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You searched for subject:(Factor VIII). Showing records 1 – 30 of 76 total matches.

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Queens University

1. Waters, Braden. Tolerance Induction and The Immunobiology of Factor VIII in Hemophilia A .

Degree: Pathology and Molecular Medicine, 2010, Queens University

 The development of inhibitory antibodies to the factor VIII (FVIII) protein is the greatest complication in the management of hemophilia A patients. These antibodies, which… (more)

Subjects/Keywords: Factor VIII ; Tolerance

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APA (6th Edition):

Waters, B. (2010). Tolerance Induction and The Immunobiology of Factor VIII in Hemophilia A . (Thesis). Queens University. Retrieved from http://hdl.handle.net/1974/6107

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):

Waters, Braden. “Tolerance Induction and The Immunobiology of Factor VIII in Hemophilia A .” 2010. Thesis, Queens University. Accessed October 22, 2020. http://hdl.handle.net/1974/6107.

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

MLA Handbook (7th Edition):

Waters, Braden. “Tolerance Induction and The Immunobiology of Factor VIII in Hemophilia A .” 2010. Web. 22 Oct 2020.

Vancouver:

Waters B. Tolerance Induction and The Immunobiology of Factor VIII in Hemophilia A . [Internet] [Thesis]. Queens University; 2010. [cited 2020 Oct 22]. Available from: http://hdl.handle.net/1974/6107.

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

Council of Science Editors:

Waters B. Tolerance Induction and The Immunobiology of Factor VIII in Hemophilia A . [Thesis]. Queens University; 2010. Available from: http://hdl.handle.net/1974/6107

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


Oregon State University

2. 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 October 22, 2020. 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. 22 Oct 2020.

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 2020 Oct 22]. 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


Western Washington University

3. Werther, Rachel. Structural studies of blood coagulation factor VIII in complexes with inhibitory antibodies.

Degree: MS, Chemistry, 2012, Western Washington University

  Normal blood clotting is regulated by blood plasma protein factors in a blood coagulation cascade. Deficiency in one of these proteins, Factor VIII (FVIII),… (more)

Subjects/Keywords: Chemistry; Blood coagulation factor VIII antibodies; Blood coagulation factor VIII antibodies – Animal models; masters theses

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APA (6th Edition):

Werther, R. (2012). Structural studies of blood coagulation factor VIII in complexes with inhibitory antibodies. (Masters Thesis). Western Washington University. Retrieved from https://doi.org/10.25710/qree-nh08 ; https://cedar.wwu.edu/wwuet/189

Chicago Manual of Style (16th Edition):

Werther, Rachel. “Structural studies of blood coagulation factor VIII in complexes with inhibitory antibodies.” 2012. Masters Thesis, Western Washington University. Accessed October 22, 2020. https://doi.org/10.25710/qree-nh08 ; https://cedar.wwu.edu/wwuet/189.

MLA Handbook (7th Edition):

Werther, Rachel. “Structural studies of blood coagulation factor VIII in complexes with inhibitory antibodies.” 2012. Web. 22 Oct 2020.

Vancouver:

Werther R. Structural studies of blood coagulation factor VIII in complexes with inhibitory antibodies. [Internet] [Masters thesis]. Western Washington University; 2012. [cited 2020 Oct 22]. Available from: https://doi.org/10.25710/qree-nh08 ; https://cedar.wwu.edu/wwuet/189.

Council of Science Editors:

Werther R. Structural studies of blood coagulation factor VIII in complexes with inhibitory antibodies. [Masters Thesis]. Western Washington University; 2012. Available from: https://doi.org/10.25710/qree-nh08 ; https://cedar.wwu.edu/wwuet/189


University of Adelaide

4. Ling, Min. Some laboratory and clinical aspects of haemophilia A.

Degree: 2010, University of Adelaide

 The hereditary bleeding disorder haemophilia A is caused by a deficiency or functional defect of coagulation factor VIII (FVIII). FVIII replacement therapy enables effective treatment… (more)

Subjects/Keywords: haemophilia A; factor VIII; Factor VIII inhibitors; thrombin generation assay; ankle arthropathy

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APA (6th Edition):

Ling, M. (2010). Some laboratory and clinical aspects of haemophilia A. (Thesis). University of Adelaide. Retrieved from http://hdl.handle.net/2440/62386

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):

Ling, Min. “Some laboratory and clinical aspects of haemophilia A.” 2010. Thesis, University of Adelaide. Accessed October 22, 2020. http://hdl.handle.net/2440/62386.

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

MLA Handbook (7th Edition):

Ling, Min. “Some laboratory and clinical aspects of haemophilia A.” 2010. Web. 22 Oct 2020.

Vancouver:

Ling M. Some laboratory and clinical aspects of haemophilia A. [Internet] [Thesis]. University of Adelaide; 2010. [cited 2020 Oct 22]. Available from: http://hdl.handle.net/2440/62386.

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

Council of Science Editors:

Ling M. Some laboratory and clinical aspects of haemophilia A. [Thesis]. University of Adelaide; 2010. Available from: http://hdl.handle.net/2440/62386

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

5. 杉田, 千泰. Elevated plasma factor VIII enhances venous thrombus formation in rabbits : contribution of factor XI, von Willebrand factor and tissue factor : 血液凝固VIII因子の血中濃度の増加は家兎静脈血栓形成を促進させる : 血液凝固XI因子、von Willebrand因子および組織因子の関与.

Degree: 博士(医学), 2013, University of Miyazaki / 宮崎大学

以下に掲載:Thrombosis and Haemostasis. 2013, 110, 1, p.62-75, doi: 10.1160/TH13-01-0069.

Elevated plasma levels of factor VIII (FVIII) are associated with increased risk of deep venous thrombosis.… (more)

Subjects/Keywords: Deep venous thrombosis; factor VIII; factor XI; von Willebrand factor

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APA (6th Edition):

杉田, . (2013). Elevated plasma factor VIII enhances venous thrombus formation in rabbits : contribution of factor XI, von Willebrand factor and tissue factor : 血液凝固VIII因子の血中濃度の増加は家兎静脈血栓形成を促進させる : 血液凝固XI因子、von Willebrand因子および組織因子の関与. (Thesis). University of Miyazaki / 宮崎大学. Retrieved from http://hdl.handle.net/10458/4705

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):

杉田, 千泰. “Elevated plasma factor VIII enhances venous thrombus formation in rabbits : contribution of factor XI, von Willebrand factor and tissue factor : 血液凝固VIII因子の血中濃度の増加は家兎静脈血栓形成を促進させる : 血液凝固XI因子、von Willebrand因子および組織因子の関与.” 2013. Thesis, University of Miyazaki / 宮崎大学. Accessed October 22, 2020. http://hdl.handle.net/10458/4705.

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

MLA Handbook (7th Edition):

杉田, 千泰. “Elevated plasma factor VIII enhances venous thrombus formation in rabbits : contribution of factor XI, von Willebrand factor and tissue factor : 血液凝固VIII因子の血中濃度の増加は家兎静脈血栓形成を促進させる : 血液凝固XI因子、von Willebrand因子および組織因子の関与.” 2013. Web. 22 Oct 2020.

Vancouver:

杉田 . Elevated plasma factor VIII enhances venous thrombus formation in rabbits : contribution of factor XI, von Willebrand factor and tissue factor : 血液凝固VIII因子の血中濃度の増加は家兎静脈血栓形成を促進させる : 血液凝固XI因子、von Willebrand因子および組織因子の関与. [Internet] [Thesis]. University of Miyazaki / 宮崎大学; 2013. [cited 2020 Oct 22]. Available from: http://hdl.handle.net/10458/4705.

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

Council of Science Editors:

杉田 . Elevated plasma factor VIII enhances venous thrombus formation in rabbits : contribution of factor XI, von Willebrand factor and tissue factor : 血液凝固VIII因子の血中濃度の増加は家兎静脈血栓形成を促進させる : 血液凝固XI因子、von Willebrand因子および組織因子の関与. [Thesis]. University of Miyazaki / 宮崎大学; 2013. Available from: http://hdl.handle.net/10458/4705

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

6. João Batista Oliveira Maia. EXPRESSÃO IMUNO-HISTOQUÍMICA DO FATOR VIII E CD31 EM CARCINOMA ESPINOCELULAR DE LÍNGUA, LÁBIO INFERIOR E ASSOALHO DE BOCA.

Degree: 2007, Universidade Potiguar

Considerando a imprevisibilidade de comportamento biológico do carcinoma espinocelular de boca (CEC), a angiogênese tumoral vem sendo estudada para correlacionar à agressividade destas neoplasias com… (more)

Subjects/Keywords: ODONTOLOGIA; Fator VIII; CD31; Squamous cell carcinomas; Carcinoma espinocelular; Angiogênese; CD31; Angiogenesis; Factor VIII

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APA (6th Edition):

Maia, J. B. O. (2007). EXPRESSÃO IMUNO-HISTOQUÍMICA DO FATOR VIII E CD31 EM CARCINOMA ESPINOCELULAR DE LÍNGUA, LÁBIO INFERIOR E ASSOALHO DE BOCA. (Thesis). Universidade Potiguar. Retrieved from http://bibliotecadigital.unp.br/tde_busca/arquivo.php?codArquivo=24

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):

Maia, João Batista Oliveira. “EXPRESSÃO IMUNO-HISTOQUÍMICA DO FATOR VIII E CD31 EM CARCINOMA ESPINOCELULAR DE LÍNGUA, LÁBIO INFERIOR E ASSOALHO DE BOCA.” 2007. Thesis, Universidade Potiguar. Accessed October 22, 2020. http://bibliotecadigital.unp.br/tde_busca/arquivo.php?codArquivo=24.

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

MLA Handbook (7th Edition):

Maia, João Batista Oliveira. “EXPRESSÃO IMUNO-HISTOQUÍMICA DO FATOR VIII E CD31 EM CARCINOMA ESPINOCELULAR DE LÍNGUA, LÁBIO INFERIOR E ASSOALHO DE BOCA.” 2007. Web. 22 Oct 2020.

Vancouver:

Maia JBO. EXPRESSÃO IMUNO-HISTOQUÍMICA DO FATOR VIII E CD31 EM CARCINOMA ESPINOCELULAR DE LÍNGUA, LÁBIO INFERIOR E ASSOALHO DE BOCA. [Internet] [Thesis]. Universidade Potiguar; 2007. [cited 2020 Oct 22]. Available from: http://bibliotecadigital.unp.br/tde_busca/arquivo.php?codArquivo=24.

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

Council of Science Editors:

Maia JBO. EXPRESSÃO IMUNO-HISTOQUÍMICA DO FATOR VIII E CD31 EM CARCINOMA ESPINOCELULAR DE LÍNGUA, LÁBIO INFERIOR E ASSOALHO DE BOCA. [Thesis]. Universidade Potiguar; 2007. Available from: http://bibliotecadigital.unp.br/tde_busca/arquivo.php?codArquivo=24

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

7. JoÃo Batista Oliveira Maia. EXPRESSION IMUNO - HISTOQUÃMICA OF the FACTOR VIII AND OF CD31 IN CARCINOMA ESPINOCELULAR OF LANGUAGE, INFERIOR LIP AND FLOOR OF MOUTH.

Degree: 2007, Universidade Potiguar

Considering the unpredictability of the biology of oral squamous cell carcinomas, tumoral angiogenesis has been evaluated as a means of correlating the level of tumor… (more)

Subjects/Keywords: Carcinoma espinocelular. AngiogÃnese. Fator VIII, CD31; ODONTOLOGIA; Squamous cell carcinomas. Angiogenesis. Factor VIII, CD31

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APA (6th Edition):

Maia, J. B. O. (2007). EXPRESSION IMUNO - HISTOQUÃMICA OF the FACTOR VIII AND OF CD31 IN CARCINOMA ESPINOCELULAR OF LANGUAGE, INFERIOR LIP AND FLOOR OF MOUTH. (Thesis). Universidade Potiguar. Retrieved from http://bibliotecadigital.unp.br/tde_busca/arquivo.php?codArquivo=26

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):

Maia, JoÃo Batista Oliveira. “EXPRESSION IMUNO - HISTOQUÃMICA OF the FACTOR VIII AND OF CD31 IN CARCINOMA ESPINOCELULAR OF LANGUAGE, INFERIOR LIP AND FLOOR OF MOUTH.” 2007. Thesis, Universidade Potiguar. Accessed October 22, 2020. http://bibliotecadigital.unp.br/tde_busca/arquivo.php?codArquivo=26.

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

MLA Handbook (7th Edition):

Maia, JoÃo Batista Oliveira. “EXPRESSION IMUNO - HISTOQUÃMICA OF the FACTOR VIII AND OF CD31 IN CARCINOMA ESPINOCELULAR OF LANGUAGE, INFERIOR LIP AND FLOOR OF MOUTH.” 2007. Web. 22 Oct 2020.

Vancouver:

Maia JBO. EXPRESSION IMUNO - HISTOQUÃMICA OF the FACTOR VIII AND OF CD31 IN CARCINOMA ESPINOCELULAR OF LANGUAGE, INFERIOR LIP AND FLOOR OF MOUTH. [Internet] [Thesis]. Universidade Potiguar; 2007. [cited 2020 Oct 22]. Available from: http://bibliotecadigital.unp.br/tde_busca/arquivo.php?codArquivo=26.

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

Council of Science Editors:

Maia JBO. EXPRESSION IMUNO - HISTOQUÃMICA OF the FACTOR VIII AND OF CD31 IN CARCINOMA ESPINOCELULAR OF LANGUAGE, INFERIOR LIP AND FLOOR OF MOUTH. [Thesis]. Universidade Potiguar; 2007. Available from: http://bibliotecadigital.unp.br/tde_busca/arquivo.php?codArquivo=26

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

8. Gangadharan, Bagirath. Structural and functional aspects of factor viii in the initiation of the anti-factor viii immune response : Aspect structurels et fonctionnels du facteur viii dans l'initiation de la réponse immunitaire anti-facteur viii.

Degree: Docteur es, Immunologie, 2014, Université Pierre et Marie Curie – Paris VI

L’apparition d’une réponse immunitaire contre le Facteur VIII (FVIII) de la coagulation est une complication majeur qui survient chez 30% des hémophile A sévères. Bien… (more)

Subjects/Keywords: Hémophilie A; Facteur VIII; Immunogénicité; Coagulation; Signaux de dangers; Inhibiteurs; Factor VIII; Hemophilia A; 571.96

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APA (6th Edition):

Gangadharan, B. (2014). Structural and functional aspects of factor viii in the initiation of the anti-factor viii immune response : Aspect structurels et fonctionnels du facteur viii dans l'initiation de la réponse immunitaire anti-facteur viii. (Doctoral Dissertation). Université Pierre et Marie Curie – Paris VI. Retrieved from http://www.theses.fr/2014PA066257

Chicago Manual of Style (16th Edition):

Gangadharan, Bagirath. “Structural and functional aspects of factor viii in the initiation of the anti-factor viii immune response : Aspect structurels et fonctionnels du facteur viii dans l'initiation de la réponse immunitaire anti-facteur viii.” 2014. Doctoral Dissertation, Université Pierre et Marie Curie – Paris VI. Accessed October 22, 2020. http://www.theses.fr/2014PA066257.

MLA Handbook (7th Edition):

Gangadharan, Bagirath. “Structural and functional aspects of factor viii in the initiation of the anti-factor viii immune response : Aspect structurels et fonctionnels du facteur viii dans l'initiation de la réponse immunitaire anti-facteur viii.” 2014. Web. 22 Oct 2020.

Vancouver:

Gangadharan B. Structural and functional aspects of factor viii in the initiation of the anti-factor viii immune response : Aspect structurels et fonctionnels du facteur viii dans l'initiation de la réponse immunitaire anti-facteur viii. [Internet] [Doctoral dissertation]. Université Pierre et Marie Curie – Paris VI; 2014. [cited 2020 Oct 22]. Available from: http://www.theses.fr/2014PA066257.

Council of Science Editors:

Gangadharan B. Structural and functional aspects of factor viii in the initiation of the anti-factor viii immune response : Aspect structurels et fonctionnels du facteur viii dans l'initiation de la réponse immunitaire anti-facteur viii. [Doctoral Dissertation]. Université Pierre et Marie Curie – Paris VI; 2014. Available from: http://www.theses.fr/2014PA066257

9. Doi, Masaaki; Sugimoto, Mitsuhiko; Matsui, Hideto; Matsunari, Yasunori. Coagulation potential of immobilised factor VIII in flow-dependent fibrin generation on platelet surfaces.

Degree: 博士(医学), 2013, Nara Medical University / 奈良県立医科大学

Coagulation factor VIII (FVIII) plays an essential role in haemostasis. To date, physiologic activity of FVIII circulating in the bloodstream (S-FVIII) is evaluated by classic… (more)

Subjects/Keywords: Haemophilia; von Willebrand factor; factor VIII; flow; Fibrin generation

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APA (6th Edition):

Doi, Masaaki; Sugimoto, Mitsuhiko; Matsui, Hideto; Matsunari, Y. (2013). Coagulation potential of immobilised factor VIII in flow-dependent fibrin generation on platelet surfaces. (Thesis). Nara Medical University / 奈良県立医科大学. Retrieved from http://hdl.handle.net/10564/2636

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

Chicago Manual of Style (16th Edition):

Doi, Masaaki; Sugimoto, Mitsuhiko; Matsui, Hideto; Matsunari, Yasunori. “Coagulation potential of immobilised factor VIII in flow-dependent fibrin generation on platelet surfaces.” 2013. Thesis, Nara Medical University / 奈良県立医科大学. Accessed October 22, 2020. http://hdl.handle.net/10564/2636.

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

MLA Handbook (7th Edition):

Doi, Masaaki; Sugimoto, Mitsuhiko; Matsui, Hideto; Matsunari, Yasunori. “Coagulation potential of immobilised factor VIII in flow-dependent fibrin generation on platelet surfaces.” 2013. Web. 22 Oct 2020.

Vancouver:

Doi, Masaaki; Sugimoto, Mitsuhiko; Matsui, Hideto; Matsunari Y. Coagulation potential of immobilised factor VIII in flow-dependent fibrin generation on platelet surfaces. [Internet] [Thesis]. Nara Medical University / 奈良県立医科大学; 2013. [cited 2020 Oct 22]. Available from: http://hdl.handle.net/10564/2636.

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

Council of Science Editors:

Doi, Masaaki; Sugimoto, Mitsuhiko; Matsui, Hideto; Matsunari Y. Coagulation potential of immobilised factor VIII in flow-dependent fibrin generation on platelet surfaces. [Thesis]. Nara Medical University / 奈良県立医科大学; 2013. Available from: http://hdl.handle.net/10564/2636

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


Queens University

10. Leonard, Jacqueline Marianna Morello. The effect of biomechanical and biochemical regulators on the expression of Factor VIII and von Willebrand Factor in endothelial cells .

Degree: Pathology and Molecular Medicine, 2016, Queens University

 The coagulant protein Factor VIII (FVIII) has been the subject of much debate and controversy regarding where, when, and how it is expressed and produced… (more)

Subjects/Keywords: TNFa ; Inflammation ; Shear Stress ; von Willebrand Factor ; Endothelial Cells ; Factor VIII

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APA (6th Edition):

Leonard, J. M. M. (2016). The effect of biomechanical and biochemical regulators on the expression of Factor VIII and von Willebrand Factor in endothelial cells . (Thesis). Queens University. Retrieved from http://hdl.handle.net/1974/13989

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):

Leonard, Jacqueline Marianna Morello. “The effect of biomechanical and biochemical regulators on the expression of Factor VIII and von Willebrand Factor in endothelial cells .” 2016. Thesis, Queens University. Accessed October 22, 2020. http://hdl.handle.net/1974/13989.

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

MLA Handbook (7th Edition):

Leonard, Jacqueline Marianna Morello. “The effect of biomechanical and biochemical regulators on the expression of Factor VIII and von Willebrand Factor in endothelial cells .” 2016. Web. 22 Oct 2020.

Vancouver:

Leonard JMM. The effect of biomechanical and biochemical regulators on the expression of Factor VIII and von Willebrand Factor in endothelial cells . [Internet] [Thesis]. Queens University; 2016. [cited 2020 Oct 22]. Available from: http://hdl.handle.net/1974/13989.

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

Council of Science Editors:

Leonard JMM. The effect of biomechanical and biochemical regulators on the expression of Factor VIII and von Willebrand Factor in endothelial cells . [Thesis]. Queens University; 2016. Available from: http://hdl.handle.net/1974/13989

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


Universidade Estadual de Campinas

11. Bittar, Luis Fernando, 1980-. Avaliação da expressão proteica e de alterações moleculares do receptor hepático LRP1 e sua correlação com os níveis plasmáticos de fator VIII: Evaluation of protein expression and molecular changes of hepatic LRP1 receptor and its correlation with plasma levels of factor VIII.

Degree: 2013, Universidade Estadual de Campinas

 Abstract: Introduction: Increased levels of factor VIII (FVIII) are a prevalent and independent risk factor for venous thromboembolism (VTE). Post-thrombotic syndrome (PTS) is a long-term… (more)

Subjects/Keywords: Tromboembolismo venoso; Inflamação; Síndrome pós-trombótica; Fator de von Willebrand; Fator VIII; Venous thrombosis; Factor VIII; Von Willebrand factor

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APA (6th Edition):

Bittar, Luis Fernando, 1. (2013). Avaliação da expressão proteica e de alterações moleculares do receptor hepático LRP1 e sua correlação com os níveis plasmáticos de fator VIII: Evaluation of protein expression and molecular changes of hepatic LRP1 receptor and its correlation with plasma levels of factor VIII. (Thesis). Universidade Estadual de Campinas. Retrieved from http://repositorio.unicamp.br/jspui/handle/REPOSIP/312768

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):

Bittar, Luis Fernando, 1980-. “Avaliação da expressão proteica e de alterações moleculares do receptor hepático LRP1 e sua correlação com os níveis plasmáticos de fator VIII: Evaluation of protein expression and molecular changes of hepatic LRP1 receptor and its correlation with plasma levels of factor VIII.” 2013. Thesis, Universidade Estadual de Campinas. Accessed October 22, 2020. http://repositorio.unicamp.br/jspui/handle/REPOSIP/312768.

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

MLA Handbook (7th Edition):

Bittar, Luis Fernando, 1980-. “Avaliação da expressão proteica e de alterações moleculares do receptor hepático LRP1 e sua correlação com os níveis plasmáticos de fator VIII: Evaluation of protein expression and molecular changes of hepatic LRP1 receptor and its correlation with plasma levels of factor VIII.” 2013. Web. 22 Oct 2020.

Vancouver:

Bittar, Luis Fernando 1. Avaliação da expressão proteica e de alterações moleculares do receptor hepático LRP1 e sua correlação com os níveis plasmáticos de fator VIII: Evaluation of protein expression and molecular changes of hepatic LRP1 receptor and its correlation with plasma levels of factor VIII. [Internet] [Thesis]. Universidade Estadual de Campinas; 2013. [cited 2020 Oct 22]. Available from: http://repositorio.unicamp.br/jspui/handle/REPOSIP/312768.

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

Council of Science Editors:

Bittar, Luis Fernando 1. Avaliação da expressão proteica e de alterações moleculares do receptor hepático LRP1 e sua correlação com os níveis plasmáticos de fator VIII: Evaluation of protein expression and molecular changes of hepatic LRP1 receptor and its correlation with plasma levels of factor VIII. [Thesis]. Universidade Estadual de Campinas; 2013. Available from: http://repositorio.unicamp.br/jspui/handle/REPOSIP/312768

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

12. Guillet, Benoît. Analyse des relations génotype-phénotype du facteur VIII : interactions avec le facteur IX, le facteur Willebrand et la LRP1 : Analysis of genotype-phenotype relations of the factor VIII : interactions with the factor IX, the factor Willebrand and the LRP1.

Degree: Docteur es, Sciences de la santé, 2009, Université Claude Bernard – Lyon I

Le facteur VIII (FVIII) est une glycoprotéine de la coagulation plasmatique, co-facteur du facteur IX activé (FIXa). Son métabolisme dépend de multiples facteurs limitant ou… (more)

Subjects/Keywords: Facteur VIII; Variations physiologiques; Hémophilie A; Facteur Willebrand; Polymorphismes; Domaine A3 du facteur VIII; VIII factor; Physiologic variations; Willebrand factor; Polymorphisms; 616.15

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APA (6th Edition):

Guillet, B. (2009). Analyse des relations génotype-phénotype du facteur VIII : interactions avec le facteur IX, le facteur Willebrand et la LRP1 : Analysis of genotype-phenotype relations of the factor VIII : interactions with the factor IX, the factor Willebrand and the LRP1. (Doctoral Dissertation). Université Claude Bernard – Lyon I. Retrieved from http://www.theses.fr/2009LYO10319

Chicago Manual of Style (16th Edition):

Guillet, Benoît. “Analyse des relations génotype-phénotype du facteur VIII : interactions avec le facteur IX, le facteur Willebrand et la LRP1 : Analysis of genotype-phenotype relations of the factor VIII : interactions with the factor IX, the factor Willebrand and the LRP1.” 2009. Doctoral Dissertation, Université Claude Bernard – Lyon I. Accessed October 22, 2020. http://www.theses.fr/2009LYO10319.

MLA Handbook (7th Edition):

Guillet, Benoît. “Analyse des relations génotype-phénotype du facteur VIII : interactions avec le facteur IX, le facteur Willebrand et la LRP1 : Analysis of genotype-phenotype relations of the factor VIII : interactions with the factor IX, the factor Willebrand and the LRP1.” 2009. Web. 22 Oct 2020.

Vancouver:

Guillet B. Analyse des relations génotype-phénotype du facteur VIII : interactions avec le facteur IX, le facteur Willebrand et la LRP1 : Analysis of genotype-phenotype relations of the factor VIII : interactions with the factor IX, the factor Willebrand and the LRP1. [Internet] [Doctoral dissertation]. Université Claude Bernard – Lyon I; 2009. [cited 2020 Oct 22]. Available from: http://www.theses.fr/2009LYO10319.

Council of Science Editors:

Guillet B. Analyse des relations génotype-phénotype du facteur VIII : interactions avec le facteur IX, le facteur Willebrand et la LRP1 : Analysis of genotype-phenotype relations of the factor VIII : interactions with the factor IX, the factor Willebrand and the LRP1. [Doctoral Dissertation]. Université Claude Bernard – Lyon I; 2009. Available from: http://www.theses.fr/2009LYO10319


Queens University

13. Georgescu, Maria. Novel Methods of Factor VIII Tolerance Induction in Hemophilia A Mouse Models .

Degree: Pathology and Molecular Medicine, Queens University

 The most serious complication of factor VIII (FVIII) replacement therapy in hemophilia A (HA) patients remains the development of anti-FVIII antibodies (inhibitors). At this time,… (more)

Subjects/Keywords: Hemophilia A; Factor VIII; inhibitors

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APA (6th Edition):

Georgescu, M. (n.d.). Novel Methods of Factor VIII Tolerance Induction in Hemophilia A Mouse Models . (Thesis). Queens University. Retrieved from http://hdl.handle.net/1974/25962

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):

Georgescu, Maria. “Novel Methods of Factor VIII Tolerance Induction in Hemophilia A Mouse Models .” Thesis, Queens University. Accessed October 22, 2020. http://hdl.handle.net/1974/25962.

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):

Georgescu, Maria. “Novel Methods of Factor VIII Tolerance Induction in Hemophilia A Mouse Models .” Web. 22 Oct 2020.

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

Vancouver:

Georgescu M. Novel Methods of Factor VIII Tolerance Induction in Hemophilia A Mouse Models . [Internet] [Thesis]. Queens University; [cited 2020 Oct 22]. Available from: http://hdl.handle.net/1974/25962.

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:

Georgescu M. Novel Methods of Factor VIII Tolerance Induction in Hemophilia A Mouse Models . [Thesis]. Queens University; Available from: http://hdl.handle.net/1974/25962

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


Queens University

14. Riches, Jonathan Jacob. Endothelial cell synthesis of Factor VIII .

Degree: Pathology and Molecular Medicine, 2013, Queens University

Factor VIII (FVIII) is an essential blood-clotting protein and mutations in the FVIII gene are the cause of hemophilia A, a severe inherited bleeding disorder.… (more)

Subjects/Keywords: Shear Stress ; Hemophilia A ; Factor VIII ; Endothelial Cells

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APA (6th Edition):

Riches, J. J. (2013). Endothelial cell synthesis of Factor VIII . (Thesis). Queens University. Retrieved from http://hdl.handle.net/1974/7853

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):

Riches, Jonathan Jacob. “Endothelial cell synthesis of Factor VIII .” 2013. Thesis, Queens University. Accessed October 22, 2020. http://hdl.handle.net/1974/7853.

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

MLA Handbook (7th Edition):

Riches, Jonathan Jacob. “Endothelial cell synthesis of Factor VIII .” 2013. Web. 22 Oct 2020.

Vancouver:

Riches JJ. Endothelial cell synthesis of Factor VIII . [Internet] [Thesis]. Queens University; 2013. [cited 2020 Oct 22]. Available from: http://hdl.handle.net/1974/7853.

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

Council of Science Editors:

Riches JJ. Endothelial cell synthesis of Factor VIII . [Thesis]. Queens University; 2013. Available from: http://hdl.handle.net/1974/7853

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

15. Huschke, Allison M. Hemostatic responses to exercise in a polycythemia vera patient.

Degree: 2016, James Madison University

 PURPOSE: To assess the hemostatic responses to exercise in a patient with Polycythemia Vera (PV). METHODS: Six female runners (≥15 miles/week) completed a maximal treadmill… (more)

Subjects/Keywords: tPA-antigen; PAI-1; Factor VIII; hematocrit; Sports Sciences

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APA (6th Edition):

Huschke, A. M. (2016). Hemostatic responses to exercise in a polycythemia vera patient. (Masters Thesis). James Madison University. Retrieved from https://commons.lib.jmu.edu/honors201019/247

Chicago Manual of Style (16th Edition):

Huschke, Allison M. “Hemostatic responses to exercise in a polycythemia vera patient.” 2016. Masters Thesis, James Madison University. Accessed October 22, 2020. https://commons.lib.jmu.edu/honors201019/247.

MLA Handbook (7th Edition):

Huschke, Allison M. “Hemostatic responses to exercise in a polycythemia vera patient.” 2016. Web. 22 Oct 2020.

Vancouver:

Huschke AM. Hemostatic responses to exercise in a polycythemia vera patient. [Internet] [Masters thesis]. James Madison University; 2016. [cited 2020 Oct 22]. Available from: https://commons.lib.jmu.edu/honors201019/247.

Council of Science Editors:

Huschke AM. Hemostatic responses to exercise in a polycythemia vera patient. [Masters Thesis]. James Madison University; 2016. Available from: https://commons.lib.jmu.edu/honors201019/247

16. Allsbrook, Robert C. The hemostatic effects of acute exposure to colored cornstarch powder during a 5k run.

Degree: 2016, James Madison University

 PURPOSE: To examine the acute hemostatic effects of particulate matter (PM) in the form of colored corn starch powder during a 5 kilometer race. METHODS:… (more)

Subjects/Keywords: PAI-1; Factor VIII; tPA; Exercise Science; Hematology; Sports Sciences

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APA (6th Edition):

Allsbrook, R. C. (2016). The hemostatic effects of acute exposure to colored cornstarch powder during a 5k run. (Masters Thesis). James Madison University. Retrieved from https://commons.lib.jmu.edu/honors201019/246

Chicago Manual of Style (16th Edition):

Allsbrook, Robert C. “The hemostatic effects of acute exposure to colored cornstarch powder during a 5k run.” 2016. Masters Thesis, James Madison University. Accessed October 22, 2020. https://commons.lib.jmu.edu/honors201019/246.

MLA Handbook (7th Edition):

Allsbrook, Robert C. “The hemostatic effects of acute exposure to colored cornstarch powder during a 5k run.” 2016. Web. 22 Oct 2020.

Vancouver:

Allsbrook RC. The hemostatic effects of acute exposure to colored cornstarch powder during a 5k run. [Internet] [Masters thesis]. James Madison University; 2016. [cited 2020 Oct 22]. Available from: https://commons.lib.jmu.edu/honors201019/246.

Council of Science Editors:

Allsbrook RC. The hemostatic effects of acute exposure to colored cornstarch powder during a 5k run. [Masters Thesis]. James Madison University; 2016. Available from: https://commons.lib.jmu.edu/honors201019/246


California State University – Sacramento

17. Cortez-Toledo, Elizabeth Jasmin. Generation of liver organoids using IPSC derived hepatocyte and endothelial cells for persistent secretion of factor VIII.

Degree: MA, Biological Science (Stem Cell, 2017, California State University – Sacramento

 Hemophilia A (HA) is a genetic disorder resulting from deficient levels of the coagulation protein factor VIII. HA is inherited through an X-linked recessive pattern… (more)

Subjects/Keywords: Stem cells; Factor VIII; Hemophilia A; Liver organoids

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APA (6th Edition):

Cortez-Toledo, E. J. (2017). Generation of liver organoids using IPSC derived hepatocyte and endothelial cells for persistent secretion of factor VIII. (Masters Thesis). California State University – Sacramento. Retrieved from http://hdl.handle.net/10211.3/190683

Chicago Manual of Style (16th Edition):

Cortez-Toledo, Elizabeth Jasmin. “Generation of liver organoids using IPSC derived hepatocyte and endothelial cells for persistent secretion of factor VIII.” 2017. Masters Thesis, California State University – Sacramento. Accessed October 22, 2020. http://hdl.handle.net/10211.3/190683.

MLA Handbook (7th Edition):

Cortez-Toledo, Elizabeth Jasmin. “Generation of liver organoids using IPSC derived hepatocyte and endothelial cells for persistent secretion of factor VIII.” 2017. Web. 22 Oct 2020.

Vancouver:

Cortez-Toledo EJ. Generation of liver organoids using IPSC derived hepatocyte and endothelial cells for persistent secretion of factor VIII. [Internet] [Masters thesis]. California State University – Sacramento; 2017. [cited 2020 Oct 22]. Available from: http://hdl.handle.net/10211.3/190683.

Council of Science Editors:

Cortez-Toledo EJ. Generation of liver organoids using IPSC derived hepatocyte and endothelial cells for persistent secretion of factor VIII. [Masters Thesis]. California State University – Sacramento; 2017. Available from: http://hdl.handle.net/10211.3/190683


Universiteit Utrecht

18. Schooten, C.J.M. van. Von Willebrand Factor: clearance as regulator of plasma levels.

Degree: 2007, Universiteit Utrecht

 Von Willebrand factor (VWF) and coagulation factor VIII (FVIII) are plasma proteins that circulate in a tight, noncovalent complex. Binding to VWF is required to… (more)

Subjects/Keywords: Geneeskunde; Von Willebrand Factor; Von Willebrand Disease; O-linked glycosylation; cysteine mutations; clearance mechanism; factor VIII; Von Willebrand factor/factor VIII complex; half-life; macrophages; Staphylococcus aureus protein A

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APA (6th Edition):

Schooten, C. J. M. v. (2007). Von Willebrand Factor: clearance as regulator of plasma levels. (Doctoral Dissertation). Universiteit Utrecht. Retrieved from http://dspace.library.uu.nl:8080/handle/1874/23898

Chicago Manual of Style (16th Edition):

Schooten, C J M van. “Von Willebrand Factor: clearance as regulator of plasma levels.” 2007. Doctoral Dissertation, Universiteit Utrecht. Accessed October 22, 2020. http://dspace.library.uu.nl:8080/handle/1874/23898.

MLA Handbook (7th Edition):

Schooten, C J M van. “Von Willebrand Factor: clearance as regulator of plasma levels.” 2007. Web. 22 Oct 2020.

Vancouver:

Schooten CJMv. Von Willebrand Factor: clearance as regulator of plasma levels. [Internet] [Doctoral dissertation]. Universiteit Utrecht; 2007. [cited 2020 Oct 22]. Available from: http://dspace.library.uu.nl:8080/handle/1874/23898.

Council of Science Editors:

Schooten CJMv. Von Willebrand Factor: clearance as regulator of plasma levels. [Doctoral Dissertation]. Universiteit Utrecht; 2007. Available from: http://dspace.library.uu.nl:8080/handle/1874/23898


University of Rochester

19. DeAngelis, Jennifer Patricia. The Mechanisms for Catalytic Inactivation of FVIIIa by APC and Factor Xa.

Degree: PhD, 2012, University of Rochester

Factor VIII (FVIII) is activated by thrombin and factor Xa (FXa) through proteolysis at Arg372, Arg740 and Arg1689 and inactivated by activated protein C (APC)… (more)

Subjects/Keywords: Factor VIII; Activated Protein C; P4-P3' Residues; Mutagenesis; Western Blotting; Factor Xa; Exosites

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APA (6th Edition):

DeAngelis, J. P. (2012). The Mechanisms for Catalytic Inactivation of FVIIIa by APC and Factor Xa. (Doctoral Dissertation). University of Rochester. Retrieved from http://hdl.handle.net/1802/25503

Chicago Manual of Style (16th Edition):

DeAngelis, Jennifer Patricia. “The Mechanisms for Catalytic Inactivation of FVIIIa by APC and Factor Xa.” 2012. Doctoral Dissertation, University of Rochester. Accessed October 22, 2020. http://hdl.handle.net/1802/25503.

MLA Handbook (7th Edition):

DeAngelis, Jennifer Patricia. “The Mechanisms for Catalytic Inactivation of FVIIIa by APC and Factor Xa.” 2012. Web. 22 Oct 2020.

Vancouver:

DeAngelis JP. The Mechanisms for Catalytic Inactivation of FVIIIa by APC and Factor Xa. [Internet] [Doctoral dissertation]. University of Rochester; 2012. [cited 2020 Oct 22]. Available from: http://hdl.handle.net/1802/25503.

Council of Science Editors:

DeAngelis JP. The Mechanisms for Catalytic Inactivation of FVIIIa by APC and Factor Xa. [Doctoral Dissertation]. University of Rochester; 2012. Available from: http://hdl.handle.net/1802/25503


McMaster University

20. Dhadwar, Singh Sukhdeep. CHITOSAN-MEDIATED ORAL GENE THERAPY FOR HEMOPHILIA TREATMENT AND PROPHYLACTIC TOLERANCE.

Degree: PhD, 2011, McMaster University

Hemophilia A and B are X-linked recessive bleeding disorders caused by the deficiency of coagulation factor VIII (FVIII) and Factor IX (FIX), respectively. Current… (more)

Subjects/Keywords: gene delivery; hemophilia; gene therapy; Factor VIII; Factor IX; blood disorders; Biological Engineering; Biological Engineering

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APA (6th Edition):

Dhadwar, S. S. (2011). CHITOSAN-MEDIATED ORAL GENE THERAPY FOR HEMOPHILIA TREATMENT AND PROPHYLACTIC TOLERANCE. (Doctoral Dissertation). McMaster University. Retrieved from http://hdl.handle.net/11375/11474

Chicago Manual of Style (16th Edition):

Dhadwar, Singh Sukhdeep. “CHITOSAN-MEDIATED ORAL GENE THERAPY FOR HEMOPHILIA TREATMENT AND PROPHYLACTIC TOLERANCE.” 2011. Doctoral Dissertation, McMaster University. Accessed October 22, 2020. http://hdl.handle.net/11375/11474.

MLA Handbook (7th Edition):

Dhadwar, Singh Sukhdeep. “CHITOSAN-MEDIATED ORAL GENE THERAPY FOR HEMOPHILIA TREATMENT AND PROPHYLACTIC TOLERANCE.” 2011. Web. 22 Oct 2020.

Vancouver:

Dhadwar SS. CHITOSAN-MEDIATED ORAL GENE THERAPY FOR HEMOPHILIA TREATMENT AND PROPHYLACTIC TOLERANCE. [Internet] [Doctoral dissertation]. McMaster University; 2011. [cited 2020 Oct 22]. Available from: http://hdl.handle.net/11375/11474.

Council of Science Editors:

Dhadwar SS. CHITOSAN-MEDIATED ORAL GENE THERAPY FOR HEMOPHILIA TREATMENT AND PROPHYLACTIC TOLERANCE. [Doctoral Dissertation]. McMaster University; 2011. Available from: http://hdl.handle.net/11375/11474


University of Pennsylvania

21. Skipwith, Christopher Gemil. Regulation of Adamts13 Function in Hemostasis by Cofactor and Substrate Exosite interactions.

Degree: 2012, University of Pennsylvania

 ADAMTS13 (A Disintegrin And Metalloprotease with ThromboSpondin type1 repeats-13) is an enzyme that is mainly synthesized in the liver and secreted into the blood stream.… (more)

Subjects/Keywords: ADAMTS13; Factor VIII; Thrombosis; TTP; von Willebrand Disease; von Willebrand Factor; Biochemistry; Biophysics; Pathology

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APA (6th Edition):

Skipwith, C. G. (2012). Regulation of Adamts13 Function in Hemostasis by Cofactor and Substrate Exosite interactions. (Thesis). University of Pennsylvania. Retrieved from https://repository.upenn.edu/edissertations/701

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):

Skipwith, Christopher Gemil. “Regulation of Adamts13 Function in Hemostasis by Cofactor and Substrate Exosite interactions.” 2012. Thesis, University of Pennsylvania. Accessed October 22, 2020. https://repository.upenn.edu/edissertations/701.

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

MLA Handbook (7th Edition):

Skipwith, Christopher Gemil. “Regulation of Adamts13 Function in Hemostasis by Cofactor and Substrate Exosite interactions.” 2012. Web. 22 Oct 2020.

Vancouver:

Skipwith CG. Regulation of Adamts13 Function in Hemostasis by Cofactor and Substrate Exosite interactions. [Internet] [Thesis]. University of Pennsylvania; 2012. [cited 2020 Oct 22]. Available from: https://repository.upenn.edu/edissertations/701.

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

Council of Science Editors:

Skipwith CG. Regulation of Adamts13 Function in Hemostasis by Cofactor and Substrate Exosite interactions. [Thesis]. University of Pennsylvania; 2012. Available from: https://repository.upenn.edu/edissertations/701

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

22. Yada, Koji; Nogami, Keiji; Ogiwara, Kenichi. Activated prothrombin complex concentrate (APCC)-mediated activation of factor (F)VIII in mixtures of FVIII and APCC enhances hemostatic effectiveness.

Degree: 博士(医学), 2013, Nara Medical University / 奈良県立医科大学

BACKGROUND AND OBJECTIVES: Activated prothrombin complex concentrates (APCCs), utilized in bypassing therapy for hemophiliacs with inhibitor, contain factors (Fs) VII, FII, FIX and FX, and… (more)

Subjects/Keywords: activation analysis;

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APA (6th Edition):

Yada, Koji; Nogami, Keiji; Ogiwara, K. (2013). Activated prothrombin complex concentrate (APCC)-mediated activation of factor (F)VIII in mixtures of FVIII and APCC enhances hemostatic effectiveness. (Thesis). Nara Medical University / 奈良県立医科大学. Retrieved from http://hdl.handle.net/10564/2635

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):

Yada, Koji; Nogami, Keiji; Ogiwara, Kenichi. “Activated prothrombin complex concentrate (APCC)-mediated activation of factor (F)VIII in mixtures of FVIII and APCC enhances hemostatic effectiveness.” 2013. Thesis, Nara Medical University / 奈良県立医科大学. Accessed October 22, 2020. http://hdl.handle.net/10564/2635.

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

MLA Handbook (7th Edition):

Yada, Koji; Nogami, Keiji; Ogiwara, Kenichi. “Activated prothrombin complex concentrate (APCC)-mediated activation of factor (F)VIII in mixtures of FVIII and APCC enhances hemostatic effectiveness.” 2013. Web. 22 Oct 2020.

Vancouver:

Yada, Koji; Nogami, Keiji; Ogiwara K. Activated prothrombin complex concentrate (APCC)-mediated activation of factor (F)VIII in mixtures of FVIII and APCC enhances hemostatic effectiveness. [Internet] [Thesis]. Nara Medical University / 奈良県立医科大学; 2013. [cited 2020 Oct 22]. Available from: http://hdl.handle.net/10564/2635.

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

Council of Science Editors:

Yada, Koji; Nogami, Keiji; Ogiwara K. Activated prothrombin complex concentrate (APCC)-mediated activation of factor (F)VIII in mixtures of FVIII and APCC enhances hemostatic effectiveness. [Thesis]. Nara Medical University / 奈良県立医科大学; 2013. Available from: http://hdl.handle.net/10564/2635

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

23. Massaro, Juliana Doblas. Dinâmica de Polimorfismos Genéticos Ligados ao Gene da Hemofilia A (F8) na População Brasileira.

Degree: PhD, Genética, 2010, University of São Paulo

A Hemofilia A é uma doença sanguínea condicionada por gene localizado no cromossomo X. É causada pela deficiência parcial ou total da atividade do Fator… (more)

Subjects/Keywords: Brazilian population; Diagnóstico indireto; Factor VIII; Fator VIII; Hemofilia A; Hemophilia A; Indirect diagnosis; Microsatellites.; miicrossatélites.; População brasileira

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APA (6th Edition):

Massaro, J. D. (2010). Dinâmica de Polimorfismos Genéticos Ligados ao Gene da Hemofilia A (F8) na População Brasileira. (Doctoral Dissertation). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/17/17135/tde-31052011-090114/ ;

Chicago Manual of Style (16th Edition):

Massaro, Juliana Doblas. “Dinâmica de Polimorfismos Genéticos Ligados ao Gene da Hemofilia A (F8) na População Brasileira.” 2010. Doctoral Dissertation, University of São Paulo. Accessed October 22, 2020. http://www.teses.usp.br/teses/disponiveis/17/17135/tde-31052011-090114/ ;.

MLA Handbook (7th Edition):

Massaro, Juliana Doblas. “Dinâmica de Polimorfismos Genéticos Ligados ao Gene da Hemofilia A (F8) na População Brasileira.” 2010. Web. 22 Oct 2020.

Vancouver:

Massaro JD. Dinâmica de Polimorfismos Genéticos Ligados ao Gene da Hemofilia A (F8) na População Brasileira. [Internet] [Doctoral dissertation]. University of São Paulo; 2010. [cited 2020 Oct 22]. Available from: http://www.teses.usp.br/teses/disponiveis/17/17135/tde-31052011-090114/ ;.

Council of Science Editors:

Massaro JD. Dinâmica de Polimorfismos Genéticos Ligados ao Gene da Hemofilia A (F8) na População Brasileira. [Doctoral Dissertation]. University of São Paulo; 2010. Available from: http://www.teses.usp.br/teses/disponiveis/17/17135/tde-31052011-090114/ ;

24. Ing, Mathieu. Immunogénicité du facteur VIII thérapeutique : importance du complément et des domaines C du facteur VIII pour son endocytose : Immunogenicity of therapeutic factor VIII : importance of complement and factor VIII C domains for its uptake.

Degree: Docteur es, Immunologie, 2016, Université Pierre et Marie Curie – Paris VI

La survenue d'anticorps neutralisant le facteur VIII de la coagulation (FVIII) chez les patients hémophiles A constitue un échec thérapeutique majeur. Si les étapes effectrices… (more)

Subjects/Keywords: Hémophilie A; Facteur VIII; Immunogénicité; Protéine thérapeutique; Système du complément; Cellules présentatrices d'antigènes; Hemophilia A; Factor VIII; Therapeutic proteins; 571.96

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APA (6th Edition):

Ing, M. (2016). Immunogénicité du facteur VIII thérapeutique : importance du complément et des domaines C du facteur VIII pour son endocytose : Immunogenicity of therapeutic factor VIII : importance of complement and factor VIII C domains for its uptake. (Doctoral Dissertation). Université Pierre et Marie Curie – Paris VI. Retrieved from http://www.theses.fr/2016PA066637

Chicago Manual of Style (16th Edition):

Ing, Mathieu. “Immunogénicité du facteur VIII thérapeutique : importance du complément et des domaines C du facteur VIII pour son endocytose : Immunogenicity of therapeutic factor VIII : importance of complement and factor VIII C domains for its uptake.” 2016. Doctoral Dissertation, Université Pierre et Marie Curie – Paris VI. Accessed October 22, 2020. http://www.theses.fr/2016PA066637.

MLA Handbook (7th Edition):

Ing, Mathieu. “Immunogénicité du facteur VIII thérapeutique : importance du complément et des domaines C du facteur VIII pour son endocytose : Immunogenicity of therapeutic factor VIII : importance of complement and factor VIII C domains for its uptake.” 2016. Web. 22 Oct 2020.

Vancouver:

Ing M. Immunogénicité du facteur VIII thérapeutique : importance du complément et des domaines C du facteur VIII pour son endocytose : Immunogenicity of therapeutic factor VIII : importance of complement and factor VIII C domains for its uptake. [Internet] [Doctoral dissertation]. Université Pierre et Marie Curie – Paris VI; 2016. [cited 2020 Oct 22]. Available from: http://www.theses.fr/2016PA066637.

Council of Science Editors:

Ing M. Immunogénicité du facteur VIII thérapeutique : importance du complément et des domaines C du facteur VIII pour son endocytose : Immunogenicity of therapeutic factor VIII : importance of complement and factor VIII C domains for its uptake. [Doctoral Dissertation]. Université Pierre et Marie Curie – Paris VI; 2016. Available from: http://www.theses.fr/2016PA066637

25. Delignat-Heudier, Sandrine. Stratégies thérapeutiques contre la réponse immunitaire anti-Facteur VIII chez l'hémophile A : par modification de la structure du FVIII, par inhibition de la signalisation des lymphocytes B : Therapeutic strategies against FVIII immune response in hemophilia A : by modifying FVIII structure, by inhibiting B cells signalisation.

Degree: Docteur es, Immunologie, 2017, Université Pierre et Marie Curie – Paris VI

L’administration de Facteur VIII thérapeutique (FVIII) chez les patients hémophiles A entraine l’apparition d’anticorps anti-FVIII appelés « inhibiteurs » chez 30% des hémophiles A sévères.… (more)

Subjects/Keywords: Hémophilie A; Facteur VIII; Inhibiteurs; Glycosylation; Cellules denritiques; Tyrosine kinase de Bruton; Hemolophilia A; Factor VIII; Glycosylation; 571.96

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APA (6th Edition):

Delignat-Heudier, S. (2017). Stratégies thérapeutiques contre la réponse immunitaire anti-Facteur VIII chez l'hémophile A : par modification de la structure du FVIII, par inhibition de la signalisation des lymphocytes B : Therapeutic strategies against FVIII immune response in hemophilia A : by modifying FVIII structure, by inhibiting B cells signalisation. (Doctoral Dissertation). Université Pierre et Marie Curie – Paris VI. Retrieved from http://www.theses.fr/2017PA066002

Chicago Manual of Style (16th Edition):

Delignat-Heudier, Sandrine. “Stratégies thérapeutiques contre la réponse immunitaire anti-Facteur VIII chez l'hémophile A : par modification de la structure du FVIII, par inhibition de la signalisation des lymphocytes B : Therapeutic strategies against FVIII immune response in hemophilia A : by modifying FVIII structure, by inhibiting B cells signalisation.” 2017. Doctoral Dissertation, Université Pierre et Marie Curie – Paris VI. Accessed October 22, 2020. http://www.theses.fr/2017PA066002.

MLA Handbook (7th Edition):

Delignat-Heudier, Sandrine. “Stratégies thérapeutiques contre la réponse immunitaire anti-Facteur VIII chez l'hémophile A : par modification de la structure du FVIII, par inhibition de la signalisation des lymphocytes B : Therapeutic strategies against FVIII immune response in hemophilia A : by modifying FVIII structure, by inhibiting B cells signalisation.” 2017. Web. 22 Oct 2020.

Vancouver:

Delignat-Heudier S. Stratégies thérapeutiques contre la réponse immunitaire anti-Facteur VIII chez l'hémophile A : par modification de la structure du FVIII, par inhibition de la signalisation des lymphocytes B : Therapeutic strategies against FVIII immune response in hemophilia A : by modifying FVIII structure, by inhibiting B cells signalisation. [Internet] [Doctoral dissertation]. Université Pierre et Marie Curie – Paris VI; 2017. [cited 2020 Oct 22]. Available from: http://www.theses.fr/2017PA066002.

Council of Science Editors:

Delignat-Heudier S. Stratégies thérapeutiques contre la réponse immunitaire anti-Facteur VIII chez l'hémophile A : par modification de la structure du FVIII, par inhibition de la signalisation des lymphocytes B : Therapeutic strategies against FVIII immune response in hemophilia A : by modifying FVIII structure, by inhibiting B cells signalisation. [Doctoral Dissertation]. Université Pierre et Marie Curie – Paris VI; 2017. Available from: http://www.theses.fr/2017PA066002

26. Jinzenji, Daniela. Desenvolvimento de processo cromatográfico para purificação de fator VIII humano. Emprego de anticorpos contra fragmentos específicos da proteína na avaliação da pureza e estabilidade durante as etapas de purificação.

Degree: Mestrado, Biotecnologia, 2008, University of São Paulo

O fator VIII de coagulação (FVIII), recombinante ou purificado de plasma, é o biofármaco necessário para o tratamento da hemofília A, a doença hemorrágica mais… (more)

Subjects/Keywords: Biofármacos derivados de plasma; Biopharmaceuticals Plasma derivation; Chromatography of proteins; Coagulation Factor VIII; Cromatografia de proteínas; Factor VIII production; Fator VIII de coagulação; Hemofília; Hemophilia; Plasma proteins purification; Produção de Fator VIII; Purificação de proteínas de plasma

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APA (6th Edition):

Jinzenji, D. (2008). Desenvolvimento de processo cromatográfico para purificação de fator VIII humano. Emprego de anticorpos contra fragmentos específicos da proteína na avaliação da pureza e estabilidade durante as etapas de purificação. (Masters Thesis). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/87/87131/tde-10032009-104314/ ;

Chicago Manual of Style (16th Edition):

Jinzenji, Daniela. “Desenvolvimento de processo cromatográfico para purificação de fator VIII humano. Emprego de anticorpos contra fragmentos específicos da proteína na avaliação da pureza e estabilidade durante as etapas de purificação.” 2008. Masters Thesis, University of São Paulo. Accessed October 22, 2020. http://www.teses.usp.br/teses/disponiveis/87/87131/tde-10032009-104314/ ;.

MLA Handbook (7th Edition):

Jinzenji, Daniela. “Desenvolvimento de processo cromatográfico para purificação de fator VIII humano. Emprego de anticorpos contra fragmentos específicos da proteína na avaliação da pureza e estabilidade durante as etapas de purificação.” 2008. Web. 22 Oct 2020.

Vancouver:

Jinzenji D. Desenvolvimento de processo cromatográfico para purificação de fator VIII humano. Emprego de anticorpos contra fragmentos específicos da proteína na avaliação da pureza e estabilidade durante as etapas de purificação. [Internet] [Masters thesis]. University of São Paulo; 2008. [cited 2020 Oct 22]. Available from: http://www.teses.usp.br/teses/disponiveis/87/87131/tde-10032009-104314/ ;.

Council of Science Editors:

Jinzenji D. Desenvolvimento de processo cromatográfico para purificação de fator VIII humano. Emprego de anticorpos contra fragmentos específicos da proteína na avaliação da pureza e estabilidade durante as etapas de purificação. [Masters Thesis]. University of São Paulo; 2008. Available from: http://www.teses.usp.br/teses/disponiveis/87/87131/tde-10032009-104314/ ;

27. Russick, Jules. Traitement de l’hémophilie A à l’aide d’ARNm codant le facteur VIII et prévention de la réponse immunitaire dirigée contre le facteur VIII thérapeutique : Treatment of hemophilia A using factor VIII-encoding mRNA and prevention of the neutralizing immune response to therapeutic factor VIII.

Degree: Docteur es, Immunologie, 2018, Sorbonne université

L’hémophilie A est une maladie hémorragique rare liée à une absence de facteur VIII (FVIII) fonctionnel de la coagulation. Les formes les plus sévères engendrent… (more)

Subjects/Keywords: Hemophilie A; Facteur VIII; Inhibiteurs du facteur VIII; ARNm transcrit in vitro; Tyrosine kinase de Bruton; Modèle murin humanisé; Hemophilia A; Factor VIII; Factor VIII inhibitors; In vitro transcribed mRNA; Bruton’s tyrosine kinase; Humanized mouse model; 616.079; 616.1572

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APA (6th Edition):

Russick, J. (2018). Traitement de l’hémophilie A à l’aide d’ARNm codant le facteur VIII et prévention de la réponse immunitaire dirigée contre le facteur VIII thérapeutique : Treatment of hemophilia A using factor VIII-encoding mRNA and prevention of the neutralizing immune response to therapeutic factor VIII. (Doctoral Dissertation). Sorbonne université. Retrieved from http://www.theses.fr/2018SORUS362

Chicago Manual of Style (16th Edition):

Russick, Jules. “Traitement de l’hémophilie A à l’aide d’ARNm codant le facteur VIII et prévention de la réponse immunitaire dirigée contre le facteur VIII thérapeutique : Treatment of hemophilia A using factor VIII-encoding mRNA and prevention of the neutralizing immune response to therapeutic factor VIII.” 2018. Doctoral Dissertation, Sorbonne université. Accessed October 22, 2020. http://www.theses.fr/2018SORUS362.

MLA Handbook (7th Edition):

Russick, Jules. “Traitement de l’hémophilie A à l’aide d’ARNm codant le facteur VIII et prévention de la réponse immunitaire dirigée contre le facteur VIII thérapeutique : Treatment of hemophilia A using factor VIII-encoding mRNA and prevention of the neutralizing immune response to therapeutic factor VIII.” 2018. Web. 22 Oct 2020.

Vancouver:

Russick J. Traitement de l’hémophilie A à l’aide d’ARNm codant le facteur VIII et prévention de la réponse immunitaire dirigée contre le facteur VIII thérapeutique : Treatment of hemophilia A using factor VIII-encoding mRNA and prevention of the neutralizing immune response to therapeutic factor VIII. [Internet] [Doctoral dissertation]. Sorbonne université; 2018. [cited 2020 Oct 22]. Available from: http://www.theses.fr/2018SORUS362.

Council of Science Editors:

Russick J. Traitement de l’hémophilie A à l’aide d’ARNm codant le facteur VIII et prévention de la réponse immunitaire dirigée contre le facteur VIII thérapeutique : Treatment of hemophilia A using factor VIII-encoding mRNA and prevention of the neutralizing immune response to therapeutic factor VIII. [Doctoral Dissertation]. Sorbonne université; 2018. Available from: http://www.theses.fr/2018SORUS362


Western Washington University

28. Smith, Ian. Structural Characterization of a Human/Porcine Chimeric FVIII Construct and an Improved Human Factor VIII Model and Progress Towards Determination of the FVIII C1 Domain In Complex With Inhibitory Antibodies.

Degree: MS, Chemistry, 2018, Western Washington University

  Blood coagulation factor VIII (FVIII) is a non-enzymatic protein cofactor, which plays a crucial role in the formation of a stable blood clot. Absence… (more)

Subjects/Keywords: Chemistry; Hemophilia – Treatment – Complications; Hemophilia – Treatment – Research; Blood coagulation factor VIII – Therapeutic use – Testing; Blood coagulation factor VIII antibodies; Chimerism – Testing; Blood coagulation disorders; Therapeutics, Experimental; masters theses

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APA (6th Edition):

Smith, I. (2018). Structural Characterization of a Human/Porcine Chimeric FVIII Construct and an Improved Human Factor VIII Model and Progress Towards Determination of the FVIII C1 Domain In Complex With Inhibitory Antibodies. (Masters Thesis). Western Washington University. Retrieved from https://doi.org/10.25710/wn94-rc05 ; https://cedar.wwu.edu/wwuet/710

Chicago Manual of Style (16th Edition):

Smith, Ian. “Structural Characterization of a Human/Porcine Chimeric FVIII Construct and an Improved Human Factor VIII Model and Progress Towards Determination of the FVIII C1 Domain In Complex With Inhibitory Antibodies.” 2018. Masters Thesis, Western Washington University. Accessed October 22, 2020. https://doi.org/10.25710/wn94-rc05 ; https://cedar.wwu.edu/wwuet/710.

MLA Handbook (7th Edition):

Smith, Ian. “Structural Characterization of a Human/Porcine Chimeric FVIII Construct and an Improved Human Factor VIII Model and Progress Towards Determination of the FVIII C1 Domain In Complex With Inhibitory Antibodies.” 2018. Web. 22 Oct 2020.

Vancouver:

Smith I. Structural Characterization of a Human/Porcine Chimeric FVIII Construct and an Improved Human Factor VIII Model and Progress Towards Determination of the FVIII C1 Domain In Complex With Inhibitory Antibodies. [Internet] [Masters thesis]. Western Washington University; 2018. [cited 2020 Oct 22]. Available from: https://doi.org/10.25710/wn94-rc05 ; https://cedar.wwu.edu/wwuet/710.

Council of Science Editors:

Smith I. Structural Characterization of a Human/Porcine Chimeric FVIII Construct and an Improved Human Factor VIII Model and Progress Towards Determination of the FVIII C1 Domain In Complex With Inhibitory Antibodies. [Masters Thesis]. Western Washington University; 2018. Available from: https://doi.org/10.25710/wn94-rc05 ; https://cedar.wwu.edu/wwuet/710


Cape Peninsula University of Technology

29. Collette, Carol Joan. Optimization of production variables governing yield and stability of factor VIII in cryoprecipitate .

Degree: 1997, Cape Peninsula University of Technology

 Cryoprecipitates are used as the raw material for the preparation of Factor VIII (FVIIIl) for replacement therapy for haemophiliacs. Routinely, cryoprecipitate only recovers 50% of… (more)

Subjects/Keywords: Blood coagulation factor VIII; Medical technology

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APA (6th Edition):

Collette, C. J. (1997). Optimization of production variables governing yield and stability of factor VIII in cryoprecipitate . (Thesis). Cape Peninsula University of Technology. Retrieved from http://etd.cput.ac.za/handle/20.500.11838/1468

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):

Collette, Carol Joan. “Optimization of production variables governing yield and stability of factor VIII in cryoprecipitate .” 1997. Thesis, Cape Peninsula University of Technology. Accessed October 22, 2020. http://etd.cput.ac.za/handle/20.500.11838/1468.

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

MLA Handbook (7th Edition):

Collette, Carol Joan. “Optimization of production variables governing yield and stability of factor VIII in cryoprecipitate .” 1997. Web. 22 Oct 2020.

Vancouver:

Collette CJ. Optimization of production variables governing yield and stability of factor VIII in cryoprecipitate . [Internet] [Thesis]. Cape Peninsula University of Technology; 1997. [cited 2020 Oct 22]. Available from: http://etd.cput.ac.za/handle/20.500.11838/1468.

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

Council of Science Editors:

Collette CJ. Optimization of production variables governing yield and stability of factor VIII in cryoprecipitate . [Thesis]. Cape Peninsula University of Technology; 1997. Available from: http://etd.cput.ac.za/handle/20.500.11838/1468

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

30. Cheung, Katharine Lana. Chronic Kidney Disease and the Risk of Venous Thromboembolism.

Degree: PhD, Clinical and Translational Science, 2018, University of Vermont

  Chronic kidney disease (CKD) affects more than 30 million adults in the U.S. and is strongly associated with cardiovascular events and mortality. Venous thromboembolism… (more)

Subjects/Keywords: Chronic kidney disease; Factor VIII; Inflammation; Procoagulation; Thrombosis; Venous thromoembolism; Epidemiology; Medical Sciences

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APA (6th Edition):

Cheung, K. L. (2018). Chronic Kidney Disease and the Risk of Venous Thromboembolism. (Doctoral Dissertation). University of Vermont. Retrieved from https://scholarworks.uvm.edu/graddis/879

Chicago Manual of Style (16th Edition):

Cheung, Katharine Lana. “Chronic Kidney Disease and the Risk of Venous Thromboembolism.” 2018. Doctoral Dissertation, University of Vermont. Accessed October 22, 2020. https://scholarworks.uvm.edu/graddis/879.

MLA Handbook (7th Edition):

Cheung, Katharine Lana. “Chronic Kidney Disease and the Risk of Venous Thromboembolism.” 2018. Web. 22 Oct 2020.

Vancouver:

Cheung KL. Chronic Kidney Disease and the Risk of Venous Thromboembolism. [Internet] [Doctoral dissertation]. University of Vermont; 2018. [cited 2020 Oct 22]. Available from: https://scholarworks.uvm.edu/graddis/879.

Council of Science Editors:

Cheung KL. Chronic Kidney Disease and the Risk of Venous Thromboembolism. [Doctoral Dissertation]. University of Vermont; 2018. Available from: https://scholarworks.uvm.edu/graddis/879

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