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You searched for subject:(PACS 2 phosphofurin acidic cluster sorting protein 2 ). Showing records 1 – 30 of 34636 total matches.

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1. Atkins, Katelyn Mae. PACS-2 regulates SIRT 1-mediated deacetylation of p53 following DNA damage.

Degree: PhD, 2012, Oregon Health Sciences University

Subjects/Keywords: Membrane proteins; Sirtuins; Carrier proteins; DNA damage; Viral proteins; p53-AIP1 (p53-regulated apoptosis inducing protein 1); PACS-2 (phosphofurin acidic cluster sorting protein-2); Apoptosis Regulatory Proteins; Sirtuin 1; Vesicular Transport Proteins; DNA Damage; Viral Regulatory and Accessory Proteins

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

APA (6th Edition):

Atkins, K. M. (2012). PACS-2 regulates SIRT 1-mediated deacetylation of p53 following DNA damage. (Doctoral Dissertation). Oregon Health Sciences University. Retrieved from doi:10.6083/M4MG7MH2 ; http://digitalcommons.ohsu.edu/etd/862

Chicago Manual of Style (16th Edition):

Atkins, Katelyn Mae. “PACS-2 regulates SIRT 1-mediated deacetylation of p53 following DNA damage.” 2012. Doctoral Dissertation, Oregon Health Sciences University. Accessed June 05, 2020. doi:10.6083/M4MG7MH2 ; http://digitalcommons.ohsu.edu/etd/862.

MLA Handbook (7th Edition):

Atkins, Katelyn Mae. “PACS-2 regulates SIRT 1-mediated deacetylation of p53 following DNA damage.” 2012. Web. 05 Jun 2020.

Vancouver:

Atkins KM. PACS-2 regulates SIRT 1-mediated deacetylation of p53 following DNA damage. [Internet] [Doctoral dissertation]. Oregon Health Sciences University; 2012. [cited 2020 Jun 05]. Available from: doi:10.6083/M4MG7MH2 ; http://digitalcommons.ohsu.edu/etd/862.

Council of Science Editors:

Atkins KM. PACS-2 regulates SIRT 1-mediated deacetylation of p53 following DNA damage. [Doctoral Dissertation]. Oregon Health Sciences University; 2012. Available from: doi:10.6083/M4MG7MH2 ; http://digitalcommons.ohsu.edu/etd/862

2. 野中, 秀樹. ミクログリアの MAP2 陽性および GFAP 陽性細胞への分化転換機構に関する研究.

Degree: 博士(学術), 2016, Kyoto Institute of Technology / 京都工芸繊維大学

 ミクログリアは遊走能・貪食能および炎症性サイトカインの放出などにより脳内の免疫反応を担っているとともに神経栄養因子を分泌して神経系の維持および修復にも関与している中枢神経系のグリア細胞である.近年,ミクログリアが高濃度血清中でニューロンやアストロサイトへと分化転換する可能性を示唆する報告が出された.しかしながら,ミクログリアの神経系細胞への分化転換を支持する報告は依然として少なく,その分子メカニズムに関してはほとんどわかっていない.そこで本研究は,単離・精製したミクログリアがニューロンやアストロサイトへと分化転換することを確認し,その分子メカニズムおよび分化転換の促進方法についての検討を行い,以下の知見を得た. 第一章 ミクログリアの microtubule-associated protein 2 (MAP2) 陽性および glial fibrillary acidic protein (GFAP) 陽性細胞への分化転換に関する研究 単離・精製したミクログリアは,ミクログリアのマーカーである CD11b および ionized calcium binding adaptor molecule 1 (IBA-1) で染色したところ約 99% と高純度であった.既報に従い高濃度血清中で 2(more)

Subjects/Keywords: ミクログリア; 分化転換; microtubule-associated protein 2 (MAP2); glial fibrillary acidic protein (GFAP); 神経幹細胞; SOX2; Smad4; basic FGF (bFGF); fibroblast growth factor 2 (FGF2); FGFR1; FGFR2; FGFR3; SU5402; PD98059

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APA (6th Edition):

野中, . (2016). ミクログリアの MAP2 陽性および GFAP 陽性細胞への分化転換機構に関する研究. (Thesis). Kyoto Institute of Technology / 京都工芸繊維大学. Retrieved from http://hdl.handle.net/10212/2333

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):

野中, 秀樹. “ミクログリアの MAP2 陽性および GFAP 陽性細胞への分化転換機構に関する研究.” 2016. Thesis, Kyoto Institute of Technology / 京都工芸繊維大学. Accessed June 05, 2020. http://hdl.handle.net/10212/2333.

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

MLA Handbook (7th Edition):

野中, 秀樹. “ミクログリアの MAP2 陽性および GFAP 陽性細胞への分化転換機構に関する研究.” 2016. Web. 05 Jun 2020.

Vancouver:

野中 . ミクログリアの MAP2 陽性および GFAP 陽性細胞への分化転換機構に関する研究. [Internet] [Thesis]. Kyoto Institute of Technology / 京都工芸繊維大学; 2016. [cited 2020 Jun 05]. Available from: http://hdl.handle.net/10212/2333.

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

Council of Science Editors:

野中 . ミクログリアの MAP2 陽性および GFAP 陽性細胞への分化転換機構に関する研究. [Thesis]. Kyoto Institute of Technology / 京都工芸繊維大学; 2016. Available from: http://hdl.handle.net/10212/2333

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


University of Manchester

3. Rodriguez-Enriquez, Ricardo. Analysis of Bcl-2 family protein interactions in live cells by fluorescence recovery after photobleaching.

Degree: 2014, University of Manchester

 The Bcl-2 family of proteins strictly regulates the intrinsic pathway of apoptosis.Direct physical interactions between Bcl-2 proteins regulate mitochondrial outerpermeabilisation (MOMP), which occurs in response… (more)

Subjects/Keywords: Bcl-2 family protein; FRAP

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APA (6th Edition):

Rodriguez-Enriquez, R. (2014). Analysis of Bcl-2 family protein interactions in live cells by fluorescence recovery after photobleaching. (Doctoral Dissertation). University of Manchester. Retrieved from http://www.manchester.ac.uk/escholar/uk-ac-man-scw:228609

Chicago Manual of Style (16th Edition):

Rodriguez-Enriquez, Ricardo. “Analysis of Bcl-2 family protein interactions in live cells by fluorescence recovery after photobleaching.” 2014. Doctoral Dissertation, University of Manchester. Accessed June 05, 2020. http://www.manchester.ac.uk/escholar/uk-ac-man-scw:228609.

MLA Handbook (7th Edition):

Rodriguez-Enriquez, Ricardo. “Analysis of Bcl-2 family protein interactions in live cells by fluorescence recovery after photobleaching.” 2014. Web. 05 Jun 2020.

Vancouver:

Rodriguez-Enriquez R. Analysis of Bcl-2 family protein interactions in live cells by fluorescence recovery after photobleaching. [Internet] [Doctoral dissertation]. University of Manchester; 2014. [cited 2020 Jun 05]. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:228609.

Council of Science Editors:

Rodriguez-Enriquez R. Analysis of Bcl-2 family protein interactions in live cells by fluorescence recovery after photobleaching. [Doctoral Dissertation]. University of Manchester; 2014. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:228609


Wake Forest University

4. Kowalczewski, Christine Jane. Natural Polymeric Carriers for Local Delivery of Therapeutic Agents to Promote Enhanced Bone Regeneration.

Degree: 2014, Wake Forest University

 Bone has the innate ability to heal, but on occasion defects surpass a critical size capable of spontaneously healing. These critically-sized bone defects pose significant… (more)

Subjects/Keywords: Bone Morphogenetic Protein -2

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APA (6th Edition):

Kowalczewski, C. J. (2014). Natural Polymeric Carriers for Local Delivery of Therapeutic Agents to Promote Enhanced Bone Regeneration. (Thesis). Wake Forest University. Retrieved from http://hdl.handle.net/10339/47453

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):

Kowalczewski, Christine Jane. “Natural Polymeric Carriers for Local Delivery of Therapeutic Agents to Promote Enhanced Bone Regeneration.” 2014. Thesis, Wake Forest University. Accessed June 05, 2020. http://hdl.handle.net/10339/47453.

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

MLA Handbook (7th Edition):

Kowalczewski, Christine Jane. “Natural Polymeric Carriers for Local Delivery of Therapeutic Agents to Promote Enhanced Bone Regeneration.” 2014. Web. 05 Jun 2020.

Vancouver:

Kowalczewski CJ. Natural Polymeric Carriers for Local Delivery of Therapeutic Agents to Promote Enhanced Bone Regeneration. [Internet] [Thesis]. Wake Forest University; 2014. [cited 2020 Jun 05]. Available from: http://hdl.handle.net/10339/47453.

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

Council of Science Editors:

Kowalczewski CJ. Natural Polymeric Carriers for Local Delivery of Therapeutic Agents to Promote Enhanced Bone Regeneration. [Thesis]. Wake Forest University; 2014. Available from: http://hdl.handle.net/10339/47453

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


University of Missouri – Columbia

5. Thomas, William Donald, 1974-. In vitro and in vivo approaches to tumor targeting by phage display.

Degree: 2010, University of Missouri – Columbia

 [ACCESS RESTRICTED TO THE UNIVERSITY OF MISSOURI AT AUTHOR'S REQUEST.] Approximately 30% of breast cancers are linked with the over-expression of ErbB2. Because of its… (more)

Subjects/Keywords: Tumor proteins; Bacteriophages; HER-2 protein; HER-2 gene; Breast  – Cancer

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APA (6th Edition):

Thomas, William Donald, 1. (2010). In vitro and in vivo approaches to tumor targeting by phage display. (Thesis). University of Missouri – Columbia. Retrieved from https://doi.org/10.32469/10355/10348

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):

Thomas, William Donald, 1974-. “In vitro and in vivo approaches to tumor targeting by phage display.” 2010. Thesis, University of Missouri – Columbia. Accessed June 05, 2020. https://doi.org/10.32469/10355/10348.

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

MLA Handbook (7th Edition):

Thomas, William Donald, 1974-. “In vitro and in vivo approaches to tumor targeting by phage display.” 2010. Web. 05 Jun 2020.

Vancouver:

Thomas, William Donald 1. In vitro and in vivo approaches to tumor targeting by phage display. [Internet] [Thesis]. University of Missouri – Columbia; 2010. [cited 2020 Jun 05]. Available from: https://doi.org/10.32469/10355/10348.

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

Council of Science Editors:

Thomas, William Donald 1. In vitro and in vivo approaches to tumor targeting by phage display. [Thesis]. University of Missouri – Columbia; 2010. Available from: https://doi.org/10.32469/10355/10348

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


Georgia Tech

6. Priddy, Lauren B. Biomaterial strategies for improved bone healing with bone morphogenetic protein-2 delivery.

Degree: PhD, Biomedical Engineering (Joint GT/Emory Department), 2015, Georgia Tech

 This thesis investigated hybrid biomaterial systems with controlled strategies for bone morphogenetic protein-2 (BMP-2) delivery to promote structural and functional restoration of segmental bone defects.… (more)

Subjects/Keywords: Bone regeneration; Bone morphogenetic protein-2 (BMP-2); Heterotopic mineralization; Biomaterials

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APA (6th Edition):

Priddy, L. B. (2015). Biomaterial strategies for improved bone healing with bone morphogenetic protein-2 delivery. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/55531

Chicago Manual of Style (16th Edition):

Priddy, Lauren B. “Biomaterial strategies for improved bone healing with bone morphogenetic protein-2 delivery.” 2015. Doctoral Dissertation, Georgia Tech. Accessed June 05, 2020. http://hdl.handle.net/1853/55531.

MLA Handbook (7th Edition):

Priddy, Lauren B. “Biomaterial strategies for improved bone healing with bone morphogenetic protein-2 delivery.” 2015. Web. 05 Jun 2020.

Vancouver:

Priddy LB. Biomaterial strategies for improved bone healing with bone morphogenetic protein-2 delivery. [Internet] [Doctoral dissertation]. Georgia Tech; 2015. [cited 2020 Jun 05]. Available from: http://hdl.handle.net/1853/55531.

Council of Science Editors:

Priddy LB. Biomaterial strategies for improved bone healing with bone morphogenetic protein-2 delivery. [Doctoral Dissertation]. Georgia Tech; 2015. Available from: http://hdl.handle.net/1853/55531


Penn State University

7. Lapp, Daniel Wesley. Molecular Mechaisms of Astrocyte Protection Following Oxidative Stress.

Degree: PhD, Neuroscience, 2013, Penn State University

 Damage to the CNS following insults such as ischemia or traumatic injury is a critical issue due to the potentially devastating consequences and largely irreversible… (more)

Subjects/Keywords: Stat3; Uncoupling Protein 2; oxidative stress; astrocyte

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APA (6th Edition):

Lapp, D. W. (2013). Molecular Mechaisms of Astrocyte Protection Following Oxidative Stress. (Doctoral Dissertation). Penn State University. Retrieved from https://etda.libraries.psu.edu/catalog/23177

Chicago Manual of Style (16th Edition):

Lapp, Daniel Wesley. “Molecular Mechaisms of Astrocyte Protection Following Oxidative Stress.” 2013. Doctoral Dissertation, Penn State University. Accessed June 05, 2020. https://etda.libraries.psu.edu/catalog/23177.

MLA Handbook (7th Edition):

Lapp, Daniel Wesley. “Molecular Mechaisms of Astrocyte Protection Following Oxidative Stress.” 2013. Web. 05 Jun 2020.

Vancouver:

Lapp DW. Molecular Mechaisms of Astrocyte Protection Following Oxidative Stress. [Internet] [Doctoral dissertation]. Penn State University; 2013. [cited 2020 Jun 05]. Available from: https://etda.libraries.psu.edu/catalog/23177.

Council of Science Editors:

Lapp DW. Molecular Mechaisms of Astrocyte Protection Following Oxidative Stress. [Doctoral Dissertation]. Penn State University; 2013. Available from: https://etda.libraries.psu.edu/catalog/23177


University of Manchester

8. Rodriguez-Enriquez, Ricardo. Analysis of Bcl-2 family protein interactions in live cells by fluorescence recovery after photobleaching.

Degree: PhD, 2014, University of Manchester

 The Bcl-2 family of proteins strictly regulates the intrinsic pathway of apoptosis. Direct physical interactions between Bcl-2 proteins regulate mitochondrial outerpermeabilisation (MOMP), which occurs in… (more)

Subjects/Keywords: 570; Bcl-2 family protein, FRAP

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APA (6th Edition):

Rodriguez-Enriquez, R. (2014). Analysis of Bcl-2 family protein interactions in live cells by fluorescence recovery after photobleaching. (Doctoral Dissertation). University of Manchester. Retrieved from https://www.research.manchester.ac.uk/portal/en/theses/analysis-of-bcl2-family-protein-interactions-in-live-cells-by-fluorescence-recovery-after-photobleaching(aa5eb271-6e43-48f3-940d-f63763ea4629).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.764284

Chicago Manual of Style (16th Edition):

Rodriguez-Enriquez, Ricardo. “Analysis of Bcl-2 family protein interactions in live cells by fluorescence recovery after photobleaching.” 2014. Doctoral Dissertation, University of Manchester. Accessed June 05, 2020. https://www.research.manchester.ac.uk/portal/en/theses/analysis-of-bcl2-family-protein-interactions-in-live-cells-by-fluorescence-recovery-after-photobleaching(aa5eb271-6e43-48f3-940d-f63763ea4629).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.764284.

MLA Handbook (7th Edition):

Rodriguez-Enriquez, Ricardo. “Analysis of Bcl-2 family protein interactions in live cells by fluorescence recovery after photobleaching.” 2014. Web. 05 Jun 2020.

Vancouver:

Rodriguez-Enriquez R. Analysis of Bcl-2 family protein interactions in live cells by fluorescence recovery after photobleaching. [Internet] [Doctoral dissertation]. University of Manchester; 2014. [cited 2020 Jun 05]. Available from: https://www.research.manchester.ac.uk/portal/en/theses/analysis-of-bcl2-family-protein-interactions-in-live-cells-by-fluorescence-recovery-after-photobleaching(aa5eb271-6e43-48f3-940d-f63763ea4629).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.764284.

Council of Science Editors:

Rodriguez-Enriquez R. Analysis of Bcl-2 family protein interactions in live cells by fluorescence recovery after photobleaching. [Doctoral Dissertation]. University of Manchester; 2014. Available from: https://www.research.manchester.ac.uk/portal/en/theses/analysis-of-bcl2-family-protein-interactions-in-live-cells-by-fluorescence-recovery-after-photobleaching(aa5eb271-6e43-48f3-940d-f63763ea4629).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.764284

9. Luczka, Emilie. Implication de la protéine Zonula Ocludens-2 (ZO-2) dans le processus d'invasion tumorale : Implication of Zonula Occludens-2 protein (ZO-2) in the tumor invasion process.

Degree: Docteur es, Médecine, 2011, Reims

Lors de l’invasion tumorale, les cellules épithéliales tumorales acquièrent des propriétésmigratoires et invasives impliquant des modifications phénotypiques importantes. Parmi ceschangements, on observe notamment une réorganisation… (more)

Subjects/Keywords: Tumeurs; ZO-2; Matrix metalloproteinases; ZEB-2; Invasion tumorale; Neoplasms; Zonula occludens-2 protein; Neoplasm invasiveness; Matrix metalloproteinases; ZEB2 protein, human

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APA (6th Edition):

Luczka, E. (2011). Implication de la protéine Zonula Ocludens-2 (ZO-2) dans le processus d'invasion tumorale : Implication of Zonula Occludens-2 protein (ZO-2) in the tumor invasion process. (Doctoral Dissertation). Reims. Retrieved from http://www.theses.fr/2011REIMM205

Chicago Manual of Style (16th Edition):

Luczka, Emilie. “Implication de la protéine Zonula Ocludens-2 (ZO-2) dans le processus d'invasion tumorale : Implication of Zonula Occludens-2 protein (ZO-2) in the tumor invasion process.” 2011. Doctoral Dissertation, Reims. Accessed June 05, 2020. http://www.theses.fr/2011REIMM205.

MLA Handbook (7th Edition):

Luczka, Emilie. “Implication de la protéine Zonula Ocludens-2 (ZO-2) dans le processus d'invasion tumorale : Implication of Zonula Occludens-2 protein (ZO-2) in the tumor invasion process.” 2011. Web. 05 Jun 2020.

Vancouver:

Luczka E. Implication de la protéine Zonula Ocludens-2 (ZO-2) dans le processus d'invasion tumorale : Implication of Zonula Occludens-2 protein (ZO-2) in the tumor invasion process. [Internet] [Doctoral dissertation]. Reims; 2011. [cited 2020 Jun 05]. Available from: http://www.theses.fr/2011REIMM205.

Council of Science Editors:

Luczka E. Implication de la protéine Zonula Ocludens-2 (ZO-2) dans le processus d'invasion tumorale : Implication of Zonula Occludens-2 protein (ZO-2) in the tumor invasion process. [Doctoral Dissertation]. Reims; 2011. Available from: http://www.theses.fr/2011REIMM205


Universiteit Utrecht

10. Palmen, E.G.A. De competentiebeleving van kinderen in het cluster 2-onderwijs. Een studie naar samenhangende factoren met de competentiebeleving van deze kinderen.

Degree: 2009, Universiteit Utrecht

 Achtergrond: Taal speelt een belangrijke rol in de ontwikkeling van het kind, maar niet bij alle kinderen verloopt deze ontwikkeling zoals het hoort. Veel kinderen… (more)

Subjects/Keywords: Sociale Wetenschappen; Competentiebeleving, Spraak- en Taal Problemen; Cluster 2-onderwijs

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APA (6th Edition):

Palmen, E. G. A. (2009). De competentiebeleving van kinderen in het cluster 2-onderwijs. Een studie naar samenhangende factoren met de competentiebeleving van deze kinderen. (Masters Thesis). Universiteit Utrecht. Retrieved from http://dspace.library.uu.nl:8080/handle/1874/34453

Chicago Manual of Style (16th Edition):

Palmen, E G A. “De competentiebeleving van kinderen in het cluster 2-onderwijs. Een studie naar samenhangende factoren met de competentiebeleving van deze kinderen.” 2009. Masters Thesis, Universiteit Utrecht. Accessed June 05, 2020. http://dspace.library.uu.nl:8080/handle/1874/34453.

MLA Handbook (7th Edition):

Palmen, E G A. “De competentiebeleving van kinderen in het cluster 2-onderwijs. Een studie naar samenhangende factoren met de competentiebeleving van deze kinderen.” 2009. Web. 05 Jun 2020.

Vancouver:

Palmen EGA. De competentiebeleving van kinderen in het cluster 2-onderwijs. Een studie naar samenhangende factoren met de competentiebeleving van deze kinderen. [Internet] [Masters thesis]. Universiteit Utrecht; 2009. [cited 2020 Jun 05]. Available from: http://dspace.library.uu.nl:8080/handle/1874/34453.

Council of Science Editors:

Palmen EGA. De competentiebeleving van kinderen in het cluster 2-onderwijs. Een studie naar samenhangende factoren met de competentiebeleving van deze kinderen. [Masters Thesis]. Universiteit Utrecht; 2009. Available from: http://dspace.library.uu.nl:8080/handle/1874/34453


University of Minnesota

11. Xu, Hongliang. Uncoupling Lipid Metabolism from Inflammation in Adipose Tissue.

Degree: PhD, Biochemistry, Molecular Bio, and Biophysics, 2016, University of Minnesota

 Obesity has become an epidemic that affects the quality of life for more than one third of the US population. Syndromes associated with obesity, such… (more)

Subjects/Keywords: fatty acid binding protein; Sirtuin3; uncoupling protein 2

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APA (6th Edition):

Xu, H. (2016). Uncoupling Lipid Metabolism from Inflammation in Adipose Tissue. (Doctoral Dissertation). University of Minnesota. Retrieved from http://hdl.handle.net/11299/182816

Chicago Manual of Style (16th Edition):

Xu, Hongliang. “Uncoupling Lipid Metabolism from Inflammation in Adipose Tissue.” 2016. Doctoral Dissertation, University of Minnesota. Accessed June 05, 2020. http://hdl.handle.net/11299/182816.

MLA Handbook (7th Edition):

Xu, Hongliang. “Uncoupling Lipid Metabolism from Inflammation in Adipose Tissue.” 2016. Web. 05 Jun 2020.

Vancouver:

Xu H. Uncoupling Lipid Metabolism from Inflammation in Adipose Tissue. [Internet] [Doctoral dissertation]. University of Minnesota; 2016. [cited 2020 Jun 05]. Available from: http://hdl.handle.net/11299/182816.

Council of Science Editors:

Xu H. Uncoupling Lipid Metabolism from Inflammation in Adipose Tissue. [Doctoral Dissertation]. University of Minnesota; 2016. Available from: http://hdl.handle.net/11299/182816


University of Pretoria

12. Anyango, Joseph Ochieng. Physico-chemical modification of kafirin microstructures for application as biomaterials.

Degree: Food Science, 2013, University of Pretoria

 Microparticles produced from kafirin, the sorghum grain prolamin protein, by molecular selfassembly using coacervation with acetic acid solvent are vacuolated. They have shown considerable potential… (more)

Subjects/Keywords: Binding; Bone morphogenetic protein-2 (bmp-2); Water stability; Cross-linking; Kafirin; Microparticles; UCTD

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APA (6th Edition):

Anyango, J. O. (2013). Physico-chemical modification of kafirin microstructures for application as biomaterials. (Doctoral Dissertation). University of Pretoria. Retrieved from http://hdl.handle.net/2263/29708

Chicago Manual of Style (16th Edition):

Anyango, Joseph Ochieng. “Physico-chemical modification of kafirin microstructures for application as biomaterials.” 2013. Doctoral Dissertation, University of Pretoria. Accessed June 05, 2020. http://hdl.handle.net/2263/29708.

MLA Handbook (7th Edition):

Anyango, Joseph Ochieng. “Physico-chemical modification of kafirin microstructures for application as biomaterials.” 2013. Web. 05 Jun 2020.

Vancouver:

Anyango JO. Physico-chemical modification of kafirin microstructures for application as biomaterials. [Internet] [Doctoral dissertation]. University of Pretoria; 2013. [cited 2020 Jun 05]. Available from: http://hdl.handle.net/2263/29708.

Council of Science Editors:

Anyango JO. Physico-chemical modification of kafirin microstructures for application as biomaterials. [Doctoral Dissertation]. University of Pretoria; 2013. Available from: http://hdl.handle.net/2263/29708


University of Pretoria

13. [No author]. Physico-chemical modification of kafirin microstructures for application as biomaterials .

Degree: 2013, University of Pretoria

 Microparticles produced from kafirin, the sorghum grain prolamin protein, by molecular selfassembly using coacervation with acetic acid solvent are vacuolated. They have shown considerable potential… (more)

Subjects/Keywords: Binding; Bone morphogenetic protein-2 (bmp-2); Water stability; Cross-linking; Kafirin; Microparticles; UCTD

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APA (6th Edition):

author], [. (2013). Physico-chemical modification of kafirin microstructures for application as biomaterials . (Doctoral Dissertation). University of Pretoria. Retrieved from http://upetd.up.ac.za/thesis/available/etd-11222012-135328/

Chicago Manual of Style (16th Edition):

author], [No. “Physico-chemical modification of kafirin microstructures for application as biomaterials .” 2013. Doctoral Dissertation, University of Pretoria. Accessed June 05, 2020. http://upetd.up.ac.za/thesis/available/etd-11222012-135328/.

MLA Handbook (7th Edition):

author], [No. “Physico-chemical modification of kafirin microstructures for application as biomaterials .” 2013. Web. 05 Jun 2020.

Vancouver:

author] [. Physico-chemical modification of kafirin microstructures for application as biomaterials . [Internet] [Doctoral dissertation]. University of Pretoria; 2013. [cited 2020 Jun 05]. Available from: http://upetd.up.ac.za/thesis/available/etd-11222012-135328/.

Council of Science Editors:

author] [. Physico-chemical modification of kafirin microstructures for application as biomaterials . [Doctoral Dissertation]. University of Pretoria; 2013. Available from: http://upetd.up.ac.za/thesis/available/etd-11222012-135328/


University of Illinois – Urbana-Champaign

14. Polak, Samantha J. Quantitative image analysis of in vivo microstructure and growth factor effects in hydroxyapatite bone scaffolds.

Degree: MS, 0408, 2011, University of Illinois – Urbana-Champaign

 Osteoinductive agents, such as BMP-2, are known to improve bone formation when combined with scaffolds. Microporosity (<20??m) has also been shown to influence bone regeneration… (more)

Subjects/Keywords: Hydroxyapatite; Bone scaffold; Bone morphogenetic protein 2 (BMP-2); Microporosity; Micro computed tomography (Micro-CT)

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APA (6th Edition):

Polak, S. J. (2011). Quantitative image analysis of in vivo microstructure and growth factor effects in hydroxyapatite bone scaffolds. (Thesis). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/18409

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):

Polak, Samantha J. “Quantitative image analysis of in vivo microstructure and growth factor effects in hydroxyapatite bone scaffolds.” 2011. Thesis, University of Illinois – Urbana-Champaign. Accessed June 05, 2020. http://hdl.handle.net/2142/18409.

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

MLA Handbook (7th Edition):

Polak, Samantha J. “Quantitative image analysis of in vivo microstructure and growth factor effects in hydroxyapatite bone scaffolds.” 2011. Web. 05 Jun 2020.

Vancouver:

Polak SJ. Quantitative image analysis of in vivo microstructure and growth factor effects in hydroxyapatite bone scaffolds. [Internet] [Thesis]. University of Illinois – Urbana-Champaign; 2011. [cited 2020 Jun 05]. Available from: http://hdl.handle.net/2142/18409.

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

Council of Science Editors:

Polak SJ. Quantitative image analysis of in vivo microstructure and growth factor effects in hydroxyapatite bone scaffolds. [Thesis]. University of Illinois – Urbana-Champaign; 2011. Available from: http://hdl.handle.net/2142/18409

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


University of New Orleans

15. Aguerrevere, Luis. Multivariate Cluster Analysis of the MMPI-2 and MMPI-2-RF Scales in Spine Pain Patients with Financial Compensation: Characterization and Validation of Chronic Pain Subgroups.

Degree: PhD, Psychology, 2010, University of New Orleans

 Different psychosocial factors influence the experience and adaptation to pain. Previous cluster analytic studies using the Minnesota Multiphasic Personality Inventory-2nd edition described psychologically different subgroups… (more)

Subjects/Keywords: MMPI-2; MMPI-2-RF; spine pain; disability; psychological overlay; cluster analysis; pre-surgical screening; malingering

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APA (6th Edition):

Aguerrevere, L. (2010). Multivariate Cluster Analysis of the MMPI-2 and MMPI-2-RF Scales in Spine Pain Patients with Financial Compensation: Characterization and Validation of Chronic Pain Subgroups. (Doctoral Dissertation). University of New Orleans. Retrieved from https://scholarworks.uno.edu/td/1267

Chicago Manual of Style (16th Edition):

Aguerrevere, Luis. “Multivariate Cluster Analysis of the MMPI-2 and MMPI-2-RF Scales in Spine Pain Patients with Financial Compensation: Characterization and Validation of Chronic Pain Subgroups.” 2010. Doctoral Dissertation, University of New Orleans. Accessed June 05, 2020. https://scholarworks.uno.edu/td/1267.

MLA Handbook (7th Edition):

Aguerrevere, Luis. “Multivariate Cluster Analysis of the MMPI-2 and MMPI-2-RF Scales in Spine Pain Patients with Financial Compensation: Characterization and Validation of Chronic Pain Subgroups.” 2010. Web. 05 Jun 2020.

Vancouver:

Aguerrevere L. Multivariate Cluster Analysis of the MMPI-2 and MMPI-2-RF Scales in Spine Pain Patients with Financial Compensation: Characterization and Validation of Chronic Pain Subgroups. [Internet] [Doctoral dissertation]. University of New Orleans; 2010. [cited 2020 Jun 05]. Available from: https://scholarworks.uno.edu/td/1267.

Council of Science Editors:

Aguerrevere L. Multivariate Cluster Analysis of the MMPI-2 and MMPI-2-RF Scales in Spine Pain Patients with Financial Compensation: Characterization and Validation of Chronic Pain Subgroups. [Doctoral Dissertation]. University of New Orleans; 2010. Available from: https://scholarworks.uno.edu/td/1267


University of Ghana

16. Bortier, E. Prevalence of Pfhrp2 and/or Pfhrp3 Gene Deletions in Plasmodium Falciparum Isolates and the Performance of Hrp2 Based Malaria Rapid Diagnostic Tests .

Degree: 2019, University of Ghana

 BACKGROUND: Malaria rapid diagnostic tests (MRDTs) are important for malaria disease management. However, performance of the RDTs is affected when the targeted antigens in the… (more)

Subjects/Keywords: Malaria; Plasmodium Falciparum; Histidine-rich protein 2 (HRP2); Plasmodium vivax; Plasmodium falciparum histidine-rich protein-2 (PfHRP2)

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APA (6th Edition):

Bortier, E. (2019). Prevalence of Pfhrp2 and/or Pfhrp3 Gene Deletions in Plasmodium Falciparum Isolates and the Performance of Hrp2 Based Malaria Rapid Diagnostic Tests . (Masters Thesis). University of Ghana. Retrieved from http://ugspace.ug.edu.gh/handle/123456789/34636

Chicago Manual of Style (16th Edition):

Bortier, E. “Prevalence of Pfhrp2 and/or Pfhrp3 Gene Deletions in Plasmodium Falciparum Isolates and the Performance of Hrp2 Based Malaria Rapid Diagnostic Tests .” 2019. Masters Thesis, University of Ghana. Accessed June 05, 2020. http://ugspace.ug.edu.gh/handle/123456789/34636.

MLA Handbook (7th Edition):

Bortier, E. “Prevalence of Pfhrp2 and/or Pfhrp3 Gene Deletions in Plasmodium Falciparum Isolates and the Performance of Hrp2 Based Malaria Rapid Diagnostic Tests .” 2019. Web. 05 Jun 2020.

Vancouver:

Bortier E. Prevalence of Pfhrp2 and/or Pfhrp3 Gene Deletions in Plasmodium Falciparum Isolates and the Performance of Hrp2 Based Malaria Rapid Diagnostic Tests . [Internet] [Masters thesis]. University of Ghana; 2019. [cited 2020 Jun 05]. Available from: http://ugspace.ug.edu.gh/handle/123456789/34636.

Council of Science Editors:

Bortier E. Prevalence of Pfhrp2 and/or Pfhrp3 Gene Deletions in Plasmodium Falciparum Isolates and the Performance of Hrp2 Based Malaria Rapid Diagnostic Tests . [Masters Thesis]. University of Ghana; 2019. Available from: http://ugspace.ug.edu.gh/handle/123456789/34636


Texas Medical Center

17. Sun, Sheng. REGULATION OF THE ESCRT FUNCTION OF ALIX.

Degree: PhD, 2016, Texas Medical Center

  The ESCRT (endosomal sorting complex required for transport) is an evolutionary conserved membrane remodeling machinery that performs membrane invagination and abscission. ALIX is a… (more)

Subjects/Keywords: ALIX; MVB sorting; EGFR; ALG-2; intramolecular interaction; CHMP4; cytokinetic abscission; retroviral budding; Life Sciences; Medicine and Health Sciences

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APA (6th Edition):

Sun, S. (2016). REGULATION OF THE ESCRT FUNCTION OF ALIX. (Doctoral Dissertation). Texas Medical Center. Retrieved from http://digitalcommons.library.tmc.edu/utgsbs_dissertations/656

Chicago Manual of Style (16th Edition):

Sun, Sheng. “REGULATION OF THE ESCRT FUNCTION OF ALIX.” 2016. Doctoral Dissertation, Texas Medical Center. Accessed June 05, 2020. http://digitalcommons.library.tmc.edu/utgsbs_dissertations/656.

MLA Handbook (7th Edition):

Sun, Sheng. “REGULATION OF THE ESCRT FUNCTION OF ALIX.” 2016. Web. 05 Jun 2020.

Vancouver:

Sun S. REGULATION OF THE ESCRT FUNCTION OF ALIX. [Internet] [Doctoral dissertation]. Texas Medical Center; 2016. [cited 2020 Jun 05]. Available from: http://digitalcommons.library.tmc.edu/utgsbs_dissertations/656.

Council of Science Editors:

Sun S. REGULATION OF THE ESCRT FUNCTION OF ALIX. [Doctoral Dissertation]. Texas Medical Center; 2016. Available from: http://digitalcommons.library.tmc.edu/utgsbs_dissertations/656


University of Adelaide

18. Kavanagh, Steven James. Characterisation of PSC1 as an acidic rich RS domain protein (ARRS) with a conserved mammalian family member.

Degree: 2006, University of Adelaide

 The Acidic Rich family of RS Domain proteins (ARRS) is defined by both the presence and arrangement of conserved domains within 2 family members. Conserved… (more)

Subjects/Keywords: acidic; protein; mammalian

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APA (6th Edition):

Kavanagh, S. J. (2006). Characterisation of PSC1 as an acidic rich RS domain protein (ARRS) with a conserved mammalian family member. (Thesis). University of Adelaide. Retrieved from http://hdl.handle.net/2440/59642

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):

Kavanagh, Steven James. “Characterisation of PSC1 as an acidic rich RS domain protein (ARRS) with a conserved mammalian family member.” 2006. Thesis, University of Adelaide. Accessed June 05, 2020. http://hdl.handle.net/2440/59642.

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

MLA Handbook (7th Edition):

Kavanagh, Steven James. “Characterisation of PSC1 as an acidic rich RS domain protein (ARRS) with a conserved mammalian family member.” 2006. Web. 05 Jun 2020.

Vancouver:

Kavanagh SJ. Characterisation of PSC1 as an acidic rich RS domain protein (ARRS) with a conserved mammalian family member. [Internet] [Thesis]. University of Adelaide; 2006. [cited 2020 Jun 05]. Available from: http://hdl.handle.net/2440/59642.

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

Council of Science Editors:

Kavanagh SJ. Characterisation of PSC1 as an acidic rich RS domain protein (ARRS) with a conserved mammalian family member. [Thesis]. University of Adelaide; 2006. Available from: http://hdl.handle.net/2440/59642

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


University of Plymouth

19. White, Desley Louise. Non-transferrin-bound iron and protein glycation in type 2 diabetes.

Degree: PhD, 2012, University of Plymouth

 Background and Methods: The involvement of iron in the risk for, and complications of, type 2 diabetes has generated substantial interest over the past 15… (more)

Subjects/Keywords: 616.4624; Type 2 diabetes : Oxidative stress : Iron : Transferrin : Protein glycation

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APA (6th Edition):

White, D. L. (2012). Non-transferrin-bound iron and protein glycation in type 2 diabetes. (Doctoral Dissertation). University of Plymouth. Retrieved from http://hdl.handle.net/10026.1/1181

Chicago Manual of Style (16th Edition):

White, Desley Louise. “Non-transferrin-bound iron and protein glycation in type 2 diabetes.” 2012. Doctoral Dissertation, University of Plymouth. Accessed June 05, 2020. http://hdl.handle.net/10026.1/1181.

MLA Handbook (7th Edition):

White, Desley Louise. “Non-transferrin-bound iron and protein glycation in type 2 diabetes.” 2012. Web. 05 Jun 2020.

Vancouver:

White DL. Non-transferrin-bound iron and protein glycation in type 2 diabetes. [Internet] [Doctoral dissertation]. University of Plymouth; 2012. [cited 2020 Jun 05]. Available from: http://hdl.handle.net/10026.1/1181.

Council of Science Editors:

White DL. Non-transferrin-bound iron and protein glycation in type 2 diabetes. [Doctoral Dissertation]. University of Plymouth; 2012. Available from: http://hdl.handle.net/10026.1/1181


Indian Institute of Science

20. Nama, Srikanth. Regulation and Characterization of Transcription Factor Activator Protein-2 Alpha (AP-2α).

Degree: 2009, Indian Institute of Science

 Introduction AP2α is a 52 kDa retinoic acid inducible and developmentally regulated activator of transcription, which binds to the DNA in a sequence-specific manner. Transcription… (more)

Subjects/Keywords: Protein Transcription; Activator Protein-2 alpha (AP-2α); Protein Binding; Histone Deacetylase Inhibitors (HDIs); Mitogen Activated Protein Kinase (MAPK); AP-2 alpha; AP-2 Transcription; MAP Kinase Pathway; AP-2 - Growth Inhibition; AP2α; HDAC Inhibitors; Biochemistry

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APA (6th Edition):

Nama, S. (2009). Regulation and Characterization of Transcription Factor Activator Protein-2 Alpha (AP-2α). (Thesis). Indian Institute of Science. Retrieved from http://hdl.handle.net/2005/3095

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):

Nama, Srikanth. “Regulation and Characterization of Transcription Factor Activator Protein-2 Alpha (AP-2α).” 2009. Thesis, Indian Institute of Science. Accessed June 05, 2020. http://hdl.handle.net/2005/3095.

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

MLA Handbook (7th Edition):

Nama, Srikanth. “Regulation and Characterization of Transcription Factor Activator Protein-2 Alpha (AP-2α).” 2009. Web. 05 Jun 2020.

Vancouver:

Nama S. Regulation and Characterization of Transcription Factor Activator Protein-2 Alpha (AP-2α). [Internet] [Thesis]. Indian Institute of Science; 2009. [cited 2020 Jun 05]. Available from: http://hdl.handle.net/2005/3095.

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

Council of Science Editors:

Nama S. Regulation and Characterization of Transcription Factor Activator Protein-2 Alpha (AP-2α). [Thesis]. Indian Institute of Science; 2009. Available from: http://hdl.handle.net/2005/3095

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

21. 紅林, 奈央子. Regulation of neuropeptide Y Y1 receptor expression by bone morphogenetic protein 2 in C2C12 myoblasts : C2C12筋芽細胞におけるNeuropeptide Y Y1受容体のBMP2による発現制御.

Degree: 博士(歯学), 2014, Hokkaido University / 北海道大学

The neuropeptide Y(NPY) system is known as one of the major neural signaling pathways. NPY, produced by peripheral tissues including osteoblasts, is known to bind… (more)

Subjects/Keywords: Bone morphogenetic protein 2; Neuropeptide Y; Osteoblasts; Y1 receptor

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APA (6th Edition):

紅林, . (2014). Regulation of neuropeptide Y Y1 receptor expression by bone morphogenetic protein 2 in C2C12 myoblasts : C2C12筋芽細胞におけるNeuropeptide Y Y1受容体のBMP2による発現制御. (Thesis). Hokkaido University / 北海道大学. Retrieved from http://hdl.handle.net/2115/56295 ; http://dx.doi.org/10.14943/doctoral.k11268

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):

紅林, 奈央子. “Regulation of neuropeptide Y Y1 receptor expression by bone morphogenetic protein 2 in C2C12 myoblasts : C2C12筋芽細胞におけるNeuropeptide Y Y1受容体のBMP2による発現制御.” 2014. Thesis, Hokkaido University / 北海道大学. Accessed June 05, 2020. http://hdl.handle.net/2115/56295 ; http://dx.doi.org/10.14943/doctoral.k11268.

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

MLA Handbook (7th Edition):

紅林, 奈央子. “Regulation of neuropeptide Y Y1 receptor expression by bone morphogenetic protein 2 in C2C12 myoblasts : C2C12筋芽細胞におけるNeuropeptide Y Y1受容体のBMP2による発現制御.” 2014. Web. 05 Jun 2020.

Vancouver:

紅林 . Regulation of neuropeptide Y Y1 receptor expression by bone morphogenetic protein 2 in C2C12 myoblasts : C2C12筋芽細胞におけるNeuropeptide Y Y1受容体のBMP2による発現制御. [Internet] [Thesis]. Hokkaido University / 北海道大学; 2014. [cited 2020 Jun 05]. Available from: http://hdl.handle.net/2115/56295 ; http://dx.doi.org/10.14943/doctoral.k11268.

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

Council of Science Editors:

紅林 . Regulation of neuropeptide Y Y1 receptor expression by bone morphogenetic protein 2 in C2C12 myoblasts : C2C12筋芽細胞におけるNeuropeptide Y Y1受容体のBMP2による発現制御. [Thesis]. Hokkaido University / 北海道大学; 2014. Available from: http://hdl.handle.net/2115/56295 ; http://dx.doi.org/10.14943/doctoral.k11268

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


Robert Gordon University

22. Gryka, Anna. Alterations in the macronutrient content of the diet and the effects on body composition, cardiovascular disease risk and the control of energy metabolism in obese patients with type 2 diabetes mellitus.

Degree: PhD, 2011, Robert Gordon University

 Background/Objective: Several studies have shown that a low carbohydrate diet (LCHOD) can improve glycaemic control in type 2 diabetes (T2DM). The objective of the current… (more)

Subjects/Keywords: 612.3; Obesity; Type 2 diabetes; Carbohydrate; Protein; Diet; Body composition

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APA (6th Edition):

Gryka, A. (2011). Alterations in the macronutrient content of the diet and the effects on body composition, cardiovascular disease risk and the control of energy metabolism in obese patients with type 2 diabetes mellitus. (Doctoral Dissertation). Robert Gordon University. Retrieved from http://hdl.handle.net/10059/703

Chicago Manual of Style (16th Edition):

Gryka, Anna. “Alterations in the macronutrient content of the diet and the effects on body composition, cardiovascular disease risk and the control of energy metabolism in obese patients with type 2 diabetes mellitus.” 2011. Doctoral Dissertation, Robert Gordon University. Accessed June 05, 2020. http://hdl.handle.net/10059/703.

MLA Handbook (7th Edition):

Gryka, Anna. “Alterations in the macronutrient content of the diet and the effects on body composition, cardiovascular disease risk and the control of energy metabolism in obese patients with type 2 diabetes mellitus.” 2011. Web. 05 Jun 2020.

Vancouver:

Gryka A. Alterations in the macronutrient content of the diet and the effects on body composition, cardiovascular disease risk and the control of energy metabolism in obese patients with type 2 diabetes mellitus. [Internet] [Doctoral dissertation]. Robert Gordon University; 2011. [cited 2020 Jun 05]. Available from: http://hdl.handle.net/10059/703.

Council of Science Editors:

Gryka A. Alterations in the macronutrient content of the diet and the effects on body composition, cardiovascular disease risk and the control of energy metabolism in obese patients with type 2 diabetes mellitus. [Doctoral Dissertation]. Robert Gordon University; 2011. Available from: http://hdl.handle.net/10059/703


University of Alberta

23. Zhou, Ying. Intestinal Uptake of Barley Protein Nanoparticles as Delivery Vehicles for Bioactive Compounds.

Degree: MS, Department of Agricultural, Food, and Nutritional Science, 2013, University of Alberta

 The use of nanoparticles as nutrient delivery vehicles enables the enhancement of the oral bioavailability and health promoting benefits of bioactive compounds. Barley protein nanoparticles… (more)

Subjects/Keywords: Barley protein; Nanoparticles; Caco-2 cells; Uptake; Bioavailability

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APA (6th Edition):

Zhou, Y. (2013). Intestinal Uptake of Barley Protein Nanoparticles as Delivery Vehicles for Bioactive Compounds. (Masters Thesis). University of Alberta. Retrieved from https://era.library.ualberta.ca/files/3t945r40m

Chicago Manual of Style (16th Edition):

Zhou, Ying. “Intestinal Uptake of Barley Protein Nanoparticles as Delivery Vehicles for Bioactive Compounds.” 2013. Masters Thesis, University of Alberta. Accessed June 05, 2020. https://era.library.ualberta.ca/files/3t945r40m.

MLA Handbook (7th Edition):

Zhou, Ying. “Intestinal Uptake of Barley Protein Nanoparticles as Delivery Vehicles for Bioactive Compounds.” 2013. Web. 05 Jun 2020.

Vancouver:

Zhou Y. Intestinal Uptake of Barley Protein Nanoparticles as Delivery Vehicles for Bioactive Compounds. [Internet] [Masters thesis]. University of Alberta; 2013. [cited 2020 Jun 05]. Available from: https://era.library.ualberta.ca/files/3t945r40m.

Council of Science Editors:

Zhou Y. Intestinal Uptake of Barley Protein Nanoparticles as Delivery Vehicles for Bioactive Compounds. [Masters Thesis]. University of Alberta; 2013. Available from: https://era.library.ualberta.ca/files/3t945r40m


University of Alberta

24. Mohamed, Amany. Amyloid beta peptide, Cholesterol and Isoprenoids in Alzheimer’s disease.

Degree: PhD, Department of Pharmacology, 2013, University of Alberta

 Alzheimer’s disease (AD) is the most common form of dementia in the elderly. The major pathological features of AD are extracellular amyloid plaques, intracellular neurofibrillary… (more)

Subjects/Keywords: Amyloid beta peptide; SREBP-2; Cholesterol; Protein prenylation

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APA (6th Edition):

Mohamed, A. (2013). Amyloid beta peptide, Cholesterol and Isoprenoids in Alzheimer’s disease. (Doctoral Dissertation). University of Alberta. Retrieved from https://era.library.ualberta.ca/files/f7623d25p

Chicago Manual of Style (16th Edition):

Mohamed, Amany. “Amyloid beta peptide, Cholesterol and Isoprenoids in Alzheimer’s disease.” 2013. Doctoral Dissertation, University of Alberta. Accessed June 05, 2020. https://era.library.ualberta.ca/files/f7623d25p.

MLA Handbook (7th Edition):

Mohamed, Amany. “Amyloid beta peptide, Cholesterol and Isoprenoids in Alzheimer’s disease.” 2013. Web. 05 Jun 2020.

Vancouver:

Mohamed A. Amyloid beta peptide, Cholesterol and Isoprenoids in Alzheimer’s disease. [Internet] [Doctoral dissertation]. University of Alberta; 2013. [cited 2020 Jun 05]. Available from: https://era.library.ualberta.ca/files/f7623d25p.

Council of Science Editors:

Mohamed A. Amyloid beta peptide, Cholesterol and Isoprenoids in Alzheimer’s disease. [Doctoral Dissertation]. University of Alberta; 2013. Available from: https://era.library.ualberta.ca/files/f7623d25p


University of Alberta

25. Chen, Chao. Effects of macrophages and noggin suppression on the BMP-2-induced osteogenesis of human bone marrow mesenchymal stem cells.

Degree: MS, Department of Surgery, 2011, University of Alberta

 The osteogenic effects of bone morphogenetic protein-2 (BMP-2) on human mesenchymal stem cells (MSCs) are less profound than expected as compared with rodent cells, and… (more)

Subjects/Keywords: bone morphogenetic protein-2; mesenchymal stem cells; macrophages; noggin; bone; osteogenesis

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APA (6th Edition):

Chen, C. (2011). Effects of macrophages and noggin suppression on the BMP-2-induced osteogenesis of human bone marrow mesenchymal stem cells. (Masters Thesis). University of Alberta. Retrieved from https://era.library.ualberta.ca/files/w9505192t

Chicago Manual of Style (16th Edition):

Chen, Chao. “Effects of macrophages and noggin suppression on the BMP-2-induced osteogenesis of human bone marrow mesenchymal stem cells.” 2011. Masters Thesis, University of Alberta. Accessed June 05, 2020. https://era.library.ualberta.ca/files/w9505192t.

MLA Handbook (7th Edition):

Chen, Chao. “Effects of macrophages and noggin suppression on the BMP-2-induced osteogenesis of human bone marrow mesenchymal stem cells.” 2011. Web. 05 Jun 2020.

Vancouver:

Chen C. Effects of macrophages and noggin suppression on the BMP-2-induced osteogenesis of human bone marrow mesenchymal stem cells. [Internet] [Masters thesis]. University of Alberta; 2011. [cited 2020 Jun 05]. Available from: https://era.library.ualberta.ca/files/w9505192t.

Council of Science Editors:

Chen C. Effects of macrophages and noggin suppression on the BMP-2-induced osteogenesis of human bone marrow mesenchymal stem cells. [Masters Thesis]. University of Alberta; 2011. Available from: https://era.library.ualberta.ca/files/w9505192t


University of Alberta

26. Wang, guilin. Bisphosphonate-modified nanoparticles as drug delivery systems for bone diseases.

Degree: PhD, Department of Chemical and Materials Engineering, 2011, University of Alberta

 The objective of this thesis is to design nanoparticle (NP)-based drug delivery systems suitable for treatment of bone diseases. Two types of nanocarriers, (1) polymer… (more)

Subjects/Keywords: liposome; bone morphogenetic protein-2; nanoparticles; bone targeting; bisphosphonate; drug delivery

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APA (6th Edition):

Wang, g. (2011). Bisphosphonate-modified nanoparticles as drug delivery systems for bone diseases. (Doctoral Dissertation). University of Alberta. Retrieved from https://era.library.ualberta.ca/files/1544bp45j

Chicago Manual of Style (16th Edition):

Wang, guilin. “Bisphosphonate-modified nanoparticles as drug delivery systems for bone diseases.” 2011. Doctoral Dissertation, University of Alberta. Accessed June 05, 2020. https://era.library.ualberta.ca/files/1544bp45j.

MLA Handbook (7th Edition):

Wang, guilin. “Bisphosphonate-modified nanoparticles as drug delivery systems for bone diseases.” 2011. Web. 05 Jun 2020.

Vancouver:

Wang g. Bisphosphonate-modified nanoparticles as drug delivery systems for bone diseases. [Internet] [Doctoral dissertation]. University of Alberta; 2011. [cited 2020 Jun 05]. Available from: https://era.library.ualberta.ca/files/1544bp45j.

Council of Science Editors:

Wang g. Bisphosphonate-modified nanoparticles as drug delivery systems for bone diseases. [Doctoral Dissertation]. University of Alberta; 2011. Available from: https://era.library.ualberta.ca/files/1544bp45j


University of Edinburgh

27. Ekiert, Robert. Analysis of partner proteins of MeCP2 and their relevance to Rett syndrome.

Degree: PhD, 2012, University of Edinburgh

 Methyl-CpG binding protein 2 (MeCP2) was discovered as a protein binding to methylated DNA more than 20 years ago. It is very abundant in the… (more)

Subjects/Keywords: 572.8; MeCP2; Methyl-CpG binding protein 2; Rett syndrome; epigenetics

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

APA (6th Edition):

Ekiert, R. (2012). Analysis of partner proteins of MeCP2 and their relevance to Rett syndrome. (Doctoral Dissertation). University of Edinburgh. Retrieved from http://hdl.handle.net/1842/9901

Chicago Manual of Style (16th Edition):

Ekiert, Robert. “Analysis of partner proteins of MeCP2 and their relevance to Rett syndrome.” 2012. Doctoral Dissertation, University of Edinburgh. Accessed June 05, 2020. http://hdl.handle.net/1842/9901.

MLA Handbook (7th Edition):

Ekiert, Robert. “Analysis of partner proteins of MeCP2 and their relevance to Rett syndrome.” 2012. Web. 05 Jun 2020.

Vancouver:

Ekiert R. Analysis of partner proteins of MeCP2 and their relevance to Rett syndrome. [Internet] [Doctoral dissertation]. University of Edinburgh; 2012. [cited 2020 Jun 05]. Available from: http://hdl.handle.net/1842/9901.

Council of Science Editors:

Ekiert R. Analysis of partner proteins of MeCP2 and their relevance to Rett syndrome. [Doctoral Dissertation]. University of Edinburgh; 2012. Available from: http://hdl.handle.net/1842/9901


University of Pennsylvania

28. Qin, Haiou. Measures of the Dynamics of G Protein Interaction With the Ribosome With Applications to Antibiotic Screening.

Degree: 2010, University of Pennsylvania

 Ribosomes catalyze protein synthesis via the translation cycle, in which the translation initiation is recognized as a key step to regulate the process. The functional… (more)

Subjects/Keywords: protein synthesis; initiation factor 2; FRET; antibiotics; Biochemistry

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

APA (6th Edition):

Qin, H. (2010). Measures of the Dynamics of G Protein Interaction With the Ribosome With Applications to Antibiotic Screening. (Thesis). University of Pennsylvania. Retrieved from https://repository.upenn.edu/edissertations/429

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):

Qin, Haiou. “Measures of the Dynamics of G Protein Interaction With the Ribosome With Applications to Antibiotic Screening.” 2010. Thesis, University of Pennsylvania. Accessed June 05, 2020. https://repository.upenn.edu/edissertations/429.

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

MLA Handbook (7th Edition):

Qin, Haiou. “Measures of the Dynamics of G Protein Interaction With the Ribosome With Applications to Antibiotic Screening.” 2010. Web. 05 Jun 2020.

Vancouver:

Qin H. Measures of the Dynamics of G Protein Interaction With the Ribosome With Applications to Antibiotic Screening. [Internet] [Thesis]. University of Pennsylvania; 2010. [cited 2020 Jun 05]. Available from: https://repository.upenn.edu/edissertations/429.

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

Council of Science Editors:

Qin H. Measures of the Dynamics of G Protein Interaction With the Ribosome With Applications to Antibiotic Screening. [Thesis]. University of Pennsylvania; 2010. Available from: https://repository.upenn.edu/edissertations/429

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


University of Kansas

29. McGreal, Kerri McGreal. TRANSMEMBRANE PROTEIN 2: A NOVEL PROTEIN IN POLYCYSTIC KIDNEY DISEASE.

Degree: MS, Clinical Research, 2016, University of Kansas

 ABSTRACT Background: Autosomal Dominant Polycystic Kidney Disease (ADPKD) is a common hereditary cause of end stage renal disease. Affected individuals have mutations in PKD1 or… (more)

Subjects/Keywords: Medicine; Biochemistry; Polycystic Kidney Disease; Polycystin-1; Transmembrane Protein 2

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

APA (6th Edition):

McGreal, K. M. (2016). TRANSMEMBRANE PROTEIN 2: A NOVEL PROTEIN IN POLYCYSTIC KIDNEY DISEASE. (Masters Thesis). University of Kansas. Retrieved from http://hdl.handle.net/1808/22495

Chicago Manual of Style (16th Edition):

McGreal, Kerri McGreal. “TRANSMEMBRANE PROTEIN 2: A NOVEL PROTEIN IN POLYCYSTIC KIDNEY DISEASE.” 2016. Masters Thesis, University of Kansas. Accessed June 05, 2020. http://hdl.handle.net/1808/22495.

MLA Handbook (7th Edition):

McGreal, Kerri McGreal. “TRANSMEMBRANE PROTEIN 2: A NOVEL PROTEIN IN POLYCYSTIC KIDNEY DISEASE.” 2016. Web. 05 Jun 2020.

Vancouver:

McGreal KM. TRANSMEMBRANE PROTEIN 2: A NOVEL PROTEIN IN POLYCYSTIC KIDNEY DISEASE. [Internet] [Masters thesis]. University of Kansas; 2016. [cited 2020 Jun 05]. Available from: http://hdl.handle.net/1808/22495.

Council of Science Editors:

McGreal KM. TRANSMEMBRANE PROTEIN 2: A NOVEL PROTEIN IN POLYCYSTIC KIDNEY DISEASE. [Masters Thesis]. University of Kansas; 2016. Available from: http://hdl.handle.net/1808/22495


Ruhr Universität Bochum

30. Becker, Kristin. Kofaktorassemblierung in Photosystem 2 : Struktur und Funktion von Psb28.

Degree: 2011, Ruhr Universität Bochum

 Während des Lebenszyklus von PS2 treten Komplexe unterschiedlicher Untereinheitenzusammensetzung auf. Das Alter der fünf bekannten Subspezies wurde durch eine pulse-chase Strategie untersucht und gezeigt, in… (more)

Subjects/Keywords: Photosystem 2; Cyanobakterien; Biogenese; Strukturanalyse; Protein-Lipid-Wechselwirkung

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

APA (6th Edition):

Becker, K. (2011). Kofaktorassemblierung in Photosystem 2 : Struktur und Funktion von Psb28. (Thesis). Ruhr Universität Bochum. Retrieved from http://nbn-resolving.de/urn/resolver.pl?urn=urn:nbn:de:hbz:294-36489

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):

Becker, Kristin. “Kofaktorassemblierung in Photosystem 2 : Struktur und Funktion von Psb28.” 2011. Thesis, Ruhr Universität Bochum. Accessed June 05, 2020. http://nbn-resolving.de/urn/resolver.pl?urn=urn:nbn:de:hbz:294-36489.

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

MLA Handbook (7th Edition):

Becker, Kristin. “Kofaktorassemblierung in Photosystem 2 : Struktur und Funktion von Psb28.” 2011. Web. 05 Jun 2020.

Vancouver:

Becker K. Kofaktorassemblierung in Photosystem 2 : Struktur und Funktion von Psb28. [Internet] [Thesis]. Ruhr Universität Bochum; 2011. [cited 2020 Jun 05]. Available from: http://nbn-resolving.de/urn/resolver.pl?urn=urn:nbn:de:hbz:294-36489.

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

Council of Science Editors:

Becker K. Kofaktorassemblierung in Photosystem 2 : Struktur und Funktion von Psb28. [Thesis]. Ruhr Universität Bochum; 2011. Available from: http://nbn-resolving.de/urn/resolver.pl?urn=urn:nbn:de:hbz:294-36489

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

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