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You searched for subject:(mouse model). Showing records 1 – 30 of 609 total matches.

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1. Lau, Bonnie W. CXCR4/SDF1 in recruitment of stem cells to orthotopic murine malignant mesothelioma spheroids.

Degree: PhD, Division of Biology and Medicine. Pathobiology, 2009, Brown University

 Malignant mesothelioma is an aggressive cancer of the mesothelial lining causally linked to asbestos exposure and is highly resistant to current therapies. We hypothesize a… (more)

Subjects/Keywords: mouse model

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APA (6th Edition):

Lau, B. W. (2009). CXCR4/SDF1 in recruitment of stem cells to orthotopic murine malignant mesothelioma spheroids. (Doctoral Dissertation). Brown University. Retrieved from https://repository.library.brown.edu/studio/item/bdr:148/

Chicago Manual of Style (16th Edition):

Lau, Bonnie W. “CXCR4/SDF1 in recruitment of stem cells to orthotopic murine malignant mesothelioma spheroids.” 2009. Doctoral Dissertation, Brown University. Accessed January 15, 2021. https://repository.library.brown.edu/studio/item/bdr:148/.

MLA Handbook (7th Edition):

Lau, Bonnie W. “CXCR4/SDF1 in recruitment of stem cells to orthotopic murine malignant mesothelioma spheroids.” 2009. Web. 15 Jan 2021.

Vancouver:

Lau BW. CXCR4/SDF1 in recruitment of stem cells to orthotopic murine malignant mesothelioma spheroids. [Internet] [Doctoral dissertation]. Brown University; 2009. [cited 2021 Jan 15]. Available from: https://repository.library.brown.edu/studio/item/bdr:148/.

Council of Science Editors:

Lau BW. CXCR4/SDF1 in recruitment of stem cells to orthotopic murine malignant mesothelioma spheroids. [Doctoral Dissertation]. Brown University; 2009. Available from: https://repository.library.brown.edu/studio/item/bdr:148/


Cape Peninsula University of Technology

2. Petrova, Antoinette. Modulation of ultrviolet light induced skin carcinogenesis by extracts of Rooibos and Honeybush using a mouse model:elucidating possible protective mechanisms .

Degree: 2009, Cape Peninsula University of Technology

 This thesis provides the first scientific evidence of the photoprotective properties of rooibos and honeybush herbal tea extracts and to some extent, two major honeybush… (more)

Subjects/Keywords: rooibos; honeybush; carcinogenesis; mouse model

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APA (6th Edition):

Petrova, A. (2009). Modulation of ultrviolet light induced skin carcinogenesis by extracts of Rooibos and Honeybush using a mouse model:elucidating possible protective mechanisms . (Thesis). Cape Peninsula University of Technology. Retrieved from http://etd.cput.ac.za/handle/20.500.11838/1487

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):

Petrova, Antoinette. “Modulation of ultrviolet light induced skin carcinogenesis by extracts of Rooibos and Honeybush using a mouse model:elucidating possible protective mechanisms .” 2009. Thesis, Cape Peninsula University of Technology. Accessed January 15, 2021. http://etd.cput.ac.za/handle/20.500.11838/1487.

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

MLA Handbook (7th Edition):

Petrova, Antoinette. “Modulation of ultrviolet light induced skin carcinogenesis by extracts of Rooibos and Honeybush using a mouse model:elucidating possible protective mechanisms .” 2009. Web. 15 Jan 2021.

Vancouver:

Petrova A. Modulation of ultrviolet light induced skin carcinogenesis by extracts of Rooibos and Honeybush using a mouse model:elucidating possible protective mechanisms . [Internet] [Thesis]. Cape Peninsula University of Technology; 2009. [cited 2021 Jan 15]. Available from: http://etd.cput.ac.za/handle/20.500.11838/1487.

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

Council of Science Editors:

Petrova A. Modulation of ultrviolet light induced skin carcinogenesis by extracts of Rooibos and Honeybush using a mouse model:elucidating possible protective mechanisms . [Thesis]. Cape Peninsula University of Technology; 2009. Available from: http://etd.cput.ac.za/handle/20.500.11838/1487

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


University of Utah

3. Arch, Dorinda Deana. Altered liver parameters in a genetic mouse model of porphyria cutanea tarda and possible involvement of ABC transporters in the disease.

Degree: PhD, Pharmacology & Toxicology;, 2010, University of Utah

 The project sought to examine the changes in the liver associated with porphyria and whether ATP binding cassette (ABC) transporters in the hepatocyte might in… (more)

Subjects/Keywords: Liver parameters; Mouse model

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APA (6th Edition):

Arch, D. D. (2010). Altered liver parameters in a genetic mouse model of porphyria cutanea tarda and possible involvement of ABC transporters in the disease. (Doctoral Dissertation). University of Utah. Retrieved from http://content.lib.utah.edu/cdm/singleitem/collection/etd2/id/62/rec/68

Chicago Manual of Style (16th Edition):

Arch, Dorinda Deana. “Altered liver parameters in a genetic mouse model of porphyria cutanea tarda and possible involvement of ABC transporters in the disease.” 2010. Doctoral Dissertation, University of Utah. Accessed January 15, 2021. http://content.lib.utah.edu/cdm/singleitem/collection/etd2/id/62/rec/68.

MLA Handbook (7th Edition):

Arch, Dorinda Deana. “Altered liver parameters in a genetic mouse model of porphyria cutanea tarda and possible involvement of ABC transporters in the disease.” 2010. Web. 15 Jan 2021.

Vancouver:

Arch DD. Altered liver parameters in a genetic mouse model of porphyria cutanea tarda and possible involvement of ABC transporters in the disease. [Internet] [Doctoral dissertation]. University of Utah; 2010. [cited 2021 Jan 15]. Available from: http://content.lib.utah.edu/cdm/singleitem/collection/etd2/id/62/rec/68.

Council of Science Editors:

Arch DD. Altered liver parameters in a genetic mouse model of porphyria cutanea tarda and possible involvement of ABC transporters in the disease. [Doctoral Dissertation]. University of Utah; 2010. Available from: http://content.lib.utah.edu/cdm/singleitem/collection/etd2/id/62/rec/68


Cornell University

4. Ko, Frank. In Vivo Noninvasive Mouse Model Of Load Induced Osteoarthritis.

Degree: PhD, Mechanical Engineering, 2014, Cornell University

 Osteoarthritis (OA) is the leading cause of disability among the elderly population, affecting approximately 27 millions Americans and costing $60 billion in related-health care costs.… (more)

Subjects/Keywords: Osteoarthritis; Mouse model; Mechanical loading

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APA (6th Edition):

Ko, F. (2014). In Vivo Noninvasive Mouse Model Of Load Induced Osteoarthritis. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/37056

Chicago Manual of Style (16th Edition):

Ko, Frank. “In Vivo Noninvasive Mouse Model Of Load Induced Osteoarthritis.” 2014. Doctoral Dissertation, Cornell University. Accessed January 15, 2021. http://hdl.handle.net/1813/37056.

MLA Handbook (7th Edition):

Ko, Frank. “In Vivo Noninvasive Mouse Model Of Load Induced Osteoarthritis.” 2014. Web. 15 Jan 2021.

Vancouver:

Ko F. In Vivo Noninvasive Mouse Model Of Load Induced Osteoarthritis. [Internet] [Doctoral dissertation]. Cornell University; 2014. [cited 2021 Jan 15]. Available from: http://hdl.handle.net/1813/37056.

Council of Science Editors:

Ko F. In Vivo Noninvasive Mouse Model Of Load Induced Osteoarthritis. [Doctoral Dissertation]. Cornell University; 2014. Available from: http://hdl.handle.net/1813/37056


McMaster University

5. Lai, Jonathan. Neurodevelopmental Outcomes in the Fragile X Mouse.

Degree: PhD, 2015, McMaster University

Fragile X Syndrome (FXS) is a neurodevelopmental disorder and the most common heritable single gene cause of Autism Spectrum Disorder (ASD). The Fragile X (FMR1-KO)… (more)

Subjects/Keywords: brain development; genetic mouse model

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APA (6th Edition):

Lai, J. (2015). Neurodevelopmental Outcomes in the Fragile X Mouse. (Doctoral Dissertation). McMaster University. Retrieved from http://hdl.handle.net/11375/17209

Chicago Manual of Style (16th Edition):

Lai, Jonathan. “Neurodevelopmental Outcomes in the Fragile X Mouse.” 2015. Doctoral Dissertation, McMaster University. Accessed January 15, 2021. http://hdl.handle.net/11375/17209.

MLA Handbook (7th Edition):

Lai, Jonathan. “Neurodevelopmental Outcomes in the Fragile X Mouse.” 2015. Web. 15 Jan 2021.

Vancouver:

Lai J. Neurodevelopmental Outcomes in the Fragile X Mouse. [Internet] [Doctoral dissertation]. McMaster University; 2015. [cited 2021 Jan 15]. Available from: http://hdl.handle.net/11375/17209.

Council of Science Editors:

Lai J. Neurodevelopmental Outcomes in the Fragile X Mouse. [Doctoral Dissertation]. McMaster University; 2015. Available from: http://hdl.handle.net/11375/17209


Brigham Young University

6. Chronis, Rhonda Nicole. Comparison of Cytokine Expression and Bacterial Growth During Periparturient and Mid Lactation Mastitis in a Mouse Model.

Degree: MS, 2017, Brigham Young University

 Clinical cases of bovine mastitis are most severe in the early stages of lactation. The causes of this increased propensity for severe mastitis during early… (more)

Subjects/Keywords: mastitis; periparturient; mouse model; Microbiology

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APA (6th Edition):

Chronis, R. N. (2017). Comparison of Cytokine Expression and Bacterial Growth During Periparturient and Mid Lactation Mastitis in a Mouse Model. (Masters Thesis). Brigham Young University. Retrieved from https://scholarsarchive.byu.edu/cgi/viewcontent.cgi?article=7847&context=etd

Chicago Manual of Style (16th Edition):

Chronis, Rhonda Nicole. “Comparison of Cytokine Expression and Bacterial Growth During Periparturient and Mid Lactation Mastitis in a Mouse Model.” 2017. Masters Thesis, Brigham Young University. Accessed January 15, 2021. https://scholarsarchive.byu.edu/cgi/viewcontent.cgi?article=7847&context=etd.

MLA Handbook (7th Edition):

Chronis, Rhonda Nicole. “Comparison of Cytokine Expression and Bacterial Growth During Periparturient and Mid Lactation Mastitis in a Mouse Model.” 2017. Web. 15 Jan 2021.

Vancouver:

Chronis RN. Comparison of Cytokine Expression and Bacterial Growth During Periparturient and Mid Lactation Mastitis in a Mouse Model. [Internet] [Masters thesis]. Brigham Young University; 2017. [cited 2021 Jan 15]. Available from: https://scholarsarchive.byu.edu/cgi/viewcontent.cgi?article=7847&context=etd.

Council of Science Editors:

Chronis RN. Comparison of Cytokine Expression and Bacterial Growth During Periparturient and Mid Lactation Mastitis in a Mouse Model. [Masters Thesis]. Brigham Young University; 2017. Available from: https://scholarsarchive.byu.edu/cgi/viewcontent.cgi?article=7847&context=etd


University of Toronto

7. Minty, Gillian Eleanor Summersgill. The Role of TLR3 in the Development of Lupus-like Autoimmunity in B6.NZBc13 Mice.

Degree: 2013, University of Toronto

The New Zealand Black (NZB) mouse chromosome 13 (c13) is linked to development of autoimmunity. B6 mice containing a portion of NZBc13 (B6.NZBc13 (c13)) develop… (more)

Subjects/Keywords: Autoimmunity; mouse model; SLE; 0982

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APA (6th Edition):

Minty, G. E. S. (2013). The Role of TLR3 in the Development of Lupus-like Autoimmunity in B6.NZBc13 Mice. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/43245

Chicago Manual of Style (16th Edition):

Minty, Gillian Eleanor Summersgill. “The Role of TLR3 in the Development of Lupus-like Autoimmunity in B6.NZBc13 Mice.” 2013. Masters Thesis, University of Toronto. Accessed January 15, 2021. http://hdl.handle.net/1807/43245.

MLA Handbook (7th Edition):

Minty, Gillian Eleanor Summersgill. “The Role of TLR3 in the Development of Lupus-like Autoimmunity in B6.NZBc13 Mice.” 2013. Web. 15 Jan 2021.

Vancouver:

Minty GES. The Role of TLR3 in the Development of Lupus-like Autoimmunity in B6.NZBc13 Mice. [Internet] [Masters thesis]. University of Toronto; 2013. [cited 2021 Jan 15]. Available from: http://hdl.handle.net/1807/43245.

Council of Science Editors:

Minty GES. The Role of TLR3 in the Development of Lupus-like Autoimmunity in B6.NZBc13 Mice. [Masters Thesis]. University of Toronto; 2013. Available from: http://hdl.handle.net/1807/43245

8. Bogni, Caroline. Développement de thérapies géniques pour les myopathies congénitales : Development of gene thérapies for congenital myopathies.

Degree: Docteur es, Sciences de la vie et de la santé, 2019, Université Paris-Saclay (ComUE)

 Les myopathies congénitales sont des maladies génétiques rares touchant les muscles qui ne possèdent pour le moment pas de traitement curatif. Elles se manifestent par… (more)

Subjects/Keywords: Modèle murin; Mouse model

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APA (6th Edition):

Bogni, C. (2019). Développement de thérapies géniques pour les myopathies congénitales : Development of gene thérapies for congenital myopathies. (Doctoral Dissertation). Université Paris-Saclay (ComUE). Retrieved from http://www.theses.fr/2019SACLE038

Chicago Manual of Style (16th Edition):

Bogni, Caroline. “Développement de thérapies géniques pour les myopathies congénitales : Development of gene thérapies for congenital myopathies.” 2019. Doctoral Dissertation, Université Paris-Saclay (ComUE). Accessed January 15, 2021. http://www.theses.fr/2019SACLE038.

MLA Handbook (7th Edition):

Bogni, Caroline. “Développement de thérapies géniques pour les myopathies congénitales : Development of gene thérapies for congenital myopathies.” 2019. Web. 15 Jan 2021.

Vancouver:

Bogni C. Développement de thérapies géniques pour les myopathies congénitales : Development of gene thérapies for congenital myopathies. [Internet] [Doctoral dissertation]. Université Paris-Saclay (ComUE); 2019. [cited 2021 Jan 15]. Available from: http://www.theses.fr/2019SACLE038.

Council of Science Editors:

Bogni C. Développement de thérapies géniques pour les myopathies congénitales : Development of gene thérapies for congenital myopathies. [Doctoral Dissertation]. Université Paris-Saclay (ComUE); 2019. Available from: http://www.theses.fr/2019SACLE038


University of Sydney

9. Chan, Alex Ho Pang. Assessment of anti-inflammatory synthetic vascular grafts in a novel mouse model .

Degree: 2018, University of Sydney

 Cardiovascular disease is the largest cause of mortality in the world with coronary artery disease (CAD) accounting for half of these mortalities. One of the… (more)

Subjects/Keywords: Vascular grafting; mouse model; Cardiovascular

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APA (6th Edition):

Chan, A. H. P. (2018). Assessment of anti-inflammatory synthetic vascular grafts in a novel mouse model . (Thesis). University of Sydney. Retrieved from http://hdl.handle.net/2123/18947

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):

Chan, Alex Ho Pang. “Assessment of anti-inflammatory synthetic vascular grafts in a novel mouse model .” 2018. Thesis, University of Sydney. Accessed January 15, 2021. http://hdl.handle.net/2123/18947.

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

MLA Handbook (7th Edition):

Chan, Alex Ho Pang. “Assessment of anti-inflammatory synthetic vascular grafts in a novel mouse model .” 2018. Web. 15 Jan 2021.

Vancouver:

Chan AHP. Assessment of anti-inflammatory synthetic vascular grafts in a novel mouse model . [Internet] [Thesis]. University of Sydney; 2018. [cited 2021 Jan 15]. Available from: http://hdl.handle.net/2123/18947.

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

Council of Science Editors:

Chan AHP. Assessment of anti-inflammatory synthetic vascular grafts in a novel mouse model . [Thesis]. University of Sydney; 2018. Available from: http://hdl.handle.net/2123/18947

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


University of Louisville

10. Gleason, Robert C., 1988-. Sexual dimorphism in periodontitis in a mouse model.

Degree: MS, 2013, University of Louisville

 Background: Periodontal disease is an infection-driven chronic inflammatory disease. It occurs primarily from excessive inflammatory reactions that arise from complex exchanges between the host immune… (more)

Subjects/Keywords: Periodontal disease; PD in mouse model; Mouse model; Ligature mouse model; P. gingivalis in mice; Sexual dimorphism in PD

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APA (6th Edition):

Gleason, Robert C., 1. (2013). Sexual dimorphism in periodontitis in a mouse model. (Masters Thesis). University of Louisville. Retrieved from 10.18297/etd/504 ; https://ir.library.louisville.edu/etd/504

Chicago Manual of Style (16th Edition):

Gleason, Robert C., 1988-. “Sexual dimorphism in periodontitis in a mouse model.” 2013. Masters Thesis, University of Louisville. Accessed January 15, 2021. 10.18297/etd/504 ; https://ir.library.louisville.edu/etd/504.

MLA Handbook (7th Edition):

Gleason, Robert C., 1988-. “Sexual dimorphism in periodontitis in a mouse model.” 2013. Web. 15 Jan 2021.

Vancouver:

Gleason, Robert C. 1. Sexual dimorphism in periodontitis in a mouse model. [Internet] [Masters thesis]. University of Louisville; 2013. [cited 2021 Jan 15]. Available from: 10.18297/etd/504 ; https://ir.library.louisville.edu/etd/504.

Council of Science Editors:

Gleason, Robert C. 1. Sexual dimorphism in periodontitis in a mouse model. [Masters Thesis]. University of Louisville; 2013. Available from: 10.18297/etd/504 ; https://ir.library.louisville.edu/etd/504


University of Alberta

11. Hsi Dickie, Belinda. Advancing the Alb-uPA/SCID/Bg Chimeric Mouse.

Degree: PhD, Department of Surgery, 2009, University of Alberta

 The feasibility of the Alb-uPA/SCID/Bg chimeric mouse as a model for Hepatitis C Virus (HCV) infection was assessed experimentally by (1) the infection and treatment… (more)

Subjects/Keywords: Hepatitis C; Mouse Model; Transgenic mice; Alb-uPA/SCID/Beige mouse

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APA (6th Edition):

Hsi Dickie, B. (2009). Advancing the Alb-uPA/SCID/Bg Chimeric Mouse. (Doctoral Dissertation). University of Alberta. Retrieved from https://era.library.ualberta.ca/files/rr171x54d

Chicago Manual of Style (16th Edition):

Hsi Dickie, Belinda. “Advancing the Alb-uPA/SCID/Bg Chimeric Mouse.” 2009. Doctoral Dissertation, University of Alberta. Accessed January 15, 2021. https://era.library.ualberta.ca/files/rr171x54d.

MLA Handbook (7th Edition):

Hsi Dickie, Belinda. “Advancing the Alb-uPA/SCID/Bg Chimeric Mouse.” 2009. Web. 15 Jan 2021.

Vancouver:

Hsi Dickie B. Advancing the Alb-uPA/SCID/Bg Chimeric Mouse. [Internet] [Doctoral dissertation]. University of Alberta; 2009. [cited 2021 Jan 15]. Available from: https://era.library.ualberta.ca/files/rr171x54d.

Council of Science Editors:

Hsi Dickie B. Advancing the Alb-uPA/SCID/Bg Chimeric Mouse. [Doctoral Dissertation]. University of Alberta; 2009. Available from: https://era.library.ualberta.ca/files/rr171x54d


University of Edinburgh

12. Rao, Chandrika. Uncovering novel regulators of neural fate commitment in embryonic stem cells.

Degree: PhD, 2019, University of Edinburgh

 How do pluripotent stem cells reliably select the neural lineage during differentiation? When embryonic stem (ES) cells are exposed to a homogeneous signalling environment, differentiation… (more)

Subjects/Keywords: pluripotent cells; mouse model; E2A; mouse embryonic stem cells; neural differentiation

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APA (6th Edition):

Rao, C. (2019). Uncovering novel regulators of neural fate commitment in embryonic stem cells. (Doctoral Dissertation). University of Edinburgh. Retrieved from http://hdl.handle.net/1842/35977

Chicago Manual of Style (16th Edition):

Rao, Chandrika. “Uncovering novel regulators of neural fate commitment in embryonic stem cells.” 2019. Doctoral Dissertation, University of Edinburgh. Accessed January 15, 2021. http://hdl.handle.net/1842/35977.

MLA Handbook (7th Edition):

Rao, Chandrika. “Uncovering novel regulators of neural fate commitment in embryonic stem cells.” 2019. Web. 15 Jan 2021.

Vancouver:

Rao C. Uncovering novel regulators of neural fate commitment in embryonic stem cells. [Internet] [Doctoral dissertation]. University of Edinburgh; 2019. [cited 2021 Jan 15]. Available from: http://hdl.handle.net/1842/35977.

Council of Science Editors:

Rao C. Uncovering novel regulators of neural fate commitment in embryonic stem cells. [Doctoral Dissertation]. University of Edinburgh; 2019. Available from: http://hdl.handle.net/1842/35977


NSYSU

13. HSIN, HUNG. Genetically Engineered Mouse Model Recapitulating LKB1 and PTEN Loss In Gastric Cancer.

Degree: Master, Institute of Biomedical Sciences, 2016, NSYSU

 Gastric cancer (GC) is an aggressive disease with the highest rate of mortality among cancers and is the second leading cause of cancer death worldwide.… (more)

Subjects/Keywords: mouse model; PTEN; LKB1; Gastric cancer; adenocarcinoma

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APA (6th Edition):

HSIN, H. (2016). Genetically Engineered Mouse Model Recapitulating LKB1 and PTEN Loss In Gastric Cancer. (Thesis). NSYSU. Retrieved from http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0628116-104605

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):

HSIN, HUNG. “Genetically Engineered Mouse Model Recapitulating LKB1 and PTEN Loss In Gastric Cancer.” 2016. Thesis, NSYSU. Accessed January 15, 2021. http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0628116-104605.

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

MLA Handbook (7th Edition):

HSIN, HUNG. “Genetically Engineered Mouse Model Recapitulating LKB1 and PTEN Loss In Gastric Cancer.” 2016. Web. 15 Jan 2021.

Vancouver:

HSIN H. Genetically Engineered Mouse Model Recapitulating LKB1 and PTEN Loss In Gastric Cancer. [Internet] [Thesis]. NSYSU; 2016. [cited 2021 Jan 15]. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0628116-104605.

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

Council of Science Editors:

HSIN H. Genetically Engineered Mouse Model Recapitulating LKB1 and PTEN Loss In Gastric Cancer. [Thesis]. NSYSU; 2016. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0628116-104605

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


University of Rochester

14. Szymaniak, Brittany M. Loss of ATM Induces Glial Cell Dysfunction in a Novel Murine Model of Ataxia-telangiectasia.

Degree: PhD, 2016, University of Rochester

 Ataxia-telangiectasia (A-T) is a rare, recessive, pediatric disorder that is primarily characterized by cerebellar degeneration of Purkinje neurons and results from mutations in the Ataxia-telangiectasia… (more)

Subjects/Keywords: ATM; Mouse model; Ataxia-telangiectasia; Cuprizone

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APA (6th Edition):

Szymaniak, B. M. (2016). Loss of ATM Induces Glial Cell Dysfunction in a Novel Murine Model of Ataxia-telangiectasia. (Doctoral Dissertation). University of Rochester. Retrieved from http://hdl.handle.net/1802/31655

Chicago Manual of Style (16th Edition):

Szymaniak, Brittany M. “Loss of ATM Induces Glial Cell Dysfunction in a Novel Murine Model of Ataxia-telangiectasia.” 2016. Doctoral Dissertation, University of Rochester. Accessed January 15, 2021. http://hdl.handle.net/1802/31655.

MLA Handbook (7th Edition):

Szymaniak, Brittany M. “Loss of ATM Induces Glial Cell Dysfunction in a Novel Murine Model of Ataxia-telangiectasia.” 2016. Web. 15 Jan 2021.

Vancouver:

Szymaniak BM. Loss of ATM Induces Glial Cell Dysfunction in a Novel Murine Model of Ataxia-telangiectasia. [Internet] [Doctoral dissertation]. University of Rochester; 2016. [cited 2021 Jan 15]. Available from: http://hdl.handle.net/1802/31655.

Council of Science Editors:

Szymaniak BM. Loss of ATM Induces Glial Cell Dysfunction in a Novel Murine Model of Ataxia-telangiectasia. [Doctoral Dissertation]. University of Rochester; 2016. Available from: http://hdl.handle.net/1802/31655


California State University – Northridge

15. Qubrosi, Mirey. The use of the wire hang test and a novel genotyping method to further determine the M712T mouse model.

Degree: MS, Biology, 2013, California State University – Northridge

 Hereditary Inclusion Body Myopathy (HIBM) is a disorder caused by a mutation in the GNE gene. Although there are 60 known mutations, this research study… (more)

Subjects/Keywords: M712T mouse model; Dissertations, Academic  – CSUN  – Biology.

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APA (6th Edition):

Qubrosi, M. (2013). The use of the wire hang test and a novel genotyping method to further determine the M712T mouse model. (Masters Thesis). California State University – Northridge. Retrieved from http://hdl.handle.net/10211.2/3644

Chicago Manual of Style (16th Edition):

Qubrosi, Mirey. “The use of the wire hang test and a novel genotyping method to further determine the M712T mouse model.” 2013. Masters Thesis, California State University – Northridge. Accessed January 15, 2021. http://hdl.handle.net/10211.2/3644.

MLA Handbook (7th Edition):

Qubrosi, Mirey. “The use of the wire hang test and a novel genotyping method to further determine the M712T mouse model.” 2013. Web. 15 Jan 2021.

Vancouver:

Qubrosi M. The use of the wire hang test and a novel genotyping method to further determine the M712T mouse model. [Internet] [Masters thesis]. California State University – Northridge; 2013. [cited 2021 Jan 15]. Available from: http://hdl.handle.net/10211.2/3644.

Council of Science Editors:

Qubrosi M. The use of the wire hang test and a novel genotyping method to further determine the M712T mouse model. [Masters Thesis]. California State University – Northridge; 2013. Available from: http://hdl.handle.net/10211.2/3644


Vanderbilt University

16. Mergy, Marc Andrew. Generation and Characterization of the First Construct-Valid Model of ADHD, the DAT Val559 Knock-In Mouse.

Degree: PhD, Neuroscience, 2013, Vanderbilt University

 Attention-deficit/hyperactivity disorder (ADHD) is the most commonly diagnosed childhood neuropsychiatric disorder. More than twenty years of genetic, behavioral, and pharmacological research support the hypothesis that… (more)

Subjects/Keywords: transporter; dopamine; ADHD; transgenic; mouse; animal model

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APA (6th Edition):

Mergy, M. A. (2013). Generation and Characterization of the First Construct-Valid Model of ADHD, the DAT Val559 Knock-In Mouse. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://hdl.handle.net/1803/14625

Chicago Manual of Style (16th Edition):

Mergy, Marc Andrew. “Generation and Characterization of the First Construct-Valid Model of ADHD, the DAT Val559 Knock-In Mouse.” 2013. Doctoral Dissertation, Vanderbilt University. Accessed January 15, 2021. http://hdl.handle.net/1803/14625.

MLA Handbook (7th Edition):

Mergy, Marc Andrew. “Generation and Characterization of the First Construct-Valid Model of ADHD, the DAT Val559 Knock-In Mouse.” 2013. Web. 15 Jan 2021.

Vancouver:

Mergy MA. Generation and Characterization of the First Construct-Valid Model of ADHD, the DAT Val559 Knock-In Mouse. [Internet] [Doctoral dissertation]. Vanderbilt University; 2013. [cited 2021 Jan 15]. Available from: http://hdl.handle.net/1803/14625.

Council of Science Editors:

Mergy MA. Generation and Characterization of the First Construct-Valid Model of ADHD, the DAT Val559 Knock-In Mouse. [Doctoral Dissertation]. Vanderbilt University; 2013. Available from: http://hdl.handle.net/1803/14625

17. Simms, Elizabeth. Ara h 1 Peptide Immunotherapy in a Mouse Model of Peanut-Induced Anaphylaxis.

Degree: PhD, 2018, McMaster University

Background: Despite the clinical severity and rising prevalence of peanut allergy, there is a marked absence of widespread, practical treatments available for peanut-allergic patients. Peptide… (more)

Subjects/Keywords: Anaphylaxis; Peanut allergy; Peptide immunotherapy; Mouse model

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APA (6th Edition):

Simms, E. (2018). Ara h 1 Peptide Immunotherapy in a Mouse Model of Peanut-Induced Anaphylaxis. (Doctoral Dissertation). McMaster University. Retrieved from http://hdl.handle.net/11375/23044

Chicago Manual of Style (16th Edition):

Simms, Elizabeth. “Ara h 1 Peptide Immunotherapy in a Mouse Model of Peanut-Induced Anaphylaxis.” 2018. Doctoral Dissertation, McMaster University. Accessed January 15, 2021. http://hdl.handle.net/11375/23044.

MLA Handbook (7th Edition):

Simms, Elizabeth. “Ara h 1 Peptide Immunotherapy in a Mouse Model of Peanut-Induced Anaphylaxis.” 2018. Web. 15 Jan 2021.

Vancouver:

Simms E. Ara h 1 Peptide Immunotherapy in a Mouse Model of Peanut-Induced Anaphylaxis. [Internet] [Doctoral dissertation]. McMaster University; 2018. [cited 2021 Jan 15]. Available from: http://hdl.handle.net/11375/23044.

Council of Science Editors:

Simms E. Ara h 1 Peptide Immunotherapy in a Mouse Model of Peanut-Induced Anaphylaxis. [Doctoral Dissertation]. McMaster University; 2018. Available from: http://hdl.handle.net/11375/23044


University of Adelaide

18. Dawson, Ruby Emily. Investigation of the GATOR1 complex genes in focal cortical dysplasia and focal epilepsy.

Degree: 2019, University of Adelaide

 Epilepsy is a complex disease characterised by seizures due to abnormal neuronal activity. Both hereditable and non-hereditable epilepsy forms of epilepsy exist, and understanding their… (more)

Subjects/Keywords: epilepsy; mTOR; neurobiology; neurodevelopment; mouse model

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APA (6th Edition):

Dawson, R. E. (2019). Investigation of the GATOR1 complex genes in focal cortical dysplasia and focal epilepsy. (Thesis). University of Adelaide. Retrieved from http://hdl.handle.net/2440/121340

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):

Dawson, Ruby Emily. “Investigation of the GATOR1 complex genes in focal cortical dysplasia and focal epilepsy.” 2019. Thesis, University of Adelaide. Accessed January 15, 2021. http://hdl.handle.net/2440/121340.

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

MLA Handbook (7th Edition):

Dawson, Ruby Emily. “Investigation of the GATOR1 complex genes in focal cortical dysplasia and focal epilepsy.” 2019. Web. 15 Jan 2021.

Vancouver:

Dawson RE. Investigation of the GATOR1 complex genes in focal cortical dysplasia and focal epilepsy. [Internet] [Thesis]. University of Adelaide; 2019. [cited 2021 Jan 15]. Available from: http://hdl.handle.net/2440/121340.

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

Council of Science Editors:

Dawson RE. Investigation of the GATOR1 complex genes in focal cortical dysplasia and focal epilepsy. [Thesis]. University of Adelaide; 2019. Available from: http://hdl.handle.net/2440/121340

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


University of Toronto

19. Nelson, Seana ML. Generating C-peptide Humanized Mice.

Degree: 2012, University of Toronto

Type 1 diabetes is primarily caused by the loss of insulin producing beta-cells. Future therapies based on transplantation of in vitro generated beta-cells hold great… (more)

Subjects/Keywords: Mouse model; Gene targeting; 0369; 0307

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APA (6th Edition):

Nelson, S. M. (2012). Generating C-peptide Humanized Mice. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/69989

Chicago Manual of Style (16th Edition):

Nelson, Seana ML. “Generating C-peptide Humanized Mice.” 2012. Masters Thesis, University of Toronto. Accessed January 15, 2021. http://hdl.handle.net/1807/69989.

MLA Handbook (7th Edition):

Nelson, Seana ML. “Generating C-peptide Humanized Mice.” 2012. Web. 15 Jan 2021.

Vancouver:

Nelson SM. Generating C-peptide Humanized Mice. [Internet] [Masters thesis]. University of Toronto; 2012. [cited 2021 Jan 15]. Available from: http://hdl.handle.net/1807/69989.

Council of Science Editors:

Nelson SM. Generating C-peptide Humanized Mice. [Masters Thesis]. University of Toronto; 2012. Available from: http://hdl.handle.net/1807/69989


University of Manitoba

20. Abyat, Zahra. Method optimization for Fourier transform infrared imaging of hippocampal sections from background and 3xTg (AD model) mice.

Degree: Biomedical Engineering, 2019, University of Manitoba

 The creatine/phosphocreatine system, regulated by Creatine kinase, plays a vital role in maintaining energy balance in the brain. Energy metabolism and the function of creatine… (more)

Subjects/Keywords: FTIR; 3XTg mouse model; creatine dietary enrichment

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APA (6th Edition):

Abyat, Z. (2019). Method optimization for Fourier transform infrared imaging of hippocampal sections from background and 3xTg (AD model) mice. (Masters Thesis). University of Manitoba. Retrieved from http://hdl.handle.net/1993/34395

Chicago Manual of Style (16th Edition):

Abyat, Zahra. “Method optimization for Fourier transform infrared imaging of hippocampal sections from background and 3xTg (AD model) mice.” 2019. Masters Thesis, University of Manitoba. Accessed January 15, 2021. http://hdl.handle.net/1993/34395.

MLA Handbook (7th Edition):

Abyat, Zahra. “Method optimization for Fourier transform infrared imaging of hippocampal sections from background and 3xTg (AD model) mice.” 2019. Web. 15 Jan 2021.

Vancouver:

Abyat Z. Method optimization for Fourier transform infrared imaging of hippocampal sections from background and 3xTg (AD model) mice. [Internet] [Masters thesis]. University of Manitoba; 2019. [cited 2021 Jan 15]. Available from: http://hdl.handle.net/1993/34395.

Council of Science Editors:

Abyat Z. Method optimization for Fourier transform infrared imaging of hippocampal sections from background and 3xTg (AD model) mice. [Masters Thesis]. University of Manitoba; 2019. Available from: http://hdl.handle.net/1993/34395

21. Li, Kailiang. Loss of basigin expression in the uterus reduces fertility in female mice.

Degree: PhD, Animal Sciences, 2020, University of Illinois – Urbana-Champaign

 Basigin (BSG), a member of the immunoglobulin superfamily, is a transmembrane glycoprotein expressed in many cell types. It is involved in neurological processes, lymphocyte migration,… (more)

Subjects/Keywords: basigin; implantation; decidualizaiton; infertility; mouse model

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APA (6th Edition):

Li, K. (2020). Loss of basigin expression in the uterus reduces fertility in female mice. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/107985

Chicago Manual of Style (16th Edition):

Li, Kailiang. “Loss of basigin expression in the uterus reduces fertility in female mice.” 2020. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed January 15, 2021. http://hdl.handle.net/2142/107985.

MLA Handbook (7th Edition):

Li, Kailiang. “Loss of basigin expression in the uterus reduces fertility in female mice.” 2020. Web. 15 Jan 2021.

Vancouver:

Li K. Loss of basigin expression in the uterus reduces fertility in female mice. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2020. [cited 2021 Jan 15]. Available from: http://hdl.handle.net/2142/107985.

Council of Science Editors:

Li K. Loss of basigin expression in the uterus reduces fertility in female mice. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2020. Available from: http://hdl.handle.net/2142/107985


Princeton University

22. Kloth, Alexander D. Probing cerebellar function and its role in autism spectrum disorders .

Degree: PhD, 2014, Princeton University

 Over the past few decades, a view has emerged in which the cerebellum learns and adapts well-timed response to unexpected events. While the cerebellum is… (more)

Subjects/Keywords: autism; cerebellum; eyeblink conditioning; mouse model

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APA (6th Edition):

Kloth, A. D. (2014). Probing cerebellar function and its role in autism spectrum disorders . (Doctoral Dissertation). Princeton University. Retrieved from http://arks.princeton.edu/ark:/88435/dsp01k643b3409

Chicago Manual of Style (16th Edition):

Kloth, Alexander D. “Probing cerebellar function and its role in autism spectrum disorders .” 2014. Doctoral Dissertation, Princeton University. Accessed January 15, 2021. http://arks.princeton.edu/ark:/88435/dsp01k643b3409.

MLA Handbook (7th Edition):

Kloth, Alexander D. “Probing cerebellar function and its role in autism spectrum disorders .” 2014. Web. 15 Jan 2021.

Vancouver:

Kloth AD. Probing cerebellar function and its role in autism spectrum disorders . [Internet] [Doctoral dissertation]. Princeton University; 2014. [cited 2021 Jan 15]. Available from: http://arks.princeton.edu/ark:/88435/dsp01k643b3409.

Council of Science Editors:

Kloth AD. Probing cerebellar function and its role in autism spectrum disorders . [Doctoral Dissertation]. Princeton University; 2014. Available from: http://arks.princeton.edu/ark:/88435/dsp01k643b3409


Colorado State University

23. Layer, Emily L. Understanding Mycobacterium abscessus pulmonary and disseminated disease.

Degree: MS(M.S.), Microbiology, Immunology, and Pathology, 2017, Colorado State University

 Mycobacterium abscessus is an emerging human pathogen which is difficult to treat and results in increased mortality. Moreover, the cause of increasing case rates and… (more)

Subjects/Keywords: animal; mouse; nontuberculous; model; abscessus; mycobacteria

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APA (6th Edition):

Layer, E. L. (2017). Understanding Mycobacterium abscessus pulmonary and disseminated disease. (Masters Thesis). Colorado State University. Retrieved from http://hdl.handle.net/10217/183863

Chicago Manual of Style (16th Edition):

Layer, Emily L. “Understanding Mycobacterium abscessus pulmonary and disseminated disease.” 2017. Masters Thesis, Colorado State University. Accessed January 15, 2021. http://hdl.handle.net/10217/183863.

MLA Handbook (7th Edition):

Layer, Emily L. “Understanding Mycobacterium abscessus pulmonary and disseminated disease.” 2017. Web. 15 Jan 2021.

Vancouver:

Layer EL. Understanding Mycobacterium abscessus pulmonary and disseminated disease. [Internet] [Masters thesis]. Colorado State University; 2017. [cited 2021 Jan 15]. Available from: http://hdl.handle.net/10217/183863.

Council of Science Editors:

Layer EL. Understanding Mycobacterium abscessus pulmonary and disseminated disease. [Masters Thesis]. Colorado State University; 2017. Available from: http://hdl.handle.net/10217/183863


University of Toronto

24. Chung, Eu Ddeum. Generation of a New Model for RB1-deficient Pineoblastoma and Lysosome-based Therapy.

Degree: PhD, 2019, University of Toronto

 Pineoblastoma is a WHO IV tumour of the pineal gland affecting primarily children. Five-year overall survival (OS) is 54%, and this level significantly drops to… (more)

Subjects/Keywords: Mouse model; p53; Pineoblastoma; Rb; 0307

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APA (6th Edition):

Chung, E. D. (2019). Generation of a New Model for RB1-deficient Pineoblastoma and Lysosome-based Therapy. (Doctoral Dissertation). University of Toronto. Retrieved from http://hdl.handle.net/1807/97349

Chicago Manual of Style (16th Edition):

Chung, Eu Ddeum. “Generation of a New Model for RB1-deficient Pineoblastoma and Lysosome-based Therapy.” 2019. Doctoral Dissertation, University of Toronto. Accessed January 15, 2021. http://hdl.handle.net/1807/97349.

MLA Handbook (7th Edition):

Chung, Eu Ddeum. “Generation of a New Model for RB1-deficient Pineoblastoma and Lysosome-based Therapy.” 2019. Web. 15 Jan 2021.

Vancouver:

Chung ED. Generation of a New Model for RB1-deficient Pineoblastoma and Lysosome-based Therapy. [Internet] [Doctoral dissertation]. University of Toronto; 2019. [cited 2021 Jan 15]. Available from: http://hdl.handle.net/1807/97349.

Council of Science Editors:

Chung ED. Generation of a New Model for RB1-deficient Pineoblastoma and Lysosome-based Therapy. [Doctoral Dissertation]. University of Toronto; 2019. Available from: http://hdl.handle.net/1807/97349


University of Toronto

25. Wang, Sharon. Cooperating Oncogenic Alterations in Aggressive Pten-Deficient Breast Cancer.

Degree: PhD, 2017, University of Toronto

PTEN is one of the most frequently inactivated tumor suppressors in human malignancies including breast cancer, and its mutation or loss is often implicated in… (more)

Subjects/Keywords: Breast; Mouse model; p53; PTEN; 0992

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APA (6th Edition):

Wang, S. (2017). Cooperating Oncogenic Alterations in Aggressive Pten-Deficient Breast Cancer. (Doctoral Dissertation). University of Toronto. Retrieved from http://hdl.handle.net/1807/91193

Chicago Manual of Style (16th Edition):

Wang, Sharon. “Cooperating Oncogenic Alterations in Aggressive Pten-Deficient Breast Cancer.” 2017. Doctoral Dissertation, University of Toronto. Accessed January 15, 2021. http://hdl.handle.net/1807/91193.

MLA Handbook (7th Edition):

Wang, Sharon. “Cooperating Oncogenic Alterations in Aggressive Pten-Deficient Breast Cancer.” 2017. Web. 15 Jan 2021.

Vancouver:

Wang S. Cooperating Oncogenic Alterations in Aggressive Pten-Deficient Breast Cancer. [Internet] [Doctoral dissertation]. University of Toronto; 2017. [cited 2021 Jan 15]. Available from: http://hdl.handle.net/1807/91193.

Council of Science Editors:

Wang S. Cooperating Oncogenic Alterations in Aggressive Pten-Deficient Breast Cancer. [Doctoral Dissertation]. University of Toronto; 2017. Available from: http://hdl.handle.net/1807/91193


University of Newcastle

26. Aryal, Ritambhara. The relationship of iron and amyloid: insights from a new mouse model of iron loading and amyloidosis.

Degree: PhD, 2020, University of Newcastle

Research Doctorate - Doctor of Philosophy (PhD)

Alzheimer’s disease (AD) is a neurodegenerative disease which has been proposed to be associated with brain iron abnormalities,… (more)

Subjects/Keywords: brain; iron; amyloid; Alzheimer's disease; mouse model

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APA (6th Edition):

Aryal, R. (2020). The relationship of iron and amyloid: insights from a new mouse model of iron loading and amyloidosis. (Doctoral Dissertation). University of Newcastle. Retrieved from http://hdl.handle.net/1959.13/1411211

Chicago Manual of Style (16th Edition):

Aryal, Ritambhara. “The relationship of iron and amyloid: insights from a new mouse model of iron loading and amyloidosis.” 2020. Doctoral Dissertation, University of Newcastle. Accessed January 15, 2021. http://hdl.handle.net/1959.13/1411211.

MLA Handbook (7th Edition):

Aryal, Ritambhara. “The relationship of iron and amyloid: insights from a new mouse model of iron loading and amyloidosis.” 2020. Web. 15 Jan 2021.

Vancouver:

Aryal R. The relationship of iron and amyloid: insights from a new mouse model of iron loading and amyloidosis. [Internet] [Doctoral dissertation]. University of Newcastle; 2020. [cited 2021 Jan 15]. Available from: http://hdl.handle.net/1959.13/1411211.

Council of Science Editors:

Aryal R. The relationship of iron and amyloid: insights from a new mouse model of iron loading and amyloidosis. [Doctoral Dissertation]. University of Newcastle; 2020. Available from: http://hdl.handle.net/1959.13/1411211


University of Edinburgh

27. Tillotson, Anne Rebekah. Identifying the key functions of MeCP2 via genetic manipulation in mice.

Degree: PhD, 2017, University of Edinburgh

 MeCP2 was identified by its ability to bind DNA in a methylation-specific manner. Yet, how it interprets the DNA methylome remains unclear. Several mechanisms have… (more)

Subjects/Keywords: MeCP2; epigenetic; mouse model; gene expression

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APA (6th Edition):

Tillotson, A. R. (2017). Identifying the key functions of MeCP2 via genetic manipulation in mice. (Doctoral Dissertation). University of Edinburgh. Retrieved from http://hdl.handle.net/1842/28917

Chicago Manual of Style (16th Edition):

Tillotson, Anne Rebekah. “Identifying the key functions of MeCP2 via genetic manipulation in mice.” 2017. Doctoral Dissertation, University of Edinburgh. Accessed January 15, 2021. http://hdl.handle.net/1842/28917.

MLA Handbook (7th Edition):

Tillotson, Anne Rebekah. “Identifying the key functions of MeCP2 via genetic manipulation in mice.” 2017. Web. 15 Jan 2021.

Vancouver:

Tillotson AR. Identifying the key functions of MeCP2 via genetic manipulation in mice. [Internet] [Doctoral dissertation]. University of Edinburgh; 2017. [cited 2021 Jan 15]. Available from: http://hdl.handle.net/1842/28917.

Council of Science Editors:

Tillotson AR. Identifying the key functions of MeCP2 via genetic manipulation in mice. [Doctoral Dissertation]. University of Edinburgh; 2017. Available from: http://hdl.handle.net/1842/28917


University of Edinburgh

28. McBride, Andrew Niall. Development of a novel mouse model for the colorectal cancer risk locus at Xp22.2.

Degree: PhD, 2016, University of Edinburgh

 Colorectal cancer (CRC) is the third most common cancer globally with around 1.3 million cases diagnosed annually. In cases of inherited CRC where none of… (more)

Subjects/Keywords: 616.99; colorectal cancer; mouse model; Shroom2; GPR143

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APA (6th Edition):

McBride, A. N. (2016). Development of a novel mouse model for the colorectal cancer risk locus at Xp22.2. (Doctoral Dissertation). University of Edinburgh. Retrieved from http://hdl.handle.net/1842/25714

Chicago Manual of Style (16th Edition):

McBride, Andrew Niall. “Development of a novel mouse model for the colorectal cancer risk locus at Xp22.2.” 2016. Doctoral Dissertation, University of Edinburgh. Accessed January 15, 2021. http://hdl.handle.net/1842/25714.

MLA Handbook (7th Edition):

McBride, Andrew Niall. “Development of a novel mouse model for the colorectal cancer risk locus at Xp22.2.” 2016. Web. 15 Jan 2021.

Vancouver:

McBride AN. Development of a novel mouse model for the colorectal cancer risk locus at Xp22.2. [Internet] [Doctoral dissertation]. University of Edinburgh; 2016. [cited 2021 Jan 15]. Available from: http://hdl.handle.net/1842/25714.

Council of Science Editors:

McBride AN. Development of a novel mouse model for the colorectal cancer risk locus at Xp22.2. [Doctoral Dissertation]. University of Edinburgh; 2016. Available from: http://hdl.handle.net/1842/25714


Universitat de Valencia

29. Calvo Hoyas, Paula. Establecimiento y optimización de modelo murino de la patología ginecológica endometriosis utilizando xenografts de endometrio humano para el estudio del potencial papel terapéutico del RNA de doble cadena (pIC-PEI) .

Degree: 2018, Universitat de Valencia

 La endometriosis es una enfermedad con elevada prevalencia en la población de mujeres en edad fértil (Goldstein y cols, 1980; Eskenazi y cols, 1997; Gazvani… (more)

Subjects/Keywords: endometriosis; angiogenesis; apoptosis; mouse model; pICPEI

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APA (6th Edition):

Calvo Hoyas, P. (2018). Establecimiento y optimización de modelo murino de la patología ginecológica endometriosis utilizando xenografts de endometrio humano para el estudio del potencial papel terapéutico del RNA de doble cadena (pIC-PEI) . (Doctoral Dissertation). Universitat de Valencia. Retrieved from http://hdl.handle.net/10550/66945

Chicago Manual of Style (16th Edition):

Calvo Hoyas, Paula. “Establecimiento y optimización de modelo murino de la patología ginecológica endometriosis utilizando xenografts de endometrio humano para el estudio del potencial papel terapéutico del RNA de doble cadena (pIC-PEI) .” 2018. Doctoral Dissertation, Universitat de Valencia. Accessed January 15, 2021. http://hdl.handle.net/10550/66945.

MLA Handbook (7th Edition):

Calvo Hoyas, Paula. “Establecimiento y optimización de modelo murino de la patología ginecológica endometriosis utilizando xenografts de endometrio humano para el estudio del potencial papel terapéutico del RNA de doble cadena (pIC-PEI) .” 2018. Web. 15 Jan 2021.

Vancouver:

Calvo Hoyas P. Establecimiento y optimización de modelo murino de la patología ginecológica endometriosis utilizando xenografts de endometrio humano para el estudio del potencial papel terapéutico del RNA de doble cadena (pIC-PEI) . [Internet] [Doctoral dissertation]. Universitat de Valencia; 2018. [cited 2021 Jan 15]. Available from: http://hdl.handle.net/10550/66945.

Council of Science Editors:

Calvo Hoyas P. Establecimiento y optimización de modelo murino de la patología ginecológica endometriosis utilizando xenografts de endometrio humano para el estudio del potencial papel terapéutico del RNA de doble cadena (pIC-PEI) . [Doctoral Dissertation]. Universitat de Valencia; 2018. Available from: http://hdl.handle.net/10550/66945


Kansas State University

30. Lang, Yuekun. Identification and evaluation of antivirals for Rift Valley fever virus.

Degree: PhD, Department of Diagnostic Medicine/Pathobiology, 2017, Kansas State University

 Rift Valley fever virus (RVFV) is an enveloped, negative-sense, ssRNA virus with a tripartite genome that causes morbidity and mortality in both livestock and humans.… (more)

Subjects/Keywords: Rift Valley fever virus; Antiviral; Mouse model

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APA (6th Edition):

Lang, Y. (2017). Identification and evaluation of antivirals for Rift Valley fever virus. (Doctoral Dissertation). Kansas State University. Retrieved from http://hdl.handle.net/2097/38195

Chicago Manual of Style (16th Edition):

Lang, Yuekun. “Identification and evaluation of antivirals for Rift Valley fever virus.” 2017. Doctoral Dissertation, Kansas State University. Accessed January 15, 2021. http://hdl.handle.net/2097/38195.

MLA Handbook (7th Edition):

Lang, Yuekun. “Identification and evaluation of antivirals for Rift Valley fever virus.” 2017. Web. 15 Jan 2021.

Vancouver:

Lang Y. Identification and evaluation of antivirals for Rift Valley fever virus. [Internet] [Doctoral dissertation]. Kansas State University; 2017. [cited 2021 Jan 15]. Available from: http://hdl.handle.net/2097/38195.

Council of Science Editors:

Lang Y. Identification and evaluation of antivirals for Rift Valley fever virus. [Doctoral Dissertation]. Kansas State University; 2017. Available from: http://hdl.handle.net/2097/38195

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