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You searched for subject:( rhBGN recombinant human diglycan). Showing records 1 – 30 of 37273 total matches.

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University of Debrecen

1. Hamed, Rashidi. Pharmacological treatment of Duchenne and Becker muscular dystrophies .

Degree: DE – Általános Orvostudományi Kar, University of Debrecen

 Currently, there is no cure for muscular dystrophy. Treatment is generally aimed at controlling the onset of symptoms to maximize the quality of life. Medical… (more)

Subjects/Keywords: AAV – adeno-associated viruses; Ad – adenoviruses; ADSCs – adipose derived stem cells; AFOs – ancle foot orthoses; BMD – Becker muscular dystrophy; CVS – chorion villus sampling; DAPC – dystrophin-associated protein complex; DMD – Duchenne muscular dystrophy; EMA – European Medical Agency; EMG – electromyography; ES – human embryonic; FAPs – fibro-adipogenic progenitors; HDACi – histone deacetylase inhibitor; IA - intraarterial; IM - intamuscular; iPSCs – induced pluripotent stem cells; IV – intravenous; KAFOs – knee ankle foot orthoses; LBM – lean body mass; MCK – muscle creatine kinase; MDSCs – muscle derived stem cells; MMT – manual muscle testing; MSCs – mesenchymal stem cells; PMO – phosphorodiamidate morpholino oligomer; PS – phosphorothioate; rhBGN – recombinant human diglycan; ROM – range of motion; ROS – reactive-oxygen species; SCs – satellita cells; SP cells – side population cells; TLRs – troll-like receptorsTMV – tight muscle volume

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APA (6th Edition):

Hamed, R. (n.d.). Pharmacological treatment of Duchenne and Becker muscular dystrophies . (Thesis). University of Debrecen. Retrieved from http://hdl.handle.net/2437/243130

Note: this citation may be lacking information needed for this citation format:
No year of publication.
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Hamed, Rashidi. “Pharmacological treatment of Duchenne and Becker muscular dystrophies .” Thesis, University of Debrecen. Accessed November 15, 2019. http://hdl.handle.net/2437/243130.

Note: this citation may be lacking information needed for this citation format:
No year of publication.
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Hamed, Rashidi. “Pharmacological treatment of Duchenne and Becker muscular dystrophies .” Web. 15 Nov 2019.

Note: this citation may be lacking information needed for this citation format:
No year of publication.

Vancouver:

Hamed R. Pharmacological treatment of Duchenne and Becker muscular dystrophies . [Internet] [Thesis]. University of Debrecen; [cited 2019 Nov 15]. Available from: http://hdl.handle.net/2437/243130.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation
No year of publication.

Council of Science Editors:

Hamed R. Pharmacological treatment of Duchenne and Becker muscular dystrophies . [Thesis]. University of Debrecen; Available from: http://hdl.handle.net/2437/243130

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation
No year of publication.


Universidade Federal de Santa Maria

2. Marlei Veiga dos Santos. ESTUDO DA INTERAÇÃO ENTRE ALUMÍNIO E OS CONSTITUINTES DE FORMULAÇÕES DE ERITROPOETINA EMPREGANDO HPLC E AAS.

Degree: 2009, Universidade Federal de Santa Maria

Erythropoietin (EPO) is a glycoprotein which stimulates the erythropoiesis (production of hemaceas) and is clinically used for the treatment of renal anemia. EPO formulations present… (more)

Subjects/Keywords: eritropoetina recombinante humana; alumínio; QUIMICA; recombinant human erythropoietin; aluminum; interaction; interação

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APA (6th Edition):

Santos, M. V. d. (2009). ESTUDO DA INTERAÇÃO ENTRE ALUMÍNIO E OS CONSTITUINTES DE FORMULAÇÕES DE ERITROPOETINA EMPREGANDO HPLC E AAS. (Thesis). Universidade Federal de Santa Maria. Retrieved from http://coralx.ufsm.br/tede/tde_busca/arquivo.php?codArquivo=2583

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):

Santos, Marlei Veiga dos. “ESTUDO DA INTERAÇÃO ENTRE ALUMÍNIO E OS CONSTITUINTES DE FORMULAÇÕES DE ERITROPOETINA EMPREGANDO HPLC E AAS.” 2009. Thesis, Universidade Federal de Santa Maria. Accessed November 15, 2019. http://coralx.ufsm.br/tede/tde_busca/arquivo.php?codArquivo=2583.

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

MLA Handbook (7th Edition):

Santos, Marlei Veiga dos. “ESTUDO DA INTERAÇÃO ENTRE ALUMÍNIO E OS CONSTITUINTES DE FORMULAÇÕES DE ERITROPOETINA EMPREGANDO HPLC E AAS.” 2009. Web. 15 Nov 2019.

Vancouver:

Santos MVd. ESTUDO DA INTERAÇÃO ENTRE ALUMÍNIO E OS CONSTITUINTES DE FORMULAÇÕES DE ERITROPOETINA EMPREGANDO HPLC E AAS. [Internet] [Thesis]. Universidade Federal de Santa Maria; 2009. [cited 2019 Nov 15]. Available from: http://coralx.ufsm.br/tede/tde_busca/arquivo.php?codArquivo=2583.

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

Council of Science Editors:

Santos MVd. ESTUDO DA INTERAÇÃO ENTRE ALUMÍNIO E OS CONSTITUINTES DE FORMULAÇÕES DE ERITROPOETINA EMPREGANDO HPLC E AAS. [Thesis]. Universidade Federal de Santa Maria; 2009. Available from: http://coralx.ufsm.br/tede/tde_busca/arquivo.php?codArquivo=2583

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

3. 古川, 克郎. Intratracheal administration of recombinant human keratinocyte growth factor promotes alveolar epithelial cell proliferation during compensatory lung growth in rat : keratinocyte growth factor蛋白の気管内投与はラットの代償性肺肥大における肺胞上皮細胞増殖を促進する.

Degree: 博士(医学), 2013, Nagasaki University / 長崎大学

 Keratinocyte growth factor (KGF) is considered to be one of the most important mitogens for lung epithelial cells. The objectives of this study were to… (more)

Subjects/Keywords: Compensatory growth; Intratracheal injection; PCNA; Recombinant human KGF; Trilobectomy

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APA (6th Edition):

古川, . (2013). Intratracheal administration of recombinant human keratinocyte growth factor promotes alveolar epithelial cell proliferation during compensatory lung growth in rat : keratinocyte growth factor蛋白の気管内投与はラットの代償性肺肥大における肺胞上皮細胞増殖を促進する. (Thesis). Nagasaki University / 長崎大学. Retrieved from http://hdl.handle.net/10069/35392

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):

古川, 克郎. “Intratracheal administration of recombinant human keratinocyte growth factor promotes alveolar epithelial cell proliferation during compensatory lung growth in rat : keratinocyte growth factor蛋白の気管内投与はラットの代償性肺肥大における肺胞上皮細胞増殖を促進する.” 2013. Thesis, Nagasaki University / 長崎大学. Accessed November 15, 2019. http://hdl.handle.net/10069/35392.

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

MLA Handbook (7th Edition):

古川, 克郎. “Intratracheal administration of recombinant human keratinocyte growth factor promotes alveolar epithelial cell proliferation during compensatory lung growth in rat : keratinocyte growth factor蛋白の気管内投与はラットの代償性肺肥大における肺胞上皮細胞増殖を促進する.” 2013. Web. 15 Nov 2019.

Vancouver:

古川 . Intratracheal administration of recombinant human keratinocyte growth factor promotes alveolar epithelial cell proliferation during compensatory lung growth in rat : keratinocyte growth factor蛋白の気管内投与はラットの代償性肺肥大における肺胞上皮細胞増殖を促進する. [Internet] [Thesis]. Nagasaki University / 長崎大学; 2013. [cited 2019 Nov 15]. Available from: http://hdl.handle.net/10069/35392.

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

Council of Science Editors:

古川 . Intratracheal administration of recombinant human keratinocyte growth factor promotes alveolar epithelial cell proliferation during compensatory lung growth in rat : keratinocyte growth factor蛋白の気管内投与はラットの代償性肺肥大における肺胞上皮細胞増殖を促進する. [Thesis]. Nagasaki University / 長崎大学; 2013. Available from: http://hdl.handle.net/10069/35392

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


University of Manchester

4. Idicula Babu, Benoy. Epigallocatechin-3-gallate and recombinant human activated protein C and the modulation of acute pancreatitis.

Degree: Thesis (M.D.), 2012, University of Manchester

 Effective management of acute pancreatitis has for centuries eluded mankind. The disease has a wide spectrum of presentation; the milder form is usually a self… (more)

Subjects/Keywords: 616.3; Green tea extracts; Recombinant human activated protein C; Acute pancreatitis

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APA (6th Edition):

Idicula Babu, B. (2012). Epigallocatechin-3-gallate and recombinant human activated protein C and the modulation of acute pancreatitis. (Doctoral Dissertation). University of Manchester. Retrieved from https://www.research.manchester.ac.uk/portal/en/theses/epigallocatechin3gallate-and-recombinant-human-activated-protein-c-and-the-modulation-of-acute-pancreatitis(5fc797e9-cf5b-4aab-841d-62c3a8cd82c6).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.566553

Chicago Manual of Style (16th Edition):

Idicula Babu, Benoy. “Epigallocatechin-3-gallate and recombinant human activated protein C and the modulation of acute pancreatitis.” 2012. Doctoral Dissertation, University of Manchester. Accessed November 15, 2019. https://www.research.manchester.ac.uk/portal/en/theses/epigallocatechin3gallate-and-recombinant-human-activated-protein-c-and-the-modulation-of-acute-pancreatitis(5fc797e9-cf5b-4aab-841d-62c3a8cd82c6).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.566553.

MLA Handbook (7th Edition):

Idicula Babu, Benoy. “Epigallocatechin-3-gallate and recombinant human activated protein C and the modulation of acute pancreatitis.” 2012. Web. 15 Nov 2019.

Vancouver:

Idicula Babu B. Epigallocatechin-3-gallate and recombinant human activated protein C and the modulation of acute pancreatitis. [Internet] [Doctoral dissertation]. University of Manchester; 2012. [cited 2019 Nov 15]. Available from: https://www.research.manchester.ac.uk/portal/en/theses/epigallocatechin3gallate-and-recombinant-human-activated-protein-c-and-the-modulation-of-acute-pancreatitis(5fc797e9-cf5b-4aab-841d-62c3a8cd82c6).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.566553.

Council of Science Editors:

Idicula Babu B. Epigallocatechin-3-gallate and recombinant human activated protein C and the modulation of acute pancreatitis. [Doctoral Dissertation]. University of Manchester; 2012. Available from: https://www.research.manchester.ac.uk/portal/en/theses/epigallocatechin3gallate-and-recombinant-human-activated-protein-c-and-the-modulation-of-acute-pancreatitis(5fc797e9-cf5b-4aab-841d-62c3a8cd82c6).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.566553


Boston University

5. Dehghani, Bijan. Development of an elastic sealant for surgical applications.

Degree: MS, Medical Sciences, 2015, Boston University

 The need to close wounds and prevent air/liquid leakage is commonly faced in surgical operations. It is a necessary step required for proper post-operative tissue… (more)

Subjects/Keywords: Biomedical engineering; Biomaterials; Elastin; Human recombinant protein; Sealant; Surgery; Tissue engineering

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APA (6th Edition):

Dehghani, B. (2015). Development of an elastic sealant for surgical applications. (Masters Thesis). Boston University. Retrieved from http://hdl.handle.net/2144/16139

Chicago Manual of Style (16th Edition):

Dehghani, Bijan. “Development of an elastic sealant for surgical applications.” 2015. Masters Thesis, Boston University. Accessed November 15, 2019. http://hdl.handle.net/2144/16139.

MLA Handbook (7th Edition):

Dehghani, Bijan. “Development of an elastic sealant for surgical applications.” 2015. Web. 15 Nov 2019.

Vancouver:

Dehghani B. Development of an elastic sealant for surgical applications. [Internet] [Masters thesis]. Boston University; 2015. [cited 2019 Nov 15]. Available from: http://hdl.handle.net/2144/16139.

Council of Science Editors:

Dehghani B. Development of an elastic sealant for surgical applications. [Masters Thesis]. Boston University; 2015. Available from: http://hdl.handle.net/2144/16139

6. Prince R Prabhu. Structural elucidation and immunoprophylactic studies of recombinant parasitic proteins for therapeutic intervention in human lymphatic filariasis;.

Degree: 2014, Anna University

Human lymphatic filariasis is an incapacitating vector borne disease and is the world s second leading cause of long-term disability. To worsen the condition there… (more)

Subjects/Keywords: Immunoprophylactic; recombinant parasitic proteins; human lymphatic filariasis; x-ray crystallographic; Glutathione-S-transferase

Page 1

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APA (6th Edition):

Prabhu, P. R. (2014). Structural elucidation and immunoprophylactic studies of recombinant parasitic proteins for therapeutic intervention in human lymphatic filariasis;. (Thesis). Anna University. Retrieved from http://shodhganga.inflibnet.ac.in/handle/10603/15514

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):

Prabhu, Prince R. “Structural elucidation and immunoprophylactic studies of recombinant parasitic proteins for therapeutic intervention in human lymphatic filariasis;.” 2014. Thesis, Anna University. Accessed November 15, 2019. http://shodhganga.inflibnet.ac.in/handle/10603/15514.

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

MLA Handbook (7th Edition):

Prabhu, Prince R. “Structural elucidation and immunoprophylactic studies of recombinant parasitic proteins for therapeutic intervention in human lymphatic filariasis;.” 2014. Web. 15 Nov 2019.

Vancouver:

Prabhu PR. Structural elucidation and immunoprophylactic studies of recombinant parasitic proteins for therapeutic intervention in human lymphatic filariasis;. [Internet] [Thesis]. Anna University; 2014. [cited 2019 Nov 15]. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/15514.

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

Council of Science Editors:

Prabhu PR. Structural elucidation and immunoprophylactic studies of recombinant parasitic proteins for therapeutic intervention in human lymphatic filariasis;. [Thesis]. Anna University; 2014. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/15514

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


University of Pretoria

7. Koorts, Alida Maria. Intracellular calcium and transmembrane calcium fluxes in chronic renal failure patients.

Degree: Physiology, 2010, University of Pretoria

 Intracellular calcium is a major determinant of a wide variety of cell functions and thus of organ function. In order to get a clear picture… (more)

Subjects/Keywords: Transmission electron microscopy; Fluorescent calcium indicator; Intracellular calcium; Haemodialysis patients; Recombinant human erythropoietin; UCTD

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APA (6th Edition):

Koorts, A. M. (2010). Intracellular calcium and transmembrane calcium fluxes in chronic renal failure patients. (Masters Thesis). University of Pretoria. Retrieved from http://hdl.handle.net/2263/28059

Chicago Manual of Style (16th Edition):

Koorts, Alida Maria. “Intracellular calcium and transmembrane calcium fluxes in chronic renal failure patients.” 2010. Masters Thesis, University of Pretoria. Accessed November 15, 2019. http://hdl.handle.net/2263/28059.

MLA Handbook (7th Edition):

Koorts, Alida Maria. “Intracellular calcium and transmembrane calcium fluxes in chronic renal failure patients.” 2010. Web. 15 Nov 2019.

Vancouver:

Koorts AM. Intracellular calcium and transmembrane calcium fluxes in chronic renal failure patients. [Internet] [Masters thesis]. University of Pretoria; 2010. [cited 2019 Nov 15]. Available from: http://hdl.handle.net/2263/28059.

Council of Science Editors:

Koorts AM. Intracellular calcium and transmembrane calcium fluxes in chronic renal failure patients. [Masters Thesis]. University of Pretoria; 2010. Available from: http://hdl.handle.net/2263/28059


Oregon State University

8. Alkhatib, Aveen K. The adsorption of human recombinant factor VIII in the presence of the nonionic triblock surfactant Pluronic® F-68 at the air-water interface.

Degree: MS, Chemical Engineering, 2010, Oregon State University

 The adsorption behavior of a human recombinant Factor VIII (rFVIII) in the presence of the nonionic, poly(ethylene oxide)-poly(propylene oxide)-poly(ethylene oxide) (PEO-PPO-PEO) triblock surfactant Pluronic® F-68… (more)

Subjects/Keywords: Human recombinant Factor VIII (rFVIII); Blood coagulation factor VIII  – Absorption and adsorption

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APA (6th Edition):

Alkhatib, A. K. (2010). The adsorption of human recombinant factor VIII in the presence of the nonionic triblock surfactant Pluronic® F-68 at the air-water interface. (Masters Thesis). Oregon State University. Retrieved from http://hdl.handle.net/1957/14013

Chicago Manual of Style (16th Edition):

Alkhatib, Aveen K. “The adsorption of human recombinant factor VIII in the presence of the nonionic triblock surfactant Pluronic® F-68 at the air-water interface.” 2010. Masters Thesis, Oregon State University. Accessed November 15, 2019. http://hdl.handle.net/1957/14013.

MLA Handbook (7th Edition):

Alkhatib, Aveen K. “The adsorption of human recombinant factor VIII in the presence of the nonionic triblock surfactant Pluronic® F-68 at the air-water interface.” 2010. Web. 15 Nov 2019.

Vancouver:

Alkhatib AK. The adsorption of human recombinant factor VIII in the presence of the nonionic triblock surfactant Pluronic® F-68 at the air-water interface. [Internet] [Masters thesis]. Oregon State University; 2010. [cited 2019 Nov 15]. Available from: http://hdl.handle.net/1957/14013.

Council of Science Editors:

Alkhatib AK. The adsorption of human recombinant factor VIII in the presence of the nonionic triblock surfactant Pluronic® F-68 at the air-water interface. [Masters Thesis]. Oregon State University; 2010. Available from: http://hdl.handle.net/1957/14013


University of Pretoria

9. Koorts, Alida Maria. Intracellular calcium and transmembrane calcium fluxes in chronic renal failure patients .

Degree: 2010, University of Pretoria

 Intracellular calcium is a major determinant of a wide variety of cell functions and thus of organ function. In order to get a clear picture… (more)

Subjects/Keywords: Transmission electron microscopy; Fluorescent calcium indicator; Intracellular calcium; Haemodialysis patients; Recombinant human erythropoietin; UCTD

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

APA (6th Edition):

Koorts, A. M. (2010). Intracellular calcium and transmembrane calcium fluxes in chronic renal failure patients . (Masters Thesis). University of Pretoria. Retrieved from http://upetd.up.ac.za/thesis/available/etd-09202010-115338/

Chicago Manual of Style (16th Edition):

Koorts, Alida Maria. “Intracellular calcium and transmembrane calcium fluxes in chronic renal failure patients .” 2010. Masters Thesis, University of Pretoria. Accessed November 15, 2019. http://upetd.up.ac.za/thesis/available/etd-09202010-115338/.

MLA Handbook (7th Edition):

Koorts, Alida Maria. “Intracellular calcium and transmembrane calcium fluxes in chronic renal failure patients .” 2010. Web. 15 Nov 2019.

Vancouver:

Koorts AM. Intracellular calcium and transmembrane calcium fluxes in chronic renal failure patients . [Internet] [Masters thesis]. University of Pretoria; 2010. [cited 2019 Nov 15]. Available from: http://upetd.up.ac.za/thesis/available/etd-09202010-115338/.

Council of Science Editors:

Koorts AM. Intracellular calcium and transmembrane calcium fluxes in chronic renal failure patients . [Masters Thesis]. University of Pretoria; 2010. Available from: http://upetd.up.ac.za/thesis/available/etd-09202010-115338/


Linköping University

10. Gärdefors, Katarina. Development and characterization of Mantle Cell Lymphoma specific IgGs.

Degree: Chemistry and Biology, 2008, Linköping University

  Mantle cell lymphoma (MCL) is one of several sub-types of B-cell lymphomas. The malignancy is very aggressive and average survival time is short. The… (more)

Subjects/Keywords: Mantle cell lymphoma (MCL); Sox11; human recombinant antibodies; single chain variable fragment (scFv); IgG.

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APA (6th Edition):

Gärdefors, K. (2008). Development and characterization of Mantle Cell Lymphoma specific IgGs. (Thesis). Linköping University. Retrieved from http://urn.kb.se/resolve?urn=urn:nbn:se:liu:diva-15255

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):

Gärdefors, Katarina. “Development and characterization of Mantle Cell Lymphoma specific IgGs.” 2008. Thesis, Linköping University. Accessed November 15, 2019. http://urn.kb.se/resolve?urn=urn:nbn:se:liu:diva-15255.

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

MLA Handbook (7th Edition):

Gärdefors, Katarina. “Development and characterization of Mantle Cell Lymphoma specific IgGs.” 2008. Web. 15 Nov 2019.

Vancouver:

Gärdefors K. Development and characterization of Mantle Cell Lymphoma specific IgGs. [Internet] [Thesis]. Linköping University; 2008. [cited 2019 Nov 15]. Available from: http://urn.kb.se/resolve?urn=urn:nbn:se:liu:diva-15255.

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

Council of Science Editors:

Gärdefors K. Development and characterization of Mantle Cell Lymphoma specific IgGs. [Thesis]. Linköping University; 2008. Available from: http://urn.kb.se/resolve?urn=urn:nbn:se:liu:diva-15255

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


Université Catholique de Louvain

11. Guichard, Marie-Julie. Development of a long-acting version of recombinant human deoxyribonuclease I for the treatment of cystic fibrosis lung disease.

Degree: 2018, Université Catholique de Louvain

Recombinant human deoxyribonuclease I (rhDNase) is the mucolytic agent most widely used in cystic fibrosis (CF) treatment. However, its rapid clearance from the lungs implies… (more)

Subjects/Keywords: Recombinant human deoxyribonuclease I; PEGylation; Cystic Fibrosis; Pulmonary drug delivery; Prolonged residence time

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APA (6th Edition):

Guichard, M. (2018). Development of a long-acting version of recombinant human deoxyribonuclease I for the treatment of cystic fibrosis lung disease. (Thesis). Université Catholique de Louvain. Retrieved from http://hdl.handle.net/2078.1/197736

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):

Guichard, Marie-Julie. “Development of a long-acting version of recombinant human deoxyribonuclease I for the treatment of cystic fibrosis lung disease.” 2018. Thesis, Université Catholique de Louvain. Accessed November 15, 2019. http://hdl.handle.net/2078.1/197736.

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

MLA Handbook (7th Edition):

Guichard, Marie-Julie. “Development of a long-acting version of recombinant human deoxyribonuclease I for the treatment of cystic fibrosis lung disease.” 2018. Web. 15 Nov 2019.

Vancouver:

Guichard M. Development of a long-acting version of recombinant human deoxyribonuclease I for the treatment of cystic fibrosis lung disease. [Internet] [Thesis]. Université Catholique de Louvain; 2018. [cited 2019 Nov 15]. Available from: http://hdl.handle.net/2078.1/197736.

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

Council of Science Editors:

Guichard M. Development of a long-acting version of recombinant human deoxyribonuclease I for the treatment of cystic fibrosis lung disease. [Thesis]. Université Catholique de Louvain; 2018. Available from: http://hdl.handle.net/2078.1/197736

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


Kansas State University

12. Sheshukova, Kseniya Alekseyevna. Bioprocess development: extraction and purification of human serum albumin from transgenic rice.

Degree: MS, Department of Biological & Agricultural Engineering, 2019, Kansas State University

 Transgenic plant systems have successfully been used to express recombinant proteins, including rice seed-expressed recombinant human serum albumin (rHSA). The development of an efficient and… (more)

Subjects/Keywords: Transgenic plants; Recombinant proteins; Downstream processing; Protein extraction; Protein purification; Human serum albumin

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APA (6th Edition):

Sheshukova, K. A. (2019). Bioprocess development: extraction and purification of human serum albumin from transgenic rice. (Masters Thesis). Kansas State University. Retrieved from http://hdl.handle.net/2097/39681

Chicago Manual of Style (16th Edition):

Sheshukova, Kseniya Alekseyevna. “Bioprocess development: extraction and purification of human serum albumin from transgenic rice.” 2019. Masters Thesis, Kansas State University. Accessed November 15, 2019. http://hdl.handle.net/2097/39681.

MLA Handbook (7th Edition):

Sheshukova, Kseniya Alekseyevna. “Bioprocess development: extraction and purification of human serum albumin from transgenic rice.” 2019. Web. 15 Nov 2019.

Vancouver:

Sheshukova KA. Bioprocess development: extraction and purification of human serum albumin from transgenic rice. [Internet] [Masters thesis]. Kansas State University; 2019. [cited 2019 Nov 15]. Available from: http://hdl.handle.net/2097/39681.

Council of Science Editors:

Sheshukova KA. Bioprocess development: extraction and purification of human serum albumin from transgenic rice. [Masters Thesis]. Kansas State University; 2019. Available from: http://hdl.handle.net/2097/39681

13. Bomfim, Aline de Sousa. Clonagem e expressão de fator IX recombinante em células 293T e SK-Hep-1 e caracterização das células produtoras.

Degree: Mestrado, Biociências Aplicadas à Farmácia, 2013, University of São Paulo

 O fator IX (FIX) da coagulação sanguínea é uma proteína dependente de vitamina K de grande valor farmacêutico no tratamento da Hemofilia B, o qual… (more)

Subjects/Keywords: fator IX recombinante; Hemofilia B; Hemophilia B; human cell lines; lentiviral vectors; linhagens celulares humanas.; recombinant factor IX; vetores lentivirais

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

APA (6th Edition):

Bomfim, A. d. S. (2013). Clonagem e expressão de fator IX recombinante em células 293T e SK-Hep-1 e caracterização das células produtoras. (Masters Thesis). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/60/60135/tde-13122013-111826/ ;

Chicago Manual of Style (16th Edition):

Bomfim, Aline de Sousa. “Clonagem e expressão de fator IX recombinante em células 293T e SK-Hep-1 e caracterização das células produtoras.” 2013. Masters Thesis, University of São Paulo. Accessed November 15, 2019. http://www.teses.usp.br/teses/disponiveis/60/60135/tde-13122013-111826/ ;.

MLA Handbook (7th Edition):

Bomfim, Aline de Sousa. “Clonagem e expressão de fator IX recombinante em células 293T e SK-Hep-1 e caracterização das células produtoras.” 2013. Web. 15 Nov 2019.

Vancouver:

Bomfim AdS. Clonagem e expressão de fator IX recombinante em células 293T e SK-Hep-1 e caracterização das células produtoras. [Internet] [Masters thesis]. University of São Paulo; 2013. [cited 2019 Nov 15]. Available from: http://www.teses.usp.br/teses/disponiveis/60/60135/tde-13122013-111826/ ;.

Council of Science Editors:

Bomfim AdS. Clonagem e expressão de fator IX recombinante em células 293T e SK-Hep-1 e caracterização das células produtoras. [Masters Thesis]. University of São Paulo; 2013. Available from: http://www.teses.usp.br/teses/disponiveis/60/60135/tde-13122013-111826/ ;

14. Cumbane, Victória Simão. Resposta de anticorpos contra proteínas recombinantes baseadas em antígenos de merozoítos de Plasmodium vivax em indivíduos de uma comunidade rural da Amazônia brasileira.

Degree: Mestrado, Análises Clínicas, 2011, University of São Paulo

Nos últimos anos, estudamos vários aspectos da resposta imune naturalmente adquirida em indivíduos de diferentes áreas endêmicas da Região Amazônica expostos à malária. Para isso,… (more)

Subjects/Keywords: Antibody response; Human malaria; Malária humana; Plasmodium vivax; Plasmodium vivax; Proteínas recombinantes; Recombinant proteins; Resposta de anticorpos

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

APA (6th Edition):

Cumbane, V. S. (2011). Resposta de anticorpos contra proteínas recombinantes baseadas em antígenos de merozoítos de Plasmodium vivax em indivíduos de uma comunidade rural da Amazônia brasileira. (Masters Thesis). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/9/9136/tde-15072011-113553/ ;

Chicago Manual of Style (16th Edition):

Cumbane, Victória Simão. “Resposta de anticorpos contra proteínas recombinantes baseadas em antígenos de merozoítos de Plasmodium vivax em indivíduos de uma comunidade rural da Amazônia brasileira.” 2011. Masters Thesis, University of São Paulo. Accessed November 15, 2019. http://www.teses.usp.br/teses/disponiveis/9/9136/tde-15072011-113553/ ;.

MLA Handbook (7th Edition):

Cumbane, Victória Simão. “Resposta de anticorpos contra proteínas recombinantes baseadas em antígenos de merozoítos de Plasmodium vivax em indivíduos de uma comunidade rural da Amazônia brasileira.” 2011. Web. 15 Nov 2019.

Vancouver:

Cumbane VS. Resposta de anticorpos contra proteínas recombinantes baseadas em antígenos de merozoítos de Plasmodium vivax em indivíduos de uma comunidade rural da Amazônia brasileira. [Internet] [Masters thesis]. University of São Paulo; 2011. [cited 2019 Nov 15]. Available from: http://www.teses.usp.br/teses/disponiveis/9/9136/tde-15072011-113553/ ;.

Council of Science Editors:

Cumbane VS. Resposta de anticorpos contra proteínas recombinantes baseadas em antígenos de merozoítos de Plasmodium vivax em indivíduos de uma comunidade rural da Amazônia brasileira. [Masters Thesis]. University of São Paulo; 2011. Available from: http://www.teses.usp.br/teses/disponiveis/9/9136/tde-15072011-113553/ ;

15. Giassetti, Mariana Ianello. Modelos para a produção de eritropoietina recombinante humana in vivo e in vitro com vetores plasmideais em ovinos.

Degree: Mestrado, Reprodução Animal, 2011, University of São Paulo

 Para produção de biofármacos protéicos, como a eritropoietina recombinante humana (EPOrh), são necessárias alterações pós-traducionais adequadas que garantam a sua especificidade e atividade biológica. Essas… (more)

Subjects/Keywords: Bioreactor; Biorreatores; Célula mamária; Eritropoietina recombinante humana; Mammary cell; Milk proteins; Ovelha; Ovine; Proteínas do leite; Recombinant human erythropoietin

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

APA (6th Edition):

Giassetti, M. I. (2011). Modelos para a produção de eritropoietina recombinante humana in vivo e in vitro com vetores plasmideais em ovinos. (Masters Thesis). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/10/10131/tde-18102012-112038/ ;

Chicago Manual of Style (16th Edition):

Giassetti, Mariana Ianello. “Modelos para a produção de eritropoietina recombinante humana in vivo e in vitro com vetores plasmideais em ovinos.” 2011. Masters Thesis, University of São Paulo. Accessed November 15, 2019. http://www.teses.usp.br/teses/disponiveis/10/10131/tde-18102012-112038/ ;.

MLA Handbook (7th Edition):

Giassetti, Mariana Ianello. “Modelos para a produção de eritropoietina recombinante humana in vivo e in vitro com vetores plasmideais em ovinos.” 2011. Web. 15 Nov 2019.

Vancouver:

Giassetti MI. Modelos para a produção de eritropoietina recombinante humana in vivo e in vitro com vetores plasmideais em ovinos. [Internet] [Masters thesis]. University of São Paulo; 2011. [cited 2019 Nov 15]. Available from: http://www.teses.usp.br/teses/disponiveis/10/10131/tde-18102012-112038/ ;.

Council of Science Editors:

Giassetti MI. Modelos para a produção de eritropoietina recombinante humana in vivo e in vitro com vetores plasmideais em ovinos. [Masters Thesis]. University of São Paulo; 2011. Available from: http://www.teses.usp.br/teses/disponiveis/10/10131/tde-18102012-112038/ ;


University of Vermont

16. Qian, Xi. Regulation of β-Casein Gene Expression by Octamer Transcription Factors and Utilization of β-Casein Gene Promoter to Produce Recombinant Human Proinsulin in the Transgenic Milk.

Degree: PhD, Animal Science, 2014, University of Vermont

  β-Casein is a major milk protein, which is synthesized in mammary alveolar secretory epithelial cells (MECs) upon the stimulation of lactogenic hormones, mainly prolactin… (more)

Subjects/Keywords: Bioreactor; Hormonal regulation; Milk protein; Octamer binding transcription factor; Recombinant human insulin; Transcriptional regulation; Biochemistry; Biomedical; Molecular Biology

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

APA (6th Edition):

Qian, X. (2014). Regulation of β-Casein Gene Expression by Octamer Transcription Factors and Utilization of β-Casein Gene Promoter to Produce Recombinant Human Proinsulin in the Transgenic Milk. (Doctoral Dissertation). University of Vermont. Retrieved from https://scholarworks.uvm.edu/graddis/316

Chicago Manual of Style (16th Edition):

Qian, Xi. “Regulation of β-Casein Gene Expression by Octamer Transcription Factors and Utilization of β-Casein Gene Promoter to Produce Recombinant Human Proinsulin in the Transgenic Milk.” 2014. Doctoral Dissertation, University of Vermont. Accessed November 15, 2019. https://scholarworks.uvm.edu/graddis/316.

MLA Handbook (7th Edition):

Qian, Xi. “Regulation of β-Casein Gene Expression by Octamer Transcription Factors and Utilization of β-Casein Gene Promoter to Produce Recombinant Human Proinsulin in the Transgenic Milk.” 2014. Web. 15 Nov 2019.

Vancouver:

Qian X. Regulation of β-Casein Gene Expression by Octamer Transcription Factors and Utilization of β-Casein Gene Promoter to Produce Recombinant Human Proinsulin in the Transgenic Milk. [Internet] [Doctoral dissertation]. University of Vermont; 2014. [cited 2019 Nov 15]. Available from: https://scholarworks.uvm.edu/graddis/316.

Council of Science Editors:

Qian X. Regulation of β-Casein Gene Expression by Octamer Transcription Factors and Utilization of β-Casein Gene Promoter to Produce Recombinant Human Proinsulin in the Transgenic Milk. [Doctoral Dissertation]. University of Vermont; 2014. Available from: https://scholarworks.uvm.edu/graddis/316


University of Hyderabad

17. Rajasekhar, S N V S. Recombinant human translational initiation factor 2 : expression of subunits, puri fication and characterization; -.

Degree: Biochemistry, 2005, University of Hyderabad

None

Bibliography p.78-106

Advisors/Committee Members: Ramaiah, K V A.

Subjects/Keywords: Recombinant human; Expression of subunits; Fication; Biochemistry

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APA (6th Edition):

Rajasekhar, S. N. V. S. (2005). Recombinant human translational initiation factor 2 : expression of subunits, puri fication and characterization; -. (Thesis). University of Hyderabad. Retrieved from http://shodhganga.inflibnet.ac.in/handle/10603/25630

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):

Rajasekhar, S N V S. “Recombinant human translational initiation factor 2 : expression of subunits, puri fication and characterization; -.” 2005. Thesis, University of Hyderabad. Accessed November 15, 2019. http://shodhganga.inflibnet.ac.in/handle/10603/25630.

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

MLA Handbook (7th Edition):

Rajasekhar, S N V S. “Recombinant human translational initiation factor 2 : expression of subunits, puri fication and characterization; -.” 2005. Web. 15 Nov 2019.

Vancouver:

Rajasekhar SNVS. Recombinant human translational initiation factor 2 : expression of subunits, puri fication and characterization; -. [Internet] [Thesis]. University of Hyderabad; 2005. [cited 2019 Nov 15]. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/25630.

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

Council of Science Editors:

Rajasekhar SNVS. Recombinant human translational initiation factor 2 : expression of subunits, puri fication and characterization; -. [Thesis]. University of Hyderabad; 2005. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/25630

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

18. 中川, 泰志郎. A Study on Retention Mechanism of Recombinant Human Monoclonal Antibodies in Hydroxyapatite Chromatography.

Degree: 博士(工学), Gunma University / 群馬大学

学位記番号:工博乙99, 学位の種類:博士(工学)

Subjects/Keywords: Hydroxyapatite chromatography; Recombinant human monoclonal antibodies; Retention mechanism

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APA (6th Edition):

中川, . (n.d.). A Study on Retention Mechanism of Recombinant Human Monoclonal Antibodies in Hydroxyapatite Chromatography. (Thesis). Gunma University / 群馬大学. Retrieved from http://hdl.handle.net/10087/8120

Note: this citation may be lacking information needed for this citation format:
No year of publication.
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

中川, 泰志郎. “A Study on Retention Mechanism of Recombinant Human Monoclonal Antibodies in Hydroxyapatite Chromatography.” Thesis, Gunma University / 群馬大学. Accessed November 15, 2019. http://hdl.handle.net/10087/8120.

Note: this citation may be lacking information needed for this citation format:
No year of publication.
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

中川, 泰志郎. “A Study on Retention Mechanism of Recombinant Human Monoclonal Antibodies in Hydroxyapatite Chromatography.” Web. 15 Nov 2019.

Note: this citation may be lacking information needed for this citation format:
No year of publication.

Vancouver:

中川 . A Study on Retention Mechanism of Recombinant Human Monoclonal Antibodies in Hydroxyapatite Chromatography. [Internet] [Thesis]. Gunma University / 群馬大学; [cited 2019 Nov 15]. Available from: http://hdl.handle.net/10087/8120.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation
No year of publication.

Council of Science Editors:

中川 . A Study on Retention Mechanism of Recombinant Human Monoclonal Antibodies in Hydroxyapatite Chromatography. [Thesis]. Gunma University / 群馬大学; Available from: http://hdl.handle.net/10087/8120

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation
No year of publication.


Dublin City University

19. Mtawae, Karima. Stability and kinetic studies on recombinant pyroglutamyl peptidase I and two mutant forms.

Degree: School of Biotechnology, 2005, Dublin City University

 This thesis investigates the kinetic and stability characteristics of recombinant human brain pyroglutamyl peptidase PAPI, an omega exopeptidase which cleaves pyroglutamic acid from the N-terminus… (more)

Subjects/Keywords: Biotechnology; Recombinant human brain pyroglutamyl peptidase; PAPI

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APA (6th Edition):

Mtawae, K. (2005). Stability and kinetic studies on recombinant pyroglutamyl peptidase I and two mutant forms. (Thesis). Dublin City University. Retrieved from http://doras.dcu.ie/18094/

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):

Mtawae, Karima. “Stability and kinetic studies on recombinant pyroglutamyl peptidase I and two mutant forms.” 2005. Thesis, Dublin City University. Accessed November 15, 2019. http://doras.dcu.ie/18094/.

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

MLA Handbook (7th Edition):

Mtawae, Karima. “Stability and kinetic studies on recombinant pyroglutamyl peptidase I and two mutant forms.” 2005. Web. 15 Nov 2019.

Vancouver:

Mtawae K. Stability and kinetic studies on recombinant pyroglutamyl peptidase I and two mutant forms. [Internet] [Thesis]. Dublin City University; 2005. [cited 2019 Nov 15]. Available from: http://doras.dcu.ie/18094/.

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

Council of Science Editors:

Mtawae K. Stability and kinetic studies on recombinant pyroglutamyl peptidase I and two mutant forms. [Thesis]. Dublin City University; 2005. Available from: http://doras.dcu.ie/18094/

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


Michigan Technological University

20. Alothaim, Tahiyat. DEVELOPMENT AND CHARACTERIZATION OF HISTIDINE-TAGGED HPV16 L2 AND MS2-ARGININE-TAGGED RECOMBINANT PROTEINS FOR DOWNSTREAM PROCESSES.

Degree: MS, Department of Biological Sciences, 2017, Michigan Technological University

Human papillomaviruses (HPVs) are the most common sexually transmitted infections. Persistent infection with HPV can lead to anogenital cancers including head and neck cancers.… (more)

Subjects/Keywords: Human papillomaviruses; HPV vaccine; purification; Tags; recombinant protein; VLPs; Diseases; Genetics and Genomics; Immunology and Infectious Disease; Microbiology; Virology

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

APA (6th Edition):

Alothaim, T. (2017). DEVELOPMENT AND CHARACTERIZATION OF HISTIDINE-TAGGED HPV16 L2 AND MS2-ARGININE-TAGGED RECOMBINANT PROTEINS FOR DOWNSTREAM PROCESSES. (Masters Thesis). Michigan Technological University. Retrieved from http://digitalcommons.mtu.edu/etdr/402

Chicago Manual of Style (16th Edition):

Alothaim, Tahiyat. “DEVELOPMENT AND CHARACTERIZATION OF HISTIDINE-TAGGED HPV16 L2 AND MS2-ARGININE-TAGGED RECOMBINANT PROTEINS FOR DOWNSTREAM PROCESSES.” 2017. Masters Thesis, Michigan Technological University. Accessed November 15, 2019. http://digitalcommons.mtu.edu/etdr/402.

MLA Handbook (7th Edition):

Alothaim, Tahiyat. “DEVELOPMENT AND CHARACTERIZATION OF HISTIDINE-TAGGED HPV16 L2 AND MS2-ARGININE-TAGGED RECOMBINANT PROTEINS FOR DOWNSTREAM PROCESSES.” 2017. Web. 15 Nov 2019.

Vancouver:

Alothaim T. DEVELOPMENT AND CHARACTERIZATION OF HISTIDINE-TAGGED HPV16 L2 AND MS2-ARGININE-TAGGED RECOMBINANT PROTEINS FOR DOWNSTREAM PROCESSES. [Internet] [Masters thesis]. Michigan Technological University; 2017. [cited 2019 Nov 15]. Available from: http://digitalcommons.mtu.edu/etdr/402.

Council of Science Editors:

Alothaim T. DEVELOPMENT AND CHARACTERIZATION OF HISTIDINE-TAGGED HPV16 L2 AND MS2-ARGININE-TAGGED RECOMBINANT PROTEINS FOR DOWNSTREAM PROCESSES. [Masters Thesis]. Michigan Technological University; 2017. Available from: http://digitalcommons.mtu.edu/etdr/402


Michigan Technological University

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

APA (6th Edition):

Hopson, S. (2017). Heterologous Expression and Purification of Full-Length Human Polybromo-1 Protein. (Doctoral Dissertation). Michigan Technological University. Retrieved from http://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 November 15, 2019. http://digitalcommons.mtu.edu/etdr/436.

MLA Handbook (7th Edition):

Hopson, Sarah. “Heterologous Expression and Purification of Full-Length Human Polybromo-1 Protein.” 2017. Web. 15 Nov 2019.

Vancouver:

Hopson S. Heterologous Expression and Purification of Full-Length Human Polybromo-1 Protein. [Internet] [Doctoral dissertation]. Michigan Technological University; 2017. [cited 2019 Nov 15]. Available from: http://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: http://digitalcommons.mtu.edu/etdr/436


University of Zululand

22. Oyinloye, Babatunji Emmanuel. Structural Characterization of the Switch domain regions of Schistosoma mansoni druggable Adenylate cyclase-stimulating Gα-protein .

Degree: 2017, University of Zululand

 Among the neglected tropical diseases (NTDs), schistosomiasis, a common human parasitic disease; continues to rank high as one of the major causes of morbidity and… (more)

Subjects/Keywords: antimicrobial peptides  – characterization  – docking  – drug resistance  – human schistosomiasis  – neglected tropical diseases  – praziquantel  – recombinant protein  – Schistosoma mansoni  – trematode

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

APA (6th Edition):

Oyinloye, B. E. (2017). Structural Characterization of the Switch domain regions of Schistosoma mansoni druggable Adenylate cyclase-stimulating Gα-protein . (Thesis). University of Zululand. Retrieved from http://hdl.handle.net/10530/1542

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):

Oyinloye, Babatunji Emmanuel. “Structural Characterization of the Switch domain regions of Schistosoma mansoni druggable Adenylate cyclase-stimulating Gα-protein .” 2017. Thesis, University of Zululand. Accessed November 15, 2019. http://hdl.handle.net/10530/1542.

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

MLA Handbook (7th Edition):

Oyinloye, Babatunji Emmanuel. “Structural Characterization of the Switch domain regions of Schistosoma mansoni druggable Adenylate cyclase-stimulating Gα-protein .” 2017. Web. 15 Nov 2019.

Vancouver:

Oyinloye BE. Structural Characterization of the Switch domain regions of Schistosoma mansoni druggable Adenylate cyclase-stimulating Gα-protein . [Internet] [Thesis]. University of Zululand; 2017. [cited 2019 Nov 15]. Available from: http://hdl.handle.net/10530/1542.

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

Council of Science Editors:

Oyinloye BE. Structural Characterization of the Switch domain regions of Schistosoma mansoni druggable Adenylate cyclase-stimulating Gα-protein . [Thesis]. University of Zululand; 2017. Available from: http://hdl.handle.net/10530/1542

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


University of Oxford

23. Amdani, Siti Nornadhirah. The oocyte-activation factor, phospholipase C zeta (PLCζ) : clinical prognosis, diagnosis, and treatment of oocyte activation deficiency.

Degree: PhD, 2018, University of Oxford

 Oocyte activation deficiency (OAD) is an infertile condition observed in patients who have experienced recurrent total fertilisation failure (TFF) following intracytoplasmic sperm injection treatment. This… (more)

Subjects/Keywords: next generation sequencing (NGS); variants; promoter; phospholipase C zeta (PLC?); human recombinant PLC? protein (hrPLC?); introns; Oocyte activation deficiency (OAD)

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APA (6th Edition):

Amdani, S. N. (2018). The oocyte-activation factor, phospholipase C zeta (PLCζ) : clinical prognosis, diagnosis, and treatment of oocyte activation deficiency. (Doctoral Dissertation). University of Oxford. Retrieved from http://ora.ox.ac.uk/objects/uuid:af4c4f98-497a-4666-9eec-a46bb579dd59 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.736166

Chicago Manual of Style (16th Edition):

Amdani, Siti Nornadhirah. “The oocyte-activation factor, phospholipase C zeta (PLCζ) : clinical prognosis, diagnosis, and treatment of oocyte activation deficiency.” 2018. Doctoral Dissertation, University of Oxford. Accessed November 15, 2019. http://ora.ox.ac.uk/objects/uuid:af4c4f98-497a-4666-9eec-a46bb579dd59 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.736166.

MLA Handbook (7th Edition):

Amdani, Siti Nornadhirah. “The oocyte-activation factor, phospholipase C zeta (PLCζ) : clinical prognosis, diagnosis, and treatment of oocyte activation deficiency.” 2018. Web. 15 Nov 2019.

Vancouver:

Amdani SN. The oocyte-activation factor, phospholipase C zeta (PLCζ) : clinical prognosis, diagnosis, and treatment of oocyte activation deficiency. [Internet] [Doctoral dissertation]. University of Oxford; 2018. [cited 2019 Nov 15]. Available from: http://ora.ox.ac.uk/objects/uuid:af4c4f98-497a-4666-9eec-a46bb579dd59 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.736166.

Council of Science Editors:

Amdani SN. The oocyte-activation factor, phospholipase C zeta (PLCζ) : clinical prognosis, diagnosis, and treatment of oocyte activation deficiency. [Doctoral Dissertation]. University of Oxford; 2018. Available from: http://ora.ox.ac.uk/objects/uuid:af4c4f98-497a-4666-9eec-a46bb579dd59 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.736166

24. Καραντζής, Παναγιώτης. Η θεραπευτική αξία της ανθρώπινης ανασυνδιασμένης ερυθροποιητίνης σε έγκυους φορείς της β-μεσογειακής αναιμίας με σοβαρή αναιμία στο τρίτο τρίμηνο της κύησης.

Degree: 2012, National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ)

The aim of this study was to investigate the benefits from the use of human recombinant erythropoietin (rhHEPO) in the third trimester of pregnancy in… (more)

Subjects/Keywords: Ανασυνδιασμένη ανθρώπινη ερυθροποιητίνη; Β-μεσογειακή αναιμία; Αναιμία; Κύηση; Αναιμία στην κύηση; Human recombinant erythropoietin; B-thalassemia; Anemia; Pregnant; Anemia in pregnancy

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

APA (6th Edition):

Καραντζής, . . (2012). Η θεραπευτική αξία της ανθρώπινης ανασυνδιασμένης ερυθροποιητίνης σε έγκυους φορείς της β-μεσογειακής αναιμίας με σοβαρή αναιμία στο τρίτο τρίμηνο της κύησης. (Thesis). National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ). Retrieved from http://hdl.handle.net/10442/hedi/29725

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):

Καραντζής, Παναγιώτης. “Η θεραπευτική αξία της ανθρώπινης ανασυνδιασμένης ερυθροποιητίνης σε έγκυους φορείς της β-μεσογειακής αναιμίας με σοβαρή αναιμία στο τρίτο τρίμηνο της κύησης.” 2012. Thesis, National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ). Accessed November 15, 2019. http://hdl.handle.net/10442/hedi/29725.

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

MLA Handbook (7th Edition):

Καραντζής, Παναγιώτης. “Η θεραπευτική αξία της ανθρώπινης ανασυνδιασμένης ερυθροποιητίνης σε έγκυους φορείς της β-μεσογειακής αναιμίας με σοβαρή αναιμία στο τρίτο τρίμηνο της κύησης.” 2012. Web. 15 Nov 2019.

Vancouver:

Καραντζής . Η θεραπευτική αξία της ανθρώπινης ανασυνδιασμένης ερυθροποιητίνης σε έγκυους φορείς της β-μεσογειακής αναιμίας με σοβαρή αναιμία στο τρίτο τρίμηνο της κύησης. [Internet] [Thesis]. National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ); 2012. [cited 2019 Nov 15]. Available from: http://hdl.handle.net/10442/hedi/29725.

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

Council of Science Editors:

Καραντζής . Η θεραπευτική αξία της ανθρώπινης ανασυνδιασμένης ερυθροποιητίνης σε έγκυους φορείς της β-μεσογειακής αναιμίας με σοβαρή αναιμία στο τρίτο τρίμηνο της κύησης. [Thesis]. National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ); 2012. Available from: http://hdl.handle.net/10442/hedi/29725

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


Cal Poly

25. Cruz, Erin E. OSSEOINTEGRATION OF TEMPORARY ANCHORAGE DEVICES USING RECOMBINANT HUMAN BONE MORPHOGENETIC PROTEIN-2.

Degree: MS, Biomedical and General Engineering, 2010, Cal Poly

 Over the past 5 years, the use of titanium implants as temporary anchorage devices (TADs) has become an important tool in clinical orthodontic practices. The… (more)

Subjects/Keywords: recombinant human bone morphogenetic protein-2 (rhBMP-2); osseointegration; temporary anchorage device; sandblasted and acid etched; titanium; Orthodontics and Orthodontology

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APA (6th Edition):

Cruz, E. E. (2010). OSSEOINTEGRATION OF TEMPORARY ANCHORAGE DEVICES USING RECOMBINANT HUMAN BONE MORPHOGENETIC PROTEIN-2. (Masters Thesis). Cal Poly. Retrieved from https://digitalcommons.calpoly.edu/theses/343 ; 10.15368/theses.2010.66

Chicago Manual of Style (16th Edition):

Cruz, Erin E. “OSSEOINTEGRATION OF TEMPORARY ANCHORAGE DEVICES USING RECOMBINANT HUMAN BONE MORPHOGENETIC PROTEIN-2.” 2010. Masters Thesis, Cal Poly. Accessed November 15, 2019. https://digitalcommons.calpoly.edu/theses/343 ; 10.15368/theses.2010.66.

MLA Handbook (7th Edition):

Cruz, Erin E. “OSSEOINTEGRATION OF TEMPORARY ANCHORAGE DEVICES USING RECOMBINANT HUMAN BONE MORPHOGENETIC PROTEIN-2.” 2010. Web. 15 Nov 2019.

Vancouver:

Cruz EE. OSSEOINTEGRATION OF TEMPORARY ANCHORAGE DEVICES USING RECOMBINANT HUMAN BONE MORPHOGENETIC PROTEIN-2. [Internet] [Masters thesis]. Cal Poly; 2010. [cited 2019 Nov 15]. Available from: https://digitalcommons.calpoly.edu/theses/343 ; 10.15368/theses.2010.66.

Council of Science Editors:

Cruz EE. OSSEOINTEGRATION OF TEMPORARY ANCHORAGE DEVICES USING RECOMBINANT HUMAN BONE MORPHOGENETIC PROTEIN-2. [Masters Thesis]. Cal Poly; 2010. Available from: https://digitalcommons.calpoly.edu/theses/343 ; 10.15368/theses.2010.66

26. A.L. de Goede (Anna). HIV Immunotherapy: Host Immunity and Virus Evolution.

Degree: 2014, Erasmus University Rotterdam

 markdownabstract__Abstract__ HIV-1 infection poses a major challenge to global public health. In spite of its huge clinical benefits, combined antiretroviral therapy fails to eradicate the… (more)

Subjects/Keywords: human immunodeficiency virus; HIV; HIV-1; immunotherapy; immunity; vaccine; vaccination; dentritic cell; evoluation; recombinant virus; viral vector; antigen delivery

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

APA (6th Edition):

(Anna), A. d. G. (2014). HIV Immunotherapy: Host Immunity and Virus Evolution. (Thesis). Erasmus University Rotterdam. Retrieved from http://hdl.handle.net/1765/51371

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):

(Anna), A.L. de Goede. “HIV Immunotherapy: Host Immunity and Virus Evolution.” 2014. Thesis, Erasmus University Rotterdam. Accessed November 15, 2019. http://hdl.handle.net/1765/51371.

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

MLA Handbook (7th Edition):

(Anna), A.L. de Goede. “HIV Immunotherapy: Host Immunity and Virus Evolution.” 2014. Web. 15 Nov 2019.

Vancouver:

(Anna) AdG. HIV Immunotherapy: Host Immunity and Virus Evolution. [Internet] [Thesis]. Erasmus University Rotterdam; 2014. [cited 2019 Nov 15]. Available from: http://hdl.handle.net/1765/51371.

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

Council of Science Editors:

(Anna) AdG. HIV Immunotherapy: Host Immunity and Virus Evolution. [Thesis]. Erasmus University Rotterdam; 2014. Available from: http://hdl.handle.net/1765/51371

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


Freie Universität Berlin

27. Andreou, Andreas. Establishment of a detection method for direct antibacterial activity of human defensins as a tool to investigate defensin production in intestinal tissues of patients with inflammatory bowel disease.

Degree: 2010, Freie Universität Berlin

 Introduction: As a part of the innate immunity, defensins support the preservation of the intestinal mucosal barrier which is affected in patients with inflammatory bowel… (more)

Subjects/Keywords: human β2-defensin; recombinant fusion proteins; glutathione S-transferase; inflammatory bowel disease; 600 Technik, Medizin, angewandte Wissenschaften::610 Medizin und Gesundheit

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

APA (6th Edition):

Andreou, A. (2010). Establishment of a detection method for direct antibacterial activity of human defensins as a tool to investigate defensin production in intestinal tissues of patients with inflammatory bowel disease. (Thesis). Freie Universität Berlin. Retrieved from https://refubium.fu-berlin.de/handle/fub188/10462

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):

Andreou, Andreas. “Establishment of a detection method for direct antibacterial activity of human defensins as a tool to investigate defensin production in intestinal tissues of patients with inflammatory bowel disease.” 2010. Thesis, Freie Universität Berlin. Accessed November 15, 2019. https://refubium.fu-berlin.de/handle/fub188/10462.

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

MLA Handbook (7th Edition):

Andreou, Andreas. “Establishment of a detection method for direct antibacterial activity of human defensins as a tool to investigate defensin production in intestinal tissues of patients with inflammatory bowel disease.” 2010. Web. 15 Nov 2019.

Vancouver:

Andreou A. Establishment of a detection method for direct antibacterial activity of human defensins as a tool to investigate defensin production in intestinal tissues of patients with inflammatory bowel disease. [Internet] [Thesis]. Freie Universität Berlin; 2010. [cited 2019 Nov 15]. Available from: https://refubium.fu-berlin.de/handle/fub188/10462.

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

Council of Science Editors:

Andreou A. Establishment of a detection method for direct antibacterial activity of human defensins as a tool to investigate defensin production in intestinal tissues of patients with inflammatory bowel disease. [Thesis]. Freie Universität Berlin; 2010. Available from: https://refubium.fu-berlin.de/handle/fub188/10462

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


Georgia Tech

28. Tang, Shiue-Cheng. Genetic engineering of non-beta-cells for regulated insulin secretion.

Degree: PhD, Chemical Engineering, 2003, Georgia Tech

Subjects/Keywords: Recombinant human insulin; Pancreatic beta cells; Diabetes; Recombinant human insulin; Pancreatic beta cells; Diabetes

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

APA (6th Edition):

Tang, S. (2003). Genetic engineering of non-beta-cells for regulated insulin secretion. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/5375

Chicago Manual of Style (16th Edition):

Tang, Shiue-Cheng. “Genetic engineering of non-beta-cells for regulated insulin secretion.” 2003. Doctoral Dissertation, Georgia Tech. Accessed November 15, 2019. http://hdl.handle.net/1853/5375.

MLA Handbook (7th Edition):

Tang, Shiue-Cheng. “Genetic engineering of non-beta-cells for regulated insulin secretion.” 2003. Web. 15 Nov 2019.

Vancouver:

Tang S. Genetic engineering of non-beta-cells for regulated insulin secretion. [Internet] [Doctoral dissertation]. Georgia Tech; 2003. [cited 2019 Nov 15]. Available from: http://hdl.handle.net/1853/5375.

Council of Science Editors:

Tang S. Genetic engineering of non-beta-cells for regulated insulin secretion. [Doctoral Dissertation]. Georgia Tech; 2003. Available from: http://hdl.handle.net/1853/5375

29. Appelman-Dijkstra, Natasha Mireille. Long-term consequences of growth hormone replacement and cranial radiation on pituitary function.

Degree: 2015, Department of Endocrinology, Faculty of Medicine, Leiden University Medical Center (LUMC), Leiden University

 This thesis covers the consequences of cranial irradiation of non-pituitary tumors, eg nasopharyngeal carcinoma, on pituitary function. In chapter 2 we have performed a meta-analysis… (more)

Subjects/Keywords: Pituitary; Cranial radiation; Growth hormone replacement; Recombinant human growth hormone; Pituitary; Cranial radiation; Growth hormone replacement; Recombinant human growth hormone

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

APA (6th Edition):

Appelman-Dijkstra, N. M. (2015). Long-term consequences of growth hormone replacement and cranial radiation on pituitary function. (Doctoral Dissertation). Department of Endocrinology, Faculty of Medicine, Leiden University Medical Center (LUMC), Leiden University. Retrieved from http://hdl.handle.net/1887/33195

Chicago Manual of Style (16th Edition):

Appelman-Dijkstra, Natasha Mireille. “Long-term consequences of growth hormone replacement and cranial radiation on pituitary function.” 2015. Doctoral Dissertation, Department of Endocrinology, Faculty of Medicine, Leiden University Medical Center (LUMC), Leiden University. Accessed November 15, 2019. http://hdl.handle.net/1887/33195.

MLA Handbook (7th Edition):

Appelman-Dijkstra, Natasha Mireille. “Long-term consequences of growth hormone replacement and cranial radiation on pituitary function.” 2015. Web. 15 Nov 2019.

Vancouver:

Appelman-Dijkstra NM. Long-term consequences of growth hormone replacement and cranial radiation on pituitary function. [Internet] [Doctoral dissertation]. Department of Endocrinology, Faculty of Medicine, Leiden University Medical Center (LUMC), Leiden University; 2015. [cited 2019 Nov 15]. Available from: http://hdl.handle.net/1887/33195.

Council of Science Editors:

Appelman-Dijkstra NM. Long-term consequences of growth hormone replacement and cranial radiation on pituitary function. [Doctoral Dissertation]. Department of Endocrinology, Faculty of Medicine, Leiden University Medical Center (LUMC), Leiden University; 2015. Available from: http://hdl.handle.net/1887/33195


Indian Institute of Science

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

Degree: 2016, 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 · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Manoharan, S. (2016). Engineering the N-Glycosylation Pathway in Pichia Pastoris for the Expression of Glycoprotein Hormones. (Thesis). Indian Institute of Science. Retrieved from http://hdl.handle.net/2005/3017

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):

Manoharan, Simna. “Engineering the N-Glycosylation Pathway in Pichia Pastoris for the Expression of Glycoprotein Hormones.” 2016. Thesis, Indian Institute of Science. Accessed November 15, 2019. http://hdl.handle.net/2005/3017.

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

MLA Handbook (7th Edition):

Manoharan, Simna. “Engineering the N-Glycosylation Pathway in Pichia Pastoris for the Expression of Glycoprotein Hormones.” 2016. Web. 15 Nov 2019.

Vancouver:

Manoharan S. Engineering the N-Glycosylation Pathway in Pichia Pastoris for the Expression of Glycoprotein Hormones. [Internet] [Thesis]. Indian Institute of Science; 2016. [cited 2019 Nov 15]. Available from: http://hdl.handle.net/2005/3017.

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

Council of Science Editors:

Manoharan S. Engineering the N-Glycosylation Pathway in Pichia Pastoris for the Expression of Glycoprotein Hormones. [Thesis]. Indian Institute of Science; 2016. Available from: http://hdl.handle.net/2005/3017

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

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