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You searched for +publisher:"University of Kansas" +contributor:("Vines, Charlotte"). Showing records 1 – 10 of 10 total matches.

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University of Kansas

1. Ruiz, Autumn Joy. Vpu Mediated Enhancement of Human Immunodeficiency Virus Pathogenesis: The Role of Conserved and Unique Domains in Protein Function.

Degree: PhD, Anatomy & Cell Biology, 2010, University of Kansas

 The work in this dissertation examined the biological characteristics of different HIV-1 Vpu subtypes, with an emphasis on subtypes B and C, and the potential… (more)

Subjects/Keywords: Cell biology; Microbiology; Hiv; Pathogenesis; Vpu

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APA (6th Edition):

Ruiz, A. J. (2010). Vpu Mediated Enhancement of Human Immunodeficiency Virus Pathogenesis: The Role of Conserved and Unique Domains in Protein Function. (Doctoral Dissertation). University of Kansas. Retrieved from http://hdl.handle.net/1808/7618

Chicago Manual of Style (16th Edition):

Ruiz, Autumn Joy. “Vpu Mediated Enhancement of Human Immunodeficiency Virus Pathogenesis: The Role of Conserved and Unique Domains in Protein Function.” 2010. Doctoral Dissertation, University of Kansas. Accessed February 23, 2019. http://hdl.handle.net/1808/7618.

MLA Handbook (7th Edition):

Ruiz, Autumn Joy. “Vpu Mediated Enhancement of Human Immunodeficiency Virus Pathogenesis: The Role of Conserved and Unique Domains in Protein Function.” 2010. Web. 23 Feb 2019.

Vancouver:

Ruiz AJ. Vpu Mediated Enhancement of Human Immunodeficiency Virus Pathogenesis: The Role of Conserved and Unique Domains in Protein Function. [Internet] [Doctoral dissertation]. University of Kansas; 2010. [cited 2019 Feb 23]. Available from: http://hdl.handle.net/1808/7618.

Council of Science Editors:

Ruiz AJ. Vpu Mediated Enhancement of Human Immunodeficiency Virus Pathogenesis: The Role of Conserved and Unique Domains in Protein Function. [Doctoral Dissertation]. University of Kansas; 2010. Available from: http://hdl.handle.net/1808/7618


University of Kansas

2. Schmitt, Kimberly Patricia. The role of the rhesus macaque (macaca mulatta) apolipoprotein B mRNA-editing enzyme catalytic polypeptide-like 3 (APOBEC3) in lentiviral replication and persistence.

Degree: PhD, Anatomy & Cell Biology, 2012, University of Kansas

 SHIV infections in rhesus macaques have been used to extensively study accessory proteins of HIV-1 involved in pathogenesis as well as in vaccine development. All… (more)

Subjects/Keywords: Virology; Microbiology; Biology; Apobec3; Shiv; Vif

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APA (6th Edition):

Schmitt, K. P. (2012). The role of the rhesus macaque (macaca mulatta) apolipoprotein B mRNA-editing enzyme catalytic polypeptide-like 3 (APOBEC3) in lentiviral replication and persistence. (Doctoral Dissertation). University of Kansas. Retrieved from http://hdl.handle.net/1808/9983

Chicago Manual of Style (16th Edition):

Schmitt, Kimberly Patricia. “The role of the rhesus macaque (macaca mulatta) apolipoprotein B mRNA-editing enzyme catalytic polypeptide-like 3 (APOBEC3) in lentiviral replication and persistence.” 2012. Doctoral Dissertation, University of Kansas. Accessed February 23, 2019. http://hdl.handle.net/1808/9983.

MLA Handbook (7th Edition):

Schmitt, Kimberly Patricia. “The role of the rhesus macaque (macaca mulatta) apolipoprotein B mRNA-editing enzyme catalytic polypeptide-like 3 (APOBEC3) in lentiviral replication and persistence.” 2012. Web. 23 Feb 2019.

Vancouver:

Schmitt KP. The role of the rhesus macaque (macaca mulatta) apolipoprotein B mRNA-editing enzyme catalytic polypeptide-like 3 (APOBEC3) in lentiviral replication and persistence. [Internet] [Doctoral dissertation]. University of Kansas; 2012. [cited 2019 Feb 23]. Available from: http://hdl.handle.net/1808/9983.

Council of Science Editors:

Schmitt KP. The role of the rhesus macaque (macaca mulatta) apolipoprotein B mRNA-editing enzyme catalytic polypeptide-like 3 (APOBEC3) in lentiviral replication and persistence. [Doctoral Dissertation]. University of Kansas; 2012. Available from: http://hdl.handle.net/1808/9983


University of Kansas

3. Shannon, Laura. The Role of the G-Protein Coupled Receptor C-C Chemokine Receptor 7 in T Lymphocyte Migration and Breast Cancer Metastasis.

Degree: PhD, Microbiology, Molecular Genetics & Immunology, 2010, University of Kansas

 C-C Chemokine Receptor 7 (CCR7) promotes migration of T lymphocytes into and throughout lymph nodes via ligands CCL21 and CCL19. The mechanisms by which CCR7… (more)

Subjects/Keywords: Cell biology; Breast cancer; Chemokine; G-protein coupled receptor; Immunology

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APA (6th Edition):

Shannon, L. (2010). The Role of the G-Protein Coupled Receptor C-C Chemokine Receptor 7 in T Lymphocyte Migration and Breast Cancer Metastasis. (Doctoral Dissertation). University of Kansas. Retrieved from http://hdl.handle.net/1808/7423

Chicago Manual of Style (16th Edition):

Shannon, Laura. “The Role of the G-Protein Coupled Receptor C-C Chemokine Receptor 7 in T Lymphocyte Migration and Breast Cancer Metastasis.” 2010. Doctoral Dissertation, University of Kansas. Accessed February 23, 2019. http://hdl.handle.net/1808/7423.

MLA Handbook (7th Edition):

Shannon, Laura. “The Role of the G-Protein Coupled Receptor C-C Chemokine Receptor 7 in T Lymphocyte Migration and Breast Cancer Metastasis.” 2010. Web. 23 Feb 2019.

Vancouver:

Shannon L. The Role of the G-Protein Coupled Receptor C-C Chemokine Receptor 7 in T Lymphocyte Migration and Breast Cancer Metastasis. [Internet] [Doctoral dissertation]. University of Kansas; 2010. [cited 2019 Feb 23]. Available from: http://hdl.handle.net/1808/7423.

Council of Science Editors:

Shannon L. The Role of the G-Protein Coupled Receptor C-C Chemokine Receptor 7 in T Lymphocyte Migration and Breast Cancer Metastasis. [Doctoral Dissertation]. University of Kansas; 2010. Available from: http://hdl.handle.net/1808/7423


University of Kansas

4. Zhang, Elizabeth Yan. THE ROLE OF ADAPTOR PROTEIN GADS IN CD8+ T CELL-MEDIATED IMMUNITY.

Degree: PhD, Microbiology, Molecular Genetics & Immunology, 2011, University of Kansas

 CD8+ T cells are the branch of the adaptive immune system responsible for recognizing and killing tumor cells or cells infected with intracellular pathogens, such… (more)

Subjects/Keywords: Immunology; Cd8+ t cells; Gads; Tcr signaling

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APA (6th Edition):

Zhang, E. Y. (2011). THE ROLE OF ADAPTOR PROTEIN GADS IN CD8+ T CELL-MEDIATED IMMUNITY. (Doctoral Dissertation). University of Kansas. Retrieved from http://hdl.handle.net/1808/9710

Chicago Manual of Style (16th Edition):

Zhang, Elizabeth Yan. “THE ROLE OF ADAPTOR PROTEIN GADS IN CD8+ T CELL-MEDIATED IMMUNITY.” 2011. Doctoral Dissertation, University of Kansas. Accessed February 23, 2019. http://hdl.handle.net/1808/9710.

MLA Handbook (7th Edition):

Zhang, Elizabeth Yan. “THE ROLE OF ADAPTOR PROTEIN GADS IN CD8+ T CELL-MEDIATED IMMUNITY.” 2011. Web. 23 Feb 2019.

Vancouver:

Zhang EY. THE ROLE OF ADAPTOR PROTEIN GADS IN CD8+ T CELL-MEDIATED IMMUNITY. [Internet] [Doctoral dissertation]. University of Kansas; 2011. [cited 2019 Feb 23]. Available from: http://hdl.handle.net/1808/9710.

Council of Science Editors:

Zhang EY. THE ROLE OF ADAPTOR PROTEIN GADS IN CD8+ T CELL-MEDIATED IMMUNITY. [Doctoral Dissertation]. University of Kansas; 2011. Available from: http://hdl.handle.net/1808/9710


University of Kansas

5. Luo, Yong. MOLECULAR MECHANISMS OF THE DNA DAMAGE RESPONSE INDUCED DURING PARVOVIRUS INFECTION.

Degree: PhD, Microbiology, Molecular Genetics & Immunology, 2012, University of Kansas

 DNA damage response (DDR) is a critical safeguarding system to protect genomic stability and integrality through a cascade of phosphorylation events of three PI-3-kinase-like kinases:… (more)

Subjects/Keywords: Microbiology; Dna damage response; Dna replication; Parvovirus

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APA (6th Edition):

Luo, Y. (2012). MOLECULAR MECHANISMS OF THE DNA DAMAGE RESPONSE INDUCED DURING PARVOVIRUS INFECTION. (Doctoral Dissertation). University of Kansas. Retrieved from http://hdl.handle.net/1808/14837

Chicago Manual of Style (16th Edition):

Luo, Yong. “MOLECULAR MECHANISMS OF THE DNA DAMAGE RESPONSE INDUCED DURING PARVOVIRUS INFECTION.” 2012. Doctoral Dissertation, University of Kansas. Accessed February 23, 2019. http://hdl.handle.net/1808/14837.

MLA Handbook (7th Edition):

Luo, Yong. “MOLECULAR MECHANISMS OF THE DNA DAMAGE RESPONSE INDUCED DURING PARVOVIRUS INFECTION.” 2012. Web. 23 Feb 2019.

Vancouver:

Luo Y. MOLECULAR MECHANISMS OF THE DNA DAMAGE RESPONSE INDUCED DURING PARVOVIRUS INFECTION. [Internet] [Doctoral dissertation]. University of Kansas; 2012. [cited 2019 Feb 23]. Available from: http://hdl.handle.net/1808/14837.

Council of Science Editors:

Luo Y. MOLECULAR MECHANISMS OF THE DNA DAMAGE RESPONSE INDUCED DURING PARVOVIRUS INFECTION. [Doctoral Dissertation]. University of Kansas; 2012. Available from: http://hdl.handle.net/1808/14837

6. Wang, Wenjia. Identification and Characterization of Novel Kinases that Regulate BRCA1 Expression and Function.

Degree: PhD, Pathology & Laboratory Medicine, 2010, University of Kansas

 Transcriptional and functional regulation of the breast cancer susceptibility gene 1 (BRCA1) in the pathogenesis of sporadic breast cancers is poorly understood. We developed a… (more)

Subjects/Keywords: Molecular biology; Brca1; Fgfr2; Hck; Ionizing radiation-induced foci (irif); Kinase sirna library screen; Map3k1

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APA (6th Edition):

Wang, W. (2010). Identification and Characterization of Novel Kinases that Regulate BRCA1 Expression and Function. (Doctoral Dissertation). University of Kansas. Retrieved from http://hdl.handle.net/1808/6758

Chicago Manual of Style (16th Edition):

Wang, Wenjia. “Identification and Characterization of Novel Kinases that Regulate BRCA1 Expression and Function.” 2010. Doctoral Dissertation, University of Kansas. Accessed February 23, 2019. http://hdl.handle.net/1808/6758.

MLA Handbook (7th Edition):

Wang, Wenjia. “Identification and Characterization of Novel Kinases that Regulate BRCA1 Expression and Function.” 2010. Web. 23 Feb 2019.

Vancouver:

Wang W. Identification and Characterization of Novel Kinases that Regulate BRCA1 Expression and Function. [Internet] [Doctoral dissertation]. University of Kansas; 2010. [cited 2019 Feb 23]. Available from: http://hdl.handle.net/1808/6758.

Council of Science Editors:

Wang W. Identification and Characterization of Novel Kinases that Regulate BRCA1 Expression and Function. [Doctoral Dissertation]. University of Kansas; 2010. Available from: http://hdl.handle.net/1808/6758

7. Chen, Yun. Molecular Mechanism of Parvovirus Infection.

Degree: PhD, Microbiology, Molecular Genetics & Immunology, 2010, University of Kansas

 The studies to be presented are composed of two parts: 1) investigating the molecular mechanisms underlying cytopathic effects induced during infections of parvovirus B19 (B19V)… (more)

Subjects/Keywords: Biology; Microbiology; Molecular biology; Cell cycle; Cell death; Epo/epor/jak2; Human parvovirus b19; Parvovirus; Tropism

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APA (6th Edition):

Chen, Y. (2010). Molecular Mechanism of Parvovirus Infection. (Doctoral Dissertation). University of Kansas. Retrieved from http://hdl.handle.net/1808/6778

Chicago Manual of Style (16th Edition):

Chen, Yun. “Molecular Mechanism of Parvovirus Infection.” 2010. Doctoral Dissertation, University of Kansas. Accessed February 23, 2019. http://hdl.handle.net/1808/6778.

MLA Handbook (7th Edition):

Chen, Yun. “Molecular Mechanism of Parvovirus Infection.” 2010. Web. 23 Feb 2019.

Vancouver:

Chen Y. Molecular Mechanism of Parvovirus Infection. [Internet] [Doctoral dissertation]. University of Kansas; 2010. [cited 2019 Feb 23]. Available from: http://hdl.handle.net/1808/6778.

Council of Science Editors:

Chen Y. Molecular Mechanism of Parvovirus Infection. [Doctoral Dissertation]. University of Kansas; 2010. Available from: http://hdl.handle.net/1808/6778

8. Sestak, Joshua. Soluble Antigen Arrays utilize molecular and physical features to suppress Experimental Autoimmune Encephalomyelitis.

Degree: PhD, Pharmaceutical Chemistry, 2011, University of Kansas

 Blockade of immune cell adhesion during antigen recognition may suppress the inflammatory immune response in autoimmune diseases. Employing a novel N-oxime chemistry, Soluble Antigen Arrays… (more)

Subjects/Keywords: Pharmaceutical sciences; Polymer chemistry; Immunology

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APA (6th Edition):

Sestak, J. (2011). Soluble Antigen Arrays utilize molecular and physical features to suppress Experimental Autoimmune Encephalomyelitis. (Doctoral Dissertation). University of Kansas. Retrieved from http://hdl.handle.net/1808/8187

Chicago Manual of Style (16th Edition):

Sestak, Joshua. “Soluble Antigen Arrays utilize molecular and physical features to suppress Experimental Autoimmune Encephalomyelitis.” 2011. Doctoral Dissertation, University of Kansas. Accessed February 23, 2019. http://hdl.handle.net/1808/8187.

MLA Handbook (7th Edition):

Sestak, Joshua. “Soluble Antigen Arrays utilize molecular and physical features to suppress Experimental Autoimmune Encephalomyelitis.” 2011. Web. 23 Feb 2019.

Vancouver:

Sestak J. Soluble Antigen Arrays utilize molecular and physical features to suppress Experimental Autoimmune Encephalomyelitis. [Internet] [Doctoral dissertation]. University of Kansas; 2011. [cited 2019 Feb 23]. Available from: http://hdl.handle.net/1808/8187.

Council of Science Editors:

Sestak J. Soluble Antigen Arrays utilize molecular and physical features to suppress Experimental Autoimmune Encephalomyelitis. [Doctoral Dissertation]. University of Kansas; 2011. Available from: http://hdl.handle.net/1808/8187

9. Smith, Sarah Ellen. Mechanisms of cellular symmetry breaking in S. cerevisiae.

Degree: PhD, Molecular & Integrative Physiology, 2013, University of Kansas

 Cell polarization is vital to diverse biological processes, from maintenance of stem cell identity to chemotaxis of neutrophils. The small GTPase Cdc42 has long been… (more)

Subjects/Keywords: Biology

…and Integrative Physiology, University of Kansas Medical Center, 3901 Rainbow Boulevard… 

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APA (6th Edition):

Smith, S. E. (2013). Mechanisms of cellular symmetry breaking in S. cerevisiae. (Doctoral Dissertation). University of Kansas. Retrieved from http://hdl.handle.net/1808/14185

Chicago Manual of Style (16th Edition):

Smith, Sarah Ellen. “Mechanisms of cellular symmetry breaking in S. cerevisiae.” 2013. Doctoral Dissertation, University of Kansas. Accessed February 23, 2019. http://hdl.handle.net/1808/14185.

MLA Handbook (7th Edition):

Smith, Sarah Ellen. “Mechanisms of cellular symmetry breaking in S. cerevisiae.” 2013. Web. 23 Feb 2019.

Vancouver:

Smith SE. Mechanisms of cellular symmetry breaking in S. cerevisiae. [Internet] [Doctoral dissertation]. University of Kansas; 2013. [cited 2019 Feb 23]. Available from: http://hdl.handle.net/1808/14185.

Council of Science Editors:

Smith SE. Mechanisms of cellular symmetry breaking in S. cerevisiae. [Doctoral Dissertation]. University of Kansas; 2013. Available from: http://hdl.handle.net/1808/14185


University of Kansas

10. Bellon, Marcia Lynn. Telomerase Regulation and Telomere Maintenance during Human T-cell Leukemia/Lymphoma Virus (HTLV-I) Transformation.

Degree: PH.D., Microbiology, Molecular Genetics & Immunology, 2008, University of Kansas

 Human T-cell leukemia/lymphoma virus (HTLV-I) is the etiological agent of the lymphoproliferative disorder, adult T-cell leukemia/lymphoma (ATLL) and the neurodegenerative disease, tropical spastic paraparesis/HTLV-I-associated myelopathy… (more)

Subjects/Keywords: Biology; Microbiology; Htlv; Telomerase; Telomere; Leukemia; Shelterin

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APA (6th Edition):

Bellon, M. L. (2008). Telomerase Regulation and Telomere Maintenance during Human T-cell Leukemia/Lymphoma Virus (HTLV-I) Transformation. (Doctoral Dissertation). University of Kansas. Retrieved from http://hdl.handle.net/1808/3948

Chicago Manual of Style (16th Edition):

Bellon, Marcia Lynn. “Telomerase Regulation and Telomere Maintenance during Human T-cell Leukemia/Lymphoma Virus (HTLV-I) Transformation.” 2008. Doctoral Dissertation, University of Kansas. Accessed February 23, 2019. http://hdl.handle.net/1808/3948.

MLA Handbook (7th Edition):

Bellon, Marcia Lynn. “Telomerase Regulation and Telomere Maintenance during Human T-cell Leukemia/Lymphoma Virus (HTLV-I) Transformation.” 2008. Web. 23 Feb 2019.

Vancouver:

Bellon ML. Telomerase Regulation and Telomere Maintenance during Human T-cell Leukemia/Lymphoma Virus (HTLV-I) Transformation. [Internet] [Doctoral dissertation]. University of Kansas; 2008. [cited 2019 Feb 23]. Available from: http://hdl.handle.net/1808/3948.

Council of Science Editors:

Bellon ML. Telomerase Regulation and Telomere Maintenance during Human T-cell Leukemia/Lymphoma Virus (HTLV-I) Transformation. [Doctoral Dissertation]. University of Kansas; 2008. Available from: http://hdl.handle.net/1808/3948

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