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You searched for subject:( Protein recombinant expression). Showing records 1 – 30 of 30895 total matches.

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Universitat de Valencia

1. Martínez Solís, María. Interacción insecto-baculovirus. Aplicaciones en la mejora de baculovirus como vector para la expresión heteróloga de proteínas.

Degree: 2018, Universitat de Valencia

 Los baculovirus forman un amplio grupo de virus patógenos de insectos que se caracterizan por su elevada especificidad. Su principal aplicación es su uso como… (more)

Subjects/Keywords: BEVS; baculovirus; expression system; recombinant protein

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

APA (6th Edition):

Martínez Solís, M. (2018). Interacción insecto-baculovirus. Aplicaciones en la mejora de baculovirus como vector para la expresión heteróloga de proteínas. (Doctoral Dissertation). Universitat de Valencia. Retrieved from http://hdl.handle.net/10550/66207

Chicago Manual of Style (16th Edition):

Martínez Solís, María. “Interacción insecto-baculovirus. Aplicaciones en la mejora de baculovirus como vector para la expresión heteróloga de proteínas. ” 2018. Doctoral Dissertation, Universitat de Valencia. Accessed April 17, 2021. http://hdl.handle.net/10550/66207.

MLA Handbook (7th Edition):

Martínez Solís, María. “Interacción insecto-baculovirus. Aplicaciones en la mejora de baculovirus como vector para la expresión heteróloga de proteínas. ” 2018. Web. 17 Apr 2021.

Vancouver:

Martínez Solís M. Interacción insecto-baculovirus. Aplicaciones en la mejora de baculovirus como vector para la expresión heteróloga de proteínas. [Internet] [Doctoral dissertation]. Universitat de Valencia; 2018. [cited 2021 Apr 17]. Available from: http://hdl.handle.net/10550/66207.

Council of Science Editors:

Martínez Solís M. Interacción insecto-baculovirus. Aplicaciones en la mejora de baculovirus como vector para la expresión heteróloga de proteínas. [Doctoral Dissertation]. Universitat de Valencia; 2018. Available from: http://hdl.handle.net/10550/66207


University of Western Ontario

2. Lama, Pravesh. Identification and Functional Characterization of GmMYB176-Specific Protein Kinases in Soybean.

Degree: 2016, University of Western Ontario

 GmMYB176 is an R1 MYB transcription factor that regulates isoflavonoid biosynthesis in soybean. The deletion of phosphorylation sites in GmMYB176 abrogates its interaction with 14-3-3… (more)

Subjects/Keywords: Isoflavonoid; protein kinase; recombinant protein expression; kinase assay; Biology; Life Sciences

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APA (6th Edition):

Lama, P. (2016). Identification and Functional Characterization of GmMYB176-Specific Protein Kinases in Soybean. (Thesis). University of Western Ontario. Retrieved from https://ir.lib.uwo.ca/etd/3823

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):

Lama, Pravesh. “Identification and Functional Characterization of GmMYB176-Specific Protein Kinases in Soybean.” 2016. Thesis, University of Western Ontario. Accessed April 17, 2021. https://ir.lib.uwo.ca/etd/3823.

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

MLA Handbook (7th Edition):

Lama, Pravesh. “Identification and Functional Characterization of GmMYB176-Specific Protein Kinases in Soybean.” 2016. Web. 17 Apr 2021.

Vancouver:

Lama P. Identification and Functional Characterization of GmMYB176-Specific Protein Kinases in Soybean. [Internet] [Thesis]. University of Western Ontario; 2016. [cited 2021 Apr 17]. Available from: https://ir.lib.uwo.ca/etd/3823.

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

Council of Science Editors:

Lama P. Identification and Functional Characterization of GmMYB176-Specific Protein Kinases in Soybean. [Thesis]. University of Western Ontario; 2016. Available from: https://ir.lib.uwo.ca/etd/3823

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


University of California – Berkeley

3. Dana, Craig Matthew. Cel7A Engineering and Expression.

Degree: Chemical Engineering, 2013, University of California – Berkeley

 Renewable fuels produced from biomass-derived sugars are receiving increasing attention. Lignocellulose-degrading enzymes derived from fungi are attractive for saccharification of biomass because they can be… (more)

Subjects/Keywords: Chemical engineering; CBHI; Cel7A; cellulase; protein engineering; recombinant expression; saccharomyces cerevisiae

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APA (6th Edition):

Dana, C. M. (2013). Cel7A Engineering and Expression. (Thesis). University of California – Berkeley. Retrieved from http://www.escholarship.org/uc/item/3sb6n3n5

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):

Dana, Craig Matthew. “Cel7A Engineering and Expression.” 2013. Thesis, University of California – Berkeley. Accessed April 17, 2021. http://www.escholarship.org/uc/item/3sb6n3n5.

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

MLA Handbook (7th Edition):

Dana, Craig Matthew. “Cel7A Engineering and Expression.” 2013. Web. 17 Apr 2021.

Vancouver:

Dana CM. Cel7A Engineering and Expression. [Internet] [Thesis]. University of California – Berkeley; 2013. [cited 2021 Apr 17]. Available from: http://www.escholarship.org/uc/item/3sb6n3n5.

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

Council of Science Editors:

Dana CM. Cel7A Engineering and Expression. [Thesis]. University of California – Berkeley; 2013. Available from: http://www.escholarship.org/uc/item/3sb6n3n5

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


Universidade Nova

4. Silva, Maria Margarida dos Santos. Assessment of Notch1 ligands production - key protein targets in breast cancer.

Degree: 2014, Universidade Nova

Cell-to-cell communication is required for many biological processes in development and adult life. One of the most common systems utilized by a wide range of… (more)

Subjects/Keywords: Notch signalling; Breast cancer; Recombinant protein expression; Macromolecular crystallisation

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APA (6th Edition):

Silva, M. M. d. S. (2014). Assessment of Notch1 ligands production - key protein targets in breast cancer. (Thesis). Universidade Nova. Retrieved from http://www.rcaap.pt/detail.jsp?id=oai:run.unl.pt:10362/13638

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):

Silva, Maria Margarida dos Santos. “Assessment of Notch1 ligands production - key protein targets in breast cancer.” 2014. Thesis, Universidade Nova. Accessed April 17, 2021. http://www.rcaap.pt/detail.jsp?id=oai:run.unl.pt:10362/13638.

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

MLA Handbook (7th Edition):

Silva, Maria Margarida dos Santos. “Assessment of Notch1 ligands production - key protein targets in breast cancer.” 2014. Web. 17 Apr 2021.

Vancouver:

Silva MMdS. Assessment of Notch1 ligands production - key protein targets in breast cancer. [Internet] [Thesis]. Universidade Nova; 2014. [cited 2021 Apr 17]. Available from: http://www.rcaap.pt/detail.jsp?id=oai:run.unl.pt:10362/13638.

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

Council of Science Editors:

Silva MMdS. Assessment of Notch1 ligands production - key protein targets in breast cancer. [Thesis]. Universidade Nova; 2014. Available from: http://www.rcaap.pt/detail.jsp?id=oai:run.unl.pt:10362/13638

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


North-West University

5. Van Vuuren, Lihandra Jansen. Identification and expression of proteases C. sonorensis and C. imicola important for African horsesickness virus replication / Lihandra Jansen van Vuuren .

Degree: 2014, North-West University

 African horsesickness (AHS) is one of the most deadly diseases of horses, with a mortality rate of over 90% in horses that have not been… (more)

Subjects/Keywords: African horsesickness virus; Culicoides imicola; Culicoides sonorensis; Protease expression; Proteolytic activity; Recombinant protein expression

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APA (6th Edition):

Van Vuuren, L. J. (2014). Identification and expression of proteases C. sonorensis and C. imicola important for African horsesickness virus replication / Lihandra Jansen van Vuuren . (Thesis). North-West University. Retrieved from http://hdl.handle.net/10394/10742

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):

Van Vuuren, Lihandra Jansen. “Identification and expression of proteases C. sonorensis and C. imicola important for African horsesickness virus replication / Lihandra Jansen van Vuuren .” 2014. Thesis, North-West University. Accessed April 17, 2021. http://hdl.handle.net/10394/10742.

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

MLA Handbook (7th Edition):

Van Vuuren, Lihandra Jansen. “Identification and expression of proteases C. sonorensis and C. imicola important for African horsesickness virus replication / Lihandra Jansen van Vuuren .” 2014. Web. 17 Apr 2021.

Vancouver:

Van Vuuren LJ. Identification and expression of proteases C. sonorensis and C. imicola important for African horsesickness virus replication / Lihandra Jansen van Vuuren . [Internet] [Thesis]. North-West University; 2014. [cited 2021 Apr 17]. Available from: http://hdl.handle.net/10394/10742.

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

Council of Science Editors:

Van Vuuren LJ. Identification and expression of proteases C. sonorensis and C. imicola important for African horsesickness virus replication / Lihandra Jansen van Vuuren . [Thesis]. North-West University; 2014. Available from: http://hdl.handle.net/10394/10742

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


San Jose State University

6. Nilasari, Dewi. Expression of Recombinant Green Fluorescent Protein in Bacillus methanolicus.

Degree: MS, Chemical and Materials Engineering, 2011, San Jose State University

  Microbial biocatalysts are used in a wide range of industries to produce large scale quantities of proteins, amino acids, and commodity chemicals. Most of… (more)

Subjects/Keywords: Bacillus methanolicus; Electroporation; Green Fluorescent Protein (GFP); Intracellular pH; Recombinant protein expression

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APA (6th Edition):

Nilasari, D. (2011). Expression of Recombinant Green Fluorescent Protein in Bacillus methanolicus. (Masters Thesis). San Jose State University. Retrieved from https://doi.org/10.31979/etd.2xyd-dbrt ; https://scholarworks.sjsu.edu/etd_theses/4107

Chicago Manual of Style (16th Edition):

Nilasari, Dewi. “Expression of Recombinant Green Fluorescent Protein in Bacillus methanolicus.” 2011. Masters Thesis, San Jose State University. Accessed April 17, 2021. https://doi.org/10.31979/etd.2xyd-dbrt ; https://scholarworks.sjsu.edu/etd_theses/4107.

MLA Handbook (7th Edition):

Nilasari, Dewi. “Expression of Recombinant Green Fluorescent Protein in Bacillus methanolicus.” 2011. Web. 17 Apr 2021.

Vancouver:

Nilasari D. Expression of Recombinant Green Fluorescent Protein in Bacillus methanolicus. [Internet] [Masters thesis]. San Jose State University; 2011. [cited 2021 Apr 17]. Available from: https://doi.org/10.31979/etd.2xyd-dbrt ; https://scholarworks.sjsu.edu/etd_theses/4107.

Council of Science Editors:

Nilasari D. Expression of Recombinant Green Fluorescent Protein in Bacillus methanolicus. [Masters Thesis]. San Jose State University; 2011. Available from: https://doi.org/10.31979/etd.2xyd-dbrt ; https://scholarworks.sjsu.edu/etd_theses/4107


University of Manchester

7. Carballo Amador, Manuel. Altering the solubility of recombinant proteins through modification of surface features.

Degree: 2015, University of Manchester

Protein solubility plays an important role whether for biophysical and structural studies, or for production and delivery of therapeutic proteins. Poor solubility could lead to… (more)

Subjects/Keywords: protein solubility; protein aggregation; recombinant expression; solubility prediction; E. coli; HEK 293-EBNA

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APA (6th Edition):

Carballo Amador, M. (2015). Altering the solubility of recombinant proteins through modification of surface features. (Doctoral Dissertation). University of Manchester. Retrieved from http://www.manchester.ac.uk/escholar/uk-ac-man-scw:262813

Chicago Manual of Style (16th Edition):

Carballo Amador, Manuel. “Altering the solubility of recombinant proteins through modification of surface features.” 2015. Doctoral Dissertation, University of Manchester. Accessed April 17, 2021. http://www.manchester.ac.uk/escholar/uk-ac-man-scw:262813.

MLA Handbook (7th Edition):

Carballo Amador, Manuel. “Altering the solubility of recombinant proteins through modification of surface features.” 2015. Web. 17 Apr 2021.

Vancouver:

Carballo Amador M. Altering the solubility of recombinant proteins through modification of surface features. [Internet] [Doctoral dissertation]. University of Manchester; 2015. [cited 2021 Apr 17]. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:262813.

Council of Science Editors:

Carballo Amador M. Altering the solubility of recombinant proteins through modification of surface features. [Doctoral Dissertation]. University of Manchester; 2015. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:262813


University of Melbourne

8. PUTRI, MARIA THERESIA KHRISDIANA. Examination of the H5N1 avian influenza virus epitopes for differentiation between infected and vaccinated animals.

Degree: 2015, University of Melbourne

 Avian Influenza Virus H5N1 has been a significant pathogen in veterinary and public health since it first appearance in 1996, particularly in countries such as… (more)

Subjects/Keywords: H5N1; Avian Influenza Virus; epitopes; DIVA; Indonesia; ELISA; peptide; recombinant protein; protein expression; epitope mapping

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APA (6th Edition):

PUTRI, M. T. K. (2015). Examination of the H5N1 avian influenza virus epitopes for differentiation between infected and vaccinated animals. (Doctoral Dissertation). University of Melbourne. Retrieved from http://hdl.handle.net/11343/56523

Chicago Manual of Style (16th Edition):

PUTRI, MARIA THERESIA KHRISDIANA. “Examination of the H5N1 avian influenza virus epitopes for differentiation between infected and vaccinated animals.” 2015. Doctoral Dissertation, University of Melbourne. Accessed April 17, 2021. http://hdl.handle.net/11343/56523.

MLA Handbook (7th Edition):

PUTRI, MARIA THERESIA KHRISDIANA. “Examination of the H5N1 avian influenza virus epitopes for differentiation between infected and vaccinated animals.” 2015. Web. 17 Apr 2021.

Vancouver:

PUTRI MTK. Examination of the H5N1 avian influenza virus epitopes for differentiation between infected and vaccinated animals. [Internet] [Doctoral dissertation]. University of Melbourne; 2015. [cited 2021 Apr 17]. Available from: http://hdl.handle.net/11343/56523.

Council of Science Editors:

PUTRI MTK. Examination of the H5N1 avian influenza virus epitopes for differentiation between infected and vaccinated animals. [Doctoral Dissertation]. University of Melbourne; 2015. Available from: http://hdl.handle.net/11343/56523


University of Manchester

9. Carballo Amador, Manuel. Altering the solubility of recombinant proteins through modification of surface features.

Degree: PhD, 2015, University of Manchester

Protein solubility plays an important role whether for biophysical and structural studies, or for production and delivery of therapeutic proteins. Poor solubility could lead to… (more)

Subjects/Keywords: 572; HEK 293-EBNA; E. coli; solubility prediction; protein aggregation; protein solubility; recombinant expression

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APA (6th Edition):

Carballo Amador, M. (2015). Altering the solubility of recombinant proteins through modification of surface features. (Doctoral Dissertation). University of Manchester. Retrieved from https://www.research.manchester.ac.uk/portal/en/theses/altering-the-solubility-of-recombinant-proteins-through-modification-of-surface-features(a2a7e7d5-3cc5-4f0c-924e-61bb817c0f3e).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.764393

Chicago Manual of Style (16th Edition):

Carballo Amador, Manuel. “Altering the solubility of recombinant proteins through modification of surface features.” 2015. Doctoral Dissertation, University of Manchester. Accessed April 17, 2021. https://www.research.manchester.ac.uk/portal/en/theses/altering-the-solubility-of-recombinant-proteins-through-modification-of-surface-features(a2a7e7d5-3cc5-4f0c-924e-61bb817c0f3e).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.764393.

MLA Handbook (7th Edition):

Carballo Amador, Manuel. “Altering the solubility of recombinant proteins through modification of surface features.” 2015. Web. 17 Apr 2021.

Vancouver:

Carballo Amador M. Altering the solubility of recombinant proteins through modification of surface features. [Internet] [Doctoral dissertation]. University of Manchester; 2015. [cited 2021 Apr 17]. Available from: https://www.research.manchester.ac.uk/portal/en/theses/altering-the-solubility-of-recombinant-proteins-through-modification-of-surface-features(a2a7e7d5-3cc5-4f0c-924e-61bb817c0f3e).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.764393.

Council of Science Editors:

Carballo Amador M. Altering the solubility of recombinant proteins through modification of surface features. [Doctoral Dissertation]. University of Manchester; 2015. Available from: https://www.research.manchester.ac.uk/portal/en/theses/altering-the-solubility-of-recombinant-proteins-through-modification-of-surface-features(a2a7e7d5-3cc5-4f0c-924e-61bb817c0f3e).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.764393


University of Sydney

10. Wu, Jiadai. Haliotis rubra hemocyanin: sequencing, recombinant expression and investigation of the binding activities of expressed function units with HSV-1 .

Degree: 2017, University of Sydney

 Hemocyanin (HrH) has been shown to possess antiviral activity against HSV-1 by selectively binding to viral glycoproteins (gB, gC, gD). Its large size however precluded… (more)

Subjects/Keywords: Haliotis rubra hemocyanin; Herpes Simplex Virus type 1; Gene Clone; Protein recombinant expression; Protein purification; Protein-protein interaction

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APA (6th Edition):

Wu, J. (2017). Haliotis rubra hemocyanin: sequencing, recombinant expression and investigation of the binding activities of expressed function units with HSV-1 . (Thesis). University of Sydney. Retrieved from http://hdl.handle.net/2123/17792

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):

Wu, Jiadai. “Haliotis rubra hemocyanin: sequencing, recombinant expression and investigation of the binding activities of expressed function units with HSV-1 .” 2017. Thesis, University of Sydney. Accessed April 17, 2021. http://hdl.handle.net/2123/17792.

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

MLA Handbook (7th Edition):

Wu, Jiadai. “Haliotis rubra hemocyanin: sequencing, recombinant expression and investigation of the binding activities of expressed function units with HSV-1 .” 2017. Web. 17 Apr 2021.

Vancouver:

Wu J. Haliotis rubra hemocyanin: sequencing, recombinant expression and investigation of the binding activities of expressed function units with HSV-1 . [Internet] [Thesis]. University of Sydney; 2017. [cited 2021 Apr 17]. Available from: http://hdl.handle.net/2123/17792.

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

Council of Science Editors:

Wu J. Haliotis rubra hemocyanin: sequencing, recombinant expression and investigation of the binding activities of expressed function units with HSV-1 . [Thesis]. University of Sydney; 2017. Available from: http://hdl.handle.net/2123/17792

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


University of Pretoria

11. [No author]. Optimization of the heterologous expression of folate metabolic enzymes of Plasmodium falciparum .

Degree: 2011, University of Pretoria

 Malaria is a fatal tropical disease affecting billions of people in impoverished countries world-wide. An alarming fact is that a child in Africa dies of… (more)

Subjects/Keywords: Folate biosynthesis; Recombinant protein expression; Guanosine 5’ triphosphate; Codon harmonization; Malaria; UCTD

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APA (6th Edition):

author], [. (2011). Optimization of the heterologous expression of folate metabolic enzymes of Plasmodium falciparum . (Masters Thesis). University of Pretoria. Retrieved from http://upetd.up.ac.za/thesis/available/etd-03302011-181338/

Chicago Manual of Style (16th Edition):

author], [No. “Optimization of the heterologous expression of folate metabolic enzymes of Plasmodium falciparum .” 2011. Masters Thesis, University of Pretoria. Accessed April 17, 2021. http://upetd.up.ac.za/thesis/available/etd-03302011-181338/.

MLA Handbook (7th Edition):

author], [No. “Optimization of the heterologous expression of folate metabolic enzymes of Plasmodium falciparum .” 2011. Web. 17 Apr 2021.

Vancouver:

author] [. Optimization of the heterologous expression of folate metabolic enzymes of Plasmodium falciparum . [Internet] [Masters thesis]. University of Pretoria; 2011. [cited 2021 Apr 17]. Available from: http://upetd.up.ac.za/thesis/available/etd-03302011-181338/.

Council of Science Editors:

author] [. Optimization of the heterologous expression of folate metabolic enzymes of Plasmodium falciparum . [Masters Thesis]. University of Pretoria; 2011. Available from: http://upetd.up.ac.za/thesis/available/etd-03302011-181338/

12. 林, 亜由美. Is D-aspartate produced by glutamic-oxaloacetic transaminase-1 like 1(Got1l1), a putative aspartate racemase? : アスパラギン酸ラセマーゼとされる Got1l1 は、本当に D-アスパラギン酸を合成するのか?.

Degree: 博士(医学), 2016, University of Toyama / 富山大学

富山大学・富生命博乙第5号・林亜由美・2015/01/22

Amino Acids. 2015 Jan;47(1):79-86. doi: 10.1007/s00726-014-1847-3.に掲載。出版社版はhttp://link.springer.com/article/10.1007%2Fs00726-014-1847-3(オープンアクセス)

2014

Subjects/Keywords: Glutamic-oxaloacetic transaminase-1 like 1; D-Aspartate; Knockout mice; Testis; Hippocampus; Recombinant protein expression

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APA (6th Edition):

林, . (2016). Is D-aspartate produced by glutamic-oxaloacetic transaminase-1 like 1(Got1l1), a putative aspartate racemase? : アスパラギン酸ラセマーゼとされる Got1l1 は、本当に D-アスパラギン酸を合成するのか?. (Thesis). University of Toyama / 富山大学. Retrieved from http://hdl.handle.net/10110/13665 ; http://dx.doi.org/10.15099/00005039

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):

林, 亜由美. “Is D-aspartate produced by glutamic-oxaloacetic transaminase-1 like 1(Got1l1), a putative aspartate racemase? : アスパラギン酸ラセマーゼとされる Got1l1 は、本当に D-アスパラギン酸を合成するのか?.” 2016. Thesis, University of Toyama / 富山大学. Accessed April 17, 2021. http://hdl.handle.net/10110/13665 ; http://dx.doi.org/10.15099/00005039.

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

MLA Handbook (7th Edition):

林, 亜由美. “Is D-aspartate produced by glutamic-oxaloacetic transaminase-1 like 1(Got1l1), a putative aspartate racemase? : アスパラギン酸ラセマーゼとされる Got1l1 は、本当に D-アスパラギン酸を合成するのか?.” 2016. Web. 17 Apr 2021.

Vancouver:

林 . Is D-aspartate produced by glutamic-oxaloacetic transaminase-1 like 1(Got1l1), a putative aspartate racemase? : アスパラギン酸ラセマーゼとされる Got1l1 は、本当に D-アスパラギン酸を合成するのか?. [Internet] [Thesis]. University of Toyama / 富山大学; 2016. [cited 2021 Apr 17]. Available from: http://hdl.handle.net/10110/13665 ; http://dx.doi.org/10.15099/00005039.

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

Council of Science Editors:

林 . Is D-aspartate produced by glutamic-oxaloacetic transaminase-1 like 1(Got1l1), a putative aspartate racemase? : アスパラギン酸ラセマーゼとされる Got1l1 は、本当に D-アスパラギン酸を合成するのか?. [Thesis]. University of Toyama / 富山大学; 2016. Available from: http://hdl.handle.net/10110/13665 ; http://dx.doi.org/10.15099/00005039

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


University of Pretoria

13. Goolab, Shivani. Optimization of the heterologous expression of folate metabolic enzymes of Plasmodium falciparum.

Degree: Biochemistry, 2011, University of Pretoria

 Malaria is a fatal tropical disease affecting billions of people in impoverished countries world-wide. An alarming fact is that a child in Africa dies of… (more)

Subjects/Keywords: Folate biosynthesis; Recombinant protein expression; Guanosine 5’ triphosphate; Codon harmonization; Malaria; UCTD

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APA (6th Edition):

Goolab, S. (2011). Optimization of the heterologous expression of folate metabolic enzymes of Plasmodium falciparum. (Masters Thesis). University of Pretoria. Retrieved from http://hdl.handle.net/2263/23647

Chicago Manual of Style (16th Edition):

Goolab, Shivani. “Optimization of the heterologous expression of folate metabolic enzymes of Plasmodium falciparum.” 2011. Masters Thesis, University of Pretoria. Accessed April 17, 2021. http://hdl.handle.net/2263/23647.

MLA Handbook (7th Edition):

Goolab, Shivani. “Optimization of the heterologous expression of folate metabolic enzymes of Plasmodium falciparum.” 2011. Web. 17 Apr 2021.

Vancouver:

Goolab S. Optimization of the heterologous expression of folate metabolic enzymes of Plasmodium falciparum. [Internet] [Masters thesis]. University of Pretoria; 2011. [cited 2021 Apr 17]. Available from: http://hdl.handle.net/2263/23647.

Council of Science Editors:

Goolab S. Optimization of the heterologous expression of folate metabolic enzymes of Plasmodium falciparum. [Masters Thesis]. University of Pretoria; 2011. Available from: http://hdl.handle.net/2263/23647


Queensland University of Technology

14. Chanson, Aurelie Heitiare. Recombinant protein production using a Tobacco yellow dwarf virus-based episomal expression vector : control of Rep activity.

Degree: 2009, Queensland University of Technology

 Over the past decade, plants have been used as expression hosts for the production of pharmaceutically important and commercially valuable proteins. Plants offer many advantages… (more)

Subjects/Keywords: recombinant protein production; tobacco yellow dwarf virus; episomal expression vector; Rep activity

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APA (6th Edition):

Chanson, A. H. (2009). Recombinant protein production using a Tobacco yellow dwarf virus-based episomal expression vector : control of Rep activity. (Thesis). Queensland University of Technology. Retrieved from https://eprints.qut.edu.au/30290/

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):

Chanson, Aurelie Heitiare. “Recombinant protein production using a Tobacco yellow dwarf virus-based episomal expression vector : control of Rep activity.” 2009. Thesis, Queensland University of Technology. Accessed April 17, 2021. https://eprints.qut.edu.au/30290/.

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

MLA Handbook (7th Edition):

Chanson, Aurelie Heitiare. “Recombinant protein production using a Tobacco yellow dwarf virus-based episomal expression vector : control of Rep activity.” 2009. Web. 17 Apr 2021.

Vancouver:

Chanson AH. Recombinant protein production using a Tobacco yellow dwarf virus-based episomal expression vector : control of Rep activity. [Internet] [Thesis]. Queensland University of Technology; 2009. [cited 2021 Apr 17]. Available from: https://eprints.qut.edu.au/30290/.

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

Council of Science Editors:

Chanson AH. Recombinant protein production using a Tobacco yellow dwarf virus-based episomal expression vector : control of Rep activity. [Thesis]. Queensland University of Technology; 2009. Available from: https://eprints.qut.edu.au/30290/

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


Universidade Nova

15. Pereira, João Nuno dos Santos. Establishing a high titer transient gene expression process in conditioned media for CHO-DG44 cells.

Degree: 2011, Universidade Nova

Dissertação para obtenção do Grau de Mestre em Biotecnologia

Transient gene expression (TGE) allows for fast protein production in mammalian cells and has become a… (more)

Subjects/Keywords: Transient gene expression; Recombinant protein production; CHO cells; Conditioned medium; Scale-up

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APA (6th Edition):

Pereira, J. N. d. S. (2011). Establishing a high titer transient gene expression process in conditioned media for CHO-DG44 cells. (Thesis). Universidade Nova. Retrieved from http://www.rcaap.pt/detail.jsp?id=oai:run.unl.pt:10362/6149

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):

Pereira, João Nuno dos Santos. “Establishing a high titer transient gene expression process in conditioned media for CHO-DG44 cells.” 2011. Thesis, Universidade Nova. Accessed April 17, 2021. http://www.rcaap.pt/detail.jsp?id=oai:run.unl.pt:10362/6149.

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

MLA Handbook (7th Edition):

Pereira, João Nuno dos Santos. “Establishing a high titer transient gene expression process in conditioned media for CHO-DG44 cells.” 2011. Web. 17 Apr 2021.

Vancouver:

Pereira JNdS. Establishing a high titer transient gene expression process in conditioned media for CHO-DG44 cells. [Internet] [Thesis]. Universidade Nova; 2011. [cited 2021 Apr 17]. Available from: http://www.rcaap.pt/detail.jsp?id=oai:run.unl.pt:10362/6149.

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

Council of Science Editors:

Pereira JNdS. Establishing a high titer transient gene expression process in conditioned media for CHO-DG44 cells. [Thesis]. Universidade Nova; 2011. Available from: http://www.rcaap.pt/detail.jsp?id=oai:run.unl.pt:10362/6149

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


Linköping University

16. Lundén, Amanda. Can Sterol Carrie Protein-2 function as a solubility tag in E.coli?.

Degree: Biology, 2016, Linköping University

  Expressing foreign proteins in E.coli is a major challenge because they often tend to develop into unsolvable and inactive proteins. They aggregate into so… (more)

Subjects/Keywords: CATΔ9; E.coli; GFP; pET-15b; protein expression; recombinant proteins; SCP-2; Solubility tag

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APA (6th Edition):

Lundén, A. (2016). Can Sterol Carrie Protein-2 function as a solubility tag in E.coli?. (Thesis). Linköping University. Retrieved from http://urn.kb.se/resolve?urn=urn:nbn:se:liu:diva-129803

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):

Lundén, Amanda. “Can Sterol Carrie Protein-2 function as a solubility tag in E.coli?.” 2016. Thesis, Linköping University. Accessed April 17, 2021. http://urn.kb.se/resolve?urn=urn:nbn:se:liu:diva-129803.

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

MLA Handbook (7th Edition):

Lundén, Amanda. “Can Sterol Carrie Protein-2 function as a solubility tag in E.coli?.” 2016. Web. 17 Apr 2021.

Vancouver:

Lundén A. Can Sterol Carrie Protein-2 function as a solubility tag in E.coli?. [Internet] [Thesis]. Linköping University; 2016. [cited 2021 Apr 17]. Available from: http://urn.kb.se/resolve?urn=urn:nbn:se:liu:diva-129803.

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

Council of Science Editors:

Lundén A. Can Sterol Carrie Protein-2 function as a solubility tag in E.coli?. [Thesis]. Linköping University; 2016. Available from: http://urn.kb.se/resolve?urn=urn:nbn:se:liu:diva-129803

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


University of Georgia

17. Barbosa, Taylor Marcelo Correa. Molecular characterization of natural recombinant ALVS and their use as vectors for gene delivery into stable cell lines.

Degree: 2014, University of Georgia

 Avian Leukosis viruses (ALV) previously found as contaminant of Marek’s Disease vaccines were molecularly characterized. All three isolates, named PDRC-1039, PDRC-3246 and PDRC-32-49, were found… (more)

Subjects/Keywords: Avian Leukosis Virus; ALV; Retrovirus; Retroviral Vector; Gene delivery; Transduction; Stable expression; Recombinant protein expression; Avian cells; Vaccine

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APA (6th Edition):

Barbosa, T. M. C. (2014). Molecular characterization of natural recombinant ALVS and their use as vectors for gene delivery into stable cell lines. (Thesis). University of Georgia. Retrieved from http://hdl.handle.net/10724/26226

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):

Barbosa, Taylor Marcelo Correa. “Molecular characterization of natural recombinant ALVS and their use as vectors for gene delivery into stable cell lines.” 2014. Thesis, University of Georgia. Accessed April 17, 2021. http://hdl.handle.net/10724/26226.

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

MLA Handbook (7th Edition):

Barbosa, Taylor Marcelo Correa. “Molecular characterization of natural recombinant ALVS and their use as vectors for gene delivery into stable cell lines.” 2014. Web. 17 Apr 2021.

Vancouver:

Barbosa TMC. Molecular characterization of natural recombinant ALVS and their use as vectors for gene delivery into stable cell lines. [Internet] [Thesis]. University of Georgia; 2014. [cited 2021 Apr 17]. Available from: http://hdl.handle.net/10724/26226.

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

Council of Science Editors:

Barbosa TMC. Molecular characterization of natural recombinant ALVS and their use as vectors for gene delivery into stable cell lines. [Thesis]. University of Georgia; 2014. Available from: http://hdl.handle.net/10724/26226

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

18. Del Greco, Elizabeth. Mammalian Cell Line Development Platform for Recombinant Protein Production: Expanding the Protein Expression Toolbox for Research and Drug Discovery Applications.

Degree: MS, Biological Sciences, 2017, Dominican University of California

Recombinant proteins have revolutionized the biomedical industry, providing therapeutics for life-threatening diseases and protein reagents for research applications. BioMarin Pharmaceutical Inc. develops recombinant protein(more)

Subjects/Keywords: recombinant protein production; protein expression; cell line development; enzyme replacement therapy; lysosomal storage disorder; SP2/0 cell line; Biotechnology

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APA (6th Edition):

Del Greco, E. (2017). Mammalian Cell Line Development Platform for Recombinant Protein Production: Expanding the Protein Expression Toolbox for Research and Drug Discovery Applications. (Masters Thesis). Dominican University of California. Retrieved from https://scholar.dominican.edu/masters-theses/283

Chicago Manual of Style (16th Edition):

Del Greco, Elizabeth. “Mammalian Cell Line Development Platform for Recombinant Protein Production: Expanding the Protein Expression Toolbox for Research and Drug Discovery Applications.” 2017. Masters Thesis, Dominican University of California. Accessed April 17, 2021. https://scholar.dominican.edu/masters-theses/283.

MLA Handbook (7th Edition):

Del Greco, Elizabeth. “Mammalian Cell Line Development Platform for Recombinant Protein Production: Expanding the Protein Expression Toolbox for Research and Drug Discovery Applications.” 2017. Web. 17 Apr 2021.

Vancouver:

Del Greco E. Mammalian Cell Line Development Platform for Recombinant Protein Production: Expanding the Protein Expression Toolbox for Research and Drug Discovery Applications. [Internet] [Masters thesis]. Dominican University of California; 2017. [cited 2021 Apr 17]. Available from: https://scholar.dominican.edu/masters-theses/283.

Council of Science Editors:

Del Greco E. Mammalian Cell Line Development Platform for Recombinant Protein Production: Expanding the Protein Expression Toolbox for Research and Drug Discovery Applications. [Masters Thesis]. Dominican University of California; 2017. Available from: https://scholar.dominican.edu/masters-theses/283


University of Manitoba

19. Thorington, Robyn. An in vitro RNA synthesis assay to measure the fidelity of the measles virus polymerase.

Degree: Medical Microbiology and Infectious Diseases, 2020, University of Manitoba

 In the year 2000, the World Health Organization began its efforts to eradicate the measles virus (MeV) that lead to both a drastic decrease in… (more)

Subjects/Keywords: Measles virus; RdRp; Viral polymerase; Recombinant protein expression; in vitro RNA synthesis; Measles large protein; Measles nucleoprotein; Measles phosphoprotein

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APA (6th Edition):

Thorington, R. (2020). An in vitro RNA synthesis assay to measure the fidelity of the measles virus polymerase. (Masters Thesis). University of Manitoba. Retrieved from http://hdl.handle.net/1993/34543

Chicago Manual of Style (16th Edition):

Thorington, Robyn. “An in vitro RNA synthesis assay to measure the fidelity of the measles virus polymerase.” 2020. Masters Thesis, University of Manitoba. Accessed April 17, 2021. http://hdl.handle.net/1993/34543.

MLA Handbook (7th Edition):

Thorington, Robyn. “An in vitro RNA synthesis assay to measure the fidelity of the measles virus polymerase.” 2020. Web. 17 Apr 2021.

Vancouver:

Thorington R. An in vitro RNA synthesis assay to measure the fidelity of the measles virus polymerase. [Internet] [Masters thesis]. University of Manitoba; 2020. [cited 2021 Apr 17]. Available from: http://hdl.handle.net/1993/34543.

Council of Science Editors:

Thorington R. An in vitro RNA synthesis assay to measure the fidelity of the measles virus polymerase. [Masters Thesis]. University of Manitoba; 2020. Available from: http://hdl.handle.net/1993/34543


Indian Institute of Science

20. Manoharan, Simna. Engineering the N-Glycosylation Pathway in Pichia Pastoris for the Expression of Glycoprotein Hormones.

Degree: PhD, Faculty of Engineering, 2018, Indian Institute of Science

 Proteins, participating in a myriad of biological function, are at the core of all cellular activities occurring within living organisms. Therapeutic proteins, hence constitute a… (more)

Subjects/Keywords: Glycoprotein Hormones; N-Glycosylation; Recombinant Protein Expression; Pichia Pastoris N-Glycosylation; Industrial Proteins; Glycosylated Protein Expression; Protein Glycosylation; Glycoengineered Pichia Pastoris; Human Chorionic Gonadotropin (hCG); Follicle Stimulating Hormone (FSH); Therapeutic Proteins; Glycoprotein Hormone Expression; Recombinant Therapeutic Proteins; Pichia pastoris; Glycoengineered Strains; Chemical Engineering

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APA (6th Edition):

Manoharan, S. (2018). Engineering the N-Glycosylation Pathway in Pichia Pastoris for the Expression of Glycoprotein Hormones. (Doctoral Dissertation). Indian Institute of Science. Retrieved from http://etd.iisc.ac.in/handle/2005/3017

Chicago Manual of Style (16th Edition):

Manoharan, Simna. “Engineering the N-Glycosylation Pathway in Pichia Pastoris for the Expression of Glycoprotein Hormones.” 2018. Doctoral Dissertation, Indian Institute of Science. Accessed April 17, 2021. http://etd.iisc.ac.in/handle/2005/3017.

MLA Handbook (7th Edition):

Manoharan, Simna. “Engineering the N-Glycosylation Pathway in Pichia Pastoris for the Expression of Glycoprotein Hormones.” 2018. Web. 17 Apr 2021.

Vancouver:

Manoharan S. Engineering the N-Glycosylation Pathway in Pichia Pastoris for the Expression of Glycoprotein Hormones. [Internet] [Doctoral dissertation]. Indian Institute of Science; 2018. [cited 2021 Apr 17]. Available from: http://etd.iisc.ac.in/handle/2005/3017.

Council of Science Editors:

Manoharan S. Engineering the N-Glycosylation Pathway in Pichia Pastoris for the Expression of Glycoprotein Hormones. [Doctoral Dissertation]. Indian Institute of Science; 2018. Available from: http://etd.iisc.ac.in/handle/2005/3017


University of Oulu

21. Nokelainen, M. (Minna). Recombinant human collagens:characterization of type II collagen expressed in insect cells and production of types I-III collagen in the yeast Pichia pastoris.

Degree: 2000, University of Oulu

 Abstract An efficient system for expressing recombinant human collagens is expected to have numerous scientific and medical applications, but this is difficult to achieve because… (more)

Subjects/Keywords: procollagen; prolyl 4-hydroxylase; recombinant protein expression

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APA (6th Edition):

Nokelainen, M. (. (2000). Recombinant human collagens:characterization of type II collagen expressed in insect cells and production of types I-III collagen in the yeast Pichia pastoris. (Doctoral Dissertation). University of Oulu. Retrieved from http://urn.fi/urn:isbn:9514257383

Chicago Manual of Style (16th Edition):

Nokelainen, M (Minna). “Recombinant human collagens:characterization of type II collagen expressed in insect cells and production of types I-III collagen in the yeast Pichia pastoris.” 2000. Doctoral Dissertation, University of Oulu. Accessed April 17, 2021. http://urn.fi/urn:isbn:9514257383.

MLA Handbook (7th Edition):

Nokelainen, M (Minna). “Recombinant human collagens:characterization of type II collagen expressed in insect cells and production of types I-III collagen in the yeast Pichia pastoris.” 2000. Web. 17 Apr 2021.

Vancouver:

Nokelainen M(. Recombinant human collagens:characterization of type II collagen expressed in insect cells and production of types I-III collagen in the yeast Pichia pastoris. [Internet] [Doctoral dissertation]. University of Oulu; 2000. [cited 2021 Apr 17]. Available from: http://urn.fi/urn:isbn:9514257383.

Council of Science Editors:

Nokelainen M(. Recombinant human collagens:characterization of type II collagen expressed in insect cells and production of types I-III collagen in the yeast Pichia pastoris. [Doctoral Dissertation]. University of Oulu; 2000. Available from: http://urn.fi/urn:isbn:9514257383


Freie Universität Berlin

22. Klatt, Stephan. Evaluierung des einzelligen Parasiten L. tarentolae als eukaryotischer Expressionswirt für die biomedizinische Forschung.

Degree: 2013, Freie Universität Berlin

 Leishmania tarentolae ist ein einzelliger, eukaryotischer Parasit, welcher zur Gattung der Leishmanien gehört. Er wird von Sandmücken übertragen und infiziert – im Gegensatz zu seinen… (more)

Subjects/Keywords: Leishmania tarentolae; recombinant protein expression; glycoprotein analysis; in-vivo biotinylation; signal peptide modification; 500 Naturwissenschaften und Mathematik::570 Biowissenschaften; Biologie

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APA (6th Edition):

Klatt, S. (2013). Evaluierung des einzelligen Parasiten L. tarentolae als eukaryotischer Expressionswirt für die biomedizinische Forschung. (Thesis). Freie Universität Berlin. Retrieved from http://dx.doi.org/10.17169/refubium-10951

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):

Klatt, Stephan. “Evaluierung des einzelligen Parasiten L. tarentolae als eukaryotischer Expressionswirt für die biomedizinische Forschung.” 2013. Thesis, Freie Universität Berlin. Accessed April 17, 2021. http://dx.doi.org/10.17169/refubium-10951.

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

MLA Handbook (7th Edition):

Klatt, Stephan. “Evaluierung des einzelligen Parasiten L. tarentolae als eukaryotischer Expressionswirt für die biomedizinische Forschung.” 2013. Web. 17 Apr 2021.

Vancouver:

Klatt S. Evaluierung des einzelligen Parasiten L. tarentolae als eukaryotischer Expressionswirt für die biomedizinische Forschung. [Internet] [Thesis]. Freie Universität Berlin; 2013. [cited 2021 Apr 17]. Available from: http://dx.doi.org/10.17169/refubium-10951.

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

Council of Science Editors:

Klatt S. Evaluierung des einzelligen Parasiten L. tarentolae als eukaryotischer Expressionswirt für die biomedizinische Forschung. [Thesis]. Freie Universität Berlin; 2013. Available from: http://dx.doi.org/10.17169/refubium-10951

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


University of Washington

23. Slogic, Patrick. Predicting expression levels of de novo protein designs in yeast through machine learning.

Degree: 2020, University of Washington

Protein engineering has unlocked potential for the biomolecular synthesis of amino acid sequences with specified functions. With the many implications in enhancing therapy development, developing… (more)

Subjects/Keywords: Deep learning; Machine learning; Molecular engineering; Protein engineering; Recombinant DNA; Yeast expression; Molecular biology; Computer science; Biomedical engineering; Bioengineering

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APA (6th Edition):

Slogic, P. (2020). Predicting expression levels of de novo protein designs in yeast through machine learning. (Thesis). University of Washington. Retrieved from http://hdl.handle.net/1773/45844

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):

Slogic, Patrick. “Predicting expression levels of de novo protein designs in yeast through machine learning.” 2020. Thesis, University of Washington. Accessed April 17, 2021. http://hdl.handle.net/1773/45844.

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

MLA Handbook (7th Edition):

Slogic, Patrick. “Predicting expression levels of de novo protein designs in yeast through machine learning.” 2020. Web. 17 Apr 2021.

Vancouver:

Slogic P. Predicting expression levels of de novo protein designs in yeast through machine learning. [Internet] [Thesis]. University of Washington; 2020. [cited 2021 Apr 17]. Available from: http://hdl.handle.net/1773/45844.

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

Council of Science Editors:

Slogic P. Predicting expression levels of de novo protein designs in yeast through machine learning. [Thesis]. University of Washington; 2020. Available from: http://hdl.handle.net/1773/45844

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


Michigan Technological University

24. Hopson, Sarah. Heterologous Expression and Purification of Full-Length Human Polybromo-1 Protein.

Degree: PhD, Department of Chemistry, 2017, Michigan Technological University

  Over the past decade, it has become apparent that the human polybromo-1 protein (BAF180) has a critical role in cancer. BAF180 is known to… (more)

Subjects/Keywords: recombinant protein expression and purification; human polybromo-1; BAF180; PBRM1; hPB1; Pichia pastoris; Biochemistry; Molecular Biology

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APA (6th Edition):

Hopson, S. (2017). Heterologous Expression and Purification of Full-Length Human Polybromo-1 Protein. (Doctoral Dissertation). Michigan Technological University. Retrieved from https://digitalcommons.mtu.edu/etdr/436

Chicago Manual of Style (16th Edition):

Hopson, Sarah. “Heterologous Expression and Purification of Full-Length Human Polybromo-1 Protein.” 2017. Doctoral Dissertation, Michigan Technological University. Accessed April 17, 2021. https://digitalcommons.mtu.edu/etdr/436.

MLA Handbook (7th Edition):

Hopson, Sarah. “Heterologous Expression and Purification of Full-Length Human Polybromo-1 Protein.” 2017. Web. 17 Apr 2021.

Vancouver:

Hopson S. Heterologous Expression and Purification of Full-Length Human Polybromo-1 Protein. [Internet] [Doctoral dissertation]. Michigan Technological University; 2017. [cited 2021 Apr 17]. Available from: https://digitalcommons.mtu.edu/etdr/436.

Council of Science Editors:

Hopson S. Heterologous Expression and Purification of Full-Length Human Polybromo-1 Protein. [Doctoral Dissertation]. Michigan Technological University; 2017. Available from: https://digitalcommons.mtu.edu/etdr/436


University of Lund

25. Lood, Rolf. Propionibacterium acnes and its phages.

Degree: 2011, University of Lund

 Microorganisms are everywhere! They can tolerate many diverse extreme environments, such as the human body. Even though many of us might associate the word microorganism… (more)

Subjects/Keywords: Other Clinical Medicine; Propionibacterium acnes; biofilm; bacteriophage; Siphovirus; pseudolysogeny; heme oxygenase; free radicals; recombinant protein expression; vector

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APA (6th Edition):

Lood, R. (2011). Propionibacterium acnes and its phages. (Doctoral Dissertation). University of Lund. Retrieved from https://lup.lub.lu.se/record/2155119 ; https://portal.research.lu.se/ws/files/3340443/2155133.pdf

Chicago Manual of Style (16th Edition):

Lood, Rolf. “Propionibacterium acnes and its phages.” 2011. Doctoral Dissertation, University of Lund. Accessed April 17, 2021. https://lup.lub.lu.se/record/2155119 ; https://portal.research.lu.se/ws/files/3340443/2155133.pdf.

MLA Handbook (7th Edition):

Lood, Rolf. “Propionibacterium acnes and its phages.” 2011. Web. 17 Apr 2021.

Vancouver:

Lood R. Propionibacterium acnes and its phages. [Internet] [Doctoral dissertation]. University of Lund; 2011. [cited 2021 Apr 17]. Available from: https://lup.lub.lu.se/record/2155119 ; https://portal.research.lu.se/ws/files/3340443/2155133.pdf.

Council of Science Editors:

Lood R. Propionibacterium acnes and its phages. [Doctoral Dissertation]. University of Lund; 2011. Available from: https://lup.lub.lu.se/record/2155119 ; https://portal.research.lu.se/ws/files/3340443/2155133.pdf


University of Melbourne

26. WEBER, DANIEL. Membrane interactions of the Alzheimer’s Aβ42 peptide and pore-forming protein equinatoxin II in atomistic detail.

Degree: 2015, University of Melbourne

 Cytolytic properties of membrane active peptides and proteins (MAPS), in particular the 42-residue isoform of the amyloid beta peptide (Aβ42) from Alzheimer’s disease and the… (more)

Subjects/Keywords: molecular dynamics; solid state NMR; solution NMR; membrane; amyloid; Equinatoxin; actinoporin; amyloid beta peptide; Alzheimer's disease; recombinant peptide; protein expression

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APA (6th Edition):

WEBER, D. (2015). Membrane interactions of the Alzheimer’s Aβ42 peptide and pore-forming protein equinatoxin II in atomistic detail. (Doctoral Dissertation). University of Melbourne. Retrieved from http://hdl.handle.net/11343/55101

Chicago Manual of Style (16th Edition):

WEBER, DANIEL. “Membrane interactions of the Alzheimer’s Aβ42 peptide and pore-forming protein equinatoxin II in atomistic detail.” 2015. Doctoral Dissertation, University of Melbourne. Accessed April 17, 2021. http://hdl.handle.net/11343/55101.

MLA Handbook (7th Edition):

WEBER, DANIEL. “Membrane interactions of the Alzheimer’s Aβ42 peptide and pore-forming protein equinatoxin II in atomistic detail.” 2015. Web. 17 Apr 2021.

Vancouver:

WEBER D. Membrane interactions of the Alzheimer’s Aβ42 peptide and pore-forming protein equinatoxin II in atomistic detail. [Internet] [Doctoral dissertation]. University of Melbourne; 2015. [cited 2021 Apr 17]. Available from: http://hdl.handle.net/11343/55101.

Council of Science Editors:

WEBER D. Membrane interactions of the Alzheimer’s Aβ42 peptide and pore-forming protein equinatoxin II in atomistic detail. [Doctoral Dissertation]. University of Melbourne; 2015. Available from: http://hdl.handle.net/11343/55101


University of Dundee

27. Sokolova, Antoaneta Y. Nitroaromatic pro-drug activation and resistance in the African trypanosome.

Degree: PhD, 2011, University of Dundee

 Sleeping sickness, caused by Trypanosoma brucei, is a deadly disease that affects some of the poorest countries in sub-Saharan Africa. Although the disease prevalence is… (more)

Subjects/Keywords: 615; Sleeping sickness; African trypanosomiasis; Trypanosome; Trypanosoma brucei; Trypanosomiasis; Resistance; Pro-drug; Nitroaromatic; Nitroheterocyclic; Nifurtimox; Fexinidazole; Nitroreductase; NTR; Recombinant expression; Protein

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APA (6th Edition):

Sokolova, A. Y. (2011). Nitroaromatic pro-drug activation and resistance in the African trypanosome. (Doctoral Dissertation). University of Dundee. Retrieved from https://discovery.dundee.ac.uk/en/studentTheses/52c1537e-4a37-446c-b62c-86df5b95b2ea ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.578815

Chicago Manual of Style (16th Edition):

Sokolova, Antoaneta Y. “Nitroaromatic pro-drug activation and resistance in the African trypanosome.” 2011. Doctoral Dissertation, University of Dundee. Accessed April 17, 2021. https://discovery.dundee.ac.uk/en/studentTheses/52c1537e-4a37-446c-b62c-86df5b95b2ea ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.578815.

MLA Handbook (7th Edition):

Sokolova, Antoaneta Y. “Nitroaromatic pro-drug activation and resistance in the African trypanosome.” 2011. Web. 17 Apr 2021.

Vancouver:

Sokolova AY. Nitroaromatic pro-drug activation and resistance in the African trypanosome. [Internet] [Doctoral dissertation]. University of Dundee; 2011. [cited 2021 Apr 17]. Available from: https://discovery.dundee.ac.uk/en/studentTheses/52c1537e-4a37-446c-b62c-86df5b95b2ea ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.578815.

Council of Science Editors:

Sokolova AY. Nitroaromatic pro-drug activation and resistance in the African trypanosome. [Doctoral Dissertation]. University of Dundee; 2011. Available from: https://discovery.dundee.ac.uk/en/studentTheses/52c1537e-4a37-446c-b62c-86df5b95b2ea ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.578815


Australian National University

28. Zelger, Renate. Detection of Plasmodium falciparum: From Biomarker Identification and Characterisation to Application .

Degree: 2016, Australian National University

 Malaria is one of the most deadly infectious diseases, responsible for 438 000 deaths and 214 million infections per year, mostly in developing countries. Ultra-sensitive… (more)

Subjects/Keywords: Plasmodium falciparum; malaria diagnosis; PfHSP20; PFC0685w; Pf08_0017; Pf14_0287; TT-lock immuno-qPCR; Dictyostelium discoideum; recombinant protein expression

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APA (6th Edition):

Zelger, R. (2016). Detection of Plasmodium falciparum: From Biomarker Identification and Characterisation to Application . (Thesis). Australian National University. Retrieved from http://hdl.handle.net/1885/118068

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):

Zelger, Renate. “Detection of Plasmodium falciparum: From Biomarker Identification and Characterisation to Application .” 2016. Thesis, Australian National University. Accessed April 17, 2021. http://hdl.handle.net/1885/118068.

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

MLA Handbook (7th Edition):

Zelger, Renate. “Detection of Plasmodium falciparum: From Biomarker Identification and Characterisation to Application .” 2016. Web. 17 Apr 2021.

Vancouver:

Zelger R. Detection of Plasmodium falciparum: From Biomarker Identification and Characterisation to Application . [Internet] [Thesis]. Australian National University; 2016. [cited 2021 Apr 17]. Available from: http://hdl.handle.net/1885/118068.

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

Council of Science Editors:

Zelger R. Detection of Plasmodium falciparum: From Biomarker Identification and Characterisation to Application . [Thesis]. Australian National University; 2016. Available from: http://hdl.handle.net/1885/118068

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

29. Marina Katia Ferreira Mazzoni. Clonagem e expressão de proteína antiapoptótica presente na hemolinfa de Lonomia obliqua WALKER 1855 (Lepdoptera: Saturniidae) em Escherichia coli.

Degree: 2015, University of São Paulo

A lagarta L. obliqua tem se destacado por apresentar em sua hemolinfa proteínas com atividade biológica demonstrada em cultivos celulares. A literatura disponível não apresenta… (more)

Subjects/Keywords: Escherichia coli; Lonomia obliqua; Antiapoptótica; Clonagem; Expressão gênica; Proteína recombinante; Escherichia coli; Lonomia obliqua; Antiapoptotic; Cloning; Gene expression; Recombinant protein

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APA (6th Edition):

Mazzoni, M. K. F. (2015). Clonagem e expressão de proteína antiapoptótica presente na hemolinfa de Lonomia obliqua WALKER 1855 (Lepdoptera: Saturniidae) em Escherichia coli. (Masters Thesis). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/87/87131/tde-07032016-134221/

Chicago Manual of Style (16th Edition):

Mazzoni, Marina Katia Ferreira. “Clonagem e expressão de proteína antiapoptótica presente na hemolinfa de Lonomia obliqua WALKER 1855 (Lepdoptera: Saturniidae) em Escherichia coli.” 2015. Masters Thesis, University of São Paulo. Accessed April 17, 2021. http://www.teses.usp.br/teses/disponiveis/87/87131/tde-07032016-134221/.

MLA Handbook (7th Edition):

Mazzoni, Marina Katia Ferreira. “Clonagem e expressão de proteína antiapoptótica presente na hemolinfa de Lonomia obliqua WALKER 1855 (Lepdoptera: Saturniidae) em Escherichia coli.” 2015. Web. 17 Apr 2021.

Vancouver:

Mazzoni MKF. Clonagem e expressão de proteína antiapoptótica presente na hemolinfa de Lonomia obliqua WALKER 1855 (Lepdoptera: Saturniidae) em Escherichia coli. [Internet] [Masters thesis]. University of São Paulo; 2015. [cited 2021 Apr 17]. Available from: http://www.teses.usp.br/teses/disponiveis/87/87131/tde-07032016-134221/.

Council of Science Editors:

Mazzoni MKF. Clonagem e expressão de proteína antiapoptótica presente na hemolinfa de Lonomia obliqua WALKER 1855 (Lepdoptera: Saturniidae) em Escherichia coli. [Masters Thesis]. University of São Paulo; 2015. Available from: http://www.teses.usp.br/teses/disponiveis/87/87131/tde-07032016-134221/


University of Manchester

30. French, Joseph. Towards an understanding of the burden of recombinant protein production.

Degree: 2016, University of Manchester

Recombinant protein technologies have emerged as important tools for the production of proteins with industrial, academic and biopharmaceutical applications. However, current process development for a… (more)

Subjects/Keywords: recombinant protein; escherichia coli; burden

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

APA (6th Edition):

French, J. (2016). Towards an understanding of the burden of recombinant protein production. (Doctoral Dissertation). University of Manchester. Retrieved from http://www.manchester.ac.uk/escholar/uk-ac-man-scw:294150

Chicago Manual of Style (16th Edition):

French, Joseph. “Towards an understanding of the burden of recombinant protein production.” 2016. Doctoral Dissertation, University of Manchester. Accessed April 17, 2021. http://www.manchester.ac.uk/escholar/uk-ac-man-scw:294150.

MLA Handbook (7th Edition):

French, Joseph. “Towards an understanding of the burden of recombinant protein production.” 2016. Web. 17 Apr 2021.

Vancouver:

French J. Towards an understanding of the burden of recombinant protein production. [Internet] [Doctoral dissertation]. University of Manchester; 2016. [cited 2021 Apr 17]. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:294150.

Council of Science Editors:

French J. Towards an understanding of the burden of recombinant protein production. [Doctoral Dissertation]. University of Manchester; 2016. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:294150

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