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You searched for subject:(Src). Showing records 1 – 30 of 195 total matches.

[1] [2] [3] [4] [5] [6] [7]

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University of Rochester

1. Spindel, Oded N. Characterization of Thioredoxin-Interacting Protein (TXNIP), an α-Arrestin Scaffold Protein, in Endothelial Signaling.

Degree: PhD, 2013, University of Rochester

 Cardiovascular diseases (CVD) are among the leading causes for morbidity and mortality in the western world. Examples of CVD include congestive heart failure, coronary artery… (more)

Subjects/Keywords: TXNIP; Endothelial; VEGFR2; Src

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APA (6th Edition):

Spindel, O. N. (2013). Characterization of Thioredoxin-Interacting Protein (TXNIP), an α-Arrestin Scaffold Protein, in Endothelial Signaling. (Doctoral Dissertation). University of Rochester. Retrieved from http://hdl.handle.net/1802/27309

Chicago Manual of Style (16th Edition):

Spindel, Oded N. “Characterization of Thioredoxin-Interacting Protein (TXNIP), an α-Arrestin Scaffold Protein, in Endothelial Signaling.” 2013. Doctoral Dissertation, University of Rochester. Accessed October 18, 2017. http://hdl.handle.net/1802/27309.

MLA Handbook (7th Edition):

Spindel, Oded N. “Characterization of Thioredoxin-Interacting Protein (TXNIP), an α-Arrestin Scaffold Protein, in Endothelial Signaling.” 2013. Web. 18 Oct 2017.

Vancouver:

Spindel ON. Characterization of Thioredoxin-Interacting Protein (TXNIP), an α-Arrestin Scaffold Protein, in Endothelial Signaling. [Internet] [Doctoral dissertation]. University of Rochester; 2013. [cited 2017 Oct 18]. Available from: http://hdl.handle.net/1802/27309.

Council of Science Editors:

Spindel ON. Characterization of Thioredoxin-Interacting Protein (TXNIP), an α-Arrestin Scaffold Protein, in Endothelial Signaling. [Doctoral Dissertation]. University of Rochester; 2013. Available from: http://hdl.handle.net/1802/27309


University of Debrecen

2. Kálnási, Béla Zsolt. A humán papillomavírus 16 e7 onkoprotein általi src aktiváció mechanizmusának vizsgálata .

Degree: DE – TEK – Természettudományi és Technológiai Kar – Biológiai és Ökológiai Intézet, 2013, University of Debrecen

 Munkám során annak a kérdésnek a megválaszolásához végeztem kísérleteimet, hogy a magas onkogén kockázatú humán papillomavírus 16 E7 onkoproteinje milyen módon eredményezi a Src kinázok… (more)

Subjects/Keywords: humán papillomavírus; onkoprotein; Src kináz

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APA (6th Edition):

Kálnási, B. Z. (2013). A humán papillomavírus 16 e7 onkoprotein általi src aktiváció mechanizmusának vizsgálata . (Thesis). University of Debrecen. Retrieved from http://hdl.handle.net/2437/176712

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):

Kálnási, Béla Zsolt. “A humán papillomavírus 16 e7 onkoprotein általi src aktiváció mechanizmusának vizsgálata .” 2013. Thesis, University of Debrecen. Accessed October 18, 2017. http://hdl.handle.net/2437/176712.

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

MLA Handbook (7th Edition):

Kálnási, Béla Zsolt. “A humán papillomavírus 16 e7 onkoprotein általi src aktiváció mechanizmusának vizsgálata .” 2013. Web. 18 Oct 2017.

Vancouver:

Kálnási BZ. A humán papillomavírus 16 e7 onkoprotein általi src aktiváció mechanizmusának vizsgálata . [Internet] [Thesis]. University of Debrecen; 2013. [cited 2017 Oct 18]. Available from: http://hdl.handle.net/2437/176712.

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

Council of Science Editors:

Kálnási BZ. A humán papillomavírus 16 e7 onkoprotein általi src aktiváció mechanizmusának vizsgálata . [Thesis]. University of Debrecen; 2013. Available from: http://hdl.handle.net/2437/176712

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


Université de Sherbrooke

3. Germain, Pascale. Shp2 régule la phosphorylation des tyrosines de l'arrestine .

Degree: 2009, Université de Sherbrooke

 Les arrestines sont connues pour leurs rôles dans la désensibilisation et l'endocytose des récepteurs couplés aux protéines G (RCPGs). Au fil des ans, plusieurs partenaires… (more)

Subjects/Keywords: Tyrosine; Src; Shp2; Phosphorylation; Arrestine

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APA (6th Edition):

Germain, P. (2009). Shp2 régule la phosphorylation des tyrosines de l'arrestine . (Masters Thesis). Université de Sherbrooke. Retrieved from http://savoirs.usherbrooke.ca/handle/11143/3968

Chicago Manual of Style (16th Edition):

Germain, Pascale. “Shp2 régule la phosphorylation des tyrosines de l'arrestine .” 2009. Masters Thesis, Université de Sherbrooke. Accessed October 18, 2017. http://savoirs.usherbrooke.ca/handle/11143/3968.

MLA Handbook (7th Edition):

Germain, Pascale. “Shp2 régule la phosphorylation des tyrosines de l'arrestine .” 2009. Web. 18 Oct 2017.

Vancouver:

Germain P. Shp2 régule la phosphorylation des tyrosines de l'arrestine . [Internet] [Masters thesis]. Université de Sherbrooke; 2009. [cited 2017 Oct 18]. Available from: http://savoirs.usherbrooke.ca/handle/11143/3968.

Council of Science Editors:

Germain P. Shp2 régule la phosphorylation des tyrosines de l'arrestine . [Masters Thesis]. Université de Sherbrooke; 2009. Available from: http://savoirs.usherbrooke.ca/handle/11143/3968


Queens University

4. D'Abreo, Carmeline. The Role of Cadherin-11 and gp130 in Transformation by Activated Src .

Degree: Pathology and Molecular Medicine, 2011, Queens University

 Signal Transducer and Activator of Transcription 3, Stat3, has been associated with cytokine-induced proliferation, anti-apoptosis and neoplastic transformation, while constitutively active Stat3 has been found… (more)

Subjects/Keywords: Cadherin-11; Src; gp130; Stat3

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APA (6th Edition):

D'Abreo, C. (2011). The Role of Cadherin-11 and gp130 in Transformation by Activated Src . (Thesis). Queens University. Retrieved from http://hdl.handle.net/1974/6887

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):

D'Abreo, Carmeline. “The Role of Cadherin-11 and gp130 in Transformation by Activated Src .” 2011. Thesis, Queens University. Accessed October 18, 2017. http://hdl.handle.net/1974/6887.

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

MLA Handbook (7th Edition):

D'Abreo, Carmeline. “The Role of Cadherin-11 and gp130 in Transformation by Activated Src .” 2011. Web. 18 Oct 2017.

Vancouver:

D'Abreo C. The Role of Cadherin-11 and gp130 in Transformation by Activated Src . [Internet] [Thesis]. Queens University; 2011. [cited 2017 Oct 18]. Available from: http://hdl.handle.net/1974/6887.

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

Council of Science Editors:

D'Abreo C. The Role of Cadherin-11 and gp130 in Transformation by Activated Src . [Thesis]. Queens University; 2011. Available from: http://hdl.handle.net/1974/6887

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


University of Vienna

5. Angerer, Gerhard. Hemmung der osteoklastären Funktion durch neue Src-Kinaseinhibitoren vom Pyrazolo[3,4-d]pyrimidin-typ.

Degree: 2010, University of Vienna

Im Rahmen dieser Diplomarbeit wurden Substanzen vom Pyrazolo[3,4 d]pyrimidin-typ mit den Kurzbezeichnungen SI83, S7, SI20, S13 und S31 auf ihre Eigenschaft hin untersucht, osteoklastäre Prozesse und Funktionen sowie die Genese von Osteoklasten zu hemmen.

Subjects/Keywords: 44.40 Pharmazie, Pharmazeutika; Osteoporose / Osteoklasteninhibierung / Src-Kinaseblocker; osteoporosis / osteoclastinhibition / src-kinaseblock

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APA (6th Edition):

Angerer, G. (2010). Hemmung der osteoklastären Funktion durch neue Src-Kinaseinhibitoren vom Pyrazolo[3,4-d]pyrimidin-typ. (Thesis). University of Vienna. Retrieved from http://othes.univie.ac.at/8219/

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):

Angerer, Gerhard. “Hemmung der osteoklastären Funktion durch neue Src-Kinaseinhibitoren vom Pyrazolo[3,4-d]pyrimidin-typ.” 2010. Thesis, University of Vienna. Accessed October 18, 2017. http://othes.univie.ac.at/8219/.

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

MLA Handbook (7th Edition):

Angerer, Gerhard. “Hemmung der osteoklastären Funktion durch neue Src-Kinaseinhibitoren vom Pyrazolo[3,4-d]pyrimidin-typ.” 2010. Web. 18 Oct 2017.

Vancouver:

Angerer G. Hemmung der osteoklastären Funktion durch neue Src-Kinaseinhibitoren vom Pyrazolo[3,4-d]pyrimidin-typ. [Internet] [Thesis]. University of Vienna; 2010. [cited 2017 Oct 18]. Available from: http://othes.univie.ac.at/8219/.

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

Council of Science Editors:

Angerer G. Hemmung der osteoklastären Funktion durch neue Src-Kinaseinhibitoren vom Pyrazolo[3,4-d]pyrimidin-typ. [Thesis]. University of Vienna; 2010. Available from: http://othes.univie.ac.at/8219/

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


University of Helsinki

6. Tuovinen, Mika-Petri. Sam68:n tyrosiinifosforylaatio v-src-transformoiduissa rotan fibroblastisoluissa.

Degree: 1995, University of Helsinki

Subjects/Keywords: src; Sam68; Perinnöllisyystiede; src; Sam68

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APA (6th Edition):

Tuovinen, M. (1995). Sam68:n tyrosiinifosforylaatio v-src-transformoiduissa rotan fibroblastisoluissa. (Thesis). University of Helsinki. Retrieved from http://hdl.handle.net/10138/157652

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):

Tuovinen, Mika-Petri. “Sam68:n tyrosiinifosforylaatio v-src-transformoiduissa rotan fibroblastisoluissa.” 1995. Thesis, University of Helsinki. Accessed October 18, 2017. http://hdl.handle.net/10138/157652.

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

MLA Handbook (7th Edition):

Tuovinen, Mika-Petri. “Sam68:n tyrosiinifosforylaatio v-src-transformoiduissa rotan fibroblastisoluissa.” 1995. Web. 18 Oct 2017.

Vancouver:

Tuovinen M. Sam68:n tyrosiinifosforylaatio v-src-transformoiduissa rotan fibroblastisoluissa. [Internet] [Thesis]. University of Helsinki; 1995. [cited 2017 Oct 18]. Available from: http://hdl.handle.net/10138/157652.

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

Council of Science Editors:

Tuovinen M. Sam68:n tyrosiinifosforylaatio v-src-transformoiduissa rotan fibroblastisoluissa. [Thesis]. University of Helsinki; 1995. Available from: http://hdl.handle.net/10138/157652

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


West Virginia University

7. Clump, David A. Genetic variant of the adaptor protein, AFAP-110, efficiently activates c-Src resulting in podosome formation.

Degree: 2008, West Virginia University

 The actin filament associated protein of 110 kDA (AFAP-110) is a well-characterized protein composed of amino-terminal binding motifs that function upstream of a carboxy-terminal actin… (more)

Subjects/Keywords: Microfilament proteins.; Oncogenes.; Microfilament Proteins.; Genes, src.

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APA (6th Edition):

Clump, D. A. (2008). Genetic variant of the adaptor protein, AFAP-110, efficiently activates c-Src resulting in podosome formation. (Thesis). West Virginia University. Retrieved from http://wvuscholar.wvu.edu:8881/R/?func=dbin-jump-full&object_id=13952

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):

Clump, David A. “Genetic variant of the adaptor protein, AFAP-110, efficiently activates c-Src resulting in podosome formation.” 2008. Thesis, West Virginia University. Accessed October 18, 2017. http://wvuscholar.wvu.edu:8881/R/?func=dbin-jump-full&object_id=13952.

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

MLA Handbook (7th Edition):

Clump, David A. “Genetic variant of the adaptor protein, AFAP-110, efficiently activates c-Src resulting in podosome formation.” 2008. Web. 18 Oct 2017.

Vancouver:

Clump DA. Genetic variant of the adaptor protein, AFAP-110, efficiently activates c-Src resulting in podosome formation. [Internet] [Thesis]. West Virginia University; 2008. [cited 2017 Oct 18]. Available from: http://wvuscholar.wvu.edu:8881/R/?func=dbin-jump-full&object_id=13952.

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

Council of Science Editors:

Clump DA. Genetic variant of the adaptor protein, AFAP-110, efficiently activates c-Src resulting in podosome formation. [Thesis]. West Virginia University; 2008. Available from: http://wvuscholar.wvu.edu:8881/R/?func=dbin-jump-full&object_id=13952

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


Kyoto University

8. Sato, Hiroki. Src regulates insulin secretion and glucose metabolism by influencing subcellular localization of glucokinase in pancreatic β-cells .

Degree: 2016, Kyoto University

Subjects/Keywords: glucokinase; insulin; src

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APA (6th Edition):

Sato, H. (2016). Src regulates insulin secretion and glucose metabolism by influencing subcellular localization of glucokinase in pancreatic β-cells . (Thesis). Kyoto University. Retrieved from http://hdl.handle.net/2433/217719

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):

Sato, Hiroki. “Src regulates insulin secretion and glucose metabolism by influencing subcellular localization of glucokinase in pancreatic β-cells .” 2016. Thesis, Kyoto University. Accessed October 18, 2017. http://hdl.handle.net/2433/217719.

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

MLA Handbook (7th Edition):

Sato, Hiroki. “Src regulates insulin secretion and glucose metabolism by influencing subcellular localization of glucokinase in pancreatic β-cells .” 2016. Web. 18 Oct 2017.

Vancouver:

Sato H. Src regulates insulin secretion and glucose metabolism by influencing subcellular localization of glucokinase in pancreatic β-cells . [Internet] [Thesis]. Kyoto University; 2016. [cited 2017 Oct 18]. Available from: http://hdl.handle.net/2433/217719.

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

Council of Science Editors:

Sato H. Src regulates insulin secretion and glucose metabolism by influencing subcellular localization of glucokinase in pancreatic β-cells . [Thesis]. Kyoto University; 2016. Available from: http://hdl.handle.net/2433/217719

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


University of Toronto

9. Lee, Ken Wing Kin. High Glucose-induced ROS Production is Mediated by c-Src in Mesangial Cells.

Degree: 2012, University of Toronto

The pathogenesis of diabetic nephropathy (DN) remains incompletely understood. In previous studies, we observed the activation of Tyr kinase Src by high glucose (HG) and… (more)

Subjects/Keywords: Diabetic nephropathy; Src; Reactive oxygen species; 0719

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APA (6th Edition):

Lee, K. W. K. (2012). High Glucose-induced ROS Production is Mediated by c-Src in Mesangial Cells. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/33753

Chicago Manual of Style (16th Edition):

Lee, Ken Wing Kin. “High Glucose-induced ROS Production is Mediated by c-Src in Mesangial Cells.” 2012. Masters Thesis, University of Toronto. Accessed October 18, 2017. http://hdl.handle.net/1807/33753.

MLA Handbook (7th Edition):

Lee, Ken Wing Kin. “High Glucose-induced ROS Production is Mediated by c-Src in Mesangial Cells.” 2012. Web. 18 Oct 2017.

Vancouver:

Lee KWK. High Glucose-induced ROS Production is Mediated by c-Src in Mesangial Cells. [Internet] [Masters thesis]. University of Toronto; 2012. [cited 2017 Oct 18]. Available from: http://hdl.handle.net/1807/33753.

Council of Science Editors:

Lee KWK. High Glucose-induced ROS Production is Mediated by c-Src in Mesangial Cells. [Masters Thesis]. University of Toronto; 2012. Available from: http://hdl.handle.net/1807/33753


University of Alberta

10. Marasinghe Arachchige, Bodhi Nirosha. Structural aspects of the interaction of the cytoplasmic domain of Mucin-1 (MUC1) with the SH3 domain of Src Kinase.

Degree: MS, Medical Sciences-Laboratory Medicine and Pathology, 2011, University of Alberta

 Abstract Breast cancer is the second most frequent cause of cancer deaths in Canadian women with death resulting from the spread of cancer cells or… (more)

Subjects/Keywords: Src Kinase; MUC1; NMR; SH3 domain

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APA (6th Edition):

Marasinghe Arachchige, B. N. (2011). Structural aspects of the interaction of the cytoplasmic domain of Mucin-1 (MUC1) with the SH3 domain of Src Kinase. (Masters Thesis). University of Alberta. Retrieved from https://era.library.ualberta.ca/files/wp988k67k

Chicago Manual of Style (16th Edition):

Marasinghe Arachchige, Bodhi Nirosha. “Structural aspects of the interaction of the cytoplasmic domain of Mucin-1 (MUC1) with the SH3 domain of Src Kinase.” 2011. Masters Thesis, University of Alberta. Accessed October 18, 2017. https://era.library.ualberta.ca/files/wp988k67k.

MLA Handbook (7th Edition):

Marasinghe Arachchige, Bodhi Nirosha. “Structural aspects of the interaction of the cytoplasmic domain of Mucin-1 (MUC1) with the SH3 domain of Src Kinase.” 2011. Web. 18 Oct 2017.

Vancouver:

Marasinghe Arachchige BN. Structural aspects of the interaction of the cytoplasmic domain of Mucin-1 (MUC1) with the SH3 domain of Src Kinase. [Internet] [Masters thesis]. University of Alberta; 2011. [cited 2017 Oct 18]. Available from: https://era.library.ualberta.ca/files/wp988k67k.

Council of Science Editors:

Marasinghe Arachchige BN. Structural aspects of the interaction of the cytoplasmic domain of Mucin-1 (MUC1) with the SH3 domain of Src Kinase. [Masters Thesis]. University of Alberta; 2011. Available from: https://era.library.ualberta.ca/files/wp988k67k


University of Edinburgh

11. Abdelhameed, Taher. Role of src splice variants in nerve terminal function.

Degree: 2010, University of Edinburgh

Src is a 60 kDa tyrosine kinase that is expressed in most of animal tissues. Src has three splice variants, C-src, which is ubiquitously expressed,… (more)

Subjects/Keywords: 573.8; src; nerve terminal; endocytosis; exocytosis

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APA (6th Edition):

Abdelhameed, T. (2010). Role of src splice variants in nerve terminal function. (Doctoral Dissertation). University of Edinburgh. Retrieved from http://hdl.handle.net/1842/4485

Chicago Manual of Style (16th Edition):

Abdelhameed, Taher. “Role of src splice variants in nerve terminal function.” 2010. Doctoral Dissertation, University of Edinburgh. Accessed October 18, 2017. http://hdl.handle.net/1842/4485.

MLA Handbook (7th Edition):

Abdelhameed, Taher. “Role of src splice variants in nerve terminal function.” 2010. Web. 18 Oct 2017.

Vancouver:

Abdelhameed T. Role of src splice variants in nerve terminal function. [Internet] [Doctoral dissertation]. University of Edinburgh; 2010. [cited 2017 Oct 18]. Available from: http://hdl.handle.net/1842/4485.

Council of Science Editors:

Abdelhameed T. Role of src splice variants in nerve terminal function. [Doctoral Dissertation]. University of Edinburgh; 2010. Available from: http://hdl.handle.net/1842/4485

12. Sato, Hiroki. Src regulates insulin secretion and glucose metabolism by influencing subcellular localization of glucokinase in pancreatic β-cells : Srcは膵β細胞においてグルコキナーゼの細胞内局在への影響を介してインスリン分泌とグルコース代謝を制御する.

Degree: 博士(医学), 2016, Kyoto University / 京都大学

新制・論文博士

乙第13062号

論医博第2120号

Subjects/Keywords: glucokinase; insulin; src

Page 1 Page 2

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APA (6th Edition):

Sato, H. (2016). Src regulates insulin secretion and glucose metabolism by influencing subcellular localization of glucokinase in pancreatic β-cells : Srcは膵β細胞においてグルコキナーゼの細胞内局在への影響を介してインスリン分泌とグルコース代謝を制御する. (Thesis). Kyoto University / 京都大学. Retrieved from http://hdl.handle.net/2433/217719 ; http://dx.doi.org/10.14989/doctor.r13062

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):

Sato, Hiroki. “Src regulates insulin secretion and glucose metabolism by influencing subcellular localization of glucokinase in pancreatic β-cells : Srcは膵β細胞においてグルコキナーゼの細胞内局在への影響を介してインスリン分泌とグルコース代謝を制御する.” 2016. Thesis, Kyoto University / 京都大学. Accessed October 18, 2017. http://hdl.handle.net/2433/217719 ; http://dx.doi.org/10.14989/doctor.r13062.

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

MLA Handbook (7th Edition):

Sato, Hiroki. “Src regulates insulin secretion and glucose metabolism by influencing subcellular localization of glucokinase in pancreatic β-cells : Srcは膵β細胞においてグルコキナーゼの細胞内局在への影響を介してインスリン分泌とグルコース代謝を制御する.” 2016. Web. 18 Oct 2017.

Vancouver:

Sato H. Src regulates insulin secretion and glucose metabolism by influencing subcellular localization of glucokinase in pancreatic β-cells : Srcは膵β細胞においてグルコキナーゼの細胞内局在への影響を介してインスリン分泌とグルコース代謝を制御する. [Internet] [Thesis]. Kyoto University / 京都大学; 2016. [cited 2017 Oct 18]. Available from: http://hdl.handle.net/2433/217719 ; http://dx.doi.org/10.14989/doctor.r13062.

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

Council of Science Editors:

Sato H. Src regulates insulin secretion and glucose metabolism by influencing subcellular localization of glucokinase in pancreatic β-cells : Srcは膵β細胞においてグルコキナーゼの細胞内局在への影響を介してインスリン分泌とグルコース代謝を制御する. [Thesis]. Kyoto University / 京都大学; 2016. Available from: http://hdl.handle.net/2433/217719 ; http://dx.doi.org/10.14989/doctor.r13062

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


Vanderbilt University

13. Arnette, Christopher R. Functional and regulatory mechanisms of microtubule-associated proteins involved in cancer progression.

Degree: PhD, Cell and Developmental Biology, 2014, Vanderbilt University

 Microtubule-associated proteins (MAPS) frequently influence microtubule (MT) dynamics and may also alter MT-dependent processes, such as protein trafficking. RASSF1A is a MAP that is frequently… (more)

Subjects/Keywords: Actin; Trafficking; Microtubules; c-Src; RASSF1A

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APA (6th Edition):

Arnette, C. R. (2014). Functional and regulatory mechanisms of microtubule-associated proteins involved in cancer progression. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://etd.library.vanderbilt.edu//available/etd-03172014-142501/ ;

Chicago Manual of Style (16th Edition):

Arnette, Christopher R. “Functional and regulatory mechanisms of microtubule-associated proteins involved in cancer progression.” 2014. Doctoral Dissertation, Vanderbilt University. Accessed October 18, 2017. http://etd.library.vanderbilt.edu//available/etd-03172014-142501/ ;.

MLA Handbook (7th Edition):

Arnette, Christopher R. “Functional and regulatory mechanisms of microtubule-associated proteins involved in cancer progression.” 2014. Web. 18 Oct 2017.

Vancouver:

Arnette CR. Functional and regulatory mechanisms of microtubule-associated proteins involved in cancer progression. [Internet] [Doctoral dissertation]. Vanderbilt University; 2014. [cited 2017 Oct 18]. Available from: http://etd.library.vanderbilt.edu//available/etd-03172014-142501/ ;.

Council of Science Editors:

Arnette CR. Functional and regulatory mechanisms of microtubule-associated proteins involved in cancer progression. [Doctoral Dissertation]. Vanderbilt University; 2014. Available from: http://etd.library.vanderbilt.edu//available/etd-03172014-142501/ ;

14. Tsang, Jennifer Lai-Yee. A Novel Reciprocal Regulatory Circuit Between Caspase-8 and c-Src.

Degree: 2014, University of Toronto

Apoptosis and cell survival are two seemingly opposing fate-determining processes that are regulated by distinct and complex signaling pathways. Caspase-8, an apical caspase, plays a… (more)

Subjects/Keywords: Survival; Apoptosis; Caspase-8; c-Src; 0307

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APA (6th Edition):

Tsang, J. L. (2014). A Novel Reciprocal Regulatory Circuit Between Caspase-8 and c-Src. (Doctoral Dissertation). University of Toronto. Retrieved from http://hdl.handle.net/1807/65760

Chicago Manual of Style (16th Edition):

Tsang, Jennifer Lai-Yee. “A Novel Reciprocal Regulatory Circuit Between Caspase-8 and c-Src.” 2014. Doctoral Dissertation, University of Toronto. Accessed October 18, 2017. http://hdl.handle.net/1807/65760.

MLA Handbook (7th Edition):

Tsang, Jennifer Lai-Yee. “A Novel Reciprocal Regulatory Circuit Between Caspase-8 and c-Src.” 2014. Web. 18 Oct 2017.

Vancouver:

Tsang JL. A Novel Reciprocal Regulatory Circuit Between Caspase-8 and c-Src. [Internet] [Doctoral dissertation]. University of Toronto; 2014. [cited 2017 Oct 18]. Available from: http://hdl.handle.net/1807/65760.

Council of Science Editors:

Tsang JL. A Novel Reciprocal Regulatory Circuit Between Caspase-8 and c-Src. [Doctoral Dissertation]. University of Toronto; 2014. Available from: http://hdl.handle.net/1807/65760


University of Illinois – Chicago

15. Bakhshi, Farnaz R. Mechanism of Caveolin-1 Degradation.

Degree: 2014, University of Illinois – Chicago

 In the present study, we tested the hypothesis that oxidative/nitrosative stress promotes caveolin-1 (Cav-1) degradation, providing an underlying mechanism of endothelial cell activation/dysfunction in patients… (more)

Subjects/Keywords: Caveolin-1; Pulmonary Arterial Hypertension; Src; degradation

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APA (6th Edition):

Bakhshi, F. R. (2014). Mechanism of Caveolin-1 Degradation. (Thesis). University of Illinois – Chicago. Retrieved from http://hdl.handle.net/10027/18852

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):

Bakhshi, Farnaz R. “Mechanism of Caveolin-1 Degradation.” 2014. Thesis, University of Illinois – Chicago. Accessed October 18, 2017. http://hdl.handle.net/10027/18852.

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

MLA Handbook (7th Edition):

Bakhshi, Farnaz R. “Mechanism of Caveolin-1 Degradation.” 2014. Web. 18 Oct 2017.

Vancouver:

Bakhshi FR. Mechanism of Caveolin-1 Degradation. [Internet] [Thesis]. University of Illinois – Chicago; 2014. [cited 2017 Oct 18]. Available from: http://hdl.handle.net/10027/18852.

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

Council of Science Editors:

Bakhshi FR. Mechanism of Caveolin-1 Degradation. [Thesis]. University of Illinois – Chicago; 2014. Available from: http://hdl.handle.net/10027/18852

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


University of Manchester

16. Rowling, Emily. Pre-clinical evaluation of novel anti-metastatic targets.

Degree: PhD, 2014, University of Manchester

 Background: Radiotherapy is used in the treatment of over 50% of cancer patients and bar surgery, is the most effective cancer intervention. However, in the… (more)

Subjects/Keywords: 615.8; Src; metastasis; Radiotherapy; PI3K; Thyroid

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APA (6th Edition):

Rowling, E. (2014). Pre-clinical evaluation of novel anti-metastatic targets. (Doctoral Dissertation). University of Manchester. Retrieved from https://www.research.manchester.ac.uk/portal/en/theses/preclinical-evaluation-of-novel-antimetastatic-targets(caa9ab41-c054-4559-b575-3fd8974005a7).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.634898

Chicago Manual of Style (16th Edition):

Rowling, Emily. “Pre-clinical evaluation of novel anti-metastatic targets.” 2014. Doctoral Dissertation, University of Manchester. Accessed October 18, 2017. https://www.research.manchester.ac.uk/portal/en/theses/preclinical-evaluation-of-novel-antimetastatic-targets(caa9ab41-c054-4559-b575-3fd8974005a7).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.634898.

MLA Handbook (7th Edition):

Rowling, Emily. “Pre-clinical evaluation of novel anti-metastatic targets.” 2014. Web. 18 Oct 2017.

Vancouver:

Rowling E. Pre-clinical evaluation of novel anti-metastatic targets. [Internet] [Doctoral dissertation]. University of Manchester; 2014. [cited 2017 Oct 18]. Available from: https://www.research.manchester.ac.uk/portal/en/theses/preclinical-evaluation-of-novel-antimetastatic-targets(caa9ab41-c054-4559-b575-3fd8974005a7).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.634898.

Council of Science Editors:

Rowling E. Pre-clinical evaluation of novel anti-metastatic targets. [Doctoral Dissertation]. University of Manchester; 2014. Available from: https://www.research.manchester.ac.uk/portal/en/theses/preclinical-evaluation-of-novel-antimetastatic-targets(caa9ab41-c054-4559-b575-3fd8974005a7).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.634898


University of Michigan

17. Kwarcinski, Frank. Developing Kinase Inhibitors as Chemical Tools and Potential Drugs.

Degree: PhD, Medicinal Chemistry, 2016, University of Michigan

 Kinase inhibitors have experienced a dramatic evolution over the last two decades, as multi-targeted kinase chemical probes have gradually given way to highly specific, clinically… (more)

Subjects/Keywords: Kinase inhibitor; Src kinase; Biological Chemistry; Science

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APA (6th Edition):

Kwarcinski, F. (2016). Developing Kinase Inhibitors as Chemical Tools and Potential Drugs. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/120774

Chicago Manual of Style (16th Edition):

Kwarcinski, Frank. “Developing Kinase Inhibitors as Chemical Tools and Potential Drugs.” 2016. Doctoral Dissertation, University of Michigan. Accessed October 18, 2017. http://hdl.handle.net/2027.42/120774.

MLA Handbook (7th Edition):

Kwarcinski, Frank. “Developing Kinase Inhibitors as Chemical Tools and Potential Drugs.” 2016. Web. 18 Oct 2017.

Vancouver:

Kwarcinski F. Developing Kinase Inhibitors as Chemical Tools and Potential Drugs. [Internet] [Doctoral dissertation]. University of Michigan; 2016. [cited 2017 Oct 18]. Available from: http://hdl.handle.net/2027.42/120774.

Council of Science Editors:

Kwarcinski F. Developing Kinase Inhibitors as Chemical Tools and Potential Drugs. [Doctoral Dissertation]. University of Michigan; 2016. Available from: http://hdl.handle.net/2027.42/120774


Queens University

18. Mak, Hannah. The Ezrin Signalling Network as a Potential Novel Marker in Breast Cancer Metastasis .

Degree: Pathology and Molecular Medicine, 2010, Queens University

 Metastasis is the leading cause of mortality in human breast cancer. However, there are few predictive, prognostic, or therapeutic targets of breast cancer metastasis. Ezrin,… (more)

Subjects/Keywords: Src; Ezrin; Breast cancer; Invasion; Metastasis

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APA (6th Edition):

Mak, H. (2010). The Ezrin Signalling Network as a Potential Novel Marker in Breast Cancer Metastasis . (Thesis). Queens University. Retrieved from http://hdl.handle.net/1974/5599

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):

Mak, Hannah. “The Ezrin Signalling Network as a Potential Novel Marker in Breast Cancer Metastasis .” 2010. Thesis, Queens University. Accessed October 18, 2017. http://hdl.handle.net/1974/5599.

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

MLA Handbook (7th Edition):

Mak, Hannah. “The Ezrin Signalling Network as a Potential Novel Marker in Breast Cancer Metastasis .” 2010. Web. 18 Oct 2017.

Vancouver:

Mak H. The Ezrin Signalling Network as a Potential Novel Marker in Breast Cancer Metastasis . [Internet] [Thesis]. Queens University; 2010. [cited 2017 Oct 18]. Available from: http://hdl.handle.net/1974/5599.

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

Council of Science Editors:

Mak H. The Ezrin Signalling Network as a Potential Novel Marker in Breast Cancer Metastasis . [Thesis]. Queens University; 2010. Available from: http://hdl.handle.net/1974/5599

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


University of Texas – Austin

19. Gravenstreter, Alicia Nicole. Design and synthesis of conformationally constrained Src SH2 ligands for protein–ligand thermodynamic evaluation.

Degree: Chemistry, 2016, University of Texas – Austin

 Predicting how small structural changes will impact the thermodynamics of binding a small molecule to a protein represents a major challenge in the fields of… (more)

Subjects/Keywords: Cyclopropane; Thermodynamic; Conformational constraint; Preorganization; Src SH2

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APA (6th Edition):

Gravenstreter, A. N. (2016). Design and synthesis of conformationally constrained Src SH2 ligands for protein–ligand thermodynamic evaluation. (Thesis). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/41737

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):

Gravenstreter, Alicia Nicole. “Design and synthesis of conformationally constrained Src SH2 ligands for protein–ligand thermodynamic evaluation.” 2016. Thesis, University of Texas – Austin. Accessed October 18, 2017. http://hdl.handle.net/2152/41737.

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

MLA Handbook (7th Edition):

Gravenstreter, Alicia Nicole. “Design and synthesis of conformationally constrained Src SH2 ligands for protein–ligand thermodynamic evaluation.” 2016. Web. 18 Oct 2017.

Vancouver:

Gravenstreter AN. Design and synthesis of conformationally constrained Src SH2 ligands for protein–ligand thermodynamic evaluation. [Internet] [Thesis]. University of Texas – Austin; 2016. [cited 2017 Oct 18]. Available from: http://hdl.handle.net/2152/41737.

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

Council of Science Editors:

Gravenstreter AN. Design and synthesis of conformationally constrained Src SH2 ligands for protein–ligand thermodynamic evaluation. [Thesis]. University of Texas – Austin; 2016. Available from: http://hdl.handle.net/2152/41737

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

20. Marli Ferreira Curcio. Effects of nitric oxide on the signaling activity of Src kinase associated with the migration of cell lines expressing or not the protein tyrosine phosphatase alpha (PTPalfa).

Degree: 2010, Universidade Federal de São Paulo

 13 Resumo A Proteína Tirosina Fosfatase do tipo receptor (PTP) desempenha funções reguladoras do metabolismo, migração, sobrevivência, proliferação e a diferenciação celular (Hunter, 2000; Tonks,… (more)

Subjects/Keywords: OXIDO NITRICO; QUINASES DA FAMILIA SRC; OXIDO NITRICO; QUINASES DA FAMILIA SRC .; BIOLOGIA MOLECULAR

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APA (6th Edition):

Curcio, M. F. (2010). Effects of nitric oxide on the signaling activity of Src kinase associated with the migration of cell lines expressing or not the protein tyrosine phosphatase alpha (PTPalfa). (Thesis). Universidade Federal de São Paulo. Retrieved from http://www.bdtd.unifesp.br/tede//tde_busca/arquivo.php?codArquivo=712 ; http://www.bdtd.unifesp.br/tede//tde_busca/arquivo.php?codArquivo=713 ; http://www.bdtd.unifesp.br/tede//tde_busca/arquivo.php?codArquivo=714

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):

Curcio, Marli Ferreira. “Effects of nitric oxide on the signaling activity of Src kinase associated with the migration of cell lines expressing or not the protein tyrosine phosphatase alpha (PTPalfa).” 2010. Thesis, Universidade Federal de São Paulo. Accessed October 18, 2017. http://www.bdtd.unifesp.br/tede//tde_busca/arquivo.php?codArquivo=712 ; http://www.bdtd.unifesp.br/tede//tde_busca/arquivo.php?codArquivo=713 ; http://www.bdtd.unifesp.br/tede//tde_busca/arquivo.php?codArquivo=714.

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

MLA Handbook (7th Edition):

Curcio, Marli Ferreira. “Effects of nitric oxide on the signaling activity of Src kinase associated with the migration of cell lines expressing or not the protein tyrosine phosphatase alpha (PTPalfa).” 2010. Web. 18 Oct 2017.

Vancouver:

Curcio MF. Effects of nitric oxide on the signaling activity of Src kinase associated with the migration of cell lines expressing or not the protein tyrosine phosphatase alpha (PTPalfa). [Internet] [Thesis]. Universidade Federal de São Paulo; 2010. [cited 2017 Oct 18]. Available from: http://www.bdtd.unifesp.br/tede//tde_busca/arquivo.php?codArquivo=712 ; http://www.bdtd.unifesp.br/tede//tde_busca/arquivo.php?codArquivo=713 ; http://www.bdtd.unifesp.br/tede//tde_busca/arquivo.php?codArquivo=714.

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

Council of Science Editors:

Curcio MF. Effects of nitric oxide on the signaling activity of Src kinase associated with the migration of cell lines expressing or not the protein tyrosine phosphatase alpha (PTPalfa). [Thesis]. Universidade Federal de São Paulo; 2010. Available from: http://www.bdtd.unifesp.br/tede//tde_busca/arquivo.php?codArquivo=712 ; http://www.bdtd.unifesp.br/tede//tde_busca/arquivo.php?codArquivo=713 ; http://www.bdtd.unifesp.br/tede//tde_busca/arquivo.php?codArquivo=714

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

21. Kousuke, Kasahara. Functional specificity of Src-family kinases regulated by their spatio-temporal localizations : 時空間的な細胞内局在解析からアプローチするSrc型チロシンキナーゼの機能解明.

Degree: Chiba University / 千葉大学

研究科: 千葉大学大学院薬学研究院

修了年:2007

学位:千大院医薬博甲第医薬22号

Advisors/Committee Members: 千葉大学大学院薬学研究院.

Subjects/Keywords: Src-family kinases; Src型チロシンキナーゼ

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APA (6th Edition):

Kousuke, K. (n.d.). Functional specificity of Src-family kinases regulated by their spatio-temporal localizations : 時空間的な細胞内局在解析からアプローチするSrc型チロシンキナーゼの機能解明. (Thesis). Chiba University / 千葉大学. Retrieved from http://opac.ll.chiba-u.jp/da/curator/900047166/

Note: this citation may be lacking information needed for this citation format:
No year of publication.
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Kousuke, Kasahara. “Functional specificity of Src-family kinases regulated by their spatio-temporal localizations : 時空間的な細胞内局在解析からアプローチするSrc型チロシンキナーゼの機能解明.” Thesis, Chiba University / 千葉大学. Accessed October 18, 2017. http://opac.ll.chiba-u.jp/da/curator/900047166/.

Note: this citation may be lacking information needed for this citation format:
No year of publication.
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Kousuke, Kasahara. “Functional specificity of Src-family kinases regulated by their spatio-temporal localizations : 時空間的な細胞内局在解析からアプローチするSrc型チロシンキナーゼの機能解明.” Web. 18 Oct 2017.

Note: this citation may be lacking information needed for this citation format:
No year of publication.

Vancouver:

Kousuke K. Functional specificity of Src-family kinases regulated by their spatio-temporal localizations : 時空間的な細胞内局在解析からアプローチするSrc型チロシンキナーゼの機能解明. [Internet] [Thesis]. Chiba University / 千葉大学; [cited 2017 Oct 18]. Available from: http://opac.ll.chiba-u.jp/da/curator/900047166/.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation
No year of publication.

Council of Science Editors:

Kousuke K. Functional specificity of Src-family kinases regulated by their spatio-temporal localizations : 時空間的な細胞内局在解析からアプローチするSrc型チロシンキナーゼの機能解明. [Thesis]. Chiba University / 千葉大学; Available from: http://opac.ll.chiba-u.jp/da/curator/900047166/

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation
No year of publication.


University of Saskatchewan

22. Smith-Windsor, Erin Lea. Src family kinase involvement in selected cancer cell phenotypes.

Degree: 2011, University of Saskatchewan

 The non-receptor tyrosine kinase Src has been found to be overexpressed and activated in many human cancers, where it has been implicated in changes in… (more)

Subjects/Keywords: proliferation; adhesion; inhibitors; Src family kinases; RNAi; cancer; migration; colony forming ability; Src

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APA (6th Edition):

Smith-Windsor, E. L. (2011). Src family kinase involvement in selected cancer cell phenotypes. (Thesis). University of Saskatchewan. Retrieved from http://hdl.handle.net/10388/etd-03302011-231143

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):

Smith-Windsor, Erin Lea. “Src family kinase involvement in selected cancer cell phenotypes.” 2011. Thesis, University of Saskatchewan. Accessed October 18, 2017. http://hdl.handle.net/10388/etd-03302011-231143.

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

MLA Handbook (7th Edition):

Smith-Windsor, Erin Lea. “Src family kinase involvement in selected cancer cell phenotypes.” 2011. Web. 18 Oct 2017.

Vancouver:

Smith-Windsor EL. Src family kinase involvement in selected cancer cell phenotypes. [Internet] [Thesis]. University of Saskatchewan; 2011. [cited 2017 Oct 18]. Available from: http://hdl.handle.net/10388/etd-03302011-231143.

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

Council of Science Editors:

Smith-Windsor EL. Src family kinase involvement in selected cancer cell phenotypes. [Thesis]. University of Saskatchewan; 2011. Available from: http://hdl.handle.net/10388/etd-03302011-231143

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


Université Paris-Sud – Paris XI

23. Ballesta, Annabelle. Approche combinée expérimentale et mathématique pour la personnalisation sur base moléculaire des thérapies anticancéreuses standards et chronomodulées : A combined experimental and mathematical approach for molecular-based personalization of chronomodulated and standard anticancer therapies.

Degree: Docteur es, Pharmacologie et modélisation mathématique, 2011, Université Paris-Sud – Paris XI

 Personnaliser les traitements anticancéreux sur base moléculaire consiste à optimiser la thérapie en fonction des profils d'expression de gènes des cellules saines et tumorales du… (more)

Subjects/Keywords: Optimisation thérapeutique; Pharmacocinétique-pharmacodynamie moléculaire; Irinotecan; SRC; Therapeutics optimization; Cancer; Mathematical modeling; Systems biology; Molecular pharmacokinetics-pharmacodynamics; Circadian rhythm; Irinotecan; SRC

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APA (6th Edition):

Ballesta, A. (2011). Approche combinée expérimentale et mathématique pour la personnalisation sur base moléculaire des thérapies anticancéreuses standards et chronomodulées : A combined experimental and mathematical approach for molecular-based personalization of chronomodulated and standard anticancer therapies. (Doctoral Dissertation). Université Paris-Sud – Paris XI. Retrieved from http://www.theses.fr/2011PA114810

Chicago Manual of Style (16th Edition):

Ballesta, Annabelle. “Approche combinée expérimentale et mathématique pour la personnalisation sur base moléculaire des thérapies anticancéreuses standards et chronomodulées : A combined experimental and mathematical approach for molecular-based personalization of chronomodulated and standard anticancer therapies.” 2011. Doctoral Dissertation, Université Paris-Sud – Paris XI. Accessed October 18, 2017. http://www.theses.fr/2011PA114810.

MLA Handbook (7th Edition):

Ballesta, Annabelle. “Approche combinée expérimentale et mathématique pour la personnalisation sur base moléculaire des thérapies anticancéreuses standards et chronomodulées : A combined experimental and mathematical approach for molecular-based personalization of chronomodulated and standard anticancer therapies.” 2011. Web. 18 Oct 2017.

Vancouver:

Ballesta A. Approche combinée expérimentale et mathématique pour la personnalisation sur base moléculaire des thérapies anticancéreuses standards et chronomodulées : A combined experimental and mathematical approach for molecular-based personalization of chronomodulated and standard anticancer therapies. [Internet] [Doctoral dissertation]. Université Paris-Sud – Paris XI; 2011. [cited 2017 Oct 18]. Available from: http://www.theses.fr/2011PA114810.

Council of Science Editors:

Ballesta A. Approche combinée expérimentale et mathématique pour la personnalisation sur base moléculaire des thérapies anticancéreuses standards et chronomodulées : A combined experimental and mathematical approach for molecular-based personalization of chronomodulated and standard anticancer therapies. [Doctoral Dissertation]. Université Paris-Sud – Paris XI; 2011. Available from: http://www.theses.fr/2011PA114810

24. Sevos, Jessica. Quand le corps n'en fait qu'à sa tête : étude des effets d'affordance dans la schizophrénie : Non communiqué.

Degree: Docteur es, Psychologie cognitive, 2013, Université Paul Valéry – Montpellier III

Ce travail a pour objet d’étude l’émergence d’effets d’affordance dans la schizophrénie. En effet, les troubles de l’action, observés chez les patients schizophrènes, pourraient être… (more)

Subjects/Keywords: Schizophrénie; Affordance; Paradigme SRC; Perception-action; Cognition incarnée; Schizophrenia; Affordance; SRC paradigm; Perception-action; Embodied cognition

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APA (6th Edition):

Sevos, J. (2013). Quand le corps n'en fait qu'à sa tête : étude des effets d'affordance dans la schizophrénie : Non communiqué. (Doctoral Dissertation). Université Paul Valéry – Montpellier III. Retrieved from http://www.theses.fr/2013MON30063

Chicago Manual of Style (16th Edition):

Sevos, Jessica. “Quand le corps n'en fait qu'à sa tête : étude des effets d'affordance dans la schizophrénie : Non communiqué.” 2013. Doctoral Dissertation, Université Paul Valéry – Montpellier III. Accessed October 18, 2017. http://www.theses.fr/2013MON30063.

MLA Handbook (7th Edition):

Sevos, Jessica. “Quand le corps n'en fait qu'à sa tête : étude des effets d'affordance dans la schizophrénie : Non communiqué.” 2013. Web. 18 Oct 2017.

Vancouver:

Sevos J. Quand le corps n'en fait qu'à sa tête : étude des effets d'affordance dans la schizophrénie : Non communiqué. [Internet] [Doctoral dissertation]. Université Paul Valéry – Montpellier III; 2013. [cited 2017 Oct 18]. Available from: http://www.theses.fr/2013MON30063.

Council of Science Editors:

Sevos J. Quand le corps n'en fait qu'à sa tête : étude des effets d'affordance dans la schizophrénie : Non communiqué. [Doctoral Dissertation]. Université Paul Valéry – Montpellier III; 2013. Available from: http://www.theses.fr/2013MON30063

25. Shi, Xiaoli. Etude de la spécificité des interactions protéine-protéine : application au complexe Alix-domaine SH3 des Src Kinases : Studies on protein-protein interaction : and its applications in ALIX/SFKs-SH3 complexes.

Degree: Docteur es, Biochimie structurale, 2011, Aix-Marseille 1

Les domaines SH3 (Src Homology domain) représentent l'un des modules protéiques le plus largement répandu dans la nature. Ils participent à des interactions intra- et… (more)

Subjects/Keywords: Interaction Protéine-Protéine; Vih; Nef; Src Kinase; Domaine SH3; Alix; Protein-Protein Interaction; Hiv; Nef; Src Kinase; SH3 domain; Alix

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

APA (6th Edition):

Shi, X. (2011). Etude de la spécificité des interactions protéine-protéine : application au complexe Alix-domaine SH3 des Src Kinases : Studies on protein-protein interaction : and its applications in ALIX/SFKs-SH3 complexes. (Doctoral Dissertation). Aix-Marseille 1. Retrieved from http://www.theses.fr/2011AIX10024

Chicago Manual of Style (16th Edition):

Shi, Xiaoli. “Etude de la spécificité des interactions protéine-protéine : application au complexe Alix-domaine SH3 des Src Kinases : Studies on protein-protein interaction : and its applications in ALIX/SFKs-SH3 complexes.” 2011. Doctoral Dissertation, Aix-Marseille 1. Accessed October 18, 2017. http://www.theses.fr/2011AIX10024.

MLA Handbook (7th Edition):

Shi, Xiaoli. “Etude de la spécificité des interactions protéine-protéine : application au complexe Alix-domaine SH3 des Src Kinases : Studies on protein-protein interaction : and its applications in ALIX/SFKs-SH3 complexes.” 2011. Web. 18 Oct 2017.

Vancouver:

Shi X. Etude de la spécificité des interactions protéine-protéine : application au complexe Alix-domaine SH3 des Src Kinases : Studies on protein-protein interaction : and its applications in ALIX/SFKs-SH3 complexes. [Internet] [Doctoral dissertation]. Aix-Marseille 1; 2011. [cited 2017 Oct 18]. Available from: http://www.theses.fr/2011AIX10024.

Council of Science Editors:

Shi X. Etude de la spécificité des interactions protéine-protéine : application au complexe Alix-domaine SH3 des Src Kinases : Studies on protein-protein interaction : and its applications in ALIX/SFKs-SH3 complexes. [Doctoral Dissertation]. Aix-Marseille 1; 2011. Available from: http://www.theses.fr/2011AIX10024

26. Hébert Chatelain, Etienne. Impact des phosphorylations sur tyrosine sur le métabolisme mitochondrial : régulation et impacts fonctionnels des phosphorylations induites par la Src kinase : Tyrosine phosphorylation impact on mitochondrial metabolism : regulation and functionnal impacts of phosphorylation mediated by the Src kinase.

Degree: Docteur es, Sciences, technologie, santé. Biologie cellulaire et physiopathologie, 2011, Université de Bordeaux Segalen

La mitochondrie est une organelle très importante vu son implication dans plusieurs processus cellulaires. Elle produit notamment la majeure partie de l'énergie qui est consommée… (more)

Subjects/Keywords: Mitochondrie; Phosphorylation oxydative; Tyrosine; Phosphorylation; Src kinase; PTP1B; Mitochondria; Oxidative phosphorylation; Tyrosine; Phosphorylation; Src kinase; PTP1B

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

APA (6th Edition):

Hébert Chatelain, E. (2011). Impact des phosphorylations sur tyrosine sur le métabolisme mitochondrial : régulation et impacts fonctionnels des phosphorylations induites par la Src kinase : Tyrosine phosphorylation impact on mitochondrial metabolism : regulation and functionnal impacts of phosphorylation mediated by the Src kinase. (Doctoral Dissertation). Université de Bordeaux Segalen. Retrieved from http://www.theses.fr/2011BOR21830

Chicago Manual of Style (16th Edition):

Hébert Chatelain, Etienne. “Impact des phosphorylations sur tyrosine sur le métabolisme mitochondrial : régulation et impacts fonctionnels des phosphorylations induites par la Src kinase : Tyrosine phosphorylation impact on mitochondrial metabolism : regulation and functionnal impacts of phosphorylation mediated by the Src kinase.” 2011. Doctoral Dissertation, Université de Bordeaux Segalen. Accessed October 18, 2017. http://www.theses.fr/2011BOR21830.

MLA Handbook (7th Edition):

Hébert Chatelain, Etienne. “Impact des phosphorylations sur tyrosine sur le métabolisme mitochondrial : régulation et impacts fonctionnels des phosphorylations induites par la Src kinase : Tyrosine phosphorylation impact on mitochondrial metabolism : regulation and functionnal impacts of phosphorylation mediated by the Src kinase.” 2011. Web. 18 Oct 2017.

Vancouver:

Hébert Chatelain E. Impact des phosphorylations sur tyrosine sur le métabolisme mitochondrial : régulation et impacts fonctionnels des phosphorylations induites par la Src kinase : Tyrosine phosphorylation impact on mitochondrial metabolism : regulation and functionnal impacts of phosphorylation mediated by the Src kinase. [Internet] [Doctoral dissertation]. Université de Bordeaux Segalen; 2011. [cited 2017 Oct 18]. Available from: http://www.theses.fr/2011BOR21830.

Council of Science Editors:

Hébert Chatelain E. Impact des phosphorylations sur tyrosine sur le métabolisme mitochondrial : régulation et impacts fonctionnels des phosphorylations induites par la Src kinase : Tyrosine phosphorylation impact on mitochondrial metabolism : regulation and functionnal impacts of phosphorylation mediated by the Src kinase. [Doctoral Dissertation]. Université de Bordeaux Segalen; 2011. Available from: http://www.theses.fr/2011BOR21830

27. Paliwal, Preeti. Role of Src family kinase, Hck, in the regulation of p73, a homolog of tumor suppressor p53; -.

Degree: Cellular and Molecular Biology, 2007, Jawaharlal Nehru University

None

References p.81-98

Advisors/Committee Members: Swarup, Ghanshyam and Radha, V.

Subjects/Keywords: Src; homolog; tumor; suppressor

Page 1

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

APA (6th Edition):

Paliwal, P. (2007). Role of Src family kinase, Hck, in the regulation of p73, a homolog of tumor suppressor p53; -. (Thesis). Jawaharlal Nehru University. Retrieved from http://shodhganga.inflibnet.ac.in/handle/10603/29525

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):

Paliwal, Preeti. “Role of Src family kinase, Hck, in the regulation of p73, a homolog of tumor suppressor p53; -.” 2007. Thesis, Jawaharlal Nehru University. Accessed October 18, 2017. http://shodhganga.inflibnet.ac.in/handle/10603/29525.

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

MLA Handbook (7th Edition):

Paliwal, Preeti. “Role of Src family kinase, Hck, in the regulation of p73, a homolog of tumor suppressor p53; -.” 2007. Web. 18 Oct 2017.

Vancouver:

Paliwal P. Role of Src family kinase, Hck, in the regulation of p73, a homolog of tumor suppressor p53; -. [Internet] [Thesis]. Jawaharlal Nehru University; 2007. [cited 2017 Oct 18]. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/29525.

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

Council of Science Editors:

Paliwal P. Role of Src family kinase, Hck, in the regulation of p73, a homolog of tumor suppressor p53; -. [Thesis]. Jawaharlal Nehru University; 2007. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/29525

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


University of Ottawa

28. Konarski, Yulia. SHP-1/ Src Complex is a Master Regulator of the IL-12/IL-23 pro- and IL-10/IL-27 Anti-inflammatory Axis in TLR4-activated Signaling Pathways in Human Monocytes and Macrophages .

Degree: 2013, University of Ottawa

 Although the etiology surrounding many autoimmune diseases remains unknown, the underlying characteristic of many of these diseases is a disruption in the balance of pro-… (more)

Subjects/Keywords: Immunology; SHP-1; Src; IL-12 family; IL-10; Autoimmune Diseases

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

APA (6th Edition):

Konarski, Y. (2013). SHP-1/ Src Complex is a Master Regulator of the IL-12/IL-23 pro- and IL-10/IL-27 Anti-inflammatory Axis in TLR4-activated Signaling Pathways in Human Monocytes and Macrophages . (Thesis). University of Ottawa. Retrieved from http://hdl.handle.net/10393/25999

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):

Konarski, Yulia. “SHP-1/ Src Complex is a Master Regulator of the IL-12/IL-23 pro- and IL-10/IL-27 Anti-inflammatory Axis in TLR4-activated Signaling Pathways in Human Monocytes and Macrophages .” 2013. Thesis, University of Ottawa. Accessed October 18, 2017. http://hdl.handle.net/10393/25999.

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

MLA Handbook (7th Edition):

Konarski, Yulia. “SHP-1/ Src Complex is a Master Regulator of the IL-12/IL-23 pro- and IL-10/IL-27 Anti-inflammatory Axis in TLR4-activated Signaling Pathways in Human Monocytes and Macrophages .” 2013. Web. 18 Oct 2017.

Vancouver:

Konarski Y. SHP-1/ Src Complex is a Master Regulator of the IL-12/IL-23 pro- and IL-10/IL-27 Anti-inflammatory Axis in TLR4-activated Signaling Pathways in Human Monocytes and Macrophages . [Internet] [Thesis]. University of Ottawa; 2013. [cited 2017 Oct 18]. Available from: http://hdl.handle.net/10393/25999.

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

Council of Science Editors:

Konarski Y. SHP-1/ Src Complex is a Master Regulator of the IL-12/IL-23 pro- and IL-10/IL-27 Anti-inflammatory Axis in TLR4-activated Signaling Pathways in Human Monocytes and Macrophages . [Thesis]. University of Ottawa; 2013. Available from: http://hdl.handle.net/10393/25999

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

29. Gouin-Boisvert, Béatrice. Implication des protéines adaptatrices Tks4 et Tks5 dans la dégradation du cartilage articulaire par les synoviocytes dans la polyarthrite rhumatoïde.

Degree: M. Sc., Immunologie, 2015, Université de Sherbrooke

 La polyarthrite rhumatoïde (PR) est une maladie inflammatoire auto-immune qui affecte environ 1% de la population. Il s’agit d’une maladie douloureuse et débilitante, caractérisée par… (more)

Subjects/Keywords: Polyarthrite rhumatoïde; Invasion cellulaire; Tks4; Tks5; Invadosome; Invadopode; Src; FLS

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

APA (6th Edition):

Gouin-Boisvert, B. (2015). Implication des protéines adaptatrices Tks4 et Tks5 dans la dégradation du cartilage articulaire par les synoviocytes dans la polyarthrite rhumatoïde. (Masters Thesis). Université de Sherbrooke. Retrieved from http://www.collectionscanada.gc.ca/obj/thesescanada/vol2/QSHERU/TC-QSHERU-11143_7612.pdf ; http://savoirs.usherbrooke.ca/bitstream/11143/7612/3/Gouin_Boisvert_Beatrice_MSc_2015.pdf

Chicago Manual of Style (16th Edition):

Gouin-Boisvert, Béatrice. “Implication des protéines adaptatrices Tks4 et Tks5 dans la dégradation du cartilage articulaire par les synoviocytes dans la polyarthrite rhumatoïde.” 2015. Masters Thesis, Université de Sherbrooke. Accessed October 18, 2017. http://www.collectionscanada.gc.ca/obj/thesescanada/vol2/QSHERU/TC-QSHERU-11143_7612.pdf ; http://savoirs.usherbrooke.ca/bitstream/11143/7612/3/Gouin_Boisvert_Beatrice_MSc_2015.pdf.

MLA Handbook (7th Edition):

Gouin-Boisvert, Béatrice. “Implication des protéines adaptatrices Tks4 et Tks5 dans la dégradation du cartilage articulaire par les synoviocytes dans la polyarthrite rhumatoïde.” 2015. Web. 18 Oct 2017.

Vancouver:

Gouin-Boisvert B. Implication des protéines adaptatrices Tks4 et Tks5 dans la dégradation du cartilage articulaire par les synoviocytes dans la polyarthrite rhumatoïde. [Internet] [Masters thesis]. Université de Sherbrooke; 2015. [cited 2017 Oct 18]. Available from: http://www.collectionscanada.gc.ca/obj/thesescanada/vol2/QSHERU/TC-QSHERU-11143_7612.pdf ; http://savoirs.usherbrooke.ca/bitstream/11143/7612/3/Gouin_Boisvert_Beatrice_MSc_2015.pdf.

Council of Science Editors:

Gouin-Boisvert B. Implication des protéines adaptatrices Tks4 et Tks5 dans la dégradation du cartilage articulaire par les synoviocytes dans la polyarthrite rhumatoïde. [Masters Thesis]. Université de Sherbrooke; 2015. Available from: http://www.collectionscanada.gc.ca/obj/thesescanada/vol2/QSHERU/TC-QSHERU-11143_7612.pdf ; http://savoirs.usherbrooke.ca/bitstream/11143/7612/3/Gouin_Boisvert_Beatrice_MSc_2015.pdf


University of Edinburgh

30. Maeda, Sayaka. GIS-based Multi-criteria Evaluation with Analytical Hierarchy Process to assess suitable areas for Willow Short Rotation Coppice production in Scotland.

Degree: 2007, University of Edinburgh

 In Scotland, agriculture remains the dominant form of land use in rural areas, indicating that the successful implementation of renewable energy strategies has the potential… (more)

Subjects/Keywords: SRC; Analytic Hierarchy Process; Network Analysis; Scotland; Willow; Biomass

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

APA (6th Edition):

Maeda, S. (2007). GIS-based Multi-criteria Evaluation with Analytical Hierarchy Process to assess suitable areas for Willow Short Rotation Coppice production in Scotland. (Thesis). University of Edinburgh. Retrieved from http://hdl.handle.net/1842/1883

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):

Maeda, Sayaka. “GIS-based Multi-criteria Evaluation with Analytical Hierarchy Process to assess suitable areas for Willow Short Rotation Coppice production in Scotland.” 2007. Thesis, University of Edinburgh. Accessed October 18, 2017. http://hdl.handle.net/1842/1883.

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

MLA Handbook (7th Edition):

Maeda, Sayaka. “GIS-based Multi-criteria Evaluation with Analytical Hierarchy Process to assess suitable areas for Willow Short Rotation Coppice production in Scotland.” 2007. Web. 18 Oct 2017.

Vancouver:

Maeda S. GIS-based Multi-criteria Evaluation with Analytical Hierarchy Process to assess suitable areas for Willow Short Rotation Coppice production in Scotland. [Internet] [Thesis]. University of Edinburgh; 2007. [cited 2017 Oct 18]. Available from: http://hdl.handle.net/1842/1883.

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

Council of Science Editors:

Maeda S. GIS-based Multi-criteria Evaluation with Analytical Hierarchy Process to assess suitable areas for Willow Short Rotation Coppice production in Scotland. [Thesis]. University of Edinburgh; 2007. Available from: http://hdl.handle.net/1842/1883

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

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