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You searched for subject:(Tissue factor). Showing records 1 – 30 of 217 total matches.

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Cornell University

1. Witter, Lauren. The Role Of Tissue Factor In Canine Hemangiosarcoma.

Degree: M.S., Veterinary Medicine, Veterinary Medicine, 2015, Cornell University

 Keywords: Hemangiosarcoma, Angiosarcoma, Tissue Factor Hemangiosarcoma (HSA) and angiosarcoma (AS) are malignant endothelial neoplasms in dogs and human beings, respectively. Canine patients suffering from hemangiosarcoma… (more)

Subjects/Keywords: Hemangiosarcoma; Angiosarcoma; Tissue Factor

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APA (6th Edition):

Witter, L. (2015). The Role Of Tissue Factor In Canine Hemangiosarcoma. (Masters Thesis). Cornell University. Retrieved from http://hdl.handle.net/1813/40672

Chicago Manual of Style (16th Edition):

Witter, Lauren. “The Role Of Tissue Factor In Canine Hemangiosarcoma.” 2015. Masters Thesis, Cornell University. Accessed November 28, 2020. http://hdl.handle.net/1813/40672.

MLA Handbook (7th Edition):

Witter, Lauren. “The Role Of Tissue Factor In Canine Hemangiosarcoma.” 2015. Web. 28 Nov 2020.

Vancouver:

Witter L. The Role Of Tissue Factor In Canine Hemangiosarcoma. [Internet] [Masters thesis]. Cornell University; 2015. [cited 2020 Nov 28]. Available from: http://hdl.handle.net/1813/40672.

Council of Science Editors:

Witter L. The Role Of Tissue Factor In Canine Hemangiosarcoma. [Masters Thesis]. Cornell University; 2015. Available from: http://hdl.handle.net/1813/40672

2. Poudel, Sashi. Variation in tissue correction factors for LiF, Al2O3 and Silicon Dosimeters as a function of tissue depth with comparison between intensity weighted mono-energetic photon and the poly-energetic photons used in brachytherapy and diagnostic radiology.

Degree: PhD, 2017, Worcester Polytechnic Institute

 "The MCNP6 radiation transport code was used to quantify changes in the absorbed dose tissue conversion factors for LiF, Al2O3, and silicon-based electronic dosimeters. While… (more)

Subjects/Keywords: Tissue Correction Factor; MCNP; Dosimeter

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APA (6th Edition):

Poudel, S. (2017). Variation in tissue correction factors for LiF, Al2O3 and Silicon Dosimeters as a function of tissue depth with comparison between intensity weighted mono-energetic photon and the poly-energetic photons used in brachytherapy and diagnostic radiology. (Doctoral Dissertation). Worcester Polytechnic Institute. Retrieved from etd-101417-143952 ; https://digitalcommons.wpi.edu/etd-dissertations/487

Chicago Manual of Style (16th Edition):

Poudel, Sashi. “Variation in tissue correction factors for LiF, Al2O3 and Silicon Dosimeters as a function of tissue depth with comparison between intensity weighted mono-energetic photon and the poly-energetic photons used in brachytherapy and diagnostic radiology.” 2017. Doctoral Dissertation, Worcester Polytechnic Institute. Accessed November 28, 2020. etd-101417-143952 ; https://digitalcommons.wpi.edu/etd-dissertations/487.

MLA Handbook (7th Edition):

Poudel, Sashi. “Variation in tissue correction factors for LiF, Al2O3 and Silicon Dosimeters as a function of tissue depth with comparison between intensity weighted mono-energetic photon and the poly-energetic photons used in brachytherapy and diagnostic radiology.” 2017. Web. 28 Nov 2020.

Vancouver:

Poudel S. Variation in tissue correction factors for LiF, Al2O3 and Silicon Dosimeters as a function of tissue depth with comparison between intensity weighted mono-energetic photon and the poly-energetic photons used in brachytherapy and diagnostic radiology. [Internet] [Doctoral dissertation]. Worcester Polytechnic Institute; 2017. [cited 2020 Nov 28]. Available from: etd-101417-143952 ; https://digitalcommons.wpi.edu/etd-dissertations/487.

Council of Science Editors:

Poudel S. Variation in tissue correction factors for LiF, Al2O3 and Silicon Dosimeters as a function of tissue depth with comparison between intensity weighted mono-energetic photon and the poly-energetic photons used in brachytherapy and diagnostic radiology. [Doctoral Dissertation]. Worcester Polytechnic Institute; 2017. Available from: etd-101417-143952 ; https://digitalcommons.wpi.edu/etd-dissertations/487


University of Illinois – Urbana-Champaign

3. Ke, Ke. The tissue factor-factor VII(a) complex in blood coagulation.

Degree: PhD, 0318, 2013, University of Illinois – Urbana-Champaign

 Initiation of the coagulation cascade in vivo is mediated by tissue factor (TF), which functions as the cell surface receptor and catalytic cofactor for factor(more)

Subjects/Keywords: blood coagulation; coagulation factors; tissue factor; factor VIIa; factor X; membranes

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APA (6th Edition):

Ke, K. (2013). The tissue factor-factor VII(a) complex in blood coagulation. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/44458

Chicago Manual of Style (16th Edition):

Ke, Ke. “The tissue factor-factor VII(a) complex in blood coagulation.” 2013. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed November 28, 2020. http://hdl.handle.net/2142/44458.

MLA Handbook (7th Edition):

Ke, Ke. “The tissue factor-factor VII(a) complex in blood coagulation.” 2013. Web. 28 Nov 2020.

Vancouver:

Ke K. The tissue factor-factor VII(a) complex in blood coagulation. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2013. [cited 2020 Nov 28]. Available from: http://hdl.handle.net/2142/44458.

Council of Science Editors:

Ke K. The tissue factor-factor VII(a) complex in blood coagulation. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2013. Available from: http://hdl.handle.net/2142/44458


University of Notre Dame

4. Haifeng Xu. FVII stands on the crossroads of coagulation and inflammation</h1>.

Degree: Chemistry and Biochemistry, 2007, University of Notre Dame

  Upregulation of the activated Factor VII (FVIIa)/Tissue Factor (TF) complex, downregulation of natural anticoagulation pathways, and inhibition of fibrinolysis, are major contributors to coagulopathies… (more)

Subjects/Keywords: tissue factor; endotoxemia

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APA (6th Edition):

Xu, H. (2007). FVII stands on the crossroads of coagulation and inflammation</h1>. (Thesis). University of Notre Dame. Retrieved from https://curate.nd.edu/show/8g84mk63s3p

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):

Xu, Haifeng. “FVII stands on the crossroads of coagulation and inflammation</h1>.” 2007. Thesis, University of Notre Dame. Accessed November 28, 2020. https://curate.nd.edu/show/8g84mk63s3p.

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

MLA Handbook (7th Edition):

Xu, Haifeng. “FVII stands on the crossroads of coagulation and inflammation</h1>.” 2007. Web. 28 Nov 2020.

Vancouver:

Xu H. FVII stands on the crossroads of coagulation and inflammation</h1>. [Internet] [Thesis]. University of Notre Dame; 2007. [cited 2020 Nov 28]. Available from: https://curate.nd.edu/show/8g84mk63s3p.

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

Council of Science Editors:

Xu H. FVII stands on the crossroads of coagulation and inflammation</h1>. [Thesis]. University of Notre Dame; 2007. Available from: https://curate.nd.edu/show/8g84mk63s3p

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


University of Oklahoma

5. Sunderland, Kegan. VIRUS-SELECTED OSTEOGENESIS-INDUCING PEPTIDES FOR ENHANCED BONE REGENERATION IN 3D PRINTED TITANIUM ALLOY IMPLANTS.

Degree: PhD, 2018, University of Oklahoma

 Bone morphogenetic proteins (BMPs) are part of the transforming growth factor-β superfamily and function as key regulators of cellular growth, differentiation, and tissue formation. While… (more)

Subjects/Keywords: Tissue Regeneration; Phage Display; Growth factor mimetic

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

APA (6th Edition):

Sunderland, K. (2018). VIRUS-SELECTED OSTEOGENESIS-INDUCING PEPTIDES FOR ENHANCED BONE REGENERATION IN 3D PRINTED TITANIUM ALLOY IMPLANTS. (Doctoral Dissertation). University of Oklahoma. Retrieved from http://hdl.handle.net/11244/316302

Chicago Manual of Style (16th Edition):

Sunderland, Kegan. “VIRUS-SELECTED OSTEOGENESIS-INDUCING PEPTIDES FOR ENHANCED BONE REGENERATION IN 3D PRINTED TITANIUM ALLOY IMPLANTS.” 2018. Doctoral Dissertation, University of Oklahoma. Accessed November 28, 2020. http://hdl.handle.net/11244/316302.

MLA Handbook (7th Edition):

Sunderland, Kegan. “VIRUS-SELECTED OSTEOGENESIS-INDUCING PEPTIDES FOR ENHANCED BONE REGENERATION IN 3D PRINTED TITANIUM ALLOY IMPLANTS.” 2018. Web. 28 Nov 2020.

Vancouver:

Sunderland K. VIRUS-SELECTED OSTEOGENESIS-INDUCING PEPTIDES FOR ENHANCED BONE REGENERATION IN 3D PRINTED TITANIUM ALLOY IMPLANTS. [Internet] [Doctoral dissertation]. University of Oklahoma; 2018. [cited 2020 Nov 28]. Available from: http://hdl.handle.net/11244/316302.

Council of Science Editors:

Sunderland K. VIRUS-SELECTED OSTEOGENESIS-INDUCING PEPTIDES FOR ENHANCED BONE REGENERATION IN 3D PRINTED TITANIUM ALLOY IMPLANTS. [Doctoral Dissertation]. University of Oklahoma; 2018. Available from: http://hdl.handle.net/11244/316302

6. Matsunari, Yasunori; Sugimoto, Mitsuhiko; Doi, Masaaki; Matsui, Hideto. Functional characterization of tissue factor in von Willebrand factor-dependent thrombus formation under whole blood flow conditions. : 全血流動下でのフォンビルブランド因子依存性血栓形成における組織因子の機能特性.

Degree: 博士(医学), 2016, Nara Medical University / 奈良県立医科大学

Von Willebrand factor (VWF) plays an important role in mediating platelet adhesion and aggregation under high shear rate conditions. Such platelet aggregates are strengthened by… (more)

Subjects/Keywords: Blood flow; Fibrin; Thrombus formation; Tissue factor; Von Willebrand factor

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APA (6th Edition):

Matsunari, Yasunori; Sugimoto, Mitsuhiko; Doi, Masaaki; Matsui, H. (2016). Functional characterization of tissue factor in von Willebrand factor-dependent thrombus formation under whole blood flow conditions. : 全血流動下でのフォンビルブランド因子依存性血栓形成における組織因子の機能特性. (Thesis). Nara Medical University / 奈良県立医科大学. Retrieved from http://hdl.handle.net/10564/3293

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):

Matsunari, Yasunori; Sugimoto, Mitsuhiko; Doi, Masaaki; Matsui, Hideto. “Functional characterization of tissue factor in von Willebrand factor-dependent thrombus formation under whole blood flow conditions. : 全血流動下でのフォンビルブランド因子依存性血栓形成における組織因子の機能特性.” 2016. Thesis, Nara Medical University / 奈良県立医科大学. Accessed November 28, 2020. http://hdl.handle.net/10564/3293.

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

MLA Handbook (7th Edition):

Matsunari, Yasunori; Sugimoto, Mitsuhiko; Doi, Masaaki; Matsui, Hideto. “Functional characterization of tissue factor in von Willebrand factor-dependent thrombus formation under whole blood flow conditions. : 全血流動下でのフォンビルブランド因子依存性血栓形成における組織因子の機能特性.” 2016. Web. 28 Nov 2020.

Vancouver:

Matsunari, Yasunori; Sugimoto, Mitsuhiko; Doi, Masaaki; Matsui H. Functional characterization of tissue factor in von Willebrand factor-dependent thrombus formation under whole blood flow conditions. : 全血流動下でのフォンビルブランド因子依存性血栓形成における組織因子の機能特性. [Internet] [Thesis]. Nara Medical University / 奈良県立医科大学; 2016. [cited 2020 Nov 28]. Available from: http://hdl.handle.net/10564/3293.

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

Council of Science Editors:

Matsunari, Yasunori; Sugimoto, Mitsuhiko; Doi, Masaaki; Matsui H. Functional characterization of tissue factor in von Willebrand factor-dependent thrombus formation under whole blood flow conditions. : 全血流動下でのフォンビルブランド因子依存性血栓形成における組織因子の機能特性. [Thesis]. Nara Medical University / 奈良県立医科大学; 2016. Available from: http://hdl.handle.net/10564/3293

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


University of Georgia

7. Krige, Lindel. Coagulation factors involved in the pathology of placental malaria.

Degree: 2014, University of Georgia

 Pregnant women and children are most vulnerable to malarial infection. Malaria in pregnancy leads to intrauterine growth restriction and preterm deliveries, resulting in low birth… (more)

Subjects/Keywords: Placental Malaria; Coagulation; Mouse Model; Tissue Factor; Tissue Factor Pathway Inhibitor; Plasminogen Activator Inhibitor; Thrombomodulin; Protease Activated Receptors

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APA (6th Edition):

Krige, L. (2014). Coagulation factors involved in the pathology of placental malaria. (Thesis). University of Georgia. Retrieved from http://hdl.handle.net/10724/26379

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):

Krige, Lindel. “Coagulation factors involved in the pathology of placental malaria.” 2014. Thesis, University of Georgia. Accessed November 28, 2020. http://hdl.handle.net/10724/26379.

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

MLA Handbook (7th Edition):

Krige, Lindel. “Coagulation factors involved in the pathology of placental malaria.” 2014. Web. 28 Nov 2020.

Vancouver:

Krige L. Coagulation factors involved in the pathology of placental malaria. [Internet] [Thesis]. University of Georgia; 2014. [cited 2020 Nov 28]. Available from: http://hdl.handle.net/10724/26379.

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

Council of Science Editors:

Krige L. Coagulation factors involved in the pathology of placental malaria. [Thesis]. University of Georgia; 2014. Available from: http://hdl.handle.net/10724/26379

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


Vanderbilt University

8. Peterson, Kristin Rose. Immunometabolism and the role of complement factor 5 in insulin action.

Degree: PhD, Pharmacology, 2019, Vanderbilt University

 Adipose tissue (AT) is a dynamic endocrine organ that contributes to metabolic health. Proper function of resident immune cells is vital to AT function, and… (more)

Subjects/Keywords: obesity; complement factor 5; insulin action; immunometabolism; adipose tissue

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APA (6th Edition):

Peterson, K. R. (2019). Immunometabolism and the role of complement factor 5 in insulin action. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://hdl.handle.net/1803/10760

Chicago Manual of Style (16th Edition):

Peterson, Kristin Rose. “Immunometabolism and the role of complement factor 5 in insulin action.” 2019. Doctoral Dissertation, Vanderbilt University. Accessed November 28, 2020. http://hdl.handle.net/1803/10760.

MLA Handbook (7th Edition):

Peterson, Kristin Rose. “Immunometabolism and the role of complement factor 5 in insulin action.” 2019. Web. 28 Nov 2020.

Vancouver:

Peterson KR. Immunometabolism and the role of complement factor 5 in insulin action. [Internet] [Doctoral dissertation]. Vanderbilt University; 2019. [cited 2020 Nov 28]. Available from: http://hdl.handle.net/1803/10760.

Council of Science Editors:

Peterson KR. Immunometabolism and the role of complement factor 5 in insulin action. [Doctoral Dissertation]. Vanderbilt University; 2019. Available from: http://hdl.handle.net/1803/10760


Jawaharlal Nehru University

9. Sindhu, K. V. Identification and characterization of stage/tissue restricted putative transcription factor(s) from developing chick heart; -.

Degree: School of Life Sciences, 2004, Jawaharlal Nehru University

Regulatory DNA elements located in the promoter/enhancer regions of various genes dictates newlinetheir temporal and spatial pattern of expression. Enormity of the metazoan genomes and… (more)

Subjects/Keywords: stage/tissue restricted putative transcription; developing chick heart; transcription factor(s)

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APA (6th Edition):

Sindhu, K. V. (2004). Identification and characterization of stage/tissue restricted putative transcription factor(s) from developing chick heart; -. (Thesis). Jawaharlal Nehru University. Retrieved from http://shodhganga.inflibnet.ac.in/handle/10603/16461

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):

Sindhu, K V. “Identification and characterization of stage/tissue restricted putative transcription factor(s) from developing chick heart; -.” 2004. Thesis, Jawaharlal Nehru University. Accessed November 28, 2020. http://shodhganga.inflibnet.ac.in/handle/10603/16461.

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

MLA Handbook (7th Edition):

Sindhu, K V. “Identification and characterization of stage/tissue restricted putative transcription factor(s) from developing chick heart; -.” 2004. Web. 28 Nov 2020.

Vancouver:

Sindhu KV. Identification and characterization of stage/tissue restricted putative transcription factor(s) from developing chick heart; -. [Internet] [Thesis]. Jawaharlal Nehru University; 2004. [cited 2020 Nov 28]. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/16461.

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

Council of Science Editors:

Sindhu KV. Identification and characterization of stage/tissue restricted putative transcription factor(s) from developing chick heart; -. [Thesis]. Jawaharlal Nehru University; 2004. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/16461

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

10. L. Facchinetti. PLATELET-ASSOCIATED TISSUE FACTOR EXPRESSION: INSIGHTS INTO THE MEGAKARYOCYTE-PLATELET AXIS.

Degree: 2014, Università degli Studi di Milano

Tissue factor is the main activator of the blood coagulation cascade and for this reason levels of TF are not easily detectable in cells in… (more)

Subjects/Keywords: tissue factor; platelets; megakaryocytes; Settore BIO/14 - Farmacologia

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APA (6th Edition):

Facchinetti, L. (2014). PLATELET-ASSOCIATED TISSUE FACTOR EXPRESSION: INSIGHTS INTO THE MEGAKARYOCYTE-PLATELET AXIS. (Thesis). Università degli Studi di Milano. Retrieved from http://hdl.handle.net/2434/229418

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):

Facchinetti, L.. “PLATELET-ASSOCIATED TISSUE FACTOR EXPRESSION: INSIGHTS INTO THE MEGAKARYOCYTE-PLATELET AXIS.” 2014. Thesis, Università degli Studi di Milano. Accessed November 28, 2020. http://hdl.handle.net/2434/229418.

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

MLA Handbook (7th Edition):

Facchinetti, L.. “PLATELET-ASSOCIATED TISSUE FACTOR EXPRESSION: INSIGHTS INTO THE MEGAKARYOCYTE-PLATELET AXIS.” 2014. Web. 28 Nov 2020.

Vancouver:

Facchinetti L. PLATELET-ASSOCIATED TISSUE FACTOR EXPRESSION: INSIGHTS INTO THE MEGAKARYOCYTE-PLATELET AXIS. [Internet] [Thesis]. Università degli Studi di Milano; 2014. [cited 2020 Nov 28]. Available from: http://hdl.handle.net/2434/229418.

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

Council of Science Editors:

Facchinetti L. PLATELET-ASSOCIATED TISSUE FACTOR EXPRESSION: INSIGHTS INTO THE MEGAKARYOCYTE-PLATELET AXIS. [Thesis]. Università degli Studi di Milano; 2014. Available from: http://hdl.handle.net/2434/229418

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


University of Manchester

11. Rees, Peter Adam. The role of extrinsic clotting pathway activation in the colorectal cancer microenvironment.

Degree: 2018, University of Manchester

 Malignancy is associated with a hypercoagulable state manifested clinically by an increased incidence of venous thromboembolism (VTE). Colorectal cancer (CRC) patients who develop VTE have… (more)

Subjects/Keywords: colorectal cancer; venous thromboembolism; tumour microenvironment; tissue factor

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APA (6th Edition):

Rees, P. A. (2018). The role of extrinsic clotting pathway activation in the colorectal cancer microenvironment. (Doctoral Dissertation). University of Manchester. Retrieved from http://www.manchester.ac.uk/escholar/uk-ac-man-scw:316936

Chicago Manual of Style (16th Edition):

Rees, Peter Adam. “The role of extrinsic clotting pathway activation in the colorectal cancer microenvironment.” 2018. Doctoral Dissertation, University of Manchester. Accessed November 28, 2020. http://www.manchester.ac.uk/escholar/uk-ac-man-scw:316936.

MLA Handbook (7th Edition):

Rees, Peter Adam. “The role of extrinsic clotting pathway activation in the colorectal cancer microenvironment.” 2018. Web. 28 Nov 2020.

Vancouver:

Rees PA. The role of extrinsic clotting pathway activation in the colorectal cancer microenvironment. [Internet] [Doctoral dissertation]. University of Manchester; 2018. [cited 2020 Nov 28]. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:316936.

Council of Science Editors:

Rees PA. The role of extrinsic clotting pathway activation in the colorectal cancer microenvironment. [Doctoral Dissertation]. University of Manchester; 2018. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:316936


University of Connecticut

12. Malinowski, Seth. Modulating the Release of Therapeutic Agents from PLGA Coated Cancellous Allografts.

Degree: MS, Biomedical Engineering, 2016, University of Connecticut

  Bone grafts are used in 2 million annual surgeries with that statistic expected to rise due to the increasing elderly population as well as… (more)

Subjects/Keywords: Cancellous Allografts; Growth Factor Delivery; Antibiotic Delivery; Bone Healing; Tissue Engineering

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APA (6th Edition):

Malinowski, S. (2016). Modulating the Release of Therapeutic Agents from PLGA Coated Cancellous Allografts. (Masters Thesis). University of Connecticut. Retrieved from https://opencommons.uconn.edu/gs_theses/926

Chicago Manual of Style (16th Edition):

Malinowski, Seth. “Modulating the Release of Therapeutic Agents from PLGA Coated Cancellous Allografts.” 2016. Masters Thesis, University of Connecticut. Accessed November 28, 2020. https://opencommons.uconn.edu/gs_theses/926.

MLA Handbook (7th Edition):

Malinowski, Seth. “Modulating the Release of Therapeutic Agents from PLGA Coated Cancellous Allografts.” 2016. Web. 28 Nov 2020.

Vancouver:

Malinowski S. Modulating the Release of Therapeutic Agents from PLGA Coated Cancellous Allografts. [Internet] [Masters thesis]. University of Connecticut; 2016. [cited 2020 Nov 28]. Available from: https://opencommons.uconn.edu/gs_theses/926.

Council of Science Editors:

Malinowski S. Modulating the Release of Therapeutic Agents from PLGA Coated Cancellous Allografts. [Masters Thesis]. University of Connecticut; 2016. Available from: https://opencommons.uconn.edu/gs_theses/926


Université Catholique de Louvain

13. Gnimassou, Olouyomi Karol. Hypoxia– and exercise-mediated effects on the muscle mass via endogenous local progenitors and the hippo signaling pathway.

Degree: 2019, Université Catholique de Louvain

Hypoxia is the state of lowered O2 tension condition that influence skeletal muscle mass when associated to resistance exercise whether after acute or chronic exposure.… (more)

Subjects/Keywords: Hypoxia-inducible factor; Differentiation; Hippo pathway; Tissue oxygenation index; Autophagy; Microarray

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APA (6th Edition):

Gnimassou, O. K. (2019). Hypoxia– and exercise-mediated effects on the muscle mass via endogenous local progenitors and the hippo signaling pathway. (Thesis). Université Catholique de Louvain. Retrieved from http://hdl.handle.net/2078.1/221012

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):

Gnimassou, Olouyomi Karol. “Hypoxia– and exercise-mediated effects on the muscle mass via endogenous local progenitors and the hippo signaling pathway.” 2019. Thesis, Université Catholique de Louvain. Accessed November 28, 2020. http://hdl.handle.net/2078.1/221012.

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

MLA Handbook (7th Edition):

Gnimassou, Olouyomi Karol. “Hypoxia– and exercise-mediated effects on the muscle mass via endogenous local progenitors and the hippo signaling pathway.” 2019. Web. 28 Nov 2020.

Vancouver:

Gnimassou OK. Hypoxia– and exercise-mediated effects on the muscle mass via endogenous local progenitors and the hippo signaling pathway. [Internet] [Thesis]. Université Catholique de Louvain; 2019. [cited 2020 Nov 28]. Available from: http://hdl.handle.net/2078.1/221012.

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

Council of Science Editors:

Gnimassou OK. Hypoxia– and exercise-mediated effects on the muscle mass via endogenous local progenitors and the hippo signaling pathway. [Thesis]. Université Catholique de Louvain; 2019. Available from: http://hdl.handle.net/2078.1/221012

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


Loughborough University

14. Lui, Yuan Siang. Developing sustained dual-drug therapy for tendon sports injuries.

Degree: PhD, 2016, Loughborough University

 Tendon plays an important role in regulating body locomotion and providing additional stability to the body. However, tendon is susceptible to injuries and the healing… (more)

Subjects/Keywords: 616.7; Tendon tissue engineering; Naproxen sodium; Insulin-like growth factor 1

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APA (6th Edition):

Lui, Y. S. (2016). Developing sustained dual-drug therapy for tendon sports injuries. (Doctoral Dissertation). Loughborough University. Retrieved from http://hdl.handle.net/2134/23739

Chicago Manual of Style (16th Edition):

Lui, Yuan Siang. “Developing sustained dual-drug therapy for tendon sports injuries.” 2016. Doctoral Dissertation, Loughborough University. Accessed November 28, 2020. http://hdl.handle.net/2134/23739.

MLA Handbook (7th Edition):

Lui, Yuan Siang. “Developing sustained dual-drug therapy for tendon sports injuries.” 2016. Web. 28 Nov 2020.

Vancouver:

Lui YS. Developing sustained dual-drug therapy for tendon sports injuries. [Internet] [Doctoral dissertation]. Loughborough University; 2016. [cited 2020 Nov 28]. Available from: http://hdl.handle.net/2134/23739.

Council of Science Editors:

Lui YS. Developing sustained dual-drug therapy for tendon sports injuries. [Doctoral Dissertation]. Loughborough University; 2016. Available from: http://hdl.handle.net/2134/23739


University of Illinois – Urbana-Champaign

15. Gajsiewicz, Joshua M. Polyphosphate and tissue factor/factor VIIA as initiators of coagulation.

Degree: PhD, Biochemistry, 2016, University of Illinois – Urbana-Champaign

 Protein-membrane interactions are a critical component of the coagulation cascade. For many coagulation factors, these interactions are mediated via γ-carboxyglutamate rich regions, or GLA domains,… (more)

Subjects/Keywords: Blood coagulation; Clotting; Protein-membrane interactions; Tissue factor (TF); Polyphosphate

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APA (6th Edition):

Gajsiewicz, J. M. (2016). Polyphosphate and tissue factor/factor VIIA as initiators of coagulation. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/95553

Chicago Manual of Style (16th Edition):

Gajsiewicz, Joshua M. “Polyphosphate and tissue factor/factor VIIA as initiators of coagulation.” 2016. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed November 28, 2020. http://hdl.handle.net/2142/95553.

MLA Handbook (7th Edition):

Gajsiewicz, Joshua M. “Polyphosphate and tissue factor/factor VIIA as initiators of coagulation.” 2016. Web. 28 Nov 2020.

Vancouver:

Gajsiewicz JM. Polyphosphate and tissue factor/factor VIIA as initiators of coagulation. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2016. [cited 2020 Nov 28]. Available from: http://hdl.handle.net/2142/95553.

Council of Science Editors:

Gajsiewicz JM. Polyphosphate and tissue factor/factor VIIA as initiators of coagulation. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2016. Available from: http://hdl.handle.net/2142/95553


University of Georgia

16. Duff, Emily. The effects of Ciliary Neurotrophic Factor on adipose tissue apoptosis.

Degree: 2014, University of Georgia

 The administration of Ciliary Neurotrophic Factor (CNTF), a neurocytokine recently implicated for its role in energy homeostasis, results in a reduction of food intake and… (more)

Subjects/Keywords: Adipose Tissue; Apoptosis; Ciliary Neurotrophic Factor; CNTF; Leptin; Obesity

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APA (6th Edition):

Duff, E. (2014). The effects of Ciliary Neurotrophic Factor on adipose tissue apoptosis. (Thesis). University of Georgia. Retrieved from http://hdl.handle.net/10724/21812

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):

Duff, Emily. “The effects of Ciliary Neurotrophic Factor on adipose tissue apoptosis.” 2014. Thesis, University of Georgia. Accessed November 28, 2020. http://hdl.handle.net/10724/21812.

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

MLA Handbook (7th Edition):

Duff, Emily. “The effects of Ciliary Neurotrophic Factor on adipose tissue apoptosis.” 2014. Web. 28 Nov 2020.

Vancouver:

Duff E. The effects of Ciliary Neurotrophic Factor on adipose tissue apoptosis. [Internet] [Thesis]. University of Georgia; 2014. [cited 2020 Nov 28]. Available from: http://hdl.handle.net/10724/21812.

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

Council of Science Editors:

Duff E. The effects of Ciliary Neurotrophic Factor on adipose tissue apoptosis. [Thesis]. University of Georgia; 2014. Available from: http://hdl.handle.net/10724/21812

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


University of New South Wales

17. Malhotra, Angad. Can platelet rich plasma improve bone healing? - An in vitro and in vivo investigation into the use of platelet rich plasma to augment bone regeneration.

Degree: Clinical School - Prince of Wales Hospital, 2013, University of New South Wales

 Introduction: The management of bone defects continues to present surgical challenges, and alternatives to autograft remain sought after. Upon activation, platelets release an array of… (more)

Subjects/Keywords: Bone healing; Platelet rich plasma; Tissue engineering; Animal model; Growth factor

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APA (6th Edition):

Malhotra, A. (2013). Can platelet rich plasma improve bone healing? - An in vitro and in vivo investigation into the use of platelet rich plasma to augment bone regeneration. (Doctoral Dissertation). University of New South Wales. Retrieved from http://handle.unsw.edu.au/1959.4/52858 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:11531/SOURCE01?view=true

Chicago Manual of Style (16th Edition):

Malhotra, Angad. “Can platelet rich plasma improve bone healing? - An in vitro and in vivo investigation into the use of platelet rich plasma to augment bone regeneration.” 2013. Doctoral Dissertation, University of New South Wales. Accessed November 28, 2020. http://handle.unsw.edu.au/1959.4/52858 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:11531/SOURCE01?view=true.

MLA Handbook (7th Edition):

Malhotra, Angad. “Can platelet rich plasma improve bone healing? - An in vitro and in vivo investigation into the use of platelet rich plasma to augment bone regeneration.” 2013. Web. 28 Nov 2020.

Vancouver:

Malhotra A. Can platelet rich plasma improve bone healing? - An in vitro and in vivo investigation into the use of platelet rich plasma to augment bone regeneration. [Internet] [Doctoral dissertation]. University of New South Wales; 2013. [cited 2020 Nov 28]. Available from: http://handle.unsw.edu.au/1959.4/52858 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:11531/SOURCE01?view=true.

Council of Science Editors:

Malhotra A. Can platelet rich plasma improve bone healing? - An in vitro and in vivo investigation into the use of platelet rich plasma to augment bone regeneration. [Doctoral Dissertation]. University of New South Wales; 2013. Available from: http://handle.unsw.edu.au/1959.4/52858 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:11531/SOURCE01?view=true


University of Western Ontario

18. Racanelli, Michael. YAP-mediated mechanotransduction promotes fibrotic activity.

Degree: 2019, University of Western Ontario

 Fibrosis, a phenotype associated with mortality for a multitude of diseases, has no disease-modifying treatment. We examine if Verteporfin (VP), an inhibitor of the YAP-TEAD… (more)

Subjects/Keywords: Fibrosis; mechanotransduction; extracellular matrix (ECM); Verteporfin (VP); connective tissue growth factor (CCN2); Skin and Connective Tissue Diseases

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APA (6th Edition):

Racanelli, M. (2019). YAP-mediated mechanotransduction promotes fibrotic activity. (Thesis). University of Western Ontario. Retrieved from https://ir.lib.uwo.ca/etd/6283

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):

Racanelli, Michael. “YAP-mediated mechanotransduction promotes fibrotic activity.” 2019. Thesis, University of Western Ontario. Accessed November 28, 2020. https://ir.lib.uwo.ca/etd/6283.

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

MLA Handbook (7th Edition):

Racanelli, Michael. “YAP-mediated mechanotransduction promotes fibrotic activity.” 2019. Web. 28 Nov 2020.

Vancouver:

Racanelli M. YAP-mediated mechanotransduction promotes fibrotic activity. [Internet] [Thesis]. University of Western Ontario; 2019. [cited 2020 Nov 28]. Available from: https://ir.lib.uwo.ca/etd/6283.

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

Council of Science Editors:

Racanelli M. YAP-mediated mechanotransduction promotes fibrotic activity. [Thesis]. University of Western Ontario; 2019. Available from: https://ir.lib.uwo.ca/etd/6283

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

19. He, Hongbin. Studies on the genetic control of infection and hepatic disease in schistosoma haematobium and schistosoma japonicum infections in human : Etudes du contrôle génétique des niveaux d'infection et des atteintes hépatiques dans les infections par Schistosoma haematobium et Schistosoma japonicum.

Degree: Docteur es, Pathologie humaine, 2010, Aix-Marseille 2

La bilharziose reste un problème de santé majeur. L'équipe du Pr Dessein a montré que les infections élevées étaient déterminées par un locus majeur en… (more)

Subjects/Keywords: Bilharziose; Génétique; Susceptibilité; Fibrose; Ctgf; Stat6; Schistosomiasis; Hepatic fibrosis; Connective tissue growth factor; Stat6 transcription factor

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APA (6th Edition):

He, H. (2010). Studies on the genetic control of infection and hepatic disease in schistosoma haematobium and schistosoma japonicum infections in human : Etudes du contrôle génétique des niveaux d'infection et des atteintes hépatiques dans les infections par Schistosoma haematobium et Schistosoma japonicum. (Doctoral Dissertation). Aix-Marseille 2. Retrieved from http://www.theses.fr/2010AIX20720

Chicago Manual of Style (16th Edition):

He, Hongbin. “Studies on the genetic control of infection and hepatic disease in schistosoma haematobium and schistosoma japonicum infections in human : Etudes du contrôle génétique des niveaux d'infection et des atteintes hépatiques dans les infections par Schistosoma haematobium et Schistosoma japonicum.” 2010. Doctoral Dissertation, Aix-Marseille 2. Accessed November 28, 2020. http://www.theses.fr/2010AIX20720.

MLA Handbook (7th Edition):

He, Hongbin. “Studies on the genetic control of infection and hepatic disease in schistosoma haematobium and schistosoma japonicum infections in human : Etudes du contrôle génétique des niveaux d'infection et des atteintes hépatiques dans les infections par Schistosoma haematobium et Schistosoma japonicum.” 2010. Web. 28 Nov 2020.

Vancouver:

He H. Studies on the genetic control of infection and hepatic disease in schistosoma haematobium and schistosoma japonicum infections in human : Etudes du contrôle génétique des niveaux d'infection et des atteintes hépatiques dans les infections par Schistosoma haematobium et Schistosoma japonicum. [Internet] [Doctoral dissertation]. Aix-Marseille 2; 2010. [cited 2020 Nov 28]. Available from: http://www.theses.fr/2010AIX20720.

Council of Science Editors:

He H. Studies on the genetic control of infection and hepatic disease in schistosoma haematobium and schistosoma japonicum infections in human : Etudes du contrôle génétique des niveaux d'infection et des atteintes hépatiques dans les infections par Schistosoma haematobium et Schistosoma japonicum. [Doctoral Dissertation]. Aix-Marseille 2; 2010. Available from: http://www.theses.fr/2010AIX20720


University of Georgia

20. Bracken, Tara Catherine. Investigating the extrinsic pathway of coagulation as a therapeutic target for severe malaria.

Degree: 2017, University of Georgia

 Malaria poses a serious threat to global health, with 3.2 billion people in 95 countries at risk of infection. Pregnant women and young children in… (more)

Subjects/Keywords: Plasmodium falciparum; placental malaria; cerebral malaria; coagulation; anticoagulant therapy; adjunctive therapy; Tissue Factor; Thrombin; coagulation Factor X; extrinsic pathway of coagulation

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APA (6th Edition):

Bracken, T. C. (2017). Investigating the extrinsic pathway of coagulation as a therapeutic target for severe malaria. (Thesis). University of Georgia. Retrieved from http://hdl.handle.net/10724/36939

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):

Bracken, Tara Catherine. “Investigating the extrinsic pathway of coagulation as a therapeutic target for severe malaria.” 2017. Thesis, University of Georgia. Accessed November 28, 2020. http://hdl.handle.net/10724/36939.

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

MLA Handbook (7th Edition):

Bracken, Tara Catherine. “Investigating the extrinsic pathway of coagulation as a therapeutic target for severe malaria.” 2017. Web. 28 Nov 2020.

Vancouver:

Bracken TC. Investigating the extrinsic pathway of coagulation as a therapeutic target for severe malaria. [Internet] [Thesis]. University of Georgia; 2017. [cited 2020 Nov 28]. Available from: http://hdl.handle.net/10724/36939.

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

Council of Science Editors:

Bracken TC. Investigating the extrinsic pathway of coagulation as a therapeutic target for severe malaria. [Thesis]. University of Georgia; 2017. Available from: http://hdl.handle.net/10724/36939

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


NSYSU

21. Huang, Sheng-feng. Association of Oct4, Sox2, Nanog and Lin28 Protein Expression Levels with the Prognosis of Invasive Mammary Ductal Carcinoma Patients.

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

 Breast cancer is the most common cancer in Taiwanese women and the invasive ductal carcinoma (IDC) is the most common type. Increasing evidence shows that… (more)

Subjects/Keywords: reprogramming factor; induce induced pluripotent stem cell; tissue microarray; Invasive ductal carcinoma

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APA (6th Edition):

Huang, S. (2012). Association of Oct4, Sox2, Nanog and Lin28 Protein Expression Levels with the Prognosis of Invasive Mammary Ductal Carcinoma Patients. (Thesis). NSYSU. Retrieved from http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0830112-143255

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, Sheng-feng. “Association of Oct4, Sox2, Nanog and Lin28 Protein Expression Levels with the Prognosis of Invasive Mammary Ductal Carcinoma Patients.” 2012. Thesis, NSYSU. Accessed November 28, 2020. http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0830112-143255.

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

MLA Handbook (7th Edition):

Huang, Sheng-feng. “Association of Oct4, Sox2, Nanog and Lin28 Protein Expression Levels with the Prognosis of Invasive Mammary Ductal Carcinoma Patients.” 2012. Web. 28 Nov 2020.

Vancouver:

Huang S. Association of Oct4, Sox2, Nanog and Lin28 Protein Expression Levels with the Prognosis of Invasive Mammary Ductal Carcinoma Patients. [Internet] [Thesis]. NSYSU; 2012. [cited 2020 Nov 28]. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0830112-143255.

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. Association of Oct4, Sox2, Nanog and Lin28 Protein Expression Levels with the Prognosis of Invasive Mammary Ductal Carcinoma Patients. [Thesis]. NSYSU; 2012. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0830112-143255

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


Universiteit Utrecht

22. Hennink, I. Tissue factor expression in thrombocytes of dogs suffering from idiopathic immune mediated haemolytic anemia.

Degree: 2015, Universiteit Utrecht

 Dogs suffering from canine idiopathic immune mediated haemolytic anaemia (cIIMHA) are at great risk of dying particularly in the first two weeks after the diagnosis… (more)

Subjects/Keywords: Tissue factor; TF; canine idiopathic immune mediated haemolytic anemia; dogs; thrombocytes; TFmRNA

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APA (6th Edition):

Hennink, I. (2015). Tissue factor expression in thrombocytes of dogs suffering from idiopathic immune mediated haemolytic anemia. (Masters Thesis). Universiteit Utrecht. Retrieved from http://dspace.library.uu.nl:8080/handle/1874/323304

Chicago Manual of Style (16th Edition):

Hennink, I. “Tissue factor expression in thrombocytes of dogs suffering from idiopathic immune mediated haemolytic anemia.” 2015. Masters Thesis, Universiteit Utrecht. Accessed November 28, 2020. http://dspace.library.uu.nl:8080/handle/1874/323304.

MLA Handbook (7th Edition):

Hennink, I. “Tissue factor expression in thrombocytes of dogs suffering from idiopathic immune mediated haemolytic anemia.” 2015. Web. 28 Nov 2020.

Vancouver:

Hennink I. Tissue factor expression in thrombocytes of dogs suffering from idiopathic immune mediated haemolytic anemia. [Internet] [Masters thesis]. Universiteit Utrecht; 2015. [cited 2020 Nov 28]. Available from: http://dspace.library.uu.nl:8080/handle/1874/323304.

Council of Science Editors:

Hennink I. Tissue factor expression in thrombocytes of dogs suffering from idiopathic immune mediated haemolytic anemia. [Masters Thesis]. Universiteit Utrecht; 2015. Available from: http://dspace.library.uu.nl:8080/handle/1874/323304


Temple University

23. Mundy, Christina Maria. The Interaction Between Connective Tissue Growth Factor and Bone Morphogenetic Protein-2 During Osteoblast Differentiation and Function.

Degree: PhD, 2014, Temple University

Cell Biology

Connective tissue growth factor (CTGF/CCN2) and bone morphogenetic protein (BMP)-2 are both produced and secreted by osteoblasts. Both proteins have been shown to… (more)

Subjects/Keywords: Cellular biology;

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APA (6th Edition):

Mundy, C. M. (2014). The Interaction Between Connective Tissue Growth Factor and Bone Morphogenetic Protein-2 During Osteoblast Differentiation and Function. (Doctoral Dissertation). Temple University. Retrieved from http://digital.library.temple.edu/u?/p245801coll10,269581

Chicago Manual of Style (16th Edition):

Mundy, Christina Maria. “The Interaction Between Connective Tissue Growth Factor and Bone Morphogenetic Protein-2 During Osteoblast Differentiation and Function.” 2014. Doctoral Dissertation, Temple University. Accessed November 28, 2020. http://digital.library.temple.edu/u?/p245801coll10,269581.

MLA Handbook (7th Edition):

Mundy, Christina Maria. “The Interaction Between Connective Tissue Growth Factor and Bone Morphogenetic Protein-2 During Osteoblast Differentiation and Function.” 2014. Web. 28 Nov 2020.

Vancouver:

Mundy CM. The Interaction Between Connective Tissue Growth Factor and Bone Morphogenetic Protein-2 During Osteoblast Differentiation and Function. [Internet] [Doctoral dissertation]. Temple University; 2014. [cited 2020 Nov 28]. Available from: http://digital.library.temple.edu/u?/p245801coll10,269581.

Council of Science Editors:

Mundy CM. The Interaction Between Connective Tissue Growth Factor and Bone Morphogenetic Protein-2 During Osteoblast Differentiation and Function. [Doctoral Dissertation]. Temple University; 2014. Available from: http://digital.library.temple.edu/u?/p245801coll10,269581

24. Ayerst, Bethanie Imogen. GDF5 Mediated Enhancement of Chondrocyte Phenotype and its Modulation by Heparin and Heparan Sulfates.

Degree: 2017, University of Manchester

 Articular cartilage plays a vital role in load-bearing joints, providing an almost frictionless surface to articulating bones. However, the avascular nature and low cell density… (more)

Subjects/Keywords: cartilage; Growth differentiation factor 5; Heparin; Heparan sulfate; Mesenchymal stem cells; Tissue engineering; Glycosaminoglycans

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APA (6th Edition):

Ayerst, B. I. (2017). GDF5 Mediated Enhancement of Chondrocyte Phenotype and its Modulation by Heparin and Heparan Sulfates. (Doctoral Dissertation). University of Manchester. Retrieved from http://www.manchester.ac.uk/escholar/uk-ac-man-scw:307032

Chicago Manual of Style (16th Edition):

Ayerst, Bethanie Imogen. “GDF5 Mediated Enhancement of Chondrocyte Phenotype and its Modulation by Heparin and Heparan Sulfates.” 2017. Doctoral Dissertation, University of Manchester. Accessed November 28, 2020. http://www.manchester.ac.uk/escholar/uk-ac-man-scw:307032.

MLA Handbook (7th Edition):

Ayerst, Bethanie Imogen. “GDF5 Mediated Enhancement of Chondrocyte Phenotype and its Modulation by Heparin and Heparan Sulfates.” 2017. Web. 28 Nov 2020.

Vancouver:

Ayerst BI. GDF5 Mediated Enhancement of Chondrocyte Phenotype and its Modulation by Heparin and Heparan Sulfates. [Internet] [Doctoral dissertation]. University of Manchester; 2017. [cited 2020 Nov 28]. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:307032.

Council of Science Editors:

Ayerst BI. GDF5 Mediated Enhancement of Chondrocyte Phenotype and its Modulation by Heparin and Heparan Sulfates. [Doctoral Dissertation]. University of Manchester; 2017. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:307032


Penn State University

25. Saravanan, Pratima. THE EFFECT OF GEOMETRY, HEMODYNAMICS, AND TISSUE FACTOR ON CLOT FORMATION IN ANEURYSM MODELS.

Degree: 2018, Penn State University

 According to a statistical report by The Centers for Disease Control and Prevention (CDC), aortic aneurysms alone constitutes 9,845 deaths in 2013, where men of… (more)

Subjects/Keywords: aneurysm; hemodynamics; tissue factor; thrombus; wall shear stress; poly (1; 8 - octane diol citrate)

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APA (6th Edition):

Saravanan, P. (2018). THE EFFECT OF GEOMETRY, HEMODYNAMICS, AND TISSUE FACTOR ON CLOT FORMATION IN ANEURYSM MODELS. (Thesis). Penn State University. Retrieved from https://submit-etda.libraries.psu.edu/catalog/15152pvs5384

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):

Saravanan, Pratima. “THE EFFECT OF GEOMETRY, HEMODYNAMICS, AND TISSUE FACTOR ON CLOT FORMATION IN ANEURYSM MODELS.” 2018. Thesis, Penn State University. Accessed November 28, 2020. https://submit-etda.libraries.psu.edu/catalog/15152pvs5384.

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

MLA Handbook (7th Edition):

Saravanan, Pratima. “THE EFFECT OF GEOMETRY, HEMODYNAMICS, AND TISSUE FACTOR ON CLOT FORMATION IN ANEURYSM MODELS.” 2018. Web. 28 Nov 2020.

Vancouver:

Saravanan P. THE EFFECT OF GEOMETRY, HEMODYNAMICS, AND TISSUE FACTOR ON CLOT FORMATION IN ANEURYSM MODELS. [Internet] [Thesis]. Penn State University; 2018. [cited 2020 Nov 28]. Available from: https://submit-etda.libraries.psu.edu/catalog/15152pvs5384.

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

Council of Science Editors:

Saravanan P. THE EFFECT OF GEOMETRY, HEMODYNAMICS, AND TISSUE FACTOR ON CLOT FORMATION IN ANEURYSM MODELS. [Thesis]. Penn State University; 2018. Available from: https://submit-etda.libraries.psu.edu/catalog/15152pvs5384

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

26. L. Rossetti. PLATELET ACTIVATION AND ASSOCIATED TRANSCRIPTIONAL SIGNATURE IN TYPE 2 DIABETIC PATIENTS WITH STABLE CORONARY ARTERY DISEASE: INSIGHTS INTO THEIR THROMBOTIC PROPENSITY.

Degree: 2014, Università degli Studi di Milano

 Platelet activation and associated transcriptional signature in type 2 diabetic patients with stable coronary artery disease: insights into their thrombotic propensity Several studies indicate that… (more)

Subjects/Keywords: Type 2 diabetes mellitus; platelet; tissue factor; stable angina; platelet transcriptome; Settore BIO/14 - Farmacologia

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APA (6th Edition):

Rossetti, L. (2014). PLATELET ACTIVATION AND ASSOCIATED TRANSCRIPTIONAL SIGNATURE IN TYPE 2 DIABETIC PATIENTS WITH STABLE CORONARY ARTERY DISEASE: INSIGHTS INTO THEIR THROMBOTIC PROPENSITY. (Thesis). Università degli Studi di Milano. Retrieved from http://hdl.handle.net/2434/246942

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):

Rossetti, L.. “PLATELET ACTIVATION AND ASSOCIATED TRANSCRIPTIONAL SIGNATURE IN TYPE 2 DIABETIC PATIENTS WITH STABLE CORONARY ARTERY DISEASE: INSIGHTS INTO THEIR THROMBOTIC PROPENSITY.” 2014. Thesis, Università degli Studi di Milano. Accessed November 28, 2020. http://hdl.handle.net/2434/246942.

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

MLA Handbook (7th Edition):

Rossetti, L.. “PLATELET ACTIVATION AND ASSOCIATED TRANSCRIPTIONAL SIGNATURE IN TYPE 2 DIABETIC PATIENTS WITH STABLE CORONARY ARTERY DISEASE: INSIGHTS INTO THEIR THROMBOTIC PROPENSITY.” 2014. Web. 28 Nov 2020.

Vancouver:

Rossetti L. PLATELET ACTIVATION AND ASSOCIATED TRANSCRIPTIONAL SIGNATURE IN TYPE 2 DIABETIC PATIENTS WITH STABLE CORONARY ARTERY DISEASE: INSIGHTS INTO THEIR THROMBOTIC PROPENSITY. [Internet] [Thesis]. Università degli Studi di Milano; 2014. [cited 2020 Nov 28]. Available from: http://hdl.handle.net/2434/246942.

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

Council of Science Editors:

Rossetti L. PLATELET ACTIVATION AND ASSOCIATED TRANSCRIPTIONAL SIGNATURE IN TYPE 2 DIABETIC PATIENTS WITH STABLE CORONARY ARTERY DISEASE: INSIGHTS INTO THEIR THROMBOTIC PROPENSITY. [Thesis]. Università degli Studi di Milano; 2014. Available from: http://hdl.handle.net/2434/246942

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

27. Darbousset, Roxane. Roles of polymorphonuclear neutrophils in thrombosis : Roles of Polymorphonuclear Neutrophils in thrombosis.

Degree: Docteur es, Pathologie humaine. Oncologie, 2013, Aix Marseille Université

L’hémostase est un processus physiologique permettant de préserver l’intégrité du système vasculaire et de prévenir une perte de sang en réponse à une blessure. En… (more)

Subjects/Keywords: Thrombose, Microscopie intravitale, Neutrophiles, Plaquettes, Facteur Tissulaire; Thrombosis, Intravital microscopy, Neutrophils, Platelets, Tissue Factor

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

APA (6th Edition):

Darbousset, R. (2013). Roles of polymorphonuclear neutrophils in thrombosis : Roles of Polymorphonuclear Neutrophils in thrombosis. (Doctoral Dissertation). Aix Marseille Université. Retrieved from http://www.theses.fr/2013AIXM5071

Chicago Manual of Style (16th Edition):

Darbousset, Roxane. “Roles of polymorphonuclear neutrophils in thrombosis : Roles of Polymorphonuclear Neutrophils in thrombosis.” 2013. Doctoral Dissertation, Aix Marseille Université. Accessed November 28, 2020. http://www.theses.fr/2013AIXM5071.

MLA Handbook (7th Edition):

Darbousset, Roxane. “Roles of polymorphonuclear neutrophils in thrombosis : Roles of Polymorphonuclear Neutrophils in thrombosis.” 2013. Web. 28 Nov 2020.

Vancouver:

Darbousset R. Roles of polymorphonuclear neutrophils in thrombosis : Roles of Polymorphonuclear Neutrophils in thrombosis. [Internet] [Doctoral dissertation]. Aix Marseille Université 2013. [cited 2020 Nov 28]. Available from: http://www.theses.fr/2013AIXM5071.

Council of Science Editors:

Darbousset R. Roles of polymorphonuclear neutrophils in thrombosis : Roles of Polymorphonuclear Neutrophils in thrombosis. [Doctoral Dissertation]. Aix Marseille Université 2013. Available from: http://www.theses.fr/2013AIXM5071

28. Lakbakbi, Souad. Adhésion et activation des cellules sanguines par une membrane d'hémodialyse (AN-69ST) : conséquence sur l'expression de facteur tissulaire et la thrombogénecité de la membrane. : Adhesion and activation of blood cells by a hemodialysis membrane (AN-69ST) : consequence on the expression of tissue factor and of the membrane thrombogenicity.

Degree: Docteur es, Sciences - STS, 2014, Reims

L'objectif de ce travail est d'évaluer le rôle du facteur tissulaire (FT) dans l'initiation de la coagulation d'un circuit d'hémodialyse. A partir de l'analyse des… (more)

Subjects/Keywords: Hemodialyse; Facteur tissulaire; Neutrophiles; Anticoagulation; Biocompatibilité; Hemodialysis; Tissue factor; Neutrophils; Anticoagulation; Biocompatibility

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

APA (6th Edition):

Lakbakbi, S. (2014). Adhésion et activation des cellules sanguines par une membrane d'hémodialyse (AN-69ST) : conséquence sur l'expression de facteur tissulaire et la thrombogénecité de la membrane. : Adhesion and activation of blood cells by a hemodialysis membrane (AN-69ST) : consequence on the expression of tissue factor and of the membrane thrombogenicity. (Doctoral Dissertation). Reims. Retrieved from http://www.theses.fr/2014REIMS012

Chicago Manual of Style (16th Edition):

Lakbakbi, Souad. “Adhésion et activation des cellules sanguines par une membrane d'hémodialyse (AN-69ST) : conséquence sur l'expression de facteur tissulaire et la thrombogénecité de la membrane. : Adhesion and activation of blood cells by a hemodialysis membrane (AN-69ST) : consequence on the expression of tissue factor and of the membrane thrombogenicity.” 2014. Doctoral Dissertation, Reims. Accessed November 28, 2020. http://www.theses.fr/2014REIMS012.

MLA Handbook (7th Edition):

Lakbakbi, Souad. “Adhésion et activation des cellules sanguines par une membrane d'hémodialyse (AN-69ST) : conséquence sur l'expression de facteur tissulaire et la thrombogénecité de la membrane. : Adhesion and activation of blood cells by a hemodialysis membrane (AN-69ST) : consequence on the expression of tissue factor and of the membrane thrombogenicity.” 2014. Web. 28 Nov 2020.

Vancouver:

Lakbakbi S. Adhésion et activation des cellules sanguines par une membrane d'hémodialyse (AN-69ST) : conséquence sur l'expression de facteur tissulaire et la thrombogénecité de la membrane. : Adhesion and activation of blood cells by a hemodialysis membrane (AN-69ST) : consequence on the expression of tissue factor and of the membrane thrombogenicity. [Internet] [Doctoral dissertation]. Reims; 2014. [cited 2020 Nov 28]. Available from: http://www.theses.fr/2014REIMS012.

Council of Science Editors:

Lakbakbi S. Adhésion et activation des cellules sanguines par une membrane d'hémodialyse (AN-69ST) : conséquence sur l'expression de facteur tissulaire et la thrombogénecité de la membrane. : Adhesion and activation of blood cells by a hemodialysis membrane (AN-69ST) : consequence on the expression of tissue factor and of the membrane thrombogenicity. [Doctoral Dissertation]. Reims; 2014. Available from: http://www.theses.fr/2014REIMS012


Australian National University

29. Bruggeman, Kiara Anaya Fay. Novel Growth Factor Delivery Systems from Self-Assembling Peptide (SAP) Hydrogels .

Degree: 2016, Australian National University

 Growth factors are important signalling molecules in regenerative medicine and tissue engineering, but their inherent instability, lasting only minute to hours in vivo, presents an… (more)

Subjects/Keywords: self-assembling peptide; drug delivery; tissue engineering; regenerative medicine; growth factor; controlled release

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

APA (6th Edition):

Bruggeman, K. A. F. (2016). Novel Growth Factor Delivery Systems from Self-Assembling Peptide (SAP) Hydrogels . (Thesis). Australian National University. Retrieved from http://hdl.handle.net/1885/117065

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):

Bruggeman, Kiara Anaya Fay. “Novel Growth Factor Delivery Systems from Self-Assembling Peptide (SAP) Hydrogels .” 2016. Thesis, Australian National University. Accessed November 28, 2020. http://hdl.handle.net/1885/117065.

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

MLA Handbook (7th Edition):

Bruggeman, Kiara Anaya Fay. “Novel Growth Factor Delivery Systems from Self-Assembling Peptide (SAP) Hydrogels .” 2016. Web. 28 Nov 2020.

Vancouver:

Bruggeman KAF. Novel Growth Factor Delivery Systems from Self-Assembling Peptide (SAP) Hydrogels . [Internet] [Thesis]. Australian National University; 2016. [cited 2020 Nov 28]. Available from: http://hdl.handle.net/1885/117065.

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

Council of Science Editors:

Bruggeman KAF. Novel Growth Factor Delivery Systems from Self-Assembling Peptide (SAP) Hydrogels . [Thesis]. Australian National University; 2016. Available from: http://hdl.handle.net/1885/117065

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

30. M. Milano. PARTICULATE MATTER PHAGOCYTOSIS INDUCES TISSUE FACTOR IN DIFFERENTIATING MACROPHAGES.

Degree: 2016, Università degli Studi di Milano

 Airborne exposure to particulate matter with diameter <10μm (PM10) has been linked to an increased risk of thromboembolic events, but the mechanisms are not completely… (more)

Subjects/Keywords: coagulation; inflammation; lung; macrophage; monocyte; particulate matter; phagocytosis; tissue factor; Settore MED/09 - Medicina Interna

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

APA (6th Edition):

Milano, M. (2016). PARTICULATE MATTER PHAGOCYTOSIS INDUCES TISSUE FACTOR IN DIFFERENTIATING MACROPHAGES. (Thesis). Università degli Studi di Milano. Retrieved from http://hdl.handle.net/2434/362958

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):

Milano, M.. “PARTICULATE MATTER PHAGOCYTOSIS INDUCES TISSUE FACTOR IN DIFFERENTIATING MACROPHAGES.” 2016. Thesis, Università degli Studi di Milano. Accessed November 28, 2020. http://hdl.handle.net/2434/362958.

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

MLA Handbook (7th Edition):

Milano, M.. “PARTICULATE MATTER PHAGOCYTOSIS INDUCES TISSUE FACTOR IN DIFFERENTIATING MACROPHAGES.” 2016. Web. 28 Nov 2020.

Vancouver:

Milano M. PARTICULATE MATTER PHAGOCYTOSIS INDUCES TISSUE FACTOR IN DIFFERENTIATING MACROPHAGES. [Internet] [Thesis]. Università degli Studi di Milano; 2016. [cited 2020 Nov 28]. Available from: http://hdl.handle.net/2434/362958.

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

Council of Science Editors:

Milano M. PARTICULATE MATTER PHAGOCYTOSIS INDUCES TISSUE FACTOR IN DIFFERENTIATING MACROPHAGES. [Thesis]. Università degli Studi di Milano; 2016. Available from: http://hdl.handle.net/2434/362958

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

[1] [2] [3] [4] [5] [6] [7] [8]

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