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You searched for subject:( experimental cell). Showing records 1 – 30 of 92 total matches.

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Univerzitet u Beogradu

1. Savić, Danijela, 1976-. Uticaj purinskih nukleozidnih analoga, ribavirina i tiazofurina, na aktivaciju mikroglije u uslovima inflamacije.

Degree: Biološki fakultet, 2013, Univerzitet u Beogradu

Biologija - neurobiologija / Biology - Neurobiology

Aktivacija mikroglije jedno je od glavnih obeležja eksperimentalnog autoimunskog encefalomijelitisa (EAE) i drugih neuroloških poremećaja koje odlikuje hronična… (more)

Subjects/Keywords: Central nervous system; inflammation; microglia; experimental autoimmune encephalomyelitis; cell culture

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APA (6th Edition):

Savić, Danijela, 1. (2013). Uticaj purinskih nukleozidnih analoga, ribavirina i tiazofurina, na aktivaciju mikroglije u uslovima inflamacije. (Thesis). Univerzitet u Beogradu. Retrieved from https://fedorabg.bg.ac.rs/fedora/get/o:2285/bdef:Content/get

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):

Savić, Danijela, 1976-. “Uticaj purinskih nukleozidnih analoga, ribavirina i tiazofurina, na aktivaciju mikroglije u uslovima inflamacije.” 2013. Thesis, Univerzitet u Beogradu. Accessed March 28, 2020. https://fedorabg.bg.ac.rs/fedora/get/o:2285/bdef:Content/get.

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

MLA Handbook (7th Edition):

Savić, Danijela, 1976-. “Uticaj purinskih nukleozidnih analoga, ribavirina i tiazofurina, na aktivaciju mikroglije u uslovima inflamacije.” 2013. Web. 28 Mar 2020.

Vancouver:

Savić, Danijela 1. Uticaj purinskih nukleozidnih analoga, ribavirina i tiazofurina, na aktivaciju mikroglije u uslovima inflamacije. [Internet] [Thesis]. Univerzitet u Beogradu; 2013. [cited 2020 Mar 28]. Available from: https://fedorabg.bg.ac.rs/fedora/get/o:2285/bdef:Content/get.

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

Council of Science Editors:

Savić, Danijela 1. Uticaj purinskih nukleozidnih analoga, ribavirina i tiazofurina, na aktivaciju mikroglije u uslovima inflamacije. [Thesis]. Univerzitet u Beogradu; 2013. Available from: https://fedorabg.bg.ac.rs/fedora/get/o:2285/bdef:Content/get

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


Purdue University

2. McGee, Reginald. MODELING, ANALYSIS, AND CONTROL OF SYK-MEDIATED SIGNALING EVENTS FOR B CELLS AND ASSOCIATED CELLULAR RESPONSE FOR B CELLS.

Degree: PhD, Mathematics, 2015, Purdue University

 Understanding the immune system and its responses to foreign threats (antigens) is a matter of understanding the immune cells involved, their individual responses, and chemicals… (more)

Subjects/Keywords: B cell signaling; Computational Modeling; Convergence Result; Experimental Design; Mutant; Syk

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APA (6th Edition):

McGee, R. (2015). MODELING, ANALYSIS, AND CONTROL OF SYK-MEDIATED SIGNALING EVENTS FOR B CELLS AND ASSOCIATED CELLULAR RESPONSE FOR B CELLS. (Doctoral Dissertation). Purdue University. Retrieved from https://docs.lib.purdue.edu/open_access_dissertations/1312

Chicago Manual of Style (16th Edition):

McGee, Reginald. “MODELING, ANALYSIS, AND CONTROL OF SYK-MEDIATED SIGNALING EVENTS FOR B CELLS AND ASSOCIATED CELLULAR RESPONSE FOR B CELLS.” 2015. Doctoral Dissertation, Purdue University. Accessed March 28, 2020. https://docs.lib.purdue.edu/open_access_dissertations/1312.

MLA Handbook (7th Edition):

McGee, Reginald. “MODELING, ANALYSIS, AND CONTROL OF SYK-MEDIATED SIGNALING EVENTS FOR B CELLS AND ASSOCIATED CELLULAR RESPONSE FOR B CELLS.” 2015. Web. 28 Mar 2020.

Vancouver:

McGee R. MODELING, ANALYSIS, AND CONTROL OF SYK-MEDIATED SIGNALING EVENTS FOR B CELLS AND ASSOCIATED CELLULAR RESPONSE FOR B CELLS. [Internet] [Doctoral dissertation]. Purdue University; 2015. [cited 2020 Mar 28]. Available from: https://docs.lib.purdue.edu/open_access_dissertations/1312.

Council of Science Editors:

McGee R. MODELING, ANALYSIS, AND CONTROL OF SYK-MEDIATED SIGNALING EVENTS FOR B CELLS AND ASSOCIATED CELLULAR RESPONSE FOR B CELLS. [Doctoral Dissertation]. Purdue University; 2015. Available from: https://docs.lib.purdue.edu/open_access_dissertations/1312


Princeton University

3. Dumitrascu, Bianca. Expanding the computational biologist’s toolkit: Experimental design and multi-modality in genomics .

Degree: PhD, 2019, Princeton University

 The traditional biological research pipeline consists of three steps: hypothesis generation, data collection, and data analysis. Data analysis is sometimes followed by a readjustment in… (more)

Subjects/Keywords: experimental design; genomics; single cell sequencing; transfer learning

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APA (6th Edition):

Dumitrascu, B. (2019). Expanding the computational biologist’s toolkit: Experimental design and multi-modality in genomics . (Doctoral Dissertation). Princeton University. Retrieved from http://arks.princeton.edu/ark:/88435/dsp01rn301425t

Chicago Manual of Style (16th Edition):

Dumitrascu, Bianca. “Expanding the computational biologist’s toolkit: Experimental design and multi-modality in genomics .” 2019. Doctoral Dissertation, Princeton University. Accessed March 28, 2020. http://arks.princeton.edu/ark:/88435/dsp01rn301425t.

MLA Handbook (7th Edition):

Dumitrascu, Bianca. “Expanding the computational biologist’s toolkit: Experimental design and multi-modality in genomics .” 2019. Web. 28 Mar 2020.

Vancouver:

Dumitrascu B. Expanding the computational biologist’s toolkit: Experimental design and multi-modality in genomics . [Internet] [Doctoral dissertation]. Princeton University; 2019. [cited 2020 Mar 28]. Available from: http://arks.princeton.edu/ark:/88435/dsp01rn301425t.

Council of Science Editors:

Dumitrascu B. Expanding the computational biologist’s toolkit: Experimental design and multi-modality in genomics . [Doctoral Dissertation]. Princeton University; 2019. Available from: http://arks.princeton.edu/ark:/88435/dsp01rn301425t


University of Texas Southwestern Medical Center

4. Moss, Lacy Reynolds. Elucidating the Anti-Cancer Mechanism of Low Density Lipoprotein-Mediated Delivery of Docosahexaenoic Acid to Hepatocellular Carcinoma Cells.

Degree: 2015, University of Texas Southwestern Medical Center

 Hepatocellular carcinoma is a lethal malignancy with few effective therapy options. New selective treatments are urgently needed to destroy hepatocellular carcinoma cells without harming the… (more)

Subjects/Keywords: Cell Death; Docosahexaenoic Acids; Lipoproteins, LDL; Liver Neoplasms, Experimental

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APA (6th Edition):

Moss, L. R. (2015). Elucidating the Anti-Cancer Mechanism of Low Density Lipoprotein-Mediated Delivery of Docosahexaenoic Acid to Hepatocellular Carcinoma Cells. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/4215

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):

Moss, Lacy Reynolds. “Elucidating the Anti-Cancer Mechanism of Low Density Lipoprotein-Mediated Delivery of Docosahexaenoic Acid to Hepatocellular Carcinoma Cells.” 2015. Thesis, University of Texas Southwestern Medical Center. Accessed March 28, 2020. http://hdl.handle.net/2152.5/4215.

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

MLA Handbook (7th Edition):

Moss, Lacy Reynolds. “Elucidating the Anti-Cancer Mechanism of Low Density Lipoprotein-Mediated Delivery of Docosahexaenoic Acid to Hepatocellular Carcinoma Cells.” 2015. Web. 28 Mar 2020.

Vancouver:

Moss LR. Elucidating the Anti-Cancer Mechanism of Low Density Lipoprotein-Mediated Delivery of Docosahexaenoic Acid to Hepatocellular Carcinoma Cells. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2015. [cited 2020 Mar 28]. Available from: http://hdl.handle.net/2152.5/4215.

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

Council of Science Editors:

Moss LR. Elucidating the Anti-Cancer Mechanism of Low Density Lipoprotein-Mediated Delivery of Docosahexaenoic Acid to Hepatocellular Carcinoma Cells. [Thesis]. University of Texas Southwestern Medical Center; 2015. Available from: http://hdl.handle.net/2152.5/4215

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


University of Minnesota

5. Chang, Yao-chung. Comparing the effects of sexual and asexual reproduction during long term adaptation of Baker's yeast Saccharomyces cerevisiae.

Degree: PhD, Ecology, Evolution and Behavior, 2013, University of Minnesota

 If the ancestors of extant organisms were well adapted to a particular environment and that environment reoccurs, the ability to recapture prior adaptations could increase… (more)

Subjects/Keywords: Cell size; Experimental evolution; Historical contingency; Multicellularity; Reversible evolution; Sexual reproduction

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APA (6th Edition):

Chang, Y. (2013). Comparing the effects of sexual and asexual reproduction during long term adaptation of Baker's yeast Saccharomyces cerevisiae. (Doctoral Dissertation). University of Minnesota. Retrieved from http://hdl.handle.net/11299/177060

Chicago Manual of Style (16th Edition):

Chang, Yao-chung. “Comparing the effects of sexual and asexual reproduction during long term adaptation of Baker's yeast Saccharomyces cerevisiae.” 2013. Doctoral Dissertation, University of Minnesota. Accessed March 28, 2020. http://hdl.handle.net/11299/177060.

MLA Handbook (7th Edition):

Chang, Yao-chung. “Comparing the effects of sexual and asexual reproduction during long term adaptation of Baker's yeast Saccharomyces cerevisiae.” 2013. Web. 28 Mar 2020.

Vancouver:

Chang Y. Comparing the effects of sexual and asexual reproduction during long term adaptation of Baker's yeast Saccharomyces cerevisiae. [Internet] [Doctoral dissertation]. University of Minnesota; 2013. [cited 2020 Mar 28]. Available from: http://hdl.handle.net/11299/177060.

Council of Science Editors:

Chang Y. Comparing the effects of sexual and asexual reproduction during long term adaptation of Baker's yeast Saccharomyces cerevisiae. [Doctoral Dissertation]. University of Minnesota; 2013. Available from: http://hdl.handle.net/11299/177060

6. Silva, Julio Cesar Rosa e. Avaliação de marcadores de proliferação celular e apoptose em tecido endometrial eutópico e ectópico em modelo experimental de endometriose em coelhas.

Degree: PhD, Ginecologia e Obstetrícia, 2007, University of São Paulo

Objetivo:Caracterizar o padrão de homeostase (proliferação celular e apoptose) de tecido endometrial eutópico e ectópico de coelhas submetidas à indução de lesões de endometriose por… (more)

Subjects/Keywords: apoptose; apoptosis; cell proliferation; coelha; endometriose experimental; Experimental endometriosis; homeostase tecidual; proliferação celular; rabbit; tissue homeostasis

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APA (6th Edition):

Silva, J. C. R. e. (2007). Avaliação de marcadores de proliferação celular e apoptose em tecido endometrial eutópico e ectópico em modelo experimental de endometriose em coelhas. (Doctoral Dissertation). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/17/17145/tde-26092013-162027/ ;

Chicago Manual of Style (16th Edition):

Silva, Julio Cesar Rosa e. “Avaliação de marcadores de proliferação celular e apoptose em tecido endometrial eutópico e ectópico em modelo experimental de endometriose em coelhas.” 2007. Doctoral Dissertation, University of São Paulo. Accessed March 28, 2020. http://www.teses.usp.br/teses/disponiveis/17/17145/tde-26092013-162027/ ;.

MLA Handbook (7th Edition):

Silva, Julio Cesar Rosa e. “Avaliação de marcadores de proliferação celular e apoptose em tecido endometrial eutópico e ectópico em modelo experimental de endometriose em coelhas.” 2007. Web. 28 Mar 2020.

Vancouver:

Silva JCRe. Avaliação de marcadores de proliferação celular e apoptose em tecido endometrial eutópico e ectópico em modelo experimental de endometriose em coelhas. [Internet] [Doctoral dissertation]. University of São Paulo; 2007. [cited 2020 Mar 28]. Available from: http://www.teses.usp.br/teses/disponiveis/17/17145/tde-26092013-162027/ ;.

Council of Science Editors:

Silva JCRe. Avaliação de marcadores de proliferação celular e apoptose em tecido endometrial eutópico e ectópico em modelo experimental de endometriose em coelhas. [Doctoral Dissertation]. University of São Paulo; 2007. Available from: http://www.teses.usp.br/teses/disponiveis/17/17145/tde-26092013-162027/ ;


University of Alberta

7. Amiri, Mohammad Saeid. Computer simulation and experimental characterization of a tubular micro- solid oxide fuel cell.

Degree: PhD, Department of Chemical and Materials Engineering, 2010, University of Alberta

 This work is focused on a state-of-the-art tubular micro-solid oxide fuel cell (TμSOFC), ~3 millimeters in diameter and ~300 microns thick, with Ni/YSZ and LSM/YSZ… (more)

Subjects/Keywords: Tubular micro- Solid Oxide Fuel Cell; Experimental validation; Computational fluid dynamics; Modeling

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APA (6th Edition):

Amiri, M. S. (2010). Computer simulation and experimental characterization of a tubular micro- solid oxide fuel cell. (Doctoral Dissertation). University of Alberta. Retrieved from https://era.library.ualberta.ca/files/z029p528k

Chicago Manual of Style (16th Edition):

Amiri, Mohammad Saeid. “Computer simulation and experimental characterization of a tubular micro- solid oxide fuel cell.” 2010. Doctoral Dissertation, University of Alberta. Accessed March 28, 2020. https://era.library.ualberta.ca/files/z029p528k.

MLA Handbook (7th Edition):

Amiri, Mohammad Saeid. “Computer simulation and experimental characterization of a tubular micro- solid oxide fuel cell.” 2010. Web. 28 Mar 2020.

Vancouver:

Amiri MS. Computer simulation and experimental characterization of a tubular micro- solid oxide fuel cell. [Internet] [Doctoral dissertation]. University of Alberta; 2010. [cited 2020 Mar 28]. Available from: https://era.library.ualberta.ca/files/z029p528k.

Council of Science Editors:

Amiri MS. Computer simulation and experimental characterization of a tubular micro- solid oxide fuel cell. [Doctoral Dissertation]. University of Alberta; 2010. Available from: https://era.library.ualberta.ca/files/z029p528k


University of Alberta

8. Miller, Samantha M. Analysis of an Open-Cathode Fuel Cell Stack in an Enclosure for Varying Operating Conditions.

Degree: MS, Department of Mechanical Engineering, 2013, University of Alberta

 Open-cathode polymer electrolyte fuel cell (PEFC) stacks use hydrogen as a fuel, are a high efficiency power source, and do not produce CO2, NOx, SOx,… (more)

Subjects/Keywords: system-level modelling; mathematical modelling; fuel cell stack; transient dynamics; open-cathode; enclosure; experimental validation

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APA (6th Edition):

Miller, S. M. (2013). Analysis of an Open-Cathode Fuel Cell Stack in an Enclosure for Varying Operating Conditions. (Masters Thesis). University of Alberta. Retrieved from https://era.library.ualberta.ca/files/m039k550b

Chicago Manual of Style (16th Edition):

Miller, Samantha M. “Analysis of an Open-Cathode Fuel Cell Stack in an Enclosure for Varying Operating Conditions.” 2013. Masters Thesis, University of Alberta. Accessed March 28, 2020. https://era.library.ualberta.ca/files/m039k550b.

MLA Handbook (7th Edition):

Miller, Samantha M. “Analysis of an Open-Cathode Fuel Cell Stack in an Enclosure for Varying Operating Conditions.” 2013. Web. 28 Mar 2020.

Vancouver:

Miller SM. Analysis of an Open-Cathode Fuel Cell Stack in an Enclosure for Varying Operating Conditions. [Internet] [Masters thesis]. University of Alberta; 2013. [cited 2020 Mar 28]. Available from: https://era.library.ualberta.ca/files/m039k550b.

Council of Science Editors:

Miller SM. Analysis of an Open-Cathode Fuel Cell Stack in an Enclosure for Varying Operating Conditions. [Masters Thesis]. University of Alberta; 2013. Available from: https://era.library.ualberta.ca/files/m039k550b


University of Notre Dame

9. Ricky Garza Villarreal. Laboratory Experiments on Dispersive Transport Across Interfaces: the Role of Flow Cell Edges and Corners</h1>.

Degree: MSin Geological Sciences, Civil Engineering and Geological Sciences, 2013, University of Notre Dame

  Contrary to solutions given by the advection dispersion equation, asymmetric break through curves dependent upon flow direction have been experimentally produced for the conceptual… (more)

Subjects/Keywords: porous media; flow cell; corners; dispersive transport; groundwater; edges; conservative transport; experimental

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APA (6th Edition):

Villarreal, R. G. (2013). Laboratory Experiments on Dispersive Transport Across Interfaces: the Role of Flow Cell Edges and Corners</h1>. (Masters Thesis). University of Notre Dame. Retrieved from https://curate.nd.edu/show/zs25x63614d

Chicago Manual of Style (16th Edition):

Villarreal, Ricky Garza. “Laboratory Experiments on Dispersive Transport Across Interfaces: the Role of Flow Cell Edges and Corners</h1>.” 2013. Masters Thesis, University of Notre Dame. Accessed March 28, 2020. https://curate.nd.edu/show/zs25x63614d.

MLA Handbook (7th Edition):

Villarreal, Ricky Garza. “Laboratory Experiments on Dispersive Transport Across Interfaces: the Role of Flow Cell Edges and Corners</h1>.” 2013. Web. 28 Mar 2020.

Vancouver:

Villarreal RG. Laboratory Experiments on Dispersive Transport Across Interfaces: the Role of Flow Cell Edges and Corners</h1>. [Internet] [Masters thesis]. University of Notre Dame; 2013. [cited 2020 Mar 28]. Available from: https://curate.nd.edu/show/zs25x63614d.

Council of Science Editors:

Villarreal RG. Laboratory Experiments on Dispersive Transport Across Interfaces: the Role of Flow Cell Edges and Corners</h1>. [Masters Thesis]. University of Notre Dame; 2013. Available from: https://curate.nd.edu/show/zs25x63614d


Queen Mary, University of London

10. Corsiero, Elisa. Characterization of peripheral and lesional single B cell autoreactivity in patients with Sjögren's syndrome and rheumatoid arthritis.

Degree: PhD, 2013, Queen Mary, University of London

 Sjögren's syndrome (SS) and rheumatoid arthritis (RA) are characterised by breach of self-tolerance with high affinity circulating autoantibodies and peripheral B cell disturbances in the… (more)

Subjects/Keywords: 616.7; Experimental Medicine and Rheumatology; Sjo¨gren's syndrome; rheumatoid arthritis; B cell disturbances

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APA (6th Edition):

Corsiero, E. (2013). Characterization of peripheral and lesional single B cell autoreactivity in patients with Sjögren's syndrome and rheumatoid arthritis. (Doctoral Dissertation). Queen Mary, University of London. Retrieved from http://qmro.qmul.ac.uk/xmlui/handle/123456789/26968 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.612583

Chicago Manual of Style (16th Edition):

Corsiero, Elisa. “Characterization of peripheral and lesional single B cell autoreactivity in patients with Sjögren's syndrome and rheumatoid arthritis.” 2013. Doctoral Dissertation, Queen Mary, University of London. Accessed March 28, 2020. http://qmro.qmul.ac.uk/xmlui/handle/123456789/26968 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.612583.

MLA Handbook (7th Edition):

Corsiero, Elisa. “Characterization of peripheral and lesional single B cell autoreactivity in patients with Sjögren's syndrome and rheumatoid arthritis.” 2013. Web. 28 Mar 2020.

Vancouver:

Corsiero E. Characterization of peripheral and lesional single B cell autoreactivity in patients with Sjögren's syndrome and rheumatoid arthritis. [Internet] [Doctoral dissertation]. Queen Mary, University of London; 2013. [cited 2020 Mar 28]. Available from: http://qmro.qmul.ac.uk/xmlui/handle/123456789/26968 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.612583.

Council of Science Editors:

Corsiero E. Characterization of peripheral and lesional single B cell autoreactivity in patients with Sjögren's syndrome and rheumatoid arthritis. [Doctoral Dissertation]. Queen Mary, University of London; 2013. Available from: http://qmro.qmul.ac.uk/xmlui/handle/123456789/26968 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.612583


University of Edinburgh

11. Cambrook, Helen Elizabeth. Investigating the role of T-bet in CD4+ T cell driven central nervous system autoimmunity.

Degree: PhD, 2014, University of Edinburgh

 Self-reactive CD4+ helper T cells (Th) are key causal agents in the pathogenesis of many autoimmune diseases. Experimental autoimmune encephalomyelitis (EAE) is a CD4+T cell(more)

Subjects/Keywords: 616.97; experimental autoimmune encephalomyelitis; EAE; CD4+T cell model; Th cells; T-bet

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APA (6th Edition):

Cambrook, H. E. (2014). Investigating the role of T-bet in CD4+ T cell driven central nervous system autoimmunity. (Doctoral Dissertation). University of Edinburgh. Retrieved from http://hdl.handle.net/1842/17608

Chicago Manual of Style (16th Edition):

Cambrook, Helen Elizabeth. “Investigating the role of T-bet in CD4+ T cell driven central nervous system autoimmunity.” 2014. Doctoral Dissertation, University of Edinburgh. Accessed March 28, 2020. http://hdl.handle.net/1842/17608.

MLA Handbook (7th Edition):

Cambrook, Helen Elizabeth. “Investigating the role of T-bet in CD4+ T cell driven central nervous system autoimmunity.” 2014. Web. 28 Mar 2020.

Vancouver:

Cambrook HE. Investigating the role of T-bet in CD4+ T cell driven central nervous system autoimmunity. [Internet] [Doctoral dissertation]. University of Edinburgh; 2014. [cited 2020 Mar 28]. Available from: http://hdl.handle.net/1842/17608.

Council of Science Editors:

Cambrook HE. Investigating the role of T-bet in CD4+ T cell driven central nervous system autoimmunity. [Doctoral Dissertation]. University of Edinburgh; 2014. Available from: http://hdl.handle.net/1842/17608


Virginia Tech

12. Davis, Mark William. Development and Evaluation of a Test Apparatus for Fuel Cells.

Degree: MS, Mechanical Engineering, 2000, Virginia Tech

 The development of a test apparatus for proton exchange membrane fuel cells is presented. The design of the prototype device is provided in detail along… (more)

Subjects/Keywords: Test Apparatus; Fuel Cell; Experimental; PEM

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APA (6th Edition):

Davis, M. W. (2000). Development and Evaluation of a Test Apparatus for Fuel Cells. (Masters Thesis). Virginia Tech. Retrieved from http://hdl.handle.net/10919/34037

Chicago Manual of Style (16th Edition):

Davis, Mark William. “Development and Evaluation of a Test Apparatus for Fuel Cells.” 2000. Masters Thesis, Virginia Tech. Accessed March 28, 2020. http://hdl.handle.net/10919/34037.

MLA Handbook (7th Edition):

Davis, Mark William. “Development and Evaluation of a Test Apparatus for Fuel Cells.” 2000. Web. 28 Mar 2020.

Vancouver:

Davis MW. Development and Evaluation of a Test Apparatus for Fuel Cells. [Internet] [Masters thesis]. Virginia Tech; 2000. [cited 2020 Mar 28]. Available from: http://hdl.handle.net/10919/34037.

Council of Science Editors:

Davis MW. Development and Evaluation of a Test Apparatus for Fuel Cells. [Masters Thesis]. Virginia Tech; 2000. Available from: http://hdl.handle.net/10919/34037

13. Drewes, Carine Cristiane. Investigação dos mecanismos de ação do Amblyomin-X sobre a angiogênese in vivo induzida pelo VEGF.

Degree: Mestrado, Toxicologia e Análises Toxicológicas, 2011, University of São Paulo

Amblyomin-X é um inibidor de serinoprotease do tipo kunitz obtido de uma biblioteca de cDNA das glândulas salivares do carrapato Amblyomma cajannense. Dados preliminares mostraram… (more)

Subjects/Keywords: Amblyomin-X; Amblyomin-X; Angiogênese; Angiogenesis; Câmara dosal; Célula endotelial; Dorsal Chamber; Endothelial cell; Experimental toxicology; Inibidores de serinoproteases do tipo kunitz; Serineprotease Kunitz-type inhibitor; Toxicologia experimental; VEGF; VEGF

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APA (6th Edition):

Drewes, C. C. (2011). Investigação dos mecanismos de ação do Amblyomin-X sobre a angiogênese in vivo induzida pelo VEGF. (Masters Thesis). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/9/9141/tde-12072011-095035/ ;

Chicago Manual of Style (16th Edition):

Drewes, Carine Cristiane. “Investigação dos mecanismos de ação do Amblyomin-X sobre a angiogênese in vivo induzida pelo VEGF.” 2011. Masters Thesis, University of São Paulo. Accessed March 28, 2020. http://www.teses.usp.br/teses/disponiveis/9/9141/tde-12072011-095035/ ;.

MLA Handbook (7th Edition):

Drewes, Carine Cristiane. “Investigação dos mecanismos de ação do Amblyomin-X sobre a angiogênese in vivo induzida pelo VEGF.” 2011. Web. 28 Mar 2020.

Vancouver:

Drewes CC. Investigação dos mecanismos de ação do Amblyomin-X sobre a angiogênese in vivo induzida pelo VEGF. [Internet] [Masters thesis]. University of São Paulo; 2011. [cited 2020 Mar 28]. Available from: http://www.teses.usp.br/teses/disponiveis/9/9141/tde-12072011-095035/ ;.

Council of Science Editors:

Drewes CC. Investigação dos mecanismos de ação do Amblyomin-X sobre a angiogênese in vivo induzida pelo VEGF. [Masters Thesis]. University of São Paulo; 2011. Available from: http://www.teses.usp.br/teses/disponiveis/9/9141/tde-12072011-095035/ ;

14. Zager, Adriano. A ativação imune materna e os efeitos sobre a imunidade, neuroinflamação e desenvolvimento da encefalomielite autoimune experimental na prole de camundongos.

Degree: PhD, Patologia Experimental e Comparada, 2013, University of São Paulo

Experiências vivenciadas durante o período pré-natal são determinantes para a saúde do feto. A ocorrência de infecções maternas e a consequente ativação do sistema imune… (more)

Subjects/Keywords: Ativação imune materna; Cell-mediated immunity; Citocinas Th1/Th2/Th17; Encefalomielite autoimune experimental; Experimental autoimmune encephalomyelitis; Imunidade mediada por células; Maternal immune activation; Neuroinflamação; Neuroinflammation; Th1/Th2/Th17 cytokines

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

APA (6th Edition):

Zager, A. (2013). A ativação imune materna e os efeitos sobre a imunidade, neuroinflamação e desenvolvimento da encefalomielite autoimune experimental na prole de camundongos. (Doctoral Dissertation). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/10/10133/tde-21112013-113642/ ;

Chicago Manual of Style (16th Edition):

Zager, Adriano. “A ativação imune materna e os efeitos sobre a imunidade, neuroinflamação e desenvolvimento da encefalomielite autoimune experimental na prole de camundongos.” 2013. Doctoral Dissertation, University of São Paulo. Accessed March 28, 2020. http://www.teses.usp.br/teses/disponiveis/10/10133/tde-21112013-113642/ ;.

MLA Handbook (7th Edition):

Zager, Adriano. “A ativação imune materna e os efeitos sobre a imunidade, neuroinflamação e desenvolvimento da encefalomielite autoimune experimental na prole de camundongos.” 2013. Web. 28 Mar 2020.

Vancouver:

Zager A. A ativação imune materna e os efeitos sobre a imunidade, neuroinflamação e desenvolvimento da encefalomielite autoimune experimental na prole de camundongos. [Internet] [Doctoral dissertation]. University of São Paulo; 2013. [cited 2020 Mar 28]. Available from: http://www.teses.usp.br/teses/disponiveis/10/10133/tde-21112013-113642/ ;.

Council of Science Editors:

Zager A. A ativação imune materna e os efeitos sobre a imunidade, neuroinflamação e desenvolvimento da encefalomielite autoimune experimental na prole de camundongos. [Doctoral Dissertation]. University of São Paulo; 2013. Available from: http://www.teses.usp.br/teses/disponiveis/10/10133/tde-21112013-113642/ ;

15. Roseta, Maria Oliveira Zenha da Cruz. Estudo laboratorial e em condições reais sobre o aglomerado de cortiça expandida aplicado como revestimento exterior.

Degree: 2013, Repositório Científico do Instituto Politécnico de Lisboa

Trabalho Final de Mestrado elaborado no Laboratório de Engenharia Civil para obtenção do grau de Mestre em Engenharia Civil na Área de Especialização de Edificações… (more)

Subjects/Keywords: Aglomerado de cortiça expandida; Revestimento exterior; Célula experimental; Condições reais; Condições em laboratório; Expanded cork agglomerate; Exterior cladding; Experimental cell; Actual conditions; Conditions in the laboratory

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APA (6th Edition):

Roseta, M. O. Z. d. C. (2013). Estudo laboratorial e em condições reais sobre o aglomerado de cortiça expandida aplicado como revestimento exterior. (Thesis). Repositório Científico do Instituto Politécnico de Lisboa. Retrieved from http://www.rcaap.pt/detail.jsp?id=oai:repositorio.ipl.pt:10400.21/3627

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):

Roseta, Maria Oliveira Zenha da Cruz. “Estudo laboratorial e em condições reais sobre o aglomerado de cortiça expandida aplicado como revestimento exterior.” 2013. Thesis, Repositório Científico do Instituto Politécnico de Lisboa. Accessed March 28, 2020. http://www.rcaap.pt/detail.jsp?id=oai:repositorio.ipl.pt:10400.21/3627.

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

MLA Handbook (7th Edition):

Roseta, Maria Oliveira Zenha da Cruz. “Estudo laboratorial e em condições reais sobre o aglomerado de cortiça expandida aplicado como revestimento exterior.” 2013. Web. 28 Mar 2020.

Vancouver:

Roseta MOZdC. Estudo laboratorial e em condições reais sobre o aglomerado de cortiça expandida aplicado como revestimento exterior. [Internet] [Thesis]. Repositório Científico do Instituto Politécnico de Lisboa; 2013. [cited 2020 Mar 28]. Available from: http://www.rcaap.pt/detail.jsp?id=oai:repositorio.ipl.pt:10400.21/3627.

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

Council of Science Editors:

Roseta MOZdC. Estudo laboratorial e em condições reais sobre o aglomerado de cortiça expandida aplicado como revestimento exterior. [Thesis]. Repositório Científico do Instituto Politécnico de Lisboa; 2013. Available from: http://www.rcaap.pt/detail.jsp?id=oai:repositorio.ipl.pt:10400.21/3627

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


University of Hong Kong

16. 許嘉森; Xu, Jiasen. A study of embryotrophic mechanism of human oviductal cells on mouse embryo development in vitro.

Degree: PhD, 2000, University of Hong Kong

published_or_final_version

Obstetrics and Gynaecology

Doctoral

Doctor of Philosophy

Subjects/Keywords: Embryology, Experimental.; Mouse - Embryos.; Cell culture.; Oviduct.

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

APA (6th Edition):

許嘉森; Xu, J. (2000). A study of embryotrophic mechanism of human oviductal cells on mouse embryo development in vitro. (Doctoral Dissertation). University of Hong Kong. Retrieved from Xu, J. [許嘉森]. (2000). A study of embryotrophic mechanism of human oviductal cells on mouse embryo development in vitro. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4389472 ; http://dx.doi.org/10.5353/th_b4389472 ; http://hdl.handle.net/10722/65328

Chicago Manual of Style (16th Edition):

許嘉森; Xu, Jiasen. “A study of embryotrophic mechanism of human oviductal cells on mouse embryo development in vitro.” 2000. Doctoral Dissertation, University of Hong Kong. Accessed March 28, 2020. Xu, J. [許嘉森]. (2000). A study of embryotrophic mechanism of human oviductal cells on mouse embryo development in vitro. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4389472 ; http://dx.doi.org/10.5353/th_b4389472 ; http://hdl.handle.net/10722/65328.

MLA Handbook (7th Edition):

許嘉森; Xu, Jiasen. “A study of embryotrophic mechanism of human oviductal cells on mouse embryo development in vitro.” 2000. Web. 28 Mar 2020.

Vancouver:

許嘉森; Xu J. A study of embryotrophic mechanism of human oviductal cells on mouse embryo development in vitro. [Internet] [Doctoral dissertation]. University of Hong Kong; 2000. [cited 2020 Mar 28]. Available from: Xu, J. [許嘉森]. (2000). A study of embryotrophic mechanism of human oviductal cells on mouse embryo development in vitro. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4389472 ; http://dx.doi.org/10.5353/th_b4389472 ; http://hdl.handle.net/10722/65328.

Council of Science Editors:

許嘉森; Xu J. A study of embryotrophic mechanism of human oviductal cells on mouse embryo development in vitro. [Doctoral Dissertation]. University of Hong Kong; 2000. Available from: Xu, J. [許嘉森]. (2000). A study of embryotrophic mechanism of human oviductal cells on mouse embryo development in vitro. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4389472 ; http://dx.doi.org/10.5353/th_b4389472 ; http://hdl.handle.net/10722/65328


University of California – Irvine

17. Lengfeld, Justin Edward. Endothelial Wnt/β-catenin modulates blood-brain barrier integrity in a mouse model of multiple sclerosis.

Degree: Biological Sciences, 2016, University of California – Irvine

 Blood-brain barrier (BBB) breakdown is a contributing factor in many neurological diseases, including Multiple Sclerosis (MS). MS is an inflammatory disease in which auto-reactive T-cells… (more)

Subjects/Keywords: Cellular biology; Blood-brain barrier; Endothelial cell; experimental autoimmune encephalomyelitis; Multiple sclerosis; Wnt/β-catenin pathway

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APA (6th Edition):

Lengfeld, J. E. (2016). Endothelial Wnt/β-catenin modulates blood-brain barrier integrity in a mouse model of multiple sclerosis. (Thesis). University of California – Irvine. Retrieved from http://www.escholarship.org/uc/item/9581w0tw

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):

Lengfeld, Justin Edward. “Endothelial Wnt/β-catenin modulates blood-brain barrier integrity in a mouse model of multiple sclerosis.” 2016. Thesis, University of California – Irvine. Accessed March 28, 2020. http://www.escholarship.org/uc/item/9581w0tw.

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

MLA Handbook (7th Edition):

Lengfeld, Justin Edward. “Endothelial Wnt/β-catenin modulates blood-brain barrier integrity in a mouse model of multiple sclerosis.” 2016. Web. 28 Mar 2020.

Vancouver:

Lengfeld JE. Endothelial Wnt/β-catenin modulates blood-brain barrier integrity in a mouse model of multiple sclerosis. [Internet] [Thesis]. University of California – Irvine; 2016. [cited 2020 Mar 28]. Available from: http://www.escholarship.org/uc/item/9581w0tw.

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

Council of Science Editors:

Lengfeld JE. Endothelial Wnt/β-catenin modulates blood-brain barrier integrity in a mouse model of multiple sclerosis. [Thesis]. University of California – Irvine; 2016. Available from: http://www.escholarship.org/uc/item/9581w0tw

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


Massey University

18. Morley, Annabel. Investigating the evolutionary changes in Crabtree-negative yeasts during a long-term evolution experiment.

Degree: PhD, Genetics, 2017, Massey University

 The Crabtree effect is a metabolic strategy that allows yeast to ferment in the presence of oxygen. This is of interest as not all yeasts… (more)

Subjects/Keywords: Saccharomyces cerevisiae; Yeasts; Evolution; Metabolism; Experimental evolution; Research Subject Categories::NATURAL SCIENCES::Biology::Cell and molecular biology::Genetics

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APA (6th Edition):

Morley, A. (2017). Investigating the evolutionary changes in Crabtree-negative yeasts during a long-term evolution experiment. (Doctoral Dissertation). Massey University. Retrieved from http://hdl.handle.net/10179/13445

Chicago Manual of Style (16th Edition):

Morley, Annabel. “Investigating the evolutionary changes in Crabtree-negative yeasts during a long-term evolution experiment.” 2017. Doctoral Dissertation, Massey University. Accessed March 28, 2020. http://hdl.handle.net/10179/13445.

MLA Handbook (7th Edition):

Morley, Annabel. “Investigating the evolutionary changes in Crabtree-negative yeasts during a long-term evolution experiment.” 2017. Web. 28 Mar 2020.

Vancouver:

Morley A. Investigating the evolutionary changes in Crabtree-negative yeasts during a long-term evolution experiment. [Internet] [Doctoral dissertation]. Massey University; 2017. [cited 2020 Mar 28]. Available from: http://hdl.handle.net/10179/13445.

Council of Science Editors:

Morley A. Investigating the evolutionary changes in Crabtree-negative yeasts during a long-term evolution experiment. [Doctoral Dissertation]. Massey University; 2017. Available from: http://hdl.handle.net/10179/13445


Universidade do Rio Grande do Sul

19. Lopes, Fernanda Martins. Caracterização da diferenciação neural induzida por ácido retinóico da linhagem de neuroblastoma humano SH-SY5Y e seu uso como ferramenta para pesquisa em neurociências.

Degree: 2012, Universidade do Rio Grande do Sul

 Os mecanismos moleculares que levam ao dano da via nigroestriatal durante a progressão da Doença de Parkinson (DP) ainda não estão totalmente elucidados. Dessa forma,… (more)

Subjects/Keywords: Doença de Parkinson; Parkinson disease; SH-SY5Y; Estresse oxidativo; Diferenciação celular; 6-hydroxydopamine; Experimental model; Neuroblastoma; Cell differentiation; Tretinoína; Oxidative stress

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APA (6th Edition):

Lopes, F. M. (2012). Caracterização da diferenciação neural induzida por ácido retinóico da linhagem de neuroblastoma humano SH-SY5Y e seu uso como ferramenta para pesquisa em neurociências. (Thesis). Universidade do Rio Grande do Sul. Retrieved from http://hdl.handle.net/10183/49007

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):

Lopes, Fernanda Martins. “Caracterização da diferenciação neural induzida por ácido retinóico da linhagem de neuroblastoma humano SH-SY5Y e seu uso como ferramenta para pesquisa em neurociências.” 2012. Thesis, Universidade do Rio Grande do Sul. Accessed March 28, 2020. http://hdl.handle.net/10183/49007.

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

MLA Handbook (7th Edition):

Lopes, Fernanda Martins. “Caracterização da diferenciação neural induzida por ácido retinóico da linhagem de neuroblastoma humano SH-SY5Y e seu uso como ferramenta para pesquisa em neurociências.” 2012. Web. 28 Mar 2020.

Vancouver:

Lopes FM. Caracterização da diferenciação neural induzida por ácido retinóico da linhagem de neuroblastoma humano SH-SY5Y e seu uso como ferramenta para pesquisa em neurociências. [Internet] [Thesis]. Universidade do Rio Grande do Sul; 2012. [cited 2020 Mar 28]. Available from: http://hdl.handle.net/10183/49007.

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

Council of Science Editors:

Lopes FM. Caracterização da diferenciação neural induzida por ácido retinóico da linhagem de neuroblastoma humano SH-SY5Y e seu uso como ferramenta para pesquisa em neurociências. [Thesis]. Universidade do Rio Grande do Sul; 2012. Available from: http://hdl.handle.net/10183/49007

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

20. Miller, Megan Michelle. Examining strategies for reducing cell phone use while driving: investigating the potential of targeting non-driving participants of cell phone conversations and testing the utility of techniques for reducing habitual responses to cell phones.

Degree: PhD, Department of Psychological Sciences, 2014, Kansas State University

 The current research investigated strategies to reduce cell phone use while driving. Anti-distracted driving campaigns, which typically communicate risk information and target driver behavior, may… (more)

Subjects/Keywords: Cell phone use while driving; Messaging; Temptation resistance; Mindfulness; Implementation intentions; Behavioral Sciences (0602); Experimental Psychology (0623); Social Psychology (0451)

Page 1 Page 2 Page 3 Page 4 Page 5 Page 6 Page 7

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APA (6th Edition):

Miller, M. M. (2014). Examining strategies for reducing cell phone use while driving: investigating the potential of targeting non-driving participants of cell phone conversations and testing the utility of techniques for reducing habitual responses to cell phones. (Doctoral Dissertation). Kansas State University. Retrieved from http://hdl.handle.net/2097/18176

Chicago Manual of Style (16th Edition):

Miller, Megan Michelle. “Examining strategies for reducing cell phone use while driving: investigating the potential of targeting non-driving participants of cell phone conversations and testing the utility of techniques for reducing habitual responses to cell phones.” 2014. Doctoral Dissertation, Kansas State University. Accessed March 28, 2020. http://hdl.handle.net/2097/18176.

MLA Handbook (7th Edition):

Miller, Megan Michelle. “Examining strategies for reducing cell phone use while driving: investigating the potential of targeting non-driving participants of cell phone conversations and testing the utility of techniques for reducing habitual responses to cell phones.” 2014. Web. 28 Mar 2020.

Vancouver:

Miller MM. Examining strategies for reducing cell phone use while driving: investigating the potential of targeting non-driving participants of cell phone conversations and testing the utility of techniques for reducing habitual responses to cell phones. [Internet] [Doctoral dissertation]. Kansas State University; 2014. [cited 2020 Mar 28]. Available from: http://hdl.handle.net/2097/18176.

Council of Science Editors:

Miller MM. Examining strategies for reducing cell phone use while driving: investigating the potential of targeting non-driving participants of cell phone conversations and testing the utility of techniques for reducing habitual responses to cell phones. [Doctoral Dissertation]. Kansas State University; 2014. Available from: http://hdl.handle.net/2097/18176

21. Savić Danijela. The effect of purine nucleoside, analogues, ribavirin and tiazofurin, on microglial activation under inflammatory conditions.

Degree: PhD, Biology, 2012, University of Belgrade

Activation of microglia is the hallmark of experimental autoimmune encephalomyelitis (EAE) and other neurodegenerative disorders associated with chronic neuroinflammation. The present study addressed the potency… (more)

Subjects/Keywords: Central nervous system; inflammation; microglia; experimental autoimmune encephalomyelitis; cell culture; Centralni nervni sistem; inflamacija; mikroglija; eksperimentalni autoimunski encefalomijelitis; ćelijska kultura

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APA (6th Edition):

Danijela, S. (2012). The effect of purine nucleoside, analogues, ribavirin and tiazofurin, on microglial activation under inflammatory conditions. (Doctoral Dissertation). University of Belgrade. Retrieved from http://dx.doi.org/10.2298/BG20121001SAVIC ; http://eteze.bg.ac.rs/application/showtheses?thesesId=29 ; https://fedorabg.bg.ac.rs/fedora/get/o:2285/bdef:Content/get ; http://vbs.rs/scripts/cobiss?command=SEARCH&base=99999&select=ID=41536015

Chicago Manual of Style (16th Edition):

Danijela, Savić. “The effect of purine nucleoside, analogues, ribavirin and tiazofurin, on microglial activation under inflammatory conditions.” 2012. Doctoral Dissertation, University of Belgrade. Accessed March 28, 2020. http://dx.doi.org/10.2298/BG20121001SAVIC ; http://eteze.bg.ac.rs/application/showtheses?thesesId=29 ; https://fedorabg.bg.ac.rs/fedora/get/o:2285/bdef:Content/get ; http://vbs.rs/scripts/cobiss?command=SEARCH&base=99999&select=ID=41536015.

MLA Handbook (7th Edition):

Danijela, Savić. “The effect of purine nucleoside, analogues, ribavirin and tiazofurin, on microglial activation under inflammatory conditions.” 2012. Web. 28 Mar 2020.

Vancouver:

Danijela S. The effect of purine nucleoside, analogues, ribavirin and tiazofurin, on microglial activation under inflammatory conditions. [Internet] [Doctoral dissertation]. University of Belgrade; 2012. [cited 2020 Mar 28]. Available from: http://dx.doi.org/10.2298/BG20121001SAVIC ; http://eteze.bg.ac.rs/application/showtheses?thesesId=29 ; https://fedorabg.bg.ac.rs/fedora/get/o:2285/bdef:Content/get ; http://vbs.rs/scripts/cobiss?command=SEARCH&base=99999&select=ID=41536015.

Council of Science Editors:

Danijela S. The effect of purine nucleoside, analogues, ribavirin and tiazofurin, on microglial activation under inflammatory conditions. [Doctoral Dissertation]. University of Belgrade; 2012. Available from: http://dx.doi.org/10.2298/BG20121001SAVIC ; http://eteze.bg.ac.rs/application/showtheses?thesesId=29 ; https://fedorabg.bg.ac.rs/fedora/get/o:2285/bdef:Content/get ; http://vbs.rs/scripts/cobiss?command=SEARCH&base=99999&select=ID=41536015


University of Miami

22. Ashbaugh, Jessica Jopek. Interleukin-7 Receptor Alpha, Nuclear Factor-Kappa B, and Tumor Necrosis Factor Contribute to Inflammatory Responses in Experimental Autoimmune Encephalomyelitis, a Model of Multiple Sclerosis.

Degree: PhD, Microbiology and Immunology (Medicine), 2012, University of Miami

  Multiple Sclerosis (MS) is a debilitating autoimmune disease whose pathological hallmarks are intermittent demyelination, axonal damage, and inflammation throughout the central nervous system (CNS).… (more)

Subjects/Keywords: experimental autoimmune encephalomyelitis; interleukin-7 receptor alpha; nuclear factor-kappa B; tumor necrosis factor; Multiple Sclerosis; T cell

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APA (6th Edition):

Ashbaugh, J. J. (2012). Interleukin-7 Receptor Alpha, Nuclear Factor-Kappa B, and Tumor Necrosis Factor Contribute to Inflammatory Responses in Experimental Autoimmune Encephalomyelitis, a Model of Multiple Sclerosis. (Doctoral Dissertation). University of Miami. Retrieved from https://scholarlyrepository.miami.edu/oa_dissertations/871

Chicago Manual of Style (16th Edition):

Ashbaugh, Jessica Jopek. “Interleukin-7 Receptor Alpha, Nuclear Factor-Kappa B, and Tumor Necrosis Factor Contribute to Inflammatory Responses in Experimental Autoimmune Encephalomyelitis, a Model of Multiple Sclerosis.” 2012. Doctoral Dissertation, University of Miami. Accessed March 28, 2020. https://scholarlyrepository.miami.edu/oa_dissertations/871.

MLA Handbook (7th Edition):

Ashbaugh, Jessica Jopek. “Interleukin-7 Receptor Alpha, Nuclear Factor-Kappa B, and Tumor Necrosis Factor Contribute to Inflammatory Responses in Experimental Autoimmune Encephalomyelitis, a Model of Multiple Sclerosis.” 2012. Web. 28 Mar 2020.

Vancouver:

Ashbaugh JJ. Interleukin-7 Receptor Alpha, Nuclear Factor-Kappa B, and Tumor Necrosis Factor Contribute to Inflammatory Responses in Experimental Autoimmune Encephalomyelitis, a Model of Multiple Sclerosis. [Internet] [Doctoral dissertation]. University of Miami; 2012. [cited 2020 Mar 28]. Available from: https://scholarlyrepository.miami.edu/oa_dissertations/871.

Council of Science Editors:

Ashbaugh JJ. Interleukin-7 Receptor Alpha, Nuclear Factor-Kappa B, and Tumor Necrosis Factor Contribute to Inflammatory Responses in Experimental Autoimmune Encephalomyelitis, a Model of Multiple Sclerosis. [Doctoral Dissertation]. University of Miami; 2012. Available from: https://scholarlyrepository.miami.edu/oa_dissertations/871


Universidad de Salamanca

23. García Hernández, Violeta. Análisis proteómico durante el desarrollo de la pancreatitis aguda experimental .

Degree: 2017, Universidad de Salamanca

 [ES]La pancreatitis aguda (PA) es una condición inflamatoria del páncreas caracterizada por una incidencia alta y creciente, que se manifiesta con una gravedad de considerable… (more)

Subjects/Keywords: Cell biology; Tesis y disertaciones académicas; Universidad de Salamanca (España); Tesis doctoral; Academic dissertations; Bioquímica; Proteínas; Patología experimental; Biología molecular

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APA (6th Edition):

García Hernández, V. (2017). Análisis proteómico durante el desarrollo de la pancreatitis aguda experimental . (Thesis). Universidad de Salamanca. Retrieved from http://hdl.handle.net/10366/136271

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):

García Hernández, Violeta. “Análisis proteómico durante el desarrollo de la pancreatitis aguda experimental .” 2017. Thesis, Universidad de Salamanca. Accessed March 28, 2020. http://hdl.handle.net/10366/136271.

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

MLA Handbook (7th Edition):

García Hernández, Violeta. “Análisis proteómico durante el desarrollo de la pancreatitis aguda experimental .” 2017. Web. 28 Mar 2020.

Vancouver:

García Hernández V. Análisis proteómico durante el desarrollo de la pancreatitis aguda experimental . [Internet] [Thesis]. Universidad de Salamanca; 2017. [cited 2020 Mar 28]. Available from: http://hdl.handle.net/10366/136271.

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

Council of Science Editors:

García Hernández V. Análisis proteómico durante el desarrollo de la pancreatitis aguda experimental . [Thesis]. Universidad de Salamanca; 2017. Available from: http://hdl.handle.net/10366/136271

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

24. Cheng, Wing Yin. Macrophage PPAR-Gamma Inhibits Gpr132 to Mediate the Anti-Tumor Effects of Rosiglitazone.

Degree: 2016, University of Texas Southwestern Medical Center

 Tumor-associated macrophage (TAM) significantly contributes to tumorigenesis. Human cancer is enhanced by PPARgamma loss-of-function mutations, and inhibited by the thiazolidinedione (TZD) class of synthetic PPARgamma… (more)

Subjects/Keywords: Antineoplastic Agents; Cell Cycle Proteins; Macrophages; Mammary Neoplasms, Experimental; PPAR gamma; Receptors, G-Protein-Coupled; Thiazolidinediones

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APA (6th Edition):

Cheng, W. Y. (2016). Macrophage PPAR-Gamma Inhibits Gpr132 to Mediate the Anti-Tumor Effects of Rosiglitazone. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/5295

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):

Cheng, Wing Yin. “Macrophage PPAR-Gamma Inhibits Gpr132 to Mediate the Anti-Tumor Effects of Rosiglitazone.” 2016. Thesis, University of Texas Southwestern Medical Center. Accessed March 28, 2020. http://hdl.handle.net/2152.5/5295.

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

MLA Handbook (7th Edition):

Cheng, Wing Yin. “Macrophage PPAR-Gamma Inhibits Gpr132 to Mediate the Anti-Tumor Effects of Rosiglitazone.” 2016. Web. 28 Mar 2020.

Vancouver:

Cheng WY. Macrophage PPAR-Gamma Inhibits Gpr132 to Mediate the Anti-Tumor Effects of Rosiglitazone. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2016. [cited 2020 Mar 28]. Available from: http://hdl.handle.net/2152.5/5295.

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

Council of Science Editors:

Cheng WY. Macrophage PPAR-Gamma Inhibits Gpr132 to Mediate the Anti-Tumor Effects of Rosiglitazone. [Thesis]. University of Texas Southwestern Medical Center; 2016. Available from: http://hdl.handle.net/2152.5/5295

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


University of Guelph

25. Leacy, Alexander. In vitro and in ovo characterization of aquatic bird bornavirus 1 in avian species .

Degree: 2019, University of Guelph

 Aquatic bird bornavirus 1 (ABBV-1) is associated with fatal inflammation of nervous tissue in avian species. Waterfowl act as the natural host, with populations of… (more)

Subjects/Keywords: aquatic bird bornavirus 1; avian bornavirus; Bornaviridae; waterfowl; poultry; cell lines; host range; growth curves; in ovo pathogenesis; experimental infection

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APA (6th Edition):

Leacy, A. (2019). In vitro and in ovo characterization of aquatic bird bornavirus 1 in avian species . (Thesis). University of Guelph. Retrieved from https://atrium.lib.uoguelph.ca/xmlui/handle/10214/16110

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):

Leacy, Alexander. “In vitro and in ovo characterization of aquatic bird bornavirus 1 in avian species .” 2019. Thesis, University of Guelph. Accessed March 28, 2020. https://atrium.lib.uoguelph.ca/xmlui/handle/10214/16110.

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

MLA Handbook (7th Edition):

Leacy, Alexander. “In vitro and in ovo characterization of aquatic bird bornavirus 1 in avian species .” 2019. Web. 28 Mar 2020.

Vancouver:

Leacy A. In vitro and in ovo characterization of aquatic bird bornavirus 1 in avian species . [Internet] [Thesis]. University of Guelph; 2019. [cited 2020 Mar 28]. Available from: https://atrium.lib.uoguelph.ca/xmlui/handle/10214/16110.

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

Council of Science Editors:

Leacy A. In vitro and in ovo characterization of aquatic bird bornavirus 1 in avian species . [Thesis]. University of Guelph; 2019. Available from: https://atrium.lib.uoguelph.ca/xmlui/handle/10214/16110

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


University of New Mexico

26. Dasgupta, Anushka. Protein carbonylation, protein aggregation and cell death in a murine model of multiple sclerosis.

Degree: Biomedical Sciences Graduate Program, 2013, University of New Mexico

 Many studies have suggested that oxidative stress plays an important role in the pathophysiology of both multiple sclerosis (MS) and its animal model experimental autoimmune… (more)

Subjects/Keywords: Experimental Autoimmune Encephalomyelitis; Multiple Sclerosis; Neuronal cell death; Protein aggregation; Protein carbonylation; Oxidative stress; glutathione depletion

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APA (6th Edition):

Dasgupta, A. (2013). Protein carbonylation, protein aggregation and cell death in a murine model of multiple sclerosis. (Doctoral Dissertation). University of New Mexico. Retrieved from https://digitalrepository.unm.edu/biom_etds/122

Chicago Manual of Style (16th Edition):

Dasgupta, Anushka. “Protein carbonylation, protein aggregation and cell death in a murine model of multiple sclerosis.” 2013. Doctoral Dissertation, University of New Mexico. Accessed March 28, 2020. https://digitalrepository.unm.edu/biom_etds/122.

MLA Handbook (7th Edition):

Dasgupta, Anushka. “Protein carbonylation, protein aggregation and cell death in a murine model of multiple sclerosis.” 2013. Web. 28 Mar 2020.

Vancouver:

Dasgupta A. Protein carbonylation, protein aggregation and cell death in a murine model of multiple sclerosis. [Internet] [Doctoral dissertation]. University of New Mexico; 2013. [cited 2020 Mar 28]. Available from: https://digitalrepository.unm.edu/biom_etds/122.

Council of Science Editors:

Dasgupta A. Protein carbonylation, protein aggregation and cell death in a murine model of multiple sclerosis. [Doctoral Dissertation]. University of New Mexico; 2013. Available from: https://digitalrepository.unm.edu/biom_etds/122

27. Wohler, Jillian E. The role of the [beta]2-integrin family on T cell subsets.

Degree: PhD, 2009, University of Alabama – Birmingham

Members of the [beta]2-integrin family of adhesion molecules, CD11a, CD11b, and CD11c, have all been shown to play a role in the pathogenesis of experimental(more)

Subjects/Keywords: Antigens, CD11  – analysis<; br>; Cell Cycle Proteins  – physiology<; br>; Cell Proliferation<; br>; Encephalomyelitis, Autoimmune, Experimental  – genetics<; br>; Encephalomyelitis, Autoimmune, Experimental  – immunology<; br>; T-Lymphocytes  – cytology

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

APA (6th Edition):

Wohler, J. E. (2009). The role of the [beta]2-integrin family on T cell subsets. (Doctoral Dissertation). University of Alabama – Birmingham. Retrieved from http://contentdm.mhsl.uab.edu/u?/etd,409

Chicago Manual of Style (16th Edition):

Wohler, Jillian E. “The role of the [beta]2-integrin family on T cell subsets.” 2009. Doctoral Dissertation, University of Alabama – Birmingham. Accessed March 28, 2020. http://contentdm.mhsl.uab.edu/u?/etd,409.

MLA Handbook (7th Edition):

Wohler, Jillian E. “The role of the [beta]2-integrin family on T cell subsets.” 2009. Web. 28 Mar 2020.

Vancouver:

Wohler JE. The role of the [beta]2-integrin family on T cell subsets. [Internet] [Doctoral dissertation]. University of Alabama – Birmingham; 2009. [cited 2020 Mar 28]. Available from: http://contentdm.mhsl.uab.edu/u?/etd,409.

Council of Science Editors:

Wohler JE. The role of the [beta]2-integrin family on T cell subsets. [Doctoral Dissertation]. University of Alabama – Birmingham; 2009. Available from: http://contentdm.mhsl.uab.edu/u?/etd,409

28. Molendijk, Ilse. Mesenchymal stromal cell therapy for Crohn's disease: from perianal fistulizing disease to experimental colitis.

Degree: 2016, Department of Gastroenterology and Hepatology, Faculty of Medicine, Leiden University Medical Center (LUMC), Leiden University

 A frequent manifestation of Crohn's disease (CD) is the formation of perianal fistulas which can greatly affect patient’s quality of life due to continuous pain,… (more)

Subjects/Keywords: Gastroenterology; Crohn's disease; Perianal fistulas; Mesenchymal stromal cell; Experimental colitis; Gastroenterology; Crohn's disease; Perianal fistulas; Mesenchymal stromal cell; Experimental colitis

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APA (6th Edition):

Molendijk, I. (2016). Mesenchymal stromal cell therapy for Crohn's disease: from perianal fistulizing disease to experimental colitis. (Doctoral Dissertation). Department of Gastroenterology and Hepatology, Faculty of Medicine, Leiden University Medical Center (LUMC), Leiden University. Retrieved from http://hdl.handle.net/1887/38545

Chicago Manual of Style (16th Edition):

Molendijk, Ilse. “Mesenchymal stromal cell therapy for Crohn's disease: from perianal fistulizing disease to experimental colitis.” 2016. Doctoral Dissertation, Department of Gastroenterology and Hepatology, Faculty of Medicine, Leiden University Medical Center (LUMC), Leiden University. Accessed March 28, 2020. http://hdl.handle.net/1887/38545.

MLA Handbook (7th Edition):

Molendijk, Ilse. “Mesenchymal stromal cell therapy for Crohn's disease: from perianal fistulizing disease to experimental colitis.” 2016. Web. 28 Mar 2020.

Vancouver:

Molendijk I. Mesenchymal stromal cell therapy for Crohn's disease: from perianal fistulizing disease to experimental colitis. [Internet] [Doctoral dissertation]. Department of Gastroenterology and Hepatology, Faculty of Medicine, Leiden University Medical Center (LUMC), Leiden University; 2016. [cited 2020 Mar 28]. Available from: http://hdl.handle.net/1887/38545.

Council of Science Editors:

Molendijk I. Mesenchymal stromal cell therapy for Crohn's disease: from perianal fistulizing disease to experimental colitis. [Doctoral Dissertation]. Department of Gastroenterology and Hepatology, Faculty of Medicine, Leiden University Medical Center (LUMC), Leiden University; 2016. Available from: http://hdl.handle.net/1887/38545


Indian Institute of Science

29. Singh, Gurbind. Studies On Embryonic Stem Cells From Enhanced Green Fluorescent Protein Transgenic Mice : Induction Of Cardiomyocyte Differentiation.

Degree: 2011, Indian Institute of Science

 Genesis of life begins with the fusion of female and male haploid gametes through a process of fertilization leading to the formation of a diploid… (more)

Subjects/Keywords: Experimental Research; Stem Cells; Transgenic Mice; Cardiomyocyte Differentiation; Embryonic Stem Cells; Enhanced Green Fluorescent Protein (EGFP); Fibroblast Growth Factor (FGF); Embryonic Stem Cell Line; ES-cells; Molecular Biology

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APA (6th Edition):

Singh, G. (2011). Studies On Embryonic Stem Cells From Enhanced Green Fluorescent Protein Transgenic Mice : Induction Of Cardiomyocyte Differentiation. (Thesis). Indian Institute of Science. Retrieved from http://hdl.handle.net/2005/2116

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):

Singh, Gurbind. “Studies On Embryonic Stem Cells From Enhanced Green Fluorescent Protein Transgenic Mice : Induction Of Cardiomyocyte Differentiation.” 2011. Thesis, Indian Institute of Science. Accessed March 28, 2020. http://hdl.handle.net/2005/2116.

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

MLA Handbook (7th Edition):

Singh, Gurbind. “Studies On Embryonic Stem Cells From Enhanced Green Fluorescent Protein Transgenic Mice : Induction Of Cardiomyocyte Differentiation.” 2011. Web. 28 Mar 2020.

Vancouver:

Singh G. Studies On Embryonic Stem Cells From Enhanced Green Fluorescent Protein Transgenic Mice : Induction Of Cardiomyocyte Differentiation. [Internet] [Thesis]. Indian Institute of Science; 2011. [cited 2020 Mar 28]. Available from: http://hdl.handle.net/2005/2116.

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

Council of Science Editors:

Singh G. Studies On Embryonic Stem Cells From Enhanced Green Fluorescent Protein Transgenic Mice : Induction Of Cardiomyocyte Differentiation. [Thesis]. Indian Institute of Science; 2011. Available from: http://hdl.handle.net/2005/2116

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


University of Oulu

30. Lappalainen, N. (Niina). The responses of ectohydric and endohydric mosses under ambient and enhanced ultraviolet radiation.

Degree: 2010, University of Oulu

 Abstract Previous reports on the effects of enhanced UV-B radiation on bryophytes have been equivocal. This study shows that mosses not only respond to enhanced… (more)

Subjects/Keywords: UV-absorbing compounds; cell wall; environmental specimen bank; experimental study; fluorescence microscopy; growth; long-term changes; methanol; mosses; natural conditions; photosynthesizing pigments; pleurozium schreberi; polytrichum juniperinum; ultraviolet radiation

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

APA (6th Edition):

Lappalainen, N. (. (2010). The responses of ectohydric and endohydric mosses under ambient and enhanced ultraviolet radiation. (Doctoral Dissertation). University of Oulu. Retrieved from http://urn.fi/urn:isbn:9789514262142

Chicago Manual of Style (16th Edition):

Lappalainen, N (Niina). “The responses of ectohydric and endohydric mosses under ambient and enhanced ultraviolet radiation.” 2010. Doctoral Dissertation, University of Oulu. Accessed March 28, 2020. http://urn.fi/urn:isbn:9789514262142.

MLA Handbook (7th Edition):

Lappalainen, N (Niina). “The responses of ectohydric and endohydric mosses under ambient and enhanced ultraviolet radiation.” 2010. Web. 28 Mar 2020.

Vancouver:

Lappalainen N(. The responses of ectohydric and endohydric mosses under ambient and enhanced ultraviolet radiation. [Internet] [Doctoral dissertation]. University of Oulu; 2010. [cited 2020 Mar 28]. Available from: http://urn.fi/urn:isbn:9789514262142.

Council of Science Editors:

Lappalainen N(. The responses of ectohydric and endohydric mosses under ambient and enhanced ultraviolet radiation. [Doctoral Dissertation]. University of Oulu; 2010. Available from: http://urn.fi/urn:isbn:9789514262142

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