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You searched for subject:(Cytomegalovirus). Showing records 241 – 270 of 284 total matches.

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241. Tay, Chin Hun. In Vivo Regulation of Murine Cytomegalovirus Infections: The Role of Cell Surface Molecules and Mechanisms of Control by Natural Killer Cells: A Dissertation.

Degree: Immunology and Microbiology, Pathology, 1997, U of Massachusetts : Med

  The overall aim of this thesis was to determine how natural killer (NK) cells regulate virus infections in vivo. Anti-viral mechanisms by which NK… (more)

Subjects/Keywords: Muromegalovirus; Cytomegalovirus Infections; Animal Experimentation and Research; Cells; Digestive System; Hemic and Immune Systems; Immunology and Infectious Disease; Tissues; Viruses

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APA (6th Edition):

Tay, C. H. (1997). In Vivo Regulation of Murine Cytomegalovirus Infections: The Role of Cell Surface Molecules and Mechanisms of Control by Natural Killer Cells: A Dissertation. (Doctoral Dissertation). U of Massachusetts : Med. Retrieved from https://escholarship.umassmed.edu/gsbs_diss/64

Chicago Manual of Style (16th Edition):

Tay, Chin Hun. “In Vivo Regulation of Murine Cytomegalovirus Infections: The Role of Cell Surface Molecules and Mechanisms of Control by Natural Killer Cells: A Dissertation.” 1997. Doctoral Dissertation, U of Massachusetts : Med. Accessed November 18, 2019. https://escholarship.umassmed.edu/gsbs_diss/64.

MLA Handbook (7th Edition):

Tay, Chin Hun. “In Vivo Regulation of Murine Cytomegalovirus Infections: The Role of Cell Surface Molecules and Mechanisms of Control by Natural Killer Cells: A Dissertation.” 1997. Web. 18 Nov 2019.

Vancouver:

Tay CH. In Vivo Regulation of Murine Cytomegalovirus Infections: The Role of Cell Surface Molecules and Mechanisms of Control by Natural Killer Cells: A Dissertation. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 1997. [cited 2019 Nov 18]. Available from: https://escholarship.umassmed.edu/gsbs_diss/64.

Council of Science Editors:

Tay CH. In Vivo Regulation of Murine Cytomegalovirus Infections: The Role of Cell Surface Molecules and Mechanisms of Control by Natural Killer Cells: A Dissertation. [Doctoral Dissertation]. U of Massachusetts : Med; 1997. Available from: https://escholarship.umassmed.edu/gsbs_diss/64

242. Florin, Luise. Inhibition of tetraspanin functions impairs human papillomavirus and cytomegalovirus infections.

Degree: 2018, MDPI Basel, Switzerland.

Subjects/Keywords: Human papillomavirus; HPV16; Human cytomegalovirus; Tetraspanin; Virus entry; Blocking peptide; IC50; Biología y Biomedicina / Biología

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APA (6th Edition):

Florin, L. (2018). Inhibition of tetraspanin functions impairs human papillomavirus and cytomegalovirus infections. (Thesis). MDPI Basel, Switzerland. Retrieved from http://hdl.handle.net/10486/685846

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):

Florin, Luise. “Inhibition of tetraspanin functions impairs human papillomavirus and cytomegalovirus infections.” 2018. Thesis, MDPI Basel, Switzerland. Accessed November 18, 2019. http://hdl.handle.net/10486/685846.

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

MLA Handbook (7th Edition):

Florin, Luise. “Inhibition of tetraspanin functions impairs human papillomavirus and cytomegalovirus infections.” 2018. Web. 18 Nov 2019.

Vancouver:

Florin L. Inhibition of tetraspanin functions impairs human papillomavirus and cytomegalovirus infections. [Internet] [Thesis]. MDPI Basel, Switzerland.; 2018. [cited 2019 Nov 18]. Available from: http://hdl.handle.net/10486/685846.

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

Council of Science Editors:

Florin L. Inhibition of tetraspanin functions impairs human papillomavirus and cytomegalovirus infections. [Thesis]. MDPI Basel, Switzerland.; 2018. Available from: http://hdl.handle.net/10486/685846

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

243. Carpentier, Kathryn Semmens. Evolution of Protein Kinase R Antagonism in Primate Cytomegaloviruses.

Degree: PhD, 2017, University of Washington

 During millions of years of coevolution with their hosts, cytomegaloviruses (CMVs) have succeeded in adapting to overcome host-specific immune defenses, including the protein kinase R… (more)

Subjects/Keywords: Arms Race; Cytomegalovirus; Protein Kinase R; TRS1; Virology; Molecular biology; microbiology

…lymphoblastoid cells and are associated with malignancies. 1 Human Cytomegalovirus HHV-5, more… …commonly known as human cytomegalovirus (HCMV), is the prototypic member of the beta… 

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APA (6th Edition):

Carpentier, K. S. (2017). Evolution of Protein Kinase R Antagonism in Primate Cytomegaloviruses. (Doctoral Dissertation). University of Washington. Retrieved from http://hdl.handle.net/1773/38178

Chicago Manual of Style (16th Edition):

Carpentier, Kathryn Semmens. “Evolution of Protein Kinase R Antagonism in Primate Cytomegaloviruses.” 2017. Doctoral Dissertation, University of Washington. Accessed November 18, 2019. http://hdl.handle.net/1773/38178.

MLA Handbook (7th Edition):

Carpentier, Kathryn Semmens. “Evolution of Protein Kinase R Antagonism in Primate Cytomegaloviruses.” 2017. Web. 18 Nov 2019.

Vancouver:

Carpentier KS. Evolution of Protein Kinase R Antagonism in Primate Cytomegaloviruses. [Internet] [Doctoral dissertation]. University of Washington; 2017. [cited 2019 Nov 18]. Available from: http://hdl.handle.net/1773/38178.

Council of Science Editors:

Carpentier KS. Evolution of Protein Kinase R Antagonism in Primate Cytomegaloviruses. [Doctoral Dissertation]. University of Washington; 2017. Available from: http://hdl.handle.net/1773/38178

244. Bachelet, Thomas. Réponse des Lymphocytes T Gamma-Delta à deux Complications de la transplantation rénale : le Cytomégalovirus et les anticorps spécifiques du donneur : γδ T cells response to two complications of kidney transplantation : cytomegalovirus and Donor Specific Antibodies.

Degree: Docteur es, Sciences, technologie, santé. Biologie cellulaire et physiopathologie, 2013, Université de Bordeaux Segalen

La transplantation rénale est la stratégie de suppléance rénale la plus performante. Le renforcement des thérapeutiques ciblant la réponse cellulaire T (i) a conduit à… (more)

Subjects/Keywords: Lymphocytes T gamma-delta, , ,; Cytomégalovirus; Anticorps spécifiques du donneur; Lésions de la microcirculation; CD16; TCR; Surveillance lymphoide du stress; Γδ T cells; Cytomegalovirus; Donor specific antibodies; Antibody mediated lesions; CD16; TCR; Stress lymphoid surveillance

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APA (6th Edition):

Bachelet, T. (2013). Réponse des Lymphocytes T Gamma-Delta à deux Complications de la transplantation rénale : le Cytomégalovirus et les anticorps spécifiques du donneur : γδ T cells response to two complications of kidney transplantation : cytomegalovirus and Donor Specific Antibodies. (Doctoral Dissertation). Université de Bordeaux Segalen. Retrieved from http://www.theses.fr/2013BOR22091

Chicago Manual of Style (16th Edition):

Bachelet, Thomas. “Réponse des Lymphocytes T Gamma-Delta à deux Complications de la transplantation rénale : le Cytomégalovirus et les anticorps spécifiques du donneur : γδ T cells response to two complications of kidney transplantation : cytomegalovirus and Donor Specific Antibodies.” 2013. Doctoral Dissertation, Université de Bordeaux Segalen. Accessed November 18, 2019. http://www.theses.fr/2013BOR22091.

MLA Handbook (7th Edition):

Bachelet, Thomas. “Réponse des Lymphocytes T Gamma-Delta à deux Complications de la transplantation rénale : le Cytomégalovirus et les anticorps spécifiques du donneur : γδ T cells response to two complications of kidney transplantation : cytomegalovirus and Donor Specific Antibodies.” 2013. Web. 18 Nov 2019.

Vancouver:

Bachelet T. Réponse des Lymphocytes T Gamma-Delta à deux Complications de la transplantation rénale : le Cytomégalovirus et les anticorps spécifiques du donneur : γδ T cells response to two complications of kidney transplantation : cytomegalovirus and Donor Specific Antibodies. [Internet] [Doctoral dissertation]. Université de Bordeaux Segalen; 2013. [cited 2019 Nov 18]. Available from: http://www.theses.fr/2013BOR22091.

Council of Science Editors:

Bachelet T. Réponse des Lymphocytes T Gamma-Delta à deux Complications de la transplantation rénale : le Cytomégalovirus et les anticorps spécifiques du donneur : γδ T cells response to two complications of kidney transplantation : cytomegalovirus and Donor Specific Antibodies. [Doctoral Dissertation]. Université de Bordeaux Segalen; 2013. Available from: http://www.theses.fr/2013BOR22091

245. Saba, Esber. Mise en évidence et caractérisation d'une spécificité anticorps "TcCRA" chez l'homme : Characterization of a novel antibody specificity “Trypanosoma cruzi Cross Reactive Antibodies ; TcCRA" in human.

Degree: Docteur es, Sciences de la vie et de la santé, 2014, Saint-Etienne

Les anticorps à réactivité croisée sont caractérisés par leur capacité à reconnaitre des épitopes différents de ceux qui ont causé leur induction. Cela se produit… (more)

Subjects/Keywords: Trypanosoma cruzi; Mimétisme moléculaire; Cardiomyopathie; VIH; Transfert adaptatif de l’immunité; Réactivation de CMV; HSCT; Reconstitution immunitaire; Trypanosoma cruzi; Molecular mimicry; Cardiomyopathy; HIV; Adaptive transfer of immunity; Reactivation of cytomegalovirus; Hematopoietic Stem Cell Transplantations; Immune reconstitution

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APA (6th Edition):

Saba, E. (2014). Mise en évidence et caractérisation d'une spécificité anticorps "TcCRA" chez l'homme : Characterization of a novel antibody specificity “Trypanosoma cruzi Cross Reactive Antibodies ; TcCRA" in human. (Doctoral Dissertation). Saint-Etienne. Retrieved from http://www.theses.fr/2014STET009T

Chicago Manual of Style (16th Edition):

Saba, Esber. “Mise en évidence et caractérisation d'une spécificité anticorps "TcCRA" chez l'homme : Characterization of a novel antibody specificity “Trypanosoma cruzi Cross Reactive Antibodies ; TcCRA" in human.” 2014. Doctoral Dissertation, Saint-Etienne. Accessed November 18, 2019. http://www.theses.fr/2014STET009T.

MLA Handbook (7th Edition):

Saba, Esber. “Mise en évidence et caractérisation d'une spécificité anticorps "TcCRA" chez l'homme : Characterization of a novel antibody specificity “Trypanosoma cruzi Cross Reactive Antibodies ; TcCRA" in human.” 2014. Web. 18 Nov 2019.

Vancouver:

Saba E. Mise en évidence et caractérisation d'une spécificité anticorps "TcCRA" chez l'homme : Characterization of a novel antibody specificity “Trypanosoma cruzi Cross Reactive Antibodies ; TcCRA" in human. [Internet] [Doctoral dissertation]. Saint-Etienne; 2014. [cited 2019 Nov 18]. Available from: http://www.theses.fr/2014STET009T.

Council of Science Editors:

Saba E. Mise en évidence et caractérisation d'une spécificité anticorps "TcCRA" chez l'homme : Characterization of a novel antibody specificity “Trypanosoma cruzi Cross Reactive Antibodies ; TcCRA" in human. [Doctoral Dissertation]. Saint-Etienne; 2014. Available from: http://www.theses.fr/2014STET009T

246. Cocita, Clément. Etude de redondances mises en place par le système immunitaire pour lutter contre l'infection par le cytomégalovirus murin : Study of redundancies established by the immune system for the protection during murine cytomegalovirus infection.

Degree: Docteur es, Immunologie, 2015, Aix Marseille Université

Chez la souris, les cellules dendritiques plasmacytoïdes (pDC) et natural killer (NK) contribuent à la résistance contre les infections systémiques par les virus herpétiques tels… (more)

Subjects/Keywords: Cytomégalovirus murin; Cellule dendritique plasmacytoïde; Cellule natural killer; Interféron de type I; MyD88; Rate; Foie; Redondance; Murine cytomegalovirus; Plasmacytoid dendritic cell; Natural killer cell; Type I interferon; MyD88; Spleen; Liver; Redundancy; 571

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APA (6th Edition):

Cocita, C. (2015). Etude de redondances mises en place par le système immunitaire pour lutter contre l'infection par le cytomégalovirus murin : Study of redundancies established by the immune system for the protection during murine cytomegalovirus infection. (Doctoral Dissertation). Aix Marseille Université. Retrieved from http://www.theses.fr/2015AIXM4061

Chicago Manual of Style (16th Edition):

Cocita, Clément. “Etude de redondances mises en place par le système immunitaire pour lutter contre l'infection par le cytomégalovirus murin : Study of redundancies established by the immune system for the protection during murine cytomegalovirus infection.” 2015. Doctoral Dissertation, Aix Marseille Université. Accessed November 18, 2019. http://www.theses.fr/2015AIXM4061.

MLA Handbook (7th Edition):

Cocita, Clément. “Etude de redondances mises en place par le système immunitaire pour lutter contre l'infection par le cytomégalovirus murin : Study of redundancies established by the immune system for the protection during murine cytomegalovirus infection.” 2015. Web. 18 Nov 2019.

Vancouver:

Cocita C. Etude de redondances mises en place par le système immunitaire pour lutter contre l'infection par le cytomégalovirus murin : Study of redundancies established by the immune system for the protection during murine cytomegalovirus infection. [Internet] [Doctoral dissertation]. Aix Marseille Université 2015. [cited 2019 Nov 18]. Available from: http://www.theses.fr/2015AIXM4061.

Council of Science Editors:

Cocita C. Etude de redondances mises en place par le système immunitaire pour lutter contre l'infection par le cytomégalovirus murin : Study of redundancies established by the immune system for the protection during murine cytomegalovirus infection. [Doctoral Dissertation]. Aix Marseille Université 2015. Available from: http://www.theses.fr/2015AIXM4061

247. Gunkel, J. Advances in congenital and postnatal cytomegalovirus infections.

Degree: 2017, University Utrecht

 Congenital CMV infection (cCMV) is the most prevalent viral infection worldwide and the leading cause of non-genetic sensorineural hearing loss. Early diagnosis of cCMV infection… (more)

Subjects/Keywords: Cytomegalovirus; congenital infection; postnatal infection; sensorineural hearing loss; screening; prematurity; neurodevelopment

…and Toddler Development-III Birthweight Cytomegalic inclusion disease Cytomegalovirus… …Congenital cytomegalovirus CMV-sepsis-like-syndrome Central nervous system Corrected age Computed… …cytomegalovirus Radial diffusivity Region of interest Respiratory distress syndrome Socio-economic… …outline of the thesis CHAPTER 1 The history of cytomegalovirus 1 The first account of… …proposed the term cytomegalovirus.10 Cytomegalovirus Human cytomegalovirus (CMV), also… 

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APA (6th Edition):

Gunkel, J. (2017). Advances in congenital and postnatal cytomegalovirus infections. (Doctoral Dissertation). University Utrecht. Retrieved from http://dspace.library.uu.nl/handle/1874/351727 ; URN:NBN:NL:UI:10-1874-351727 ; urn:isbn:978-94-028-0660-1 ; URN:NBN:NL:UI:10-1874-351727 ; http://dspace.library.uu.nl/handle/1874/351727

Chicago Manual of Style (16th Edition):

Gunkel, J. “Advances in congenital and postnatal cytomegalovirus infections.” 2017. Doctoral Dissertation, University Utrecht. Accessed November 18, 2019. http://dspace.library.uu.nl/handle/1874/351727 ; URN:NBN:NL:UI:10-1874-351727 ; urn:isbn:978-94-028-0660-1 ; URN:NBN:NL:UI:10-1874-351727 ; http://dspace.library.uu.nl/handle/1874/351727.

MLA Handbook (7th Edition):

Gunkel, J. “Advances in congenital and postnatal cytomegalovirus infections.” 2017. Web. 18 Nov 2019.

Vancouver:

Gunkel J. Advances in congenital and postnatal cytomegalovirus infections. [Internet] [Doctoral dissertation]. University Utrecht; 2017. [cited 2019 Nov 18]. Available from: http://dspace.library.uu.nl/handle/1874/351727 ; URN:NBN:NL:UI:10-1874-351727 ; urn:isbn:978-94-028-0660-1 ; URN:NBN:NL:UI:10-1874-351727 ; http://dspace.library.uu.nl/handle/1874/351727.

Council of Science Editors:

Gunkel J. Advances in congenital and postnatal cytomegalovirus infections. [Doctoral Dissertation]. University Utrecht; 2017. Available from: http://dspace.library.uu.nl/handle/1874/351727 ; URN:NBN:NL:UI:10-1874-351727 ; urn:isbn:978-94-028-0660-1 ; URN:NBN:NL:UI:10-1874-351727 ; http://dspace.library.uu.nl/handle/1874/351727


University of Queensland

248. Trindade Oliveira, Martha. Cell-type specific activities of cytomegalovirus GPCR homologues.

Degree: School of Chemistry & Molecular Biosciences, 2016, University of Queensland

Subjects/Keywords: cytomegalovirus; viral GPCR; migration; chemokines; trophoblast; endothelial cells; intranasal dissemination; footpad dissemination; LysM; CD11c; 0605 Microbiology; 110804 Medical Virology

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APA (6th Edition):

Trindade Oliveira, M. (2016). Cell-type specific activities of cytomegalovirus GPCR homologues. (Thesis). University of Queensland. Retrieved from http://espace.library.uq.edu.au/view/UQ:406757

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):

Trindade Oliveira, Martha. “Cell-type specific activities of cytomegalovirus GPCR homologues.” 2016. Thesis, University of Queensland. Accessed November 18, 2019. http://espace.library.uq.edu.au/view/UQ:406757.

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

MLA Handbook (7th Edition):

Trindade Oliveira, Martha. “Cell-type specific activities of cytomegalovirus GPCR homologues.” 2016. Web. 18 Nov 2019.

Vancouver:

Trindade Oliveira M. Cell-type specific activities of cytomegalovirus GPCR homologues. [Internet] [Thesis]. University of Queensland; 2016. [cited 2019 Nov 18]. Available from: http://espace.library.uq.edu.au/view/UQ:406757.

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

Council of Science Editors:

Trindade Oliveira M. Cell-type specific activities of cytomegalovirus GPCR homologues. [Thesis]. University of Queensland; 2016. Available from: http://espace.library.uq.edu.au/view/UQ:406757

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


University of Ottawa

249. Theriault, Mylene A. Development and Validation of Quantitative PCR Assays for DNA-Based Newborn Screening of 22q11.2 Deletion Syndrome, Spinal Muscular Atrophy, Severe Combined Immunodeficiency and Congenital Cytomegalovirus Infection .

Degree: 2013, University of Ottawa

 The development of new high throughput technologies able to multiplex disease biomarkers as well as advances in medical treatments has lead to the recent expansion… (more)

Subjects/Keywords: 22q11.2 deletion syndrome; spinal muscular atrophy; severe combined immunodeficiency; congenital cytomegalovirus; qPCR; TaqMan; relative quantification; copy number variation; T-cell receptor excision circle; newborn screening; OpenArray; multiplex; TBX1; CRKL; UFD1L; COMT; HIRA; UL54; UL55; US17; dried blood spot; contiguous gene deletion; SMN1; SMN2

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APA (6th Edition):

Theriault, M. A. (2013). Development and Validation of Quantitative PCR Assays for DNA-Based Newborn Screening of 22q11.2 Deletion Syndrome, Spinal Muscular Atrophy, Severe Combined Immunodeficiency and Congenital Cytomegalovirus Infection . (Thesis). University of Ottawa. Retrieved from http://hdl.handle.net/10393/30318

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):

Theriault, Mylene A. “Development and Validation of Quantitative PCR Assays for DNA-Based Newborn Screening of 22q11.2 Deletion Syndrome, Spinal Muscular Atrophy, Severe Combined Immunodeficiency and Congenital Cytomegalovirus Infection .” 2013. Thesis, University of Ottawa. Accessed November 18, 2019. http://hdl.handle.net/10393/30318.

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

MLA Handbook (7th Edition):

Theriault, Mylene A. “Development and Validation of Quantitative PCR Assays for DNA-Based Newborn Screening of 22q11.2 Deletion Syndrome, Spinal Muscular Atrophy, Severe Combined Immunodeficiency and Congenital Cytomegalovirus Infection .” 2013. Web. 18 Nov 2019.

Vancouver:

Theriault MA. Development and Validation of Quantitative PCR Assays for DNA-Based Newborn Screening of 22q11.2 Deletion Syndrome, Spinal Muscular Atrophy, Severe Combined Immunodeficiency and Congenital Cytomegalovirus Infection . [Internet] [Thesis]. University of Ottawa; 2013. [cited 2019 Nov 18]. Available from: http://hdl.handle.net/10393/30318.

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

Council of Science Editors:

Theriault MA. Development and Validation of Quantitative PCR Assays for DNA-Based Newborn Screening of 22q11.2 Deletion Syndrome, Spinal Muscular Atrophy, Severe Combined Immunodeficiency and Congenital Cytomegalovirus Infection . [Thesis]. University of Ottawa; 2013. Available from: http://hdl.handle.net/10393/30318

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

250. Pereboom, M.T.R. The role of clients, midwives and health policy in preventing infectious diseases during pregnancy: Toxoplasmosis, Listeriosis. Cytomegalovirus & Chlamydia trachomatis .

Degree: 2014, Vrije Universiteit Amsterdam

Subjects/Keywords: Prevention; Midwives; Pregnant Women; Toxoplasmosis; Listeriosis; Cytomegalovirus; Chlamydia trachomatis; Infectious Diseases

…MF. Toxoplasmosis, cytomegalovirus, listeriosis, and preconcepƟon care. DĂƚĞƌŶŚŝůĚ,ĞĂůƚŚ… …cytomegalovirus: Results from the 2005 HealthStyles survey. J Womens Health ;>ĂƌĐŚŵƚͿ͘2008; 17(5… …cytomegalovirus among women. /ŶĨĞĐƚŝƐKďƐƚĞƚ'LJŶĞĐŽů͘2006; 2006: 1-7 Jones JL, Ogunmodede F, ScheŌel… …child-to-mother transmission of cytomegalovirus. WƌĞǀDĞĚ͘ 2012; 54(5): ϯ51-7… …and cytomegalovirus in pregnancy. ůŝŶ>ĂďDĞĚ͘2010; ϯ0(ϯ): 709-20. ϱϭ 2 … 

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APA (6th Edition):

Pereboom, M. T. R. (2014). The role of clients, midwives and health policy in preventing infectious diseases during pregnancy: Toxoplasmosis, Listeriosis. Cytomegalovirus & Chlamydia trachomatis . (Doctoral Dissertation). Vrije Universiteit Amsterdam. Retrieved from http://hdl.handle.net/1871/51612

Chicago Manual of Style (16th Edition):

Pereboom, M T R. “The role of clients, midwives and health policy in preventing infectious diseases during pregnancy: Toxoplasmosis, Listeriosis. Cytomegalovirus & Chlamydia trachomatis .” 2014. Doctoral Dissertation, Vrije Universiteit Amsterdam. Accessed November 18, 2019. http://hdl.handle.net/1871/51612.

MLA Handbook (7th Edition):

Pereboom, M T R. “The role of clients, midwives and health policy in preventing infectious diseases during pregnancy: Toxoplasmosis, Listeriosis. Cytomegalovirus & Chlamydia trachomatis .” 2014. Web. 18 Nov 2019.

Vancouver:

Pereboom MTR. The role of clients, midwives and health policy in preventing infectious diseases during pregnancy: Toxoplasmosis, Listeriosis. Cytomegalovirus & Chlamydia trachomatis . [Internet] [Doctoral dissertation]. Vrije Universiteit Amsterdam; 2014. [cited 2019 Nov 18]. Available from: http://hdl.handle.net/1871/51612.

Council of Science Editors:

Pereboom MTR. The role of clients, midwives and health policy in preventing infectious diseases during pregnancy: Toxoplasmosis, Listeriosis. Cytomegalovirus & Chlamydia trachomatis . [Doctoral Dissertation]. Vrije Universiteit Amsterdam; 2014. Available from: http://hdl.handle.net/1871/51612

251. Slayton, Mark D. Protein-DNA Interactions of pUL34, an Essential Human Cytomegalovirus DNA-Binding Protein.

Degree: PhD, Molecular and Cellular Biology (Arts and Sciences), 2018, Ohio University

 Human cytomegalovirus (HCMV) is primarily an opportunistic pathogen in human, causing significant disease in immunocompromised individuals. A large, double-stranded DNA genome (~230 kilobases) provides the… (more)

Subjects/Keywords: Virology; Molecular Biology; Genetics; Human cytomegalovirus; DNA binding; viral replication; ChIP-seq; DNA replication

…104 11 CHAPTER 1: INTRODUCTION Medical Significance Human cytomegalovirus (HCMV)… …Cytomegalovirus Classification Human cytomegalovirus, or human herpesvirus 5, is a member of the… …x28;chicken pox); betaherpesvirinae which includes cytomegalovirus, human herpesvirus… …and Johnson, 2012). Genome organization Human cytomegalovirus has one the largest… …et al., 1996). Viral infection and replication Human cytomegalovirus, like all known… 

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APA (6th Edition):

Slayton, M. D. (2018). Protein-DNA Interactions of pUL34, an Essential Human Cytomegalovirus DNA-Binding Protein. (Doctoral Dissertation). Ohio University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=ohiou1533638730703166

Chicago Manual of Style (16th Edition):

Slayton, Mark D. “Protein-DNA Interactions of pUL34, an Essential Human Cytomegalovirus DNA-Binding Protein.” 2018. Doctoral Dissertation, Ohio University. Accessed November 18, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=ohiou1533638730703166.

MLA Handbook (7th Edition):

Slayton, Mark D. “Protein-DNA Interactions of pUL34, an Essential Human Cytomegalovirus DNA-Binding Protein.” 2018. Web. 18 Nov 2019.

Vancouver:

Slayton MD. Protein-DNA Interactions of pUL34, an Essential Human Cytomegalovirus DNA-Binding Protein. [Internet] [Doctoral dissertation]. Ohio University; 2018. [cited 2019 Nov 18]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ohiou1533638730703166.

Council of Science Editors:

Slayton MD. Protein-DNA Interactions of pUL34, an Essential Human Cytomegalovirus DNA-Binding Protein. [Doctoral Dissertation]. Ohio University; 2018. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ohiou1533638730703166

252. CHEE KIE LIN, MELISSA. DNA vaccines for murine cytomegalovirus.

Degree: 2004, National University of Singapore

Subjects/Keywords: Cytomegalovirus; immediate early gene 1; DNA vaccine; lysosome associated membrane protein; immune response; virus challenge

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APA (6th Edition):

CHEE KIE LIN, M. (2004). DNA vaccines for murine cytomegalovirus. (Thesis). National University of Singapore. Retrieved from http://scholarbank.nus.edu.sg/handle/10635/13663

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):

CHEE KIE LIN, MELISSA. “DNA vaccines for murine cytomegalovirus.” 2004. Thesis, National University of Singapore. Accessed November 18, 2019. http://scholarbank.nus.edu.sg/handle/10635/13663.

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

MLA Handbook (7th Edition):

CHEE KIE LIN, MELISSA. “DNA vaccines for murine cytomegalovirus.” 2004. Web. 18 Nov 2019.

Vancouver:

CHEE KIE LIN M. DNA vaccines for murine cytomegalovirus. [Internet] [Thesis]. National University of Singapore; 2004. [cited 2019 Nov 18]. Available from: http://scholarbank.nus.edu.sg/handle/10635/13663.

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

Council of Science Editors:

CHEE KIE LIN M. DNA vaccines for murine cytomegalovirus. [Thesis]. National University of Singapore; 2004. Available from: http://scholarbank.nus.edu.sg/handle/10635/13663

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


Virginia Commonwealth University

253. Meza, Benjamin. The Effect of Cell Type on the Efficacy of CMV Antiviral Drugs.

Degree: MS, Physiology, 2008, Virginia Commonwealth University

  Until recently, all in vitro drug susceptibility assays of cytomegalovirus (CMV) were performed in clinically irrelevant fibroblast cells. This study sought to test if… (more)

Subjects/Keywords: Cytomegalovirus; CMV; Antiviral; Drug; Ganciclovir; Maribavir; Fibroblast; Epithelial; ARPE-19; Retinitis; Life Sciences; Physiology

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APA (6th Edition):

Meza, B. (2008). The Effect of Cell Type on the Efficacy of CMV Antiviral Drugs. (Thesis). Virginia Commonwealth University. Retrieved from https://scholarscompass.vcu.edu/etd/1567

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):

Meza, Benjamin. “The Effect of Cell Type on the Efficacy of CMV Antiviral Drugs.” 2008. Thesis, Virginia Commonwealth University. Accessed November 18, 2019. https://scholarscompass.vcu.edu/etd/1567.

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

MLA Handbook (7th Edition):

Meza, Benjamin. “The Effect of Cell Type on the Efficacy of CMV Antiviral Drugs.” 2008. Web. 18 Nov 2019.

Vancouver:

Meza B. The Effect of Cell Type on the Efficacy of CMV Antiviral Drugs. [Internet] [Thesis]. Virginia Commonwealth University; 2008. [cited 2019 Nov 18]. Available from: https://scholarscompass.vcu.edu/etd/1567.

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

Council of Science Editors:

Meza B. The Effect of Cell Type on the Efficacy of CMV Antiviral Drugs. [Thesis]. Virginia Commonwealth University; 2008. Available from: https://scholarscompass.vcu.edu/etd/1567

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


Virginia Commonwealth University

254. Parikh, Hardik. Understanding Molecular Interactions: Application of HINT-based Tools in the Structural Modeling of Novel Anticancer and Antiviral Targets, and in Protein-Protein Docking.

Degree: PhD, Pharmaceutical Sciences, 2013, Virginia Commonwealth University

 Computationally driven drug design/discovery efforts generally rely on accurate assessment of the forces that guide the molecular recognition process. HINT (Hydropathic INTeraction) is a natural… (more)

Subjects/Keywords: Hydropathic Interaction; HINT; Hydrophobicity; Molecular Docking; Homology Modeling; 3D Virtual Screening; Protein Protein Docking; Sphingosine Kinase 2 Inhibitor; Human cytomegalovirus UL98 Alkaline Nuclease; Medicine and Health Sciences; Pharmacy and Pharmaceutical Sciences

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APA (6th Edition):

Parikh, H. (2013). Understanding Molecular Interactions: Application of HINT-based Tools in the Structural Modeling of Novel Anticancer and Antiviral Targets, and in Protein-Protein Docking. (Doctoral Dissertation). Virginia Commonwealth University. Retrieved from https://scholarscompass.vcu.edu/etd/3116

Chicago Manual of Style (16th Edition):

Parikh, Hardik. “Understanding Molecular Interactions: Application of HINT-based Tools in the Structural Modeling of Novel Anticancer and Antiviral Targets, and in Protein-Protein Docking.” 2013. Doctoral Dissertation, Virginia Commonwealth University. Accessed November 18, 2019. https://scholarscompass.vcu.edu/etd/3116.

MLA Handbook (7th Edition):

Parikh, Hardik. “Understanding Molecular Interactions: Application of HINT-based Tools in the Structural Modeling of Novel Anticancer and Antiviral Targets, and in Protein-Protein Docking.” 2013. Web. 18 Nov 2019.

Vancouver:

Parikh H. Understanding Molecular Interactions: Application of HINT-based Tools in the Structural Modeling of Novel Anticancer and Antiviral Targets, and in Protein-Protein Docking. [Internet] [Doctoral dissertation]. Virginia Commonwealth University; 2013. [cited 2019 Nov 18]. Available from: https://scholarscompass.vcu.edu/etd/3116.

Council of Science Editors:

Parikh H. Understanding Molecular Interactions: Application of HINT-based Tools in the Structural Modeling of Novel Anticancer and Antiviral Targets, and in Protein-Protein Docking. [Doctoral Dissertation]. Virginia Commonwealth University; 2013. Available from: https://scholarscompass.vcu.edu/etd/3116

255. Goulidaki, Nektaria. Ο ρόλος των microRNAs και της πρωτεΐνης RhoB στην ιική μόλυνση από τον ανθρώπινο κυτταρομεγαλοϊό.

Degree: 2015, University of Crete (UOC); Πανεπιστήμιο Κρήτης

 Human Cytomegalovirus (HCMV), an ubiquitous β-herpesvirus, is a significant pathogen that causes medically severe diseases in immunocompromised individuals and in congenitally infected neonates. RhoB belongs… (more)

Subjects/Keywords: Ανθρώπινος κυτταρομεγαλοϊός; Rho GTPάσες; RhoB GTPάση; Kυτταροπλασματικό διαμέρισμα συναρμολόγησης; Κυτταροσκελετός ακτίνης; MicroRNAs; Kυτταρικές προσεκβολές; Πρωτεΐνη pUL32; Πρωτεΐνη pp65; Πρωτεΐνη pUL97; Ερπητοϊός; HCMV; Human cytomegalovirus; Rho GTPases; RHOB GTPase; Assembly complex; Assembly compartment; Actin cytoskeleton; miRNAs; Cellular projections; pUL32; pp65; pUL97; HERPESVIRUS

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APA (6th Edition):

Goulidaki, N. (2015). Ο ρόλος των microRNAs και της πρωτεΐνης RhoB στην ιική μόλυνση από τον ανθρώπινο κυτταρομεγαλοϊό. (Thesis). University of Crete (UOC); Πανεπιστήμιο Κρήτης. Retrieved from http://hdl.handle.net/10442/hedi/36314

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):

Goulidaki, Nektaria. “Ο ρόλος των microRNAs και της πρωτεΐνης RhoB στην ιική μόλυνση από τον ανθρώπινο κυτταρομεγαλοϊό.” 2015. Thesis, University of Crete (UOC); Πανεπιστήμιο Κρήτης. Accessed November 18, 2019. http://hdl.handle.net/10442/hedi/36314.

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

MLA Handbook (7th Edition):

Goulidaki, Nektaria. “Ο ρόλος των microRNAs και της πρωτεΐνης RhoB στην ιική μόλυνση από τον ανθρώπινο κυτταρομεγαλοϊό.” 2015. Web. 18 Nov 2019.

Vancouver:

Goulidaki N. Ο ρόλος των microRNAs και της πρωτεΐνης RhoB στην ιική μόλυνση από τον ανθρώπινο κυτταρομεγαλοϊό. [Internet] [Thesis]. University of Crete (UOC); Πανεπιστήμιο Κρήτης; 2015. [cited 2019 Nov 18]. Available from: http://hdl.handle.net/10442/hedi/36314.

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

Council of Science Editors:

Goulidaki N. Ο ρόλος των microRNAs και της πρωτεΐνης RhoB στην ιική μόλυνση από τον ανθρώπινο κυτταρομεγαλοϊό. [Thesis]. University of Crete (UOC); Πανεπιστήμιο Κρήτης; 2015. Available from: http://hdl.handle.net/10442/hedi/36314

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

256. Castillo, Jonathan Patrick. The Role of Human Cytomegalovirus Immediate Early Proteins in Cell Growth Control: A Dissertation.

Degree: Immunology and Microbiology, Microbiology and Physiological Systems, 2002, U of Massachusetts : Med

  The proper maintenance of the pathways governing cell growth is critical to ensure cell survival and DNA fidelity. Much of our understanding of how… (more)

Subjects/Keywords: Cytomegalovirus; Immediate-Early Proteins; Protein p53; Retinoblastoma Protein; DNA Replication; S Phase; Amino Acids, Peptides, and Proteins; Cells; Genetic Phenomena; Viruses

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APA (6th Edition):

Castillo, J. P. (2002). The Role of Human Cytomegalovirus Immediate Early Proteins in Cell Growth Control: A Dissertation. (Doctoral Dissertation). U of Massachusetts : Med. Retrieved from https://escholarship.umassmed.edu/gsbs_diss/49

Chicago Manual of Style (16th Edition):

Castillo, Jonathan Patrick. “The Role of Human Cytomegalovirus Immediate Early Proteins in Cell Growth Control: A Dissertation.” 2002. Doctoral Dissertation, U of Massachusetts : Med. Accessed November 18, 2019. https://escholarship.umassmed.edu/gsbs_diss/49.

MLA Handbook (7th Edition):

Castillo, Jonathan Patrick. “The Role of Human Cytomegalovirus Immediate Early Proteins in Cell Growth Control: A Dissertation.” 2002. Web. 18 Nov 2019.

Vancouver:

Castillo JP. The Role of Human Cytomegalovirus Immediate Early Proteins in Cell Growth Control: A Dissertation. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 2002. [cited 2019 Nov 18]. Available from: https://escholarship.umassmed.edu/gsbs_diss/49.

Council of Science Editors:

Castillo JP. The Role of Human Cytomegalovirus Immediate Early Proteins in Cell Growth Control: A Dissertation. [Doctoral Dissertation]. U of Massachusetts : Med; 2002. Available from: https://escholarship.umassmed.edu/gsbs_diss/49

257. Sun, Kefeng. Improved Targeting and Biopharmaceutical Properties of Prodrugs of Anti-infective Agents.

Degree: PhD, Pharmaceutical Sciences, 2013, University of Michigan

 The prodrug strategy has been frequently used as a chemical approach for the enhancement of certain disadvantages of parent drugs. In this dissertation, I synthesized… (more)

Subjects/Keywords: Prodrug; Human Cytomegalovirus Protease; Targeted Activation; Solubility; Intestinal Permeability; Pharmacy and Pharmacology; Health Sciences

…x28;L)-glycine hCMV human cytomegalovirus hCMVP human cytomegalovirus protease… …cytomegalovirus (hCMV) protease, a serine protease that possesses intrinsic esterase… …protease, the herpes simplex virus-1 (HSV-1) protease, the human cytomegalovirus (… 

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APA (6th Edition):

Sun, K. (2013). Improved Targeting and Biopharmaceutical Properties of Prodrugs of Anti-infective Agents. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/97781

Chicago Manual of Style (16th Edition):

Sun, Kefeng. “Improved Targeting and Biopharmaceutical Properties of Prodrugs of Anti-infective Agents.” 2013. Doctoral Dissertation, University of Michigan. Accessed November 18, 2019. http://hdl.handle.net/2027.42/97781.

MLA Handbook (7th Edition):

Sun, Kefeng. “Improved Targeting and Biopharmaceutical Properties of Prodrugs of Anti-infective Agents.” 2013. Web. 18 Nov 2019.

Vancouver:

Sun K. Improved Targeting and Biopharmaceutical Properties of Prodrugs of Anti-infective Agents. [Internet] [Doctoral dissertation]. University of Michigan; 2013. [cited 2019 Nov 18]. Available from: http://hdl.handle.net/2027.42/97781.

Council of Science Editors:

Sun K. Improved Targeting and Biopharmaceutical Properties of Prodrugs of Anti-infective Agents. [Doctoral Dissertation]. University of Michigan; 2013. Available from: http://hdl.handle.net/2027.42/97781

258. Tichelaar, Ynse Ieuwe Gerardus Vladimir. Infections, inflammation and venous thrombosis; an epidemiological perspective.

Degree: Faculty of Medical Sciences, 2012, NARCIS

 Alledaagse, relatief onschuldige ontstekingsklachten zoals luchtweginfecties, diarree of een grieperig gevoel, brengen een verhoogde kans op trombose met zich mee. Hierdoor vergroot het risico op… (more)

Subjects/Keywords: Proefschriften (vorm); Factor VIII; Bloedstolling; Glucose; Bloedsuiker; HIV; Cytomegalovirus; Epidemiologie; Infecties; Trombose; cardiologie; infectieziekten, parasitaire ziekten

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APA (6th Edition):

Tichelaar, Y. I. G. V. (2012). Infections, inflammation and venous thrombosis; an epidemiological perspective. (Doctoral Dissertation). NARCIS. Retrieved from https://www.rug.nl/research/portal/en/publications/infections-inflammation-and-venous-thrombosis-an-epidemiological-perspective(815ec81f-f5df-447c-b75c-589ddc858473).html ; urn:nbn:nl:ui:11-dbi/4f44caf4a2b44 ; 815ec81f-f5df-447c-b75c-589ddc858473 ; 11370/815ec81f-f5df-447c-b75c-589ddc858473 ; urn:isbn:9789036753012 ; urn:nbn:nl:ui:11-dbi/4f44caf4a2b44 ; https://www.rug.nl/research/portal/en/publications/infections-inflammation-and-venous-thrombosis-an-epidemiological-perspective(815ec81f-f5df-447c-b75c-589ddc858473).html

Chicago Manual of Style (16th Edition):

Tichelaar, Ynse Ieuwe Gerardus Vladimir. “Infections, inflammation and venous thrombosis; an epidemiological perspective.” 2012. Doctoral Dissertation, NARCIS. Accessed November 18, 2019. https://www.rug.nl/research/portal/en/publications/infections-inflammation-and-venous-thrombosis-an-epidemiological-perspective(815ec81f-f5df-447c-b75c-589ddc858473).html ; urn:nbn:nl:ui:11-dbi/4f44caf4a2b44 ; 815ec81f-f5df-447c-b75c-589ddc858473 ; 11370/815ec81f-f5df-447c-b75c-589ddc858473 ; urn:isbn:9789036753012 ; urn:nbn:nl:ui:11-dbi/4f44caf4a2b44 ; https://www.rug.nl/research/portal/en/publications/infections-inflammation-and-venous-thrombosis-an-epidemiological-perspective(815ec81f-f5df-447c-b75c-589ddc858473).html.

MLA Handbook (7th Edition):

Tichelaar, Ynse Ieuwe Gerardus Vladimir. “Infections, inflammation and venous thrombosis; an epidemiological perspective.” 2012. Web. 18 Nov 2019.

Vancouver:

Tichelaar YIGV. Infections, inflammation and venous thrombosis; an epidemiological perspective. [Internet] [Doctoral dissertation]. NARCIS; 2012. [cited 2019 Nov 18]. Available from: https://www.rug.nl/research/portal/en/publications/infections-inflammation-and-venous-thrombosis-an-epidemiological-perspective(815ec81f-f5df-447c-b75c-589ddc858473).html ; urn:nbn:nl:ui:11-dbi/4f44caf4a2b44 ; 815ec81f-f5df-447c-b75c-589ddc858473 ; 11370/815ec81f-f5df-447c-b75c-589ddc858473 ; urn:isbn:9789036753012 ; urn:nbn:nl:ui:11-dbi/4f44caf4a2b44 ; https://www.rug.nl/research/portal/en/publications/infections-inflammation-and-venous-thrombosis-an-epidemiological-perspective(815ec81f-f5df-447c-b75c-589ddc858473).html.

Council of Science Editors:

Tichelaar YIGV. Infections, inflammation and venous thrombosis; an epidemiological perspective. [Doctoral Dissertation]. NARCIS; 2012. Available from: https://www.rug.nl/research/portal/en/publications/infections-inflammation-and-venous-thrombosis-an-epidemiological-perspective(815ec81f-f5df-447c-b75c-589ddc858473).html ; urn:nbn:nl:ui:11-dbi/4f44caf4a2b44 ; 815ec81f-f5df-447c-b75c-589ddc858473 ; 11370/815ec81f-f5df-447c-b75c-589ddc858473 ; urn:isbn:9789036753012 ; urn:nbn:nl:ui:11-dbi/4f44caf4a2b44 ; https://www.rug.nl/research/portal/en/publications/infections-inflammation-and-venous-thrombosis-an-epidemiological-perspective(815ec81f-f5df-447c-b75c-589ddc858473).html


Freie Universität Berlin

259. Le, Vu Thuy Khanh. Characterization of the virus-mediated inhibition of interferon beta gene induction and identification of interferon modulating genes of mouse cytomegalovirus.

Degree: 2007, Freie Universität Berlin

 To investigate the interaction between mouse cytomegalovirus (MCMV) and the type I interferon (IFN) system IFNbeta and IFNalpha4 gene transcription and activation of related transcription… (more)

Subjects/Keywords: interferon beta; inhibition; mouse cytomegalovirus; NF-kappaB;

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APA (6th Edition):

Le, V. T. K. (2007). Characterization of the virus-mediated inhibition of interferon beta gene induction and identification of interferon modulating genes of mouse cytomegalovirus. (Thesis). Freie Universität Berlin. Retrieved from http://dx.doi.org/10.17169/refubium-12947

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):

Le, Vu Thuy Khanh. “Characterization of the virus-mediated inhibition of interferon beta gene induction and identification of interferon modulating genes of mouse cytomegalovirus.” 2007. Thesis, Freie Universität Berlin. Accessed November 18, 2019. http://dx.doi.org/10.17169/refubium-12947.

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

MLA Handbook (7th Edition):

Le, Vu Thuy Khanh. “Characterization of the virus-mediated inhibition of interferon beta gene induction and identification of interferon modulating genes of mouse cytomegalovirus.” 2007. Web. 18 Nov 2019.

Vancouver:

Le VTK. Characterization of the virus-mediated inhibition of interferon beta gene induction and identification of interferon modulating genes of mouse cytomegalovirus. [Internet] [Thesis]. Freie Universität Berlin; 2007. [cited 2019 Nov 18]. Available from: http://dx.doi.org/10.17169/refubium-12947.

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

Council of Science Editors:

Le VTK. Characterization of the virus-mediated inhibition of interferon beta gene induction and identification of interferon modulating genes of mouse cytomegalovirus. [Thesis]. Freie Universität Berlin; 2007. Available from: http://dx.doi.org/10.17169/refubium-12947

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


Freie Universität Berlin

260. Frömmel, Claudia Bettina. Analysis of the Expression of Killer Inhibitory Receptor CD158b on CD8 T-Lymphocytes specific for human Cytomegalovirus.

Degree: 2006, Freie Universität Berlin

 HCMV-specific CD8 T-lymphocytes play an important role in control of viral replication and preventing HCMV disease. Direct assessment of virus specific cells by peptide specific… (more)

Subjects/Keywords: Killer Inhibitory Receptors; CD158b; CD8 T-Lymphocytes; Cytomegalovirus; 600 Technik, Medizin, angewandte Wissenschaften::610 Medizin und Gesundheit::610 Medizin und Gesundheit

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APA (6th Edition):

Frömmel, C. B. (2006). Analysis of the Expression of Killer Inhibitory Receptor CD158b on CD8 T-Lymphocytes specific for human Cytomegalovirus. (Thesis). Freie Universität Berlin. Retrieved from http://dx.doi.org/10.17169/refubium-6823

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):

Frömmel, Claudia Bettina. “Analysis of the Expression of Killer Inhibitory Receptor CD158b on CD8 T-Lymphocytes specific for human Cytomegalovirus.” 2006. Thesis, Freie Universität Berlin. Accessed November 18, 2019. http://dx.doi.org/10.17169/refubium-6823.

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

MLA Handbook (7th Edition):

Frömmel, Claudia Bettina. “Analysis of the Expression of Killer Inhibitory Receptor CD158b on CD8 T-Lymphocytes specific for human Cytomegalovirus.” 2006. Web. 18 Nov 2019.

Vancouver:

Frömmel CB. Analysis of the Expression of Killer Inhibitory Receptor CD158b on CD8 T-Lymphocytes specific for human Cytomegalovirus. [Internet] [Thesis]. Freie Universität Berlin; 2006. [cited 2019 Nov 18]. Available from: http://dx.doi.org/10.17169/refubium-6823.

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

Council of Science Editors:

Frömmel CB. Analysis of the Expression of Killer Inhibitory Receptor CD158b on CD8 T-Lymphocytes specific for human Cytomegalovirus. [Thesis]. Freie Universität Berlin; 2006. Available from: http://dx.doi.org/10.17169/refubium-6823

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


Freie Universität Berlin

261. Mokros, Thilo. Molecular mechanisms of immune evasion by the cytomegalovirus-encoded chemokine receptor US28.

Degree: 2004, Freie Universität Berlin

 The ubiquitous human cytomegalovirus encodes four putative G-protein coupled receptors with sequence homology to human chemokine receptors: US27, US28, UL33 and UL78. To date, only… (more)

Subjects/Keywords: G-protein; receptor; US28; phosphorylation; cytomegalovirus; endocytosis; 500 Naturwissenschaften und Mathematik::570 Biowissenschaften; Biologie::570 Biowissenschaften; Biologie

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APA (6th Edition):

Mokros, T. (2004). Molecular mechanisms of immune evasion by the cytomegalovirus-encoded chemokine receptor US28. (Thesis). Freie Universität Berlin. Retrieved from https://refubium.fu-berlin.de/handle/fub188/11695

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):

Mokros, Thilo. “Molecular mechanisms of immune evasion by the cytomegalovirus-encoded chemokine receptor US28.” 2004. Thesis, Freie Universität Berlin. Accessed November 18, 2019. https://refubium.fu-berlin.de/handle/fub188/11695.

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

MLA Handbook (7th Edition):

Mokros, Thilo. “Molecular mechanisms of immune evasion by the cytomegalovirus-encoded chemokine receptor US28.” 2004. Web. 18 Nov 2019.

Vancouver:

Mokros T. Molecular mechanisms of immune evasion by the cytomegalovirus-encoded chemokine receptor US28. [Internet] [Thesis]. Freie Universität Berlin; 2004. [cited 2019 Nov 18]. Available from: https://refubium.fu-berlin.de/handle/fub188/11695.

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

Council of Science Editors:

Mokros T. Molecular mechanisms of immune evasion by the cytomegalovirus-encoded chemokine receptor US28. [Thesis]. Freie Universität Berlin; 2004. Available from: https://refubium.fu-berlin.de/handle/fub188/11695

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

262. Chavoshi, Sara Sadat. Investigating Interaction Partners Of Yeast UBPS and Human USP7 Deubiquitinases.

Degree: PhD, Biology, 2019, York University

 Ubiquitin-specific proteases (USPs; Ubps) are the most abundant family of deubiquitinating enzymes. Their involvement in various cellular processes, which are implicated in development and diseases… (more)

Subjects/Keywords: Molecular biology; Protein expression; Cloning; Protein purification; Structural biology; Protein interaction; Human herpesviruses; Human Cytomegalovirus; Kaposi's sarcoma-associated herpesvirus; Deubiquitinating enzymes; Human USP7; Yeast Ubp15; Protein crystallography; Saccharomyces cerevisiae Ubps; USP7-p53-Hdm2 pathway

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APA (6th Edition):

Chavoshi, S. S. (2019). Investigating Interaction Partners Of Yeast UBPS and Human USP7 Deubiquitinases. (Doctoral Dissertation). York University. Retrieved from http://hdl.handle.net/10315/36239

Chicago Manual of Style (16th Edition):

Chavoshi, Sara Sadat. “Investigating Interaction Partners Of Yeast UBPS and Human USP7 Deubiquitinases.” 2019. Doctoral Dissertation, York University. Accessed November 18, 2019. http://hdl.handle.net/10315/36239.

MLA Handbook (7th Edition):

Chavoshi, Sara Sadat. “Investigating Interaction Partners Of Yeast UBPS and Human USP7 Deubiquitinases.” 2019. Web. 18 Nov 2019.

Vancouver:

Chavoshi SS. Investigating Interaction Partners Of Yeast UBPS and Human USP7 Deubiquitinases. [Internet] [Doctoral dissertation]. York University; 2019. [cited 2019 Nov 18]. Available from: http://hdl.handle.net/10315/36239.

Council of Science Editors:

Chavoshi SS. Investigating Interaction Partners Of Yeast UBPS and Human USP7 Deubiquitinases. [Doctoral Dissertation]. York University; 2019. Available from: http://hdl.handle.net/10315/36239


ETH Zürich

263. Ghielmetti, Maddalena. Human leukocyte recruitment to the porcine endothelium: implications for xenotransplantation.

Degree: 2009, ETH Zürich

Subjects/Keywords: HISTOKOMPATIBILITÄT + BIOKOMPATIBILITÄT + TRANSPLANTATIONSIMMUNOLOGIE (IMMUNOLOGIE); XENOTRANSPLANTATION (BIOMEDIZINISCHE TECHNIKEN); LEUKOZYTEN + AMÖBOIDE BLUTZELLEN (BLUTZELLEN); CYTOMEGALOVIRUS (VIROLOGIE); SUS SCROFA DOMESTICA (ZOOLOGIE); ENDOTHEL (CYTOLOGIE, HISTOLOGIE); HISTOCOMPATIBILITY + BIOCOMPATIBILITY + TRANSPLANTATION IMMUNOLOGY (IMMUNOLOGY); XENOTRANSPLANTATION (BIOMEDICAL TECHNIQUES); LEUKOCYTES + AMOEBOID BLOOD CELLS (BLOOD CELLS); CYTOMEGALOVIRUS (VIROLOGY); SUS SCROFA DOMESTICA (ZOOLOGY); ENDOTHELIUM (CYTOLOGY, HISTOLOGY); info:eu-repo/classification/ddc/610; Medical sciences, medicine

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APA (6th Edition):

Ghielmetti, M. (2009). Human leukocyte recruitment to the porcine endothelium: implications for xenotransplantation. (Doctoral Dissertation). ETH Zürich. Retrieved from http://hdl.handle.net/20.500.11850/151361

Chicago Manual of Style (16th Edition):

Ghielmetti, Maddalena. “Human leukocyte recruitment to the porcine endothelium: implications for xenotransplantation.” 2009. Doctoral Dissertation, ETH Zürich. Accessed November 18, 2019. http://hdl.handle.net/20.500.11850/151361.

MLA Handbook (7th Edition):

Ghielmetti, Maddalena. “Human leukocyte recruitment to the porcine endothelium: implications for xenotransplantation.” 2009. Web. 18 Nov 2019.

Vancouver:

Ghielmetti M. Human leukocyte recruitment to the porcine endothelium: implications for xenotransplantation. [Internet] [Doctoral dissertation]. ETH Zürich; 2009. [cited 2019 Nov 18]. Available from: http://hdl.handle.net/20.500.11850/151361.

Council of Science Editors:

Ghielmetti M. Human leukocyte recruitment to the porcine endothelium: implications for xenotransplantation. [Doctoral Dissertation]. ETH Zürich; 2009. Available from: http://hdl.handle.net/20.500.11850/151361


ETH Zürich

264. Torti, Nicole. What drives memory T cell inflation during MCMV infection?.

Degree: 2011, ETH Zürich

Subjects/Keywords: CYTOMEGALOVIRUS (VIROLOGIE); VIRALE INFEKTIONEN (MEDIZIN); TIERISCHE MODELLE IN DER MEDIZIN; TRANSGENE MÄUSE (TIERGENETIK); HELFERZELLEN (IMMUNOLOGIE); ANTIKÖRPERBINDUNGSSTELLE + ANTIGENDETERMINANTE + EPITOP (IMMUNOLOGIE); CYTOMEGALOVIRUS (VIROLOGY); VIRUS INFECTIONS (MEDICINE); ANIMAL MODELS IN MEDICINE; TRANSGENIC MICE (ANIMAL GENETICS); HELPER T LYMPHOCYTES (IMMUNOLOGY); ANTIBODY-BINDING SITE + ANTIGENIC DETERMINANT + EPITOPE (IMMUNOLOGY); info:eu-repo/classification/ddc/610; Medical sciences, medicine

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APA (6th Edition):

Torti, N. (2011). What drives memory T cell inflation during MCMV infection?. (Doctoral Dissertation). ETH Zürich. Retrieved from http://hdl.handle.net/20.500.11850/152896

Chicago Manual of Style (16th Edition):

Torti, Nicole. “What drives memory T cell inflation during MCMV infection?.” 2011. Doctoral Dissertation, ETH Zürich. Accessed November 18, 2019. http://hdl.handle.net/20.500.11850/152896.

MLA Handbook (7th Edition):

Torti, Nicole. “What drives memory T cell inflation during MCMV infection?.” 2011. Web. 18 Nov 2019.

Vancouver:

Torti N. What drives memory T cell inflation during MCMV infection?. [Internet] [Doctoral dissertation]. ETH Zürich; 2011. [cited 2019 Nov 18]. Available from: http://hdl.handle.net/20.500.11850/152896.

Council of Science Editors:

Torti N. What drives memory T cell inflation during MCMV infection?. [Doctoral Dissertation]. ETH Zürich; 2011. Available from: http://hdl.handle.net/20.500.11850/152896


ETH Zürich

265. Thom, Jenny Tosca. Immune Control of Cytomegalovirus in the Salivary Glands.

Degree: 2015, ETH Zürich

Subjects/Keywords: CYTOMEGALOVIRUS (VIROLOGIE); PATHOGENESE VIRALER INFEKTIONEN (VIROLOGIE); SPEICHELDRÜSEN + SPEICHEL (ANATOMIE UND PHYSIOLOGIE); LOKALE IMMUNITÄT + GEWEBSIMMUNITÄT + SCHLEIMHAUTIMMUNITÄT (IMMUNOLOGIE); T-LYMPHOZYTEN-AKTIVIERUNG (IMMUNOLOGIE); CYTOMEGALOVIRUS (VIROLOGY); PATHOGENESIS OF VIRAL INFECTIONS (VIROLOGY); SALIVARY GLANDS + SALIVA (ANATOMY AND PHYSIOLOGY); LOCAL IMMUNITY + TISSUE IMMUNITY + MUCOSAL IMMUNITY (IMMUNOLOGY); T LYMPHOCYTE ACTIVATION (IMMUNOLOGY); info:eu-repo/classification/ddc/610; Medical sciences, medicine

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APA (6th Edition):

Thom, J. T. (2015). Immune Control of Cytomegalovirus in the Salivary Glands. (Doctoral Dissertation). ETH Zürich. Retrieved from http://hdl.handle.net/20.500.11850/155252

Chicago Manual of Style (16th Edition):

Thom, Jenny Tosca. “Immune Control of Cytomegalovirus in the Salivary Glands.” 2015. Doctoral Dissertation, ETH Zürich. Accessed November 18, 2019. http://hdl.handle.net/20.500.11850/155252.

MLA Handbook (7th Edition):

Thom, Jenny Tosca. “Immune Control of Cytomegalovirus in the Salivary Glands.” 2015. Web. 18 Nov 2019.

Vancouver:

Thom JT. Immune Control of Cytomegalovirus in the Salivary Glands. [Internet] [Doctoral dissertation]. ETH Zürich; 2015. [cited 2019 Nov 18]. Available from: http://hdl.handle.net/20.500.11850/155252.

Council of Science Editors:

Thom JT. Immune Control of Cytomegalovirus in the Salivary Glands. [Doctoral Dissertation]. ETH Zürich; 2015. Available from: http://hdl.handle.net/20.500.11850/155252

266. Kalpoe, Jaijant Satishkumar. Quantum virology: improved management of viral infections through quantitative measurements.

Degree: 2007, Department of Medical Microbiology, Medicine / Leiden University Medical Center (LUMC), Leiden University

 Real-time monitoring of PCR has strongly supported the increased diagnostic use of nucleic acid detection assays in clinical virology. Particularly the improvements in the ability… (more)

Subjects/Keywords: Adenovirus; Area under the viremia curve; Cytomegalovirus; Epstein-Barr virus; Nasopharyngeal disease; Post transplant lymphoproliferative; Real-time PCR; (Val)ganciclovir; Varicella-zostervirus; Virus quantitation; Adenovirus; Area under the viremia curve; Cytomegalovirus; Epstein-Barr virus; Nasopharyngeal disease; Post transplant lymphoproliferative; Real-time PCR; (Val)ganciclovir; Varicella-zostervirus; Virus quantitation

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APA (6th Edition):

Kalpoe, J. S. (2007). Quantum virology: improved management of viral infections through quantitative measurements. (Doctoral Dissertation). Department of Medical Microbiology, Medicine / Leiden University Medical Center (LUMC), Leiden University. Retrieved from http://hdl.handle.net/1887/12100

Chicago Manual of Style (16th Edition):

Kalpoe, Jaijant Satishkumar. “Quantum virology: improved management of viral infections through quantitative measurements.” 2007. Doctoral Dissertation, Department of Medical Microbiology, Medicine / Leiden University Medical Center (LUMC), Leiden University. Accessed November 18, 2019. http://hdl.handle.net/1887/12100.

MLA Handbook (7th Edition):

Kalpoe, Jaijant Satishkumar. “Quantum virology: improved management of viral infections through quantitative measurements.” 2007. Web. 18 Nov 2019.

Vancouver:

Kalpoe JS. Quantum virology: improved management of viral infections through quantitative measurements. [Internet] [Doctoral dissertation]. Department of Medical Microbiology, Medicine / Leiden University Medical Center (LUMC), Leiden University; 2007. [cited 2019 Nov 18]. Available from: http://hdl.handle.net/1887/12100.

Council of Science Editors:

Kalpoe JS. Quantum virology: improved management of viral infections through quantitative measurements. [Doctoral Dissertation]. Department of Medical Microbiology, Medicine / Leiden University Medical Center (LUMC), Leiden University; 2007. Available from: http://hdl.handle.net/1887/12100

267. Beek, Martha Trijntje van der. Herpesvirus infections in immunocompromised patients: treatment, treatment failure and antiviral resistance.

Degree: 2012, Department of Medical Microbiology, Faculty of Medicine, Leiden University Medical Center (LUMC), Leiden University

 The research described in this thesis aims to study determinants of the course and outcome of treatment of herpesvirus infections in immunocompromised patients. Both viral… (more)

Subjects/Keywords: Herpes simplex virus type 1; Varicella-zoster virus; Cytomegalovirus; antiviral treatment; antiviral resistance; hematopoietic stem cell transplantation; renal transplantation; liver transplantation; Herpes simplex virus type 1; Varicella-zoster virus; Cytomegalovirus; antiviral treatment; antiviral resistance; hematopoietic stem cell transplantation; renal transplantation; liver transplantation

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APA (6th Edition):

Beek, M. T. v. d. (2012). Herpesvirus infections in immunocompromised patients: treatment, treatment failure and antiviral resistance. (Doctoral Dissertation). Department of Medical Microbiology, Faculty of Medicine, Leiden University Medical Center (LUMC), Leiden University. Retrieved from http://hdl.handle.net/1887/20141

Chicago Manual of Style (16th Edition):

Beek, Martha Trijntje van der. “Herpesvirus infections in immunocompromised patients: treatment, treatment failure and antiviral resistance.” 2012. Doctoral Dissertation, Department of Medical Microbiology, Faculty of Medicine, Leiden University Medical Center (LUMC), Leiden University. Accessed November 18, 2019. http://hdl.handle.net/1887/20141.

MLA Handbook (7th Edition):

Beek, Martha Trijntje van der. “Herpesvirus infections in immunocompromised patients: treatment, treatment failure and antiviral resistance.” 2012. Web. 18 Nov 2019.

Vancouver:

Beek MTvd. Herpesvirus infections in immunocompromised patients: treatment, treatment failure and antiviral resistance. [Internet] [Doctoral dissertation]. Department of Medical Microbiology, Faculty of Medicine, Leiden University Medical Center (LUMC), Leiden University; 2012. [cited 2019 Nov 18]. Available from: http://hdl.handle.net/1887/20141.

Council of Science Editors:

Beek MTvd. Herpesvirus infections in immunocompromised patients: treatment, treatment failure and antiviral resistance. [Doctoral Dissertation]. Department of Medical Microbiology, Faculty of Medicine, Leiden University Medical Center (LUMC), Leiden University; 2012. Available from: http://hdl.handle.net/1887/20141

268. Tomazin, Roman Anton. Evasion of CD8+ and CD4+ T cell recognition by herpesviruses.

Degree: PhD, 1999, Oregon Health Sciences University

Subjects/Keywords: ATP-Binding Cassette Transporters; CD4-Positive T-Lymphocytes; CD8-Positive T-Lymphocytes; Simplexvirus; Cytomegalovirus; Genes, MHC Class I; Genes, MHC Class II; Immediate-Early Proteins

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APA (6th Edition):

Tomazin, R. A. (1999). Evasion of CD8+ and CD4+ T cell recognition by herpesviruses. (Doctoral Dissertation). Oregon Health Sciences University. Retrieved from doi:10.6083/M4KS6PVS ; http://digitalcommons.ohsu.edu/etd/3340

Chicago Manual of Style (16th Edition):

Tomazin, Roman Anton. “Evasion of CD8+ and CD4+ T cell recognition by herpesviruses.” 1999. Doctoral Dissertation, Oregon Health Sciences University. Accessed November 18, 2019. doi:10.6083/M4KS6PVS ; http://digitalcommons.ohsu.edu/etd/3340.

MLA Handbook (7th Edition):

Tomazin, Roman Anton. “Evasion of CD8+ and CD4+ T cell recognition by herpesviruses.” 1999. Web. 18 Nov 2019.

Vancouver:

Tomazin RA. Evasion of CD8+ and CD4+ T cell recognition by herpesviruses. [Internet] [Doctoral dissertation]. Oregon Health Sciences University; 1999. [cited 2019 Nov 18]. Available from: doi:10.6083/M4KS6PVS ; http://digitalcommons.ohsu.edu/etd/3340.

Council of Science Editors:

Tomazin RA. Evasion of CD8+ and CD4+ T cell recognition by herpesviruses. [Doctoral Dissertation]. Oregon Health Sciences University; 1999. Available from: doi:10.6083/M4KS6PVS ; http://digitalcommons.ohsu.edu/etd/3340

269. Loo, Christopher P. Characterization of CD8 T cells in a Replication-deficient Murine Cytomegalovirus Infection.

Degree: PhD, 2013, Oregon Health Sciences University

Subjects/Keywords: Cytomegalovirus; CD8-Positive T-Lymphocytes; Virus Replication; Inflammation; Dendritic Cells; Medical Immunology; Medical Microbiology; Medicine and Health Sciences

…cells response in a replication-deficient murine cytomegalovirus (MCMV) infection… …Murine cytomegalovirus infection, like Human CMV, produces a robust chronic immune response… …Overview The scope of this thesis is the CD8 T cell response in murine Cytomegalovirus (MCMV… …be used to influence the study of immune therapy. 14 1.2 Cytomegalovirus 1.2.1… …icosahedral capsid (triangulation number 16). Cytomegalovirus belongs to the… 

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APA (6th Edition):

Loo, C. P. (2013). Characterization of CD8 T cells in a Replication-deficient Murine Cytomegalovirus Infection. (Doctoral Dissertation). Oregon Health Sciences University. Retrieved from doi:10.6083/M437772M ; http://digitalcommons.ohsu.edu/etd/3495

Chicago Manual of Style (16th Edition):

Loo, Christopher P. “Characterization of CD8 T cells in a Replication-deficient Murine Cytomegalovirus Infection.” 2013. Doctoral Dissertation, Oregon Health Sciences University. Accessed November 18, 2019. doi:10.6083/M437772M ; http://digitalcommons.ohsu.edu/etd/3495.

MLA Handbook (7th Edition):

Loo, Christopher P. “Characterization of CD8 T cells in a Replication-deficient Murine Cytomegalovirus Infection.” 2013. Web. 18 Nov 2019.

Vancouver:

Loo CP. Characterization of CD8 T cells in a Replication-deficient Murine Cytomegalovirus Infection. [Internet] [Doctoral dissertation]. Oregon Health Sciences University; 2013. [cited 2019 Nov 18]. Available from: doi:10.6083/M437772M ; http://digitalcommons.ohsu.edu/etd/3495.

Council of Science Editors:

Loo CP. Characterization of CD8 T cells in a Replication-deficient Murine Cytomegalovirus Infection. [Doctoral Dissertation]. Oregon Health Sciences University; 2013. Available from: doi:10.6083/M437772M ; http://digitalcommons.ohsu.edu/etd/3495


Freie Universität Berlin

270. Deckers, Jonas Merlin S. Variability of a glycoprotein and a G-protein-coupled receptor (UL55, UL33) of cytomegalovirus.

Degree: 2009, Freie Universität Berlin

Cytomegalovirus infections can cause serious problems in fetus, newborns and immunocompromised patients, and viral DNA is usually detected with specific PCR. An unprejudiced way of… (more)

Subjects/Keywords: cytomegalovirus; CMV; glycoprotein B; UL55; UL33; G-protein-coupled receptor; primate; gorilla; chimpanzee; genotype; 600 Technik, Medizin, angewandte Wissenschaften::610 Medizin und Gesundheit

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APA (6th Edition):

Deckers, J. M. S. (2009). Variability of a glycoprotein and a G-protein-coupled receptor (UL55, UL33) of cytomegalovirus. (Thesis). Freie Universität Berlin. Retrieved from http://dx.doi.org/10.17169/refubium-4301

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):

Deckers, Jonas Merlin S. “Variability of a glycoprotein and a G-protein-coupled receptor (UL55, UL33) of cytomegalovirus.” 2009. Thesis, Freie Universität Berlin. Accessed November 18, 2019. http://dx.doi.org/10.17169/refubium-4301.

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

MLA Handbook (7th Edition):

Deckers, Jonas Merlin S. “Variability of a glycoprotein and a G-protein-coupled receptor (UL55, UL33) of cytomegalovirus.” 2009. Web. 18 Nov 2019.

Vancouver:

Deckers JMS. Variability of a glycoprotein and a G-protein-coupled receptor (UL55, UL33) of cytomegalovirus. [Internet] [Thesis]. Freie Universität Berlin; 2009. [cited 2019 Nov 18]. Available from: http://dx.doi.org/10.17169/refubium-4301.

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

Council of Science Editors:

Deckers JMS. Variability of a glycoprotein and a G-protein-coupled receptor (UL55, UL33) of cytomegalovirus. [Thesis]. Freie Universität Berlin; 2009. Available from: http://dx.doi.org/10.17169/refubium-4301

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

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