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You searched for subject:(Apical Membrane Antigen 1). Showing records 1 – 30 of 25916 total matches.

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University of Illinois – Urbana-Champaign

1. Milan Noris, Evelia Maria. Development of a plant-based vaccine against malaria.

Degree: PhD, Nutritional Sciences, 2015, University of Illinois – Urbana-Champaign

 Malaria is the most prevalent tropical human disease reported worldwide, caused by protozoan parasites. Half of the world's population is at risk of malaria, and… (more)

Subjects/Keywords: Malaria; Plant-based vaccine; Plasmodium faciparum; Apical Membrane Antigen 1 (AMA1); Merozoite Surface Protein 1 (MSP1); Plastid transformation; Adjuvant; GK1.

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APA (6th Edition):

Milan Noris, E. M. (2015). Development of a plant-based vaccine against malaria. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/89223

Chicago Manual of Style (16th Edition):

Milan Noris, Evelia Maria. “Development of a plant-based vaccine against malaria.” 2015. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed April 13, 2021. http://hdl.handle.net/2142/89223.

MLA Handbook (7th Edition):

Milan Noris, Evelia Maria. “Development of a plant-based vaccine against malaria.” 2015. Web. 13 Apr 2021.

Vancouver:

Milan Noris EM. Development of a plant-based vaccine against malaria. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2015. [cited 2021 Apr 13]. Available from: http://hdl.handle.net/2142/89223.

Council of Science Editors:

Milan Noris EM. Development of a plant-based vaccine against malaria. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2015. Available from: http://hdl.handle.net/2142/89223

2. Baradji, Issa. The Role of Apical Membrane Antigen-1 in Erythrocyte Invasion by the Zoonotic Apicomplexan Babesia microti.

Degree: PhD, Veterinary Microbiology, 2010, Texas A&M University

 Babesia microti is a tickborne hemoprotozoan parasite that causes the disease babesiosis in humans. Babesia microti Apical Membrane Antigen-1 (AMA-1) is a micronemal protein suspected… (more)

Subjects/Keywords: Babesia microti; Apical Membrane Antigen-1; AMA-1; erythrocyte; parasite ligand; red blood cell; receptor; protein-protein interaction

…viii NOMENCLATURE AMA-1 Apical Membrane Antigen1 BmAMA-1 Babesia microti Apical… …internalization, and multiplication in the host cell. Apical membrane antigen-1 (AMA-1) is one… …Proteins 1 (RAP-1), Babesia bovis Apical membrane Antigen 1 ( BbAMA1), and… …played by parasites ligands Apical Membrane Antigen-1 (AMA-1), Rhoptries Associated… …Membrane Antigen-1 B. microti ama-1 gene Babesia microti ama-1 gene BmAMA-1 protein Babesia… 

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APA (6th Edition):

Baradji, I. (2010). The Role of Apical Membrane Antigen-1 in Erythrocyte Invasion by the Zoonotic Apicomplexan Babesia microti. (Doctoral Dissertation). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/ETD-TAMU-2008-08-68

Chicago Manual of Style (16th Edition):

Baradji, Issa. “The Role of Apical Membrane Antigen-1 in Erythrocyte Invasion by the Zoonotic Apicomplexan Babesia microti.” 2010. Doctoral Dissertation, Texas A&M University. Accessed April 13, 2021. http://hdl.handle.net/1969.1/ETD-TAMU-2008-08-68.

MLA Handbook (7th Edition):

Baradji, Issa. “The Role of Apical Membrane Antigen-1 in Erythrocyte Invasion by the Zoonotic Apicomplexan Babesia microti.” 2010. Web. 13 Apr 2021.

Vancouver:

Baradji I. The Role of Apical Membrane Antigen-1 in Erythrocyte Invasion by the Zoonotic Apicomplexan Babesia microti. [Internet] [Doctoral dissertation]. Texas A&M University; 2010. [cited 2021 Apr 13]. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-2008-08-68.

Council of Science Editors:

Baradji I. The Role of Apical Membrane Antigen-1 in Erythrocyte Invasion by the Zoonotic Apicomplexan Babesia microti. [Doctoral Dissertation]. Texas A&M University; 2010. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-2008-08-68


University of Queensland

3. Pattinson, David. Evaluation of chimeric virus-like particles, capsomeres and bacterial minicells as vaccine delivery platforms.

Degree: School of Medicine, 2014, University of Queensland

Subjects/Keywords: Vaccine; Murine polyomavirus; Virus-like particles; Capsomeres; Bacterial minicells; Malaria; Circumsporozoite protein; Apical membrane antigen-1; Ovalbumin; Cell-mediated immunity; 1107 Immunology

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APA (6th Edition):

Pattinson, D. (2014). Evaluation of chimeric virus-like particles, capsomeres and bacterial minicells as vaccine delivery platforms. (Thesis). University of Queensland. Retrieved from http://espace.library.uq.edu.au/view/UQ:347062

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):

Pattinson, David. “Evaluation of chimeric virus-like particles, capsomeres and bacterial minicells as vaccine delivery platforms.” 2014. Thesis, University of Queensland. Accessed April 13, 2021. http://espace.library.uq.edu.au/view/UQ:347062.

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

MLA Handbook (7th Edition):

Pattinson, David. “Evaluation of chimeric virus-like particles, capsomeres and bacterial minicells as vaccine delivery platforms.” 2014. Web. 13 Apr 2021.

Vancouver:

Pattinson D. Evaluation of chimeric virus-like particles, capsomeres and bacterial minicells as vaccine delivery platforms. [Internet] [Thesis]. University of Queensland; 2014. [cited 2021 Apr 13]. Available from: http://espace.library.uq.edu.au/view/UQ:347062.

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

Council of Science Editors:

Pattinson D. Evaluation of chimeric virus-like particles, capsomeres and bacterial minicells as vaccine delivery platforms. [Thesis]. University of Queensland; 2014. Available from: http://espace.library.uq.edu.au/view/UQ:347062

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

4. フローレス, マリアジョリナルー. Characterization of glycosylphosphatidylinositol-anchored ceruloplasmin enriched in the apical plasma membrane of rat hepatocytes : ラット肝細胞の頂端面側細胞膜に局在するGPI-セルロプラスミンの特性に関する研究.

Degree: 博士(医学), 2017, Akita University / 秋田大学

 Aim: Ceruloplasmin (Cp) is an acute-phase protein and a member of the multicopper oxidase family of enzymes. It has been implicated in iron metabolism because… (more)

Subjects/Keywords: apical membrane; ceruloplasmin; GPI-Cp; hepatocyte

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APA (6th Edition):

フローレス, . (2017). Characterization of glycosylphosphatidylinositol-anchored ceruloplasmin enriched in the apical plasma membrane of rat hepatocytes : ラット肝細胞の頂端面側細胞膜に局在するGPI-セルロプラスミンの特性に関する研究. (Thesis). Akita University / 秋田大学. Retrieved from http://hdl.handle.net/10295/2509

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):

フローレス, マリアジョリナルー. “Characterization of glycosylphosphatidylinositol-anchored ceruloplasmin enriched in the apical plasma membrane of rat hepatocytes : ラット肝細胞の頂端面側細胞膜に局在するGPI-セルロプラスミンの特性に関する研究.” 2017. Thesis, Akita University / 秋田大学. Accessed April 13, 2021. http://hdl.handle.net/10295/2509.

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

MLA Handbook (7th Edition):

フローレス, マリアジョリナルー. “Characterization of glycosylphosphatidylinositol-anchored ceruloplasmin enriched in the apical plasma membrane of rat hepatocytes : ラット肝細胞の頂端面側細胞膜に局在するGPI-セルロプラスミンの特性に関する研究.” 2017. Web. 13 Apr 2021.

Vancouver:

フローレス . Characterization of glycosylphosphatidylinositol-anchored ceruloplasmin enriched in the apical plasma membrane of rat hepatocytes : ラット肝細胞の頂端面側細胞膜に局在するGPI-セルロプラスミンの特性に関する研究. [Internet] [Thesis]. Akita University / 秋田大学; 2017. [cited 2021 Apr 13]. Available from: http://hdl.handle.net/10295/2509.

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

Council of Science Editors:

フローレス . Characterization of glycosylphosphatidylinositol-anchored ceruloplasmin enriched in the apical plasma membrane of rat hepatocytes : ラット肝細胞の頂端面側細胞膜に局在するGPI-セルロプラスミンの特性に関する研究. [Thesis]. Akita University / 秋田大学; 2017. Available from: http://hdl.handle.net/10295/2509

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

5. SONG ZHENYING. Amino acid substitutions in the epstein-barr virus associated oncogene latent membrane protein 1 impact upon the immunogenicity of Nasopharyngeal carcinoma cells.

Degree: 2009, National University of Singapore

Subjects/Keywords: Epstein-Barr Virus; latent membrane protein 1; nasopharyngeal carcinoma; antigen presentation

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APA (6th Edition):

ZHENYING, S. (2009). Amino acid substitutions in the epstein-barr virus associated oncogene latent membrane protein 1 impact upon the immunogenicity of Nasopharyngeal carcinoma cells. (Thesis). National University of Singapore. Retrieved from https://scholarbank.nus.edu.sg/handle/10635/28156

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):

ZHENYING, SONG. “Amino acid substitutions in the epstein-barr virus associated oncogene latent membrane protein 1 impact upon the immunogenicity of Nasopharyngeal carcinoma cells.” 2009. Thesis, National University of Singapore. Accessed April 13, 2021. https://scholarbank.nus.edu.sg/handle/10635/28156.

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

MLA Handbook (7th Edition):

ZHENYING, SONG. “Amino acid substitutions in the epstein-barr virus associated oncogene latent membrane protein 1 impact upon the immunogenicity of Nasopharyngeal carcinoma cells.” 2009. Web. 13 Apr 2021.

Vancouver:

ZHENYING S. Amino acid substitutions in the epstein-barr virus associated oncogene latent membrane protein 1 impact upon the immunogenicity of Nasopharyngeal carcinoma cells. [Internet] [Thesis]. National University of Singapore; 2009. [cited 2021 Apr 13]. Available from: https://scholarbank.nus.edu.sg/handle/10635/28156.

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

Council of Science Editors:

ZHENYING S. Amino acid substitutions in the epstein-barr virus associated oncogene latent membrane protein 1 impact upon the immunogenicity of Nasopharyngeal carcinoma cells. [Thesis]. National University of Singapore; 2009. Available from: https://scholarbank.nus.edu.sg/handle/10635/28156

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


Johannes Gutenberg Universität Mainz

6. Fine, Tamir. Mapping the elastic response of epithelial apical cell membranes suspended across porous array.

Degree: 2009, Johannes Gutenberg Universität Mainz

 As the elastic response of cell membranes to mechanical stimuli plays a key role in various cellular processes, novel biophysical strategies to quantify the elasticity… (more)

Subjects/Keywords: AFM, Elasticity, Apical Membrane, Indentation; Natural sciences and mathematics

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APA (6th Edition):

Fine, T. (2009). Mapping the elastic response of epithelial apical cell membranes suspended across porous array. (Doctoral Dissertation). Johannes Gutenberg Universität Mainz. Retrieved from http://ubm.opus.hbz-nrw.de/volltexte/2010/2174/

Chicago Manual of Style (16th Edition):

Fine, Tamir. “Mapping the elastic response of epithelial apical cell membranes suspended across porous array.” 2009. Doctoral Dissertation, Johannes Gutenberg Universität Mainz. Accessed April 13, 2021. http://ubm.opus.hbz-nrw.de/volltexte/2010/2174/.

MLA Handbook (7th Edition):

Fine, Tamir. “Mapping the elastic response of epithelial apical cell membranes suspended across porous array.” 2009. Web. 13 Apr 2021.

Vancouver:

Fine T. Mapping the elastic response of epithelial apical cell membranes suspended across porous array. [Internet] [Doctoral dissertation]. Johannes Gutenberg Universität Mainz; 2009. [cited 2021 Apr 13]. Available from: http://ubm.opus.hbz-nrw.de/volltexte/2010/2174/.

Council of Science Editors:

Fine T. Mapping the elastic response of epithelial apical cell membranes suspended across porous array. [Doctoral Dissertation]. Johannes Gutenberg Universität Mainz; 2009. Available from: http://ubm.opus.hbz-nrw.de/volltexte/2010/2174/


University of Guelph

7. Lackeyram, Dale, Anthony. Expression of the Small Intestinal Apical Membrane Hydrolases in the Early-Weaned Piglet.

Degree: PhD, Department of Animal and Poultry Science, 2012, University of Guelph

 The small intestinal mucosal apical hydrolases are essential to the terminal digestion of enteral nutrients such as carbohydrates, proteins, fats and phosphates, and non-immune defense.… (more)

Subjects/Keywords: Early Weaning; Small Intestinal Hydrolases; Apical membrane hydrolases

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APA (6th Edition):

Lackeyram, Dale, A. (2012). Expression of the Small Intestinal Apical Membrane Hydrolases in the Early-Weaned Piglet. (Doctoral Dissertation). University of Guelph. Retrieved from https://atrium.lib.uoguelph.ca/xmlui/handle/10214/3628

Chicago Manual of Style (16th Edition):

Lackeyram, Dale, Anthony. “Expression of the Small Intestinal Apical Membrane Hydrolases in the Early-Weaned Piglet.” 2012. Doctoral Dissertation, University of Guelph. Accessed April 13, 2021. https://atrium.lib.uoguelph.ca/xmlui/handle/10214/3628.

MLA Handbook (7th Edition):

Lackeyram, Dale, Anthony. “Expression of the Small Intestinal Apical Membrane Hydrolases in the Early-Weaned Piglet.” 2012. Web. 13 Apr 2021.

Vancouver:

Lackeyram, Dale A. Expression of the Small Intestinal Apical Membrane Hydrolases in the Early-Weaned Piglet. [Internet] [Doctoral dissertation]. University of Guelph; 2012. [cited 2021 Apr 13]. Available from: https://atrium.lib.uoguelph.ca/xmlui/handle/10214/3628.

Council of Science Editors:

Lackeyram, Dale A. Expression of the Small Intestinal Apical Membrane Hydrolases in the Early-Weaned Piglet. [Doctoral Dissertation]. University of Guelph; 2012. Available from: https://atrium.lib.uoguelph.ca/xmlui/handle/10214/3628

8. Lentini, Gaëlle. Identification de nouvelles protéines régulées différentiellement au cours du cycle cellulaire de Toxoplasma gondii : Identification of new proteins differentially regulated along the cell cycle of Toxoplasma gondii.

Degree: Docteur es, Biologie Santé, 2015, Montpellier

Toxoplasma gondii est un protiste apicomplexe responsable de la toxoplasmose. Ce parasite intracellulaire obligatoire possède des organites sécrétoires apicaux dont les rhoptries qui contiennent des… (more)

Subjects/Keywords: Toxoplasma gondii; Apicomplexes; Rhoptries; Protease; Complexe membranaire interne; Complexe apical; Toxoplasma gondii; Apicomplexa; Rhoptry; Protease; Inner membrane complex; Apical complex

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APA (6th Edition):

Lentini, G. (2015). Identification de nouvelles protéines régulées différentiellement au cours du cycle cellulaire de Toxoplasma gondii : Identification of new proteins differentially regulated along the cell cycle of Toxoplasma gondii. (Doctoral Dissertation). Montpellier. Retrieved from http://www.theses.fr/2015MONTT049

Chicago Manual of Style (16th Edition):

Lentini, Gaëlle. “Identification de nouvelles protéines régulées différentiellement au cours du cycle cellulaire de Toxoplasma gondii : Identification of new proteins differentially regulated along the cell cycle of Toxoplasma gondii.” 2015. Doctoral Dissertation, Montpellier. Accessed April 13, 2021. http://www.theses.fr/2015MONTT049.

MLA Handbook (7th Edition):

Lentini, Gaëlle. “Identification de nouvelles protéines régulées différentiellement au cours du cycle cellulaire de Toxoplasma gondii : Identification of new proteins differentially regulated along the cell cycle of Toxoplasma gondii.” 2015. Web. 13 Apr 2021.

Vancouver:

Lentini G. Identification de nouvelles protéines régulées différentiellement au cours du cycle cellulaire de Toxoplasma gondii : Identification of new proteins differentially regulated along the cell cycle of Toxoplasma gondii. [Internet] [Doctoral dissertation]. Montpellier; 2015. [cited 2021 Apr 13]. Available from: http://www.theses.fr/2015MONTT049.

Council of Science Editors:

Lentini G. Identification de nouvelles protéines régulées différentiellement au cours du cycle cellulaire de Toxoplasma gondii : Identification of new proteins differentially regulated along the cell cycle of Toxoplasma gondii. [Doctoral Dissertation]. Montpellier; 2015. Available from: http://www.theses.fr/2015MONTT049

9. Tulio Lorenzo Olano Dextre. Susceptibilidade genética a periodontite apical crônica em indivíduos com fissura labiopalatina: estudo caso-controle.

Degree: 2016, University of São Paulo

 A periodontite apical é um processo inflamatório que ocorre na região do periápice, em decorrência de contaminação microbiana do sistema de canais que se origina… (more)

Subjects/Keywords: Fenda Labial; Fissura Palatina; Metaloproteinase da Membrana; Periodontite Apical; Apical Periodontitis; Cleft Lip; Cleft Palate; Matrix Metalloproteinases; Membrane-Associated

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APA (6th Edition):

Dextre, T. L. O. (2016). Susceptibilidade genética a periodontite apical crônica em indivíduos com fissura labiopalatina: estudo caso-controle. (Doctoral Dissertation). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/61/61132/tde-18102016-154607/

Chicago Manual of Style (16th Edition):

Dextre, Tulio Lorenzo Olano. “Susceptibilidade genética a periodontite apical crônica em indivíduos com fissura labiopalatina: estudo caso-controle.” 2016. Doctoral Dissertation, University of São Paulo. Accessed April 13, 2021. http://www.teses.usp.br/teses/disponiveis/61/61132/tde-18102016-154607/.

MLA Handbook (7th Edition):

Dextre, Tulio Lorenzo Olano. “Susceptibilidade genética a periodontite apical crônica em indivíduos com fissura labiopalatina: estudo caso-controle.” 2016. Web. 13 Apr 2021.

Vancouver:

Dextre TLO. Susceptibilidade genética a periodontite apical crônica em indivíduos com fissura labiopalatina: estudo caso-controle. [Internet] [Doctoral dissertation]. University of São Paulo; 2016. [cited 2021 Apr 13]. Available from: http://www.teses.usp.br/teses/disponiveis/61/61132/tde-18102016-154607/.

Council of Science Editors:

Dextre TLO. Susceptibilidade genética a periodontite apical crônica em indivíduos com fissura labiopalatina: estudo caso-controle. [Doctoral Dissertation]. University of São Paulo; 2016. Available from: http://www.teses.usp.br/teses/disponiveis/61/61132/tde-18102016-154607/


University of Southern California

10. Sura, Asmiti Vivek. Characterization of the retromer complex of proteins in gastric parietal cells.

Degree: MS, Biochemistry and Molecular Biology, 2013, University of Southern California

 Gastric acid secretion involves the regulated recycling of the H, K-ATPase to and from the apical membrane of parietal cells. All of the steps in… (more)

Subjects/Keywords: apical membrane recycling; gastric microsomes; H K-ATPase; hydrogen-potassium-adenosinetriphosphatase; retromer; tubulovesicles

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APA (6th Edition):

Sura, A. V. (2013). Characterization of the retromer complex of proteins in gastric parietal cells. (Masters Thesis). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/307627/rec/1312

Chicago Manual of Style (16th Edition):

Sura, Asmiti Vivek. “Characterization of the retromer complex of proteins in gastric parietal cells.” 2013. Masters Thesis, University of Southern California. Accessed April 13, 2021. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/307627/rec/1312.

MLA Handbook (7th Edition):

Sura, Asmiti Vivek. “Characterization of the retromer complex of proteins in gastric parietal cells.” 2013. Web. 13 Apr 2021.

Vancouver:

Sura AV. Characterization of the retromer complex of proteins in gastric parietal cells. [Internet] [Masters thesis]. University of Southern California; 2013. [cited 2021 Apr 13]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/307627/rec/1312.

Council of Science Editors:

Sura AV. Characterization of the retromer complex of proteins in gastric parietal cells. [Masters Thesis]. University of Southern California; 2013. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/307627/rec/1312

11. Brar, Harmenjit Singh. Triple Positive Microparticles as a “Liquid Biopsy” for Risk Stratification of Prostate Cancer.

Degree: 2017, University of Western Ontario

 Prostate cancer remains a substantial contributor to cancer-related mortality worldwide. Current screening methods include obtaining a PSA blood test. However, controversy surrounds its use as… (more)

Subjects/Keywords: Prostate Cancer; Extracellular Vesicles; Prostate Specific Membrane Antigen; Six-transmembrane Epithelial Antigen of the Prostate-1; GHSR1a; CD151; Surgery; Urology

…Doubling Time PSMA Prostate Specific Membrane Antigen ROC Receiver Operating Curve ROI… …transmembrane Epithelial Antigen of the Prostate-1 TCGA The Cancer Genome Atlas TMA Tissue… …using metastatic prostate cancer patient plasma. For Prostate Specific Membrane Antigen clone… …study (A). For Six Transmembrane Antigen of Prostate-1 conjugated with Alexa Fluor… …secretagogue receptor HG PIN High Grade Prostatic Intraepithelial Neoplasia IGF-1 Insulin-like… 

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APA (6th Edition):

Brar, H. S. (2017). Triple Positive Microparticles as a “Liquid Biopsy” for Risk Stratification of Prostate Cancer. (Thesis). University of Western Ontario. Retrieved from https://ir.lib.uwo.ca/etd/4933

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):

Brar, Harmenjit Singh. “Triple Positive Microparticles as a “Liquid Biopsy” for Risk Stratification of Prostate Cancer.” 2017. Thesis, University of Western Ontario. Accessed April 13, 2021. https://ir.lib.uwo.ca/etd/4933.

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

MLA Handbook (7th Edition):

Brar, Harmenjit Singh. “Triple Positive Microparticles as a “Liquid Biopsy” for Risk Stratification of Prostate Cancer.” 2017. Web. 13 Apr 2021.

Vancouver:

Brar HS. Triple Positive Microparticles as a “Liquid Biopsy” for Risk Stratification of Prostate Cancer. [Internet] [Thesis]. University of Western Ontario; 2017. [cited 2021 Apr 13]. Available from: https://ir.lib.uwo.ca/etd/4933.

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

Council of Science Editors:

Brar HS. Triple Positive Microparticles as a “Liquid Biopsy” for Risk Stratification of Prostate Cancer. [Thesis]. University of Western Ontario; 2017. Available from: https://ir.lib.uwo.ca/etd/4933

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


Cornell University

12. Brown, Joel. INVESTIGATING MAMMALIAN DEVELOPMENT USING MOUSE FORWARD GENETICS.

Degree: PhD, Genetics and Development, 2018, Cornell University

 Forward genetics allows the identification of novel genes involved in a particular biological process. We performed an ENU forward mutagenesis screen in mice aimed at… (more)

Subjects/Keywords: calcium; Actomyosin; Apical Constriction; Cofilin 1; Neural Tube; SPCA1; Developmental biology; Genetics; Molecular biology

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APA (6th Edition):

Brown, J. (2018). INVESTIGATING MAMMALIAN DEVELOPMENT USING MOUSE FORWARD GENETICS. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/59291

Chicago Manual of Style (16th Edition):

Brown, Joel. “INVESTIGATING MAMMALIAN DEVELOPMENT USING MOUSE FORWARD GENETICS.” 2018. Doctoral Dissertation, Cornell University. Accessed April 13, 2021. http://hdl.handle.net/1813/59291.

MLA Handbook (7th Edition):

Brown, Joel. “INVESTIGATING MAMMALIAN DEVELOPMENT USING MOUSE FORWARD GENETICS.” 2018. Web. 13 Apr 2021.

Vancouver:

Brown J. INVESTIGATING MAMMALIAN DEVELOPMENT USING MOUSE FORWARD GENETICS. [Internet] [Doctoral dissertation]. Cornell University; 2018. [cited 2021 Apr 13]. Available from: http://hdl.handle.net/1813/59291.

Council of Science Editors:

Brown J. INVESTIGATING MAMMALIAN DEVELOPMENT USING MOUSE FORWARD GENETICS. [Doctoral Dissertation]. Cornell University; 2018. Available from: http://hdl.handle.net/1813/59291


NSYSU

13. Kao, Pei-Hsiu. Molecular mechanism of membrane components on modulating membrane-damaging activity of Naja naja atra cardiotoxins.

Degree: PhD, Institute of Biomedical Sciences, 2012, NSYSU

 Naja naja atra Cardiotoxins (CTXs), basic polypeptides of 60 amino acid residues adopt a three-fingered loop-folding topology and show cytotoxicity for human tissues in targeting… (more)

Subjects/Keywords: phospholipid vesicle; H-antigen; cardiolipin; cardiotoxin; membrane-damaging activity; sphingomyelin

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APA (6th Edition):

Kao, P. (2012). Molecular mechanism of membrane components on modulating membrane-damaging activity of Naja naja atra cardiotoxins. (Doctoral Dissertation). NSYSU. Retrieved from http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0706112-155756

Chicago Manual of Style (16th Edition):

Kao, Pei-Hsiu. “Molecular mechanism of membrane components on modulating membrane-damaging activity of Naja naja atra cardiotoxins.” 2012. Doctoral Dissertation, NSYSU. Accessed April 13, 2021. http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0706112-155756.

MLA Handbook (7th Edition):

Kao, Pei-Hsiu. “Molecular mechanism of membrane components on modulating membrane-damaging activity of Naja naja atra cardiotoxins.” 2012. Web. 13 Apr 2021.

Vancouver:

Kao P. Molecular mechanism of membrane components on modulating membrane-damaging activity of Naja naja atra cardiotoxins. [Internet] [Doctoral dissertation]. NSYSU; 2012. [cited 2021 Apr 13]. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0706112-155756.

Council of Science Editors:

Kao P. Molecular mechanism of membrane components on modulating membrane-damaging activity of Naja naja atra cardiotoxins. [Doctoral Dissertation]. NSYSU; 2012. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0706112-155756


University of Maryland

14. Miller, Heather. The regulation of B cell activation by membrane damage and antigen density.

Degree: Cell Biology & Molecular Genetics, 2015, University of Maryland

 Antibodies generated by B cells neutralize pathogens and pathogen-secreted toxins and flag them for immune clearance. Antibody responses are initiated via binding of cognate antigen(more)

Subjects/Keywords: Immunology; Cellular biology; antigen density; B cell; membrane repair

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APA (6th Edition):

Miller, H. (2015). The regulation of B cell activation by membrane damage and antigen density. (Thesis). University of Maryland. Retrieved from http://hdl.handle.net/1903/16960

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):

Miller, Heather. “The regulation of B cell activation by membrane damage and antigen density.” 2015. Thesis, University of Maryland. Accessed April 13, 2021. http://hdl.handle.net/1903/16960.

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

MLA Handbook (7th Edition):

Miller, Heather. “The regulation of B cell activation by membrane damage and antigen density.” 2015. Web. 13 Apr 2021.

Vancouver:

Miller H. The regulation of B cell activation by membrane damage and antigen density. [Internet] [Thesis]. University of Maryland; 2015. [cited 2021 Apr 13]. Available from: http://hdl.handle.net/1903/16960.

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

Council of Science Editors:

Miller H. The regulation of B cell activation by membrane damage and antigen density. [Thesis]. University of Maryland; 2015. Available from: http://hdl.handle.net/1903/16960

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


University of New South Wales

15. Jin, Dongbin. Stimulation of CD8 T cells with membrane vesicles prepared from antigen presenting cells.

Degree: Clinical School - St Vincent's Hospital, 2015, University of New South Wales

 Immunotherapy has emerged as a promising tool to treat diseases via enhancing or suppressing immune responses of T cells. For infectious diseases and cancer, inducing… (more)

Subjects/Keywords: Membrane vesicle; Immunotherapy; CD8 T cell; Antigen presenting cell; Dendritic cell

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APA (6th Edition):

Jin, D. (2015). Stimulation of CD8 T cells with membrane vesicles prepared from antigen presenting cells. (Doctoral Dissertation). University of New South Wales. Retrieved from http://handle.unsw.edu.au/1959.4/54605 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:35345/SOURCE02?view=true

Chicago Manual of Style (16th Edition):

Jin, Dongbin. “Stimulation of CD8 T cells with membrane vesicles prepared from antigen presenting cells.” 2015. Doctoral Dissertation, University of New South Wales. Accessed April 13, 2021. http://handle.unsw.edu.au/1959.4/54605 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:35345/SOURCE02?view=true.

MLA Handbook (7th Edition):

Jin, Dongbin. “Stimulation of CD8 T cells with membrane vesicles prepared from antigen presenting cells.” 2015. Web. 13 Apr 2021.

Vancouver:

Jin D. Stimulation of CD8 T cells with membrane vesicles prepared from antigen presenting cells. [Internet] [Doctoral dissertation]. University of New South Wales; 2015. [cited 2021 Apr 13]. Available from: http://handle.unsw.edu.au/1959.4/54605 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:35345/SOURCE02?view=true.

Council of Science Editors:

Jin D. Stimulation of CD8 T cells with membrane vesicles prepared from antigen presenting cells. [Doctoral Dissertation]. University of New South Wales; 2015. Available from: http://handle.unsw.edu.au/1959.4/54605 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:35345/SOURCE02?view=true


University of Pennsylvania

16. Santoro, Stephen. T Cells Bearing a Chimeric Antigen Receptor Against the Tumor Vasculature Destroy the Tumor Endothelium and Result in Tumor Regression.

Degree: 2014, University of Pennsylvania

 Aberrant blood vessels enable tumor growth, provide a barrier to immune infiltration, and serve as a source of pro-tumorigenic signals. Targeting tumor blood vessels for… (more)

Subjects/Keywords: Adoptive therapy; Chimeric antigen receptor; Endothelial cells; Prostate-specific membrane antigen; Vascular disruption; Biology; Cell Biology; Oncology

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APA (6th Edition):

Santoro, S. (2014). T Cells Bearing a Chimeric Antigen Receptor Against the Tumor Vasculature Destroy the Tumor Endothelium and Result in Tumor Regression. (Thesis). University of Pennsylvania. Retrieved from https://repository.upenn.edu/edissertations/1432

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):

Santoro, Stephen. “T Cells Bearing a Chimeric Antigen Receptor Against the Tumor Vasculature Destroy the Tumor Endothelium and Result in Tumor Regression.” 2014. Thesis, University of Pennsylvania. Accessed April 13, 2021. https://repository.upenn.edu/edissertations/1432.

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

MLA Handbook (7th Edition):

Santoro, Stephen. “T Cells Bearing a Chimeric Antigen Receptor Against the Tumor Vasculature Destroy the Tumor Endothelium and Result in Tumor Regression.” 2014. Web. 13 Apr 2021.

Vancouver:

Santoro S. T Cells Bearing a Chimeric Antigen Receptor Against the Tumor Vasculature Destroy the Tumor Endothelium and Result in Tumor Regression. [Internet] [Thesis]. University of Pennsylvania; 2014. [cited 2021 Apr 13]. Available from: https://repository.upenn.edu/edissertations/1432.

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

Council of Science Editors:

Santoro S. T Cells Bearing a Chimeric Antigen Receptor Against the Tumor Vasculature Destroy the Tumor Endothelium and Result in Tumor Regression. [Thesis]. University of Pennsylvania; 2014. Available from: https://repository.upenn.edu/edissertations/1432

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

17. Suresh, Shruthy. The Integrated Stress Response Pathway Regulates PD-L1 Translation in Human Lung Cancer.

Degree: 2019, University of Texas Southwestern Medical Center

The student had requested that her name appear as "Shruthy Suresh" on the ETD record even though her name appears as "Shruthy Suresh Aggarwal" in… (more)

Subjects/Keywords: B7-H1 Antigen; Immunotherapy; Lung Neoplasms; Programmed Cell Death 1 Receptor

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APA (6th Edition):

Suresh, S. (2019). The Integrated Stress Response Pathway Regulates PD-L1 Translation in Human Lung Cancer. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/6624

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):

Suresh, Shruthy. “The Integrated Stress Response Pathway Regulates PD-L1 Translation in Human Lung Cancer.” 2019. Thesis, University of Texas Southwestern Medical Center. Accessed April 13, 2021. http://hdl.handle.net/2152.5/6624.

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

MLA Handbook (7th Edition):

Suresh, Shruthy. “The Integrated Stress Response Pathway Regulates PD-L1 Translation in Human Lung Cancer.” 2019. Web. 13 Apr 2021.

Vancouver:

Suresh S. The Integrated Stress Response Pathway Regulates PD-L1 Translation in Human Lung Cancer. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2019. [cited 2021 Apr 13]. Available from: http://hdl.handle.net/2152.5/6624.

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

Council of Science Editors:

Suresh S. The Integrated Stress Response Pathway Regulates PD-L1 Translation in Human Lung Cancer. [Thesis]. University of Texas Southwestern Medical Center; 2019. Available from: http://hdl.handle.net/2152.5/6624

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


University of Melbourne

18. Selck, Claudia. New approaches to induce tolerance in autoantigen-specific memory T cells in type 1 diabetes.

Degree: 2018, University of Melbourne

 Autoimmune disorders like type 1 diabetes (T1D) result from the failure of immune tolerance mechanisms. Antigen-specific therapy constitutes an attractive approach to re-establish a tolerant… (more)

Subjects/Keywords: Type 1 diabetes; tolerance; antigen; memory T cells

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APA (6th Edition):

Selck, C. (2018). New approaches to induce tolerance in autoantigen-specific memory T cells in type 1 diabetes. (Doctoral Dissertation). University of Melbourne. Retrieved from http://hdl.handle.net/11343/220001

Chicago Manual of Style (16th Edition):

Selck, Claudia. “New approaches to induce tolerance in autoantigen-specific memory T cells in type 1 diabetes.” 2018. Doctoral Dissertation, University of Melbourne. Accessed April 13, 2021. http://hdl.handle.net/11343/220001.

MLA Handbook (7th Edition):

Selck, Claudia. “New approaches to induce tolerance in autoantigen-specific memory T cells in type 1 diabetes.” 2018. Web. 13 Apr 2021.

Vancouver:

Selck C. New approaches to induce tolerance in autoantigen-specific memory T cells in type 1 diabetes. [Internet] [Doctoral dissertation]. University of Melbourne; 2018. [cited 2021 Apr 13]. Available from: http://hdl.handle.net/11343/220001.

Council of Science Editors:

Selck C. New approaches to induce tolerance in autoantigen-specific memory T cells in type 1 diabetes. [Doctoral Dissertation]. University of Melbourne; 2018. Available from: http://hdl.handle.net/11343/220001


Georgia Tech

19. Li, Kaitao. 2D kinetic study of of PD-1 interaction and its inhibition of T-cell antigen recognition.

Degree: PhD, Biomedical Engineering (Joint GT/Emory Department), 2016, Georgia Tech

 Programmed death-1 (PD-1) is an immune-checkpoint receptor with its primary function to maintain peripheral tolerance of the adaptive immune responses. The importance of PD-1 is… (more)

Subjects/Keywords: Programmed death-1; 2D kinetics; T-cell antigen recognition; CD8, CD222

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APA (6th Edition):

Li, K. (2016). 2D kinetic study of of PD-1 interaction and its inhibition of T-cell antigen recognition. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/58608

Chicago Manual of Style (16th Edition):

Li, Kaitao. “2D kinetic study of of PD-1 interaction and its inhibition of T-cell antigen recognition.” 2016. Doctoral Dissertation, Georgia Tech. Accessed April 13, 2021. http://hdl.handle.net/1853/58608.

MLA Handbook (7th Edition):

Li, Kaitao. “2D kinetic study of of PD-1 interaction and its inhibition of T-cell antigen recognition.” 2016. Web. 13 Apr 2021.

Vancouver:

Li K. 2D kinetic study of of PD-1 interaction and its inhibition of T-cell antigen recognition. [Internet] [Doctoral dissertation]. Georgia Tech; 2016. [cited 2021 Apr 13]. Available from: http://hdl.handle.net/1853/58608.

Council of Science Editors:

Li K. 2D kinetic study of of PD-1 interaction and its inhibition of T-cell antigen recognition. [Doctoral Dissertation]. Georgia Tech; 2016. Available from: http://hdl.handle.net/1853/58608

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

Degree: 2016, James Madison University

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

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

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APA (6th Edition):

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

Chicago Manual of Style (16th Edition):

Huschke, Allison M. “Hemostatic responses to exercise in a polycythemia vera patient.” 2016. Masters Thesis, James Madison University. Accessed April 13, 2021. https://commons.lib.jmu.edu/honors201019/247.

MLA Handbook (7th Edition):

Huschke, Allison M. “Hemostatic responses to exercise in a polycythemia vera patient.” 2016. Web. 13 Apr 2021.

Vancouver:

Huschke AM. Hemostatic responses to exercise in a polycythemia vera patient. [Internet] [Masters thesis]. James Madison University; 2016. [cited 2021 Apr 13]. Available from: https://commons.lib.jmu.edu/honors201019/247.

Council of Science Editors:

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


Lehigh University

21. Plucinsky, Sarah. The Biophysical Characterization of Caveolin-1.

Degree: PhD, Chemistry, 2018, Lehigh University

 The main topic of this doctoral dissertation is the biophysical characterization of caveolin-1. Caveolin-1 is an integral membrane protein that has been shown to be… (more)

Subjects/Keywords: Caveolae; Caveolin-1; Membrane protein Structure; Biochemistry

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APA (6th Edition):

Plucinsky, S. (2018). The Biophysical Characterization of Caveolin-1. (Doctoral Dissertation). Lehigh University. Retrieved from https://preserve.lehigh.edu/etd/4314

Chicago Manual of Style (16th Edition):

Plucinsky, Sarah. “The Biophysical Characterization of Caveolin-1.” 2018. Doctoral Dissertation, Lehigh University. Accessed April 13, 2021. https://preserve.lehigh.edu/etd/4314.

MLA Handbook (7th Edition):

Plucinsky, Sarah. “The Biophysical Characterization of Caveolin-1.” 2018. Web. 13 Apr 2021.

Vancouver:

Plucinsky S. The Biophysical Characterization of Caveolin-1. [Internet] [Doctoral dissertation]. Lehigh University; 2018. [cited 2021 Apr 13]. Available from: https://preserve.lehigh.edu/etd/4314.

Council of Science Editors:

Plucinsky S. The Biophysical Characterization of Caveolin-1. [Doctoral Dissertation]. Lehigh University; 2018. Available from: https://preserve.lehigh.edu/etd/4314

22. Brodovitch, Alexandre. Détection et première analyse d'antigènes par les lymphocytes T : Antigen detection and initial analysis by T lymphocytes.

Degree: Docteur es, Immunologie, 2014, Aix Marseille Université

Les lymphocytes T (LT) doivent analyser efficacement un nombre important de cellules présentatrices d'antigène (CPA) afin de détecter un antigène spécifique et d'initier une réponse… (more)

Subjects/Keywords: Lymphocyte T; Détection des Antigènes; Étalement; Mouvements de membrane; Tirfm; Irm; T-Lymphocyte; Antigen detection; Spreading; Membrane movement; Tirfm; Irm; 571

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APA (6th Edition):

Brodovitch, A. (2014). Détection et première analyse d'antigènes par les lymphocytes T : Antigen detection and initial analysis by T lymphocytes. (Doctoral Dissertation). Aix Marseille Université. Retrieved from http://www.theses.fr/2014AIXM4050

Chicago Manual of Style (16th Edition):

Brodovitch, Alexandre. “Détection et première analyse d'antigènes par les lymphocytes T : Antigen detection and initial analysis by T lymphocytes.” 2014. Doctoral Dissertation, Aix Marseille Université. Accessed April 13, 2021. http://www.theses.fr/2014AIXM4050.

MLA Handbook (7th Edition):

Brodovitch, Alexandre. “Détection et première analyse d'antigènes par les lymphocytes T : Antigen detection and initial analysis by T lymphocytes.” 2014. Web. 13 Apr 2021.

Vancouver:

Brodovitch A. Détection et première analyse d'antigènes par les lymphocytes T : Antigen detection and initial analysis by T lymphocytes. [Internet] [Doctoral dissertation]. Aix Marseille Université 2014. [cited 2021 Apr 13]. Available from: http://www.theses.fr/2014AIXM4050.

Council of Science Editors:

Brodovitch A. Détection et première analyse d'antigènes par les lymphocytes T : Antigen detection and initial analysis by T lymphocytes. [Doctoral Dissertation]. Aix Marseille Université 2014. Available from: http://www.theses.fr/2014AIXM4050

23. Brocqueville, Guillaume. Dualité fonctionnelle de LMP1 : implication dans l’apoptose et la transformation cellulaire : Functionnal duality of LMP1 : involvement in apoptosis and cellular transformation.

Degree: Docteur es, Biochimie et biologie moléculaire, 2011, Université Lille II – Droit et Santé

Le virus d’Epstein-Barr (EBV) est un herpèsvirus humain qui infecte plus de 90% de la population généralement de façon bénigne et asymptomatique. Cependant, de nombreuses… (more)

Subjects/Keywords: Survie cellulaire; LMP-1 (Latent membrane Protein-1); Cell survival

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APA (6th Edition):

Brocqueville, G. (2011). Dualité fonctionnelle de LMP1 : implication dans l’apoptose et la transformation cellulaire : Functionnal duality of LMP1 : involvement in apoptosis and cellular transformation. (Doctoral Dissertation). Université Lille II – Droit et Santé. Retrieved from http://www.theses.fr/2011LIL2S030

Chicago Manual of Style (16th Edition):

Brocqueville, Guillaume. “Dualité fonctionnelle de LMP1 : implication dans l’apoptose et la transformation cellulaire : Functionnal duality of LMP1 : involvement in apoptosis and cellular transformation.” 2011. Doctoral Dissertation, Université Lille II – Droit et Santé. Accessed April 13, 2021. http://www.theses.fr/2011LIL2S030.

MLA Handbook (7th Edition):

Brocqueville, Guillaume. “Dualité fonctionnelle de LMP1 : implication dans l’apoptose et la transformation cellulaire : Functionnal duality of LMP1 : involvement in apoptosis and cellular transformation.” 2011. Web. 13 Apr 2021.

Vancouver:

Brocqueville G. Dualité fonctionnelle de LMP1 : implication dans l’apoptose et la transformation cellulaire : Functionnal duality of LMP1 : involvement in apoptosis and cellular transformation. [Internet] [Doctoral dissertation]. Université Lille II – Droit et Santé 2011. [cited 2021 Apr 13]. Available from: http://www.theses.fr/2011LIL2S030.

Council of Science Editors:

Brocqueville G. Dualité fonctionnelle de LMP1 : implication dans l’apoptose et la transformation cellulaire : Functionnal duality of LMP1 : involvement in apoptosis and cellular transformation. [Doctoral Dissertation]. Université Lille II – Droit et Santé 2011. Available from: http://www.theses.fr/2011LIL2S030


NSYSU

24. Lin, Tung-cheng. Antiserum titer determination and adherence comparison of three major outer membrane proteins TSA56, TSA47 and TSA22 in Orientia tsutsugamushi.

Degree: Master, Biological Sciences, 2011, NSYSU

 Orientia tsutsugamushi, the causative agent of scrub typhus, is an obligate intracellular pathogen. Recent studies show that the complete genome sequence of Orientia tsutsugamushi have… (more)

Subjects/Keywords: antiserum immunoblots; outer membrane protein; type-specific antigen; Orientia tsutsugamushi; scrub typhus; adhesion assay

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APA (6th Edition):

Lin, T. (2011). Antiserum titer determination and adherence comparison of three major outer membrane proteins TSA56, TSA47 and TSA22 in Orientia tsutsugamushi. (Thesis). NSYSU. Retrieved from http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0907111-024719

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):

Lin, Tung-cheng. “Antiserum titer determination and adherence comparison of three major outer membrane proteins TSA56, TSA47 and TSA22 in Orientia tsutsugamushi.” 2011. Thesis, NSYSU. Accessed April 13, 2021. http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0907111-024719.

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

MLA Handbook (7th Edition):

Lin, Tung-cheng. “Antiserum titer determination and adherence comparison of three major outer membrane proteins TSA56, TSA47 and TSA22 in Orientia tsutsugamushi.” 2011. Web. 13 Apr 2021.

Vancouver:

Lin T. Antiserum titer determination and adherence comparison of three major outer membrane proteins TSA56, TSA47 and TSA22 in Orientia tsutsugamushi. [Internet] [Thesis]. NSYSU; 2011. [cited 2021 Apr 13]. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0907111-024719.

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

Council of Science Editors:

Lin T. Antiserum titer determination and adherence comparison of three major outer membrane proteins TSA56, TSA47 and TSA22 in Orientia tsutsugamushi. [Thesis]. NSYSU; 2011. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0907111-024719

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


Washington State University

25. [No author]. PROSTATE CANCER CELL CAPTURE USING IMMOBILIZED INHIBITORS OF PROSTATE-SPECIFIC MEMBRANE ANTIGEN .

Degree: 2011, Washington State University

 Prostate cancer, especially its metastasis to the bone, is the leading cause of death for men in the US. The development of bone metastasis is… (more)

Subjects/Keywords: Chemistry; circulating tumor cells; flow cytometry; magnetic beads; Prostate cancer; prostate-specific membrane antigen

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APA (6th Edition):

author], [. (2011). PROSTATE CANCER CELL CAPTURE USING IMMOBILIZED INHIBITORS OF PROSTATE-SPECIFIC MEMBRANE ANTIGEN . (Thesis). Washington State University. Retrieved from http://hdl.handle.net/2376/3543

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):

author], [No. “PROSTATE CANCER CELL CAPTURE USING IMMOBILIZED INHIBITORS OF PROSTATE-SPECIFIC MEMBRANE ANTIGEN .” 2011. Thesis, Washington State University. Accessed April 13, 2021. http://hdl.handle.net/2376/3543.

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

MLA Handbook (7th Edition):

author], [No. “PROSTATE CANCER CELL CAPTURE USING IMMOBILIZED INHIBITORS OF PROSTATE-SPECIFIC MEMBRANE ANTIGEN .” 2011. Web. 13 Apr 2021.

Vancouver:

author] [. PROSTATE CANCER CELL CAPTURE USING IMMOBILIZED INHIBITORS OF PROSTATE-SPECIFIC MEMBRANE ANTIGEN . [Internet] [Thesis]. Washington State University; 2011. [cited 2021 Apr 13]. Available from: http://hdl.handle.net/2376/3543.

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

Council of Science Editors:

author] [. PROSTATE CANCER CELL CAPTURE USING IMMOBILIZED INHIBITORS OF PROSTATE-SPECIFIC MEMBRANE ANTIGEN . [Thesis]. Washington State University; 2011. Available from: http://hdl.handle.net/2376/3543

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

26. [No author]. The Evolution of Phosphoramidates from Small-Molecule Inhibitors to Tunable Cleavable Linkers .

Degree: 2016, Washington State University

 During the development of a series of phosphoramidate-based inhibitors to prostate-specific membrane antigen, we observed a trend in increasing acid stability as the distance between… (more)

Subjects/Keywords: Organic chemistry; Cleavable linker; Drug conjugate; Drug delivery; Phosphoramidate; pH-tunable; Prostate-specific membrane antigen

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

APA (6th Edition):

author], [. (2016). The Evolution of Phosphoramidates from Small-Molecule Inhibitors to Tunable Cleavable Linkers . (Thesis). Washington State University. Retrieved from http://hdl.handle.net/2376/12074

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):

author], [No. “The Evolution of Phosphoramidates from Small-Molecule Inhibitors to Tunable Cleavable Linkers .” 2016. Thesis, Washington State University. Accessed April 13, 2021. http://hdl.handle.net/2376/12074.

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

MLA Handbook (7th Edition):

author], [No. “The Evolution of Phosphoramidates from Small-Molecule Inhibitors to Tunable Cleavable Linkers .” 2016. Web. 13 Apr 2021.

Vancouver:

author] [. The Evolution of Phosphoramidates from Small-Molecule Inhibitors to Tunable Cleavable Linkers . [Internet] [Thesis]. Washington State University; 2016. [cited 2021 Apr 13]. Available from: http://hdl.handle.net/2376/12074.

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

Council of Science Editors:

author] [. The Evolution of Phosphoramidates from Small-Molecule Inhibitors to Tunable Cleavable Linkers . [Thesis]. Washington State University; 2016. Available from: http://hdl.handle.net/2376/12074

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

27. DAI XILEI. Differential Signal Induction, Membrane Trafficking and Immune Effector Mediated by FcyRl Versus FcyRlla.

Degree: 2009, National University of Singapore

Subjects/Keywords: Fcgamma receptors; Membrane trafficking; Antigen presentation

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APA (6th Edition):

XILEI, D. (2009). Differential Signal Induction, Membrane Trafficking and Immune Effector Mediated by FcyRl Versus FcyRlla. (Thesis). National University of Singapore. Retrieved from https://scholarbank.nus.edu.sg/handle/10635/160955

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):

XILEI, DAI. “Differential Signal Induction, Membrane Trafficking and Immune Effector Mediated by FcyRl Versus FcyRlla.” 2009. Thesis, National University of Singapore. Accessed April 13, 2021. https://scholarbank.nus.edu.sg/handle/10635/160955.

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

MLA Handbook (7th Edition):

XILEI, DAI. “Differential Signal Induction, Membrane Trafficking and Immune Effector Mediated by FcyRl Versus FcyRlla.” 2009. Web. 13 Apr 2021.

Vancouver:

XILEI D. Differential Signal Induction, Membrane Trafficking and Immune Effector Mediated by FcyRl Versus FcyRlla. [Internet] [Thesis]. National University of Singapore; 2009. [cited 2021 Apr 13]. Available from: https://scholarbank.nus.edu.sg/handle/10635/160955.

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

Council of Science Editors:

XILEI D. Differential Signal Induction, Membrane Trafficking and Immune Effector Mediated by FcyRl Versus FcyRlla. [Thesis]. National University of Singapore; 2009. Available from: https://scholarbank.nus.edu.sg/handle/10635/160955

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


University of California – Irvine

28. Neek, Medea Babaie. Protein-Based Nanoparticles for Cancer Immunotherapy.

Degree: Chemical and Biochemical Engineering, 2019, University of California – Irvine

 Although progress has been made in conventional cancer therapy, cancer is still the second leading cause of death in the United States. Recently, a new… (more)

Subjects/Keywords: Immunology; Chemical engineering; Animal Survival; anti-PD-1; Cancer Antigen; Cancer Vaccine; Nanoparticles; Vaccine platform

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APA (6th Edition):

Neek, M. B. (2019). Protein-Based Nanoparticles for Cancer Immunotherapy. (Thesis). University of California – Irvine. Retrieved from http://www.escholarship.org/uc/item/0nq864zk

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):

Neek, Medea Babaie. “Protein-Based Nanoparticles for Cancer Immunotherapy.” 2019. Thesis, University of California – Irvine. Accessed April 13, 2021. http://www.escholarship.org/uc/item/0nq864zk.

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

MLA Handbook (7th Edition):

Neek, Medea Babaie. “Protein-Based Nanoparticles for Cancer Immunotherapy.” 2019. Web. 13 Apr 2021.

Vancouver:

Neek MB. Protein-Based Nanoparticles for Cancer Immunotherapy. [Internet] [Thesis]. University of California – Irvine; 2019. [cited 2021 Apr 13]. Available from: http://www.escholarship.org/uc/item/0nq864zk.

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

Council of Science Editors:

Neek MB. Protein-Based Nanoparticles for Cancer Immunotherapy. [Thesis]. University of California – Irvine; 2019. Available from: http://www.escholarship.org/uc/item/0nq864zk

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


University of Toronto

29. Liu, Feiyang (Victoria). Antigen-binding Fragments: Production for and Use in Crystallographic Studies.

Degree: 2013, University of Toronto

An immunoglobulin (IgG) consists of two antigen-binding fragments (Fab) connected to a crystallisable fragment through hinge regions. This thesis mainly investigates the production methods of… (more)

Subjects/Keywords: antigen-binding fragment; X-ray crystallography; HIV-1; broadly neutralizing monoclonal antibody; 0307

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

APA (6th Edition):

Liu, F. (. (2013). Antigen-binding Fragments: Production for and Use in Crystallographic Studies. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/43090

Chicago Manual of Style (16th Edition):

Liu, Feiyang (Victoria). “Antigen-binding Fragments: Production for and Use in Crystallographic Studies.” 2013. Masters Thesis, University of Toronto. Accessed April 13, 2021. http://hdl.handle.net/1807/43090.

MLA Handbook (7th Edition):

Liu, Feiyang (Victoria). “Antigen-binding Fragments: Production for and Use in Crystallographic Studies.” 2013. Web. 13 Apr 2021.

Vancouver:

Liu F(. Antigen-binding Fragments: Production for and Use in Crystallographic Studies. [Internet] [Masters thesis]. University of Toronto; 2013. [cited 2021 Apr 13]. Available from: http://hdl.handle.net/1807/43090.

Council of Science Editors:

Liu F(. Antigen-binding Fragments: Production for and Use in Crystallographic Studies. [Masters Thesis]. University of Toronto; 2013. Available from: http://hdl.handle.net/1807/43090


Boston University

30. Randhawa, Anantbir. A reduction in the RNA binding protein TIA1 protects against neurodegeneration, rescues behavioral deficits and prolongs survival.

Degree: MS, Medical Sciences, 2018, Boston University

 RNA binding proteins (RBPs) have been found to be frequently involved in neurodegenerative diseases (Ash 2014). Mutations in RBPs cause amyotrophic lateral sclerosis (ALS), spinocerebellar… (more)

Subjects/Keywords: Medicine; Neurodegeneration; Neuroinflammation; Stress granules; Tau; Tauopathies; T-cell intracellular antigen 1

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

APA (6th Edition):

Randhawa, A. (2018). A reduction in the RNA binding protein TIA1 protects against neurodegeneration, rescues behavioral deficits and prolongs survival. (Masters Thesis). Boston University. Retrieved from http://hdl.handle.net/2144/31265

Chicago Manual of Style (16th Edition):

Randhawa, Anantbir. “A reduction in the RNA binding protein TIA1 protects against neurodegeneration, rescues behavioral deficits and prolongs survival.” 2018. Masters Thesis, Boston University. Accessed April 13, 2021. http://hdl.handle.net/2144/31265.

MLA Handbook (7th Edition):

Randhawa, Anantbir. “A reduction in the RNA binding protein TIA1 protects against neurodegeneration, rescues behavioral deficits and prolongs survival.” 2018. Web. 13 Apr 2021.

Vancouver:

Randhawa A. A reduction in the RNA binding protein TIA1 protects against neurodegeneration, rescues behavioral deficits and prolongs survival. [Internet] [Masters thesis]. Boston University; 2018. [cited 2021 Apr 13]. Available from: http://hdl.handle.net/2144/31265.

Council of Science Editors:

Randhawa A. A reduction in the RNA binding protein TIA1 protects against neurodegeneration, rescues behavioral deficits and prolongs survival. [Masters Thesis]. Boston University; 2018. Available from: http://hdl.handle.net/2144/31265

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