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You searched for subject:(Wnt catenin signaling). Showing records 1 – 30 of 61 total matches.

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Vanderbilt University

1. Jernigan, Kristin Kalie. Role of LRP6 in the Wnt/beta-catenin pathway and its regulation by heterotrimeric G proteins.

Degree: PhD, Cell and Developmental Biology, 2010, Vanderbilt University

 The Wnt/beta-catenin signaling pathway is a well-conserved signal transduction pathway that is highly regulated during metazoan development and is associated with various human diseases. In… (more)

Subjects/Keywords: LRP6; G protein signaling; wnt signaling; beta-catenin

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APA (6th Edition):

Jernigan, K. K. (2010). Role of LRP6 in the Wnt/beta-catenin pathway and its regulation by heterotrimeric G proteins. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://etd.library.vanderbilt.edu/available/etd-03022010-112411/ ;

Chicago Manual of Style (16th Edition):

Jernigan, Kristin Kalie. “Role of LRP6 in the Wnt/beta-catenin pathway and its regulation by heterotrimeric G proteins.” 2010. Doctoral Dissertation, Vanderbilt University. Accessed December 08, 2019. http://etd.library.vanderbilt.edu/available/etd-03022010-112411/ ;.

MLA Handbook (7th Edition):

Jernigan, Kristin Kalie. “Role of LRP6 in the Wnt/beta-catenin pathway and its regulation by heterotrimeric G proteins.” 2010. Web. 08 Dec 2019.

Vancouver:

Jernigan KK. Role of LRP6 in the Wnt/beta-catenin pathway and its regulation by heterotrimeric G proteins. [Internet] [Doctoral dissertation]. Vanderbilt University; 2010. [cited 2019 Dec 08]. Available from: http://etd.library.vanderbilt.edu/available/etd-03022010-112411/ ;.

Council of Science Editors:

Jernigan KK. Role of LRP6 in the Wnt/beta-catenin pathway and its regulation by heterotrimeric G proteins. [Doctoral Dissertation]. Vanderbilt University; 2010. Available from: http://etd.library.vanderbilt.edu/available/etd-03022010-112411/ ;


UCLA

2. Kershaw, Kathleen. Divergent regulation and function of Wnt/β-catenin signaling and TCF transcription factors in pancreatic cancer.

Degree: Cellular & Molecular Pathology, 2018, UCLA

 With steadily increasing incidence and an 8-9% 5-year survival rate, pancreatic ductal adenocarcinoma (PDA) treatment represents an urgent, unmet clinical need. Hindered by long asymptomatic… (more)

Subjects/Keywords: Molecular biology; pancreatic cancer; pancreatic ductal adenocarcinoma; TCF/LEF; Wnt signaling; Wnt/β-catenin

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APA (6th Edition):

Kershaw, K. (2018). Divergent regulation and function of Wnt/β-catenin signaling and TCF transcription factors in pancreatic cancer. (Thesis). UCLA. Retrieved from http://www.escholarship.org/uc/item/50q4r472

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):

Kershaw, Kathleen. “Divergent regulation and function of Wnt/β-catenin signaling and TCF transcription factors in pancreatic cancer.” 2018. Thesis, UCLA. Accessed December 08, 2019. http://www.escholarship.org/uc/item/50q4r472.

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

MLA Handbook (7th Edition):

Kershaw, Kathleen. “Divergent regulation and function of Wnt/β-catenin signaling and TCF transcription factors in pancreatic cancer.” 2018. Web. 08 Dec 2019.

Vancouver:

Kershaw K. Divergent regulation and function of Wnt/β-catenin signaling and TCF transcription factors in pancreatic cancer. [Internet] [Thesis]. UCLA; 2018. [cited 2019 Dec 08]. Available from: http://www.escholarship.org/uc/item/50q4r472.

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

Council of Science Editors:

Kershaw K. Divergent regulation and function of Wnt/β-catenin signaling and TCF transcription factors in pancreatic cancer. [Thesis]. UCLA; 2018. Available from: http://www.escholarship.org/uc/item/50q4r472

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


NSYSU

3. Tai , Po-han. Therapeutic potential and mechanism of LECT2 for liver cancer.

Degree: Master, Institute of Biomedical Sciences, 2014, NSYSU

 Hepatocellular carcinoma (HCC) is one of the most common cancers in the world. However, current therapeutic modalities for HCC, including surgery, transendothelial embolization (TAE) and… (more)

Subjects/Keywords: β-catenin; Hepatocellular carcinoma; Wnt signaling pathway; Cancer stem cell; LECT2

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APA (6th Edition):

Tai , P. (2014). Therapeutic potential and mechanism of LECT2 for liver cancer. (Thesis). NSYSU. Retrieved from http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0621114-111413

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):

Tai , Po-han. “Therapeutic potential and mechanism of LECT2 for liver cancer.” 2014. Thesis, NSYSU. Accessed December 08, 2019. http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0621114-111413.

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

MLA Handbook (7th Edition):

Tai , Po-han. “Therapeutic potential and mechanism of LECT2 for liver cancer.” 2014. Web. 08 Dec 2019.

Vancouver:

Tai P. Therapeutic potential and mechanism of LECT2 for liver cancer. [Internet] [Thesis]. NSYSU; 2014. [cited 2019 Dec 08]. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0621114-111413.

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

Council of Science Editors:

Tai P. Therapeutic potential and mechanism of LECT2 for liver cancer. [Thesis]. NSYSU; 2014. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0621114-111413

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


NSYSU

4. Wu, Ping-Hsuan. The role of LECT2 in liver carcinogenesis.

Degree: Master, Biological Sciences, 2011, NSYSU

 Leukocyte cell-derived chemotaxin 2 (LECT2) is first isolated as a 16-kDa secreted protein from cultured fluid of phytohemagglutinin-activated human T-cell leukemia SKW-3 cells. Recently LECT2… (more)

Subjects/Keywords: Wnt pathway; β-catenin; Hepatocellular carcinoma; cellular signaling; LECT2

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APA (6th Edition):

Wu, P. (2011). The role of LECT2 in liver carcinogenesis. (Thesis). NSYSU. Retrieved from http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0824111-001511

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):

Wu, Ping-Hsuan. “The role of LECT2 in liver carcinogenesis.” 2011. Thesis, NSYSU. Accessed December 08, 2019. http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0824111-001511.

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

MLA Handbook (7th Edition):

Wu, Ping-Hsuan. “The role of LECT2 in liver carcinogenesis.” 2011. Web. 08 Dec 2019.

Vancouver:

Wu P. The role of LECT2 in liver carcinogenesis. [Internet] [Thesis]. NSYSU; 2011. [cited 2019 Dec 08]. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0824111-001511.

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

Council of Science Editors:

Wu P. The role of LECT2 in liver carcinogenesis. [Thesis]. NSYSU; 2011. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0824111-001511

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


University of Illinois – Chicago

5. Huang, Shuo. The Role of Damaged DNA Binding Protein 2 in Colon Cancer.

Degree: 2017, University of Illinois – Chicago

 Deregulation of the Wnt/β-catenin signaling pathway drives the development of colorectal cancer (CRC) but understanding of this pathway remains incomplete. Here we report that the… (more)

Subjects/Keywords: Colon Cancer; Wnt/ β-catenin Signaling; DDB2; RNF43

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APA (6th Edition):

Huang, S. (2017). The Role of Damaged DNA Binding Protein 2 in Colon Cancer. (Thesis). University of Illinois – Chicago. Retrieved from http://hdl.handle.net/10027/22150

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):

Huang, Shuo. “The Role of Damaged DNA Binding Protein 2 in Colon Cancer.” 2017. Thesis, University of Illinois – Chicago. Accessed December 08, 2019. http://hdl.handle.net/10027/22150.

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

MLA Handbook (7th Edition):

Huang, Shuo. “The Role of Damaged DNA Binding Protein 2 in Colon Cancer.” 2017. Web. 08 Dec 2019.

Vancouver:

Huang S. The Role of Damaged DNA Binding Protein 2 in Colon Cancer. [Internet] [Thesis]. University of Illinois – Chicago; 2017. [cited 2019 Dec 08]. Available from: http://hdl.handle.net/10027/22150.

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

Council of Science Editors:

Huang S. The Role of Damaged DNA Binding Protein 2 in Colon Cancer. [Thesis]. University of Illinois – Chicago; 2017. Available from: http://hdl.handle.net/10027/22150

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

6. Okuda, Yukiko; Keisuke, Nakano; Koji, Suzuki; Yoshihiko, Sugita; Katsutoshi, Kubo; Hatsuhiko, Maeda; Norimasa, Okafuji; Hiromasa, Hasegawa. Wnt signaling as a possible promoting factor of cell differentiation in pleomorphic adenomas : 多形腺腫における細胞分化の促進因子としての Wnt シグナルの可能性.

Degree: 博士(歯学), 2015, Matsumoto Dental University / 松本歯科大学

There are well known that Wnt signaling was some roles of cell differentiation at the development tissues, especially the oral and maxillofacial regions of some… (more)

Subjects/Keywords: pleomorphic adenoma; Wnt signaling; β-catenin; cytokeratin; immunohistochemistry; cell differentiation

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APA (6th Edition):

Okuda, Yukiko; Keisuke, Nakano; Koji, Suzuki; Yoshihiko, Sugita; Katsutoshi, Kubo; Hatsuhiko, Maeda; Norimasa, Okafuji; Hiromasa, . H. (2015). Wnt signaling as a possible promoting factor of cell differentiation in pleomorphic adenomas : 多形腺腫における細胞分化の促進因子としての Wnt シグナルの可能性. (Thesis). Matsumoto Dental University / 松本歯科大学. Retrieved from http://id.nii.ac.jp/1070/00002398/

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):

Okuda, Yukiko; Keisuke, Nakano; Koji, Suzuki; Yoshihiko, Sugita; Katsutoshi, Kubo; Hatsuhiko, Maeda; Norimasa, Okafuji; Hiromasa, Hasegawa. “Wnt signaling as a possible promoting factor of cell differentiation in pleomorphic adenomas : 多形腺腫における細胞分化の促進因子としての Wnt シグナルの可能性.” 2015. Thesis, Matsumoto Dental University / 松本歯科大学. Accessed December 08, 2019. http://id.nii.ac.jp/1070/00002398/.

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

MLA Handbook (7th Edition):

Okuda, Yukiko; Keisuke, Nakano; Koji, Suzuki; Yoshihiko, Sugita; Katsutoshi, Kubo; Hatsuhiko, Maeda; Norimasa, Okafuji; Hiromasa, Hasegawa. “Wnt signaling as a possible promoting factor of cell differentiation in pleomorphic adenomas : 多形腺腫における細胞分化の促進因子としての Wnt シグナルの可能性.” 2015. Web. 08 Dec 2019.

Vancouver:

Okuda, Yukiko; Keisuke, Nakano; Koji, Suzuki; Yoshihiko, Sugita; Katsutoshi, Kubo; Hatsuhiko, Maeda; Norimasa, Okafuji; Hiromasa H. Wnt signaling as a possible promoting factor of cell differentiation in pleomorphic adenomas : 多形腺腫における細胞分化の促進因子としての Wnt シグナルの可能性. [Internet] [Thesis]. Matsumoto Dental University / 松本歯科大学; 2015. [cited 2019 Dec 08]. Available from: http://id.nii.ac.jp/1070/00002398/.

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

Council of Science Editors:

Okuda, Yukiko; Keisuke, Nakano; Koji, Suzuki; Yoshihiko, Sugita; Katsutoshi, Kubo; Hatsuhiko, Maeda; Norimasa, Okafuji; Hiromasa H. Wnt signaling as a possible promoting factor of cell differentiation in pleomorphic adenomas : 多形腺腫における細胞分化の促進因子としての Wnt シグナルの可能性. [Thesis]. Matsumoto Dental University / 松本歯科大学; 2015. Available from: http://id.nii.ac.jp/1070/00002398/

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


University of Ottawa

7. Bastarache, Sophie. Studies on the Expression and Phosphorylation of the USP4 Deubiquitinating Enzyme .

Degree: 2011, University of Ottawa

 The USP4 is a deubiquitinating enzyme found elevated in certain human lung and adrenal tumours. USP4 has a very close relative, USP15, which has caused… (more)

Subjects/Keywords: USP4; Ubiquitin; Proteasome; B-catenin; Wnt signaling; GRK2

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APA (6th Edition):

Bastarache, S. (2011). Studies on the Expression and Phosphorylation of the USP4 Deubiquitinating Enzyme . (Thesis). University of Ottawa. Retrieved from http://hdl.handle.net/10393/20184

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):

Bastarache, Sophie. “Studies on the Expression and Phosphorylation of the USP4 Deubiquitinating Enzyme .” 2011. Thesis, University of Ottawa. Accessed December 08, 2019. http://hdl.handle.net/10393/20184.

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

MLA Handbook (7th Edition):

Bastarache, Sophie. “Studies on the Expression and Phosphorylation of the USP4 Deubiquitinating Enzyme .” 2011. Web. 08 Dec 2019.

Vancouver:

Bastarache S. Studies on the Expression and Phosphorylation of the USP4 Deubiquitinating Enzyme . [Internet] [Thesis]. University of Ottawa; 2011. [cited 2019 Dec 08]. Available from: http://hdl.handle.net/10393/20184.

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

Council of Science Editors:

Bastarache S. Studies on the Expression and Phosphorylation of the USP4 Deubiquitinating Enzyme . [Thesis]. University of Ottawa; 2011. Available from: http://hdl.handle.net/10393/20184

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


Vanderbilt University

8. Saito-Diaz, Vicente Kenyi. Regulation of Wnt Receptor Activation by the Tumor Suppressor APC.

Degree: PhD, Cell and Developmental Biology, 2017, Vanderbilt University

 The Wnt pathway is a highly-conserved pathway that controls many developmental processes and is mutated in many human diseases (e.g., cancer). The tumor suppressor adenomatous… (more)

Subjects/Keywords: endocytosis; beta-catenin; LRP6; APC; Wnt signaling; clathrin; caveolin; colorectal cancer

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APA (6th Edition):

Saito-Diaz, V. K. (2017). Regulation of Wnt Receptor Activation by the Tumor Suppressor APC. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://etd.library.vanderbilt.edu/available/etd-03272017-113107/ ;

Chicago Manual of Style (16th Edition):

Saito-Diaz, Vicente Kenyi. “Regulation of Wnt Receptor Activation by the Tumor Suppressor APC.” 2017. Doctoral Dissertation, Vanderbilt University. Accessed December 08, 2019. http://etd.library.vanderbilt.edu/available/etd-03272017-113107/ ;.

MLA Handbook (7th Edition):

Saito-Diaz, Vicente Kenyi. “Regulation of Wnt Receptor Activation by the Tumor Suppressor APC.” 2017. Web. 08 Dec 2019.

Vancouver:

Saito-Diaz VK. Regulation of Wnt Receptor Activation by the Tumor Suppressor APC. [Internet] [Doctoral dissertation]. Vanderbilt University; 2017. [cited 2019 Dec 08]. Available from: http://etd.library.vanderbilt.edu/available/etd-03272017-113107/ ;.

Council of Science Editors:

Saito-Diaz VK. Regulation of Wnt Receptor Activation by the Tumor Suppressor APC. [Doctoral Dissertation]. Vanderbilt University; 2017. Available from: http://etd.library.vanderbilt.edu/available/etd-03272017-113107/ ;


University of Toronto

9. Hong, Helen. Identifying Pharmacological Therapeutics for Aggressive Fibromatosis.

Degree: 2011, University of Toronto

Aggressive fibromatosis is a fibroproliferative tumour that can occur as a sporadic lesion or a manifestation in FAP patients. Tumours are characterized by the stabilization… (more)

Subjects/Keywords: aggressive fibromatosis; beta-catenin; wnt signaling; mouse model; 0307; 0992

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APA (6th Edition):

Hong, H. (2011). Identifying Pharmacological Therapeutics for Aggressive Fibromatosis. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/27340

Chicago Manual of Style (16th Edition):

Hong, Helen. “Identifying Pharmacological Therapeutics for Aggressive Fibromatosis.” 2011. Masters Thesis, University of Toronto. Accessed December 08, 2019. http://hdl.handle.net/1807/27340.

MLA Handbook (7th Edition):

Hong, Helen. “Identifying Pharmacological Therapeutics for Aggressive Fibromatosis.” 2011. Web. 08 Dec 2019.

Vancouver:

Hong H. Identifying Pharmacological Therapeutics for Aggressive Fibromatosis. [Internet] [Masters thesis]. University of Toronto; 2011. [cited 2019 Dec 08]. Available from: http://hdl.handle.net/1807/27340.

Council of Science Editors:

Hong H. Identifying Pharmacological Therapeutics for Aggressive Fibromatosis. [Masters Thesis]. University of Toronto; 2011. Available from: http://hdl.handle.net/1807/27340


Rice University

10. Massey, Joseph Kyle. Wnt/ß-catenin Signaling Dynamics in Human Cells.

Degree: PhD, Natural Sciences, 2019, Rice University

 Many biological processes are coordinated by intercellular signaling, and all intercellular signaling pathways have been implicated in multiple roles throughout an organism’s lifetime. While the… (more)

Subjects/Keywords: stem-cells; signaling; differentiation; wnt; ß-catenin; developmental biology; systems biology

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APA (6th Edition):

Massey, J. K. (2019). Wnt/ß-catenin Signaling Dynamics in Human Cells. (Doctoral Dissertation). Rice University. Retrieved from http://hdl.handle.net/1911/105976

Chicago Manual of Style (16th Edition):

Massey, Joseph Kyle. “Wnt/ß-catenin Signaling Dynamics in Human Cells.” 2019. Doctoral Dissertation, Rice University. Accessed December 08, 2019. http://hdl.handle.net/1911/105976.

MLA Handbook (7th Edition):

Massey, Joseph Kyle. “Wnt/ß-catenin Signaling Dynamics in Human Cells.” 2019. Web. 08 Dec 2019.

Vancouver:

Massey JK. Wnt/ß-catenin Signaling Dynamics in Human Cells. [Internet] [Doctoral dissertation]. Rice University; 2019. [cited 2019 Dec 08]. Available from: http://hdl.handle.net/1911/105976.

Council of Science Editors:

Massey JK. Wnt/ß-catenin Signaling Dynamics in Human Cells. [Doctoral Dissertation]. Rice University; 2019. Available from: http://hdl.handle.net/1911/105976


University of Vienna

11. Vonbrüll, Matthias. Manipulation of Wnt signaling in tumorcells with antisense molecules.

Degree: 2018, University of Vienna

Seit der Erfindung von Antisense Molekülen gab es zahlreiche Versuche diese therapeutisch anzuwenden. Die FDA Zulassungen von Fomivirsen, Pegaptanib und Mipomersen heben das große Potential… (more)

Subjects/Keywords: 42.13 Molekularbiologie; Antisense Molekül / β-catenin / Morpholino / PNA / Wnt Signalweg; Antisense / β-catenin / Morpholino / PNA / Wnt signaling

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APA (6th Edition):

Vonbrüll, M. (2018). Manipulation of Wnt signaling in tumorcells with antisense molecules. (Thesis). University of Vienna. Retrieved from http://othes.univie.ac.at/53305/

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):

Vonbrüll, Matthias. “Manipulation of Wnt signaling in tumorcells with antisense molecules.” 2018. Thesis, University of Vienna. Accessed December 08, 2019. http://othes.univie.ac.at/53305/.

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

MLA Handbook (7th Edition):

Vonbrüll, Matthias. “Manipulation of Wnt signaling in tumorcells with antisense molecules.” 2018. Web. 08 Dec 2019.

Vancouver:

Vonbrüll M. Manipulation of Wnt signaling in tumorcells with antisense molecules. [Internet] [Thesis]. University of Vienna; 2018. [cited 2019 Dec 08]. Available from: http://othes.univie.ac.at/53305/.

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

Council of Science Editors:

Vonbrüll M. Manipulation of Wnt signaling in tumorcells with antisense molecules. [Thesis]. University of Vienna; 2018. Available from: http://othes.univie.ac.at/53305/

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


University of Southern California

12. Ou, Chen-Yin. Differential role of two coactivators, CCAR1 and CARM1, for dysregulated beta-catenin activity in colorectal cancer cell growth and gene expression.

Degree: PhD, Genetic, Molecular & Cellular Biology, 2012, University of Southern California

 Aberrant activation of Wnt/beta-catenin signaling is recognized as a critical factor in the etiology of colorectal cancer. Evidence has suggested that dysregulated beta-catenin activity is… (more)

Subjects/Keywords: colorectal cancer; colon cancer; transcriptional regulation; Wnt signaling; beta-catenin; CARM1; CCAR1; coactivator

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APA (6th Edition):

Ou, C. (2012). Differential role of two coactivators, CCAR1 and CARM1, for dysregulated beta-catenin activity in colorectal cancer cell growth and gene expression. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/310293/rec/1987

Chicago Manual of Style (16th Edition):

Ou, Chen-Yin. “Differential role of two coactivators, CCAR1 and CARM1, for dysregulated beta-catenin activity in colorectal cancer cell growth and gene expression.” 2012. Doctoral Dissertation, University of Southern California. Accessed December 08, 2019. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/310293/rec/1987.

MLA Handbook (7th Edition):

Ou, Chen-Yin. “Differential role of two coactivators, CCAR1 and CARM1, for dysregulated beta-catenin activity in colorectal cancer cell growth and gene expression.” 2012. Web. 08 Dec 2019.

Vancouver:

Ou C. Differential role of two coactivators, CCAR1 and CARM1, for dysregulated beta-catenin activity in colorectal cancer cell growth and gene expression. [Internet] [Doctoral dissertation]. University of Southern California; 2012. [cited 2019 Dec 08]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/310293/rec/1987.

Council of Science Editors:

Ou C. Differential role of two coactivators, CCAR1 and CARM1, for dysregulated beta-catenin activity in colorectal cancer cell growth and gene expression. [Doctoral Dissertation]. University of Southern California; 2012. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/310293/rec/1987


University of Rochester

13. Paris, Nicole. Role of Wilms Tumor 1 and β-Catenin in Embryonic Diaphragm Development.

Degree: PhD, 2015, University of Rochester

 Congenital diaphragmatic hernia (CDH) is a relatively common birth defect that causes significant mortality and morbidity in newborns. Diaphragm development is currently not well understood,… (more)

Subjects/Keywords: Wt1; β-Catenin; Congenital Diaphragmatic Hernia; CDH; Wnt Signaling; Diaphragm Development; Mesotheliur

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APA (6th Edition):

Paris, N. (2015). Role of Wilms Tumor 1 and β-Catenin in Embryonic Diaphragm Development. (Doctoral Dissertation). University of Rochester. Retrieved from http://hdl.handle.net/1802/30259

Chicago Manual of Style (16th Edition):

Paris, Nicole. “Role of Wilms Tumor 1 and β-Catenin in Embryonic Diaphragm Development.” 2015. Doctoral Dissertation, University of Rochester. Accessed December 08, 2019. http://hdl.handle.net/1802/30259.

MLA Handbook (7th Edition):

Paris, Nicole. “Role of Wilms Tumor 1 and β-Catenin in Embryonic Diaphragm Development.” 2015. Web. 08 Dec 2019.

Vancouver:

Paris N. Role of Wilms Tumor 1 and β-Catenin in Embryonic Diaphragm Development. [Internet] [Doctoral dissertation]. University of Rochester; 2015. [cited 2019 Dec 08]. Available from: http://hdl.handle.net/1802/30259.

Council of Science Editors:

Paris N. Role of Wilms Tumor 1 and β-Catenin in Embryonic Diaphragm Development. [Doctoral Dissertation]. University of Rochester; 2015. Available from: http://hdl.handle.net/1802/30259


University of California – San Francisco

14. Statman, Lauren Yael. Mechanosensitive β-Catenin Signaling Modulates Mesenchymal Stem Cell Chondrogenesis.

Degree: Bioengineering, 2012, University of California – San Francisco

 Bone marrow-derived mesenchymal stem cells are a promising source of cells for cartilage regeneration therapies due to their ease of isolation and capacity to differentiate… (more)

Subjects/Keywords: Biomedical engineering; Cellular biology; β -Catenin; Cartilage; Chondrogenesis; Hydrostatic Pressure; Mesenchymal Stem Cells; Wnt Signaling

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

APA (6th Edition):

Statman, L. Y. (2012). Mechanosensitive β-Catenin Signaling Modulates Mesenchymal Stem Cell Chondrogenesis. (Thesis). University of California – San Francisco. Retrieved from http://www.escholarship.org/uc/item/26z9t3fg

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):

Statman, Lauren Yael. “Mechanosensitive β-Catenin Signaling Modulates Mesenchymal Stem Cell Chondrogenesis.” 2012. Thesis, University of California – San Francisco. Accessed December 08, 2019. http://www.escholarship.org/uc/item/26z9t3fg.

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

MLA Handbook (7th Edition):

Statman, Lauren Yael. “Mechanosensitive β-Catenin Signaling Modulates Mesenchymal Stem Cell Chondrogenesis.” 2012. Web. 08 Dec 2019.

Vancouver:

Statman LY. Mechanosensitive β-Catenin Signaling Modulates Mesenchymal Stem Cell Chondrogenesis. [Internet] [Thesis]. University of California – San Francisco; 2012. [cited 2019 Dec 08]. Available from: http://www.escholarship.org/uc/item/26z9t3fg.

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

Council of Science Editors:

Statman LY. Mechanosensitive β-Catenin Signaling Modulates Mesenchymal Stem Cell Chondrogenesis. [Thesis]. University of California – San Francisco; 2012. Available from: http://www.escholarship.org/uc/item/26z9t3fg

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


University of Michigan

15. Pedersen Schuler, Elisabeth. The Function of Wnt/beta-catenin Signaling in Ewing Sarcoma and its Contribution to Pathogenesis.

Degree: PhD, Molecular & Cellular Path PhD, 2018, University of Michigan

 Ewing sarcoma is an aggressive bone and soft tissue tumor with a high propensity for metastasis; however, the mechanisms that contribute to this process are… (more)

Subjects/Keywords: The role of Wnt/beta-catenin signaling in Ewing sarcoma; Pathology; Health Sciences

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APA (6th Edition):

Pedersen Schuler, E. (2018). The Function of Wnt/beta-catenin Signaling in Ewing Sarcoma and its Contribution to Pathogenesis. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/144020

Chicago Manual of Style (16th Edition):

Pedersen Schuler, Elisabeth. “The Function of Wnt/beta-catenin Signaling in Ewing Sarcoma and its Contribution to Pathogenesis.” 2018. Doctoral Dissertation, University of Michigan. Accessed December 08, 2019. http://hdl.handle.net/2027.42/144020.

MLA Handbook (7th Edition):

Pedersen Schuler, Elisabeth. “The Function of Wnt/beta-catenin Signaling in Ewing Sarcoma and its Contribution to Pathogenesis.” 2018. Web. 08 Dec 2019.

Vancouver:

Pedersen Schuler E. The Function of Wnt/beta-catenin Signaling in Ewing Sarcoma and its Contribution to Pathogenesis. [Internet] [Doctoral dissertation]. University of Michigan; 2018. [cited 2019 Dec 08]. Available from: http://hdl.handle.net/2027.42/144020.

Council of Science Editors:

Pedersen Schuler E. The Function of Wnt/beta-catenin Signaling in Ewing Sarcoma and its Contribution to Pathogenesis. [Doctoral Dissertation]. University of Michigan; 2018. Available from: http://hdl.handle.net/2027.42/144020


University of Western Ontario

16. Grol, Matthew W. P2X7 Nucleotide Receptor Signaling in Osteoblasts.

Degree: 2013, University of Western Ontario

 Nucleotides are released from cells of the osteoblast lineage in response to mechanical stimulation, and signal through two families of P2 nucleotide receptors – G… (more)

Subjects/Keywords: osteoblast; ATP; P2Y and P2X nucleotide receptors; calcium/NFAT signaling; Wnt/beta-catenin signaling; proton efflux; Cell Biology

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APA (6th Edition):

Grol, M. W. (2013). P2X7 Nucleotide Receptor Signaling in Osteoblasts. (Thesis). University of Western Ontario. Retrieved from https://ir.lib.uwo.ca/etd/1470

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):

Grol, Matthew W. “P2X7 Nucleotide Receptor Signaling in Osteoblasts.” 2013. Thesis, University of Western Ontario. Accessed December 08, 2019. https://ir.lib.uwo.ca/etd/1470.

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

MLA Handbook (7th Edition):

Grol, Matthew W. “P2X7 Nucleotide Receptor Signaling in Osteoblasts.” 2013. Web. 08 Dec 2019.

Vancouver:

Grol MW. P2X7 Nucleotide Receptor Signaling in Osteoblasts. [Internet] [Thesis]. University of Western Ontario; 2013. [cited 2019 Dec 08]. Available from: https://ir.lib.uwo.ca/etd/1470.

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

Council of Science Editors:

Grol MW. P2X7 Nucleotide Receptor Signaling in Osteoblasts. [Thesis]. University of Western Ontario; 2013. Available from: https://ir.lib.uwo.ca/etd/1470

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


University of Toronto

17. Poliszczuk, Peter. The Search for Novel Wnt Pathway Modulators.

Degree: 2010, University of Toronto

Signaling pathways are complex and function to transmit signals from the extracellular environment into the cell. Analysis of results obtained from a high throughput siRNA… (more)

Subjects/Keywords: Wnt Signaling; Receptor Tyrosine Kinase; Beta-Catenin; Frizzled; Cell Signaling; Leukocyte Tyrosine Kinase; Membrane Protein Palmitoylated 3; LTK; MPP3; MAGUK; 0473

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

APA (6th Edition):

Poliszczuk, P. (2010). The Search for Novel Wnt Pathway Modulators. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/25895

Chicago Manual of Style (16th Edition):

Poliszczuk, Peter. “The Search for Novel Wnt Pathway Modulators.” 2010. Masters Thesis, University of Toronto. Accessed December 08, 2019. http://hdl.handle.net/1807/25895.

MLA Handbook (7th Edition):

Poliszczuk, Peter. “The Search for Novel Wnt Pathway Modulators.” 2010. Web. 08 Dec 2019.

Vancouver:

Poliszczuk P. The Search for Novel Wnt Pathway Modulators. [Internet] [Masters thesis]. University of Toronto; 2010. [cited 2019 Dec 08]. Available from: http://hdl.handle.net/1807/25895.

Council of Science Editors:

Poliszczuk P. The Search for Novel Wnt Pathway Modulators. [Masters Thesis]. University of Toronto; 2010. Available from: http://hdl.handle.net/1807/25895

18. Chin, Alana. Elucidating a novel WNT/?-CATENIN Signaling-Independent Environment that Precedes Villus Morphogenesis in the Embryonic Intestine.

Degree: PhD, Cell and Developmental Biology, 2017, University of Michigan

 The intestine is a vital organ responsible for several functions, including excretion of waste, acting as a major site of host immunity, and most importantly,… (more)

Subjects/Keywords: intestinal development; villus morphogenesis; cell signaling; Wnt/beta-catenin signaling pathway; Molecular, Cellular and Developmental Biology; Health Sciences

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APA (6th Edition):

Chin, A. (2017). Elucidating a novel WNT/?-CATENIN Signaling-Independent Environment that Precedes Villus Morphogenesis in the Embryonic Intestine. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/136965

Chicago Manual of Style (16th Edition):

Chin, Alana. “Elucidating a novel WNT/?-CATENIN Signaling-Independent Environment that Precedes Villus Morphogenesis in the Embryonic Intestine.” 2017. Doctoral Dissertation, University of Michigan. Accessed December 08, 2019. http://hdl.handle.net/2027.42/136965.

MLA Handbook (7th Edition):

Chin, Alana. “Elucidating a novel WNT/?-CATENIN Signaling-Independent Environment that Precedes Villus Morphogenesis in the Embryonic Intestine.” 2017. Web. 08 Dec 2019.

Vancouver:

Chin A. Elucidating a novel WNT/?-CATENIN Signaling-Independent Environment that Precedes Villus Morphogenesis in the Embryonic Intestine. [Internet] [Doctoral dissertation]. University of Michigan; 2017. [cited 2019 Dec 08]. Available from: http://hdl.handle.net/2027.42/136965.

Council of Science Editors:

Chin A. Elucidating a novel WNT/?-CATENIN Signaling-Independent Environment that Precedes Villus Morphogenesis in the Embryonic Intestine. [Doctoral Dissertation]. University of Michigan; 2017. Available from: http://hdl.handle.net/2027.42/136965

19. Jonge, W.J. de. Wnt/β-catenin’s regulatory role in embryonic stem cell pluripotency and differentiation.

Degree: 2014, Universiteit Utrecht

 Stem cells need to tightly regulate the switch between self-renewal and differentiation. Several external signaling pathways contribute to this regulation, together with the internal regulatory… (more)

Subjects/Keywords: Wnt signaling; β-catenin; embryonic stem cell

…stabilization of β-catenin Wnt signaling starts with secretion of Wnt ligands that are palmitoylated… …x29; In the absence of Wnt signaling, β-catenin is phosphorylated by the destruction complex… …catenin, targeting it for destruction by the proteasome. B) When Wnt signaling is present… …Image modified from Clevers, 2006. When β-catenin is stabilized during Wnt signaling, it… …canonical Wnt signaling pathway determines whether its main effector, β-catenin, is stabilized or… 

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

APA (6th Edition):

Jonge, W. J. d. (2014). Wnt/β-catenin’s regulatory role in embryonic stem cell pluripotency and differentiation. (Masters Thesis). Universiteit Utrecht. Retrieved from http://dspace.library.uu.nl:8080/handle/1874/289238

Chicago Manual of Style (16th Edition):

Jonge, W J de. “Wnt/β-catenin’s regulatory role in embryonic stem cell pluripotency and differentiation.” 2014. Masters Thesis, Universiteit Utrecht. Accessed December 08, 2019. http://dspace.library.uu.nl:8080/handle/1874/289238.

MLA Handbook (7th Edition):

Jonge, W J de. “Wnt/β-catenin’s regulatory role in embryonic stem cell pluripotency and differentiation.” 2014. Web. 08 Dec 2019.

Vancouver:

Jonge WJd. Wnt/β-catenin’s regulatory role in embryonic stem cell pluripotency and differentiation. [Internet] [Masters thesis]. Universiteit Utrecht; 2014. [cited 2019 Dec 08]. Available from: http://dspace.library.uu.nl:8080/handle/1874/289238.

Council of Science Editors:

Jonge WJd. Wnt/β-catenin’s regulatory role in embryonic stem cell pluripotency and differentiation. [Masters Thesis]. Universiteit Utrecht; 2014. Available from: http://dspace.library.uu.nl:8080/handle/1874/289238


University of Southern California

20. Danopoulos, Soula. The role of Wnt signaling in organogenesis: limb and lung.

Degree: PhD, Cranio-Facial Biology, 2016, University of Southern California

Wnt signaling is important in a variety of cellular processes, including cell proliferation, differentiation, migration, and polarity. All of these cellular events are critical during… (more)

Subjects/Keywords: Wnt signaling; Fgf; limb development; soluble FGFR2b; beta-catenin; lung branching; Rac1; epithelium; mesenchyme; vasculature; cross-talk; transgenic animals

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APA (6th Edition):

Danopoulos, S. (2016). The role of Wnt signaling in organogenesis: limb and lung. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/480344/rec/7272

Chicago Manual of Style (16th Edition):

Danopoulos, Soula. “The role of Wnt signaling in organogenesis: limb and lung.” 2016. Doctoral Dissertation, University of Southern California. Accessed December 08, 2019. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/480344/rec/7272.

MLA Handbook (7th Edition):

Danopoulos, Soula. “The role of Wnt signaling in organogenesis: limb and lung.” 2016. Web. 08 Dec 2019.

Vancouver:

Danopoulos S. The role of Wnt signaling in organogenesis: limb and lung. [Internet] [Doctoral dissertation]. University of Southern California; 2016. [cited 2019 Dec 08]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/480344/rec/7272.

Council of Science Editors:

Danopoulos S. The role of Wnt signaling in organogenesis: limb and lung. [Doctoral Dissertation]. University of Southern California; 2016. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/480344/rec/7272


The Ohio State University

21. Hankey, William C, IV. Chromatin-associated functions of the APC tumor suppressor protein.

Degree: PhD, Biomedical Sciences, 2016, The Ohio State University

 Biallelic mutation of the APC tumor suppressor gene occurs in a high percentage ofcolorectal tumors and is considered the critical event driving tumor initiation in… (more)

Subjects/Keywords: Biomedical Research; APC; tumor suppressor; colorectal cancer; canonical WNT signaling; chromatin; transcription; AP-1; transcription factor; ChIP-seq; beta-catenin

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APA (6th Edition):

Hankey, William C, I. (2016). Chromatin-associated functions of the APC tumor suppressor protein. (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1480198247672881

Chicago Manual of Style (16th Edition):

Hankey, William C, IV. “Chromatin-associated functions of the APC tumor suppressor protein.” 2016. Doctoral Dissertation, The Ohio State University. Accessed December 08, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=osu1480198247672881.

MLA Handbook (7th Edition):

Hankey, William C, IV. “Chromatin-associated functions of the APC tumor suppressor protein.” 2016. Web. 08 Dec 2019.

Vancouver:

Hankey, William C I. Chromatin-associated functions of the APC tumor suppressor protein. [Internet] [Doctoral dissertation]. The Ohio State University; 2016. [cited 2019 Dec 08]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1480198247672881.

Council of Science Editors:

Hankey, William C I. Chromatin-associated functions of the APC tumor suppressor protein. [Doctoral Dissertation]. The Ohio State University; 2016. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1480198247672881

22. I. Spadoni. IDENTIFICATION AND CHARACTERIZATION OF THE 'GUT VASCULAR BARRIER'.

Degree: 2014, Università degli Studi di Milano

 In order to protect the body from a wide range of harmful environmental agents, the intestine has developed a number of barrier mechanisms to limit… (more)

Subjects/Keywords: intestine; endothelial cells; barrier; vascular permeability; Salmonella typhimurium; Wnt/b-catenin signaling pathway; Settore BIO/11 - Biologia Molecolare

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APA (6th Edition):

Spadoni, I. (2014). IDENTIFICATION AND CHARACTERIZATION OF THE 'GUT VASCULAR BARRIER'. (Thesis). Università degli Studi di Milano. Retrieved from http://hdl.handle.net/2434/234155

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):

Spadoni, I.. “IDENTIFICATION AND CHARACTERIZATION OF THE 'GUT VASCULAR BARRIER'.” 2014. Thesis, Università degli Studi di Milano. Accessed December 08, 2019. http://hdl.handle.net/2434/234155.

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

MLA Handbook (7th Edition):

Spadoni, I.. “IDENTIFICATION AND CHARACTERIZATION OF THE 'GUT VASCULAR BARRIER'.” 2014. Web. 08 Dec 2019.

Vancouver:

Spadoni I. IDENTIFICATION AND CHARACTERIZATION OF THE 'GUT VASCULAR BARRIER'. [Internet] [Thesis]. Università degli Studi di Milano; 2014. [cited 2019 Dec 08]. Available from: http://hdl.handle.net/2434/234155.

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

Council of Science Editors:

Spadoni I. IDENTIFICATION AND CHARACTERIZATION OF THE 'GUT VASCULAR BARRIER'. [Thesis]. Università degli Studi di Milano; 2014. Available from: http://hdl.handle.net/2434/234155

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


McMaster University

23. Padwal, Manreet. The Role of MMP9 and WNT Signaling in Peritoneal Angiogenesis.

Degree: PhD, 2017, McMaster University

 Patients on peritoneal dialysis (PD) are reliant on the peritoneum to provide a semi-permeable barrier to allow for dialysis (solute clearance), salt and water removal… (more)

Subjects/Keywords: Peritoneal Dialysis; Angiogenesis; Fibrosis; Matrix Metalloproteinase 9; WNT/b-catenin signaling; TGFB; Epithelial to Mesenchymal Transition; WNT5A; Ror2; VEGF; Ultrafiltration

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

APA (6th Edition):

Padwal, M. (2017). The Role of MMP9 and WNT Signaling in Peritoneal Angiogenesis. (Doctoral Dissertation). McMaster University. Retrieved from http://hdl.handle.net/11375/22089

Chicago Manual of Style (16th Edition):

Padwal, Manreet. “The Role of MMP9 and WNT Signaling in Peritoneal Angiogenesis.” 2017. Doctoral Dissertation, McMaster University. Accessed December 08, 2019. http://hdl.handle.net/11375/22089.

MLA Handbook (7th Edition):

Padwal, Manreet. “The Role of MMP9 and WNT Signaling in Peritoneal Angiogenesis.” 2017. Web. 08 Dec 2019.

Vancouver:

Padwal M. The Role of MMP9 and WNT Signaling in Peritoneal Angiogenesis. [Internet] [Doctoral dissertation]. McMaster University; 2017. [cited 2019 Dec 08]. Available from: http://hdl.handle.net/11375/22089.

Council of Science Editors:

Padwal M. The Role of MMP9 and WNT Signaling in Peritoneal Angiogenesis. [Doctoral Dissertation]. McMaster University; 2017. Available from: http://hdl.handle.net/11375/22089

24. Theologis, Thomas. Συσχέτιση μεταξύ επιπέδων Dickkopf-1 στο αρθρικό υγρό και στο αίμα σε άτομα με πρωτοπαθή οστεοαρθρίτιδα γόνατος και κλινικής βαρύτητας της νόσου.

Degree: 2017, National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ)

Introduction: Primary knee osteoarthritis (OA) contributes to disability among middle-aged and elderly people. Dickkopf-1(Dkk-1) is a natural inhibitor of Wnt/β-catenin signaling pathway implicated in regulation… (more)

Subjects/Keywords: Οστεοαρθρίτιδα; Γόνατο; Σηματοδοτική οδός; Dickkopf-1; Wnt/β-catenin signaling pathway; Knee; Osteoarthritis; Kellgren and Lawrence grading system

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APA (6th Edition):

Theologis, T. (2017). Συσχέτιση μεταξύ επιπέδων Dickkopf-1 στο αρθρικό υγρό και στο αίμα σε άτομα με πρωτοπαθή οστεοαρθρίτιδα γόνατος και κλινικής βαρύτητας της νόσου. (Thesis). National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ). Retrieved from http://hdl.handle.net/10442/hedi/42448

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):

Theologis, Thomas. “Συσχέτιση μεταξύ επιπέδων Dickkopf-1 στο αρθρικό υγρό και στο αίμα σε άτομα με πρωτοπαθή οστεοαρθρίτιδα γόνατος και κλινικής βαρύτητας της νόσου.” 2017. Thesis, National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ). Accessed December 08, 2019. http://hdl.handle.net/10442/hedi/42448.

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

MLA Handbook (7th Edition):

Theologis, Thomas. “Συσχέτιση μεταξύ επιπέδων Dickkopf-1 στο αρθρικό υγρό και στο αίμα σε άτομα με πρωτοπαθή οστεοαρθρίτιδα γόνατος και κλινικής βαρύτητας της νόσου.” 2017. Web. 08 Dec 2019.

Vancouver:

Theologis T. Συσχέτιση μεταξύ επιπέδων Dickkopf-1 στο αρθρικό υγρό και στο αίμα σε άτομα με πρωτοπαθή οστεοαρθρίτιδα γόνατος και κλινικής βαρύτητας της νόσου. [Internet] [Thesis]. National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ); 2017. [cited 2019 Dec 08]. Available from: http://hdl.handle.net/10442/hedi/42448.

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

Council of Science Editors:

Theologis T. Συσχέτιση μεταξύ επιπέδων Dickkopf-1 στο αρθρικό υγρό και στο αίμα σε άτομα με πρωτοπαθή οστεοαρθρίτιδα γόνατος και κλινικής βαρύτητας της νόσου. [Thesis]. National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ); 2017. Available from: http://hdl.handle.net/10442/hedi/42448

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

25. Noort, Mascha van. Non-phosphorylated b-catenin in Wnt signaling.

Degree: 2002, University Utrecht

 The Wnt signaling cascade plays an important role in development and carcinogenesis. Under non-signaling conditions, a large cytoplasmic complex, consisting of the kinase GSK-3?, the… (more)

Subjects/Keywords: b-catenin; Wnt signaling; phosphorylation; monoclonal antibody; signal transduction

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

APA (6th Edition):

Noort, M. v. (2002). Non-phosphorylated b-catenin in Wnt signaling. (Doctoral Dissertation). University Utrecht. Retrieved from http://dspace.library.uu.nl/handle/1874/421 ; URN:NBN:NL:UI:10-1874-421 ; URN:NBN:NL:UI:10-1874-421 ; http://dspace.library.uu.nl/handle/1874/421

Chicago Manual of Style (16th Edition):

Noort, Mascha van. “Non-phosphorylated b-catenin in Wnt signaling.” 2002. Doctoral Dissertation, University Utrecht. Accessed December 08, 2019. http://dspace.library.uu.nl/handle/1874/421 ; URN:NBN:NL:UI:10-1874-421 ; URN:NBN:NL:UI:10-1874-421 ; http://dspace.library.uu.nl/handle/1874/421.

MLA Handbook (7th Edition):

Noort, Mascha van. “Non-phosphorylated b-catenin in Wnt signaling.” 2002. Web. 08 Dec 2019.

Vancouver:

Noort Mv. Non-phosphorylated b-catenin in Wnt signaling. [Internet] [Doctoral dissertation]. University Utrecht; 2002. [cited 2019 Dec 08]. Available from: http://dspace.library.uu.nl/handle/1874/421 ; URN:NBN:NL:UI:10-1874-421 ; URN:NBN:NL:UI:10-1874-421 ; http://dspace.library.uu.nl/handle/1874/421.

Council of Science Editors:

Noort Mv. Non-phosphorylated b-catenin in Wnt signaling. [Doctoral Dissertation]. University Utrecht; 2002. Available from: http://dspace.library.uu.nl/handle/1874/421 ; URN:NBN:NL:UI:10-1874-421 ; URN:NBN:NL:UI:10-1874-421 ; http://dspace.library.uu.nl/handle/1874/421

26. Noort, Mascha van. Non-phosphorylated b-catenin in Wnt signaling.

Degree: 2002, University Utrecht

 The Wnt signaling cascade plays an important role in development and carcinogenesis. Under non-signaling conditions, a large cytoplasmic complex, consisting of the kinase GSK-3?, the… (more)

Subjects/Keywords: b-catenin; Wnt signaling; phosphorylation; monoclonal antibody; signal transduction

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APA (6th Edition):

Noort, M. v. (2002). Non-phosphorylated b-catenin in Wnt signaling. (Doctoral Dissertation). University Utrecht. Retrieved from http://dspace.library.uu.nl/handle/1874/421 ; URN:NBN:NL:UI:10-1874-421 ; URN:NBN:NL:UI:10-1874-421 ; http://dspace.library.uu.nl/handle/1874/421

Chicago Manual of Style (16th Edition):

Noort, Mascha van. “Non-phosphorylated b-catenin in Wnt signaling.” 2002. Doctoral Dissertation, University Utrecht. Accessed December 08, 2019. http://dspace.library.uu.nl/handle/1874/421 ; URN:NBN:NL:UI:10-1874-421 ; URN:NBN:NL:UI:10-1874-421 ; http://dspace.library.uu.nl/handle/1874/421.

MLA Handbook (7th Edition):

Noort, Mascha van. “Non-phosphorylated b-catenin in Wnt signaling.” 2002. Web. 08 Dec 2019.

Vancouver:

Noort Mv. Non-phosphorylated b-catenin in Wnt signaling. [Internet] [Doctoral dissertation]. University Utrecht; 2002. [cited 2019 Dec 08]. Available from: http://dspace.library.uu.nl/handle/1874/421 ; URN:NBN:NL:UI:10-1874-421 ; URN:NBN:NL:UI:10-1874-421 ; http://dspace.library.uu.nl/handle/1874/421.

Council of Science Editors:

Noort Mv. Non-phosphorylated b-catenin in Wnt signaling. [Doctoral Dissertation]. University Utrecht; 2002. Available from: http://dspace.library.uu.nl/handle/1874/421 ; URN:NBN:NL:UI:10-1874-421 ; URN:NBN:NL:UI:10-1874-421 ; http://dspace.library.uu.nl/handle/1874/421


University of Toronto

27. Silkstone, David. Age Related Tissue Fibrosis During Fracture Repair Is Mediated by Wnt/β-catenin Signaling.

Degree: 2010, University of Toronto

The regenerative potential of tissue injury declines with age. Recently, a significant role for Wnt/β-catenin signaling has been shown in tissue specific stem cell aging,… (more)

Subjects/Keywords: Fracture Repair; Elderly; Osteoblasts; Tissue Fibrosis; Wnt/β-catenin Signaling; Multipotent Mesenchymal Stem Cells; 0433; 0410; 0379

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APA (6th Edition):

Silkstone, D. (2010). Age Related Tissue Fibrosis During Fracture Repair Is Mediated by Wnt/β-catenin Signaling. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/25802

Chicago Manual of Style (16th Edition):

Silkstone, David. “Age Related Tissue Fibrosis During Fracture Repair Is Mediated by Wnt/β-catenin Signaling.” 2010. Masters Thesis, University of Toronto. Accessed December 08, 2019. http://hdl.handle.net/1807/25802.

MLA Handbook (7th Edition):

Silkstone, David. “Age Related Tissue Fibrosis During Fracture Repair Is Mediated by Wnt/β-catenin Signaling.” 2010. Web. 08 Dec 2019.

Vancouver:

Silkstone D. Age Related Tissue Fibrosis During Fracture Repair Is Mediated by Wnt/β-catenin Signaling. [Internet] [Masters thesis]. University of Toronto; 2010. [cited 2019 Dec 08]. Available from: http://hdl.handle.net/1807/25802.

Council of Science Editors:

Silkstone D. Age Related Tissue Fibrosis During Fracture Repair Is Mediated by Wnt/β-catenin Signaling. [Masters Thesis]. University of Toronto; 2010. Available from: http://hdl.handle.net/1807/25802


Erasmus University Rotterdam

28. Liu, Pengyu. The mutant components of Wnt/ß-catenin signaling in liver cancer.

Degree: 2019, Erasmus University Rotterdam

Subjects/Keywords: HCC; Wnt signaling; β-catenin; AXIN1; TCGA

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

APA (6th Edition):

Liu, P. (2019). The mutant components of Wnt/ß-catenin signaling in liver cancer. (Doctoral Dissertation). Erasmus University Rotterdam. Retrieved from http://hdl.handle.net/1765/116676

Chicago Manual of Style (16th Edition):

Liu, Pengyu. “The mutant components of Wnt/ß-catenin signaling in liver cancer.” 2019. Doctoral Dissertation, Erasmus University Rotterdam. Accessed December 08, 2019. http://hdl.handle.net/1765/116676.

MLA Handbook (7th Edition):

Liu, Pengyu. “The mutant components of Wnt/ß-catenin signaling in liver cancer.” 2019. Web. 08 Dec 2019.

Vancouver:

Liu P. The mutant components of Wnt/ß-catenin signaling in liver cancer. [Internet] [Doctoral dissertation]. Erasmus University Rotterdam; 2019. [cited 2019 Dec 08]. Available from: http://hdl.handle.net/1765/116676.

Council of Science Editors:

Liu P. The mutant components of Wnt/ß-catenin signaling in liver cancer. [Doctoral Dissertation]. Erasmus University Rotterdam; 2019. Available from: http://hdl.handle.net/1765/116676


Erasmus University Rotterdam

29. Wang, Wenhui. Targeting Wnt/β-catenin Signaling in Liver Cancers.

Degree: 2018, Erasmus University Rotterdam

 textabstractAs one of the critical contributing factors to hepatocellular carcinoma (HCC) growth, aberrant activation of Wnt/β-catenin signaling derives from a variety of molecular alterations involved… (more)

Subjects/Keywords: Wnt/β-catenin Signaling; liver cancer; hepatocellular carcinoma

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

APA (6th Edition):

Wang, W. (2018). Targeting Wnt/β-catenin Signaling in Liver Cancers. (Doctoral Dissertation). Erasmus University Rotterdam. Retrieved from http://hdl.handle.net/1765/105989

Chicago Manual of Style (16th Edition):

Wang, Wenhui. “Targeting Wnt/β-catenin Signaling in Liver Cancers.” 2018. Doctoral Dissertation, Erasmus University Rotterdam. Accessed December 08, 2019. http://hdl.handle.net/1765/105989.

MLA Handbook (7th Edition):

Wang, Wenhui. “Targeting Wnt/β-catenin Signaling in Liver Cancers.” 2018. Web. 08 Dec 2019.

Vancouver:

Wang W. Targeting Wnt/β-catenin Signaling in Liver Cancers. [Internet] [Doctoral dissertation]. Erasmus University Rotterdam; 2018. [cited 2019 Dec 08]. Available from: http://hdl.handle.net/1765/105989.

Council of Science Editors:

Wang W. Targeting Wnt/β-catenin Signaling in Liver Cancers. [Doctoral Dissertation]. Erasmus University Rotterdam; 2018. Available from: http://hdl.handle.net/1765/105989


Universitat Pompeu Fabra

30. Theka, Ilda, 1984-. Wnt/beta-catenin activity controls the stability of imprinted genes in mouse embryonic stem cells.

Degree: Departament de Ciències Experimentals i de la Salut, 2017, Universitat Pompeu Fabra

 Mouse embryonic stem cells (ESCs) derive from the inner cell mass of the blastocyst and they are able to generate the three germ layers. Many… (more)

Subjects/Keywords: Wnt/β-catenin signaling; Embryonic stem cell; Genomic imprinting; Pluripotent; Cell reprogramming; Ruta de Wnt/β-catenina; Células madre embrionarias; Impronta genética; Pluripotente; Reprogramación celular; 576

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

APA (6th Edition):

Theka, Ilda, 1. (2017). Wnt/beta-catenin activity controls the stability of imprinted genes in mouse embryonic stem cells. (Thesis). Universitat Pompeu Fabra. Retrieved from http://hdl.handle.net/10803/565761

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):

Theka, Ilda, 1984-. “Wnt/beta-catenin activity controls the stability of imprinted genes in mouse embryonic stem cells.” 2017. Thesis, Universitat Pompeu Fabra. Accessed December 08, 2019. http://hdl.handle.net/10803/565761.

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

MLA Handbook (7th Edition):

Theka, Ilda, 1984-. “Wnt/beta-catenin activity controls the stability of imprinted genes in mouse embryonic stem cells.” 2017. Web. 08 Dec 2019.

Vancouver:

Theka, Ilda 1. Wnt/beta-catenin activity controls the stability of imprinted genes in mouse embryonic stem cells. [Internet] [Thesis]. Universitat Pompeu Fabra; 2017. [cited 2019 Dec 08]. Available from: http://hdl.handle.net/10803/565761.

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

Council of Science Editors:

Theka, Ilda 1. Wnt/beta-catenin activity controls the stability of imprinted genes in mouse embryonic stem cells. [Thesis]. Universitat Pompeu Fabra; 2017. Available from: http://hdl.handle.net/10803/565761

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

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