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You searched for subject:(lung cells). Showing records 1 – 30 of 146 total matches.

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1. 稲村, 幸雄. Recruitment of distinct immune cell populations to the lung after intratracheal TLR4 signaling activation by two different stimulations : 異なる二種類の刺激による気管内Toll様受容体4(TLR4)シグナル伝達活性化に伴う、特徴的な免疫細胞集団の肺への遊走.

Degree: 博士(医学), 2017, Nagasaki University / 長崎大学

 The toll-like receptor 4 (TLR4)-mediated immune response is considered as one of the triggers of acute respiratory distress syndrome. The agonistic monoclonal antibody UT12 specific… (more)

Subjects/Keywords: lung; TLR4; neutrophils; dendritic cells

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APA (6th Edition):

稲村, . (2017). Recruitment of distinct immune cell populations to the lung after intratracheal TLR4 signaling activation by two different stimulations : 異なる二種類の刺激による気管内Toll様受容体4(TLR4)シグナル伝達活性化に伴う、特徴的な免疫細胞集団の肺への遊走. (Thesis). Nagasaki University / 長崎大学. Retrieved from http://hdl.handle.net/10069/37068

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):

稲村, 幸雄. “Recruitment of distinct immune cell populations to the lung after intratracheal TLR4 signaling activation by two different stimulations : 異なる二種類の刺激による気管内Toll様受容体4(TLR4)シグナル伝達活性化に伴う、特徴的な免疫細胞集団の肺への遊走.” 2017. Thesis, Nagasaki University / 長崎大学. Accessed August 22, 2019. http://hdl.handle.net/10069/37068.

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

MLA Handbook (7th Edition):

稲村, 幸雄. “Recruitment of distinct immune cell populations to the lung after intratracheal TLR4 signaling activation by two different stimulations : 異なる二種類の刺激による気管内Toll様受容体4(TLR4)シグナル伝達活性化に伴う、特徴的な免疫細胞集団の肺への遊走.” 2017. Web. 22 Aug 2019.

Vancouver:

稲村 . Recruitment of distinct immune cell populations to the lung after intratracheal TLR4 signaling activation by two different stimulations : 異なる二種類の刺激による気管内Toll様受容体4(TLR4)シグナル伝達活性化に伴う、特徴的な免疫細胞集団の肺への遊走. [Internet] [Thesis]. Nagasaki University / 長崎大学; 2017. [cited 2019 Aug 22]. Available from: http://hdl.handle.net/10069/37068.

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

Council of Science Editors:

稲村 . Recruitment of distinct immune cell populations to the lung after intratracheal TLR4 signaling activation by two different stimulations : 異なる二種類の刺激による気管内Toll様受容体4(TLR4)シグナル伝達活性化に伴う、特徴的な免疫細胞集団の肺への遊走. [Thesis]. Nagasaki University / 長崎大学; 2017. Available from: http://hdl.handle.net/10069/37068

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


Temple University

2. Stabler, Collin Turner. Optimizing Endothelial Repopulation of Decellularized Lung.

Degree: PhD, 2016, Temple University

Bioengineering

Decellularized lung tissue has been recognized as a potential platform to engineer whole lung organs suitable for transplantation or for modeling a variety of… (more)

Subjects/Keywords: Biomedical engineering;

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APA (6th Edition):

Stabler, C. T. (2016). Optimizing Endothelial Repopulation of Decellularized Lung. (Doctoral Dissertation). Temple University. Retrieved from http://digital.library.temple.edu/u?/p245801coll10,388434

Chicago Manual of Style (16th Edition):

Stabler, Collin Turner. “Optimizing Endothelial Repopulation of Decellularized Lung.” 2016. Doctoral Dissertation, Temple University. Accessed August 22, 2019. http://digital.library.temple.edu/u?/p245801coll10,388434.

MLA Handbook (7th Edition):

Stabler, Collin Turner. “Optimizing Endothelial Repopulation of Decellularized Lung.” 2016. Web. 22 Aug 2019.

Vancouver:

Stabler CT. Optimizing Endothelial Repopulation of Decellularized Lung. [Internet] [Doctoral dissertation]. Temple University; 2016. [cited 2019 Aug 22]. Available from: http://digital.library.temple.edu/u?/p245801coll10,388434.

Council of Science Editors:

Stabler CT. Optimizing Endothelial Repopulation of Decellularized Lung. [Doctoral Dissertation]. Temple University; 2016. Available from: http://digital.library.temple.edu/u?/p245801coll10,388434


University of Alberta

3. Ionescu, Lavinia Iuliana. Evaluation of Mesenchymal Stem Cell-Based Therapies for Inflammatory Lung Diseases.

Degree: PhD, Department of Physiology, 2012, University of Alberta

 Recent discoveries in stem cell biology have generated enthusiasm about the possibility of harnessing stem cells for organ repair and regeneration. The ability of pluri-… (more)

Subjects/Keywords: asthma; mesenchymal stem cells; acute lung injury; lung; lipopolysaccharide; ovalbumin

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APA (6th Edition):

Ionescu, L. I. (2012). Evaluation of Mesenchymal Stem Cell-Based Therapies for Inflammatory Lung Diseases. (Doctoral Dissertation). University of Alberta. Retrieved from https://era.library.ualberta.ca/files/kh04dq54w

Chicago Manual of Style (16th Edition):

Ionescu, Lavinia Iuliana. “Evaluation of Mesenchymal Stem Cell-Based Therapies for Inflammatory Lung Diseases.” 2012. Doctoral Dissertation, University of Alberta. Accessed August 22, 2019. https://era.library.ualberta.ca/files/kh04dq54w.

MLA Handbook (7th Edition):

Ionescu, Lavinia Iuliana. “Evaluation of Mesenchymal Stem Cell-Based Therapies for Inflammatory Lung Diseases.” 2012. Web. 22 Aug 2019.

Vancouver:

Ionescu LI. Evaluation of Mesenchymal Stem Cell-Based Therapies for Inflammatory Lung Diseases. [Internet] [Doctoral dissertation]. University of Alberta; 2012. [cited 2019 Aug 22]. Available from: https://era.library.ualberta.ca/files/kh04dq54w.

Council of Science Editors:

Ionescu LI. Evaluation of Mesenchymal Stem Cell-Based Therapies for Inflammatory Lung Diseases. [Doctoral Dissertation]. University of Alberta; 2012. Available from: https://era.library.ualberta.ca/files/kh04dq54w


University of Manchester

4. Gieschen-Krische, Mary. The role of NKT cells following solid organ transplantation.

Degree: PhD, 2014, University of Manchester

 Introduction: NKT cells are categorised as borderline between NK and T cells, sharing phenotypic and functional characteristics of both cells, demonstrating their capacity to contritube… (more)

Subjects/Keywords: acute lung injury; immunosuppression; NKT cells; lung; transplantation

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APA (6th Edition):

Gieschen-Krische, M. (2014). The role of NKT cells following solid organ transplantation. (Doctoral Dissertation). University of Manchester. Retrieved from https://www.research.manchester.ac.uk/portal/en/theses/the-role-of-nkt-cells-following-solid-organ-transplantation(321a0a4b-336e-44dd-a608-58f7ea58e27e).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.764287

Chicago Manual of Style (16th Edition):

Gieschen-Krische, Mary. “The role of NKT cells following solid organ transplantation.” 2014. Doctoral Dissertation, University of Manchester. Accessed August 22, 2019. https://www.research.manchester.ac.uk/portal/en/theses/the-role-of-nkt-cells-following-solid-organ-transplantation(321a0a4b-336e-44dd-a608-58f7ea58e27e).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.764287.

MLA Handbook (7th Edition):

Gieschen-Krische, Mary. “The role of NKT cells following solid organ transplantation.” 2014. Web. 22 Aug 2019.

Vancouver:

Gieschen-Krische M. The role of NKT cells following solid organ transplantation. [Internet] [Doctoral dissertation]. University of Manchester; 2014. [cited 2019 Aug 22]. Available from: https://www.research.manchester.ac.uk/portal/en/theses/the-role-of-nkt-cells-following-solid-organ-transplantation(321a0a4b-336e-44dd-a608-58f7ea58e27e).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.764287.

Council of Science Editors:

Gieschen-Krische M. The role of NKT cells following solid organ transplantation. [Doctoral Dissertation]. University of Manchester; 2014. Available from: https://www.research.manchester.ac.uk/portal/en/theses/the-role-of-nkt-cells-following-solid-organ-transplantation(321a0a4b-336e-44dd-a608-58f7ea58e27e).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.764287


University of Manchester

5. Gieschen-Krische, Mary. The role of NKT cells following solid organ transplantation.

Degree: 2014, University of Manchester

 Introduction: NKT cells are categorised as borderline between NK and T cells, sharing phenotypic and functional characteristics of both cells, demonstrating their capacity to contritube… (more)

Subjects/Keywords: NKT cells; lung; transplantation; immunosuppression; acute lung injury

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APA (6th Edition):

Gieschen-Krische, M. (2014). The role of NKT cells following solid organ transplantation. (Doctoral Dissertation). University of Manchester. Retrieved from http://www.manchester.ac.uk/escholar/uk-ac-man-scw:242866

Chicago Manual of Style (16th Edition):

Gieschen-Krische, Mary. “The role of NKT cells following solid organ transplantation.” 2014. Doctoral Dissertation, University of Manchester. Accessed August 22, 2019. http://www.manchester.ac.uk/escholar/uk-ac-man-scw:242866.

MLA Handbook (7th Edition):

Gieschen-Krische, Mary. “The role of NKT cells following solid organ transplantation.” 2014. Web. 22 Aug 2019.

Vancouver:

Gieschen-Krische M. The role of NKT cells following solid organ transplantation. [Internet] [Doctoral dissertation]. University of Manchester; 2014. [cited 2019 Aug 22]. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:242866.

Council of Science Editors:

Gieschen-Krische M. The role of NKT cells following solid organ transplantation. [Doctoral Dissertation]. University of Manchester; 2014. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:242866


University of Toronto

6. Kim, Bo Ram. Investigation of the Oncogenic Role of Sox2 in the Pathogenesis of Lung Squamous Cell Carcinoma using Normal Human Lung Basal Progenitors.

Degree: 2012, University of Toronto

Sox2 is the most frequently amplified oncogene in lung squamous cell carcinoma (SCC). Lung SCC arises in the proximal to central airways and is thought… (more)

Subjects/Keywords: lung squamous cell carcinoma; Sox2; basal cells; lung progenitor; 0379

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APA (6th Edition):

Kim, B. R. (2012). Investigation of the Oncogenic Role of Sox2 in the Pathogenesis of Lung Squamous Cell Carcinoma using Normal Human Lung Basal Progenitors. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/32250

Chicago Manual of Style (16th Edition):

Kim, Bo Ram. “Investigation of the Oncogenic Role of Sox2 in the Pathogenesis of Lung Squamous Cell Carcinoma using Normal Human Lung Basal Progenitors.” 2012. Masters Thesis, University of Toronto. Accessed August 22, 2019. http://hdl.handle.net/1807/32250.

MLA Handbook (7th Edition):

Kim, Bo Ram. “Investigation of the Oncogenic Role of Sox2 in the Pathogenesis of Lung Squamous Cell Carcinoma using Normal Human Lung Basal Progenitors.” 2012. Web. 22 Aug 2019.

Vancouver:

Kim BR. Investigation of the Oncogenic Role of Sox2 in the Pathogenesis of Lung Squamous Cell Carcinoma using Normal Human Lung Basal Progenitors. [Internet] [Masters thesis]. University of Toronto; 2012. [cited 2019 Aug 22]. Available from: http://hdl.handle.net/1807/32250.

Council of Science Editors:

Kim BR. Investigation of the Oncogenic Role of Sox2 in the Pathogenesis of Lung Squamous Cell Carcinoma using Normal Human Lung Basal Progenitors. [Masters Thesis]. University of Toronto; 2012. Available from: http://hdl.handle.net/1807/32250


University of Kashmir

7. Qazi Danish Mushtaq. A study on crosstalk between lung carcinoma and immune cells;.

Degree: 2013, University of Kashmir

newlineTumor cells are seen to modulate the phenotype of all major immune cells to newlineexpress tumor favouring phenotypes. Inflammation associated with tumors, a result of… (more)

Subjects/Keywords: Cross-Talk; Immune Cells; Lung Carcinoma

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APA (6th Edition):

Mushtaq, Q. D. (2013). A study on crosstalk between lung carcinoma and immune cells;. (Thesis). University of Kashmir. Retrieved from http://shodhganga.inflibnet.ac.in/handle/10603/14385

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):

Mushtaq, Qazi Danish. “A study on crosstalk between lung carcinoma and immune cells;.” 2013. Thesis, University of Kashmir. Accessed August 22, 2019. http://shodhganga.inflibnet.ac.in/handle/10603/14385.

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

MLA Handbook (7th Edition):

Mushtaq, Qazi Danish. “A study on crosstalk between lung carcinoma and immune cells;.” 2013. Web. 22 Aug 2019.

Vancouver:

Mushtaq QD. A study on crosstalk between lung carcinoma and immune cells;. [Internet] [Thesis]. University of Kashmir; 2013. [cited 2019 Aug 22]. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/14385.

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

Council of Science Editors:

Mushtaq QD. A study on crosstalk between lung carcinoma and immune cells;. [Thesis]. University of Kashmir; 2013. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/14385

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


University of Arizona

8. Calderon, Stephanie Marie. CC16 Depletion in the Lung Due to Early Life Biomass Exposures .

Degree: 2019, University of Arizona

 Millions of people across the globe are affected by respiratory diseases that include chronic obstructive pulmonary disease (COPD), asthma, emphysema, as well as cancer. COPD… (more)

Subjects/Keywords: Lung; CC16; Club cells; Biomass exposure

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APA (6th Edition):

Calderon, S. M. (2019). CC16 Depletion in the Lung Due to Early Life Biomass Exposures . (Masters Thesis). University of Arizona. Retrieved from http://hdl.handle.net/10150/631918

Chicago Manual of Style (16th Edition):

Calderon, Stephanie Marie. “CC16 Depletion in the Lung Due to Early Life Biomass Exposures .” 2019. Masters Thesis, University of Arizona. Accessed August 22, 2019. http://hdl.handle.net/10150/631918.

MLA Handbook (7th Edition):

Calderon, Stephanie Marie. “CC16 Depletion in the Lung Due to Early Life Biomass Exposures .” 2019. Web. 22 Aug 2019.

Vancouver:

Calderon SM. CC16 Depletion in the Lung Due to Early Life Biomass Exposures . [Internet] [Masters thesis]. University of Arizona; 2019. [cited 2019 Aug 22]. Available from: http://hdl.handle.net/10150/631918.

Council of Science Editors:

Calderon SM. CC16 Depletion in the Lung Due to Early Life Biomass Exposures . [Masters Thesis]. University of Arizona; 2019. Available from: http://hdl.handle.net/10150/631918


University of Toronto

9. Clifford, Monica Allison. Identification of Molecular and Functional Heterogeneity of Epithelial Progenitor Cells in the Upper Airway.

Degree: 2013, University of Toronto

Upper airways are lined with a pseudostratified mucociliary epithelium maintained by basal cells. To investigate functional and phenotypic heterogeneity within the human basal cell compartment,… (more)

Subjects/Keywords: airway epithelium; lung progenitor cells; 0379; 0307

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APA (6th Edition):

Clifford, M. A. (2013). Identification of Molecular and Functional Heterogeneity of Epithelial Progenitor Cells in the Upper Airway. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/35590

Chicago Manual of Style (16th Edition):

Clifford, Monica Allison. “Identification of Molecular and Functional Heterogeneity of Epithelial Progenitor Cells in the Upper Airway.” 2013. Masters Thesis, University of Toronto. Accessed August 22, 2019. http://hdl.handle.net/1807/35590.

MLA Handbook (7th Edition):

Clifford, Monica Allison. “Identification of Molecular and Functional Heterogeneity of Epithelial Progenitor Cells in the Upper Airway.” 2013. Web. 22 Aug 2019.

Vancouver:

Clifford MA. Identification of Molecular and Functional Heterogeneity of Epithelial Progenitor Cells in the Upper Airway. [Internet] [Masters thesis]. University of Toronto; 2013. [cited 2019 Aug 22]. Available from: http://hdl.handle.net/1807/35590.

Council of Science Editors:

Clifford MA. Identification of Molecular and Functional Heterogeneity of Epithelial Progenitor Cells in the Upper Airway. [Masters Thesis]. University of Toronto; 2013. Available from: http://hdl.handle.net/1807/35590


University of Rochester

10. DiPiazza, Anthony Thomas. Insights into CD4 T Cell-Mediated Immunity to Influenza Viruses.

Degree: PhD, 2019, University of Rochester

 Influenza A viruses continue to pose a threat to human health worldwide and virusspecific CD4 T cells are key to protective immunity. The goal of… (more)

Subjects/Keywords: Antigen presenting cells; Infection; Influenza; Lung; T cells.

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APA (6th Edition):

DiPiazza, A. T. (2019). Insights into CD4 T Cell-Mediated Immunity to Influenza Viruses. (Doctoral Dissertation). University of Rochester. Retrieved from http://hdl.handle.net/1802/34970

Chicago Manual of Style (16th Edition):

DiPiazza, Anthony Thomas. “Insights into CD4 T Cell-Mediated Immunity to Influenza Viruses.” 2019. Doctoral Dissertation, University of Rochester. Accessed August 22, 2019. http://hdl.handle.net/1802/34970.

MLA Handbook (7th Edition):

DiPiazza, Anthony Thomas. “Insights into CD4 T Cell-Mediated Immunity to Influenza Viruses.” 2019. Web. 22 Aug 2019.

Vancouver:

DiPiazza AT. Insights into CD4 T Cell-Mediated Immunity to Influenza Viruses. [Internet] [Doctoral dissertation]. University of Rochester; 2019. [cited 2019 Aug 22]. Available from: http://hdl.handle.net/1802/34970.

Council of Science Editors:

DiPiazza AT. Insights into CD4 T Cell-Mediated Immunity to Influenza Viruses. [Doctoral Dissertation]. University of Rochester; 2019. Available from: http://hdl.handle.net/1802/34970

11. Svensson, Susanne. In vitro and in vivo inhibition of Chk1 sensitize lung cancer stem cells to chemotherapy.

Degree: 2011, Università degli Studi di Catania

 Development of resistance to radiation and chemotherapy turns the treatment of solid cancers into a therapeutic challenge. One of the most exciting breakthroughs being explored… (more)

Subjects/Keywords: Non-small cell lung cancer; Lung cancer stem cells; DNA damage; Chk1 inhibitors

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APA (6th Edition):

Svensson, S. (2011). In vitro and in vivo inhibition of Chk1 sensitize lung cancer stem cells to chemotherapy. (Thesis). Università degli Studi di Catania. Retrieved from http://hdl.handle.net/10761/98

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):

Svensson, Susanne. “In vitro and in vivo inhibition of Chk1 sensitize lung cancer stem cells to chemotherapy.” 2011. Thesis, Università degli Studi di Catania. Accessed August 22, 2019. http://hdl.handle.net/10761/98.

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

MLA Handbook (7th Edition):

Svensson, Susanne. “In vitro and in vivo inhibition of Chk1 sensitize lung cancer stem cells to chemotherapy.” 2011. Web. 22 Aug 2019.

Vancouver:

Svensson S. In vitro and in vivo inhibition of Chk1 sensitize lung cancer stem cells to chemotherapy. [Internet] [Thesis]. Università degli Studi di Catania; 2011. [cited 2019 Aug 22]. Available from: http://hdl.handle.net/10761/98.

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

Council of Science Editors:

Svensson S. In vitro and in vivo inhibition of Chk1 sensitize lung cancer stem cells to chemotherapy. [Thesis]. Università degli Studi di Catania; 2011. Available from: http://hdl.handle.net/10761/98

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


University of Cincinnati

12. Richie, Nicole. The Retinoblastoma Tumor Supressor Protein is a Critical Regulator of Lung Epithelial Repair after Injury.

Degree: PhD, Medicine : Pathobiology and Molecular Medicine, 2008, University of Cincinnati

 Airway remodeling is associated with the vast majority of lung diseases including chronic obstructive pulmonary disease, asthma, and lung cancer. Epithelial regeneration is a key… (more)

Subjects/Keywords: Molecular Biology; Oncology; Pathology; Retinoblastoma (Rb); Cre-LoxP; Lung injury; Lung progenitor and stem cells

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APA (6th Edition):

Richie, N. (2008). The Retinoblastoma Tumor Supressor Protein is a Critical Regulator of Lung Epithelial Repair after Injury. (Doctoral Dissertation). University of Cincinnati. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=ucin1225203307

Chicago Manual of Style (16th Edition):

Richie, Nicole. “The Retinoblastoma Tumor Supressor Protein is a Critical Regulator of Lung Epithelial Repair after Injury.” 2008. Doctoral Dissertation, University of Cincinnati. Accessed August 22, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1225203307.

MLA Handbook (7th Edition):

Richie, Nicole. “The Retinoblastoma Tumor Supressor Protein is a Critical Regulator of Lung Epithelial Repair after Injury.” 2008. Web. 22 Aug 2019.

Vancouver:

Richie N. The Retinoblastoma Tumor Supressor Protein is a Critical Regulator of Lung Epithelial Repair after Injury. [Internet] [Doctoral dissertation]. University of Cincinnati; 2008. [cited 2019 Aug 22]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ucin1225203307.

Council of Science Editors:

Richie N. The Retinoblastoma Tumor Supressor Protein is a Critical Regulator of Lung Epithelial Repair after Injury. [Doctoral Dissertation]. University of Cincinnati; 2008. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ucin1225203307


University of Florida

13. Jimenez, Elizabeth. Generation of DNA Aptamers for Lung Cancer Studies.

Degree: PhD, Chemistry, 2013, University of Florida

 The overall objective of this proposal is to develop a strategy for the detection and isolation of circulating tumor cells(CTC's) from peripheral blood of lung(more)

Subjects/Keywords: Adenocarcinoma; Blood; Cancer; Cell lines; Cells; Lung neoplasms; Lungs; Molecules; Small cell lung carcinoma; Tumors; aptamers  – cancer  – cell-selex  – lung

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APA (6th Edition):

Jimenez, E. (2013). Generation of DNA Aptamers for Lung Cancer Studies. (Doctoral Dissertation). University of Florida. Retrieved from http://ufdc.ufl.edu/UFE0045913

Chicago Manual of Style (16th Edition):

Jimenez, Elizabeth. “Generation of DNA Aptamers for Lung Cancer Studies.” 2013. Doctoral Dissertation, University of Florida. Accessed August 22, 2019. http://ufdc.ufl.edu/UFE0045913.

MLA Handbook (7th Edition):

Jimenez, Elizabeth. “Generation of DNA Aptamers for Lung Cancer Studies.” 2013. Web. 22 Aug 2019.

Vancouver:

Jimenez E. Generation of DNA Aptamers for Lung Cancer Studies. [Internet] [Doctoral dissertation]. University of Florida; 2013. [cited 2019 Aug 22]. Available from: http://ufdc.ufl.edu/UFE0045913.

Council of Science Editors:

Jimenez E. Generation of DNA Aptamers for Lung Cancer Studies. [Doctoral Dissertation]. University of Florida; 2013. Available from: http://ufdc.ufl.edu/UFE0045913

14. Santos, Angela Batista Gomes dos. Perfil celular do tecido pulmonar em crianças de até dois anos: um estudo em autópsias.

Degree: Mestrado, Fisiopatologia Experimental, 2011, University of São Paulo

Introdução: Doenças pulmonares ou infecções que ocorrem no início da vida podem ter permanente impacto na vida adulta. Pouco se sabe sobre o perfil de… (more)

Subjects/Keywords: Autópsia; Autopsy; Células dendríticas; Dendritic cells; Infants; Lactante; Linfócitos; Lung; Lymphocytes; Mast cells; Mastócitos; Pulmão

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APA (6th Edition):

Santos, A. B. G. d. (2011). Perfil celular do tecido pulmonar em crianças de até dois anos: um estudo em autópsias. (Masters Thesis). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/5/5160/tde-24052011-153742/ ;

Chicago Manual of Style (16th Edition):

Santos, Angela Batista Gomes dos. “Perfil celular do tecido pulmonar em crianças de até dois anos: um estudo em autópsias.” 2011. Masters Thesis, University of São Paulo. Accessed August 22, 2019. http://www.teses.usp.br/teses/disponiveis/5/5160/tde-24052011-153742/ ;.

MLA Handbook (7th Edition):

Santos, Angela Batista Gomes dos. “Perfil celular do tecido pulmonar em crianças de até dois anos: um estudo em autópsias.” 2011. Web. 22 Aug 2019.

Vancouver:

Santos ABGd. Perfil celular do tecido pulmonar em crianças de até dois anos: um estudo em autópsias. [Internet] [Masters thesis]. University of São Paulo; 2011. [cited 2019 Aug 22]. Available from: http://www.teses.usp.br/teses/disponiveis/5/5160/tde-24052011-153742/ ;.

Council of Science Editors:

Santos ABGd. Perfil celular do tecido pulmonar em crianças de até dois anos: um estudo em autópsias. [Masters Thesis]. University of São Paulo; 2011. Available from: http://www.teses.usp.br/teses/disponiveis/5/5160/tde-24052011-153742/ ;


RMIT University

15. Elbaz, A. Investigating the immune and cytotoxic responses of mast and lung epithelial cells to engineered nanoparticles.

Degree: 2012, RMIT University

 The applications for engineered nanoparticles have increased dramatically in recent years. They have been introduced into the industrial, electrical, agricultural, pharmaceutical and medical fields due… (more)

Subjects/Keywords: Fields of Research; nanoparticles; mast cells; lung epithelial cells; immune responses and cytotoxicity

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APA (6th Edition):

Elbaz, A. (2012). Investigating the immune and cytotoxic responses of mast and lung epithelial cells to engineered nanoparticles. (Thesis). RMIT University. Retrieved from http://researchbank.rmit.edu.au/view/rmit:161007

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):

Elbaz, A. “Investigating the immune and cytotoxic responses of mast and lung epithelial cells to engineered nanoparticles.” 2012. Thesis, RMIT University. Accessed August 22, 2019. http://researchbank.rmit.edu.au/view/rmit:161007.

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

MLA Handbook (7th Edition):

Elbaz, A. “Investigating the immune and cytotoxic responses of mast and lung epithelial cells to engineered nanoparticles.” 2012. Web. 22 Aug 2019.

Vancouver:

Elbaz A. Investigating the immune and cytotoxic responses of mast and lung epithelial cells to engineered nanoparticles. [Internet] [Thesis]. RMIT University; 2012. [cited 2019 Aug 22]. Available from: http://researchbank.rmit.edu.au/view/rmit:161007.

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

Council of Science Editors:

Elbaz A. Investigating the immune and cytotoxic responses of mast and lung epithelial cells to engineered nanoparticles. [Thesis]. RMIT University; 2012. Available from: http://researchbank.rmit.edu.au/view/rmit:161007

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

16. Salvati, Valentina. Development of effective lung cancer therapies based on lung cancer stem cella targeting.

Degree: 2015, Università degli Studi di Catania

 Il carcinoma polmonare non a piccole cellule (NSCLC) rappresenta circa l 80% di tutti i tumori al polmone ed è il cancro più comune e… (more)

Subjects/Keywords: Area 05 - Scienze biologiche; Cancer stem cells, EGFR phosphorylation, lung cancer

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APA (6th Edition):

Salvati, V. (2015). Development of effective lung cancer therapies based on lung cancer stem cella targeting. (Thesis). Università degli Studi di Catania. Retrieved from http://hdl.handle.net/10761/4035

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):

Salvati, Valentina. “Development of effective lung cancer therapies based on lung cancer stem cella targeting.” 2015. Thesis, Università degli Studi di Catania. Accessed August 22, 2019. http://hdl.handle.net/10761/4035.

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

MLA Handbook (7th Edition):

Salvati, Valentina. “Development of effective lung cancer therapies based on lung cancer stem cella targeting.” 2015. Web. 22 Aug 2019.

Vancouver:

Salvati V. Development of effective lung cancer therapies based on lung cancer stem cella targeting. [Internet] [Thesis]. Università degli Studi di Catania; 2015. [cited 2019 Aug 22]. Available from: http://hdl.handle.net/10761/4035.

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

Council of Science Editors:

Salvati V. Development of effective lung cancer therapies based on lung cancer stem cella targeting. [Thesis]. Università degli Studi di Catania; 2015. Available from: http://hdl.handle.net/10761/4035

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


University of Alberta

17. Strueby, Lannae L. Paracrine Effect of Mesenchymal Stromal Cells on Multifactorial Lung Injury in Neonatal Mice.

Degree: MS, Department of Physiology, 2014, University of Alberta

 Bronchopulmonary dysplasia (BPD) is a common complication of extreme prematurity. Preterm infants often require mechanical ventilation and supplemental oxygen for survival. These interventions increase the… (more)

Subjects/Keywords: Paracrine; Conditioned Media; Mesenchymal Stromal Cells; Lung Injury; Bronchopulmonary Dysplasia

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APA (6th Edition):

Strueby, L. L. (2014). Paracrine Effect of Mesenchymal Stromal Cells on Multifactorial Lung Injury in Neonatal Mice. (Masters Thesis). University of Alberta. Retrieved from https://era.library.ualberta.ca/files/1g05ff203

Chicago Manual of Style (16th Edition):

Strueby, Lannae L. “Paracrine Effect of Mesenchymal Stromal Cells on Multifactorial Lung Injury in Neonatal Mice.” 2014. Masters Thesis, University of Alberta. Accessed August 22, 2019. https://era.library.ualberta.ca/files/1g05ff203.

MLA Handbook (7th Edition):

Strueby, Lannae L. “Paracrine Effect of Mesenchymal Stromal Cells on Multifactorial Lung Injury in Neonatal Mice.” 2014. Web. 22 Aug 2019.

Vancouver:

Strueby LL. Paracrine Effect of Mesenchymal Stromal Cells on Multifactorial Lung Injury in Neonatal Mice. [Internet] [Masters thesis]. University of Alberta; 2014. [cited 2019 Aug 22]. Available from: https://era.library.ualberta.ca/files/1g05ff203.

Council of Science Editors:

Strueby LL. Paracrine Effect of Mesenchymal Stromal Cells on Multifactorial Lung Injury in Neonatal Mice. [Masters Thesis]. University of Alberta; 2014. Available from: https://era.library.ualberta.ca/files/1g05ff203


University of Oulu

18. Mäkelä, T. (Tuomas). Systemic transplantation of bone marrow stromal cells:an experimental animal study of biodistribution and tissue targeting.

Degree: 2014, University of Oulu

Abstract Bone marrow mesenchymal stromal cells (MSCs) and mononuclear cells (BM-MNCs) have shown great therapeutic potential in various clinical settings. Although intravascular transplantation of the… (more)

Subjects/Keywords: biodistribution; imaging; lung entrapment; stem cells; kantasolut; keuhkoläpäisevyys; kudosjakautuminen; kuvantaminen

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APA (6th Edition):

Mäkelä, T. (. (2014). Systemic transplantation of bone marrow stromal cells:an experimental animal study of biodistribution and tissue targeting. (Doctoral Dissertation). University of Oulu. Retrieved from http://urn.fi/urn:isbn:9789526206547

Chicago Manual of Style (16th Edition):

Mäkelä, T (Tuomas). “Systemic transplantation of bone marrow stromal cells:an experimental animal study of biodistribution and tissue targeting.” 2014. Doctoral Dissertation, University of Oulu. Accessed August 22, 2019. http://urn.fi/urn:isbn:9789526206547.

MLA Handbook (7th Edition):

Mäkelä, T (Tuomas). “Systemic transplantation of bone marrow stromal cells:an experimental animal study of biodistribution and tissue targeting.” 2014. Web. 22 Aug 2019.

Vancouver:

Mäkelä T(. Systemic transplantation of bone marrow stromal cells:an experimental animal study of biodistribution and tissue targeting. [Internet] [Doctoral dissertation]. University of Oulu; 2014. [cited 2019 Aug 22]. Available from: http://urn.fi/urn:isbn:9789526206547.

Council of Science Editors:

Mäkelä T(. Systemic transplantation of bone marrow stromal cells:an experimental animal study of biodistribution and tissue targeting. [Doctoral Dissertation]. University of Oulu; 2014. Available from: http://urn.fi/urn:isbn:9789526206547


University of Illinois – Chicago

19. Yazbeck, Pascal. Focal Adhesion Kinase, Maintenance of Sphingosine 1 Phosphate Receptor 1 Expression and Barrier Function.

Degree: 2017, University of Illinois – Chicago

 Formation of leaky blood vessels remains a persistent pathology in several diseases including acute lung injury. Sphingosine-1-phosphate (S1P) is a lipid mediator well known for… (more)

Subjects/Keywords: Endothelial cells; Epigenetics; S1PR1; KLF2; lung vascular permeability

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APA (6th Edition):

Yazbeck, P. (2017). Focal Adhesion Kinase, Maintenance of Sphingosine 1 Phosphate Receptor 1 Expression and Barrier Function. (Thesis). University of Illinois – Chicago. Retrieved from http://hdl.handle.net/10027/21883

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):

Yazbeck, Pascal. “Focal Adhesion Kinase, Maintenance of Sphingosine 1 Phosphate Receptor 1 Expression and Barrier Function.” 2017. Thesis, University of Illinois – Chicago. Accessed August 22, 2019. http://hdl.handle.net/10027/21883.

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

MLA Handbook (7th Edition):

Yazbeck, Pascal. “Focal Adhesion Kinase, Maintenance of Sphingosine 1 Phosphate Receptor 1 Expression and Barrier Function.” 2017. Web. 22 Aug 2019.

Vancouver:

Yazbeck P. Focal Adhesion Kinase, Maintenance of Sphingosine 1 Phosphate Receptor 1 Expression and Barrier Function. [Internet] [Thesis]. University of Illinois – Chicago; 2017. [cited 2019 Aug 22]. Available from: http://hdl.handle.net/10027/21883.

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

Council of Science Editors:

Yazbeck P. Focal Adhesion Kinase, Maintenance of Sphingosine 1 Phosphate Receptor 1 Expression and Barrier Function. [Thesis]. University of Illinois – Chicago; 2017. Available from: http://hdl.handle.net/10027/21883

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


University of Cincinnati

20. Akunuru, Shailaja. Regulation of cancer stem cell activity and epithelial mesenchymal transition by Rac1 in Human lung adenocarcinoma cells.

Degree: PhD, Medicine: Molecular and Developmental Biology, 2011, University of Cincinnati

 The cancer stem cell (CSC) theory predicts that a small fraction of cancer cells possesses unique self-renewal, expansion and differentiation activities in tumorigenesis. While this… (more)

Subjects/Keywords: Cellular Biology; Cancer stem cells; EMT; Rac1; Metastasis; Lung cancer; NSCLA

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APA (6th Edition):

Akunuru, S. (2011). Regulation of cancer stem cell activity and epithelial mesenchymal transition by Rac1 in Human lung adenocarcinoma cells. (Doctoral Dissertation). University of Cincinnati. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=ucin1314301864

Chicago Manual of Style (16th Edition):

Akunuru, Shailaja. “Regulation of cancer stem cell activity and epithelial mesenchymal transition by Rac1 in Human lung adenocarcinoma cells.” 2011. Doctoral Dissertation, University of Cincinnati. Accessed August 22, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1314301864.

MLA Handbook (7th Edition):

Akunuru, Shailaja. “Regulation of cancer stem cell activity and epithelial mesenchymal transition by Rac1 in Human lung adenocarcinoma cells.” 2011. Web. 22 Aug 2019.

Vancouver:

Akunuru S. Regulation of cancer stem cell activity and epithelial mesenchymal transition by Rac1 in Human lung adenocarcinoma cells. [Internet] [Doctoral dissertation]. University of Cincinnati; 2011. [cited 2019 Aug 22]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ucin1314301864.

Council of Science Editors:

Akunuru S. Regulation of cancer stem cell activity and epithelial mesenchymal transition by Rac1 in Human lung adenocarcinoma cells. [Doctoral Dissertation]. University of Cincinnati; 2011. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ucin1314301864


University of Western Australia

21. McCoy, Melanie Jane. The effect of chemotherapy on the anti-tumour immune response in patients with thoracic malignancies.

Degree: PhD, 2011, University of Western Australia

[Truncated abstract] Chemotherapy and immunotherapy have historically been considered antagonistic treatment options due to the variable lymphopaenia experienced as a side effect of most cytotoxic… (more)

Subjects/Keywords: Mesothelioma; Lung cancer; Chemotherapy; T Cells; Flow cytometry; Anti-tumour immunity

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APA (6th Edition):

McCoy, M. J. (2011). The effect of chemotherapy on the anti-tumour immune response in patients with thoracic malignancies. (Doctoral Dissertation). University of Western Australia. Retrieved from http://repository.uwa.edu.au:80/R/?func=dbin-jump-full&object_id=30870&local_base=GEN01-INS01

Chicago Manual of Style (16th Edition):

McCoy, Melanie Jane. “The effect of chemotherapy on the anti-tumour immune response in patients with thoracic malignancies.” 2011. Doctoral Dissertation, University of Western Australia. Accessed August 22, 2019. http://repository.uwa.edu.au:80/R/?func=dbin-jump-full&object_id=30870&local_base=GEN01-INS01.

MLA Handbook (7th Edition):

McCoy, Melanie Jane. “The effect of chemotherapy on the anti-tumour immune response in patients with thoracic malignancies.” 2011. Web. 22 Aug 2019.

Vancouver:

McCoy MJ. The effect of chemotherapy on the anti-tumour immune response in patients with thoracic malignancies. [Internet] [Doctoral dissertation]. University of Western Australia; 2011. [cited 2019 Aug 22]. Available from: http://repository.uwa.edu.au:80/R/?func=dbin-jump-full&object_id=30870&local_base=GEN01-INS01.

Council of Science Editors:

McCoy MJ. The effect of chemotherapy on the anti-tumour immune response in patients with thoracic malignancies. [Doctoral Dissertation]. University of Western Australia; 2011. Available from: http://repository.uwa.edu.au:80/R/?func=dbin-jump-full&object_id=30870&local_base=GEN01-INS01


University of Sydney

22. McKnight, Lauren Anne. The role of natural regulatory T cells in the regulation of asthma .

Degree: 2014, University of Sydney

 Allergic asthma is a chronic inflammatory disease of the airways characterised by Th2 sensitisation and inflammation, which represents a failure of tolerance to environmental antigens.… (more)

Subjects/Keywords: Asthma; Flow Cytometry; Lung; Mice; Transgenic; T-Lymphocytes; Regulatory; Th2 Cells

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APA (6th Edition):

McKnight, L. A. (2014). The role of natural regulatory T cells in the regulation of asthma . (Thesis). University of Sydney. Retrieved from http://hdl.handle.net/2123/13593

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):

McKnight, Lauren Anne. “The role of natural regulatory T cells in the regulation of asthma .” 2014. Thesis, University of Sydney. Accessed August 22, 2019. http://hdl.handle.net/2123/13593.

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

MLA Handbook (7th Edition):

McKnight, Lauren Anne. “The role of natural regulatory T cells in the regulation of asthma .” 2014. Web. 22 Aug 2019.

Vancouver:

McKnight LA. The role of natural regulatory T cells in the regulation of asthma . [Internet] [Thesis]. University of Sydney; 2014. [cited 2019 Aug 22]. Available from: http://hdl.handle.net/2123/13593.

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

Council of Science Editors:

McKnight LA. The role of natural regulatory T cells in the regulation of asthma . [Thesis]. University of Sydney; 2014. Available from: http://hdl.handle.net/2123/13593

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


Harvard University

23. Lau, Allison Nicole. Characterization of lung tumor-propagating cells reveals a role for CD24 and Yap/Taz in lung cancer progression and metastasis.

Degree: PhD, Biology: Medical Sciences, Division of, 2014, Harvard University

Lung cancer is the leading cause of cancer deaths worldwide. A large part of this high mortality rate is due to the onset of metastatic… (more)

Subjects/Keywords: Genetics; CD24; lung cancer; metastasis; Taz; tumor propagating cells; Yap

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APA (6th Edition):

Lau, A. N. (2014). Characterization of lung tumor-propagating cells reveals a role for CD24 and Yap/Taz in lung cancer progression and metastasis. (Doctoral Dissertation). Harvard University. Retrieved from http://nrs.harvard.edu/urn-3:HUL.InstRepos:12269822

Chicago Manual of Style (16th Edition):

Lau, Allison Nicole. “Characterization of lung tumor-propagating cells reveals a role for CD24 and Yap/Taz in lung cancer progression and metastasis.” 2014. Doctoral Dissertation, Harvard University. Accessed August 22, 2019. http://nrs.harvard.edu/urn-3:HUL.InstRepos:12269822.

MLA Handbook (7th Edition):

Lau, Allison Nicole. “Characterization of lung tumor-propagating cells reveals a role for CD24 and Yap/Taz in lung cancer progression and metastasis.” 2014. Web. 22 Aug 2019.

Vancouver:

Lau AN. Characterization of lung tumor-propagating cells reveals a role for CD24 and Yap/Taz in lung cancer progression and metastasis. [Internet] [Doctoral dissertation]. Harvard University; 2014. [cited 2019 Aug 22]. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:12269822.

Council of Science Editors:

Lau AN. Characterization of lung tumor-propagating cells reveals a role for CD24 and Yap/Taz in lung cancer progression and metastasis. [Doctoral Dissertation]. Harvard University; 2014. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:12269822


University of Washington

24. McKinney, Bonnie Lewis. Cell-specific transcriptional analysis in complex tissues.

Degree: 2017, University of Washington

 Cell-type specific transcriptional analysis can yield important information about the role of a certain cell type in the context of its tissue microenvironment. Previous methods… (more)

Subjects/Keywords: Lung stromal cells; Ribotag; Translating ribosome affinity purification; Pathology; Medicine; pathology

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APA (6th Edition):

McKinney, B. L. (2017). Cell-specific transcriptional analysis in complex tissues. (Thesis). University of Washington. Retrieved from http://hdl.handle.net/1773/38194

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):

McKinney, Bonnie Lewis. “Cell-specific transcriptional analysis in complex tissues.” 2017. Thesis, University of Washington. Accessed August 22, 2019. http://hdl.handle.net/1773/38194.

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

MLA Handbook (7th Edition):

McKinney, Bonnie Lewis. “Cell-specific transcriptional analysis in complex tissues.” 2017. Web. 22 Aug 2019.

Vancouver:

McKinney BL. Cell-specific transcriptional analysis in complex tissues. [Internet] [Thesis]. University of Washington; 2017. [cited 2019 Aug 22]. Available from: http://hdl.handle.net/1773/38194.

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

Council of Science Editors:

McKinney BL. Cell-specific transcriptional analysis in complex tissues. [Thesis]. University of Washington; 2017. Available from: http://hdl.handle.net/1773/38194

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


McGill University

25. Dubois, Anthony E. J. The Isolation and Characterization of an Organ-Specific Neoantigen from a Human Lung Cancer Cell Line Grown in Tissue Culture.

Degree: PhD, Department of Surgery, 1986, McGill University

Antitumor immunity in cancer patients as measured by the in vitro assay of leukocyte adherence inhibition (LAI) is directed to a tumor cell surface component… (more)

Subjects/Keywords: Neoantigen; Human lung cancer cells

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APA (6th Edition):

Dubois, A. E. J. (1986). The Isolation and Characterization of an Organ-Specific Neoantigen from a Human Lung Cancer Cell Line Grown in Tissue Culture. (Doctoral Dissertation). McGill University. Retrieved from http://digitool.library.mcgill.ca/thesisfile154185.pdf

Chicago Manual of Style (16th Edition):

Dubois, Anthony E J. “The Isolation and Characterization of an Organ-Specific Neoantigen from a Human Lung Cancer Cell Line Grown in Tissue Culture.” 1986. Doctoral Dissertation, McGill University. Accessed August 22, 2019. http://digitool.library.mcgill.ca/thesisfile154185.pdf.

MLA Handbook (7th Edition):

Dubois, Anthony E J. “The Isolation and Characterization of an Organ-Specific Neoantigen from a Human Lung Cancer Cell Line Grown in Tissue Culture.” 1986. Web. 22 Aug 2019.

Vancouver:

Dubois AEJ. The Isolation and Characterization of an Organ-Specific Neoantigen from a Human Lung Cancer Cell Line Grown in Tissue Culture. [Internet] [Doctoral dissertation]. McGill University; 1986. [cited 2019 Aug 22]. Available from: http://digitool.library.mcgill.ca/thesisfile154185.pdf.

Council of Science Editors:

Dubois AEJ. The Isolation and Characterization of an Organ-Specific Neoantigen from a Human Lung Cancer Cell Line Grown in Tissue Culture. [Doctoral Dissertation]. McGill University; 1986. Available from: http://digitool.library.mcgill.ca/thesisfile154185.pdf


Utah State University

26. Watterson, Todd L. Effects of Cache Valley Particulate Matter on Human Lung Cells.

Degree: PhD, Animal, Dairy, and Veterinary Sciences, 2012, Utah State University

  During wintertime temperature inversion episodes the concentrations of particulate air pollution, also defined as particulate matter (PM), in Utah’s Cache Valley have often been… (more)

Subjects/Keywords: Cache Valley; particulate matter; lung cells; inversion; pollution; Animal Sciences

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APA (6th Edition):

Watterson, T. L. (2012). Effects of Cache Valley Particulate Matter on Human Lung Cells. (Doctoral Dissertation). Utah State University. Retrieved from https://digitalcommons.usu.edu/etd/1341

Chicago Manual of Style (16th Edition):

Watterson, Todd L. “Effects of Cache Valley Particulate Matter on Human Lung Cells.” 2012. Doctoral Dissertation, Utah State University. Accessed August 22, 2019. https://digitalcommons.usu.edu/etd/1341.

MLA Handbook (7th Edition):

Watterson, Todd L. “Effects of Cache Valley Particulate Matter on Human Lung Cells.” 2012. Web. 22 Aug 2019.

Vancouver:

Watterson TL. Effects of Cache Valley Particulate Matter on Human Lung Cells. [Internet] [Doctoral dissertation]. Utah State University; 2012. [cited 2019 Aug 22]. Available from: https://digitalcommons.usu.edu/etd/1341.

Council of Science Editors:

Watterson TL. Effects of Cache Valley Particulate Matter on Human Lung Cells. [Doctoral Dissertation]. Utah State University; 2012. Available from: https://digitalcommons.usu.edu/etd/1341


University of Rochester

27. Bello-Irizarry, Sheila Ninoshka. MyD88-Dependent Signaling Pathways Contribute to both Host Defense and Immunopathogenesis during Pneumocystis Infection.

Degree: PhD, 2013, University of Rochester

 Pneumocystis Pneumonia (PcP) is a common respiratory infection of HIV patients and other immunocompromised individuals. A functional immune system is critical for host defense against… (more)

Subjects/Keywords: Pneumocystis; Inflammation; Lung Injury; Opportunistic Pathogen; Alveolar Epithelial Cells; MyD88

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APA (6th Edition):

Bello-Irizarry, S. N. (2013). MyD88-Dependent Signaling Pathways Contribute to both Host Defense and Immunopathogenesis during Pneumocystis Infection. (Doctoral Dissertation). University of Rochester. Retrieved from http://hdl.handle.net/1802/27245

Chicago Manual of Style (16th Edition):

Bello-Irizarry, Sheila Ninoshka. “MyD88-Dependent Signaling Pathways Contribute to both Host Defense and Immunopathogenesis during Pneumocystis Infection.” 2013. Doctoral Dissertation, University of Rochester. Accessed August 22, 2019. http://hdl.handle.net/1802/27245.

MLA Handbook (7th Edition):

Bello-Irizarry, Sheila Ninoshka. “MyD88-Dependent Signaling Pathways Contribute to both Host Defense and Immunopathogenesis during Pneumocystis Infection.” 2013. Web. 22 Aug 2019.

Vancouver:

Bello-Irizarry SN. MyD88-Dependent Signaling Pathways Contribute to both Host Defense and Immunopathogenesis during Pneumocystis Infection. [Internet] [Doctoral dissertation]. University of Rochester; 2013. [cited 2019 Aug 22]. Available from: http://hdl.handle.net/1802/27245.

Council of Science Editors:

Bello-Irizarry SN. MyD88-Dependent Signaling Pathways Contribute to both Host Defense and Immunopathogenesis during Pneumocystis Infection. [Doctoral Dissertation]. University of Rochester; 2013. Available from: http://hdl.handle.net/1802/27245


University of Texas Southwestern Medical Center

28. Guo, Wei. Roles of MicroRNAs in Fetal Lung Development.

Degree: 2016, University of Texas Southwestern Medical Center

Lung alveolar type II cells uniquely synthesize surfactant, a developmentally-regulated lipoprotein that is essential for breathing. Expression of the major surfactant protein, SP-A, in midgestation… (more)

Subjects/Keywords: Alveolar Epithelial Cells; Lung; MicroRNAs; Nuclear Proteins; Transcription Factors

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APA (6th Edition):

Guo, W. (2016). Roles of MicroRNAs in Fetal Lung Development. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/5729

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):

Guo, Wei. “Roles of MicroRNAs in Fetal Lung Development.” 2016. Thesis, University of Texas Southwestern Medical Center. Accessed August 22, 2019. http://hdl.handle.net/2152.5/5729.

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

MLA Handbook (7th Edition):

Guo, Wei. “Roles of MicroRNAs in Fetal Lung Development.” 2016. Web. 22 Aug 2019.

Vancouver:

Guo W. Roles of MicroRNAs in Fetal Lung Development. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2016. [cited 2019 Aug 22]. Available from: http://hdl.handle.net/2152.5/5729.

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

Council of Science Editors:

Guo W. Roles of MicroRNAs in Fetal Lung Development. [Thesis]. University of Texas Southwestern Medical Center; 2016. Available from: http://hdl.handle.net/2152.5/5729

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


University of Texas Southwestern Medical Center

29. El-Ashmawy, Mariam A. Protecting Healthy Cells Against the Negative Effects of Radiation Therapy for Lung Cancer.

Degree: 2017, University of Texas Southwestern Medical Center

 Although radiation therapy is a commonly used treatment for many human diseases including cancer, ionizing radiation produces reactive oxygen species that can damage both cancer… (more)

Subjects/Keywords: Antioxidants; Epithelial Cells; Lung; Oleanolic Acid; Radiation-Protective Agents

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

APA (6th Edition):

El-Ashmawy, M. A. (2017). Protecting Healthy Cells Against the Negative Effects of Radiation Therapy for Lung Cancer. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/4145

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):

El-Ashmawy, Mariam A. “Protecting Healthy Cells Against the Negative Effects of Radiation Therapy for Lung Cancer.” 2017. Thesis, University of Texas Southwestern Medical Center. Accessed August 22, 2019. http://hdl.handle.net/2152.5/4145.

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

MLA Handbook (7th Edition):

El-Ashmawy, Mariam A. “Protecting Healthy Cells Against the Negative Effects of Radiation Therapy for Lung Cancer.” 2017. Web. 22 Aug 2019.

Vancouver:

El-Ashmawy MA. Protecting Healthy Cells Against the Negative Effects of Radiation Therapy for Lung Cancer. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2017. [cited 2019 Aug 22]. Available from: http://hdl.handle.net/2152.5/4145.

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

Council of Science Editors:

El-Ashmawy MA. Protecting Healthy Cells Against the Negative Effects of Radiation Therapy for Lung Cancer. [Thesis]. University of Texas Southwestern Medical Center; 2017. Available from: http://hdl.handle.net/2152.5/4145

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


University of Texas Southwestern Medical Center

30. LaRanger, Ryan. Differentiation of Normal and Cystic Fibrosis Human Lung Epithelial Cells in a Decellularized and Reconstituted Mouse Lung.

Degree: 2017, University of Texas Southwestern Medical Center

 Engineered lung tissue may eventually address the chronic shortage of transplantable lung tissue and permit modeling of lung disease in a controlled ex vivo environment.… (more)

Subjects/Keywords: Cell Culture Techniques; Epithelial Cells; Lung; rho-Associated Kinases; Tissue Engineering

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

APA (6th Edition):

LaRanger, R. (2017). Differentiation of Normal and Cystic Fibrosis Human Lung Epithelial Cells in a Decellularized and Reconstituted Mouse Lung. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/6619

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):

LaRanger, Ryan. “Differentiation of Normal and Cystic Fibrosis Human Lung Epithelial Cells in a Decellularized and Reconstituted Mouse Lung.” 2017. Thesis, University of Texas Southwestern Medical Center. Accessed August 22, 2019. http://hdl.handle.net/2152.5/6619.

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

MLA Handbook (7th Edition):

LaRanger, Ryan. “Differentiation of Normal and Cystic Fibrosis Human Lung Epithelial Cells in a Decellularized and Reconstituted Mouse Lung.” 2017. Web. 22 Aug 2019.

Vancouver:

LaRanger R. Differentiation of Normal and Cystic Fibrosis Human Lung Epithelial Cells in a Decellularized and Reconstituted Mouse Lung. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2017. [cited 2019 Aug 22]. Available from: http://hdl.handle.net/2152.5/6619.

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

Council of Science Editors:

LaRanger R. Differentiation of Normal and Cystic Fibrosis Human Lung Epithelial Cells in a Decellularized and Reconstituted Mouse Lung. [Thesis]. University of Texas Southwestern Medical Center; 2017. Available from: http://hdl.handle.net/2152.5/6619

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

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