (Masters Thesis). University of Central Florida. Retrieved from https://stars.library.ucf.edu/etd/587

Chicago Manual of Style (16th Edition):

Limaye, Arati. “Receptor Mediated Oral Delivery Of Bioencapsulated Green Fluorescent Protein Expressed In Transgenic Chloroplasts.” 2005. Masters Thesis, University of Central Florida. Accessed July 20, 2019. https://stars.library.ucf.edu/etd/587.

MLA Handbook (7th Edition):

Limaye, Arati. “Receptor Mediated Oral Delivery Of Bioencapsulated Green Fluorescent Protein Expressed In Transgenic Chloroplasts.” 2005. Web. 20 Jul 2019.

Vancouver:

Limaye A. Receptor Mediated Oral Delivery Of Bioencapsulated Green Fluorescent Protein Expressed In Transgenic Chloroplasts. [Internet] [Masters thesis]. University of Central Florida; 2005. [cited 2019 Jul 20]. Available from: https://stars.library.ucf.edu/etd/587.

Council of Science Editors:

Limaye A. Receptor Mediated Oral Delivery Of Bioencapsulated Green Fluorescent Protein Expressed In Transgenic Chloroplasts. [Masters Thesis]. University of Central Florida; 2005. Available from: https://stars.library.ucf.edu/etd/587


RMIT University

6. Ravi, R. The effect of UV radiation on furin activity in human keratinocyte cell lines.

Degree: 2010, RMIT University

 UV light is acknowledged to be the main carcinogen involved in the formation of skin cancer. It generates a range of biological responses in the… (more)

Subjects/Keywords: Fields of Research; Ultraviolet radiation; furin; TACE; TNFa; MMP; Keratinocytes

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APA (6th Edition):

Ravi, R. (2010). The effect of UV radiation on furin activity in human keratinocyte cell lines. (Thesis). RMIT University. Retrieved from http://researchbank.rmit.edu.au/view/rmit:160550

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):

Ravi, R. “The effect of UV radiation on furin activity in human keratinocyte cell lines.” 2010. Thesis, RMIT University. Accessed July 20, 2019. http://researchbank.rmit.edu.au/view/rmit:160550.

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

MLA Handbook (7th Edition):

Ravi, R. “The effect of UV radiation on furin activity in human keratinocyte cell lines.” 2010. Web. 20 Jul 2019.

Vancouver:

Ravi R. The effect of UV radiation on furin activity in human keratinocyte cell lines. [Internet] [Thesis]. RMIT University; 2010. [cited 2019 Jul 20]. Available from: http://researchbank.rmit.edu.au/view/rmit:160550.

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

Council of Science Editors:

Ravi R. The effect of UV radiation on furin activity in human keratinocyte cell lines. [Thesis]. RMIT University; 2010. Available from: http://researchbank.rmit.edu.au/view/rmit:160550

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


Penn State University

7. Cruz, Linda Marie. Diversity in Papillomavirus Host Interactions During Attachment and Entry.

Degree: PhD, Cell and Molecular Biology, 2013, Penn State University

 Infections by high-risk human papillomaviruses (HPV) are the main causative agents for the development of cervical cancer. HPVs are uniquely associated with and dependent on… (more)

Subjects/Keywords: Human papillomavirus; HPV; Viral Entry; Virus Attachment; Cell Binding; Glycosaminoglycans; Furin

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APA (6th Edition):

Cruz, L. M. (2013). Diversity in Papillomavirus Host Interactions During Attachment and Entry. (Doctoral Dissertation). Penn State University. Retrieved from https://etda.libraries.psu.edu/catalog/20497

Chicago Manual of Style (16th Edition):

Cruz, Linda Marie. “Diversity in Papillomavirus Host Interactions During Attachment and Entry.” 2013. Doctoral Dissertation, Penn State University. Accessed July 20, 2019. https://etda.libraries.psu.edu/catalog/20497.

MLA Handbook (7th Edition):

Cruz, Linda Marie. “Diversity in Papillomavirus Host Interactions During Attachment and Entry.” 2013. Web. 20 Jul 2019.

Vancouver:

Cruz LM. Diversity in Papillomavirus Host Interactions During Attachment and Entry. [Internet] [Doctoral dissertation]. Penn State University; 2013. [cited 2019 Jul 20]. Available from: https://etda.libraries.psu.edu/catalog/20497.

Council of Science Editors:

Cruz LM. Diversity in Papillomavirus Host Interactions During Attachment and Entry. [Doctoral Dissertation]. Penn State University; 2013. Available from: https://etda.libraries.psu.edu/catalog/20497


Brigham Young University

8. Gross, Andrew Jacob. Discovery of an Allosteric Site on Furin, contributing to Potent Inhibition: A Promising Therapeutic for the Anemia of Chronic Inflammation.

Degree: PhD, 2014, Brigham Young University

 Anemia of chronic inflammation (ACI) is a condition that develops in a setting of chronic immune activation. ACI is characterized and triggered by inflammatory cytokines… (more)

Subjects/Keywords: furin; anemia of chronic inflammation; hepcidin; protease inhibitors; ferroportin; Chemistry

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APA (6th Edition):

Gross, A. J. (2014). Discovery of an Allosteric Site on Furin, contributing to Potent Inhibition: A Promising Therapeutic for the Anemia of Chronic Inflammation. (Doctoral Dissertation). Brigham Young University. Retrieved from https://scholarsarchive.byu.edu/cgi/viewcontent.cgi?article=7537&context=etd

Chicago Manual of Style (16th Edition):

Gross, Andrew Jacob. “Discovery of an Allosteric Site on Furin, contributing to Potent Inhibition: A Promising Therapeutic for the Anemia of Chronic Inflammation.” 2014. Doctoral Dissertation, Brigham Young University. Accessed July 20, 2019. https://scholarsarchive.byu.edu/cgi/viewcontent.cgi?article=7537&context=etd.

MLA Handbook (7th Edition):

Gross, Andrew Jacob. “Discovery of an Allosteric Site on Furin, contributing to Potent Inhibition: A Promising Therapeutic for the Anemia of Chronic Inflammation.” 2014. Web. 20 Jul 2019.

Vancouver:

Gross AJ. Discovery of an Allosteric Site on Furin, contributing to Potent Inhibition: A Promising Therapeutic for the Anemia of Chronic Inflammation. [Internet] [Doctoral dissertation]. Brigham Young University; 2014. [cited 2019 Jul 20]. Available from: https://scholarsarchive.byu.edu/cgi/viewcontent.cgi?article=7537&context=etd.

Council of Science Editors:

Gross AJ. Discovery of an Allosteric Site on Furin, contributing to Potent Inhibition: A Promising Therapeutic for the Anemia of Chronic Inflammation. [Doctoral Dissertation]. Brigham Young University; 2014. Available from: https://scholarsarchive.byu.edu/cgi/viewcontent.cgi?article=7537&context=etd


University of Helsinki

9. Sariola, Merja. Localization of endogenous furin and regulation of its cleavage activity.

Degree: 1997, University of Helsinki

Subjects/Keywords: furin; Semliki Forest virus; Kexin; Biokemia; furin; Semliki Forest virus; Kexin

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APA (6th Edition):

Sariola, M. (1997). Localization of endogenous furin and regulation of its cleavage activity. (Thesis). University of Helsinki. Retrieved from http://hdl.handle.net/10138/159231

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):

Sariola, Merja. “Localization of endogenous furin and regulation of its cleavage activity.” 1997. Thesis, University of Helsinki. Accessed July 20, 2019. http://hdl.handle.net/10138/159231.

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

MLA Handbook (7th Edition):

Sariola, Merja. “Localization of endogenous furin and regulation of its cleavage activity.” 1997. Web. 20 Jul 2019.

Vancouver:

Sariola M. Localization of endogenous furin and regulation of its cleavage activity. [Internet] [Thesis]. University of Helsinki; 1997. [cited 2019 Jul 20]. Available from: http://hdl.handle.net/10138/159231.

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

Council of Science Editors:

Sariola M. Localization of endogenous furin and regulation of its cleavage activity. [Thesis]. University of Helsinki; 1997. Available from: http://hdl.handle.net/10138/159231

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


Tampere University

10. Martinez Cordova, Zuzet. Anti-inflammatory function of Proprotein Convertase FURIN .

Degree: 2017, Tampere University

 Riittävä muttei ylimitoitettu immuunivaste mahdollisesti haitallisia patogeenejä ja epänormaaleja soluja vastaan on välttämätön, muuten seurauksena voi olla autoimmuunisairauksia, krooninen tulehdus tai syöpä. Puolustusjärjestelmä koostuu useiden… (more)

Subjects/Keywords: FURIN; makrofagi; T-solu; synnynnäinen immuniteetti; syöpä; macrophage; T cell; innate immunity; cancer

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APA (6th Edition):

Martinez Cordova, Z. (2017). Anti-inflammatory function of Proprotein Convertase FURIN . (Doctoral Dissertation). Tampere University. Retrieved from http://tampub.uta.fi/handle/10024/100816

Chicago Manual of Style (16th Edition):

Martinez Cordova, Zuzet. “Anti-inflammatory function of Proprotein Convertase FURIN .” 2017. Doctoral Dissertation, Tampere University. Accessed July 20, 2019. http://tampub.uta.fi/handle/10024/100816.

MLA Handbook (7th Edition):

Martinez Cordova, Zuzet. “Anti-inflammatory function of Proprotein Convertase FURIN .” 2017. Web. 20 Jul 2019.

Vancouver:

Martinez Cordova Z. Anti-inflammatory function of Proprotein Convertase FURIN . [Internet] [Doctoral dissertation]. Tampere University; 2017. [cited 2019 Jul 20]. Available from: http://tampub.uta.fi/handle/10024/100816.

Council of Science Editors:

Martinez Cordova Z. Anti-inflammatory function of Proprotein Convertase FURIN . [Doctoral Dissertation]. Tampere University; 2017. Available from: http://tampub.uta.fi/handle/10024/100816


Brigham Young University

11. Schuler, Jeffrey Thomas. Forward Chemical Genetics Drug Screen Yields Novel Proteases and Proteolytic Inhibitors of HGF–induced Epithelial–Mesenchymal Transition.

Degree: MS, 2016, Brigham Young University

 Hepatocyte Growth Factor (HGF)–induced Epithelial–Mesenchymal Transition (EMT) is a complex cellular pathway that causes epithelial cell scattering by breaking cell–cell contacts, eliminating apical–basal polarity, and… (more)

Subjects/Keywords: EMT; cell spreading; cell compaction; HGF; BACE; EphA2; Furin; MMP–9; MMP–12; Physiology

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APA (6th Edition):

Schuler, J. T. (2016). Forward Chemical Genetics Drug Screen Yields Novel Proteases and Proteolytic Inhibitors of HGF–induced Epithelial–Mesenchymal Transition. (Masters Thesis). Brigham Young University. Retrieved from https://scholarsarchive.byu.edu/cgi/viewcontent.cgi?article=7257&context=etd

Chicago Manual of Style (16th Edition):

Schuler, Jeffrey Thomas. “Forward Chemical Genetics Drug Screen Yields Novel Proteases and Proteolytic Inhibitors of HGF–induced Epithelial–Mesenchymal Transition.” 2016. Masters Thesis, Brigham Young University. Accessed July 20, 2019. https://scholarsarchive.byu.edu/cgi/viewcontent.cgi?article=7257&context=etd.

MLA Handbook (7th Edition):

Schuler, Jeffrey Thomas. “Forward Chemical Genetics Drug Screen Yields Novel Proteases and Proteolytic Inhibitors of HGF–induced Epithelial–Mesenchymal Transition.” 2016. Web. 20 Jul 2019.

Vancouver:

Schuler JT. Forward Chemical Genetics Drug Screen Yields Novel Proteases and Proteolytic Inhibitors of HGF–induced Epithelial–Mesenchymal Transition. [Internet] [Masters thesis]. Brigham Young University; 2016. [cited 2019 Jul 20]. Available from: https://scholarsarchive.byu.edu/cgi/viewcontent.cgi?article=7257&context=etd.

Council of Science Editors:

Schuler JT. Forward Chemical Genetics Drug Screen Yields Novel Proteases and Proteolytic Inhibitors of HGF–induced Epithelial–Mesenchymal Transition. [Masters Thesis]. Brigham Young University; 2016. Available from: https://scholarsarchive.byu.edu/cgi/viewcontent.cgi?article=7257&context=etd


University of Michigan

12. Tippett, Larry D. Substrate Specificity of the Widely Expressed Subtilisin-like Proprotein Convertases (SPCs): A Role for the Substrate Amino Acid Directly Downstream of the Endoproteolytic Cleavage Site.

Degree: Master's, College of Arts and Sciences: Biology, 2001, University of Michigan

 Substrate specificity was investigated among four of the eukaryotic, widely expressed subtilisin-like proprotein convertases (SPCs): furin, PACE4, PC5, and PC7. Through site-directed mutagenesis, amino acid… (more)

Subjects/Keywords: furin; PACE4; PC5; PC7; substrate specificity

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APA (6th Edition):

Tippett, L. D. (2001). Substrate Specificity of the Widely Expressed Subtilisin-like Proprotein Convertases (SPCs): A Role for the Substrate Amino Acid Directly Downstream of the Endoproteolytic Cleavage Site. (Masters Thesis). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/117758

Chicago Manual of Style (16th Edition):

Tippett, Larry D. “Substrate Specificity of the Widely Expressed Subtilisin-like Proprotein Convertases (SPCs): A Role for the Substrate Amino Acid Directly Downstream of the Endoproteolytic Cleavage Site.” 2001. Masters Thesis, University of Michigan. Accessed July 20, 2019. http://hdl.handle.net/2027.42/117758.

MLA Handbook (7th Edition):

Tippett, Larry D. “Substrate Specificity of the Widely Expressed Subtilisin-like Proprotein Convertases (SPCs): A Role for the Substrate Amino Acid Directly Downstream of the Endoproteolytic Cleavage Site.” 2001. Web. 20 Jul 2019.

Vancouver:

Tippett LD. Substrate Specificity of the Widely Expressed Subtilisin-like Proprotein Convertases (SPCs): A Role for the Substrate Amino Acid Directly Downstream of the Endoproteolytic Cleavage Site. [Internet] [Masters thesis]. University of Michigan; 2001. [cited 2019 Jul 20]. Available from: http://hdl.handle.net/2027.42/117758.

Council of Science Editors:

Tippett LD. Substrate Specificity of the Widely Expressed Subtilisin-like Proprotein Convertases (SPCs): A Role for the Substrate Amino Acid Directly Downstream of the Endoproteolytic Cleavage Site. [Masters Thesis]. University of Michigan; 2001. Available from: http://hdl.handle.net/2027.42/117758


Kyoto University / 京都大学

13. Doi, Keiko. Crucial role of the Rap G protein signal in Notch activation and leukemogenicity of T-cell acute lymphoblastic leukemia : RapG蛋白シグナルによるT細胞性急性白血病細胞のNotch活性化と白血病原性の制御.

Degree: 博士(医科学), 2015, Kyoto University / 京都大学

新制・課程博士

甲第18905号

医科博第61号

Subjects/Keywords: Rap signal; Notch signal; Adam10; Furin; Notch ligand

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APA (6th Edition):

Doi, K. (2015). Crucial role of the Rap G protein signal in Notch activation and leukemogenicity of T-cell acute lymphoblastic leukemia : RapG蛋白シグナルによるT細胞性急性白血病細胞のNotch活性化と白血病原性の制御. (Thesis). Kyoto University / 京都大学. Retrieved from http://hdl.handle.net/2433/199214 ; http://dx.doi.org/10.14989/doctor.k18905

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):

Doi, Keiko. “Crucial role of the Rap G protein signal in Notch activation and leukemogenicity of T-cell acute lymphoblastic leukemia : RapG蛋白シグナルによるT細胞性急性白血病細胞のNotch活性化と白血病原性の制御.” 2015. Thesis, Kyoto University / 京都大学. Accessed July 20, 2019. http://hdl.handle.net/2433/199214 ; http://dx.doi.org/10.14989/doctor.k18905.

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

MLA Handbook (7th Edition):

Doi, Keiko. “Crucial role of the Rap G protein signal in Notch activation and leukemogenicity of T-cell acute lymphoblastic leukemia : RapG蛋白シグナルによるT細胞性急性白血病細胞のNotch活性化と白血病原性の制御.” 2015. Web. 20 Jul 2019.

Vancouver:

Doi K. Crucial role of the Rap G protein signal in Notch activation and leukemogenicity of T-cell acute lymphoblastic leukemia : RapG蛋白シグナルによるT細胞性急性白血病細胞のNotch活性化と白血病原性の制御. [Internet] [Thesis]. Kyoto University / 京都大学; 2015. [cited 2019 Jul 20]. Available from: http://hdl.handle.net/2433/199214 ; http://dx.doi.org/10.14989/doctor.k18905.

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

Council of Science Editors:

Doi K. Crucial role of the Rap G protein signal in Notch activation and leukemogenicity of T-cell acute lymphoblastic leukemia : RapG蛋白シグナルによるT細胞性急性白血病細胞のNotch活性化と白血病原性の制御. [Thesis]. Kyoto University / 京都大学; 2015. Available from: http://hdl.handle.net/2433/199214 ; http://dx.doi.org/10.14989/doctor.k18905

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


University of Oulu

14. Peltonen, T. (Tuomas). Endothelial factors in the pathogenesis of aortic valve stenosis.

Degree: 2008, University of Oulu

 Abstract Calcified aortic valve disease represents a spectrum of disease spanning from mild aortic valve sclerosis to severe aortic valve stenosis (AS), being an actively… (more)

Subjects/Keywords: APJ; C-type natriuretic peptide; aortic valve stenosis; apelin; endothelin receptors; endothelin-1; furin; natriuretic peptide receptors

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APA (6th Edition):

Peltonen, T. (. (2008). Endothelial factors in the pathogenesis of aortic valve stenosis. (Doctoral Dissertation). University of Oulu. Retrieved from http://urn.fi/urn:isbn:9789514289880

Chicago Manual of Style (16th Edition):

Peltonen, T (Tuomas). “Endothelial factors in the pathogenesis of aortic valve stenosis.” 2008. Doctoral Dissertation, University of Oulu. Accessed July 20, 2019. http://urn.fi/urn:isbn:9789514289880.

MLA Handbook (7th Edition):

Peltonen, T (Tuomas). “Endothelial factors in the pathogenesis of aortic valve stenosis.” 2008. Web. 20 Jul 2019.

Vancouver:

Peltonen T(. Endothelial factors in the pathogenesis of aortic valve stenosis. [Internet] [Doctoral dissertation]. University of Oulu; 2008. [cited 2019 Jul 20]. Available from: http://urn.fi/urn:isbn:9789514289880.

Council of Science Editors:

Peltonen T(. Endothelial factors in the pathogenesis of aortic valve stenosis. [Doctoral Dissertation]. University of Oulu; 2008. Available from: http://urn.fi/urn:isbn:9789514289880


Kyoto University

15. Doi, Keiko. Crucial role of the Rap G protein signal in Notch activation and leukemogenicity of T-cell acute lymphoblastic leukemia .

Degree: 2015, Kyoto University

Subjects/Keywords: Rap signal; Notch signal; Adam10; Furin; Notch ligand

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

APA (6th Edition):

Doi, K. (2015). Crucial role of the Rap G protein signal in Notch activation and leukemogenicity of T-cell acute lymphoblastic leukemia . (Thesis). Kyoto University. Retrieved from http://hdl.handle.net/2433/199214

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):

Doi, Keiko. “Crucial role of the Rap G protein signal in Notch activation and leukemogenicity of T-cell acute lymphoblastic leukemia .” 2015. Thesis, Kyoto University. Accessed July 20, 2019. http://hdl.handle.net/2433/199214.

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

MLA Handbook (7th Edition):

Doi, Keiko. “Crucial role of the Rap G protein signal in Notch activation and leukemogenicity of T-cell acute lymphoblastic leukemia .” 2015. Web. 20 Jul 2019.

Vancouver:

Doi K. Crucial role of the Rap G protein signal in Notch activation and leukemogenicity of T-cell acute lymphoblastic leukemia . [Internet] [Thesis]. Kyoto University; 2015. [cited 2019 Jul 20]. Available from: http://hdl.handle.net/2433/199214.

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

Council of Science Editors:

Doi K. Crucial role of the Rap G protein signal in Notch activation and leukemogenicity of T-cell acute lymphoblastic leukemia . [Thesis]. Kyoto University; 2015. Available from: http://hdl.handle.net/2433/199214

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

16. ZHANG WEI. The characterization of a new small gtpase arf like protein 8.

Degree: 2007, National University of Singapore

Subjects/Keywords: SMALL GTPASE; Arl8; Golgi; trafficking; furin; ARFRP-1

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APA (6th Edition):

WEI, Z. (2007). The characterization of a new small gtpase arf like protein 8. (Thesis). National University of Singapore. Retrieved from http://scholarbank.nus.edu.sg/handle/10635/13349

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):

WEI, ZHANG. “The characterization of a new small gtpase arf like protein 8.” 2007. Thesis, National University of Singapore. Accessed July 20, 2019. http://scholarbank.nus.edu.sg/handle/10635/13349.

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

MLA Handbook (7th Edition):

WEI, ZHANG. “The characterization of a new small gtpase arf like protein 8.” 2007. Web. 20 Jul 2019.

Vancouver:

WEI Z. The characterization of a new small gtpase arf like protein 8. [Internet] [Thesis]. National University of Singapore; 2007. [cited 2019 Jul 20]. Available from: http://scholarbank.nus.edu.sg/handle/10635/13349.

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

Council of Science Editors:

WEI Z. The characterization of a new small gtpase arf like protein 8. [Thesis]. National University of Singapore; 2007. Available from: http://scholarbank.nus.edu.sg/handle/10635/13349

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


University of Toronto

17. Zhou, Jing-Jing Aileen. Enhancing Production of Recombinant BMP-2 in Mammalian Cell Culture Systems by Inhibition of Pro-protein Cleavage using 9DR Peptides.

Degree: 2008, University of Toronto

Introduction: Mammalian cell recombinant bone morphogenetic protein (rBMP) synthesis is reported to be poor. The BMP pro-domain may be involved in folding, stability and secretion.… (more)

Subjects/Keywords: recombinant BMP-2 production; furin cleavage; 0567

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APA (6th Edition):

Zhou, J. A. (2008). Enhancing Production of Recombinant BMP-2 in Mammalian Cell Culture Systems by Inhibition of Pro-protein Cleavage using 9DR Peptides. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/11175

Chicago Manual of Style (16th Edition):

Zhou, Jing-Jing Aileen. “Enhancing Production of Recombinant BMP-2 in Mammalian Cell Culture Systems by Inhibition of Pro-protein Cleavage using 9DR Peptides.” 2008. Masters Thesis, University of Toronto. Accessed July 20, 2019. http://hdl.handle.net/1807/11175.

MLA Handbook (7th Edition):

Zhou, Jing-Jing Aileen. “Enhancing Production of Recombinant BMP-2 in Mammalian Cell Culture Systems by Inhibition of Pro-protein Cleavage using 9DR Peptides.” 2008. Web. 20 Jul 2019.

Vancouver:

Zhou JA. Enhancing Production of Recombinant BMP-2 in Mammalian Cell Culture Systems by Inhibition of Pro-protein Cleavage using 9DR Peptides. [Internet] [Masters thesis]. University of Toronto; 2008. [cited 2019 Jul 20]. Available from: http://hdl.handle.net/1807/11175.

Council of Science Editors:

Zhou JA. Enhancing Production of Recombinant BMP-2 in Mammalian Cell Culture Systems by Inhibition of Pro-protein Cleavage using 9DR Peptides. [Masters Thesis]. University of Toronto; 2008. Available from: http://hdl.handle.net/1807/11175


University of Michigan

18. Subramani, Araskumar. Substrate Specificity of the Widely Expressed Subtilisin-like Proprotein Convertases.

Degree: Master's, College of Arts and Sciences: Biology, 2009, University of Michigan

 Limited endoproteolysis plays a key role in the activation and maturation of proteins that traverse the secretory pathway. Subtilisin-like Proprotein Convertases (SPCs) are a family… (more)

Subjects/Keywords: subtilisin-like proprotein convertases (SPCs); amino acids; endoproteolysis; furin

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APA (6th Edition):

Subramani, A. (2009). Substrate Specificity of the Widely Expressed Subtilisin-like Proprotein Convertases. (Masters Thesis). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/117754

Chicago Manual of Style (16th Edition):

Subramani, Araskumar. “Substrate Specificity of the Widely Expressed Subtilisin-like Proprotein Convertases.” 2009. Masters Thesis, University of Michigan. Accessed July 20, 2019. http://hdl.handle.net/2027.42/117754.

MLA Handbook (7th Edition):

Subramani, Araskumar. “Substrate Specificity of the Widely Expressed Subtilisin-like Proprotein Convertases.” 2009. Web. 20 Jul 2019.

Vancouver:

Subramani A. Substrate Specificity of the Widely Expressed Subtilisin-like Proprotein Convertases. [Internet] [Masters thesis]. University of Michigan; 2009. [cited 2019 Jul 20]. Available from: http://hdl.handle.net/2027.42/117754.

Council of Science Editors:

Subramani A. Substrate Specificity of the Widely Expressed Subtilisin-like Proprotein Convertases. [Masters Thesis]. University of Michigan; 2009. Available from: http://hdl.handle.net/2027.42/117754

19. Maxson, Julia Elizabeth. Processing and trafficking of the iron regulatory protein, hemojuvelin.

Degree: PhD, 2011, Oregon Health Sciences University

Subjects/Keywords: Membrane proteins; Hemojuvelin; Furin; Matriptase-2; Membrane Proteins; Protein Transport; Iron-Regulatory Proteins

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APA (6th Edition):

Maxson, J. E. (2011). Processing and trafficking of the iron regulatory protein, hemojuvelin. (Doctoral Dissertation). Oregon Health Sciences University. Retrieved from doi:10.6083/M4T43R2S ; http://digitalcommons.ohsu.edu/etd/667

Chicago Manual of Style (16th Edition):

Maxson, Julia Elizabeth. “Processing and trafficking of the iron regulatory protein, hemojuvelin.” 2011. Doctoral Dissertation, Oregon Health Sciences University. Accessed July 20, 2019. doi:10.6083/M4T43R2S ; http://digitalcommons.ohsu.edu/etd/667.

MLA Handbook (7th Edition):

Maxson, Julia Elizabeth. “Processing and trafficking of the iron regulatory protein, hemojuvelin.” 2011. Web. 20 Jul 2019.

Vancouver:

Maxson JE. Processing and trafficking of the iron regulatory protein, hemojuvelin. [Internet] [Doctoral dissertation]. Oregon Health Sciences University; 2011. [cited 2019 Jul 20]. Available from: doi:10.6083/M4T43R2S ; http://digitalcommons.ohsu.edu/etd/667.

Council of Science Editors:

Maxson JE. Processing and trafficking of the iron regulatory protein, hemojuvelin. [Doctoral Dissertation]. Oregon Health Sciences University; 2011. Available from: doi:10.6083/M4T43R2S ; http://digitalcommons.ohsu.edu/etd/667

20. Ravindranath, Shreyas Raj. Elucidating the biomechanical aspects of mammalian Notch Signaling.

Degree: Biomedical Engineering, 2016, University of California – Irvine

 Canonical Notch Signaling Pathway is a critical signaling pathway that is required for cell fate specification and as such for the development of cells of… (more)

Subjects/Keywords: Biomedical engineering; Biophysics; Developmental biology; Furin; Notch Signaling

…Force Extension Curve FI Furin Inhibitor – Decanoyl Chloromethyl Ketone Jag Jagged MNNL… …contains the human IgG Fc with the CH2-CH3 hinge) N1ΔFC Notch 1 with deleted Furin… …Force RFS Rupture Force Spectra S1 Site 1 – Furin Cleavage site S1 Rupture Breakage at… …Publications  S.Ravindranath & M.Oltmann et al., “The Role of Furin Processing in Mammalian Notch… …cleaved into a heterodimer by furin in the trans-golgi network at a xiv region known as S1… 

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APA (6th Edition):

Ravindranath, S. R. (2016). Elucidating the biomechanical aspects of mammalian Notch Signaling. (Thesis). University of California – Irvine. Retrieved from http://www.escholarship.org/uc/item/1jm9p7kf

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):

Ravindranath, Shreyas Raj. “Elucidating the biomechanical aspects of mammalian Notch Signaling.” 2016. Thesis, University of California – Irvine. Accessed July 20, 2019. http://www.escholarship.org/uc/item/1jm9p7kf.

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

MLA Handbook (7th Edition):

Ravindranath, Shreyas Raj. “Elucidating the biomechanical aspects of mammalian Notch Signaling.” 2016. Web. 20 Jul 2019.

Vancouver:

Ravindranath SR. Elucidating the biomechanical aspects of mammalian Notch Signaling. [Internet] [Thesis]. University of California – Irvine; 2016. [cited 2019 Jul 20]. Available from: http://www.escholarship.org/uc/item/1jm9p7kf.

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

Council of Science Editors:

Ravindranath SR. Elucidating the biomechanical aspects of mammalian Notch Signaling. [Thesis]. University of California – Irvine; 2016. Available from: http://www.escholarship.org/uc/item/1jm9p7kf

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


Virginia Commonwealth University

21. Ross, Heather Hamilton. Characterization and Functional Analysis of a Newly Identified Human MT5-MMP Transcript Variant Isolated from Multipotent NT2 Cells.

Degree: PhD, Anatomy & Neurobiology, 2006, Virginia Commonwealth University

 Membrane-type 5 matrix metalloproteinase (MT5-MMP) is unique among MMP family members as it is predominately expressed in the CNS. Its expression is ubiquitous during brain… (more)

Subjects/Keywords: endopeptides; plasmin system; cysteine; furin; Anatomy; Medicine and Health Sciences; Nervous System

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

APA (6th Edition):

Ross, H. H. (2006). Characterization and Functional Analysis of a Newly Identified Human MT5-MMP Transcript Variant Isolated from Multipotent NT2 Cells. (Doctoral Dissertation). Virginia Commonwealth University. Retrieved from https://scholarscompass.vcu.edu/etd/839

Chicago Manual of Style (16th Edition):

Ross, Heather Hamilton. “Characterization and Functional Analysis of a Newly Identified Human MT5-MMP Transcript Variant Isolated from Multipotent NT2 Cells.” 2006. Doctoral Dissertation, Virginia Commonwealth University. Accessed July 20, 2019. https://scholarscompass.vcu.edu/etd/839.

MLA Handbook (7th Edition):

Ross, Heather Hamilton. “Characterization and Functional Analysis of a Newly Identified Human MT5-MMP Transcript Variant Isolated from Multipotent NT2 Cells.” 2006. Web. 20 Jul 2019.

Vancouver:

Ross HH. Characterization and Functional Analysis of a Newly Identified Human MT5-MMP Transcript Variant Isolated from Multipotent NT2 Cells. [Internet] [Doctoral dissertation]. Virginia Commonwealth University; 2006. [cited 2019 Jul 20]. Available from: https://scholarscompass.vcu.edu/etd/839.

Council of Science Editors:

Ross HH. Characterization and Functional Analysis of a Newly Identified Human MT5-MMP Transcript Variant Isolated from Multipotent NT2 Cells. [Doctoral Dissertation]. Virginia Commonwealth University; 2006. Available from: https://scholarscompass.vcu.edu/etd/839


University of Waikato

22. McFarlane, Craig Desmond. Mechanism of myostatin action during satellite cell activation and muscle wasting.

Degree: 2007, University of Waikato

 Myostatin, a Transforming Growth Factor-beta (TGF-β) superfamily member, has been well characterised as a negative regulator of muscle growth and development. In support, inactivation or… (more)

Subjects/Keywords: Myostatin; furin; processing; pax7; self-renewal; atrogin-1; muscle wasting; microtubules; myosac; cxxc5

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APA (6th Edition):

McFarlane, C. D. (2007). Mechanism of myostatin action during satellite cell activation and muscle wasting. (Doctoral Dissertation). University of Waikato. Retrieved from http://hdl.handle.net/10289/3516

Chicago Manual of Style (16th Edition):

McFarlane, Craig Desmond. “Mechanism of myostatin action during satellite cell activation and muscle wasting. ” 2007. Doctoral Dissertation, University of Waikato. Accessed July 20, 2019. http://hdl.handle.net/10289/3516.

MLA Handbook (7th Edition):

McFarlane, Craig Desmond. “Mechanism of myostatin action during satellite cell activation and muscle wasting. ” 2007. Web. 20 Jul 2019.

Vancouver:

McFarlane CD. Mechanism of myostatin action during satellite cell activation and muscle wasting. [Internet] [Doctoral dissertation]. University of Waikato; 2007. [cited 2019 Jul 20]. Available from: http://hdl.handle.net/10289/3516.

Council of Science Editors:

McFarlane CD. Mechanism of myostatin action during satellite cell activation and muscle wasting. [Doctoral Dissertation]. University of Waikato; 2007. Available from: http://hdl.handle.net/10289/3516


Universiteit Utrecht

23. Bosch, B.J. The coronavirus spike protein : mechanisms of membrane fusion and virion incorporation.

Degree: 2004, Universiteit Utrecht

 The coronavirus spike protein is a membrane-anchored glycoprotein responsible for virus-cell attachment and membrane fusion, prerequisites for a successful virus infection. In this thesis, two… (more)

Subjects/Keywords: Diergeneeskunde; coronavirus; SARS-CoV; MHV; virus entry; virus inhibition; membrane fusion; heptad repeat; furin; virus assembly

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

APA (6th Edition):

Bosch, B. J. (2004). The coronavirus spike protein : mechanisms of membrane fusion and virion incorporation. (Doctoral Dissertation). Universiteit Utrecht. Retrieved from http://dspace.library.uu.nl:8080/handle/1874/1706

Chicago Manual of Style (16th Edition):

Bosch, B J. “The coronavirus spike protein : mechanisms of membrane fusion and virion incorporation.” 2004. Doctoral Dissertation, Universiteit Utrecht. Accessed July 20, 2019. http://dspace.library.uu.nl:8080/handle/1874/1706.

MLA Handbook (7th Edition):

Bosch, B J. “The coronavirus spike protein : mechanisms of membrane fusion and virion incorporation.” 2004. Web. 20 Jul 2019.

Vancouver:

Bosch BJ. The coronavirus spike protein : mechanisms of membrane fusion and virion incorporation. [Internet] [Doctoral dissertation]. Universiteit Utrecht; 2004. [cited 2019 Jul 20]. Available from: http://dspace.library.uu.nl:8080/handle/1874/1706.

Council of Science Editors:

Bosch BJ. The coronavirus spike protein : mechanisms of membrane fusion and virion incorporation. [Doctoral Dissertation]. Universiteit Utrecht; 2004. Available from: http://dspace.library.uu.nl:8080/handle/1874/1706

24. Bosch, B.J. The coronavirus spike protein : mechanisms of membrane fusion and virion incorporation.

Degree: 2004, University Utrecht

 The coronavirus spike protein is a membrane-anchored glycoprotein responsible for virus-cell attachment and membrane fusion, prerequisites for a successful virus infection. In this thesis, two… (more)

Subjects/Keywords: coronavirus; SARS-CoV; MHV; virus entry; virus inhibition; membrane fusion; heptad repeat; furin; virus assembly

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

APA (6th Edition):

Bosch, B. J. (2004). The coronavirus spike protein : mechanisms of membrane fusion and virion incorporation. (Doctoral Dissertation). University Utrecht. Retrieved from http://dspace.library.uu.nl/handle/1874/1706 ; URN:NBN:NL:UI:10-1874-1706 ; URN:NBN:NL:UI:10-1874-1706 ; http://dspace.library.uu.nl/handle/1874/1706

Chicago Manual of Style (16th Edition):

Bosch, B J. “The coronavirus spike protein : mechanisms of membrane fusion and virion incorporation.” 2004. Doctoral Dissertation, University Utrecht. Accessed July 20, 2019. http://dspace.library.uu.nl/handle/1874/1706 ; URN:NBN:NL:UI:10-1874-1706 ; URN:NBN:NL:UI:10-1874-1706 ; http://dspace.library.uu.nl/handle/1874/1706.

MLA Handbook (7th Edition):

Bosch, B J. “The coronavirus spike protein : mechanisms of membrane fusion and virion incorporation.” 2004. Web. 20 Jul 2019.

Vancouver:

Bosch BJ. The coronavirus spike protein : mechanisms of membrane fusion and virion incorporation. [Internet] [Doctoral dissertation]. University Utrecht; 2004. [cited 2019 Jul 20]. Available from: http://dspace.library.uu.nl/handle/1874/1706 ; URN:NBN:NL:UI:10-1874-1706 ; URN:NBN:NL:UI:10-1874-1706 ; http://dspace.library.uu.nl/handle/1874/1706.

Council of Science Editors:

Bosch BJ. The coronavirus spike protein : mechanisms of membrane fusion and virion incorporation. [Doctoral Dissertation]. University Utrecht; 2004. Available from: http://dspace.library.uu.nl/handle/1874/1706 ; URN:NBN:NL:UI:10-1874-1706 ; URN:NBN:NL:UI:10-1874-1706 ; http://dspace.library.uu.nl/handle/1874/1706

.